COMPOSITES TECHNOLOGIES FOR 2020
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COMPOSITES TECHNOLOGIES FOR 2020
ACCM-4
Proceedings of the Fourth Asian-Australasian Conference on Composite Materials (ACCM-4) University of Sydney, Australia 6 - 9 July 2004
Edited by L. Ye, Y.-W. Mai and Z. Su
Organised by The Asian-Australasian Association for Composite Materials (AACM) The University of Sydney
x e
The University of Sydney
WOODHEAD PUBLISHING LIMITED Cambridge England
Published by Woodhead Publishing Limited, Abington Hall, Abington Cambridge CB1 6AH, England www.woodhead-publishing.com First published 2004, Woodhead Publishing Limited © 2004, Woodhead Publishing Limited The authors have asserted their moral rights. This book contains information obtained from authentic and highly regarded sources. Reprinted material is quoted with permission, and sources are indicated. Reasonable efforts have been made to publish reliable data and information, but the authors and the publisher cannot assume responsibility for the validity of all materials. The publisher makes no representation, express or implied, with regard to the accuracy of the information contained in this book and cannot accept any legal responsibility or liability for any errors or omissions. Neither the authors nor the publisher, nor anyone else associated with this publication, shall be liable for any loss, damage or liability directly or indirectly caused or alleged to be caused by this book. Neither this book nor any part may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, microfilming and recording, or by any information storage or retrieval system, without permission in writing from the publisher. The consent of Woodhead Publishing Limited does not extend to copying for general distribution, for promotion, for creating new works, or for resale. Specific permission must be obtained in writing from Woodhead Publishing Limited for such copying. Trademark notice: Product or corporate names may be trademarks or registered trademarks, and are used only for identification and explanation, without intent to infringe. British Library Cataloguing in Publication Data A catalogue record for this book is available from the British Library.
ISBN 1 85573 831 7 Printed by Antony Rowe Limited, Chippenham, Wilts, England
Contents Preface Conference Organisation ACCM-4 Sponsors
xix xxi xxiv
Part I: Bio/Eco-Composites All-plant Fiber Composites Zhang, M. Q., Rong, M. Z, Lu, X.
3
Compression Molding and Mechanical Properties of Composite Materials from Post Consumer Type Fiber Waste Hatta, S., Kimura, T., Gonno, H., Kadokura, K.
9
Various Lignocellulosics Fibre Reinforced Polyester Composites: The Study on Mechanical, Physical and Biological Properties Abdul Khalil, H. P. S., Issam, A.M.
15
Development of Eco-Cement Containing High Volumes of Waste Glass Sobolev, K., Iscioglu, G, Tiirker, P., Yeginobali, A., Ertiin, T.
21
Screwless Extrusion of Natural Fibre-Reinforced Thermoplastic Composites Galea, T., Mills, T., Halliwell, R., Jayaraman, K.
27
Mechanical Properties of "Green" Composites Made from Starch-Based Biodegradable Resin and Bamboo Powder Takagi, H., Takura, R., Ochi, S.
33
Part II: Characterisation Effect of Fibre-Orientation on Mechanical Properties of Polypropylene Composites Houshyar, S., Shanks, R. A., Hodzic, A.
41
Friction and Wear Properties of Potassium Titanate Whiskers Reinforced PTFE Composites Feng, X., Chen, D. H., Jiang, X. H., Sun, S, Lu, .X, Jin, Y.
46
Study on Jute Fiber Reinforced Polypropylene (PP) Composite Ma, S., Zhang, A. D., Ding, X., Wang, Y. M. Mechanical and Thermal Properties of Composites of Epoxy Resin Derived from Kraft Lignin Filled with Cellulose Particles Funabashi, M., Hirose, S., Hatakeyama, H.
52
57
vi
Contents
Effects of Microcracks and Surface Roughness on Thermal Oxidation of CarbonFiber Reinforced Polyimide Composite Kung,H.-K., Chen,H.-S.
62
Effects of Fillers on the Tensile Properties of Polyimide Composite Films at Room and Cryogenic Temperatures Zhang, Y. H., Fu, S. Y, Li, M., Li, Y., Li, L. F., Yan, Q.
68
Processing Effects on Electrical Conductivity and Mechanical Properties of Particulate Composite Mohafezatkar, F., Haddadi-asl, V., Nazokdast, H.
72
Study on the Hydrolysis-resistant Polyethylene Terephthalate (PET) Fibers Wang, Y. P., Wang, Y. M. Size Effect on the Compressive Strength of T300/924C Carbon Fiber-Epoxy Laminates in Considering Influence of an Anti-buckling Device Lee, J. W., Kong, C. D., Soutis, C. Environment Effect of Natural Sisal Fibre Reinforced Epoxy Composites Manufactured by Resin Transfer Molding Zhang, X. P., Yuan, Q., Ngatimin, W., Whitbourn, J., Ye, L. Effective Thermomechanical Properties of Interpenetrating-Structured Composites Tilbrook, M., Moon, R., Rutgers, L., Hoffman, M.
78
83
88
94
Mechanical and Thermal Properties of Phenolic Composites Reinforced with Hybrid of Spun and Continuous Carbon Fabrics Kang, T. J, Shin, S. J., Jung, K, Cho, Y. J.
100
Specific Properties vs. Microstructures for Syntactic Foam Wouterson, K, Boey, F., Hu, X., Wong, S.-C.
106
Functionally-Graded Structure and Properties in Human Teeth Low, I. M., Mahmood, U.
112
Experimental Investigation of Porosity in Carbon/Epoxy Composite Laminates Zhang, B.M., Liu, L, Wu, Z. J., Wang, D. F. Characterisation of a Reinforced PPS Thermoplastic Laminate For Forming Simulations Chen, Z. P., Phung, T., Paton, R., de Bruijn, P.
118 124
Characterisation of the Thermo-mechanical Behaviour of a Glass Reinforced Vinyl Ester Composite St John, N. A., Gardiner, C. P., Dunlop, LA. 131 Experimental Study on the Flexural Behavior Using Polyethylene Coated Bars Kim, Y. J.
137
Contents Moisture Absorption by Cyanate Ester Modified Epoxy Resin Matrices: Effect of Resin Structure Karad, S., Jones, F. New Epoxy Resins Based On Azomethine Groups For Potential Polymer Applications Issam, A. M., Abdul Khalil, H. P. S., Wan Rosli, W. D.
vii
143
149
Mechanical Properties of Rotational Moulded Polyethylene Composites Experiments and Theories Yan, W., Lin, R. J. T., Bhattacharyya, D.
154
Morphology and Mechanical Properties of HDPE Reinforced with PET Microfibres Seltzer, R., Fasce, L., Frontini, P., Rodriguez Pita, V. J., Pacheco, E. B. A. V., Dias, M. L.
163
Mechanistic Evaluation of Environments on Degradation of E-Glass/Vinylester Composites Karbhari, V. M., Chu, W., Wu, L. X.
169
High Value Composites from Recycled Polyolefins and Rubbers Fainleib, A., Grigoryeva, O., Tolstov, A., Starostenko, O.
175
Viscoelastic Behaviour, Thermal Properties and Morphology for New Composites from Recycled HDPE, EPDM, Ground Tyre Rubber (GTR) and Bitumen Grigoryeva, O., Tolstov, A., Starostenko, O., Fainleib, A., Lievana, E., Karger-Kocsis, J.
181
Effect of Coupled Long-Term Seawater Exposure and Bi-Axial Creep Loading (2:1) on Durability of Fiber-Reinforced Polymer-Matrix Composites Chen, X. H., Gokdag, E., Wang, S. S. 187
Part III: Composite Structures Deformation Analysis of Kinematically Constrained Thermoplastic Composite Plates in Forming Temperature Daghyani, H. R., Abadi, M. T., Fariborz, S.
195
Stability Analysis of Loaded Columns Made of Pultruded Composites Mahajerin, E.
201
Identification of Elastic Parameters for Cross-ply Laminated Plates and Shells Hosokawa, K., Matsumoto, K.
207
Parametric Instability Analysis and Experiment of Laminated Composite Shell Yeh,M.-K., Huang, H.-C.
212
viii
Contents
Bending Properties of Braided Composite Tubes Okano, M., Sugimoto, K, Nakai, A., Hamada, H.
218
Analytical Stress Analysis of Rotating Composite Beams Due to Material Discontinuities Tahani, M., Nosier, A., Rezaeepazhand, J., Zebarjad, S. M.
223
Thin-plate Splines for Thick Composite Plate Analysis Ferreira, A. J. M.
229
Part IV: Delamination Evaluation of Fatigue Delamination Behavior in Hybrid Composite Material using the Delamination Shape Parameters Song, S.-K, Kim, C.-W., Oh, D.-J. The Effect of Stitch Distribution and Stitch Pattern on Mode I Delamination Toughness of Stitched Laminated Composites Wood, M. D. K, Sun, X. N., Tong, L. Y., Katzos, A., Rispler, A. Dynamic Analysis for Delaminated Composites with Arbitrary Shaped Multiple Delaminations Based on Higher-Order Zig-Zag Theory Cho, M., Oh, J., Kim, J.S., Kim, G.-I.
237 243
249
Part V: Design and Optimisation Application of Stochastic Optimization to Reconstruction of Random Microstructures Pyrz, R-, Bochenek, B. 257 Optimal Design of Filament Wound Structures Based on the Semi-geodesic Path Algorithm Kim, C.-U., Kang, D.-H., Hong, C.S., Kim, C.-G.
264
Development of a Material Mixing Method for Topology Optimization of Multiple Material Structures Han, S. Y., Lee, S. K, Park, J. Y. 270 Structural Design of a 750kW Composite Wind Turbine Blade Jung, C. K, Park, S. K, Han, K. S.
276
Axiomatic Design of Composite Track Pin Park, D. C, Kim, S. S., Lee, S. M., Lee, D. G.
282
Characterization and Design Optimization of FRP Composite Modular System for Slab-on-Girder Bridges Cheng, L. J., Karbhari, V. M.
288
Contents
ix
Design of Composite-Antenna-Structures with High Electrical and Mechanical Performances You, C.S., Hwang, W.
294
Filament Wound Spherical Composite Pressure Vessel Design by an Energy Method KimB.-S., Joe, C.-R.
299
Part VI; Failure Analysis Numerical Study on Buckling of Z-pinned Composite Laminates Yan, W. Y., Liu, H.-Y., Mai, Y.-W.
307
A Three Dimensional Approach of Fatigue Crack Propagation for Aluminum Panels Repaired with Single-Sided Composite Laminates Hosseini-Toudeshky, H., Sadeghi, G., Daghyani, H. R.
313
Time-temperature-water Absorption Superposition Principle for Flexural Fatigue Strength of Unidirectional CFRP Laminates Ichimura, J., Sekine, N., Nakada, M., Miyano, Y.
319
Buckling of Composite Plates with Cutouts Rezaeepazhand, J., Darbari, A. M.
325
Fatigue Crack Propagation in Graded Composites Tilbrook,M., Rutgers, L., Moon, R., Hoffman, M.
331
Dynamic Response Behavior of Stiffened Delaminated Plates Considering Failure Bai,R.X., Chen,H.R,, Wang, M.
337
Tensile Behaviour of Polymer Coated Optical Fibres Law, S., Yan, C, Ye, L.
343
Statistical Model for Multiaxial Fatigue Behavior of Unidirectional Laminates Diao.X.X, Lessard,L.B.
349
Part VII: FEM/Simulation Simulation of Three-dimensional Flow in Compression Resin Transfer Molding by the Control Volume/Finite Element Method Shojaei, A., Boorboor, D., Ghaffarian, S. R.
357
Modeling of Two Dimensional Cellular Solids with Two Types of Imperfections Li,K., Gao,X.-L.
363
Finite Element Modeling of Fine Structure of Natural Plant Fibers for Statistical Characterization of Their Tensile Strengths Suzuki, K., Kimpara, I., Funami, K.
370
x
Contents
Multilayered and Selective Higher-Order-Deformable Sandwich Finite Element Modeling for Numerical Accuracy Improvement Suzuki, K., Kimpara, I.
376
Adhesion Measures of Elasto-plastic Thin Film via Buckle-driven Delamination Li, Q. Y., Yu, S. W.
382
Evaluation of Intra-ply Shearing Stiffness for a Plain Weave Fabric Prepreg
Yu,X.B., Ye,L, McGuckin, D.
388
Part VIII: Fracture Initial Fracture Behaviour of the Weft-Knitted Textile Composites Having WeltKnit Architectures Khondker, O. A., Fukui, T., Nakai, A., Hamada, H.
397
Mixed-mode Fracture of a CF/PEI Composite Material Choupani, N., Ye, L, Mai, Y.-W.
403
Effects of Molecular Structure on the Essential Work of Fracture of Amorphous Copolyester at Various Deformation Rates Chen,H.B., Wu, J. S., Karger-Kocsis, J.
409
How to Eliminate Buckling in the Essential Work of Fracture Measurement with Very Thin Plastic Films Chen, H. B., Liu, S. L, Wu, J. S.
416
Fracture Behaviour of Sandwich Laminates Reinforced by Short-Glass Fibres Khatibi, A. A.
422
Analytical and Numerical Simulations of Plastic Zone at Crack Tip in Anisotropic Solids Liu,H.-X., Ye,Z.-M., Liu, H.-Y.
428
Application of Essential Work of Fracture Methodology to Polymer Fracture Duan, K., Hu, X. Z, Mai, Y.-W.
433
Three-Dimensional Micromechanics Analysis of Strain Energy Release Rate Distribution along Delamination Crack Front in FRP Tanaka, H., Nakai, Y.
439
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour During Mode I Fracture in Glass Fibre Composites Feih, S., S0rensen, B. F. 445 Behavior of Brittle Reinforced Composites Fracture at Elevated Temperatures Mohamed, A. T.
452
Contents
xi
Part IX: Impact Non-woven Fabric Reinforced Cellular Textile Composites with Improved Energy Absorption Capacity Lam, S. W., Tao, X. M., Yu, T. X.
461
Energy Absorption Properties of Braided Composite Tubes Okano, M., Sugimoto, K., Nakai, A., Hamada, H.
466
Characterization of Damage Resistance and Damage Tolerance of Composite Materials Shen, Z, Yang, S. C, Fu, S. Y., Ye, L.
472
Simplified Prediction Method of Impact Response on Composite Laminates Kim, S. J., Hwang, I. H.
All
Indentation Responses and Damage in Kaolin/Cellulose-Fibre Epoxy Nanocomposites Vaihola, S., Vilaiphand, W., Lopez, A., Low, I. M.
482
Impact Performance of 3D Interlock Textile Composites Byun, J.-K, Urn, M.-K., Hwang, B.S., Song, S.-W.
488
The Ballistic Impact Behavior of Composites Reinforced by Biaxial Weft Knitted UHMWPE Fabrics Liang, Z.-Q., Qiu, G.-X., Yi, X.-S. Low Speed Impact Behavior of Aluminum Honeycomb Sandwich Panel Song,J.-L, Bae,S.-I., Han, M.S., Ham, K.-C.
494
500
Part X: Industrial Applications Thermomechanical Analysis of Water Aged Pultruded Composites Al-Assafi, S.
509
Secondary Bonding in the Construction of Large Marine Composite Structures Simpson, G. J., Burchill, P. J.
515
Surface Analysis of "Class A" Polymer Composite Substrates for the Automotive Industry Schubel, P. J., Harper, L. T., Turner, T. A., Warrior, N. A., Rudd, C. D., Kendall, K. N.
521
Injection Molding of Silk Composite from Industrial Fiber Waste Kimura, T., Suzuki, T., Hatta, S.
527
Test of Full Scale Integrally Stiffened Composite Spoiler Rispler, A.
533
xii
Contents
Study on the Polypropylene(PP) Fiber/Cement Mortar Workability Zhang, H., Zou, L. M., Ni, J. H., Wang, Y. M. Hybrid Composites for Engineering Application Ahmad, F., Latif, M. Ridzuan. A., Nisar, H.
539 545
Development of a Knowledge Warehouse for Intelligent Risk Mapping and Assessment System Savci, S., Kayis,B.
551
Opportunities for Nanocomposites in the Oil & Gas Industry Varley,R., Leong, K. H.
557
Part XI; Interface Interfacial Properties of Polypropylene Fibre-Matrix Composites Houshyar, S., Shanks, R. A., Hodzic, A. Surface Grafting of Nano-SiC with Glycidyl Methacrylate in Emulsion and Its Effect on the Tribological Performance of Epoxy Composites Rong, M. Z, Luo, Y., Zhang, M. Q., Wetzel, B., Friedrich, K.
565
571
Influence of Matrix Type and Processing Conditions on the Morphology of the Interface and the Interfacial Adhesion of PE/PE Composites Masoomi, M., Ghaffarian, S. R., Mohammadi, N.
577
Filler-Elastomer Interactions: Effect of Ozone Treatment on Adhesion Characteristics of Carbon Black/Rubber Composites Park, S.-J., Lee, H.-Y., Lee, J.-R., Min, B.-G.
583
Interface End Theory and Fragmentation Test Ji, X, Dai, Y., Ye, L, Mai, Y.-W.
588
Stress Singularity Analysis of Interface End and Specimen Design for Fiber Pullout Test Dai, Y, Ji, X., Ye, L, Mai, Y.-W. 594
Part XII; Joint Evaluation of Strength of SiC/SiC Composite Joint Using New Interface Potential Serizawa, H., Lewinsohn, C. A., Murakawa, H.
603
Static and Fatigue Analysis of Double-Bolted-Joints for Gr/Epoxy after Thermal Cyclic Loading Yip, M.-C, Li, R.-Y., Yang, C.-H.
609
Tensile Strength and Fatigue Properties of Z-Pinned Composite Lap Joints Chang, P., Mouritz, A. P., Cox, B. N.
615
Contents
xiii
The Effect of Thickness on Joint Property of Mechanical Joint with Washer and Torque Ochi, A., Sugimoto, K., Nakai, A., Hamada, H.
621
Part XIII: Metal Matrix Composites Micromechanical Modelling of Hybrid Metal Matrix Composites Babu, P. E. J., Savithri, S., Pillai, U. T. S., Pai, B. C.
629
Formation of Nanostructured Magnesium Composite Reinforced by in-situ TiC Lu, L, Gupta, M., Toy, K. W.
635
Preparation of Mg-based Hydrogen Storage Nano-composite by Reaction Ball Milling Hu, Y. Q., Yan, C, Zhang, H. F., Ye, L, Hu, Z. Q.
639
A Tin-based Composite Solder Reinforced by Nano-sized Particulates and its Soldering Ability Zhang, X. P., Shi, Y. W., Ye, L, Mai, Y.-W.
645
Suitability of Metal Composite Suspensions for Injection Moulding Ahmad, F.
651
Effect of Intermetallic Volume Fraction on the Mechanical Properties of Intermetallic/Metal Micro-laminated Composites
Kim, H. Y., Hong, S. H., Chung, D. S., Enoki, M.
Part XIV: Nanocomposites Fracture Behaviour of Nano-composite Ceramics Soh,A.K., Fang,D.-N., Dong, Z.-X.
665
Structure-property Relationships of Polymer Nanocomposites Filled with Mechanochemically Grafted Nanoparticles Ruan, W. K, Zhang, M. Q., Rong, M. Z, Friedrich, K.
671
A Numerical Model for Evaluating Elastic Properties of Carbon Nanotube Reinforced Composites Hu, N., Fukunaga, H, Kameyama, M.
677
Interfacial Bonding Strength between Carbon Nanotubes and Epoxy Resin Matrix: Experimental and Computational Studies Wang, B., Liang, Z. Y., Gou, J. H, Jiang, T. H., Zhang, C, Kramer, L.
683
Epoxy-clay Nanocomposites: Morphology, Moisture Absorption Behavior and Thermo-mechanical Properties Hu, C. G., Kim, J.-K., Ban, S.
689
xiv
Contents
Study on Fabrication and Properties of Nano-alumina Particles Reinforced Thermosetting Matrix Composites Cui, Y. H, Tao, J., Wo, D. Z. Investigating High Strain Rate Responses of Nylon 6/ Clay Nanocomposites Huang, J. C, Tsai, J.-L. Mechanical Properties of SiC>2/Epoxy Nanocomposites at Cryogenic Temperature Huang, C. J., Fu, S. Y., Zhang, Y. H, Li, L. F.
695 701 707
Mechanical Properties and Fracture Performance of Nanoclay-reinforced Polypropylene modified with Maleic Anhydride Wong, S.-C, Chen, L, Liu, T. X., He, C. B., Lu, X. H.
713
Nanoclay reinforced UV Curable High-barrier Coatings Uhl, F. M., Davuluri, S. P., Wong, S.-C, Webster, D. C.
719
A Comprehensive Study on Intercalation and Exfoliation of Epoxy/Clay Nanocomposites Liu, J., Wu,J.S. Hydrogen Bonding, Mechanical and Physical Property, and Surface Morphology of Waterborne Polyurethane / Clay Nanocomposite Ma, C.-C. M., Kuan, H.-C, Chuang, W.-P., Su, H.-Y. Thermal Mechanical and Electrical Properties of Multiwall Carbon Nanotube/Waterborne Polyurethane Nanocomposite Kuan, H.-C, Ma, C.-C. M.
725
731
736
Preparation and Properties of Toughened Novolac Type Phenolic /SiO2 Flame Retardant Nanocomposite Ma, C.-C. M., Tai.H., Chiang, C.-L, Kuan, H.-C, Yang, J.-C, Hsu, C.-W.
742
Synthesis, Thermal Properties and Flame Retardance of Novel Phenolic Resin/Silica Nanocomposites Chiang, C.-L, Ma, C.-C. M., Kuan, H.-C, Chang, H. R., Lu, S.-C.
748
On the Enhancement of the Creep Resistance of Polymer by Inorganic Nanoparticles Zhang, Z., Yang, J.-L, Friedrich, K.
754
The Stress Transfer in a Single-Walled Carbon Nanotube-Reinforced Epoxy Xiao, K. Q., Zhang, L. C.
760
A Study on Mechanical Properties of MWNT/PMMA Nanocomposites Kim, H.-C, Lee, S.-E., Kim, C.-G., Lee, J.-J.
766
Fabrication and Microstructure of Si3N4-TiCnano Composites Zhao, J., Huang, X. P., Ai, X, Lu, Z. J.
772
Contents
xv
Synthesis, Thermal and Wear Properties of Waterborne Polyurethane/Polysilicic Acid Nanocomposite Su, H.-Y., Ma, C.-C. M., Kuan, H.-C, Wang, C. P.
778
Preparation and Properties of Epoxy-Bridged Polyorganosiloxanes NanoComposite Lee, T.-M., Ma, C.-C. M., Hsu, C.-W., Chiang, C.-L.
784
Moisture Absorption and Hygrothermal Aging of Organo-montmorillonite Reinforced Polyamide 6/Polypropylene Nanocomposites Chow, W. S., Mohdlshak, Z. A., Karger-Kocsis, J.
790
Geopolymer Reinforced Polyethylene Nanocomposites Yuan, X. W., Easteal, A. J., Bhattacharyya, D.
796
Part XV; Processing Understanding the Thermoforming Issues of Carbon Fibre Reinforced Polyphenylene Sulphide [PPS] Composite Hou,M., Ye,L.
805
A Numerical Approach to Analyze the Curing Process of Railroad Composite Brake Shoe Shojaei, A., Abbasi, F.
811
Possibility of Fabricating Mixed cx/(3 Sialon Ceramics as Composite Materials Karunaratne, B. S. B.
817
High Quality and Low Cost Manufacture of Potassium Titanate Whiskers Lu, X. H, Liu, C, He, M., Yang, Z. H, Bao, N. Z, Feng, X.
823
What Darcy Really Meant - the Truth on Permeability Bechtold, G.
828
Study on Re-pull Force in Pultrusion Processes—I. Experimental Observations Smith, C, Johnstone, B., Lu, M., Ye, L, Mai, Y.-W.
834
Study on Re-pull Force in Pultrusion Processes—II. Theoretical Analysis Lu, M., Ye, L, Mai, Y.-W., Smith, C, Johnstone, B. Influence of Foaming Temperature and Time on the Hardness of Cellular Al-Si-Cu-Mg Alloys Hasan, MD. A., Kim, A., Lee, H.-J., Cho, S.-S.
840
846
Forming Characteristics of Aluminium and Glass-Reinforced Thermoplastic FibreMetal Laminates Mosse, L., Compston, P., Kalyanasundaram, S., Cardew-Hall, M., Cantwell, W. 852
xvi
Contents
Compaction of Single Layer Plain Weave Fabric Preform Chen, Z.-R., Ye, L, Kruckenberg, T. A Study on the Control Strategy to Minimize Voids in Resin Transfer Mold Filling Process Park, Y.-H., Lee, D. H., Lee, W. II, Rang, M. K.
858
864
Fabrication Process and Characterization of Conductive Composite for PEFC Bipolar Plates Heo, S. I., Yun, J. C, Yang, Y. C, Han, K. S. 870 SiO2/Sulfonated PEEK Doped with Dodecatunstophosphoric Acid Hybrid Materials — Preparation and Properties Wu, H.-L, Ma, C.-C. M.
876
Thermoplastic Composite Access Cover Manufactured by Co-Consolidation after Thermoforming Stiffers Wang,K.J., Yi,X.-S.
882
Dome Forming of Triaxial Non-Crimp Fabrics Kong, H., Mouritz, A. P., Paton, R.
888
In situ Microfibrillar Reinforced Composites of PET/PC Liang, G. G., Easteal, A. J.
894
Part XVI: Smart Composites EPR and Magnetic Susceptibility Studies on the Structure and Polaron Dynamics on V2O5-, MOO3- and CuO- Containing Glasses Das, B. B., Ambika, R., Ageetha, S., Vimala, P.
903
Increase of High Burst Pressure in CFRP Vessels Reinforced by SMA Fibers Ben, G., Sakata, K.
908
Monitoring the Strain in the CFRP Laminates and CFRP/Concrete Structures Ogi, K., Takao, Y.
914
Free Vibration of Perforated Aluminum Plates Reinforced with Bonded Composite Patches Rezaeepazhand, J., Sabouri, H.
920
Design Method for SMA Super Hybrid Composite Materials Zhang, B. M., Li, S. L, Wu, Z. J., Du, S. Y, Li, Q. F. Control of Crack Closure in Shape Memory Alloy TiNi Fiber embedded CFRP Composite Materials Shimamoto, A., Lee, C.-C.
926
931
Contents Influence of Stress Induced Birefringence on FBG Sensors Embedded in CFRP Laminates Mizutani, T, Takeda, N., Nishi, T, Tsuji, R., Okabe, Y.
xvii
937
Magnetoelectric Properties of Piezoelectric and Magnetostrictive Composites with 2-2 and 3-1 Connectivity Huang, H. T, Zhou, L. M.
943
Shape Memory Effect on Interfacial Strength of SMA-reinforced Composites Poon, C.-K., Zhou, L. M.
949
Part XVII: Structural Health Monitoring Modified Acoustic Emission Generated in a Full-Scale Aircraft Wing Subjected to Simulated Flight Loading Paget, C. A., Atherton, K, O'Brien, E.
957
In-situ Health Monitoring of Filament Wound Pressure Tanks using Embedded FBG Sensors Rang, D.-K, Kim, C.-U., Park, S.-W., Hong, C.S., Kim, C.-G.
963
An Approach towards Predicting the Evolution of Fire Damage for Marine Composites Mathys, Z., Gardiner, C. P., Burchill, P. J.
969
A Bayesian Artificial Neural Network Method to Characterise Laminar Defects using Dynamic Measurements Lam, H. F., Veidt, M., Kitipornchai, S. 975 A Damage Detection Technique of Composite Laminates with Embedded FBG Sensors Kim, W.S., Kim, S.-H, Lee, J.-J.
981
Damage Detection in Composites Using Fiber Bragg Grating Sensors as Ultrasonic Receivers Okabe, Y., Tamaue, H, Kuwahara, J., Takeda, N. 987 Inverse Analysis for Damage Identification in CFRP Laminates with Embedded FBG Sensors Yashiro, S., Okabe, T, Takeda, N.
993
Parameterised Modelling Technique & Its Application to Artificial Neural Networkbased Structural Health Monitoring Huang, N., Ye, L, Su, Z. 999 Information Fusion in Distributed Sensor Network for Structural Damage Detection Wang, X. M., Foliente, G, Su, Z, Ye, L.
1005
xviii
Contents
Remaining Life of FRP Rehabilitated Bridge Structures Lee, L. S., Atadero, B., Karbhari, V. M., Sikorsky, C.
1012
Delamination Monitoring of CFRP Laminates Using Electrical Potential Method Ueda, M., Todoroki, A., Shimamura, Y., Kobayashi, H.
1018
Damage Detection in Glare plate-like structures Rosalie, S. C, Chiu, W. K.
1025
Quantitative Nondestructive Evaluation in Composites Beam Using Piezoelectrics Choi, Y.-G., Su, Z, Chen, Z.-R., Ye, L. 1032
Part XVIII: Textile Composites Mechanical Properties of Textile Hybrid Composite Inoda, M., Sugimoto, K., Nakai, A., Hamada, H.
1041
Effects of Fabrication and Processing Techniques of Aramid/Nylon Weft-Knitted Thermoplastic Composites on Tensile Behaviour Khondker, O. A., Fukui, T., Nakai, A., Hamada, H.
1047
Modeling and Characterization of 3D Heterogeneous Tissue Scaffolds Fang, Z., Starly, B., Darling, A., Sun, W.
1052
Continuative Fabrication and Mechanical Properties of Multi-axial Warp Knitted Thermoplastic Composites Using Micro-braided Yarn Narita, T., Nakai, A., Hamada, H, Komiya, I., Fukui, E.
1058
Multi-Scale Analysis for Material Characterization of Textile Composites Liang, J., Wang, K. S., Du, S. Y.
1064
Study on Damage Development of Woven Fabric Composites with Spread Tow Kurashiki, T., Zako, M., Hayashi, Y., Verpoest, I.
1070
Measurement of Material Damping Properties of Triaxial Woven Fabric Composites in Low-Pressure Condition Zako, M., Kurashiki, T., Nakanishi, Y., Matsumoto, K.
1076
CTE Model of 3D Orthogonal Textile Reinforced Aluminum Matrix Composites Lee,S.-K., Byun, J.-H, Hong, S. H.
1081
Permeability of Sisal Textile Reinforced Composites by Resin Transfer Molding Li, Y., Mai, Y.-W., Ye, L. Index of Authors
1087 1093
Preface Over the past three decades, the terminology of composite materials has been well acknowledged by the technical community, and composite materials have been gaining exponential acceptance in a diversity of industries, serving as competitive candidates for traditional structural and functional materials to realise current and future trends imposed on high performance structures. Striking examples of breakthroughs based on utilisation of composite materials are increasingly found nowadays in transportation vehicles (aircraft, space shuttle and automobile), civil infrastructure (buildings, bridge and highway barriers), and sporting goods (Fl, golf club, sailboat) etc., owing to an improved understanding of their performance characteristics and application potentials, especially innovative, cost-effective manufacturing processes. As the equivalent of ICCM in the Asian-Australasian regions, the Asian-Australasian Association for Composite Materials (AACM) has been playing a vital leading role in the field of composites science and technology since its inception in 1997 in Australia. AACM aims to encourage the interchange of knowledge in all aspects of composite materials amongst both the scientific and engineering communities. The first three ACCM conferences were successfully held in Osaka-Japan, Kyongju-Korea, and Auckland- New Zealand, respectively, every two years since 1998. Following the excellent reputations and traditions of previous ACCMs, ACCM-4 is held in scenic Sydney, Australia, 6-9 July 2004. The theme of ACCM-4, Composites Technologies for 2020, provides a forum to present state-of-the-art achievements and recent advances in composites sciences and technologies, and discuss and identify key and emerging issues for future pursuits. By bringing together leading experts and promising innovators from the research institutions, end-use industries and academia, ACCM-4 intends to facilitate broadband knowledge sharing and identify opportunities for long-term cooperative research and development ventures. We are very pleased with many contributions from authors and overwhelming response from participants. Nearly 200 manuscripts were received from 25 countries and regions, and 65% of them were from areas of the Asian-Australasian region. The proceedings were published from camera-ready manuscripts prepared by the authors. Each paper was vigorously peer-reviewed by at least two independent referees from the local scientific committee and other selected referees. Some papers required multiple revisions. The selected papers, classified under 25 categories, are in a wide spectrum, ranging from general manufacturing and processing techniques to the latest and hottest topics such as nano-composites and eco-bio composites. Together they represent an authoritative documentation of current advances in the field of composite materials. We wish to thank the following for their contributions to the success of this Conference: Air Force Office of Scientific Research, and Asian Office of Aerospace Research and Development. We are also grateful to the Cooperative Research Centre-Advanced Composite Structures (CRC-ACS), the Sydney University Centre for Advanced Materials Technology (CAMT) and the DSTO-AED Centre of Expertise in Damage
xx
Preface
Mechanics, Australian Composite Structures Society (ACSS) and University of Sydney, for their financial and other forms of supports to this Conference. Finally, we would like to thank all members of the ACCM International Advisory and Scientific Committees in promoting this Conference. Special thanks are due to all the authors for the careful preparation of their manuscripts; and conscientious reviewers for maintaining the high scientific quality of the ACCM-4 proceedings.
Lin Ye Yiu-Wing Mai Zhongqing Su Sydney, Australia July 2004
Conference Organisation ACCM-4 Co-Chairmen L. Ye, University of Sydney S.Y. Du, Harbin Institute of Tech. T. Uenoya, Tech. Research Institute of Osaka Prefecture
AACM Steering Committee M. Zako (President), Osaka University L. Ye (Vice-President), University of Sydney J.K. Kim (General Secretariat), Hong Kong Uni. Sci. & Tech.
International Advisory Committee (AACM Council) D. Bhattacharyya, University of Auckland O.I. Byon, Nihon University H.R. Daghyani, Amirkabir University of Tech. Iran T. Fujii, Doshisha University T. Fukuda, Osaka City University K.S. Han, Pohang University of Sci. & Tech. C.S. Hong, KA1ST S.H. Hong, KAIST D.A.L. Juwono-Soenarso, University of Indonesia S.J. Kim, Seoul National University I. Kimpara, Kanazawa Institute of Tech. W.I. Lee, Seoul National University K.H. Leong, Petronas Research & Scientific Services C.C.M. Ma, National Tsing Hua University Y.W. Mai, University of Sydney Y. Miyano, Kanazawa Institute of Tech. M. Nasir, University of Sains Malaysia V.A. Phan, Institute of New Tech. Promotion of Vietnam S. Ramakrishina, National University of Singapore D.Z. Wo, Nanjing University of Aero. & Astro. M.C. Yip, National Tsing Hua University
International Scientific Committee A. Baker, Platforms Sciences Laboratory/DSTO B. Banks, University of Strathclyde T.-W. Chou, University of Delaware I. Crivelli-Visconti, Univerista' Degli Studi Di Napoli Federico II K. Friedrich, University of Kaiserslautern H. T. Hahn, University of California, Los Angeles Y. Hamada, Kyoto Institute of Technology
xxii S. V. Hoa, Concordia University H. Ishida, Case Western Reserve University T. Katayama, Doshisha University D. Kelly, University of New South Wales F. K. Ko, Drexel University W. I. Lee, Seoul National University A. C. Loos, Virginia Tech I. Marshall, Monash University K. Niihara, Osaka University T. K. O'Brien, NASA Langley Research Centre R. Byron Pipes, University of Akron A. Pousartip, University of British Columbia F. Rose, Platforms Sciences Laboratory/DSTO M. Scott, Royal Melbourne Institute of Technology P. Smith, University of Surrey C.-T. Sun, Purdue University N. Takano, Osaka University N. Takeda, University of Tokyo X. Tao, Hong Kong Polytechnic University J. S. Wu, Hong Kong University ofSci. & Tech. X.-S. Yi, Institute of Aerospace Materials/China M. Zhang, Zhongshan University Z. Zhang, University of Kaiserslautern L. Zhou, Hong Kong Polytechnic University
Local Scientific Committee A. Afaghi-Khatibi, Melbourne University M. Bannister, CRC-Advanced Composite Structures A. Beehag, CRC-Advanced Composite Structures W.K. Chiu, Monash University A Crosky, University of New South Wales S. Galea, Platforms Sciences Laboratory/DSTO Israel Herszberg, Royal Melbourne Institute of Tech. M. Hoffman, University of New South Wales M. Hou, CRC-Advanced Composite Structures X.-Z. Hu, University of Western Australia J. Li, University of Technology Sydney I. M. Low, Curtin University of Technology A. Mouriz, Royal Melbourne Institute of Technology Rowan Paton, CRC-Advanced Composite Structures L. Tong, University of Sydney C. Wang, Platforms Sciences Laboratory/DSTO X. Wang, Manufacturing and Infrastru. TechJCSIRO D.-Y. Wu, Manufacturing and Infrastru. TechJCSIRO
Conference Organisation
Conference Organisation Local Organising Committee Z. Chen, University of Sydney R. Connell, University of Sydney N. Huang, University of Sydney K.-Y. Kim, University of Sydney T. Krunkenberg, University of Sydney W. Liang, University of Sydney M. Lu, University of Sydney Y. Lu, University of Sydney Z. Su, University of Sydney C. Yan, University of Sydney
xxiii
ACCM-4 Sponsors We wish to thank the following for their contributions to the success of this conference
Air Force Office of Scientific Research (AFOSR) Asian Office of Aerospace Research and Development (AOARD)
Cooperative Research Centre-Advanced Composite Structures (CRC-ACS), Australia
Australian Composite Structures Society (ACSS)
The University of Sydney
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AEROMECH @usyd
School of Aerospace, Mechanical and Mechatronic Engineering, University of Sydney
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Bio/Eco-Composites
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All-Plant Fiber Composites Ming Qiu Zhang , Min Zhi Rong, Xun Lu Materials Science Institute, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Zhongshan University, Guangzhou 510275, P. R. China
ABSTRACT Plasticization of fir sawdust was carried out in the present work to prepare natural resources based plastics. It was found that thermoplasticity and mechanical properties of the chemically modified wood flour changed with the substitution reaction conditions. By compounding sisal fibers and the plasticized fir sawdust, unidirectional laminates were manufactured similar to conventional thermoplastic composites. Such an all-plant fiber composite material is characterized by easy processing, environment friendly and low cost. Instead of chemical heterogeneity of conventional composites, physical heterogeneity of the current natural fiber composite is favorable for interfacial interaction.
INTRODUCTION Fiber reinforced polymer composites have been widely used in many fields mainly because of their high specific stiffness and strength. Recently, with increasing energy crisis and ecological problems, material scientists began to take interests in vegetable fibers serving as substitutes for man-made fibers in the area of composites [1]. In fact, however, these composites are not environment friendly enough due to the fact that the matrix resins are synthesized products from earth oil and mostly non-biodegradable. Considering the existing dilemma, the authors of the present work use modified plant fiber that can be processed like conventional polymers as matrix to make plant fiber reinforced plasticized plant fiber composite. The following benefits will be gained accordingly, (i) As natural fibers are slightly modified as a whole by chemical methods, cost effectiveness characterized by the renewable raw materials is maintained, (ii) Fully biodegradable ability is associated with the composite because both the reinforcer and matrix are biomaterials. (iii) Instead of chemical heterogeneity of conventional composites, physical heterogeneity of the all-plant fibers composite is favorable for interfacial interaction. Plant fiber consists of cellulose, hemicellulose, lignin and a small amount of extractives. Cellulose is the essential component and belongs to an isotactic /3-1, 4polyacetal of cellulose. High degree of crystallinity of cellulose as well as three dimensional reticulate structure of lignin make plant fibers far from thermoplastic materials. However, the crystalline structure of cellulose might be disrupted by substituting its hydroxyl group with some chemical reagent [2, 3]. This decrystallization process helps to improve thermoplasticity of cellulose since the substitution groups act as plasticizer. Etherification, esterification and graft-copolymerization are proved to be * Corresponding Author, Prof. M. Q. Zhang, Materials Science Institute, Zhongshan University, Guangzhou 510275, P. R. China. Fax: +86-20-84036576, e-mail: ceszmq(5),zsu.edu.cn.
4
All-plant Fiber Composites
effective to introduce plasticization into cellulose. Therefore, plant fibers can thus be converted into thermoplastics by using these techniques [4]. EXPERIMENTAL China fir sawdust was ground into a mesh size of 80-100 and then dried under vacuum at 80°C overnight. After being pre-swelled by ION NaOH for 1 hour, the powder was transferred into a flask containing (CFFj^NI and benzyl chloride. The reaction was carried out under vigorous stirring at 120°C for 4-10 hours to get benzylated products with various reaction extents. The products were purified through washing for 2-3 times with distilled water to remove inorganic salts, and with ethanol to remove residues of benzyl chloride and by-products, respectively. Finally the treated sawdust was dried again under vacuum at 80°C overnight for being used as composite matrix. As the modified fir exhibits rather high viscosity which can not be measured by a conventional melt indexer, a home-made tester was used to assess its flowability in terms of melt index (MI, defined as the weight of the material flowing out of the nozzle in gram within 10 minutes under given pressure and temperature) and flow temperature (defined as the temperature at which the material begins to flow out of the nozzle during heating under a given pressure). To produce plates of neat matrix and unidirectional sisal laminates, benzylated fir sawdust alone and its mixture with continuous sisal fiber at a desired proportion were compressed into sheets using a hot press at 130°C under lOMPa. The molding conditions were chosen based on the viscosity measurements. RESULTS AND DISCUSSION Benzylation of wood is a typical Williamson synthesis reaction, which involves nucleophilic substitution of an alkoxide or a phenoxide ion for a halide ion [5]. Since cellulose constitutes the majority of wood and lignin contains little hydroxyl, benzyl chloride has to react mainly with the hydroxyl of cellulose. Hon et al reported that wood species have little effect on the rate of benzylation [5], but the reaction turned out to be quite slow in the case of fir powder when the conditions suggested in ref.[5] were followed. Our experimental results show that the reaction is remarkably influenced by the concentration and amount of NaOH, amount of benzyl chloride, reaction temperature and time. Based on these findings, the extent of benzylation of fir can be adjusted by taking appropriate measures. Figure 1 illustrates that the chemical structure of benzylated fir is
3700
3300
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2500
2100
1700
1300
900
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1
Wavenumber [cm ]
FIGURE 1 FTIR spectra of (1) unmodified fir sawdust and (2, 3) benzylated fir sawdust with different weight gains (curve 2: 47%, curve 3: 98%).
All-plant Fiber Composites
5
quite different from that of the untreated version. Hydroxyl absorption at about 3400cm"1 diminishes after benzylation as a result of etherification. Because the appearance of the bands at 1800-1950,1600, 736 and 695cm"1 is indicative of the mono-substituted benzene rings in benzyl groups, it can be concluded that the hydroxyl groups of cellulose have been substituted by benzyl groups. By comparing curves 2 and 3, it is seen that the characteristic peaks of benzyl group become stronger with a rise in the amount of the substituent. For an accurate analysis of the reaction and the resultant, degree of substitution originating from benzylation process should be known. Due to the chemical heterogeneity of wood, this parameter is factually hard to be measured. Instead, the extent of benzylation reaction can be evaluated by the percentage weight gain, which has explicit engineering meaning. As exhibited in Figure 2, an increase in the weight gain of the benzylated fir sawdust corresponds to an improvement of its thermal flowability. That is, the more hydroxyl groups of cellulose are substituted by benzyl groups, the higher the melt index and the lower flow temperature. The data in Figure 2, on one hand, demonstrate that the fir sawdust has been converted into a thermoplastic material after benzylation and acquired thermoforming ability. On the other hand, they reveal that the processing window of bezylated fir sawdust is a function of molding temperature and pressure.
20
40
60
Weight gain [%] FIGURE 2 Effect of weight gain on flow temperature and MI of benzylated fir sawdust (pressure=6MPa)
FIGURE 3 WAXD patterns of (1) unmodified fir sawdust and (2, 3) benzylated fir sawdust with different weight gains (curve 2: 47%. curve 3: 98%).
6
All-plant Fiber Composites
Figure 3 gives the WAXD patterns of untreated and treated fir sawdust. It is seen that the peak at 20=22.2° of the as-received sawdust (curve 1), which is derived from the reflection of (002) plane of cellulose I lattice, diminishes after benzylation (curve 2) and forms broader scattering when the extent of benzylation is significantly increased (curve 3). As the diffraction peak profiles shown in curves 2 and 3 resemble those of ball-milled cellulose which had been decrystallized [6], it can be concluded that the above-stated variation in (002) reflection is a result of decrystallization. Such a decrystallization process helps to improve thermoplasticity of cellulose by breaking hydrogen bonds between cellulose molecules. It is believed that the large benzyl groups introduced onto cellulose bring in more free volumes and account for the change in the supramolecular structure. It is worth noting that an increased molecular mobility of cellulose is hard to result in an increased flowability of fir sawdust if the network of lignin keeps intact. Therefore, partial removal and damage of lignin structure as reflected by the absence of the carbonyl band at 1760cm"1 and aromatic ether band at 1275cm"1 (Figure 1) is necessary to get rid of the fetter, which further improves the extent of substitution of cellulose. Prior to the discussion of sisal laminates, mechanical properties of the matrix, benzylated fir sawdust, should be known at first. As shown in Table 1, the molded sheet of modified fir sawdust with a weight gain of 72.8% has the highest performance except for the flexural modulus. Similar to the case of original wood material, crystallinity and molecular weight of cellulose determine the mechanical properties of its plasticized version. For highly substituted wood, more crystalline regions of cellulose are destroyed, while a higher reaction temperature or longer reaction time that is required to increase substitution degree would result in severer degradation than the slightly substituted one. These contradictory effects are responsible for the reduced mechanical properties coupled with increased thermoplasticity (cf. Table 1 and Figure 2). On the other hand, if the degree of substitution is so low that the modified fir sawdust can not be sufficiently melted, a sheet with lower mechanical properties but higher crystallinity retention would be yielded. Evidently, the benzylated fir sawdust with a weight gain of 72.6% seems to be well balanced. As a result, the benzylated products with weight gains of 70%-80% were selected as the matrix material for making sisal laminates in this work. Compared with cyanoethylated pine [4], the benzylated fir sawdust has much higher impact toughness but lower static strength and modulus. The difference should be attributed to the modification techniques rather than wood species. Tensile and flexural properties of unidirectional sisal reinforced benzylated fir sawdust composites are shown in Figure 4 as a function of sisal volume fraction, Vf. It is seen that moduli increase with sisal content in an approximately linear way, while the TABLE I Mechanical properties of thermoformed sheets of benzylated fir sawdust Weight Gain [%] 37.0 54.5 65.2 72.8 81.2 96.7 105.3
Tensile Strength [MPal 12.5 13.8 15.2 17.5 16.3 15.1 12.7
Young's Modulus [GPa] 1.92 1.98 2.21 2.39 2.30 2.24 2.12
Flexural Strength [MPa] 33.6 34.3 34.9 36.8 35.5 34.5 33.9
Flexural Modulus [GPa] 2.20 2.18 2.33 2.47 2.51 2.55 2.50
Impact Strength [kJ/m2] 3.9 4.4 4.7 5.6 5.1 4.5 3.7
All-plant Fiber Composites
7
strengths reach a maximum at Vf=30vol%. Although the latter phenomenon can be attributed to the competition between the effects of reinforcement and micro-crack initiation as a result of fiber incorporation, this drop in strengths appears too early. This is different from the results of thermosetting polymer based plant fiber composites. For example, a linear relationship between tensile strength and fiber loading were found up to Vf=60vol% in unidirectional jute/unsaturated polyester and sisal/epoxy systems [1, 7]. Obviously, wetting and absorption problems at the fiber/matrix interface should be responsible for this behavior, hi the case of thermosetting resins, the low molecular weight monomers before curing facilitate impregnation of the reinforcing fiber bundles to form intimate adhesion. For benzylated fir sawdust that has a quite high melt viscosity, it is somewhat difficult to impregnate sisal fibers under the current processing conditions. That is, the kinetic barrier leads to insufficient interfacial bonding in spite of the fact the fiber reinforcement and matrix are thermodynamically compatible. Consequently, the strengthening effect of sisal fibers can not brought into full play especially at a fiber content higher than 30vol%.
.
—D—Tensile strength —0—Young's modulus
20
20 a. O
8s
15 2 10
10
20
30
10
40
20
30
I
40
Sisal content [vol%]
Sisal content [vol%]
FIGURE 4 Tensile (a) and flexural properties (b) of unidirectional sisal/benzylated fir sawdust laminates as a function of sisal content
100
2
3
Strain [%] Figure 5 Typical stress-strain curves obtained from tensile tests of (1) benzylated fir sawdust, (2) sisal/benzylated fir sawdust laminates (V(=19.7vol%), (3) sisal/benzylated fir sawdust laminates (Vf=31vol%) and (4) sisal/benzylated fir sawdust laminates (Vf=40.4vol%).
It is interesting to examine the failure behavior reflected by the tensile stress-strain plots in Figure 5. Unlike unidirectional sisal/epoxy laminates that are characterized by
8
All-plant Fiber Composites
brittle failure [7], the current composites show long tails after the predominant damage. Such a post-failure crack propagation resistance improves the safety of use and must be related to the interfacial failure characteristics. That is, the localized shear deformation of the ductile matrix induced by the reinforcing fiber accounts for the phenomenon. It is thus expected that an increased interfacial interaction in the present laminates would result in a higher elongation to break. CONCLUSIONS (1) By means of benzylation, fir sawdust can be converted into a thermoplastic material. In comparison with cyanoethylated products, benzylated wood flour has higher thermoplasticity and toughness. (2) Melt viscosity and mechanical performance of benzylated fir sawdust is a function of the extent of benzylation, which provides posibilities for tailoring the structure-properties relationship. From technical point of view, the modified fir sawdust melt is thermally sensitive but not pressure sensitive. (3) Unidirectional sisal reinforced plasticized fir sawdust laminates can be manufactured by similar techniques available for conventional thermoplastic composites and exhibit moderate modulus and strength. To improve the mechanical properties, the flow behavior of the matrix should be greatly improved to ensure sufficient impregnation and interfacial adhesion. Another possible solution might lie in the production of self-reinforced composites, i.e. surface of the reinforcing plant fibers is appropriately plasticized and then the fibers are bound together without additional matrix resin under the joint action of temperature and pressure. In this way, uncoiling of the spirally arranged micro fibrils inside plant fibers, which consumes substantial energy, would occur and provide the composite with enhanced performance. A paper on this topic will be published in the near future. ACKNOWLEDGMENT The financial support by the National Natural Science Foundation of China (Grant: 50173032) is gratefully acknowledged. REFERENCES 1. 2. 3. 4.
5. 6. 7.
Bledzki, A. K. and J. Gassan 1999. "Composites Reinforced with Cellulose Based Fiber", Progr. Polym. Sci, 24:221-274. Morita, M. and I. Sakata 1986. "Chemical Conversion ofWood to Thermoplastic Materials", J. Appl. Polym. Set, 31:832-840. Hon, D. N. S. 1992. "Chemical Modification of Lignocellulosic Materials: Old Chemistry, New Approaches", Polym, News, 17:102-107. Lu, X., M. Q. Zhang, M. Z. Rong, G. Shi, G. C. Yang, and H. M. Zeng. 1999. "Natural Vegetable Fiber/Plasticized Natural Vegetable Fiber - A Candidate for Low Cost and Fully Biodegradable Composite", Adv. Compos. Lett, 8:231-236. Hon, D. N. S. and M. S. L. Josefina. 1989. "Thermoplastization of Wood. I. Benzylation of Wood", J. Polym. Sci, Part A: Polym. Chem., 27:2457-2482. Heritage, K. J., J. Mann, and L. Roldan-Gonzalez. 1963. "Crystallinity and the Structure of Celluloses", J. Polym. Sci, Part A: Polym. Chem., 1:671-695. Rong, M. Z., M. Q. Zhang, Y. Liu, G. C. Yang, and H. M. Zeng. 2001. "The Effect of Fber Treatment on the Mechanical Properties of Unidirectional Sisal-Reinforced Epoxy Composites", Compos. Sci. Techno!., 61:1437-1447.
Compression Molding and Mechanical Properties of Composite Materials from Post Consumer Type Fiber Waste
SeijiHatta* Kyoto Municipal Industrial Research Institute, Textile Technology Center, Japan Teruo Kimura, Hirohisa Gonno Kyoto Institute of Technology, Advanced Fibro Science, Japan Kenzo Kadokura Kadokura Trading Company Co.LTD., Japan
ABSTRACT The composite materials consisted with rag were molded by using the compression molding method and their mechanical properties were investigated. The rag was pre-treated by opener and card machine and mixed with Polypropylene fiber to make the web. After that the felt was made from the web by using the needle punch method. Polypropylene fiber was used for the matrix material, and the volume content of PP was varied in the experiments. The results suggest that the molding method described herein shows promise for contributing toward the material recycling of post consumer type fiber wastes as raw materials of composites. INTRODUCTION In recent years, increased emphasis has been placed on developing the recycling system of fiber waste with the goal ofprotecting the environment. However, relatively little investigation has been conducted regarding such a recycling system. There are two types of fiber wastes such as industrial fiber waste resulted from the process of manufacturing products and fiber waste named "rag" as a post consumer. It is estimated that the used fibers in Japan are released about two million tons per year. Although 10 per cent of waste fiber have been recycled or reused as the used cloths, the industrial wiping cloths, the shoddy and the felt, almost 90 % of waste fiber is destroyed by fire and buried underground. These conditions have raised the concerns about the necessity of the finding innovative usage of rag and new recycling technologies are strongly required. Meanwhile, to meet a wide variety of recent engineering requests, many research efforts related to the development of new materials have been carried out actively in many fields. In this paper, to establish the new material recycling system of the •rags, the compression molding method in which the rags were used as reinforcements of the composite materials was proposed.
* Corresponding Author, kamigyo-ku, Kyoto, 602-0898, Japan, +81-75-441-3165,
[email protected]
10
Compression Molding and Mechanical Properties
The rag was used as a reinforcement of composite materials. Figure 1 shows the aspect of rag. Various kind of fibers were mixed in the rag, and the fibers used here are shown in Table 1. As can be seen in this Table, the rag used here is mainly consisted by the cellulose fibers. The measured mechanical properties and the size of fibers are shown in Table 2.The monofilament PP fiber wastes were used as a matrix material.
FIGURE 1 Aspect ofragused TABLE I Materials and component of rag used 2
2 PP30Wt% l3kg/m 2 ) PP50Wt% t5kg/m ) PP70Wt% t5kg/m )
Cellulose fibers (Cotton,Rayon,another) Polyesters Wool Another fiber PP
45— 54%
43— 4 5 %
15— 20%
12— 15% 5— 8% 2— 3% 2 7 - 33%
10— 15% 3— 4% 2— 3% 3 8 - 48%
10— 5— 2r^ 59-
12% 7% 3% 68%
TABLE II Properties of each fiber
Cotton Rayon Polyester PP
Tensile strength(MPa) Young's modulus(GPa) Fiber length(mm) Fineness(D) 1 0 -- 3 0 2 0 0 --350 9 . 3 - -12.7 1.5- - 2 . 3 1 5 0 -- 4 0 0 4 . 5 - - 8.3 1 5 -- 3 5 1.5- - 3 . 0 3 2 0 -- 4 5 0 13--35 3 . 1 - - 7.5 1.5- - 2 . 5 10--55 3 5 0 -- 5 3 0 4 . 5 - - 7.5 2 5 -- 5 0
PRE-MOLDING OF FELT The rag was pre-treated by opener and card machine and mixed with PP fiber to make the web. After that the felt was made from the web by using the needle punch method. Figures 2(a) and (b) show the aspects of molded felt and the cross section. As can be seen in the figure, the various fibers are mixed at randomly together with the PP fiber. The content of PP fiber was varied in the wide range in the experiment.
Compression Molding and Mechanical Properties
(a) Aspect of pre-molded felt
11
(b) Cross section of felt
FIGURE 2 Pre-molded felt
COMPRESSION MOLDING METHOD AND MECHANICAL TESTS For molding of composite materials, the compression molding method was performed. The molding process was as follows. Namely, the pre-molded felts were firstly heated in the furnace with forced convection air flow at 190 degree during 25 minutes in order to melt the PP fibers. After the heating process, the felts were compressed in the die of 190 degree with dimensions of 250 mm x 250 mm until 3 mm or 5 mm thickness. Then the natural cooling was done by keeping the proper pressure. The aspect of molded composite material is shown inFig.3.
FIGURE 3 Molded composite
The tensile, three-point bending and Izod impact tests were performed in accordance with JIS K 7054, JIS K 7055 and JIS K 7062, respectively. The aspects of cross section of composites were also observed by using SEM and micro scope. RESULTS AND DISCUSSION Figures 4(a), (b) and (c) show the aspects of cross section of composites for Wf=30%, 50% and 70%, respectively. Here Wf means the weight fraction of waste fibers in the composite. The good penetration of matrix material can be seen for Wf=30% and 50%. However, the many voids can be clearly seen for Wf=70% because of the lack of matrix material. The adhesion between fiber and PP matrix is not good as shown in these figures because of no-treatment of fiber surface and PP matrix in this experiment.
12
Compression Molding and Mechanical Properties
(a)Wf-=30%
(b)Wf=50% FIGURE 4 SEM observation of molded composites
Figure 5 shows the tensile stress-strain curves for molded composites. The stress-strain curve shows an inflection after the initial linear portion and the tensile strain is found to be maximum for matrix material. The tensile strength and modulus of composite were evaluated from the maximum tensile stress and the slope of initial linear portion of stress-strain curve, respectively.
0.05 Strain E t
0.1
FIGURE 5 Tensile stress-strain curves
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0
0 20 40 60 80 Weight fraction of waste fiber Wf (%) (a)Tensile strength
0 20 40 60 80 Weight fraction of waste fiber Wf (%) (b)Tensile modulus
FIGURE 6 Relationship between weightfractionof wastefiberand tensile properties
13
Compression Molding and Mechanical Properties
Figures 6(a) and (b) show the tensile strength and modulus as a function of Wf. As can be seen from the figures, the strength and modulus increase with increasing Wf. However, the notable increase of tensile strength can not be expected for the composite molded here. This may be caused by the lack of adhesion between matrix and waste fibers. Meanwhile, the fairly large value of modulus can be obtained at Wf=50%. It should be noted here that in the large range of Wf such as 70%, the strength and modulus take smaller values than those of matrix material. This may be caused bay the lack of matrix resin in the larger Wf in addition to the lack of adhesion between matrix and waste fibers. Figure 7 shows the bending stress-strain curves. The stress-strain curve shows an inflection after the initial portion as same as the result of tensile stress. The slope of initial linear portion for composites was severe in comparison with that of matrix material.
0
0.05 Strain E b
0.1
FIGURE 7 Bending stress-strain curves
Figures 8(a) and (b) show the bending strength and modulus as a function of Wf. Similar tendency to the tensile properties can be obtained for the results of bending tests. Namely, the strength and modulus take maximum values at Wf=50%, and decrease in the larger Wf. 153.5
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m o 0 20 40 60 80 Weight fraction of waste fiber Wf (%) (a) Bending strength
0 20 40 60 80 Weight fraction of waste fiber Wf (%) (b) Bending modulus
FIGURE 8 Relationship between Weight faction of wastefiberand bending properties
14
Compression Molding and Mechanical Properties
Figure 9 shows the Izod impact values as a function of Wf. It should be noted here that the impact value increases largely with increasing Wf. It is seen from the figure that the impact value becomes larger for larger Wf. For example, the impact value at Wf=70% is the value of about six times of that of matrix material. The said large impact value may be caused by the large energy absorption of flexible long fibers used here.
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80
Weight fraction of waste fiber Wf (%) FIGURE 9 had impact value
CONCLUSIONS The composite materials based on the post consumer type waste fiber such as rag have been molded, and their mechanical properties were investigated. The tensile, bending and impact properties were improved with the increasing of waste fiber content in the range of Wf =£50%. Especially, the fairly larger values of modulus and Izod impact value can be obtained in comparison with those of matrix material. Although minor problem were encountered, the molding method of composite materials described in the present paper showed promise as a contribution towards the recycling of waste fibers such as rag.
Various Lignocellulosics Fibre Reinforced Polyester Composites: The Study on Mechanical, Physical and Biological Properties Abdul Khalil, H. P. S. and Issam, A. M. Bio-Resources, Paper and Coating Technology, School of Industrial Technology, Universiti Sains Malaysia, 11800 Minden, Penang, Malaysia.
ABSTRACT Non-woven lignocellulosic fibres (oil palm empty fruit bunches (EFB), bamboo fibres and pineapple leaf fibres) reinforced thermoset composites were fabricated at different fibre weight fractions, i.e. 10, 20, 30, 40 and 50%. The polyester resin (unsaturated) and MEKP as catalyst were used. The mechanical, physical and biological properties of composites were analyzed with and without fibre treatments (control untreated, acetylation, prepreg ABS and silane) in composites. In general, as increased the weight fraction in matrix, the composite properties increased. The mechanical properties followed the order: bamboo (highest) > pineapple > EFB (lowest). Fibres treatments with ABS exhibited the highest mechanical strength and lowest water absorption of composites followed by acetic anhydride, silane and untreated fibres composites. However, the value was still lower as compared to the glass fibre composites. INTRODUCTION Lignocellulosics or plant fibres have been used by mankind as structural materials since prehistoric times. More recently, interest in the use of materials derived from natural resources has increased dramatically. The use of lignocellulosic fibres (oil palm empty fruit bunches (EFB), bamboo fibres, pineapple leaf fibres etc) as a replacement for glass in the reinforcement of composites is currently generating much interest in the research community. Lignocellulosic fibres offer a number of advantages over glass in such applications because of low costs [1,2], a very high performance/weight ratio [2], light weight [3], easy processing [4], reactive surface chemistry [5] and the fact that they maybe burned at the end of their product life-cycle [6]. Since lignocellulosic fibres are hydrophilic surfaces and polyester matrix is generally hydrophobic, poor fibre-matrix dispersion and wetting of the fibres occur. This incompatibility leads to poor mechanical properties and higher water absorption. The uses of lignocellulosic fibre with or without [5-7] chemical modification and the coupling agent's treatments [7] for polymer composites application have been increasingly studied in recent times. In this study, non-woven lignocellulosics fibres such EFB, bamboo and pineapple leaf fibres reinforced thermoset composites were fabricated using unsaturated polyester resin as a matrix. The mechanical, physical and * Corresponding Author, Email: Email: akhalil(%usm.mv
16
Lignocellulosics Fibre Reinforced Polyester Composites
biological properties were evaluated with and without fibre treatments. The properties of the composites were then compared with glass fibre composites. EXPERIMENTAL Fibre Preparation and Treatments The empty fruit bunches fibres was supplied by Sabutek Ltd. (Malaysia); bamboo fibres and pineapple leaf fibres were supplied by Malaysian Palm Oil Board. Non woven fibre mats of various fibres were prepared using wet process. The fibres were dried in oven at 105°C overnight. The fibre was the extracted before fibre treatments. Silane [7], acetylation [8] and ABS treatments [9] were carried out using method as explained in detailed in the previous study. Formation of Composites The unsaturated polyester resin, type W-1905, used was a commercial product supplied by Euro-Pharma Sdn Bhd, Malaysia. The formulation used consists of 100 parts of resin by weight for 1.5 parts catalyst (methyl ethyl ketone peroxide). Extracted fibres (without modification) and modified fibre (with acetic, silane and ABS prepreg) mats were used to make laminates of non-woven hybrid (random) polyester composites. Composites of varying fibre weight fraction (Wf) of 10%, 20%, 30%, 40% and 50% were prepared using a Resin Transfer Moulding (RTM) machine as explained in detailed in the previous study [10]. Mechanical, Biological and Water Absorption Testing Flexural and impact properties were studied in the test. Flexural tests were carried out on an Instron model 5582 according to ASTM D 790 respectively. For water absorption test, the samples were cut to a size of 5 x 5 x 0.6 cm and immersed in deionised water at ambient temperature. Mechanical and water absorption testing were carried out according to method as explained in detailed in the previous study [10]. Biological Testing The test was performed for 12 months, following the BS standard EN ISO 846:1997. The samples were completely buried in natural soil at 90% water holding capacity (WHC) and 50% soil moisture content. The test was carried out according to the method explained in detailed in previous study [10]. RESULTS AND DISCUSSION Mechanical Properties The results for flexural strength and modulus tests were presented in Table I. It showed that, flexural strength (FS) and flexural modulus (FM) for all unmodified and modified fibres increased steadily as the percentage of fibre increased from 10% to 50%. In general, the flexural properties of treated and untreated fibres composites followed in the order; EFB (lowest) > pineapple leaf > bamboo (highest). As compared to various treatment, fibres treated with ABS showed higher flexural
Lignocellulosics Fibre Reinforced Polyester Composites
17
properties, followed by acetylated and silane treated fibres composites, as compared to unmodified fibres. TABLE I Flexural strength and modulus for different fibre reinforced polyester composites Silane
ABS
Unmodified
Flexural strength (MPa) 45.6 45.6 40.0 37.3 40.0 37.3 43.4 46.6 48.1 51.6 50.2 53.9
45.6 45.5 45.5 53.0 58.7 61.3
3220 3457 3520 3621 3876 3942
45.6 48.6 51.9 53.8 54.5 58.5
45.6 61.8 66.0 68.5 63.3 74.4
3220 3445 3756 3926 4220 4286
45.6 48.8 51.3 54.2 55.0 59.9
45.6 65.2 68.4 72.4 73.3 79.8
3220 3720 4025 4511 4620 4482
Fibre
Fibre/ matrix (Wf)%
Unmodified
EFB
0 10 20 30 40 50
45.6 34.5 34.5 40.2 44.5 46.5
0 10 20 30 40 50
45.6 44.2 47.2 48.9 49.5 53.2
45.6 53.0 56.6 58.7 59.4 63.8
0 10 20 30 40 50
45.6 43.4 45.6 48.2 48.9 53.2
45.6 54.3 57.0 60.3 61.1 66.5
Pineapple Leaf
Acetylated
Acetylated
Silane
ABS
(MPa) 3220 3664 3731 3838 4108 4179
3220 4287 4364 4489 4806 4888
3220 3962 4319 4515 4853 4929
3220 3703 4038 4220 4536 4607
3220 4479 4882 5104 5486 5572
3220 4278 4629 5188 5313 5154
3220 4092 4428 4962 5082 4430
3220 4836 5233 5865 6006 5826
Flexural modulus 3220 3872 3942 4055 4341 4415
Bamboo
Table II showed the results of impact strength for all types of fibres at different fibre treatments. It showed that impact strength of all unmodified and modified composites increased gradually as the fibre loading increased. For unmodified composites, EFB showed the highest value of impact strength at fibre loading more than 40%. Same phenomenon was observed with all treated fibres composites. TABLE II Impact strength for different fibre reinforced polyester composites Fibre
Fibre/matrix (Wf) (%)
Unmodified
Acetylated
Impact strength (kJm"2) 5.5 5.5 6.0 6.6 9.4 8.5 10.2 11.2 14.8 16.3 15.2 16.7
Silane
ABS
5.5 6.3 8.9 10.7 15.5 15.9
5.5 7.2 10.3 12.2 17.8 18.2
EFB
0 10 20 30 40 50
Pineapple leaf
0 10 20 30 40 50
5.5 9.2 10.8 11.7 13.2 13,0
5.5 10.7 12.5 13.6 15.3 15.7
5.5 9.9 11.6 12.6 14.3 14.7
5.5 12.2 14.2 15.5 17.4 17.8
Bamboo
0 10 20
5.5 8.2 9.1
5.5 9.8 10.92
5.5 9.0 10.0
5.5 11.4 12.7
18
Lignocellulosics Fibre Reinforced Polyester Composites 30 40 50
12.24 14.16 15.84
10.2 11.8 13.2
11.2 12.9 14.5
14.2 16.6 18.4
Water Absorption Results for water absorption showed at Figure 1-3. The results showed that after 20 days exposure in water, the rate of water uptake for all types of composites remain almost constant except for the unmodified composites. Comparison with different types of fibres, bamboo showed the highest moisture absorption, followed by pineapple leaf and EFB fibres. This was due to the hydrophilic nature of the lignocellulosic, as well as due to the higher cellulose content in bamboo. -•-Unmodified -•-Acetylated -±-Silane -S-S-ABS HI-Cast Resin -•-CSM
Time {days)
Time (days)
FIGURE 1: Water absorption of bamboo reinforced composites
FIGURE 2: Water absorption of pineapple leaf reinforced composites
Time (Days)
FIGURE 3: Water absorption of EFB reinforced composites
Biological Properties The effect of fibre treatment upon the resistance of fibres to microbiological attack was showed in Figure 4-12. Flexural properties of the composites deteriorated when samples were exposed in soil burial tests. Whereas, no significant changes in properties were observed when unreinforced resins samples were exposed, all of the composites exhibited deterioration to varying extent. Both ABS and silane treatment of fibres provided a significant degree of protection.
Lignocellulosics Fibre Reinforced Polyester Composites H 0 month
Unmodified Aealylated
Sllana
ABS
Cast resin
n 3 rnonth
Unmodified Acotylated
CSM
19 E3 6 month
SI la no
9 12 n
ABS
Cast resin
CSM
Types of treatment
Types of treatment
FIGURE 4: Effect of biological test on flexural strength of EFB reinforced composites
FIGURE 5: Effect of biological test on flexural strength of pineapple leaf reinforced composites
• 0 month G3 month B6 month • 12 month!
• 0 month Q 3 month E 6 month a 12 month
Unmodified Acotylated Types of treatment
Types of treatment
FIGURE 6: Effect of biological test on flexural strength of bamboo reinforced composites
Flexural mo dulus
g 5
=
• 3 month
i|
Unmodified Acetylalsd
B 6 month
iTTTT
• 0 month
1 Silane
FIGURE 7: Effect of biological test on flexural modulus of EFB reinforced composites
B12 month
E
["•Omil onth
a 3 month
B 6 month
B12 month
• . =
II 1
ABS
Cast resin
CSM
Unmodified Acstylatad
Types of treatment
Silane
ABS
Cast resin
CSM
Types of treatment
FIGURE 8: Effect of biological test on flexural mod. of pineapple leaf reinforced composites
FIGURE 9: Effect of biological test on flexural modulus of bamboo reinforced composites
Figure 10-12 showed the effect of biological tests on impact properties of the composites. All figure showed similar phenomenon that CSM composites exhibited the highest impact strength which was more than 50 kJm2.
-•-Asetilasl -•-Sllana -*-ABS -K-Castrasin -«-CSM 52
FIGURE 10: Effect of biological test on impact strength of EFB reinforced composites
1
«
FIGURE 11: Effect of biological test on impact strength of pineapple leaf reinforced composites
20
Lignocellulosics Fibre Reinforced Polyester Composites
Masa(BuIan)
FIGURE 12: Effect of biological test on impact strength of bamboo reinforced composites
CONCLUSIONS The conclusions from above study were summarized as followed: • In general, mechanical properties of unmodified and modified composites increased gradually as the weight fraction of the composites increased from 10%-50% • Mechanical properties of the unmodified and modified (acetylated, silane, ABS) composites followed the order: bamboo (highest) > pineapple leaf > EFB (lowest) • According to types of treatment, mechanical properties of the composites followed the order: ABS pre-preg (highest) > acetylated > silane > unmodified (lowest) • For all types of composites and fibre treatments, the rate of water absorption decreased in the order: unmodified (highest) > silane > acetylated > ABS > CSM > cast resin (lowest). • The results of biological studies showed that changes in impact and flexural strength for pineapple leaf, bamboo and EFB reinforced composites were as followed: CSM (highest) > ABS > acetylated > silane > unmodified > cast resin (lowest). ACKNOLEDGMENTS The authors would like to thank to Universiti Sains Malaysia, Penang, Yayasan FELDA Grant No. P/TEKIND/650214/Y 104 and Kementerian Sains, Teknologi dan Alam Sekitar (MOSTE) Project Number: 09-02-05-1071 RM8 EA001 that has made this work possible. REFERENCES 1. 2. 3.
Bolton, A. J. 1994. "Natural Fibres For Plastic Reinforcement," Mater Tech., 9:12 Sreekala, M. S., Thomas, S. and Neelakantan, N. R. 1997. Journal Polym Engin., 16:265 Matsuda, H. 1993. "Preparation and Utilisation of Esterified Woods Bearing Caboxyl Groups," Wood Sci Tech., 27:23 4. Bisanda, E. T. N. and Ansell, M. P. 1991. Comp Sci Tech., 41:165 5. Abdul Khalil, H. P. S. and Ismail, H. Polym Test., 9:42-56 6. Gassan, J. and Bledzki, A. K. 1996. "Modification Method on Natural Fibres and Their Influence on the Properties of the Composites," ANTEC, 2:225 7. Rozman, H. D., Abdul Khalil, H. P. S., Kumar, R. N., Abusamah, A and Kon, B. K. 1995. Int J Polym Mater., 32:247 8. Hill, C. A. S., Abdul Khalil, H. P. S and Hale, M. D. 1998. "A Study of The Potential of Acetylation to Improve The Properties of Plant Fibre," Industrial Crops and Products., 8:53 9. Abdul Khalil, H. P. S., Maulida and Nasir, M. 2000. Mechanical and Water Absorption Properties of Lignocellulosic-Based Hybrid Composites. In: The 3 rd Regional IMT-GT Conference, Medan, Indonesia: 101-110 10. Abdul Khalil, H. P. S., Rozman, H. D., Ahmad, M. N. and Ismail, H. 2000. "Acetylated Plant Fibre Reinforced Composites: A Study On Mechanical, Hygrothermal and Ageing Characteristic," Polymer Plastics Technology Engineering., 39:757
Development of Eco-Cement Containing High Volumes of Waste Glass Konstantin Sobolev* Division de Estudios de Postgrado, Facultad de Ingenieria Civil Universidad Autonoma de Nuevo Leon, Mexico Gunsel Iscioglu BEM Cement, TRNC Pelin Tilrker, Asim Yeginobali, Tomris Ertiin R&D Institute, Turkish Cement Manufacturers' Association, Turkey
ABSTRACT Waste glass is a serious environmental problem in many countries, mainly because of the inconsistency of the waste glass streams. Consequently the ability of glass industry to recycle waste glass is limited. Therefore, alternative technologies are needed to boost the recycling of waste glass beyond the present restraints of the glass industry. The application of waste glass as a finely ground mineral additive (FGMA) in cement is one of the promising directions for the recycling of waste glass. Based on the method of mechano-chemical activation, a new group of ECO- cements was developed. In ECO- cement, relatively large amounts (up to 70%) of portland cement clinker can be replaced with waste glass or another locally available mineral additives. This report examines the effect of waste glass materials (window glass, black-andwhite monitor glass, brown and green bottle glass) on the micro structure and strength of ECO-cement based materials. According to the research results, the developed ECO-cement (with 50% of waste glass) possessed compressive strength at a level similar to normal portland cement, in the range of 44.5 - 66.7 MPa. Best compressive strength values were demonstrated by the ECO-cement based on waste window and green bottle glass. SEM observations detected a visible densification around the glass grains, due to partial hydration of glass grains and formation of C-S-H. INTRODUCTION Glass, one of the earliest man-made materials, has been known for over 9000 years. Because of its availability, cost effectiveness and unique mechanical, chemical, thermal, and optical properties, glass has many useful applications. In the USA alone about 20 million tons of glass products are manufactured annually with a shipment value of about $29 billion [1].
* Corresponding Author, A.P.#17, Ciudad Universitaria, San Nicolas de los Garza, Nuevo Leon, Mexico, 66450; Fax: (+l)-925-663-0491; e-mail:
[email protected]
22
Development of Eco-Cement
Theoretically, glass is a 100% recyclable material and it can be indefinitely recycled without any loss of quality. According to EPA official statistics [2-3], the municipal solid waste (MSW) stream in the USA contains about 5.5% of waste glass which yields 12.8 million tons per year. In 2000, only 23% of this volume was recycled [2-6]. Therefore, in spite of the apparent simplicity of glass recovery, its recycling rate is still insufficient (at an average MSW recovery level of 30%) [3]. Waste glass comes from different sources: glass containers (bottles and jars), construction glass (windows), and electrical equipment (lamps, monitors and TVs). Most (89%) of the waste glass comes from various containers [2-3]. Generally, recovered glass containers are recycled into new glass containers, others are used in newly emerging sectors such as fiberglass insulation, abrasives, light-weight aggregates, yet others are used for concrete and asphalt [2-25]. When waste glass is proposed as a constituent of cement (as a mineral additive) and concrete (as aggregate), concern about the strength reduction and potentially deleterious alkali-silica reaction (ASR) is often raised [18-25]. The usual precautions to avoid ASR (such as the application of low alkali cement and pozzolanic additives) were found to be effective when waste glass was used in concrete [22-25]. The application of waste glass as a finely ground mineral additive (FGMA) in cement is another promising direction for waste glass recycling [20, 26]. According to [20], FGMA glass with its high surface area, participates in the relatively quick pozzolanic reactions that eliminates the danger of a slower alkali-silica reaction at a later stage. It was demonstrated that the technology of High Performance (HP) Cement can be used for engineering ECO-cement with a high volume of mineral additives (HVMA) [26, 27]. Supersilica, a reactive silica-based complex admixture is added during the cement grinding process, promotes the mechano-chemical activation of cement and imparts high strength and extreme durability to the concrete or mortar made from such cement [27]. hi ECO-cement, relatively large amounts (up to 70%) of portland cement clinker can be replaced with inexpensive locally available mineral additives, including waste glass. It was proposed that the complex admixture and FGMA glass containing significant amounts of amorphous, reactive silicon dioxide can participate in simultaneous pozzolanic reactions [27]. RESEARCH SIGNIFICANCE The effect of FGMA glass (waste sital glass) on the strength behavior of HP cement- based materials has been reported in the literature [26], At the same time the recycling of different types of waste glass in ECO-cement was proposed [27]. Consequently, the evaluation of the effect of various groups of waste glass on the properties and microstructure of ECO-cement is important for the development and realization of this alternative way of waste glass recycling. EXPERIMENTAL PROGRAM Materials Used Four different waste glass materials (in a form of glass cullet) were used in the research: window glass (WG), black-and-white monitor glass (MG), brown and green bottle glass (BBG and GBG, respectively). The reference cement was portland cement CEM-I 42.5 (NPC) [28]. The ASTM Type I [29] clinker and reactive silica- based complex admixture Supersilica were used for the preparation of waste glass ECO-
Development of Eco-Cement
23
cement samples. The chemical composition of these materials was analyzed using XRD technique (Table I). It is noticeable that no lead was detected in the MG sample. TABLE I Chemical Analysis of Cement Components Composition SiO 2 A12O3 Fe 2 O 3 TiO 2
CaO MgO Na 2 O
K2O SO3 Cr 2 O 3 Loss of Ignition
Clinker
Window Glass
Monitor Glass
20.84 5.52 3.61 0.29 65.57 2.13 0.82 0.19 0.91 0.03 0.23
71.71 1.26 0.09 0.07 8.44 4.16 13.61 0.40 0.25 -
83.96 2.03 0.04 0.20 0.37 0.01 7.98 5.35 0.05 -
Bottle Glass Brown Green 71.19 2.38 0.29 0.15 10.38 1.70 13.16 0.70 0.04 -
71.12 1.71 0.24 0.07 10.02 3.01 13.17 0.19 0.25 0.23 -
Notations Used The following notations were used to distinguish the ECO-cement samples: WGC - for window glass (WG) cement; MGC - for monitor glass (MG) cement; BBGC - for brown bottle glass (BBG) cement; GBGC - for green bottle glass (GBG) cement. Mixture Proportioning The strength properties of five cement samples were investigated. These included cements based on high performance cement technology with different types of waste glass (WG, MG, BBG and GBG) and reference cement. 50% (by weight) of waste glass and 10% complex admixture were used to produce the waste glass containing cements. The composition and properties of investigated cements are presented in Table II. The mortars for compressive strength tests were prepared according to ASTM C109 [29]. Sand-to-cement ratio (S/C) of 2.75 was used for all mortars. These mortars were produced at a reduced water /cement ratio (W/C) adjusted to obtain a flow range of 140-190 mm. For SEM investigations, cement pastes of window glass (WG) cement with W/C of 0.5 were used. Preparation of Specimens Clinker was pre-ground in a ball mill for 60 minutes for subsequent use in the research program. Waste glass samples were washed to remove organic contaminants and crushed in the laboratory jaw crusher to a maximum size of 4 mm. Samples of glass cement were obtained by grinding a mixture composed of 35% pre-ground clinker, 5% gypsum, 10% complex admixture and 50% waste glass. The sample weight was 5 kg and the grinding media weight was 65 kg. Grinding time for all cement samples was 60 minutes. The investigated mortars were mixed following EN 196 [30]. The mortars were cast into three-gang (40x40x160 mm) prism molds, and compacted in accordance
24
Development of Eco-Cement
with EN 196 [30]. After the compaction procedure, the molds were placed in a humidity cabinet for 24 hours (keeping a relative humidity of 95% and a temperature of 20±l°C). Following this period, the specimens were removed from the molds and kept in water until the testing age. For SEM investigations, the cement pastes were prepared by the same mixing and molding method. Then, these pastes were cured for 28-day at 20+1 °C. After the curing period, the fractured specimens were dried, treated with acetone and coated with a thin layer of gold. Tests Performed The mortar samples were tested at the age of 2, 7 and 28 days for compression. Compressive strength tests were conducted using the portions of prisms broken in flexure [31]. The compressive strength results indicated are the average of the four values. SEM observations were performed using LEO Scanning Electron Microscope operated at an accelerating voltage of 15 kV. TEST RESULTS Compressive Strength of Mortars The compressive test results of glass cement mortars (following ASTM) are given in Table II. According to the test results, the best 28-day compressive strength value of 50.1 MPa was obtained from cement produced with window glass. The monitor glass, brown bottle and green bottle glass based cements reached a 28-day compressive strength in the range of 44.5 - 46.0 MPa, which is close to the strength of reference NPC (45.4 MPa). The compressive strength values at the 2-day age are almost the same for the investigated group of glass cements. Glass cement based on WG demonstrated the best compressive strength at the early ages. Similar behavior of waste glass ECOcements was observed at the 7- day age (Table II). Delay in the strength development of waste glass ECO-cements at early age: e.g. 50% at 2 days and 26% at 7 days can be explained by very low clinker content (35%) in these cements. Pozzolanic reaction of glass, as well as low W/C helps to offset this trend at later stages of hardening. TABLE II Compressive Strength of Investigated Mortars Composition Type NPC WGC MGC BBGC GBGC
Clinker
Gypsum
Glass
95 35 35 35 35
5 5 5 5 5
0 50 50 50 50
Compressive Strength, MPa Super Silica 0 10 10 10 10
W/C 0.45 0.30 0.30 0.30 0.30
2 days
7 days
28 days
26.5 16.4 12.1 13.2 11.6
36.1 31.0 25.0 25.0 25.5
45.4 50.1 44.5 45.3 46.0
SEM Observations It was observed that glass particles are well dispersed in the paste, resulting in a dense structure with low porosity (Figure 1). It is also noted that the glass grains are well connected to matrix and are coated with a thin layer of reticulated gel of C-S-H (Figure 1). Further, it was found that there is a visible densification around the glass
Development of Eco-Cement
25
grains, possibly due to partial hydration of glass grains, leading to an additional formation of C-S-H. SEM detected no sign of ASR in the investigated samples.
FIGURE 1 Microstructure of ECO Cement
CONCLUSIONS The developed ECO-cement containing 50% of waste glass possessed compressive strength properties at a level similar to normal portland cement, in the range of 44.5- 66.7 MPa. Best compressive strength values were demonstrated by the ECO-cement based on waste window and green bottle glass. It should be pointed out that the low-water demand property of ECO-cements results in high workability at low W/C. It helps to improve the strength of mortars based on these cements and also to offset the use of mineral additives in the cement composition. SEM observations detected a visible densification around the glass grains, due to partial hydration of glass grains and an additional formation of C-S-H. No sign of ASR was found in the investigated samples of waste glass cement. The research leads to the conclusion that the application of HP cement technology helps to recycle waste glass in ECO cement. Additional investigations may be necessary to improve the chemical activity of waste glass in the cement system. Further research is also required to explain and quantify the hydration mechanism and the microstructural development of ECO cement containing large volumes of waste glass, as well as to examine their resistance to a number of detrimental factors including the possible adverse effects of the alkali-silica reaction. ACKNOWLEDGEMENT The authors would like to acknowledge the receipt of samples of Supersilica from SCI Con Technologies. The author is grateful to the staff of Quality Control Laboratory of BEM Cement, Cement and Concrete Research Institute of TCMA, R&D Division of SISECAM Holding and Environmental & Educational Research Center of FAST at LAU for their help in conducting the experiments. The suggestions of Dr. U. Kersting and Dr. C. Podmore are highly appreciated. REFERENCES 1.
U.S. Department of Energy. 2002. "Glass Industry of the Future - Energy and Environmental Profile of the U.S. Glass Industry", pp. 1-23.
26 2. 3. 4. 5. 6. 7. 8. 9. 10. 11.
12. 13. 14. 15. 16. 17. 18. 19.
20. 21. 22. 23. 24.
25. 26. 27. 28. 29. 30.
31. 32.
Development of Eco-Cement U.S. Environmental Protection Agency. 1992. "Markets for Recovered Glass", pp. 1-15. (EPA530-SW-90-071A) U.S. Environmental Protection Agency. 2002. "Characterization of Municipal Solid Waste in the United States: 2000 Update", pp. 7-41. Geiger, G. 1994. "Environmental and Energy Issues in the Glass Industry", American Ceramic Society Bulletin 73(2), pp. 32-37. Stewart, G. 1986. "Cullet and Glass Container Manufacture", Resource Recycling, 2. "Americans Continue to Recycle More Than One in Three Glass Containers", October 27, 1999, Glass Packaging Institute, www.gpi.org/98rate.htm Apotheker, S. 1989. "Glass Processing: the Link between Collection and Manufacture", Resource Recycling, 7, p. 38. Rodriguez, D. 1995. "Application of Differential Grinding for Fine Cullet Production and Contaminant Removal", Ceramic Engineering Science Procedures, 2(16), pp. 96-100. Mayer, P. 2000. "Technology Meets the Challenge of Cullet Processing", Glass Industry, 2. Guter, E. 1996. "Quality Cullet Is Required for Fiberglass", Glass Industry, 1, pp. 13-35. Pascoe, R.D., Barley, R.W. and Child, P.R. 2001. "Autogenous Grinding of Glass Cullet in a Stirred Mill", in Recycling and Reuse of Glass Cullet, R.K. Dhir, M.C. Limbachiya and T.D. Dyer, eds. London: Thomas Telford, pp. 15-29. Clean Washington Center. 1995. "Evaluation of Crushed Recycled Glass as a Filtration Medium in Slow Rate Sand Filtration". Clean Washington Center. 1994. "Glass Feedstock Evaluation Project: Engineering Suitability Evaluation. Evaluation of Cullet as a Construction Aggregate". (GL-93-3) Day, D.E., and Schaffer, R., Glasphalt Paving Handbook, University of Missouri-Rolla, p. 53. Malisch, W.R., Day, D.E., and Wixson, B.G. 1975. "Use of Domestic Waste Glass for Urban Paving: Summary Report", U.S. Environmental Protection Agency. (EPA-670/2-75-053) "Glasphalt May Pave the Way for Worldwide Aviation in the 21 st Century", March 1, 2003, http://www.sciencedaily.eom/releases/1997/l 1/971110064723.htm Nash, P.T., Jayawickrama P., et al. 1995. "Use of Glass Cullet in Roadway Construction", FHWATCEQ. (0-1331) Shin, C.J., and Sonntag, V. 1994. "Using recycled glass as construction aggregate", Transportation Research Board, National Research Council. (No. 1437) Shao, Y., Lefort, T., Moras, S., and Rodriguez, D. 1998. "Waste Glass: A Possible Pozzolanic Material for Concrete", International Symposium on Sustainable Development of the Cement and Concrete Industry, CANMET/ACI, Ottawa, pp. 317-326. Dyer, T.D., and Dhir, R.K. 2001. "Chemical Reactions of Glass Cullet Used as Cement Component", Journal of Materials in Civil Engineering, 13(6), pp. 412-417. Naik, T.R., and Kraus, R.N. 1999. "Use of Glass Cullet as Aggregates in Flowable Concrete with Fly Ash", CBU. (CBU-1999-03) Meyer C. 2003. "Glass Concrete", Concrete International, Vol. 25, No. 6, pp. 55-58. National Research Council - Strategic Highway Research Program. 1993. "Eliminating or Minimizing Alkali-Silica Reactivity". (SHRP-C-343) Xie, Z., Xiang, W., and Xi, Y. 2003. "ASR Potentials of Glass Aggregates in Water-Glass Activated Fly Ash and Portland Cement Mortars", Journal of Materials in Civil Engineering, (15)1, pp. 67-74. "Making Concrete with Glass - Now Possible", May 13, 2002, Ref: 2002/90, http://www.dbce.csiro.au/news/viewpress.cfm/109 Sobolev, K., and Arikan, M. 2002. "High Volume Mineral Additive ECO- Cement", American Ceramic Society Bulletin, 81(1), pp. 39-43. Sobolev, K. 1999. "High Performance Cement: Solution for Next Millennium", Materials Technology, 14(4), pp. 191-193. American Society for Testing and Materials. 1999. "Standard Specification for Portland Cement", Annual Book of ASTM Standards, ASTM C150. European Committee for Standardization. 1994. "European Standard Specification for Cement", European Standard, EN 197-1. American Society for Testing and Materials. 1999. "Compressive Strength of Hydraulic Cement Mortars (Using Portions of Prisms Broken in Flexure)", Annual Book of ASTM Standards, ASTM C349. American Society for Testing and Materials. 1999. "Compressive Strength of Hydraulic Cement Mortars Using 2-in or 50-mm Cube Specimens", Annual Book of ASTM Standards, ASTM C109. European Committee for Standardization. 1994. "Test Method for Determining Compressive Strength of Cement Mortar", European Standard, EN 196.
Screwless Extrusion of Natural Fibre-Reinforced Thermoplastic Composites Timothy Galea, Tony Mills, Rex Halliwell and Krishnan Jayaraman Centre for Advanced Composite Materials, Department of Mechanical Engineering, The University of Auckland, Private Bag 92019, Auckland, New Zealand.
ABSTRACT Natural fibres possess good reinforcing capability when properly compounded with polymers. These fibres are relatively inexpensive, originate from renewable resources and possess favourable values of specific strength and specific modulus. Thermoplastic polymers possess shorter manufacturing cycle times and reprocessability despite problems with high viscosities and poor fibre wetting. The renewability of natural fibres and the recyclability of thermoplastic polymers provide an attractive eco-friendly quality to the resulting natural fibre-reinforced thermoplastic composite materials. Common methods for manufacturing natural fibre-reinforced thermoplastic composites, injection moulding and extrusion, often require compounding of the constituents in mixers leading to degradation of the fibres. Development of a screwless extruder, that minimises fibre degradation and employs a reliable and low technology process for compounding the constituents, is the main objective of this study.
INTRODUCTION Natural fibres come from renewable resources and are relatively inexpensive. These fibres are now well recognised to impart good reinforcing capability to composites. While their tensile strengths and moduli are generally inferior to those of polymeric fibres, they often exhibit significantly larger elongation giving them better damage tolerance [1,2]. A relatively large body of published literature [3-9] in the area of wood fibrereinforced virgin thermoplastic composites exists. These studies have examined the mechanical properties of the composites and the effects of various coupling agents on the interfacial bonding between the fibres and the polymer. The presence of a suitable coupling agent has been shown to be important for the achievement of significant gains in the mechanical properties of these composites in a recent review [10]. Common methods for manufacturing natural fibre-reinforced thermoplastic composites are injection moulding and extrusion. These techniques often require compounding of the constituents in mixers leading to the degradation of natural fibres. Hence, there is a need for a simple and reliable screwless extruder that minimises fibre degradation during compounding of the constituents.
* Corresponding Author: Department of Mechanical Engineering, The University of Auckland, Private Bag 92019, Auckland, New Zealand; Fax: + 64 9 373 7479; E-mail:
[email protected]
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Screwless Extrusion of Natural Fibre-Reinforced Thermoplastic Composites
A screwless extrusion technique for plastication and extrusion of thermoplastics, called elastic melt extrusion, has been developed by Maxwell and Scalora [11] based on the normal force effect. When a visco-elastic material is sheared between a stationary plate and a rotating plate, a normal force will be generated which will tend to push the two plates apart. Therefore, if an orifice is made in one of the plates, and both plates are constrained axially, the viscous material will be extruded though this orifice due to the normal force effect. The elastic melt extrusion technique results in much shorter material residence times than typical, and has a complete lack of contact between moving parts. It also subjects the material to a high degree of mixing compared with screw extrusion, the most common short fibre composite compounding method [12]. Since natural fibres will not be damaged through abrasion with moving parts, and shorter exposure times should reduce degradation due to high temperatures, it seems that the elastic melt extrusion process should result in a better fibre quality than screw extrusion. The purpose of this investigation is to assess the feasibility of the elastic melt extrusion process for compounding woodfibre-high density polyethylene and woodfibre-polypropylene composites. MATERIALS The woodfibres used in this study were Pinus Radiata fibres supplied by the New Zealand Forest Research Institute in Rotorua. They were light brown in colour with widths varying from 15 urn to 40 urn, lengths ranging from 1.5 mm to 5 mm, density of 400 kg/m3 and a nominal tensile strength and stiffness of 125-150 MPa and 2.5-4 GPa, respectively [13]. It should be noted that these values are very dependent on the source of woodfibres and their fibril angles. The high density polyethylene (HDPE) used was obtained from recycled milk bottles shredded into flake form. The flakes were roughly circular with a diameter of 5-10 mm. There were remnants of coloured bottle components present in the HDPE flakes, which caused the HDPE extrudate to be of a green colour rather than the clear extrudate that would occur from extrusion quality HDPE. The Polypropylene (PP) used was Cotene grade JE6100 in granular form with a diameter of 1-2 mm. The PP was reasonably free of impurities and a clear transparent extrudate was achieved. The requisite mass of woodfibres was put into an open top container followed by the required mass of HDPE or PP to achieve specific fibre mass fractions. The fibres and the polymer were mixed in the container by hand and efforts were made to separate the clumps of fibres so that the mixture would be as homogeneous as possible. ELASTIC MELT EXTRUDER The elastic melt extruder, shown in Figure 1, is powered by a 3-phase motor with variable speed control. The motor runs the internal drum of the extruder, which is in the shape of a cone, through an elliptical reduction gearbox (6.41:1). The machine is heated by four heating coils mounted in the front or orifice plate. These coils are controlled by a thermocouple attached to the exterior of the orifice plate and a variable temperature controller. The fibre-polymer mixture, dropped into the feed tube, is forced into the shearing zone between the front face of the cone and the front plate. During initial operation, heat is introduced to the conical section by conduction between the front face of the cone and the front plate through the molten material. Once the machine is running, most of the heat is provided through shear of the molten material lying between
Screwless Extrusion of Natural Fibre-Reinforced Thermoplastic Composites
29
the cone and the outer walls. The rear of the drum is thermally insulated from the front by a heat resistant gasket.
Polymer feed tube Shaft support bearings
A
Orifice plate ;one/drive assembly Extrudate
FIGURE 1 Schematic diagram of the elastic melt extruder
EXTRUSION OF COMPOSITES Preliminary studies were carried out on the elastic melt extruder using HDPE and PP to determine the effects of the drum speed, gap size (distance between the front face of the cone and the front plate) and the operating temperature on the extrusion rate or the material output from the extruder. The process variables that would provide maximum material output were then selected for the rest of this study, Table 1. The operation and output of the elastic melt extruder was sensitive to feed rates. An excessive rate of material addition created localised clumps of partially melted polymer and fibres in the melt, causing the drum to seize up. If the amount of material in the melt cavity was low, the output was significantly reduced causing material residence time to increase. Further, a decreased rate of material addition can cause the melt temperature to increase by up to 20°C. The feed rate was approximate for this study, Table 1. TABLE I Process variables used in elastic melt extrusion
Variable Drum rotational speed Gap size Temperature Feed rate
Unit rpm mm °C g/s
Value 15-20 10 + 0.5 180-200 0.2+0.1
Once the elastic melt extruder had reached the operatmg temperature, the fibrepolymer mixture was added to the hopper. Roughly a handful of fibre-polymer mixture was added for every 20-30cm of extrudate produced. The fill level was visually gauged by the amount of melt covering the drum. These rough approximations were sufficient for the small volume batches of composites produced in these initial studies, Table 2.
30
Screwless Extrusion of Natural Fibre-Reinforced Thermoplastic Composites TABLE II Materials produced using elastic melt extrusion
Material type Wood-PP Wood-HDPE
Fibre mass fractions as mixed before extrusion 30% 10% 15% 20% 25% 40%
0%
Y V
•
/
•
/
S
•
•
/
m
/
x
The woodfibre-HDPE and woodfibre-PP extradates contained a number of small voids. These voids may have been due to the moisture released by the woodfibres at the high temperatures of extrusion. Microscopic examination revealed that the fibres were aligned in the direction of extrusion. With higher fibre mass fractions, a degree of fibre clumping occurred at irregular intervals. These clumps were approximately 5 mm in diameter and did not have any polymer penetration. PRODUCTION OF COMPOSITE SPECIMENS The individual batches of the extradates were fed piece by piece into the loading hopper of an industrial granulator. Once a batch had been granulated, the collected material was bagged and labelled for injection moulding, and the granulator opened and cleaned to prevent cross contamination of samples. A BOY50M screw injection moulder was used to mould the tensile specimens. Machine variables were set to those typically used in the extrusion of HDPE or PP depending on the matrix of the composite material being moulded. TESTING OF COMPOSITE SPECIMENS The tensile properties of the woodfibre-thermoplastic composite specimens at room temperature and humidity (23°C and 50% RH) were determined in a computercontrolled Instron universal testing machine (Model 5567) using five replicates for each test by following the standard ASTM D 638M - 02. These specimens were conditioned at room temperature and humidity for 24 hours prior to the tests. The tensile strengths of the composites generally increase with increasing fibre content, with significant improvements over the tensile strengths of the base polymers occurring after 15% fibre mass fraction for woodfibre-HDPE composites and 20% fibre mass fraction for woodfibre-PP composites, Figure 2. The tensile moduli of the composite materials show significant improvements over the tensile moduli of the base polymers with increasing fibre content, Figure 3. SUMMARY A screwless extruder has been built based on a similar extruder intended for the extrusion of thermoplastics. Some of the advantages of this extruder include: complete lack of contact between moving parts, strong mixing action, shorter material residence times and the direct addition of natural fibres to the melt. The pressure developed during this extrusion process is low compared to that developed in conventional screw extruders. However, the laboratory prototype that has been built is smaller than the conventional screw extruders. Woodfibre-HDPE and woodfibre-PP composites have been successfully compounded by means of the elastic melt extruder. Mixing and dispersion of the
Screwless Extrusion of Natural Fibre-Reinforced Thermoplastic Composites
31
Wood-PP -
Wood-HDPE PP
—
15
20
25
30
-
HDPE 35
40
Fibre mass fraction (%)
FIGURE 2 Tensile strengths of woodfibre-PP and woodfibre-HDPE composites as a function of fibre content
15
20
25
30
Fibre mass fraction (%) FIGURE 3 Tensile moduli of woodfibre-PP and woodfibre-HDPE composites as a fimction of fibre content
45
32
Screwless Extrusion of Natural Fibre-Reinforced Thermoplastic Composites
constituents have been achieved in a short time due to intensive local shearing of the fibre-polymer mixture. Heat degradation of the fibres has also been minimised due to the heating of a small amount of feed material at any given time. Tensile properties of the composite specimens produced through granulation and injection moulding of the extrudates show reasonable improvements over the tensile properties of the base polymers. REFERENCES 1. 2.
3. 4. 5. 6. 7. 8. 9. 10. 11. 12.
13.
Chand, N., R. K. Tiwary and P. K. Rohtagi. 1988. "Structure - properties of natural cellulosic fibres an annotated bibliography," Journal of Materials Science, 23: 381-387. Groom, L.H., S. M. Shaler and M. Mott. 1995. "The mechanical properties of individual lignocellulosic fibres," in Virgin and Recycled Wood Fiber and Polymers for Composites. Proceedings of the Third Woodfiber-Plastic Composites Conference, 1-3 May, 1995, Madison, USA, pp. 33-40. Woodhams, R.T., Q. Thomas and D. K. Rodgers. 1984. "Woodfibres as reinforcing fillers for polyolefins," Polymer Engineering and Science, 24: 1166-1171. Beshay, A.D., B. V. Kokta and C. Daneault. 1985. "Use of wood fibers in thermoplastic composites II: Polyethylene," Polymer Composites, 6(4): 261-271. Zadorecki, P. and A. J. Mitchell. 1989. "Future prospects for wood cellulose as reinforcement in organic polymer composites," Polymer Composites, 10(2): 69-77. Bataille, P., L. Ricard and S. Sapieha. 1989. "Effects of cellulose fibres in Polypropylene composites," Polymer Composites, 10(2): 103-108. Balatinecz, J J. and R. T. Woodhams. 1993. "Wood-plastic composites: Doing more with less," Journal of Forestry, 11: 22-26. Sain, M.M., B. V. Kokta and C. Imbert. 1994. "Structure-property relationships of wood fiber-filled Polypropylene composite," Polymer-Plastic Technology and Engineering, 33(1): 89-104. Bhattacharyya, D., M. Bowis and K. Jayaraman. 2003. "Thermoforming of woodfibre-polypropylene composite sheets," Composites Science and Technology, 63: 353-365. Lu, J.Z., Q. Wu and H. S. McNabb. 2000. "Chemical coupling in wood fiber and polymer composites: A review of coupling agents and treatments," Wood and Fiber Science, 32(1): 88-104. Maxwell, B. and A. J. Scalora. 1959. "The elastic melt extruder- works without screw," Plastics Engineering, 10:107-114, 202-210. Bledzki, A.K., V. E. Sperber and O. Faruk. 2002. "Natural and Wood Fibre Reinforcement in polymers," Rapra Review Reports, Volume 13 number 8, Rapra Technology, Shrewsbury, United Kingdom. Bowis, M.E. 1997. Thermoforming Woodfibre-Polypropylene Composite Sheets. PhD thesis, Department of Mechanical Engineering, University of Auckland, Auckland, New Zealand.
Mechanical Properties of "Green" Composites Made from Starch-Based Biodegradable Resin and Bamboo Powder Hitoshi Takagi* Department of Mechanical Engineering, Faculty of Engineering, The University of Tokushima, Japan Ryuki Takura and Shinji Ochi Department of Ecosystem Engineering, Graduate School of Engineering, The University of Tokushima, Japan
ABSTRACT Recently, bamboo has been reevaluated from an environment-friendly viewpoint. The reason for this is that bamboo is typical of the yearly-renewable bioresource and that it inherently has an advantage in its high growing speed. With the increase in the volume of the bamboo used in the near future, it is anticipated that the quantity of bamboo powder discharged in various cutting processes will increase accordingly. It is therefore important to develop an adequate technology utilizing the bamboo powder. For this purpose, we developed totally biodegradable "green" composites with bamboo powder and a starch-based resin. These "green" composites were fabricated by the hot-pressing using at 10 MPa and 130°C for 10 minutes. It is found that the "green" composites fabricated with bamboo powder of 0.5 mm in diameter had an acceptably high flexural strength and high flexural modulus. It is also shown that an alkali treatment applied to the bamboo powder affects the mechanical properties of the "green" composites with an increased flexural strength of about 20 percent. Furthermore, it was seen from biodegradation tests that the "green" composites could be easily biodegrade as they are buried in compost environment.
INTRODUCTION Since general-purpose plastics have several features such as lightweight, durable and, above all, easy to mold, the plastics are used abundantly in commercial goods in our daily life. However, the waste disposal of the used plastic becomes an urgent social problem with increasing both mass production and mass consumption of the plastics. Since general plastic products are non-biodegradable and are chemically stable in the environment, the increases in the volume of waste plastics become one of the biggest sources for a landfill shortage problem. hi these situations, as an approach to solve the waste problem, the use of biodegradable resin products is supposed to reduce the volume of plastic waste in landfills [1]. In addition, the biodegradable resin fully produced from natural crops, such as corn, * Corresponding Author, 2-1 Mmajijosanjima-cho Tokushima 770-8506, Japan, fax: +81-886-656-9082 and e-mail:
[email protected]
34
Mechanical Properties of "Green" Composites
sugar beet and potato, has been recognized as a circulating material, because after full biodegradation, the biodegradable resin breaks down into water and carbon dioxide, and then these two substances are absorbed into crops again. Biodegradable plastic products should be rapidly replacing petroleum-based plastics in many industrial applications. The cost of the biodegradable resin, however, is higher than that of general-purpose plastics, and moreover, the biodegradable resins have relatively poor mechanical properties as compared with those of general-purpose plastics. Especially, since there exists no high-strength biodegradable material, the social demand for the development of high-strength biodegradable composite materials is continually expanding. hi recent years, a wide variety of research projects have been performed on the biodegradable composite materials, which are composed of a biodegradable resin and biodegradable reinforcement, such as natural plant fibers, and are often called as "green" composites [2-6]. The use of natural fibers as reinforcement for polymer composites contributes not only to strengthening of matrix but also reducing the total material cost of the composites, since many common plant fibers are much cheaper than biodegradable resins. Since the combination of natural plant fibers and thermoplastics is attractive from an ecological viewpoint, many researches tried to use a wide variety of natural plant fibers; bamboo [6-8], hemp [3], MAO [4], henequen [5], cotton [9], flax [9], and pineapple [10]. Bamboo fiber is recognized as one of the most attractive candidates for strengthening natural fiber [11]. It has been proposed, therefore, that bamboo has several advantages such as (1) the environmental load is small, since it is yearly renewable and its growing speed is fast, thus it is easy to regenerate after cutting, and (2) the bamboo fiber has relatively high strength as compared with other natural fibers such as jute, cotton, etc. The discharge volume of the bamboo powders (saw dust) is expected to increase year by year with increasing the amount of consumption of bamboo fibers and bamboo products. However, no studies have ever tried to utilize the bamboo powders discharged from bamboo factories as ingredient in "green" composites. hi this study, we tried to fabricate "green" composites made from starch-based biodegradable resin and bamboo powders. The mechanical properties of the composites are evaluated using tensile tests and fiexural tests. The effect of alkali treatment of the bamboo powder on the mechanical properties of "green" composites was also investigated. EXPERIMENTAL METHODS Raw Materials A water-dispersive biodegradable resin (Miyoshi Oil & Fat Co., Ltd., CP-300) was used as matrix material. This resin has several features; high-strength, emulsion type with average particle size of 6 jum and non-volatile components of 40% by weight. The bamboo powder is prepared from the saw dust of Moso-bamboo (Phyllostachys pubescens) discharged from a bamboo factory. Bamboo powder less than 0.5 mm in diameter was obtained by using a sieve with a mesh size of 0.5 mm. Alkali Treatment of the Bamboo Powder hi order to increase the adhesion strength of fiber/matrix interface, we applied alkali treatment to bamboo powder. Since it is the surface treatment method for using alkali treatment abundantly even in the inside for naturalfiber,in this study, the bamboo powder was treated with alkali by following procedures. First, aqueous NaOH solution of 5% by
Mechanical Properties of "Green" Composites
35
weight was prepared, and then bamboo powder was put in the alkali solution. The fraction of bamboo powder to the solution is fixed to 10% by weight. After stirring of the mixture at room temperature for 100 minutes, the bamboo powder was taken out, and then rinsed with distilled water. Bamboo powder was dried at 105°C for 2 hours in an oven. Sample Preparation Method The mixture of bamboo powder and biodegradable resin, which are weighed out into a predetermined composition, was well mixed in a beaker of 500 milliliter, then put into a rectangular metal frame, followed by drying at 105°C for 2 hours in an oven. Next, the metallic molds, which have the dimensions of 100x15 mm for flexural test and 100x10 mm for tensile test, were used to hot-press the dried sample. The samples were hot-pressed at 130°C and 10 MPa for 10 minutes. Then, the metallic mold was cooled to room temperature using an electric fan. The density of "green" composites with bamboo powder of 66.6% by weight was 1.18 g/cm3 and the water content was 3% by weight. Mechanical Testing Both tensile tests and flexural tests were carried out using an Instron Mechanical Tester (Model 5567) in order to evaluate the mechanical properties of "green" composites reinforced with bamboo powder. The flexural strength was measured using a three point flexural test, with a span length of 50 mm and a crosshead speed of 1.0 mm / min. Shapes of specimen for flexural test were 100 mm in length, 15 mm in width and 1.5 mm in thickness. The tensile test was also carried out at a crosshead speed of 1.0 mm / min. The specimen configuration for tensile test was 100 mm in length, 10 mm in width, 1.5 mm in thickness, with a gage length of 30 mm. Furthermore, 2 mm thick aluminum tabs were glued at the both ends of the tensile specimen to prevent from damage introduced during fixing. Biodegradation Testing Biodegradation tests were carried out by using a home-use garbage-processing machine (Hitachi, Ltd., BGD-150). After trial operation for several days in order to activate microorganisms, "green" composite sample was placed within the processing media (wood chips), and the biodegradation behavior of the composites was investigated. The sample was put into a nylon baggy net to avoid the difficulty in recovering of degraded sample scattered in the media, and then this net including sample was buried in the compost media. After biodegradation test, the appearance of the sample was examined by using stereoscopic microscope and optical microscope. EXPERIMENTAL RESULTS AND DISCUSSIONS Effect of the Bamboo Powder Content on the Bending Strength A representative flexural stress-deflection diagram for composites with different bamboo powder content is shown in Fig. 1. Data for a neat resin sample is also given in this graph for reference. It can be seen that flexural strength and flexural modulus increase with increasing the bamboo powder content, and that maximum deflection decreases with increasing the content. It is therefore clear that the strengthening of the biodegradable resin is accomplished by the addition of bamboo powder.
36
Mechanical Properties of "Green" Composites
Figure 2 shows the relationship between both flexural strength and flexural modulus and bamboo powder content. It can be seen that both flexural strength and flexural modulus linearly increase with increasing the bamboo powder content. At the content of 66.6% by weight, both flexural strength and flexural modulus show peak values of 36.7 MPa and 4.3 GPa, respectively. These strength values are higher than those of bamboo powder particle boards reported elsewhere (flexural strength of 27.0 MPa and flexural modulus of 4.0 GPa) [12]. In addition, Shibusawa reported that the flexural strength of bamboo particle board produced using small pieces of bamboo was 39 MPa and that this value was higher than the regulated flexural strength of 19.6 MPa in JIS (Japan Industrial Standards) [13]. Thus, it is shown that the "green" composites have also enough strength comparable to the regulation value of JIS. Effect of the Bamboo Powder Content on the Tensile Strength The representative tensile stress-strain diagram for the composite with different bamboo powder content and that for neat resin are show in Fig. 3. A similar dependence of bamboo powder content on mechanical properties has been found in this figure. The relationship between both tensile strength and Young's modulus and bamboo powder content is shown in a Fig. 4. It can be seen that both tensile strength and Young's modulus increase with increasing the bamboo powder content. The "green" composites with bamboo powder content of 66.6 % by weight have a maximum tensile strength of 25.8 MPa and a maximum Young's modulus of 2.9 GPa. Effect of Alkali Treatment The chemical surface treatment of natural fibers is of the great importance and is considered as a low-cost method, therefore a considerable number of studies have been made on alkali treatment [14-16]. Figure 5 shows the result offlexuraltest for the "green" composites fabricated using bamboo powder with and without alkali treatment. It can be seen that alkali-treated composites shows highflexuralstrength showing the improvement about 20% and large maximum deflection. The reason for these increases in mechanical properties is that adhesion strength between bamboo powder and resin increases by alkali treatment of bamboo powder and that the increases in surface roughness derived from alkali treatment enhance the stress transfer between bamboo fiber and resin. The decrease in lignin on the surface of bamboo powder directly contributes to increases in strength, because alkali treatment has an action of removing hydrophobic lignin existing on the surface vicinity of natural fiber as reported by Mohanty et al. [14]. Biodegradation Behavior The results of biodegradation tests shows that sample buried in composting media for seven days macroscopically breaks down into a lot of small pieces. Especially, the superficial resin of the sample is preferentially decomposed, and the surface morphology changes from flat surface to rugged one. Similar experimental results were reported by Luo and Netravali for poly(hydroxybutyrate-co-hydroxyvalerate) resin composted in soil [17]. It is thus concluded from the biodegradation results that the "green" composites are biodegradable. CONCLUSIONS Environment friendly biodegradable "green" composites were made from bamboo powder and a starch-based biodegradable resin. Their tensile andflexuralproperties were
Mechanical Properties of "Green" Composites
37
evaluated, and the effect of alkali treatment on their strength was also investigated. As the result, the "green" composites with bamboo powder of 66.6% by weight has flexural strength of 36.7 MPa and flexural modulus of 4.3 GPa. These mechanical properties exceed the regulation of 18 MPa in Japan Industrial Standards (JIS) for a high strength particleboard. These composites, therefore, have a potential to apply to commercial products. The effectiveness of the alkali treatment for bamboo powder was confirmed experimentally, showing the improvement about 20% in flexural strength in comparison with the strength for the composites fabricated with untreated bamboo powder. REFERENCES 1.
2. 3.
4.
5.
6.
7. 8.
9.
10.
11.
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13. 14.
15.
16.
17.
Cutter, C. N., J. L. Willett, and G. R. Siragusa. 2001. "Improved Antimicrobial Activity of Nisin-Incorporated Polymer Films by Formulation Change and Addition of Food Grade Chelator," Letters in Applied Microbiology, 33(4): 325-328. Netravali, A. N. and S. Chabba. 2003. "Composites Get Greener," Materials Today, 6(4): 22-29. Takagi, H. and S. Ochi. 2002. "Characterization of High-Strength 'Green' Composites Using Manila Hemp Fibers and Starch-Based Resin," presented at the Third Japan-Canada Joint Conference on New Applications of Advanced Composites (JCJC-JJI), May 14-15, 2002. Takagi, H., C. W. Cindy, and A. N. Netlavali. 2002. "Tensile Properties of Starch-Based 'Green' Composites Reinforced with Randomly Oriented Discontinuous MAO Fibers," presented at the International Workshop on "Green" Composites, November 19-20, 2002. Chabba, S. and A. N. Netravali. 2002. "Characterization o f Green" Composites Using Henequen Fibers and Modified Soy Protein," presented at the International Workshop on "Green" Composites, November 19-20, 2002. Takagi, H. and R. Takura. 2003. "The Manufacture and Mechanical Properties of Composite Boards Made from Starch-Based Biodegradable Plastic and Bamboo Powder," Zairyo, 52: 357-361 (in Japanese). Chen, X., G. Qipeng and M. Yongli. 1998. "Bamboo Fiber-Reinforced Polypropylene Composites: A Study of the Mechanical Properties," Journal of Applied Polymer Science, 69: 1891-1899. Okubo, K. and T. Fujii. 2002. "Eco-Composites Using Bamboo and Other Natural Fibers and Their Mechanical Properties," presented at the International Workshop on "Green"' Composites, November 19-20, 2002. Jiang, L. and G. Hinrichsen. 1999. "Flax and Cotton Fiber Reinforced Biodegradable Polyester Amide Composites, 1 Manufacture of Composites and Characterization of Their Mechanical Properties," Die Angewandte Makromolekulare Chemie, 268(1): 13-17. Luo, S. and A. N. Netlavali. 1999. "Mechanical and Thermal Properties of Environmental-Friendly 'Green' Composites Made from Pineapple Leaf Fibers and Poly(hydroxybutyrate-co-vallerate) Resin," Polymer Composites, 20(3): 367-378. Ochi, S., H. Takagi, and R. Nflri. 2002. "Mechanical Properties of Heat-Treated Natural Fibers," presented at the International Conference on High Performance Structures and Composites, March 11-13,2002. Fujimoto, Y., Y. Nakashima, J. Kawabe, Y. Mataki, and S. Kumon. 1998. "Manufacturing of Particleboard from Bamboo Particles - Influence of Particle Size on Properties of Bamboo Particleboard," Mokuzaikogyo, 53(5): 212-217 (in Japanese). Shibusawa, T. 1998. "New Material -Bamboo-," Ringyogijutsu, 672: 23-26 (in Japanese). Mohanty, A. K., M. A. Khan, S. Sahoo, and G. Hinrichsen. 2000. "Effect of Chemical Modification on the Performance of Biodegradable Jute Yara-Biopol® Composites," Journal of Materials Science, 35(10): 2589-2595. Ray, D. B. K. Sarkar, and N. R. Base. 2002. "Impact Fatigue Behaviour of Vinyleester Resin Matrix Composites Reinforced with Alkali Treated Jute Fibers," Composites Part A: applied science and manufacturing, 33(2): 233-241. Valadez-Gonzales, A., J. M. Cervantes-Uc, R. Olayo, and P. J. Herrera-Franco. 1999. "Effest of Fiber Surface Treatment on the Fiber-Matrix Bond Strength of Natural Fiber Reinforced Composites," Composites PartB: engineering, 30(3): 309-320. Luo, S. and A. N. Netlavali. 2003. "A Study of Physical and Mechanical Properties of Poly(hydroxybutyrate-co-hydroxyvalerate) during Composting," Polymer Degradation and Stability, 80(1): 59-66.
Mechanical Properties of "Green" Composites
38
IS
BP66.6%-BDP33.3% BP50.0%-BDP50.0% BP33.3%-BDP66.6% BDP(CP-300)
50
1
• Bending strength A Bending modulus
PH
S 40 § 30
}
1 20
i
bo
I 10 5 10 Deflection (mm)
-
•
f o
' .
]
i
I
x
25
1
1
50
75
(BDP:CP-300)
Content of bamboo powder (mass%)
FIGURE 1 Typical stress-deflection curves as a function of content of bamboo powder.
FIGURE 2 The relationship between flexural strength and flexural modulus and content of bamboo powder.
1
BP66.6%-BDP33.3% BP50.0%-BDP50.0% BP33.3%-BDP66.6% •--BDP100%(CP-300)
30
-
30
t
20
o Tensile strength ^ Young's modulus
20
I
0 10
10
\
'£•-;• 0.01
• • ''
0.02 Strain E
:
f
I
1
T
.-
f
:
8
-4
o
2
i
1 0.03
0
0
25
50
75
0
CBDP:CP-300)
Content of bamboo powder (mass%
FIGURE 3 Typical stress-strain curves as a function of content of bamboo powder.
FIGURE 4 The relationship between tensile strength and Young's modulus and content of bamboo powder.
1 PQ
2
4 6 8 Deflection (mm)
10
FIGURE 5 Effect of alkali treatment on the flexural behavior of "green" composites.
Part II
Characterisation
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Effect of Fibre-Orientation on Mechanical Properties of Polypropylene Composites S. Houshyar, R. A. Shanks*, A. Hodzic** Applied Chemistry, RMIT University, GPO Box 2476V, Melbourne, 3001, Australia
ABSTRACT The mechanical and structural properties of a composite consisting of polypropylene fibres (PP) in a random poly(propylene-co-ethylene) (PPE) has been prepared and its properties evaluated. The mechanical properties of PPE laminates were largely determined by the presence of a complex fibre orientation distribution in the composite. The results showed that all-PP composites demonstrated enhanced stiffness and creep resistance with decrease in the orientation angle, 9, between the fibre axis and the load direction; the friction coefficient decreased linearly as 9 increased from 0° to 90°. Composites with zero angle (unidirectional composites) between fibre axis and applied load (9 = 0°) possess the highest stiffness, because the fibre efficiency is inherently strong for this system as all the fibres are able to contribute to the composite stiffness and to carry the load. An increase in 9 leads to a decrease in composite stiffness, which indicates that by increasing 9, a lower proportion of the applied load is transferred to the fibres and thus it is not completely distributed among the fibres. The composite with 8 = 90° showed the highest relative creep, whereas the composite with 9 = 0° displayed the lowest creep. In general, the relative creep increased steadily with increasing 9; also the increment in 9 produced a decrease in the creep modulus, and it was observed up to 90°. Composites with woven fabric showed the best properties, after the unidirectional composites, due to the interlaced structure of the woven fabric. The bundles of plain fibre cloth restrict displacement in each other and result in high stiffness. In addition the mechanical properties of the composite with random fibres are somewhat between the composite with 0°< 9 < 90°, due to alignment of fibers along any direction in the composite.
INTRODUCTION There are some important parameters, which affect the properties of thermoplastic composites. These are: (a) the fibre-matrix bond (b) the type and volume of fibre, (c) the distribution and orientation of fibres within the matrix, (d) the ability to obtain isotropic and orthotropic behavior if required (e) ease of handling of the reinforcement and a (f) suitable method of manufacture [1,2,3]. A crucial parameter for design of composite material is the fibre orientation, as it controls the mechanical response. In order to obtain the favoured materials properties for a particular application, it is important to know the function of performance ' * Correspondence Author, Applied Chemistry, RMIT University, GPO Box 2476V, Melbourne, 3001, Australia, Tel and fax: +613 9925 2122, robert.shanks (ftjrmit.edu.au ** Current address: School of Engineering, James Cook University, Townsville, Australia
42
Effect of Fibre-Orientation on Mechanical Properties
change with the fibre orientation under given loading conditions. The mechanical properties of polymer composite systems as a function of fibre orientation have been studied in the past [4,5]. Krenchel [6] presented an analytical approach, which suggested that the mechanical properties of a laminated composite depend on the individual mechanical properties of its constituents. The mechanical properties of these thermoplastic composites can be modified by changing fibre orientation. EXPERIMENTAL The materials employed in this investigation were random poly(propylene-coethylene) matrix (PPE) (density, p = 0.905 gem"3 , MFI = 0.8 dg/min, melting temperature= 147.5 °C, ~ 5 % ethylene) and PP fibres, woven and non-woven mat (fibre diameters = 50 (j.m, fibre tensile strength = 250-350 MPa, tensile modulus = 4.7 GPa and length = 2-3 cm, fabric modulus = 5.2 GPa with plain weave). The fibres were washed with acetone to remove any processing lubricants. The fibres were obtained from Melded Fabrics Pty Ltd, the PPE from Basell Australia Pty Ltd. According to DSC results [7], 155 -160 °C was selected as the molding temperature range. A heated press was used in two stages. In the first stage, long PP fibres, woven or non-woven mat were distributed according to Table 1, on top of a PPE film and placed between two Teflon sheets, then pressed at 155 -160 °C for 5-7 minutes. TABLE I. Designations of the samples with different orientation angles
Sample Number of Plies Ply one
Cl
C2
C3
C4
C5
C6
C7
C8
One& three Woven
One& three Random
One& three
Three
Three
Three
Three
0°
0°
45°
0°
45°
Ply two
Woven
Random
0°
90°
0°
45°
90°
Ply three
Woven
One& three Nonwoven Nonwoven Nonwoven
Random
0°
0°
45°
0°
45°
After initial pressing, 11-14 kPa pressure was applied for 8-10 minutes. In the second stage, three layers of the composite were laminated together under the same conditions as in the first stage, to provide a more uniform composite. The PP fibre concentration in the composite was 50 %v/v. The mechanical properties were measured with a Perkin-Elmer DMA7e in extension and three-point bend mode at 25°C. The static force was scanned from 100 mN to 8000 mN at 100 mN/min and 0.0 mN to 6400 mN at 400mN/min for three-point bend and extension modes, respectively. The samples were cut from sheets, with dimensions 1x12x5 mm and 1x10x5 mm for three-point bend and extension modes, respectively. Creep recovery was recorded with a Perkin-Elmer DMA7e in extension mode at 25 °C with constant time (~15min) for creep and recovery. To investigate the effect of different PP fibre orientation in one layer composites, creep tests were carried out with a constant static force of 2000 mN at room temperature and duration time of 25 minutes. A small residual load (~ 200 mN) was left on each specimen in the unload condition to maintain the integrity of the loading assembly. For composites with three plies, creep tests were carried out with the same parameters except for the values of static force of 3000 mN and residual load of 400 mN. The samples were cut from the sheets with dimensions 1x10x5 mm. In order to test the reliability of experimental
Effect of Fibre-Orientation on Mechanical Properties
43
results, at least five specimens for each type of composite were used for creep recovery behavior tests. RESULT AND DISCUSSION PP-PPE composite with one ply The effect of fibre orientation on the mechanical properties of PP-PPE composites was analysed by DMA. Mechanical properties such as tensile modulus of the composites were measured and the results are shown in Figure l(a,b). Figure l(b) shows that the composite with zero angle between fibre axis and applied load (9 = 0°) posses the highest stiffhess. The fibre efficiency is inherently strong for this system as all the fibres are able to contribute to the composite stiffness and to carry the load. An increase in 6 leads to a decrease in composite stiffness, which indicates that by increasing 8, a lower proportion of the applied load is transferred to the fibres and it is not completely distributed among the fibres. In other words, a decrease in the fibre efficiency results in a decrease of the composite stiffness. In the composite where 9 = 90°, the fibres cannot act as a reinforcement in the matrix and fibre efficiency is minimal. The fibres cannot support the matrix, which flows and deforms under the stress. 1400-1 12001000-
— re o. 5 ~~ UJ
800-
6004002000-
Different type of fibre orientation
FIGURE 1. Tensile modulus of the one layer composite system different type of fibre orientation
On the other hand, the composite reinforced with the woven fabric (Figure 1 (a)) shows an inherently strong stiffness, due to the well-proportioned structure of the woven fabric. The bundle of plain fibre cloth restricts displacement of each fibre and result in a high stiffness. Also, the results provide information on the composites with non-woven and random mat. Although the composite with non-woven mat provides better stiffness than the composite with random fibres due to the high entanglement of fibres in some parts, they have the same properties in both directions. In addition, the modulus of the composite with random fibres is somewhat between the composites with 0° < 9 < 90°, due to alignment of fibres along any direction in the composite.
Effect of Fibre-Orientation on Mechanical Properties
44 PP-PPE composite with 3 plies
Figure 2 shows the tensile modulus as a function of fibre orientation in the composite with three plies. There is a decrease in the tensile properties of the composite with increasing 9 of each ply. In both data sets, one and three plies, it can be assumed that the composite stiffness clearly expresses a dramatic increase with decreasing 9. This is due to the fact that the reinforcement imparted by the fibres allows stress transfer from the matrix to the fibres. The load transmittance is a function of fibre orientation and magnitude of the fibre-matrix interfacial bond. As the angle (6) increases, the stiffness of the composite will decrease and lead to breakage of the composite at lower stress [5,6]. According to these results, different fibre orientations can be used in each ply depending on the direction of the applied load on the composite. D longitudinal E3 Transverse
Different type of fibre orientation
FIGURE 2. Tensile modulus of the three layers composite
CREEP BEHAVIOUR The effect of PP fibre orientation on the creep response of the composite is shown in Figure 3. The load transmittance is a function of fibre orientation and fibre/matrix interfacial bond. The composite with 6 = 90° showed the highest relative creep value, whereas the composite with 9 = 0° displayed the lowest value. In general, the relative creep increased steadily with increasing 9; also the increment in 9 produces a decrease in the creep modulus, and is observed up to 90°. As 6 increased, fibres were not able to contribute to the stiffness of the composite, which resulted in a decrease of the composite stiffness at lower stress. The results clearly indicate that the creep resistance is dependant on fibre orientation and the quality of the fibre-matrix interface.
Effect of Fibre-Orientation on Mechanical Properties
45
Time (min)
FIGURE 3. Creep response of the composite with different orientation
CONCLUSION The effect of fibre orientation on the creep and mechanical properties of PPE has been analyzed by static and dynamic mechanical analysis [DMA], The results clearly indicate that there is a decrease in composite modulus by increasing 6, between the fibre axis and applied load direction, due to a decrease in the contribution of the fibres in carrying the applied load. The study proves that the composite with woven fabric has the best properties due to the stiffness of the reinforcement. ACKNOWLEDGEMENTS Financial support from International Postgraduate Scholarship (IPRS) is acknowledged. REFERENCES 1. N. Barkoula, J. Karger-Kocsis. 2002," Effects of fibre content and relative fibre-orientation on the solid particle erosion of GF/PP composites " Wear, 252, 80-87. 2. Y. Liang, S. Li, R. Zhang, S. Li. 1996." Effect of fiber orientation on a graphite fiber composite in single pendulum scratching," Wear, 198, 122-128. 3. Karger-Kocsis, J. 1995. Polypropylene: Struct. Blends Composites, Vol. 1, Chapman & Hall, UK, pp. 1-50. 4. M.A. Lopez-Manchado, M. Arroyo. 2000. "Thermal and dynamic mechanical properties of polypropylene and short organic fiber composites," Polymer, 41, 7761. 5. J. Rosenthal. 1992. "A model for determining fibre reinforcement efficiencies and fibre orientation in polymer composites, " Polymer Composites, 13(6), 462-466. 6. William, D.J. 1994. Materials Science and Engineering, an Introduction, John Wiley and sons, pp. 106. 7. S. Houshyar , R. A. Shaiiks. 2003. "Morphology, thermal and mechanical properties of polypropylene fibre-matrix composites," Macromolecular Materials and Engineering, 288, 599.
Friction and Wear Properties of Potassium Titanate Whiskers Reinforced PTFE Composites Xin FENG *, Donghui CHEN, Xiaohong JIANG, Shenghua SUN, Xiaohua LU Nanjing University of Technology, P. R. China Yuansheng JIN National Key Laboratory of Tribology, Tsing-Hua University, P. R. China
ABSTRACT Potassium titanate whiskers (PTW) is a promising reinforcer with good abrasion proof properties. Tribological performance of PTW reinforced PTFE composites (PTW-PTFE) was investigated. The results showed that addition of PTW caused an increase in wear resistance of PTFE. The wear of PTW-PTFE composites was only about one tenth of PTFE. Compare to PTFE, both of the limit loading and the limit sliding speed of PTW-PTFE increase 10% and 60% respectively. The friction coefficient and hardness of PTW-PTFE were slightly changed. The friction coefficient of PTW-PTFE was much steadier than that of PTFE. Both PTFE and PTW-PTFE had lower wear mass loss but higher wear traces surface at 200 °C than that at 25 °C. The PTW with larger size had better wear resistance. SEM showed that PTW were effective in impeding large-scale fragmentation of PTFE, thereby reducing the wear.
INTRODUCTION Polytetrafiuoroethylene (PTFE) is a thermoplastic with a variety of high performance like extremely low friction coefficient and high temperature stability. However, PTFE exhibits poor wear, abrasion resistance and severe creep deformation, leading to early failure and leakage problems in sealing material [1, 2]. Potassium titanate whiskers (PTW, K2O-6TiO2) is a promising reinforcer for the composites, due to its unique properties such as outstanding mechanical performance, excellent heat resistance and good abrasion proof properties. Its tensile strength is higher than carbon fibers. PTW is tiny which brings about a micro-reinforcing effect in PTW composites. It is suitable to produce ware with complex shape, high precision and high degree finish of surface [3, 4]. hi this paper, tribological performance of PTW-PTFE of various filler contents at different load, sliding speed was investigated. EXPERIMENTAL Materials The PTFE powder (30um diameter) was provided by Shanghai Tianyuan resin * Corresponding Author, College of Chemical engineering, Nanjing University of Technology, Nanjing 210009, P.R.China, Tel:0086-25-83588063, Fax:0086-25-83588063, e-mail:
[email protected]
Friction and Wear Properties of Potassium Titanate Whiskers
47
group (China). PTW, with an average diameter 1.86/xm and length 10.47 jtm, was supplied by Shengyang Jinjian Co. in China. PTW was modified with surface modifier [4]. Preparation of PTW- PTFE composites sample is same as Glass Fibers-PTFE composites. Friction and Wear Testing Friction and wear tests were carried out in an Optimol SRV( Germany) on the dry friction condition. Before testing, specimens ( $24mm><7.95mm ) should be running-in against steel ball (GCrl5, $ 12.5mm) . Parameters of test were load(50N, 200N), friction duration (25min), frequency (lOHz), stroke (2mm), sliding speed (0.04m/s). Parameters of running-in were friction duration (5min), load (30N corresponded to test load 50N, 50N corresponded to test load 200N), frequency (lOHz), stroke (2mm), sliding speed (0.04m/s). The wear mass loss of specimens was detected by weighing with an accuracy of 0.1 mg. Scanning electron microscope (JSM-6300, Japan) was used for studying worn disc surfaces. RESULTS AND DISCUSSION Friction and Wear Properties at 25 °C Effect of PTW Content on Friction and Wear Properties Table 1 showed that addition of PTW to PTFE caused a significant improvement of wear (mass loss) not only under load 50N but also 200N. The wear of PTW-PTFE composites was just one tenth of pure PTFE, while friction coefficients and hardness values were slightly affected. Therefore, PTW-PTFE composites is a potential sealing material. TABLE I PTW content effect on friction coefficients (fi) and wear and hardness and ratio of SPTFE and SPTW of PTW-PTFE composite PTW / wt% 0 5 10 15 20
Shore hardness (HD/15) 63.5 63.8 63.9 64.2 64.5
c
/c
° PTFE ' ° PTW
1 2.455 1.335 0.732 0.517
n Load /50N 0.156 0.158 0.153 0.164 0.162
wear /mg Load /200N 0.153 0.153 0.152 0.154 0.153
Load /50N 7.5 0.8 0.8 0.8 1.2
Load /200N 17.1 1.6 1.9 2.1 2.3
It was obvious from Table 1, when content of PTW in PTFE was more than 5wt%, the wear increased. This phenomenon was different from conventional filler such as Glass fibers and Carbon fibers and copper powder with 20~40wt% optimum content in PTFE [2]; however which was similar to the nano-composites [5]. This phenomenon caused by tiny size of PTW. Specific surface area of PTW( SPTW )is 0.713m2/g, it is 2.5 times as large as that of Glass fibers (Its diameter and length are 6.7^m and 117.3/xm respectively) . Table 1 indicated that when PTW content reached 20wt%, the ratio of SPTFEI SPTIV was very small. It means that PTW was very poorly
48
Friction and Wear Properties of Potassium Titanate Whiskers
wrapped by PTFE (SPTFE is 0.605m2/g). At this state, PTW tended to aggregate with each other and the cohesive strength of interface in PTW-PTFE weakened rapidly. Variation of Friction Coefficients of PTW-PTFE and Pure PTFE
0.16o
|
|
-AAA-
_
1
-
0.15-
lonci
!
- -
Load=50N ^
A
A
-
0.16- Load=200N
Defficie
Figure 1 showed variation of friction coefficient of 5wt%PTW-PTFE composites and pure PTFE with friction time under 50N and 200N respectively, which indicated that the variation value of friction coefficient of PTW-PTFE was smaller than pure PTFE. The former was 0.150-0.159, the later was 0.120-0.160. It revealed that PTW made the friction coefficient of PTFE composites steadier.
0.15
6
/
A
W
AA'
A'
0.14-
0.14i
0.13-
—•—5wt% PTW-PTFE - A — PTFE
A
0.130.12-
n 19 10
15 20 time/min
25
30
— 5wt% PTW-PTFE -PTFE
A^
10
15 20 time/min
25
30
FIGURE 1 The variation of friction coefficient of 5wt%PTW-PTFE and PTFE with friction time under 50N and 200N
Load Limit and Sliding Speed Limit Table 2 exhibited that both of the loading limit and the sliding speed limit of 5wt%PTW-PTFE increased 10% and 60% respectively compare to PTFE. It indicated that addition of PTW improved the PV limit value (The PV limit value is defined as the product of the system pressure and the surface velocity), so that material can work under more rigorous condition. TABLE II Load limit and Sliding speed limit of 5wt%PTW-PTFE and PTFE
Specimen PTFE 5wt%PTW-PTFE
Sliding speed /m-s"1 0.04 0.04
Load limit Load Vlimit at load /N limit 0.169 500 550 0.209
Load /N 50 50
Sliding speed limit Sliding speed limit at speed / m-s"1 limit 0.06 0.257 0.096 0.296
Effect of Temperature on Friction and Wear Properties Table 3 showed that wear properties of material were different at 25 °C and 200 °C. Wear properties included wear (mass loss, mg), wear traces surface ( mm2 ). The study indicated that wear traces surface of PTW-PTFE and PTFE at 200 °C was higher than that at 25 °C; however wear (mass loss) at 200°C is slightly lower than that at 25 °C.
Friction and Wear Properties of Potassium Titanate Whiskers
49
There are two causes resulting material failure under work condition. First, wear leads seal material mass loss, and then seal material becomes thin. Second, elevated temperature leads to seal material soft and dent, and then seal material becomes thin, however, at same time the mass of seal material has not been lost. Therefore, it is notable that both wear mass loss and wear traces surface should be as criterion whether the material is out of work or not. Especially when the friction temperature is elevated, the criterion of wear traces surface is very important. TABLE III Specimen
PTFE PTFE 10wt%PTW-PTFE 10wt%PTW-PTFE
Wear properties of PTW-PTFE and PTFE at 25 °C and 200 °C Surrounding Temperature IV 25 200 25 200
0.23: 0.22: 0.21 % o
o o ••8
Load /N
Frequency /Hz
Stroke /mm
50 50 200 200
10 10 10 10
2 2 2 2
Sliding speed / m-s' 0.04 0.04 0.04 0.04
Wear /mg 3.8 3.7 1.9 1.4
WearTraces Surface /mm2 12.46 21.55 27.34 41.90
Load: 50N Frequency: 10 Hz Stroke: 2mm Step-risen temperature (°C)
0.20^
0.19-1 0.180.17: 0.16: 0.15: 10
FIGURE 2
20
30
40 50 time/min
60
70
80
Change of friction coefficient of 10wt% PTW-PTFE with increased temperature
Figure 2 was the curve of friction coefficient change of 10wt% PTW-PTFE with increased surrounding temperature, which showed that the change of friction coefficient was only 0.015 (from 0.152 to 0.167) when temperature from 25°C to 240 °C, but friction coefficient increases suddenly when temperature more than 280 "C.The reason was 280 °C closed to the melting point of PTFE 320 "C.The surface becomes soft, which resulted contact surface increasing quickly and then a lot of adhesive point was produced. Hence, the friction coefficient increased sharply [6]. Effect of PTW Size on Wear Properties Figure 3 showed that the size of PTW also influenced the tribological properties. PTFE composites reinforced by larger size PTW had higher abrasive resistance than by smaller size PTW not only under 50N but also under 200N. The thick and thin PTW were with an average diameter 1.86^.m, 0.77jiim and length 10.47/xm, 11.12/xm
Friction and Wear Properties of Potassium Titanate Whiskers
50
respectively in figure 3. 2.42.22.01.8-
] ThickPTW 3 ThinPTW
— 1.6O) 1
r 1.2-1 IB
1
> 0.80.60.40.20.0 50N
200N
10wt%PTW-PTFE
FIGURE 3 Effect of PTW size on Wear properties
SEM Analysis of Worn Surfaces Figure 4 (a) and (b) showed micrographs of worn surfaces of PTFE and 20wt%PTW-PTFE composite respectively under 50N load, at 0.04m-s"1 sliding speed and 25 °C, which revealed that worn surface of PTFE was with severe crack, however worn surface of 20wt%PTW-PTFE was very smooth. It indicated that addition of PTW prevented PTFE from large-scale fragmentation generated and grown, thereby reducing fatigue wear, and then increasing the abrasive resistance.
(a) PTFE (b) 20wt%PTW-PTFE FIGURE 4 SEM photographs of worn surfaces of PTFE and 20wt%PTW-PTFE
CONCLUSIONS 1. Filler PTW is effective in impeding large-scale fragmentation of PTFE, thereby addition of PTW causes PTFE composites an increase in wear resistance, meanwhile makes the friction coefficient steadier, while the friction coefficient and hardness is slightly affected. 2. The wear of PTW-PTFE composites was only about one tenth of PTFE.
Friction and Wear Properties of Potassium Titanate Whiskers
51
Compare to PTFE, both of the limit loading and the limit sliding speed of PTW-PTFE composites increase 10% and 60% respectively. It indicated that PTW-PTFE composites with higher PV limit value can work under more rigorous condition. 3. There is the highest wear resistance for PTW-PTFE composites when content of PTW is about 5wt%. 4. Both PTFE and PTW-PTFE have lower wear mass loss but higher wear traces surface at 200 °C than that at 25°C.It is notable that both wear mass loss and wear traces surface should be as criterion whether the material is out of work or not. 5. The size of PTW also influences the tribological properties. The PTW with larger size has better wear resistance. ACKNOWLEDGMENTS Authors appreciate the Outstanding Youth Fund of National Natural Science Foundation of P. R. China (29925616) and National High-tech Research Development Program(863 Program: 2003AA333010) and The Tribology Science Fund of National Tribology Laboratory (SKLT02-2) REFERENCES 1.
Khedkar, J., I.Negulescu, and E. I. Meletis. 2002. "Sliding wear behavior of PTFE composites, " Wear, 252 (5-6): 361-369.
2.
Bijwe, J., S. Neje, J. Indumathi, and M. Fahim. 2002. "Friction and wear performance evaluation of carbon fibre reinforced PTFE composite, " Journal of Reinforced Plastics and Composites, 21(13): 1221-1240.
3.
Feng X.i J. Z. Lii,> X. H. Lu. et al. 1999, "Application of potassium titanate whisker in composite," ACTA MATERIAE COMPOSITAESINICA, 16(4): 1-7
4.
Lii, J. Z., and X. H. Lu. 2001. "Elastic Interlayer Toughening of Potassium Titanate Whiskers-Nylon66 Composites and Their Fractal Research," J. Appl. Polym. Set, 82(2):368-374.
5.
He, C. X., L. P. Shi, and H. P. Shen. 2000. "Friction and Wear Properties of Nanocrystalline A12O3 Filled-PTFE Composite," Tribology, 20(2):153-155.
6.
Wu, R.J. 1998. The Surface and Interface of Polymer. Beijing: Science Press
Study on Jute Fiber Reinforced Polypropylene (PP) Composite Ma Sheng and Wang Yimin State Key Laboratory for Chemical Fibers and Polymer Materials Donghua University, Shanghai, 200051, P. R. China Zhang Anding and Ding Xin College of textile, Donghua University, Shanghai, 200051, P. R. China
ABSTRACT Jute fiber reinforced PP composites are studied in this article. The composites are made of jute fiber as reinforcement for thermoplastic polypropylene. The effect of different fiber content and different fiber length on composite properties, such as the tensile strength, the flexural strength and impact strength are studied. The process conditions for making the composite and the invalidation theory of the composite are also discussed. The results indicate that the comprehensive properties of the composites with 12mm fiber length and 10% fiber weight content are improved obviously. INTRODUCTION Composite materials made of cellulose-based fibers such as jute fiber demonstrate remarkable environmental and economical advantages. This is because the cellulosic fibers have many advantages, such as low cost, low density, high specific strength and modulus, limited requirements on processing equipments, no health problems, ease of fiber surface modification, and availability as renewable natural resources. And this composite combines good mechanical properties with a low specific mass and offers an alternative material to glass-fiber reinforced plastics in some technical applications. However, their high level of moisture absorption, poor wettability by non-polar plastics, and insufficient adhesion between untreated fibers and the polymer matrix frequently exhibit unsatisfactory mechanical properties. Despite this intrinsical disadvantages, the study of jute fiber-reinforced plastic composites is continually increasing. For example, some scientists and experts of India have given lots of studies about jute fiber reinforced thermoplastic composites. Through these earlier papers, it is summarized that mechanical performance of a fiber-reinforced plastic composite primarily depends on three factors: (a) strength and modulus of the reinforced materials, (b) strength and chemical stability of the matrix, and (c) effectiveness of the bond between the fibers and the polymer matrix in transferring stress across the interface. Most of the composite properties are strongly depended on microstructure parameters such as fiber length, fiber content and
* Corresponding author, Donghua University, Tel: 86-21-62379785, Fax: 86-21-62379309, E-mail address:
[email protected]
Jute Fiber Reinforced Polypropylene Composite
53
alignment and packing arrangement of fibers. In randomly oriented short fiber composites, the fiber length and fiber content play an important role in determining their mechanical performance. The optimal length of the jute fiber depends on the bonding between the fiber and the resin. And similarly, the volume fraction of the fiber lies on the interfacial bonding exists between the fiber and the matrix. Several types of thermoplastics like polyethylene, polypropylene and polystyrene have been reported as matrices for natural fiber composites. These polymers may have different agglutination towards the fiber due to the difference in their chemical structure. As a consequence, the reinforcement effect of the fibers in these matrices may vary widely. It is well known that some polymers are susceptible to reinforcement; others are not with respect to particular filler. For fiber filled composites it has been found that the higher the flow limit of the matrix the lower the critical length of the fiber. This paper selected polypropylene (PP) as the matrix. However, the studies reported in the literature on the use of jute fiber as reinforcement in thermoplastic polymer like PP have been scanty. This can be attributed to the invalidation behavior for jute fiber reinforced PP composite is less well understood than for glass fiber reinforced plastic composite because of the lack of systematic and detailed information available. Base on this reason, this article deals with the effects on the mechanical properties of jute fiber reinforced PP composite with different fiber length and fiber content. By comparison, the parameter and process optimization of the composite is introduced in this paper. EXPERIMENTAL Materials Jute fiber was obtained from Zhejiang Jute Co., Ltd, China. And PP was gained from Jin Shan Petrochemical Corporation Ltd, Shanghai, China. The properties of jute fiber and the matrix PP are presented in Table 1. Jute fiber was cut to 3mm, 5mm and 10mm in length respectively. And the average value of the diameter of the jute fiber is 54um. The melt flow index (MFI) of PP is 5g/10min. TABLE I Properties of jute fiber and PP
,, . . , Materials
_ ., Density , 4
Tensile ,, strength
Tensile , . modulus
Elongation ., , at break
Moisture . regain
rpastern
-
/MPa
/GPa
/%
/%
r
J/°
1.41 0.91
424 28.5
14.13 0.867
2.54 10.34
12.6 —
4.24 —
/g cm
,.
I/O
Jute fiber PP
Sample Preparation A screw mixing technique was used to make the jute fiber reinforced PP composite. The composite containing 10, 20 and 30% by weight of fiber was prepared using fiber of length in 3mm, 5mm and 10mm. The temperature of the screw head is controlled no more than 180°C because of the degradability of the jute fiber. The tensile specimen, the flexional specimen and the impact specimen were prepared by injection
54
Jute Fiber Reinforced Polypropylene Composite
molding according to the standard of ASTM D63814, ASTM D790 and ASTM D256. Testing of Composite Tensile testing and flexural testing of thermoplastic composite was carried out using a Universal testing machine of Tianshui Sansi of China at a crosshead speed of 5mm/min and a gauge length of 100mm and 95mm respectively. The tensile modulus and elongation at break of the composite were calculated from the stress-displacement curve. At least five specimens were tested for each set of samples. Impact testing was carried out using a pendulum RESILIMPACTOR of Italy. RESULTS AND DISCUSSIONS Effect of Fiber Content Table II Effect of jute content on mechanical properties of jute/PP composite
B D Materials PP C 29.88 29.82 29.78 Tensile strength/MPa 28.5 1.875 1.634 1.157 Tensile modulus/GPa 0.867 34.68 39.2 40.7 Flexural strength/MPa 30.16 1.184 1.768 2.5 Flexural modulus/GPa 0.776 4.95 4.75 6.57 4.78 Impact strength/J • m"2 The weight content of the jute fiber in the composite is 10, 20 and 30%; and corresponding volume content is about 5.6, 13.1, and 20.5%. The effect of jute content on mechanical properties of jute fiber reinforced PP composite is presented in Table II. From the results it is observed that all mechanical properties except impact strength improve with the adding jute fiber to the resin. From T Table II, the most remarkable observations are: (a) The tensile strength of the composite increases by about 4.5% compare to PP. However, the improvement quantity is slightly falling with increase of jute content. And it was easy to find that the improvement is the most remarkable when the fiber weight content is 10%. (b) The flexural strength of jute fiber reinforced PP composite improves greatly compare to PP, and the increase of the flexural strength with increase of jute fiber. The flexural strength increases by 35% compare to PP. (c) Similarly, both the tensile modulus and the flexural modulus improve more or less. The improvement quantity is increasing with increase of jute fiber for the tensile modulus and contrarily for the flexural modulus. This can be found clearly from figure 1.
Jute Fiber Reinforced Polypropylene Composite
2
4
6
55
8 10 Elongation/%
FIGURE 1 The stress-elongation curve of the composites with different fiber content Note: Apresents for PP, and B, C and D present for 10%, 20%, and 30% jute/PP composite respectively
In contrast to the tensile and flexural properties, the work of impact test is found to be pessimistic. The impact strength of the composite has a slightly decline compare to PP. The reason for low impact strength of jute/PP composite is due to the high bonding of the fiber with polypropylene resin, which resulted in the fracture of fiber at the crack without any fiber pull-out.
Effect of Fiber Length In this paper, the jute fiber was cut 3mm, 5mm and 10mm respectively. Generally speaking, the fiber reinforced thermoplastics composite showed an increasing trend in their mechanical properties with the fiber length. However, the flexural properties of the composite demonstrate an unusual change. Table III shows all the variation in tensile and flexural and impact properties of the thermoplastics composite. Table III Effect of jute length on mechanical properties of jute/PP composite
Materials PP Tensile strength/MPa 28.5 Tensile modulus/GPa 0.867 Flexural strength /MPa 30.16 Flexural modulus /GPa 0.776 Impact strength /J • m"2 6.57
B 29.66 1.833 35.8 1.334 5.78
C 29.88 1.875 34.68 1.184 4.78
D 29.99 1.976 37.7 1.365 4.41
From Table III, the jute/PP composite shows an enhancement in their tensile strength and modulus by increasing the fiber length from 3mm to 10mm, whereas the flexural strength and modulus go through a decrease with the fiber length from 3mm to 5mm and followed a significant increase with the fiber length from 5mm to 10mm. This decreasing trend in flexural properties of the composite may be due to the jute fiber didn't completely disperse and the fiber-to-fiber contact occurred. In terms of
56
Jute Fiber Reinforced Polypropylene Composite
impact strength, the change rule is approximate with effect of fiber content.
Elongation/%
FIGURE 2 The stress-elongation curve of the composites with different fiber length Note: This time A presents for PP, and B, C and D present for 3mm, 5mm, and 10mm jute/PP composite respectively
Figure 2 shows the stress-elongation curve of the composite with the change fiber length. CONCLUSIONS In this paper, the mechanical properties of short jute fiber reinforced PP composite have been investigated as a function of fiber content and fiber length. The various parameters lead to the various properties of the composite. As a consequence, the reinforcement effect of the fiber to the resin varies widely. By comparison, the composite with 10mm fiber length and 10% fiber weight content is improved most obviously.
REFERENCES [1] A.C.Karmaker, J.A.Youngquist. 1996. "Injection Molding Polypropylene Reinforced with Short Jute Fibers," Journal ofApplied Polymer Science, 62(8): 1142-1151. [2] Karmaker A. C, Schneider J. P. 1996. "Mechanical performance of short jute fiber reinforced polypropylene," Journal of Materials Science Letters, 1(2): 201-202. [3] A.K.Rana, A.Mandal, B.C.Mitra, R.Jacobson. 1998. "Short Jute Fiber-Reinforced Polypropylene Composites: Effect of Compatibiliar," Journal of Applied Polymer Science, 69: 329-338. [4] Rana A.K., Mitra B.C, Banerjee A.N. 1999. "Short jute fiber-reinforced polypropylene composites: dynamic mechanical study," Journal of Applied Polymer Science, 71(4): 531-539. [5] Jochen Gassan, Andrzej, K.Bledzki. 1999. "Influence of Fiber Surface Treatment on the Creep Behavior of Jute Fiber-Reinforced Polypropylene," Journal of Thermoplastic Composite Materials, 12: 388-398. [6] Saha AK, Das S, Bhatta D, Mitra BC. 1999, "Study of jute fiber reinforced polyester composites by dynamic mechanical analysis," Journal of Applied Polymer Science, 71(9): 1505-1513. [7] Ghosh P, Bose NR, Mitra BC, Das S. 1997. "Dynamic mechanical analysis of FRP composites based on different fiber reinforcements and epoxy resin as the matrix material," Journal of Applied Polymer Science, 64(12): 2467-2472.
Mechanical and Thermal Properties of Composites of Epoxy Resin Derived from Kraft Lignin Filled with Cellulose Particles Masahiro Funabashi*, Shigeo Hirose National Institute of Advanced Industrial Science and Technology, Japan Hyoe Hatakeyama Fukui University of Technology, Japan
ABSTRACT A mixture of ester-carboxylic acid derivatives (KL polyacid, KLP A) was obtained by reaction of an ethylene glycol solution of Kraft lignin (KL) and succinic anhydride in the presence of a catalytic amount of dimethylbenzylamine at 100 °C. Cellulose particles were added to the above mixture with various mixing ratios from 0 to 60 wt%. A prepolymer of lignin-based epoxy resin was prepared by a reaction of the mixture of KLPA and cellulose particles with ethylene glycol diglycidyl ether (EGDGE) at 100 °C. The above mixtures were molded into sheets at 130 °C for 5 hours. The mechanical properties of the samples were investigated by tensile tests using plate type specimens. The elastic modulus and tensile strength were determined by the tensile tests. Thermal properties of composite samples were measured by differential scanning calorimetry (DSC) and thermogravimetry (TG). Glass transition temperatures of samples were determined by DSC. Thermal decomposition temperatures and mass residues were determined by TG. The values of strength and modulus determined by tensile tests were maximum at cellulose content of 60 wt% for composite samples with cellulose particles of 25 mm diameter. Thermal properties such as peak temperatures of thermal decomposition and glass transition temperature determined by TG and DSC were not affected by cellulose contents.
INTRODUCTION Polymer composites consisting of polymer matrices and fillers are used in various industrial fields, such as the automobile, construction, and aerospace industries, etc., since they have high specific modulus, high specific strength and are lightweight, easy to process and corrosion resistant. Polymer composites are difficult to dispose of, because they are highly durable. Large amounts of bio-waste are produced in the agricultural and industrial fields. The above problem can be solved by the production of biodegradable polymer composites using plant components from bio-waste. Biodegradable polymers can be prepared by the combination of polymers derived from plant components and fillers from solid parts of plants [1-6]. Plant components such as saccharides and lignin * Corresponding Author, National Institute of Advanced Industrial Science and Technology, AIST Tsukuba Central 5, Tsukuba, Ibaraki 305-8565, Japan, Tel. +81-(0)29-861-4584, Fax. +81-(0)29-861-6250,
[email protected]
58
Properties of Composites of Epoxy Resin
have been recognized as important raw materials for polymer processing, since they are produced abundantly in nature. Polyurethane composites consisting of the polyurethanes, which were derived from saccharides and lignin, and solid plant materials were also studied at our laboratory [1-6]. Biodegradable polymer composites consisting of the poly-lactones, such as poly(lactic acid) and poly(caprolactone), and cellulose fillers were also studied in our laboratory [7-8]. In this study, the polymer composites were prepared by combining epoxy resin derived from Kraft lignin (KL) and cellulose particles. The mechanical and thermal properties of the above composite samples were investigated. EXPERIMENTAL Materials Kraft lignin (KL) was used as a lignin in this study. KL was dried in a vacuum oven at 60°C for 2 days. Cellulose particles, Avicel (Asahi Chemical Industry CO., LTD) were used in this study. Avicel (PH-M25) was used as fillers of composite samples, where the average diameter of particles was 25 |^m. Sample preparation An ethylene glycol solution of KL was reacted with succinic anhydride in the presence of a catalytic amount of dimethylbenzylamine at 100 °C. A mixture of ester-carboxylic acid derivatives (KLPA) was obtained by the above reaction. Cellulose particles were added to the above mixture with various mixing ratios from 0 to 60 wt% and were mixed well by a mechanical mixer at 70 °C for 2 hours. A prepolymer of lignin-based epoxy resin was prepared by a reaction of KLPA with ethylene glycol diglycidyl ether (EGDGE) at 100 °C for 20 min. The above mixtures were poured into mold to form sheets at 130 °C for 5 hours. The sheets were removed from the mold after cooling and were cut into plate shaped specimens for density measurements and mechanical tests. Density measurements The apparent density (/?a) was determined as the ratio of sample weight to the apparent volume of the plate shaped specimens. Tensile tests Mechanical properties of samples were investigated by tensile tests using a Shimadzu AG-10TB. The sizes of plate type specimens were 15 mm wide, 3 mm thick and 150 mm long. Span was 100 mm. Test speed was 5 mm min"1. The tensile strength and tensile modulus were determined from the stress-strain curves of tensile tests. Tensile strength (Oi) was defined as the maximum stress of the stress-strain curves. Elastic modulus (Et) was defined as the gradient of the linear part of stress-strain curve. The specific strength ((Tts) and the specific modulus (E^) were calculated as Oi and Et divided by apparent density of samples, /?a. Differential scanning calorimetry (DSC) DSC was carried out using a Seiko DSC 220 at a heating rate of 10 °C min"1 in the
Properties of Composites of Epoxy Resin
59
temperature range from -60 to 70 °C. The initial glass transition temperature (Tig) of samples was determined from DSC curves according to the method reported by Hatakeyama [9]. Thermogravimetry (TG) TG was carried out in a nitrogen flow at flow rate 300 ml min 1 using a Seiko TG 220 at a heating rate of 10 °C min"1 in the temperature range from 30 to 550°C. The peak temperatures (DTn and DT^) were observed from derivative thermogravimetry (DTG) curves. Mass residue of samples at 500°C (MR500) was determined from TG curves.
RESULTS AND DISCUSSION Density measurements The relationship between content of cellulose particles and density of samples is shown in Figure 1. Density of samples increases with increasing cellulose content when content reached 40 wt%, and then density slightly decreases with increasing content. In the range of cellulose content from 0 to 30 wt%, the increase of cellulose makes the density increase. At the same time, the viscosity of mixture of epoxy pre-polymer and cellulose particles increases with increasing cellulose content. It was thought that when content reached 30 wt%, the air bubbles could not escape during the sample preparation. The presence of void in the samples caused the density decrease at content more than 40 wt%.
0
20
40
60
80
content /wt% FIGURE 1 Relationship between content of cellulose and density of samples; cellulose particles, PH-M25
Mechanical tests The mechanical properties of samples were investigated by tensile tests using plate-shape specimen. The strength and modulus of samples are shown in Figure 2. Both values of strength and modulus of samples increase with increasing cellulose content, and when content exceeds 40 wt%, both values rapidly increase. The reinforcement effect of cellulose particles can be clearly observed as shown in Figure 2. These results indicated
60
Properties of Composites of Epoxy Resin
that KL epoxy resin used in this study could be used as a good adhesive for polymer composites.
1500
V) _3 3 •D
O
E
20
80
40 60 content /wt%
FIGURE 2 Relationships between content of cellulose and, strength and modulus of samples by tensile tests; cellulose particles, PH-M25
Thermal properties measurements The thermal properties of samples were investigated by TG and DSC analyses. TG curves and derivative TG (DTG) curves were obtained by TG analysis. Relationship between cellulose content and mass residues at 500 °C (M?5Oo) determined by TG analysis are shown in Figure 3. MRsoo increases with increasing cellulose content. The above results suggest that cellulose molecular changed to component in the residue after heating up to 500 °C. Peak temperatures of DTG curves were also determined by TG. DTG curve of KL epoxy sample without cellulose particles showed one peak at 376 °C. The DTG curves of KL epoxy samples with cellulose particles of PH-M25 showed two peaks at almost the same temperatures, that is, the higher temperature DTA2 was ca. 377 °C and the lower temperature D7d2 ca. 315 °C. The height of peak at DTdi increases with increasing cellulose content. In contrast, the height of peak at T)T&2 decreases with increasing content.
20
40
60
80
content /wt% FIGURE 3 Relationship between content of cellulose particles and mass residues at 500 °C in DTG curves; cellulose particles, PH-M25
Properties of Composites of Epoxy Resin
61
The initial glass transition temperatures (7jg) and heat capacity gap at Tig were determined by DSC analysis. 7ig of all the composite samples with cellulose particles of PH-M25 including pure epoxy sample were almost the same ca. -17 °C. The heat capacity gaps at Tig (ACP) of composites samples decreased linearly with increasing cellulose content and the extrapolated value of ACP at 100 wt% content was estimated as 0.
CONCLUSIONS Elastomeric polymer composites of lignin-based epoxy resin filled with cellulose particles were prepared by a reaction of an ethylene glycol solution of Kraft lignin and succinic anhydride with ethylene glycol diglycidyl ether in the presence of a catalytic amount of dimethylbenzylamine. Mechanical and thermal properties of the composite samples were investigated by the tensile tests, TG and DSC. Tensile strength and tensile modulus increase with increasing content of cellulose particles and reach the maximum values at cellulose content 60 wt%. Results of thermal analyses by TG and DSC indicated that there is no interaction between epoxy polymer and cellulose particles detected by the thermal analyses.
REFERENCES 1.
2.
3.
4.
5.
6.
7. 8.
9.
D. Kamakura, H. Hatakeyama, H. Kasahara, S. Hirose and T. Hatakeyama, Thermal and mechanical properties of polyurethane composites containing wood particles, the proceedings of 10th International Symposium on Wood and Pulping Chemistry, 1999, 3,442 H. Hatakeyama, D. Kamakura, S. Hirose and T. Hatakeyama, Biodegradable polyurethane composites containing coffee bean parchments, "Recent Advanced in Environmentally Compatible Polymers", J. F. Kennedy, G. O. Phillips, P. A. Williams and H. Hatakeyama, Eds., Woodhead Publishing Ltd., 2001, p.191 M. Funabashi, S. Hirose and H. Hatakeyama, Thermal and mechanical properties of polyurethane composites containing residue from palm oil production, the proceedings of 5th Pacific Rim Bio-Based Composites Symposium, Canberra, 2000, 591 M. Funabashi, S. Hirose, M. Sibaja, M. Moya and H. Hatakeyama, Thermal and mechanical properties of polyurethane composites consisting of pineapple molasses and banana fibers, the proceedings of USM-JIRCAS Joint International Symposium "Lignocellulose- Material of the Millennium: Technology and Application", Penang, 2001, 203 M. Funabashi, S. Hirose, T. Hatakeyama and H. Hatakeyama, Effect of filler shape on mechanical properties of rigid polyurethane composites containing plant particles, Macromolecular Symposia, 2003, 197,231-241 M. Funabashi, S. Hirose and H. Hatakeyama, Mechanical properties of polyurethane composites using fibers of oil palm empty fruit bunches, the proceedings of 3rd Asian-Australasian Conference on Composite Materials, Auckland, 2002, 345 M. Funabashi and M. Kunioka, Composites consisting of poly(e-caprolactone) and cellulose fibers directly molded during polymerization by yttrium triflate, Green Chemistry, 2003, 5,591 M. Funabashi and M. Kunioka, Biodegradable Composites of Poly(lactic acid) with Cellulose Fibers Polymerized by Aluminum Triflate, the proceedings of 1st IUPAC International Conference on Bio-based Polymers, Saitama, 2003, P2-1 T. Hatakeyama and F. X. Quinn, Thermal analysis: fundamentals and applications to polymer science 2nd edition, John Wiley & Sons, 1999, pp.59
Effects of Microcracks and Surface Roughness on Thermal Oxidation of Carbon-Fiber Reinforced Polyimide Composite Huang-Kuang Kung and Hung-Shyong Chen Graduate Institute of Mechatronic Engineering Cheng Shiu University, Taiwan, R.O.C.
ABSTRACT In high temperature applications, the oxidation of polymer composites will lead to micro structure change and mechanical property degradation and both of them have harmful effects on service life. In the literature, some researchers have suggested the fiber-matrix interface model to explain the discrepancy while others believed it had something to do with the surface preparation. In this research, a microstructure-based oxidation model with microcrack and surface roughness is proposed to predict the high-temperature oxidation of fiber-reinforced polymer composite. Consequently, predictions concerning high-temperature oxidation are favorably supported by experimental data.
INTRODUCTION Many studies on the high-temperature thermal oxidation of polyimide-matrix composites have focused on polyimide-matrix composites. Bowles [1] and Nowak [2] evaluated both the effects of different fiber reinforcements on the stability of oxidation and the properties of various fiber-reinforced PMR-15 composites. Scola et al. [3,4] studied changes in mechanical properties and the associated degradation mechanisms of a series of graphite-fiber/PMR-15 composites during isothermal aging at 316 °C (600 °F). Bowles [1], Nam and Seferis [5-7] took the principal directions of the material into account in investigating the anisotropic nature of thermal oxidation in a composite system. Furthermore, oxidation may induce chemical and microstructural changes, cause loss of material, and crack material [8]. Nam and Seferis[7] studied a unidirectional bismaleimide/carbon fiber composite, and showed that the oxidation rate of a composite may be determined from oxidation rates in the principle material directions. Alston [9] and Scola et al [3,4] found that the weight loss of a composite exceeds that of the neat resin. The findings in [3-4,9] contradict the expectation that the oxidation of a composite should be lower than that of neat resin owing to the shielding of high thermo-resistance fibers. In the literature, some researchers have suggested a fiber-matrix interface model to explain the discrepancy[8,10]. However, others believe that it is associated with the preparation of the surface [5-7].
* Corresponding Author, 840, Cheng-Ching Rd., Neausong, Kaohsiung 833, TAIWAN, R.O.C, Tel: +886-7-7310555; Fax: +886-7-7337100, E-mail address:
[email protected]
Effects of Microcracks and Surface Roughness on Thermal Oxidation
63
THEORETICAL DEVELOPMENT Microstructure-based oxidation models are applied to evaluate the anisotropic oxidation of the fibers and the matrix and considering aspects of the micro structure. The oxidation correction factors may be included to account for the additional oxidation area, leading to a transverse oxidation weight loss, Aw'r) of,
where A^ and A^J are the actual and apparent oxidation area of matrix in the transverse direction; AfT) and AfTJ are the actual and apparent oxidation area of fiber in the transverse direction ; A ^ and A ^ are the microcrack-related oxidation area for matrix and fiber in the transverse direction, respectively. The ratio of actual matrix oxidation area, A^, to apparent matrix oxidation area, A(JJ, for the matrix in the transverse composite direction can be easily shown to be, bL + R
L bL
'V n
«£1
(2)
=
where R is the radius of the fiber; R^x is the surface roughness in the transverse direction, and b is half the mean distance between fibers. For the oxidation of the fiber, neglecting any loose fibers on the surface, a similar procedure yields, n A
f
f
ji
-Af-^L—2
V
where AfT) is the actual fiber oxidation area and AjJ is the apparent fiber oxidation area. The microcrack-induced oxidation area may relate to crack density, crack length and crack depth. Then, the microcrack-induced oxidation area for matrix and fiber in the transverse direction can be written as, Amd
( O
_
?
_
(T) „ (T)r
(7-)
(7)
(A\
(T) A
*
where c(dT)is the microcrack density in the transverse direction ; c, ( r | is the average microcrack length in the transverse direction', c[T) is the average microcrack depth in the transverse direction ; r^' is the geometry-related correction factor for matrix in the transverse direction ; rf > is the geometry-related correction factor for fiber in the transverse direction. Including the effects of surface roughness and microcracks, the isothermal composite weight change per unit apparent oxidation area in the axial direction of a
64
Effects of Microcracks and Surface Roughness on Thermal Oxidation
composite may be expressed using the modified rule of mixtures as, A(A)
A™
A\A) fa
A{A)
(6)
fa
where A(A) and AmAJ are the actual and apparent oxidation area of matrix in the axial direction ; A(A) and A(fA) are the actual and apparent oxidation area of fiber in the axial direction ; , 4 ^ and Affare microcrack-related oxidation area for matrix and fiber in the axial direction, respectively. Following the same procedure as used for the transverse oxidation model, the ratio between the actual matrix oxidation area and the apparent matrix oxidation area in the axial oxidation of the composite is,
(7) (7)
where S^ is the surface roughness of the composite in the axial direction, and A(nA) and A^fJ are the actual and apparent matrix oxidation areas in the axial direction, respectively. Using a similar approach as taken to the fibers, 71
A
Afa
2
— =l
(8)
ER2 4
where A{A) and A(fA) are the actual and apparent fiber oxidation areas in the axial direction, respectively. Similarly, the microcrack-induced oxidation area for matrix and fiber in the axial direction can be written as, AA) A(A)
AA) fd
~AAT A fa
~;
d
(A) = 2C
"
C
I
-m
~*
(A) (A) C r
"
(A)
f
where c(dA)is microcrack density in the axial direction I c'^'is average microcrack length in the axial direction ; c[A) is average microcrack depth in the axial direction ; r^A) is the geometry-related correction factor for matrix in the axial direction ; r{fA) is the geometry -related correction factor for fiber in the axial direction. EXPERIMENTS Composite panels of carbon fiber/PEEK are cut by a water-cooled diamond-plated saw. The specimens had nominal dimensions of 25 mm long, 25mm
Effects of Microcracks and Surface Roughness on Thermal Oxidation
65
wide and 3mm thick. Silicon carbide CC-Cw emery papers with 80, 100, 120, 240, 400, 600, 800 and 1200 grit respectively, and lum alumina paste were used to polish the surface of the composite. All surfaces of specimens were checked using an optical microscope to ensure that they had been thoroughly polished. Average measurements were obtained using three of specimens to eliminate experimental error. Theoretically, the surface roughness should be the same in all directions on the surface since specimens are isotropic. However, the reinforced fibers make the surface roughness of composite specimens anisotropic. The surface roughness can be defined at the point at which the profile curve is perpendicular to the movement of stylus. The surface roughness of the composite was measured using Mitutoyo Surftest-4 and all the values of Ra, R2 and Rmil were recorded. The cut-off value was 0.8 mm and the traversed length was 4.8 mm, six times the cut-off value, for all measurements. The pre-polished specimens (polished with 80, 100, 120, 240, 400, 600, 800 and 1200 grit and lum alumina paste) were placed on the work stage to measure their surface roughness. RESULTS AND DISCUSSIONS The surface roughness parameters of the Carbon Fiber / PEEK composite are determined for specimens polished with different grits of emery papers. The finest surfaces of the specimens are polished with 1 um alumina paste. Figure 1 plots the surface roughness of the Carbon Fiber/ PEEK composite vs. emery grit size in the axial and transverse directions. The transverse surface roughness consistently exceeds the axial surface at any given grit level. The G3O-5OO/PMR-15 oxidation data in a parallel study [10] are used to verify the surface-roughness oxidation model. All specimens were hand-polished down to the 600 grit level. The corresponding surface roughness R^ and R^ at 600 grit are obtained from Fig. 1 as 3.34 /urn and 2.61 jum, respectively. The development of microcracks of PMR15/G30-500 subjected to 316°Cfor 1000 hours in the axial surface can be observed in Figure 2. The density, length and depth of microcracks are increasing with the exposure time. Figure 3 shows the microcrack density evolution of PMR15/G3O-5OO subjected to 316°Cin the axial direction. As can be seen in the figure, up to 1000 hour, the microcrack density still increasing rapidly. Figure 4 shows the statistic measurement of the average microcrack length and depth of PMR15/G30-500 composite. The average length of microcrack evolves increasingly with time in the first stage and then levels off at 400 hour. The restriction of growing of microcrack length may be due to the specimen width limited in 3 mm for current experimental data. The value of geometry-related correction factors r,(nA) and rjA) are assumed to be unity. Based on the data of Figures 1, 3 and 4, the predictions of weight loss flux AmlcA) of PMR15/G30-500 with the effect of surface roughness and microcrack-related oxidation at 316°C are presented in Figure 5. Compared with experimental data, the prediction of the rule of mixture is the least accurate. As shown in Figure 5, predictions with the effect of surface roughness only, and the effect of surface roughness and microcrack have better agreement with experimental results.
66
Effects of Microcracks and Surface Roughness on Thermal Oxidation
Emery grain size (jim)
FIGURE 1 Surface roughness of Carbon Fiber/ PEEK composite vs. emery grain size.
FIGURE 2 Microcrack observation of PMR15/G3O-5OO subjected to 316°C for 1000 hours.
FIGURE 3 Microcrack density of PMR15/G30-500 subjected to 316 " C on the axial surface.
FIGURE 4 Average microcrack length and depth of PMR15/G30-500 subjected to 316 "C .
Effects of Microcracks and Surface Roughness on Thermal Oxidation
67
Rule of Mixture ~~
Prediction w/ Roughness Only Prediction w/ Roughness & Damage
FIGURE 5 Predictions and experimental data of weight loss flux Am*"' of
PMR15/G30-500.
CONCLUSIONS 1. The fibers are more resistant than the matrix to abrasion. Thus, the polished specimens of the composite might exhibit surface roughness during surface treatment. 2. The transverse surface roughness is consistently larger than the axial surface roughness at a given grit level, because of the fiber-reinforced geometry in the axial and transverse directions. 3. The longer the oxidation time, the more microcracks on the oxidation surface. Therefore, discrepancies between experimental data and predictions are expected, due to severe cracking on the surface. 4. Experimental data confirm the predictions of the high-temperature oxidation by the proposed surface roughness and microcrack model over those of the rule of mixtures. REFERENCES 1.
Bowles, K. J., 1992."Effect of Fiber Reinforcements on Thermo-Oxidative Stability and Mechanical Properties of Polymer Matrix Composites", SAMPE Quarterly, April, pp. 2-12. 2. Bowles, K. J. and G. Nowak, 1988."Thermo-Oxidative Stability Studies of Celion- 6000/PMR-15 Unidirectional Composites, PMR-15, and Celion-6000 Fiber", J. Composite Materials., 22, pp. 966-985. 3. Scola, D. A. and J. H. Vontell, 1991."Mechanical Properties and Mechanism of the Degradation Process of 316 C Isothermally Aged Graphite Fiber/PMR-15 Composites", Polymer Engineering Science, 31, pp. 6-13. 4. Scola, D. A. and M. Wai, 1994."The Thermo-Oxidative Stability of Fluorinated Polyimides and Polyimide/Graphite Composites at 371 °C", J. Applied Polymer Science, 52, pp. 421-429. 5. Nam, J. D. and J. C. Seferis, 1992. "Anisotropic Thermo-Oxidative Stability of Carbon Fiber Reinforced Polymeric Composites", SAMPE Quarterly, October, pp. 10-18. 6. Nam, J. D. and J. C. Seferis, 1991. "A Composite Methodology for Multistage Degradation of Polymers", Journal of Polymer Science, Part B, 29, pp. 601-608. 7. Nam, J. D. and J. C. Seferis, 1992. "Generalized Composite Degradation Kinetics for Polymeric Systems Under Isothermal and Nonisothermal Conditions", J. of Polymer Science, Part B, 30, pp. 455-463. 8. Skontorp, A. and S. S. Wang, 1995. "High-Temperature Anisotropic Thermal Oxidation of Carbon Fiber Reinforced Polyimide Composites: Theory and Experiment", The Tenth International Conference on Composite Materials (ICCM-10), Whistler, British Columbia, Canada, 14-18. 9. Alston, W. B., 198O."Resin/fiber thermo-oxidative interactions in PMR polyimide/graphite composites", Polymer Composites, 1, 66-70. 10. Skontorp, A., 1995. Ph.D. Dissertation, Department of Mechanical Engineering, University of Houston, Houston, TX, USA.
Effects of Fillers on the Tensile Properties of Polyimide Composite Films at Room and Cryogenic Temperatures Y. H. Zhang1'2, S.Y. Fu1*, M. Li1'2, Y. Li1'2, L.F. Li1, Q.Yan1 1 Cryogenic Materials Laboratory, Technical Institute of Physics and Chemistry Chinese Academy of Sciences, Beijing 100080, China 2Graduate School, Chinese Academy of Sciences, Beijing 100039, China
ABSTRACT Nano- and micro-filler reinforced polyimide composite films with a high thermal conductivity and a low thermal expansion while still remaining high modulus and strength are desirable in cryogenic applications. Polyimide composite films were prepared by incorporation of fillers such as clay and silica particles into polyimide matrix. The silica particles were made by sol-gel process. The tensile properties of polyimide composite films were studied at room and cryogenic temperatures (77K) taking into account the effects of filler contents for involved fillers. SEM study was carried out on the fracture surfaces of the polyimide composite films. The results for the dependence of the tensile properties of polyimide composite films at room and cryogenic temperatures were discussed on filler contents for the involved fillers. INTRODUCTION Polyimide (PI) is one of the most promising thermally stable polymers with good mechanical properties. With the rapid developments in space, superconducting magnet and electronic technologies, the cryogenic properties of PI films have recently drawn much attention. So far, remarkable progress has been made in syntheses of PI/MMT, Pl/mica and Pi/silica nanocomposites, and properties of PI nanocomposite films at room temperature have been extensively studied [1-6]. Nonetheless, the conclusions obtained at room temperature cannot simply be transferred to the cryogenic case. Moreover, data for these properties at cryogenic temperature cannot be derived from those obtained at room temperature. Thus, it is important and necessary to study the mechanical and thermal properties at cryogenic temperature of PI nanocomposites for cryogenic engineering applications. However, up to now little report has been presented of the cryogenic properties of the PI hybrid nanocomposite films. Lately, a series of polyimide hybrid films such as PI/MMT, Pi/mica and Pi/silica etc have been synthesized in our laboratory. In this paper, the tensile properties of polyimide composite firms were studied at room and cryogenic temperatures (77K) taking into account the effects of filler contents for the involved fillers. The results for the dependence of the tensile properties of polyimide nanocomposite films at room and cryogenic temperatures were discussed on filler contents.
* Corresponding author, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, P.O. Box 2711, Beijing 100080, P.R. China, Tel: +86-10-62659040/80669735; Fax: +86-10-62564049, Email: [email protected]/ [email protected]
Effects of Fillers on Tensile Properties of Polyimide Composite Films
69
EXPERIMENTAL WORK The hybrid nanocomposite films were synthesized in our laboratory. The polyimide was prepared from pyromellitic dianhydride (PMDA), 4, 4'—diamine—diphenyl ether (ODA) and the solvent of N, N—dimethylacetamide (DMAc). The PI/MMT composite films were prepared via intercalation method, and the Pi/silica hybrid films were synthesised by sol-gel process. The sizes of film specimens for the tensile tests were respectively 10 mm><90 mm (room temperature) and 10 mmxl20 mm (cryogenic temperature). The tensile properties of polyimide nanocomposite films at room temperature were measured by an Instron 1122 universal tensile tester at the loading rate of 50 mm/min, and the tensile testing at cryogenic temperature (77K) was performed using a Reger 20A universal testing machine at the loading rate of 2 mm/min. The thickness of films was 25-39 um, and the specimens were cut from free films. The gauge length was 50 mm. More than 6 samples were tested for each composition. RESULTS AND DISCUSSION The tensile strength, modulus and elongation at break of hybrid films with various MMT contents are shown in Figs. 1-3. The tensile strength and elongation at break of hybrid films with lower MMT content exhibited higher levels than that of the original neat polyimide film. It was observed in Fig. 1 that the tensile strength of hybrid films was higher than that of the pure PI film when MMT content was lower than 3 wt %, and then decreased with increasing MMT content at both room and cryogenic temperatures. The tensile strength at cryogenic temperature was generally higher than that at room temperature. An exception is that the tensile strength at cryogenic temperature was lower than that at room temperature for the case of 20 wt % MMT. The aggregations of MMT at a high MMT content would prick up the stress concentration more severely at cryogenic temperature than at the room temperature at the sites of PI/MMT interfaces in the PI/MMT hybrid composites because PI matrix became more brittle at cryogenic temperature and would easily form cracks as the applied load increased, bringing about a dramatic decrease in the composite strength. As shown in Fig. 2, the modulus increased with increasing MMT content at both room and cryogenic temperatures. Moreover, the modulus at cryogenic temperature is higher than that at room temperature. This is mainly due to the fact that the matrix modulus at cryogenic temperature is higher than that at room temperature because of the tight arrangement of PI molecules. The tensile elongation at break is shown in Fig. 3. It can be seen that at low MMT contents, the tensile elongation at break at cryogenic temperature is much lower than that at room temperature. On the other hand, at high MMT contents, the tensile elongation at break at cryogenic temperature is slightly lower than that at room temperature. This is caused by the fact that at high MMT contents, both the MMT content and MMT-PI matrix interface would dominate the failure of the composite. The interface adhesion strength is higher at cryogenic temperature than that at room temperature while the aggregations at cryogenic temperature would lead to earlier failure. As a result, the difference in the failure strain between at room and cryogenic temperature at high MMT contents was not so large as at low MMT contents. Moreover, it can be seen that when the MMT was at low contents (1-5 wt %), the elongation at break of the films was ^ 10 %, showing good ductility and usefulness for cryogenic engineering applications.
70
Effects of Fillers on Tensile Properties of Polyimide Composite Films
5
10 15 MMT content (%)
FIGURE 1 Effects of the clay content on the tensile strength of Pi/clay hybrid films at room and cryogenic (77K) temperatures.
5
10 15 MMT content (%)
FIGURE 3 Effects of the clay content on the elongation at break of Pi/clay hybrid films at room and cryogenic (77K) temperatures
0
5
10 15 MMT content (%)
FIGURE 2 Effects of the clay content on the tensile modulus of Pi/clay hybrid films at room and cryogenic (77K) temperatures
0
1
2 3 4 Silica Content (wt %)
FIGURE 4 Tensile strength of Pi/silica hybrid films at room and cryogenic temperature
Fig. 4 showed that the tensile strength of the hybrid films was higher at cryogenic temperaturre than at room temperature. This is because on the one hand, the molecules of polymer matrix tightly arranged at cryogenic temperature, the matrix played an important role in determining strength of the composites, leading to a higher tensile strength at cryogenic temperature than that at room temperature. On the other hand, the interface adhesion strength between silica particles and PI matrix was higher at cryogenic temperature because of higher compressive stress at the interfaces than that at room temperature, bringing about a higher hybrid composite strength at cryogenic temperature. When silica content was above 3 wt %, the tensile strength decreased at cryogenic temperature, this is because the silica particles pricked up the stress concentration in the Pi/silica hybrid composites and the matrix became more brittle at cryogenic temperature and easily bringing about formation of cracks and then a dramatic decrease in the composite strength as the silica particle content increased. Moreover, it was observed in Fig. 4 that the tensile strength of hybrid films increased with the increase of silica content up to a content of 3 wt %, and then decreased monotonically at cryogenic temperature. Fig. 5 displayed that the Young's modulus was improved by the addition of silica particles content at both room and cryogenic temperatures. Moreover, the modulus at cryogenic temperature is higher than that at room temperature. This is due to the fact that the matrix modulus at cryogenic temperature is higher than that at room temperature. Fig. 6 indicated that the tensile elongation at break was as a function of silica content.
Effects of Fillers on Tensile Properties of Polyimide Composite Films
71
The elongation at break showed a decreasing tendency with increasing the silica content. Moreover, it can be seen that the tensile elongation at break at cryogenic temperature was much lower than that at room temperature. This is because the matrix controlled the failure of the hybrid composite film, and the matrix fractured in a brittle manner at cryogenic temperature while in a relatively ductile mode at room temperature. cryogenic temperatun .room temperature
Silica Content ( w t % )
FIGURE 5 Tensile modulus of Pi/silica hybrid films at room and cryogenic temperature
• cryogenic temperatui 1 room temperature
2 3 silica Content (wt %)
FIGURE 6 Elongation at break of Pi/silica hybrid films at room and cryogenic temperature
CONCLUSIONS The cryogenic tensile properties of polyimide/clay and polyimide/silica hybrid films have been studied. It has been shown that the cryogenic tensile strength and Young's modulus could be effectively enhanced while the cryogenic elongation at break might maintain its level by the addition of clay and silica particles at appropriate particle contents. Moreover, the tensile strength and Young's modulus of the hybrid films at cryogenic temperature were generally higher than at room temperature while the elongation at break was lower at cryogenic temperature than at room temperature. There appeared to exist an optimal particle content that corresponded to the maximum cryogenic tensile strength for both Pi/clay and Pl/silica hybrid films. ACKNOWLEDGEMENTS The authors thank associate Professor Xishu Wang at Department of Engineering Mechanics, Tsinghua University for assistance in obtaining SEM micrographs. We would acknowledge that this work was funded by the Hundred Talents Program of Chinese Academy of Sciences ; Key Research Programme of Beijing City Science and Technology Committee (No H020420020230); National High Technical Research and Development Programme of China (No 2002AA306171); Foundation of State Key Lab of New Ceramics and Fine Processing (SKLNCFP) at Tsinghua University. Thanks are also given to Prof. S. Y. Yang etc. from Institute of Chemistry, CAS for their help in preparation of some samples. REFERENCES 1. 2. 3. 4. 5 6
A. Gu, S. Kuo, F. C. Chang. Journal ofApplied Polymer Science, 2001, 79: 1902. D. M. Delozier, R.A. Orwoll, J.F. Cahoon, J. S. Ladislaw, J.G. Smith Jr. J. W. Cornell. Polymer, 2003, 44:2231. G. H. Hsiue, J. K. Chen, Y. L. Liu. Journal of Applied Polymer Science, 2000, 76: 1609 C.V Avadhani,, Y. Chujo. Appl Org Chem, 1997, 11: 153. A. Morikawa; Y, Iyoku, M. Kakimoto, Y. Imrai. Polym J. 1992, 24: 107. L. Mascia, A. Kioul. Polymer, 1995, 36(19): 3649.
Processing Effects on Electrical Conductivity and Mechanical Properties of Particulate Composite Farshad Mohafezatkar, Vahid Haddadi-asl & Hossein Nazokdast Department of Polymer Engineering, Amirkabir University P.O.Box No.15875-4413, Tehran, Iran
ABSTRACT The effect of various parameters on electrical resistivity and mechanical properties of HDPE/CB, EPDM/CB and HDPE/EPDM/CB composites were studied. The percolation threshold was obtained for the HDPE/EPDM/CB composites occurred at lower than 3 wt% carbon black. This threshold was significantly lower than those found for individually filled HDPE or EPDM. The impact strength of HDPE/EPDM/CB composite was also about 20 times greater than HDPE/CB composite. The composite preparation sequence, rotor speed and filled factor were among the effective variable studied. Result indicated that, composite prepared by fist compounding CB with EPDM followed by HDPE feeding has the lowest resistivity value relative to those samples prepared by other two mixing procedures. The volume resistivity was found to be decrease with increasing rotor speed up to 50 rpm and decreasing filled factor.
INTRODUCTION The electrical conductive polymeric composite has received a great attention during the last two decades. These composites can be used in application such as antistatic, sensors [1], auto regulating resistors [2,3], electrostatic discharge dissipation [4], electromagnetic interference shielding [5, 6], and electrodes [7]. The carbon black is among the most important conductive filler used in this group of composites. At a critical amount of the electrically conductive filler the volume resistivity decreased by about 8 orders of magnitudes known as percolation threshold. This critical weight of CB particles required for building an electrically conductive network throughout the polymer matrix depends on the structure, porosity, average size and size distribution of CB particles [8], and on the polymer rheology [9] and processing conditions as well[10]. Low content of carbon black in composite is desirable, since increasing amount of CB commonly has a detrimental effect on the mechanical properties and processing of thermoplastics and in addition increases the cost of final composites. The important way to reduce the CB content in these composites is selective localization of CB in an immiscible polymer blend matrix [11,12]. In this paper, conductive composites with low percolation threshold based on HDPE/EPDM blend were studied and the effects
* Correspondence author, Department of Polymer Engineering, Amirkabir University, Fax: ^98(21)8039907, E-mail: [email protected]
Processing Effects on Electrical Conductivity and Mechanical Properties
73
of composite preparation sequence, rotor speed and filled factor on electrical and mechanical properties were investigated. EXPERIMENTAL High density polyethylene (HDPE, Iran Petrochemical, HD 5218 EA) and ethylene-propylene-diene monomer (EPDM, Exxonmobil, Vistalon 7500) were used in this study. Carbon black Printex XE2-B which is a highly conductive black, was supplied by Degussa-Hules (iodine adsorption: 1124 mg/g; surface area: 1000 m2/g; DBP absorption: 406 ml/lOOg; PH=7). For evaluation of percolation threshold the polymer first mixed in a Brabender PL at 160°C for 2 min and then CB was added. After 15 min, compounds were removed from the mixer. In order to study the influence of the preparation procedure on the properties of composites, three modes of feeding sequence were selected: addition of CB to the polymer blend, (HDPE+EPDM)+CB; CB compounding with HDPE followed by EPDM addition, (HDPE+CB)+EPDM; or CB compounding with EPDM followed by HDPE addition, (EPDM+CB)+HDPE. For evaluation of the rotor speed and filled factor, three levels were selected as follow: 40, 50, 60 for rotor speed and 0.7, 0.75, 0.8 for filled factor. All compounds were molded between aluminum foils at pressure of ca. 23 MPa for 5 min at 160°C to produce 2 mm thick specimens and cooled under pressure to room temperature. The mechanical and electrical properties of the specimens were tested according to ASTM test methods D-257 for volume resistivity, D-256 for Izod impact, and D-638for tensile strength. RESULTS AND DISCUSSION Electrical Resistivity The effect of carbon black content on the volume resistivity of the individually filled polymers (i.e., HDPE/CB and EPDM/CB) and the blend of them (i.e., HDPE/EPDM/CB) are depicted in Figure 1. As expected the ternary composites exhibited a low percolation threshold, lower than 3 wt%, which is lower than the percolation thresholds of CB in HDPE, 5 wt%, and EPDM, 15 wt%.
1.00E+16 _
1.00E+14
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.
3. 1.00E+10
\ \
I 1
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£ 1.00E+06 J 1.00E+04 o •* 1.00E+02
\ —t—he30 \
-•—hdpe
\ \
—,:,— epdm
V '\
1.00E+00 15
20
25
30
35
CB(Wt%)
FIGURE 1 Volume resistivity of HDPE/CB, EPDM/CB and HDPE/EPDM/CB composites
74
Processing Effects on Electrical Conductivity and Mechanical Properties 6.00E+02
5.00E+02
I 4.00E+02 £. 1
3.00E+02
'55 % 2.00E+02 E §•
1.00E+02
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(HDPE+CB)+EPDM
(EPDM+CBJ+HDPE
(HDPE+EFDM)+CB
Sample name
FIGURE 2 Effect of feeding sequence on volume resistivity
This reduction is related to double percolation effect or selective localization of CB in one continuous phase or at the interface of co-continuous binary polymer blend [13]. Figure 2 show that the composite prepared by compounding CB with EPDM followed by HDPE addition has the lowest volume resistivity. The transfer of CB from one phase to another phase may be the reason for this reduction. The transfer of CB from PP to Ny in PP/Ny blend was illustrated by Narkis [14]. As illustrated in Figure 3, the volume resistivity of composite decreased with increasing the rotor speed up to 50 rpm that related to better distribution of CB particles in the matrix. Increasing rotor speed above this will result in breaking down CB network structure in polymeric matrix and hence increase the volume resistivity. 4000
40
50
60
Rotor speed(rpm)
FIGURE 3 Effect of rotor speed on volume resistivity
70
Processing Effects on Electrical Conductivity and Mechanical Properties
75
The effect of filled factor on volume resistivity of the composite is depicted in Figure 4. The volume resistivity of the composite enhanced with increasing filled factor, because it cause to break down of CB structure and hence damage the network connection.
6000 5000 % o 4000
•5 5. 3000 2000 •
1000
0.65
0.7
0.75
0.8
0.85
Filled factor
FIGURE 4 Effect of filled factor on volume resistivity
Mechanical Properties It is well known that the elastomer has been used to increase the toughness of the polymer composites, and the impact strength of elastomer-toughend polymer composites depends on the morphology of the composites, the characteristics of the rubber, and the nature of the interface between these phases [15]. Figure 5 shows the Izod impact strength of 20 wt% CB filled HDPE and HDPE/EPDM (70/30) composites. With addition of 30 wt% EPDM to the composite, the impact strength increases about 20 times which shows a good interface between phases. But as illustrated in Figure 6 the tensile strength decrease that related to increasing flexibility of the composite.
"
16-
i 14-
i\l O)
8
| «
6 4 -
1 2^
1 °-
HDPBCB
HDFeEPDWCB Sample name
FIGURE 5 Effect of elastomer on impact strength
76
Processing Effects on Electrical Conductivity and Mechanical Properties 16-j
ir £ 10--
I «
6 4-
I
4 0 4HDPBCB
HDPBEPDWCB Sample name
FIGURE 6 Effect of elastomer on tensile strength
The mechanical properties of HDPE/EPDM/CB composites are listed in Table I. From the table it could be seen that, in general the impact strength and tensile strength increased with increasing rotor speed and filled factor TABLE I The effect of rotor speed and filled factor on mechanical properties of composites
Rotor speed(rpm) 60 40 50 Average of tensile strength (MPa) Average of impact strength (kgf. cm/cm)
0.7
Filled factor 0.75 0.8
8.12
8.20
8.31
8.16
8.21
8.33
13.78
16.65
16.93
15.56
16.32
16.48
CONCLUSION The experimental results reported in this paper convincingly emphasize that blends of HDPE with EPDM can be endowed with electrical conductivity by using very small amounts of conductive CB particles, and blending is an effective way for reducing the percolation threshold in respect to double percolation threshold. Also the addition of EPDM increases the impact strength of the composite. The sequence of blend preparation affect not only on electrical resistivity, but also the mechanical properties of the composites. Rotor speed and filled factor are importance factors that influence on electrical and mechanical properties of polymer/CB composites. REFERENCES 1. 2. 3. 4. 5. 6.
Ruschau, G. R., R.E. Newnham, J. Runt, and B.E. Smith.1989. Sens. Actuators., 20: 269. Horsma, D. A., and T. J. Hannack. 1979. Ger. Patent DE 2543346. Cheng, T. C , and B. A. Mckinley. 1985. Eur. Patent EP 138424. Rupprecht, L. 1999. Conductive Polymers and Plastics, in Industrial Application. Plastics Design Library., pp. 209-217. Jana, P. B., A. K. Mallick, S. K. De.1992. IEEE Trans on Electromagnet Compatibility. 34:10. Abolins, V., J. M. Caraber, R. C. Bopp, and E. m. Lovgren. 1983. Eur. Patent EP77059.
Processing Effects on Electrical Conductivity and Mechanical Properties 7.
77
Haddadi-asl, V., M. Kazacos, and M. Skyllas-kazacos.1995. "Carbon-Polymer Composite Electrodes for Redox Cells", J. Apply. Polym. Sci., 57: 1455-1463. 8. Medalia, A.I. 1986. "Electrical Conduction in Carbon Black Composites", Rubber chem. Techno., 59: 432-454. 9. Soares, B.G., F. Gubbels, R. Jerome, E. Vanlathem, and r. Deltour. 1997." Electrical Conductivity of Polystyrene-Rubber Blends Loaded with Carbon Black". Rubber Chem. Techno., 70: 60-70 10. Gubbels, F., R. Jerome, E. Vanlathem, R. Deltor, S. Blacher, and F. Brouers, 1998" Kinetic and Thermodynamic Control of the Selective Localization of Carbon Black at the Interface of Immiscible Polymer Blends". Chem.mater., 10:1227-1235 11. Sumita, M., K. Sakata, S. Asai, andK. Miyasaka 1991. Polym. Bull., 25:265 12. Asai, S., K. Sakata, M. Sumita, and K. Miyasaka. 1992". Effect of Interfacial Free Energy on the Heterogeneous Distribution of Oxidized Carbon Black in Polymer Blends", PolymJour,, 24(5):41420. 13. Levon, K., A.Margolina, and A. Z. Patashinsky. 1993 " Multiple Percolation in Conducting Polymer Blends", Macromolecules, 26:4061-4063 14. Tchoudakov, R., O. Breuer, and M. Narkis. 1996" Conductive Polymer Blends with Low Carbon Black Loading: Polypropylene/ Polyamide", J. Polym. Eng. Sci., 36(10): 1336-1345. 15. Park, S.J., M.K. Seo, and j.R. Lee.2001."PTC/NTC Behaviors of Nanostructured Carbon Black • filled HDPE Polymer Composites", Carbon Science. 2(3&4):159-164.
Study on the Hydrolysis-resistant Polyethylene Terephthalate (PET) Fibers Yanping Wang, Yimin Wang State Key Laboratory for Chemical Fibers and Polymer Materials Donghua University, Shanghai, 200051, P. R. China
ABSTRACT In the industrial field, the mechanical properties of PET fibers could be deteriorated because the terminal carboxylic groups resulted in degradation of macromolecules in high moisture, namely hydrolysis reaction of PET, which limited the application of PET fibers in some special cases. In this paper, three hydrolysis stabilizers, which are chain extenders for polyester at the same time, were selected to improve its hydrolysis stability. PET pellets were blended with these additives before spinning and melt spun into fibers. The fibers were then hydrolyzed in an autoclave with saturated vapor at 140°C for a period of time. Measurements of intrinsic viscosity, terminal carboxylic groups value and strength of polyester fibers were employed to study the effects of hydrolysis resistance. Results show that 2,2'-bis(2-oxazoline) has the best hydrolysis-resistibility and the most chain-extension effect.
INTRODUCTION PET fiber is one of the most important synthetic fibers because of its high performance. It is employed in a variety of industrial applications such as textile, belts, and tire cords. PET fibers, however, are known to have a serious problem.[l] Generally a number of ester groups existed in PET macromolecule chains will be easily hydrolyzed by moisture at elevated temperature, which leads to the degradation of macromolecules. All the more, the acidic carboxyl end groups promote hydrolysis of ester bonds, resulting in fiber strength reduction. [2] The shortcoming restricts remarkably the applications of PET fiber. In order to prevent the properties deterioration of polyester as hydrolysis, a large number of experiments have been made to add various additives to PET during its polymerization or spinning to trap the carboxyl groups and slow down the hydrolysis rate. The used additives include oxazoline, epoxy, monocarbodiimides and polycarbodiimides. Of them, oxazoline and epoxy show a obvious anti-hydrolysis effect.[3] On the other hand, the industrial application promotes the development of high-performance PET fibers, which have high molecular weight. And high molecular weight PET was achieved by solid-state polycondensation [4] or chain-extender [5]. Especially, chain-extender can increase the molecular weight in less time. In this work, three bifunctional additives, which were chain-extender at the same * Corresponding author, Donghua University, Tel: 86-21-62379785, Fax: 86-21-62379309, E-mail address: [email protected]
Hydrolysis-resistant Polyethylene Terephthalate (TEP) Fibers
79
time, were blended with PET pellet respectively. The blends were then melt spun through screw extruder and drawn into fibers. The effects of these additives were evaluated by the measurement of intrinsic viscosity, carboxyl end group value and fiber strength. EXPERIMENTAL Materials Fiber grade PET was received from Yizheng Corp. in the form of pellets with intrinsic viscosity([r?]) of 0.65dl/g at 25 °C in 50:50(wt/wt) phenol/ 1,1,2,2-tetrachloroethylene and carboxyl end group value(CV) of 35eq/106g, which represents its molecular weight of 18,100g/mol. The structures of three hydrolytic stabilizers employed in this study are shown in Scheme 1. 2,2'-Bis(2-oxazoline) (BOZ) and l,3-Bis(4,5-dihydro-2-oxazolyl) benzene (BOB)was synthesized according to Ref.[6]. 2,2-Bis(4-glycidyloxyphenyl) propane (BGP) was purchased from TCI Corp.
(HI) SCHEME 1.
( I ) 2,2'-Bis(2-oxazoline) (abbrev. BOZ) (II) l,3-Bis(4,5-dihydro-2-oxazolyl) benzene (abbrev. BOB) (III) 2,2-Bis(4-glycidyloxyphenyl) propane (abbrev. BGP)
Sample preparation PET pellets were dried in vacuum for 12h at 90 °C and for 24h at 130°C. The moisture content was less than 40ppm. Three additives were dried in vacuum for 12h at 60 °C. Pellets were removed from vacuum oven and mixed with calculated amounts of stabilizer for 3min in a sealed container. A screw extruder was employed to extrude and spin PET fiber. The extruder has four heating zones to control temperature separately. The spinning temperature was 285 °C. Fibers were taken up at a rate of 600m/min. The as-spun fibers were two-stage drawn with drawn ratio of 3.5- 4 at drawing temperature of 90 °C, and then 220 °C immediately.
80
Hydrolysis-resistant Polyethylene Terephthalate (TEP) Fibers
Hydrolytic Experiments All hydrolyses were carried out in a sealed autoclave at 140±5°C. The fibers were clamped on the shelves in the autoclave. After adding of some water the oven was sealed and heated to 140°C. The fibers were hydrolyzed in the vapor at the relative humidity of 100%. Every 24h some fiber samples were taken out and dried in vacuum at80°C for testing. Testing The intrinsic viscosity ([*/]) of pellets arid fibers was measured with an Ubbelodhe viscometer in 50/50(wt/wt) phenol/1,1,2,2-tetrachloroethylene at 25 °C. Samples were solved in 50/50(v/v) o-cresol/chloroform and titrated by potassium hydroxide/benzyl alcohol. Carboxyl end group value (CV) was calculated by the method. The titre and strength were tested by Tensiltester, Textechno Co.. RESULTS AND DISCUSSION PET melt reacted with these additives while it was melting extruded through screw extruder. As-spun fibers without finishing oil were taken before winding for different measurements. Fiber samples with and without additive were tested and the results were shown in table I . TABLE I Effects hydrolysis-stabilizers on [rj] and [COOH]
Type of stabilizer
Blank
BOZ
BOB
BGP
Intrinsic viscosity [r?] (dl/g)
0.65
0.91
0.76
0.70
Molecular weight (g/mol)
18100
27200
21760
19600
Carboxyl end groups value (CV) (eq/106g PET)
,, 35
, 6
,_ 13
8
o
These data indicated that additives tested here were effective chain extenders although effects were rather varied. Of them, BOZ is the best one. Reaction of PET with BOZ leads to an increase in the molecular weight from 18100 to 27200g/mol, the intrinsic viscosity from 0.65 to 0.91dl/g. Meanwhile, these additives reduced remarkably the content of carboxyl end groups. Especially BOZ and BGP result in the reduction of the carboxyl end group value from 35 to 6 and 8eq/106g PET, respectively. Because the carboxyl end groups can auto-catalyzed the hydrolytic reaction of PET, the great decrease of CV and the increase of PET molecular weight indicate that three additives can react with the carboxyl end groups, which predicts that these additives are likely to have anti-hydrolysis effect to PET. All hydrolysis experiments were carried out in the saturated vapor at 140°C. Every 24h some fibers were removed from the sealed autoclave. The carboxyl end group value, the intrinsic viscosity and tensile strength were measured, respectively.
Hydrolysis-resistant Polyethylene Terephthalate (TEP) Fibers
20
40
81
60
Hydrolytic treating time(hr)
FIGURE 1 Variation of intrinsic viscosity with hydrolytic treating time
The decrease of intrinsic viscosity induced by hydrolysis was shown in Fig. 1. Apparently, the intrinsic viscosity of the fiber sample without any additive decreased from 0.65 to 0.20dl/g, namely, molecular weight reduced from 18100 to 4300g/mol in 72 hours. However, the intrinsic viscosity of fibers with additives reduced less. Especially, the intrinsic viscosity for fiber with BOZ was 0.59dl/g after it had been hydrolyzed for 96h, which is almost the same as that of the unhydrolysed sample.
20
40
60
Hydrolytic treating time(h)
FIGURE 2. Variation of carboxyl end group value (CV) with hydrolytic treating time
Figure.2 presents the data for carboxyl group concentration as a function of hydrolysis time at 140 °C. With the increase of treating time, carboxyl end group value (CV), which indicated result of hydrolysis, increased fast and fast due to the
Hydrolysis-resistant Polyethylene Terephthalate (TEP) Fibers
82
auto-catalyzing effect of free carboxyl groups. Comparing the [COOH] results, it was obvious that these additives were beneficial for reduction of carboxyl as compared to the pure PET fibers in the hydrolysis process. And BOZ and BOB reduced the formation rate of carboxyl group, which indicate they can efficiently reduce PET hydrolysis. •-—— —
—
^
-z. S 3o —•— BLANK —•—BOZ
n 0
>
1
20
<
1
1
40
1
60
1
80
Hydrolytic treating time(hr) FIGURE 3 Variation of Strength with hydrolytic treating time
The primary effect of hydrolytic stabilizers is for the retaining of fiber mechanical properties. The drawn fibers were hydrolyzed and degraded in the saturated vapor. The relations between the fiber strength and hydrolytic time at 140°C are shown in Figure 3. With the increase of treating time, carboxyl end group contents increased, which accelerated the decrease of strength due to auto-accelerating effect of carboxyl end groups, hi the same way, three additives slow down the decline rate of strength as hydrolysis. Namely, these additives have hydrolysis resistance for PET fibers. And BOZ has the best effect. CONCLUSION PET pellets were blended with three additives. The blends were spun and drawn. Measurements of intrinsic viscosity, carboxyl group value and strength of PET fibers with and without additives were used to evaluate the hydrolysis resistance. Results showed that three additive have the doubtless hydrolytic resistance and chain-extension effect. Of them, BOZ is the best hydrolytic stabilizer. REFERENCES [1] Carlsson, D. J., Milnera, S. M. 1982. "Hydrolysis Of Resin-Coated Poly (Ethylene Terephthalate) Yarns," Journal of Applied Polymer Science, 27( 5): 1589-1600 [2] Olson L. M., Wentz M. 1984. "Moisture Related Properties Of Hydrolyzed Polyester Fabrics," Textile Chemist and Colorist, 16(2): 48-54 [3] J. R. Reither. 1998. "Industrial fabric and yarn made from recycled polyester," USP 6,147,128 [4] Ben Duh. 2002. "Effects of the Carboxyl Concentration on the Solid-State Polymerization," Journal of Applied Polymer Science, 83(6): 1288-1304 [5] Nicoletta C , Riccardo P., Giorgio G, Ernesto O., Fabio G., Giuseppe M., 1993, "Chain extension of recycled poly(ethylene terephthalate) with 2,2-Bis(2-oxazoline)," Journal of Applied Polymer Science, 50(9): 1501-1509 [6] Henry Wenker. 1938. "Syntheses from Ethanolamine. V. Synthesis of A2-Oxazoline and of 2,2'-A2-Dioxazoline," J. Am. Chem. Soc, 60(9): 2152-2153
Size Effect on the Compressive Strength of T300/924C Carbon Fiber-Epoxy Laminates in Considering Influence of an Anti-buckling Device Jungwhan Lee, Changduk Kong Department of Aerospace Engineering, Sheffield University, U. K. Department of Aerospace Engineering, Chosun University, S. Korea* C. Soutis Department of Aerospace Engineering, Sheffield University, U. K.
ABSTRACT The size effect of specimen gauge section (length x width) was investigated on the compressive behavior of a T300/924 [45/-45/0/90]3s, carbon fiber-epoxy laminate in considering influence of an anti-buckling device. A modified compression test fixture was used together with an anti-buckling device to test 3mm thick specimens with 30mm x 30mm, 50mm x 50mm, 70mm x 70mm and 90mm x 90mm gauge length by width section, hi all cases failure was sudden and occurred mainly within the gauge length. Post failure examination suggests that 0° fiber microbuckling is the critical damage mechanism that causes final failure. This is the matrix dominated failure mode and its triggering depends very much on initial fiber waviness. It is suggested that manufacturing process and quality may play a significant role in determining the compressive strength. When an anti-buckling device was used on specimens, it was showed that the compressive strength with the device was slightly greater than that without the device due to surface friction between the specimen and the device by pre-torque in bolts of the device. In the analysis result on influence of the anti-buckling device using the finite element method, it was found that the compressive strength with the anti-buckling device loaded by bolts was about 7% higher than real compressive strength.
INTRODUCTION Since the 1960s, there is a significant, but inconclusive, amount of evidence that there is a size effect in composites. For instance, the tensile strengths of glass, carbon and ararmd filaments decrease with increasing length [1, 2]; the flexural strength of unidirectional specimens can exceed tensile strengths by as much as 44% and compressive strengths by as much as 56% [3, 4]; the flexural strength of 100-ply unidirectional specimens is 15% lower than for 25-ply specimens and apparent size effect occur in both tension and compression [5]. The stress gradient and associated through-thickness effect can explain the difference between flexural and unidirectional strengths. A recent study by Lavoie et al [6] indicates that strength* Corresponding author, #375 Seosuk-dong, Dong-gu, Gwangju, S. Korea, Fax: +82-62-230-7188, E-mail: cdgong(o>,mail.chosun,ac.kr
84
Compressive Strength of T300/924C Carbon Fiber-Epoxy Laminates
scaling in 0° fiber-dominated laminates should be regarded as an artifact of the test procedure and failure mode. For investigation of the size effect on the compressive strength of a carbon fiberepoxy laminate, specimens with four different gauge sections are tested statically in uniaxial compression. In order to avoid buckling of the relatively large specimens, the anti-buckling device was used. In this case, it was found that the compressive strength with the device was slightly greater than that without the device due to surface friction between the specimen and the device by pre-torque in bolts of the device. For investigation of influence by the anti-buckling device, the finite element method was used. SPECIMENS AND COMPRESSIVE TESTING The material used was Toray T300 carbon fiber in a Ciba-Geigy 924C epoxy resin (T300/924C). The pre-impregnated tapes (pre-preg) were laid up by hand into a [45/45/0/90]3s quasi-isotropic lay-up and cured according to the manufacturer's recommended procedure. The quality of the module laminates was examined by using ultrasonic C-scanning. Several specimens were cut from the 3 mm thick panels and glass fiber-epoxy reinforcement tabs were bonded giving gauge section of 30 x 30, 50 x 50, 70 x 70 and 90 mm x 90 mm. The geometry of the 30 mm long by 30 mm wide specimen is based on the Airbus Industry test method (AITM-1.008) [7]. Static compressive tests were carried out on a screw-driven Zwick 1488 universal testing machine with a load capacity of 200kN; a crosshead displacement rate of 1 mm/min was used. Load introduction to the specimen was mainly by end loading using modified ICSTM fixture [8]. For all 50mm x 50mm, 70mm x 70mm and 90mm x 90mm specimens an anti-buckling device similar to that used by Soutis [9] was employed to prevent column buckling. It contains a window at the device center, allowing damage around the hole to occur but restraining the specimen from general bending. In order to minimize frictional effect, the clearance between the antibuckling device and the specimen face was less than 100 urn. In case of 30mm x 30mm specimen, the clearance can be successfully kept, but in case of larger specimens than the 30mm x 30mm, the clearance cannot be sustained due to contact by some amount of pre-torque of bolts of the anti-buckling device to prevent buckling from the specimen. TEST STRENGTH RESULTS Failure of specimens was sudden and occurred mainly within the specimen gauge length. Post-failure examination suggests that in-plane fiber micro buckling in the 0° plies is the critical damage mechanism, which causes the catastrophic fracture. Longitudinal splits, fiber/matrix de-bonding and delamination between neighboring plies do not occur gradually but take place suddenly and concurrently with the final failure. This is supported by failure strain measurements. The average failure strain measured by the two back-to-back strain gauges at the point of failure was in the region of 1 %, which similar to the strain of the 0° unidirectional material, hi general, test results for all sizes were good and reproducible. The scatter in axial stiffness and strength for all specimen configurations was less than 5%, see Table 1; the results quoted in Table 1 are based on the average of five specimens tested for each different size.
Compressive Strength of T300/924C Carbon Fiber-Epoxy Laminates
85
TABLE I Average compressive strength of specimens
Compressive Strength of Unnotched Specimen Modified ICSTM
Test Fixture 30x30
30x30
50x50
70x70
90x90
Anti-buckling Device
No
Yes
Yes
Yes
Yes
Average Failure Strength
575
690
736
750
711
Coefficient Variation (%)
3.34
4.92
4.28
4.86
2.77
Specimen Size(mm)
The scatter in strength is probably due to imperfections introduced during manufacturing of the laminates resulting is fabrication defects and non-uniform laminate thickness. Imperfections in specimen geometry can produce misalignment of the specimen in the testing fixture that causes bending and reduction in the measured compressive strength. The average elastic modulus (measured at 0.25% applied strain) for all specimens was 66GPa, which is in a good agreement with that estimated by the laminate plate theory (62 GPa). However, the average strength of the specimen with the 30mm x 30mm gage section was at least 20% lower than that of the bigger size specimens. For this configuration (30mm x 30mm gage section), no anti-buckling device was used and failure occurred prematurely due to global Euler buckling. In the typical stress-strain curve of such a specimen, the strain readings of the two back-to back strain gauges are almost the same up to 0.6% applied strain and start to deviate at higher applied loads indicating out-of-plane deflection that leads to premature failure of the laminate and lower overall strength. However the compressive strengths of 50mm x50mm, 50mm x 70mm and 90mm x 90mm gauge length specimens using the anti-buckling device are 6-7% higher values than compressive strength of 30mm x 30mm gauge length specimen. It can be considered that the reason would be caused by frictional contact due to pre-torque of connecting bolts of the anti-buckling device to guide failure at specimen center as well as to avoid the buckling. From the limited strength data presented in Table 1, there is no evidence of a size effect which is not the case for specimens loaded in tension or flexure. Under compressive load, such a size effect does not seem to exist probably because of the different failure mechanism. The mechanism of failure under compressive loading is fiber micro buckling that initiates in regions of maximum fiber misalignment or waviness introduced during the fabrication process [10]. The fiber waviness is sensitive to thickness change of the specimen rather than the two-dimensional area charge introduced in this study. Therefore, an investigation on thickness effects should be performed. According to a compressive strength prediction model of Slaughter, Fleck and Budiansky [11] based on the microbuckling theory, the compressive strength of a composite, in the state of the axial normal stress, the loading directional shear stress and the transverse normal stress, was estimated. In the microscopic measurement of the quasi-isotropic [45/-45/0/90]3s laminate made of T300/924C, it was confirmed that the fiber waviness angle of the 0°-ply is average 2.5°, and the post failure kink band inclination angle is 25°. When the in-plane shear yielding strength of the used matrix is 63 MPa, and the compressive strength of the [45/-45/0/90]3s laminate predicted by the microbuckling theory is 690.3 MPa. This predicted result is in good agreement with the measured strength of the 30mm x 30mm size specimen, 690 MPa, which is
86
Compressive Strength of T300/924C Carbon Fiber-Epoxy Laminates
obtained from using the anti-buckling device without the pre-torque of bolts of the device. However in case of the measured compressive strengths of 50mm x 50mm, 70mm x 70mm, and 90mm x 90mm size specimens using the anti-buckling device as shown in Table 1, the measured values are 6-7% higher than the predicted values and the compressive strength of the 30mm x 30 mm size specimen. It was concerned as the reduction effect of the applied load on the anti-buckling device due to the surface friction and the deformation constrained boundary condition between the device and the specimen by the applied pre-torque of four bolts to guide failure at the center of specimen within the window of the device. The anti-buckling device has the 20 mm width by 20 mm length window and the thick steel plate of the device is closely contacted by pre-torque of four 1/4 inches bolts. When the applied torque Tis 10.16 N-m which is almost same as the nominal torque, the frictional pressure load Px on the contact surfaces can be expressed as the following equation. When the applied torque T is 10.16 N-m which is almost same as the nominal torque, the frictional pressure load Px on the contact surfaces can be expressed as the following equation. Px=juTm/(0.2d0A)
(1)
where T is the applied torque of the bolt, it is assumed as T = 0.2 Ft d0 by Faupel et al. [12]. The Fi is the axial force due to the torque, do is the bolt nominal diameter, m is the total number of bolts, A is the frictional surface area, and the ft is the frictional coefficient. In this study, d0 = 1/4 inch, m = 4, and /u = 0.245 that is measured at experimental tests. The contact surface boundary condition is assumed that the thickness directional displacements are constrained because of very stiff thick steel plate of the anti-buckling device. Using the finite element method the 1/2 model is analyzed, and the used finite element is the 2-D composite element [13]. The analysis results show equivalent stress distribution Sxxeq / So in width direction due to friction of the anti-buckling device, the equivalent stress decrease with increasing the frictional coefficient. In case of // = 0.245, it is noted that the equivalent stress at the center of the specimen is 7% higher than the compressive stress without the antibuckling device. In other word, it means that the compressive strength of the specimen with the anti-buckling device is 7% higher than that without the antibuckling device due to frictional effect and deformation constraints. Therefore it would be concerned that the realistic compressive strengths of 50mm x 50mm, 70mm x 70mm, and 90mm x 90mm size specimens using the anti-buckling device should be corrected to 684.5Mpa, 697.5Mpa, and 663.2 Mpa respectively which are 7% less than the measured values. CONCLUSION The effect of gauge section was investigated on the static compressive strength of a currently used carbon fiber-epoxy system; the lay-up was a quasi-isotropic and the specimen thickness was kept constant. The anti-buckling device was used on the unnotched specimens, and it was showed that the compressive strength with the anti-buckling device was slightly greater than that without the anti-buckling device due to surface friction between the specimen and the device by pre-torque in connecting bolts. In the analysis result on influence of the anti-buckling device using the finite element method, it was found that the compressive strength of the laminate with the anti-buckling device loaded by bolts was about 7% higher than real compressive strength and the corrected
Compressive Strength of T300/924C Carbon Fiber-Epoxy Laminates
87
compressive strength is in good agreement with the predicted strength based on the fiber micobuckling theory. From these limited data, it appears that the compressive strength does not depend on specimen size. Failure is matrix dominated and occurs due to fiber micro buckling in the 0° plies. The initiation of this failure mode is greatly dependent on initial fiber waviness, which highlights the importance of manufacturing processes. REFERENCE 1.
2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13.
Zwen, C , Smith, W. S. and Wardle, M. W., 1979. "Test method for fiber tensile strength, composite flexural modulus and properties of fabric reinforced laminates". Composite Materials: Testing & Design, 5th Conf. ASTM STP674 (American Society for Testing and Materials, Philadelphia), 228-262. Herring, H. W., 1966. "Selected mechanical physical properties of boron filaments", NASA TN D3202, Bullock, R. E. 1974. "Strength of composite materials in flexure and in tension", J. Composite Mater., 8,, 200-206. Berg, K. R. and Ramsey, J., 1972. "Metal aircraft structural elements reinforced with graphite filamentary composites", NASA CR-112162, August Wisnom, M. R., 1991. "The effect of specimen size on the bending strength of unidirectional carbon fiber-epoxy", Composite Structures, 18, 47-63. Lavoie, J. A., Soutis, C. and Morton, J., 2000. "Apparent strength scaling in continuous fiber composite laminates", Composite Science & Technology, 60, 283-299. Soutis, C , Fleck N.A. and Smith, P.A., 1991. "Failure prediction technique for compression loaded in carbon fiber-epoxy laminate with open hole " Journal of Composite Materials, 25, 1476-1498 Airbus Industrie Test Method, 1994. AITM 1.0008. Issue 2 Haberle J. G., 1991. "Strength and failure mechanics of unidirectional carbon fiber-reinforced plastics under axial compression", PhD Thesis, University of London, Soutis, C , 1989. "Compressive failure of notched carbon fiber-epoxy panels", PhD Thesis, University of Cambridge Slaughter, S., Fleck, N. A., Budiansky, B., 1992. "Micrbuckling of fiber composite: the role of multi-axial loading and creep", J. of Engineering Mater. Tech., 115(5), 308-313. Faupel, J. H., and Fisher, A. E., 1980. "Engineering Design: A Synthesis of Stress Analysis and Materials Engineering", 2nd Edition, John Wiley & Son, EMRC, 1992. NISAII-Users Manual, version5.2,
Environment Effect of Natural Sisal Fibre Reinforced Epoxy Composites Manufactured by Resin Transfer Molding 1
X. P. Zhang1*, Q. Yuan2, W. Ngatimin1, J. Whitbourn1 and L. Ye1 Center for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering, the University of Sydney, NSW 2006, Australia 2 Division of Manufacturing and Infrastructure Technology, CSIRO, Heighett, Vic. 3190, Australia
ABSTRACT Moisture/water absorption in fibre reinforced composites and the subsequent influence on properties of the composites are very important issues, in particular for natural fibre reinforced epoxy composites. In this work, the moisture absorption feature in a natural sisal fibre reinforced epoxy composite fabricated using Resin Transfer Molding (RTM) technology was studied, and the degradation of mechanical properties of both composites with treated and untreated fibre was characterized. The results show that increasing the content of water (moisture) in the composite results in an apparent reduction in tensile strength and impact toughness, and the deterioration in microstructure. The fibre surface treatment is an efficient method to improve the water/moisture resistance of the composite. These results may provide a sound theoretical basis for natural fibre composite design and engineering applications. INTRODUCTION In most environments, the moisture (or water) can penetrate into composites, which may result in obvious changes in the constituents and acute deteriorations in their interaction. These changes often compromise the load-carrying properties of the composites with the level of degradation increasing as the absorbed moisture content increases. Moreover, from micro-bonding point of view, a serious effect caused by moisture-absorption is the debonding between the fibre and matrix, which leads to a reduction in load transfer potential and a fall in mechanical properties of the composites. Reduction in stiffness, strength and toughness, as well as changes in thermo-mechanical behavior can often be related to the amount of moisture absorbed by the composites. For these reasons, recent years many studies have been focusing on characterization of moisture absorption (or water uptake) and the subsequent influence on properties of the composites. Most of these studies were performed for carbon and glass fibre reinforced epoxy resin composites destined for use by the aeronautical and aerospace industry [1-4]. However, little is known about natural fibre reinforced epoxy matrix composites which have been employed in some civil applications such as in roofing, building materials, and even automotive parts. Using natural fibres as a replacement for glass or carbon fibres in the reinforcement of composites has attracted increasingly the attention from materials researchers and engineers. These natural fibres include wood, bamboo, sisal, lignocellulos, flax, Correspondence author. Tel: 61-2-93517146; fax: 61-2-93517060; Email: [email protected]
Natural Sisal Fibre Reinforced Epoxy Composites
89
pineapple leaf, coir etc. Use of these natural fibres in fabricating composites broadens the applications for these agricultural by-products. Due to the potentially biodegradable feature, these natural fibres reinforced composites are also called eco-composites or environmentally benign composites. Among these natural fibres, sisal fibre is one of the strongest naturalfibres,just after flax. Sisal is extracted from the leaves of the sisal plant. The sisal leaf contains mechanical, ribbon and xylem fibres. Of these, the mechanical fibres are the most useful part [5]. In this study, a natural sisal fibre reinforced epoxy matrix composite was fabricated using resin transfer molding (RTM) technology which has become increasingly interested for the composites manufacturing industry over the last decade or more. The composite samples were then subjected to an elevated temperature moisture environment to investigate the effects of the environment on composite mechanical properties and microstructure. The moisture absorption feature in the composite was characterized for both treated and untreated fibres. The mechanical properties of composites with different moisture contents were estimated, and the fracture mechanism of both dry and wet composites was studied. COMPOSITE FABRICATION AND EVALUATION Materials, RTM System and Composite Fabrication In this work, 0-90° plain woven sisal fibre was used in fabrication of the composite. The used epoxy system is commercial materials, i.e., Araldite F resin and HY951 hardener. The mixture ratio of resin and hardener is 1:9 (wt%). The volume fraction of sisal fibre was about 0.50. The RTM system used in this work is a HYPAJECT portable injection machine which consists of a control unit, a vacuum pump, connection hoses and a steel mold. In order to investigate the influences of fibre surface conditions on water absorption feature and the bonding quality between the fibre and the resin, as well as, subsequently, the mechanical properties of the composite, a chemical solution, containing 0.05% 3-aminopropyltrethoxysilane, was used to modify the fibre surface. During the chemical treatment, the woven sisal fibre mats were immersed in the solution for 2 minutes followed by a cleaning in acetone for 2 minutes. The sisal fibre mats were dried in an oven at 80 °C for about 20 hours. The injection mold had a geometry of 410 x 205 x 5 (length x width x height, mm), which may fabricate a composite panel with the maximum size about 400 x 200 x 5 mm3. The post curing process was carried out in an oven at 80°C for three days, and the Differential Scanning Calorimetry (DSC 2920, TAInstruments) tests were conducted to evaluate the residual active chemical group in the composite panels and confirm all composite panels fully cured. Estimation of Environment Effects To characterize the effects of environmental exposure on the natural fibre reinforced epoxy composites, the specimens were immersed in a stainless steel container full of water, which was placed an oven at 70 °C for a period of one to two weeks. Over this time the specimens were taken out periodically to weight so as to determine the amount of water absorbed by the specimens. The percentage uptake of water by weight, Rw, can be defined as follows: W-W ^ l 0 0 %
(l)
90
Natural Sisal Fibre Reinforced Epoxy Composites
where W is the measured specimen weight corresponding to different dwell times, and Wo the original dry specimen weight. Both W and Wa were measured by an electronic microbalance (model: BP-210D, Sartorius) with an accuracy of 0.01 mg. During the first three days, 2 measurements were conducted due to the rapid moisture uptake of the composite, and then followed by one reading per day for the remainder of the first week as well as for the second week (in this work, readings were taken only till the 9th day due to the approximate saturation of moisture absorption). After moisture measurements each day, three tensile samples and three impact samples were taken out for mechanical property tests. Mechanical Property Estimation Tests Mechanical property tests include: tensile strength and impact resistance of the composite. The dog-bone specimens (the total length of specimens is 150 mm; gauge part length and width are 50 and 10 mm, respectively; and the specimen thickness 5 mm) were used to evaluate the tensile strength of the composite. The tensile tests were conducted using an Instron 5567 test machine with a loading speed of 0.5mm/min, referring to ASTM D638-96 [6]. The impact test specimens had a dimension of 60 x 13 x 5 (length X width x thickness, mm) with a small V-notch (2 mm in depth) cut on one edge of the specimen. Impact tests were conducted on an Izod Impact tester according to ASTM D256-02 [7]. The fractographies of the composite samples were alanyzed using an optical microscope and an SEM.
RESULTS AND DISCUSSION Mechanical Properties and Microstructures of the Composites The fabricated composite panels were inspected by optical microscopy. The surface examinations show that the composite panels had very fine quality. The microstructure observation of the polished cross-section area shows that no air bubbles existed both on surface and interior, and there existed very satisfactory bonding between the fibre and the resin, typically see Figure 1. The results of tensile strength and energy absorption for both composites with and without fibre surface treatment are shown in Table 1. Clearly, the fibre surface treatment can increase the mechanical properties of the composite. >jd:i-_.i-ibv, iii
N:i;iir,tE fritr in
2 dirci-iim
Y-J:>-.nm
FIGURE 1 Microstructure of the fabricated sisal fibre reinforced epoxy composite
Natural Sisal Fibre Reinforced Epoxy Composites
91
TABLE I Mechanical properties of the composite at different conditions Mechanical properties Tensile strength (MPa) Surface treated No treatment Absorbed energy (J) Surface treated No treatment
Dry
Day 1
Day 2
Day 3
Day 4
Day 5
Day 6
Day 7
Day 8
39.2 34.7
36.1 30.2
33.4 27.9
31.5 25.3
29.4 23.4
27.2 22.6
25.4 21.3
24.5 19.5
23.1 18.1
1.72 1.54
1.52 1.34
1.32 1.23
1.20 1.12
1.06 0.96
0.96 0.87
0.84 0.75
0.75 0.67
0.71 0.62
Water Absorption and its Influence on Property of the Composite The percentage uptake of water in the sisal fibre reinforced epoxy composite, for either untreated and treated fibres, is plotted against dwell time as shown in Figure 2. Clearly, the rate of water uptake is fairly rapid in the early stage, this is, during the first few days. Thereafter, percentage uptake of water reaches nearly saturation. But the composite without fibre surface treatment shows a longer time to reach the saturation condition of water uptake. Moreover, the composite with fibre surface treated has a lower water absorption rate compared with that of untreated one. This means that the untreated sisal fibre composite can absorb more water than treated one. The results of tensile strength and impact energy absorption for the composites with and without fibre treatment are also shown in Table 1. It can be seen that the composite exposed to the elevated temperature and moisture environment has a lower tensile strength and impact resistance compared to the original dry one, and an increase in water uptake leads to decrease in both tensile strength and impact resistance. However, the water/moisture absorption effect can be reduced by the fibre surface treatment. The composite with the treated fibres has a better resistance to water uptake, thus a relatively less degradation of mechanical properties compared to the untreated one. The main reason is that the surface treatment of sisal fibres has changed the chemical function group from hydrophilic to hydrophobic, and improved the bonding between sisal fibres and polymer matrices, and thus reduced the moisture absorption in the composite. As known, the interface plays a predominant role on the load transfer between fibre and matrix. Good interfacial bonding is crucial for the fulfillment of the advantages of both reinforcing fibre and matrix. 2.00 -fiber surface untreated -fiber surface treated
1.60 0)
1c
1.20
o
0.80
0.40
0.00 0
1
2
3
4
5
6
7
8
9
10
Dwell time (day)
FIGURE 2 Results of water absorption rate versus dwell time (at 70 DC)
92
Natural Sisal Fibre Reinforced Epoxy Composites
Figure 3 shows optical microscope images of a broken specimen after fracture test, which was immersed in 70 °C hot water for 9 days. The failure of the fibre bundle shows a fracture with less ductility; and no obvious fibre pull-out, which generally presents the relatively satisfactory bonding quality between the fibre and matrix, was observed. The moisture absorption resulted in serious swelling of the fibres, as shown in Figure 3(b).
(a) Cross-section of the broken specimen
(b) A: Breakage of a fibre bundle
v- • (c) B: Debonding along a poor interface
(d) C: Debonding along a well-bonded interface
FIGURE 3 Microstructure observation of a broken specimen immersed in 70 °C water for 9 days (without fibre surface treatment)
The studies showed that the major content of natural sisal fibre is cellulose [8, 9] which is a hydrophilic glucan polymer consisting of a linear chain of 1, 4-p-bonded anhydroglucose unit [10]. This large numbers of hydroxyl groups result in the hydrophilic properties of sisal fibre, that is, sisal fibre is prone to absorbing moisture (or water). This results in a very poor interface between sisal fibre and the hydrophobic polymer matrices and very poor moisture absorption resistance [11]. For the composite samples exposed in an elevated temperature moisture environment, therefore, the main reasons for the degradation of mechanical properties
Natural Sisal Fibre Reinforced Epoxy Composites
93
and microstructure are as follows: (1) the swelling of the fibres due to the moisture absorption; (2) the moisture absorption deteriorates the bonding quality between the fibre and matrix, leading to a poor interfacial property between sisal fibres and polymer matrices caused by the hydrophilic properties of the sisal fibre and hydrophobic characteristics of organic polymers. The interfacial adhesion and resistance to moisture absorption can be improved by fibre surface treatment with appropriate chemical solutions. Thus the mechanical properties of the composite can also be improved.
CONCLUSIONS 1. There exists an obvious water uptake in natural sisal fibre reinforced epoxy composite. The rate of water uptake is fairly rapid in the early stage of dwelling, before it reaches a saturation condition. 2. The moisture absorption in sisal fibre reinforced epoxy composite results in serious property deterioration of the composite. 3. The main mechanisms of the water uptake induced property deterioration are the swelling of the fibres in moisture environment, and the degradation of the bonding quality between the fibre and matrix. 4. Appropriate fibre surface treatments could improve the bonding quality between the fibre and matrix, and decrease the moisture absorption, thus improve the mechanical properties of the composites.
REFERENCES 1.
Dewimille, B. and Bunsell, A. R. 1982. "The modeling of hydrothermal aging in glass fibre reinforced epoxy composites." J. Phys. D: Appl. Phys, 12: 2079-2091. 2. Vaddadi, P., Nakamura, T. and Singh, S. P. 2003. "Transient hydrothermal stresses in fiber reinforced composites: a heterogeneous characterization approach," Composites Part A: Applied Science and Manufacturing, 34: 719-730. 3. Vaddadi, P., "Nakamura, T. and Singh, R. P. 2003. "Inverse analysis for transient moisture diffusion through fiber-reinforced composites," Acta Materialia, 51: 177-193. 4. Kootsookos, A and Mouritz, A. P. 2004. "Seawater durability of glass- and carbon-polymer composites," Composites Science and Technology, 64 (in press, and web on-line). 5. Bisanda, E. T. N. and Ansell, M. P. 1992. "Properties of sisal-CNSL composites." Journal of Materials Science, 27: 1690-1700. 6. ASTM D638-96. Standard Test Method for Tensile Properties of Plastics. ASTM, Philadelphia. 7. ASTM D256-02. Standard Test Methods for Determining the Izod Pendulum Impact Resistance of Plastics. ASTM, ASTM, Philadelphia. 8. Joseph, K. and Thomas, S. 1996. "Effect of chemical treatment on the tensile properties of short sisal fibre-reinforced polyethylene composites." Polymer, 37: 5139-5149. 9. Paul, A., Joseph K. and Thomas, S. 1997. "Effect of surface treatments on the electrical properties of low-density polyethylene composites reinforced with short sisal fibers," Composites Science and Technology, 57: 67-79. 10. Li, H., Pawel, Z. and Per, F. 1987. "Cellulose fiber-polyester composites with reduced water sensitivity (1) - Chemical treatment and mechanical properties," Polymer Composites, 8: 199-207. 11. Li, Y., Mai, Y.W. and Ye, L. 2000. "Sisal fibre and its composites: a review of recent developments," Composites Science and Technology, 60: 2037-2055.
Effective Thermomechanical Properties of Interpenetrating-Structured Composites Matthew Tilbrook*, Robert Moon, Lyndal Rutgers and Mark Hoffman. School of Materials Science & Engineering, University of New South Wales, Australia
ABSTRACT Composites exhibiting an interpenetrating structure have received recent attention for their potential improved toughness properties. Numerous models for prediction of effective properties of composite materials have been developed, however these have tended to focus on traditional composite structures. Alumina/epoxy and alumina/aluminium composites with interpenetrating structures were produced via a multi-step infiltration process, and their mechanical properties investigated via the impulse excitation technique. Effective properties of these specimens and other interpenetrating-structured composites appear to be predicted most successfully using the effective medium approximation (EMA). The EMA does not specify internal geometry, but rather considers inclusions of each constituent phase situated within an effective medium, which is appropriate for the non-periodic structures of the composites investigated.
INTRODUCTION Composites exhibiting an interpenetrating structure, in which both phases are continuously connected networks, have received significant interest recently for applications requiring high toughness, temperature resistance or multifunctionality [1], Most models developed for effective property predictions have tended to focus on traditional composite structures: particle/matrix, fibre/matrix and laminates; though there are models which do not assume a particular internal geometry [2], That interpenetrating structures do not usually display a periodic regularity suggests that the non-geometryspecific models may be more valid. Thermoelastic properties of particular composites with interpenetrating structures have variously been predicted with the HashinShtrikmann bounds [3,4], the effective medium approximation (EMA) [5,6] and the Tuchinskii unit-cell model [7,8]. The effective medium approximation was found to be the most appropriate of these for predicting the elastic properties of alumina-epoxy composites [9]. The extreme contrast in elastic properties of these two phases (Table 1) has two implications: amplified variation between predictions from different models; and possible aberrant behaviour due to high strain mismatch at phase interfaces. In this paper, it is shown that the effective medium approximation is appropriate for a range of composites with interpenetrating structures. The results of mechanical property measurements, on alumina-epoxy and alumina-aluminium composites and porous alumina specimens, are presented. These results and those of other researchers for similarly structured composites are shown to be simulated well using the EMA. * Correspondence Author, School of Materials Science & Engineering, University of New South Wales, Sydney NSW 2052 Australia. Email: [email protected] Fax: (02) 9385 5956.
Thermomechanical Properties of Interpenetrating-Structured Composites
95
EFFECTIVE MEDIUM APPROXIMATION The effective medium approximation, or self-consistent approach, was derived from the work of Eshelby [10], Hill [11] and others. It is based on the assumption that regions of each phase within the composite may be treated as being embedded in an effective medium. This results in a set of equations relating constituent phase properties to effective properties via weight functions, dependent on volume fraction and assumed inclusion shapes.
{(Kn-K*)-TK) = 0
((Gn-G*)-TG} = 0
(1)
The strain relation tensors TKW and TQ W are determined from a matrix A which is defined in terms of Eshelby's inclusion shape tensor P and shape functions f(v|/), where \|/ is the shape parameter describing the ellipsoid aspect ratio (prolate for V|/ < 1, spherical for v|/ = 1, and oblate for \|/ > 1). These tensors and functions are given elsewhere [5,9]. The EMA does not specifically assume continuity of phases, which can lead to problems: porous structures with >50% porosity are predicted to have zero stiffness, for example. This issue must be considered when interpreting EMA predictions.
A
200 um _
*
<*
"X, - > "*
FIGURE 1 Microstructural images of composite samples with interpenetrating-network structures: A) 5% epoxy. B) 20% epoxy. C) 30% epoxy. D) 25% aluminium. Alumina appears as the light phase, epoxy is the grey phase and the darker spots are pores, except in D: alumina dark; aluminium light.
EXPERIMENTAL PROCEDURE Alumina/epoxy and alumina/aluminium composites with interpenetrating structures have been produced via a multi-step infiltration process [9,12]. Polyurethane foam (Bulpren S-31048, Eurofoam, Troisdorf, Germany) was compressed to required density and used as an imprint for the interpenetrating structure. Alumina slip (99.99% AI2O3,
96
Thermomechanical Properties of Interpenetrating-Structured Composites
Taimicron TM-DAR, Taimei Chemicals Co Ltd, Japan) was then infiltrated into the foam under varying pressure conditions and allowed to dry over several days. The foam was burnt out at 800°C, then the alumina sintered at 1500°C for one hour. The resulting densified alumina bodies, containing a continuous network of pores, were machined to size. These were infiltrated, either with epoxy (Epofix, Struers, Denmark) at room temperature under cycled pressure conditions, or with aluminium at high temperature and pressure in an argon atmosphere. Specimens were then machined to size, and polished using diamond paste, down to a diamond particle size of 1 \xm, to enable microstructural characterisation with an optical microscope. Representative microstructural images are shown in Figure 1. The elastic properties were determined using the impulse excitation technique. This involved striking the sample gently to stimulate vibration, and measuring the resonant frequencies for flexural and torsional modes using a microphone and signal analysis software (Analyzer2000, www.brownbear.de). Elastic properties were measured for alumina-epoxy and alumina-aluminium composites, and also for alumina preforms at various stages throughout the production process. RESULTS The measured elastic property values for alumina-epoxy composites are presented in Figures 3 and 4, showing the variation of properties with composition. Predictions using the EMA, with shape factor (\j/) values between 1 and 6 show reasonable agreement with measured values for Young's modulus and Poisson's ratio. The predictions from Tuchinskii's unit cell model [7] and the finite-element model of Wegner and Gibson [13] agree with experiment for alumina volume fractions above 0.8, however below this there is significant disagreement. This may be attributed to the fact that the geometrically regular structures assumed for these models (unit-cell and stacked spheres) differ significantly from the real structures, as seen in Figure 1. Accordingly, the success of the EMA predictions is associated with its non-geometry specific nature. 0.4
(a)
0.35
h
1,+'
__
. 0-1 A
0.05
Experimental results I EMA prediction I
0 20
40
60
Composition [%vol Alumina]
I
20
40
60
80
100
Composition [%vol Alumina]
FIGURE 2 Effective mechanical property values for alumina-epoxy composites, (a) Young's Modulus: experimental results (A), computational predictions (•) [15], Tuchinskii model predictions [5], and EMA with ip = 1 and \p = 6. B) Poisson's Ratio: Experimental results (A) and EMA predictions (\p = 6).
Thermomechanical Properties of Interpenetrating-Structured Composites
97
TABLE I Experimentally determined constituent properties
Material Alumina Epoxy Aluminium
EJGPa] 397 3.4 69
Nu[v] 0.23 0.35 0.33
= 250 o « 200 c J> 150
B •« 100
I
EMA - porous (Si)
Expt - porous 0.1 0.2 0.3 0.4 Composition [Phase 2 Volume fraction]
0.7
0.75
0.8
0.S5
0.9
0.95
Volume Fraction of Alumina
FIGURE 3 Effective composite properties, (a) Young's Modulus for porous alumina specimens, before (o) and after (•) infiltration with epoxy, and EMA with \j/ = 8. (b) Alumina-aluminium - Young's modulus and thermal expansion, experiment (•) and refs [13] (•) and [14 ] (»,°), and EMA with ip = 10.
Figure 3(a) displays Young's modulus values for several alumina preforms at different stages of processing which are concordant with EMA predictions. These were specifically measured to enable calculation of stresses during processing. Results for alumina-aluminium obtained by the authors and others [13,14] are displayed in Figure 3(b) along with EMA predictions, demonstrating good correlation for Young's modulus and also for thermal expansion coefficient, as discussed by Hoffman et al [6]. FURTHER APPLICATIONS To demonstrate the general applicability of the Effective Medium Approximation method to composites with interpenetrating structures, EMA predictions have been obtained for several composite systems investigated experimentally by other researchers. Tuchinskii compared theoretical predictions, from his model for co-continuous structured composites, to experimental results for Fe-Pb, W-Cu and Ti-Mg composites [7]. As shown in Figure 4(a), the EMA predictions are very close to the measured values. The Tuchinskii model also provides good predictions, however these are given as upper and lower bounds, and hence are less precise. Both Tuchinskii and Jedamzik et al. showed that Tuchinskii's model could be used for tungsten-copper composites [7,8]. Figure 4(b) shows that the EMA and Tuchinskii's model provide very similar good predictions across a wide range of volume fractions. Wegner and Gibson have conducted a significant investigation into mechanical properties of interpenetrating-phase composites [13,16,17]. They produced and characterised steel-bronze and steel-resin composites, and simulated their mechanical response using a three-dimensional finite-element model. Whilst their computational
98
Thermomechanical Properties of Interpenetrating-Structured Composites
model provided good predictions, it would be very time-consuming to set up, and cannot be applied across the full range of compositions due to the geometric assumptions involved. As shown in Figure 5, the EMA provides sufficiently accurate predictions, which can be improved by considering porosity in some specimens, as discussed by Wegner and Gibson, or by varying the shape factor, \\i. The steel-resin composites are of particular interest, due to the extreme disparity in constituent properties, providing a useful comparison with results obtained for aluminaepoxy composites. The sharp drop-off in stiffness with increase in compliant phase volume fraction is even more significant in the steel-resin system, which could be due to differences in stress transfer at phase boundary interfaces. A good fit was obtained with a shape factor \\i = 10. This suggests that the optimum choice of shape factor may depend on the disparity in constituent material properties as well as the geometry of the composite structure. As the appropriate choice of shape factor for a particular composite system is not clear however, experimental measurement of properties is recommended.
EMA Predictions Jedamzik ' Results
0.2 0.4 0.6 0.8 Volume Fraction (Second Phase)
0.2
0.4 0.6 0.8 Volume Fraction of Copper
FIGURE 4 Comparison of EMA predictions with experimental values and Tuchinskii model predictions for Young's modulus of (a) iron-lead and titanium-magnesium composites [7] and (b) tungsten-copper composites [7,8] with interpenetrating structures.
0.2
0.4
0.6
0.8
Volume Fraction of Steel
FIGURE 5 Comparison of EMA predictions with experimental measurements [15] of Young's modulus of steel-resin (o) and steel-bronze (•) composites with interpenetrating structures.
Thermomechanical Properties of Interpenetrating-Structured Composites
99
CONCLUSIONS The mechanical properties of composites with interpenetrating structures have been investigated. The measured elastic properties of alumina-epoxy and alumina-aluminium composites produced by infiltration were more precisely simulated with the effective medium approximation (EMA), than with other models. The EMA was also applied successfully to a range of composite systems investigated by other researchers, indicating a general suitability for use with interpenetrating structured composites. Investigation of composites with significantly disparate constituent properties allows improved differentiation between predictions from different models, which highlighted the general applicability of the EMA in preference to other models. For composites with significantly differing constituent properties, EMA predictions appear to be reasonably accurate, and are preferable to the model of Tuchinskii in this regard. The advantages of the EMA over the unit-cell model of Tuchinskii, or more involved models such as those of Wegner and Gibson, is that internal phase geometry is not specified and that exact values, rather than a range, are predicted. Nevertheless, experimental determination of properties for validation of models is recommended. REFERENCES 1. 2. 3. 4.
5. 6. 7. 8. 9. 10. 11. 12. 13. 14.
15. 16. 17.
Wegner L.D., LJ. Gibson, 2001. "The fracture toughness behaviour of interpenetrating phase composites"Int. J. Mech. Sci. 43:1771-1791. Hashin Z., 1983. "Analysis of Composite Materials - A Survey," J. Appl. Mech. 50:481-505. Hashin, Z., S. Shtrikman, 1963. "A variational approach to the theory of the elastic behaviour of multiphase materials,"./ Mech. Phys. Solids 11:127-140. Torquato S, Yeong CLY, Rintoul MD, Milius DL, Aksay IA. Elastic Properties and Structure of Interpenetrating Boron Carbide/Aluminum Multiphase Composites. J Am Ceram Soc 1999; 82(5):1263-1268. Kreher W., W. Pompe, 1989. "Internal Stresses in Heterogeneous Solids," Akademie Verlag, Berlin. Hoffman M., S. Skirl, W. Pompe and J. Rodel, 1999. "Thermal Residual Strains and Stresses in A12O3/A1 Composites with Interpenetrating Networks," Acta Mater. 47(2):565-577. Tuchinskii, L.I., 1983. "Elastic Constants of Pseudoalloys with a Skeletal Structure," Porosh Metall 7(247):85-92 (Russian). Translated in: Powder Metallurgy and Metal Ceramics, Plenum. Jedamzik R., A. Neubrand, J. Rodel, 2000. "Characterisation of electrochemically processed graded tungsten/copper composites," Mat. Sci. Forum 308-311:782-787. Tilbrook M.T., RJ. Moon and M. Hoffman, 2003. "On the Mechanical Properties of Alumina-Epoxy Composites with an Interpenetrating Network Structure," Mat. Sci. Engng. A (submitted). Eshelby J.D., 1957. "The determination of the elastic field of an ellipsoidal inclusion, and related problems," Proc. Roy. Soc. A 349:376-396. Hill, R., 1965. "A self-consistent mechanics of composite materials," J. Mech. Phys. Sol. 13:213-222. Cichocki FR Cichocki, KP Trumble, J Rodel, "Tailored Porosity Gradients via Colloidal Infiltration of Compression Molded Sponges," J. Am. Ceram. Soc. 81[6] (1998) 1661-64. Wegner, L.D., LJ. Gibson, 2000. "The mechanical behaviour of interpenetrating phase composites I: modelling," Int. J. Mech. Sci. 42:925-942. H Prielipp, M Knechtel, N Claussen, SK Streiffer, H Miillejans, M Riihle, J Rodel, 1995. "Strength and fracture toughness of aluminum/alumina composites with interpenetrating networks," Mat. Sci. Eng.A 197:19-. Neubrand, A., T.-J. Chung, J. Rodel, E.D. Steffler and T. Fett, 2002. "Residual stresses in functionally graded plates," J. Mater. Res., 17 (11): 2912-2920. Wegner, L.D., LJ. Gibson, 2000. "The mechanical behaviour of interpenetrating phase composites II: a case study of a three-dimensionally printed material," Int. J. Mech. Sci. 42:943-964. Wegner, L.D., LJ. Gibson, 2001. "The mechanical behaviour of interpenetrating phase composites III: resin-impregnated porous stainless steel," Int. J. Mech. Sci. 43:1061-72.
Mechanical and Thermal Properties of Phenolic Composites Reinforced with Hybrid of Spun and Continuous Carbon Fabrics Tae Jin Kang*, Seung Jun Shin, Kyungho Jung and Young Jun Cho School of Materials Science and Engineering, Seoul National University, Korea
ABSTRACT The mechanical and thermal properties of continuous carbon fabric/spun carbon fabric interply hybrid composite materials have been studied. The hybrid composites with continuous carbon fabric of high tensile, flexural strength and spun carbon fabric of better interlaminar shear strength and lower thermal conductivity are investigated in terms of mechanical properties as well as thermal properties. Through hybridization, tensile strength and modulus of the spun reinforced composites were increased by about 28% and 20%, respectively. The hybrid composite also shows better interlaminar shear strength than continuous carbon reinforced composites. The thermal conductivity of the hybrid composite is lower approximately only 4~8% along the in-plane direction than that of the continuous carbon reinforced composite. The transverse thermal conductivity of the hybrid composite decreases with increasing continuous carbon fiber volume fraction. We predicted the thermal conductivity of textile composites using thermal-electrical analogy. The predicted thermal conductivities showed good agreement with experimental results. The erosion rate and insulation index were calculated through torch test. The spun reinforced composite has a higher insulation index than the continuous carbon reinforced composite and hybrid composites over the entire range of the back-face temperature of the specimen. The different stacking sequence has influence on the insulation index and erosion rate of hybrid composites.
INTRODUCTION Carbon/phenolic composites show excellent ablation resistance so that they have been widely applied to the thermal protection system for reentry vehicles or rocket engine components [1]. One of the most critical variables to govern the ablation performance of the composite is reinforcing materials [2], For solid rocket motor applications, one of the key requirements of the composite is low thermal conductivity to minimize the thickness of pyrolyzed carbon layer and temperature rise at the back-face of the composite [3]. The rayon-based carbon fibers were commonly used in the past due to the low thermal conductivity. In these days, however, it's not easy to get rayon-based carbon fibers because the manufacturing process causes serious environmental problems. So the PAN-based carbon fibers have gradually replaced the rayon-based carbon fibers. But PAN-based carbon fibers show high thermal conductivity in comparison with rayon-based carbon fibers. Corresponding Author, San 56-1, Shillim-dong, Kwanak-gu, 151-742, Korea, +82-2-885-1748, [email protected]
Mechanical and Thermal Properties of Phenolic Composites
101
One of the methods to reduce thermal conductivity of carbon/phenolic composites is using spun carbon yarn. Continuous carbon fibers show high thermal conductivity in the direction of fiber axis. There is feasibility of reducing thermal conductivity of composite using spun carbon fabric as reinforcement. Moreover, the protruded fibers on the staple yarn in spun composites play an important role in suppressing delamination due to the effect of fiber bridging as supplementary reinforcement [4-6]. We produced spun carbon yarn from staple Oxi-PAN fiber and fabricated carbon fabric using spun carbon yarn. We manufactured phenolic composites reinforced with spun carbon fabric, continuous carbon fabric and both of them. The mechanical and thermal properties of composite materials have been studied. The hybrid composites with continuous carbon fabric of high tensile, flexural strength and spun carbon fabric of better mterlaminar shear strength and lower thermal conductivity are investigated in terms of mechanical properties as well as thermal properties. EXPERIMENTAL Preparation of Composites The continuous and spun carbon fabric was prepared from stabilized PAN fiber supplied by Zoltek Co.. Spun stabilized PAN yarns were manufactured through woolen spinning and then woven into eight harness satin fabric. The maximum treatment temperature was maintained at 1100 °C, which is relatively lower value than conventional ones for the purpose of lowering the thermal conductivity of carbon fabric. Nitrogen gas was purged throughout carbonization process. The continuous carbon fabric was fabricated using low temperature heat-treated carbon filament tows. The spun carbon fabric was made from the spun Oxi-PAN fabric by carbonization. The resol-type phenolic resin KC-98, supplied from Kang Nam Chemical Co., was used as matrix for composite materials. The phenolic composites were fabricated at 150 °C for 2 hours. The debulking process at 105 °C for 30 minutes was done to remove possible entrapped air and voids in the resulting composite. Five kinds of composites are manufactured. Those are continuous fabric reinforced composite, spun fabric reinforced composite and three kinds of continuous/spun fabric interply hybrid composites. Characterization of Composites The tensile, flexural and short-beam shear tests were performed using MTS Sintech 10/GL based upon ASTM D3039, D790 and D2344, respectively. The thermal conductivities were measured by employing a comparative steady-state method using a tailor-made apparatus based on ASTM E-1225-87 [7]. Fig.l shows the schematic illustration of the apparatus for thermal conductivity measurement. The erosion rate and insulation index were calculated through torch test based on ASTME-285-80[8]. PREDICTION OF THERMAL CONDUCTIVITY We predicted the thermal conductivity of laminated composite using thermal-electrical analogy. We assumed that the cross-section of the fiber bundle was horse-track shape. We adopted several assumptions. First, we neglect the thermal contact resistance between fiber and matrix. Second, the heat flows rectilinearly and the heat flow
102
Mechanical and Thermal Properties of Phenolic Composites Pressure
Insulating/ Materials^
FIGURE 1 Schematic illustration of the apparatus for thermal conductivity Measurement
are parallel one another. Finally, the thermal conductivity of unit cell represents the whole composite structure. Figure 2 shows the idealized unit cell of eight harness satin fabric. The unit cell is divided into four kinds of elements for the analysis of thermal conductivity in transverse direction. On the other hand, six kinds of elements are defined for the analysis of in-plane direction thermal conductivity. Most elements are divided again into several regions. We derived the thermal conductivity of textile composites in transverse direction and in-plane direction. We can predict the thermal conductivity of textile composites in transverse and in-plane direction using Equations (1) and (2).
01 / /
//
A4W
// // •' to
/r <»
m
(l)
A
m,
M /(" \\W f/-\ km
/ft '" A w
„ ^ h h
.*
/ y
(2i
/
V/m
FIGURE 2 Idealized unit cell of 8-harness satin fabric lamina
Mechanical and Thermal Properties of Phenolic Composites
103
Skta2 f {kxhm + 2kmhz
kxhz (4 - Ji) + 4kxhm +(x + 4)hzkm
2
64kmkxh z (16 - HTC)W
\6kmk2ghz
+16hmkx + 4nhzkm
%kmk2ag
hz + jchzkm
(1)
|
k1{2h + hz) + 2kmhz Ukmkxag hmkx
+ hz
,
, + lnhzkm
(16-
*kmg2 hm + 2hz
h{8R(x)+2Ri2)+6R{3)
6R,
(2) (6)
where kji] (4 - K) + 7[kvlh] + 4kw2ahz
knh
(4-
kr,h (4-
h +4ak Z
- = 4x
64g2
4g
ffi
32g2
4kmkwXahz
1
_
kmghm
R{4) K R(5)
a + hz
f
kmghz
|
4kmknghz
a + hz
R (6)
kmg(2hz+hj
The constant ^m represents the thermal conductivity of matrix region and kj is the thermal conductivity of the region defined as /. hz and hm represent the depth of fiber domain and matrix domain, respectively. The length of the straight line in the horse track shape cross-section is a and the width of the region that contains matrix only. RESULTS AND DISCUSSION Table I shows the mechanical properties of composite materials. Through hybridization, tensile strength and modulus of the spun reinforced composites were increased by about 28% and 20%, respectively. The hybrid composite also shows better interlaminar shear strength than continuous carbon reinforced composites. The thermal conductivities of composite materials are shown in Table II. The thermal conductivity of the hybrid composite is lower approximately only 4~8% along the
104
Mechanical and Thermal Properties of Phenolic Composites
in-plane direction than that of the continuous carbon reinforced composite. The transverse thermal conductivity of the hybrid composite decreases with increasing continuous carbon fiber volume fraction. The spun reinforced composite has a higher insulation index than the continuous carbon reinforced composite and hybrid composites over the entire range of the back-face temperature of the specimen as shown in Figure 3. TABLE I Mechanical properties of composite materials Coiitiiiuoius composite 436.3 331.5 16.8
Tensile strength (MPa) Flexural strength (MPa) ILSS (MPa)
Spun composite 174.6 248.0 26.2
1:3 227.0 289.0 19.2
TABLE II Thermal conductivity
Transverse In-Plane
Continuous composite 0.62 2.25
1:3
1:5
1:7
0.57 2.17
0.58 2.08
0.66 2.04
Spun composite 0.69 2.07
• continuous Ohybrid(1:3) Hhybrid(1:5) •hybrid(1:7)
250 °C
450 °C
Backface Temperature of Specimen (°Q FIGURE 3 Insulation index
The predicted thermal conductivity of spun carbon composite in two directions using Equations (1) and (2). The predicted values were 0.79 and 2.37. They differ from the experimental values by 10%.
Mechanical and Thermal Properties of Phenolic Composites
105
CONCLUSIONS The mechanical and thermal properties of spun carbon fabric/continuous carbon fabric interply hybrid composite materials have been studied. Through hybridization, tensile strength and flexural strength of hybrid composites were increased by about 28% and 20% respectively, compared with spun carbon composites. The thermal conductivity of the hybrid composite is lower approximately 4~8% along the direction parallel to the laminar plane than that of the continuous/phenolic composite. Erosion resistance and insulation index of hybrid composites increased with the spun carbon volume fraction. We are modifying the prediction method to increase the accuracy.
REFERENCES 1. 2. 3. 4. 5. 6. 7. 8.
J. R. Diefendorf. 1988. Carbon Fibers and Their Composites, pp. 46. D. F. D'Alelio and J. A. Parker. 1971. Ablative plastics. New York: Marcel Dekker, pp. 1-39. R. L. Noland. 1994. "Ablative and Insulative Structures and Microcellular Carbon Fibers Forming Same," US Patent 5,298,313. R. B. Krieger Jr.. 1984. 29th international SAMPE Symposium, pp. 1587. G. L. Dolan and J. E. Masters. 1988. 20th international SAMPE technical conference, 34. C. T. Sunand and S. Rechak. 1988. in composite materials: Testing and design(Eight Conf), ASTM STP 972, J.D. Whitcomb, Ed. ASTM, Philadelphia, 97. Standard Test Method for thermal conductivity of solid by means of the guarded-comparative longitudinal heat flow technique, ASTM E 1225-87 Standard Test Method for oxyacetylene ablation testing of thermal insulation materials, ASTM E 285-80.
Specific Properties vs. Microstructures for Syntactic Foam Erwin Wouterson, Freddy Boey, Xiao Hu School of Materials Engineering, Nanyang Technological University, Nanyang Avenue, Singapore 639798, Singapore Shing-Chung Wong^ Department of Mechanical Engineering and Applied Mechanics, North Dakota State University, Fargo, ND 58105, USA
ABSTRACT This paper addresses the specific mechanical properties from different microstructures of syntactic foam. In this study we assessed the specific tensile, compressive and flexure strength and modulus for syntactic foam containing various volume fractions of hollow microspheres. Three different types of hollow microspheres were studied. Preliminary tensile and flexure results showed a decreasing trend for the specific strength of syntactic foam with increasing filler content. Interestingly, the specific tensile and flexure modulus elicited a different trend for each type of filler. Especially the increase in specific Young's modulus for the K46 glass microspheres was noteworthy since this trend has not been reported before. Compression tests showed the specific compressive strength decreased with increasing filler content. The specific compressive modulus, however, increased with increasing filler content. INTRODUCTION Syntactic foam is a ternary material system made in a mechanical way by mixing microballoons (the filler) with a resin system (the binder). The filler microspheres may be made of polymer, ceramic, carbon, or metal. Mostly thermoset resins are used as the binder. Dispersion of the hollow microspheres creates a porous material with closed cells. By changing the amount of microspheres, different densities and thus microstructures of syntactic foam can be created. Syntactic foam is known to possess low density, high stiffness, excellent compressive and hydrostatic strength and good impact behavior [1-5]. Unlike most other foams, syntactic foam is a material whose density before curing is the same as that after curing. Such predictability and attribute are advantageous in the manufacturing process in aerospace structures. Most of the studies on the mechanical properties focus on syntactic foam contain high volume fractions of hollow microspheres as these structures have the lowest density. In addition to high volume fractions, most studies focus on one type of microsphere and the results are not normalized against the density. From design point of view it is of more interest to view the results in the light of specific properties 5
Corresponding Author. Prof. S.-C. Wong. Fax:(701)231-8913. Email: [email protected]
Specific Properties vs. Microstructures for Syntactic Foam
107
allowing the comparison of the performance of syntactic foam to other materials. This study focuses on the effect of different microstructures on specific mechanical properties of syntactic foam. Results from tensile, compressive and flexure tests will be discussed for three different types of microspheres. EXPERIMENTAL WORK Materials The syntactic foam for this research was produced by mechanical dispersion of hollow microspheres in epoxy resin. Epicote 1006 epoxy resin was used as the binder and three different types of hollow microspheres, namely 3M Scotchlite™ Glass Bubbles K15 and K46 and Phenoset BJO-093 phenolic microspheres, were used for the filler. Properties of the different types of microspheres can be found in Table 1. The microspheres were added to the resin while slowly stirring the mixture to minimize gas bubbles in the resin. After dispersion, the syntactic foam was compression molded using an aluminum mold. The syntactic foam was left under the press for 18-22 hours to cure at room temperature. By adding different amounts of microspheres to the matrix, syntactic foams with various densities were created. Mechanical Tests Three types of mechanical tests, namely tensile, flatwise compression and flexure were performed on different microstructures of syntactic foam. For the tensile tests, syntactic foam was machined into rectangular shapes of 170 x 18 x 6 mm3. Each specimen was then cut into a standard 'dog-bone' shape by means of a TensilKut machine. The tests were carried out at room temperature using an Instron Testing Machine (Model 5567) at a crosshead speed of 5.0 mm.min"1. For each test the strain was recorded with a clip-on strain gauge. The Young's modulus, E, was measured from the initial region of deformation. For the flatwise compression test, syntactic foam was machined to blocks of 25 x 25 x 12.5 mm3. The length and width were chosen according to ASTM C365-00 [6] as in future work the syntactic foam will be used as the core material in sandwich composites. The height of the specimen was chosen based on the studies performed by Gupta et al. [1]. According to Gupta, it is recommended to use specimens with a low aspect ratio to minimize the effect of the shear stress component. The tests were carried out at room temperature using an Instron Testing Machine (Model 4206) with a maximum capacity of lOOkN. The crosshead speed was 0.5 mm.min"1. TABLE I Properties of different microspheres
Type of Microsphere BJO-093 K15 K46
True Density [g/cc] 0.21-0.25 0.15 0.46
Static Pressure [MPa] 3.44 2.07 41.37
Effective Top Size [/fm] 90 115 80
For the flexure tests, syntactic foam was machined to 127 x 12.7 x 3 mm3 in dimensions. The tests were performed by an Instron 5567. The span of the support
108
Specific Properties vs. Microstructures for Syntactic Foam
was chosen to be 48 mm to achieve a span-to-depth ratio of about 16 as recommended by the ASTM D790-00 [7]. The strain rate was 0.01 mm.mm"1.mm1. RESULTS AND DISCUSSION Specific Tensile Properties Syntactic foam behaves like a linear-elastic material up to fracture when loaded in tension. The material experiences catastrophic fracture across a plane perpendicular to the tensile axis. According to Luxmoore and Owen [8], the crack initiates from an oversized void. Fig. la shows clearly that the specific tensile stress decreases with increasing fractions of hollow microspheres. The trends and values are rather similar for the three different types of microspheres, which suggest that the specific tensile strength is independent of the constituent microsphere and the difference in the microsphere size, see table 1. According to Luxmoore, the failure of the foam is connected primarily with the failure of the resin matrix. This observation is confirmed in our previous work [9]. The decreasing trend can be explained by assuming that the presence of radial and/or annular cracks associated with the pores cause crack opening displacement [10-11]. It is suggested that the non-linearity is caused by the reduction in the area of the epoxy matrix. Introduction of hollow microspheres reduces the epoxy volume fraction consequently reducing the tensile strength. It is believed that 40 vol% of microspheres is to be the maximum amount of filler which can be fully wetted by the epoxy matrix. The change in properties and behavior of syntactic foam around 40 vol% was also observed by Bunn and Mottram [4]. Often the literature reports a decreasing trend for the Young's modulus with increasing filler content [10-11]. Only Bardella and Genna [12] report an increasing trend for K37 microspheres, which have density of 37 g.cm"3. However, their results are mostly based on analytical and numerical calculations. The results from the current research, as presented in Figure lb, show similarity to the results of [12] in the sense that the trend for the specific Young's modulus with increasing filler content is depending on the type of microsphere. K46 microspheres show an almost linear increase in the specific Young's modulus, whereas K15 microspheres show a constant
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Specific Properties vs. Microstructures for Syntactic Foam
109
specific Young's modulus and phenolic microspheres show a decrease with increasing filler content. The difference between the results for K46 and K15 microspheres suggests that for microspheres of the same material composition, higher specific Young's modulus is obtained for the microspheres with a higher density. The difference between the phenolic and K15 glass microspheres explains that besides the size of the microsphere, the composition of the microsphere is of critical importance for the subsequent mechanical properties. Phenol-formaldehyde has an E of about 6.8 GPa whereas soda lime glass has an E of about 70 GPa. The difference in E is believed to be the main reason for the difference in the trends of hollow glass and phenolic microspheres. Specific Compressive Properties Under compression, syntactic foam behaves in an elastic way first. Once the material reaches its yield point, the microspheres will be crushed and severe damage occurs. The behavior observed was similar to that reported by Gupta [1] and Bunn [4]. Similar to the tensile test, failure of the foam is primarily connected to failure of the matrix. The results of the compression tests are shown in Figs. 2a and 2b. Figure 2a reveals that the specific compressive yield strength decreases with increasing filler content for phenolic and K15 microspheres. Introduction of microspheres reduces the compressive strength. K46 microspheres also reduce the compressive strength but after normalization of the strength against the density, an increasing trend in the specific compressive yield strength can be observed. The results for the specific compressive modulus are shown in Figure 2b. Again K46 performs better as shown. The anomaly displayed by the 10 vol% composition of K46 is attributed to the presence of voids in curing. Using K46 microspheres allows for higher strength and stiffness at a lower weight. K15 and phenolic microspheres show a rather similar behavior in specific compressive modulus. Both show a minimum around 20 vol% after which the specific compressive modulus slightly increases. The increase is higher for K15 microspheres.
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110
Specific Properties vs. Microstructures for Syntactic Foam
In this study, different values for the specific Young's and compressive moduli are reported. The main cause for the difference is attributed to the deformation mechanisms under different stress states. Deviatoric stresses are more pronounced in uniaxial tension as compared to hydrostatic compression. The influence of crosshead speeds in testing may play a role but is believed to be minimal, hi general lower crosshead speed leads to a lower modulus [13]. Specific Flexural Properties For most compositions of syntactic foam, some plastic deformation was detected before the specimen failed. The amount of plastic deformation decreases with increasing filler content and is much higher for syntactic foam containing hollow phenolic microspheres. It was observed that each flexure test failed at specimen side under tensile stresses. The comparable failure mode in three-point-bending explains the resemblance in trends in Fig. 3 to Fig. 1. For the specific flexure strength, some differences between the different compositions are observed. Introduction of K46 microspheres leads to a drop in the specific flexure strength, which reaches a minimum around 30 vol% after which the specific flexure strength increases almost linearly up to 50 vol%. K15 microspheres show a similar drop in the specific flexure strength and also reach a minimum around 30 vol%. However, for K15 microspheres, the specific flexure strength remains constant after 30 vol%. Phenolic microspheres do not show a sudden drop in the specific flexure strength but instead show more linear decrease. The trends and values in the specific flexure modulus are similar to the results observed in Fig. lb. The K46 microspheres show an increase in the specific flexure modulus with increasing filler content. K15 microspheres show a constant value for the specific flexure modulus where phenolic microspheres show a decrease with increasing filler content.
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Specific Properties vs. Microstructures for Syntactic Foam
111
CONCLUSIONS From the results presented in this paper, it can be concluded that the specific properties of syntactic foam depend on the type and volume fraction of microspheres utilized in the syntactic foam. The results for the tensile and flexure tests are rather similar due to the fact that both types of tests exhibit the same failure mode. Both tests elicit a decreasing trend in specific strength with increasing filler content. Interestingly and useful for future design work, the specific modulus is different for each type of microsphere. The compression tests revealed the superior performance of K46 microspheres, giving rise to a higher compressive yield strength and modulus compared to K15 and phenolic microspheres. REFERENCES 1. Gupta, N., Kishore, E. Woldesenbet, and S. Sankaran. 2001. "Studies on compressive failure features in syntactic foam material", /. Mat. Sci., 36:4485-4491. 2. Gupta, N. and E. Woldesenbet. 2002. "Compressive fracture features of syntactic foamsmicroscopic examination", J. Mat. Sci., 37:3199 -320. 3. Ho, S.K. and H.H. Oh. 2000. "Manufacturing and impact behavior of syntactic foam", J. ofAppl. Pol. Set, 76:1324-1328. 4. Burm, P. and J.T. Mottram. 1993. "Manufacture and compression properties of syntactic foams", Composites, 24(7):565-571. 5. Shutov, F.A. 1991. "Syntactic Polymer Foams" in Handbook of Polymer Foams and Foam Technology, D Klempner and K.C. Frisch, eds. Hanser Publishers, pp. 355-374. 6. Anon. April 2000. "Standard test method for flatwise compression of sandwich cores", ASTM C365-00. 7. Anon. January 2001. "Standard test methods for flexural properties of unreinforced and reinforced plastics and electrical insulating materials", ASTM D790-00. 8. Luxmoore, A.R. and D.R.J. Owen. 1982. "Syntactic Foams" in Mechanics of Cellular Plastics, N.C. Hilyard, ed. London: Applied Science, pp. 359-391. 9. Wouterson, E.M, F.Y.C. Boey, X. Hu, and S.-C.Wong. "Specific properties of syntactic foam: Effect of filler content", to be submitted. 10. El-Hadek, M.A. and H.V. Tippur. 2002. "Simulation of porosity by microballoon dispersion in epoxy and urethane: mechanical measurements and models", J. Mat. Sci., 37:1649-1660. ll.Kristic, V. and W. Erickson. 1987. "A model for the porosity dependence of Young's modulus in brittle solids based on crack opening displacement", J. Mat. Sci., 22:2881-2886. 12. Bardella, L. and F. Genna. 2001. "On the elastic behavior of syntactic foams", Int. Journal of Solids and Structures, 38:7235-7260. 13.Hertzberg, R.W. 1996. "Deformation and Fracture Mechanics of Engineering Materials", Fourth Edition, John Wiley and Sons, Inc.
Functionally-Graded Structure and Properties in Human Teeth I.M. Low* and U. Mahmood Materials Research Group, Department of Applied Physics, Curtin University of Technology, GPO Box U1987, Perth, WA, 6845, Australia
ABSTRACT The graded composition, texture and indentation responses of human enamel has been characterised by grazing-incidence synchrotron radiation diffraction and Vickers indentation. Results show that the composition of tooth enamel consists mainly calcium-apatite or hydroxyapatite (HAP). The HAP crystals formed near the occlusal surface are aligned approximately orthogonal to each other between the axial- and occlusal-sections. Pn addition, the tooth enamel has been shown to be a hierarchical graded biomaterial with a distinct gradation in structure, texture and hardness, which is reminiscent of the fibrous-microstructures found in natural plants such as bamboo and corn. A "graded-interface" approach is proposed as a biomimetic model for designing new dental or restorative materials as well as for joining of dissimilar materials. INTRODUCTION Natural biomaterials such as teeth, bamboo and oyster shells possess enviable strength and damage resistance properties [1-3]. These materials are essentially inorganic/organic composites with hierarchical graded micro structures designed by nature to withstand high stresses, hi human teeth, these stresses are borne by the highly mineralised [96% hydroxyapatite (HAP) Cai0(PO4)6(OH)2] enamel layer which also provides hardness and wear resistance but it is brittle. The enamel is shielded from catastrophic failure by the less mineralised dentin (68% HAP) which provides toughness to the otherwise brittle tooth [4-7]. The tooth enamel has often been viewed as a homogeneous solid with uniform composition and mechanical properties. However, recent investigations have shown the existence of significant variations in the mechanical properties of enamel that can be attributed to its highly oriented microstructure as well as its location, local chemistry and prism orientation [8], This idea of enamel heterogeneity within individual teeth has been recently confirmed by various researchers [9-11] through atomic force microscopy and nanoindentation mapping of hardness and elastic modulus. This paper describes the use of Vickers indentation and synchrotron radiation diffraction to depth-profile and quantify any significant local variations in microhardness, contact-damage, composition and texture within and across the depth of human enamel. * Corresponding author. Email: [email protected]
Functionally-Graded Structure and Properties in Human Teeth
113
EXPERIMENTAL METHODS Thin slices of two adult human third molars were used for this diffraction study. A precision diamond blade cutter was used to cut each tooth into two 1.0 mm thick slices that were either parallel (occlusal-section) or perpendicular (axial-section) to the occlusal surface. Prior to the diffraction measurement, the buccal and lingual sides were ground with SiC paper to obtain a planoparallel flat plate. Two separate adult human third molars were used for the measurement of indentation responses and damage. The teeth were cut either parallel or perpendicular to the occlusal surface using a precision diamond blade. The cut specimens were then cold mounted in epoxy resin and polished to 1 |Xm surface finish. Figure 1 shows the cross-section view of a polished tooth sample. The microstructures of polished and gold-coated tooth samples were examined using a Phillips XL-20 scanning electron microscope. Ex situ atomic force microscopy investigations were carried out using a Digital Instrument Dimension 3000 scanning probe microscope. Figures 2 and 3 show the highly textured microstructures of the occlusal- and the axial-section of human enamel. Long prismatic enamel rods can be seen in Fig. 3 while key-hole shaped enamel rods are shown in Fig. 2.
FIGURE 1 Optical micrograph of a human tooth FIGURE 2 The microstructure of the occlusalshowing the axial-section of a human tooth. Also s e c t i o n o f t o o t h e n a m e l a s revealed by scanning shown is a Vickers indent with microdamage electron microscopy
Depth-profiling of the near-surface composition and texture of enamel was conducted using grazing-incidence synchrotron radiation diffraction. Imaging plates were used to record the diffraction patterns at a wavelength of 0.8 A and grazing angles (a) of 0.2, 0.4, 0.8, 1.0, 3.0, and 5.0°. A typical diffraction pattern for the axialsection of a human tooth is shown in Fig. 4 where the predominant phase is HAP [12]. The relative degree of crystallinity of HAP present at various a or depths was estimated from the reflection (211) using the relative intensity ratio method. The load-dependence and depth-profiling of hardness were measured using a Zwick microhardness tester. The former was measured over a load range of 5-100 N and the latter was measured at a load of ION. The lengths of the diagonal (2a) were used to calculate the hardness, determined here as Hv = P/2a2, where P is the load used. The values of fracture toughness (Kic) were calculated as K\c = 0.025P/c15 where c is the average crack length.
114
Functionally-Graded Structure and Properties in Human Teeth
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FIGURE 4 Synchrotron radiation diffraction pattern collected at a = 0.2° for the axial section of the tooth enamel.
RESULTS AND DISCUSSION The presence of a graded structural crystallinity and/or disorder within the human enamel is shown in Fig. 5. This clearly suggests that the human enamel is a functionallygraded material with a distinct gradation in organised structure at the nanometre and micrometre scale. The degree of this organised structure is not maximum at the occlusal surface but several micrometer beneath it. It follows that the mechanical properties such as hardness and elastic modulus will not be uniform within the human enamel but show a distinct gradation. Indeed, the recent work of Cuy et al. [9] and Habelitz et al. [10] have alluded the existence of structural gradation or heterogeneity within the enamel which is confirmed by our GISRD results. As would be expected, there is a distinct contrast in the texture index (R) between the occlusal-section and the axial-section of human enamel (Fig. 6). This implies that the HAP crystals of both microstructures are roughly orthogonal to each other [3,7] which is reminiscent of the fibrous-microstructures in natural hierarchical graded materials such as bamboo, corn and barley [13]. It is also interesting to note the R values of both occlusal- and axial sections show a modest but distant variation with depth which indicates the presence of gradation in preferred orientation within the complex enamel microstructure. This display of gradation in texture within the enamel suggests that the presence of a three-dimensional interlocking HAP structure has been designed by nature to impart strength and hardness for wear resistance and stress-bearing capability.
Functionally-Graded Structure and Properties in Human Teeth
0
1
2
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4
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0.3
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Load (N)
FIGURE 8 Variations of hardness as a function of load.
The hardness profile of a human tooth in cross-section is shown in Fig. 7. The hardness is seen to decrease sharply from enamel to dentin. The display of a loaddependent hardness behaviour in the enamel is evident in Fig. 8. In contrast, the dentin layer did not display any observable load-dependence behaviour. The display of loaddependent hardness behaviour in human enamel is unique and has never been reported. This phenomenon is well-known in coarse-grained metals and ceramics such as Ti3SiC2 and can be attributed to a grain-size effect [14]. The load-dependent hardness in the enamel may be attributed to its highly textured microstructure which favours the stochastic nature of deformation damage by virtue of a statistical variation in crystallographic orientation of individual grains. Only those grains of correct orientation will favour the occurrence of intergrain deformation along certain specified grainboundaries. The expansion of deformation zone is a combination result of the activation of additional grain-boundaries as the pressure intensifies within the Vickers compressionshear zone.
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Functionally-Graded Structure and Properties in Human Teeth
An extensive damage in the vicinity of a distorted indent but with no cracks were observed in enamel at small loads (Fig. 1). Indentation cracks were only seen to form for loads greater than 50 N but not in dentine. In the former, an extensive damage in the vicinity of the indent was also observed on the axial surface but not on the occlusal surface. In both cases, there was a pronounced display of anisotropy in the cracking pattern which suggests a highly heterogeneous or textured micro structure. The fracture toughness of the axial- and acclusal-section was 1.32 ± 0.05 and 0.49 ± 0.08 MPa.Vm respectively. The results show a clear distinction in the propensity of crack propagation across the different brittle enamel microstructures. In contrast, no radial cracks were observed for dentin. The implications of the results obtained or inferred in this work are wide-ranging. For instance, future attempts to design high performance synthetic dental structures should consider at least the gradation of structure at the interfaces. This "graded-interface" approach has been currently neglected by the various researchers in developing new dental or restorative materials [15,16]. In addition, this approach is essential as a biomimetic model for joining dissimilar materials to minimise the development of undesirable residual stresses, due to a large mismatch in composition, thermal expansion and elastic moduli, which can lead to interfacial debonding, cracking and structural failure [17,18]. CONCLUSIONS The graded properties of the human tooth in terms of structural disorder and texture have been verified by the grazing-incidence synchrotron radiation diffraction. The tooth enamel has been shown to be a hierarchical graded biomaterial with a distinct gradation in structure, texture and perhaps crystallite size, which is reminiscent of the fibrousmicro structures found in natural plants such as bamboo and corn. The design implications for developing new dental or restorative materials as well as joining of dissimilar materials are discussed in the light of a "graded-interface" approach. ACKNOWLEDGMENTS This work was funded by an ASRP grant (ANBF 03/04 AB06) We thank Dr. M. Tan of the Frementle Dental Hospital for providing the tooth samples. REFERENCES 1. 2.
3. 4.
Lucas, P.W., in: B. Kurten (Ed.) 1979. Basic Principles of Tooth Design, Teeth, Form, Function, Evolution, Columbia Univ. Press, New York, pp. 154-162. Waters, N.E., 1980. "Some Mechanical and Physical Properties of Teeth", in: J.F.V. Vincent, J.D. Currey (Eds.), Mechanical Properties of Biological Materials, Cambridge Univ. Press, Cambridge, UK, pp. 99-135. Ten Cate, A.R. 1994. Oral Histology: Development, Structure, and Function (4th Edn.), 1994. Mosby, St. Louis, MO. Wang, R.Z. and S. Weiner. 1997. "Strain-Structure Relations in Human Teeth using Moire Fringes,"/ Biomech., 31[1]: 135-142.
Functionally-Graded Structure and Properties in Human Teeth 5.
6. 7.
8.
9.
10.
11. 12. 13. 14. 15. 16. 17. 18.
117
Fong, H., M. Sarikaya, S.N. White and M.L. Snead. 2000. "Nano-Mechanical Properties Profiles Across Dentin-Enamel Junction of Human Incisor Teeth", Mater. Sci. & Eng. C, 7[1]: 119-129. Lin, C.P. and W.H. Douglas. 1994. "Structure-Property Relations and Crack Resistance at the Bovine Dentin-Enamel Junction," /. Dent. Res., 73[4]: 1072-1078. Xu, H.H.K., D.T. Smith, S. Jahanmir, E. Romberg, J.R. Kelly, V.P. Thompson and E.D. Rekow. 1998. "Indentation Damage and Mechanical Properties of Human Enamel and Dentin," J. Dent. Res., 77[2]: 472-480. Low, I.M., J. Fulton, P. Cheang and K.A. Khor. 2000. "Designing New Dental Materials Through Mimicking Human Teeth," In: K.A. Khor, T.S. Srivatsan, M. Wang, W. Zhou, F. Boey (Eds). Processing and Fabrication of Advanced Materials VIII. World Scientific, Singapore, pp. 365-373. Meredith, N., M. Sherriff, D.J. Setchell and S.A.V. Swanson. 1996. "Measurement of the Microhardness and Young's Modulus of Human Enamel and Dentin using an Indentation Technique," Arch. Oral Biology, 41[3]: 539-545. Cuy, J.L., A.B. Mann, K.J. Livi, M.F. Teaford and T.P. Weihs. 2002. "Nanoindentation Mapping of the Mechanical Properties of Human Molar Tooth Enamel," Arch. Oral Biology, 47[2]: 281-291. Habelitz, S., S.J. Marshall, G.W. Marshall and M. Balooch. 2001. "Mechanical Properties of Human Dental Enamel on the Nanometre Scale," Arch. Oral Biology, 46[1]: 173-183. Sudarsanan, K. and R.A. Young. 1969. "Significant Precision in Crystal Structural Details: Holly Springs Hydroxyapatite,'Mcto Crystallogr. Sec. B, 25[6]: 1534-1543. Amada, S. 1995. "Hierarchical Functionally Gradient Structures of Bamboo, Barley and Corn," MRS Bull, 20[l]: 35-36. Low, I.M., Lee, S.K., Barsaum, M. & Lawn, B.R. (1998) "Contact Hertzian Response of Ti3SiC2 Ceramics." J. Am. Ceram. Soc. 81[1]: 225-228. Kelly, J.R. 1997. "Ceramics in Restorative and Prosthetic Dentistry," Ann. Rev. Mater. Sci., 27[2]: 443-468. Probster, L. 2001. "Survival Rate of In-Ceram Restorations," Int. J. Prosthodont., 6[1]: 259-263. Suresh, S. 2001. "Graded Materials for Resistance to Contact Deformation and Damage," Science, 292[12]: 2447-2450. Luo, Y., W. Pan, S. Li, R. Wang, and J. Li. 2003. "A Novel Functionally-Graded Material in the Ti-Si-C system," Mater. Sci. & Eng. A, 345[1]: 99-105.
Experimental Investigation of Porosity in Carbon/Epoxy Composite Laminates Boming Zhang*, Ling Liu, Zhanjun Wu, Dianfu Wang Center for Composite Materials, Harbin Institute of Technology, Harbin 150001 P.R. China
ABSTRACT Presence of porosity in composite laminates is mainly due to the improper control of processing parameters. Pressures in autoclave process are usually applied to minimize void percentage. An experimental program was designed to investigate the effects of cure pressures on the void contents. Qualitative and quantitative characteristics of porosity in terms of void distribution, shape, size and volume fraction was carried out by ultrasonic C-scan, microscopic analysis and acid digestion method. Effects of porosity on the interlaminar shear strength for the laminates were discussed. The results show that there is a decrease of 35% in ILSS when the void content goes from 0 to 4%, each 1% increase in void content decreases ILSS approximately by 8.5% for this material, and the effects of porosity on the strength mainly contribute to the void content, void distribution, size and shape, and the void content has little connection with the generation method.
INTRODUCTION Voids are one of the most common flaws encountered within the carbon/epoxy composite laminates. They are formed primarily due to the mechanical air entrapment during the lay-up, and due to moisture absorbed during the material storing[l-4]. The presence of voids have detrimental effects on the mechanical properties such as interlaminar shear strength [1-7], compressive strength, flexural strength and tensile strength et al[2-5,7]. The influence of voids on the mechanical behavior of composite laminates is a complex problem due to the large number of variables involved. Among those factors are: shape, size and location of the voids; mechanical properties of fiber, matrix and interface; mechanical loads present and their nature and so on [6]. Also, environmental factors should be accounted for as service temperature and moisture absorption may affect the mechanical behavior of the composite constituents and their effects[6]. Many efforts have been made to characterize quantitatively the relationship between void content and mechanical properties[l-7]. All have had a difference in those results. The first reason is that there is not a sufficiently accurate method for estimation of void content. The second one is the importance of select properly the mechanical test, because some mechanical properties are not so sensitive as others to the presence of voids and so happen with the scattering of test results[l-7].
Correspondence Author, Center for Composite Materials, Harbin Institute of Technology, Harbin 150001, China, +86-451-86414323, zbm(5),hit.edu.cn
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We have employed flat composite laminates cured at several pressures. Different void contents were obtained for those laminates. Ultrasonic inspection and density determination/matrix digestion methods have been employed to measure the porosity in the laminates. Optical image analysis was carried out to analyze the distribution, size and shape of voids. We have chosen short-beam test because the interlaminar shear strength is sensitive to the occurrence of voids. The data from short-beam test were calibrated to the void contents and ultrasonic absorption coefficients. EXPERIMENTAL PROCEDURE Specimen Preparation The material under research is carbon/epoxy prepreg. The reinforced carbon fiber is T700 and matrix is TDE85 epoxy resin. Laminates with 12 plies, [0, 90]3s, were manufactured with 300mm in length and 300mm in width and 2mm in thickness. All plates were cured using autoclave process under different cure pressures. Temperature was risen up to 120°C at a rate of 2°C/minute and was held for two hours, then risen up to 180°C at the same rate and was held for some hours. Then it was cooled down to room temperature. Pressures were applied mechanically with pressure pump. Different void contents appeared in each laminate, cured with a unique pressure, so it was possible to cut test specimens from each plate. Ultrasonic C-scan All the plates were inspected by using an ultrasonic double-through-transmission technique. The host machine is SONIC—138VFD and working frequency is 5 MHz. An actual size map of the plate is generated after scanning associating a color to each attenuation level. Then areas of constant porosity level were marked on the plate and specimens were cut for porosity measurement and strength testing. Porosity Measurement The porosity was measured by matrix digestion in heated concentrated sulfuric acid according to ASTM 3171. This procedure determined the volume fraction of fibers. The void volume fraction was then calculated from the known densities of the composite and fiber. The porosity measurement was made with five test pieces on each plates and the average was taken to be as the normal void content. Optical Image Analysis Optical image analysis were employed to characterize the void location, void size, and void shape in the carbon/epoxy laminates. The specimens were mounted, polished, and desiccated. Then an image processing system equipped with a Zeiss MC80DX inverted camera microscope was used for all analyses. ILSS testing To assess the influence of voids on the mechanical strength of the laminates, the ILSS was obtained from the short beam shear test according to ASTM D2344 standard, which is widely used for the mechanical characterization of composites and, because of its simplicity and small amount of material required. Twelve specimens of each laminate
Porosity in Carbon/Epoxy Composite Laminates
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with dimensions of 25 mm long and 6.5 mm wide were tested. The span-to-depth ratio is approximately 4:1. Tests were performed in a universal test machine (DSS—10T—S) using a test speed of 1 mm/min. RESULTS AND DISCUSSION Ultrasonic Absorption Coefficient and Porosity Ultrasonic inspection method has been used for porosity measurement through the lammates. An absorption coefficient measured in dB/mm is obtained for each plate. But the coefficient is an average value for the whole area under the scan. It should be calibrated by reference to another method. Density determination/matrix digestion method was taken as the reference method. Figure 1 shows a plot of the porosity versus the measured absorption coefficient of the studied laminates. As expected the smallest absorption coefficient correspond to the low porosity laminates. A linear correlation between the void content and absorption coefficient can be observed for laminates with void content between 0 and 4%. It can be seen that a 1% void content increase will cause an approximate 1.5dB/mm attenuation in this carbon/epoxy laminates.
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Absorption coefficient (db/mm)
FIGURE 1 Porosity/ultrasonic absorption coefficient correlation curve
ILSS Analysis Figures 2 and 3 present the interlaminar shear strength as a function of ultrasonic attenuation coefficient and porosity for the studied laminates respectively. As expected, the strength values decreases with the absorption coefficient and with the porosity of the laminates. As can be seen from figure 2 that for 1.7dB/mm of attenuation coefficient a 90% of ideal strength remains, and for 2.7 dB/mm the strength is only 70%. It can be seen in Figure3 that the ILSS values are very sensitive to the void content. There is a decrease of 35% in ILSS when the void content goes from 0 to 4%, each 1% increase in void content decreases ILSS approximately by 8.5% for this material. The result indicates that the drop-off rate of ILSS closely follows the strength drop-off rate
Porosity in Carbon/Epoxy Composite Laminates
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found in the literature results[l-6]. With the increase of void content, a higher void sensitivity of ILSS is obtained that is due mainly to the increasing loss of interfacial area.
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Optical Image Analysis Figure 4 presents a typical microstructure of the laminates with (a) low porosity and (b) high porosity. It shows that the laminate with low porosity in Figure 4 (a) shows typically small and spherical voids. The voids are mainly located between the plies or the fiber
Porosity in Carbon/Epoxy Composite Laminates
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tows. Figure 4 (b) shows the occurrence of much larger and flattened and elongated voids distributed in the samples, the voids are typically located at the interlaminar interface or fiber tows and even having triangular shape and cause local deformation of the surrounding fibres. It can be seen from Figure 3 that the ILSS values decrease nonlinearly with increasing void content. The case is that the void content measured by density determination/matrix digestion method is a volume fraction, and void location and void shape must be taken into account in order to predict the influence of voids on mechanical properties. So, optical assessment of porosity increased our understanding of the void sensitivity of ILSS.
•4
(a)
(b) FIGURE 4 Micrographs of laminates with (a) low porosity and (b) high porosity
CONCLUSIONS The porosity and its effects on interlaminar shear strength have been investigated experimentally for T700/TDE85 carbon/epoxy composites. A linear relationship between
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the void content and the absorption coefficient was obtained within the range of porosity from 0 to 4%. It was concluded that for 1.7dB/mm of attenuation coefficient a 90% of ideal strength remains, and for 2.7 dB/mm the strength is only 70%. There is a decrease of 35% in ILSS when the void content goes from 0 to 4%, each 1% increase in void content decreases ILSS approximately by 8.5% for this material. The voids are mainly located between the plies or between fiber tows and even have elongated and triangular shape for high porosity laminates. Optical image analysis of porosity increased our understanding of the void size, location, and shape. REFERENCES 1. Bowles, K. J., S. Frimpong. 1992. "Voids Effects on the Interlaminar Shear Strength of Unidirectional Graphite-Fiber-Reinforced Composites," J. Comp. Mater., 26 (10): 1487-509. 2. Ghiorse, S. R. 1993. "Effect of Void Content on the Mechanical Properties of Carbon/Epoxy Laminates," SAMPE QUARTERLY., (l):54-59. 3. Almeida, S.F.M., Z.S. Nogueira Neto. 1994. "Effects of Void Content on the Strength of Composite Laminates," Comp. Struct, 28: 139-48. 4. Olivier P., J.P. Cottu, and B. Ferret. 1995. "Effects of Cure Cycle Pressure and Voids on Some Mechanical Properties of Carbon/Epoxy Laminates," Composites, 26 (7):509—515. 5. Jeong, H. 1997. "Effects of Voids on the Mechanical Strength Ultrasonic Attenuation of Laminated Composites," J. Comp. Mater.,31(3):276-292. 6. Michelle L. C , S.F.M. Almeida, and M. C. Rezende. 2001. "The Influence of Porosity on the Interlaminar Shear Strength of Carbon/Epoxy and Carbon/Bismaleimide Fabric Laminates," Comp. Sci. Technol.,61(14):2101-2108. 7. Nightingale C, R. J. Day. 2002. "Flexural and Interlaminar Shear Strength Properties of Carbon Fibre/Epoxy Composites Cured Thermally and With Microwave Radiation," Composites Part A.,33(7): 1021-1030.
Characterisation of a Reinforced PPS Thermoplastic Laminate For Forming Simulations Zhiping Chen* Hawker de Havilland, 226 Lorimer Street, Fishermans Bend, Victoria, 3207, Australia Tran Phung, School of Aerospace, Mechanical and Manufacturing Engineering, RMIT University, GPO Box 2476V, Melbourne, Vic 3001 Australia Rowan Paton Cooperative Research Centre for Advanced Composite Structures Ltd (CRC-ACS Ltd), 506 Lorimer Street, Fishermans Bend, Victoria, 3207, Australia Patricia de Bruijn Faculty of Aerospace Engineering, Delft University of Technology, Kluyverweg 1,2629 HS Delft, The Netherlands
ABSTRACT Continuous fibre Reinforced Thermoplastic Laminate (RTL) composites are an attractive alternative to materials currently being used in lightweight aircraft structures. Their potential rapid-processing capabilities have attracted lots of attention and several manufacturing methods have been developed over the last decade [1]. Among these techniques, press forming, adapted from a process used for metal forming, has received considerable industrial interest in recent years: rubber pad forming has been the most widely used method. CRC-ACS is developing rubber pad forming of RTL and has used PAM-FORM™ [2] to carry out forming simulations to assist in the understanding of the effects of process conditions and in the design of forming tools and processes. This paper reports results from bias-extension tests carried out to characterise the in-plane shear behaviour of PPS-RTL at different processing temperatures and rates. From these results some of the essential material input data for forming simulations such as viscosity, shear modulus, and locking angle can be derived. Detailed discussion on the effects of forming temperatures and forming rates on the flow behaviour of the PPS-RTL is also presented.
INTRODUCTION Composites made from Reinforced Thermoplastic Laminate (RTL) are increasingly being considered in aerospace structural applications. The main drive is to produce lowcost components using out-of-autoclave processes. Considerable work has been conducted in the past on Polyetheretherketone (PEEK) and Polyetherimide [PEI] composites for application in aerospace structures [3,4]. However, Polyphenylene * Correspondence Author, 226 Lorimer St., Fishermens Bend, Vic. 3207, Australia. Fax: +61 3 9646 0583; Email: [email protected]
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125
Sulphide (PPS) composites have emerged recently as a prime candidate for secondary structural components [5]. Over the last decade, several manufacturing methods for these RTL composites have been developed [1]. Among these techniques, press forming, adapted from the process used in the metal forming industry, has received considerable industrial interest in recent years and the rubber pad forming has been the most widely used method. In a rubber pad forming process, a preconsolidated sheet or a stack of individual plies of RTL is heated to the processing temperature, transferred to the press placed between a rigid die and a rubber pad, and pressed into shape. However, it is still a challenging task to press-form good quality and more complex components. Therefore, it is necessary to further investigate the effects of process conditions on the structure and behaviours of the material. In the CRC-ACS, the software PAM-FORM™ [2] has been used to carry out process simulations to assist in the understanding of the effects of process conditions and in the design of forming tools and processes. In PAM-FORM™, each ply of the RTL material is represented by thin shell elements with a thermo-visco-elastic matrix and an elastic fibre material (Material Type 140). This model is a "biphase" model, in which the elastic fibre and viscous matrix components are treated separately. Detailed description of the model is given in references 6 and 7 The CRC-ACS has proposed three test methods for determining material characteristics for this model: the biasextension test, the ply pull-out test and the fabric self-weight bend test for characterising intra-ply shear, inter-ply shear and out-of-plane bending respectively [8]. In the present paper, the bias-extension test is used to obtain key input data required for the PAMFORM material model. The effects of processing parameters on the flow behaviour of the PPS-RTL will be discussed in detail. EXPERIMENTAL Material The investigation used flat pre-consolidated laminates made from carbon fabric / Polyphenylene sulphide (PPS) supplied by Ten Cate Advanced Composites. Details of the material are presented in TABLE I. TABLE I RTL Material description SUPPLIER
RESIN
FABRIC
FORM
Ten Cate Advanced Composites
Polyphenylene sulphide (PPS)
Carbon 5 Harness Satin
Consolidated sheet
LAYU P 1-ply
THICKNESS 0.31mm
The melting point of the PPS resin is 280 °C and its thermal decomposition temperature is370°C. Specimens The bias extension test specimen used in the present investigation is 325mm long by 80mm wide with a gauge length of 200mm, cut from the pre-consolidated sheet with the fibre directions at ± 45° to its long axis. In order to measure the change of the fibre angle during the test, a white pattern as shown in Figure 1 was painted on the specimen.
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Characterisation of a Reinforced PPS Thermoplastic Laminate
Test Set-up The test set up is shown in Figure 2. A heating box made of four Infra-Red heating panels and insulation material was mounted on an Instron Test Machine. The Infra-Red heating panels were used to ensure rapid heating of the test specimen. Tests were carried out at four temperatures above the melting point and below the decomposition temperature of the PPS (290 °C, 300 °C, 320 °C, 340 °C), and at three crosshead speeds (lOmm/min, 50mm/min, lOOmm/min).
(a) (b) FIGURE 1 Test specimens, (a) Before test; (b) After test.
heating panel
- fixture system
- instron connection ~ moving bottom
FIGURE 2 Test set-up using the Infra-Red heating box.
FIGURE 3 Three regions on the specimen with different deformation patterns.
Characterisation of a Reinforced PPS Thermoplastic Laminate
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Test Methodology From bias-extension test results, key input parameters for PAMFORM™ such as intra-ply viscosity, the locking angle, and pre- and post-locking in-plane shear modulus can be derived. It can be seen from the tested specimen in Figure lb that three regions with different deformation patterns can be identified on the specimen. These are marked "1", "2" and "3" in Figure 3. The two triangular regions (region 1) at the two clamped ends of the specimen are undeformed mainly due to the inextensibility of the fibre. Regions marked as "2" undergo a combination of shear and inter-tow slip. It is only in the diamond-shaped region 3 that there is "pure" shear and the test results of stress and strain relationships are valid. A typical force-extension curve from the test is shown in Figure 4. This curve can be converted into a true stress-true strain curve from which the intra-ply viscosity and inplane shear modulus can be derived. The locking angle can be measured directly from the specimen.
0 2 4 (t 8 K) 12 14 16 18 30 22 2436 38 30
, FIGURE 4 A typical force-extension curve from the test.
RESULTS AND DISCUSSION Effects of Temperature Figures 5a to 5c show the tensile stress response of the PPS-RTL specimen at test temperatures ranging from 290°C to 340°C at lQrnm/min, 20mm/min and 50mm/min, respectively. Interestingly, the material is much stiffer at the lowest and highest processing temperatures for all displacement rates (i.e. 290cC and 340°C). The material stiffness is less at intermediate temperatures (i.e. 300°C and 320°C). It was found that the material exhibits little variation in initial stiffness for temperatures between 300°C to 320°C at all displacement rates. This temperature range is used for processing thermoplastic composites in rubber pad forming. Effects of Displacement Rate The effect of displacement rate at elevated temperatures on the intraply shear response of the PPS-RTL was investigated. Figures 6a to 6d show the results from experiments carried out at various cross-head rates for 290°C, 300°C, 320°C and 340°C, respectively. In general, the load increases as the displacement rate increases although at
128
Characterisation of a Reinforced PPS Thermoplastic Laminate
320°C, the apparent stiffness of the material at the three displacement rates is very similar. From the experimental results, the intraply shear viscosity is derived using Johnson's model [7] and is plotted against the processing temperatures (see Figure 7). It is found that the optimum conditions are a temperature between 300°C to 320°C and a crosshead speed between 50 to 100 mm/min.
o - * •
0 G
290degC 300degC 320degC 340degC
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o 0
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True Strain (c)
FIGURE 5 True Stress-True Strain Graph (a) Test at 10 mm/min, (b) Test at 50 mm/min and (c) Test at 100 mm/min.
CONCLUSIONS A simplified form of the fibre reinforced thermoplastic fabric prepreg rheology first proposed by Johnson and Costalas [7] has been used to characterise the intraply shear behaviour of the PPS-RTL. The essential material input data were successfully derived from simple bias extension tests at different temperatures and crosshead speeds. It was found that the lowest intraply shear forces are measured for tests at a temperature between 300°C to 320°C and a crosshead speed between 50 to 100 mm/min. Intraply shear forces were found to be higher at 340°C, indicating that some degree of crosslinking may be taking place in the PPS at higher temperatures. Further work is in progress to simulate the intraply shear deformation of PPS-RTL using finite element modelling.
Characterisation of a Reinforced PPS Thermoplastic Laminate
0
0.05
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FIGURE 6 True Stress-True Strain Graph (a) Test at 290°C, (b) Test at 300°C, (c) Test at 320°C and (d) Test at 340°C.
310
320
Temperature (degree Q
FIGURE 7 Viscosity of the PPS RTL derived using the model by Johnson and Costalas[7] from bias-extension test results
REFERENCES 1.
2.
K. Friedrich, M. Hou and J. Krebs, Thermoforming of Continuous Fibre/Thermoplastic Composite Sheets, Composite Sheet Forming, edited by D. Bhattacharyya, Elsevier Science B.V., 1997, pp.91162. PAM-FORM™, Engineering Systems International, 20 rue Saarinen, 94578 Rungis Cedex, France.
130 3.
4. 5.
6. 7.
Characterisation of a Reinforced PPS Thermoplastic Laminate
W. Schijve., Fofcker 50 Thermoplastic Main Undercarriage Door: Design and Cost Effectiveness of Thermoplastic Parts, Proceedings 14* European SAMPE Symposium, Birmingham, Oct. 19-21, 1993, pp. 421-432. A.R. Offringa, R.T. Cole, C.R. Davies, R. Schott, Gulfstream V Carbon/PEI Floor Panels, Proceedings 40th International SAMPE Symposium, May 8-11 1994, Vol. 40, pp. 396-409. A.R. Offringa, D. Myers, A. Buitenhuis., Redesigned A340-500/600 Fixed Wing Leading Edge (JNose) in Thermoplastics, Proceedings 46*1 International SAMPE Symposium, Long Beach, CA, May 6-10,2001, pp. 331-343. PAM-STAMP™ Solver Reference Manual, Engineering Systems International, 20 rue Saarinen, 94578 Rungis Cedex, France. A.F. Johnson and E. Costalas, Forming Models for Fabric Reinforced Thermoplastics, 4th Int. Conf. On Automated Composites ICAC '95, Nottingham, 6-7 September, 1995,pp.l-12.
Characterisation of the Thermo-mechanical Behaviour of a Glass Reinforced Vinyl Ester Composite Nigel A. St John*, Craig P. Gardiner Maritime Platforms Division, Defence Science and Technology Organisation, Australia Luke A. Dunlop Department of Mechanical and Materials Engineering, University of Western Australia, Australia
ABSTRACT Changes at elevated temperatures in the mechanical properties of a cast epoxy novolac based vinyl ester resin and an E-glass reinforced laminate are investigated. Dynamic Mechanical Thermal Analysis (DMTA) and tensile tests were conducted on resin castings and tension, flexure, in-plane shear and interlaminar shear tests were conducted on laminates. A significant sensitivity of resin tensile and laminate shear and flexure properties to temperature changes below the glass transition temperature of the resin were observed. Correlations between resin and laminate properties were determined. An example being that while the initial tensile modulus of laminates reflected changes in resin properties, after a knee point the tensile modulus was independent of resin properties.
INTRODUCTION The use of composite materials in large structures such as ships requires an ability to predict the structural response to a range of service conditions, which can include a wide range of thermal exposure conditions. Elevated temperatures can occur due to solar heating, poor ventilation in machinery spaces and in the extreme case, a fire. Low temperature cure resins, such as vinyl ester resins used in ship construction, are particularly sensitive to increases in temperature. The ability to accurately calculate the mechanical response of polymer matrix marine composites at elevated temperatures is thus an essential requirement for predicting structural performance. There have been limited results reported in the literature on elevated temperature mechanical properties of composites and so assumptions have generally been made on property changes for modelling purposes [1]. The research described in this paper was undertaken to characterise the effect of rising temperature on the mechanical properties of a glass-reinforced composite and relate this to corresponding resin properties. The resin used was a high glass transition temperature epoxy novolac based vinyl ester resin with E-glass woven roving chosen as reinforcement as it is typically used in composites for marine structures. * Corresponding author, Maritime Platforms Division, DSTO, PO Box 4331, Melbourne, VIC 3204, Australia; Fax: 61-3-9626 8409; email: [email protected]
132
Thermo-mechanical Behaviour of Glass Reinforced Vinyl Ester Composite
EXPERIMENTAL The novolac epoxy based vinyl ester resin Derakane Momentum 470-300 (Dow Chemical Co.) was used and cured using 0.36 phr 1% cobalt naphthenate solution and 1.0 phr Triganox 239A (Akzo Nobel) at room temperature and postcured at 90°C for 1 hour. The glass reinforcement used was an 800 g.m"2 E-glass slightly unbalanced plain weave woven roving (Colan Products). Laminates were fabricated using vacuum assisted resin transfer molding (VARTM) and the fibre content was determined by burn-off according to ASTM D 2584-94. Mechanical property tests were conducted using an Instron 5500 fitted with an oven. Resin tensile properties were measured according to ASTM D638-99. Resin dynamic mechanical properties were recorded using a Polymer Labs DMTA. Laminate tensile, flexural and short beam shear properties measured according to ASTM D3039M-00, ASTM 790M and ASTM D2344-84 on six ply laminates (67.3 wt% fibre) in the warp direction except for tensile properties where the weft direction was also tested. Laminate in-plane shear properties were measured according to ASTM 3518M-94 on ±45° eight ply laminates fabricated with plies symmetric about the mid-plane and balanced by alternating the direction of warp rovings (69.5 wt% fibre). Three specimens were generally tested at each temperature. RESULTS AND DISCUSSION Resin Casting Properties The change in resin tensile modulus with temperature is shown in Figure 1. Modulus is seen to decrease with increasing temperature, with a more rapid decrease starting at about 140°C, and by 160°C the modulus has decreased by two orders of magnitude. DMTA measurements of the resin casting showed the glass transition temperature, Tg, occurred at 169°C at scan rate of FCmin"1, as defined by the tan 5 maxima. Based on the tensile test data the onset of modulus decrease is a more relevant definition of Tg, which yields a value of 149°C using DMTA.
20
40
60
80
100
120
140
160
180
200
Temperature (°C) FIGURE 1 Tensile modulus of resin casting versus temperature
The change in tensile strength and the percent strain at failure with temperature of the resin casting is shown in Figure 2. The tensile strength follows a similar trend to
Thermo-mechanical Behaviour of Glass Reinforced Vinyl Ester Composite
133
the modulus except the change in rate of decrease with temperature occurs around the temperature used for postcuring. This reflects the greater dependence of strength on degree of postcure compared to modulus. This is because increased crosslinking due to postcure will increase strength but only be reflected in the modulus changes above theT g . The changes in percent elongation to failure of the resin are very sensitive to temperature, increasing substantially up to 140°C then beyond this point dropping rapidly. The failure was observed to be brittle at low temperatures, becoming ductile as temperature increased, and then above 140°C the resin appeared to tear indicating a rubbery state. This supports the view that the real Tg for the resin is in the range 140150°C.
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100
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140
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Temperature (°C) FIGURE 2 Change with temperature of resin casting tensile failure stress (strength) (•) and failure strain (•).
Laminate Tensile Properties The stress-strain curves for the tensile loading of laminates showed a distinctive "knee point" as has been reported previously for woven roving reinforced laminates [2]. This change in modulus was measured as an initial modulus (chord modulus between O.Oland 0.1% strain) before the knee point and as interquartile modulus (between 25 and 75% of strain to the onset of delamination) after the knee point. Figure 3 (a) shows the changes in these values with temperature for samples loaded in the warp direction. It is seen that the initial modulus decreases steadily with temperature, while the interquartile modulus remains essentially constant. The modulus of E-glass is 72.6 GPa, hence a modulus of 19.2 GPa is predicted and considering only the fibres aligned in the loading direction (warp fibres). This is close to measured interquartile modulus of 20.7 GPa and thus the initial modulus must reflect the additional contribution to laminate modulus of the fibres in the weft (90°) direction, with the effectiveness of this being related to the resin properties. The knee effect has previously been attributed to the straightening out of crimped fibres in the plane of the fabric, causing a resin tensile failure [1] or initial transverse fibre debonding [3]. The strain at which the knee point is observed initially increases with temperature, reflecting the increasing elongation to failure of the resin rather than the decreasing resin strength (Figure 2). This is consistent with the view that the knee point is due to localised resin failure caused by strain induced through straightening of the warp fibres.
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Thermo-mechanical Behaviour of Glass Reinforced Vinyl Ester Composite
Tests conducted loading in the weft direction showed similar trends to those observed in the warp direction, although the strength and moduli were lower due to fewer rovings in the weft direction for the reinforcement used. For example, room temperature tests gave a tensile strength of 310 MPa and initial and interquartile moduli of 25 GPa and 16 GPa respectively. 32-,
(a) 2824-
1 CA
1
20.
I
•
t
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16m *
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initial Modulus Interquartile Modulus
8-
1
4-
n80
80
100 120 140 160 180 200
100
120
140
160
180
200
Temperature (°C)
Temperature fC)
FIGURE 3 Change with temperature of laminate (a) tensile modulus showing initial and interquartile values and (b) tensile strength, measured in the warp direction.
The tensile strength values for the laminate loaded in the warp direction are shown in Figure 3(b) and it is seen that the strength steadily decreases with increasing temperature. The decrease up to resin Tg can be attributed to the decreasing contribution of resin strength to laminate strength due to the reduction in resin strength with temperature (Figure 2). The decrease above resin Tg probably reflects the reducing ability of the resin to transfer load between fibres in the laminate.
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Temperature (°C) FIGURE 4 Change of laminate in-plane shear strength (•) and in-plane shear modulus (•) with temperature.
Laminate In-plane Shear Properties The in-plane shear properties of the laminate were measured using the ±45° tensile coupon test that has been previously identified [4] as the most suitable shear
Thermo-mechanical Behaviour of Glass Reinforced Vinyl Ester Composite
135
test for elevated temperature testing. The in-plane shear strength and modulus are seen in Figure 4 to follow the same trend, decreasing rapidly with increasing temperature to low values around the resin Tg. Laminate Flexural and Interlaminar Shear Properties While laminate flexural and interlaminar shear strength properties are not directly of use in modelling composite properties, as they are not fundamental material properties, they are widely used because flexural tests provide a measure of the performance under bending and interlaminar shear strength provides a simple measure of the "quality" of a laminate in terms of the bonding between plies. Figure 5 shows the change in flexural modulus and strength with temperature. The tests used three point loading with large span-to-depth ratio of 32:1 to minimise shear contribution to the modulus. All specimens primary mode of failure was observed to be compression associated with macrobuckling. At higher temperatures the fabric "curled" out of the matrix slowly allowing the mode of failure to be clearly visible.
20
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100 120 140 160 180 200 220 Temperature (°C)
FIGURE 5 Change in laminate flexural modulus (•) and strength (•) with temperature.
The flexural modulus is observed to decrease slightly until the Tg of the resin is reached and then undergoes an apparent step change with approximately a 5 GPa drop followed by a continued steady decline. This is probably a reflection of the decrease in shear modulus of the laminate with increasing temperature (Figure 4) and the effect of this on measured flexural modulus. The flexural strength is observed to remain constant up to 60°C and then decreases apparently linearly with increasing temperature to below 100 MPa at the end of the resin glass transition. Considering the observed moderate changes in tensile properties (Figure 3), it is clear that compression properties are much more sensitive to changes in temperature below the resin Tg and this is seen in the flexural strength behaviour. The interlaminar shear strength values obtained by short beam shear tests with a span-to-depth ratio of 5:1 showed a similar trend to the flexural strength result with a room temperature value of 40 MPa decreasing to under 5 MPa by 170°C. Correlation of Resin and Laminate Properties One objective of the study undertaken was to identify what would be the minimum data that is necessary to make reasonable predictions of the changes in
136
Thermo-mechanical Behaviour of Glass Reinforced Vinyl Ester Composite
mechanical properties of a composite for modelling purposes. To this end correlations between resin matrix and laminate properties were explored. An example is seen in Figure 6 which shows that a linear relationship (R=0.993) exists between laminate inplane shear modulus and resin tensile modulus.
0.0
0.5
1.0
1.5
2.0
2.5
3.0
3.5
4.0
Resin Tensile Modulus (GPa)
FIGURE 6. Plot of laminate in-plane shear modulus versus resin tensile modulus for values at all temperatures
Similar relationships were obtained for laminate in-plane shear strength and resin tensile strength; laminate tensile modulus and resin tensile modulus; and laminate interlaminar shear strength and flexural strength. CONCLUSION The decrease with increasing temperature of in-plane shear, interlaminar shear and flexural laminate properties was seen to be highly dependent on the resin properties. While this was not unexpected, the large decrease in these properties prior to reaching the glass transition temperature of the resin matrix is an important observation with consequences for designers of composite structures that may experience a range of service temperatures. The laminate tensile results revealed interesting insights into the behaviour of woven reinforcements and the interactions of the resin matrix in the composite under tensile loading. Finally, results obtained in this study highlight the importance of maintaining accurate temperature control and suitable specimen conditioning for conducting mechanical tests of composites. REFERENCES 1.
2. 3. 4.
Wong, P.M.H, Davies, J.M. and Wang, Y.C. 2004, "An experimental and numerical study of the behaviour of glass fibre reinforced plastics (GRP) short columns as elevated temperatures". Compos. Struct. 63: 33-43. Zhou, G. and Davies, G.A.O. 1995 "Characterization of thick glass woven roving/polyester laminates: 1. Tension, compression and shear", Composites, 26:579-586. Johnson, A.F. 1986. Engineering Design Properties of GRP. The British Plastics Federation, pp 83-121. Lee, S. and Munro, M. 1986. "Evaluation of in-plane shear test methods for advanced composite materials by the decision analysis technique". Composites. 17:13-22.
Experimental Study on the Flexural Behavior Using Polyethylene Coated Bars Young Jin Kim* Korea Land Corporation (KOLAND), 217 BunDangGu,Sungnam City, Kyonggi Do, Korea
ABSTRACT Recently, Corrosions of reinforced concrete structures are severe problems of economical/social effects. Polyethylene coated bars protecting from corrosion and enhancing durability of reinforced concrete structures are testified to evaluate corrosion protection properties. Tests are verified by comparative bending tests of the three type materials of without coating, polyethylene coating and epoxy coating. Load-deflection relations are superior in polyethylene coated bar than any other materials (bare bar and epoxy bar). These are proved bonding properties enhancement by using cement powder. However, there were some problems to improve bond property and it wish to improve gradually. Cement is more effective than pure polyethylene-coated bars from bending and pull-out tests. It maybe connects polyethylene and concrete.
INTRODUCTION In Severe marital condition, Reinforced concrete has been regarded composite structure as durable composite materials. The anti-corrosion of the reinforced concrete is very important civil and architectural engineers. Rust expands volume increase and splitting pressure due to corrosion decrease durability of life time. Carbonation of concrete is caused by the reaction of the atmospheric carbon dioxide with alkaline substances of the pore water and the phases of the hydrated cement (silicates, aluminates and ferrite-aluminates). The presence of chloride ions (CL~) is widely recognized as causing accelerated attack on reinforcing steel. Even at high pH-values, the chlorides depassivate the steel and increase the conductivity of the concrete electrolyte, thereby speeding up the rate of attack. Today, coated bar is widely used in construction and preventive materials. The general principle of the protection provided by epoxy(or polyethylene)-coating is to furnish the steel with an insulating and isolating layer to separate it from aggressive ions and inhibit corrosion. The insulating nature of the coating ensures that any corrosion occurring is reduced compared with uncoated steel because of the elimination of available cathodic sites. No special influences on the properties of the steel have been reported or are * Corresponding author, Korea Land Corporation, Sungnam, Kyonggi, Republic of Korea. Tel;+82-31-738-7790, Fax;+82-31-738-8965, e-mail; [email protected]
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Flexural Behavior Using Polyethylene Coated Bars
known. The reinforcing steel used as raw material for epoxy (or polyethylene)-coating can have two significant influences on the finished coating products : 1) Bars with longitudinal as well as transverse ribs may well prove difficult to blast clean thoroughly and coat at the base of the longitudinal ribs. Experience has shown that longitudinal ribs frequently result in higher levels of pinholes in the coating. 2) The bond to concrete of epoxy (or polyethylene)-coated bars can be sensitive to the rib profiles of the reinforcement. Bond to concrete may be defined either as the ultimate stress at pull-out, or as a certain slip between bar and concrete at lower stress. Regarding the ultimate bond stress, it seems the epoxy-coating reduces strongly the adhesive bond to concrete. Plain and poorly ribbed bars have shown large drops in bond when epoxy-coated. It seems that the mechanical bond caused by the ribs has to be relied upon. In paper1', Coating thickness larger than 500/zni decrease the bond distinctly. If the thickness is 300//m or below, the bond values are not far from those of uncoated bars. Reductions up to 20% are reported in more normal cases. The development of polyethylene coated reinforcement can be traced to the expand use of composites after polyethylene coated pipe. This paper represents simple beam tests (L=3,000mm) within uncoated, Polyethylene-coated and epoxy-coated bars in which bending failure2). FLEXURAL BEHAVIOR OF RC-BEAM Failure Modes Of Coat Materials And Bending Tests Three types coated bars tested by uncoated, polyethylene and epoxy coated bars using RC-beams under bending conditions of Reinforced Concrete Structures. A stirrup is prevented rapid shear failure and structural behavior. Failure mode of coat material Bending failure tests of coating materials in no coat, polyethylene coat and epoxy coat section is 100xl00x400(mmxmm><mm). 2-point loading conditions are tested by high strength bars with 13, 19 and 29mm, This tests are purpose for adhesive conditions with bar and coating materials. Test results are as follows figure 1
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. .""ptirHjB!™^
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Test mould
I
.
jut . x
Concrete pouring
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Flexural Behavior Using Polyethylene Coated Bars
139
J .iMlllIll!- !
Figure after failure(no, epoxy, pe)
No coat(left), epoxy(middle), PE(right) j
FIGURE 1 Test procedures
Failure mode of bending test Section is 200x300(mmxmm). Total length is 3,000mm(span=2,700rnm), The bar ratio of reinforced concrete beam is 0.007%, eventually bending failure induced. The cases of bars are three-types in Bare-Bar(BS), Polyethylene-Bar(PE), Epoxy-Bar(EY) using HD-13(main bar). The constitutions of testing materials are followed by Table 1 TABLE I Experimental apparatus of RC-beams in three types coating bars Class
Classifications
BS, PE, EY
HD13
Coating Thickness
About 200 im
Load Condition And Test Apparatus The following figure 2 is 2-point load conditions that point loads have been located in simple beam of structural behavior. Stiffener has been constructed to prevent brittle failure of concrete and load-deflection behavior of beam within test apparatus. 2-point load conditions are as shown figure 3 in which LVDT installed at middle beam to evaluate load-vertical displacement.
140
Flexural Behavior Using Polyethylene Coated Bars
Testing lodel
FIGURE 2 Modeling
FIGURE 3 Apply Loading
TEST RESULTS AND ANALYSIS Figure 4 figured out RC-beam(no coat), PE-beam and Epoxy-beam with crack diagram to evaluate crack propagation.
1 nr-M
fit
•"fir""""* p r y
I
bY^l
1 20
40
60
80
100
1:
Displacement(mm}
FIGURE 4 Load-Displacement curve in case of coating condition
hi Figure 4, Un-coat and epoxy-coat bars have been first cracked as shown in 1.5tons (PE-bar is 4.3tons) load condition. Crack surface reached at upper place in lO.ltons and lOtons (PE-bar is lltons) respectively. Eventually, plastic deformation runs long standing without increasing load. Compressive bar has been elongate ductility and stiffness in service load. Also, Compressive force bars increased beam load condition. The crack patterns propagate to the point of load and spread entire beam section. PE coated bars added cement power enhanced PE-coated bars to bonding properties. Therefore, The relations between maximum crack load and vertical displacement are 10.07tons, 20.38mm in case of uncoated bar, 10.55tons, 20.53mm in case of PE-coated bars and 9.74tons, 30.92mm in case of epoxy coated bars. It means that upper compressive bars and stirrups control crack load and distribute crack propagation. The combinations of PE-coated bars and cement powers enhance bending stress and bonding pressure. These results summarized in Table 2.
Flexural Behavior Using Polyethylene Coated Bars
141
TABLE II Test results (Allowable Displacement: 15mm) .. . sin on Uncoated PE-coated Epoxy-coated
Failure (Ultimate loadjPercentagc of noVertical displacement in ! mode (tons) and coat bar(%) condition of ultimate load(mm) 20.38 Bending 100 10.07 Bending 104.8 20.53 10.55 Bending 9.74 96.7 30.92
FEM Analysis of Crack Propagation RC, EY beam's experiment result of FEM analysis3) represented same behaviors and distribution chart of crack showed aspect that range on the whole equally and this is judged that effect of cement. Crack of RC and EY came when vertical displacement was gone about 0.45 mm in 2.04 tons, and PE when equal vertical displacement occurrence (0.45 mm) by 2.07 tons in small load difference of displacement. When vertical displacement of RC and EY show 5.4 mm, 7.85 tons, PE's case was receiving 8.71 tons when vertical displacement show 5.4 mm. Vertical displacement of RC and EY show 56.9 mm 10.1 tons, PE's case when vertical displacement show 86.82 mm, it could receive 10.6 tons. See Figure 5-6.
I"!" n n
(a) 0.45mm, 2.04tons
(
a) 0.45mm, 2.07tons
-U i •/
Ij I 1*' f |j
'/
f
I*1 i
1 (b) 5.44mm, 7.85tons
f
*' "
ii''
\i
u i
i
rj ij
ii
""*
•
rj
ff It ||
n *\ (b) 5.47mm, 8.71tons 'f
I
_ U
\t
1tf
if If
i f
JH
ju
i ti
f i f IJ
(c) 56.92mm, 10.1 tons
FIGURE 5 Crack Propagation of RC, EY
„ if
M
1
H 11
1 T'
4
\
II
<J 11
I
-r-i
ois
Vi
,(
If '(
u 'A
*?'
y •j
|
if
IV •V
fi rj
(c) 86.82mm, 10.60tons FIGURE 6 Crack Propagation of PE
RESULTS In some case, uncoated bars and epoxy coated bars are represented same crack propagation with smooth surface condition. PE coated reinforcing bar of state that surface is scratch keeps conduct as composite material between reinforcing bar and concrete. 1) Polyethylene coating bar encased cement connect concrete and bar as composite materials. The limit of vertical displacement is 15mm within allowable deformation. 2) From table 2, percentage of uncoated bar and coated bars are compared uncoated bar with coated bars, 96.7% and 104.8% (based on 100% uncoated bar) respectively. 3) Generally Crack concentrates load action point in RC,
142
Flexural Behavior Using Polyethylene Coated Bars
EY and PE, but PE beam equally diversify overall beam section. REFERENCES 1. State of the art report, 1995, "Coating Protection for Reinforcement," pp. 25-39. 2. A Department of Construction and Transportation, 1995, "The Development of Reinforcement Concrete Structures by Repair and Reconstruction," pp. 68-93. 3. TOTAL RC, 1996, "RC-Structure Nonlinear FEM Analysis System Users Manual," Total Information Service.
Moisture Absorption by Cyanate Ester Modified Epoxy Resin Matrices: Effect of Resin Structure Sunil Karad", Frank Jones Maharashtra Institute of Technology, Paud Road, Pune 411038, India Department of Engineering Materials, University of Sheffield, Mappin Street, Sheffield SI 3JD, UK
ABSTRACT Functionality is defined as the number of reactive functional groups per unit mass of resin. The functionality of resin has a profound effect on the physical properties of thermosetting materials, and for hydrophilic systems influences the rate of moisture diffusion and the equilibrium moisture concentration. Both were found to increase in magnitude as the functionality of the epoxy resin in cyanate ester/epoxy blend was increased. The tetra functional epoxy (MY 720) gives a more polar network than the di-functional (Epon 828) epoxy and hence a greater affinity towards water, and a higher moisture concentration.
INTRODUCTION hi the early stages of the evolution of advanced composites, most requirements for improved matrix resins were satisfied by reformulating epoxy resins. One of the most important factors affecting the development of new matrix resins is the environmental durability of the current epoxy resin systems. Moisture absorption under highly humid conditions has been shown to have a deleterious effect on the properties of current epoxy matrix resins at elevated temperature [1-3]. The absorption of water by epoxies can be attributed to the affinity of the functional groups, which are highly polar, to water molecules. Since many applications in the aerospace industry cannot accept the moisture sensitive nature of epoxy resin matrix composites, intensive research work has been undertaken to identify new thermosetting resins with reduced moisture absorption but without compromising their processability. One important example of this achievement was the synthesis of the polycyanurates or cyanate ester resins for use as matrices in composites. By the co-reaction of cyanate esters with epoxies not only can the branch density of the network be modified drastically, but also its chemical composition [4-6]. The present work investigates the effect of resin functionality on the moisture absorption characteristics and viscoelastic properties of cyanate ester modified epoxy resin blends.
Corresponding author, Maharashtra Institute of Technology, Paud Road, Kothrude, Pune 411038, India, Fax: 0091-20-5442770 E-mail: [email protected]
144
Moisture Absorption by Cyanate Ester Modified Epoxy Resin Matrices
EXPERIMENTAL Three cyanate ester/Epoxy blends were used. The cyanate ester was the difunctional AroCy LIO resin (Ciba-Geigy). The epoxy resins were a difunctional Epon 828 (Shell Chemicals), an approximately trifunctional DEN 431 (Dow Chemicals), and a tetra-functional MY 720 (Ciba-Geigy). Stoichiometry of reactive groups was kept constant across blends at 1.1 epoxy groups: 1 cyanate group. The resins were thermally cured without the use of catalysts. The curing cycle, which was recommended by the manufacturer, involved 2 hours, at 180°C followed by postcuring for 4 hours, at 250 ° C. Samples of dimensions 55x25 and 1 mm thickness were used for conditioning carried out at 96% R.H. Thermal spiking to temperatures 120, 140, 160, and 180°C was performed as per the procedures designed by Xiang et al [7]. DMTA was performed in dual cantilever bending mode using a Polymer Laboratories Mk II analyser. RESULTS AND DISCUSSION TABLE I Moisture concentrations for AroCy LlO/Epon 828, AroCy L10/DEN 431, and AroCy L10/MY 720 resin samples, after 4,000 hours conditioning at 96% R.H./50 ° C , and 17 thermal spikes.
Spike Temp. (°C) Control 120 140 160 180
Final moisture concentration (wt.%) and moisture enhancement (%) AroCy LlO/Epon 828 AroCy L10/DEN 431 AroCy LI 0/MY 720 1.76 2.18 2.28 2.13 2.04
0 23 29 21 16
2.04 2.45 2.70 2.74 2.60
0 20 34 35 27
3.77 4.43 4.81 4.98 4.74
0 17 27 32 25
The moisture content was found to be higher for the resins manufactured from the higher functional epoxy resins. That is with a constant stoichiometry, the tetrafunctional epoxy resin cured with the difunctional cyanate absorbed a higher concentration of moisture than the similarly cured difunctional epoxy resin. Apicella et al [8] identified three sorption mechanisms, which were dependent on the interactions between the penetrant and the polymer: 1. Dissolution of moisture into the polymer to form a conventional solution. 2. Occupation of unoccupied volume. 3. Strong interaction of water molecules with hydrophilic sites on the polymer chain, through hydrogen bonding. Therefore the equilibrium moisture concentration is strongly dependent on the polarity and crosslinking density of the cured resin structure. Generally, the more polar the resin, the higher the equilibrium moisture concentration. The tetra-functional glycidyl amine epoxy (MY 720) is more polar in nature than DGEBA epoxy (Epon 828), so that the cured resin has more hydrophilic sites, which strongly interacts with water molecules to form hydrogen bonds. This results in a higher equilibrium moisture concentration for the AroCy L10/MY 720 blend compared to the AroCy LlO/Epon 828 blend.
Moisture Absorption by Cyanate Ester Modified Epoxy Resin Matrices
145
The moisture content reached a maximum at a specific temperature referred to as, the maximum moisture enhancement temperature (Tmax). Above or below this temperature the enhancement was much less. Tmax for AroCy LlO/Epon 828 was 140, while for AroCy L10/MY 720 was 160. However, at these temperatures maximum moisture enhancement was similar at 32±3%. Above these temperatures the trend in enhancement was comparable to the maximum concentrations of absorbed water. From Table I, it can be seen that the resin samples absorb less moisture above or below Tmax. It is proposed here that when the resin matrix is spiked at or below the Tmax, the unoccupied volume is redistributed through molecular conformational change. The resultant non-equilibrium structure is "frozen-in" when the matrix is rapidly cooled to below its wet Tg. More moisture can then be accommodated at the conditioning temperature without reducing the bulk Tg. This is seen for the AroCy LlO/Epon 828 resin samples spiked to temperatures of between 120 and 140°C. When the matrix is spiked to above TmaX] the wet Tg (wet> is also exceeded considerably. Thus, more time is available during cooling to below the Tg (wet) for the network to equilibrate through molecular conformational reorganization before the network becomes frozen. The resulting network structure can be considered to be in equilibrium with a lower unoccupied volume (in the form of free volume and micro voids). Thus, these samples will absorb less moisture than those spiked at the Tmax. This is observed for all of these three resin blends. TABLE II Thermomechanical data for AroCy LlO/Epon 828, AroCy L10/DEN 431, and AroCy L10/MY 720 resin samples, after 4,000 hours conditioning at 96% R.H./50 ° C , and 17 thermal spikes
Spike Temp
AroCy LI0/DEN 431 TgE' Tg
(°C)
AroCy LlO/Epon 828 TgE' Tg (°C) (°C)
(°C)
(°C)
AroCy LI 0/MY 720 TgE' Tg,/ Tg2 Tg (°C)
As-cured Control 120 140 160 180
187 176 169 166 165 165
201 185 177 163 162 158
185 162 150 142 143 137
259 240 240 236/198 230/188 227/168
(°C) 172 156 144 136 130 128
237 199 194 177 166 144
The Tg of the cyanate ester/epoxy blend increased from 187°C to 259 °C when the epoxy resin was changed from the di-functional (Epon 828) to tetrafunctional (MY 720). This is an expected result as a higher cross-link density will be obtained for tetra-functional epoxy resin. Many investigations [9-10] have shown that, increasing the glass transition temperature and crosslink density results in more unoccupied volume in the resin network, which will result in higher moisture absorption. From Figure I it can be seen that the isothermal diffusion coefficient and moisture content increased with increase in epoxy functionality which supports the hypothesis
146
Moisture Absorption by Cyanate Ester Modified Epoxy Resin Matrices
Figure 1 Effect of epoxy functionality on glass transition temperature (Tg) of as-cured samples, moisture content (Mt), and isothermal diffusion coefficient (Dc) for resin samples conditioned for 4000 hoursat96%R.H./50°C.
The Tg for AroCy LlO/Epon 828 difunctional blended resin falls continuously with moisture absorption and thermal spiking to 140°C. Spiking to 160°C and 180°C caused no further reduction in Tg. Above the maximum moisture enhancement spike temperature of 140°C, Tg is unaffected. This concluded that spiking above 140 °C does not result in thermal degradation of resin samples. As can be seen from Figure I, the diffusion coefficient appeared to increase with the increase in the functionality of the epoxy resin in the blend. In Figure II it can be seen that the main tan5 peak for AroCy L10/MY 720 (tetra-functional blend) resin samples is split into two when thermally spiked to 140°C. The secondary peak, which is defined asTg 2 , occurred at 198°C. This was found to drop further at higher spiketemperatures. As shown in Figure II, Tg2 fell by 30 °C when spike temperature was increased from 140°C to 180°C while Tgj fell by 9 ° C . The large decrease in Tg2 for the 180 °C-spiked samples without a concomitant increase in moisture content suggests that thermally induced hydrolytic degradation is responsible for the reduction in Tg2 and not conventional plasticisation of the polymer matrix.
Moisture Absorption by Cyanate Ester Modified Epoxy Resin Matrices
147
0.35
0.00 40
90
140
190
240
Temperature (°C) • as-cured • control A 140 o180
Figure 2 DMTA tan 8 traces for AroCy L10/MY 720 as-cured, control samples, and samples spiked to 140 and 180 ° C conditioned at 96% R.H./50 ° C .
In a recent report [11] we showed that the epoxy resin concentration in the blend significantly influenced the likelihood of hydrolysis. FTIR data indicated that the aryl triazine crosslinks were reduced in concentration when thermally spiked at 160 and 180°C. The commercial version of MY 720, MY 721 has been shown to contain a range of synthesis by-products [12]. Therefore, when the network forms by reaction with the cyanate ester, it will have a complex structure, with potential for differential plasticisation and hydrolysis [13]. The efficiency of the network formation through triazine ring crosslinks will be compromised. It is therefore concluded that the tetra functional epoxy cured cyanate ester is more susceptible to hydration at temperatures above 140°C. CONCLUSIONS The concentration of moisture which is absorbed and the moisture diffusion coefficient were shown to increase with the functionality of the epoxy resin employed in the cyanate ester/epoxy blend. The cured resin from the tetra functional epoxy (MY 720) has a more polar network than that from the di-functional (Epon 828) epoxy and hence a greater affinity towards water, which led to a higher moisture concentration on approaching saturation isothermally and under thermal spiking. Splitting of the tan 5 peak after thermal spiking was observed for the resin blend containing the tetrafunctional epoxy. From the DMTA data, it can be concluded that degradation occurred as a result of thermal spiking at a temperature > 140°C and was postulated to be associated with the incomplete reaction of the functional groups during cure. Since more unreacted functional groups will be present in tetra-functional blend, there is a higher potential for hydrolytic degradation at the higher temperatures used for thermal spiking.
148
Moisture Absorption by Cyanate Ester Modified Epoxy Resin Matrices
ACKNOWLEDGEMENTS The authors acknowledge the University of Sheffield for a scholarship and ORS award to Dr. Sunil Karad. We also acknowledge BAe Systems Ltd. for additional financial support. We thank Advanced Composites Group for the supply of resins. We acknowledge valuable discussions with Mr. E. Shahidi (ACG Ltd.). REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13.
Browning, C. E., 1978. Polymer Engineering and Science, 18 (1):16. Jiming, Z., L. James. 1995. Composites Science and Technology, 53:57. Adams, R. D., M.M. Singh. 1996. Composites Science and Technology, 56:977. Bauer, J., M. Bauer. 1988. Ada Polymerica, 39:4. Lin, R.H. 2000. Journal of Polymer Science: Chem Edition, 38:934 Guo, B.C., W.W. Fu, D.M. Jia, Q.H. Qui, L. L. Wang. 2002. Polymer Composites, 10:237. Xiang Z. D., F.R. Jones. 1997. Composites Science and Technology, 57:451. Apicella A., R. Tessieri, C. De Cataldis. 1984. Journal of Membrane Science, 18:211. Jeffrey K., R.A. Pethric. 1994. European Polymer Journal, 30:153. Enns J.B., J.K. Gillham. 1983. Journal of Applied Polymer Science, 28:2831. Karad S.K., D. Attwood, F.R. Jones. 2002. Composites -.Part A, 33:1665. Gumen V.R., F.R. Jones. 2002 In Proceedings of 9th International Conference on Fibre Reinforced Composites A.G. Gibson , editor. 151. Gumen V.R., F.R. Jones, D. Attwood. 2001. Polymer, 42:5717.
New Epoxy Resins Based on Azomethine Groups for Potential Polymer Applications A. M.ISSAM*, H. P. S. ABDUL KHALIL and W. D. WAN ROSLI School of Industrial Technology. Universiti Sains Malaysia
ABSTRACT A series of new epoxy resins containing azomethine groups were synthesized by condensation reaction. The structures were characterized and confirmed by FTIR, 1H— NMR, 13C-NMR, UV and elemental analysis. Thermal stability and degradation behavior of these epoxy resins were examined by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The results of thermal analysis showed that, all resins possess high thermal stability. The epoxy resins based on p hydroxybenzaldehyde exhibited high thermal stability as compared to 4-hydoxy-3methoxybenzaldehyde. The resins produced showed good properties and can be used as matrix in polymer composites. INTRODUCTION Epoxy resins are among the most important thermosetting polymers in wide use as a matrix for fiber-based composites, structural adhesives, surface coatings, etc. [1,2]. Most of the commercially available epoxy resins are oligomers of DGEBA [1-3]. The epoxy resins are characterized by the presence of the oxirane group which is able to react with compounds possessing active hydrogen atoms, including amines, amides, or mercaptans. Various glycidyl esters, glycidyl amine derivatives and thioethers have been synthesized using this approach [3,4]. The synthesis, characterization, and polymerization of epoxy resins of various glycidyl ethers and esters containing azomethine groups have already been reported [5-7]. Owing to the relatively high thermal stability given by the presence of azomethine linkages [8-11], heat-resistant epoxides were prepared by reacting hydroxy and/or carboxy substituted azomethines or bis-azomethines with epichlorohydrin in the presence of a quaternary ammonium bromide as catalyst. The present paper deals with the synthesis of some new epoxy resin with azomethine linkages included in the main chain. The products, obtained by the direct reaction between DGEBA epoxy resin and various azomethine bisphenols, were characterized by both spectral and thermoanalytical techniques, the results being related to the chemical structure of the synthesized polymers.
* Corresponding Author, School of Industrial Technology, Universiti Sains Malaysia, 11800 Penang, [email protected]
150
New Epoxy Resins Based on Azomethine Groups
EXPERIMENTAL Materials P-phenylenediamine and ethylene diamine (Fluka Co.) were used without further purification. Vanillin, 4-hydroxy-3—methoxybenzaldehyde, p-hydroxybenzaldehyde and epichlorohydrine (Aldrich Co.) were used without further purification. Preparation of Azomethine Bisphenols Aldehyde (0.1 mol) was added dropwise to a solution of diamine (0.05 mol) in absolute ethanol. The mixture was refluxed for 6 h with stirring in 500 ml flask to allow complete reaction, followed by precipitation, filtration and washing several times with diethylether. The precipitate was finally dried for 24 h in a vacuum oven at 70 °C. Final purification was carried out by re-crystallization from 1-butanol and then dried for 24 h in a vacuum oven at 75 °C. Preparation of the Epoxy Resins Containing Azomethine Groups Preparation of the epoxy resins with azomethine groups in the main chain of the polymer was carried out in bulk using DGEBA epoxy resin and the azomethine compounds, synthesized as previously described. The reagents, taken in the molar ratio DGEBA/azomethine of 2:1, were first heated at 100 CC for 1 hr, then nbutylamine, used as a selective catalyst for the ring opening of the epoxide compound [12], was added. The mixture was stirred at 100 °C for 2-4 hr, and at 130 °C for 1 h to complete the polymerization process. The product, obtained as a solid glassy resin, was purified by dissolution in acetone, filtered several times and precipitated in toluene. Finally, the product was dried in vacuum at 80 °C for 10 h. The yields ranged from 75 to 80%. Instrumentation The FTIR spectra of the newly synthesized epoxy resins were recorded on Perkin Elmer 2000. ^ - N M R spectra were obtained using Brucker 300 MHz NMR spectrometer in CDCI3 as the solvent and TMS as the internal reference. The glass transition temperature ( Tg) was obtained by differential scanning calorimetry (DSC) by means of a Perkin Elmer DSC7 Series at a heating rate of 20 °C min"1 in a nitrogen atmosphere. The epoxy equivalent was evaluated by dissolution of the sample in pyridine (HC1) solution) and titration with aqueous NaOH solution in the presence of phenolphthalein, as previously described [13].
RESULTS AND DISCUSSION The general reaction yielding the epoxy resins containing azomethine linkages is given in Scheme 1.
New Epoxy Resins Based on Azomethine Groups
151
•0—CH 2 —CH—CH 2
2 CH,—CH—CH,—0-
amme
Scheme 1 The chemical nature of the A radical and elemental analysis of the synthesized epoxy resins are listed in Table 1. The ring opening of the epoxide compound (Scheme 1) is followed by the appearance of the secondary alcohol group [14-15]. The degree of the selectivity of the reaction depends on the active hydrogen compound used, on the catalyst and on reaction temperature. The use of the selective amine catalyst and reaction temperatures higher than 90 °C determines a 100-fold increase in the epoxide-phenol reaction [13]. The experimental conditions used and the experimental data obtained confirm the linear structure of the obtained epoxy resins containing azomethine. TABLE I Elemental analysis of the synthesized epoxy resins (1-4) Sample 1
Aldehyde
O=C^
V-OH /OCH3
2
3
O=C—/
\-OH
O=C—^
V-OH
A
-(CH2)2-
-(CH2)2O=C-/
^OH
Values in brackets are calculated
H (%)
N (%)
(11.23)
(11.23)
(11.23)
11.24
11.24
11.24
(11.23)
(11.23)
(11.23)
11.24
11.24
11.24
(11.23)
(11.23)
(11.23)
11.24
11.24
11.24
(11.23)
(11.23)
(11.23)
11.24
11.24
11.24
-n-n-
/OCH3 4
C (%)
152
New Epoxy Resins Based on Azomethine Groups
The FTIR spectra of the epoxy resins containing azomethine linkages showed the presence of the characteristic absorption bands at 900, 1200, and 1250 cm"1, attributed to the epoxy group. The 575 - 585 cm"1 and 1120 cm"1 bands correspond to the vibration of the ether group (-CH 2 -O-C 6 H 4 -), while the bands within the 1615 - 1635 cm"1 range assigned to the -CH=N- bond. The bands indicating the presence of the aromatic ring are placed at 3100 and 1500 cm"1, respectively. The 'H-NMR spectra of the synthesized epoxy resins showed a singlet at 1.7 ppm, specific to the methylenic protons, a multiplet situated in the 2.6-3.8 ppm interval for the protons of the epoxy group, a multiplet observed in the 6.5-7.3 ppm interval for the aromatic protons and a singlet at 8.69 ppm, assigned to the azomethine protons. Figure 1 shows a typical 'H-NMR spectrum recorded for sample 1. The UV spectra of the epoxides showed absorption bands placed in the 330-360 nm interval (characteristic to the epoxy groups). Compounds with methoxy groups in the backbone (2,4) showed a little blue shift as compared to the compounds (1,3).
FIGURE 1 'H - NMR spectrum of Sample 1
The DSC curves recorded with repeated heating-cooling cycles allowed the evaluation of Ts values of the synthesized epoxy resin. The Tg values are situated in the 35-60 °C temperature range. It is obvious that they depend on the structure of the epoxides, Tg increasing with increasing polymer molecular weight [16]. One might expect the polymers with azomethine segments in the main chain to have high thermal stability. The thermal behaviour of the synthesized epoxides was evaluated by dynamic TG experiments in nitrogen and air. Epoxides containing azomethine groups in the main chain showed an apparent •thermal stability higher than that of the DGEBA epoxy resin. The polymers 1 to 4 suffer a degradation starting from about 200 °C in air whereas about 250 °C in nitrogen. An increased decomposition rate being observed in the 300-450 °C temperature range, when the weight losses reach about 60-70%. The very close similarity of the thermograms suggests that the heat stability of the synthesized epoxy resin is not significantly influenced by the structure of the azomethines introduced in the main chain of the DGEBA resin. Considering that the compounds incorporating azomethine groups (i.e. mesogenic units) and flexible spacers in the main chain could
New Epoxy Resins Based on Azomethine Groups
153
possess both heat resistance and liquid crystalline properties [17-18], further investigations will concentrate on this aspect. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18.
May, C. A. (ed.). 1988. Epoxy Resins : Chemistry and Technology, 2nd edn, Marcel Dekker, New York. Goulding, T. M. 1994. in Handbook of Adhesive Technology, (edited by A. Pizzi and K. L. Mattel), p.531. Marcel Dekker, New York. Lee, H. and Neville, K. 1967. Handbook of Epoxy Resins, Mc-Graw Hill, New York. Wright, C. D. and Muggee, J. M. 1986. Structural Adhesives: Chemistry and Technology (edited by S. R. Hartshorn), p. 113. Plenum Press, New York. Mikroyannidis, J. A. 1989. Makromol. Chem. 190, 1867. Mikroyannidis, J. A. 1990. J. Appl. Polym. Sci. 41, 2625. Mikroyannidis, J. A. 1991. Polym. Int. 25, 91. D'Alelio, G. F. D., Strazik, W. F., Feigel, D.M., and Schoenig, R. K. 1968. J. Macromol. SciChem. A2, 1457. Preston, J. 1982. Angew. Makromol. Chem. 109/110, 1. Kricheldorf, H. R. and Awe, J. 1989. Makromol. Chem. 190, 2579. Aharoni,S.M. 1988. Macromolecules 21, 1941. Cascaval, C. N., Mustata, F., and Rosu, D. 1993. Angew. Makromol. Chem. 209, 157. Alvey, F. B. 1969. J. Appl. Polym. Sci. 13, 1473. Shechter, L. and Wynstra, 1956. J. Ind. Engng. Chem. 48, 86. Enikolopyan, N. S., Markevitch, M. A., Sakhonenko, L. S., Rogovina, S. Z., and Oshmyan, V. G. 1982. J. Polym. Sci., Polym. Chem. Edn 20, 1231. Turi, E. A. 1981. Thermal Characterization of Polymeric Materials. Academic Press, New York. Sek, D. 1984. Eur. Polym. J. 20, 923. Tang, J. C. and Chang, T. C. 1994. Eur. Polym. J. 30, 1059.
Mechanical Properties of Rotational Moulded Polyethylene Composites - Experiments and Theories W. Yan, R.J.T. Lin* and D. Bhattacharyya Centre for Advanced Composite Materials Department of Mechanical Engineering The University of Auckland, Private Bag 92019, Auckland, New Zealand
ABSTRACT The dominant usage of linear polyethylene as the raw material for rotational moulding, a fast growing industrial method, has shown insufficient mechanical properties for certain applications where the strength and stiffness of a product are of importance. Worldwide rotational moulders have an urgent need for stronger, stiffer materials to be available; therefore, the introduction of reinforcements into rotomoulding process is attracting increasing attention. However, the incorporation of reinforcements in rotational moulding process has often shown difficulty of achieving a uniform distribution within the matrix material, which results in unsatisfactory mechanical properties. This paper describes an investigation using various particles of different volume fractions as the reinforcements, and verifying the various mechanical properties of rotomoulded products using different mathematical models. The results show that the Halpin-Tsai-Nielsen equation and the Nicolais-Narkis equation are well suited to predict the tensile modulus and tensile strength respectively for the rotomoulded particulate reinforced structure. A very good agreement can be achieved between the experimental results and the predictive models for the composites with particle volume fractions of 20% or less.
INTRODUCTION Rotational moulding is a method using plastic in powder or liquid form to produce hollow plastic products in a rotating mould, hi principle, rotational moulding comprises four stages: material charging, heating, cooling and de-moulding. The rapid development of this process as a mainstream plastics manufacturing method is attributed to its many advantages, such as the absence of residual stresses (no external pressure needed), low manufacturing and material costs, and the capability of manufacturing large and high quality products. However, some limitations also exist such as high mould cost, long processing time, limited mouldable material selection and mould shape complexity [1]. In order to improve the efficiency of rotational moulding, research has been carried out in various aspects, such as using special geometrical features for mould
Corresponding author, Centre for Advanced Composite Materials (CACM), Department of Mechanical Engineering, School of Engineering, University of Auckland, Private Bag 92019, Auckland, New Zealand; Phone: +64-9-3737599 Ext. 84543; Fax: +64-9-3737479; E-mail: ii.lin(fl),auckland.ac.nz
Rotational Moulded Polyethylene Composites
155 TM
design to provide stiffness for thin wall products [1,2], using ROTOLOG wireless temperature acquisition system for facilitating process control [2], identifying critical factors and enhancing heat transfer properties of moulds for the reduction of cycle time in rotational moulding [3,4]. However, incorporating reinforcements into the rotationally moulded components has created new challenges [5,6]. The first critical step for producing rotomoulded composite structures with better mechanical properties is to achieve uniformity of the reinforcement distribution. However, because of the high aspect ratio of most fibrous reinforcement, poor results have been reported when attempting to produce long glass fibre reinforced rotomoulded parts [6]. Other research has shown that the incorporation of short glass fibres or flax fibre can obtain some improvement of the mechanical properties by modifying the rotomoulding process, such as introduction of inner air pressure or double shot mould charging process [7-10]. However, the distribution of the fibres is still not completely satisfying. On the other hand, due to the low aspect ratio of particulate reinforcements, good distribution has been achieved in rotational moulding [11,12]. Some improvements in tensile modulus and impact strength can be obtained but there are some problems with the deterioration of the tensile strength [6-8,11-12]. With the addition of rigid particles to polymers or other matrices, a number of effects on mechanical properties, such as an increase in stiffness, reductions in tensile strength and the coefficient of thermal expansion, improvements of creep resistance and fracture toughness can be observed [13]. The degree of change in the mechanical properties of the composites can be affected by the size, shape, aspect ratio and the distribution of the reinforcing particles. In the case of non-spherical particles, the degree of orientation with respect to the applied stress is also important. Previously developed theories for modelling mechanical properties of particulate reinforced composites manufactured by different processes have shown good agreement with the experimental results obtained from composite parts [14-19]. However, for the pressure-free rotational moulding process, verification of the mechanical properties using these models has not been attempted yet. All these models are based on Einstein's equation for the viscosity of suspension with rigid spherical inclusions [20] to evaluate the reinforcing effect of particles in polymeric materials. However, they have their inherent weaknesses when predicting the mechanical properties of the composite products resulting in no single theory being suitable for analysing the overall composite material performance. In this study, for modelling the mechanical properties of rotomoulded products, several theories have been discussed and the predictions from these mathematical models have been compared with the experimental results obtained from composites rotomoulded with different kinds of particulate reinforcements. EXPERIMENTAL DETAILS The polymer matrix used in this study was Linear Polyethylene (LMDPE) Cotene 9042 with Melt Flow Index of 4.0g/10 min. This material is generally suitable for rotational moulding of large tanks and products that require a high degree of rigidity. The particulate reinforcements used are shown in Table I. The moulded parts had a wall thickness of 3.2 mm with the reinforcement volume fraction of up to 20 %. The sizes of the particles were in the same order of magnitude as that of the plastic powder. One laboratory designed rock-and-roll machine was used for rotational moulding experiments. The aluminium mould used had the dimensions of 100mm x 100mm x 220mm, and the wall thickness of 3mm. During the moulding process, the oven
156
Rotational Moulded Polyethylene Composites
temperature and internal air temperature were constantly monitored and recorded. The rotational speed ratio of the two axes was set at 10 to 3 with the main longitudinal axis rotating at 25 rpm. The oven temperature was set at 220°C and the heating process was stopped when the internal air temperature had reached 185°C. Forced air-cooling was used until the internal temperature dropped down to 40°C for demoulding. TABLE I Particulate reinforcement
A12O3
SiC
Irregular
Spherical glass beads with coupling agent (SGB+CA) Spherical
Irregular
Irregular
90-150
240
90-150
105-149
105-149
1
1.35
1
1.25
1.21
Spherical glass beads (SGB)
Recycled glass particles (RGP)
Shape Major dimension
Spherical
Aspect ratio
Reinforcements
The test specimens were cut out of the walls of rotomoulded boxes (94mm x 94mm x 214mm) and standard tests (stiffness - 0.1% secant modulus, BS2782; tensile strength ASTM D638-00 and impact strength, ASTM D6110-97) were conducted to determine the mechanical properties of the moulded composite specimens at room temperature. THEORETICAL MODELLING For polymer manufacturing processes such as injection moulding, compression moulding etc, there have been several theoretical models developed to predict the tensile moduli and tensile strengths of the particulate reinforced polymers, which are summarised in Table II. In general, it has been pointed out that, based on the assumption of a composite material failing when fracture is initiated from a stress concentration around a reinforcing particle, the theories for predicting the strength of a particulate reinforced system are less developed than those for predicting the moduli [20,21]. When applying these models for predicting the composite strength and modulus, the values of some important constants or parameters have to be decided. The first important parameter is the maximum packing factor of particulate reinforcement, <j>m, which can be obtained either theoretically or experimentally once the particle distribution condition is determined. In this study, random close packing is considered for deciding this factor. The other important parameter is the Einstein Coefficient, KE, which can be calculated by knowing the Poisson's ratio of the matrix material and the relative Einstein Coefficient ratio, KE/2.5, where 2.5 is the KE value of a material with a Poisson's ratio of 0.5 [20]. TABLE II Mathematical models for tensile modulus and tensile strength Name Guth model (ref[17])
Models For spherical particles
Ec=Ep(l + KEVf+U.Wf2) For non-spherical particles
Ec = Ep(l + 0.67aVf
+\.62a2V/)
Nomenclature Ec = Tensile modulus of the reinforced polymer Ep = Tensile modulus of the matrix KE = Einstein coefficient Vf= Reinforcement volume
Rotational Moulded Polyethylene Composites
Halpin-TsaiNielsen Model (ref [20])
157
1 + ABVf c
where: B -
\-B
"
"
\m Vf
p
with spherical reinforcements:
8-lOv, with nearly spherical shaped reinforcements:
A = KE-\ Verbeek model for tensile modulus (ref [18,19])
^ = Void content of composite Vp = Volume fraction of polymeric matrix (associated with zero void) X = Modified void content (void relative to polymer phase) MRF - Modulus reduction factor
(y-vPY$m A
vp{\-
,h-zfGp P
1
Vf
Em
fraction a = Reinforcement aspect ratio A = A constant which takes into account such factors as geometry of the reinforcing phase and Poisson's ratio of the matrix B = A constant which takes into account the relative modulus of the reinforcing and matrix phases Em = Tensile modulus of the reinforcement cp = A factor which depends on the maximum packing fraction 0m of the reinforcement m = Maximum packing fraction of reinforcement V! = Poisson's ratio of matrix
1-V,
GpVf
f
^
a
1
1
u
tanh(w)
u
<Jc=VpGp+KlzpMPF Nielsen model (ref [22]) Nicolais Narkis model (ref [16])
ac=ap(l-V/'3)K
Gp = Shear modulus of the polymer ac = Tensile strength of the composite TP - Shear strength of the polymer K3 — Correction factor MPF = Strength reduction factor
The values for all the constants and parameters used in these theoretical models are listed in Table III. TABLE III Value of parameters used in models Correction factor K3 Stress concentration factor K Einstein coefficient for MDPE matrix KE Poisson's ratio of matrix (MDPE) v, Maximum packing fraction of spherical glass beads (SGB) >m
0.75 ref [191 1.0 ref [22] 2.25 ref [20] 0.4 ref [23] 0.63 ref [20]
158
Rotational Moulded Polyethylene Composites
Maximum packing fraction of irregular shaped reinforcements <j)m Tensile modulus of matrix (MDPE) Ep Tensile modulus of glass beads (SGB RGP) Em Tensile modulus of A12O3 Em Tensile modulus of SiC Em Tensile strength of the polymer aD Shear strength of the polymer rn
0.60 ref [24] 0.88GPa ref [121 64.4GPa ref [23] 54.7GPa ref [23] 58.2GPa ref [231 16.2MPa ref [12] 12MPa ref [18]
RESULTS AND DISCUSSION Tensile modulus of glass bead reinforced composites
In the case of spherical glass bead reinforced composites, Fig. 1 shows that the modulus values obtained from both the Halpin-Tsai-Nielsen and Guth models agree reasonably well with the experimental results. However, Guth model tends to overpredict the modulus when the volume fraction of reinforcement becomes higher than 10%. Despite the proven ability of the Verbeek model to predict the moduli of composites with some particulate reinforcements [18], it appears to be inadequate in modelling composites with spherical reinforcement as it constantly under-predicts the stiffness as shown in Fig. 1. With a close study of Verbeek model, it can be determined that the aspect ratio of the particle plays an important role in deciding the composite modulus. From Fig. 2, it is evident that the reinforcing effect of the added particles can only happen when their aspect ratio is larger than a critical value, which in this case is around 7. Due to the fact that all the particles used in this study have aspect ratios between 1.0 and 1.35, the Verbeek theory becomes unsuitable for modeling the composites properties. -Experiment results "Halpin-Tsai-Nielsen equation ~Guth equation -Verbeek equation
Volume fraction %
FIGURE 1. Comparison of the results between theoretical models and experiment showing the effects of different theoretical models on tensile modulus at various volume fractions of glass beads.
Rotational Moulded Polyethylene Composites =1
159
AR= 3 - - - -AR-6 — - -AR-9 — - -AR-12
1.5 "\
Increa sing Aspect Ratio
y
Matrix Polymer
y'
•
•
09 -
0.3
0.0 100%
90%
80%
70%
60%
50%
40%
30%
20%
10%
Polymer Volume Fraction
FIGURE 2. The effect of changing aspect ratio on the predicted composite modulus at various polymer volume fractions according to Verbeek Model.
As demonstrated in Fig. 1, the Halpin-Tsai-Nielsen model appears to be the most accurate for predicting the tensile modulus of the particulate reinforced rotationally moulded products with a low volume fraction of reinforcement (<20%). This theoretical model will be adopted for modulus analyses in the later part of this study. Tensile strength of glass bead reinforced composites The comparison of tensile strengths obtained from different theoretical models and experimental results is shown in Fig. 3. Among the three models employed, Nicolais-Narkis model gives the best agreement with the experimental results, but the Verbeek's model again predicts less accurately than the other two models. As explained previously, the aspect ratios of the particles used in this study are too small to effectively use this the Verbeek theory for predicting the composite tensile
-Experimental results —Verbeek's mode -Nicolais-Narkis model "•Nielsen's model 10 Volume fraction %
FIGURE 3. Comparison of the results between theoretical models and experiment showing the effects of different theoretical models on tensile strength at various volume fractions of glass beads.
160
Rotational Moulded Polyethylene Composites
strengths. On the other hand, Nielsen's equation with stress concentration factor K (Table II) of 1.0 (i.e. no stress concentration) gives the results lying between those from Nicolais-Narkis and Verbeek models. A proper stress concentration factor can get the values of the composite tensile strength closer to the experimental results (in this case, K should be around 0.85). However, in order to determine a more accurate stress concentration factor to enable the effective application of Nielson model, it will need to systematically carry out more experiments. Therefore, the Nicolais-Narkis model is chosen for further analyses regarding the composite tensile strength. The effects of particle type on the tensile modulus and strength When different types of particles are used as reinforcements in rotomoulding composites, the tensile modulus get affected as shown in Fig. 4 with the volume fraction of up to 20%. It indicates that, when Halpin-Tsai-Nielsen model is used, the prediction of tensile modulus remains generally unaffected by the type of particle used in this study. The reasons may be attributed to the facts that the Poisson's ratio of the PE matrix is kept constant (0.4) resulting in the same value for the parameter A (Table II) irrespective of the type and shape of the reinforcement used, and secondly, the tensile moduli of the different particles do not vary much. In general, it can be seen from the experimental results that the moduli of the various particulate reinforced composite materials follow similar trends: that the reinforcing effect on the composite stiffness increases with the addition of particles up to 10 vol%; with further
10 Volume fraction %
15
FIGURE 4. The comparison of the results from Halpin-Tsai-Nielsen model (M) and experiments (E) showing the effects of particle types on tensile modulus at various volume fractions.
increase of particle content, the modulus either becomes stabilised or starts to decrease. This is different from what is predicted from the Halpin-Tsai-Nielsen model that shows a constantly increasing tendency. This discrepancy can be explained by the growing clustering of particles with the increasing particle volume fraction during the stress free rotational moulding that allows the particles to distribute naturally through a tumbling action. These particle clusters/chains can then cause stress concentrations due to the bridging between the boundaries of the particlepolyethylene system, which consequently affect the tensile modulus.
Rotational Moulded Polyethylene Composites
161
-•-Math model -*-RGP -#-AI2O3
-*-SCI
-•-SGB
-f-SGB +CA 10 Volume fraction °
FIGURE 5. The comparison of the results from Nicolais-Narkis model and experiments showing the effects of particle types on tensile strengths at various volume fractions.
When the Nicolais-Narkis equation is applied to evaluate the effects of different types of particulate reinforcement on the composite tensile strength, it produces a single set of predicted tensile strengths for the rotomoulded composites regardless of the different particles used, Fig. 5 because the theory solely depends on the matrix tensile modulus and the reinforcement volume fraction. Generally speaking, the tensile strengths calculated from this model agrees reasonably well with the experimental results when the volume fraction is less than 10%, but becomes overpredictive with a higher particle content. With the range of particles used in this study, both the experimental and theoretical results show a trend of decreasing strength with the volume fraction increasing. This could be due to the rising possibility of the formation of large particle clusters, resulting in a decrease of the load bearing capacity due to their inherent weak bonding. This undesirable effect warrants future study for finding a proper solution. Due to the lower aspect ratios of particles, it may be expected that the particulate systems could be more easily distributed in the rotational moulding process compared to the fibrous systems. Therefore, it is important to establish the validity of the theoretical predictions of final product properties. CONCLUSIONS From the research results described above, the following remarks may be made: > The theoretical models of Halpin-Tsai-Nielsen and Nicolais-Narkis can be used to predict the tensile modulus and the tensile strength respectively for the particulate reinforced composites produced by the rotational moulding process. > Different reinforcing particles, such as spherical shaped glass beads (90|am150um), irregular shaped glass beads (average 240|am), irregular shaped aluminium oxide (105|am -149um), irregular shaped silicon carbide (105(im 149um), do not make significant difference in the tensile moduli and tensile strengths of the final rotationally moulded products. > With the addition of small quantities of particulates (up to 10 %), the tensile modulus of the rotomoulded component increases, whereas the tensile strength always decreases with the addition of particulates in rotomoulding.
162
Rotational Moulded Polyethylene Composites
ACKNOWLEDGEMENTS The authors are thankful to the Foundation for Research Science & Technology New Zealand for providing the financial support for this research. Special thanks are also due to J. R. Courtenay (NZ) Ltd for supplying LMDPE material and allowing the free use of their industrial rotational moulding machine for producing the rotomoulded products. REFERENCE 1. Crawford, R.J., Rotational moulding of plastics (second edition). 1996: Research Studies Press LTD. 2. Crawford, R.J. and S. Gibson, Rotational moulding, the basics for designers. Rotation, 2000(July/August): p. 36. 3. Crawford, R.J. and P.J. Nugent, Impact strength of rotationally moulded polyethylene articles. Plastics, Rubber and Composites Processing and Applications, 1992.17(33-41). 4. Abdullah, M.Z., S. Bickerston, and D. Bhattacharyya. Enhanced Heat Transfer in Polymer Moulding Processes. Polymer Processing Society Asia/Australia Regional Meeting (PPS-2002), Taipei, Taiwan, November 4-8, 2002, G6. Thermoforming, Blow Molding and Rotational Molding, Paper No. 116. 5. Martin, D., et al., A summary of recent Australian R&D activities in rotational moulding. Rotation, 2001. January - February: p. 44-50. 6. Crawford, R.J. and A. Robert. Reinforcement of rotomoulded plastic parts - a challenge, in The 3rd Asian-Australasian Conference on Composite Materials. 2002. Auckland, New Zealand. 7. Harkin-Jones, E. and R.J. Crawford, Mechanical properties of rotationally molded Nyrim. Polymer Engineering and Science, 1996. 36(5): p. 615-625. 8. Harkin-Jones, E. and R.J. Crawford, Rotational molding of liquid Nyrim in biaxially rotating heated moulds. Plastics, Rubber and Composites Processing and Applications, 1995. 24(1): p. 1-7. 9. Blackburn, D.R. and O.K. Ademosu. An investigation of the production of rotationally moulded composites, in Fibre Reinforced Composites - International Comference - 9th. 2002. 10. Ward, J., Panigrahi, S., Tabil, L. G., Crerar, W. J. and Powell, T., Rotational Molding of Flax Fibre Reinforced Thermoplastics, Paper No: MBSK 02-209, An ASAE Meeting Presentation, 2002. 11. Yan, W., R. J. T. Lin, S. Bickerton, D. Bhattacharyya, Performance Evaluation of Moulded Polymeric Composites, Polymer Processing Society Asia/Australia Regional Meeting (PPS-2002), Taipei, Taiwan, November 4-8, 2002, G6. Thermoforming, Blow Molding and Rotational Molding, Paper No. 204. 12. Yan, W., R. J. T. Lin, S. Bickerton, D. Bhattacharyya, Rotational Moulding of Particulate Reinforced Polymeric Shell Structures, Materials Science Forum, Vol 437-438 (2003): p. 235-238. 13. Ahmed, S. and F.R. Jones, A review of particulate reinforcement theories for polymer composites. Journal of Materials Science, 1990. 25: p. 4933-4942. 14. Nielsen, L. E., Generalized equation for the elastic moduli of composite materials. Journal of applied physics, 1970. 41(11): p. 4626. 15. Gao, Z. and A. H. Tsou, Mechanical properties of polymers containing fillers. Journal of Polymer Science: Part B: Polymer Physics, 1999. 37: p. 155-172. 16. Nicolais, L. and M. Narkis, Stress-strain behavior of styrene-acrylonitrile/glass bead composites in the glassy region. Polymer Engineering and Science, 1971. 11(3): p. 194-199. 17. Guth, E., Theory of filler reinforcement. Journal of applied physics, 1945. 16(January): p. 20-25. 18. Verbeek, C.J.R., The influence of interfacial adhesion, particle size and size distribution on the predicted mechanical properties of particulate thermoplastic composites. Materials Letters, 2003. 57: p. 1919-1924. 19. Verbeek, C.J.R. and W.W. Focke, Modelling the Young's modulus of platelet reinforced thermoplastic sheet composites. Composites Part A: applied science and manufacturing, 2002. 33: p. 1697-1704. 20. Nielsen, L.E. and R.F. Landel, Mechanical properties of polymers and composites. 1994: Marcel Dekker, Inc. 21. Sahu, S. and L.J. Broutman, Mechanical properties of particulate composites. Polymer Engineering and Science, 1972. 12(2): p. 91-100. 22. Nielsen, L.E., Simple Theory of Stress-Strain Properties of Filled Polymers. Journal of Applied Polymer Science, 1966.10: p. 97-103. 23. Shackelford, J.F., W. Alexander, and J.S. Park, CRC Practical Handbook of Materials Selection. 1995: CRC Press, Inc. 24. Scott, G.D., Packing of spheres. Nature, 1960. 188: p. 908-909.
Morphology and Mechanical Properties of HDPE Reinforced with PET Microfibres R. Seltzer*, L. Fasce, P. Frontini INTEMA, Univ. Nac. Mar del Plata, Mar del Plata, Argentina V. J. Rodriguez Pita, E.B.A.V. Pacheco, M.L. Dias Instituto de Macromoleculas Professora Eloisa Mano, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brasil
ABSTRACT In this work compatibilized blends of PET and high density polyethylene (HDPE) with 1% and 7% ethylene/methacrylic acid copolymer (Nucrel®) have been prepared and their morphology and mechanical properties have been compared with those of the same uncompatiblized blends. Aiming to induce different morphologies the pellets of the blends were processed by three different procedures: compression molding, extrusion and extrusion followed by annealing. In every case, HDPE constituted the matrix and PET was the dispersed phase. PET adopted a nodular morphology in the compression molded samples, it took the form of microfibers (microfibrillar reinforced composites) in extruded samples, and it appeared flake like in the annealed extruded samples. According to tensile and fracture tests, extruded blends having 7% Nucrel appeared as the optimum combination of processing method and compatibilizer content.
INTRODUCTION Poly (ethylene terephtalate) (PET) and high density polyethylene) (HDPE) are extensively used in packaging of consumer and industrial products, being the most found in urban waste streams. One of the best way of reducing urban waste is by recycling. Then, it would be highly convenient, in economical terms, to blend both polymers. The obstacle is that these two polymers are incompatible, i.e. PET and HDPE are inmiscible in liquid state and there is lack of adhesion in solid state. The development of new multiphase blend materials is dependent primarily on two key requirements: control the interfacial chemistry and control of the microstructures [1]. Through this paper, the mechanical behavior of 50/50 PET/HDPE blends were assessed. Blends were prepared by reactive blending using an ethylene/methacrylic acid copolymer (Nucrel®) in different percentages as a compatibilizer agent. Guerrero et al. [2] reported a an increase in elongation at break and impact strength in the ternary blends due to compatibilization between PET and HDPE with similar agents. The blends were processed following three different procedures to promote de developing of different morphologies.
* Corresponding author, Universidad National de Mar del Plata, Argentina, fax:54-223-4810046, e-mail: [email protected]
164
HDPE Reinforced with PET Microfibres
MATERIALS AND PROCESSING The materials used were HDPE (Novatec JV060, Tm=133°C) provided by Poliaden and PET (Polyclear T86, Tm=260°C) provided by Hoechst. The compatibilizer was an ethylene/methacrilic acid copolymer (Nucrell202HC Tm=99°C) (Nu) provided by Du Pont. Before blending, the polymers were dried in an oven for 16 hours at 160°C (PET) and 60°C (acid copolymers and ionomers). PET/HDPE blends were prepared in 50/50 proportion, and the amount of compatibilizers varied from 0% to 7% weight. 50/50/xNu pellets were compounded in a Haake Rheocord 9000 extruder at 280°C and 60 rpm. Extruded ribbons of 1 mm thick were obtained from the same extruder by changing the die (50/50/xNu/E). In order to change ribbons structural properties [3], isotropization of the lower melting component (HDPE) with preservation of the oriented microfibriUar structure of the higher melting (PET) component was done (5O/5O/XNU/ET) by annealing them at 160 °C under a pressure of 10 Mpa for 15 minutes followed by cooling with running water. Compression molded plaques of 1 mm thick were processed by compression molding the pellets (50/50/xNu/C) at 270 °C and 75 MPa during 15 minutes followed by cooling with running water.
CHARACTERIZATION Morphology Blends morphology was examined by means of scanning electron microscopy, SEM (JEOL JMS-53OO), on samples broken in liquid nitrogen. Depending on the phase to be seen, these broken samples were etched dissolving selectively PET (trichlore benzene) or HDPE (xylene). Finally, they were gold coated.
FIGURE 1 SEM micrographs. Magnification xlOOO taken from the fracture surface of -a) 50/50/0Nu; b) 50/50/ONu/C after extraction of HDPE; c) 50/50/0Nu/C after extraction of HDPE; d) 50/50/lNu/C; e) 50/50/lNu/C after extraction of HDPE; f) 50/50/lNu/C after extraction of HDPE.
HDPE Reinforced with PET Microfibres
165
FIGURE 2 SEM micrographs. Magnification xlOOO taken from the fracture surface of -a) 50/50/ONu/E; b) 50/50/ONu/E after extraction of HDPE; c) 50/50/ONu/E after extraction of HDPE; d) 50/50/lNu/E; e) 50/50/lNu/E after extraction of HDPE; f) 50/50/lNu/E after extraction of HDPE; g) 50/50/7Nu/E; h) 50/50/7Nu /E after extraction of HDPE; i) 50/50/7Nu/E after extraction of HDPE
FIGURE 3 SEM micrographs. Magnification xlOOO taken from the fracture surface -a) 50/50/0Nu/ET; b) 50/50/ONU/ET after extraction of HDPE; c) 50/50/ONu/Er after extraction of HDPE; d) 50/50/lNu/Er; e) 50/50/lNu/Er after extraction of HDPE; f) 50/50/lNu/ET after extraction of HDPE; g) 50/50/7NU/ET; h) 50/50/7Nu/Br after extraction of HDPE; i) 50/50/7Nu/ET after extraction of HDPE
166
HDPE Reinforced with PET Microfibres
In the compression molded blends the dispersed PET domains are spherical in shape (Figure 1). In the binary blends (Figurelb) there is no evidence of adhesion between the two phases .The voids occurring where the particles were located show that they were attached only by weak mechanical adherence . Compatibilized blends (Figures le-f) show higher dispersion of the PET phase, i.e. more particles of smaller dimensions, though some inhomogenity is still displayed (Figure Id). The addition of the Nucrel to extruded blends (Figure 2) resulted in remarkable changes in the morphology. It can be seen that the dimension of the dispersed particles have decreased to a certain size so that the surface appearance is now quasihomogenous PET discontinuous phase is shaped into microfibers (Figure 2b). As compatibilizer content increases dissolution and extraction of HDPE from PET structure becomes less effective. This fact evidences compatibilization between both phases (Figure 2h, i). In annealed extruded blends (Figure 3) unfortunately the microfiber structure of the PET phase did not maintain although blends were reprocessed far below the melting temeprature of PET. As Nucrel content increases, higher deformation and coarsening of PET fibers is obtained upon annealing (Figures 3b, c, e, f, h, i) is detected. Thermal Properties Melting curves of two blends are shown in Figure 4. Each melting trace is characterized by two peaks: one peak around 130 °C corresponding to HDPE and the other at higher temperature, around 245 °C, corresponding to PET. It can be seen that compatibilized blends present displacements to the lower temperatures in PET and HDPE melting points. This behavior is indicative of compatibility between components [4]-
j
AH == 20.5 J/g peak = 253 °C
1—-—-__
O
Q Z LLI
;1
—-\
AH = 27 J/g peak = 248 °C
AH = 99 J/g AH = 74 J/g peak= 130 °C i peak=131°C
11
50
100
150
T°C FIGURE 4 DSC curves for blends.
200
250
50/50/0Nu;
300
50/50/lNu
Mechanical Properties Tensile properties were measured using an Instron machine mod. 4467, performing the tests on dumbell specimens cut from ribbons and plaques. The tensile properties, elastic modulus, E, tensile yield stress, ay, and elongation at break, £b, of all the investigated blends are reported in Table I. Compression molded and annealed extruded blends behave in a brittle manner and the elongation at break falls to very lows values. The latter arises from the photographs of the tested specimens (Figures 5-7), as well. Both extruded type blends display higher yield point than the compression
HDPE Reinforced with PET Microfibres
167
molded blends. The addition of 7% of Nucrel significantly improves elongation at break of the extruded blend promoting fibrillation during stretching (Figure 6). TABLE I Tensile properties Material 50/50 E (GPa) o v (Mpa) «*(%)
ONu/C
INu/C
ONu/E
INu/E
7Nu/E
ONu/Er
INU/ET
7NU/ET
1.7 12
1.9
1.1
1.6
1.9
1.7
33
35
1.5 29
2.0
22
28
29
33
1
1
4
60
>100
2
3
4
FIGURE 5 Fraelure pattern -n) 50/50/ONu/C; b) 50/50/lNu/C,
FIGURE 6 Fracture pattern of a) 50/50/ONu/E; b) 50/50/lNu/E; e)50/50/7Nu/E.
FIGURE 7 Fracture pnltorn ol -a) 50/50/0Nu/Br; b) 50/50/lNu/Er; o) 50/50/7Nu/Er.
Fracture tests were performed on an Instron machine mod. 4467 at Imm/min. DDENT cut from compression molded plaques, extruded ribbons and annealed extruded ribbons were used. Specimens nominal width, W, was 30 mm and a/W was 0.3, where a is the crack length. Blends were characterized by the stress intensity factor at maximum load, Kmax, K
=
1.122-0.564- - 0 . 2 0 5 ^ + 0 . 4 7 1 - + 0 . 1 9 ^ -
J where P is the maximum load in the load-displacement trace, B is the specimen thickness; and by the work of fracture , Wf, calculated as the total fracture energy divided by twice the ligament area. Kmax and Wf values displayed by each sample are presented in Table n. The highest values were found for the extruded blends while the lowest ones were obtained when compression molded samples were tested. Annealed samples showed intermediate behavior. Figures 8-10 show fracture patterns of the specimens. It is clearly observed that compression molded and annealed extruded blends behave in a brittle manner, while extruded blends do not present "in plane" crack propagation. Ligament stretches and fibrillates, instead. In uncompatibilized extruded and annealed extruded samples crack path deflects from mode I to mode II. This is due to lack of miscibility and adhesion between the uniaxially oriented phases. The energy required to separate the phases longitudinally is lower than the one involved in breaking the fibers transversally. The latter effect is not enhanced by the addition of Nucrel (Figures 9b, c; 10b, c). Material 50/50 K^MPa-m1") Sd K m a x wf(N/mm) Sd™,
ONu/C 0.90 0.03 3.1 0.2
TABLE II Fracture parameter values 7Nu/E ONu/E INu/E INu/C 1.47 0.85 1.56 1.44 0.12 0.08 0.05 0.08 40.3 1.3 39.5 30.2 2.6 0.1 1.0 5.1
0Nu/ET 1.11 0.14 6.8 0.6
INU/ET
1.29 0.07 4.2 0.5
7Nu/ET 1.39 0.30 8.4 1.2
168
HDPE Reinforced with PET Microfibres
-a FIGURE 8 Fracture pattern -a) 50/50/ONu/C; b) 50/50/lNu/C.
FIGURE 9 Fracture pattern of -a) 50/50/ONu/E; b) 50/50/lNu/E; c] 50/50/7Nu/E.
FIGURE 10 Fracture pattern of-a) 50/50/0Nu/ET; b) 50/50/lNu/Er; c) 50/50/7Nu/Er
CONCLUSIONS PET/HDPE blends are fragile materials with poor mechanical properties because of the incompatibility between the two phases. It emerges from the phase morphology generated that Nucrel can act as a compatibilizing agent when used as a third component. A significant improvement of the mechanical properties, in particular of the elongation at break and fracture toughness, can be achieved by inducing fibrillation of the PET phase in PE matrix by extruding the blends under adequate conditions. Processing techniques , like compression molding of extruded pellets, which are not capable of inducing fibrillation of the PET phase lead to blends having poor properties. Far from improving the mechanical properties, annealing of extruded blends disrupted PET microfiber structure which is responsible for high elongation and strength. The best overall properties were displayed by extruded blends compounded with 7% of Nucrel. ACKNOWLEDGEMENTS This work was supported by a SECyT-CAPES (BR/A00-EXII011) grant. REFERENCES 1.
2. 3. 4.
Davis BD, 2000. "Factors influencing the morphology of immiscible polymer blends in melt processing", in Polymer blends: performance. Paul DR, Bucknall CB, eds. New York: John Wiley & Sons; pp. 501-38. C. Guerrero, T. Lozano, V. Gonzalez, E. Arroyo, 2001,Vol 82 "Journal of Applied Polymer Science " 1382-1390. M. Evstatieva and N. Nicolova, S. Fakirovb, 1996, Polymer 37, 4455-4465 Utracki, L. A. Polymer Alloys and Blends; Hanser: Munich, 1989.
Mechanistic Evaluation of Environments on Degradation of E-Glass/Vinylester Composites Vistasp M. Karbhari, Wellington Chu and Lixin Wu Department of Structural Engineering, MC-0085 University of California San Diego. La Jolla, CA 92093-0085, USA
ABSTRACT E-Glass/Vinylester composite components, fabricated using processes that incorporate ambient and moderate-temperature cures, are increasingly being used in marine, offshore and civil infrastructure applications. This often results in the component being placed in use when cure progression has not reached one hundred percent result in competing mechanisms of deterioration associated with moisture and solvent sorption, and slow residual post-cure. This paper presents results of a detailed program aimed at the investigation of effects of water immersion on the durability and progressive degradation of this class of composites. Results are based on mechanical characterization, Dynamic Mechanical Thermal Analysis, and microscopy.
INTRODUCTION Due to their corrosion resistance, relatively high ultimate failure strains, and damage tolerance, E-glass/vinylester composites are increasingly being considered for use in cost-sensitive primary structural components in marine, offshore and civil infrastructure applications. Due to geometrical size requirements and those related to cost, nonautoclave processes such as wet layup, resin infusion, and pultrusion are the primary processes under consideration, with cure being achieved under ambient, or in the case of pultrusion, moderate temperature conditions with high throughput. Styrene in the monomeric form is used as a diluent in the resin in quantities between 20% and 60%. Although increases in styrene content can result in increases in hydrophobicity (and thus an effective decrease in the level of moisture absorption) it also results in an increase in shrinkage (resulting in the potential for significant microcracking in resin rich areas and high residual stresses in composites having high fiber volume fractions) as well as the possibility of incomplete polymerization. Incomplete polymerization not only leads to changes in properties with time due to slow changes in degree of cure, but also induces lower heat stability, lower resistance to hydrolysis and a greater degree of susceptibility of swelling in solvents [1,2]. In addition, the hydrolysis of ester groups can result in the formation of carboxyl groups, resulting in further decomposition due to autocatalysis [3]. In evaluating the applicability of composites for use in primary structural elements, for applications expected to show long service life, the assessment of effects of aqueous and hygrothermal exposure are critical. The diffusion and sorption of moisture in a polymer and the resulting composite is related to the availability of molecular sized * Corresponding author, Department of Structural Engineering; MC-0085; University of California San Diego; Building 409 University Center; La Jolla, CA 92093-0085, USA; Fax: (858) 534-6470; Email: [email protected]
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holes, the affinity of the polymer for moisture, and the extent to which wicking can take place along the fiber-matrix interface. The overall kinetics, and the resulting materials level deterioration, thus depend on microstructure, morphology, cross-link density, molecular weight, fiber chemistry, and interfacial bonds. The results reported in this paper are part of an ongoing comprehensive investigation into the long-term durability of pultruded E-glass/vinylester composites. MATERIALS AND TEST DETAILS Unidirectional composites were pultruded in 1.6 mm thick strips using Hybon 2001 Eglass rovings of 23 m/kN (112 linear yards/lb) yield with a Dow Derakane 441-400 vinylester having a viscosity of 400 cps at 23°G and a styrene content of 33% by weight. Fiber loading, assessed through burn-off procedures, was determined to be approximately 62%. All specimens were preconditioned at 23°C and 46% relative humidity prior to initiation of the test program. In order to adequately assess changes in characteristics of the composite as well as mechanisms of degradation as a result of water sorption, the material was subjected to mechanical testing through tension (ASTM D3039) and short-beam-shear (ASTM D2344) modes. Dynamic mechanical thermal analysis (DMTA) was conducted at a frequency of 1 hz between 25°C and 200°C. Inductively coupled plasma (ICP) analysis was also conducted on solutions in which the material was immersed in order to assess leachate elements, and fourier transform infrared (FTIR) spectroscopy was used to assess changes in the polymer itself. Moisture uptake was assessed through gravimetric means and both optical and scanning electron microscopy (SEM) were used to study degradation. Composite and neat resin specimens, as appropriate, were immersed in deionized water at 23°, 40°, 60°, 80°C for periods of time up to 75 weeks, hi addition specimens were also stored at 23°C and 46% relative humidity RH, taken to be representative of ambient, "unexposed" conditions. In order to assess reversibility of moisture sorption effects, selected tests were also conducted on specimens that were reconditioned at 23°C and 46% RH for 28 days (equal to the original period of conditioning) after removal from the immersion environments. RESULTS AND DISCUSSION Mass uptake in the specimens immersed in deionized water showed Fickian response with rates of uptake and moisture content increasing with temperature of water. Overall uptake results in terms of maximum percentage weight gain over the period of time of investigation and diffusion coefficients are listed in Table I. TABLE I Characteristics of Moisture Kinetics Temperature Of Deionized Water (°C) 23 40 60 80
Neat Resin Maximum Coefficient of Moisture Uptake Diffusion (Wt. %) (xlO"7 mm2/s) 6.25 0.64 10.00 0.93 1.26 15.31 1.40 24.31
Composite Maximum Coefficient of Moisture Uptake Diffusion (Wt. %) (xl0"7mm2/s) 0.164 1.39 0.529 2.17 0.569 2.70 0.623 3.14
From theoretical considerations the maximum uptake can in the composite be determined to be 0.139%, 0.203%, 0.275% and 0.305%, at 23°C, 40°C, 60°C and 80°C, respectively. It is noted that at temperatures higher than 23°C the experimentally
Degradation of E-Glass/Vinylester Composites
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determined values of maximum moisture uptake are higher than the theoretical ones. This is due to the activation of damage at the interface and bulk resin level resulting in additional uptake due to wicking along debonds and microcracks which results in additional flow and storage of water. Figure 1 shows paths at the interface due to debonding and initiation of fiber pitting and degradation through cracking can be seen in Figure 2 due to longer term immersion at the higher temperature levels.
FIGURE 1 Interface Debonding
FIGURE 2 Fiber Pitting and Cracking
A progression of change in tensile strength as a function of time and temperature of immersion is shown in Figure 3 from which it can clearly be seen that the level of degradation increases substantially with increase in temperature of the aqueous medium. At the end of 75 weeks, levels of retention are noted as 65.22%, 51.45%, 37.43% and 28.22% for the 23°C, 40°C, 60°C and 80°C cases, respectively. It is also noted that there is a relatively large loss in the first 5-10 weeks most of which is recovered on drying and is due to effects of matrix plasticization as a result of moisture uptake. Pitting seen on the fiber surface (Figure 2) is due to loss of K2O and Na2O from the fiber by dissolution and is corroborated by the ICP results. In a large number of applications, composites are unlikely to remain in a saturated condition due to loss of sorbed moisture with changes in the surrounding environment and it is thus not only of interest to compare changes in tensile strength prior to, and after reconditioning, but also to assess the level of regain due to "drying out" during reconditioning.
23 c
0
10
20
30
40
50
60
70
Time (Weeks)
FIGURE 3 Change in Tensile Strength
80
0
10
20
30 40 50 Time (Weeks)
60
70
FIGURE 4 Effect of Reconditioning
Figure 4 provides a comparison of level of percentage regain [4] due to reconditioning and it is seen that at almost all time periods percentage regain decreases with increase in the temperature of the deionized water emphasizing the increasing effect of temperature
Degradation of E-Glass/Vinylester Composites
172
(and by analogy of extended periods of exposure) on the level of irreversible change and damage. It can also be seen that percentage regain in each case reaches a minimum value and then increases again at the time corresponding to when degradation at the interface takes place resulting in additional wicking. Since the tests are conducted on unidirectional composites the effect of interfacial degradation is not as large as it would be in an off-axis case. Short-beam-shear (SBS) tests are often used to assess interlaminar shear strength and to compare the relative effects of environmental exposure As can be seen in Figure 5 there are significant losses in short-beam-shear strength as a function of time and temperature of immersion. While the reduction in SBS strength with time of immersion is almost linear at 23°C, it follows a stepped approach at 40°C, and the more commonly observed curve having a rapid initial decrease followed by a retardation is noted at 60°C and 80°C. The 23°C results are indicative of an almost pure interlaminar failure wherein changes in strength are dependent on interfacial mechanisms only [5] without substantial physical/mechanical degradation of the matrix. The step seen in the 40°C case is indicative of damage, primarily irreversible, occurring at the interfacial level in the form of fiber-matrix debonding, and osmotic cracking at the interface, resulting in enhanced moisture sorption due to wicking. This form of damage is irreversible, and this is clearly seen in comparing the results of SBS strength of samples tested after reconditioning (redryhig at 23°C and 46% RH for 28 days) wherein an identical stepped response is seen. Beyond this level changes to the material are not merely associated with plasticization and debonding, but also to resin hydrolysis and microcrack coalescence to form macro-transverse cracks. The latter also serve as a mechanism for enhanced wicking of moisture along the fiber. Fiber pitting and some longitudinal cracking is also seen as a result of the higher temperatures and longer periods of immersion, similar to the phenomena reported in [6-8].
-—I
-
23 C, after reconditioning
10
• - - - - 40 C
- - • - 80 C
40 C, after reconditioning
0
10
60 C
- * — 60 C, after reconditioning
20
30
40
"M— 8 0 C, after reconditioning
50
60
70
80
Time (W eeks)
FIGURE 5 Change in SBS Strength as a Function of Immersion Temperature and Time
Since the diffusion data for the 4 temperature levels provides a linear fit to the Arrhenius equation, in the form ,gri(D) = £n(DJ-Eil/(RT) it can reasonably be assumed, for purposes offirst-orderapproximation, that the material follows the same mechanisms of degradation thereby allowing for use of a time-temperature based acceleration procedure initially proposed in Litherland et al [9] and Proctor et al [10] wherein the results of plotting the logarithm of time to attain a set of levels of normalized performance versus 1000/T (where T is temperature in degrees Kelvin) can be used to predict service life at a given temperature (normally taken as the ambient, or serious
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Degradation of E-Glass/Vinylester Composites
temperature) based on performance at higher temperatures. Using data from tests conducted on specimens immersed at 40°, 60° and 80°C predictions can be made for property retention as a function of time for the 23°C case for both tensile strength and short-beam-shear-strength and it is seen that the predictions compare well with experimental results till the 75 week level providing some level of assurance of accuracy. It can be noted that at the end of the 50 year prediction period the specimens immersed in water show 31.15% and 47.05% retention in tensile strength in the "wet" and "dry" cases, respectively, whereas the retention in. SBS strength is 62.42% and 74.37%, respectively. Water uptake by vinylesters and their composites is known to cause plasticization in the short-term and hydrolysis over the long-term through attack of the ester linkages. Both these phenomena induce higher levels of molecular mobility resulting in consequent decreases in the glass transition temperature, Tg, although the decrease can often be offset through residual cure of the vinylester itself in the aqueous solution. These competing phenomena result in fluctuations in the glass transition temperature as a function of period of exposure as shown in Figure 6. It is noted that the highest values of Tg, after initiation of immersion, are measured at the 10-15 week period, which coincides with the point at which the storage modulus shows a decrease after an initially significant increase. A significant increase in E is generally indicative of progression of cure with a decrease being representative of hydrolysis and plasticization dominating effects. The progression of hydrolysis was confirmed at a preliminary level through infrared spectroscopy wherein a decrease in the ester band intensity was noted with a change in peaks at about 1452 cm"1, which had been earlier noted by Ghorbel and Valentin [11] at 1450 cm"1 in their study on glass fiber reinforced vinylesters.
0
10
20
30
40
50
60
70
80
Time (weeks)
FIGURE 6 Effect on Glass Transition Temperature
0
10
20
30
40
50
60
70
80
Time (Weeks)
FIGURE 7 Effect on Crosslink Density
A study of Figure 6 shows further that the higher temperatures of immersion result in an overall lower level of decline in glass transition temperatures from the unexposed control (decreases of 8%, 8.3%, 4.9% and 5.7%, determined from values in °K are seen at the 75 week level at 23°C, 40°, 60°C and 80°C, respectively). This is due to increased leaching of hydrolyzed low molecular weight flexibilizing segments of the matrix at the higher temperatures which leads to network embrittlement, followed by further degradation through chain scission, while at lower temperatures this effect is not dominant. It is noted that the free hydroxyl groups are known to cause autocatalyzation of hydrolysis of ester groups in the bulk resin as well leading to a reduction in crosslink density which is also seen by a visible change in color of the composite specimens. As can be seen in Figure 7 the normalized average intercrosslink molecular weight shows a
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Degradation of E-Glass/Vinylester Composites
level of correlation to Tg in that it decreases with Tg. However, it is noted that the glass transition temperature is also affected by leaching and thus there is some variation at the higher temperatures of immersion over longer time periods. SUMMARY Although fiber reinforced polymer matrix composites show good durability as compared to conventional materials used in the marine, offshore and civil infrastructures areas, there is at present a lack of a comprehensive understanding of their response over long time periods. It is seen that due to specifics of the resin and fiber systems, as well as the progression of cure realized by the processes favored, deterioration mechanisms can be fairly different from those observed in prepreg based composites. The simultaneous sorption of moisture and slow progression of cure results in a competition between mechanisms that requires an indepth understanding of moisture kinetics and changes in the polymer system as a function of exposure type and time period. ACKNOWLEDGEMENTS The support of the California Department of Transportation is gratefully acknowledged. REFERENCES 1.
Apicella, A., C. Migliaresi, L. Nicolais, L. Iaccarino, and S. Roccotelli 1983. "The Water Aging of Unsaturated Polyester-Based Composites: Influence of Resin Composite Structure," Composites, 14 [4]:. 387-392. 2. Karbhari, V.M. and S. Zhang 2002. "E-Glass/Vinylester Composites in Aqueous Environments - I: Experimental Results," Applied Composite Materials, 34[1]: 19-48. 3. Apicella, A., C. Migliaesi, L. Nicodemo, L. Nicolais, L. Iaccarino, and S. Roccotelli 1982. "Water Sorption and Mechanical Properties of a Glass-Reinforced Polyester Resin," Composites, 13: 406-410. 4. Chu, W. and V.M. Karbhari 2003. "Effect of Water Sorption on Performance of Pultruded EGlass/Vinylester Composites," submitted to ASCE Journal of Materials in Civil Engineering. 5. Gautier, L., B. Mortaigne, and V. Bellenger. 1999. "Interface Damage Study of Hydrothermally Aged Glass-Fibre-Reinforced Polyester Composites," Composites Science and Technology, 59: 2329-2337. 6. Ishai, O. 1975. "Environmental Effects of Deformation, Strength and Degradation of Unidirectional Glass-Fiber Reinforced Plastics. I. Surveyr," Polymer Engineering and Science, 15 [7]: 486-499. 7. Ehrenstein, G.W. and R. Spaude 1984. "A Study of the Corrosive Resistance of Glass Fiber Resin Polymers," Composite Structures, 2: 191-200. 8. Karbhari, V.M. 2004. "E-Glass/Vinylester Composites in Aqueous Environments: Effects on SBS Strength," ASCE Journal ofComposites for Construction in press. 9. Litherland, K.L., D.R. Oakley, and B.A. Proctor 1981. "The Use of Accelerated Ageing Procedures to Predict the Long-Term Strength of GRC Composites," Cement and Concrete Research, 11: 455-466. 10. Proctor, B.A., D.R. Oakley, and K.L. Litherland 1982. "Developments in the Assessment and Performance of GRC Over 10 Years," Composites, 13 [2], pp. 73. 11. Ghorbel, I. and D. Valentin, D. 1993. "Hydrothermal Effects on the Physico-Chemical Properties of Pure and Glass-Fiber Reinforced Polyester and Vinylester Resins," Polymer Composites, 14 [4]: 324334.
High Value Composites from Recycled Polyolefins and Rubbers Alexander Fainleib*, Olga Grigoryeva, Alexander Tolstov, Olga Starostenko Institute of Macromolecular Chemistry of the National Academy of Sciences of Ukraine, Kharkivske shose 48, 02160 Kyiv, Ukraine
ABSTRACT The novel technology for producing high value thermoplastic dynamic vulcanizates (TDVs) from recycled polyolefins and ground tire rubber (GTR) has been developed. The producing high performance composites of tensile properties on the level of TDVs based on virgin components is assured by using ethylene-propylene-diene monomer rubber (EPDM) as a rubber compatibilizer, bitumen as a devulcanizing agent for GTR as well as plasticizing and compatibilizing agent for TDV components.
INTRODUCTION Polymer blends are an important class of engineering materials, as they exhibit synergetic effects due to their comprising useful properties. However most of them (for example - polyolefm/rubber) consist of incompatible components, i.e. they show a limited mutual solubility and often high interfacial tension [1]. As a result properties of such systems are poor [2-5]. Solving the problem of poor interfacial adhesion and use the post-consumer polyolefins and ground tire rubber (GTR) instead of virgin components could bring up such a material to a commercially leading position due to a favorable cost-performance [6-9]. In this study we have tried to solve the problem of poor properties of GTRcontaining TDVs. The only way to improve the properties is a development of a fine structure through increasing an interfacial adhesion between the TDV components. For this purpose we have sequentially applied a new technology of GTR surface activation by thermal-mechanical-chemical devulcanization and reactive compatibilization of the components through dynamic co-vulcanization of pre-devulcanized GTR with EPDM and unsaturated components of bitumen inside thermoplastic (polyolefin) matrix. EXPERIMENTAL Two methods of melt blending of recycled polyolefins HDPER, LDPER or PPR with EPDM as a fresh rubber and ground tyre rubber (GTR) were developed using Brabender plasticorder or extruder. First method includes blending of GTR with bitumen, mastication of GTR/bitumen blend with recycled thermoplastics (HDPER, LDPER or PPR) and EPDM in Brabender plasticorder and (optional) rolling of the * Correspondence Author, Institute of Macromolecular Chemistry of the National Academy of Sciences of Ukraine, Kharkivske shose 48, 02160 Kyiv, Ukraine, fax: (380)445524064, e-mail: fainleib(S>,i.kiev.ua
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High Value Composites from Recycled Polyolefins and Rubbers
blend after mastication. In all cases, polyolefin (HDPER, LDPER or PPR) was melted first for 2 min, then EPDM was added and melted for 2 min before the addition of the GTR/bitumen composition, and final mixing was continued for a further 10 min. Second method consists of blending of GTR with bitumen, extrusion of GTR/bitumen blend at 135/145/155 °C, mixing of extrudate with recycled thermoplastics (HDPER, LDPER or PPR) and EPDM in extruder at 155/165/175 °C, followed by granulation and second run in extruder. A GTR fraction with a particle size of 0.4 to 0.7 mm was kindly provided by Scanrub AS (Viborg, Danmark). The EPDM containing rubber (Buna® EP G 6470 of Bayer) with 71 wt.% ethylene and 4.5 wt.% ethylidene norbornen contents was used. The bitumen used was a BN-4 grade according to the State Standard SS 6617-76. The influence of heating and rolling GTR/bitumen blends on degree of GTR devulcanization have been studied by sol-gel analysis in o-xylene. For the rheological measurements disks of TDVs with diameter 32 mm and thickness 0.7 mm were pressed on a hydraulic press at temperature of 180°C. The shear viscosity of TDVs under study was measured with PIRS-03 rheometer with a cone-plane working unit. The shear rate (7) and shear stress (7) were calculated from the equations: y = 6.28 n /tan a , T = 3M l2nR\ where n is the cone rotation frequency, a is the cone angle, Mis the torque, R is the cone radius. The cone with R=0.02 m and a=0.035 radian was used. RESULTS AND DISCUSSION Sol-gel Analysis The gel-fraction content for different compositions is shown in Table I. Comparison of gel-fraction content for GTR and GTR/bitumen pre-heated and rolled blends shows that heating at 170°C for 4 hours leads to decreasing the gel-fraction content and the additional rolling pre-heated blends for 40 minutes increases the difference in the gel-fraction content between initial GTR and treated GTR or GTR/bitumen blends (AX=XGT«-Xlreated) providing the further devulcanization. It was concluded that the bitumen plays a role of softening and devulcanizing agent, which conduces a process of breaking sulphur bridges at high temperature, then extracts part of sulphur released and next is covulcanized (by extracted and own sulphur) with devulcanized GTR during reclaimed GTR revulcanization. Table I The gel-fraction content for TDV and components used Composition
Bitumen GTR GTR GTR/bitumen (1/1) GTR/bitumen (1/1)
Treatment conditions no no heating heating heating + rolling
Gel-fraction content (per GTR), X{%\
[%]
0 86.5 78.2 73.6 73.0
0 0 8.3 12.9 13.5
Thermal Stability Thermal stability of the TDV samples prepared in Brabender plasticorder was studied by TGA method. It is shown (see Figures 1-3) that the introduction of GTR to
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basic TDV decreases a thermal oxidative destruction in TDVs based on polyethylenes and completely suppresses it in TDV based on PP. Simultaneously the stages of intensive and high temperature decompositions shift to higher temperatures and a char residue increases. The best thermal stability is observed for TDVs containing GTR/bitumen component. The stage of thermal oxidative destruction at 150-250°C characterized for basic TDV is completely suppressed for all TDVs containing GTR/bitumen component independently of type of the recycled thermoplastics used. Am, %
Am x" , % min" o *
HDPE n EPDM HDPE :EPDM:GTR
0
HDPE < :EPDM:GTR/bitumen
-20 -
\
-40 -60 -80
-
l\
-
V
-100 1
i
,
i
I
400
.
I
,
I
600 o Temperature, C
200
200 400 600 o Temperature, C Temperature, C FIGURE 1. Thermograms of TDVs based on HDPER. 200
600
400
Am, %
Am x , % min LDPE :EPDM o
LDPE K :EPDM:GTR
»
LDPE R :EPDM:GTR/bitumen
if
0
w
-20 -40
1
-60 -80
-0,
^
-
u ll
-
ll
-100 200 400 600 o Temperature, C
-1,0
i
200
,
400
1
1
600
o Temperature, C
I
200
1
I
400
>
I
600
Temperature, C
FIGURE 2. Thermograms of TPVs based on LDPER.
200 400 600 o Temperature, C
200 400 600 o Temperature, C
FIGURE 3. Thermograms of TPVs based on PPR.
200 400 600 o Temperature, C
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Rheological Properties Rheological characteristics, i.e. the logarithmic dependencies of shear stress (7) and the apparent viscosity (rj) on the shear rate (7), of the TDV samples prepared in Brabender Plasticorder are shown in Figure 4. As one can see from the Figure 4 (b), the considerable decrease of the apparent viscosity (17) of HDPER based TDVs with GTR/bitumen component in comparison with the basic TDVs takes place. An increase of rj with rise of temperature in the range of the low shear rate (7) (see Figure 4, b) for HDPER/EPDM based TDV may be connected with additional cross-link of samples at the temperature of the measurement. At increase of a shear rate the locations of flow curves change in such manner as if they rotate around a hinge "secured" in the region of log 7= 0.132 and log T = 7-104. The prominent decrease of "apparent viscosity" of TDVs in the range of the high shear rate (see Figure 4, f) probably is connected with a slip of samples relatively surface of a cone and plane. Note that the samples of LDPER/EPDM basic blend and all TDVs with GTR (without bitumen) were impossible to load into the working unit of a rheometer because of their very high viscosity (>105 Pa-s). The high viscosity of LDPE/EPDM basic blend is perhaps explained by partial crosslinking during TDV preparation. It should be concluded here that the TDVs containing GTR treated with bitumen could be easy reprocessed by injection molding, pressing and extrusion. HDPE -based TDVs :
a)
LDPE -based TDVs
c)
FIGURE 4. Rheological properties of TDVs: open symbols - recycled polyolefin/EPDM based TDVs; solid symbols - recycled polyolefiri/EPDM/(GTR/biturneri) based TDVs.
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Tensile Properties and Chemical Resistance The tensile strength of different TDVs prepared are shown in Figure 5. One can see that introducing GTR into TDV decrease tensile properties drastically (especially for HDPER). However, using GTR modified with bitumen allows us to produce TDVs with tensile properties on the level of basic ones and even higher (for LDPER). From the analysis of data presented in Figures 5 one can conclude that such an improvement of tensile properties of GTR/bitumen-containing TDVs is a result of both the better compatibility of HDPER (LDPER) with EPDM rubber, as well as a significant effect of bitumen as a universal devulcanizing, plasticizing and compatibilizing agent. Some properties of few TDV samples obtained in extruder have been measured and are presented in Table 2. As can be clearly seen from the Table 2 the sample HDPER /EPDM/(GTR/bitumen)=40/35/25(l/l) is characterized by complex of properties required for TDVs.
• • TS, MPa EB,
15
900
r
600 CO LU CO 300
f
1
FIGURE 5. Tensile properties for TDVs studied, wt.%: LDPER/EPDM/(GTR/bitumen) = 40/60/(0/0) (1), 40/35/(25/0) (2), 40/35/(12,5/12,5) (3); HDPER/EPDM/(GTR/bitumen) = 40/60/(0/0) (4), 40/35/(25/0) (5) and 40/35/(12,5/12,5) (6).
Table II Characteristics for TDVs obtained by extrusion method HDPER/EPDM/ TS EB (GTR/bitumen) [MPa] [%]
50/25/25(1/1) 60/20/20(1/1) 40/35/25(1/1) 40/20/40(1/1) 40/0/60(1/1) b c
Hardness Frost[Shore A] resistance,
95 8.1 42 12.6 32 83 6.2 400 82 5.9 57 89 3.8 15 84 d- the temperature of destruction. Standard range of the values: 0-^45%. Standard range of the values: -30 - 20%.
Chemical resistance
Petrol", ;20% NaOH", 20% HC1C, Oil, id 1 Vl AV [ %] AM [ %] AM [ %] AM [ %] -39 -36 -41 -34 >0
63 42 115 48
22.5 13.7 37.8 20.2 0.6
-2.6 -2.7 -3.5 -3.1 -3.4
-3.3 -3.1 -3.5 -3.4 -3.4
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High Value Composites from Recycled Polyolefins and Rubbers
CONCLUSIONS The high value high performance composites from polyolefin and rubber waste have been developed. This is provided by using EPDM as a rubber compatibilizer, bitumen as a devulcanizing agent for GTR, as well as plasticizing and compatibilizing agent for TDV components and technology of dynamic vulcanization. ACKNOWLEDGEMENT The work was fulfilled under the financial support of EU (INCO-Copernicus contract No.: ICA2-CT-2001-10003 and STCU Agreement No.: 3009). REFERENCES 1. Karger-Kocsis, J. 1999. "Thermoplastic rubbers via dynamic vulcanization," in Polymer Blends and Alloys, G.O. Shonaike and G.P Simon, eds. New York: Marcel Dekker, pp. 125-153. 2. Y. Li, Y. Zhang and Y.X. Zhang. 2003. "Structure and Mechanical Properties of SRP/HDPE/POE (EPR or EPDM) composites," Polym. Test, 22:859-865. 3. Y. Li, Y. Zhang and Y.X. Hnsn%. 2003. "Morphology and Mechanical Properties of HDPE/SRP/elastomer composites: Effect of Elastomer Polarity," Polym. Test, 23:83-90. 4. Fainleib, O. Grigoryeva, O. Starostenko, I. Danilenko and L. Bardash. 2003. "Reactive Compatibilization of Recycled Low Density Polyethylene/Butadiene Rubber Blends During Dynamic Vulcanization," Macromol. Symp., 202:117-126. 5. O. Grigoryeva, A. Fainleib, O. Starostenko, A. Tolstov and W. Brostow. 2003. "Thermoplastic Elastomers from Rubber and Recycled Polyethylene. Structure and Property Enhancement through Chemical Reactions in Interphase," Polym. International, accepted for publication. 6. F. Cavalieri, F. Padella and F. Cataldo. 2003. "Mechanochemical Surface Activation of Ground Tire Rubber by Solid-State Devulcanization and Grafting," J. Appl. Polym. Sci., 90:1631-1638. 7. O. Grigoryeva, A. Fainleib, O. Starostenko, I. Danilenko, N. Kozak and G. Dudarenko. 2003. "Ground Tyre Rubber (GTR) Reclamation. Virgin Rubber / Reclaimed GTR (Re)vulcanizates," Rubber Chem. Tech., accepted for publication. 8. S. Rudheshkumar, I. Fuhrmann and J. Karger-Kocsis. 2002. "LDPE-Based Thermoplastic Elastomers Containing Ground Tire Rubber with and without Dynamic Curing;" Polym. Degr. Stab., 76:137-144. 9. O. Grigoryeva, A. Fainleib, O. Starostenko and A. Tolstov. 2003. "Structure-Property Relationships for Reactively Compatibilized Thermoplastic Elastomers from Recycled Polyolefins and Rubbers," Nonlinear Optics. Quantum Optics, accepted for publication.
Viscoelastic Behaviour, Thermal Properties and Morphology for New Composites from Recycled HDPE, EPDM, Ground Tyre Rubber (GTR) and Bitumen Olga Grigoryeva*, Alexander Tolstov, Olga Starostenko, Alexander Fainleib Institute of Macromolecular Chemistry of the National Academy of Sciences of Ukraine, Kharkivske shose 48, 02160 Kyiv, Ukraine Emilio Lievana, J. Karger-Kocsis Institut fur Verbundwerkstoffe GmbH (Institute for Composite Materials), University of Kaiserslautern, POBox 3049, D-67653 Kaiserslautern, Germany,
ABSTRACT Structure-property relationships for new composites prepared from recycled HDPE, EPDM, ground tyre rubber (GTR) and bitumen have been studied by a combination of DMTA, DSC and SEM techniques and tensile tests. The better mechanical performance determined for a composition containing a preheated and rolled mixture of GTR and bitumen have been explained by a better mixing of the components and formation of the essential interface layer due to the reclaiming (for GTR) and compatibilizing (for composite) role of the bitumen.
INTRODUCTION Thermoplastic elastomers (TPEs), especially blends of elastomer and thermoplastic obtained by dynamic vulcanization of rubber in thermoplastic and having characteristics of elastomers while maintaining the thermoplasticity [1] attract a great interest of scientists and producers. High value composites can be produced by a replacement of virgin components of TPEs (fully or partly) by recycled polymers. Obtaining materials of beneficial properties is not easy task due to very poor compatibility of the components. To be reactively compatibilized (it seems to be most effective method) the components (at least their surface) of high value composites including GTR should be activated by thermal, thermal-mechanical, thermal-chemical and other methods [2,3] and additional compatibilizers should be used [3-5]. In our previous works we have compared [6] behaviour of virgin and recycled polyethylenes (low and high density polyethylenes, LDPER and HDPER, respectively) in basic and compatibilized [7] composite formulations and combined [8-11] the methods of GTR devulcanization and the following reactive compatibilization of a reclaimed GTR with other components.
* Correspondence Author, Institute of Macromolecular Chemistry of the National Academy of Sciences of Ukraine, Kharkivske shose 48, 02160 Kyiv, Ukraine, fax:(380)445524064, e-mail: fainleib(a>.i.kiev.ua
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New Composites from Recycled HDPE, EPDM, GTR and Bitumen
hi this study the reactively compatibilized high value composites based on recycled HDPE (HDPER), EPDM and partially devulcanized GTR were prepared. A new modifier, bitumen, contributing to GTR devulcanization and further compatibilization of all the composite components have been utilized. The structure-property relationships were investigated using DSC, DMTA and SEM techniques. EXPERIMENTAL Recycled high-density polyethylene (HDPER) from post-consumer bottle transportation crates collected in Kyiv (Ukraine) was used, the HDPER melt flow index (MF1) was: MFIm/2.i6 = 2.13 g/10 min. GTR fraction with a particle size of 0.4 to 0.7 mm was kindly provided by Scanrub AS (Viborg, Danmark). Ethylene/propylene/diene monomer (EPDM) containing rubber (Buna® EP G 6470 of Bayer) was used. The EPDM rubber with 71 wt % of ethylene and 4.5 wt % of ethylidene norbornen contents, respectively, had a Mooney viscosity, ML(l+4) 125°C, 59. Bitumen used was a BN-4 grade according to the State Standard SS 6617-76. HDPER and EPDM were used as received. GTR was used as received and in some TPE formulations it was mixed with bitumen (1/1 by weight) and the mixture was preheated at 170°C for 4 hours and further rolled for 40 min prior to introducing to TPE recipes. In all cases, the mastication of composition by Brabender Plasticorder was carried out at 160°C and 80 rpm for 15 min. The viscoelastic behaviour of the resulting TPEs was investigated using a DMTA device (Eplexor 150N of Gabo Qualimeter, Ahlden, Germany). Rectangular sheets having a dimension of 6x1x0.25 cnw were subjected to oscillating tensile loading. The testing temperature ranged from -105°C to 150°C selecting a heating rate of 3°C/min. Differential scanning calorimetric studies were carried out using a DuPont thermal analyzer model 910. The scans were taken in the temperature range from -100°C to 200°C with a programmed heating rate of 20°C/min. Melting temperature (7m) corresponding to the maximum in fusion endotherm, was noted. Tensile tests were performed on dumbbell specimens at ambient temperature at a crosshead speed of 100 mm/min using Instron-1122 type universal testing machine. The average data for 6-7 specimens were taken for consideration. The parameters such as tensile strength at break (75) and elongation at break (EB) were determined. The fracture surface of the specimens was inspected by using a scanning electron microscope JSM-5400 of Jeol (Tokyo, Japan). RESULTS AND DISCUSSION Dynamic Mechanical Thermal Analysis (DMTA) It was found that the damping behaviour (i.e., the character of E'=f(T) dependencies) of all of the blends studied is quite similar to HDPER and it is typical for thermoplastic compositions. We infer that in all the blends HDPER forms continuous thermoplastic phase (matrix) while crosslinked rubber components (EPDM, reclaimed GTR) form a dispersed phase. The Tg values of the TPEs and the individual components as well as the corresponding E" values at Tg are listed in Table I. HDPER/EPDM blend produced by the mastication in Brabender plasticorder exhibits the transition at -31°C (Tg2) as a result of overlapping Tg's of amorphous phases of EPDM (Tg2) and HDPER (Tg3), while a second transition at 68°C (7^) is characteristic for HDPER. Shifting the first
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183
lower Tg2 on 5°C towards higher temperature compared to (Tg2) of individual EPDM evidences of mixing amorphous phases of EPDM and HDPER. The damping behaviour of HDPER/EPDM/GTR TPE is characterized by appearance of new relaxation transition at -50°C (Tgi) characteristic for introduced GTR and by shifting other Tg's peaks towards lower temperatures. This, along with the lower values of storage moduli (E1) and higher values of E" at Tg evidences of significant growth of chain flexibility of the components, especially in rubber rich phases. It can be caused mainly by disordering the matrix due to dispersion of GTR crosslinked particles. The latter is confirmed by a significant growth of E" values (from ~ 20 up to 90 MPa) in the temperature region below Tgi. Table I DMTA data for individual components and TPEs Sample code
-
Composition [wt%]
Tg[°C] for Phases Rich in: GTR EPDM HDPEK Tg2
-
-
EPDM
-
-36
-
-
-
-31
-
68
-
134
-50
-42
54
160
150
Bl
HDPE /EPDM = 61.5/38.5*
B2
HDPE R /EPDM/GTR** = 4 0 / 2 5 / 3 5 R
Tg4
h, -
Tgi
HDPER
R
Tgi
E" Value at Tgl [MPal
4 5 6 0
h2
-
h3
ioo~
-
30
102
42 121 158 HDPE /EPDM/(GTR/bitumen)** = -49 -35 40/25/17.5/17.5 B4 HDPE R /EPDM/(GTR/bitumen)*** = -48 -33 53 63 110 40/25/17.5/17.5 * ratio of HDPER/ EPDM=61.5/38.5 wt % is equal to 40/25 wt % in the ternary blends; ** the TPE was obtained by mastication in Brabender Plasticorder; *** the TPE was obtained by preheating of GTR/bitumen blend followed by its rolling and then by mastication in Brabender Plasticorder. B3
h4
65
21 35
41
As for the damping behaviour of HDPER/EPDM/ (GTR/bitumen) TPEs one can see a shift of Tgi and 7b towards higher temperatures compared to the recipes without bitumen. This, along with decreasing E" values in the temperature region below TgJ} as well as increasing E' values in the region above Tgi transition, evidences of increasing crosslinking degree of the blends. It can be explained by the dynamic vulcanization of dispersed rubbers inside plastic HDPER matrix, confirming the role of bitumen as a curing agent for the rubbers. In addition, it was found that the B4 TPE is characterized by significant decrease of segmental motion onset (onset of Tgi) from -65°C to -75°C that means improving GTR chain flexibility, obviously due to bitumen induced degradation of GTR followed by (re)covulcanization of devulcanized GTR, EPDM and bitumen. Differential Scanning Calorimetry (DSC) DSC curves for individual polymers and TPEs produced are shown in Figure 1. First off all, both EPDM and FTDPER show a melting of their crystallites in the blends, i.e. have both amorphous and crystalline phases. Second, some depression of the melting temperature (7m) values for both EPDM and HDPER in the blends is observed in comparison to the individual polymers depending on the composition and processing conditions used (cf. Table II). The maximal reduction of Tm reaches ~5°C for EPDM and
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New Composites from Recycled HDPE, EPDM, GTR and Bitumen
~6°C for HDPER for HDPER/EPDM/GTR/bitumen TPEs. It may be caused by formation of crystallites having a smaller size or by increasing unsoundness of crystallites formed. For HDPER matrix of the TPEs a significant shift of onset of melting temperature, Tmonset, towards higher temperature and narrowing a temperature interval of crystallites melting, ATm, is observed in comparison to individual HDPER. We suppose that the growth of Tmomet from 37°C (for individual HDPER) up to 70-75°C (for HDPER as a component in blend) observed can be caused by a disappearance of smaller less perfect crystallites involved into the amorphous phase. The narrowing the melting interval, ATm, for HDPER crystallites from 123°C (for individual polymer) up to 85°C (in HDPER/EPDM blends), and further to 71-76°C (for GTR-containing TPEs) testifies of decrease of dispersion of dimensions of HDPER crystallites in the blends. a)
EPDM
HDPE -100
-50
50
100
150
200
b) EM
B3
B2 B1
-100
-50
50 Temperature,
1 00
150
200
C
FIGURE 1. DSC traces for: (a) individual EPDM, HDPER and bitumen (indicated in the plot); (b) TPEs produced (the codes of the curves correspond to the compositions in the Table I).
New Composites from Recycled HDPE, EPDM, GTR and Bitumen
185
Table II DSC data and tensile properties of TPEs Sample code
Composition
7m
ATm = Tme:nd " Tmonset
[°iC]
[°C] EPDM HDPE K
EPDM HDPE K Bl B2 B3 B4
HDPEK EPDM HDPE R /EPDM HDPE R /EPDM/GTR HDPE R / EPDM / (GTR/bitumen) HDPE R / EPDM / (GTR/bitumen)
47 45 45 42 45
136 135 132 130 133
37 43 21 35 26
123 85 76 72 71
TS [MPa]
EB [%]
17.7 11.2
10 820 750 40 65 300
11.6 3.9 4.0 6.3
Scanning Electronic Microscopy (SEM) Figure 2 depicts SEM photomicrographs taken from the cut surface of the sheets of GTR-based TPEs listed in Tables I and H One can clearly see that GTR particles directly dispersed in HDPER/EPDM blend (sample B2) are very poorly bonded to the matrix and a lot of large and small strip breakages are observed. The GTR particles debond from the matrix indicating for lacking interaction between them and, as a result, the sample exhibits low tensile properties (cf. Table II).
FIGURE 2. SEM photomicrographs of surfaces for the TPE samples produced (the codes of the curves correspond to the compositions in the Tables I and II).
A better bonding between GTR particles and matrix is observed for the formulations produced by using bitumen (sample B3) and especially for TPE produced with GTR/bitumen preheating, rolling and further mastication by Brabender plasticorder (sample B4). It can be seen that surface of the last sample of TPE looks very homogeneous and there are no visible strip breakages that is a result of better bonding between GTR particles and thermoplastic matrix via formation of an improved interface layer. Understandably, the TPE sample (sample B4) exhibits high tensile properties (cf. Table II). CONCLUSIONS Thermoplastic elastomers containing recycled HDPER and GTR have been prepared by using technology of dynamic vulcanization and reactive compatibilization. Structureproperty relationships for TPEs produced have been investigated and the effectiveness of producing methods used has been compared. A significant improvement of both TS and EB values has been achieved for HDPER/EPDM/GTR/bitumen TPEs produced with preheating and rolling of GTR/bitumen before mastication of the formulation by
186
New Composites from Recycled HDPE, EPDM, GTR and Bitumen
Brabender plasticorder. The comparative analysis of DMTA, DSC and SEM experimental results has shown that significant improvement of tensile properties achieved in comparison to TPEs containing unmodified GTR is a result of the effect of bitumen as a suitable reclaiming agent for GTR, and further as a compatibilizer for GTR/bitumen containing TPEs. ACKNOWLEDGEMENT The work was fulfilled under the financial support of EU (INCO-Copernicus contract No.: ICA2-CT-2001-10003 and STCU Agreement No.: 3009). REFERENCES 1.
Karger-Kocsis, J. 1999. "Thermoplastic rubbers via dynamic vulcanization," in Polymer Blends and Alloys, G.O. Shonaike and G.P Simon, eds. New York: Marcel Dekker, pp. 125-153. 2. F. Cavalieri, F. Padella and F. Cataldo. 2003. "Mechanochemical Surface Activation of Ground Tire Rubber by Solid-State Devulcanization and Grafting," J. Appl. Polym. Sci., 90:1631-1638. 3. O. Grigoryeva, A. Fainleib, O. Starostenko, I. Danilenko, N. Kozak and G. Dudarenko. 2003. "Ground Tyre Rubber (GTR) Reclamation. Virgin Rubber / Reclaimed GTR (Re)vulcanizates," Rubber Chem. Tech., accepted for publication. 4. Y. Li, Y. Zhang and Y.X. Zhang. 2003. "Structure and Mechanical Properties of SRP/HDPE/POE (EPR or EPDM) composites," Polym. Test, 22:859-865. 5. Y. 'Li, Y. Zhang and Y.X. Zhang. 2003. "Morphology and Mechanical Properties of HDPE/SRP/elastomer composites: Effect of Elastomer Polarity," Polym. Test, 23:83-90. 6. O. Grigoryeva, A. Fainleib, O. Starostenko, A. Tolstov and W. Brostow. 2003. "Thermoplastic Elastomers from Rubber and Recycled Polyethylene. Structure and Property Enhancement through Chemical Reactions in Interphase," Polym. International, accepted for publication. 7. Fainleib, O. Grigoryeva, O. Starostenko, I. Danilenko and L. Bardash. 2003. "Reactive Compatibilization of Recycled Low Density Polyethylene/Butadiene Rubber Blends During Dynamic Vulcanization," Macromol. Symp., 202:117-126. 8. S. Rudheshkumar and J. Karger-Kocsis. 2002. "," Plastics, Rubber and Composites, 31:1-. 9. S. Rudheshkumar, I. Fuhrmann and J. Karger-Kocsis. 2002. "LDPE-Based Thermoplastic Elastomers Containing Ground Tire Rubber with and without Dynamic Curing;" Polym. Degr. Stab., 76:137-144. 10. O. Grigoryeva, A. Fainleib, O. Starostenko and A. Tolstov. 2003. "Structure-Property Relationships for Reactively Compatibilized Thermoplastic Elastomers from Recycled Polyolefins and Rubbers," Nonlinear Optics. Quantum Optics, accepted for publication. 11. A. Fainleib, O. Grigoryeva, A. Tolstov and O. Starostenko. 2003. "Reactively Compatibilized Recycled LDPE / Ground Tire Rubber Thermoplastic Elastomers," Macromol. Symp., submitted for publication.
Effect of Coupled Long-Term Seawater Exposure and BiAxial Creep Loading (2:1) on Durability of Fiber-Reinforced Polymer-Matrix Composites Xiaohong Chen, Emrah Gokdag and Su Su Wang* Composites Engineering & Applications Center (CEAC) and Department of Mechanical Engineering, University of Houston, Houston, TX 77204-0931, USA
ABSTRACT Lightweight, high-strength fiber-reinforced polymer-matrix composites have attracted increasingly interests in their use for offshore operations. It is well known that long-term environmental attack and mechanical loading may cause microstructural damage and property degradation. The composite property degradation during long-term multi-axial loading in seawater has been a major concern because offshore structural systems are designed on the basis of either their stiffness or strength. Advanced composite systems must be capable of withstanding severe environments and still maintain their structural integrity in the designed life, hi this paper, the effect of coupled long-term seawater exposure and bi-axial loading (2:1) on durability of advanced fiber composites is investigated. Accelerated bi-axial creep experiments have been conducted on carbon fiber/epoxy and glass fiber/epoxy composites in seawater. Critical material degradation and life prediction models are developed for the composite systems. With the aid of SEM observations, damage mechanisms and failure modes in the composites subject to combined long-term seawater exposure and bi-axial creep loading have also been identified. More general loading cases and their effects are reported elsewhere due to space limitation.
INTRODUCTION Lightweight, high-strength advanced fiber composites have attracted significant interests in their applications to offshore exploration and production (E & P) operations. Coupled long-term offshore environmental exposure and mechanical loading are expected to cause microstructural damage and composite property degradation. Understanding the effect of coupled long-term seawater exposure and bi-axial creep loading on durability of fiber-reinforced polymer-matrix composites is of vital importance for long-term safe and reliable applications of advanced fiber composites for offshore operations. A significant amount of research [1-6] has been reported on moisture, water or saltwater diffusion in neat epoxy resins and their fiber composites in a stress-free state. Since diffusion in a fiber composite depends on the fiber direction, the amount and properties of matrix resin, filler phase and the fiber/matrix interface, more complex behavior is expected than that in a monolith epoxy resin. It is also recognized that an * Corresponding author, CEAC, University of Houston, Houston, TX 77204-0931, USA, 1-713-743-5063, [email protected].
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Durability of Fiber-Reinforced Polymer-Matrix Composites
external stress affects diffusivity in a neat resin [7, 8]. Nevertheless, little is known about the effect of a multi-axial stress state on diffusion in the composites. Severe degradation in mechanical properties, such as tensile strength, has been observed in epoxies and their composites when exposed to water [9, 10]. Matrixdominant properties such as transverse and shear strengths have been noted to degrade with moisture or water exposure, while fiber-dominated properties such as longitudinal strength is little affected except in glass/epoxy composite where fibers are known to degrade in water [11]. The fiber/matrix interface has been recognized to be a weak link and is a subject of many studies [12-15]. The bond strength is found to decrease with immersion time and its failure modes change with immersion time also. A wet environment significantly affects long-term composite creep behavior, especially for the transverse loading cases [16]. Creep rupture time is found to decrease with increasing temperature and moisture, hi fact, creep rupture occurs within a few hours in a glass/epoxy even at a low load when temperature and moisture content are high. Hale et al [17-19] have conducted three-point bending creep tests, and also uniaxial and bi-axial tensile tests, on E-glass fiber composite pipe with winding angles of + 55° after its elevated-temperature water exposure till saturation. The biaxial tensile failure envelopes have been given in terms of hoop and axial stresses, which are not in principal material directions. Hence, it is difficult to extend to other loading cases. Moreover, the coupled effects of combined water exposure and mechanical loading have not been investigated. hi this research, accelerated biaxial creep experiments are performed on filamentwound carbon fiber/epoxy and glass fiber/epoxy tubular specimens with winding angles of ±88.5° in seawater at an elevated temperature. The effect of coupled long-term seawater exposure and bi-axial creep loading on property degradation and failure life is assessed, hi conjunction with the experimental results, critical material degradation and life prediction models are then developed for the offshore composites. EXPERIMENTS The material systems used in the study are E-glass/epoxy (PPG1062/Epon862 with Epicure W agent) and carbon/epoxy (Grafil 34-700/Epon 862-Epicure W), typical for offshore applications. The vast amount of research conducted at the CEAC over the past years has provided a database for composite properties in the dry state [20]. Filamentwound tubular specimens with winding angles of ±88.5° with respect to the tube axis were used. The seawater was prepared by mixing tap water and Instant Ocean (2.3% NaCl by weight) [15]. Two sets of experimental facilities were used, depending on hoop-to-axial stress ratios. For instance, for the hoop-to-axial stress ratio ahlaa = 2, specially designed grip fixtures were used together with fluid pumps to add pressure on the tubular composite specimens soaked in a seawater tank at a prescribed temperature [Fig.l(a)]. Such an experimental set up with specially designed grip fixtures was relatively simple without resorting to a complex loading frame. However, it had a limitation on the range of applied ah/aa. Experimental facilities for achieving any combination of axial loading and internal pressure are shown in Fig.l(b). A creep test frame was used for applying axial loading, while a pressure intensifier with an aluminum mandrel for applying internal pressure. Specially designed grips were used to mount the aluminum mandrel and the specimen soaked in a seawater gasket on the test machine.
Durability of Fiber-Reinforced Polymer-Matrix Composites
(a)
189
(b)
FIGURE 1 Biaxial creep-diffusion experimental facilities.
THEORETICAL CONSIDERATIONS For a polymer composite under combined seawater exposure and mechanical loading, its leakage failure life, tf, may be considered as result of a rate process with the time required to cause polymer matrix fracture. Thus, the commonly used kinetic fracture model [21] for polymers is modified with inclusion of both stresses and seawater absorption, i.e.,
tf
[
RT
where t0 is a reference time; R, the gas constant; T, the absolute temperature; and AH, the activation energy, depending on stresses {cr,} and seawater absorptionM. Taking the first-order expansion of AH, one has AH(ai,M) = AH0- aiVi - AM + H.O.T.(CT,.,M)
(2)
where AH0 is the stress- and absorption-free activation energy; V,, activation volumes; and A, the seawater-polymer affinity. Expressing the first-stage seawater diffusion with the Fickian law, one may obtain the following creep stress-sorption-life equation for the composite in seawater at a constant temperature Tsubject to proportional pressure and axial loading: ^f- = Ao + 4 \og(tf ) + A2JlJ where tf=tf/t0; strength.
(3)
At = ,4/(f0,.Ar,7T); K = <Jh/cra], and X2 is the transverse tensile
Durability of Fiber-Reinforced Polymer-Matrix Composites
190
RESULTS AND DISCUSSION Owing to the space limit, selected results are presented here on long-term failure behavior of carbon fiber/epoxy and glass fiber/epoxy composites subject to combined seawater exposure and biaxial creep loading (K=2). More general loading cases and their effects are reported in [22]. Based on the aforementioned kinetic failure equation, the creep stress-sorption-life relationships have been established for carbon fiber/epoxy and glass fiber/epoxy composites in the following two forms: (a) transverse stress versus logarithmic failure time; and (b) transverse stress versus square root failure time. In Figs.2(a) and (b), composite creep failure lives clearly follow the creep stresssorption-life equation for both composite systems in seawater under 2:1 biaxial loading at 70°C. Solid lines are determined from a regression analysis of experimental data. When a high load and/or a short-time seawater exposure is applied, composite failure is governed by the stress level, as seawater diffusion takes time to reach a critical level. On the other hand, long-term failure of the composites in seawater under a low load is affected by the amount of seawater absorption and the stresses. The relationship is clearly shown in the a221X2~^t7T^ graph [Fig.2(b)]. It is also noted that the glass fiber/epoxy composite degrades more rapidly than the carbon fiber/epoxy composite with the same amount of seawater exposure time and biaxial creep loading.
K=2
Carbon/Epoxy
\ A
X. AA
Glass/Epoxy \ ,
0
(a)
1
2
(Vto)"2
3
(b)
FIGURE 2 Failure lives of carbon/epoxy and glass/epoxy composites in seawater at 70oC subject to proportional biaxial creep loading at K=2. (a) Logarithmic time scale, (b) Square root time scale.
Durability of Fiber-Reinforced Polymer-Matrix Composites
(a)
191
(b)
FIGURE 3 Fracture surfaces of fiber composites in seawater at 70oC subject to proportional biaxial creep loading (K=2) for 30 days, (a) Carbon/epoxy composite (320 psi), (b) Glass/epoxy composite (248 psi).
SEM observations have also been conducted on fracture surfaces of carbon/epoxy and glass/epoxy composites subject to combined seawater exposure and biaxial loading at K=2 [Figs.3(a) and(b)]. The composite failure modes are found to involve fiber-matrix interface degradation besides matrix cracking, fn comparison with that of the carbon/epoxy composite, severe interface degradation is observed in the glass/epoxy composite due to coupled seawater exposure and biaxial loading at 70°C for about 30 days. The degradation of advanced fiber composites is clearly governed by the time of seawater exposure, and the bi-axial stress state and magnitude. Based on the experimental data and the stress-sorption-life equation, one may construct failure envelops (or map) for fiber composites subject to long-term loading with any stress biaxial ratio. With such a failure map, it becomes possible to estimate the service lives of advanced fiber composites in a seawater environment in given loading conditions. REFERENCES 1.
2.
3.
4. 5.
6. 7. 8. 9.
Loos, A.C. and Springer, G.S. 1981. "Moisture Absorption of Graphite-Epoxy Composition Immersed in Liquids and in Humid Air," Environmental Effects on Composite Materials, Vol. 1., G.S. Springer, ed. Technomic Publishing Company, Inc., Westport, CT, pp.34-50. Woo, M. S. and Piggot, M.R. 1987. "Water Absorption of Resins and Composites: II Diffusion in Carbon and Glass Reinforced Epoxies," ASTM Journal of Composites Technology & Research, 9, 162-166. Chateauminois, A., Vincent, L., Chabert, B., Soulier, I P . 1994. "Study of the Interfacial Degradation of a Glass-Epoxy Composite During Hygrothermal Aging Using Water Diffusion Measurements and Dynamic Mechanical Thermal Analysis," Polymer, 35,4766-4774. Schutte, C.L. 1994. "Environmental Durability of Glass-Fiber Composites", Material Science and Engineering, R13, 265-322. Tsotsis, T.K. and Weitsman, Y. 1994. "A Simple Graphical Method for Determining Diffusion Parameters for Two-Stage Sorption in Composites," Journal of Materials Science Letters, 13, 16351636. Zhou, J. and Lucas, P. 1996. "Effects of Water on a Graphite/Epoxy Composite," Journal of Thermoplastic Composite Materials, 9,316-322. Fahmy, A. A. and Hurt, J.C. 1980. "Stress Dependence of Water Diffusion in Epoxy Resin," Polymer Composites, 1, 77-80. Neumann, S. and Marom, G. 1987. "Prediction of Moisture Diffusion Parameters in Composite Materials under Stress," Journal of Composite Materials, 21, 68-80. Browning, C.E., Husman, G.E. and Whitney, J.M. 1977. "Moisture Effects in Epoxy/Matrix Composites", ASTMSTP 617,481-496.
192
Durability of Fiber-Reinforced Polymer-Matrix Composites
10. Long, E.R. 1979. "Moisture Diffusion Parameter Characteristics for Epoxy Composites and Neat Resins," NASA TP-1474. 11. Hogg, P J. and Hull, D. 1983. "Corrosion and Environmental Deterioration of GRP", in Developments in GRP technology-I, B. Harris, ed. Applied Science Publishers, pp. 37-90. 12. Carlsson, L.A. 1993. "Influence of Seawater on Transverse Tensile Properties of PMC," NIST Special Publication 887,203-211. 13. Wagner, H.D., Lustiger, A. and Lin, S. 1993. "Assessing the Glass Epoxy Interface after Environmental Exposure", NIST Special publication 887, 213-225. 14. Bradley, W.L. and Grant, T. S. 1995. "The Effect of the Moisture Absorption on the Interfacial Strength of Polymeric Matrix Composites," Journal of Materials Science, 30, 5537-5542. 15. Wood, C. A. and Bradley, W. L. 1997. "Determination of the Effect of Seawater on the Interfacial Strength of an Interlayer E-Glass/Graphite/Epoxy Composite by In Situ Observation of Transverse Cracking in an Environmental SEM," Composites Science and Technology, 57, 1033-1043. 16. Scott, D.W., Lai, J.S. and Zureick, A.H. 1995. "Creep Behavior of Fiber-Reinforced Polymeric Composites: A Review of the Technical Literature," Journal of Reinforced Plastics and Composites, 14, 588-6.17. 17. Hale, J.M., Gibson, A.G. and Speake, S.D. 1998. "Tensile Strength Testing of GRP Pipes at Elevated Temperatures in Aggressive Offshore Environments," Journal of Composite Materials, 32 (10), 969987. 18. Hale, J.M., Gibson, A.G. and Speake, S.D. 2002. "Biaxial Failure Envelope and Creep Testing of Fibre Reinforced Plastic Pipes in High Temperature Aqueous Environments," Journal of Composite Materials, 36 (3), 257-270. 19. Hale, J.M., Shaw, B.A., Speake, S.D., Gibson, A.G. 2002. "High Temperature Failure Envelopes for Thermosetting Composite Pipes in Water," Plastics, Rubber, and Composites, 29 (10), 539-548. 20. Wang, S.S. and Srinivasan, S. 1996. "Long-Term Leakage Failure of Filament-Wound Fiberglass Composite Laminate Tubing under Combined Internal Pressure and Axial Loading," Technical Report CEAC-TR-96-0101, CEAC, University of Houston, Houston, TX, USA. 21. Hertzberg, R. W. 1989. Deformation and Fracture Mechanics of Engineering Materials, 3rd edition, John Wiley & Sons, Inc., New York. 22. Wang, S.S., Chen, X. H. andGogdak, E. 2003. "Coupled Long-Term Multi-Axial Creep and Diffusion in Advanced Fiber Composites in Saltwater Environment," Technical Report CEAC-TR-02-0102, CEAC, University of Houston, Houston, TX, USA.
Part III
Composite Structures
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Deformation Analysis of Kinematically Constrained Thermoplastic Composite Plates in Forming Temperature Hamid Reza Daghyani*, Mohammad Tahaye Abadi and Shahriar Fariborz Faculty of Mechanical Eng., Amirkabir University of Technology, Tehran, Iran
ABSTRACT A finite element (FE) formulation is developed to analyze the sheet forming process of multiply thermoplastic laminates reinforced with unidirectional continuous fibers. Each ply is analyzed using the plate theory considering the applied tractions over the ply surfaces as well as the kinematical constrains of matrix incompressibility and fiber inextensibility. The inter-ply shear deformation mechanism is modeled as a viscose film between plies that couples the deformation of plies. In order to avoid penetration of each ply into each other and into the tool surface, the Lagrange multipliers are defined in contact surfaces. The results of FE analysis are compared to the analytical and experimental outcomes.
INTRODUCTION Thermo forming is the most effective method in mass production of reinforced thermoplastic finished parts. High viscosity of thermoplastic materials in forming temperature and kinematical constrains of continuous fibers cause to consider some special requirements in order to produce defect free parts. Due to high expenses of the experimental investigations for production of high quality finished parts, a sheet forming model is needed to analyze the optimum conditions of geometry and loading parameters for production process. In previous research works two models were presented [1]: the kinematical model and the continuum mechanical model. In the kinematical model, the reinforced ply is mapped over the tool surface considering viscose matrix incompressibility, fiber inextensibility and fixed fiber distance constrains. The assumption of fixed fiber distance during forming process yields to incompatible results with experimental observations [2]. In the continuum mechanical models, the process is analyzed by defining a constitutive equation and solving equilibrium and continuity equations with respect to the kinematical constrains and boundary conditions. The later model gives stress states and deformation analysis of forming process during forming process while the first model gives kinematical results only in the fmial shape. Due to the difficulty of analytical solution in a continuum model, Bradaigh and Pipes [3] derived FE formulations and Bradaigh et al. [4, 5] solved them for plane stress and plane strain conditions without considering the ply interactions. Johnson and Pickett [6] derived shell formulations for deformation analysis of theroplastic plates ignoring out of plane stress and transverse shear strains. In our recent work [7], a FE formulation * Corresponding Author, Faculty of Mech. Eng., Amirkabir Uni. Of Tech. Tehran, 15914, Iran, Fax+98 21 6419736, e-mail: [email protected]
196
Kinematically Constrained Thermoplastic Composite Plates
was derived using the plate theory to analyze the deformation of a thermoplastic composite ply considering transverse intra-ply shear mechanism and applied surface tractions. In the present work, a FE formulation is developed to analyse the deformation and stress states during the sheet forming of multiply thermoplastic laminates reinforced with unidirectional continuous fibers. PLATE FORMULATION For the analysis of deformation state in composite laminates, it is most effective to describe the deformation of each thin ply in term of the deformation of its middle surface. The experimental observations show that the intra-ply shear strain causes the initial normal transverse plate to be rotated respect to the middle surface. Hence, The Kirchhoff hypothesis yields to the invalid results for sheet forming analysis of reinforced thermoplastic plies in forming temperature. Therefore, the velocity component y in each point (xux2,x3) of ply is stated by means of the ReissnerMindlin approximation [7] as:
^ , , V 3 ) = yvoUvX2)+x3wHxuXi)
+~xi2w1(v2)
(lc)
where v,. is the velocity component of middle plane, . is the rate of transverse plate rotation, w0 is the normal velocity component of middle plane, w, is the rate of thickness change and w2 is the rate of middle plane movement in thickness direction. The second order approximation of velocity in thickness direction is used for considering thickness variation and satisfying kinematical constrains. KINEMATICAL CONSTRAINS Three major assumptions are defined for kinematical constrains as: incompressibility of viscose matrix which is satisfied if the trace of strain rate tensor sets to zero, inextensibility of fibers which is satisfied if the projection of strain rate tensor along the fiber direction sets to zero and impenetrability to avoid the penetration of adjacent plies into each other or into the tool surface during numerical forming analysis where the kinematical constrains are applied to contact surfaces. Assuming an external normal pressure, the plies have similar normal velocities at contact surfaces. It can be stated as: Vjl) =K(1+I) i = 0,....n+\ (2) where n is the number of plies, F3(l)(z=l,....w) is the normal velocity of z'th ply, F3<0),F3("+1)are the normal velocities of lower and upper tool surfaces, respectively, (x1,x2,h/2)is a point on upper surface of zth ply and (x-l,x2,-h/2)is the corresponding point on lower surface of (/' +1) th ply.
Kinematically Constrained Thermoplastic Composite Plates
197
POTENTIAL FUNCTION The total potential function (PF) n is the sum of internal PF [/'„'', the external PFt/^J and the terms of kinematical constrains Uj£ considered with Lagrange multipliers for all layers [7]: ;=i
1=1
The internal PF can be calculated assuming the behavior of ply as an ideal fiber reinforced fluid (IFRF) [7].The external PF is given by: (0
„ (<)\
c+Wa
\
(4)
. (0 where W c is the contact work done by traction in lower and upper surfaces and °
(0
Wa is the work done by traction in the edge of i' ply. The contact work is due to the slip of adjacent plies relative each other or tool surface in resin rich film. If the resin rich layer in forming temperature behaves as Newtonian viscose fluid, the traction applied to the upper and lower surfaces can be stated as:
L
>~ V ( w»% w < V ' v> V l w,-*% w < ' V 0=1,2)
(5) where r\ is the resin shear viscosity and 8 is the resin rich layer thickness. Thus, the contact work can be written as:
(6) that Q(l) is the surface of ith ply. The work done in the edge of all plies can be given by:
-y2 (7) where tm,tnl and t are the normal, tangential and transverse tractions, respectively. The potential function due to previous defined constrains can be written as:
^ - t [ |»« Q
A
(8) where, T{>) ,p(i) and /l(Oare Lagrange multipliers, d^n is the component of strain rate tensor and a^is the component of unit vector in fiber direction of r'th layer. Integrating Eq. (8) over thickness yields: .n<"
(9)
198
Kinematically Constrained Thermoplastic Composite Plates
FINITE ELEMENT FORMULATION The FE formulations are derived by minimizing the potential function respect to the velocity functions defined in Eq. (1) and Lagrange multipliers. The velocity in each element of ith layer can be written in term of nodal values as: V(i)=Naf Using Eq. (1),N
(10)
anda(v()
can be stated in term of the velocity shape function Nv and '' as follows: the nodal values of velocity functions v .'\( a.. =
TV =
(11)
Nv
0
0
X}NV
0
Nv
0
0
0
0
Nu
0
0
0
( 12 )
0 0
Lagrange multipliers in each element of i' layer is stated in term of the nodal values as: T (0 = Nj.T(0 , P ( O s N p P ( O , A ' ^ N ^ 1 0 (13) Using shape function^, the terms in Eq. (13) can be defined as: 0
T<')lr •'l
Nr=N;>
J '
p(0 _ [p(
(14)
"I'll
_ IX o
~ [ o NL
Employing Eqs. (10) and (11), the PF in the whole plies can be written as follows: (15)
The matrices K ^ K ^ a n d K^were defined in our previous work [7] and for the sake of shortage, they are not brought here. The other matrices are defined as:
(16c)
-L
(16d)
where, G is defined as: 1 0 0" 0 1 0 0 0 0 The potential function must be minimized respect to the nodal values:
(17)
Kinematically Constrained Thermoplastic Composite Plates dU = 0. Sa!k> that yields to:
an Saf
C«)a«k) + 2C <
K ( T k) V v k) =0.
= 0.
k +1) ( k+ ) a v "
K« T a c v k ) =0.
an 3a
an
= 0.
199 (18)
= 0.
(k)
+ K =
«
•
(19) RESULTS AND DISSCUSSIONS During the sheet forming process of reinforced laminates, the fiber direction and thickness of each ply may be locally changed. Hence, a time dependent incremental analysis is processed to solve the equations. A software is developed to analyze the laminate deformed geometry, fiber directions, thickness, velocity, strain and stress in the whole elements. The meshes are generated using Q9/4/4/4 elements with nine points biquadratic shape functions for velocity and four Gaussian points bilinear shape functions for Lagrange multipliers. As an example, the pull out test used normally in experimental analysis to assess the shear properties of sheet forming process, is analyzed. As shown in Figure 1, a rigid plate that stacked in the middle of several plies is pulled out while compressed by two rigid plates. Hull et al. [8] proposed an analytical solution for such a problem by ignoring the normal pressure and Murtagh et al. [9] investigated it experimentally. This problem is analyzed using developed FE formulation for a Peek-Carbon fiber laminate with a longitudinal shear viscosity rjL = 6000Pa.s, transverse shear viscosity r/T = 4000Pa.s and the ratio of shear viscosity to thickness r//S = 2.2xlO7 Pa.s/m in resin-rich film. Because of symmetry only the upper plies are analyzed. Consider the normal velocity of upper and lower rigid plate is zero and the middle plate is pulled out with velocity of Vo .The velocity change in a two-ply laminate is calculated that is correlated well with the analytical solution as shown in Figure 2. Due to different fiber directions in
Fixed plate
FIGURE 1 Pull out test.
— •
Analytical results Finite element results
FIGURE 2 Analytical [8] and finite element results of pull out test.
200
Kinematically Constrained Thermoplastic Composite Plates
two plies and resin rich layer in their interfaces, the slips are observed, which are shown by horizontal jumps at the ply interfaces (Figure 2). The required pulling force for different pulling velocities in a constant normal pressure of 400 kPa is compare to the experimental results [9] shown in Figure 3. The experimental pulling force changes nonlinearly that is due to nonlinear behavior of resin-rich layer. Since in derivation of FE formulation, a Newtonian viscose fluid
- + - finite element results O Experimanlal analysis [91
o
| i I »
behavior is assumed for the resin rich film, some deviation from experimental results is observed in Figure 3.
y °
if
° ,f 0.15 0.2 0.25 0.3 shear velocity (mm/s)
FIGURE 3 Required shear stress for pulling out of the middle plate in different velocities.
CONCLUSIONS A FE is developed using Reissner-Mindlin approximation for sheet forming analysis of multiplies laminates reinforced with unidirectional fibers. The Kinematical constrains defined in each ply and in the interfaces of plies are well satisfied with this approximation. This formulation can be used for analysis of intra-ply shear and interply slip mechanisms in forming temperature while in-plane and out-of-plane tractions applied to the laminate surfaces. REFERENCES 1. 2. 3. 4.
5.
6. 7.
8.
9.
Lim, T.C., Ramakrishna, S., 2002, "Modeling of Composite Sheet Forming: A Review", Composites Part A, 33, pp. 515-537. Tucker, C.L., "Sheet Forming of Composite Materials", 1997, Advanced Composites Manufacturing, Editor: T.G. Gutowski, John Wiley, New York. CM. 6 Bradaigh and R.B. Pipes, 1991, "Finite Element Analysis of Composite Sheet-Forming Processes", Composites Manufacturing, Vol.2, Nos. 3 & 4, pp. 164-170. C. M. 6 Bradaigh, G.B. McGuinness and S.P. McEntee, 1997, "Implicit Finite Element Modeling of Composites Sheet Forming Processes", Composite Sheet Material, Composite Material Series, Vol.11, editor D.Bhattacharyya, Elsevier Pub.. S.P.McEntee and 6 Bradaigh, CM., 1998, "Large Deformation Finite Element Modeling of Single-Curvature Composite Sheet Forming With Tool Contact", Composites Manufacturing, 6, pp. 269-280. Johnson AF and Pickett AK, 1996, "Numerical simulation of the forming process in long fiber reinforced thermoplastic", CADCOMP '96, Udine, Italy. H. R. Daghyani, M. Tahaye Abadi and Sh. Fariborz, 2003, "Finite Element Analysis of Thermoplastic Composite Plates in Forming Temperature", submitted to Journal of Composite Materials. B.D.Hull, T.G.Rogers and AJ.M.Spencer, 1994, "Theoretical Analysis of Forming Flows of Continuous-fiber-Resin Systems", Flow and Rheology in Polymer Composite Manufacturing, Composite Materials Series, Vol. 10, editor S, G, Advani, Elsevier Pub. A.M. Murtagh and P.J. Mallon, 1997, "Characterizations of Shearing and Frictional Behavior during Sheet Forming", Composite Sheet Material, Composite Material Series, Vol.11, editor D.Bhattacharyya, Elsevier Pub.
Stability Analysis of Loaded Columns Made of Pultruded Composites Enayat Mahajerin* Saginaw Valley State University, U.S.A.
ABSTRACT In Pultrusion, a single reinforcement or a collection of reinforcements, saturated with a reactive resin, is pulled through a heated die that imparts a desired final geometry to the profile. Generally, the cross section of the profile is constant but it can be of arbitrary shape. These products have become very popular because they can be made to exhibit features found in components produced by other processes. In this paper, a method based on the combination of theoretical and numerical methods is developed to investigate effects of pertinent variables including geometric parameters, reinforcement types, and volume fractions of the constituents on the strength and stability of such composites. The energy method is used to establish the buckling criterion which leads to a two-dimensional, orthotropic partial differential equation (pde), for determination of the warping function. A numerical approach based on the Fundamental Collocation Method (FCM) is used for determination of the warping function. Consequently, the buckling criterion can be established, the eigenvalues of which are related to the critical buckling loads.
INTRODUCTION Recently, attention has been shifted, and toward manufacturing of pultruded composites because of their interesting characteristics including high strength-toweight ratios. Additionally, pultrusion can utilize a variety of fibers and produce complex thin or thick-walled shapes such as solid and hollow bars. The majority of pultruded components employ /^er-g/aM-reinforced polyester resins. Because of orthotropic physical and mechanical properties, and the arbitrary-shaped nature of the cross section, investigation of stability under applied loads requires a numerical method. Here, an approach based on the combination of the energy method and FCM is described.
FORMULATION We consider a general column made of a pultruded composite (Figure 1). The cross- section, R, lies in the x-y plane, and the normal, n, to the boundary, MR, makes an angle 0 (ccw) with the horizontal axis. The ends are at z=0 and z=L, and the column is subjected to an axial compression load P. Observations show that * Corresponding author, Professor of Mechanical Engineering, Saginaw Valley State University, University Center, MI 48710 USA. Phone:(989)964-4188, E-mail: mahaieri(a)/svsu.edu
202
Loaded Columns Made of Pultruded Composites
buckling of thin-walled columns often accompany twisting. A common theory that accounts for the combined effects of bending and twisting is to minimize the second variation of the strain energy, U, i.e., 8(82U )=0. Following the process for isotropic materials [1, 2], we extend the theory for orthotropic materials, and also integrate FCM in the formulation. Because 8 U is a second order, homogeneous quadratic function, it is written as (1) where q's are the amplitudes of displacements u, v, and w, in the x, y, and z directions, respectively. It can be shown that 8(82U)=0 leads to the following eigenvalue problem or the buckling criterion: an an au Det ai\ an an = 0
(2)
an O32 O33
in which 1
A T
-U1
flll = Ez
[lyy - (
I
e
—
(3)
an = Ez — - Le2 [Lx - (—^—
(4)
L
(5)
EzTI
(6)
= Ez
(7)
3 = a3i = Ez
(8)
= \\y dA
lyy =
\\X
dA
(9)
(10)
Loaded Columns Made of Pultruded Composites
203 (li)
(12)
dx
yf+Gzy{
+ xfdA
dy
l
dA
(14)
dA
(15)
= jjxw dA
(16)
where w(x,y) is the warping function of the Saint Venant torsion theory [3], s is the axial strain, and Le is the effective length of the column [4]. It can be shown that,
dx dn
=0,
dy
x,ysR
(17)
- xsm£>, x,yedR
(18)
Once (17) and (18) are solved for w(x,y), elements of the buckling criterion (2) can be determined from (3)-(8). The eigenvalues of (2) represent three principal strains, the smallest of which corresponds to the critical buckling load. For a special case in which Ixy=0, and the region R is symmetrical about the x- and y-axes, the buckling criterion becomes 011022033=0
(19)
This equation is satisfied if an=0, a22=0or a33=0, corresponding to: A
Flexural buckling in the x-direction: Flexural buckling in the y-direction:
.
JT Iyy
an = 0, i.e., £=—— t
a22 = v, i.e., e-
2
(20)
T
lxx
Ah a
Torsional buckling:
^ 3 = 0 , i.e., &r = — ( — S \ + — S i ) lp
Lz
(22)
Le
Using Hooke's law, s=a/E, (20) arid (21) lead to Euler's formulas for the flexural buckling, whereas (22) gives the critical strain causing torsional buckling.
204
Loaded Columns Made of Pultruded Composites
Infinite Plane
Q
W O
/
*
\
*
1
/
*
_/ o ft
R Xv^—_--~*"'""^ ^-^ •
o
FIGURE 1 Geometry
o
*
Field Points
•
Boundary Points
0
Source Points
FIGURE 2 Numerical Setup
NUMERICAL PROCEDURE Determination of the buckling criterion requires w(x,y) because parameters Si, S2, S3, and S4 are functions of w(x,y) and its derivatives. In the FCM process, the cross section, R, is imagined to be embedded inside an infinite plane of the same material where a series of point loads of initially unknown strengths, ck, is applied at source points (Xk,Yk), k=l,2,..,N. Normally, the sources are located outside the boundary, MR, at a finite distance, s, away (Figure 2). At any internal field point (x,y) we can write [5],
(23)
(24)
(25)
— = — cos 9 + — sin 6 dn dx dy
(26)
where ¥(x,y; Xk,Yk) denotes the influence function of (17), which is the solution at (x,y) due to a unit point load applied at the source point (Xk,Yk), and is given in [6],
Loaded Columns Made of Pultruded Composites
205
(27)
The weights, Ck, k=l,..,N, are the point load strengths, and can be adjusted via collocation so that the specified boundary conditions are satisfied at N boundary points, (Xj,yj), j=l,2,..,N. The procedure leads to a system of N simultaneous linear equations of the form
Kc=f
(28)
where K (kjj) is the NxN influence matrix, c is a column containing the unknown source strengths, and column f contains the prescribed boundary conditions. The system of equations (28) can be solved via Gaussian elimination for the weights, Ck, k=l,2,...,N. The computed weights can be inserted in (23)-(28) to find the warping function and its derivatives at any internal (field) point. Once w(x,y) and its derivatives are determined, the elements ay, i=l,..,N; j=l,...,N, of the buckling criterion (2), the eigenvalues, and consequently, the critical buckling loads can be determined.
EXAMPLES A series of pin-ended, axially loaded, "L-shaped" columns, 0.2- inch thick, made of composites with known properties (Table 1), with variable lengths and the "flange-to-web " aspect ratios, b/h, was analyzed. The critical buckling loads were computed using N=18 boundary points. Sources were distributed on a congruent boundary at a distance s (b<s
No.
Exx
GZy
Gzx
G2y
A
4166
2602
5105
1081
935
896
B
1991
1991
8105
810
810
711
C
3810
1564
5233
711
634
583
D
1462
611
2545
398
341
341
E
yy
CONCLUSIONS A suitable combination of the analytical and numerical methods for solving stability of pultruded composite columns has been presented. The method may be regarded as an efficient and straightforward tool for solving flexural-torsional buckling in any thin or thick composite column in which the cross section shape remains constant. Such characteristics are associated with bars made via pultrusion.
Loaded Columns Made of Pultruded Composites
206
I Oil
Hi)
14*
htt FIGURE 3 Critical load vs. L
Itt
02
«.3
0.4
(i.$
ft*
a?
OS
<
toft
FIGURE 4 Critical load vs. b/h
REFERENCES 1. Langhaar, H. L., Energy Methods in Applied Mechanics, J. Wiley, 1962. 2. Kappus, R. "Twisting Failure of Centrally Loaded Open-Section Columns in the Elastic Range," NACATM851, 1938. 3. Timoshenko, S. P. and Goodier, J. N., Theory of Elasticity, McGraw-Hill, 1970. 4. Gere, J. M. and Timoshenko, S. P., Mechanics of Materials, PWS, 1997. 5. Burgess, G. and Mahajerin, E., On the Numerical Solution of Laplace's Equation, International J. ofMech. Eng. Ed., vol. 13, no. 1, 45-54, 1985. 6. Kythe, P. K.. , "An Introduction to Boundary Element Method, "CRC, 1995. 7. Lekhnitskii, S. G., Theory of Elasticity of an Anisotropic Body, Mir Publishers, 1981.
Identification of Elastic Parameters for Cross-ply Laminated Plates and Shells Kenji Hosokawa* Faculty of Engineering, Chubu University, Japan Kin'ya Matsumoto Faculty of Education, Mie University, Japan
ABSTRACT An inverse analysis method has already been proposed by one of the authors to identify elastic parameters of laminated composite materials using the FEM eigenvalue analysis and the nonlinear optimization method. The purpose of this study is to apply the proposed method to a laminated square plate and a laminated shallow cylindrical shell made of the same composite material. The identified elastic parameters for the lamina of the plate were compared, and found to agree well, with that for the lamina of the shell.
INTRODUCTION Since composite materials such as fiber reinforced plastics (FRP) have high specific strength and high specific modulus, they have been used in many structural applications. It is therefore very important to make clear the dynamical properties of the laminated composites for the design and the structural analysis. Especially, elastic parameters are essential for the structural analysis. The elastic parameters of laminated composite materials, however, are difficult to determine by either theoretical or experimental approaches because of their anisotropy. On the other hand, one of the authors has already proposed an inverse analysis method to identify the elastic parameters for laminated composite materials using the FEM eigenvalue analysis and the sensitivity analysis [1], [2]. It is an advantage of this method that one can obtain nondestructively the elastic parameters of the products made of composite materials. Also, the authors applied the proposed inverse analysis method to a symmetrically and an antisymmetrically laminated square plate [3]. Furthermore, the inverse analysis method was applied to a laminated circular cylindrical shell [4]. From the comparison of these identified elastic parameters of the lamina and ones obtained by another experimental method, one can see the good agreements. However, in respect to the identification of elastic parameters, we can find few reports of the simultaneously identified elastic parameters for the laminated plates and shells made of the same composite material. For the above reason, in this paper, the proposed method is applied to a cross-ply laminated square plate and a cross-ply laminated shallow cylindrical shell. Naturally, the laminae of the plate and shell are made of the same prepreg sheets. The proposed method mainly consists of the FEM eigenvalue analysis and the nonlinear optimization method * Corresponding Author, Dept. of Mech. Eng., Chubu University, 1200 Matsumotocho, Kasugai, Aichi, 487-8501, Japan, fax:+81-568-51-1194, email:[email protected]
208
Elastic Parameters for Cross-ply Laminated Plates and Shells
considering the relation between elastic parameters and naturalfrequenciesas a nonlinear system. Firstly, by applying the experimental modal analysis technique to the cross-ply laminated square plate and shallow cylindrical shell, naturalfrequenciesand mode shapes are obtained. Secondly, from the obtained natural frequencies and mode shapes, the elastic parameters of the lamina are identified. Finally, in order to confirm the identified elastic parameters, it is shown that the estimated natural frequencies and mode shapes of the test pieces by using these identified elastic parameters. IDENTIFICATION METHOD The proposed identification method mainly consists of the FEM eigenvalue analysis and the nonlinear optimization method considering the relation between elastic parameters and naturalfrequenciesas a nonlinear system. Since the identification method was described in detail in Ref. [4], in the present paper, only an outline will be presented. Figure 1 shows the flow chart of the identification program. Firstly, the data about the geometrical configuration, initial material properties of the test piece, and natural frequencies measured by excitation test are given. Secondly, to calculate the natural frequencies and mode shapes, the eigenvalue analysis is carried out using the initial parameters. Next, the error function g(x) is estimated by the difference of the natural frequencies obtained by the eigenvalue analysis and the experiment, hi this phase, since the order of the natural modes may be replaced by the ratio of the elastic moduli of
START
)
Input of initial data Calculation of natural frequencies Calculation of error function Calculation of Jacobian matrix
g(x) J(x)
Improving the Hessian matrix H by SSR formulation or BFGS method Solving the equation Hd = —J (x)g(x) the Incomplete Cholesky method
by
Determination of step size by line searcher
Calculation of error function
g(x) No
FIGURE 1 Flow chart of identification
Elastic Parameters for Cross-ply Laminated Plates and Shells
209
anisotropic materials, the order of the natural modes is investigated by MAC (Modal Assurance Criterion). After that, elastic parameters are identified by the quasi-Newton method. Finally, if the calculated natural frequencies are converged into the experimental ones, the identification program is terminated. IDENTIFICATION OF ELASTIC PARAMETERS To identify the elastic parameters for the lamina of the laminated square plate and shallow cylindrical shell, experimental studies were carried out. As shown in Fig. 2, the configuration of the shallow cylindrical shell is a square planform (a=b=0.2[m\). The shell's thickness h is 1.60x10 [m]. The inside radius R of the shell is 0.4[m]. The density and the stacking sequence of the cross-ply laminated shallow cylindrical shell are 1557 [kg/m3] a n d [ 0 V 9 0 o 2 / 9 0 V 0 o 2 ] , respectively. The stacking sequence of the cross-ply laminated square plate is the same that of the laminated shallow cylindrical shell. The density of the laminated plate is 1549 [kg/m3]. The dimensions of the plate are of 0.2[m] long and 0.2[m] wide. The inside radius R of the plate is °°. The thickness of the laminated square plate is 1.59x10" [m]. Each layer material is graphite/epoxy. The laminae of these test pieces are made of the same prepreg sheets. Therefore, the elastic moduli for the laminae of the square plate and shallow cylindrical shell are due to have few differences. Natural Frequency and Mode Shape To satisfy the free boundary conditions, each test piece was hung from the ceiling by a
FIGURE 2 Laminated shallow cylindrical shell
Accelerometer Test piece impulse force hammer
FIGURE 3 Measurement of natural frequencies and mode shapes by experimental modal analysis technique
Elastic Parameters for Cross-ply Laminated Plates and Shells
210
fine string. The plate was divided into 7x7 points and 49 dividing points were used as reference points. Also, the shell was divided into 9x9points and 81 dividing points were used. To measure the transfer function (accelerance), an accelerometer was attached to one of the reference points and then all reference points were impacted by an impulse force hammer (See Fig. 3). The mass of the accelerometer is 0.48 [g]. From the obtained transfer function, the natural frequencies and mode shapes of the test pieces were estimated by applying the experimental modal analysis technique. Figure 4 shows the experimentally obtained natural frequencies and mode shapes of the each test piece. In this paper, for the mode shapes of the laminated shell, upper and lower edges are the curved edges. Identified Elastic Parameters From the experimental natural frequencies and mode shapes shown in Fig. 4, the elastic parameters for the lamina of the laminated square plate and shallow cylindrical shell were estimated by the proposed inverse analysis method. The computations were carried out using the FEM eigenvalue program with triangular shell elements. Each test piece is divided into 800 elements with 441 nodal points. In the numerical calculations, the mass of the accelerometer was not considered because the mass of the accelerometer is very small. The identified elastic parameters of the lamina are shown in Table 1. In Table 1, the elastic moduli EL, ET in the direction of the parallel and normal to the fiber and shear modus GLT are shown. Poisson's ratio vLT is assumed to be 0.32. From this table, one can find the good agreements between the identified elastic parameters for the lamina of the cross-ply laminated square plate and that of the cross-ply laminated shallow cylindrical shell. The difference between the identified elastic parameters of the plate and that of the shell is about 6.3% at the most. To confirm the identified elastic parameters, the FEM eigenvalue analysis was carried out by using the identified results. For the computation of natural frequencies and mode shapes, the mass of accelerometer was neglected because of it is very small compared to the test pieces' mass. Figure 5 shows the natural frequencies and mode shapes of these test pieces estimated by the eigenvalue analysis. From Figure 4 and Figure 5, one can see that the difference between the experimental natural frequencies and the numerically calculated ones is about 0.7% at the most and one can find the excellent agreements between these mode shapes of the test pieces. Test piece
Modal order
Cross-ply laminated plate
Mode shape Natural frequency [Hz]
Cross-ply laminated shell
1st
2nd
3rd
4th
5th
71.64
153.7
210.4
324.3
355.5
68.39
151.8
205.8
420.7
469.7
5
Mode shape Natural frequency [Hz]
FIGURE 4 Experimental natural frequencies and mode shapes of test pieces
Elastic Parameters for Cross-ply Laminated Plates and Shells
211
TABLE I Identified elastic parameters of lamina
Test piece Cross-ply laminated plate Cross-ply laminated shell Test piece
Modal order
Cross-ply laminated plate
Mode shape Natural frequency [Hz]
Cross-ply laminated shell
[GPa]
ET [GPa]
G LT [GPa]
119
8.19
4.36
122
8.51
4.10
1st
2nd
3rd
4th
5th
71.57
153.4
211.2
326.0
353.2
68.40
151.9
205.8
420.7
469.1
Mode shape Natural frequency [Hz]
FIGURE 5 Numerical natural frequencies and mode shapes of test pieces
CONCLUSIONS The inverse analysis method to identify elastic parameters of the laminated composite materials was applied to the cross-ply laminated square plate and the cross-ply laminated shallow cylindrical shell. One can find the good agreements between the identified elastic parameters for the lamina of the cross-ply laminated square plate and that of the cross-ply laminated shallow cylindrical shell. Also, to confirm the identified elastic parameters, the FEM eigenvalue analysis was carried out by using the above mentioned ones. From the results, one can see the good agreements with respect to the natural frequencies and mode shapes. Accordingly, it follows that one can accurately estimate elastic parameters for the lamina of the laminated composite materials by using the inverse analysis method proposed by the authors. REFERENCES 1.
2.
3.
4.
Matsumoto, K., M. Zako, and M. Furuno. 1996. "Identification of Anisotropic Parameters for Hybrid Laminated Composites Using FEM Eigenvalue Analysis," Transactions of the Japan Society of Mechanical Engineers (in Japanese), 62(596): 1341-1346. Matsumoto, K., M. Zako, M. Furuno, and T. Fujita. 1997. "Inverse Problem to Identify Equivalent Elastic Parameters of Honeycomb Sandwich Panels," Transactions of the Japan Society of Mechanical Engineers (in Japanese), 63(611):2256-2261. Hosokawa, K., K. Matsumoto, and M. Zako. 1998. "Identification of Elastic Parameters for Laminated Composites Using FEM Eigenvalue Analysis (Comparison of Numerical and Experimental Results)," Fatigue, Environmental Factors, and New Materials (Proceedings of PVP Conference), PVP-374:325-329. Hosokawa, K. and K. Matsumoto. 2002. "Identification of Elastic Parameters for Laminated Circular Cylindrical Shells (Comparison of Numerical and Experimental Results)," JSME International Journal, Series C,45(l):26-31.
Parametric Instability Analysis and Experiment of Laminated Composite Shell Meng-Kao Yeh and Hung-Chang Huang Department of Power Mechanical Engineering National Tsing Hua University Hsinchu 30013 Taiwan R.O.C.
ABSTRACT The parametric instability of graphite/epoxy laminated composite shell was investigated analytically and experimentally. The dynamic system of the laminated composite shell was derived based on the finite element modeling and the Lagrange's equation. The normalized modal expansions of the composite shells were then applied to obtain a dynamic equation of Mathieu's type, which contains parametric excitation terms. In experiment an electromagnetic device, acting like a spring with alternating stiffness, was used to excite the laminated shell parametrically in the transverse direction. The instability regions of the composite shell were identified by the transition curves, which were functions of the modal parameters of the composite shell and the position, the stiffness of the electromagnetic device attached on the composite shell. The experimental results were found to agree well with the analytical ones. INTRODUCTION Structural instability has been an important factor for the failure of structures, hi Bazant's review paper [1], several structural failure examples were pointed out due to their instability behavior, such as the failure of Quebec bridge at St. Lawrence in 1907, the collapse of Tacoma Narrows Bridge due to aerodynamic resonance in 1940, and the failure of Hartford Arena space frame in 1978. Dynamic instability is one of the significant issues in the structural instability. Bolotin [2] summarized the parametrically excited instability problems for various structural elements. Researchers also investigated the parametrically excited instability problem of the basic structural elements, such as beams, columns, plates and shells for different material properties, different boundary conditions, and different excitation forces analytically. Composite materials, with high specific strength, high specific stiffness and the ability of variable lamination to have required mechanical property, becomes an competitive substitute for use in various aerospace structures. Like the traditional metal structures, the composite structure may become unstable due to external dynamic disturbances resulted from external resonance or parametrically excited resonance, caused by periodic forces. Chen and Yeh [3] investigated the parametric instability of a beam under electromagnetic excitation. Yeh and Kuo [4] studied the dynamic instability of composite beams under parametric excitation analytically and experimentally. Yeh et al. [5] reported the measurement of dynamic regions for structures under parametric Professor, the corresponding author; Department of Power Mechanical Engineering, National Tsing Hua University, Hsinchu 30013 Taiwan, R.O.C, Fax: 886-3-5726414, E-mail: [email protected]
Parametric Instability Analysis of Laminated Composite Shells
213
excitation. Ng et al. [6] studied the dynamic stability of cylindrical panels with transverse shear effects; they found larger instability regions occurred for thicker panels. Lam and Ng [7] analyzed the dynamic stability of laminated composite cylindrical shells subjected to conservative periodic axial loads. Ganapathi et al. [8] studied the dynamic instability of laminated composite curved panels using finite element method. Argento [9] investigated the dynamic stability of a composite circular cylindrical shell subjected to combined axial and torsional loading. Bert and Birman [10] studied the parametric instability of thick orthotropic circular cylindrical shells; they found the compressive load reduced the vibration frequencies. From the above-mentioned literature, most researchers investigated the parametrically excited instability problem of structures analytically or numerically. The experimental work for parametrically excited composite shell is, to our knowledge, not reported yet. In this paper, the dynamic instability of graphite/epoxy laminated shells under parametric excitation was investigated analytically and experimentally. The electromagnetic device, acting as a spring of alternating stiffness, was used as a non-contacting transverse exciter in experiment, and the effects caused by the geometric imperfection, the eccentricity of the planar excitation forces could be avoided. INSTABILITY ANALYSIS OF COMPOSITE SHELL The dynamic instability equation of laminated shell is derived in this section and the instability regions of the laminated shell under parametric excitation were found. The laminated shell under electromagnetic excitation is idealized as shown in Figure 1. The electromagnetic device was modeled as a concentrated mass wo and a spring connected at point P(x0, yOi z0) on the mid-plane. The laminated shell, a part of a circular cylindrical shell, has length b=250 mm, radius of curvature R=100 mm, and arc span on the curved side 6 = ±35°, thickness h, and density p. The laminated shell, symmetric to the mid-plane, satisfies the Kirchhoff assumption and the Hooke's law. The gravitational effect was ignored FIGURE 1 Idealized model for laminated shell in analysis. under an electromagnetic excitation Finite Element Modal Analysis
Since one end of the laminated shell is clamped and the other three sides arefree,the exact solution for the vibration modes is not available. The finite element code ANSYS® [11] was used to obtain the natural frequencies and natural modes of the laminated shell. The three-dimensional Shell99 element was used in the analysis. Each element has 8 nodes and each node has 6 degrees of freedom. The attached electromagnetic device was modeled as a concentrated mass element, Mass21, located at the center of the device. After applying the boundary conditions, the natural frequencies and the corresponding modal vectors of the laminated shell can be obtained by using ANSYS code. Parametric excitation equation of composite shell The system dynamic equation can be derived from the Lagrange's equation {O}
(i)
214
Parametric Instability Analysis of Laminated Composite Shells
where [ M ] is the global mass matrix; [C] is the global damping matrix; [K\ is the global stiffness matrix; {Q} is the global nodal displacement vector, hi this study, the electromagnetic exciter is modeled as a spring of varying stiffness; therefore, the external force is zero. The nodal displacement vector {Q} can be assumed as
fe}= 1*^,(0
(2)
n=\
where <]>„ is the modal vector; Vn (t), function of time, is the modal displacement. Assuming the proportional damping, from the modal orthogonality relation and considering the effect of the electromagnetic spring, one obtain
n=l,2,...N (3) The above equation can be modified by the following dimensionless quantities: x = co/ ; 2c0j
C0j
2Mco,
the total mass of the composite shell. If the stiffness of spring is a constant, e(x) = 8. The natural frequencies of the transverse vibration of laminated shell shift from coM to Sw due to the spring effect. This was used to identify the spring stiffness s in experiment. If the spring has variable stiffness, say, s(x)= scos cox , then equation (3) becomes 'ra(x) = 0,n=l,2,...N
(4)
The above equation is a Mathieu equation, in which the excitation term contains the modal displacement Vn and the parametric excitation coefficient fnm, a function of the modes §n and the mass M of the composite shell. Criterion for Parametric Instability After obtaining the parametric excitation coefficient fnm, the instability bandwidth parameter Gnm can be calculated. The instability regions can be found from the instability bandwidth parameter Gnm, the amplitude of the spring, and the natural frequencies of the laminated shell <»„, coOT [3-5]. The transition curves separating the stable and unstable regions for simple resonance, combination resonance of sum type and difference type are co = 2coK + £G^< whenGnn > 0
_ _ _
V
co = con + com ± sG/2, when Gnm > 0
— —
(5) (6)
V
co = an - am ± sG/2, when Gnm > 0 (7) where Gnm is the instability bandwidth parameter as defined in reference [3-5]. The instability regions of the system, each separated by two transition curves, were found to be
Parametric Instability Analysis of Laminated Composite Shells
215
functions of the modal parameters of the laminated shell and the position and the excitation amplitude of the electromagnetic device on the laminated shells. PARAMETRIC INSTABILITY EXPERIMENT The instability experiment for graphite/epoxy composite shells using electromagnetic exciter was performed to verify the analytical solutions [3-5]. The laminated shell is made from the prepreg, which is assumed orthotropic with material principal axis on the mid-plane. The non-contacting electromagnetic exciter used is considered as a spring with alternating stiffness. The first part of the experiment was to identify the relation between the stiffness of the electromagnetic spring attached on the composite shell specimen and the DC coil current through the spring. The relationship between the fundamental frequency of the composite shell specimen and the DC coil current of the electromagnetic spring was obtained first. Giving different spring stiffness, the fundamental frequency of the shell-spring system was obtained from modal eigenvalue analysis. After comparing the experimental results with the analytical ones, the relations between the stiffness s and the DC coil current I of the electromagnetic spring were obtained for the specimen. The experiments were performed for each different specimen and repeated at each varied DC coil current. Figure 2 shows the experimental setup for measuring the parametric instability behavior of composite shells. The electromagnetic spring, powered with an AC source, was used to excite the shell specimen. The dynamic signal analyzer was used to analyze and to observe the dynamic signal from the accelerometer. During the experiment, the frequency was tuned step by step from a lower limit to a higher limit near twice the fundamental frequency. At each tuned frequency, the AC coil current of the electromagnetic spring was increased from zero to the maximum saturated current to observe the dynamic response of the composite shell. The instability of the composite shell was observed as rapidly increasing amplitude of transverse vibration occurred. Once the instability occurred, the AC current was cut off and the frequency and amplitude of the excitation current were recorded. Shell Specii
(a) Mode 1
(b) Mode 2 I
Signal Conditioner
Dynamic Signal Analyzer
FIGURE 2 Experimental setup for measuring the parametric instability of composite shells
(c)Mode 3 (d) Mode 4 FIGURE '3 Mode shapes of the composite shell ( J9O°]8 , R=100 mm, b=250 mm, 9 = +35° )
RESULTS AND DISCUSSION The laminated shell used has length b=250 mm, radius of curvature R=100 mm, and arc span on the curved side 9 = ±35°. The SHELL99 element was used in ANSYS analysis. To have efficient analytical results, the mesh density was studied. The first five natural frequencies of the composite shell become steady values for the model with
216
Parametric Instability Analysis of Laminated Composite Shells
element number higher than 100. Figure 3 shows the first four mode shapes of the composite shell with [90°]8. The first mode is a torsional one, the second a bending one and the rest are modes of coupling bending and torsion. The relations between the stiffness and the DC coil current of the electromagnetic spring were obtained for the specimen. The resonant frequencies and the corresponding modes were obtained by using ANSYS code. The relationship between the fundamental frequency of the composite shell specimen and the DC coil current through the electromagnetic spring was obtained from experiment. Giving different spring stiffness, the fundamental frequency of the shell-spring system was obtained from modal eigenvalue analysis. After comparing the experimental results with the analytical ones, the relations between the stiffness and the DC coil current of the electromagnetic spring were obtained for each specimen. For composite shell ([o°]4 , R=100 mm, b=250 mm, 9 = ±35°), a good linear relationship can be seen between the stiffness s and the DC coil current /of the electromagnetic spring was found. = 0.616/-0.002
(8)
00 0
1
2
3 4 5 Excitation Frequency ©
6
(a) 2co,, (b) to, + oo2, (c) 2co2, (d) 3 FIGURE 4 Dynamic instability regions of laminated shell ([o°\, R=100 mm, b=250 mm, 9 = ±35° ). analytical results; experimental results.
1.0
1.2
1.4
16 1.8 2.0 2.2 2,4 Excitation Frequency ta
2.6
28
3.0
FIGURE 5 Instability region at 2 co, for the laminated shell with [o°\ . results;
analytical
experimental results.
The instability regions of laminated shells were obtained from their modal parameters at the position of electromagnetic device,fromwhich the parametric excitation coefficient fnm, the instability bandwidth parameter Gnn and the transition curves separating the stable and unstable regions were found. In this study, the simple resonances, 2&\, 2co2,2co3, and the combination resonances up to ©2+CO5 are obtained. Figure 4 shows the dynamic instability regions at simple and combination resonant frequencies of the laminated shell with [0°]8, radius of curvature R=100 mm, length b=250 mm, and arc span 6 = ±35°. © is the ratio between the parametric excitation frequency and the fundamental natural frequency coj. co2 and ro3 denote the second and the third resonance frequencies after normalization by coj. The analytical results contain transition curves for the cases with damping coefficients ranging from 0 to 0.05. A maximum instability region occurs at twice the fundamental frequency 2c5j as shown in Figure 5. The reason is that the instability bandwidth parameter Gnm, related with the mass of the shell and the modal parameters at the position of the electromagnetic device, has higher value for the fundamental mode. The experimental results agree well with the analytical ones for the simple resonances at twice the fundamental frequency.
Parametric Instability Analysis of Laminated Composite Shells
217
CONCLUSIONS In this paper, the parametric instability of graphite/epoxy laminated shell was investigated analytically and experimentally. The system dynamic equation of the composite shell is derived to be an equation of Mathieu's type, in which the excitation term contains the modal displacement and the parametric excitation coefficient. The instability regions of the composite shell, each separated by two transition curves, were found to be functions of the modal parameters of the laminated shell and the position and the excitation amplitude of the electromagnetic device on it. The non-contacting electromagnetic device, attached on the laminated shell, excites the composite shell transversely. The effects caused by the geometric imperfection, the eccentricity of the in-plane excitation forces could be avoided effectively. The instability region agreed well with the analytical one for the simple resonance at twice the fundamental frequency. ACKNOWLEDGEMENTS The authors would like to thank the National Science Council, Taiwan, the Republic of China through grant NSC92-2212-E-007-061, for supporting this work.
REFERENCES 1. 2. 3.
Bazant, Z. P., 2000. "Structural Stability," International Journal of Solids and Structures, 37:55-67. Bolotin, V. V., 1965. The Dynamic Stability of Elastic Systems, New York, Holden-Day Inc. Chen, C. C. and M. K. Yeh. 2001. "Parametric Instability of a Beam under Electromagnetic Excitation," Journal of Sound and Vibration, 240:747-764. 4. Yeh, M. K., and Y. T. Kuo. 2002. "Dynamic Instability of Composite Beams Under Parametric Excitation," Proceedings of the 3rdAsian-Australasian Conference on Composite Materials, ACCM-3, July 15-17, Auckland, New Zealand, pp. 779-788. 5. Yeh, M. K., Y. T. Kuo, C. S. Liu and C. C. Chen. 2002. "Dynamic Instability Measurement of Structures Under Parametric Excitation," International Symposium on Experimental Mechanics, ISEM, December 28-30, Taipei, Taiwan, ROC, Paper No. A244. 6. Ng, T. Y., K. Y. Lam and J. N. Reddy. 1999. "Dynamic Stability of Cylindrical Panels with Transverse Shear Effects," International Journal of Solids and Structures, 36:3483-3496. 7. Lam, K. Y. and T. Y. Ng. 1998. "Dynamic Stability Analysis of Laminated Composite Cylindrical Shells Subjected to Conservative Periodic Axial Loads," Composites PartB, 29B:769-785. 8. Ganapathi, M., T. K. Varadan and V. Balamurugan. 1994. "Dynamic Instability of Laminated Composite Curved Panels Using Finite Element Method," Computer & Structures, 53:335-342. 9. Argento, A., 1993. "Dynamic Stability of a Composite Circular Cylindrical Shell Subjected to Combined Axial and Torsional Loading," Journal of Composite Materials, 27(18): 1722-1738. 10. Bert, C. W. and V. Birman. 1988. "Parametric Instability of Thick, Orthotropic, Circular Cylindrical Shells," Ada Mechanica, 71: 61-76. 11. ANSYS Theory Reference. 001369. Twelfth. SAS IP, Inc.
Bending Properties of Braided Composite Tubes Masanori Okano, Kenichi Sugimoto, Asami Nakai* and Hiroyuki Hamada Kyoto Institute of Technology, Japan
ABSTRACT In this paper, the effects of braiding angle on bending properties of braided composite tubes were investigated. The braided composite tubes with different braiding angle and number of layer were used and three-point bending tests were performed. Although the elastic modulus in longitudinal direction was high in the tube with small braiding angle, a large flat deformation was generated due to the low rigidity of circumferential direction compared to the tube with large braiding angle. Aimed at fabrication of the tube which has both high elastic modulus and low flatness ratio, the tube with hybrid laminate constitution was fabricated. In the tube that was combination of a large braiding angle in the inner part and a small braiding angle in the outer part, elastic modulus was as high as the tube with small braiding angle and the flatness ratio was the lowest.
INTRODUCTION Tubular structures are often used in the frame and a shaft part of structures. Hence in such tubular structure, not only tensile and compressive properties but also bending and torsional properties are important, and wide ranges of material design to satisfy various requirements are needed. In these circumstances, braiding technique can be adopted into tubular structure. As shown in Figure 1, braiding has a characteristic of yielding fibers that are oriented continuously in different directions. With braiding technique, the braiding angle can be changed easily and straight fibers can be inserted into braided fabric as middle-end fiber. The number and type of reinforcing fibers can be also selected. Consequently, the mechanical properties of pipe in longitudinal and circumferential direction can be controlled to meet requirements. It is expected that a wide range of material design can be carried out with braided fabrics. Concerning fabrication process of braided composites, it is possible to produce tubes with fiber bundle in three axes in one layer and a continuous fabrication process of braiding results in the reduction of manufacturing costs. Therefore, braided fabric is more suitable for reinforcements of pipe than not only unidirectional composite but also other textile fabrics. In the case of braided composite, the architecture of the braided fabric is complex and therefore, the parameters controlling its mechanical properties become numerous. In other words, the parameters such as braiding angle, the distance between braiding fiber bundles, the cross-sectional area, the geometry of cross section of the fiber bundles and fiber volume fraction within the fiber bundles exist. * Corresponding author, Gosyo-kaidoucyo, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, JAPAN FAX: +81-75-724-7800 E-mail: [email protected]
Bending Properties of Braided Composite Tubes
219
These parameters are not independent each other and change with other parameters. Based on these parameters, crimp ratio of fiber bundle and fiber volume fraction of composite were decided. Therefore, it is difficult to evaluate only the braiding angle, and it is necessary to develop a design methodology for braided composites. In this study, bending properties of tubular braided composites have been studied with respect to braiding angle. Three types of the tube with different braiding angle were fabricated and three-point bending test were carried out. MATERIALS AND EXPERIMENTAL METHOD Glass fibers (ER1150 F-165N; Nippon Electric Glass Co. Ltd.) were used as reinforcement and vinylester (R-806B; SHOWA HIGHPOLYMER Co. Ltd.) was used as matrix resin. In order to clarify the effect of braiding angle on bending properties, three braiding angles 30°, 45° and 60° were chosen and six kinds of braided composite tubes with different braiding angle and number of layer were fabricated. The specification of each tube fabricated is shown in Table 1. A group " 1 " of the tube was a composite tube with small thickness and a group "2" of the tube was a composite tube with large thickness. The three-point bending test was performed by using special pulley unit. The pulley unit is capable of decreasing the stress concentration generated at the point of support and loading nose because of transference of load by contacting the tube at two points. A strain gage with three axes was stuck on the surface opposite to the loading point to measure the local strain of the tube and to calculate the principal strain. The bending test was performed by using an INSTRON testing machine at a constant cross-head speed of 5.0mm/min. The load-deflection curves and the load-principal strain curves are shown in Figure 2 and Figure 3. Here, the principal strain value is displayed from 0// e to 10000// e to explain the slope of the curves in the load-principal strain. Thus, the strain value does not correspond to the deflection value in the load-deflection curves. For example, the strain value 8000 ju e vs> corresponded to approximately 2mm in the deflection. Concerning the load-deflection curves, in the case of the group "1", the S30-1 tube showed the highest maximum load value of the three tubes. In the case of the group "2", the maximum load value of S30-2 tube displayed the highest of the three tubes. Thus, it may be inferred that tendencies of load-deflection curves depended on the thickness and laminate constitution. Concerning the load-principal strain curves, in the case of both the group " 1 " and the group "2", the slope of load-principal strain curve of S30 tube showed the largest of the three tubes. TABLE I Specification of the fabricated tube
Fiber bundle FIGURE
1 Schematic illustration of tubular braided fabric
Inside Outside The type of Number Braiding angle Thickness diameter diameter specimen of layer [degree] [mm] [mm] [mml 6 30 26.0 29.3 S30-1 1.65 26.0 5 45 29.3 1.67 S45-1 4 60 26.0 S60-1 30.1 2.03 S30-2 9 30 26.0 31.0 2.48 8 45 26.0 30.9 S45-2 2.47 6 60 26.0 32.0 2.98 S60-2
Bending Properties of Braided Composite Tubes
220
2
4 6 Deflection [mm]
2000 4000 6000 8000 Principal strain [ p. t ]
10000
FIGURE 2 Load-deflection curve of each tube
2000 4000 6000 8000 Principal strain [ y £ ]
10000
FIGURE 3 Load-principal strain curve of each tube
Then, the elastic modulus Ep.y calculated from the load-deflection curve, the elastic modulus Ep. c calculated from load-principal strain curve of all tubes and bending strength a/, are shown in Table 2 and Table 3. In the case of both the group " 1 " and the group "2", the bending strength of the S30 tube also showed highest value of the three tubes. The difference between maximum value and minimum value of the bending strength was approximately 50%. For the tube with braiding angle 60°, the difference of the bending strength between the S60-1 tube and the S60-2 tube was not seen. However, for the tubes with braiding angles 30° and 45°, when the thickness was large, the bending strength increased at approximately 15%. Surprisingly, the elastic modulus Ep.y and Ep. c evaluated from load-displacement curve and load-principal curve showed a different value. The differences between Ep.y and Ep. c were approximately 3.0 times in the case of the tube with braiding angle 30°, 2.5 times in the case of the tube with braiding angle 45° and 2.0 times in the case of the tube with braiding angle 60°. This difference which was not the error of the experiment should be noticed.
Bending Properties of Braided Composite Tubes
221
TABLE II Results of bending strength
TABLE III Results of bending modulus
Bending The type of strength specimen <7b[MPa] S30-1 168.8 S45-1 158.4 S60-1 114.4 S30-2 197.3 S45-2 189.7 S60-2 117.7
Bending Bending The type of modulus modulus specimen E^T[GPa] En.f [GPa] 13.8 45.6 S30-1 13.6 S45-1 30.5 9.7 20.4 S60-1 S30-2 16.4 45.8 34.1 S45-2 15.5 S60-2 10.5 22.0
FLAT DEFORMATION AND FLATNESS RATIO In this section, the actual flatness ratio was calculated for each tube. Here flatness ratio was defined as the ratio of actual deflection to theoretical deflection obtained by the strain. We can calculate the theoretical deflection of three-point bending performance of the tube, from the relationship between stress and strain. And we can also calculate the relationship between the experimental deflection yexp. and strain e as a slopes of load-strain and load-deflection were obtained from experiments. Consequently, as flatness ratio was defined as the ratio of actual deflection to theoretical deflection obtained by the strain, the flatness ratio is given by
(1)
The flatness ratio calculated from equation (1) is shown in Table 4. In the case of both the group " 1 " and the group "2", it was confirmed that the tube with braiding angle 30° was easily flattened by transverse load. On the contrary, in the tube with braiding angle 45° and 60°, those tubes were not easily flattened compared to the tube with braiding angle 30°.
TABLE IV Results of flatness ratio
The type of specimen yexp/ytheo. S30-1 S45-1 S60-1 S30-2 S45-2 S60-2
3.3 2.2 2.1 2.8 2.2 2.1
TABLE V Specification of the tube with hybrid laminate constitution Inside Outside Thickness The type of Number Laminate constitution diameter diameter [mm] specimen of layer H-1
5
H-2
5
In a30 o /3 + a60°/2 In a60°/2 + a3O°/3
rmmi 26.0
[mml 29.9
1.96
26.0
29.7
1.85
222
Bending Properties of Braided Composite Tubes
THE SUGGESTION OF HYBRID LAMINATE CONSTITUTION A hybrid laminate constitution which was a combination of braiding angle of 60° and braiding angle of 30° was suggested in order to obtain a tube with the high elastic modulus in longitudinal direction and the low flatness ratio. Table 5 shows the specification of the fabricated two tubes. The H-1 tube had hybrid laminate constitution which was a combination of braiding angle of 30° in inner part and braiding angle 60° in outer part. On the other hand, the H-2 tube had a hybrid laminate constitution which was a combination of braiding angle of 60° in inner part and braiding angle of 30° in outer part. And the same static bending test was carried out by using these tubes and the elastic modulus and the flatness ratio calculated from the equation (1) are shown in Table 6 and Table 7. With respect to the elastic modulus, the H-1 tube showed lower value than the S30 tube and S45 tube, however, showed higher than the S60 tube. On the other hand, the H-2 tube displayed higher value than the tubes of the group "1". Secondary, the flatness ratio of H-1 tube was 2.4. However the flatness ratio of H-2 tube was 1.8. The value showed the lowest of all fabricated tubes. That is to say, the tube in which elastic modulus in longitudinal axis is high and the flatness ratio is low could be fabricated by designing it to have high rigidity of circumferential direction in the inner part with low rigidity of circumferential direction in outer part. CONCLUSIONS In this study, the bending properties of braided composite tubes were investigated and static three-point bending testing was carried out. The effect of braiding angle on bending properties was clarified experimentally. It found that; 1. hi the tube with braiding angle 30°, the large flat deformation was generated because of the low rigidity of the circumferential direction and when the thickness of the tube was large, the flat deformation was improved. 2. The tube with braiding angle 60° was not easy to flatten because of the high rigidity of the circumferential direction and an increase in thickness of the tube was ineffective for improving the flat deformation. 3. The tube that consisted of a combination of braiding angle of 60° in the inner part and braiding angle 30° in the outer part, showed values that were comparable to the tube with braiding angle 30°, and it showed the lowest flatness ratio of all the tubes. TABLE VI Results of bending modulus of the all tubes
Name of specimen
H-1 H-2
Bending Bending modulus modulus Ep.y [GPa] Ep* [GPa] 11.9 28.8 14.4 25.6
TABLE VII Results of flatness ratio of the all tubes
Name of specimen
yexp/ytheo.
H-1 H-2
2.4 1.8
Analytical Stress Analysis of Rotating Composite Beams Due to Material Discontinuities M. Tahani1'*, A. Nosier2, J. Rezaeepazhand3, S. M. Zebarjad4 Department of Mechanical Engineering, Faculty of Engineering, Ferdowsi University of Mashhad, P.O.Box 91775-1111, Mashhad, Iran 2 Department of Mechanical Engineering, Sharif University of Technology, P.O.Box 11365-9567, Azadi Ave., Tehran, Iran 4 Department of Materials Science and Metallurgy, Faculty of Engineering, Ferdowsi University of Mashhad, P.O.Box 91775-1111, Mashhad, Iran u
ABSTRACT Material discontinuity could cause in-plane stress gradients that it arises interlaminar stresses in regions of sudden transition of material properties. A layerwise laminated beam theory that is a modification of a layerwise laminated plate theory is developed and it is used to analyze analytically the interlaminar stresses at material discontinuities in rotating composite beams. Equations of motion are obtained by using Hamilton's principle. It is assumed that the beam is divided into two regions with different layups which are joined together. The predicted interlaminar stress distributions at the ply interfaces are shown to be in good agreement with comparative three-dimensional finite element analysis.
INTRODUCTION The problem of interlaminar stress analysis at the free edges and bonded joints of composite structures have been under investigation continuously ever since the original paper of Pipes and Pagano [1], Numerous papers have been published on the subject over three decades (see, for example, [1-7]). In these studies, interlaminar stresses appear at the free edges of finite composite laminates under different loading conditions have been considered. It is well known that interlaminar stresses arise in order to satisfy equilibrium at locations with in-plane stress gradients. Material discontinuity (i.e., a sudden change of material properties) is another source of arising in-plane stress gradients and, therefore, interlaminar stresses appear near the material discontinuities. Bhat and Lagace [6] evaluated interlaminar stresses at material discontinuities using the principle of minimum complementary energy. They analyzed laminates with different layups which had been joined together. They mentioned such cases occurred at regions of implants within adaptive structures. The advent of adaptive structures has resulted in sensors made of various materials being implanted within laminated composites by cutting some plies of the laminate and placing the sensor in that location. Also a damaged region such as that caused by impact is another example of material Corresponding author. Tel: +98-511-8615100; fax: +98-511-8629541, E-mail address: [email protected] (M. Tahani)
224
Analytical Stress Analysis of Rotating Composite Beams
discontinuity. They showed interlaminar stresses are produced in the vicinity of these material discontinuities. Investigations of interlaminar stresses in rotating composite beams have been rare. Rotating beams are often used as the simple model for propellers, turbine blades, and satellite booms. Hence, in this paper, analysis of interlaminar stresses in composite beams especially due to material discontinuities are interested. A layerwise laminated plate theory is used to develop a layerwise laminated beam theory. The results obtained from this theory are compared with those obtained by using a finite element method. The correlation among the results indicates the theoretical approach is feasible as a conceptual design tool. THEORETICAL FORMULATION It is intended here to determine interlaminar stresses in a rotating composite beam with uniform cross-section. Displacements of the beam are defined in a rotating rectangular Cartesian coordinate system, rigidly tied to the beam (see Figure 1). The beam is assumed to has the length 2L and thickness h. It is noted that only one symmetric half of the beam is shown in Figure 1. Here a layerwise laminated plate theory is developed and then it is simplified for analysis of beam structures. It is considered that the beam rotates with a constant angular velocity O.. Therefore, the displacement field is assumed to be independent of time.
Region B
Region A O'Ply 90" Ply 90" Ply O'Ply a
O'Ply O"Ply O'Ply O'Ply L
FIGURE 1 The geometry of problem with a [0° / 90° ] s laminated beam in transition to a [0° ] 4 laminated beam.
Plate Equations In this study, a layerwise laminated plate theory is used in deriving the laminated beam theory. Therefore, the following displacement field is considered:
u2(x,y,z) = Vk(x,y)<&k(z), u3(x,y,z) = Wk(x,y)®k(z)
(1)
where the displacement components, the global interpolation function, and N have been defined in [7]. It is to be noted that a repeated index indicates summation over all values of that index. Upon substitution of Eqs. (1) into the linear strain-displacement relations of elasticity, the following results will be obtained:
Analytical Stress Analysis of Rotating Composite Beams
225
Yy.=vk<&k+wkjbk, r»=u,P'k+wkjbk,
(2)
rxy = {uk,y+vktI)ok
where a prime indicating an ordinary derivative with respect to the independent variable z and a comma followed by a variable indicates differentiation respect to that variable. Using the Hamilton principle, 3(N+1) equations of motion corresponding to unknowns Uh Vk, and Wk can be shown to be: 5Uk: Mkxx +
Mkxyy-Qk=-Ikn2x-IkJUp2
5 Vk : MkViX + Mky - Qk = -IkQ2y - f'Vp2
(3)
where the generalized stress resultants have been defined in [7] and the mass terms are defined as follows: (/*,IkJ)= [h'2 p(O,,O, O.)dz J-A/2
*
*
(4)
;
V
'
It is noted that the underlined terms in Eqs. (3) may be neglected in contrast to IkCl2x and IkQ2y. The boundary conditions for a laminated plate with a rectangular platform in the layerwise theory at an edge parallel to y axis involves the specification of Uk or Mk, Vk or Mky and Wk or Rk. Similarly, at an edge parallel to x axis, the required boundary conditions can be specified. It is assumed that the laminate is laminated of orthotropic laminae, with respect to the x-axis. The constitutive relations for the Mi orthotropic lamina with respect to the laminate coordinate axes are {af =[C]m {sf' where [C] w are the transformed stiffness matrix of the Mi layer. Using Eqs. (2) and the constitutive relations the generalized stress resultants are obtained which can be represented as follows:
y
j
k
hy
(5)
k
{Q x,R x) = (A*B%)Uj + (A%,BlWj + (B£M)WLx + (B*,Di)Why where therigidityterms are given in [7]. Beam Equations It is assumed that the stress resultants are functions of x only. Hence, Eqs. (3) yields to: K.*-Q*=-Ik&x,
M^-g;=0,
RXiX-Nk=O
(6)
Also it is supposed that the strains are functions of x and z only. Therefore, Eqs. (2) are simplified as follows: ex=Uk'
sy=0,
ez=WkO't,
ry,=Vk^'k,
rxz=Uk
Yxy=Vk'Q>t
(7)
226
Analytical Stress Analysis of Rotating Composite Beams
According to the Eqs. (7), it is more reasonable for a beam to let M* be equal to zero. Substitution of this condition into the stress resultants in Eqs. (5) results in:
y
j
(8)
where the coefficients are defined in Appendix. Upon substitution of Eqs. (8) into Eqs. (6) the following governing equations of motion are obtained:
j
^
!
j (Bki - B*) w; = 0
(9)
k
(B&-B*)Uj' +{B i -B*)Vj' +D*sWj' -A^Wj = 0
ANALYTICAL SOLUTIONS In this study the local linear Lagrangian interpolation functions (j>'k through the thickness are used (see [7]). It is to be noted that there exist repeated zero roots (or eigenvalues) in the characteristic equation of the set of equations in (9). The procedure used here for solving Eqs. (9) are similar to the one suggested by Tahani and Nosier [7] and for brevity are not taken up here. RESULTS AND DISCUSSION In what follows a numerical example is presented for a rotating composite beam that composed of two different layups which are joined together (see Figure 1). The regions A and B are made up of [0°/90"]J and [0°]4beam, respectively, as shown in Figure 1. Also it is assumed that the beam has the length 2L, thickness h, with L=5h and a=U2, and is rotating with a constant angular velocity. In this particular problem, it is assumed that Q = 1000rad/sec and h = 0.0lm . To analyze this problem, two coupled differential equations for regions A and B have to be solved. The boundary conditions for this problem are:
where the superscripts (A) and (B) show regions A and B, respectively. Also the following continuity conditions at x=a must be satisfied:
= u(kB),
v{kA) = vtB), R^=R^->
(11)
This particular problem is chosen because interlaminar stresses arise only near the material discontinuities. Due to identical ply orientations in region B no free-edge effects exist at x=L. Also because the beam has length 2L and it has symmetric boundary conditions at x=0 no interlaminar stresses arise at this point.
Analytical Stress Analysis of Rotating Composite Beams
227
The material properties of the layers are taken to be those of a T300/5208 lamina [8]: £,=132 GPa, £ 2 =£ 3 =10.8 GPa , Gl2 = G13 = 5.65 GPa, G23= 3.38 GPa vl2 = v13 = 0.24 , v23=0.59, p = 1540kg/m3 (12) where the subscripts 1,2, and 3 indicate the on-axis (i.e., principal) material coordinates, hi what follows, the interlaminar stresses are determined by using Hooke's law with six numerical layers in each physical lamina (see [7]). The in-plane stress ax at z=h/4 in 0° plies in regions A and B is shown in Figure 2a. Also the in-plane stress <JX at z=h/4 in 90° ply in region A and 0° ply in region B is presented in Figure 2b. It is seen that stress distributions are discontinues near x=a. It is seen that there are close agreements between the present solutions and those obtained by the finite element method using ANSYS software [9].
4 3.5 3
5
2
D
"1.5
1.5
05
1 0.5
1 0.5 0
0.2
0.4
0.6
0
0.8
0.2
0.4
0.6
x/L
x/L
(a)
(b)
0.8
FIGURE 2 Distributions of in-plane normal stress ax at z=h/4 (a) in 0° plies in regions A and B and (b) in 90° ply in region A and 0° ply in region B.
0.1 0.05 0 2-0.05
s X-o.
[ :
/
~ ~ — ^
-0.1 O-
Present FEM
i
-0.15
s B
-0.2 -
-0.2 -0.25
i
0-
0.2
< • < < • • •
0.4
0.6
0.8
-0.3,
x/L
(a) FIGURE 3 Distributions of interlaminar stresses (a) az at the middle plane and (b) aa at z=h/4 along the 0790° interface in region A and along the 070° interface in region B.
228
Analytical Stress Analysis of Rotating Composite Beams
Distribution of interlaminar normal stress <JZ at the middle plane is shown in Figure 3a. The results show that there are sharp interlaminar stress gradients near the material discontinuity and decays away from the region of discontinuity as expected. The current solutions are seen to match the finite element solutions reasonably well except in the region close to the material discontinuity where the stresses have a steep gradient. Also Figure 3b illustrates the distribution of interlaminar shear stress <JXZ at z=h/4 along the 0°/90° interface in region A and along the 0°/0° interface in region B. It is noted that <JXZ at the free edge (x=L) meet the stress free boundary condition with a good approximation, even though this condition has not been enforced a priori. CONCLUSIONS A layerwise laminated beam theory are developed by using a layerwise laminated plate theory and it is used to predict interlaminar stresses in the vicinity of material discontinuities in rotating composite beams with general laminations. Governing equations of motion are obtained by using Hamilton's principle. The results obtained from this theory are compared with those obtained by a finite element method. The results indicate that there are severe interlaminar stresses in regions near the sudden transition of material properties (material discontinuities). These stresses may initiate heterogeneous damage in the forms of delamination and transverse cracking and may cause the damage to propagate to a substantial region of the beam, resulting in a significant loss of strength and stiffness. To this end, these stresses must be considered in design of such structures. APPENDIX The coefficients appearing in Eqs. (8) are defined as: [Aii] = [An]-[B23]T[D22T'[B2i],
[Bn] = [Bti]-[Dl2][D22T'[B2i]
[B,6 ] = [5 36 ] - [D26 ] [D22 r ' [5 23 ] , [ A , ] = [ A , ] - [Dl2 ] [D22 ]"' [Dl2 ] [A.] = [Di6l-[Dl2][D22r[D26],
[D66] = [D66]-[D26][D22y[D26]
REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9.
Pipes, R. B. and N. J. Pagano. 1970. "Interlamiiiar Stresses in Composite Laminates under Uniform Axial Extension," J. Compos. Mater., 4: 538-548. Hsu, P. W. and C. T. Herakovich. 1977. "Edge Effects in Angle-Ply Composite Laminates," J. Compos. Mater., 11: 422-428. Wang, A. S. D. and F. W. Crossman. 1977. "Some New Results on Edge Effect in Symmetric Composite Laminates," J. Compos. Mater., 11: 92-106. Pagano, N. J. 1978. "Free Edge Stress Fields in Composite Laminates," Int. J. Solids Structures, 14: 401-406. Wang, S. S. and I. Choi. 1982. "Boundary-Layer Effects in Composite Laminates: Part 2- Free-Edge Stress Solutions and Basic Characteristics," J. Appl. Meek, 49: 549-560. Bhat, N. V. and P. A. Lagace. 1994. "An Analytical Method for the Evaluation of Interlaminar Stresses Due to Material Discontinuities," J. Compos. Mater., 28(3): 190-210. Tahani, M. and A. Nosier. 2003. "Three-Dimensional Interlaminar Stress Analysis at Free Edges of General Cross-Ply Composite Laminates," Materials & Design, 24(2): 121-130. Herakovich, C. T. 1998. Mechanics of Fibrous Composites, John Wiley, New York. ANSYS, Release 5.4 UP19970828, SAS IP, Inc., 1997.
Thin-Plate Splines for Thick Composite Plate Analysis Antonio J. M. Ferreira* Departamento de Engenharia Mecanica e Gestao Industrial, Faculdade de Engenharia da Universidade do Porto, Portugal
ABSTRACT Composite laminated plates are a typical and relevant application of composite materials in various industries. Such structures are heterogeneous in the thickness direction and orthotropic in each lamina plane. Most of the methods for plate analysis are based on the finite element method. In this paper it is proposed to interpolate the system of partial differential equations by radial basis functions, in particular by thin-plate splines. The thin-plate splines (TPS) method represents an alternative to multiquadrics (MQ) radial basis functions. The TPS method does not rely on a shape-parameter like the MQ method, being this a more stable approach. Composite structures can be analysed by various sets of shear deformation theories: the classical Love-Kirchhoff plate theory, the first-order shear-deformation theory, the third-order shear deformation theory and layerwise theories. In this paper we apply the TPS method together with the third-order shear deformation theory for the analysis of moderately thick laminated plates. The methodology proves to be stable and accurate. INTRODUCTION Collocation with radial basis functions is a recent meshfree collocation method with global basis functions. The multiquadric method for the solution of partial differential equations (PDEs) was first introduced by Kansa in the early 1990s and showed exponential convergence for interpolation problems. In this paper we formulate and discuss the use of thin-plate splines radial basis functions in the solution of moderately thick laminated composite plates using a third-order shear deformation theory. Composite materials are a very important class of engineering materials with great properties and applications in a variety of complex structures, such as those typically found in space, automobile and civil applications. The correct design of such structures requires adequate stress analysis and in particular numerical tools. The proper modeling of composite laminates remains an open field of discussion and developments as a consequence of their complex behavior. It is very important to accurately determine the transverse shear stresses since they are the reason why delamination mechanisms are active. A proper laminate theory that accounts for shear deformation and an adequate numerical tool are needed in order to capture all such effects. Several laminate theories have been proposed in the literature. The simplest one is the classical laminate theory (CLT) [1] which is based on the Kirchhoff-Love theory of plates. The CLT neglects shear deformations and can lead to inaccurate results for moderately thick composite laminated or sandwich plates. The first-order shear deformation theory (FSDT) for laminated composite plates was developed as an * Corresponding Author, Departamento de Engenharia Mecanica e Gestao Industrial, FEUP, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal, Fax +351 22 9537352, email: [email protected]
Thin-plate Splines for Thick Composite Plate Analysis
230
extension of the theory of Mindlin [2] for isotropic plates which considers shear deformations and gives satisfactory results for a wide range of structures, in particular for moderately thick laminates [3-5]. The FSDT efficiency is dependent on a good choice of shear correction factors. This is not trivial and is dependent on the lamination scheme and on the deformation. Whitney [4] and Ferreira [5,6] have developed procedures for such calculation, based on cylindrical bending. The higherorder shear deformation theories (HSDT) have been developed to obviate the limitations of FSDT [7]. Following the research by the author with FSDT and MQ in the analysis of laminated composite plates [8], this paper addresses the application of thin-plate radial basis functions and HSDT to the analysis of moderately thick composite laminated plates. THIRD-ORDER THEORY OF PLATES The third-order theory of Reddy [7] is based on the same assumptions than the classical and first-order plate theories, except that the assumption of straightness and normality of a transverse normal after deformation is relaxed by expanding the displacements (u,v,w) as cubic functions of the thickness coordinate. The displacement field is then obtained as dw u(x,y,z)=u\x,y)+z(j)x '—f (1) ~dx dw (2) ' V" ) ^ 1" ) • V~ >J I ' " Yy 11,2 ~dy~ w(x,y,z)=w°(x,y) (3) where u and v are the inplane displacements at any point (x,y,z), u° and v° denote the inplane displacement of the point (x,y,0) on the midplane, w is the deflection, (j>x and <j)y are the rotations of the normals to the midplane about the y and x axes, respectively. The strain-displacement relationships are given as: ^xx
e
yy
y(0) /xy
city tiyy
'xy
du0 dx dv^ dy dun _ dvn
t XZ
fy?
(0) / xz
eO)
yy y(3) 1 xy
+ z2
/yz
ri 2)
y(l) /xy
dx dx
dx Cyy
~?>y
dx
dy
dy
dx
y(2) 1 xz
(4)
y(2) 1 yz
dx
-+ •
dy
+ z3
+ Z
%
(5)
dy
/xy
dy
dx
dw0 x
dx dwn
i
(6)
dy + dy = 3c,. Neglecting az for each orthotropic material layer, the stresswhere c, = strain relations in the fiber local coordinate system can be expressed as
Thin-plate Splines for Thick Composite Plate Analysis Qn
2,2
0
0
Qn
222
0
0
0
0
233
0
0
0
0
244
0
0
0
0
231
(7) Qs.
Here subscripts 1 and 2 are, respectively, the fiber and the normal to fiber inplane directions, 3 is the direction normal to the plate, and the reduced stiffness components, Qy are given by ii
=
~
ten
-
>
1 — 1/1/
I — V
V
=G 23 ;g 55 =G 3I ;v 21 = v ] 2 - ^
Qn =
(8)
in with £ , , £ 2 ) v12, G12, G23 and G31 are materials properties of the lamina. By performing a coordinate transformation, the stress-strain relations in the global x-y-z coordinate system can be obtained as X
Gy
Txy Tyz
Tzx
Qn
2,2
2,6
0
0 0
By
0
Yxy
245 255
Yyz
Qn
222
226
0
= 2,6
226
266
0
0
0
0
0
0
0
244
£
x
(9)
Yzx
The third-order theory of Reddy [7] satisfies zero transverse shear stresses on the bounding planes. The equations of equilibrium of the third-order theory are derived from the principle of virtual displacements as: dx dx
dy
3h2 { 8x2
^-2>o;'
\., d • + •
dx
(10)
dy2
dxdy dy
•-O
=0
(11)
with (12) In previous equations Q^R^M^^y, are the shear forces and bending moments, respectively. The Euler-Lagrange equations can be written in terms of the displacements by substituting strains and stress resultants into this equation. For example, equation (10) is given as
232
3h2
Thin-plate Splines for Thick Composite Plate Analysis
n
[dxdy2
dx2dy J
9h4
i
\dy2dx
' dx2dy ' "dy2dx2
hi this equation, stiffness components are obtained as A
a = tMl'J
= 4 ' 5 ;^ = T £ ^ W + . -zt3J,7 = 1,2,3,4,5 L ~z5JJ = 1.2.3JH, = ^£ei;W + 1 -^>-J = 1,2,3
(15)
hi (14) and (15), zk and zt+l are the lower and upper z coordinates of the A:'* layer. RADIAL BASIS FUNCTIONS The radial basis function method relies on the Euclidian distance between nodes and in some cases on a shape parameter, user-defined and object of various discussions. The influence of such parameters not only defines the RBF but also may provide illconditioned problems with inadequate solutions. To obviate the use of such parameter it is proposed in this paper the use of thin-plate splines. An RBF depends only on the distance to a center point x ; and is of the form g (Ik - x;. |h. Consider a set of nodes xux2,...,xN
EQCJ!",
The radial basis functions centered at xy. are defined as R\j=l,...,N
(16)
where x - x ; is the Euclidian norm. The thin-plate splines RBFs are given as = ||x - x.|2m logfx - Xjf ;m = 1,2,... (17) An important feature of the RBF method is that is does not require a grid. The only geometric properties needed in an RBF approximation are the pairwise distances between points. Working with higher dimensional problems is not difficult as distances are easy to compute in any number of space dimensions, hi this paper it is proposed to use Kama's unsymmetric collocation method [11]. Consider a boundary-valued problem with a domain Q c R" and a linear elliptic partial differential equation of the form Lu(x)=s(x)cR";Bu(x)]BQ =f(x)eR" (18) where dQ represents the boundary of the problem. We use points along the boundary (Xj,j = l,...,NB) and in the interior (xy., j = NB +1,...,N). Let the RBF interpolant to the solution w(x) be gj(x)
Thin-plate Splines for Thick Composite Plate Analysis
233
Collocation with the boundary data at the boundary points and with PDE at the interior points leads to equations
sB(x,c) =
(20)
= O(xi),i=NB
X -X;
(21)
where -^(x,), (x;) are the prescribed values at the boundary nodes and the function values at the interior nodes, respectively. This corresponds to a system of equations with an unsymmetric coefficient matrix, structured in matrix form as
(22)
NUMERICAL EXAMPLE A square laminate of side a and thickness h is composed of four equally thick layers oriented at (0°/90°/90°/0°). It is simply supported on all edges and subjected to a sinusoidal vertical pressure of the form:
. (nx\ . (ny\ pz =Psm — sin —
V a ) \ a ) being the origin of the coordinate system located at the lower left corner of the middle plane. The material properties are given as Ei = 25.0£2;G12 = Gn = 0.5E2;G23 = 0.2E2;v12 = 0.25 The numerical results are presented in table I, in a normalized form, as _ \02w(a/2,a/2,0)h3E2_ axx{al2,al2,hl2)h2 _ _ ayy(a/2,a/2,h/4)h2 ~<Jxx
=•
Pa' Pa2 Pa2 Tzx{0,a 12,first _ layer)h _ Txy(a,a,h/2)h Pa '* Pa2 In this table a laminated composite plate is analyzed with N = 11x11,15x15 and 21 x21 points. It can be seen that the present methodology is very accurate for the analysis of composite laminates. Both the transverse displacement, normal and transverse stresses are accurately predicted. Transverse shear stresses are calculated by the equilibrium equations. CONCLUSIONS In this paper the thin-plate splines radial basis function method and a third-order shear deformation theory were applied to the structural analysis of isotropic and symmetric laminated composite thick beams and plates. Results were compared with existing solutions showing excellent performance. Results obtained using an unsymmetric collocation strategy give very good agreement with available theories or previous results. This method, based on radial basis functions has very large potential for the
234
Thin-plate Splines for Thick Composite Plate Analysis
solution of structural problems, as a real meshless method, insensible to spatial dimension. TABLE I Composite plate a/h 100
20
10
4
N
w
11 15 21 Exact [12] 11 15 21 Exact [12] 11 15 21 Exact [12] 11 15 21 Exact [12]
0.5250 0.4575 0.4409 0.4347 0.5116 0.5029 0.5084 0.517 0.7050 0.7115 0.7133 0.743 1.8288 1.8509 1.8686 1.954
°* 0.6421 0.5650 0.5463 0.539 0.5465 0.5364 0.5423 0.543 0.5376 0.5452 0.5433 0.559 0.6289 0.6601 0.6614 0.720
a
y
0.3684 0.3434 0.3373 0.271 0.3663 0.3623 0.3657 0.309 0.4333 0.4368 0.4374 0.403 0.6175 0.6212 0.6261 0.666
0.4701 0.4295 0.4011 0.339 0.2149 0.2056 0.5906 0.328 0.1341 0.3553 0.3551 0.301 0.4422 0.1796 0.2208 0.270
0.0304 0.0238 0.0219 0.0214 0.0207 0.0221 0.0214 0.0230 0.0218 0.0238 0.5252 0.0276 0.0225 0.0315 0.0372 0.0467
REFERENCES I.
Reissner, E. and Stavsky, Y., 1961, "Bending and stretching of certain types of heterogeneous aelotropic elastic plates", J. Appl. Mech., 28 :402-412. 2 . Mindlin, R. D., 1951, "Influence of rotary inertia and shear in flexural motions of isotropic elastic plates", J. Appl. Mech., 18: 31-38. 3 . Yang, P. C. and Norris, C. H. and Stavsky, Y., 1966, "Elastic wave propagation in heterogeneous plates", Int. J. Solids and Structures, 2:665-684. 4 . Whitney, J. M., 1973, "Shear correction factors for orthotropic laminates under static load", J. Appl. Mech., 40:302-304. 5 . Ferreira, A. J. M. and Barbosa, J. T., 2000, "Buckling behaviour of composite shells", Composite Structures, 50:93-98. 6 . Ferreira, A. J. M. and Camanho, P. P. and Marques, A. T. and Fernandes, A. A., 2001, "Modelling of concrete beams reinforced with FRP re-bars", Composite Structures, 53:107-116. 7. Reddy, J. N., 1984, "A simple higher-order theory for laminated composite plates", J. Appl. Mech., 51:745-752. 8 . Ferreira, A. J. M., 2003, "A formulation of the multiquadric radial basis function method for the analysis of laminated composite plates", Composite Structures, 59(3):385-392. 9 . Reddy, J. N., 1997, Mechanics of laminated composite plates, CRC Press, New York 10 . Hardy, R. L., 1971, "Multiquadric equations of topography and other irregular surfaces", Geophys. Res., 176:1905-1915. II. Kansa, E. J., 1990, "Multiquadrics- A scattered data approximation scheme with applications to computational fluid dynamics. I: Surface approximations and partial derivative estimates", Comput. Math. Appl., 19(8/9): 127-145. 12 . Pagano, N. J., 1970, "Exact solutions for rectangular bidirectional composites and sandwich plates", J. Comp. Mater, 4, 20-34.
Part IV
Delamination
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Evaluation of Fatigue Delamination Behavior in Hybrid Composite Material Using the Delamination Shape Parameters Sam-Hong Song Department of Mechanical Engineering, Korea University 1, 5ga, Anam-dong, Sungbuk-gu, Seoul 136-701, Korea Cheol-Woong Kim Mechanical System, fnduk Institute of Technology San 76, Wolgye-dong, Nowon-gu, Seoul 139-749, Korea Dong-Joon Oh Department of Mechanical Education, Andong National University 388, Songchun-dong, Andong, Kyoungbuk 769-749, Korea
ABSTRACT The applicability of the hybrid composite materials such as Al/GFRP laminates is restricted due to the frequent delamination of different materials at interlaminar. The previous researches showed that the major parameter to control the delamination of Al/GFRP laminates was a crack (a). On the other hand, it was also shown that a delamination width (b) could strongly effect on the delamination behavior. Therefore, the aim of this research is to define the delamination behavior using the above correlation. We obtained result as follow. The delamination aspect ratio (b/a) that was suggested from the increasing a-b relationship was decreased with increasing of a/W. The suggested the delamination area rate ((^DVAXDW) which represented the growth rate of delamination area (Ap), was going higher while a/Wv/as increasing.
INTRODUCTION Hybrid composite materials such as Al/GFRP laminates show a superior fatigue behavior to general metallic materials [1-4]. In spite of it, the reason why the applicable fields were restricted is the delamination caused between the Al layer and fiber/epoxy one. This delamination greatly decreases the fiber bridging effect. Therefore, the fatigue behavior of Al/GFRP laminates based on the delamination had been evaluated. The delamination was not determined just by the crack even though the first parameter to control the delamination was the crack. The second parameter to control the delamination was delamination width (b). However, it is difficult to fine the quantitative study of delamination using the a-b relationship. Therefore, the aim of this study is to evaluate the delamination behavior by a-b relationship. The details are as follows. 1) Analysis of crack (a) - delamination width (b) relationship. 2) Estimation of delamination aspect ratio (b/a) * Correspondence Author, Address : San76, Wolgye-dong, Nowon-gu, Seoul 139-749, Korea Fax : +82-2-921-8532, E-mail: woong25(a!korea.ac.kr
238
Evaluation of Fatigue Delamination Behavior 4-O10.5
2.1 Cross-section of A-A1 Drilled holes ••s
!
80 150
(a) Geometries of AI/GFRP laminates specimen
Bending f I J Moment! E 3
f
Saw-Cut
i_^..0^^=^-——J E B ^ S ^ ^ p l
Q Attending H Moment
Aluminum alloy UD Glass/epoxy: [0]2 (b) Cross-section of AI/GFRP laminates specimen
F I G U R E 1 Geometries and cross-section o f AI/GFRP laminates (unit: mm)
delamination area rate {(AD)N/(AD)Aii) relationship. 3) The effect of the b/a on the delamination shape factor (fs) and delamination growth rate (dAr/da). Through the above facts, the new parameters required for the delamination evaluation of the AI/GFRP laminate was proposed and the applied results were discussed. FABRICATION OF SPECIMEN AND EXPERIMENTAL METHOD Fabrication of AI/GFRP Laminates Specimen AI/GFRP laminates were manufactured as the 2/1 type that the unidirectional glass fiber/epoxy was inserted between two A15052 alloy sheets. During the curing, the postheating procedure was used to reflect the Differential Scanning Calorimeter (DSC) results of GFRP prepreg and it made the specimens more stable chemically. The geometries of AI/GFRP laminates were shown in Figure 1. Pre-crack was made at the low edge of the specimens by a wheel cutter and four holes were drilled at the fixing area of specimens. Fatigue Test Method The fatigue tests were performed by the bending & torsion fatigue testing machine (TB-10B, Shimadzu Co.) whose maximum moment was 98 N-m. The cyclic bending moment of 3.92 N-m was applied and the fatigue cracks were measured at 100 magnifications by the traveling microscope. C-scan (Mi-SCOPE exla, Hitachi Co.) was used to obtain the delamination images between the Al alloys sheet and glass-fiber/epoxy one and those of corresponding cyclic delamination were recorded. RESULTS AND DISCUSSION Relationship Between Crack Length (a) and Delamination Width (b) Unlike the monolithic Al alloy, AI/GFRP laminates did not show the sudden change of the crack growth with increasing of cycles [3]. During the second half of loading, this crack growth was the same as that of the first half of loading even though increasing of the crack length caused decreasing of ligament. Consequently, linear a-N relationship was obtained as Figure 2 (i). This phenomenon resulted from the stress bridging effect of fiber laminates. However, if the crack propagated the delamination field between the Al alloy layer and the glass-fiber/epoxy one was initiated and grown. When the major axes of delamination expansion direction were determined as x- andy- direction, it was know that the delamination length of x-axis direction was equal to the crack length. In the meantime, the delamination width (b) corresponding to ^-direction was broadened normal to the crack growth direction. From these facts, a lot of information about delamination behavior could be obtained using the a-b relationship. The triangle model (c=l) was selected for this study. If the triangle model was applied, the contour (c) and delamination area (AD) could be obtained easily by the a-b. The calculation of the b was carried out by the C-scan
Evaluation of Fatigue Delamination Behavior
239
c = 1, Triangle*
Bendin<| Momer t = 3.9N Stress Ratio (R) = -1
40
c = 2, Ellipse-I* B
I 30
c = 3, Ellipse-M* Delamination zone
Crack Length, a
CO D) 2 0
10
o
r 0
\DelE
Bending Fiber moment | Orientaion
Vidth. b
u y
1x10 5
2x10 5
3x10 5
4x10 5
L.
5x10 ;
*: Delamination contour type
Number of cycles, N (No.) (i) Crack length (a) - delamination width (b) relationship
(ii) Configuration of delamination zone
FIGURE 2 The relationship between the crack length (a) and the delamination width (b)
images of Figure 3. They were used to measure the basic elements of delammation such as width (b), contour length (2c) and area (AD). The a-b relationship in Figure 2 and Figure 3 was investigated. It was as follows. While the crack growth showed linearity from the beginning to the end of cyclic loading, the increase rate of b became lower along a quadric curve. Examining the increase of a and b, a seemed to be equal to bfromthe beginning to N = 1.5 x 105 cycles but a was greater than b after N~ 1.5 x 105 cycles. After b became about 18 mm, the growth rate of b was slow. This phenomenon could be observed by the delamination images in Figure 3. The above regions (a) ~ (e) of Figure 3 showed a = b and the middle ones (f) ~ (k) of Figure 3 mean a > b. The bottom ones (1) ~ (o) of Figure 3 were the independent area where only the delamination grow after Al alloy sheet was fully fractured. Relationship Between the Delamination Aspect Ratio (b/a) and the Delamination Area Rate ((AD)N/(AD)AU)
It was known that the growth rate of crack was constant but that of b was decreased with increasing of Nor a/Wby the examination of the a-b relationship. Using a-b relationship,
(a) 3.0x10" cycle
(b) 6.0 x 10" cycle
(c) 9.0 x 10" cycle
(d) 1.2 x 10 5 cycle
(e) 1.5 x 10 5 cycle
(f) 1.8 x 1 0 5 cycle
(g) 2.1 x 10= cycle
(h) 2.4 x 10 5 cycle
(i) 2.7 x 10 5 cycle
(j) 3.0 x 10 5 cycle
(k) 3.3 x 1 0 5 cycle
(I) 4.2 x 10 5 cycle
(m) 4.5 x 10 5 cycle
(n) 4.9 x 10 5 cycle
(o) 5.1 x 10 5 cycle
FIGURE 3 Ultrasonic C-scan images of the delamination shape parameters (a, b, c) in Al/GFRP laminates
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Evaluation of Fatigue Delamination Behavior
a new parameter such as the delamination aspect ratio (b/a) was suggested to obtain the delamination growth characteristic of the longitudinal direction (x-direction) and the longitudinal transverse direction (y-direction). A new parameter such as the delamination area rate ((AD)NI(AD)AU) was also proposed to calculate the growth rate of AD using an area rate (the total area ((AD)AH) to be observed for the delamination over the delamination area ((AD)N) at the specific cycle), b/a - a/W relationship as well as (AD)NI(AD)AU - a/W was shown in Figure 4. b/a was steadily decreased as a/W was increased. The reason was while the growth rate of crack was constant with increasing of a/W. The growth rate of b was gradually decreased. On the other hand, the growth rate of (AD)NI(AD)AII was slowly increased as a/W was increased. While a/W was increased, the growth rate of b was decreased but that of a was constant. It resulted in the gradual increase of (AD)N/(AD)AH- If the growth rate of b was arithmetic, which of AD could be geometric. It was possible to observe the sudden increase of the delamination after a/W= 0.8. At first, it was guessed that the growth rate of crack would be faster due to the expansion of the damaged region if (AD)NI(AD)AU became increased. Consequently, the crack growth characteristic was linear tendency as shown in Figure 2 (i). In other words, it was clear that the magnitude of AD did not affect the crack growth characteristics. The Effect of Delamination Aspect Ratio (b/a) on the Delamination Shape Factor (fs) and on the Delamination Area Rate ((AD)NI(AD)AU) It was shown that b/a was decreased as a/W was increased. It was believed that the change of b/a could affect a major parameter to determine the delamination shape factor (fs) and the delamination growth rate (dAo/da). Considering b/a as well z&fs and dAo/da proposed by previous research [5], it was discussed at this section whether any change could be made. It was confirmed that the delamination growth depended on the crack length (a) rather than on the number of cycle (N) from the previous researches. The equation to relate the expansion ratio of AD to the increase of crack length was called the delamination growth rate (dAo/da) and was written as Equation (1). Where, fs was called the delamination shape factor. fs would be changed by the delamination type of the triangle (c=l), the ellipse-I (c=2) or the ellipse-I (c=3) like c suggested in Figure 2 (ii). Considering b/a,fs could be written as Equation (2). Where, s and D were the saw-cut length and the sum of the saw-cut and the crack lengths, respectively. Number of Cycles, N 1x105
2x105
3x105
4x105
1.4
5
1.2
1.2
b/a
1.0 DC •3
0.8
2
0.8 S TO
0.6 0.4
0.4
0.2
O oo0
0.0 -0.2 0.0
0.0 JS 0.2
0.4
0.6
0.8
1.0
Normalized Crack Size, a/W
FIGURE 4 Delamination aspect ratio (b/a) - normalized crack size (a/W) relationship and delamination area rate ((AD)i/(AD)Aii) - normalized crack size (a/W) relationship in Al/GFRP laminates
Evaluation of Fatigue Delamination Behavior
241
They were clearly demonstrated in Figure 2 (ii). c = 1,2 and 3 represent the delamination of triangle, ellipse-I and ellipse-II, respectively. (1)
= 1. / , = i l 4 ,
C = 2, / , = * ! - -M
-C = 3, / , = & , ! - ^
(2)
Figure 5 (i) showed the changing appearance of/j (fsi,fs2,fs3) obtained from the above equations as a/W was increased. The fs of ellipse-II (fsi) was greater than that of ellipse-I (fsi) and that of triangle (fsi) was the smallest in Figure 5 (i). While fS3 was three times bigger than/j; at the beginning, the difference between^ andfsi was slowly decreased as a/W was increased. Especially, the change offsi,fs2 and/j? was not observed from a/W= 0.8 and their differences were also very small. Consequently, it was known that the effect of delamination shape on the delamination behavior was strong at the beginning but it was diminished as the crack grew. The effect of three delamination shape factors (fsnfs2 and fsi) on the behavior of dAr/da was considered in Figure 5 (ii). Figure 5 (ii) showed the behavior of dAr/da according to the increase of JV. There were two cases that three/? (fsi, fs2,fsi) were considered for dAr/da and were neglected. In general, dAr/da of the former was lower than that of the latter. Particularly, dAr/da offsi became lower than those of/b and fss. hi other words, it was known that dAr/da of the triangle was distributed at lower part than those of the ellipses. For ellipses, it was clear that dAr/da oifs2 was also lower than that of/sj. The average offsi,fs2 and/jj obtained from Figure 5 (i) were fsi = 0.57, fS2 = 0.70, fs3 = 0.87. Comparing them with Figure 5 (ii), they were as follows. When dAr/da to consider/s compared with dAr/da to neglect fs, the latter was regarded as 100%. It was shown that dAr/da to consider fsi,fs2 and/s, were decreased about 43 %, 30 % and 13 %, respectively. Therefore, among three dAr/da to consider fs, dAr/da of the ellipse-II (fsi) was the greatest but dAr/da of the triangle was the smallest. It was reported by Roebroeks [6] that the fiber bridging effect of the triangular delamination was superior to that of the ellipse ones. For this reason, it was believed that the superiority of thefiberbridging effect
2.0
10J
- Delamination Contour Factor C = 1 : Triangle, fs1 = (b/a) (1 - (s/D)) C = 2 : Ellipse-I, f = (b/a) (1 - (s/D))"2 C = 3 : Ellipse-II, fs3 = (b/a) (1 - (s/D)2)"
T3 CD
102
• o A V
dAD/da c = 1, dAD/da = fs,(dAD/da) c = 2, dAD/da = y d A D / d a ) c = 3, dAD/da = fS3(dAD/da)
e CD
E c = 2,fS2 = (b/a) ( 1 - (s/D))"
ID Q
0.2
0.4
0.6
0.8
1.0
Normalized Crack Size, a/W (i) fs — a/W relationship
S2
10'
c = 3, f
S3
= (b/a) (1 - (s/D) 2 ) 1 ' 2
JX!
10°
10b
Number of Cycles, N (ii) dAc/da - N relationship
FIGURE S The effect of delaminaion shape factors (fsi,fs2 and_/jj) on the delamination growth rate {dAjJdd) in Al/GFRP laminates
242
Evaluation of Fatigue Delamination Behavior
made dAr/da lower. It implied that dAz/da of the triangular delamination became lower than that of the elliptical ones. This result agreed well with the conventional ones. CONCLUSIONS Using the crack (a) - delamination width (b) relationship, the delamination behavior of Al/GFRP laminates was evaluated and the next conclusions were obtained. (1) While the crack growth of Al/GFRP laminates showed linearity from the beginning to the end of cyclic loading, the growth of delamination width (b) was lowered along the quadric curve as the number of cycles (N) was increased. Therefore, it was known that the a-b relationship reminded a = b at the beginning of cyclic loading but a was greater than b after the middle of cycling. (2) It was shown that the delamination aspect ratio (b/a) was slowly decreased and the delamination area rate ((AD)N/(AQ)AH) was increased as the normalized crack size (a/W) was increased. However, the crack growth was nearly constant from the beginning to the end of loading even though (AD)V'(AD)'AH was increased. Consequently, it was believed that the magnitude of delamination area was not the parameter to control the crack growth characteristic. (3) The delamination shape factor (fs) was changed by the delamination shape such as the triangle or ellipse./? of the ellipse-H (fsi) was greater than that of the ellipse-I (fsi) but that of the triangle (fsi) was less than that of the ellipse-I (fsi)- While the differences among fsi,fs2 sn&fs3 seemed greater at the beginning of loading, these differences were decreased and became constant as the crack grew. Namely, the effect of the delamination shape on the delamination behavior was strong at the beginning of the cyclic loading but it was gradually diminished according to the increase of a/W. (4) Considering the effect of the delamination shape factors {fsi,fs2 and/b) on dAp/da, it was clear that dAr/da of the triangle was lower than that of the ellipse. This result was well coincident with the previous work that the fiber bridging effect of the delamination triangular shape was superior to that of the elliptical ones. ACKNOWLEDGEMENT This work supported by grant No. R01-2003-000-10567-0 from the Korea Science & Engineering Foundation.
REFERENCES 1.
Marissen, R. 1988. "Fatigue Crack Growth in ARALL ; A Hybrid Aluminum-Aramid Composite Material : Crack Growth Mechanism and Quantitative Prediction of the Crack Growth Rates," Ph. D. Thesis, Delft Univ. of Tech., Netherlands. 2. Guo, Y. J. and Wu, X. R. 1999. "Bridging Stress Distribution in Center-Cracked Fiber Reinforced Metal Laminates: Modeling and Experiment," Engineering Fracture Mechanics, Vol. 63, pp. 147-163. 3. Takamatsu, T., Matsumura, T., Ogura, N., Shimokawa, T. andKakuta, Y. 1999. "Fatigue Crack Growth Properties of a GLARE3-5/4 Fiber/Metal Laminates," Engineering Fracture Mechanics, Vol. 63, pp. 253-272. 4. Jin, Z. H. and Mai, Y. W. 1997. "Residual Strength of an ARALL Laminate Containing a Crack," Journal of Composite Materials, Vol. 31, No. 8, pp. 746-761. 5. Song, S. H. and Kim, C. W. 2003, "The Analysis of Fatigue Behavior Using the Delamination Growth Rate and Fiber Bridging Effect Factor in Al/GFRP Laminates," Transactions of the KSME, A, Vol. 27, No. 2, pp. 317-326. 6. Roebroeks, G. H. J. J. 1987. "Constant Amplitude Fatigue of ARALL-2 Laminates," Report LR-539, Dept. of Aerospace Engineering, Delft Univ. of Tech., Netherlands.
The Effect of Stitch Distribution and Stitch Pattern on Mode I Delamination Toughness of Stitched Laminated Composites Michael D. K. Wooda, Xiannian Suna, Liyong Tonga*, Anthony Katzos and Adrian Rispler a School of Aerospace, Mechanical and Mechatronic Engineering, The University of Sydney University, New South Wales 2006, Australia b
Boeing subsidiary, Hawker de Havilland, Australia
This research is part of the ARC SPIRT program in collaboration with Boeing subsidiary, Hawker de Havilland and Boeing Phantom Works, Seattle, USA
ABSTRACT In this paper, a modified double cantilever beam (MDCB) test is performed on Vectran® stitched laminated composites with varying stitch distributions and stitching patterns. The woven carbon fibre plies were laid-up in a symmetrical manner [0,±45,90]2 then stitched in a dry preform state followed by a resin film infusion (RFI) stage. To prevent the stitched specimens from failing in flexure, a known failure mode for such samples, thick aluminium Al-1050 reinforcing tabs were adhesively bonded to either side of the composite specimen along with loading blocks. An INSTRON5567 screw-driven testing machine was used to test the specimens at a crosshead velocity of 0.5mm/min with crack lengths, crack opening displacements (COD) and peak load data being recorded after the crack front had propagated several millimetres. A variation of the compliance method was used to post process the test data revealing differences in strain energy release rates (SERR), G/r, for both plain stitched and zigzag stitched specimens, with varying stitch distributions and with stitch densities of approximately 0.033 stitches/mm2. Keywords: Modified Double Cantilever Beam, Stitching, Stitching Distribution, Stitching Pattern, Strain Energy Release Rate
INTRODUCTION Laminated carbon composites are well known to possess excellent specific strength in weight critical applications but poor interlaminar strength especially in relation to damage tolerance. It is this specific strength that has ensured composites their outstanding suitability for the aircraft industry [1]; however the second factor reduces the materials resistance to damage, in particular low velocity impact.
* Correspondence Author. Email: rtong(a),aeromech.usyd.edu.au Fax:+61-2-93514841 Phone:+61-293516949
244
Effect of S titch Distribution and S titch Pattern
To retard progressive delamination and subsequent catastrophic failure, laminated composites can be reinforced in the through-the-thickness (TTT) direction by means of stitching [2] or z-pin reinforcement [3]. Z-pinning, as it has come to be known, involves the mechanical insertion of solid or fibrous independent pins aligned in the TTT direction of the laminate. Stitching of laminated composites is similar to its textile counterpart, differing only in stitch type, where a modified lock stitch is used. Stitching can be interconnected or independent with the latter requiring an extra machining process to shear off the surface loop of the continuous stitch. Presently there is significant empirical [4] and analytical [2] data available supporting the positive contribution of TTT reinforcement in bridging delamination cracks, with many researchers reporting the importance of stitch fibre diameter, stitching density and interfacial shear stress. Recent finite element analysis (FEA) conducted by Sun et al [5] has shown that stitch distribution is an influential parameter when predicting the improvement in mode I delamination toughness. The research showed that for identical stitch densities with varying stitch distributions, the resulting R-curve behaviour can be highly dissimilar. Furthermore, Lui et al [6] concluded through compression after impact (CAI) experiments that stitch pattern can change the shape of the impending delamination but not the affected area. hi this paper, Mode I delamination toughness experiments are conducted on stitched laminated woven carbon fibre modified double cantilever beam (MDCB) specimens. Both plain (straight interconnected) and zigzag (interconnected) stitching are used. The results bore behavioural resemblance to those found in [5] with patterns of identical stitch densities but varying stitch distributions producing different results. DCB SPECIMENS AND TESTING PROCEDURE Ideal for quantifying the mode I delamination toughness of a laminated composite is the mode I interlaminar fracture toughness test for fibre-reinforced polymer matrix composites [7]. The test specifies specimen (Figure 1) dimensions of at least 125.0mm (5.0 in.) long and nominally 20.0 to 25.0mm (0.8 to 1.0 in.) wide, however, specimen width is not a critical parameter. The laminate thickness should be between 3.0 and 5.0mm (0.12 and 0.2 in.) with a variation over the length of the specimen of no more than 0.1mm. A release film insert 15/an in thickness was placed in between the centre plies of the laminate lay-up to facilitate crack initiation. To avoid premature failure, in the specimen substrate arms, in flexure; thick aluminium tabs were bonded to either side of the test specimen. Loading blocks were subsequently adhesively bonded to the 1050 Aluminium tabs to enable loading. In order to assist in crack initiation and avoid any instability due to bonding through the release film insert, the pre-crack can be wedged open with a razor blade. The specimen is then mounted on an INSTRON 5567 testing machine equipped with a 10£N load cell. The specimen is then pin-loaded using displacement control where the cross-head rate is preset at 0.5mm/min in order to enable slow crack propagation. Once the crack has progressed several millimetres the specimen is unloaded at the same rate and the crack tip marked; this cycle of loading and unloading takes place 15-20 times for every specimen or until failure occurs. A digital data logger was used to continuously record the load verses cross-head displacement over time.
Effect of Stitch Distribution and Stitch Pattern
245
FIGURE 1 Specimen geometry concealing the lower tab-loading block assembly
STITCHING Four specimen groups were manufactured in this program using an industrial sewing machine adjusted to produce a modified lock stitch (MLS). A control batch with no TTT reinforcement, two sets of plain stitched specimens and one set of zigzag specimens. It should be noted that the zigzag stitch is incapable of incorporating a MLS. Over all the stitched specimens the stitch density was maintained constant at approximately 0.033stmm"2. Shown below are schematics of the stitched specimens.
.Stitching
4.06
i
W
W
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-•
•
o
-•
•
o
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•
o
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•
o
5.0 ' 5.0' 25.0
1
5.0'
25.0
5.0'
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(a)
(b)
(c)
FIGURE 2 (a) Plain short pitch (PSP) (b) Plain long pitch (PLP) and (c) Zigzag stitched
INTERLAMINAR FRACTURE TOUGHNESS CALCULATION The direct method [8], like all compliance methods, depends on the Irwin-Kies equation relating strain energy release rate (SERR) Gic to the compliance, C, which is the ratio of deflection over load. The method allows for mode I SERR values to be calculated as long as the crack propagation is stable. The mode I interlaminar fracture toughness may be written as follows
.EL w
El
5Guhcw
(1)
Effect of Stitch Distribution and Stitch Pattern
246
Where P is the peak load, w and h the specimen width and thickness respectively, El, the flexural rigidity takes into account the thick aluminium tabs as well as the carbon composite, x is t n e correction factor which takes into account the additional deflection due to rotation of the beams, Gn is the interlaminar shear modulus and a is the crack length, hi this paper, the critical strain energy release rate is taken to be the peak value prior to the first stitch breaking. RESULTS AND DISCUSSION Shown in Figure 3 are the results of the MDCB test for the unstitched specimens. Figure 3a depicts the load versus crack opening displacement (COD) curve for the first specimen only. The peak load for this specimen type occurs, on average for unstitched specimens, at approximately 1050N. The composite toughness follows an almost linear path until it reaches an asymptotic or steady state value. The length of this linear path is due to the increased length of the process zone present in MDCB tests. This SERR value is referred to as the critical SERR Gic and occurs at a crack length of roughly 60.0mm for the unstitched specimens. At this stage if the SERR value continued to increase it was noted in the experimental log that some form of fibre bridging across the crack wake was present. The average critical SERR for the unstitched specimens was 0.78KJ/m2. The G/c value, presented in this paper, is taken to be the point at which the first stitch has failed.
1.4 . UnstitchecM 1.2
600
400
I III!/, 1
1
x
»
x
x Unstit ched4 ••
x Unstit ched 5
•
x
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*
*
' A
S 0.6 0.4 I
0.2 0
2
ched2 . Unstitched3
3 COD (mm)
4
: • "
60 a (mm)
100
120
FIGURE 3 a) Load verses COD for unstitched specimen 1, b) GIr - Aa curve for all unstitched specimens
In comparison to the unstitched specimens; the zigzag stitched specimens with a stitching density of 0.0336stmm"2, shown in Figure 4a and 4b, performed considerably better with an average peak load of 2500N, roughly 2.5 times greater than that of the unstitched specimens. As the crack front reached the first row of stitches, the R-curve slope raises rapidly with an increase in the number of bridging entities until the crack wake is saturated. The critical average SERR, G/c, is achieved in the region of 53.0mm at a value of 3.47KJ/m2. The scatter of data points after 53.0mm can be attributed to the fracture behaviour of the stitch fibres. Since the zigzag stitch cannot produce an ideally modified lock stitch [9], due to the necessity for even tension on both the needle and bobbin threads respectively, the lock location cannot be controlled effectively. This reason alone contributed to the variability in asymptotic GIr values
Effect of Stitch Distribution and Stitch Pattern
247
for zigzag stitches with close to 50% of all stitches failing and pulling out to either side of the MDCB specimen.
5
At
x Stitch .ocatior
4.5
• Zigzag 1
4
• Zigzag 2
1000
• . . .
x Zigzag 4 « Zigzag 5
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\
A
-
• Zigzag 3
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•
*
* * x
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*
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1
X—X—X-) —X—X—X-
1 0.5 ***** 0 COD (mm)
20
40
60 a (mm)
80
100
120
FIGURE 4 a) Load verses COD for zigzag stitched specimen 1, b) Glr - Aa curve for all zigzag stitched specimens
For both PLP and PSP stitched specimens shown in Figure 5a, 5b, with stitching densities of 0.0372stmm"2 and 0.0348stmm"2 respectively, the results show clear differences in Gjc values and R-curve behaviour. With a critical Gjc of 2.82KJ/m2 achieved at a crack length of 55.0mm, the PSP specimens obtained an average peak load of 2275N. The PLP stitched specimens attained a critical GIc equal to 4.47KJ/m2 at roughly 55.0mm, 58% and 29% higher than for PSP and zigzag stitched specimens respectively. The PLP distributed stitch pattern reached the highest peak load of 2780N, 22% and 11.2% larger than for PSP and zigzag specimens respectively. The main reason for this increased load capacity of the PLP stitch distribution could be put down to a larger number of bridging fibres being utilised in the first row of the PLP specimens. As the crack front propagates, the induced moment at the first stitch row increases with increasing crack growth making the distribution of the stitches in the crack wake significant. The increased potential for stitching fibre abrasion sustained during the PLP sewing process as well as increased stress concentrations at the stitch lock due to the small stitch pitch distances involved in this stitch pattern may have also reduced the peak load and critical G/c values. This is reflected in the failure data where 88% of all PLP stitches failed at the surface loop and pulled out to the needle thread side where as 96% of all PSP stitches failed at the surface loop. However, the results show that stitch density alone, as a defining parameter, is not sufficient in predicting the potential resistance to crack propagation. Stitch distribution defined by stitch pitch distance and stitch line spacing must be thoroughly considered when tailoring material properties.
248
Effect of Stitch Distribution and Stitch Pattern 4.5 x Stitch Location
x Stitch Location -
• PLP 1
4
• PLP 2
3.5
. PSP 1 .PSP2 •
• PSP 3
• PLP 3 • PLP 5 • •
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x
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. *
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i
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i
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p
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60 a (mm)
40
60 a (mm)
FIGURE 5 a) Glr - ha curve for all plain long pitch stitched specimens, b) G/r — ha curve for all plain short pitch stitched specimens
CONCLUSION The results suggest that for identical stitching densities, the R-curve behaviour, peak loading and asymptotic strain energy release rates can be highly dissimilar. When tailoring stitched CFRP properties, stitch distribution should be thoroughly considered. REFERENCES [1]
[2] [3]
[4]
[5]
[6] [7] [8]
[9]
A. P. Mouritz, M. K. Bannister, P. J. Falzon, and K. H. Leong, "Review of applications for advanced three-dimensional fibre textile composites," Composites Part A, vol. 30, pp. 14451461, 1999. K. A. Dransfield, L. Jain, and Y.-W. Mai, "On the Effects of Stitching in CFRPs-I. Mode I Delamination Toughness," Composites Science and Technology, vol. 58, pp. 815-827, 1998. G. Freitas, C. Magee, P. Dardzinski, and T. Fusco, "Fiber Insertion Process for Improved Damage Tolerance in Aircraft Laminates," Journal of Advanced Materials, vol. 25, pp. 36-43, 1994. A. P. Mouritz and L. K. Jain, "Further Validation of the Jain and Mai models for Interlaminar Fracture Toughness of Stitched Composites," Composites Science and Technology, vol. 59, pp. 1653-1662, 1999. X. Sun, L. Tong, M. D. K. Wood, and Y.-W. Mai, "Effect of stitch distribution on mode I delamination toughness of laminated DCB specimens," Composites Science and Technology, Accepted, 2004. D. Liu, "Delamination Resistance in Stitched and Unstitched Composite Plates Subjected to Impact Loading," Journal of Reinforced Plastics and Composites, vol. 9, pp. 59-69, 1990. ASTM D5528-01, "Standard Test Method for Mode I Interlaminar Fracture Toughness of Unidirectional Fiber-Reinforced Polymer Matrix Composites," 2001. L. K. Jain, K. A. Dransfield, and Y.-W. Mai, "Effect of Reinforcing Tabs on the Mode I Delamination Toughness of Stitched CFRPs," Journal of Composite Materials, vol. 32, pp. 2016-2026, 1998. K. Dransfield, C. Baillie, and Y.-W. Mai, "Improving The Delamination Resistance of CFRP by Stitching - A Review," Composites Science and Technology, vol. 50, pp. 305-317, 1994.
Dynamic Analysis for Delaminated Composites with Arbitrary Shaped Multiple Delaminations Based on Higher-Order Zig-Zag Theory Maenghyo Cho , Jinho Oh School of Mechanical and Aerospace Engineering, Seoul National University San 56-1, Shillim-Dong, Kwanak-Ku, Seoul 151-744, Korea Jun-Sik Kim Department of Aerospace Engineering, The Pennsylvania State University, University Park, U.S.A. Gun-In Kim Department of Weapon Engineering, Korea Military Academy, P. O. Box 77, Gongnung, Nowon, Seoul, Korea
ABSTRACT A finite element based on the efficient higher order zig-zag theory with multiple delaminations is developed to refine the predictions of frequency and mode shapes. Displacement fields through the thickness are constructed by superimposing linear zig-zag field to the smooth globally cubic varying field. The layer-dependent degrees of freedom of displacement fields are expressed in terms of reference primary degrees of freedom by applying interface continuity conditions as well as bounding surface conditions of transverse shear stresses including delaminated interfaces. Thus the proposed theory is not only accurate but also efficient. This displacement field can systematically handle the number, shape, size, and locations of delaminations. Through the dynamic version of variational approach, the dynamic equilibrium equations and variationally consistent boundary conditions are obtained. Through the natural frequency analysis and time response analysis of composite plate with delaminations, the accuracy and efficiency of the present finite element are demonstrated. The present finite element is suitable in the predictions of the dynamic response of the thick composite plate with multiple delaminations.
INTRODUCTION Recently, development of advanced composite materials is paid special attentions to their potential applications of aircraft, marine, and automobiles owing to their high specific strength and stiffness. In particular, analysis of dynamic characteristics is quite important to understand the stability and strength of structures. Especially for structural design in the critical environments, highly accurate dynamic analysis is required. For the enhanced analysis of laminated composite plates, so-called "zig-zag" theories have been paid a lot of attentions because of their accuracy and efficiency in the ply-level analysis. Correspondence Author : Maenghyo Cho, Fax : +82-2-886-1693, E-mail address: [email protected]
250
Dynamic Analysis for Delaminated Composites
Most of the theories assume that interfaces are perfectly bonded. However, in many applications, this assumption is not adequate for the prediction of the behaviors of composite laminates. Low-speed impacts by foreign objects or imperfections in the manufacturing process may generate multiple delaminations in composite laminates. Strength and stiffness of composite structures with delaminations decrease significantly compared to the undelaminated composite plates. For the analysis of laminated plates with arbitrary shaped multiple delaminations, finite element method is a suitable choice to treat the general loading, boundary conditions, layups, and geometry. Even though finite element based on layerwise plate theory [ 1 ] can provide an adequate framework for the delamination analysis, this theory is not computationally efficient since the number of degrees-of-freedom of this theory depends upon the number of layers. Thus to reduce the active degrees-of-freedom of the problem, a global-local approach has been proposed in the refs [2-4]. In the present study, we focus on the dynamic version of composite laminated plates with multiple delaminations. The model is based on the efficient higher order zig-zag plate theory with minimal degrees of freedom. The violation of unilateral contact conditions in the delaminated region is prohibited by imposing contact constraints through the Lagrange multipliers. Eigenvalue problems and time responses are analyzed. The present results of natural frequencies and time responses are compared to those of the previously reported results. The numerical verification for the developed finite element is made on laminated composites with circular, elliptic, and rectangular shaped delaminations, respectively. The present finite element is suitable in the predictions of the dynamic response of the thick composite plate with multiple delaminations. Displacement Model Displacement field of composite plates with multiple delaminations is considered. The deformation behavior is assumed within the range of linear elasticity. The configuration of composite plate with multiple delaminations is shown in Fig. 1. Higher-order zig-zag in-plane displacement field with delaminations is obtained by superimposing zig-zag linear field and piecewise constant delamination field to the globally cubic varying field. The starting displacement field can be written as follows,
f
tfCz-z,)
i Delaminations
FIGURE 1 Configuration of laminated composite plate with multiple delaminations
(2)
Dynamic Analysis for Delaminated Composites
251
where u°a, w denote the displacement of a point O J on the reference plane. y/a are the rotations of the normal to the reference plane about xa axis. N is the number of total layers. D is the number of the delamination interfaces. H(z - zk) is the Heaviside unit step function. The terms u^,wd represent possible jumps in the slipping and opening displacements, which permit incorporation of delamination for laminated composites. The deformed schematic configuration and the kinematic variables are shown in Fig. 2. By applying top and bottom surface transverse shear stress free conditions and interface transverse shear stress continuity conditions, the following displacement field is obtained. (3) (4) 3A ,
in which,
(5)
The displacement field is the same as that proposed by Cho and Parmerter [5,6]. Finite Element Formulation To assess the validity of the dynamic version of EHOPTWD (Efficient Higher Order Plate Theory With Delamination) [7], a finite element is developed for two-dimensional problems. The present laminated plate theory which have been developed has second derivative of w(transverse deflection at the reference plane). Thus C1 continuous (slope-continuous) functions are required. However, it is well known in plate theory that it is difficult to impose normal slope continuity conditions at the interfaces between elements in arbitrarily oriented quadrilateral and triangular elements. The DKQ element developed by Batoz and Tahar [8] is the simplest elements which pass the patch test and satisfy Kirchhoff constraints. In the present study, we adopted the concept of DKQ element to overcome the continuity problem of deflection w and delamination deflection wd. For the four-noded quadrilateral element, nodal displacement vector is given by {a}e = [u°a, w ,
>a, u * , w'', w* f
(6)
Natural coordinates £ and 77 are used in the shape functions and coordinate transformation functions. The primary displacement unknowns are expressed in terms of nodal variables and shape functions as
FIGURE 2 Deformed configuration of laminates with multiple delaminations
252
Dynamic Analysis for Delaminated Composites u°=YN,u°., ud = u
I cct '
^^j
(7)
j
ex
(8)
K = 2] w.,
(9)
where Nt are the conventional bilinear shape functions, and Nai, Pai, and Haj are shape functions of the DKQ element. However, the DKQ element cannot define the transverse deflection inside an element. It only specifies along the edge of the element. When a mass matrix is required, the transverse deflection needs to be described within an element. Therefore to compute element mass matrix, a refined nonconforming quadrilateral element proposed by Cheung Y. K. [9] is adopted. NUMERIC EXAMPLES Eigenvalue Problems For the numerical evaluation of the performance of the proposed model, cantilever composite plate with center delamination is considered. The stacking sequence of the delaminated composite is [(0/90)2]s and the thickness of plate is 1.016mm. The plate has length a=127mm, and width b=12.7mm. The density is 1477kg/m2. The material properties employed in the present numerical examples are given in the ref. [10]. As shown in the Table. 1. First, second, and third bending natural frequency are predicted very accurately compared to the results of ref. [10]. First bending natural frequency is higher than those of the experiment results [10]. As the size of delaminated zone increases, natural frequency decreases. TABLE I (a) First bending frequency HOT 1 0
Present
81.75(Hz)
82.1
81.7(Hz)
78.16(Hz)
80.429(Hz)
80.8
80.2(Hz)
Delamination
Experi-ment
Nastran 10
length
10
3D (element)
0(mm)
79.83(Hz)
25.4(mm)
Theory
50.8(mm)
75.37(Hz)
75.136(Hz)
77.7
76.1 (Hz)
76.2(mm)
66.95(Hz)
66.531(Hz)
68.3
67.2(Hz)
101.6(mm)
57.54(Hz)
55.809(Hz)
59.8
56.1(Hz)
(b) Second bending frequency
Delamination
Nastran 10
length
3D (element)
0(mm) 25.4(mm)
HOT"'
Present
510.7(Hz)
513.4(Hz)
510.1(Hz)
504.1 (Hz)
499.6(Hz)
509.2(Hz)
Theory
50.8(mm)
478.6(Hz)
515.7(Hz)
488.1 (Hz)
76.2(mm)
399.3(Hz)
420.8(Hz)
385.7(Hz)
101.6(mm)
305.7(Hz)
346.7(Hz)
325.4(Hz)
Dynamic Analysis for Delaminated Composites
253
Dynamic Responses Deflection of intact zone and delaminated zone are obtained by using time integration considering Lagrange multiplier for penetration violation. fn the delaminated zone, when the relative displacement is positive, contact spring force is set to zero. On the contrary, if the relative displacement is negative, contact spring force is imposed. Dynamic response considering unilateral contact constraint is simulated in the Fig. 3. Dynamic response with rectangular and circular delamination is shown in Fig. 3. The rectangular and circular delamination size is 40% of whole structure. Thus, in the dynamic analysis, we can obtain the result that unilateral contact spring constraint can prevent penetration violation.
FIGURE 3(a) Dynamic response with one rectangular delamintion
0.010 •
— • — upper 1 IBVBT
— — uPpar2layer 0.005-
\ /
'
1
N "°°
0.00
0.01
0.02
0.03
0.04
0.05
0.06
FIGURE 3(b) Dynamic response with two rectangular delamintions Circular shape delamination
FIGURE 3(c) Dynamic response with one circular delamintion
254
Dynamic Analysis for Delaminated Composites
CONCLUSIONS In the present study, a finite element based on higher order zig-zag theory with multiple delaminations has been developed in order to analyze the dynamic behavior of composite plates with multiple and arbitrary shape delaminations. By imposing transverse shear stress free condition of top and bottom surfaces and stress interface continuity conditions between layers with delaminations, layer-dependent displacement variables were eliminated. Final displacement fields of undelaminated zone have only reference primary variables. In the delaminated zone, the minimal number of degrees-of-freedom is still retained. Thus this theory can be applied to the problems with many thick layers and multiple delaminations. Also, this theory can analyze composite structure with arbitrary shape delamination since the present non-conforming element can pass the bending patch test in arbitrary shaped quadrilateral mesh. Through the analysis of eigenvalue problem of composite plate with multiple delaminations, it is observed that the natural frequencies predicted by the present EHOPTWD are in good agreement with experiment data, HOT, and Nastran-3D solutions. The present finite element based on the zig-zag higher order theory demonstrated accurate predictions of natural frequencies and mode shapes for various types of delaminations in the thick plate range. REFERENCES 1.
Lee, J., Gurdal, Z., and Griffin, O. H. 1993. "Layer-Wise Approach for the Bifurcation Problem in Laminated Composites With Delaminations," AIAA J, Vol.31, pp. 331-338 2. Cho, M., and Kim, J. S. 1997. "Bifurcation Buckling Analysis of Delaminated Composites Using Global-Local Approach," AIAA J, Vol.35, pp. 1673-7676. 3. Cho, M., and Lee, S. G. 1998. "Global/Local Analysis of Laminated Composites With Multiple Delaminations of Various Shapes," Proceedings of the AIAA/ASME/ASCE/AHS/ASC 39th Structures, Structural Dynamics and Materials Conference, Long Beach, CA, AIAA, Reston, VA, pp. 76-86. 4. Kim, J. S., and Cho, M. 1999. "Postbuckling of Delaminated Composites Under Compressive Loads Using Global-Local Approach," AIAA J, Vol.37, pp. 774-777. 5. Cho, M , and Parmerter, R. R. 1992. "An Efficient Higher-order Plate Theory for Laminated Composites," Composite Struc, Vol.20, pp.113-123. 6. Cho, M., and Parmerter, R. R. 1993. "Efficient Higher Order Composite Plate Theory for General Lamination Configurations," AIAA J., Vol.31, No.7, pp.1299-1306. 7. Kim, J. S., and Cho, M., 2002. "Buckling Analysis for Delaminated Composites Using Plate Bending Elements Based on Higher-Order Zig-Zag Theory," Int. J. for Num. Meth. in Eng., Vol.55, No. 11, pp.1323-1343. 8. Batoz, J. L., Tahar, M. B. 1982. "Evaluation of a New Quadrilateral Thin Plate Bending Element," Int. J. for Num. Meth. in Eng., Vol.18, pp. 1655-1677. 9. Cheung, Y. K., Zhang, Y. X., and Wanji, C. 2000. "The Application of a Refined Non-Conforming Quadrilateral Plate Bending Element in Thin Plate Vibration and Stability Analysis," Finite Element in Anal, and Design, Vol.34, pp. 175-191. 10. Chattopadhyay, A., Radu, A. G., and Dragomir-Daescu, D. 2000. "A Higher Order Plate Theory for Dynamic Stability Analysis of Delaminated Composite Plates," Computational Mechanics, Vol.26, pp. 302-308.
PartV
Design and Optimisation
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Application of Stochastic Optimization to Reconstruction of Random Microstructures Ryszard Pyrz Aalborg University, Denmark Bogdan Bochenek Cracow University of Technology, Poland
ABSTRACT In the present paper the simulated annealing procedure is used to reconstruct plane and spatial dispersions of inclusions as observed on reference images of respective microstructures. The dispersion of centres of particles serve as reference distributions for reconstruction. The integral correlation function is used to define an objective function, which is identified as a sum of squared differences of nodal points of the integral correlation function for a reference and reconstructed dispersions. The reconstruction process is subject to various types of constraints. The geometrical constraint of topological entropy introduces a measure of arbitrariness of the polygonal or polyhedral tessellation associated with the point pattern of inclusion centers. The second geometrical constraint can be taken either as a pre-selected difference between a mean and standard deviation of distances of neighbouring inclusions or as a fulfilment of statistical t-tests and F-test for mean and standard deviation of distances, respectively. An attempt to implementation of constraints related to maximal stresses calculated at the inclusion interfaces has been also made and for plane dispersions effective results have been obtained. The results show, that reconstructed families of dispersions resemble the reference patterns with respect to selected criteria and, therefore, can be used for a further analysis to predict overall properties of underlying materials.
INTRODUCTION Mesoscopic modelling of microstructures can be performed for different systems. We may draw a major difference between those systems for which a volume averaging of selected representative volume element is sufficient, and those for which one has to construct many realizations of the microstructure. Volume averaging is often done by an effective medium approach, and is suitable for predicting properties such as stiffness or conductivity. Combination of ensemble-volume averaging has been used in [1-3] for determination of effective moduli of elastic particulate composites at not dilute concentrations and effective elastoplastic behaviour. However, fracture or electrical breakdown will depend on specific details in the microstructure and usually volume averaging is not acceptable. A short range * Corresponding Author, Institute of Mechanical Engineering, Aalborg University, Pontoppidanstraede 101, 9220 Aalborg East, Denmark, fax: (+45) 9815 9305, e-mail: [email protected]
258
Application of Stochastic Optimization
interactions between microstructural entities which are sensitive to their exact positions and sizes play a dominant role in non-homogeneous local variations of field quantities. For not dilute concentrations where the interaction effects between neighbouring inclusions are highly influential on the overall behaviour of the material, one must check the specific observable property for many realizations of the micro structure. Furthermore, only a tiny fraction of the original material specimen can actually be analyzed. Modern experimental techniques such as X-ray microtomography provide tools for visualization and non-destructive microstructural measurements on material samples [4-8]. In order to assess all details of the microstructure the sampling volume must necessarily be on a scale of a few hundred microns. Then an appropriate sampling procedure has to be applied to macrospecimen to guarantee that measured volume is statistically representative for a bulk material [9]. A destructive sampling procedure and the cost and labour associated with experiments might be not acceptable for many practical applications aiming to model material behaviour. It is mandatory to reconstruct the microstructure that would have similar geometrical characteristics as the microstructure acquired from the limited experimental observations. From this limited view we have tried to understand how the properties of the material relate to microstructure. The approach must necessarily be statistical in particular with respect to the measurements of the microstructure. A virtual experiment that allows to reconstruct the microstructure and subsequently to find an ensemble average of a given property provides means for this statistical assessment. The principle of this experiment is that we want to produce a statistical sample of the microstructure. The reference microstructure is characterized by a set of geometrical parameters and functions, which assign the microstructure to a certain family. Rather than simply generating and sampling the microstructure we pose an inverse problem of reconstructing the reference microstructure based upon the limited information contained in the descriptors. The solution is not unique as we are not in a position to know all necessary information for the reference microstructure. Nevertheless, this procedure may result in generation of realizations, which at least match the reference microstructure to the degree embraced by the selected geometrical descriptors [10,11]. In the present paper the methodology is presented for reconstruction of two- and three-dimensional microstructures of unidirectional fiber reinforced composites and particulate composites, respectively. The reference images are acquired with X-ray microtomography. The pair correlation function or its counterpart, integral correlation function serves as an objective function in the optimization procedure. Topological entropy and the stress interaction parameter are used as constraints for reconstructions of two-dimensional microstructures. The stress interaction parameter is expressed in geometrical terms but is correlated with stresses occurring at the fiber-matrix interphase. Thus not only the microstructure geometry but also field quantities are indirectly included in the reconstruction procedure. The three-dimensional reconstruction is formulated slightly differently. The calculation of stresses at an arbitrary point within a representative volume element with several hundreds of inclusions presents still computational problems [12,13]. Using the same objective functions as for the two-dimensional case and a first constraint on the topological entropy the second constraint is imposed either as a pre-selected difference between a mean and standard deviation of distances between neighbouring inclusions or as a fulfillment of statistical t-test and F-test for mean and standard deviation of distances, respectively.
Application of Stochastic Optimization
259
RECONSTRUCTION OF PLANAR DISPERSIONS The problem of reconstruction of dispersion pattern can be formulated as an optimization task. A sum of squared differences of nodal points of integral correlation function X(r) for a reference and optimized pattern is then the objective function and coordinates of inclusions center points are treated as the design variables for that problem. The objective function is minimized subject to two constraints. First constraint is imposed on values of topological entropy S, which represents first order correlation of the pattern [14]. A physical interaction between embedded inclusions is controlled by a second constraint imposed on stress interaction parameter C, which represents maximal radial stresses at inclusions interfaces [15]. A regular pattern with constraints, which correspond to the values of C and S selected for the reference dispersion is chosen as the starting configuration. Subsequent new configurations are generated by randomly disturbing coordinate of inclusion position. The Simulated Annealing global method has been chosen to solve the optimization problem [16]. The major advantage of Simulated Annealing over other methods is the ability to avoid becoming trapped at local minima. The reference image has been taken from X-ray microtomographic image of unidirectional glass-epoxy composite material, as illustrated in Fig.l. After several morphological image transformations, the centre points of fibres are recovered, which constitutes reference dispersion of points.
V-::-:::-.>"ri:-.':^/; ••.•;.•••::•. .'••'••.••'.•••• *'• ' , * * ' . ' • ' . ' .
(b)
(c)
FIGURE 1 Original reference image and three reconstructed patterns (a,b,c)
As can be seen from Fig.2, the optimization procedure leaves integral correlation functions of the reference and reconstructed pattern very close to each other. The constraints for reference pattern were found to be S=1.37 and C=13.6. The same parameters for reconstructed patterns a, b and c are respectively 1.31, 1.38 and 1.32 for the topological entropy S and 12.2, 13.0 and 12.4 for the stress interaction parameter. Lower values of C for reconstructed patterns indicate that we may expect slightly higher maximal radial interfacial stresses present in the reconstructed dispersion as compared with reference dispersion. This conclusion is supported in Fig.3, which shows longer tail values of the distribution functions for reconstructed patterns than for the reference pattern.
260
Application of Stochastic Optimization REFERENCE L JSTRUCTED
REFERENCE
L
02
0.25
\
\
\
-'
T 01
0.05
mum 0.2
, • 1'" 01b
- • i l l
025
0.05
0.1
distance r
0.15
(b)
distance r I
REFERENCE L JSTRUCTED
\ —
,
0.05
0.1
. , T-_• • « • _ • _ 0.15 02
0.25
(c)
distance r
FIGURE 2 Comparison of X(r) functions for reference and reconstructed patterns
1.2
1.4
1.6
1.8
2.0
1.2
Maximal radial stress [MPa]
A
I 3
1.4
1.6
1.8
2.0
2.2
Maximal radial stress [MPa]
reference — - reconstructed (c)
82 1.0
12
1.4
1.6
1.8
2.0
2.2
2.4
Maximal radial stress [MPa]
FIGURE 3 Stress density distributions for reconstructed patterns
If generated patterns are subject to the only constraint of non-overlapping, the corresponding density functions for the maximal radial stresses at fibre interfaces are shown in Fig.4 for three simulated patterns. There is a significant difference between stress density functions for this case and corresponding functions for reconstructed patterns. Tails of simulated dispersions are wider as compared with the reference pattern. It means that there are more fibres in the simulated dispersions than in the reference pattern, which are subject to interfacial stresses having values from the tails of the density distribution. Further discrepancies between reconstructed and simulated dispersions can be observed on the diagrams representing nearest neighbour distance distribution, Fig.5. While reconstructed dispersions provide reasonable distribution of
Application of Stochastic Optimization
261
nearest neighbour distances, the simulated patterns yield far too short nearest neighbour distances. The consequence of this fact is that corresponding stress density distribution exhibits longer and higher tails for larger stress ranges as observed in Fig.4.
— •°
reference simulated (a)
" • " reference — simulated (b)
3
I
1.0
1.2
1.4
1.6
1.8
2.0
2.2
2.4
1.0
Maximal radial stress [MPa]
k 1.5
2.0
2.5
3.0
3.5
Maximal radial stress [MPa]
reference simulated jc)
4
Der sity fu iction
u 0.85 1.10
Jl v^ 1.35
1.60
1.85 2.10 2.35 2-60
2.85
Maximal radial stress [MPa]
FIGURE 4 Stress density distributions for simulated patterns
0.10 0.08
A //X\\
. , ,-' ' *
I feference| I — simulated |
c g
? 0.06 t 004
1 1
; )L
-. \ V *•
0) Q
0.02-
20
Nearest neighbour distance [urn]
30
Nearest neighbour distance [u.m]
FIGURE 5 Nearest neighbour distance distribution for reconstructed and simulated patterns
RECONSTRUCTION OF SPATIAL DISPERSIONS The procedure for the reconstruction of spatial dispersions is slightly different as compared with similar procedure for planar dispersions. An efficient method to predict local stresses in representative volume element containing several hundreds of inclusions is non-existent [13] and, therefore the physical constraint related to the local stress distribution at interphases is not taken into account. Instead, the procedure of reconstruction of spatial reference pattern is performed with integral correlation function taken as the objective function and for the two cases of constraints set. The constraint imposed on values of topological entropy S is common for both cases but
262
Application of Stochastic Optimization
the second constraint is taken either as a pre-selected difference between a mean and standard deviation of distances of neighbouring inclusions (A) or as a fulfillment of statistical t-test and F-test for mean and standard deviation of distances (B). The t-test is performed to check if mean values for the analyzed distributions are equal (or not) at some confidence level. The result of F-test indicates whether variances (standard deviations) for these two distributions are (or are not) significantly different. The suitable significance level values are calculated for both tests in order to determine if these values fall within the zone of acceptance. This allows treat the distributions as consistent. Otherwise they have to be treated as different.
FIGURE 6 Reference dispersion (a) and its reconstructed counterpart (b) with Gauss radii distribution
- REFERENCE . RECONSTRUCTED
REFERENCE RECONSTRUCTED
— — »
-A \ "" 0.1
—
n.
- 1
0.15
distance r
Reference pattern
Reference pattern
Reconstructed pattern
Reconstructed pattern
IV
)5
Density line of distances to the neighbours
0.030
0.055
OQBO
0105
0.130
0.155
0.1E
Density line of distances to the neighbours
FIGURE 7 Integral correlation function and density of distances to the near neighbours for reference and reconstructed patterns with constraints A (left) and B (right)
Figure 6 shows reference and reconstructed patters for spatial dispersion with Gauss radii distribution. The comparison of results is shown in Fig. 7 where integral correlation functions and density of distances to the near neighbours are plotted for
Application of Stochastic Optimization
263
reconstructed patterns obtained when first (A) or second (B) constraints set has been applied. Values of topological entropy, mean neighbour distance and its standard deviation for the reference pattern differ from corresponding values of the reconstructed pattern by 2.8%, 9.9% and 6.2%, respectively. For constraints imposed on entropy and significance level values from t-test (for means) and F-test (for variances) values of topological entropy, mean neighbour distance and its standard deviation for the reference pattern differ from corresponding values of the reconstructed pattern by 1.7%, 2.6% and 2.7%, respectively. It is worth noting that a good agreement of results obtained for various formulations of optimization tasks is observed. CONCLUSIONS We have analysed reconstruction algorithm for spatial dispersions of inclusions. It can be used both as a method of data analysis or as a structural modelling tool to make predictions about the system, which are based on ensemble averaging methodology. The obtained solutions are not unique and a true test of their usefulness has to be performed on locally dependent physical phenomena such as nucleation and evolution of damages and initiation of failure. The reconstruction algorithm can be further extended to take into account other lower or higher order statistical descriptors that characterize the microstructure. Identification and reconstruction of micro structures with several descriptors would determine the extent to which a variety of statistical descriptors can reproduce the reference microstructure, thus shedding light on the nature of information contained in the descriptors. Furthermore, one can construct microstructures that correspond to a given set of descriptors and employ them to investigate and simulate physical phenomena where spatial patterns are of primary importance. REFERENCES 1. 2. 3. 4.
J.W. Ju and T.M. Chen, Ada Meek, 103, (1994), 103. J.W. Ju and T.M. Chen, Ada Meek, 103, (1994), 123. J.W. Ju and H. Tseng, Int. J. Solids Structures, 33, (1996), 4267. Kinney,J.H., Haupt, D.L., Nicols, M.C., Breunig, T.M., Marshall, G.W & Marshall, S.J. Nucl. Inst. andMeth. in Phys. Res. A., 347; (1994) 480. 5. Erre, D., Thomas, X., Mouze, D., Patat, J.N., Trebbia, P. & Cazaux, J. Surf. Interface Anal, 19, (1992), 89. 6. Pyrz., R. in Proc. World Aviation Conf. San Francisco, CA, paper no. 1999-01-5614,(1999). 7. Pyrz, R., in Porous, Cellular and Microcellular Materials, V. Kumar (ed), ASME MD-Vol.91, New York, 2000, p. 63. 8. Pyrz, R. & Nygaard, J., in Proc. Int. Conf. Composites in Construction - CCC2003, D. Bruno et al (eds.), Editoriale Bios, Cosenza 2003, p. 189. 9. E.R. Weibel, Stereological Methods, Academic Press, London, 1980, vol. 1 and vol. 2. 10.C.L. Yeong and S. Torquato, Phys. Rev. B, 57, (1998), 495. 11 .C.L. Yeong and S. Torquato, Phys. Rev. B, 58, (1998), 224 12.SchJ0dt-Thomsen, J. and R. Pyrz, in Proc. Int. Conf. Mesomechanics 2002, R. Pyrz et al. (eds.), Aalborg University, 2002, p. 75. 13,SchJ0dt-Thomsen, J. and R. Pyrz, in Proc. 14th Int. Conf Comp. Mat., H.T. Hahn and M. Martin (eds.), July 2003, San Diego, CD-ROM edition, ISBN 0-87263-685-2, paper no. 999. 14.Pyrz R., in Comprehensive Composite Materials, Vol.1 Fibre Reinforcement and General Theory of Composites, ed. T W Chou, Elsevier, 2000, London, 465. 15.Pyrz, R. and B. Bochenek, Int. J. Solids Structures, 35, (1998), 2413. 16.S. Kirkpatrick, C D . Gelatt Jr. and M.P. Vecchi, Science, 220, (1983), 671.
Optimal Design of Filament Wound Structures Based on the Semi-geodesic Path Algorithm Cheol-Ung Kim, Dong-Hoon Kang, Chang-Sun Hong and Chun-Gon Kim Division of Aerospace Engineering, KAIST, Korea
ABSTRACT This research aims to establish an optimal design method of filament wound structures. Filament winding is one of the most reliable and affordable production techniques for high performance composite structures such as pressure tanks, pipes and motor cases of rockets which are widely used in the aerospace application. However, the problem with filament winding is that the trajectory of the fiber path and the corresponding fiber angles cannot be chosen freely because of the stability requirement of fiber path. Most design and manufacturing of filament wound structures are based on manufacturing experiences, and there is no established design rule. In this research, possible winding patterns considering the windability and the slippage between fiber and mandrel surface were calculated using the semi-geodesic path algorithm. In addition, finite element analyses using commercial code, ABAQUS, were performed to predict the behavior of filament wound structures. On the basis of the semi-geodesic path algorithm and the verified finite element analysis method, an optimal design algorithm for filament wound structures was suggested using the genetic algorithm.
INTRODUCTION Finite element analyses, which can predict the deformation of filament wound structures, have been performed by many researchers. However, the results have been utilized only to understand structural characteristics of filament wound structures because some limited path equations were applied to the analyses. Even though such finite element analyses are helpful to design filament wound structures, most design and manufacturing of filament wound structures have been based on manufacturing experience and experiment. Thus, most designs are not optimized to account for filament wound structures. Previous research about filament wound structures are categorized into fiber path predictions, structural analyses and designs. However, there is no established design method for general filament wound structures under internal pressure satisfying given design requirements. In this study, an optimal design method of filament wound structures under internal pressure was established. Possible winding patterns considering the windability and the slippage between fiber and mandrel surface were calculated using the semi-geodesic path algorithm. In addition, finite element analyses using commercial code, ABAQUS, were performed to predict the behavior of filament wound structures. On the basis of the Correspondence Author : Division of Aerospace Engineering, KAIST, 373-1 Guseong-dong, Yuseong-gu, Daejeon, 305-701, Republic of Korea. Tel: (82-42) 869-3719, Fax: (82-42) 869-3710, Email: [email protected]
Optimal Design of Filament Wound Structures
265
semi-geodesic path algorithm and the finite element analysis method, an optimal design algorithm was suggested using the genetic algorithm and applied to a symmetric composite pressure vessel. SEMI-GEODESIC PATH ALGORITHM The design of a filament wound structure consists of the design of the mandrel shape and the calculation of the fiber path. In general, the mandrel shape can be determined by imposed design requirements such as internal pressure, volume and manufacturing convenience. When the liner or mandrel surface is given without considering winding patterns, various slip conditions must be taken into account. In this study, the semi-geodesic path equation was utilized in order to describe the realistic winding pattern on general filament wound structures [1]. da dx
1(A2 sin2 a-rr" cos2 a)~r'A2 sin a rA1 cos a
(1)
Equation (1) is defined on an arbitrary surface where a, x, 0, r, X are the winding angle, the axial coordinate parameter, the circumferential coordinate parameter, the radial coordinate parameter and the slippage tendency between the fiber and the mandrel. And more detailed derivation is shown in Reference [1]. By integrating Equation (1) with a known value, the winding angle can be calculated for the entire mandrel surface. There are two assumptions in the calculation of the thickness: the fiber volume fraction is maintained consistently and the number of fibers in a cross section is always constant. With these assumptions, the thickness along the longitudinal direction can be derived as follows:
Im, cos a, w 27ircosa
t =
r, cos a r cos a
(2)
where rc, ac, tc, np , w are radius, winding angle, thickness, number of fiber bands in a layer, and band width, respectively.
input
calculate B of • whole structure '
r(x), A,W.
calculate a range ! i
find possible a 1 i n S
^
1
^''
calci Iculate possible! wiiinding patterns |
FIGURE 1 Semi-geodesic path algorithm
266
Optimal Design of Filament Wound Structures
Windability is very important because some of the patterns calculated by Equation (1) maybe useless for the manufacture of filament wound structures unless uniform coverage is considered. The concept of windability was presented concurrently by Lossie [2] and Lowery [3]. Though notations used in the two studies are different, fundamental concepts are identical. The semi-geodesic path algorithm suggested in this study considers the fiber slippage and the windability. Figure 1 is the flow chart of the semi-geodesic path algorithm. In this research, a GUI (graphic user interface) based program was developed using Microsoft Visual C++ to perform the semi-geodesic path algorithm. PROGRESSIVE FAILURE ANALYSIS In this research, the 3-D layered solid element was utilized for finite element modeling. Progressive failure analysis was performed for the forward part of the ASTEB by the commercial code, ABAQUS. The finite element model are shown in Figure 2. In the modeling, C3D20 type elements with 20 nodes per element were used. The model has 100 elements and 1113 nodes. The modeling was performed for a 1.5 ° strip of a full tank using a cyclic symmetry boundary condition. The element size is larger at the center of the dome than that near the interface of the dome/cylinder and dome/polar opening. In the cylindrical part, 20 elements to the x-axial direction were enough to gain a converged result, but 60 elements to the meridian direction were used in the dome area. The winding path was calculated using the established semi-geodesic path algorithm. And, a preprocessor PREAFT which imposes the calculated path information on each element was developed and used. The inner pressure is 13.79 MPa (2000psi).
layered solid element 100elem. 1113nodes
cyclic symmetric
/•G plane symmetric -
x 5 scale
FIGURE 2 Finite element model and deformed shape
Optimal Design of Filament Wound Structures
267
In order to perform the progressive failure analysis, the modified Hashin's failure criterion, which is commonly used in recent studies and has many failure modes, was selected and applied to the analysis and optimal design in this research. For the purpose of failure analysis, a subroutine, USDFLD of ABAQUS ver 6.3 was coded to define the change of mechanical properties due to failure. An element failure is first identified and later the failed element is replaced with a degraded element. The degradation method should be carefully chosen because the results of progressive failure analyses often depend on the mesh size, degree of reduction, the increment size, etc. The equivalent properties of the damaged element might exist between zero values and solid ones. In this study, the stiffness reduction coefficient(SRC) varies from 0.1 to 0.9 by using Reddy's method [4]. When SRC is 0.1, the failed elements almost lose their load-carrying capacity. SRC of 0.9 means that the mechanical properties of the failed element do not decrease much compared to those of unfailed ones. The case of SRC<0.1 was excluded because the analysis becomes a conservative one. The deformation of each case is magnified 5 times in Figure 2. Figure 3 shows the comparison of results between the finite element analysis using the modified Hashin's failure criterion and the water-pressurizing test of our previous research [5]. It shows good agreement between them both in trend and quantity. Therefore, this analysis method is suitable for applying to the optimal design.
0.011 0.010
-FEM Experiment
0.009 0.008
°C
c
0.007
2
0.006
a
0.005
LL
0.004 0.003 0.002
0.001 0.000 -100
-80
-60
-40
-20
0
20
40
60
80
100
x (mm) FIGURE 3 Comparison of fiber strains between analysis and experiment
OPTIMAL DESIGN USING GENETIC ALGORITHM Design algorithm hi this study, the optimal design algorithm was established, which includes the semi-geodesic path algorithm, progressive failure analysis and genetic algorithms [6]. Figure 4 shows the flow chart of the suggested optimal design algorithm. The genetic algorithm controls the overall procedure. The windows based program for this algorithm was developed using C++ language, and it was named TDOTCOMFW.
Optimal Design of Filament Wound Structures
268 SL.11
y | Confirm design requirements Set winding angle
Calculate the range of winding angle
3: Find possible winding angles
Calculate the circumferential angfe of the whole structure
Calculate possible winding patterns
Generate initial population
Make input for FEA w
—i
save to winding f angle database V
Finite element analysis using ABAQUS -M
Change winding angle
Read output of FEA I I Genetic algorithm I I MSG path algorithm r^pa FEA
Calculate fitness
FIGURE 4 Optimal design procedure for axisymmetric filament wound structures
Application and verification The established optimal design algorithm was applied to a symmetric pressure tank of type 3 with a load sharing metallic liner for verification. The half shape of the tank is the same as the forward part of the ASTEB. The material of the composites is T800/Epoxy, and the liner is aluminum alloy 7075-T6. Basic design requirements are as follows: 1. Maximum operating inner pressure is 13.79 MPa(2000 psi). 2. The yield of the liner is not permitted. 3. The safety factor of the composite is 3.0. 4. The weight reduction is the most important goal of this design. The objective function is defined as follows J
>^Iiner
w r
yield ®yield ^^fiber
~
^f,design
>
^f,design
fiber
_ >°'liner ^ °'yield J
&
°fiber
fiber
>°'liner > °'yield
where Wmm , W, af4esign, aflber, ayidi, aliner are the possible maximum weight, the weight of the design point, the fiber directional strength considering the safety factor, the maximum fiber directional stress of the design point, the yield strength of the liner, and the maximum von Mises stress of the liner of the design point, respectively. Four design variables(the number of helical layers, the number of hoop layers, the winding angle of the cylinder part and the thickness of the liner) were set up and used in this optimal design because the goal of this application is the verification of the suggested algorithm and program. Each of them was separated to discrete values as many as 2 bits, 4
Optimal Design of Filament Wound Structures
269
bits, 5 bits and 4 bits in order to be applied to the genetic algorithm. From our previous researches, we determined the required parameters for genetic algorithm as follows; the population size was set as 100, the maximum number of generations as 100, the probability of crossover as 0.7, the probability of mutation as 0.1 and the tournament size for the genetic algorithm as 10. The initial seed value was generated randomly, and a total often optimal designs were performed. Table 1 shows the design results. Results of seven kinds were drawn. Among them, the best case, which satisfies the given design requirements, is a tank with a weight of 4.44 kg. TABLE I Design results Cases
Helical layer
Hoop layer
Winding angle
Liner
Weight
1
2
9
33.5°
1.9 mm
4.44 kg
2
3
10
34.5°
1.7 mm
4.47 kg
3
2
9
31.5°
1.9 mm
4.45 kg
4
3
10
28.0°
1.7 mm
4.50 kg
5
2
10
33.0°
1.9 mm
4.51kg
6
2
9
33.5°
1.9 mm
4.44 kg
7
2
9
33.5°
1.9 mm
4.44 kg
8
3
10
33.0°
1.7 mm
4.48 kg
9
3
9
34.0°
1.8 mm
4.58 kg
10
2
9
31.5°
1.9 mm
4.45 kg
CONCLUSION In this research, possible winding patterns considering windability and slippage were calculated using the semi-geodesic path algorithm. In addition, progressive failure analyses were performed to predict the behavior of filament wound structures. In particular, suitable element types and failure criteria for filament wound structures were studied, hi addition, on the basis of the semi-geodesic path algorithm and the finite element analysis method, an optimal design algorithm was suggested using the genetic algorithm. Finally, the developed design code was applied to a symmetric composite pressure vessel for verification. REFERENCES 1. 2. 3. 4. 5.
6.
J. Scholliers. 1992. "Robotic Filament Winding of Asymmetric Composite Parts," Ph. D Thesis (K.U.Leuven) M. Lossie. 1990, "Production Oriented Design of Filament Wound Composites," Ph. D Thesis (K.U.Leuven) P. A. Lowery. 1990. "Continued Fractions and the Derivation of Uniform-Coverage Filament Winding Patterns," SAMPE Journal, 26:57-64. Y. S. N. Reddy, C. M. Dakshina Moorthy, J. N. Reddy. 1995. "Non-linear Progressive Failure Analysis of Laminated Composite Plates," Int. J. Non-Linear Mechanics, 30(5):629-649. J. S. Park, C. S. Hong, C. G. Kim, C. U. Kim. 2002. "Analysis of Filament Wound Composite Structures Considering the Change of Winding Angles through the Thickness Direction," Composite Structures, 55:33-71. D. E. Goldberg. 1989. Genetic Algorithm in Search, Optimization, and Machine Learning, Addison-Wesley Publishing Company
Development of a Material Mixing Method for Topology Optimization of Multiple Material Structures Seog Young Han*, Soo Kyoung Lee, Jae Yong Park School of Mechanical Engineering, Hanyang University, 17 Haendang-dong, Sungdong-Gu, Seoul, 133-791, Korea
ABSTRACT This paper suggests a material mixing method to mix several materials in a structure. This method is based on ESO(Evolutionary Structural Optimization), which has been used to optimize topology of only one material structure. In this study, two criterions for material transformation and element removal are implemented for mixing several materials in a structure. Optimal topology for a multiple material structure can be obtained through repetitive application of the two criterions at each iteration. Two practical design examples of a short cantilever are presented to illustrate validity of the suggested material mixing method. It is found that the suggested method works very well and a multiple material structure has more stiffness than one material structure has under the same mass.
INTRODUCTION Topology optimization is very useful in making a conceptional design when considering weight and cost in the early design stage. An important development in topology optimization was made by Bendsoe and Kikuchi[l] who proposed the homogenization method, in which a material with an infinite number of microscale voids is introduced and the optimization problem is defined by seeking the optimal porosity of a porous medium using an optimality criterion. Mlejnek et al.[2] has accomplished shape and topology optimization using a simple energy method and a special type of function, that is, Kreisselmeier-Steinhauser function[3] for calculating effective properties. Recently, a simple method for shape and topology optimization, called Evolutionary Structural Optimization(ESO), has been proposed by Xie and Steven [4] and Chu[5], which is based on the concept of gradually removing redundant elements of the low stressed part of the material from a structure to achieve an optimal design. hi the area of MEMS, topology optimization techniques have also been actively applied. Especially, one of the thermal actuators, microgripper, has been designed by a bimorph structure[6] consisted of two materials with the different thermal strains, so that the improvement of its performance has been achieved by controlling the direction and magnitude of overall displacement effectively. hi this study, a material mixing method was suggested in order to obtain an optimal topology of a multiple material structure with the maximum stiffness under a static load based on ESO.
Correponding Author, School of Mechanical Engineering, Hanyang University, 17 Haendang-dong, Sungdong-Gu, Seoul, 133-791, Korea, FAX : 082-02-2298-46341, Email: [email protected]
Material Mixing Method for Topology Optimization
271
MATERIAL MIXING METHOD The explanation of the material mixing method for a bimaterial structure is given here in brief. Let the larger and the smaller stiffness and density of the two materials set material 1 and material 2, respectively. First of all, consider a design region made of material 1. Apply both the transformation and the removal lines for material transformation and element removal, respectively. As the first step, the elements having lower level of strain energy than the transformation line are transformed into material 2. As the second step, the elements having lower level of strain energy than the removal line which is established as the lower level of strain energy than the transformation line, are removed. An optimal topology can be obtained by iteration of this procedure at each iteration. Transformation and Removal Line TRANSFORMATION LINE The transformation line defined as eq. (1) is obtained from a journal paper [7] in this study. And the efficiency factor, a of strain energy in each element after stress analysis is defined as eq. (2). If a of a certain element is smaller than the transformation line, that is, eq. (3) is satisfied, the element is transformed from material 1 to material 2. TL = amm+Aax(
vol
5=1)"
(1)
V l
° ini,ial
« e = J ^r
(2)
a"
(3)
where, t] is the penalty factor and the threshold ratio Aa can be selected as very small value depending on the problem since it controls the range of the elements to be transformed. The elements on the area of diagonal lines under the transformation line as shown in Fig. 1 are to be transformed. This concept is similarly applied to the removal line. Penalty factor is induced to obtain an optimal topology effectively by controlling the range of the transformed elements, that is, gradually reducing the range as the number of iteration increases. It can be seen in Fig. 2 that the number of the transformed elements is reducing as iteration goes on. REMOVAL LINE The removal line was defined as eq. (4) in this study. If a of a certain element is smaller than the removal line, that is, eq. (5) is satisfied, the element is removed from the structure. The threshold ratio and the penalty factor were similarly applied for determination of the removal line. The removal line under the transformation line was obtained by controlling the sizes of the threshold ratio and the penalty factor. Procedure of Topology Optimization Optimal topology based on ESO has been obtained through stress analysis by the finite element method, material transformation by the transformation line and element
272
Material Mixing Method for Topology Optimization
removal by the removal line. Theflowchartof topology optimization process is shown in Fig. 3. This procedure is iterated until satisfying the prescribed mass or deflection constraint. = amiR+Aax(
vol
presen
'y
(4)
V0l
ini,ial
ae
(5)
EXAMPLES A Short Cantilever Beam Subject to a Concentrated Force at the Center of Free End When a short cantilever shown in Fig. 4 was subjected to a concentrated force of 300 kN at the center of free end, optimal topologies of single and two-multiple material structures were obtained using the suggested material mixing method. The quadilateral element was used and the beam was divided into the grid of 32 x 20. The used elastic modulii are listed in Table I . It was assumed that the elastic modulus of material 2 is 40% of material 1.
Element Number
FIGURE 1 Transformation and removal line
10
20
30
40
50
60
Iteration number
FIGURE 2 Reduction of the number of transformed elements
Material Mixing Method for Topology Optimization
273
FEA nf a stn inti im
Calculation of transformation & removal lines
Transformation of low strain energy efficiency elements
Removal of low strain energy efficiency elements
No
Yes
Yes
Output of topology optimization
FIGURE 3 Flowchart of the optimization process
TABLE I Material property
Material 1 Material 2
Young's Modulus 207 GPa 82.8 GPa
Density 7280 kg/mJ 3128kg/mJ
Poison's Ratio 0.3 0.3
Lx= 0.16 m
t = 0.001 m
L y = 0.10 m p ,
r
FIGURE 4 Conditions of a short cantilever
In order to investigate the topology optimization process as the materials are mixing, topology optimizations were performed for the following four cases. Those are, (1) a single material structure of material 1 with 50% mass constraint of initial mass of material 1 (2) two-multiple material structure with 40% mass constraint (3) two-multiple material
Material Mixing Method for Topology Optimization
274
structure with 30% mass constraint and (4) a single material structure of material 2 with 20% mass constraint. The obtained optimal topology of each case is shown in Fig. 5. The optimal topologies of the cases (1) and (4) are shown in Fig. 5(a) and 5(d). The results are the same as those obtained using ESO[8]. Figure 5(b) and 5(c) indicate the material mixing process of two materials properly as the mass of a structure decreases. And the deflections tend to increase as the mass of a structure decreases. Therefore, it can be verified that topology optimization was properly performed.
safes
,,K (c)
(a)
(b)
Material 2
" Material 1
FIGURE 5 Optimized topology obtained for;
(a) case(l), (b) case(2), (c) case(3), (d) case(4)
TABLE II Material property
Material 1 Material 2 Material 3
Young' s Modulus 207 GPa 144.9 GPa 82.8 GPa
Material 1
Density 7280kg/mJ 5474 kg/mJ 3128kg/mJ
(b) Material 2
Poison's Ratio 0.3 0.3 0.3
Material 3
FIGURE 6 Optimized topology obtained for a structure consisted of (a) one material (b) two materials (c) three materials
Material Mixing Method for Topology Optimization
275
TABLE IH Final masses of optimal topologies
Constitution Mass
1 Material 0.0500 kg
2 Materials 0.0475 kg
3 Materials 0.0449 kg
A Short Cantilever Beam Subject to a Concentrated Force at the Right End of Free End When a short cantilever beam is subjected to a concentrated force of 300 kN, and the maximum deflection is limited to 0.8 mm at the right end of free end instead of the center of free end in Fig. 4, optimal topologies of single, two and three multiple structures were obtained using the suggested material mixing method. The elastic modulii used in this example are listed in Table II. Since this example dealt with a three multiple material structure, two transformation and one removal line were implied. The obtained three optimal topologies are shown in Fig. 6, and the final masses were obtained under the maximum deflection constraint as shown in Table IH. Since the optimal topology of a three-multiple material structure has the smallest mass, it is known that a three-multiple material structure has the largest stiffness comparing with the other optimal structures under the same mass constraint. CONCLUSIONS hi this study, a material mixing method has been developed based on ESO in order to obtain an optimal topology of a multiple material structure. From the results of the presented examples, the following conclusions are obtained: (1) Introducing the concepts of the transformation and removal lines, optimal topologies have been obtained by iterating material transformation and removal. (2) Inducing the threshold ratio and penalty factor to establish the transformation and removal lines, the removal ratio was varied from 20% at the beginning to 1% at the last iteration. Therefore, it is known that the convergence rate in this study is much faster than the ordinary ESO, of which removal ratio is usually chosen as 1 or 2% in static problems. (3) It was found that the optimal topology of multiple materials has larger stiffness than that of single material under the same mass. REFERENCES 1. 2. 3. 4. 5. 6.
7. 8.
Bends0e M. P. and Kikuchi N., 1988, "Generating Optimal Topologeis in Structural Design Using a Homogenization Method," Comp. Meth. Appl. Meek Engng., Vol. 71, pp. 197-224. Mlejnek H. P. and Schumacher R., 1993, "An Engineer's Approach to Optimal Material Distribution & Shape Finding," Comp. Meth.. Appl. Mech. Engng., Vol. 106, pp. 1-26. Kreisselmeier G. and Steinhauser R., 1979, "Systematic Control Design by Optimizing a Vector Performance Index," IFAC Symp. Computer Aided Design of Control Systems, Zurich, Switzerland. Xie Y. M. and Steven G. P., 1993, "A Simple Evolutionary Procedure for Structural Optimization," Comput. Struc. Vol. 49, pp. 885-896. Chu D. N., Xie Y. M., Hira A. and Steven G. P., 1996, "Evolutionary structural optimization for problems with stiffness constraints," Finite Elements in Analysis and Design, No. 21, pp. 239-251. Luzhong Yin, G. K. Ananthasuresh, 2002, "A novel topology design scheme for the multi-physics problems of electro-thermally actuated compliant micromechanisrns," Sensors and Actuators A: Physical, Vol. 97-98, pp. 599-609. Qing Li, Steven G.P., Querin, O.M., Xie Y.M., 2000, "Structural Topology Design with Multiple Thermal Criteria," Engineering Computations Vol. 17, pp. 715-734. Han S. Y., 2000, "An Improved Element Removal Method for Evolutionary Structural Optimization," KSME International Journal, Vol. 14, No. 9, pp. 913-919.
Structural Design of a 750kW Composite Wind Turbine Blade C. K. Jung, S. H. Park and K. S. Han* Department of Mechanical Engineering, Pohang University of Science and Technology, Pohang, KOREA
ABSTRACT A GFRP based composite blade was developed for a 750kW wind energy conversion system of type class I. The blade sectional geometry was designed to have a general shell-spar structure. The load cases specified in the IEC61400-1 international specification were considered. For withstanding all relevant extreme loads and fatigue loads, the structural analysis for the complete blade was performed using a commercial FEM code. The static load carrying capacity, buckling stability, blade tip deflection, natural frequencies at various rotational speeds and fatigue strength were evaluated to satisfy the strength requirements in accordance with the D3C61400-1 and GL Regulations. The fatigue life more than 20 years was calculated on the basis of the Miner's rule and the Goodman diagram. For designing a lightweight blade, the thickness and the lay-up pattern of the skin-foam sandwich structures were optimized iteratively using the DOT program. T-bolts were used for joining the blade root and the hub, which were modeled using a 3D FE volume model. In order to confirm the safety of the root connection, the static stresses of the thick root laminate and the steel bolts were predicted by taking account of the bolt pretension and the root bending moments. The calculated stresses were compared with the material strengths.
INTRODUCTION As the wind turbine size grows to MW class, the wind turbine blade also becomes bigger. Therefore the material of the blade has been changed from metals and woods to composites to achieve high structural performance. Nowadays most wind turbine blades are made of GFRP to reduce the weight though CFRP is also used for limited case because of high price. The wind turbine blade should have an operation life more than 20 years. During operation, continuous loads such as drag, lift and gyroscopic force, exist. Also the wind fluctuation and yawing of thee turbine cause the blade to vibrate. Accordingly, a wind turbine blade should be designed in consideration of these static, vibration and fatigue problem to obtain the structural stability. And the blade-hub connection should sustain all the loads from blade in lifetime, hi the connection, the laminate and bolts are deformed unevenly because of their differing forms and stiffnesses, so the detail analysis of this part should be considered [1]. hi this paper, the structural design and analysis for a 750kW wind turbine blade are presented. The stress analysis for extreme loads, natural frequency extraction, buckling * Corresponding Author, Department of Mechanical Engineering, Pohang University of Science and Technology, San31 Hyoja-dong, Nam-gu, Pohang, 790-784, KOREA, fax: +82-54-279-2845, [email protected]
277
Structural Design of a 750kW Composite Wind Turbine Blade
stability analysis, fatigue life estimation and T-bolt connection analysis are performed. For light blade design, the thickness and lay-up pattern of laminate are optimized by iterative calculations. STRUCTURAL DESIGN Structure and Materials The blade is designed for type class I system according to the IEC61400-1 [2]. The total length of the blade is 24.3m. A typical structure of wind turbine blade is Fig. 1. It consists of an upper and a lower shell with spar consisting of UD(uni-directional) spar caps and one multi-axial sandwich spar web each as supporting structure. The spar caps are designed in UD glass/epoxy prepreg, the shells and the spar webs in biaxial glass/epoxy prepreg and the blade root reinforcement in a mixture of UD and biaxial glass/epoxy prepreg. Where the UD spar caps do not support the shell, it is built as sandwich structure with glass reinforced PUR(polyurethane) foam. Material properties are listed in Table I. The ultimate strength and strain are the characteristic value [3]. FINITE ELEMENT ANALYSIS Model The finite element program is ABAQUS. The element is 4-node S4 shell element [4] and the total number of element is 5600. 33 element groups along the span direction are used to model the thickness distribution of each material. Along the chord direction, the skin is separated into three parts that have different material thickness. Basically the thickness is maximum value at the blade root and becomes thin along the span direction. Total mass of the model is 1900kg.
Trailing Edge
FIGURE 1 Typical configuration of wind turbine blade
TABLE I Material properties
Ei(MPa) E 2 (MPa) V
G 12 (MPa) p(kg/m3) SL(MPa) eL(%)
U D prepreg 41600 7300 0.3 4000 1768 959 2.15
Biaxial prepreg 22000 22000 0.3 5500 1518 401 2.12
PUR foam 70 70 0.2 19 119 -
Structural Design of a 750kW Composite Wind Turbine Blade
278
TABLE II Flapwise deflection and maximum stress/strain Wind Speed [m/s]
Deflection|m]
Max. Stress[Mpa]
Max. Strainfus]
10 25 70
1.45 1.30 2.14
41.6/-33.8 38.3A32.6 82.1/-79.7
1547/-1334 1416/-1191 3184/-3190
Static Analysis Three load cases are considered for stress/strain analysis. First two are lOm/s and 25m/s wind condition during normal operation. The last is 50-year extreme wind speed case. The load safety factor is 1.35 and the material safety factor is 2.70. The flapwise tip deflection, maximum stress and strain for each load case are listed in Table H Comparing with the ultimate strength, the maximum stress of 70m/s wind case results in the minimum reserve factor of 1.81. The stain is also small and the reserve factor is 6.7. Fig.2 and Fig.3 are the stress contours of the skin and the web for 70m/s wind condition. The maximum stress occurs in the middle of blade where the thickness changes steeply from thick root area to thin profile area. The allowable stress in the skin is 148Mpa and the results show the stress is low to have sufficient static safety.
FIGURE 2 Stress contour for 70m/s wind (skin)
FIGURE 3 Stress contour for 70m/s wind (web)
Structural Design of a 750kW Composite Wind Turbine Blade
15
20 25 rpm
30
35
279
40
FIGURE 4 Campbell diagram
The stress in the web is low but the stress concentration occurs at the joint between the webs and the spar caps. Like the stress distribution of the skin, the upper side is under compression and the lower side is under the tension. Natural Frequency Analysis The blade should be designed to avoid resonance during operation. The 1st flapwise and edgewise natural frequencies are calculated as 2.4 and 3.9, respectively. Fig. 4 is the Campbell diagram which shows the natural frequencies vs. various rotational speed of the blade. Fl and LI mean the 1st flapwise and 1st lead-lag(edgewise) frequency, respectively. To avoid resonance, the 1st flapwise natural frequency should have ±10% difference from the excitation frequencies at the nominal rotational speed of 25rpm. For three-bladed wind turbine, 3P is most important excitation frequency. The Campbell diagram shows that the resonance will not occur in the operation range of 9-27 rpm. Buckling Analysis The buckling modes and corresponding eigenvalues are analyzed for the load case of 70m/s wind condition. First three eigenvalues(or load factors) are 1.479,1.481 and 1.499. The buckling load factor of 1.479 means the 1st mode buckling occurs at the base load times the load factor. The buckled positions are R=19m, R=7m and R=l 3m at middle skin area where the maximum compressive stresses occur. It can be concluded that the buckling stability is fairly obtained, because the base condition of the buckling analysis is 70m/s wind condition. Fatigue Analysis 14 load cases are simulated numerically as 10-minites time series for fatigue. To estimate the load series during 20-year operation, Rayleigh distribution is assumed for one-year wind distribution. This load-time series are converted into strain-time series using unit load and unit strain concept. Then the random strain-time series are transformed via a rainflow cycle counting method into a sequence of bins of constant strain mean and amplitude, which generate the From-To-matrix(Markov matrix) that contains the number of cycles counted at an combination of mean and range. The allowable cycles for each
280
Structural Design of a 750kW Composite Wind Turbine Blade
Laminate Extension bolt \
Pitch bearing \
\ Transverse bolt FIGURE 5 Composition of T-bolt connection
combination of mean and range can be calculated with S-N curve and strain based Goodman diagram for the composite laminate. Finally, the total fatigue damage is estimated using Eq.(l). The damage cannot exceed 1 for 20-year fatigue life [5,6]. The reserve factor of element 3464(R=llm, lower middle skin) and element 4145(R=8.8m, lower middle skin) shows the minimum value of 1.2. This area is the weakest point against fatigue.
where D is the fatigue damage, ns is the counted cycle, N{ is the allowable cycle at a certain mean and amplitude combination, R is the reserve factor and k is the reciprocal gradient for S-N curve [3]. T-bolt Connection Analysis The blade connection to the' pitch bearing is established with so called T-bolt-connection consisting of an extension bolt and a cylindrical cross bolt. Fig. 5 is a typical view of the T-bolt connection [7]. The cross bolt transmits the loadsfromthe blade root to the extension bolt and the loads passed through the extension bolt reach the pitch bearing. The laminate thickness of the root is 75mm. The diameters of the extension bolt and the cross bolt are 27mm and 54mm, respectively. The total number of T-bolt is 40. The stress is calculated for the maximum root bending moment. The result is listed in Table III. Comparing with the ultimate strength of the bolt, the static safety factor comes to be 1.3. It can be concluded the connection is safe for all load cases. TABLE III Maximum stress and strength of T-bolt connection
Root Laminate Bolts
Max. Stress[Mpa] 44/-230 809/-376
Strength[Mpa] 690/-900 1040
S.F. 65~ 1.3
Structural Design of a 750kW Composite Wind Turbine Blade
281
CONCLUSIONS A structural design procedure for IEC type class I composite wind turbine blade using finite element analysis is presented. Our conclusions are as follows 1. The blade structure is analyzed by means of static stress/strain, natural frequencies, buckling and fatigue analysis according to IEC standard. 2. The material thickness is optimized by iterative calculations of stress, natural frequencies, buckling stability and fatigue life to minimize the weight of the blade. 3. The T-bolt connection is designed with 3D volume FE model and the safety is calculated.
ACKNOWLEDGMENTS This work was supported by Korea Energy Management Corporation and UNISON.
REFERENCES 1.
2. 3. 4. 5.
6. 7.
Ladean R. McKittric, Douglas S. Cairns, P.I. John Mandell, David C. Combs, Donald A. Rabern and R. Daniel VanLuchene. 2001. "Analysis of a Composite Blade Design for the AOC 15/50 Wind Turbine Using Finite Element Model", SAND2001-1441 IEC. 1999. IEC Standard 61400-1 Part I : Safety Requirements Germanischer Lloyd. 1999. Regulations for the Certification of Wind Energy Conversion Systems HKS Inc. 2002. ABAQUS6.3 User's Manual T.P. Philippidis, A.P. Vassilopoulos, K.G. Katopis and S.G. Voutsinas. 1996. "THIN/PROBLEM : A Software for Fatigue Design and Analysis of Composite Rotor Blades", Wind Engineering, 20(5):349-362 Marshall, L. Buhl. 2002. GPP Version 6 User's Guide, NWTC, pp. 28-29. R. Osthorst, R.Fuhrhoff and R.Kortemkamp. 2002. "Measurements and Calculations with the Aim of Optimizing the T-bolt Blade-Connection Joint", Technical Report, Aerodyn
Axiomatic Design of Composite Track Pin Dong Chang Park, Seong Su Kim, Seung Min Lee, Dai Gil Lee Department of Mechanical Engineering, Korea Advanced Institute of Science and Technology, Korea
ABSTRACT Track links for high mobility tracked vehicles usually consist of track shoe bodies, track pins, rubber pads, end-connectors, and rubber bushings. Since the track pin is subjected to large transverse track tension from the track link, conventional track pins for high mobility vehicles are usually made of high strength steel, such as forged chrome-molybdenum steel, which increases the weight of tracked vehicles due to the high density of steel. Weight reduction has been the principal goal of many of the experimental track programs since World War II. However, great weight reduction in the track pin has not been achieved for several decades except a few experimental works. Therefore, in this paper, the axiomatic design approach was employed to design a lower weight track pin with composite materials. From the design of composite track pin, the weight reduction of 50% as well as better endurance life was achieved.
INTRODUCTION In these days, the weight reduction of track links for military vehicles has been great concern to improve the mobility and operational cost of tracked vehicles. The operational cost is mainly due to high fuel consumption and short life of the track components of military tracked vehicles. Therefore, the weight reduction of track links with the required durability is indispensable. Track links for high mobility tracked vehicles usually consist of track shoe bodies, track pins, rubber pads, end-connectors, and rubber bushings. In general, the conventional track link occupies about 10% of the gross vehicle weight (GVW), and the track pin's weight is about 25% of the track link weight. For example, the weight of the track pin comes up to 1500 kg for the GVW of 60 tons. Therefore, the weight reduction of track pin is necessary to develop the light weight track. The track link transfers the driving torque from the engine to the vehicle by the friction force between the ground and the track rubber pad. In addition to torque transmission, the track link absorbs impact load from the ground. The required strength of the track link is order of 105N in the longitudinal direction, in addition to various smaller loads from the ground and roadwheels. Since the track pin is subjected to large transverse track tension from the track link, conventional track pins for high mobility vehicles are usually made of high strength steel, such as forged chrome-molybdenum steel rods, which increases the weight of tracked vehicles due to the high density of steel. The increase of track weight also increases the rolling resistance of tracked vehicles, which decreases the fuel efficiency and mobility of the tracked vehicle. Therefore, the weight reduction of track * Corresponding Author, Department of Mechanical Engineering, KAIST, 373-1, Guseong-dong, Yuseong-gu, Daejeon 305-701, Republic of Korea, Phone: +82-42-869-3261,5202, Fax: +82-42-869-5221, e-mail: [email protected]
Axiomatic Design of Composite Track Pin
283
pins is an important design factor for tracked vehicles. Another design requirement for the track pin is high flexural rigidity to distribute track tension load uniformly on the rubber bushing. Pins with low flexible rigidity cause uneven load distribution and excessive bushing wear at the ends of pin due to the pin bending [1], which results in the decrease of bushing life. Another important requirement for the new track pin is easy maintenance requirements that the new track pins should be fully replaceable and interchangeable with the conventional ones. These three requirements of "to transmit the required track tension load", "to make the endurance life of the rubber bushing longer than the required life"," and "to provide an easy maintenance", under the constraints such as cost and weight reduction target, are not easy to satisfy simultaneously with conventional metal, but can be satisfied by fiber reinforced composite materials. Carbon fiber reinforced composite materials might be employed to solve the problem of cylindrical pins owing to its high specific stiffness and high strength [2]. However, there have been few attempts on the composite track pins, and the relation between the rubber bushing life and the composite track pin stiffness was little investigated. Therefore, in this paper, several composite materials were employed for the track pin design to reduce the weight of track pin as well as to enhance the fatigue life of rubber bushings. Especially the effects of shear stiffness of the composites on the life of rubber bushing were investigated. CONCEPT OF AXIOMATIC DESIGN The basic postulate of the axiomatic approach to design is that there are fundamental axioms that govern the design process [3]. Two axioms were identified by examining the common elements that are always present in good design. They were also identified by examining actions taken during the design stage that resulted in dramatic improvements. The first axiom is called the 'Independence Axiom'. It states that the independence of functional requirements (FRs) must always be maintained, where FRs are defined as the minimum set of independent requirements that characterizes the design goals. The second axiom is called the 'Information Axiom', and it states that among those designs that satisfy the Independence Axiom, the design that has the smallest information contents is the best design. When the information content is greater than zero, information must be supplied to satisfy the FRs at all times. Because the information content is defined in terms of probability, the second axiom also states that the design that has the highest probability of success is the best design. DESIGN OF COMPOSITE TRACK PIN hi the double pin type track link as shown in Figure 1, the shoe bodies are connected with each other by the track pin and the end-connectors. When the track tension force, F, is applied on the track link, the concentration of shear forces occurs at both ends of the track pin near the end-connectors. Also the shear force in the rubber bushing is produced as the rubber bushing is pressed on the pin. The calculated maximum stress for the current steel pin was 1080 MPa, due to the track tension based on the simply supported beam under a central concentrated load. The high strength steel pin of 1200 MPa has been used for the track pin. During the operation of tracked vehicles, relative rotation between the adjacent track shoe body and the pin was ±8 degrees. Figure 2 shows the free body diagram of the track pin during rotation.
284
Axiomatic Design of Composite Track Pin
rubber bush
shoe body
TRACK PIN
T/L
FIGURE 2 Torque on the track pin and rubber bushings
FIGURE 1 Schematic diagram of a track assembly
The functional requirements of the track pin are FRi = Transmit the required track tension (100,000 N). FR2 = Make the rubber bushing life longer than the required life. FR3 = Provide an easy maintenance. Three DPs for satisfying these FRs are stated as DPi = Strength of pin material DP2 = Stiffness of pin material DP3 = Pin end shape To be competitive with the conventional steel track pin, the cost of the composite track pin with maintenance cost should be lower than the conventional high strength steel track pin. Also, the weight reduction of the new track pin should be larger than at least 50% compared with the conventional track pin to earn the budget to develop the new track pin. Therefore, the constraints for the new track pin design may be dictated as follows. Ci = Weight of the track pin (smaller than 50% of the conventional track pin weight). C2 = Minimize the total life cost of the track pin. The design equation for the track pin may be written as FR X FR [- 0 FR X
0 X 0
0 \DPA 0 X
W k
(1)
Since the configuration of a track pin is limited by the dimension of the track shoe body, there is littlefreedomto change the shape of track pin to reduce the pin weight and to meet the bushing life requirement. The only way to fulfill the FRi and through DPi is to use fiber reinforced composite materials without violating the constraint Ct because metal materials such as steel or aluminum have low specific strength. Therefore, unidirectional glass fiber/epoxy composites (UGN 150, SK Industries) and carbon fiber/epoxy composites (USN 150, SK Industries) were chosen as substitutes for the present high
Axiomatic Design of Composite Track Pin
285
in
Track Tension
Rubber bushing FIGURE 3 Finite element model of the bushing and pin
strength steel, because the tensile strengths of the glass and carbon fiber/epoxy composites are 1000 MPa and 2300 MPa, respectively. Decomposition of FR 2 and DP 2 Branch The endurance life of the rubber bushing is affected by its compressive and shear strains because the rubber bushing is deformed in shear and compressive modes as shown in Figure 3. Therefore decompositions of FR2 and DP 2 branch were performed considering both shear and compressive strains. The decompositions of FR 2 and DPs for satisfying the decomposed FRs are stated as FR2i = Reduce the compressive strain of the rubber bushings FR22 = Reduce the shear strain of the rubber bushings DP12 = Flexural stiffness of pin material DP 22 = Shear stiffness of pin material The design equation for the impact beam may be written as
FR.
X
0
DR
FR12
0
X
DP,
(2)
Since the design matrices are half triangular and diagonal, respectively, the new track pin with composite materials can be realized. EFFECTS OF PIN STIFFNESS ON THE RUBBER BUSHING LIFE hi order to investigate the relation between the rubber bushing strains and the pin stiffness, the stresses and strains of the rubber bushing under torque were calculated using finite element analysis using ABAQUS 6.3 (Hibbitt, Karlsson & Sorensen, Inc., USA) - a commercial software. Besides the finite element analysis, the closed form solution for the shear strain distribution of single lap joint was adopted [4]. The track pin and shoe body were considered as the inner and outer adherends, respectively. The rubber bushing was considered as an adhesive with linear elastic material properties. Even though the strain of the bushing could be calculated easily using the closed form solution, the strains from the linear analytic model were found to be much smaller than those of the finite element analysis results because the linear joint model could not depict well the nonlinear elastic behavior of the rubber bushing when the shear strain was above 50%. Therefore, the finite element analysis was employed to calculate the strain of the bushing with the nonlinear elastic rubber properties.
Axiomatic Design of Composite Track Pin
286 - Track Pin -Rubber Bushing
(a) - Track Pin -Rubber Bushing
1
z
— Center Line
z = 280
(b) FIGURE 4 Finite element model of the bushing and pin, (a) solid pin, (b) hollow pin
Figure 4 shows the finite element mesh for the rubber bushing and the track pin in which quadratic quadrilateral axisymmetric elements with torsion (CGAX8R) were used for the track pin and the rubber bushing. Figure 4(a) shows the finite element model of the solid pin. Figure 4(b) shows the finite element model of hollow type track pin in which the total numbers of nodes and elements were 800 and 2641, respectively. The size of the elements was decreased towards both ends of rubber bushing range for the accurate calculation of the shear strain. All the nodes on the outer surface of the rubber bushing were fixed because there is no sliding between the bushing and the shoe body. The Mooney Rivlin model with constants Cio = 0.25 MPa and Coi= 0.18 MPa were used to model the hyper-elastic properties of the rubber bushing as follows:
+ x3 -:
(3)
where, W'x& strain energy function, Xis extension ratio. ANALYSIS AND EXPERIMENTAL RESULTS In order to investigate the effect of torsional rigidity of the pin on the strain of the rubber bushing, four kinds of material were employed for the track pin such as steel, unidirectional glass fiber/epoxy composites, hybrid composites composed of glass and carbon fiber/epoxy, and carbon fiber/epoxy laminates. The cross sections of the three pins were same. The shear moduli of the materials were 80 GPa, 4.4 GPa, 11 GPa, and 24 GPa, respectively. The rubber bushing has the maximum shear strain at the both ends (z=0, z=280 mm), and the minimum strain at the center of the track pin (z=140 mm) as shown in Figure 5(a). The shear strains of the rubber bushing on the four kinds of pins were compared as shown in Figure 5(b), where shear strain ratio value is 1.0 for the maximum strain of the bushing on the solid steel pin. The shear strain of the rubber bushing decreased as the shear modulus of the pin material decreased. The strains of the steel solid pin and hollow pin were almost same with each other. The shear strain of the rubber bushing on the glassfiber/epoxycomposite pin was 31% ~ 60% less than that on the steel pin, which was caused by the low torsional rigidity of the composite pin (5.5% of the steel pin). The low shear strain of the bushing might increase the endurance life of the bushing, because the fatigue life of rubber part, Nf, is given by Nf = oW*3 (a and j3: material constants, and W: strain density) [5]. Flexural tests were performed for the conventional steel track pin and the newly developed composite track pin, and the deformations of the pins were measured as shown in Figure 6. The maximum compressive strain of the rubber bushing could be obtained from the above pin deformation. The composite pins satisfied
Axiomatic Design of Composite Track Pin
287
the FR], and the compressive strain of the rubber bushing on the composite pin is bigger than that on the steel pin by 13%. But, rubber bushing is more vulnerable to fail under high shear strain than under high compressive strain. Therefore, the life of rubber bushing on the composite track pins will be longer than that on the steel pin. Figure 7 shows the newly developed composite track pin whose weight is only 50 % compared with the conventional steel pin. Pin end was designed to have grooves at both ends to satisfy FR3 through DP3.
Solid Steel Hollow Steel UGN150 Hybrid USNLam. ...
% 0.6
120
150 180 210 240
-+~ Max Strain • • • M i n . Strain
270
10 20 30 40 50 60 70 SO Shear Modulus of Track Pin (GPa)
Z (mm)
(a) (b) FIGURE 5 Rubber bushing strain w.r.t the composite track pin stiffness, (a) rubber bushing strain variation in longitudinal axis, (b) effects of pin shear modulus on the bushing shear strain
Steel Cap
1.5
2.0
2.5
3.0
3.5
Displacement (mm) Composite Tube 2"
FIGURE 6 Deformation of the bushing
Composite Tube 1
FIGURE 7 Configuration of the composite track pin
DISCUSSIONS hi this research, composite track pins for high mobility tracked vehicles were designed using the axiomatic design approach. The weight reduction for the composite pin was 50% compared to the conventional steel pin while the composite track pin satisfied all the functional requirements or the track pin. It is expected that the endurance life of the rubber bushing will be increased because the shear strain of the rubber bushing on the composite pin is 31% less than that of the conventional steel pin. REFERENCES 1. 2. 3. 4. 5.
U.S. Army Material Command. 1967 AMCP 706-356, Automotive Series Automotive Suspensions, Engineering Design Handbook. Wiesner et al. 1988. "Arrangement for the connection of the track links of endless crawler track vehicles", U.S patent no. 4735465. Lee, D.G., and Suh, N.P. 2004(will be published). Axiomatic Design and Fabrication of Composite Structures, Oxford University Press Adams and Peppiatt. 1977. "Stress analysis of adhesive bonded tubular lap joints," Journal of Adhesion, Vol. 9, pp. 1-18. Mars and Fatemi. 2002. "A literature survey on fatigue analysis approaches for rubber," International Journal of Fatigue, Vol. 24, pp. 949-961.
Characterization and Design Optimization of FRP Composite Modular System for Slab-on-Girder Bridges Lijuan Cheng and Vistasp M. Karbhari Department of Structural Engineering, MC-0085 University of California, San Diego, La Jolla, CA 92093-0085, USA
ABSTRACT This paper presents the analytical and experimental characterization results of a modular slab-on-girder bridge system consisting of a steel-free concrete slab reinforced by fiber reinforced polymer (FRP) composite deck panels and composite rectangular girders. The analytical predictions using finite element method compared well with the full-scale experimental results of the components and system tests.
INTRODUCTION Concrete slab-on-girder bridges have conventionally been the most common and basic solutions for short and medium span bridges. However, many existing reinforced concrete bridges have been found to be structurally deficient due to steel corrosion and subsequent concrete degradation [1]. Fiber Reinforced Polymer (FRP) composite materials have been found to have potential as replacements for the steel reinforcement in concrete slabs in the form of tendons, 2D/3D continuous grids and gratings [2] and flat panels [3]. Research work on bridge girders made of composite materials has also been performed [4,5]. Recent investigations on bridge systems have been focused on configurations consisting of all-FRP decks supported by steel/concrete or FRP beams [3,6]. However, research work on hybrid FRP/concrete modular bridge systems via both component/system level investigation and field demonstrating project has been limited. This paper presents results of an ongoing study on a new steel-free FRP/concrete slab-on-girder bridge system recently developed at UCSD. The system uses rectangular box girders made of hybrid E-glass-carbon fiber reinforced composites and a steel-free concrete slab cast on carbon fiber reinforced composite deck panels that are snap-locked to the girder top as shown in Figure 1. Prefabricated carbon fiber reinforced composite snap-in stirrups are provided for the horizontal shear transfer between the slab and girders. The objective of this study is to fully characterize structural response at both component and system levels through full-scale experiments and numerical analysis.
'Correspondence Author. Department of Structural Engineering, University of California, San Diego, 9500 Gilman Dr., Mail Code 0085, La Jolla, CA 92093-0085, Fax: (858) 534-6373, Email: [email protected]
FRP Composite Modular System for Slab-on-Girder Bridges
© Shsar Stirrup
289
(Unit: mm)
© Fiber Reinforced Concrete Deck
FIGURE 1 Steel-free FRP/concrete modular slab-on-girder bridge system
STEEL-FREE FRP/CONCRETE DECK The deck panel, serving as both flexural reinforcement and permanent formwork for concrete slab, includes a bottom plate with end hooks and rectangular stiffeners as well as surface shear ribs. Figure 2 shows good correlation between Finite Element Analysis (FEA) based simulations [7] and test results from full-scale flexural test of two simply supported 610-mm wide slabs with an AASHTO wheel load applied at mid-span. Diagonal cracks initiated at the shear ribs were observed due to combined flexural compression and tension shear. In the FEA model, 4-node linear-elastic shell elements were used for the FRP composites and 8-node brick elements with nonlinear response were used for concrete. Perfect bond was assumed for the slab-deck interface. 0.2
5
Mdspan Displacement (in) 04 <X6_
10 15 tvfidspan Displacement (mm)
-4500 -3000 -1500
0 1500 3000 Mdspan Strain (le-6)
4500
6000
FIGURE 2 Flexural test of steel-free FRP/concrete deck
FRP COMPOSITE RECTANGULAR GIRDER The rectangular composite girders are formed of E-glass/vinylester with an additional layer of unidirectional carbon fiber within the girder bottom flange. A "dovetail" shape is designed for the girder cap to provide an anchorage zone for the panels and the shear stirrups and the cavities are filled with polymer concrete to stabilize the composite walls. Shear ribs are included along the central strip of the cap for shear interlock. Figure 3 shows good correlation between a FEA model and test
FRP Composite Modular System for Slab-on-Girder Bridges
290
results from a 8.534-m long wet lay-up composite girder tested under four-point bending with simple supports at the ends. The encountered failure mode seen after large displacement was initiated by debonding of the short lap splice length in the glass fabric at girder bottom flange at mid-span and followed by debonding and rupture of the unidirectional carbon fiber layers. ~—Test * Beam
Midspan displacement (in) . __ _4 6 8_...
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FIGURE 3 Four-point bending test of composite rectangular girder
A refined numerical analysis of the laminated composite girder was performed using CLT and the Tsai-Wu failure criterion. First-Ply-Failure (FPF) Criterion was implemented and the results compared well with test data as seen in Figure 3. 2500( 2000
Midspan displacement (m) 4 6 8
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100 150 200 250 Midspan displacement (mm)
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FIGURE 4 Girder load-displacement response using ply failure criteria TABLE I Failure progression history Failure sequence 1 2 3 4 5 6 7 8 9 10 11 12 13
Location
Ply #
GBOT' GBOT GBOT GBOT GBOT GBOT GWEB" GWEB GWEB GWEB GWEB GWEB GBOT
1 4 24 36 43 46 1 4 33 30 23 11 48
When Scathon reaches the design ultimate
Failure load kN[kip] 1592 [358] 1600 [359.5] 1642 [369] 1641 [368.8] 1642 [369] 1646 [370] 1736 [390] 1738 [390.5] 1562(3511 1584 [356] 1602 [360] 1651 [371] 2059[463]
Displacement at failure mm [in] 197 [7.756] 198 [7.795] 200 [7.884] 204 [8.039] 205 [8.069] 206 [8.128] 219 [8.629] 220 [8.655] 198 [7.8141 203 [7.981] 206 [8.124] 214 [8.4171 268 [10.54]
Failure mode TRT'" TRT TRT TRT TRT TRT TRT TRT TRT TRT TRT TRT TRT
Strain in carbon (mm/mm) 0.008471 0.008554 0.008720 0.008763 0.008814 0.008882 0.009419 0.009467 0.009014 0.009197 0.009359 0.009699 0.012160
220 [8.673]
--
0.010000
1694 [381]
GBOT - girder bottom flange; GWEB - girder web;
100
Dead load i
TRT - transverse resin tension failure
FRP Composite Modular System for Slab-on-Girder Bridges
291
In addition, a simple beam theory model was used based on the criteria that the carbon fiber in the bottom flange reaches strain design limit of 0.01. Figure 4 shows the girder mid-span displacement response using Ply-by-Ply-Failure (PPF) Criterion and the sequence of ply failures is shown in Table 1. A parametric study was conducted to assess the effect of girder overall depth, carbon fiber amount and girder span length (Figure 5). The FPF load was found to increase with carbon fiber amount and this increase was more substantial for deeper girders at shorter spans than for shallower girders with longer spans. Total Thickness of Carbon Fiber Layer (in)
¥ 6000
¥
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5 10 15 Total Thickness of Carbon Fiber Layer (mm)
FIGURE 5 Parametric study of rectangular girder
SLAB-ON-GIRDER SYSTEM ASSEMBLY The entire bridge can be assembled from the modular components by first placing the deck panels on the top of the girders, then installing the shear stirrups by snapping them through the girder top groves, and finally casting the polypropylene fiber reinforced concrete slab mixed with fibers on top of the panels. A full-scale twogirder system assembly was experimentally tested with pins at one end and rollers at the other. No visible damage was observed under flexural loading under simulated wheel loads equivalent to 2 times the factored axial load applied on the center of the slab (Figure 6). Midspan Displacement (in) 0
0.1
0.2
0.3
0.4
0.5
0.6
0.7 150
2 x Factored wheel load 600
400
Factored wheel load
j
200
5
10 15 Midspan Displacement (mm)
20
FIGURE 6 Load-displacement response of slab flexural test of system assembly
292
FRP Composite Modular System for Slab-on-Girder Bridges
Application of wheel loads on the slab directly above the girders (instead of slab center) to simulate global flexural behavior showed linear elastic response (Figure 7). Slippage at the girder-deck interface was observed at the shear span regions with the maximum value of 1 mm in the middle of the shear span but not in the middle pure bending region. Midspan Displacement (in) 0.8 1.2 1.6
0.4
400
3.5 x Factored shear demand /•* [Factored F
H400
>
flexural demand
z\ 300 S
[Factored shear "
Test •• YEA (nonlinear) •-— M-C- analysis • Beam analysis J
500
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200 .
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tensile in composite
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20 30 40 Midspan Displacement (mm)
•i * -I 100
, , , 1 1000 2000 3000 4000 Microstrain FEA M-C Analysis Beam analysis v Girderbot Gircierbol * Girderbot - Slab top -"— Slab top • Slab top 0
FIGURE 7 Global flexural test results of system assembly
At final failure, the load-displacement response of the system displayed essentially bi-linear response with a "softening point" (Figure 8), beyond which both cracking in the slab and slippage at deck-girder interface began to develop substantially. A quarter-span finite element model with idealized rigid connections for the deck-slab and deck-girder interfaces was used and results were seen to correlate closely to the test results (Figures 6, 7, and 8). c
1
Midspan DispU cement (in) 2 3 4
>t: Phase5 4000 _—•—Te • -Tc t: Ptase3 * FCA (Strain Criteria)
A
5
1000
•
4
£3000 600 e
/
J* Factored / flexural demanc
•J2000 -
1
1000
°c
400-a
A
t Factored shear demand , ! 1. .L-J— L-.!...!.-1.-J 40 60 8( 100 120 Midspan Displacement (mm)
20
200 ~ 140
Quarter span finite element model of two-girder system: Number of elements Number of nodes Number of D.O.F.'s
: 18363 :24023 : 90078
FIGURE 8 Final failure of system global flexural and finite element model
SUMMARY The characterization results for the structural behavior of the steel-free FRP/concrete modular slab-on-girder bridge system are presented in this paper. Good performance was obtained at both the full-scale component and system levels. Finite element analysis method and moment-curvature analysis method were found to be capable of predicting the structural response of the bridge components and the assembled system.
FRP Composite Modular System for Slab-on-Girder Bridges
293
ACKNOWLEDGMENTS The research presented in this paper was supported by the Federal Highway Administrations, State of California Governor's Office, and the California Department of Transportation, support of which is gratefully acknowledged.
REFERENCES 1. 2. 3.
4.
5. 6. 7.
Dunker K.R. and Rabbat, B.G. 1995. "Assessing infrastructure deficiencies: the case of highway bridges," Journal of Infrastructure Systems, 1(2): 100-119. Yost, J.R. and Schmeckpeper, E.R. 2001. "Strength and serviceability of FRP grid reinforced bridge deck," Journal of Bridge Engineering, 6(6):605-612. Reising, R.M.W., Shahrooz, B.M., Hunt, V.J., Lenett, M.S., Christopher S., Neumann, A.R., Helmicki, A.J., Miller, R.A., Kondury, S., and Morton, S. 2001. "Performance of five-span steel bridge with fiber-reinforced polymer composite deck panels," Transportation Research Record 1770, Paper No. 01-0337, pp.113-123. Salim, H.A., Davalos J.F., Qiao, and Barbero, E.J. ,1995. "Experimental and analytical evaluation of laminated composite box beams," 4tfh International SAMPE Symposium, May 8-11, pp.532539. Deskovic, N., Triantafillou, T.C., and Meier, U. 1995. "Innovative design of FRP combined with concrete: short-term behavior," Journal of Structural Engineering, 121(7): 1069-1078. Salim H.A. and Davalos J.F. 1999. "FRP composite short-span bridges: analysis, design and testing," Journal of Advanced Materials, 31(l):18-26. ABAQUS/Standard User's Manual, Version 5.8, 1998, Version 6.3, 2002.
Design of Composite-Antenna-Structures with High Electrical and Mechanical Performances Chi-Sang You and Woonbong Hwang Department of Mechanical Engineering, Pohang University of Science and Technology, Korea
ABSTRACT hi this paper we developed load-bearing outer surface that provides antenna performances, and it is termed Composite-Antenna-Structures(CAS). CAS is composite sandwich structure in which antenna part is inserted between honeycomb core and lower facesheet. Design procedure is presented including structure design, material selection and design of antenna elements in order to obtain high electrical and mechanical performances. Optimized honeycomb thickness is selected, in which maximum gain is obtained by resonance condition. Measured electrical performances show that CAS has wide bandwidth over 10% and higher gain by 3.5 dBi than initially designed antenna, and no doubt it has excellent mechanical performances by composite laminates and honeycomb cores. The CAS concept can be extended to give a useful guide for manufacturers of structural body panels as well as antenna designers, promising innovative future communication technology.
INTRODUCTION "Structural surface becomes an antenna." Structures, materials and antenna designers have recently joined forces to develop a new high payoff technology called smart skin or CLAS, for "conformal load-bearing antenna structure" [1-4]. The embedding of radio frequency (RP) antennas in load-bearing skin is a new approach to the integration of antennas into structural body panels. It emerged from the need to improve structural efficiency and antenna performances. It demands integrated product development from disparate technologies including structures, electronics, materials and manufacturing in order to generate a realistic design. The classic of division between structures and antennas is bridged in CLAS and the technical challenge is to satisfy structural and electrical requirements that often conflict. The present study aims to design electrically and structurally effective antenna structures for the next generation of structural surface technology [5,6]. This is termed Composite-Antenna-Structures (CAS). Design procedure is focused on high gain and wide bandwidth in the electrical part, and high strength, stiffness and environmental resistance in the mechanical part. Direct-feeding stacked patch antenna is used for the antenna performances and composite sandwich structure for structural performances. Measured electrical performances are presented.
Corresponding author, Department of Mechanical Engineering, Pohang University of Science and Technology, San 31, Pohang, Kyungbuk, 790-784, Republic of Korea, Tel: +82-54-279-2174, Fax: +82-54-279-5899, E-mail: [email protected]
Composite-Antenna-Structures
295
STRUCTURE AND MATERIALS The fundamental design concept for the CAS panel is an organic composite multi-layer sandwich panel in which microstrip antenna elements are inserted. As shown in Fig. 1 direct-feeding stacked patch antenna elements are used for the antenna performances. The basic panel layers are: two facesheets, two honeycomb cores and antenna elements with dielectrics. The facesheets carry a significant portion of the in-plane loads, contribute to overall panel buckling resistance, and provide low velocity impact and environmental resistance, however outer facesheet that is placed above upper patch provides signal loss by its high electrical loss (tan8). For the facesheet Glass/Epoxy[0/90]2s (UGN200, SK chemicals) of 1 mm is used. The honeycomb cores transmit shear load between layers induced from bending loads in the panel, support the outer facesheet against compression wrinkling, provide impact resistance and increase the overall panel buckling resistance. The thickness of honeycomb core contributes to the overall rigidity that they should be selected between panel thickness requirement and structural rigidity. Between outer facesheet and upper patch Nomex honeycomb core is inserted for mechanically high flexural strength. The thickness of this honeycomb core (h) will be selected for the most efficient antenna performances. For wideband performance, two radiating patches are used. Upper patch is placed on the Duroid 5880 (Rogers corp.) of 0.254 mm, and lower patch and feedline on the Duroid 5880 of 0.762 mm with ground plane on the other face. Upper patch and lower patch are separated by air gap that is provided by Nomex honeycomb of 2.54 mm. Though Duroid 5880 has good electrical properties of low dielectric constant and electrical loss, it doesn't contribute to structural performances. Consequently, CAS is composite sandwich structure in which antenna part is inserted between honeycomb core and lower facesheet. In order not to lower antenna efficiency by outer facesheet that is structural material with high electrical loss, the thickness of honeycomb core must be adjusted in the design procedure.
Glass/Epoxy[0/90]2s (1 mm) o= 4, tanS=0.03
Honeycomb (h mm) er=1.1
Upper Patch
Duroid 5880 (0.254 mm) er= 2.2, tanb=0.0009
Honeycomb (2.54 mm) zr=1.1
Lower Patch Feedline
Duroid 5880 (0.762 mm) er= 2.2, tan&=0.0009
Ground Glass/Epoxy[0/90]2s (1 mm) er= 4, fan8=0.03
FIGURE 1 Configuration of Composite-Antenna-Structures
Composite-Antenna-Structures
296 DESIGN PROCEDURE
In our design procedure, antenna performances are aimed for Ku-band satellite communication, frequency range between 11.7 and 12.75 GHz. At first, antenna elements are designed. The sizes of rectangular patches are 7.6 and 8 mm for upper and lower patches respectively. And then facesheets and honeycomb core are added. Fig. 2 and 3 show reflection coefficient and radiation pattern variations respectively for honeycomb thickness h by computer simulation and the performances of initially designed antenna are also presented by h = infinite. Gain in the broadside direction reaches maximum at h = 10 mm, at which it is approximately half a wavelength between lower patch and outer facesheet at central frequency 12.2 GHz, and reflection coefficient is also satisfied in the desired frequency range with bandwidth of 1.5 GHz.
1
CO
Nci
-10<4—
0
o O
-20-
\ \
8 mm —•—10 mm —<^14mm
\
—A—
.g -30"o
«etle
—o— infinite —•— 4 mm
—T—18 mm
v x ? ^A^ \|»3 0 /\^x
A " \ / W X
-4D-
11
12
14
13
Frequency (GHz)
FIGURE 2 Reflection coefficients for the thickness of honeycomb core (h)
12-,
8-
4-
m
o-
"c" -40
-8-12-16 -90
-60
-30
0
30
60
90
Degrees
FIGURE 3 Radiation patterns for the thickness of honeycomb core (h) at 12.2 GHz (H-plane)
Composite-Antenna-Structures
297
ELECTRICAL MEASUREMENTS In the design procedure, optimized honeycomb thickness h of 10 mm is selected, in which maximum gain is obtained by resonance condition [7], half a wavelength distance between lower patch and outer facesheet at central frequency 12.2 GHz. Measured electrical performances of initially designed antenna and CAS with honeycomb thickness of 10 mm are shown in Fig. 4 and 5. Reflection coefficient variation of CAS is almost same as that of antenna, which means that outer facesheet above antenna elements doesn't affect impedance characteristic of antenna for the designed CAS. Radiation patterns are measured at 12.2 GHz in the compact range. The pattern is narrower and gain is higher by 3.5 dBi for the CAS, compared with radiation characteristics of initially designed antenna. It is considered that structural resonance condition by outer facesheet make beam more concentrated to the broadside direction.
QQ
11
12
13
Frequency (GHz)
FIGURE 4 Reflection coefficients of CAS and antenna
20-i
15-
CAS(/?=10mm) --Q-- Antenna
10CO
2, c "co CD
50-5-10-15 -90
-60
-30
0
30
60
Degrees
FIGURE 5 Radiation patterns of CAS and antenna
90
298
Composite-Antenna-Structures
CONCLUSIONS Composite-Antenna-Structures having both high electrical and mechanical performances is designed. CAS is composite sandwich structure in which microstrip antenna is placed between honeycomb core and lower facesheet. For the wide bandwidth, two radiating patches of different sizes are used. Honeycomb thickness between outer facesheet and upper radiating patch is selected for structural resonance condition, at which the maximum gain is obtained. The outer facesheet rearranges the radiation field distribution. It can be considered as a structure invoking multiple reflections used to concentrate the radiated power in broadside direction. Measured electrical performances show that CAS has wide bandwidth over 10% and higher gain by 3.5 dBi than initially designed antenna, and no doubt it has excellent mechanical performances by composite laminates and honeycomb cores. The CAS concept can be extended to give a useful guide for manufacturers of structural body panels as well as antenna designers, promising innovative future communication technology. REFERENCES 1. 2.
3.
4. 5.
6.
7.
A. J. Lockyer, et al. 1994. "A Qualitative Assessment of Smart Skins and Avoinics/Structures Integration," SPIE Smart Structures and Materials: Smart Materials, 2189: 172-183 A. J. Lockyer, et al. 1999. "Design and Development of a Conformal Load-Bearing Smart-Skin Antenna: Overview of the AFRL Smart Skin Structures Technology Demonstration (S3TD)," SPIE Smart Structures and Materials: Industrial and Commercial Application of Smart Structures Technologies, 3674: 410-424 A. J. Lockyer, et al. 1997. "Conformal Load-Bearing Antenna Structure (CLAS): Initiative for Multiple Military and Commercial Applications," SPIE Smart Structures and Materials: Smart Electronics and MEMS, 2189: 182-196 A. J. Lockyer, et al. 1996. "Conformal Loadbearing Antenna Structure," presented at 37th AIAA SDM Conference, Salt Lake City, UT, April 1996 C. S. You , R. M. Lee, W. Hwang, H. C. Park and W. S. Park. 2003. "Microstrip Antenna for SAR Application with Composite Sandwich Construction: Surface Antenna Structure Demonstration," Journal of Composite Materials, 37(4): 351-364 J. H. Jeon, C.S. You, C. K. Kim, W. Hwang, H. C. Park and W. S. Park. 2002. "Design of Microstrip Antennas with Composite Laminates Considering their Structural Rigidity," Mechanics of Composite Materials, 38(5): 447-460 X. H. Shen, P. Delmotte and G. A. E. Vandenbosch. 2001. "Effect of Superstrate on Radiated Field of Probe Fed Microstrip Patch Antenna." IEE Proc.-Microw. Antennas Propag., 148(3): 141-146
Filament Wound Spherical Composite Pressure Vessel Design by an Energy Method 1
Byung-Sun Kim , Chee-Ryong Joe Composite Materials Lab, Korea Institute of Machinery & Materials(KIMM) 66 Sangnam-dong, Changwon, Kyungnam, 641-010, Korea 2
Department of Mechanical Design and Manufacturing Engineering, Changwon National University 9 Sarim-dong, Changwon, Kyungnam, 641-773, Korea
ABSTRACT A design method for filament wound spherical composite pressure vessels is suggested. This method utilizes an energy method to yield a simple equation, which can easily be applied to design spherical pressure vessels by on-site engineers. Generally, the design of a filament wound pressure vessel involves repeated and complicated structural analysis to find an optimal fiber orientation. But the orientation of fibers to form a spherical vessel cannot be decided just by the aspect of structural effectiveness. The way of winding a spherical vessel may vary due to the manufacturing hardware conditions as well as the software. The out look appearance of the surface of the vessel is also an important aspect. Thus, it takes prolonged time to design a filament wound pressure vessel using a general structural analysis. In this study, a simple design equation for filament wound spherical composite pressure vessels is suggested. This equation can be applied to design any spherical composite pressure vessel as long as the end-boss diameter of the vessel is relatively small, and the total thickness of the filament composite layers over the inner liner is equal, no matter what the winding sequence is. This equation can easily be used by on-site engineers to design spherical composite pressure vessels.
DESIGN OF COMPOSITE LAYERS Selection of Design Method The Composite Group of KIMM has developed two computer programs suitable for Composite Pressure Vessel Design, which are called 'KJMMPV and 'DOME' [1, 2]. 'DOME' decides the profiles of the dome area for cylinder type vessel by the tensile stress only without any bending stress. Under the assumption that Helical winding is applied on entire vessel and Hoop winding is for the cylinder part only, 'KHVIMPV' decides the number of Helical and Hoop layers, respectively, under the constant winding tension. 'KIMMPV' design concentrates more on the cylinder than dome area. Near spherical vessel in present study, does not require design in the cylinder area. The design in this case may be carried out by Laminated Plate Theory [4]. The theory may be applied appropriately when the vessel is composed of uniform ply angles or finite number of uniform plies. * Corresponding author, KIMM, 66SangnamDong, Changwon, Korea, 641-010, Fax : 82-55-280-3883, [email protected]
300
Filament Wound Spherical Composite Pressure Vessel
For the case of near spherical vessel, the finite number of various angle plies may be wound since the optimized design could be achieved when the symmetric winding shape is maintained with respect to the center of the sphere. Thus, instead of following up with Classical Plate Theory, it is more appropriate to design with Virtual Energy Method by introducing Virtual Displacement concept for the reinforcing fibers that provides endless variation of stacking angles. Virtual Energy Method
FIGURE 1. Spherical vessel with thickness much smaller than its radius
When internal pressure, P, is applies to a vessel in Fig. 1, the stress on the vessel when rearranged from P • n r1 = a • t • 2nr is Pr
m (1)
When the same situation is applied with Virtual Energy Method, under the assumption that the vessel contains non-compressible liquid and a small amount of same liquid is added by A V and the diameter, r, is increased to a • r. Then, the surface area and the volume of the vessel becomes Surface Area: 4 n r1 -» 4 n {a • r ) 2
(2)
4 4 Volume: — n r 3 -» — n (a • r ) 3 3 3 Here, the work for the pressure applied to the volume, A V, is £1=P-AF = ^-JP{(ar)3-r3}
(3)
The energy stored by elastic energy due to the increase in the surface area, AS, is E2 = a • t • AS = a • t • 4 n {{arf
- r2 }
(4)
(here, a is the tensile stress on the vessel) Since the work and the stored energy are equal, E{ = E2 Substituting equations (3) and (4) into equation (5),
(5)
Filament Wound Spherical Composite Pressure Vessel Pr(a3
301
-1)
3 t ( a 2 - 1) Since the radius increase is extremely small and limiting above equation, ,. P-r(a3 - 1 ) P-r .. ( a 3 - 1 ) hm a = lim —^ = hm - — «-*' "^ 3t(a2 - 1 ) 3; «-i(a2-l) According to the Lopital's Theorem,
(7)
,. ( a 3 - l ) ,. 3 a 2 3 hm -— = hm =«-' ( a 2 -1) «-i 2a 2
(8)
Thus, from equations (7) and (8), Pr a - -
(9,
Equation (9) is exactly same as equation (1), proving that Virtual Energy Method can also be applied accurately for the stress analysis of the composite pressure vessel.
Stress Analysis of Filament Wound Spherical Pressure Vessel by Virtual Energy Method A spherical composite pressure vessel with radius, r, and composite thickness, t, much smaller than radius is completely filled with incompressible fluid that provides pressure, P. To the vessel, a small amount of same liquid is add by AV and the diameter, r, is increased to a • r. Then, the volume of the vessel becomes 4 4 Volume: - n r3 -+-n{arf
(10)
Here, the work by adding AV to pressure, P, is same as equation (3). When the radius is increased to a • r, the total length of composite robin wrapped on the vessel is also increases b y a . Total Length of Composite Robin: /—>«;/ All reinforcing fibers should withstand uniform tension. If the tension on one reinforcing fiber robin is assumed to be F under the pressure, the energy stored for the elastic extension A/ by AV is E3 =F -Al = Fl(a - 1 )
(11)
When the manufactured vessel is pressurized, the elastic deformation will also occur in the matrix and some energy will be stored in the matrix. However, since the presence of
302
Filament Wound Spherical Composite Pressure Vessel
the micro cracks in the matrix during the internal pressure test was reported [2], it is not safe to rely on the strength of the matrix. In the present study, the reinforcing fibers' strengths were only considered in the stress analysis for safer design. Since the work and the stored energy are same = E3
(12)
Substituting equations (3) and (11) into (12) and rearranging for F F-
03,
(2-1
Applying lim on equation (13)
lim F =
-\
3/
a
APnP 3/
J
-
-I
3/
«->' >'
1
—
Arranging equation (14) for/,
Since F is the tension on a single fiber, F = as-
df-tf
(16)
<JS : Fiber Tensile Strength df : Fiber Robin Width tf : Fiber Robin Thickness
Combining equations (16) and (15), the total length,/, of reinforcing fiber robin is An r • P as
• df
• tf
Thus, the total volume, Vr, becomes Vr=l-df-tf=
4 n r3 • P
(18)
If the Fiber Volume Fraction of Filament Wound Pressure Vessel is vf, the total volume of the composite part is
Filament Wound Spherical Composite Pressure Vessel 4 ri p Vc=L-= « -
303
(19)
For composite thickness, t, and radius, r, the volume of the composite is Vc = An r2 • t
(20)
Equating equations (19) and (20), and arranging for t t
P-r =
—
(21)
This equation can easily be used by on-site engineers to figure out the thickness of the composite layer in near spherical composite pressure vessels. Even if it is not used as the final design value, it can be at least a good estimation to start with.
DESIGN EXAMPLE hi equation (21), substituting as = 4902 (MPa ), Vf = 0.5 P = 62 (MPa ) 0.5, r = Ro = 495 .7 (mm )
The composite thickness, t, becomes 62x495.7 t =
= 12.6 (mm) 4902x0.5
Since the outer radius of PE Liner is 497.5 mm and the composite thickness is 12.6 mm, the outer diameter of the final vessel becomes 1016.6mm which exceeds the required max, diameter of 994.2mm. Therefore, the vessel needs to have small portion of cylinder shape in the middle part of the vessel maintaining near spherical shape. Now, when the outer diameter of the vessel is 994.2mm and the Skirt's thickness is 5.4mm, the outer diameter of the cylinder is 983.4mm. Since the diameter of the vessel is reduced, the thickness of the composite could become thinner slightly. However, adopting the thickness of 12.6mm to this, the vessel design would be safer on the sidewall. The thickness of the PE liner is 6.7mm, and the inner diameter of the PE in the cylinder area is 944.8mm. If the length of the cylinder is L, the vessel's internal volume is
K, =„ ( »*£>.. I + ± , <»£«,.
(22)
However, the required final total volume is v, = 0.4883 x 109 mm 3 and the volume will be reduced by the insertion of the Metal End Boss at each ends of the vessel. Equating v, = 0.4883 x 109 • ' to equation (22)
304
Filament Wound Spherical Composite Pressure Vessel
0.4882 x 10' =
(23)
L+-.
Rearranging, 0.4883 x 109 - - K (472.4)3 L =
= 67 (mm)
n (472.4)'
Finally, Inner diameter of the liner on the cylinder = 944.8 mm Length of the liner on the cylinder = 67 mm Radius of the liner in Dome area = 472.4 mm Total thickness of the composites = 12.6 mm And the Schematic drawing of the composite pressure vessel is shown in figure 2.
FIGURE 2. Schematic Diagram of the Pressure Vessel
REFERENCES 1. 2. 3.
KIMM Report, 'Development of FRP Pressure Vessel©', MOST, BSM 160-1244.C, 1989 KIMM Report, 'Development of FRP Pressure Vessel(II)', MOST, BSM 203-1426«C, 1990 E. J. Jun, W.I. Lee, K. J. Yoon and T. W. Kim, 'Latest Composites', Kyohaksa Pub. Co., ISBN 89-09-01638-8 93580, 1995
Part VI
Failure Analysis
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Numerical Study on Buckling of Z-pinned Composite Laminates Wenyi Yan* Computational Engineering Research Centre, Faculty of Engineering and Surveying, the University of Southern Queensland, Toowoomba, QLD 4350, Australia Hong-Yuan Liu and Yiu-Wing Mai Centre for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering, the University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT Z-pinning is a newly developed technique to enhance the strength of composite laminates in the thickness direction. Recent experimental and theoretical researches manifest that z-pins can significantly improve mode I fracture toughness in doublecantilever-beam tests and mode II fracture toughness in end-notched-flexure beam tests. From a practical point of view, buckling accompanying delamination is a typical failure mode in laminated composite structures. For the purpose of a complete understanding on the z-pinning technique towards an improvement of the mechanical behaviour of laminated composites, in the present study, a numerical approach is applied to investigate the buckling of z-pinned composite laminates with initial delaminations under compression. The numerical results indicate that z-pinning can effectively increase the compressive strength of composite laminates provided that the initial imperfection is within a certain range. The magnitude of the improvement is consistent with available experimental data.
INTRODUCTION While recognizing the superiorities of composite laminates with high strength/ weight ratio and designable in-plane strength, the weak point of composite laminates with low delamination toughness has never been neglected. Over the last decade, many techniques have been developed to enhance the strength of composite laminates in the thickness direction, that is, z-direction. Among them, a novel approach, so-called zpinning has been developed by Foster-Miller hie in the USA [1]. In this technique, short stiff fibres initially contained in foam are inserted into the uncured composite in the zdirection through a combination of heat and pressure compacting the foam. After curing, a simple 3D structured laminated composite is created. Well designed z-pinning process can minimize the amount of in-plane fiber damage. Compared to other techniques of through-thickness reinforcement, such as stitching and weaving, z-pinning is reckoned as a convenient and cost-effective approach. The size of pin diameter is normally from 0.15 mm to 1 mm. The pin can be made of composite, such as carbon fibre/BMI or metallic materials from titanium to stainless steel [2]. * Corresponding author, Faculty of Engineering and Surveying, the University of Southern Queensland, Toowoomba, QLD 4350, Australia, Fax: ++61 7 4631 2526 Email: [email protected]
308
Buckling of Z-pinned Composite Laminates
Recent experimental and theoretical researches confirm that z-pins can significantly improve mode I fracture toughness in double-cantilever-beam (DCB) and mode II fracture toughness in end-notched-flexure (ENF) tests [3-6]. Depending on pin density, experimental data shows that the mode I fracture toughness of pinned laminates can be improved by about 20 times and mode II fracture toughness can be improved by about 9 times [3]. Theoretical and numerical investigations reveal that a large amount of energy absorption is caused by the pull-out process of the z-pins, which results in a much higher fracture energy release rate during delamination growth in the z-pinned laminates [4-6]. In practice, buckling accompanying delamination under compression is a typical failure mode in laminated composite. Compression after impact becomes a routine test either to evaluate the impact damage or to investigate the influence of delamination on buckling strength, or damage tolerance. Generally, two kinds of buckling modes have been observed in practice: local buckling and global buckling, which are illustrated in Fig. 1 for z-pinned laminates. Z-pins IP
a. Local buckling mode
Z-pins IP
-*—
4d
IP
b. Global buckling mode
FIGURE 1. Global and local buckling modes in z-pinned composite laminate under compression.
Figure 1 (a) shows a case of local buckling. Under edge compression the composite laminates might separate along the initial delamination (damage) plane, or one of the initial delamination planes in the case of multiple delaminated plies due to impact. After that, the separated sub-laminates collapse simultaneously. Due to the relatively low interlaminar fracture toughness, local buckling can normally trigger an unstable delamination growth. On the contrary, the initial delamination surfaces will not separate in a global buckling and the sub-laminates collapse in the same direction, as shown in Fig. l(b). Clearly, initial delamination has minor influence on global buckling. For the purpose of examining damage tolerance, or the reduction of compression strength resulted from the delamination, boundary conditions are normally set properly to avoid global buckling in experiments so that only local buckling is allowed to take place [7, 8]. In a z-pinned laminated composite, due to opening of the delamination under the bending moment in local buckling, the pins will be forced to pull out, which is shown in Fig. l(a). Certainly, the reaction of the pulling force on the pins will try to bridge the sub-laminates together, i.e., resist the buckling deformation. Furthermore, similarly to the case of fracture in a double-cantilever-beam, the pins will provide bridging forces to hinder delamination from growing. Hence, it is expected that z-pins will enhance the local buckling strength
Buckling of Z-pinned Composite Laminates
309
of a composite laminate under edgewise compression, fn 1993, Shu and Mai presented their original studies on delamination buckling with stitching [9, 10]. It was found that through-thickness stitching delayed both buckling and delamination extension. The present study is aimed to numerically quantify the influence of z-pinning on the local buckling strength. It is obvious that z-pinning should only have a minor effect on global buckling because the pins will not be pulled out in this case. Some experimental studies on compression after impact tests on z-pinned laminates were conducted at Cranfield University [11-13]. In these tests, the initial delamination damage in the pinned laminates was induced by low velocity impact. After that, in-plane compression experiments were carried out to measure the compression strength/buckling strength, which is generally called compression after impact (CAT) test. The first stage of the test to initiate delamination by impact also served to evaluate the influence of zpinning on impact damage, which was quantified by the projected delamination area. Zhang et al. [13] reported that z-pinning reduced impact damage area by 19% to 63% in their tests and the mechanism is that z-pins can effectively improve the mode II fracture toughness against shear-induced delamination under impact loading. In their CAI tests, an averaged 45% increase of compression strength was measured in z-pinned laminates. To obtain a complete understanding of z-pinning technique towards improvement of the mechanical behaviour of composite laminates, in the present study, a numerical approach is applied to investigate the buckling of a z-pinned composite laminate with initial delaminations under edge compression. The influence of z-pins is demonstrated by comparing with the results derived from unpinned samples. NUMERICAL ANALYSIS Description of buckling model To analyze the effect of z-pinning on the buckling strength of composite laminates, only the local buckling failure mode with z-pins pulling out during the buckling process will be considered. Generally, the damage due to impact is quite complicated, which includes multi-layer delaminations, fibre breaking and matrix cracking. For simplicity, a symmetrical structure with three initial interlaminar delaminations is considered in our study. The major longer initial delamination is assumed to locate in the middle plane of the laminate and two minor shorter initial delaminations are in the middle of the sublaminates. Due to symmetry, only a quarter of the whole problem is simulated in our finite element model, which is illustrated in Figure 2.
U(P)
] /
•
(m hr> pp pp pp (m qp o"o pp pp go op 1 1 1 1 1 1 1 1 1 1 1 1 1 111 1 1 1 11 I I I I I I I 1 1 1 1 1
da
FIGURE 2. Numerical model for local buckling analysis.
Here, we consider a plane strain problem with the y-axis in the direction with zero normal strain. The symmetrical planes, one horizontal and one vertical, are replaced by simply supported boundary conditions in the FE model. L in Figure 2 represents the half
310
Buckling of Z-pinned Composite Laminates
length of the laminate and h is the half-thickness. The compressive displacement, U, corresponding to the compressive force per unit width, P, for half of the laminate is applied at the right end of the model. The initial damage of the major delamination is represented by two parameters, da and du da is the half-size of the delamination area and di is the initial displacement from the separated surfaces of the major delamination to the middle plane at the centre of the initial delamination zone, which represents the out-ofplane damage and is called an imperfection here. This initial displacement is assumed to disappear linearly towards the border of the delamination zone, which is the crack-tip in terms of fracture mechanics. The thickness of the minor delamination with a length of dm is treated as zero. This simplified damage description can be viewed as a proper approximation of a typical practical case. The distance between adjacent pins is represented by dc. The values of all the parameters are summarized in Table I, which are consistent with similar experimental tests [13]. TABLE I. Values of parameters to describe FE model and z-pinning. h (mm) 2
L (mm) 75
da (mm) 20
4(mm)
rf, (mm) 0.01-0.3
15
dc(mm) 1.75
Sa (mm) 0.1
2
The composite laminate is simplified as transversely isotropic elastic with the x-y plane, i.e., 1-2 plane, as the plane of isotropy. According to the elasticity of anisotropic materials, 5 independent material constants are required to determine the elastic behavior and which are chosen based on [12] and listed in Table II. TABLE II. The material constants of the composite laminate. E, (GPa) 67.8
E2 (GPa) 11
Vl2
Vl3
M-12 ( G P a )
0.34
0.3
15
Z-pin pullout simulation During the buckling process, the z-pins in the delamination zone will be pulled out. General discussion and experimental work on the z-pin pullout can be found in [14, 15]. In this paper, a simple bi-linear bridging model is adopted, which was proven to be very effective to capture the z-pinning bridging effect in previous studies [5, 6]. This model is represented by the function between the bridging force, P, and the pullout displacement, S, which is: P=
\ \PB-Pa(S-Se)Hh-Sa),
0<5<8a 8<5
(1)
where Pa is peak bridging force and its corresponding pullout displacement is 8a. The ultimate pull-out displacement, h, is equal to half-thickness of the laminate. The bridging force is zero when the pin is completely pulled out from the composite, that is, when 5 = h. The values of P a and 8a are listed in Table I. The deterioration of the impact on the z-pin bridging behavior is reflected by choosing a lower value of Pa than that in our previous study. A set of non-linear springs are used in the finite element model to simulate the pullout process of the individual pins [5].
Buckling of Z-pinned Composite Laminates
311
RESULTS AND DISCUSSION The buckling problem without delamination growth is studied in this paper, which corresponds to the composite laminates with high fracture toughness. Figure 3 shows the variation of the compressive force per unit width, IP, with the applied compressive displacement, U, for a given imperfection 4=0.08 mm. Both unpinned sample and zpinned specimen are analyzed. As shown in Fig. 3, the compressive force increases linearly with the displacement at the initial stage. The unpinned sample bifurcates first and no more compressive force can be applied, which leads to buckling of the structure. In contrast, the z-pinned specimen can continuously support an increasing force linearly over the bifurcation point of the unpinned sample until the force reaches a higher value. After that, it collapses quickly with a sudden force reduction and reaches the postbuckling state. Here, Riks method is applied to capture the post-buckling state of the zpinned laminate [16]. To obtain the compressive critical force, 2Pcr, simple static analysis can give exactly the same result. Figure 3 clearly manifests that the compressive strength has been increased from 0.84 to 1.28 kN/mm caused by z-pinning. This increase is in good agreement with available experimental results of Zhang et al. [13].
Unpinned sample Z-pinned specimen with Riks method
Compressive displacement, U, (mm)
FIGURE 3. The compressive force versus compressive displacement for unpinned sample and z-pinned specimen with 4=0.08 mm.
Our analysis indicates that the predicted compressive strength, oc=Pc/h, depends on the imperfection, dt. Figure 4 shows a c as a function of dt. To demonstrate the effect of zpinning on the compressive strength, the results from the unpinned samples are also shown by the solid curve in Figure 4, which indicates that the compressive strength is slightly reduced with increasing imperfection size. However, the compressive strength of z-pinned specimens is reduced more sharply with increasing size of the imperfection. Eventually, the two curves merge together when d, reaches 0.3 mm, which means the influence of z-pinning can be neglected if dt is over 0.3 mm. Larger di means higher initial bending moment applied on the sub-laminates under a given compressive force, which in turn creates a higher bending deflection. Thus, the pins can be forced out more easily due to the higher deflection. No experimental evidence, however, is yet available to verify this prediction. SUMMARY A finite element model is developed to evaluate the influence of z-pinning on the buckling behavior of composite laminates with initial interlaminar delaminations. The bridging effect of z-pins during local buckling is simulated by a set of non-linear springs.
312
Buckling of Z-pinned Composite Laminates
Our results indicate that z-pinning can effectively increase the compressive strength of composite laminates due to the failure of local buckling provided that the initial size of the imperfection is no larger than a certain value. Further parametric study is under way to examine this problem in detail, especially buckling-induced delamination growth.
- Unpinned sample • Z-pinned specimen
Imperfection, d}, (mm)
FIGURE 4. Predicted compressive strength as a function of imperfection size, dj.
ACKNOWLEDGEMENT The authors would like to thank the Australian Research Council for the support of this project on the effect of z-pinning on composite laminates. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13.
14.
15. 16.
Freitas, G., C. Magee, P. Dardzinski and T. Fusco. 1994. "Fiber insertion process for improved damage tolerance in aircraft laminates," J. Adv. Mater., 25(4):36-43. http://www.aztex-z-fiber.com/ Cartie, D. D. R., I. K. Partridge. 1999. "Delamination Behaviour of Z-pinned Laminates," in Proceedings of the 12'h international conference on composite materials, ICCM12, Paris 5th-9th July. Liu, H.-Y., Y.-W. Mai, 2001. "Effects of z-pin reinforcement on interlaminar mode I delamination," in Proceedings of the 13th International Conference on Composite Materials, ICCM13, Beijing. Yan, W., H.-Y. Liu, Y.-W. Mai. 2003. "Numerical study on the mode I delamination toughness of Zpinned laminates'" Comp. Sci. Tech., 63:1481-1493. Yan, W., H.-Y. Liu, Y.-W. Mai. "Mode II delamination toughness of Z-Pinned Laminates," to appear in Comp. Sci. Tech. Pavier, M. J. and M. P. Clarke, 1995. "Experimental techniques for the investigation of the effects of impact damage on carbon fibre composites," Comp. Sci. Tech., 55:157-169. Short, G. J., F. J. Guild and M. J. Pavier, 2001. "The effect of delamination geometry on the compressive failure of composite laminates," Comp. Sci. Tech., 61:2075-2086. Shu, D. and Y.-W. Mai, 1993. " Delamination Buckling with Bridging", Comp. Sci. Tech., 47:25-33. Shu, D. and Y.-W. Mai, 1993. "Effect of Stitching on Interlaminar Delamination Extension in Composite Laminates," Comp. Sci. Tech., 49:165-171. Cartie, D. D. R. 2000. "Effect of z-fibres on the delamination behaviour of carbon fibre/epoxy laminates," PhD thesis, Cranfield University, U. K. Negre, P. 2000. "Compression-after-impact performance of z-pinned carbon fibre/epoxy laminates," Master thesis, Cranfield University, U. K. Zhang, X., L. Hounslow and M. Grassi, 2003. "Improvement of low-velocity impact and compressionafter-impact performance by z-fibre pinning," in Proceedings of the 14th international conference on composite materials, ICCM14, San Diego, California. Liu, H.-Y., W. Yan and Y.-W. Mai, "Z-pin bridging force in composite delamination," Fracture of Polymers, Composites and Adhesives II", ESIS Publication 32, Editors: B. R. K. Blackman, A. Pavan and J. G. Williams, 491-502. Dai, S.-C, W. Yan, H.-Y. Liu and Y.-W. Mai. "Experimental study on z-pin bridging law by pullout test," submitted to Comp. Sci. Tech. ABAQUS 2002 Version 6.3. Providence, RI: HKS Inc.
A Three Dimensional Approach of Fatigue Crack Propagation for Aluminum Panels Repaired with Single-Sided Composite Laminates H. Hosseini-Toudeshky*, G. Sadeghi Aerospace Engineering Dept. - Amirkabir University of Technology, Tehran, Iran H. R. Daghyani Mechanical Engineering Dept. - Amirkabir University of Technology, Tehran, Iran
ABSTRACT hi this paper fatigue crack growth of centrally cracked aluminum plates repaired with single-sided composite patches are studied. Three dimensional finite elements analysis of the repaired aluminum panels were performed to obtain the crack-front shape and fatigue crack growth life of them. The crack front shape was obtained using the variation of stress intensity factors along the crack-tip during the propagation, hi this procedure crack-tip fracture parameters of J and Ki were calculated using Equivalent Domain Integral (EDI) method. Fatigue crack growth lives for a certain crack growth length calculated from this procedure are also compared with those obtained assuming that the crack front is perpendicular to the plate surfaces.
INTRODUCTION Adhesively bonded composite patches or reinforcements are structurally efficient and much less damaging to the structure than traditional repairs based on mechanically fasteners metallic patches. Baker and Jones [1] studied the repair technique using adhesively bonded Boron/Epoxy composite patches which is widely considered as a cost effective and reliable method. One of the most challenging aspects of bonded composite repair technology has been the stress analysis of repaired panels and the subsequent fracture parameters calculations. The difficulty arises from the fact that a metallic panel under in-plane loading would develop highly complicated three dimensional stresses, if composite patches are bonded to its surface un-symmetrical (single-sided repair). In many studies, the variation of stresses over the thickness of the cracked plate has not been considered in the fracture analyses or crack propagation procedure [1-4]. In many studies the stresses and strains fields of the mid-plane have been used to calculate the fracture parameters, however, the maximum stresses and strains occur on the un-patched surface of the cracked plate [5]. In this paper, three dimensional finite elements analysis of the repaired aluminum panels with single-sided composite patches were performed to obtain the crack front shape during the propagation and fatigue crack growth life of them. The crack front shape was calculated using the obtained stress intensity factors along the crack-tip. * Corresponding author, E-mail: [email protected]
314
A Three Dimensional Approach of Fatigue Crack Propagation
Crack-tip fracture parameters of J and Ki were calculated using Equivalent Domain Integral (EDI) method. Fatigue crack growth life of the panels obtained from this procedure are also compared with those obtained assuming that the crack front remains perpendicular to the plate surfaces during the crack propagation. EDI TECHNIQUE AND 3D CRACK GROWTH In general, 3-D crack problems can be analyzed using finite elements method. Arbitrary crack configurations can be modeled using different methods such as Crack Opening Displacement (COD) and Virtual Crack Closure Technique (VCCT) to evaluate strain energy release rate and stress intensity factor, but they can be used for linear elastic problems only. EDI can be used for elastic-plastic fracture analysis of the components. This method is based on three dimensional calculation of J-integral parameter, taking into account the non-elastic strains. It is a path independent integration and could be used for arbitrary crack front shapes. It can be used to calculate the variations of fracture parameters along the crack front of the single sided repaired panels during the crack propagation. The J-integral definition considers a balance of mechanical energy for a translation in front of the crack. Using the divergence theorem, in linear elastic condition and in the absence of surface loads the following representation of J for 3-D problems [6] is obtained: J f = -[
\W
dxt
IJ
8xk8xj
where W is strain-energy density; tj is traction component; u,- are displacements components, the value of S at crack-tip is zero and varies through the crack-tip elements in radial direction, and f is the width of crack-tip element. Having the Jintegral value from the above equation the stress intensity factors are obtained using K, = TJE'JJ [6]. Where E* is equal to E in plane stress and E* = £7(1-o 2 ) in plane strain conditions. Having the variations of stress intensity factors and material properties along the crack-front one may use Paris law to calculate the crack propagation life for a certain crack growth length. In the current study variation of crack growth length are calculated along the crack-front for a certain number of loading cycles in each step. FINITE ELEMENTS MODELING Several aluminum panels repaired with single sided adhesively bonded composite laminates were analyzed using finite elements method. Typical geometry and loading of aluminum panels, adhesive layer and composite patch are shown in figure 1. The panels were assumed to be made of 2024-T3 aluminum alloy. Material properties and dimensions of panels, adhesive layer and composite patches are listed in Tables 1 and 2. The Paris Law constants are c = 2.44E-8 and m = 2.601 for the aluminum alloy [5]. hi these three dimensional modeling a 20-node singular solid elements was used to model the crack front. This element gives enough strains to calculate equation (1) numerically at 8 gauss points for in each element. An isotropic 8-node-solid element was used to model the aluminum panels and adhesive. Furthermore, a layered 8-nodesolid element was used to model the laminated composite patch. 10 and 2 elements
A Three Dimensional Approach of Fatigue Crack Propagation
315
t t t t t t t t t t
,rTTTTTTT7V |^
2W (Plate)
^J
FIGURE 1 Typical geometry and loading of single-sided repaired panels TABLE I Material properties
E (MPa) V
Al. panel 71.3E+3 0.33
adhesive 1.89E+3 0.33
patch Ex = 208E+3, Ey = 25.4E+3 v
xr -vxz
=
0.1677 ,vm
=0.035
TABLE II Dimensions of the models
L (mm) W(mm) t (mm)
Aluminum panel 75 50 2.29,3.50
Adhesive 30 20 0.1016
patch 30 20 0.127 per layer
were used in the thickness of plate and adhesive respectively and a very fine mesh was generated for the area near the crack-tip. The patches material was Boron/Epoxy composite and unidirectional lay-ups were used for the patches in all models. The stress and strain fields of the repaired panels were obtained using ANSYS finite elements program. A macro program was also developed to handle the crack growth modeling procedure and to find the crack front shape during the crack propagation. In this analysis we assumed that there is no debonding between the cracked plate and patch. A dynamic mesh generation using automesh capability of the code was also used to generate the mesh of the repaired panels at each crack growth step. The Jintegral and Ki values were computed for the crack-front in each step. Then the crack growth increment was calculated and the geometry was updated for "the new crack shape. The above procedure was repeated for several steps to find the crack-front shape along the crack propagation. RESULTS AND DISCUSSIONS Figures 2(a) and 2(b) show the variations of normalized stress intensity factor versus normalized thickness of the panel and patch respectively for initial crack condition. Stress intensity factor (SIF) is normalized using the following expression: - * * - \ln*m
"
(2)
In this equation a = 5 mm is half of the initial crack length and a^ is remotely applied unit tensile stress. Panels are bonded with 2, 6, 12 and 18 layers Boron/Epoxy
316
A Three Dimensional Approach of Fatigue Crack Propagation
composite patches. For panels without repair SIF is uniformly distributed along the crack-tip except at edges. When the composite laminates are bonded, SIF has a nonuniform distribution along the thickness. The SIF value at the un-patched surface of the repaired panels is larger than those obtained for the mid-plane and patched surface of the panel. The un-patched SIF are increased for small patch thicknesses with respect to the un-repaired panels SIF. But, by more increasing the number of patch layers the SIF at un-patched surface is reduced. This is due to the effect of composite laminates to stop the opening of the crack faces and decreasing the displacements against the induced extra bending. Therefore by increasing the number of patch layers the un-patched surface SIF is reduced. Mid-plane SIF is significantly decreased by increasing the number of patch layers. 1.4 1.2-
o 0. 0.204
0.6
Normalized thickness.
(a)
0.5
1
1.5
2
Patch thickness (mm)
(b)
FIGURE 2 (a)Normalized SIF along the thickness at crack-tip for various patches (b) Normalized SIF versus patch thickness at un-patched surface and mid-plane Panel thickness t = 2.29 mm
Figure 3 shows the crack front curve during the propagation for various numbers of load cycles and for a typical repaired panel with panel thickness of 2.29mm and 18 layers patch. This figure shows that the crack is quickly started to grow from unpatched surface side of the initial crack-tip to generate the new crack-front shape. Then it will grow along the panel thickness in an almost uniform manner after a few steps. The crack growth rate on the free surface is bigger than the mid-plane and patched surface of the cracked panel. Figure 4 shows the variation of normalized crack growth life versus patch thickness of the repaired panels for two typical panels. These lives were estimated for a certain crack growth from a=5mrn to a=8rnm and were normalized with respect to the un-repaired panel life. This curves show that the fatigue crack growth life of the repaired panels are increased significantly using small patch thicknesses, but there is a small and almost steady changes in the crack growth life for the patch thicknesses of bigger than 0.3mm (2 layers). Crack growth life extension of the repaired panels using various number of layers are listed in table 3. These lives were obtained for a certain crack growth from a=5.0mm to 3=8.0"™ at un-patched surface of the panel. The remotely applied stresses were the same for all repaired panels. These tables show that the patches are more efficient in life extension for thin plates. The life extension rate of the panels resulted from the panels with thin patches are much bigger than those obtained from the thick patches.
A Three Dimensional Approach of Fatigue Crack Propagation nitial crack
= ^
317
•— 465000 <~ 909000 »~1176500 — 1382400 »—1568700
056000 2S3500 4 78200 807500
I ! 5
1i 6
7
Crack front shape after 1807500 cycles
8
Crack-tip position along the thickness of cracked plate (m
FIGURE 3 Crack-front configurations for several loading cycles
0
0.5
1
1.5
2
Patch thickness (mm) FIGURE 4 Normalized crack growth life versus patch thickness for various panels Table III Life extension of composite laminates for different repaired panels a- Panel thickness t = 3.50 mm Number of Layers 0 2 6 12 18
Cycles (10*6) 0.798 1.112 1.179 1.230 1.276
Life extension (%) 0 39.42 47.76 54.21 60.02
b- Panel thickness t = 2.29 mm Number of Layers 0 2 6 12 18
Cycles (10*6) 0.775 1.213 1.446 1.586 1.664
Life extension (%) 0 56.60 86.68 104.74 114.89
Fatigue crack growths of the repaired panels were also studied based on the assumption that the crack front remains perpendicular to the panel surfaces during the propagation using three dimensional finite elements analysis. Figures 5(a) and 5(b) show the normalized fatigue life versus patch thickness of the repaired panels with 2.29 mm thickness based on the new assumption and real crack-front shape. The performed results in figures 5 (a) and 5(b) were obtained for a certain crack growth from a=5.0mm to a=8.0mm at mid-plane and un-patched surface of the panels respectively. As figure 5 (a) shows, the estimated lives based on the mid-plane crack growth length and fracture parameters considering the real crack-front shape are smaller than those obtained using the assumption of crack-front perpendicular to the
A Three Dimensional Approach of Fatigue Crack Propagation
318
panel surfaces, but they have similar general behaviors. Therefore the estimated life extension based on this assumption may lead to the non-conservative results. Figure 5(b) shows that the estimated lives based on the un-patched surface crack growth length and fracture parameters considering the real crack-front shape are bigger than those obtained using the assumption of crack-front perpendicular to the panel surfaces. The calculated lives based on the new assumption leads to the un-valid results especially for the repaired panels with small patch thickness.
1
1.5
Patch thickness (mm)
(a)
0.5
1
1.5
Patch thickness (mm)
(b)
FIGURE 5 Normalized life versus patch thickness of repaired panels (panel thickness = 2.29 mm) (a) using mid-plane parameters, (b) using un-patched surface
CONCLUSION Fatigue crack growth was studied for centrally cracked aluminum plates repaired with single-sided composite patches. The crack front shape during the crack propagation and fatigue crack growth life of the repaired panels were obtained using three dimensional finite elements analysis. The un-patched SIF are increased for small patch thicknesses with respect to the un-repaired panels SIF. But, by more increasing the number of patch layers the SIF at un-patched surface is reduced. Mid-plane SIF is also significantly decreased by increasing the number of patch layers. The estimated lives based on the mid-plane crack growth length considering the real crack-front shape are smaller than those obtained using the assumption of crack-front perpendicular to the panel surfaces, but they have similar general behaviors. Therefore the estimated life extension based on this assumption may lead to the nonconservative results. The calculated lives based on the new assumption using unpatched surface parameters leads to the un-valid results. REFERENCES 1. Baker, A. A. and Jones, R.," Bonded repair of aircraft structures", Martinus Nijhoff Publisher, Dordrecht, Netherlands, 1988, 2. Ratwani, M. M., "Analysis of Cracked Adhesively Bonded Laminated Structures", AIAA J., Vol.17, No. 4, 1979, PP. 988-994 3. Rose, L. R. F., "A Cracked Plate Repaired by Bonded Reinforcements", Int. J. Fract, Vol. 18, No. 2, 1982, PP: 135-144. 4. Hosseini-Toudeshky H., Shahverdi H., and Daghyani H. R., "Fatigue life assessment of repaired panels with adhesively bounded composite plates" (Second Asian Australian Conference on Composite Materials, ACCM- 2000, Kyonju, Korea, 18-20 August, 2000) 5. Hosseini-Toudeshky, H., Mohammadi, B., and Daghyani, H. R., "Effects of patch lay-up configuration on fracture parameters and fatigue life of single-sided repaired panels in mixedmode conditions", 4th Iranian Aerospace Society Conference, 23-27 Jan. 2003, Tehran 6. G. P. Nikishkov, S. N. Atluri 1987. "Calculation of Fracture Mechanics Parameters for an Arbitrary Three Dimensional Crack, by the 'Equivalent Domain Integral' Method" Int. J. for Numerical Methods in Eng., 24:1801-1821.
Time-temperature-water Absorption Superposition Principle for Flexural Fatigue Strength of Unidirectional CFRP Laminates Jun Ichimura* and Naoyuki Sekine Graduate School, Kanazawa Institute of Technology, Japan Masayuki Nakada and Yasushi Miyano Materials System Research Laboratory, Kanazawa Institute of Technology, Japan
ABSTRACT This paper is concerned with the influence of water absorption on the time-temperature dependent flexural fatigue strength of unidirectional CFRP laminates, which consist of carbon fiber and epoxy resin. The CFRP laminates were prepared under three conditions of Dry, Wet (percentage of water content: 1.0% and 2.0%) and Wet+Dry. Three-point bending constant strength rate (CSR) and fatigue tests for these three kinds of CFRP laminates were carried out under various loading rates and temperatures. It is cleared that the flexural CSR and fatigue strengths of CFRP laminates strongly depend on the water absorption as well as time and temperature, and the time-temperature-water absorption superposition principle holds for there flexural CSR and fatigue strengths.
INTRODUCTION Recently carbon fiber reinforced plastics (CFRP) has been used for the primary structures of airplanes, ship, spacecraft and others, in which the high reliability should be kept during the long operating period. Therefore, it is strongly expected that the accelerated testing methodology is established for the long-term life prediction of composite structures exposed under the actual environment of temperatures, water and others. The mechanical behavior of polymer resins exhibits time and temperature dependence, which is called viscoelastic behavior, not only above the glass transition temperature Tg but also below Tg. [1-8] Furthermore, the viscoelastic behavior of polymer resins also depends on water absorption.[9-12] Thus, it can be presumed that the mechanical behavior of polymer composites significantly depends on water absorption as well as time and temperature. This paper is concerned with the influence of water absorption on the time-temperature dependent flexural strength of unidirectional CFRP laminates. The CFRP laminates which consist of PAN-based carbon fiber and epoxy resin were treated under three conditions of Dry, Wet and Wet + Dry after molding. Three-point bending constant strength rate (CSR) and fatigue tests for these three kinds of CFRP laminates were carried out under various loading rates and temperatures. The influence of water absorption on time-temperature dependent flexural CSR and fatigue strengths is * Corresponding author, 3-1 Yatsukaho, Matto, Ishikawa 924-0838, Japan, Fax:+81-76-274-9251,
Time-Temperature-Water Absorption Superposition Principle
320
evaluated, and the applicability of time-temperatures-water absorption superposition principle is discussed for the flexural fatigue strength as well as the flexural CSR strength for this CFRP laminates.
EXPERIMENTAL PROCEDURE The CFRP pre-preg sheets are made of unidirectional carbon fiber (Fortafil 510, Fortafil) and epoxy resin (Cape 2002, Cape). The CFRP laminates were formed by hot pressing these 15 pre-preg sheets at 130°C for lhour. The fiber volume fraction of the laminates was approximately 53%. The thickness of CFRP laminates was 3mm. These laminates were cut to the transverse direction of fibers, and the length and width were 80mm and 10mm, respectively. The test specimens were treated under three conditions of Dry, Wet and Wet + Dry. Details of treated conditions are shown in Table 1. The Dry specimens were obtained by holding the cured specimen in the oven at 150°C for 2 hours. The Wet specimens were obtained by soaking the Dry specimens in hot water at various temperatures and times. The Wet + Dry specimens were obtained by dehydrating the Wet specimens in the oven at 150°C for 2 hours. TABLE I
Treated conditions for Dry, Wet and Wet + Dry
Water content Dry
0%
Wetl.O-a Wetl.O-b Wet2.0 Wetl.O+Dry Wet2.0+Dry
1.0% 1.0% 2.0% 0% 0%
hi oven 150°Cx2h 150°Cx2h 150°Cx2h 150°Cx2h 150°Cx2h 150°Cx2h
f
hi water
f (-
80°C x 144h 95°Cx24h
f +f
95°Cx48h 80°C x 144h 95°C x 48h
H^
In oven
HH HH
150°Cx2h 150°Cx2h
RESULTS AND DISCUSSION Flexural CSR Strength The left side of Fig. 1 (a)-(f) shows the flexural CSR strengthCTSversus time to failure ts at various temperatures T for Dry, Wetl.O and Wet2.0 and Wetl.O + Dry and Wet2.0+Dry specimens, where ts is the time period from initial loading to maximum load during testing. The master curves of a s versus the reduced time to failure ts' were constructed by shifting a s at various constant temperatures along the log scale of ts. Since the smooth master curve of a s for each specimen can be obtained as shown in the right side of each graph, the time-temperature superposition principle is applicable for each as. From Fig.l (b) and (d), it was cleared that c s decreases with water absorption. The chain line in Fig.l(c) show the master curve of a s for Wetl.O-a. Since the master curve of o"s for Wetl.O-a and Wetl.O-b agree well with each other, the master curve of as for wet specimens depend on the amount of water absorption regardless of soaking time and temperature. The 0S for Wetl .0+Dry specimen return perfectly to that of Dry specimen by drying after water absorption, however o s for Wet2.0+Dry specimen did not return to that of Dry specimen by drying after water absorption as shown in Fig.l (e) and (f).
Time-Temperature-Water Absorption Superposition Principle Reduced temperature T' f ] 25 50 70 80 90100 120 1 1 i I 1 1
321
Reduced temperature T' [°C] 25 50 70 B0 90 Dry
V1mln
5
20
""
Q,
-
A*
A X
25°C 50DC
-
o 70t O 80°C
O 100°C n 120°c 1 i rO i i i 0 2 •2 0 2 4 - 2 log t, [mini
i 4
1 1 1 6 8 10 12 14 16 18 log V [min]
log ts [min]
log V [mini
(b)Wetl.O-a
(a) Dry Reduced temperature T' pc] 25 50 70 80 90
Reduced temperature T [°C] 25 50 70 80 90
(c)Wetl.O-b
(d) Wet 2.0
Reduced temperature T [°C] 25 50 80 100 120
Reduced temperature T' [°C] 25 50 80 100 120
•51100
1
I
P
Dry 80
±JL ml
W= 0% (Wet2.0+Dry) T0=25"C_ ^Imin
A
\
\\ Vo
I
4
6 8 10 12 14 16 18 log ts' [min]
-
25"C 50"C o 70°C O 80-C 90°C o 100"C D 120°C A X
^4-2 0 2 4 - 2 log t« [min]
0
Jo
40 > t3
20 i 2
i 4
i i 6 8 10 12 14 16 1 log y [min]
0
(e)Wetl.0+Dry (f) Wet2.0+Dry FIGURE 1 Master curves of flexural CSR strength
25 I
f. -2
I
~J -4
I I I
f
I
5
Temperature T [°C] 50 SO 100 120 1 I ' I 1 T 0 =25°C W 0 =0%
"12 -16 -18
O Dry AWeH.O - AWet2.0 DWet1.0+Dry l I l 34 32 30
1 28
1 26
24
FIGURE 2 Time-temperature shift factors of flexural CSR strength
The time-temperature shift factors aTo(T) of crs for all specimens are shown in Fig.2. These aTo(T) are in good agreement with two Arrhenius' equations with different activation energy AH. The knee point temperature of aTo(T) decreases with water absorption and returns to that for Dry specimen by drying after water absorption. Figure 3 shows the SEM photographs of fracture surface for Dry, Wet and Wet + Dry specimens after flexural CSR test at temperature T=25°C. The Dry, Wetl.O-b and Wetl.O+Dry specimens were failed mainly by cohesive fracture of matrix resin.
Time-Temperature-Water Absorption Superposition Principle
322
The Wet 2.0 and Wet2.0 + Dryspecimens were failed mainly by interfacial fracture of carbon fiber between matrix resin. It can be considered that this change of fracture mode is caused by water absorption, and the imperfect recovery by dehydratiy of the CTS for Wet2.0+Dry specimen is caused by this change offracturemode.
(a)Dry
(b)Wetl.O-b
(c)Wetl.0+Dry
(d)Wet2.0 FIGURE 3 SEM photographs of flexural CSR strength
(e)Wet2.0+Dry
The left side of Fig.4 shows the master curves of crs for Dry, Wetl.O and Wet2.0 specimens. A smooth gland- master curve of crs was obtained by shifting the master curves of as for Wet 1.0 and Wet2.0 specimens along the log scale of reduced time to failure t s ' until they overlapped each other. There fore, the timetemperature-water absorption superposition principle (TTWSP) holds for CTS. The time-temperature-water absorption shift factor a-ro,wo(T,W) obtained experimentally from Fig.4 were plotted in Fig.5. 1Q0 -4
-2
0
Reduced time to failure log t,' [min] 2 4 ' 6 8 10 12 14
16
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TD=25°C
25 \
Temperature T [°C] 50 80 100 120 Do of Wetl.O
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-
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FIGURE 4 Grand-master curve of flexural CSR strength
FIGURE 5 TTWSP shift factor of flexural CSR strength
24
323
Time-Temperature-Water Absorption Superposition Principle Fatigue Strength
The flexural fatigue strength Cf versus number of cycles to failure Nf for the Dry and Wet 1.0 specimens at frequency f=2Hz and stress ratio (minimum stress/ maximum stress)R=0.05 are shown in Fig.6. The upper portion of Fig.7 shows a f versus the reduced time to failure tf' obtained from the S-N curves at various temperatures shown in Fig.6 based on the time-temperature superposition principle for CSR strength. Each point on these curves of constant reduced frequency represents the number of cycles to failure. Connecting the points of the same Nf with these curves, the master curves of c?f for constant Nf are constructed as shown in the lower side of Fig.7. The left side of Fig.8 shows the master curves of af for Dry and Wet 1.0 specimens obtained in Fig.7. These fatigue master curves can be superimposed by shifting there curves along the log scale of reduced time to failure tf' using the time-temperature-water absorption shift factor aTO,wo(T,W) for CSR strength as. Therefore, the TTWSP for a s also holds for af.
Wet1.0(Tv,=80'C) f=2Hz R=0.05
0
1
2 3 4 5 Number of cycles to failure log N,
0
1
2 3 4 Number of cycles to failure log N,
(a) Dry (b) Wet 1.0 FIGURE 6 Flexural fatigue strength versus number of cycles to failure at frequency 2Hz
25
Reducedtemperaturer f C] 50 80 1QQ
2 4 6 8 10 12 14 Reduced time to failure log tf' [min]
25
16
18
-2
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Reduced temperature V p 50
2 4 6 8 10 12 14 Reduced time to failure log tf' [min]
(a) Dry (b)Wetl.O FIGURE 7 Master curves of flexural fatigue strength
16
18
Time-Temperature-Water Absorption Superposition Principle
324
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FIGURE 8 Grand-master curve of flexural fatigue strength
CONCLUSION The influence of water absorption on the time-temperature dependent flexural fatigue strength of unidirectional CFRP laminates, which consist of carbon fiber and epoxy resin were discussed. The CFRP laminates were prepared under three conditions of Dry, Wet and Wet+Dry. Three-point bending CSR and fatigue tests for these three kinds of CFRP laminates were carried out under various loading rates and temperatures. It is cleared that the flexural CSR and fatigue strengths of CFRP laminates strongly depend on the water absorption as well as time and temperature and the time-temperature-water absorption superposition principle holds for these flexural CSR and fatigue strengths. ACKNOWLEDGEMENTS This work was supported by the National Science Foundation (No. CMS-9812758), and the Asian Office of Aerospace R&D (No.AOARD-03-4062). REFERENCES 1. 2. 3. 4.. 5.
Aboudi, J. and Cederbaum, G, Composite Structures, 12: 243-256 (1989). Sullivan, J. L., Composite Science and Technology, 39:207-232 (1990). Gates, T., Experimental Mechanics, 68-73 (1992). Miyano, Y, Kanemitsu, M., Kunio, T. and Kuhn, H., J. Composite Materials, 20: 520-538 (1986). Miyano, Y, McMurray, M. K., Enyama, I , and Nakada, M., J. Composite Materials, 28: 1250-1260 (1994). 6. Miyano, Y, K. McMurray, M., Kitade, N., Nakada, M. and Mohri, M., Advanced Composite Materials, 4: 87-99 (1994). 7. Miyano, Y, Nakada, M., and McMurray, M. K., J. Composite Materials, 29:1808-1822 (1995). 8. Miyano, Y, Nakada, M., McMurray, M. K. and Muki, R., J. Composite Materials, 31:619-638 (1997). 9. Shen, C. H and Springer, G S., J. Composite Materials, 10: 2-20 (1976). 10. Kibler, K. G, AGRD Conference Proceedings, 8-1, (1980). 11. Neumann, S. and Marom, G, Polymer Composites, 6: 9-12 (1985). 12. Selzer, R., and Friedrich, K., Composites Part A, 28A: 595-604 (1997).Aboudi, J. and Cederbaum, G, Composite Structures, 12: 243-256 (1989).
Buckling of Composite Plates with Cutouts Jalil Rezaeepazhand* and Ali Moein Darbari Department of Mechanical Engineering, Ferdowsi University of Mashhad P.O. Box: 91775-1111, Mashhad, Iran
ABSTRACT Thin-walled shells and panels of various constructions find wide use as primary structural elements in simple and complex configuration. In aerospace structures, panels with variously shaped cutout are often used. The understanding of the effects of cutout on the buckling behavior of such plates has grown in importance with the increasing need for lightweight structures. The excellent mechanical properties of advanced composite materials make them prime candidates for a wide variety of application in aerospace, mechanical, civil and other branches of engineering. A finite element analysis, using commercial finite element software, is used to study the buckling behavior of laminated composite plates with different central cutout. Particular emphasis is placed on fiat square plates subjected to a uni-axial compression load. The main objective of this study is to demonstrate the buckling behavior of composite plates with central cutout. The effect of cutout geometry (circular, square, or special cutout), fiber angle, stacking sequences, and cutout size are discussed.
INTRODUCTION Use of reinforced composites in light-weight aerospace structures has increased steadily over the years. The outstanding mechanical properties of advanced composites provide the engineer with potential to optimize properties specific to application. The increasing use of laminated composite components for a wide variety of applications in aerospace, mechanical and other branches of engineering requires extensive experimental evaluation of any new design. The enormous design flexibility of advanced composites is obtained because of the large number of design parameters. The correct and effective use of advanced composite materials requires complex analyses in order to achieve good understanding of the system response characteristics to external causes. Different cutout shapes in structural elements are needed to provide access to other parts of the structure and to reduced the weight of the system. With a view to better understanding of buckling behavior of composite plates with central cutout, a numerical investigation was undertaken. This type of investigation can save considerable expense and time, and provide the necessary information on behavior of systems. Particular emphasis is placed on the case of simply supported square laminated composite plates with a central cutout. In the
"Corresponding Author, Department of Mechanical Engineering, Ferdowsi University of Mashhad, P.O. Box 91775-111, Mashhad, Iran, [email protected].
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Buckling of Composite Plates with Cutouts
present studies, the material behavior is assumed to be linearly elastic. Furthermore, it is assumed that the plate is without any imperfections. LITERATURE REVIEW Studies on the buckling behaviors of isotropic and composites plates with and without cutout are reported extensively. Nemathfl] presented an interesting review on earlier works on buckling behavior of composite plates with centrally located cutouts. The effect of cutout size and shape on the buckling and postbuckling response of quasi-isotropic plates subjected to uniaxial compression is presented by Bailey and Wood[2]. They investigated stability of perfect and imperfect square plates with circular and square cutouts. Both finite element and experimental results are presented. Ko[3] investigated the effect of plates aspect ratio, hole sizes, and boundary conditions on buckling of MMC composite plates with central square cutouts. Waas et al.[4] conducted a series of experiments to determine the failure mechanisms in compressively loaded laminated composite plates with a circular cutout. Hilburger et al.[5] presented a numerical and experimental study on the buckling behavior of quasi-isotropic curve panels with a centrally located cutout. Due to complexity involved in analysis of perforated plates, the closed form buckling solution are practically unobtainable. Numerical analysis using commercial finite element software is an attractive option for study the buckling behavior of perforated plates. This study investigates the problem of elastic buckling of simply supported laminated composite square plates with central cutout subjected to uniaxial compression load. Numerical studies using commercial finite element code, Ansys, were conducted to investigate the effects of variation in cutout geometries and shapes, laminate stacking sequences and fiber orientation on linear buckling responses of laminated composite plates with centrally located cutout. MATERIALS AND METHODS A square plate of dimensions 1000xl000x5mm is considered in this study. A circular cutout of diameter D is located at center of plate. The cutout ratio(DAV) is defined as the ratio of the cutout diameter to width(W) of the plate. Similar models were considered for rectangular, triangular and rhombic shape cutouts. Figure 1 shows these types of cutouts.
circular
square
triangular
rhombic
FIGURE 1: Different cutout shapes
Two types of compression loads, uniform displacing (displacement-loading) and uniform stressing (stress-loading) can be modeled [1]. Different types of loading, boundary conditions and plates aspect ratios have been investigated[6]. hi this paper, only results of displacement-loading are presented. A uniform inplane compression
Buckling of Composite Plates with Cutouts
327
load which applied in the edges perpendicular to longitudinal axis presents this type of loading. Both, simply supports and clamped supports are considered. The material properties of each ply are boron/epoxy with material properties given in Table 1. TABLE I : Material properties Al2024-T6 E = 70.02 GPa v = 0.32
Boron/Epoxy E, = 208 GPa E2 = E3 = 25.4 GPa G12 = 7.2. GPa v !2 = 0.1677
FINITE ELEMENT MODELS A finite element model is created for each case. The shell91 layered element is used to model the composite plates. This element has 8 nodes with 6 DOF at each node[7]. For each case, mesh sensitivity is performed in order to achieve an acceptable mesh density. Validation study for finite element modeling is carried out by comparing the analytical buckling loads of perfect aluminum and boron/epoxy square plates with those results from Ansys software. Good agreement is achieved[6]. RESULTS AND DISCUSSION Various cutout shapes and laminate parameters such as fiber angles, and stacking sequences are considered in this study. Effect of Boundary Conditions Figure 2 presents critical loads of especially orthotropic plates with a central circular cutout as a function of cutout ratios for simply(S-S) or clamped (C-S) supported boundary conditions. It is clear that, for S-S plates, increases in cutout diameter, increases the load carrying capacity(critical load) of the perforated plates. However, for C-S plates, introducing a small size cutout reduces the critical load. But large size cutouts increase the load caring capacity of plates. Effect of Cutout Shapes In order to study the effect of cutout shapes on buckling response of composite plates, three different central cutouts, rectangular, triangular and rhombic shape cutouts are compared with circular cutouts. Figure 3 compares change in critical loads of plates with rectangular and circular cutouts for different cutout dimensions. For identical cutout area, circular cutout has higher critical loads than rectangular cutouts. Similar results are shown in figure 4 for triangular and rhombic cutouts. Based on
Buckling of Composite Plates with Cutouts
328
0.2
D/w
0.6
0.4
CUTOUT AREA(m2)
FIGURE 2 Buckling loads of simply and clamped supported orthotropic plates with circular cutouts.
0.1
0.2
0.3
FIGURE 3 Buckling loads of S-S plates with circular and rectangular cutouts.
0.1
CUTOUT AREA (m )
FIGURE 4 Buckling loads for S-S orthotropic plates with triangular and rhombic cutouts.
0.2
0.3
0.4
0.5
0.6
0.7
D/W
2
FIGURE 5 Buckling loads of orthotropic and cross-ply plates with circular cutouts.
presented results, triangular cutouts yield higher critical loads than rhombic and rectangular shape. Effect of Stacking Sequences and Fiber Orientations To demonstrate the effect of fiber orientation and stacking sequence in critical load of perforated plates, different lay ups with equal number of plies are considered in this section. It is assumed that, all plates have a central circular cutout and S-S boundary conditions. Figure 5 compares the critical buckling loads of 20 layers especially orthotropic plates( 0 = 0 or 90) with a symmetric cross ply (0/90)5S plate with the same number of plies. It is clear that, cutout dimensions have similar effect
Buckling of Composite Plates with Cutouts
329
on these laminate configurations. However, when all fibers are located in load direction (9 = 0), increase in critical loads is higher than two other configurations. The effect of fiber orientation on buckling response of symmetric angle ply laminates (±9)5S is presented in figure 6. Three different cutout ratios(D/W=0.1,0.3, and 0.5) are considered. It is shown that, fiber angle has considerable influence on critical loads of perforated plates. For small cutout ratios, a maximum critical load can be achieved when 6 = 30. Figure 7 presents variations of critical loads as a function of cutout ratio for isotropic, quasi-isotropic and orthotropic materials. It is clear that, as cutout ratio increases orthotropic plates achieved higher critical load than quasi-isotropic and isotropic ones.
0
15
30
45
60
75
90
Angle FIGURE 6 Effect of fiber orientation on buckling loads of (±8)5s perforated plates.
FIGURE 7 Buckling loads for isotropic, quasiisotropic and orthotropic perforated plates.
CONCLUSIONS AND RECOMMENDATIONS This study investigates problems associated with laminated composite plates with centrally located cutouts. Such study is important since it provides the necessary design information for buckling behavior of perforated composite plates. Linear elastic buckling responses of laminated composite plates with various cutout shapes and sizes, stacking sequences and fiber orientation have been studied. The results presented indicated that, buckling response of laminated composite plates is significantly changed by cutout size and shape, fiber orientation, stacking sequences, and boundary conditions of perforated plates. The results presented herein indicate that, for a perforated composite plate a set of cutout shape and size can be found which increase the load carrying capacity of the perforated plates. Some recommendations for future research include a) study the effect of initial geometric imperfection, b) study of the effect of other boundary and load conditions, and c) initiation of an experimental program for validation.
330
Buckling of Composite Plates with Cutouts
REFERENCES 1. Nemeth, M. P., 1996. "Buckling and Post buckling behavior of laminated composite plates with a cutout" , NASA technical paper 3587. 2. Bailey, R and Wood, J. 1996. "Stability characteristics of composite panels with various cutout geometries", Composite Structures 35 , pp 21-31 3. Ko, W. L, 1998. "Anomalous buckling characteristics of laminated MMC plates with central square holes", NASA/TP-1998-206559. 4. Waas, A.M., Babcock, C. D. Jr. and Knauss, W.G., 1998 "An experimental study of compressive failure of fibrous laminated composites in the presence of stress gradients", International Journal of Solids and Structures, Vol. 26, No. 9/10, pp. 1071-1098. 5. Hilburger, M. W. et al., 1999. "Buckling behavior of compression-loaded quasi-isotropic curved panels with a circular cutout", Proceeding of 40' AIAA/ASME/ASCE/AHS/ASC, SDM conference, April 12-15, St. Louis, Missuri, AIAA paper 99-1279. 6. Moein Darbari, A. 2003, Buckling analysis of plates with central cutouts, MS. Thesis, Ferdowsi University of Mashhad, Iran.(in Persian). 7. ANSYS User's Manuals.
Fatigue Crack Propagation in Graded Composites Matthew Tilbrook*, Lyndal Rutgers, Robert Moon and Mark Hoffman School of Materials Science & Engineering, University of New South Wales, Australia
ABSTRACT Material structures exhibiting- a tailored variation in properties are collectively termed functionally graded materials (FGMs). Despite the considerable advances in understanding of FGMs over the past decade, several key areas require further work, including the fatigue behaviour of, and crack propagation paths in, FGMs. Graded alumina-epoxy composite samples, exhibiting an approximately continuous spatial variation in composition and properties, have been produced via an infiltration process. Fatigue cracks have been initiated and propagated under cyclic four-point bend loading. Crack deflection has been observed, along with subsequent deviation and curvature as the crack moves through the graded region. A variation in fatigue crack growth resistance was observed as the crack moved through regions of varying composition. A finite element model, which employs automatic crack extension and remeshing, has been developed to simulate the propagation process. Particular attention was paid to the criteria used for crack propagation and deflection, and to the effects of bridging on crack path. Experimental results and modeling predictions are presented and compared.
INTRODUCTION Functionally graded materials (FGMs) represent a solution to problems that can arise at interfaces between different materials, due to elastic property mismatch and poor adhesion. FGMs, which are usually composite materials, have been a key focus in composites [1] and fracture [2] research over the past decade. In spite of this and the fact that high performance materials often fail due to damage sustained under cyclic loading [3], research on fatigue crack propagation in graded materials has been limited [4-6]. This paper details an investigation, through experiment and simulation, of crack propagation in functionally graded material specimens. Graded alumina/epoxy composite samples have been produced via an infiltration process, and fatigue cracks have been initiated and propagated within them under cyclic four-point bend loading. To enable simulation of crack propagation, effective composite properties were quantified and a finite element model, which employs automatic crack extension and remeshing, was developed. Experimental results and modeling predictions are presented and compared in Section 4, demonstrating good agreement. EXPERIMENTAL PROCEDURE Graded alumina-epoxy composite specimens, exhibiting an interpenetrating network structure, were produced by a multi-step infiltration process, as in [6] and [7]. * Correspondence Author, School of Materials Science & Engineering, University of New South Wales, Sydney NSW 2052 Australia. Email: [email protected] Fax: (02) 9385 5956.
332
Fatigue Crack Propagation in Graded Composites -40 mm
Length -130 mm
95%A"-iv..
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FIGURE 1 Schematic of graded composite four-point bend specimen. Approximate compositions for the gradient steps: A: 30% alumina/70% epoxy, B: 45/55, C: 55/45, D: 70/30, E: 85/15.
The processing steps were as follows: (1) Open-celled polyurethane (PU) foam (Bulpren S-31048, Eurofoam, Troisdorf, Germany, 90 pores/inch) was used as an preform for the interpenetrating network structure. Foam pieces were compressed from an initial density of 2.5% to obtain the required volume fractions of foam and air. (2) These were positioned in a stepped configuration and infiltrated with a suspension of alumina particles (99.99% AI2O3, Taimicron TM-DAR, Taimei Chemicals Co Ltd, Japan) under cycled pressure conditions then allowed to dry. (3) The foam was then pyrolysed at 800°C, leaving a ceramic green-body (approximate dimensions: 60 x 35 x 9mm3) with a network of interconnecting pores, and a graded pore distribution. The ceramic was sintered at 1500°C for one hour leading to ~ 10% shrinkage in each dimension. (4) Ceramic pieces machined to remove excess material with rotary grinding wheel. (5) Ceramic pieces were positioned in silicone moulds and epoxy resin (Epofix, Struers, Germany) was infiltrated into the ceramic under varying pressure then cured at room temperature. (6) Specimens were then ground to size (approximate dimensions: 130 x 30 x 6 mm3) with a 600 grit diamond grinding wheel, and polished with an automatic polisher and diamond paste down to a diamond particle size of 1 micron in the final step. The final dimensions of a typical graded specimen are shown in Figure 1. A variety of gradient specimens were produced and tested, enabling examination of the effects of variation in gradient and notch parameters on crack propagation. Microstructural characterisation of the graded composite samples was conducted via optical microscopy. Optical micrographs are shown in Figure 2, in which phase continuity at step-interfaces may be clearly observed. Phase volume fractions were determined from relative areafractionsof each phase in the micrographs. Crack propagation in graded samples under cyclic four-point bend loading was conducted using an hydraulic MTS in load control. Crack initiation occurred from a notch sawn into the graded region. The notches were sharpened using a razor blade and diamond paste to obtain a notch root radius around 10-20 microns. Crack extension was observed with a microscope (Olympus ) and digital camera (Optronics ) which enabled fatigue crack growth rates to be measured. COMPOSITE PROPERTY DISTRIBUTION Accurate prediction of crack propagation in graded specimens requires detailed knowledge of the spatial distribution of effective composite properties within the graded region. Elastic properties of homogeneous alumina-epoxy composites have previously been quantified, from which the distributions of properties within the graded samples were estimated. Non-graded specimens, with compositions ranging from 95% alumina to 50% alumina, were produced in a manner similar to that in Figure 1, and characterised via microanalysis and impulse excitation measurements, with results published in full elsewhere [9].
Fatigue Crack Propagation in Graded Composites
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Fatigue testing was also conducted on notched homogeneous composite beams under cyclic four-point bend loading. They generally exhibited Paris-law behaviour, as illustrated in Figure 3(a), with large values (-24) for the exponent, m, as expected for brittle materials. An increase in crack-growth resistance with crack extension was observed, and attributed to crack-wake effects. This is demonstrated in Figure 3(b), which shows that, while the applied SIF for crack propagation tended to increase with crack extension, the resultant crack propagation rate tended to decrease. In general, composite specimens with increased epoxy volume fractions exhibited significantly decreased stiffness and intrinsic toughness, as illustrated in Figure 4 which shows the compositional and corresponding property distributions across one of the graded specimens.
i ii •
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5% epoxy
45° o epoxy
epoxy
FIGURE 2 Optical micrographs of graded composite specimens showing interfaces between steps. Approximate compositions of steps are given and positions of the interfaces are indicated.
; 30% Epoxy
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0.5
1
1.5
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FIGURE 3 Results of fatigue tests on homogeneous composite samples, (a) Fatigue crack growth rates for several different compositions, showing Paris law behaviour, (b) Systematic decrease in crack growth rate with crack extension, with increased applied SIF range, indicative of crack-extension toughening effects.
Fatigue Crack Propagation in Graded Composites
334 1
— ID
- Volume fraction (epoxy) - Relative E - Relative Kc
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-
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n
I
5
i
1
10
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15
20
Position across gradient, x [mm]
FIGURE 4 Material Gradient: Measured compositional distribution for a graded composite sample, along with stiffness and toughness distributions calculated from experiments on homogeneous specimens.
FINITE ELEMENT SIMULATION A finite element model has been developed to simulate the process of fatigue crack propagation in graded specimens. The commercial FEA software package ANSYS (Version 6.1, ANSYS Inc, Canonsburg, Pennsylvania) was utilised, with a number of modifications specific to graded materials. Full details of this model, and various aspects of its validation, are given by Tilbrook et al. [10] however several key aspects warrant mention here: 1) The spatial distributions of effective properties, in particular stiffness and fatigue resistance, were calculated from the compositional distribution and the experimental results for homogeneous composites described above. 2) Application of material stiffness gradient. As ANSYS does not allow graded elements, this was achieved by defining temperature-dependent properties, and assigning nodal temperatures individually, leading to a spatial temperature and property gradient. 3) Calculation of fracture parameters. Mode I and II stress intensity factors were determined from crack-opening and crack-sliding displacement values respectively for nodes near the crack-tip. Crack propagation was assumed to occur for: where Kc(x, Aa) was estimated to include crack-extension toughening effects. 4) Determination of crack propagation direction. The local symmetry criterion (Kn = 0) was used. A test kink was extended from the crack-tip and its angle varied to minimise Kii. The size of the test kink was 50 microns, which corresponded to <0.5% of the original crack length. 5) Crack propagation was simulated automatically with a routine to delete the mesh and areas around the crack, extend the crack, and then redefine the geometry and mesh. The crack was extended in increments of 0.5 mm, <5% of original crack length. This model has been used previously [10] to investigate the influence of various gradient parameters on crack-tip stresses and crack paths. In the current work, the model was used firstly to predict crack paths for comparison with experiments, and secondly to analyse the experimental fatigue data, as expressions relating applied load to crack-tip stress intensity factor are not known for graded materials, particularly for curved cracks.
Fatigue Crack Propagation in Graded Composites
335
RESULTS & DISCUSSION Initial deflection of cracks toward the more compliant epoxy section was observed as expected [12], followed by further deviation as the crack progressed through the graded region, as shown in Figure 5. Some key results of fatigue experiments on FGMs and corresponding FE simulations are presented and compared in Figures 6 and 7. Figure 6 shows crack paths in FGM specimens with similar gradient profiles but differing gradient widths. The effect of gradient steepness on deflection is clearly observed as cracks in the narrower, steeper, gradients deflected more (-50°) than those in wider gradients (-25°). This comparison is illustrated in Figure 5(b) and (c). The effects of varying initial notch position and length do not appear significant over the ranges investigated, which is concordant with previous conclusions from FE simulations [10]. In Figure 7, the variation in applied cyclic loading with crack length is shown for an FGM specimen. These loads are close to those required for fracture, because the range of cyclically applied loads over which crack propagation occurs is very small for brittle materials (Figure 3(a)). The experimental load variation is compared with FE predictions, and demonstrates far better agreement with predictions for which R-curve behaviour was taken into consideration, than with those for which it was neglected. This indicates that R-curve behaviour can influence failure strength significantly, although it does not appear to affect crack propagation path significantly.
(b)
(a)
(O
FIGURE 5 Images of cracks in graded specimens, (a) initial deflection from notch-tip and further propagation across specimens with (b) wide and (c) narrow gradient.
:
(a)
16 -
E
14 -
y
*= 12
10 -
6
8
10 •
12
14
16
18
20
Displacment from ceramic-gradient interface, x [mm]
0
2
4
6
8
10
12
Displacement from ceramic-gradient interface, x [mm]
FIGURE 6 Crack propagation paths in graded samples under four-point bending - experimental results and modeling predictions for cracks in gradients of (a) 20mm and (b) 10 mm approximate width.
336
Fatigue Crack Propagation in Graded Composites
Experiment - FEM - with R-curve • FEM - without R-curve
Crack Extension, Aa [mm]
FIGURE 7 Applied loading profile for crack propagation in a graded sample under four-point bending.
CONCLUSIONS Graded alumina-epoxy samples have been produced via infiltration for investigating the effect of material property gradient on crack propagation, in conjunction with homogeneous composite characterisation and finite element modelling. Crack deflection was observed, with close agreement between measured and predicted deflection angles. Higher deflection was observed for steeper gradients and for cracks initially situated within the epoxy-rich region of the gradient. Crack-wake effects were observed for both homogeneous and graded composites. Whilst these effects have a notable influence on crack propagation resistance, they do not appear to influence the crack path significantly.
REFERENCES 1.
Neubrand A., J. Rodel, 1997. "Gradient Materials: An Overview of a Novel Concept," Zeit. f. Met. 88:358-71. 2. Paulino G.C. (ed), 2002. "Fracture of Functionally Graded Materials," Eng. Fract. Mech. 69:1667-78. 3. Ritchie R.O., 1999. "Mechanisms of fatigue crack propagation in ductile and brittle solids," Int. J. Fract. 100:55-83. 4. Tilbrook, M.T., RJ. Moon, and M. Hoffman, 2003. Crack Propagation in Graded Composites, Comp. Set. Technol. (accepted). 5. Forth S.C., L.H. Favrow, W.D. Keat, J.A. Newman, 2003. "Three-dimensional mixed-mode fatigue crack growth in a functionally graded titanium alloy", Engng. Fract. Mech. 70:2175-2185. 6. Xu F.M., S.J. Zhu, J. Zhao, M. Qi, F.G. Wang, S.X. Li, Z.G. Wang, 2003. "Fatigue crack growth in SiC particulates reinforced Al matrix graded composite," Mat. Sci. Engng. A 1-6. 7. Cichocki F.R., K.P. Trumble, and J. Rodel. 1998. "Tailored Porosity Gradients via Colloidal Infiltration of Compression Molded Sponges," J. Am. Ceram. Soc, 81(6): 1661-1664. 8. Neubrand, A., T.-J. Chung, J. Rodel, E.D. Steffler and T. Fett, 2002. "Residual stresses in functionally graded plates,"./. Mater. Res., 17 (11): 2912-2920. 9. Tilbrook M.T., R J. Moon and M. Hoffman, 2003. "On the Mechanical Properties of Alumina-Epoxy Composites with an Interpenetrating Network Structure," Mat. Sci. Engng. A (submitted). 10. Tilbrook M.T., RJ. Moon and M. Hoffman, 2003. "Finite Element Analysis of Crack-Tip Stresses and Crack Propagation in Functionally Graded Materials," Engng. Fract. Mech. (submitted). 11. Bittencourt T.N., P.A. Wawrzynek, A.R. Ingraffea and J.L.A. Sousa, 1996. "Quasi-automatic simulation of crack propagation for 2D LEFM problems," Engng. Fract. Mech. 55:321-324. 12. Gu P. and Asaro R.J., 1997. "Crack Deflection in Functionally Graded Materials," Int. J. Sol Struct. 34(24):3085-98.
Dynamic Response Behavior of Stiffened Delaminated Plates Considering Failure Ruixiang Bai, Haoran Chen* State Key Laboratory of Structural Analysis for Industrial Equipment, Dalian University of Technology, Dalian 116024, P.R.China Man Wang. Dalian Institute of Light Industry 116034, P.R.China
ABSTRACT The paper is to study on dynamic response behavior of the stiffened delaminated composite plates considering failure process. A formula of element stiffness and mass matrices for the composite laminated plate and beam are deduced by using the first-order shear deformation theory. A damping model is constituted on the basis of Raleigh damping model in conjunction with Adams' strain energy method (MSE). A delaminated constrained model and a virtual interface element are also developed for avoiding the overlap and penetration phenomenon between the upper and lower sub-laminates at the delamination region. The failure analysis method is established by Tsai's failure criterion and corresponding reduced stiffness role. Some numerical examples show that the effects of frequency of dynamic load, delamination location, and reduction of structure stiffness during the failure process dynamic behavior of the delaminated composite laminates are significant.
INTRODUCTION The initial-delamination caused by the external low velocity impact by foreign objects during the manufacturing process and/or in the service life and the progressive failure under dynamic load for the stiffened composite plates can significantly alter the dynamic properties and response of composite structures, hence a clear understanding of their dynamics behaviors is of extremely importance in designing and maintaining the laminated composite structures. The investigation and analysis of dynamic response for stiffened delaminated plates are of great interest to engineers and mechanics scientists and so far many valuable papers have been published [1-6], however they haven't considered the progressive failure. Therefore, the investigation in this paper is a significant engineering subject need to be solved. The paper is to deal with dynamic response behavior of the stiffened delaminated plates, especially, considering progressive failure process. The methodology, model and corresponding analysis method method established and conclusions given by some typical examples would be useful for composite structures designers.
* Corresponding Author, Email: [email protected].
338
Dynamic Response Behavior of Stiffened Delaminated Plates
ANALYSIS THEORY For the sake of simplicity, consider a stiffened laminated plate with an arbitrarily located through-width delamination, which can be divided into three spans wise regions, namely one delamination and two perfect regions, as shown in Fig.l.
X
—\ y \
\
\ \
\
\
\ \ /^—— \ "l '^
\ Upper sublami.
FIGURE 1 Delamination model of stiffened composite laminated plate
Based on first-order shear deformation theory and Hamilton's principle, The formulae of element stifmess and mass matrices for the plate have been deduced by authors in Refs. [2,4,7], as
K=L BTDBdQ M = \a NTRNdQ
(1)
Where D and R denote the generalized stiffness and mass density matrix, and B and N are the geometry and shape function matrix, respectively. Assuming the damping behavior of the laminates to be slight weakness, an approximate energy method proposed by Adams can be employed in the dynamic analysis of the structures [8]. According to the measured specimen's loss factor matrix 77, the specific damping capacity y/j corresponding toj-th mode can be determined by the following formulation:
y/ . =
AU
i
'- = -^—'
(2)
Here {$•} is the j-th modal shape of the structures, [K"] and [^5] denote the structural stiffhess and the damped structural stiffhess matrix, respectively. If § i s defined as the modal damping ratio for the y'-th mode, thus y/j=AnZj
(3)
Furthermore, the damping matrix [C] can be given by Raleigh damping model. Employing Hamilton's principle, the motion equation can be given as
Dynamic Response Behavior of Stiffened Delaminated Plates Mu + Cu+Ku=P(t)
339 (4)
where M> C and K are the total mass matrix, stiffness and the damping matrix, while u and P(t) are the total displacement and the force vector of the structure. To ensure integral stability in time domain, the Eq. (4) is transformed into the following precise time-integration iteration formulation [9]: v = Hv + r
(5)
Where
H = \°
7
\B G\ B = -M'K
0
l v = R r-M-'P(t) \U\
G=
-MC
hence, PD-S(Sinusoidal) formulation as[10]: v
(^i+i) = ^(T)[v(.h ) ~
a
sin(o^) - b cos(ft)^)] + a sin(e#k+1 ) + b cos(atk+l)
(6)
Here
b = (a I + H 2 / a}' (-r, - Hr2 / w)\
MEDELING AND FAILURE CRITERION In accordance with the requirement of displacement continuity at the nodes along the delaminated front between perfect and delamination regions, the following additional continuity conditions must be imposed as [7]: M
u2
v
v2 =vs+0x3(H-hu)/2 w2= w3
i =u,+0y,(H-h,)/2
i =v3-6x3(H-h,)/2 w, =w3
=u3-0yi(H-hu)/2 (8)
H, hu and hi are the thickness of the base, upper and lower sub-laminates respectively. Next, the virtual interface piecewise linear spring elements are inserted along the delamination interface surfaces for preventing penetration of the upper and lower sub-laminates during dynamic analysis process [5,7], The stiffness matrix of element as "" 1 - 1 " (9)
['•M-.
Here k is a specified stiffened factor, which is defined to be zero in the separated state or a linear function of the transverse relative displacement between the upper and lower sub-laminates in contact. In addition, Tsai-Hill failure criteria is employed for
340
Dynamic Response Behavior of Stiffened Delaminated Plates
predicting the local damage failure occurrence and the following stiffness degradation rules are applied to determine the reduced material properties during the dynamic analysis process [11]: E2 =0.56E2 =
(10)
G,*2=0.44G12
jul
NUMERICAL EXAMPLE AND DISCUSSION Dynamic Response and Failure of Perfect Bare and Stiffened Laminated Plates Excited by Sinusoidal Uniform Distributed Load Consider a [0/90/90/0]4S perfect bare and stiffened laminated square plates with simply support along the four edges. The length and thickness are 400mm and 10mm for both plates; and the width and distance between the [0]64 stiffeners are 10mm and 200mm; respectively. The mechanical properties and strength parameters for both plates are£,=135.0Gpa, £2=8.80Gpa, v12=0.33, Gn = G23 = G13 =4.47Gpa, p= 1380Kg / m \ yl =0.43%, y/2 = 3.86%, tf/4 =i//5 =y/6 = 5.72% and Xt =Xc = 1447Mpa, Yt = 52Mpa, Yc = 206Mpa, S = 93Mpa, respectively. The exciting sinusoidal uniform distributed load q = 530 sin (a aot) kpa, here, a>0 denotes the natural frequency in the first mode for the laminates and a is a specified constant. Fig.2 plots the normalized dynamic midpoint deflections (w/H) versus the normalized time t / T within the first period for a = 0.691 case. The curves marked land 1 denote the midpoint deflections for the bare laminates ignoring and considering failure, while the curves marked 2 and 2 represent the midpoint deflections of stiffened laminates for ignoring and considering failure effect, respectively. It is clear that the dynamic deflections for stiffened plate are obviously lower than that for bare plate; and the normalized dynamic midpoint deflections of the both laminates for considering failure effect case are significantly larger than that for ignoring failure effect case. Hence the stiffeners can improve the dynamic stiffness of the laminates considerably and the effect of stiffness degradation caused by progressive failure upon the dynamic stiffness cannot be ignored for both laminates.
0.20
0.40
0.60
0.80
1.00
FIGURE 2 Dynamic deflections at middle point with and without considering failure for perfect bare and stiffened laminated plates in CC=0.691case
1.00 0.00
1.00
2.00
3.00
4.00
5.00
6.00
7.00
FIGURE 3 Variation of magnification parameters with a for perfect stiffened laminated plate
Dynamic Response Behavior of Stiffened Delaminated Plates
341
Fig.3 illustrates the variation of magnification parameters with a for the stiffened laminated plate, in which the curves marked 1 and 2 represent the results for ignoring and considering failure effect cases, respectively. Compared curve 1 and 2 shows that the values of X in the first three resonant peak points for ignoring failure effect are less than that for considering failure effect, and the variation rate of X with the exciting load frequencies approaching to the resonance stage for former is not steeper than the latter. The reason is the plate near the resonance stage appears in grave failure. Thus the stiffness degradation and exciting load frequency are two significant aspects affecting the dynamic deflection of stiffened laminated plate. Dynamic Response and Failure of Stiffened Delaminated Laminates Excited by Sinusoidal Uniform Distributed Load Consider a [O2 /904]s stiffened delaminated plate with boundary conditions as simply supports along the x directional edges and free along the y directional edges, which is excited by a sinusoidal uniform line distributed load q =1000sin (200 ^t) kPa in the middle span, The length, width and thickness the base-plate are 600mm, 200mm and 15mm; the thickness and distance between [0]e4 stiffeners are 10mm and 100mm respectively. A through width delamination with length 120mm is located at middle span of the plate. The material properties of the plate are the same as foregoing example. The Fig.4 (a) and (b) depict the curves of (w/H) - (t / T) for the plates with different delaminaton locations along the thickness direction for ignoring or considering failure effect respectively: where the cures from the bottom to the up denote that for hi/ h=l/6, 1/4, 1/2, 3/4 and 5/6; respectively.
0.00 0.05 0.10 0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50
( a ) Ignoring failure
-0.50 L 0.05 0.10 0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50
( b ) Considering failure
FIGURE 4 D dynamic deflection at middle point for upper sub-laminates with deferent delamination locations
It can be also indicated that the effect of delamination and progressive failure decrease the dynamic stiffness of the stiffened plates, significantly, which depend on the frequency of dynamic load, delamination location and shapes. ACKNOWLEDGEMENTS The authors are grateful to the support of National Natural Science Foundation in China, Grant No. 10272025
342
Dynamic Response Behavior of Stiffened Delaminated Plates
REFERENCES 1.
Saravanos D A and Hopkins D A. 1996. "Effects of Delaminations on the Damped Dynamic Characteristics of Composite Laminates: Analysis and Experiments," Sound Vibration, 195(5): 977-993. 2. Hong M and Chen H R. 1999. "Vibration frequency, mode and damping behavior of laminated composite plates with delamination," J. Ship Mechanics, 3(6):28-38. 3. Luo H and Hanagud S. 2000. "Dynamics of delaminated beams," / Solids and Struct., 37:1501-1519. 4. Hong M and Chen H R. 2000. "Dynamic behavior of laminated composite plates with delamination," J of Shipbuilding Structural Mechanics, 4(6): 28-38. 5. Wang J, Tong L. 2002. "A study of the vibration of delaminated beams using a nonlinear anti-interpenetration constrained model," Compos Struc, 57:483-488. 6. Kim H Y, Hwang W B. 2002. "Effect of debonding on natural frequencies and frequency response functions of honeycomb sandwich beams," Compos Struct., 55:51-62. 7. Chen H R and Bai R X. 2003. "Study on failure process of delaminated stiffened composite plates under compression," Ada Mechanica SINICA, 19(4):289-299. 8. Adams R D and Bacon D G C. 1973. "Effect fiber-orientation and laminate geometry on properties of CFRP. J. Comp Mater., 7:402-428. 9. Zhong W X. 1994. "On precise time-integration method for structural dynamics," J. Dalian University of Technology, 34(2):131-136.(in Chinese) 10. Lin J H. 1995. "On precise time-integration method for structures under random exciting dynamic load," J. Dalian University of Technology, 35(5):600-606.(in Chinese) 11. Tsi S W. 1986. "Composites Design," United State Air Force Materials Laboratory Press.
Tensile Behaviour of Polymer Coated Optical Fibres Susan Law Australian Photonics/Optical Fibre Technology Centre, The University of Sydney, NSW 2006, Australia Cheng Yan and Lin Ye Centre for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering, The University of Sydney, NSW 2006, Australia
ABSTRACT It is still arguable if the standard testing method for fibre using a mandrel can be used to investigate the tensile behavior of a coated optical fibre. In this work, the failure mode of an optical fibre with polymer coating was examined using different gripping methods. The results indicated that the tensile behavior of the fibre was closely associated with the gripping methods. If the fibre was only gripped on the coating, the failure was dominated by delamination between the fibre core and the coating due to high shear stress. The maximum failure load was observed in the sample when the gripping point (epoxy drop) was over the fibre core and the end of the coating. The implications of these results on the design of photonic packaging were also discussed.
INTRODUCTION Fibre termination assemblies pervade photonics in all its forms from connectors in networks to hermetic feedthrough terminations in components to sensor tips in photonic thermometers. Wherever optical fibre is used, there is a requirement at some point for it to be engineered into a structure for connection to some other device. The recognition that failure of these terminations was a major cause of failure in photonic devices has led to work such as Suhir's studies of the structural mechanics of polymer-coated silica fibre [1] and Matthewson's work on the reliability of silica fibre [2]. Despite this, the intrinsic brittle nature of glass means much more work needs to be done [3], especially on the failure mechanisms of fibres and coating under mechanical and thermal loading. Traditionally "pigtailing fibre", the fibre used to provide the optical connection in packaging photonic devices, has been the poor cousin to transmission fibre and specialty fibre for devices. In general standard transmission fibre has been used and the only attempt to produce specialty packaging fibre to meet the mechanical requirements of packaging was the release of a fibre with 90 |^m cladding diameter to reduce the tensile and compressive stresses experienced by the fibre within a package [4, 5]. The reliability of optical fibre has principally been studied in respect of durability of cabling,, and the only mechanical test applied to optical fibre in manufacture is the * Corresponding author, Optical Fibre Technology Centre, University of Sydney, 206 National Innovation Centre, Australian Technology Park, Eveleigh NSW 1430. Fax: +612 9351 1911; Email: [email protected]
344
Tensile Behaviour of Polymer Coated Optical Fibres
strength proof test [6] to eliminate sections of fibre containing microcracks. Short lengths of fibre, such as those used in connectorising, are regarded as "strong" in that there is a low probability of a significant microcrack within the length [2]. No discussion has been devoted to the structural mechanics of anchoring fibre in the standard reference on photonic packaging [7] and the only standard pertaining to the durability of the fibre termination is a simple tension test between the device casing and the external cable based on a test developed for connectors [8]. As Trewhella et al. pointed out [9], the conclusions which can be drawn from this particular test are somewhat limited. Understanding the failure modes of a joint or anchor point is a key preliminary to developing more reliable joints, hi this work we carried out a preliminary investigation on the tensile behaviour of a polymer coated optical fibre. The attention was directed to the effects of griping (anchoring) methods on the failure modes. EXPERIMENTAL PROCEDURE The tensile test was carried out in accordance with the American Standard for Test and Measurement ASTM D 3379-75 [10]. An Instron 5567 with a load cell of 10 and 100 N and pneumatic grips was used. Samples were prepared by mounting a single fibre on a pre-prepared paper frame. Two styles of paper frame were tried, one with a diamond cut-out and one with a rounded rectangular cut-out (Figure 1).
FIGURE 1: Two types of paper frame used.
FIGURE 2 Three methods of mounting the fibre.
The length of the cut-out is equal to the gauge length, i.e. the length over which the strain is measured. It was found that the adhesive was more likely to conform to the gauge length when the rectangular cut out was used. A comparison was also made between the use of 2-part epoxy and Acrylate superglue. The former can form a small solid drop after curing, which was found to be more suitable for griping the fibre due to the absence of interaction between the grips and the coating. The fibre tested was a standard commercial single mode fibre with an 8.5 urn doped silica core, 125 |j.m silica cladding and a dual-layer acrylate coating of final diameter 250 |j.m. The fibre was mounted using the epoxy in three different ways, i.e., mounting on the coating directly, mounting only on the bare fibre core after stripping off the coating and mounting on the stripped fibre and the end of the coating, as shown in Figure 2. The fibre was stripped with a mechanical stripper and cleaned with methanol (a common but not optimal method of removing the coating from a fibrefl 1]). Several gauge lengths (10, 25 50 and 100 mm) were used to examine the effect of fibre length on the tensile behavior of this fibre. The same loading rate of 1 mm/min was used for all samples.
Tensile Behaviour of Polymer Coated Optical Fibres
345
RESULTS AND DISCUSSION Gripping on Coating Figure 3 give a typical load-extension curve for the sample with 50 mm gauge length. The load drops after reaching a peak value. An almost constant load is maintained with further increase of the extension. The peak load varies over the range 6~8 N. A similar result has been observed in the samples with 10 and 25 mm gauge lengths. 10
2 0 -2* Extension (mm)
FIGURE 3 Load versus extension curves for the sample with 50 mm gauge length.
FIGURE 4 Tensile stress (CTf) and shear stress (x) at the fibre/matrix interface
Observation of the failed fibres indicated that the fibre was not broken during the test but the polymer coating was stripped from the cladding. Obviously, delamination took place first during the loading. It is interesting to note that the location of the delamination was very close to the gripping points and changed a little among the samples tested. Nairn's stress analysis [11] on an embedded fibre showed that the maximum shear stress (T) is located at a short distance from the loading points, as shown in Figure 4. This is why the delamination always starts from the sites close to gripping points. Consequently, the coating itself breaks as a result of load shift from the fibre to the coating because the load is applied to the coating and the fibre does not bear any loading due to the delamination (Figure 5). In all cases this occurred at or close to the anchor point. Following this the coating is stripped from the fibre with further delamination under an almost constant load.
Tensile Behaviour of Polymer Coated Optical Fibres
346
FIGL'KK 5 Coating dulamination and failure.
The consistency of coating failure indicates that no uniform deformation/strain can be established along the full length of the fibre/coating structure due to the weak interface strength between the coating and the fibre. This implies the sites close to anchoring points of optical fibres can be the potential failure sites in a photonic device. Shorter samples also showed evidence of delamination at the interface between the two coating layers Gripping on Fibre When the gripping point was on bare fibre, the failure mode was dominated by the fibre breaking. The relationship between load and extension is shown in Figure 6 where a typical elastic behavior is observed as expected for a material like silica. Compared with the sample gripped only on the coating (Figure 3), a lower extension but a higher load corresponding to failure point is observed due to the high elastic modulus of silica fibre. 20 15
0 (I
0.5
1
1
-5 Extension (mm)
FIGURE 6 Load vs extension for sample gripped on bare fibre.
Gripping on Fibre and End of Coating In the case where the gripping point (epoxy drop) was over the fibre and end of the coating (Figure 2), the fibre typically failed at one end. Failure occurred in the coated section under the epoxy drop with the fibre stub sliding out of the coating. Examination of the failed samples under the microscope indicated that the failure occurred between
Tensile Behaviour of Polymer Coated Optical Fibres
347
0.5 and 1 mm from the end of the coating (Figure 7). Failure loads were significantly higher than for gripping on bare fibre, as shown in Figure 8. End of Coating
End of Coating
EIVJ
of Fibre
Fibre sliding ou: of anchored coating
FIGURE 7 Failure of fibre under epoxy droplet when gripping over the end of the coating.
One reason is the contribution of coating to the elastic load. Another possible reason is the high constraint imposed by the epoxy drop on the end of the coating, which can increase the load bearing capacity but limit the development of high shear stress for possible delamination. 30 y 25 20' 15 o 10 50 0.5
1
1.5
25
-5 Extension (mm)
FIGURE 8 Load vs extension plot for sample gripped over fibre and end of coating.
Implications for Photonic Packaging Based on above results, the strongest joints for fibre connection in terms of failure load are those where the bond is over the end of the coating although the failure mode is very complex. While anchoring over the coating generally results in delamination close to the anchor point with the fibre left intact, such a failure can have dire consequences both for the optical alignment of a system, and for the durability of the delaminated fibre section (even if the coating does not fail) [12, 13]. hi the case of two anchor points in close proximity (e.g. a fibre end mount and a package feed through) it would appear that significant shear stress can develop on the interface between coating layers for a dual coated fibre. Further work on the effect of mechanical properties of both optical fibre and polymer coating on failure mode is required.
348
Tensile Behaviour of Polymer Coated Optical Fibres
CONCLUDING REMARKS The tensile behavior of polymer coated silica optical fibre was closely associated with how the fibre was gripped. If the fibre was only gripped on the coating, the failure was dominated by delamination between the fibre core and the coating close to the gripping point, followed by stripping of the coating from the fibre. The maximum failure load was observed in the sample when the gripping point (epoxy drop) was over the fibre core and the end of the coating. When the gripping point was on bare fibre the failure mode was dominated by fibre breaking. These results can provide some useful guidelines for packaging design in a photonic system. ACKNOWLEDGEMENTS The authors would like to acknowledge the support of the Australian Government via the ARC and the Australian Photonics CRC. In particular C. Yan acknowledges the receipt of an ARC Australian Research Fellowship. They would also like to acknowledge the support received from their colleagues at the OFTC and the CAMT respectively. Dr Law would also like to thank her daughter for assistance with cutting out numerous paper frames. REFERENCES 1. Suhir, E. (2001). Structural mechanics of polymer coated optical glass fibres: review. First International IEEE Conference on Polymers and Adhesives in Microelectronics and Photonics. Incorporating POLY, PEP & Adhesives in Electronics. Proceedings (Cat. No.01TH8592), 270-275. 2. Matthewson, M J. (1994). Optical fiber reliability models. Proceedings of the SPIE - The International Society for Optical Engineering CR50, 3-31. 3. Gebizlioglu, O.S., Kurkjian, C.R., and Reith, L.A. (1999). Materials issues in the development and use of lightguide fibers, cables, and components. Proceedings of the SPIE - The International Society for Optical Engineering CR73, 68-111. 4. Suhir, E. (1996). Predicted curvatures and stresses in a fiber-optic interconnect subjected to bending. Journal of Lightwave Technology vol. 14, no.2, 144-147. 5. Suhir, E. (1997). Stresses in a partially coated optical glass fiber subjected to the ends off-set. Journal of Lightwave Technology vol.15, no.ll, 2091-2094. 6. TIA/EIA-455-31-C (1999). FOTP-31 - Proof Testing of Optical Fibers by Tension, Telecommunications Industry Association. 7. Mickelson, A.R., Basavanhally, N.R., and Lee, Y.-C. (1997). Optoelectronic Packaging (New York: Wiley Interscience). 8. TIA/EIA-455-6-B (2003). FOTP-6 - Cable Retention Test Procedure for Fiber Optic Cable Interconnecting Devices, Telecommunications Industry Association. 9. Trewhella, J.M., DeCusatis, C , and Fox, J. (1999). Performance comparison of small form factor fiber optic connectors. 1999 Proceedings. 49th Electronic Components and Technology Conference (Cat. No.99CH36299), 398-407. 10. ASTM-D-3379-75 (1982). Standard test method for tensile strength and Young's modulus for highmodulus single-filament materials, American Society for Testing and Materials: Philadelphia. 11. Matthewson, M.J., Kurkjian, C.R., and Hamblin, J.R. (1997). Acid stripping of fused silica optical fibers without strength degradation. Journal of Lightwave Technology vol.15, no. 3,490-497. 12. Hand, R.J., Ellis, B., Whittle, B.R., and Wang, F.H. (2003). Epoxy based coatings on glass: strengthening mechanisms. Journal of Non-Crystalline Solids vol.315, no.3, 276-287. 13. Shiue, Y.S., Matthewson, M.J., Stupak, P.R., and O'Connor, M.J. (2001). Coating additives for enhanced mechanical reliability of fused silica optical fibers: effect on mechanical and optical performance. Proceedings of the SPIE - The International Society for Optical Engineering vol.4215, 129-133.
Statistical Model for Multiaxial Fatigue Behavior of Unidirectional Laminates Xiaoxue Diao* PreciCad Inc. 350 Sharest Est, Quebec, QC, G1K 3H4, CANADA Larry B. Lessard Department of Mechanical Engineering, McGill University, Montreal, QC, H3A 3K6, CANADA
ABSTRACT In this paper a statistical model was developed to simulate the fatigue behavior of a unidirectional composite laminate subjected to multiaxial fatigue loading based on the experimental data of static and fatigue behavior of that laminate subjected to uniaxial fatigue loading and under in-plane shear conditions. The statistical model was applied to evaluate fatigue life and residual strength of the unidirectional graphite/epoxy AS4/3501-6 composite lamina subjected to off-axis fatigue loading Simulation of the S-N curve for a 30° off-axis laminate showed a good agreement with experimental data.
INTRODUCTION Although some models have been proposed to study the biaxial/multiaxial fatigue of composites [1,2], all these models are deterministic in approach. However, The large scatter in residual strength and fatigue life measurements of composite materials is a well-known fact, which should be included in the design of composite structures. In this paper, a statistical approach is employed to study the fatigue failure of fiber reinforced composite lamina subjected to multiaxial loading. The generalized residual material property degradation model developed by Shokrieh and Lessard [3,4] is used to generalize the statistical model for composite lamina under fatigue loading with arbitrary stress ratio.
DEVELOPMENT OF STATISTICAL MODEL Consider a unidirectional lamina under a biaxial state of fatigue stress in longitudinal (an), transverse (022) and shear (012) directions. Sims and Brogdon [5] proposed a fatigue failure criterion,
* Corresponding author. Email: xdiao(3)hotmail.com
350
Multiaxial Fatigue Behavior of Unidirectional Laminates
R22(n,a22,K)J
{Rl2(n,a 12,K)
=1
where Rii(n,crn,K), R22(n,a22,K) and Ri2(n,ai2,K) are the residual strengths in the longitudinal, transverse and in-plane shear directions, respectively. In this research, the equation presented by Harris et al [6] is adopted to describe the degradation of residual strength, R(n,a,K):
^n, a,,
=
K)
flog(n)-108(0.25)]'
where Rs;, a; and b, (i=l 1,22,12) are the static strength and curve fitting parameters. Nfi (i=ll, 22, 12) are fatigue cycles to failure of the unidirectional lamina under uniaxial loading a n , a22 and du, respectively. From Eqs. (1) and (2), the number of cycles to failure can be numerically solved as an explicit function of static strength and stress state. It is also an implicit function of stress ratio by means of the Goodman-type diagram. n = g(R sll ,R i22 ,R J12 ,o 11 ,a 22 ,CT 12 )
(3)
In the statistical description [7], the fatigue strength of a lamina in the longitudinal, transverse and in-plane shear directions is a random variable. Fatigue life of the lamina subjected to multi-axial loading must be determined statistically in terms of distribution functions of the random variables R s n, Rs22, Rsi2It is assumed here that the static strengths in the longitudinal, transverse and inplane shear modes are independent of each other and their distribution functions are of the form of Weibull functions [8], f
'(R-)=f(f!)"rl«PH|i)a},
1 = 11,22, 12
(4)
where i, i (i=ll, 22, 12) are the shape and scale parameters of the Weibull function, which are determined from the experimental data of static strength in three loading modes, respectively. The density distribution function of the random variable n can be calculated based on Eq. (4) if the failure criterion Eq. (1) is utilized [9]. f(n,CT11>a22,CT12) = JdR.» ]dR ffi JdR i .28(n-g(a 11 ,CT H ,CT 12 ,R sll ,R C2) R, 12 )f 11 (R !l ,)f 22 (R a2 )f 12 (R sl2 )(5) 0
0
0
The average fatigue life of the composite lamina under multi-axial loading can be calculated [9] N F ( o n , 0 2 2 , a 1 2 ) = Jnf(n,a11)CT22,a12)dn
/" = JdR,.. jdR,22
.
(6) }dRsl2g(RI11,Rs22,R,,2,an,a22;a12)f1,(R,,1)f22(Rs22)f12(R!l2)
Multiaxial Fatigue Behavior of Unidirectional Laminates
351
The dependence of residual strength on the stress ratio K is reflected by a relationship between number of cycles to failure and the corresponding state of stress in Eq. (2). The generalized relation between the alternating stress ca=(amax-<7miii)/2, tensile strength at, compressive strength a c was presented by Harris [6] based on Adam's model [10-12] as
where a=a a /a t , q=am/at, c=oc/at, and f u, v are curve fitting constants. Experimental results by Harris and his co-workers [6] showed that u can be expressed by a linear function of logarithmic fatigue life Nf, i.e. u = A + BlogNf (8) where A and B are curve fitting parameters. Combining Eqs. (7) and (8) yields U=
ln[(l 1 - ( q)(l ) +q )] =A + B l 0 g N f
(9)
Eq. (9) is fitted with experimental data from different stress ratios so that a master curve for u versus logNf for different stress ratios is extracted, consequently, A and B are found. For a better simulation of the fatigue life of the unidirectional lamina under shear fatigue loading, a modified formulation was proposed [3,4]
hi order to apply the statistical model to predict the fatigue life of a unidirectional lamina under biaxial loading, the following tests must be conducted to characterize the properties of the lamina under uniaxial load in longitudinal, transverse and in-plane shear directions, respectively: 1. tests of static tensile, compressive and shear strength and their deviation for unidirectional lamina, from which the Weibull parameters a; and p\ (i=ll, 22, 12),are determined; 2. tests of residual strength of the unidirectional lamina for determination of strength degradation parameters a\ and fy (i=l 1, 22,12) based on Eq. (2); 3. tests of fatigue life of the unidirectional lamina under different stress ratios (at least two) for determination of curve fitting parameters Aj and Bf (i=ll, 22, 12) fromEq. (9)orEq. (10).
MATERIAL CHARACTERIZATION A unidirectional lamina under biaxial fatigue loading ((Tn=0 in Eq. (1)) was considered. A series of tests were conducted on graphite/epoxy AS4/3501-6 unidirectional lamina under transverse and in-plane shear loading conditions for material characterization. The results of fatigue life of unidirectional lamina under transverse tension-tension (R=0.1) and compression-compression (R=10) fatigue loading [4] are shown in Fig. 1. Similar results are shown in Fig. 2 for the unidirectional lamina under in-plane shear loading with the maximum stress of 40%
Multiaxial Fatigue Behavior of Unidirectional Laminates
352
and 80% of static strength and two different stress ratios 0.1 and 0.0. The results are converted to a relation between the life parameter U22, U12 and logarithmic fatigue life based on Eqs. (9) and (10), shown in Figs. 3 and 4, from which a master curve can be extracted with fitting A; and B; (i=22,12) determined consequently. The parameter/ =1.06 for better fitting to the experimental results [6]. The residual strength of a unidirectional lamina under transverse tension-tension and in-plane shear loading with different maximum stresses [4] are presented in Figs. 5 and 6. The fitting parameters a; and bj (i=22, 12) in the degradation formula of normalized residual strength Eq. (2) are thus determined, shown in Table 1. 1.2
£
1.0
c
0
O In
o .
0.2
0.8
A8DA ^
ISo
OO
O A
O
'g 0.4
OO
o static (T) • static (C) o R=0.1 AR=10
O static O R=0.1 A R=0.0
O
0.0 -
1
0
1
2
3
4
5
6
7
-
1
1
0
1
2
3
4
5
6
7
8
LogNf
LogNf
FIGURE 1 Experimental data of static and fatigue life of unidirectional lamina under transverse loading with different stress ratios.
FIGURE 2 Experimental data of static and fatigue life of [0/90]s laminate undeT in-plane shear loading with different stress ratios.
3.0 CN
u22 = 0.0937LogNf+ 1.0117
2.5
= 0.1785LogNf+ 0.1245
mel
CD
2.0
S3 urv Life
S.
1.5 1.0
O R=0.1 AR=10
0>
0.5
ter
O [0
0-0 0
1
2
2
3
4
5
6
7
8
LogNf
FIGURE 3 Normalized fatigue life curve for a unidirectional lamina under transverse tensile loading conditions.
FIGURE 4 Normalized fatigue life curve for a [0/90]s laminate under in-plane shear loading conditions.
TABLE I. Model parameters obtained from material characterization. Loading Mode (i) Trans. Tension (22) In-plane Shear (12)
Rsi [MPa] 52.56 136.33
OC;
16. 1 3 18. 6 3
P.
[MPa] 54.31 139.42
Ai
Bj
ai
bi
1.011 7 0 .124 5
0.093 7 0.178 5
9 .628 7 0 .160 0
7 .968 1 9.110 0
Multiaxial Fatigue Behavior of Unidirectional Laminates
353
1.2
6
i
£ 1.0 •a 2 $ 8
£ 0.8
1
<"
8
o static 0 60% A 40%
">,
0 ^
E ra
o-S0'6 a: 0.4 0.2
a22=9.6287 b22=0.1255
0.0 0.0
0.2
0.4
0.6
0.8
1.0
0.2
Normalized Cycles
0.4
0.6
0.8
1.0
Normalized Cycles
FIGURE 6 Normalized residual strength curve for a [0/90]s laminate under in-plane shear loadin
FIGURE 5 Normalized residual strength curve for a unidirectional lamina under transverse tensile loading.
STATISTICAL EVALUATION With all the model parameters obtained from materials characterization in Table 1, the statistical model can be applied to calculate the S-N curve of a lamina under a 30° off-axis loading. The calculated residual strength of the laminate subjected to 30° off-axis fatigue loading with maximum of 70% static strength is shown in Fig. 7. Similar calculations can be made for other applied stress levels. These results are normalized and shown in Fig. 8. If the normalized residual strength of unidirectional laminates with off-axis angle 9 is of the same form as Eq. (2): R e (n,q e ,K)-CT e
•[-
log(n)-log(0.25) f
(11)
vlog(Nffi)-log(0.25)j
where Rse, Re(n,ae,K) and OQ are the off-axis static strength, residual strength and applied stress, the value of parameters ae and be (9=30°) are determined to be 3.272 and 1.346, respectively. Therefore, if the fatigue life of an off-axis laminate under different applied stress levels is known, the normalized residual strength of the laminate can be determined based on Eq. (11). The fatigue life of unidirectional laminate with 30° off-axis angles is calculated from Eq. (6), shown in Fig. 9, which shows a good agreement with experiments [4].
E" 1S0 CD
Maximum Applied Stress - FVediction 95% - 1 0
1
2
3
4
5
6
LogN
FIGURE 7 Residual strength of [30] 16 offaxis laminate under an applied stress with maximum of 70% static strength.
0.2
0.4
0.6
0.8
Normalized Cycles
FIGURE 8 Normalized residual strength of [30] i6 off-axis laminate.
354
Multiaxial Fatigue Behavior of Unidirectional Laminates 1.0 I 0.8 0.6 0.4 •
n0.8
0.2 •
A 0.7 O 0.6
X0.5 0.0 i 0.0 0.2
§ ^l jF at i 0.4
i 0.6
i 0.8
Td 1.0
Normalized Cycles FIGURE 9 Calculated S-N curve and deviations for [30]]6 off-axis laminate.
SUMMARY 1) The residual strength and fatigue life of an off-axis laminate can be determined from the statistical model if the fatigue behavior of unidirectional lamina under longitudinal, transverse and in-plane shear loading are known through material characterization. 2) The normalized residual strength of an off-axis laminate against normalized fatigue cycles for different applied stress levels converges to a master curve, which can be used to determined the residual strength of the laminate under any applied stress levels if the corresponding fatigue life is known. 3) The fatigue life calculated for the unidirectional laminate with off-axis angle 30° agrees well with experimental data, indicating the usability of the statistical model. REFERENCES 1.
Garud, Y. S., 1981. "Multiaxial Fatigue: A Survey of the State of the Art", Journal of Testing and Evaluation, JTEVA, 9:165-178 2. Found, M. S., 1985. "A Review of the Multiaxial Fatigue Testing of Fiber Reinforced Plastics", Multiaxial Fatigue, ASTM STP 853, K. J. Miller and M. W. Brown, Eds., American Society for Testing and Materials, Philadelphia, pp.381-395 3. Shokrieh M. M. and L. B. Lessard, 1997 "Multiaxial Fatigue Behaviour of Unidirectional Plies Based on Uniaxial Fatigue Experimental: Part I. Modeling", International Journal of Fatigue, 4. Shokrieh, M. M. and L. B. Lessard, 1997, "Multiaxial Fatigue Behaviour of Unidirectional Plies Based on Uniaxial Fatigue Experimental: Part II. Experimental Evaluation", International Journal of Fatigue, 5. Sims, D. F. and V. H. Brogdon, 1977. "Fatigue Behavior of Composites Under Different Loading Modes", in Fatigue of Filamentary Composite Materials, ASTM STP-636, ASTM, Philadelphia, pp. 185-205 6. Harris, B., H. Feiter, R. Adam, R. F. Dickson and G. Fernando, 1990. "Fatigue Behaviour of Carbon Fibre Reinforced Plastics", Composites, 21:232-242 7. Diao, X.X, Lin Ye and Yiu-Wing Mai, 1995. "Statistical Prediction of Fatigue Failure of Fibre Reinforced Composite Materials", Applied Composite Materials, 2:153-173 8. Weibull, W. 1951. "A Statistical Distribution Function of Wide Applicability", Journal of Applied Mechanics, 18:293-297 9. Melsa, J. L. and A. P. Sage, 1973. An Introduction to Probability and Stochastic Processes, Prentice-Hall, Inc. Englewood Cliffs, New Jersey, 10. Adam, T., G. Fernando, R. F. Dickson, H. Reiter and B. Harris, 1989. "Fatigue Life Prediction for Hybrid Composites", International Journal of Fatigue, 11:233-237 11. Adam, T., R. F. Dickson, G. Fernando, B. Harris and H. Reiter, 1986. "The Fatigue Behaviour of Kevlar/Carbon Hybrid Composites", IMechE Conference Publications (Institution of Mechanical Engineers), 2:329-335 12. Fernando, G., T. Adam, B. Harris and H. Reiter, 1994. "Life Prediction for Fatigue of T800/5234 Carbon-Fibre Composites: I Constant-Amplitude Loading", International Journal of Fatigue, ' 16:523-532.
Part VII
FEM/Simulation
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Simulation of Three-dimensional Flow in Compression Resin Transfer Molding by the Control Volume/Finite Element Method Akbar Shojaei* Chemical and Petroleum Engineering Department, Sharif University of Technology, Tehran, Iran Davood Boorboor and S. Reza Ghaffarian Polymer Engineering Department, Amirkabir University of Technology, Tehran, Iran
ABSTRACT In compression resin transfer molding (CRTM), resin injection and mold closing occur during the mold filling stage. In this paper, numerical simulation of threedimensional flow in compression resin transfer molding (CRTM) is presented. Numerical method is based on the control volume/finite element method (CVFEM) and the numerical algorithm to update the flow front at each time step is based on quasi-steady state approach. Numerical scheme presented in this article can be used to predict the flow progression, pressure distribution, mold clamping force in full threedimensional mold. Numerical example provided in the paper demonstrates the effectiveness of the developed numerical simulation in analyzing the CRTM process.
INTRODUCTION Due to advantages of Resin transfer molding (RTM), it increasingly becomes an important processing technology to fabricate net-shape polymer-matrix composites, ranging from nonstructural components with simple shapes, to structural parts with complex geometries. Despite various advantages of the RTM process, there are still some problems in the fabrication of part with large dimensions or high fiber content, including long mold filling time and presence of considerable void content in the final product. In order to overcome the above mentioned problems, various methodologies have been presented to modify the conventional RTM process. One important improvement in RTM is to combine the compression into the resin transfer molding. This process is called compression resin transfer molding (CRTM) and consists of resin injection and mold clamping or compression during the filling stage. Numerical simulation is known as effective tool to analyze filling stage in CRTM. Recently, numerical simulation of the CRTM process has been addressed in literature [1-4]. But, all of these simulations are restricted to two-dimensional flow in the CRTM mold. In some practical applications, two-dimensional flow assumption is no longer valid, and then three-dimensional simulation is needed to estimate the processing parameters accurately. Corresponding author. Chemical and Petroleum Engineering Department, Sharif University of Technology, Tehran 11365-9465, Iran. Fax: +98-21-6022853. Email: [email protected]
358
Three-dimensional Flow in Compression Resin Transfer Molding
The objective of the present article is to propose a numerical method for the full three-dimensional simulation of filling stage in the CRTM process. First, the current mathematical model of CRTM process, continuity equation, is extended to threedimensional domain. Then the control volume/finite element method (CV/FEM) is used to solve the governing equation. Various capabilities are provided in the computer code, permitting prediction of the flow front progression in threedimensional domain, pressure distribution and clamping force. Finally, application of three-dimensional simulation is demonstrated by providing a numerical case study. THEORETICAL MODELING During filling stage in the CRTM process, the liquid resin flows through the fibrous reinforcement. This can be assumed as flow through porous media. Mathematical models governing filling stage for pure injection process, namely RTM, have been well documented in literature [5]. Resin flow for both RTM and CRTM can be modeled by Darcy's law, but the continuity equation for CRTM needs to be modified for considering the mold closing effect. Resin flow through porous media described by Darcy's law is given as follows in three-dimensional domain: dP - dx xz dP yz (1) dy zz dP
Eq. 1 can be rewritten in tensor notation as:
=-~[K].\
(2)
where v is the superficial velocity vector with three components v, u and w in x, y and z directions, respectively, [K] represents the permeability tensor, Ky are its components, P is the pressure and u. is the resin viscosity. The general continuity equation for a deformable medium is given as follows: V.v=—L-^
dV dr
(3)
where dV is the infinite small elemental volume at time t and the term d(dv)/dt represents the rate of deformation of this elemental volume. This deformation rate depends on the mold closing speed and fiber preform deformation behavior. Eq. 3 had been first derived in soil mechanics [6,7], then it was rederived by Pham et al. [2] for CRTM in which the fiber deformation may be large. Substituting Darcy's law into Eq. 3 leads to single equation for pressure as: dV dt
(4)
Three-dimensional Flow in Compression Resin Transfer Molding
359
Eq. 4 is a general form of governing equation for three-dimensional flow in the CRTM process. By solving Eq. 4 with the aid of appropriate boundary conditions, one can obtain the pressure field in saturated zone and consequently estimate the flow front progression during filling stage. The total force exerted on the mold is composed of two components, including the resin pressure in saturated region and fiber bed stress. The total force may be estimated by the following model [2,4]: PdS
(5)
where Ftoal is total force exerted on the mold, S the surface area of the mold, P the resin pressure in saturated zone and af the fiber bed stress. NUMERICAL METHOD In the present formulation, control volume/finite element method (CV/FEM) is used to discretize the governing equation, i.e. Eq. 4. The volume of mold cavity is first divided into eight-node three-dimensional elements and then control volumes are constructed around a node as shown in Fig. 1.
^<>" -« '/:••
/
/-
J. /FIGURE 1 An eight node element and its subcontrol volumes used in this study
In order to track the flow front progression, a scalar parameter, /, called nodal fill fraction, showing the status of each control volume, is used. The fill fraction for each control volume represents the ratio of occupied volume by the resin to its total pore volume. During the filling stage, each control volume may have three different statuses:/= 1 for main region,/= 0 for empty region and 0
icA »
)
icv. dV
dt
=
dV = dt\['c.v.
(6)
360
Three-dimensional Flow in Compression Resin Transfer Molding
where S and V represent the control surface and control volume, respectively, C.S. and C.V. are the subscripts that denote integration over the control surface and control volume, respectively, n is the unit normal vector of the control surface and V is the rate of volume change of a control volume. Eq. 6 is valid for a complete control volume and can be applied for all control volumes within the domain. In the present paper, the global stiffness matrix is constructed based on element by element assembling procedure. The parameters available in the left hand side of Eq. 6 are identical to parameters in the numerical formulation of pure RTM [8], but major concern in the numerical formulation of three-dimensional flow in CRTM is to establish a correlation between rate of volume change of a SCV, i.e. SCV , and upper mold closing speed. In the present work, the following relation is proposed to calculate 'SCV for a SCV based on the rate of volume change of relevant element: SCV, =
^
Ve
(7)
where Ve and Vscv are volumes of element and SCV, respectively, and Ve is the rate of volume change of an element. This is an important point from the viewpoint of numerical scheme, because according to Eq. 7, SCV is directly calculated based on elemental deformation rate. For an element which is compressed only in the thickness direction, we propose the following relation between Ve and Un as: Ve=SnUn
(8)
where Un is the normal component of the preform deformation rate through the thickness of the part, and Sn is a characteristic surface area of an element. According to Eq. 8, Ve can be obtained if Sn is known for an element. For three-dimensional elements, calculation of Ve is not straightforward and it is dependent on the geometry of the element. Based on the numerical formulation presented, an algorithm is developed to simulate the filling process of CRTM in full three-dimensional space. A computer code is written in FORTRAN computer language based on the numerical algorithm and the validity of the numerical algorithm was checked with analytical solution of 1dimensional flow. NUMERICAL RESULTS AND DISCUSSION In order to demonstrate the effectiveness of the numerical algorithm used in this study, numerical simulation of CRTM is performed for a mold cavity whose shape and finite element mesh is shown in Fig. 2. The resin injection and the mold closing are performed simultaneously throughout the mold filling stage.
Three-dimensional Flow in Compression Resin Transfer Molding
361
I Mold closing direction
100 Time (sec)
150
FIGURE 3 Flow front positions at three different times during filling stage; (a) t=50s, (b) t=100s, (c) t=150s and (d) Force exerted on the mold wall during filling process
362
Three-dimensional Flow in Compression Resin Transfer Molding
The mold closing speed is 5><10"5 m/s. The resin is injected through an inlet gate located at top of the flat section of the mold under the constant flow rate of 4.485 xlO"5 m3/s. The flow rate is set so that a final fiber volume fraction of 0.65 is met at the end of filling stage. Other parameters are: jx= 0.1 Pa.s, kx=k/=kz = 5><10"12 exp(6<£) and P = 2A06VJ531 where J^is the fiber volume percentage and cp is the porosity. It is assumed that the reinforcement deforms elastically during the compression process. Figures 3(a)-3(c) show the flow front positions at three different times during the mold filling stage. As shown in Fig. 3, fluid progresses radially from the injection port and then it becomes flat in the inclined section. The simulated mold filling time is 196 sec. Comparison of this simulation result with analytical value, i.e. 200 sec, shows a 2% error in filling time. As the injection process holds throughout the filling stage, analytical filling time can be simply calculated by dividing the final pore volume of the cavity to the injection flow rate. Fluid pressure force, reinforcement force and total amount of force exerted on the top of the mold calculated by the present numerical scheme are shown in Fig. 3(d). As seen in the figure, contribution of resin pressure force on total force exerted on the mold wall is negligible in comparison with fiber compaction force at early stage of mold filling. However, when the flow front reaches to the mold wall and flow front reaches to the inclined section of the mold, resin pressure force is considerable. This is reasonable, because at latter stage of mold filling, flow length and resistance against flow increase, needing a high pressure to hold a constant flow rate at the inlet port. CONCLUSION Numerical simulation based on the CV/FEM is presented to analyze the isothermal three-dimensional flow in the CRTM process. The numerical formulation for flow progression is based on the concept of quasi-steady state approach. The numerical scheme developed in this study provides necessary information for filling stage such as flow front progression, pressure distribution, and mold clamping force. This information is helpful in designing the optimum processing conditions before the mold is actually built. Numerical example provided shows the effectiveness of the numerical algorithm developed in this paper. REFERENCES 1.
2.
3. 4. 5. 6. 7. 8.
Phelan, Jr. F. 1996. "Analysis of Injection/Compression Liquid Composite Molding Process Variants," ASME International Mechanical Engineering Congress and Exhibition, Atlanta, GA, pp. 1-10. Pham, X. T., F. Trochu, and R. Guavin. 1998. "Simulation of Compression Resin Transfer molding with Displacement Control," Journal of Reinforced Plastics and Composites, 17:15251556. Han, K., J. Ni, J. Toth, L. J. Lee and J. P. Greene. 1998. "Analysis of an Injection/Compression Liquid Composite Molding Process," Polymer Composites, 19:487-496. Kang, M. K. and W. I. Lee. 1999. "Analysis of Resin Transfer/Compression Molding Process," Polymer Composites, 20:293-304. Shojaei, A., S. R. Ghaffarian and S. M. Ff. Karimian. 2003. "Modeling and Simulation Approaches in the Resin Transfer Molding Process- A Review," Polymer Composites, 24:525-544. Taylor, D. W. 1948. Fundamentals of Soil Mechanics. John Wiley & Sons, New York. Bear, J. 1971. Dynamics of Fluids in Porous Media. American Elsevier. Shojaei, A. S. R. Ghaffarian, and S. M. H. Karimian. 2002. "Numerical Simulation of ThreeDimensional Mold Filling Process in Resin Transfer Molding Using Quasi-Steady State and Partial Saturation Formulations," Composites Science and Technology, 62:861-879.
Modeling of Two-Dimensional Cellular Solids with Two Types of Imperfections K. Li, X.-L. Gao* Department of Mechanical Engineering-Engineering Mechanics, Michigan Technological University, 1400 Townsend Drive, Houghton, MI 49931-1295, USA
ABSTRACT The Voronoi tessellation technique and the finite element method are utilized to investigate the microstructure-property relations of two-dimensional cellular solids having irregular cell shapes and non-uniform cell wall thickness. Twenty finite element models are constructed for honeycomb samples (specimens) to obtain the mean values and standard deviations of the effective elastic properties. Spatially periodic boundary conditions are applied to each specimen. The simulation results indicate that the Young's moduli increase as cell shapes become more irregular, but decrease as cell wall thickness gets less uniform. The Poisson's ratios are insignificantly affected by the presence of these imperfections. The effect of the interaction between the two types of imperfections appears to be weak. In addition, it is found that such imperfect honeycombs can be regarded as isotropic.
INTRODUCTION Cellular solids (foams) are prevalent in nature and ubiquitous in engineering applications. A successful model that links the observed properties to the complex microstructures of foams can help us to understand how the microstructures affect the mechanical properties and enable us to optimize the microstructural parameters for a given application. Although unit cell-based models [1-3] can provide important results, they are significantly limited by their inability to account for microstructural imperfections inherent in most real cellular materials, whose cell structures are typically non-periodic, non-uniform and disordered. Thus, more complex, statistical models are necessitated to obtain improved predictions. Efforts have been made to investigate the effects of imperfections, such as irregular cell shapes, non-uniform cell wall thickness, wavy cell walls, and missing or fractured cell walls, on mechanical properties of cellular materials; most of these studies are based on the finite element method (FEM) [1, 4-7]. However, in each of the existing studies, only one type of imperfections was included at a time. In general, two or more types of imperfections are simultaneously involved in the microstructure of a cellular material. Therefore, models incorporating two or more types of imperfections are still in need.
* Corresponding Author, Department of Mechanical Engineering-Engineering Mechanics, Michigan Technological University, 1400 Townsend Drive, Houghton, MI 49931-1295, USA. Tel: +1-906-4871898; fax: +1-906-487-2822. E-mail: [email protected].
364
Two-Dimensional Cellular Solids
, V---{• /----<' •')-—(• y»-/ • \---( • \—(• Vr y _ / • ) — < T v < V ) — < • ) - . { • v < • >- \ • >—< • >—< * >--< • / v
/'
\ Seed 6
, Regular Voronoi cell \
/
\ • }-—\ * ) — < , «
-/ • >—(* v ~ < • \—<" •;—~< * >—< # / — { <
^>--< • y-G}-<' )-< • M • > —( • >—( • )—s i , \—/ • -J
, \ _ - ( . V—< t >—( • ; — ( • ) — ; • } . \
-(.
\ — { . V—< • V - < • •>—( -
x
Delauiiay triangulatioii • Seed 4 Voronoi boundary
. V_y . v_y , V / , y _ / . \ / . v / . v. v_y . V.1/ . FIGURE 1 Voronoi diagram based on regularly packed seeds
FIGURE 2 Coordinate perturbations of the Jthseed(x 1 ',Jj)
The objective of this paper is to address the combined effects of two co-existing imperfections - irregular cell shapes and non-uniform cell wall thickness - on the elastic properties of two-dimensional (2-D) foams. ANALYSIS The Voronoi tessellation technique is often used to capture random features of foam micro structures. When a set of seeds, placed in space simultaneously in a random fashion, grow in all directions with a uniform speed, a 2-D or 3-D Voronoi diagram is formed, depending on the space dimension. The Voronoi tessellation structure is fully determined by the initial locations of the seeds. Using regularly positioned seeds produces regular Voronoi diagrams. The current analysis starts with a reference model, which is a hexagonal honeycomb structure with perfectly ordered, regular cell shapes and uniform cell wall thickness. This reference model can be constructed from a set of regularly packed seeds using the Voronoi tessellation technique, as shown in Figure 1. Perturbations are then introduced to the reference model to generate Voronoi diagrams with irregular cell shapes and non-uniform cell wall thickness. Spatially Periodic Honeycombs with Cell Shape and Cell Wall Thickness Variations There are two methods to construct 2-D random foam models using the Voronoi tessellation technique [8]. The second method, which uses a set of seeds of periodic symmetry [9], is adopted here to construct spatially periodic models. First, a preset number of seeds are generated within a rectangle. Then, the position of each seed within the rectangle is copied to eight identical rectangles adjacent to or sitting at the corners of the original rectangle. Finally, the Voronoi tessellation technique is applied to all of the seeds within the nine rectangles. Part of the resulting Voronoi tessellation that is inscribed by the center (original) rectangle can be taken out as a unique periodic specimen. The irregularity of cell shapes is determined by the irregular distribution of the seeds. The locations of the seeds used to construct Voronoi diagrams with irregular cell shapes are perturbed from a regular lattice of seeds. Figure 2 shows the coordinate
Two-Dimensional Cellular Solids
365
perturbations of a regularly packed seed. The perturbed coordinates of seed i, x\ and x\, may be represented by
=x\ + a(d0 sin 6'. where *,', Xj are the two coordinates of the same seed in the regular lattice, do is the distance between two regularly packed (unperturbed) seeds, 6t (e[0, 2n]) is a stochastic angle (with a uniform distribution) between the x r axis and the line connecting the unperturbed and perturbed seeds,
N
I 7=1
where R is the relative foam density, L\ and L2 are, respectively, the width and height of the foam sample (specimen), /, is the length of cell wall j , and N is the total number of cell walls. To this end, each cell wall is assigned a random thickness given by
(a)
(b)
(c)
FIGURE 3 Honeycomb samples with varying a: (a) a = 0, (b) a = 0.5, (c) a = 1.0
366
Two-Dimensional Cellular Solids j
0)
j
where b (e [0, 1]) is the amplitude used to quantify the non-uniformity of cell wall thickness, y/j (e [-1, 1]) is a random variable with a uniform distribution, and c, called the normalizing factor, is defined by N
to ensure that the relative density (R) remains unchanged with the variation of the cell wall thickness. Given R, a, b, 9i and
j
r
hzxL2
£2=—^-, vI2=—^K '
Z
f
r
'
l
hE2Li
Z
r
v2, = - - ^ - , '
£jL2
Zl
r
(5) '
\
/
E2L-l
where h is the thickness of the honeycomb, F\ and F2 are, respectively, the total reaction forces along x\ and xi directions on the prescribed boundary, and u\ and ui are the lateral displacements (extensions) perpendicular to the loading directions x2 and x\, respectively. Also, biaxial strains £\ = 0.001 and £2 = - 0.001 are applied simultaneously along the two orthogonal directions to determine the effective shear modulus Gn, defined by G12 = Tnlyn, as
_FJL2-F2ILX 12
~
2/,(se)
;
(6)
Two-Dimensional Cellular Solids
367
Note that F\ and Fi in Eqs. (5) and (6) are obtained from the finite element analysis. In modeling uniaxial or biaxial loading tests, displacement boundary conditions are usually used [1,4-6]. However, since the specimen is cut out of an infinite structure that can be regarded as periodic, spatially periodic boundary conditions need to be applied to ensure that the predicted properties of the specimen are representative of those of the honeycomb [12]. Before proceeding to model honeycombs having irregular cell shapes and nonuniform cell wall thickness, a mesh sensitivity study is performed, which reveals that the appropriate number of cells to be included in a specimen is 360 [8]. RESULTS AND DISCUSSIONS Isotropy of the Effective Properties A total of 29 cases with different combinations of the three controlling parameters a, b and R are analyzed here. The maximum and minimum mean values of three ratios, i.e., E\IEi, vnlvii and G\ilGyi, are evaluated. Here, GuT is calculated using G\i = i?i/[2(l+vi2)], which is the shear relation required for material isotropy. Numerical results indicate that the mean values ofEi/E2, vu/vn and GulG\2T are very close to unity for all cases [8]. Therefore, it can be concluded that the elastic response of the honeycombs studied is isotropic regardless of changes in cell shape irregularity, cell wall thickness non-uniformity, and relative density. Effects of Cell Shape Irregularity The effects of irregular cell shapes on elastic properties are analyzed for honeycombs having a fixed relative density R = 0.01 and some uniform cell wall thickness (i.e., b = 0). For each value of a, twenty independent lists of random variables 6>,- and #>,- (z e{l, ..., M}) are used to generate twenty honeycomb samples, each of which has a unique arrangement of cell walls. Finite element analyses are then conducted on the twenty samples, and the mean values and standard deviations of the effective properties, i.e., the Young's moduli and Poisson's ratios, are obtained. Figures 4 and 5 graphically show the predicted elastic properties at different values of a. From Figure 4 it is observed that, on average, the Young's moduli increase considerably with a. Poisson's ratios, however, are insignificantly affected by the cell shape irregularity, as shown in Figure 5. The strong dependence of the Young's moduli on a may be attributed to the changes in the microstnicture as cells become less regular. In addition to hexagons, other types of polyhedrons, such as pentagons, quadrangles, and triangles, appear in the microstructure, as shown in Figures 3(b) and 3(c). The stiffness of each of these fewer-sided polyhedrons is higher than that of a hexagon, thereby leading to a significant increase of the Young's moduli. 40
0.9998 -, < 0.9996
~ 30 LU
•^ 0.9994
,,f 25 i
*
20
0.9992 0.999
0.2
0.4
0.6 a
0.8
1
0
0.2
0.4
0.6 a
0.8
368
Two-Dimensional Cellular Solids 1.002 i
-a = O 40 n a
30
'
S
*
= 10
'
1001
^
! 0,991
uj
J 20 J
0.998 0.997
10
0.996 0
0.2
0.4
0.6
0.8
1
b
FIGURE 6 Young's moduli
0
-a = 0 -a=1.0 02
0.4
0.6
0.8
1
b
FIGURE 7 Poisson's ratios
Effects of Cell Wall Thickness Non-Uniformity For 2-D foams, the influence of cell wall thickness variations on the elastic properties is still unclear. The regular honeycomb (a = 0) and the completely irregular honeycomb (a = 1.0) with non-uniform cell wall thickness are therefore analyzed here. Four values of the thickness non-uniformity amplitude, i.e., b = 0.2, 0.5, 0.8 and 1.0, are used for each of the two values of a. When b - 1.0, cell wall thickness variations are completely random. For each pair of a and b, twenty honeycomb samples are modeled using independent lists of random variables ,•, q>i (i E { 1 , ..., M}) and y/j (J e{l, ..., N}). The relative density R remains to be 0.01 for all of the samples. The predicted effective elastic properties are shown in Figures 6 and 7. Figure 6 reveals that the Young's moduli significantly decrease in a monotonic fashion as b increases for both values of a considered, while Poisson's ratios are insignificantly influenced by the varying values of b, as shown in Figure 7. Furthermore, it can be seen that the differences between the mean values of the Young's moduli for the honeycombs with a = 1.0 and those with a = 0 are insignificantly affected by varying b. This implies that the effect of the interaction between the cell shape and cell wall thickness variations on the elastic properties is weak. A further examination of Figure 6 shows that the Young's moduli are affected more by the cell wall thickness nonuniformity than by the cell shape irregularity. This follows from the fact that the Young's moduli for the case with a = 1.0 and b = 1.0 are smaller than the corresponding ones for the case with a = 0 and b = 0 (i.e., honeycombs without imperfections), although the two Young's moduli are found to increase as a rises (for fixed b) and to decrease with the increase of b (for fixed values of a), as discussed earlier. Moreover, for the special cases without the interaction (i.e., with a or b being zero but the other one varying), it is found that the maximum gain of moduli is 45% as a varies from 0 to 1.0 with the cell wall thickness being uniform (i.e., b = 0), while the maximum loss of moduli is 47% as b changes from 0 to 1.0 for a regular honeycomb. ACKNOWLEDGEMENTS The work reported here is partially funded by a grant from the AFOSR (Grant # F49620-03-1-0004) and by a contract from L & L Products. These supports are gratefully acknowledged. The public access to the Qhull program initially made available by the Geometry Center at the University of Minnesota - Twin Cities is also thankfully appreciated.
Two-Dimensional Cellular Solids
369
REFERENCES 1.
Silva, M. J., W. C. Hayes, and L. J. Gibson. 1995. "The effects of non-periodic microstructure on the elastic properties of two-dimensional cellular solids," Int. J. Mech. Sci, 37: 1161-1177. 2. Gibson, L. J. and M. F. Ashby. 1997. Cellular Solids: Structures and Properties, 2nd edition. Cambridge: Cambridge University Press. 3. Li, K., X.-L. Gao, and A. K. Roy. 2003. "Micromechanics model for three-dimensional open-cell foams using a tetrakaidecahedral unit cell and Castigliano's second theorem," Compos. Sci. Tech., 63: 1769-1781. 4. Simone, A. E. and L. J. Gibson. 1998. "Effects of solid distribution on the stiffness and strength of metallic foams," Ada. mater., 46: 2139-2150. 5. Simone, A. E. and L. J. Gibson. 1998. "The effects of cell face curvature and corrugations on the stiffness and strength of metallic foams," Acta. mater., 46: 3929-3935. 6. Silva, M. J. and L. J. Gibson. 1997. "The effects of non-periodic microstructure and defects on the compressive strength of two-dimensional cellular solids," Int. J. Mech. Sci., 39: 549-563. 7. Chen, C , T. J. Lu and N. A. Fleck. 1999. "Effect of imperfections on the yielding of twodimensional foams," J. Mech. Phys. Solids, 47: 2235-2272. 8. Li, K., X.-L. Gao, and G. Subhash. 2003. Manuscript submitted for publication. 9. Nygards M. and P. Gudmundson. 2002. "Micromechanical modeling of ferritic/pearlitic steels," Mat. Sci. Eng. A, 24: 435-443. 10. ABAQUS Theory and User's Manuals, Version 6.3. Pawtucket (RI): Hibbitt, Karlson and Sorenson, Inc., 2002. 11. Li, K., X.-L. Gao, and A. K. Roy. 2003. "Micromechanical analysis of three-dimensional open-cell foams using the matrix method for space frame structures," in: Proceedings of the 14th International Conference on Composite Materials (ICCM-14), July 14-18, 2003, San Diego, CA. 12. Laroussi, M., K. Sab, and A. Alaoui. 2002. "Foam mechanics: nonlinear response of an elastic 3Dperiodic microstructure," Int. J. Solids Struc, 39: 3599-3623.
Finite Element Modeling of Fine Structure of Natural Plant Fibers for Statistical Characterization of Their Tensile Strengths Kohji Suzuki Chiba Institute of Technology, Department of Mechanical Engineering Science, Japan Isao Kimpara Kanazawa Institute of Technology, Advanced Materials Science R&D Center, Japan Kunio Funami Chiba Institute of Technology, Department of Mechanical Engineering Science, Japan
ABSTRACT Natural plant fibers can be environmentally-preferable industrial raw materials owing to their renewable, biodegradable and carbon-neutral features. However, those natural plant fibers have not yet been fully examined from the standpoint of engineering, and hence are hardly said to have acquired any credentials in the field of structural applications. Furthermore, the plant fibers, made up of numerous plant cells (elementary fibrous cells) glued to each other with the inter-cell material, may exhibit a certain unique statistical characteristics regarding the physical and geometrical properties reflecting their unique internal fine (cellular) structures. In this study, first the biologic internal fine structures of natural plant fibers were carefully discussed about mostly using the optical microscopic images of kenaf (Hibiscus cannabinus L.) bast fibers. After that, a simple but well-devised numerical, i.e. finite element, modeling framework was proposed for the stress analysis and strength simulation of natural plant fibers. By using the proposed numerical modeling, probabilistic simulations of tensile strength of natural plant fibers were conducted with the Monte Carlo direct method invoked, which was followed by a few statistical treatments to the simulation results. The statistically-treated results foretold importance of considering the shear stresses induced in the inter-cell material as well as the axial stresses in the elementary fibrous cells for estimating the fiber breaking loads. INTRODUCTION Fibers extracted from the natural fiber-producing plants such as jute, bamboo, flax, ramie, sisal, abaca and kenaf are cheap, easy to handle, biodegradable and renewable, non-petroleum and carbon-neutral, and hence considerably environmentally-preferable and harmless-to-human-body cellulose-based natural resources, and now are seeking use which can be counted on ever-growing mass production as well as profitability for reducing the environmental burdens to Earth. For instance, kenaf (Hibiscus cannabinus L.) bast fibers are currently looked upon as a promising reinforcing agent for the biodegradable polymers such as poly L. lactic acid (PLLA) in the automobile and house-hold appliance industries. The plants and the fibers shown in Fig.l were actually grown by the first author in the year of 2002 [1]. However, when one tries to put this kind of plant biomass into the mainstream in the industry, especially in the fields of structural * Correspondence Author, 2-17-1 Tsudanuma, Narashino, Chiba 275-0016, JAPAN fax number: +81-(0)47-478-0261, email: [email protected]
Fine Structure of Natural Plant Fibers
371
4/N 9
•• f | ''i • **-.
r
(a)
(b)
(c)
FIGURE 1 (a) Fully grown-up kenaf plants, (b) kenaf fibers in the bast layer and (c) air-dried kenaf fibers.
composite materials, he surely encounters one serious problem, i.e. the issue of assurance of strength reliability and quality. Natural plant fibers are not rigorously-quality-managed products but essentially botanical and agronomy things and by nature they do not fit in engineering ways of thinking so well. Therefore, some careful treatments to these natural resources should be employed toward their practical applications to the industries [2]. In this study, in order to investigate the actual fracture process commonly occurring in the natural plant fibers and the resulting phenomenological tensile-strength statistics, the authors will advocate the merit of numerical modeling in an engineering finite element manner for the fine (cellular) structure of natural plant fibers with kenaf fibers chosen as a typical example. The authors will propose a numerical modeling methodology for fine (cellular) structures of a plant fiber, which are actually a kind of composite material by itself and made up of numerous elementary fibrous cells and inter-cell material (binder gluing elementary fibrous cells together). Beam elements will be used for modeling elementary fibrous cells while solid elements for inter-cell material. By using the finite element models of plant fibers, probabilistic simulations based on the conventional Monte Carlo direct method [3] will also be invoked to obtain some useful numerical statistics in terms of the fiber strength. The validity and benefit of the present framework of numerical modeling and probabilistic simulation will be partly shown by a preliminary case study. INTERNAL FINE STRUCTURE IN NATURAL PLANT FIBERS Figure 2 (a) and (b) respectively show a general illustration and a cross-sectional view of a kenaf (Hibiscus cannabinus L.) bast fiber as an example of plant fiber anatomy. As can be seen in these figures, the natural plant fibers are definitely not a monolithic and homogeneous single fiber with a circular cross section but rather a bundle or a composite with an elliptic or polygonal cross section consisting of several fibrous plant cells which are approximately 10 urn wide and 3mm long in the case of kenaf and can be compared to
Plant Fiber (Technical Fiber) Elementary Fibrous Cells Inter-C»ll V .:• -i.-l
Elementary Fibrous Cell
-
^
- ~
Lumen Secondary Cell Walls
l_/^_,
(a)
Kenaf Bast (Technical) Fiber
(b)
FIGURE 2 Internal fine (meso-scopic and cellular) structures of natural plant fibers, (a) a schematic of a plant fiber, (b) a cross-sectional view of a plant (kenaf) fiber and (c) cell wall fine structure.
372
Fine Structure of Natural Plant Fibers
tiny spindle-shaped hollow structures or macaroni fibers with their both ends capped. In this study, those ultimate plant cells are to be called "elementary fibrous cells". One of the most prominent features commonly seen in the morphology of those elementary fibrous cells is the open hole at the center, so-called "lumen". Note also that, once the elementary fibrous cells are separated from each other through a certain specific series of chemical and mechanical processes, then they will be called "pulp" and, notoriously, have been used as an important raw material for paper. In fact, as shown in Fig.l (c), the past researches have revealed that the elementary fibrous cells themselves are filament winding composite pipes with cellulose micro fibrils (CMF), which are helically winding in the cell wall and give stiffness and strength to the wall, as the reinforcement, and the mixture of the other non-cellulose substances such as pectin, hemi-cellulose and lignin as the matrix resin. Generally speaking, plant fibrous cells have a thick and stiff secondary cell wall, which can be further divided into three layers, Si, S2 and S3 as shown in Fig. 1 (c). Above all, the winding angle of CMF in the thickest S2 layer has a strong positive relation to the cell's physical properties such as stiffness, strength, elongation at break and so on. In addition to the elementary fibrous cells, the inter-cell material, which glues the elementary cells together, is also an important constituent of the plant fiber. It is a kind of binder a few Lim thick filling the space between the neighboring elementary fibrous cells. This adhesive material is primarily made up of non-cellulose polysaccharides such as pectin and hemi-cellulose, and occasionally including a small ratio of lignin. Since there is scarcely any cellulose content in this material, its stiffness and strength are by two or three orders of magnitude smaller than those of materials reinforced by CMF. Although its stiffness and strength are considerably small compared to those of elementary cells, almost all of the loads from one elementaryfibrouscell to the others will be carried via the shear stresses in this interfacial region, and hence the mechanical properties of this binder can govern the overall mechanical performance of the plant fibers. For instance, the present authors have already obtained several evidences that fractures in the plant fibers can be initiated as shear failures in the inter-cell material regions. Figure 3 (a) is a cross sectional view of a fractured plant fiber in which cracks in the inter-cell regions can be clearly seen longitudinally running through along the elementary fibrous cells just like the transverse matrix cracks often seen in the unidirectional fiber-reinforced plastics. Since that fractured fiber could hardly experience any tensile load in transverse direction, those "transverse cracks" might be driven by "shear stress concentrations around adhesive rich regions". This hypothesis is indirectly but quantitatively supported by the dependence of the frequency percentage of the two typical fiber fracture patterns on the fiber gauge length as schematically shown in Fig.3 (b). Thefracturepattern, A, is for the shear failure in the inter-cell material, on the other hand, the latter pattern, B, is for the axial tensile breakage of the elementary fibrous cells. When the fiber increases in gauge length from 3
* \H\. * • Transverse Cracks
(a)
G.L. = 2mm G.L. = 3mm G.L. = 6mm pattern percentage pattern percentage pattern percentage 47.1% A A 30.0% A 58.8% 52.9% B B B 70.0% 41.2% 100% total 100% total total 100%
(b)
FIGURE 3 Some evidences on fractures arising from the inter-cell material, (a) a cross-sectional view of one of the fractured fibers with transverse cracks, (b) the two typical patterns of fiber fracture and the dependence of those fracture patterns on the gauge length of fiber tensile specimens.
Fine Structure of Natural Plant Fibers
373
to 6 mm, then the pattern, A, also increases in frequency from 30.0% to 58.8%. This fact implies that fiber fractures are more easily initiated as a shear failure in the inter-cell material than as a tensile breakage of an elementary cell as long as the gauge length is large enough for shear stress concentrations in resin rich regions to occur at a sufficient frequency which may depend primarily upon the averaged length of elementary cells. FINITE ELEMENT MODELING In this study, after all the discussions about the internal fine structure and failure mechanisms of the plant fibers previously made and also about another anatomical observations in terms of longitudinal cross-sectional morphologies as shown in Fig.4 (a), the following numerical modeling with a combination of beam and continuum solid elements as schematically shown in Fig.4 (b) are proposed for the stress analysis and strength simulation of this natural biomass. Each of the elementary fibrous cells is to be modeled with beam elements. Cross sectional figurations and areas of the elementary fibrous cells can vary, so they will need to be statistically measured and then modeled with a mean, a coefficient of variation (CV) and a most plausible type of the probabilistic distributions. Otherwise, they might be idealized as an ellipse or a rectangle with an open-hole (lumen). Note also that, in the cases that only the axial forces are mainly concerned with, the shape and moduli of the sections are redundant. Similarly, the allover fiber length and flaw density along fiber length (nearly equal to axial tensile strength assigned to each of the beam elements) should be allowed to probabilistically vary. Spatial arrangements of elementary fibrous cells packed in the fibers are randomly generated. On the other hand, the inter-cell material regions are to be meshed with continuum solid elements. As already mentioned, the major ingredients of this cementing material are polysaccharide fractions such as pectin and hemi-cellulose. There is no observation on an existence of cellulose contents, in this interfacial regions, and therefore its stiffness and strength will be very small compared to those of elementary cells reinforced with CMF. A strength data sampled from an appropriate probabilistic distribution representing the strength properties of the elementary cells or the inter-cell material should be assigned to each element. Overall fracture of the plant fibers will be judged at the first moment when the actual stress of a certain element exceeds its strength. The component of stress and strength for that comparison is the axial tensile component for the beam elements (i.e. the elementary fibrous cells) and the shear component for the solid elements (i.e. the inter-cell material). Thisfracturejudgment is fairly applicable to brittle materials and the load-elongation curves of the kenaf fibers experimentally obtained by the present authors clearly indicated the nature of brittle facture in natural plant fibers. Elementary Fibrous Cells
Inter-Cell Material
43Beam Elements for Elementary Fibrous Cells ec n ar;
ell
alls
Kenaf Bast (Technical} Fiber (a)
Solid Elements for Inter-Cell Material (b)
FIGURE 4 (a) longitudinal section of kenaf fiber, (b) the present finite element modeling for plant fibers.
374
Fine Structure of Natural Plant Fibers
NUMERICAL EXAMPLE By using the proposed finite element modeling of natural plant fibers, a preliminary probabilistic simulation for statistical evaluations of their tensile strength were conducted with the Monte Carlo method invoked [3]. The simulation flow was charted in Fig.5. The finite element code, ANSYS 7.0, was used as the mesh generator, the solver and the result visualization tool. Probabilistic Design System (PDS), one of the ANSYS program extensions was also utilized to conduct the present probabilistic simulation. The key tasks up to the point of simulation execution are, (a) to construct a complete set of deterministic finite element analysis in the form of batch files written in APDL (ANSYS Parametric Design Language), (b) to define geometrical or physical parameters as "random input variables" and to specify their statistical data such as mean, standard deviation, and probabilistic distribution, and then (c) to select the resulting output parameters of interest. hi Table 1, the problem description, the dimensions and material properties of the plant fibers, the elementary fibrous cells and the inter-cell material are respectively shown. For the purpose of examining how the fiber strength depends on its gauge length, twelve different cases of the gauge length, L, from 0.1 to 40mm were simulated, hi order to eliminate the so-called "end effects", the numerical fiber models were so created that their length will always longer than the gauge length by the average length of the elementary fibrous cells. In Fig.6 (a), a typical finite element meshes (both of the entire and the zoomed-up views) are shown. On the other hand, Figure 6 (b) shows the shear stress distribution in the inter-cell material at one of the simulation steps. In that distribution are clearly seen the shear stress concentrations which can be a starting point offiberbreakage. TABELI The problem description and the simulation input data. Model dimension Total number of simulation samples
Monte Carlo direct simulation (ANSYSPDS) jrandomnumber generation ana then ''random input variable sampling
Problem Descriptions
i
20
at least 30 Elementary fibrous ceils are generated based on spatially uniform random distribution. The generated cells are dlscretlzed by 2D beam elements. Intercell materials are modeled by 2D plane-stress solid elements. Length, cross-sectional area and axial strength for each of the elementary fibrous cells are assumed to have normal (Gauss) distributions. Fiber strengths are calculated by using an axial reaction force for the first failure of the cells and averaged fiber cross-sectional area.
• modify the APDL file (rased on the | snput variable sampling results ana j prooiem solution ana evaluation of j output parameters tor this step
Gauge length : L [mm] Fiber Cross section height: H [mm] Max. numbers of elementary fibrous cells per cross section Mean of cell length : /_mean [mm] Standard deviation of cell length : STDevJ [mm] Length of beam elements : /_beam [mm] Elementary Mean of cross^ectional area i A mean [mm J Fibrous Cell Standard deviation of cross-sectional area : STDev__<4 [mm1] Young's modulus ; E Cell [N/mm1] Mean of cell axial strength : X_Cell [N/mm2] Standard deviation of ceil axial strength : STDev X [N/mm2]
inter-Cell
FIGURE 5 The simulation flow.
(a)
Young's modulus : E mat [N/mm2] Poisson's ratio : nu mat Mean of shear strength : S_Cell [N/mmJ] Standard deviation of shear strength : STDev S [N/mm2] Thickness: b [mm]
0.1,0.3,0.5, 1,2,3,4,5,6, 10,16,25,40 0.1 11 3 0.6 0.1 0.0001 0.00005 70000 1000 100 10000 0.3 60 12 0.01
(b)
FIGURE 6 (a) Typical FE mesh (Z=6mm) and its zoomed view, (b) shear stress in the inter-cell material.
Fine Structure of Natural Plant Fibers
375
TABLE II Means and CV of the strengths obtained by the simulation and percentage of the shear fracture. L
Q
(mm)
(MPa)
0.1 0.3 0.5 1 2 3 4 5 6 10 16 25 40
817 602 537 513 412 369 350 319 311 261 239 202 184
cv,, (%>
o DL=0.1mm e GL=0.5mm a GL=2.Qmm • GL=3.0n x GL=4.0mm • GL=16mm + GL=4Qmm
T «lit( ojnean) a percentage of inter-cell material fracture
percentage of shear fracture in inter-cell material
0.0
19.5 21.6 20.4
20.0 30.0
16.2 18.5 25.5 17.2 23.0 25.5 27.2 33.2 31.1 32.0
51.7 38.5 50.0 57.4 72.0 58.0 56.0 54.0 56.0 70.0
-2.0
-1.0
0.0
(a)
1.0
2.0
3.0
4.0
(b)
FIGURE 7 (a) Mean strengths and percentages of cases of fracture initiation in the inter-cell materials, (b) Weibull plots of the strengths.
In Table 2, as the simulation results, the means, the coefficient of variations and the percentage of the specimens which were broken by the shear failure in the inter-cell material regions, are summarized against the gauge length, hi Fig.7 (a), the means of strengths and the percentages of cases of fracture which initiated in an inter-cell material region are simultaneously plotted against the gauge length. Generally, as the gauge length increases, the fiber strength tends to decrease and the percentage of occurrence of shear failure increases, which, as previously mentioned in this paper, foretells importance of considering the shear stresses which will occur in the inter-cell material of plant fibers, as well as the axial stresses in the elementary fibrous cells, for the estimation of the fiber breaking loads. Finally, Weibull plots of the strengths of different gauge lengths are shown in Fig.7 (b). Some of the gauge length cases, e.g. G.L. = 0.5, 2.0 and 4.0mm, are seen to make not straight but kinked lines, which implies that strength characteristics of natural plant fibers are not necessarily represented by the classical two-parameter Weibull distribution. This is probably because of the multiple seeds of fracture, that is, the axial tensile breakage of the elementary fibrous cells and the shear failure at the stress concentrations in the inter-cell material regions. CONCLUDING REMARKS A numerical modeling with a combination of beam and continuum solid finite elements for stress analysis and strength simulation of natural plant fibers has been newly developed after carefully discussing about the internal fine (cellular) structure of kenaf (Hibiscus cannabinus L.) bast fibers. By using the present numerical model, Monte Carlo probabilistic simulations for statistical characterizations of tensile strength properties of natural plant fibers were also carried out, and the preliminary simulation results in a general case of natural plants partly indicated importance of considering the shear stresses which will occur in the inter-cell material regions in plant fibers, in addition to the axial stresses in the elementary fibrous cells, for the estimation of the fiber breaking loads. REFERENCES 1. Suzuki, K. 2004. "Research Report on Test Growing Kenaf', Report ofChiba Institute of Technology, 51, (in press). 2. Suzuki, K., Kimpara, L, Funami, K. and Kageyama, K. 2003. "Natural Bast Fibers with Large Variations in Geometrical and Mechanical Properties", Proc. 8th Japan International SAMPE Symposium (JISSE-8), pp. 139-142. 3. Suzuki, K., Funami, K., Kimpara, I and Kageyama, K. 2003. "The Stochastic Finite Element Analysis of Natural Fiber Reinforced Composites with Large Variations in Geometrical and Mechanical Properties", Proc. the 14th International Conference of Composite Materials (ICCM-14), CD-ROM pp.1-10.
Multilayered and Selective Higher-Order-Deformable Sandwich Finite Element Modeling for Numerical Accuracy Improvement Kohji Suzuki Chiba Institute of Technology, Department of Mechanical Engineering Science, Japan Isao Kimpara Kanazawa Institute of Technology, Advanced Materials Science R&D Center, Japan ABSTRACT Multilayered, higher-order-deformable and hybrid treatments are keys to numerical accuracy improvements of finite element analysis of composite and sandwich structures. In this context, the conventional displacement-based equivalent-single-layered and first-order-shear-deformable isoparametric shell finite element models are quite powerless for the multilayered composite and sandwich structures. This is especially true when one needs to numerically analyze composites and sandwiches in unusual states such as considerably severe transverse shear deformed situations and delamination-like damage states. In this study, new multilayered and higher-order-deformable finite element models will be proposed for accurate displacement and stress analysis of structural sandwich composite materials. The proposed model employed the flexible and versatile displacement assumptions for each of the three layers in sandwich-type constructions. The displacement assumptions for the core layer should be higher-order-deformable since this intermediate layer is thick and low modulus, while those of the upper and lower layers can be modeled as lower-order-deformable, such as first-order-shear-deformable, since they are thin and stiff. In the present finite element formulation, the displacement continuity constraints at the layer interfaces are enforced by invoking the penalty function method, in which the adhesions between the adjacent layers can be achieved with the penalty parameter virtually set to be infinitely large. In addition to the finite element formulation and then the program coding, a numerical example of a square sandwich plate subjected to uniformly distributing load were also shown, which showed, for the displacements of the core layer to be accurately modeled, the higher-order-deformable model should be used.
INTRODUCTION Sandwich structures have long been served as high-performance structural parts in many industries such as aerospace, marine and sports, and the demands for this sort of structural component won't be diminished for years to come. A sandwich-typed plates and shells are usually realized by facing the both surfaces of the intermediate core layer with the upper and lower skin layers. The upper and lower skin layers are most commonly formed with very thin but very stiff laminated composite materials like carbon fiber reinforced plastics (CFRPs), while the intermediate core layer with relatively thick, * Correspondence Author, 2-17-1 Tsudanuma, Narashino, +81-(0)47-478-0261, email: [email protected]
Chiba
275-0016, JAPAN;
Fax:
Multilayered and Selective Higher-Order-Deformable Sandwich
377
considerably low-modulus with a minimum transverse-shear resistance and light-weight porous materials like polyurethane foam and aramid honeycomb. This fact leads to a suspicion of multilayered (ML) deformations through the thickness. Apparently, for thick and soft-core sandwich structures, equivalent-single-layer (ESL) models [1-3] are not applicable and instead more-than-three-layered, i.e. ML, models considering the jumping discontinuity through the thickness in terms of the material properties and the kinematical assumptions will be probably indispensable if one wants to numerically model fairly accurate layer-by-layer displacements and in-plane stresses and then inter-laminar stresses in those structures. However, the conventional ML models [4-5] employ lower-order displacement fields for each of the three layers, in spite of the fact that the geometrical and mechanical properties of skins faces and the core are quite different from each other and hence there is possibility of some higher-order-deformable (HOD) states in the structures. This is especially true when one needs to numerically analyze composites and sandwiches in unusual states such as in transversely-shear-deformed situations, in delamination-like damagings, and so on. hi this study, a new multilayered and higher-order-deformable (ML/HOD) model will be proposed for accurate numerical analysis of structural sandwich composite materials, which can selectively consider ML and HOD assumptions in a flexible and versatile manner, hi addition, by using the proposed sandwich modeling, a few different finite elements will be developed and applied to a case of a square sandwich plate. FINITE ELEMENT FORMULATION The multilayered (ML) and higher-order-deformable (HOD) finite element model will be presented herein. For preserving its generality, summation conventions are implied for repeated subscripts in the mathematical formulae. hi the present finite element formulation, the three displacement components in each discrete layer are assumed to be expressed with power series expansions in terms of the thickness coordinates, xf), as follows:
where the superscript'T' denotes either of the upper skin (U), the core (C) or the lower skin (L) layers, and U\kp are the unknown coefficients in the series expansions. The geometric configuration of a laminate and the deformation of the typical layer "&" are respectively shown in Fig.l. Geometrically, U{^, Uf^ and Uf^ are the translational components i n ^ , x2 and x3 directions, respectively, while U\k) and Uf^ respectively stand for small rotations about x2 and —xl axes. The rest of the coefficients of power series expansions are higher-order influences such as warping of the cross-section and elongation of a transverse normal. The series in Eqn.(l) can be truncated at a proper order of expansion (practically at most up to the third order), however, at this moment, the orders of truncation is not yet determined for preserving the generality and flexibility of the present theory. For conceptual sake, when the orders of the series for k^ layer areiVf', JV<*> and N™ f o r < \ uf and uf\ respectively, the notation (N[k) N™ N\k)) will be used to express the order of displacement assumptions, and the notation,
Multilayered and Selective Higher-Order-Deformable Sandwich
378
^ir *•*: translation
\j. M • rotation
Upper
Lower face
~-h(k>/2 Ui P (P > 2).- higher-order terms
(a) through-the-thickhess configurations
(b) Deformation of the layer' k'
FIGURE 1 Sandwich plate element, notations and displacement assumptions.
[(Af> A f > Nlv) ) (Af > N(2C) A f > )(Af > Af } A f >)] will also be used for the entire sandwich laminate. Note that the brackets are for the entire sandwich and three columns of parentheses within the brackets, respectively from the left side to the right, denote the upper skin (U), the core (C) and the lower skin (L) layers. Three integers in each of the parentheses denote, respectively, the order of truncation of the polynomial series of three displacement components. Based on the small deformation elasticity, the strain-displacement relations are expressed in the following expansion forms:
ey=-2{
dXj
ax, )
V
*
3
J
'
^i/P^
•
i'
2)
(2, j = 1,2,3; i < j and P = 0,1,2, • • •, max (Af>,
(2) Nf))
where Efl are general strain components. Physically, E^ are strains at the middle plane of the &* layer, and Ef? are curvatures of that layer. E\k)0 stand for the first approximations of transverse shear strains. When E\k\ are set equal to zero, then the same displacement / strain assumptions as the classical plate (CP) theory are modeled in the kth layer (not in the entire laminate). On the other hand, when these terms are set non-zero, then the first-order-shear-deformable (FOSD) theory, i.e., Reissner-Mindline assumption, (110), are assigned in that layer. The rest of the general strains are higher-order components corresponding to the higher-order-deformable (HOD) displacements. Obviously, the orders of through-the-thickness variations of strains depend upon the displacement orders ( A f ' A f A f J ) . For instance, when the displacement assumption (332) is adopted, then cubic variations of in-plane strains, parabolic variations of transverse shear strains and linear variations of transverse normal strain can be modeled. The aim of the HOD assumptions is placed on an optimization in the numerical modeling of displacement and strain variations over the thickness of the laminates and sandwiches as close to the actual as possible. Appropriate and practical orders of displacements should be determined in accordance with the actual sandwich configurations to be modeled. After assuming the higher-order-deformable (HOD) displacements in each layer, next comes assemblage of layers to form the entire sandwich. In the present formulation, the
Multilayered and Selective Higher-Order-Deformable Sandwich
379
displacement continuity constraints at the perfectly adhered interfaces between the k01 and the (k + l)'h layers are given as follows: fr(k)(x i ) - « ( i t I ) \x x Si
\X1>X2) ~Ui
x
\iX2-:
(3)
(z= 1,2,3 and/> = 0,1,2,---, hi order to consider above constraints, the following modified potential energy functional with displacement continuities relaxed at layer interfaces will be utilized,
where the first two terms are the potential energy in the system obtained after summing the ones stored in all the three layers without interface constraints. 7] andwj, respectively, denote mechanical and geometrical boundary conditions on the upper and lower exterior surfaces of the sandwiches. On the other hand, the last term is the auxiliary energy term due to the interfacial displacement constrains, and Xt stands for each of the three components of the so-called inter-laminar stress, and, in this formulation by the penalty method, can be estimated by, Ajk) - a^k)gjk), in which a\k) are called the penalty parameters. When each a\k) for each layer interface is set virtually infinite, then the displacement continuities will be approximated and the auxiliary energy term will vanish, hi the present finite element formulation, the allover domain of a sandwich plate will be discretized into Ne elements such that: (5) The generalized displacement vector 5 are defined as a collection of each sub-vectors for those in the Ar"1 (k = U, C or L) layer:
Finally, taking the first variation of the functional in Eqn.(5), and then collecting the contributions from all elements yields the following equilibrium equation system: 5
0
^> ^
[K + K J d = f
(7)
55
in which K is the global stiffness matrix without displacement constraints and K a , on the other hand, is the interface constraint stiffness portion including the penalty parameters, d and f are respectively the assembled nodal displacement and force vectors.
Multilayered and Selective Higher-Order-Deformable Sandwich
380
y l
-V2-
simply supported conditions for all four edges
0 (a) the problem definitions
1/2
I
x
(b) top view of the plate
FIGURE 2 A simply-supported CFRP/honeycomb-core sandwich plate to be analyzed.
NUMERICAL EXAMPLE hi order to assess the degree of improvement of the accuracy and convergence properties of the finite element modeling by HOD assumptions, comparative results are presented in the case of a simply-supported CFRP/honeycomb-core sandwich plate subjected to an uniformly distributed load over the whole area of the upper face surface as shown in Fig.2. The dimensions and the material properties and the load intensity applied used in the numerical analysis are as follows: for the entire sandwich plate; / = 200mm, h = 9.6mm, q0 = 1 .OMPa for the faces; = £ , = 560GPa,
£ z =91.7GPa
vxy =0.0813, vYz= 0.450, v z x = 0.0237, G xy =259GPa,
Gyz = Gzx = 29.5GPa
and for the core of aluminum honeycomb with the following properties;
F=8.0mm, Ex=0.5lGPa, Ey=0.63GP&, £z=14.1GPa vxy = 0.83, vyz = 0.015, v2x = 0.34, Gxy = 0.49GPa, Gyz = 2.46GPa, Gzx = 3.03GPa Three different types of sandwich elements, that is, [(110)(110)(l 10)] element, [(110)(332X110)] element and [(332)(332)(332)] element based on the selective formulations shown in the previous section were used for the analysis. As a baseline for numerical accuracy, a detailed 3-D continuum solid element model was also generated using the general purpose finite element package MARC (version k-5) with the use of 20-node isoparametric 3-D continuum solid elements. The total number of nodes in the 3-D solid FEM model was 15236, and the total number of elements was 3125. The variation of the central deflection (normalized with the result by 3-D solid FE) against square mesh refinement is shown in Fig.3. It is observed that, as the degrees of freedom are increased in number, every of the present FEs' solutions are converging to the constant value a little bit smaller than the result obtained with the detailed 3-D continuum solid FE. It is also observed that [(110)(332)(110)] and [(332)(332)(332)] element, the results obtained by which were almost identical, gave more accurate results than [(110)(l 10)(l 10)] did. On the other hand, the other analytical models, all of which are
Multilayered and Selective Higher-Order-Deformable Sandwich
381
[(110)(110)(110)] FE solution [(332)(332)(332)] or [(110)(332)(110)] FE solution
1.1 3-D solid FE solution 1,(0.982) '(0.951) Allen's analytical solution (0.841) HOT of Reddy (0.773) FOSDT (0.694) CLT (0.609)
10
15
20
25
Number of elements FIGURE 3 Central deflections against square mesh refinement.
based on the existing classical and equivalent-single-layered (ESL) theory, without any exception, provided poor (too stiff) results. CONCLUDING REMARKS Some accurate FE models for sandwich plates were presented, based on the selective multilayered and higher-order-deformable (ML/HOD) assumption, i.e. [(110)(l 10)(l 10)], [(110)(332)(H0)] and [(332)(332)(332)]. The numerical example on a square sandwich plate with uniform distributing load clearly illustrated that those ML/HOD models proposed in this study were more accurate than the ESL-based models such CLT, FOSDT, which showed, for the displacements of the core layer to be accurately modeled, the higher-order-deformable models should be used. In addition, since the numerical accuracy of [(110)(l 10)(l 10)] model was slightly inferior to the other two models, i.e. [(110)(332)(110)] and [(332)(332)(332)] and also from the view point of computational efficiency, the optimum numerical model will be [(110)(332)(110)] among the three models taken into consideration in this study. REFERENCES 1. Yang, P.C., Norris, C.H. and Stavsky, Y. 1966. "Elastic wave propagation in heterogeneous plates", Int. J. Solid Struct, 2, pp.665-684. 2. Lo, K.H., Christensen, R.M. and Wu, E.M. 1977. "A higher-order theory plate deformation. Part 2: Laminated plates", J. Appl. Meek, 44, pp.669-676. 3. Reddy, I N . 1984. "A simple higher-order theory for laminated composite plates", J. Appl. Meek, 51, pp.745-752. 4. Mau, S.T. 1973, "A refined laminated plate theory", J. Appl. Meek, 40, pp.606-607. 5. Ferreira, A.J.M., Barros, J.A.O. and Marques, A.T. 1991, "Finite element analysis of sandwich structures", Proc. 8th Int. Conf. Compos. Mater. (ICCM/8), Honolulu, 3A2.
Adhesion Measures of Elasto-plastic Thin Film via Buckle-driven Delamination Qunyang Li and Shouwen Yu* Key Lab .of Failure Mechanics of MoE, Tsinghua University, Beijing 100084, China
ABSTRACT Indentation test is becoming increasingly used to quantitatively assess the thin film interfacial adhesion for its simplicity and ability to mechanically probe the smallest of solids. The conventional technique is based on the analysis of Marshall and Evans which is a combination of Linear Elastic Fracture Mechanics (LEFM) and simplified post-buckling theory. In this paper a full post-buckling response of elasto-plastic thin film is investigated by FEM calculation; the contributions plastic buckling to the indentation test is discussed. The results show that plasticity is a significant factor for those films with low yield stress and must be taken in account in adhesion measurement. INTRODUCTION Thin films have a wide range of applications in microelectronics and magnetic recording industries. Because of the importance of thin film adhesion, there are more than 200 different methods [1] to measuring interfacial adhesion at present, suggesting them to be material, geometry and even industry specific. While many of these tests are semi-quantitatively measurements and are useful for functional or comparative purposes [2-5]. For brittle, weakly bonded films, indentation can be used to delaminate the films from the substrates, thus measuring the thin film interfacial strength [1]. During this process, the thin film experiences five stages of deformation from elastic contact and dislocation nucleation to film decohesion and buckling [6]. This indentation technique is mainly based on the pioneer works of Marshall & Evans [7] and Evans & Hutchinson [8] which gave the theoretical analysis for the conical indentation-induced thin film delamination. Consider an indentation-induced interface crack in a residually stressed film, shown in Fig.l. The film has a thickness t and stick on a semi-infinite substrate, loaded by a hard angular indenter which leaves a permanent impression, and the residual stress is assumed to be aR. The strain energy release rate G is obtained as follows [6,8].Denote V, E as Poisson ratio and elastic miduli, <7Q = 2?(a7a)/(l- V), <JC express the critical buckling stress of the plate,we have
G = t(l - v) {(1 - cc)aR2 + <x02 [(1 + v) / 2 - (1 - a)(l - ac I
(1)
Correspondence Author, Department of Engineering Mechanics, Tsinghua University, Beijing 100084, China, Fax: ++86 10 62781824, E-mail: [email protected]
Adhesion Measures of Elasto-plastic Thin Film
383
Film , T.1 *• T Substrate Crack Plastic Zone FIGURE 1 Schematic of indentation-induced delamination at the interface of a thin film and substrate
where a—radius of delamination, a'—increment of radius a induced by plastic deformation, a = 1 for <JO+CTR <<JC (no buckling) or a = (1 + 1.207(1 + v))
for
ao+crR > <7C (buckling). After measuring the strain energy release rate G, the interfacial adhesion between the thin film and substrate can be calculated. The equation (1) is only valid for initial stage of post-buckling, and the assumption of the buckling of plate is taken without considering the plastic behavior of thin films. Experiment of Kriese et al. [9] found that during indentation the interfacial fracture toughness was reproducibility high for shallow indents, 8-10 J/m 2 , but dropped to a fairly steady 0.7-1.2 J/m2 for deeper indents. It is hard to explain these experimental data via conventional analysis. As we know, the plasticity of materials will greatly affect the buckling process; can it be a reason for this phenomenon? In the paper, we will emphasize on some aspects of thin film bucking and their influences to the indentation test. Based on finite element method (FEM) code ABAUQS, the full post-buckling responses of thin films are obtained .The material plasticity are taken into consideration and their contributions are discussed. LARGE DEFORMATION BUCKLING FOR THIN FILM DELAMINATION Model for FEM Analysis A circular delamination at a film/substrate interface is considered, as shown in Fig.2(a), with a uniform biaxial compression a exiting in the film. For this axisymmetric problem, only one cross-section of the buckled film (i.e. the buckled film disc) is modeled, shown in Fig.2(b). The film disc has a thickness t and a radius a, and is subject to uniform biaxial compression a on the perimeter (BC2). Boundary conditions are applied, such that the perimeter (BC2) is always fixed in r direction while the film center (BC1) is fixed in r direction for single-buckling case FEM Results of Full Single-buckling Response The procedure of 'Eigenvalue Buckling Prediction' in ABAQUS is used to obtain the critical buckling stress. For various values of tl a, using the non-dimensional stress uc = 12(1 - v2 )
tV with k = 14.3876, which coincides the theoretical Euler buckling stress A; = 14.68 very well. To calculate the film response when a > <JC , RIKS procedure is used to perform post-buckling analyses :For the case of tl a = 1/20, the edge stress a as a
384
Adhesion Measures of Elasto-plastic Thin Film
function of displacement A for this film disc is plotted in Fig.3. The Fig.3 gives the full post-buckling response of the elastic thin film, from which we can clearly observe the whole process of buckling and the stiffness of the film (i.e. the slope of the curve) is greatly reduced after the critical point of buckling.
(a)
BC2 Film
BC1
(b)
FIGURE2 (a) Circular delamination at a film/substrate interface; (b) Model for FEM calculation
1
"i
— • — Single-buckling ) 4 3 2 1
-
•
n 12
16
A/A
FIGURE 3 Plot of edge stress <J as a function of inward displacement A (Uc
and Ac are the
critical stress and displacement for single-buckling)
The FEM results of the initial slope well fit the theoretical prediction, which is provided by Evans & Hutchinson [8] and assumed to be a = (l +1.207(1 + v))~l. But from Fig.5, it can be seen that the slope of the post-buckled brunch goes down as the increase of inward displacement. To consider the deviation from the initial slope value, we assume the slope a has the following form a = aa-/3
—
(3)
where a0 is the initial slop value and p is fitted from the FEM data to be around 0.01973 for different values of v. Thus the equation of energy rate is modified as .1 + v G=-^)2]} (4) c £ ^ " 2 ° c RJ where a , ft are determined by equation (3).
Adhesion Measures of Elasto-plastic Thin Film
385
POST-BUCKLING OF ELASTO-PLASTIC THIN FILMS All the discussion above is based on the assumption of elastic deformation. But because of the large deformation during the post-buckling stage, it may be very helpful if we take the plasticity of the film into consideration to investigate its influence, especially for the film with low value of yield stress ay. This section will carry out the FEM analysis on the effects of plasticity to the single-buckling process. Model for FEM Analysis The schematic of the model is similar as Fig.2, but the thin film is modified as an elasto-plastic material which obeys the power hardening law a
=
(5) o\,
where ay and sy are the initial yield stress and yield strain, and n is the hardening exponent. FEM Post-buckling Analysis for Elasto-plastic Films First, we calculate the case of ay IE = 2xlO~3, i.e. ac Iay * 1.7 .From Fig.4, the energy release rate decreases significantly when considering the film plasticity. For the perfect plastic case, the energy release rate decreases to one half of the elastic one when a » ac, to 20% when a « 2<xc and to less than 5% when a » 3ac (it should be noted that the result is not yet valid and only serve a qualitative analysis when the stress reaches such a high value, such expressed in Fig. 5.
Elastic 1.5
O
n=3 n=7 n=20 Perfect plastic
/
y /
1.0
0.5
nn 0
/*
"^ 1
2
3
4
5
a la
FIGURE 4 Energy release rate for elasto-plastic films with different values of hardening exponent n (<Jcla*
1.7)
386
Adhesion Measures of Elasto-plastic Thin Film 2.0 Elastic
/
n=2 n=3 n =7
''""""" ^
1.5 \
Perfect plastic
1.0 • \
'•
\
\ \ '
0.5 •
\ \v
0.0
0
1
2
3
4 cr/cr
5
6
7
I
FIGURE 5 Energy release rate for elasto-plastic films with different value of hardening exponent n «Jc/ay*0.3)
As we has been mentioned above, experiment of Kriese et al.[9] found that during indentation the interfacial fracture toughness was reproducibility high for shallow indents, but dropped to a fairly steady value for deeper indents. If we assume that the radius of the buckled film increases from 30 um for shallow indent to 100 um for deeper indent, the value of ac I ay for deeper indent will reduce to about one tenth of the shallow one. According to the discussion above, the influence of the film plasticity will be a dominant factor for shallow indent, so it must be included to interpreter the results correctly. This might be one of the reasons for the discrepancy between shallow and deeper indent. CONCLUSION An investigation on the post-buckling of thin film is carried out by FEM calculation. Some of the important factors, such as the material plasticity, are discussed in this paper .The results show that for the case of a < 3<7C, the asymptotical solution is satisfactory with a relative error less than 10%.The plasticity has significant influence on the post-buckling responses and should be considered in interpreting the indentation test results. The greater the value of ac/ay, the more contributions of the plasticity. The abnormal experimental results of Kxiese [9] can be explained by this calculation. We can say that if the conventional method of indentation test is considered, the deeper indent the more precise of the results. ACKNOWLEDGEMENT This project is supported by NSFC (10172050) and SRFDP 3064, Key grant project of Chinese MoE-No-0306. REFERENCES 1
Volinsky, A.A., N.R. Moody,and W.W. Gerberich. 2002. Interfacial toughness measurements for thin films on substrates. Acta Materialia., 50:441-466.
Adhesion Measures of Elasto-plastic Thin Film 2
3 4 5 6 7 8 9
387
Jindal, P.C., D.T. Quinto, and GJ .Wolfe. 1987. Adhesion measurements of chemically vapor deposited and physically vapor deposited hard coating on WC-Co substrates. Thin Solid Films, 154:361-375. Rickerby ,D.S. 1988.A review of the methods for the measurement of coating substrate adhesion. Surf. Coat. Tech., 36:541-559. Steinmann PA, and H.E. Hintermann. 1989.A review of the mechanical tests for assessment of thin film adhesion. J. Vac. Set TechnoX. A, 7:2267-2272. McCabe ,A. R., A.M. Jones, and S.J. Bull. 1994. Mechanical properties of ion-beam deposited diamond like carbon on polymers. Diamond and Related Technol, 3:205-209. Gerberich, W.W., and D.E. Kramer, et al.1999. Nanoindentation-induced defect-interface interactions: phenomena, methods and limitations. Ada. Mater, 47(15):4115-4123. Marshall, D.B., and A.G. Evans. 1984. Measurement of adherence of residually stressed thin films by indentation. I. Mechanics of interface delamination. J. Appl. Phys,, 56(10):2632-2638. Evans, A.G., and J.W. Hutchinson. 1984. On the mechanics of delamination and spalling in compressed films. Int. J. Solids Structures, 20(5):455-466. Kriese ,M.D., D.A. Boismier, N.R. Moody, and WW Gerberich. 1998. Nanomechanical fracture-testing of thin films. Engineering Fracture Mechanics, 61:1-20.
Evaluation of Intra-ply Shearing Stiffness for a Plain Weave Fabric Prepreg Xiaobo Yu , Lin Ye School of Aerospace, Mechanical and Mechatronic Engineering The University of Sydney, NSW 2006, Australia Damian McGuckin Pacific Engineering Systems International Ltd 22/8 Campbell St., Artarmon, NSW 2064, Australia
ABSTRACT It has been found that forming simulations give poor predictions of the formability of simple cup shapes during double-diaphragm forming of fabric prepreg stacks. In response, this study evaluated the available test results, as well as test set ups, for intraply shearing stiffness measurement. Parametric studies using multiple simulations indicated that the effective intra-ply shearing stiffness of a plain weave prepreg may be more than ten times higher than currently available experimental data indicates. This finding is supported by a modelling analysis that attempts to predict the effect of compaction pressure on the intra-ply shearing stiffness.
INTRODUCTION Carbon fibre reinforced epoxy composites are well accepted in the aerospace industry. A typical aerospace composite part is assembled from 3 to 60 plies of carbon fabric impregnated with epoxy resin (prepreg) [1]. Traditionally, it is formed by successive hand lamination of individual plies. This is appropriate and efficient for small production runs, but makes composite parts expensive for high-volume production [2]. To achieve automation and reduce manufacturing costs, aerospace industries and research institutes around the world have been developing alternative manufacturing approaches in the last decade. In Australia, diaphragm forming has been identified and developed by the Cooperative Research Centre for Advanced Composite Structures (CRC-ACS) to be the leading solution to automated preforming of a large variety of aerospace parts [2]. Numerical simulations on diaphragm forming are also in development [3-6] for the purpose of establishing a virtual prototyping approach to quickly identify optimum forming parameters. So far, better numerical simulations have been achieved by a number of improvements including the better understanding of diaphragm material properties, improved finite element treatment of intra-ply shearing stiffness [3-4], more accurate experimental data and simulation of inter-ply friction [5], and the awareness of, and a remedy to, an intra-ply shear locking problem [6]. With all these improvements however, as will be demonstrated in this paper, it still remains a
f
Correspondence author, fax: +61 2 9351 3760, e-mail: [email protected]
Intra-ply Shearing Stiffness for Plain Weave Fabric Prepreg
389
challenge to accurately predict forming quality based on given forming parameters and available material properties. The present study was investigated following poor predictions of wrinkling in benchmark simulations of double diaphragm forming of a simple cup. The study evaluated the reasonableness of available test results for intra-ply shearing stiffness, by means of parameter studies and modelling analyses. Even with all the efforts of a more accurate and repeatable measurement of intra-ply shearing stiffness, for example [7-13], the present study gives rise to the suspicion that the effective prepreg intra-ply shearing stiffness encountered during double diaphragm forming cannot be reproduced in a test set up without prepreg compaction. BENCHMARK SIMULATIONS CRC-ACS has performed a number of experimental studies on double diaphragm forming of a simple cup shape, using stacks of CF/EP plain weave fabric prepreg, to investigate the effects of various forming parameters [14]. The current benchmark simulations consider two of the tests. One was a 3-ply [±45/0,90/±45] simple cup where the part was formed without wrinkles. The other was a 6-ply [±45/0,90/±45]s simple cup where significant wrinkles developed in the flange of the part. Except for the number of prepreg plies, the two tests were performed under identical set up (see Figure 1) and forming conditions. The 2002 version PAM-FORM software [15] was used for the benchmark simulations. The diaphragm was modelled by membrane elements degenerated from Type 107 shell elements. The diaphragm material properties were measured from uniaxial tension tests. The stack of prepreg was modelled following the concept described in Figure 2. Each ply was discretized individually and was connected to its neighboring plies by a Type 13 segment-to-segment large sliding contact. The inter-ply friction was calculated considering compaction pressure and sliding velocity within a user subroutine using non-linear functions determined by ply pullout tests [5]. The transition from static (high) to dynamic (low) friction was ignored. By using static friction, the benchmark Stack of prepreg-—,.
Top diaphragm
1 J
Bottom diaphragm 1
Dimensions: Box: diameter = 420mm, depth = 100mm; Tool: diameter = 100mm, height = 80mm; Stack of prepreg: diameter = 140mm.
FIGURE 1. Schematic section showing the test set up for double diaphragm forming of a simple cup.
Inter-ply friction
Intra-ply shearing stiffness
Out-of-plane bending stiffness
FIGURE 2. Illustration showing how a stack of woven fabric prepreg is decomposed in a PAM-FORM simulation.
390
Intra-ply Shearing Stiffness for Plain Weave Fabric Prepreg
simulations produce conservative, or more likely to wrinkle, predictions. Type 140 shell elements were used to model each ply of woven fabric. The fabric was decomposed into two directions according to their orientations. Each was assigned an axial stiffness that represents the equivalent Young's modulus of the prepreg along the fibre direction, and an out-of-plane bending stiffness that was scaled by a bending factor to correlate with ply self-weight tests [16]. The prepreg also had an intra-ply shearing stiffness to resist trellis deformations. The intra-ply stiffness was determined from bias extension test results [17] using the improved Ideal Fibre Reinforced Fluid (FRF) model [4]. To implement the improvement on the FRF model, each Type 140 shell element was overlapped by a Type 107 shell as reported in [3]. It was known that the IFRF model, in spite of being improved, may still be not as accurate as desired, and might induce up to 70% error in reproducing experimental data [4]. However, as will be demonstrated later, this error may be minor compared to those from other sources. Figure 3 shows the meshes used in the benchmark simulations. Triangle elements were used to avoid warping and hourglass mode deformations. For each triangle element, two of its three edges were aligned with fibre directions. The aligned mesh was introduced to avoid so-called intra-ply shear locking, a phenomenon of numerical overestimation of intra-ply stiffness [6]. The aligned mesh differentiates the present simulations from most previous ones. Based on the aforementioned modelling and material properties, the 3-ply forming simulation predicted no wrinkles, in agreement with the test result. However, the 6-ply forming simulation predicted no wrinkles as well, in contrast to the experimental result. The inaccurate simulation could be attributed to a number of possibilities, including misinterpretation of forming mechanisms, inappropriate implementation in finite element codes and incorrect material properties. A couple of these possibilities were checked. Altering the diaphragm material properties within a large range had little effect on predicted forming quality in this particular case. The inter-ply friction has been found to be an important parameter for wrinkle development. However, it was calculated in a user friction subroutine that accurately reproduced reliable test results. In addition, static friction values were used, so that the inter-ply friction value used was more likely to predict wrinkles. The fibre out-of-plane bending stiffness can affect wrinkle development in a single ply but it has little effect on a stack of plies connected by interply friction. It was found that no wrinkles developed even if the fibre out-of-plane bending stiffness was set to zero. In comparison, there appeared to be considerable inaccuracy when the IFRF model was used to describe the intra-ply shearing stiffness. Furthermore, it is suspected that the effective intra-ply shearing stiffness of a prepreg ply in diaphragm forming cannot be accurately measured in a bias extension test without compaction pressure. In view of these, parametric simulation studies were performed to "back-calculate" a more likely intra-ply shearing stiffness. 0/90 ply
± 45 ply
FIGURE 3. Aligned meshes used in the benchmark simulations, (only a quarter of the full model is shown for clarity)
Intra-ply Shearing Stiffness for Plain Weave Fabric Prepreg
391
A wide range of intra-ply shearing stiffness was tried. Figure 4 shows force versus displacement relationships when three representative intra-ply shearing stiffness properties were applied in bias extension test simulations. The force responses corresponding to A, B and C are approximately 30, 20 and 10 times as high as the test result [17]. When applied to simple cup forming simulations, the intra-ply shearing stiffness A appears too stiff because wrinkles developed in the 3-ply forming simulation as well. Intra-ply shearing stiffness B seems appropriate as the simulations of 3-ply and 6-ply forming, as shown in Figure 5, both agree with the experiment. In the case of intraply shearing stiffness C, wrinkles predicted in the 6-ply forming are not as pronounced as in the experiment.
10
20
30
Displacement {mm)
FIGURE 4. Force versus displacement relationship in bias extension test simulations.
•V FIGURE 5. Benchmark simulations based on intra-ply shearing stiffness B.
MODELLING OF INTRA-PLY SHEARING STIFFNESS The parametric studies suggest that the intra-ply shearing stiffness needs to be scaled up by more than 10 times from the current experimental data in order to get the benchmark simulations to make the correct predictions. The increase required is thought to be far greater than the possible inaccuracy in the IFRF model or experimental randomness. The authors suspect that the intra-ply shearing stiffness of a prepreg ply during diaphragm forming may not be measured by a bias extension (or picture frame) test which does not include the effect of the compaction pressure experienced by the fabric stack during diaphragm forming. As further evidence for this concern, a modelling analysis is presented as follows. As explained in [18], we assume that the intra-ply shearing stiffness is mainly caused by the viscous friction at fibre cross-over and between neighboring tows contacts. It is noted that due to differences in fabric structure, the conclusion of [18], stating that the friction at fibre cross-over is negligible, does not apply to this study. As shown in Figures 6(a) and 6(b), the adjacent tows in a plain weave fabric are separated at the top
392
Intra-ply Shearing Stiffness for Plain Weave Fabric Prepreg
and bottom halves of a ply thickness. The friction at fibre cross-over therefore plays a predominant role on intra-ply shearing stiffness. This study goes one step further to incorporate the effects of compaction pressure. It is assumed that the friction over a unit area can be described by a function ^(q, v), where q and v are local compaction pressure and sliding velocity, respectively. Introducing the virtual work principle, the pulling force of a bias extension test, F(p, u), under nominal compaction pressure p and pulling velocity u, can be calculated by Eq. (1), where the integration calculates energy rate over a single cross-over, and "2" sums up the energy rate of all cross-over points. We further assume the q and v effects can be decoupled [5] so that function *¥(q, v) takes the form of Eq. (2). Substituting Eq. (2) into Eq. (1) and considering Figure 6(c), Eq. (3) can be obtained for a given pulling velocity (M) and deformation, where Sd is the tow width. Now the effect of compaction pressure can be examined. Assume that the pressure dependency of inter-tow friction takes the pattern of inter-ply friction as shown in Figure 6(d). The slight difference caused by the local and nominal pressure was ignored. It can be seen that when the compaction pressure increases from zero to the range of 60 to 100 kPa, f(q) increases to approximately nine times as much. When combined with 10%, 15%, or 20% Sd increment due to tow flattening under compaction pressure, the pulling force increases to approximately 12, 13.5, or 15.5 times as much, even if the cS"d term in Eq. (3) is ignored. If cSd is included, Eq.(3) predicts a larger pulling force. ,v)dA
(1) (2) (3)
No compaction Individual test data -Averaged test data
Compaction Normal Pressure (kPa) b
( )
FIGURE 6. (a) A woven fabric; (b) Tow flattening due to compaction pressure; (c) A fibre cross-over; (d) The pressure dependency of inter-ply friction.
FINAL REMARKS AND SUGGESTIONS The previous simulations show that the intra-ply shearing stiffness needs to be increased by more than ten times the measured figures to obtain good results. The implication that the current intra-ply shearing stiffness is incorrect is supported by a modelling analysis that incorporates the effect of compaction pressure. These two analyses suggest that a bias extension test or a picture frame test performed without compaction pressure may significantly under-estimate the effective intra-ply shearing stiffness of a plain woven prepreg ply during double diaphragm forming. The present work highlights the necessity to clarify the effect of compaction pressure experimentally. As a starting point, a diaphragm packaging method as reported in [19] is suggested as a possible test for measurement of intra-ply shearing stiffness. This approach is currently being investigated by the authors.
Intra-ply Shearing Stiffness for Plain Weave Fabric Prepreg
393
ACKNOWLEDGEMENTS This work was supported by the Australian government under the ARC-Linkage Project Scheme, and the Auslndustry R&D Tax Concession/Offset Scheme, and ESI Group who provided a copy of the PAM-FORM software. The ongoing and underlying support of the Cooperative Research Centre for Advanced Composite Structures Ltd is also gratefully acknowledged. The help given to the authors by their colleagues Allen Chhor and Bruce Cartwright of Pacific ESI was invaluable.
REFERENCES 1.
2. 3.
4. 5.
6.
7.
8.
9. 10. 11.
12.
13.
14. 15. 16.
17. 18.
19.
Paton, R., G. Clayton, P. Falzon and D. Do. 2000. "Automated manufacture of advanced composite aerospace components," 8th International Conference on Manufacturing Engineering, Sydney, Australia, August 2000, Paper Number 62. Young, M. 2003. "Diaphragm forming guidelines," CRC-ACS TM 03016. Yu, X., B. Cartwright, L. Zhang, Y.-W. Mai and R. Paton. 2000. "Finite element simulations of the diaphragm forming process," presented at 15th Annual Technical Conference of the American Society for Composite. Texas, USA, 2000. Yu, X., L. Zhang and Y.-W. Mai. 2003. "Modelling and finite element treatment of intra-ply shearing of woven fabric," Journal of Materials Processing Technology, 138(1-3): 47-52. Cartwright, B., A. Chhor, S. Howlett, D. McGuckin, R. Paton, L. Ye and X. Yu. 2003. "Industrially robust modelling of viscous friction effects in composites," presented at EuroPAM 2003, October 1617, 2003. Mainz, Germany. Yu, X., B. Cartwright, D. McGuckin, L. Ye and Y.-W. Mai. 2004. "Intra-ply shear locking in finite element analyses of woven fabric forming processes," submitted to Composites Science and Technology. McGuinness, G.B. and C.M.O. Bradaigh. 1997. "Development of rheological models for forming flows and picture-frame shear testing of fabric reinforced thermoplastic sheets," Journal of NonNewtonian Fluid Mechanics, 73(1-2): 1-28. McGuinness, G.B. and C.M.O. Bradaigh. 1998. "Characterisation of thermoplastic composite melts in rhombus-shear: the picture-frame experiment," Composites Part a-Applied Science and Manufacturing, 29(1-2): 115-132. Wang, J., J.R. Page and R. Paton. 1998. "Experimental investigation of the draping properties of reinforcement fabrics," Composites Science and Technology, 58(2): 229-237 Nguyen, M., I. Herszberg and R. Paton. 1999. "The shear properties of woven carbon fabric," Composite Structures, 47(1-4): 767-779. Harrison, P., M.J. Clifford and A.C. Long. 2002. "Shear characterisation of woven textile Composites', presented at 10th European Conference on Composite Materials, 3-7th June, Brugge, Lebrun, G., M.N. Bureau and J. Denault. 2003. "Evaluation of bias-extension and picture-frame test methods for the measurement of intraply shear properties of PP/glass commingled fabrics," Composite Structures, 61(4): 341-352. Peng, X.Q., J. Cao, J. Chen, P. Xue, D.S. Lussier and L. Liu. 2004. "Experimental and numerical analysis on normalization of picture frame tests for composite materials," Composites Science and Technology, 64:11 -21. Young, M. and R. Paton. 2001. "Investigation on the forming of a simple cup," CRC-ACS TM01003. ESI Software. 2002. PAM-FORM 2002 Solver Reference Manual. Young, M., B. Cartwright, R. Paton, X. Yu, L. Zhang and Y.-W. Mai. 2001. "Material characterisation tests for finite element simulation of the diaphragm forming process," presented at ESAFORM 2001 Conference. Wang, J., R. Paton and J.R. Page. 1997. "Forming properties of thermoset fabric prepregs at room and elevated temperature," CRC-ACS TM 97028. Harrison, P., MJ. Clifford, A.C. Long and CD. Rudd. 2002. "Constitutive modelling of impregnated continuous fibre reinforced composites micromechanical approach," Plastics, Rubber and Composites, 31(2): 76-86. Nestor, T.A., and CM. O'Bradaigh. 1995. "Experimental investigation of the intraply shear mechanism in thermoplastic composites sheet forming," Key Engineering Materials, 99-100: 19-36.
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Part VIII
Fracture
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Initial Fracture Behaviour of the Weft-Knitted Textile Composites Having Welt-Knit Architectures Omar Khondker*, Tatsuro Fukui, Asami Nakai and Hiroyuki Hamada Advanced Fibro-Science, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan
ABSTRACT Initial fracture behaviour of the weft-knitted glass/epoxy composites was investigated to study their dependence upon the welt-knit architectures with varying structural parameters, such as the length of the non-loop welt-stitches and the lineal density of held-stitches within the welt-length. Strain gages were bonded onto the test specimens at different locations of the structural unit-cell. Knee points of the stress-strain curves were closely studied in order to characterize the first onset of local failure. Postfailure examination was carried out on the test specimens using stereo-optical and scanning electron microscopy to analyze their microscopic fracture behaviour. No significant changes were recorded in the stiffness and strength values with increasing welt-lengths and number of held stitches, in either test directions. In general, crack propagated almost normal to the direction of the two principal loading axes. According to the SEM micrographs, fracture plane for the wale-tested specimens coincided along the length of the welt-stitches and continued through the fibre crossover regions of the same course, whereas for the course-tested specimens, fracture plane ran along the fibre crossover regions transverse and adjacent to the length of the welt-stitches. Initial fracture modes in either test directions combined transverse and debonding cracks, inside and between the fibre bundles, respectively. These observations agreed well with the knee point responses obtained from the local stress-strain curves.
INTRODUCTION Considerable research [1-11] has been directed on the macro-mechanical properties of textile composites, such as their static tensile, bending and fatigue properties with regard to their overall fracture behaviour, hi textile composites, several modes of micro fractures, such as transverse cracks inside the fibre bundles, delamination at the fibre cross parts, matrix and filament failure occur and accumulate before final rupture of the composite. The initiation of micro fracture termed as 'initial fracture' is particularly important, in order to carry out a precise investigation on the overall mechanical properties of textile composite materials. Knitting is ideally suited for the cost-effective production of intricately-shaped composites. Lack of comprehensive investigation on the initial fracture behaviour of knitted composites towards understanding their overall mechanical properties, still acts as an impediment to the wider acceptance of these materials and, hence, expanded application. In an earlier work [12,13], initial fracture * Correspondence Author, Advanced Fibro-Science, Kyoto Institute of Technology, Matsugasaki, Sakyoku, Kyoto 606-8585, Japan Phone: (81-75) 724 7844 Fax: (81-75) 724 7800 Email: [email protected]
398
Initial Fracture Behaviour of Weft-Knitted Textiles Composites
behaviour of the weft-knitted glass/epoxy composite having a plain architecture was investigated. The effects of lengths and locations of the strain gages on the knee point stress-strain behaviour were investigated. Strain gage with a small gage length (up to 3 mm) was recommended and used for this study to measure the strain values at the local areas of the plain-loop architecture. It was concluded that for the plain weft-knitted composites, initial fracture mode was primarily dictated by a transverse crack inside the fibre bundle within the loop head in the wale direction, and a fibre bundle debonding at the fibre crossover regions in the course direction. Fractographic observation agreed well with the knee point responses obtained from the stress-strain characteristics. The present work concentrated on various welt-knit architectures and their effects on the initial fracture behaviour of the welt-knitted glass/epoxy composites. A typical loop configuration of a plain knit architecture, as shown in Figure 1, creates heterogeneous type of structure at unit-cell level, consisting of four major parts namely loop head, fibre cross part, slant loop and resin rich area. This heterogeneous loop-structure causes local variation in the strain values, and is believed to have an important effect on the overall fracture behaviour of knitted composites.
' '
FIGURE 1 A typical plain knitted loop
Held-stitch
' '
Non-loop welt-stitch
' '
FIGURE 2 Schematic of the welt-knitted architectures
EXPERIMENTAL Materials, Manufacture and Mechanical Test Weft-knitted fabrics from D-Glass fibre of density 2.17 gm/cm3 (D B450 1/2 4.4S Y23, Nippon Electrical Glass Co., Ltd.) were produced as the reinforcements and Bisphenol-A type epoxy resin (Epikote 828, lapan Epoxy Resin Co., Ltd.) was used as the matrix. The fabric materials under investigation comprise of three different welt-knit architectures such as (2,2,2), (2,4,2) and (2,6,2). Figure 2 represents schematic diagrams of these welt-knit structures. Welt-stitch, also known as non-loop float-stitch, can be defined as the length of yarn, not received by the needle(s), and which connects two other loops (not adjacent to each other) of the same course. The loop which, having been pulled through the loop of the previous course, is retained by the needle(s) during the knitting of the welt-stitch, can be defined as the held-stitch. Through manipulation of welt and held stitches, various welt-knit architectures can be created in the fabric structure, by changing the length of the non-loop welt-stitches and the number of heldstitches within the welt-length in a unit cell. The expression for welt architecture, for example (2,2,2), (2,4,2) or (2,6,2) in Figure 2, implies the number of wale-stitches ahead of the non-loop welt-length (1st numeral), the lineal density of the held-stitches within the welt-length (2nd numeral) and the number of courses between the non-loop weltstitches (3rd numeral). 1 ply composite panels, having 1 mm nominal thickness, were fabricated by hand lamination method. The average fibre volume fraction was estimated as 16.4% for all the three types of welt-knit structures under investigation. The composite panels were cured at room temperature for approximately 48 hours, followed
Initial Fracture Behaviour of Weft-Knitted Textiles Composites
399
by a two-hour postcure at 100°C to optimise resin properties. Tensile tests were conducted on an Instron universal testing machine (type 4206) under a nominal test speed of 1.00 mm min"1 in both wale and course directions. Deformation and fracture behaviour at each loop component were expected to be different. Strain gages with 1 mm gage length, were bonded onto these different loop segments of the welt-knit structural unit-cell to measure the local responses at these points. It is noteworthy that strain gages were deliberately avoided in the resin rich areas where knee stresses were found to be much higher than any other location in the entire knit structure [12]. Post-failure examinations were carried out on the selected test specimens using a scanning electron microscope (SEM) to study the fracture behaviour of composites at micro-level. RESULTS AND DISCUSSIONS Macro-Mechanical Properties Figures 3a and 3b show typical tensile stress-strain characteristics and tensile properties of welt-knitted composites in either test directions. It should be noteworthy that, contrary to the case of the course specimens, the wale specimens were able to maintain loads over a relatively larger strain interval before ultimate failure occurred, hi the current study, knee point is defined as the measure of the initial micro-fracture and was identified by a simple statistical approach [14].
a 5 M 4 1 3 c. Wale
1
d Wa e p 10 H
0
8
s,6
Strain (%)
Ss
S
Tensile Modulu
Strain (%)
«60
° e. Course
J
g-
2 S
S.50 Sij40 2 20
«u
f. Course
FIGURE 3 Stress-strain characteristics and tensile properties of welt-knitted composites
As shown in Figures 3c to 3f, both modulus and strength values were improved in the course direction than in the wale direction for each type of the welt-knit structures. This was attributed to the simple fact that the straight lengths of the non-loop weltstitches have their yarn orientation in the course direction only. Manipulation of weltlength and held-stitch density appeared to have noticeable effects on the tensile properties of welt knitted composites, in either knitting directions. Both modulus and strength values slightly decreased with the increase in welt-lengths and held-stitch densities for the wale-tested specimens, whereas the course-tested specimens exhibited an opposite trend. A closer observation on the wale-tested specimens reveals that 2,2,2 specimens have the orientation of non-loop welt-stitches (with shorter lengths) at a denser proportion in the cut-out test specimens as compared to other welt structures (2,4,2 and 2,6,2). This also resulted in a slightly higher fibre content in 2,2,2 wale specimens as compared to other welt counterparts. Hence, while tested in the wale
400
Initial Fracture Behaviour of Weft-Knitted Textiles Composites
directions, the fracture path of 2,2,2 specimens had a better chance to get bridged intermittently by the un-fractured fibre bundles as compared to 2,4,2 and 2,6,2 structures, so that load could be re-distributed to the fibres to delay the final rupture by improving fibre loading efficiencies. The slightly higher modulus value for the wale-tested 2,2,2 composite specimens was attributed to their higher fibre content as compared to 2,4,2 and 2,6,2 specimens. On the contrary, while-tested in the course direction, the fibre orientation of non-loop welt-stitches behaved like course-inserted fibre tows, and the proportion of these straight fibres obviously increased in 2,6,2 specimens than 2,2,2 and 2,4,2 specimens. This has resulted in the increased strength value in 2,6,2 composites. In the course direction, the slightly higher modulus value for 2,6,2 composites as compared to 2,2,2 and 2,4,2 composites, was obviously due to their better fibre directionality and higher proportion of straight fibres along the loading direction. Fracture plane for the wale-tested specimens coincided along the length of the non-loop welt-stitches and continued through the fibre crossover regions of the same course, whereas for the course-tested specimens, fracture plane ran along the fibre crossover regions transverse and adjacent to the length of the welt-stitches. In the knit structures, fibre crossover regions are the areas experiencing crucial fibre bending and high stress concentration, and were predominantly considered to be the failure nuclei [15]. Initial Fracture Behaviour The initial fracture behaviour of composites defined more on the local aspects than on the average properties. A knee point was not the intersection between the linear and the non-linear segment of the stress-strain curve. These points were rather defined so as to correspond to the values of the initial fracture stress and strain. A statistical approach [14], was applied to estimate these knee points as a quantitative evaluation of initial fracture - the first onset of failure. Knee point stress values varied at different characteristic locations of the welt loop configurations, and were also affected by the welt knit-structural parameters, in either knitting directions (Figure 4).
Stress at Initial Fracture
Cross (1)
aWale
Cross (2)
Stress at Initial Fracture
(1)
b Course
-
Cross (2)
FIGURE 4 Knee stresses at different characteristic locations of the welt architectures
It was quite noticeable from Figure 4a that, for the wale-tested specimens, the lowest knee stress occurred at the welt loop of 2,2,2 composites and at the cross parts 1 of 2,4,2, and 2,6,2 composites. On the other hand, for the course-tested specimens, the lowest knee stress or the first imtial fracture occurred at the cross parts 1 of 2,2,2 and 2,4,2 composites and at the slant-cross part of 2,6,2 composites, as observed in Figure 4b. Micro-fracture aspects of the welt knitted composites were examined from the photomicrographs taken at the weakest areas of welt architectures, as illustrated in
Initial Fracture Behaviour of Weft-Knitted Textiles Composites
401
Figures 5. As discussed earlier, for the wale-tested specimens, fracture initiation occurred at the welt loops and at the cross parts 1, whereas for the course-tested specimens, cross parts 1 and slant-cross parts were the areas suffering initial fracture. Fracture modes for the wale specimens consisted of a transverse crack inside the fibre bundle of the welt loops and a fibre-bundle-debonding at the cross parts (Figure 5a). For the course specimens, fracture modes were the combination of debonding between the fibre bundles at the cross parts and transverse crack inside the slant-cross loops (Figure 5b). Transverse Crack
Debonding
Debonding
Transverse Crack
*!»'
Welt loop Transverse crack
0
Welt loop
Cross part (1) Fibre Bundle Debonding
WtuaadloV----'
Cross part (1)
Cross part (1) Fibre Bundle Debonding
\MherllniKlk >
Slant-Cross loop Transverse crack
•—y
Cross part (1)
Slant-Cross loop
FIGURE 5 Photomicrographs and the schematic representation of micro-fractures in the welt knitted composites
A closer observation on the cross sections offibrebundles at the welt-stitch revealed that, the width of fibre bundle at the welt loops increased with the increase in the weltlengths and/or held stitches, and so did the aspect ratios of the fibre bundles at the welt loops. The higher aspect ratios in 2,4,2 and 2,6,2 wale specimens, seemed to have resulted in the higher knee stresses at their corresponding welt loops, whereas a low knee stress value at the welt loops of 2,2,2 wale specimens was due to their low aspect ratio at the cross section of the fibre bundles. SUMMARY Manipulation of welt-length and held-stitch density appeared to have noticeable effects on the tensile properties of the welt knitted composites in either knitting directions. Whilst strength is mechanically controlled, modulus is predominantly controlled by factors such as fibre content and fibre directionality. There was a gradual degradation in the tensile properties with the increase in the welt-lengths and held-stitch densities for the wale-tested specimens, while the course-tested specimens exhibited an opposite trend. In the knit structures, fibre crossover regions were believed to have experienced crucial fibre bending and high stress concentration, and due to which, fracture plane for the wale-tested specimens coincided along the length of the non-loop welt-stitches and continued through the fibre crossover regions of the same course. On the other hand, fracture plane in the course-tested specimens ran along the fibre crossover regions transverse and adjacent to the length of the welt-stitches. These observations agreed well with the responses obtained at the knee points of the local stress-strain curves. The knee stresses varied at different characteristic locations of the welt knit architectures, and were also affected by the welt knit-structural parameters, in either knitting directions. The
402
Initial Fracture Behaviour of Weft-Knitted Textiles Composites
initial fracture behaviour of composites defined more on the local aspects than on the average properties. For the wale-tested specimens, initial fracture resulted from the fibre fractures at the welt loops and at the cross parts 1, whereas, for the course-tested specimens, cross parts 1 and slant-cross parts were the areas suffering initial fracture. Fracture modes consisted of transverse and debonding cracks, inside the fibre bundle of the welt loops and at the cross parts for the wale specimens, whereas, for the course specimens,fracturemodes were the combination of debonding between the fibre bundles at the cross parts and transverse crack inside the slant-cross loops. Observations on the cross sections of fibre bundles at the welt-stitch revealed that the higher aspect ratios seemed to have resulted in the higher knee stresses at the corresponding welt loops while comparing the wale-tested composite specimens with regard to their different welt architectures. References 1.
2. 3.
4.
5. 6. 7.
8.
9.
10. 11. 12.
13.
14.
15.
Leong, K.H., Falzon, P.J., Bannister, M.K. and Herszberg, I. 1998."An investigation of the mechanical performance of weft-knit milano-rib glass/epoxy composites", Comp. Sci. and Tech., 58:239-251. Ramakrishna, S., Hamada, H., Cheng, K.B. 1997. "Analytical Procedure for the Prediction of Elastic Properties ofPlain Knitted Fabric-reinforced Composites", Composites Part A, 28:25-37. Wu, W.L., Kotaki, M., Hamada, H., Inoda, M., Maekawa, Z., Kanamaru, R. and Sanae, N. 1992. "Bending Properties of 2.5 Dimensional Warp Knitted Fabric Reinforced Composites", Advanced Composite Letter, 1:197-200. Kitagawa, K., Kankawa, Y., Shimamura, T., Wu, W.L., Kotaki, M., Inoda, M., Hamada, H., Fujita, A., Goto, A. and Maekawa, Z. 1992. "Effects of Surface Treatments on Mechanical Properties of Knitted Structural Composites", Advanced Composite Letter, 1:201-204. Ramakrishna, S. and Hamada, H. 1995. "Impact Damage Resistance of Knitted Glass Fibre Fabric Reinforced Polypropylene Composites", Science and Engineering of Composite Materials, 4:61-72. Hamada, H., Nakai, A., Fujita, A. and Inoda, M. 1995. "Mechanical Properties of Weft Knitted Fabric Reinforced Composites", Advanced Composites Letters, 4:83-85. Wu, W.L., Inoda, M., Hamada, H. and Maekawa, Z. 1993. "Study of Mechanical Properties in Kitted Structural Composites-Computer Simulation of Deformation of Knitted Fabrics", Proceedings of 36th JAPAN Congress on Materials Research, 205-212. Wu, W.L., Inoda, M., Hamada, H., Maekawa, Z., Kanamaru, R. and Sanae, N. 1993. "Influence of Knitted Structure on Mechanical Properties in Knitted Structural Composites", Proceedings of 36th JAPAN Congress on Materials Research, 213-218. Ramakrishna, S., Hamada, H. and Hull, D. 1995. "The Effect of Knitted Fabric Structure on the Crushing Behaviour of Glass-Epoxy Composite Tubes", Impact and Dynamic Fracture of Polymers and Composites, 453-464. Verpoest, I. and Dendauw, J. 1992. "Mechanical Properties of Knitted Glass Fibre/Epoxy Resin Laminates", Proceedings of The 37' International SAMPE Symposium, 369-377. Kameo, K., Haan, J. DE., Nakai, A. and Hamada, H. 1999. "Open Hole Tensile Behaviours of Knitted Fabric Composites", Journal of Reinforced Plastics and Composites; 18(17): 1605-1617. Fukui, T., Osada, T., Nakai, A., Inoda, M. and Hamada, H. 2002. "Initial Fracture Behaviour of Plain Knitted Composites", Proceedings of the Tenth U.S.-Japan Conference on Composite Materials, 1618 September, 2002, 849-858. Osada, T., Nishiyabu, K., Fukui, T., Nakai, A., Inoda, M. and Hamada, H. 2002. "Initial Fracture Behaviour of Knitted Composites", Proceedings of the Third Asian-Australian Conference on Composite Materials, 15-17 My, 2002, 715-721. Osada, T., Mizoguchi, M., Kotaki, M., Nakai, A. and Hamada, H. 2001. "Initial Micro Fracture Behaviour of Woven Fabric Composites", Proceedings of the 13th International Conference on Composite Materials, 25-29 June, 2001, ID 1083. Khondker, O.A., Leong, K.H. and Herszberg, I. 2001. "An Investigation of the Structure-Property Relationship of Knitted Composites", Journal of Composite Materials, 35(6):489-508.
Mixed-mode Fracture of a CF/PEI Composite Material Naghdali Choupani, Lin Ye* & Yiu-Wing Mai Centre for Advanced Materials Technology School of Aerospace, Mechanical and Mechatronic Engineering J07 The University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT This study reports investigation on mixed-mode interlaminar fracture behavior in CF/PEI composite material based on experimental and numerical analyses. Experiments were conducted on modified Arcan specimens using the special test loading device. By varying the angle,oc from 0° to 90°, mode-I, mixed-mode and mode-II data are obtained experimentally. Using the finite-element results, correction factors were applied to the CF/PEI fracture specimen. Based on experimentally measured critical loads and by the aid of the finite-element method, mixed-mode interlaminar fracture toughness for the composite under consideration has been determined. Numerical results indicate that for pure mode-I loading, mode-I stress intensity factor is maximum and as a increases, Ki decreases down to 0 for pure mode-II loading. Stress intensity factor for mode-II loading shows the opposite trend; as the ratio of mode-II to mode-I increases, Kn increases. It should be noted that for loading angles close to pure mode-I and pure mode-II loadings, very high ratios of strain energy release rates are dominant. As expected, it is confirmed that by varying the loading angle of Arcan specimen, pure mode-I, pure mode-II and a wide range of mixed-mode loading conditions can be created and tested.
INTRODUCTION Failures in composite materials occur mainly due to the interlaminar fracture between laminates. This indicates that characterizing interlaminar fracture toughness is the most effective factor in the fracture of composite materials. The critical strain energy release rate, Gc, which is the energy released due to extension of a crack is often used for prediction of fracture, hi recent years, many test methods have been proposed by many researchers to determine interlaminar fracture toughness for each of the three modes of loading (I, II, and III) and also under mixed-mode conditions [1]. The double cantilever beam (DCB) test is the most widely used method for measuring mode-I (opening) interlaminar fracture toughness. The end-notched flexure (ENF) has emerged as one of the most convenient mode-II (sliding shear) interlaminar fracture specimens. A crack rail shear (CRS) specimen has been proposed to determine the mode-Ill (tearing) critical strain energy release rate [2]. However, due to the strong anisotropy of composite structures, the fracture is usually not a result of pure mode-I or pure mode-II loading, and the delamination occurs in the mixed-mode loading conditions. For this reason, the study of the mixed-mode interlaminar fracture toughness is very important.
" Corresponding author. Tel: +61-2-9351 4798, Fax: +61-2-9351 3760, e-mail: ve(oiaeromech.usvd.edu.au
404
Mixed-mode Fracture of a CF/PEI Composite Material
Various attempts have been made to characterize interlaminar fracture toughness under mixed-mode loading conditions, but mostly beam type specimens were used [3-5]. Some of these include: the mixed-mode flexure (MMF) test, the end loaded split (ELS) TABLE I Elastic Properties of CF/PEI composite E,[GPa]
E2[GPa]
E3[GPa]
G12[GPa]
G13[GPa]
G23[GPa]
57.6
57.6
8.7
3.1
2.8
2.8
0.03
Ul3
"23
0.4
0.4
specimen, the single leg bending (SLB) specimen, the crack lap shear (CLS) test, the edge delamination tension (EDT) specimen, and the asymmetric double cantilever beam [3,4]. However, for all these test methods there are problems to create a wide range of mixed-mode ratios which limit their usefulness. The mixed-mode bending (MMB) test, has been proposed by combining the schemes used for DCB and ENF tests, which can produce a wide range of the ratios of mode-I and mode-II components by varying the lever arm of the specimen [4,5]. But in order to obtain reliable results for interlaminar fracture toughness for pure mode-I, pure mode-II, and mixed-mode loading conditions different beam type specimens would be required. In this study, a modified version of Arcan specimen is made for the mixed-mode fracture test of CF/PEI specimens, which allows mode-I, mode-II, and almost any combination of mode-I and mode-II loading to be tested with the same test specimen configuration [6]. Therefore, disadvantages presented in the previous mixed-mode toughness test methods can be avoided. This investigation seeks to extend the understanding of the interlaminar fracture behavior of a CF/PEI composite under mixedmode loading conditions. EXPERIMENTAL PROCEDURES Material In the experiment, a woven plate consisting of 22 plies of CF/PEI prepergs, in order to obtain a plate thickness of approximately 6mm were used. During the lay up prepergs by hand to the required number of plies, a non-adhering film placed between the central plies in order to introduce a starter crack. The composite plates were produced using hot press. The specimens were cut with a diamond wheel and machined to the dimensions of 30x10x6 mm. This composite is similar to the material investigated previously by Kim [7] and elastic constants of plate used in FEM analyses are summarized in Table 1. Test method and setup In Figure 1, the loading device and modified version of Arcan specimen are shown. This specimen is used in order to study the mixed-mode interlaminar fracture toughness of a CF/PEI composite material. The composite strip was attached into aluminum plates using adhesive. For surface preparation of aluminum plates, FPL-Etch method was applied [8]. Composite surface preparation method involved degreasing with methyl ethyl ketone (MEK), rinse and check for water break, hand abrasion with 320 grit aluminum oxide abrasive papers and clean for bonding [9]. The specimens were pinned into the loading device in order to transmit the applied loads. With the application of load P and by varying the loading angle,a from 0° to 90° , pure mode-I, pure mode-II, and all mixed-mode loading conditions can be created and tested. Fracture tests were conducted by controlling the constant displacement rate of 0.2 mm/min and the fracture
Mixed-mode Fracture of a CF/PEI Composite Material
405
loads and displacements were recorded. All tests were carried out using an Instron 5567 testing machine. Tests were repeated 3 times for every loading angle.
i .
t
(a) FIGURE 1 Overview of test rig and set up: (a) Mode-I test; (b) Mixed-mode test; (c) Mode-II test
ANALYSIS OF MIXED-MODE INTERLAMINAR FRACTURE The energy release rates for orthotropic material with the crack in one plane of symmetry can be calculated from the following relationships [2,10]: j-
K,
(1) where Ej and En are effective moduli, and Kj and Kn are mode-I and mode-II stress intensity factors, respectively. It is assumed that the specimens are orthotropic linear elastic material. For plane strain conditions, effective moduli Ei and En are defined as: E - I
T
l
"
E
\b12
+2bi2+b66
1
^ \b22
2bn
(2) +2bn+b66
2bn
where the terms of the constants btj are defined in terms of the following nonzero entries a{j of the orthotropic compliance matrix: b
-a
WJL
(ij = 1,2,4,5,6)
(3)
\Y\Tx FIGURE 2 Finite element mesh pattern of the entire specimen and around the crack tip
406
Mixed-mode Fracture of a CF/PEI Composite Material
The stress intensity factors ahead of the crack tip for a modified version of Arcan specimen were calculated by using the following equations [11,12]: cosaf^alw) wt K,,=
Pc4na
(4)
wt
where Pc is critical load at fracture, a is loading angle, w is specimen length, t is specimen thickness and a is crack length. In turn Ki and Kn are obtained using geometrical factors/J (a/w) and/ 2 (a/w), respectively, which are obtained through finite element analysis of Arcan test specimen. Numerical analyses were also carried out. Figure 2 shows example of the mesh pattern of the specimen, which were performed with ABAQUS 6.2.4 [13]. The entire specimen was modeled using 2424 eight node collapsed quadrilateral element and the mesh was refined around crack tip, so that the smallest element size found in the crack tip elements was approximately 0.25mm relative to the crack length. A linear elastic finite element analysis was performed under a plain strain condition using 1/r0'5 stress field singularity. To obtain a 1/r05 singularity term of the crack tip stress field, the elements around the crack tip were focused on the crack tip and the mid side nodes were moved to a quarter point of each element side. The method used to calculate the stress intensity factor was an interaction method performed in the ABAQUS [13]. The J integral was also calculated, hi linear elastic fracture mechanics, the J integral coincides with total energy release rate, GT=GI+GH. These J values were compared with those obtained by the method mentioned above. RESULTS AND DISCUSSION In order to assess stress intensity factors at fracture, Ki and KD using Equations (4), geometrical factors fx (a I w) and f2 (a I w) for both loading modes were determined. The a I w ratio was varied between 0.3 and 0.7 at 0.1 intervals and a fourth order polynomial was fitted through finite element analysis as:
Loading angle (degree) FIGURE 3 The ratio of mode-II to mode-I Gn/Gi (in logarithmic scale) vs. loading angle,ct
Mixed-mode Fracture of a CF/PEI Composite Material
407
250
15
30
45
60
75
90
Loading angle (degree) FIGURE 4 Energy release rates G,, Gu, GT=Gi+Gn and J integral vs. loading angle,a
= 182.12(a/w) 4 -293.81(a/w) 3 +187.87 (a/w) 2 -51.492(a/w) +6.1137 (5) = -18.622(a/w)4 + 36.753 (a/w) 3 -25.182(a/M')2 + 7.759(a/w) + 0.0944 The energy release rates were calculated using conventional Equations (1). The relationship between the mixed-mode ratios of energy release rates and the loading angles a is shown in Figure 3. For loading angles close to pure mode-I loading, very high ratios of mode-I to mode-II is dominant. The ratios of strain energy release rates close to pure mode-II loading exhibits the opposite trend. As expected, it is confirmed that by varying the loading angle of Arcan specimen pure mode-I, pure mode-II and a wide range of mixed-mode loading conditions can be created and tested. In Figure 4, energy release rates Gi and Gn obtained by Equations (1), the total energy release rate obtained by Gr=Gi+Gn and the J integral are compared for a constant value of the load P=1000 N. It is seen that for loading angles oc<60° the mode-I fracture becomes dominant. As mode-II loading contribution increases, mode-I strain energy release rate Gi decreases and mode-II strain energy release rate Gn increases. For a>75° mode-II fracture becomes dominant. Total strain energy release rate under mixed-mode
12
15
18
Crack length (mm) FIGURE 5 The relation between energy release rate and crack length
21
408
Mixed-mode Fracture of a CF/PEI Composite Material
loading conditions decreases with the loading angle. The results of total strain energy rates values obtained by Equations (1) and the J integral agree with each other very well. Figure 5 shows the changes in energy release rates due to change in the crack length under different loading conditions. Although the mode-I energy release rate value changes largely due to the change in the crack length ratio, the mode-II value does not change markedly. It is also confirmed that as the mode-II fracture becomes dominant, the mixed-mode fracture toughness decreases. In the present experiments, bond failures limited the Arcan test use for tough CF/PEI laminates, especially under pure mode-II and mixed-mode loading conditions. The experimental work is still in progress and will be reported later. CONCLUSION hi this paper the mixed-mode interlaminar fracture behaviour for CF/PEI composite specimens was investigated based on experimental and numerical analyses. A modified version of Arcan specimen was employed to conduct mixed-mode test using the special test loading device. The full range of mixed-mode loading conditions including pure mode-I and pure mode-II loading can be created and tested. It is a simple test procedure, clamping/unclamping the specimens is easy to achieve and only one type of specimen is required to generate all loading conditions. The large scatter of the results was observed and unstable crack growth occurred in all cases, hi the Arcan test configuration, composite specimens were bonded between two metal fixtures that bond failures limited the test use for tough composite materials, especially under pure mode-II and mixed-mode loading conditions. The method of bonding needs improvement and more work is needed for the Arcan test method. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8.
9. 10. 11. 12. 13.
O'Brien, T. K. 1998. "Interlaminar Fracture Toughness: The Long and Winding Road to Standardization," The 4th International Conference on Composites Engineering, July 6-11,1997. Gillespie, J. W. and L. A. Carlsson. 1990. Delaware Composites Design Encyclopedia-Volume 6. Technomic Publishing Co. Inc., pp. 113-119. Rikards, R. 2000. "Interlaminar Fracture Behaviour of Laminated Composites," Computers and Structures, 76:11-18. Reeder, J.R. and J.H. Crews 1990. "Mixed-mode Bending Method for Delamination Testing," J. AIAA, 28: 1270-1276. Ducept, F., D. Gamby, and P. Davies. 1999. "A Mixed-mode Failure Criterion Derived from Tests on Symmetric and Asymmetric Specimens," Compos. Sci. Tech., 59:609-619. Arcan, M., Z. Hashin, and A. Voloshin. 1978. "A Method to Produce Plane-stress States with Applications to Fiber-reinforced Materials," Experimental Mechanics, 18:141-6. Kim, K.-Y. and L. Ye., Private Communication (2003). Glyn, L., L. Ye, Y.-W. Mai, and C.-T Sun. 1997. "The Effect of Adhesive Bonding between Aluminum and Composite Preperg on the Mechanical Properties of Carbon-fiber-reinforced Metal Laminates," Compos. Sci. Tech., 57:35-45. Daghyani, H. R., L. Ye, and Y.-W. Mai. 1996. "Mixed-mode Fracture of Adhesively Bonded CF/Epoxy Composite Joints,"/. Compos. Mater, 30:1248-65. Sih, G. C. andE. P. Chen. 1981. Crack in Composite Materials. Martinus Nijhoff Publishers, pp. 1-9. Yoon, S. H. and C. S. Hong. 1990. "Interlaminar Fracture Toughness of Graphite/Epoxy Composite Under Mixed-mode Deformations," Experimental Mechanics, 30:234-9. Jurf, R. A. and R. B. Pipes. 1982. "Interlaminar Fracture of Composite Materials," J. Compos. Mater, 16:386-94. Habbit, Karlsson and Sorensen, 2001. ABAQUS User's Manual version 6.2.4.
Effects of Molecular Structure on the Essential Work of Fracture of Amorphous Copolyester at Various Deformation Rates H. B. Chen and J. S. Wu Materials Research Group, Department of Mechanical Engineering, The Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong J. Karger-Kocsis Institute of Composite Materials, University of Technology Kaiserslautern, Kaiserslautern, Germany
ABSTRACT The fracture behavior of amorphous copolyesters with different molecular structure was studied with double edge notched tensile loaded specimens (DENT) using the essential work of fracture (EWF) approach. Various deformation rates ranging from 1 mm/min to 1000 mm/min were employed. Amorphous poly(ethylene terephthalate) (aPET) exhibited considerably higher specific essential and nonessential work of fracture than the copolyesters containing either cyclohexylenedimethylene (aPET-C) or neopentyl glycols (aPET-N). At high deformation rates, ductile/brittle fracture transition was observed with aPET-C and aPET-N, while aPET always fractured in ductile mode within the entire deformation rate range. These phenomena were ascribed to the different molecular flexibility and entanglement density of the copolyesters. The specific essential work of fracture of the aPET as a function of deformation rate went through a minimum. The initial decrease in toughness was caused by the hampered segmental mobility due to the increased deformation rate. The subsequent increase in toughness was attributed to the adiabatic heating induced temperature rise in the process and plastic zones.
INTRODUCTION Amorphous linear polyester and its copolymers are widely used in various applications, particularly, for packaging. Amorphous polyesters, such as polyethylene terephthalate) (PET) and polyethylene terephthalate glycol) (PETG), have good optical properties (e.g. high transparency, gloss and low haze) and high ductility. However, some of them are prone to physical aging and crystallization, which result in material embrittlement. To diminish the tendency to crystallization, one can incorporate certain stiff moieties in the PET main chain to violate the regularity of the chain structure to a certain degree, for example, replacing a part of ethylene glycol with 1,4-cyclohexylene dimethylene units (CHDM) or neopentyl glycol [1]. With the above-mentioned modification, the molecular chain flexibility * Correspondence Author, Tel: (852) 2358 7200; Fax: (852) 2358 1543; E-mail: [email protected]
410
Essential Work of Fracture of Amorphous Copolyester
and entanglement characteristics of the copolyesters are changed, which must have influences on the mechanical and fracture properties of the materials. Obviously, a good understanding on the mechanical property-molecular structure relationships of the copolyesters will provide useful guidance to R&D practice of the industry. In this work, fracture toughness of three amorphous copolyesters with different molecular structures and entanglement densities were investigated using the essential work of fracture approach. The correlations between the fracture toughness and their molecular built-up were discussed with the hope of making a contribution to a better understanding of the important relationships. Moreover, various deformation rates ranging from 1 mm/min up to 1000 mm/min were employed to study the strain-rate dependent fracture behavior. THE ESSENTIAL WORK OF FRACTURE The essential work of fracture (EWF) is a useful method to characterize the fracture toughness for ductile polymeric materials and is becoming popular due to its simplicity [1-7]. As illustrated in Figure 1, the fracture zone of a double-edge notched tensile (DENT) specimen can be separated into the inner process zone and the outer plastic zone. Accordingly, the total energy, Wf, required to fracture a pre-cracked specimen may be divided into two related components: the essential (We) and nonessential (Wp) work of fracture, corresponding to the energy dissipated in the process zone and plastic zone, respectively. Physically, We is the energy needed to create two new fracture surfaces, thus is proportional to the area of fracture surface; Wp is the energy dissipated in the plastic zone through various deformation mechanisms, thus is proportional to the volume of the plastically deformed zone. Accordingly, the basic equations of the EWF can be written as: wt = we + wp = •
It2
(1)
Wf
(2)
where t the specimen thickness, / the ligament length and /? the shape factor of the plastic zone. The specific essential work of fracture (we) and the specific non-essential work of fracture (wp) can be obtained by plotting wf against /. we is considered a material constant under plane stress conditions, at least for a given specimen thickness. wp, on the other hand, may change with the specimen geometry, gauge length etc.
Process Zone (WJ at2
\
Plastic Zcm ( Wf)
FIGURE 1 DENT specimen used in the EWF study
Essential Work of Fracture of Amorphous Copolyester
411
EXPERIMENTAL Materials Three amorphous copolyesters used in this study were aPET (amorphous polyethylene terephthalate), aPET-C (amorphous copolyester synthesized from terephthalic acid and two diols: ethylene glycol and 1,4-Cyclohexane dimethylene glycol), and aPET-N (amorphous copolyester synthesized from terephthalic acid and two diols: ethylene glycol and neopentyl glycol). All the specimens were in the form of films with a thickness of 0.25 mm. Table 1 shows their basic properties. TABLE I Basic characteristics of the amorphous copolyesters studied. Materials aPET aPET-N aPET-C
I.V. [dl/g] 0.74 0.75 0.70
E-Modulus IGPa] 2.4 2.2 2.1
Yield Strength [MPa] 52.4 48.1 45.5
Fracture Tests The EWF tests were performed on a Zwick 1445 universal testing machine at room temperature. Double edge notched tensile (DENT) specimens with various ligament lengths ranging from 5 mm to 25 mm were employed. The width, gauge length was 35 mm and 70 mm, respectively. For each ligament length, at least three specimens were tested. Various deformation rates, viz. 1, 10, 100, 500 and 1000 mm/min, were applied. Dynamic Mechanical Analysis Dynamic mechanical analysis (DMA) was performed using a TA instruments DMA 983 at the resonance mode with displacement amplitude of 0.2 mm and frequency of 1 Hz. The temperature scanning ranged from — 100°C to the softening point at a heating rate of 2°C/min. RESULTS AND DISCUSSION Validity of Current EWF Tests Before discussing the relationships between the molecular structure and the EWF parameters, the validity of current EWF measurements should be assessed first, particularly at high deformation rate. For a valid EWF test, two basic requirements must be satisfied [8]. One is that the load-displacement curves obtained with samples of different ligament lengths have geometric similarity; the other is that the ligament of the specimen must undergo fully yielding prior to the onset of crack growth. To our best knowledge, there are little EWF tests performed at very high deformation rate, hi this study, to check the validity of the EWF method at high deformation rate, an infrared thermographic camera was employed to monitor the entire fracture process. The observations as illustrated in Figure 2 demonstrate that the fracture process at high deformation rates occurred in the same way that satisfies the prerequisites for a valid EWF measurement.
Essential Work of Fracture of Amorphous Copolyester
412
FIGURE 2 Serial infrared frames reflecting the fracture process of aPET at v = 1000 mm/min.
Fracture Behavior at Low Deformation Rate Table 2 lists the EWF parameters of the copolyesters obtained at a deformation rate of 1 mm/min. Clearly, all the parameters do depend on the copolyester's molecular build-up. The ranking of the specific essential work of fracture is same as the ranking of their yield strength (cf. Table 1), i.e. aPET > aPET-N > aPET-C. TABLE II The fracture parameters of the amorphous copolyesters at a deformation rate of 1 mm/min
v=l mm/min aPET aPET-N aPET-C
P 2
[kJ/m ] 50.6 ± 1 8 46.2 ± 1 5 38.7 ± 2 2
Sic
3
[MJ/m ] 10.6 ±0.2 6.8 ±0.2 7.5 ±0.2
3
[MJ/m 99.5 72.3 76.7
0.107 0.091 0.099
1
[mm] 1.9 1.6 1.4
Theoretically, we in mode I fracture consists of two components [5]: w=d(°
(3)
ade + (*' cr(A, )dA
where (a,e) the true stress/strain, sn and sn the true and engineering necking strains., a and A, the stress and crack tip opening displacement within the fracture process zone. 8]C is the mode I critical value of A[, d is the width of the fracture process zone as illustrated in Figure 3 and is of the order of the specimen thickness. Physically, the first term is the plastic work to necking and the second term refers to the fracture work of the neck. For the samples with same specimen thickness, one can expect that the width of the fracture process zone will be similar. Thus the parameters dictating the value of we will be the stress ( a ) in the ligament and the critical crack tip opening displacement (CTOD) (Slc). S T
Crack
FIGURE 3 A fully developed fracture process zone under mode I loading schematically
Essential Work of Fracture of Amorphous Copolyester To determine the CTOD, the method used by Hashemi et al [9] was adopted. eb=e0+epL
413
(4)
where eb the extension to break for the specimen with a ligament length of L; e0 the extrapolated value of eb at zero ligament length and can be identified to equal to Slc. The critical CTOD results obtained in this way are listed in Table 2, together with the yield stress (<jy) of the tested samples. Apparently, both Slc and ay values are in the order of aPET > aPET-N > aPET-C. If we is calculated using Eq. (3) with the 8lc and ay values in Table 2, the aPET would have the highest we value, followed by aPET-N and aPET-C, this is in agreement with our experimental results. Fracture Behavior at High Deformation Rate Figure 4 illustrates the changes of the specific essential work of fracture of the copolyesters under different deformation rates. The results indicate that we decreased with increasing the deformation rate in the range of 1 mm/min to 100 mm/min. Further increasing the deformation rate, aPET-C and aPET-N failed in a brittle mode, whereas we of the aPET started to increase. This trend suggests that the dominant influence of deformation rate on the fracture behavior of polymers is different at different rate range. At the rate above 100 mm/min, the adiabatic heating ahead of the crack tip due to high rate dominates, resulting in an increase of the temperature in the process and plastic zones. This temperature rise is beneficial to the molecular chain mobility, thus, the fracture toughness. On the other hand, increasing the deformation rate can also lower down the fracture toughness if the chain relaxation cannot response to the loading induced deformation in the time scale at high rate (wellknown as strain-rate embrittlement). The segmental mobility of molecular chains at high deformation rate is seriously hampered so that only a part of the entangled chains may be involved in the stress distribution process and the network deformation is limited [10]. Given the above-mentioned two competing factors, it seems that in the rate rang between 1-100 mm/min, the effect of stain-rate embrittlement has a dominant effect; whereas at higher deformation rates, the effect of adiabatic heating becomes dominant for the aPET. 70.
—•— aPET aPET-C aPET-N
60.
g
50-
u E 40.
s.
in 30.
\ Brittle Failure 1
10
100
500
1000
Deformation Rate [mm/min]
FIGURE 4 Deformation rate dependence of the specific essential work of fracture
In agreement with the changes of EWF parameters against the deformation rate, different failure modes at different rates were also observed. The failure of the aPET was always ductile within the entire deformation rate range studied, whereas two different failure modes, i.e. stable ductile fracture and unstable brittle fracture were
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Essential Work of Fracture of Amorphous Copolyester
observed with both aPET-C and aPET-N specimens. The onset deformation rate for the ductile/brittle transition was at 500 mm/min and 100 mm/min for the aPET-C and aPET-N, respectively, which reflects again the molecular flexibility of the two samples, as discussed in the following text. Figure 5 shows the dynamic mechanical analysis (DMA) results of the amorphous copolyesters studied. Besides the obvious primary dissipation, i.e. oc-relaxation peak at Tg temperature (about 75°), there is also a broad but distinct secondary dissipation, i.e. P-relaxation peak at about -60°C. When the EWF tests are carried out at room temperature and low deformation rate, the heat generated during tension is not significant and has sufficient time to exchange with the ambient; therefore, the temperature around the ligament of the tested specimens is close to or slightly higher than the ambient temperature. For instance, at v = 100 mm/min, the temperature ahead of the crack tip of the aPET specimen was about 35°C, as recorded by the infrared camera. Therefore, the fracture of the specimen at low deformation rate was completed at a temperature between the arelaxation and p-relaxation, which means that the P-relaxation was activated and achieved to a substantial degree, while the a-relaxation was not activated at all. In other words, only p-relaxation has contributions to the fracture behavior. Furthermore, the peak temperature (PMT) and the peak height (PH) of tan8 represent the characteristics of the molecular chain relaxation. The higher the temperature and/or the larger the tan8 peak, the more flexible is the molecular chain [11]. Though the PMT of the P-relaxation of the three copolyesters in Figure 5 is quite close, the PH of each sample has obvious difference, which indicates that the three copolyesters have different chain rigidity. Based on the peak height, it is obvious that the molecular chain of aPET-N is most rigid. Therefore, the low ductile/brittle transition rate for the aPET-N can be attributed to its lower molecular flexibility. Based on the same DMA argument, the molecular chain flexibility of the aPET-C is better than that of the aPET, which is probably because the cyclohexylene rings in the aPET-C promote the longrange cooperative chain motions in the copolyester, leading to increased chain flexibility [12]. Since the aPET has the highest ductility at high deformation rate, it may suggest that high entanglement density plays a more important role on the stress transfer ahead of the crack tip, as discussed below. t
aPET aPET-C • • -aPET-N
-100
-50
ad' 0
50
100
150
Temperature [°C] FIGURE 5 Loss tangent (tan8) vs. temperature curves of the amorphous copolyesters at 1.0 Hz
It was noted that the brittle fracture occurred only at relatively large ligament lengths. For instance, the DENT specimens of the aPET-N with a short ligament length (e.g. 5 mm) would still fail in ductile manner at v = 100 mm/min. The reason behind this phenomenon may be explained as follows. When ligament length is large, considerable elastic energy will be stored in the tested body when it is loaded. Although the ligament yielding and the formation of the outer plastic zone can
Essential Work of Fracture of Amorphous Copolyester
415
dissipate some of the stored energy, however, at high deformation rate, the energy dissipation due to the plastic deformation of the materials in the plastic zone may not be fast enough for complete release of the stored energy. Therefore, once the crack starts to propagate after the full ligament yielding, the stored elastic energy is suddenly released through fast unstable fracture of the ligament. This brittle fracture behavior should depend strongly on the stress and energy transferring ability of the molecular network. Since the aPET has the highest entanglement density, the applied stress and energy can be transferred to and dissipated efficiently in a relatively large area surrounding the crack tip, leading to a bigger plastic zone and higher toughness. In addition, at high deformation rate, the strain-induced temperature rise makes the temperature of the material ahead of the crack tip and around the ligament of the aPET sample close to or above its Tg, which may activate the primary relaxation and enhance the molecular chain mobility. Therefore, no brittle failure was observed with the aPET. CONCLUSION This work studied the essential work of fracture (EWF) and molecular structure relationships using three amorphous (co)polyesters with different molecular build-up (viz. aPET, aPET-C and aPET-N) at different deformation rates. Based on the results obtained, the following conclusions can be drawn: • Both specific essential and non-essential work of fracture of the (co)polyester films strongly depend on the molecular architecture, particularly the entanglement density. Higher entanglement density will results in greater EWF parameters. • Effects of deformation rate on the EWF parameter were investigated at very high deformation rate up to 1000 mm/min for the first time. It was found that the deformation rate affects the specific essential work of fracture via two competing mechanisms, i.e. strain rate embrittlement and adiabatic heating. The former will results in a decrease in toughness with deformation rate increase, while the latter does the opposite. • Ductile/brittle (D/B) transition was observed with the aPET-C and aPET-N. The offset deformation rates for the D/B transition depends on the molecular build-up of the films. The brittle unstable failure was ascribed to the sudden release of the elastically stored energy in the specimens. REFERENCES 1.
Karger-Kocsis J, in Williams JG and Pavan A, editors, Fracture of Polymers, Composites and Adhesives - ESIS Publ.27, Elsevier Sci., Oxford, 2000, pp.213-230. 2. Mai YW and Cotterell B, Eng. Fract. Mech. 1985; 21(1): 123-128. 3. Mai YW and Cotterell B, Int. J. Fract. 1986; 30(2): R37-R40. 4. Mai YW, Cotterell B, Int. J. Fract. 1986; 32(5): 105-125. 5. Mai YW, Int. J. Mech. Sci. 1993; 35(12): 995-1005. 6. Wu JS, Mai YW and Cotterell B, J. Mater. Sci. 1993; 28(12): 3373-3384. 7. Wu JS and Mai YW, Polym. Eng. Sci. 1996; 36(18): 2275-2288. 8. Clutton, E. in Moore, D. R.; Pavan, A.; Williams, J. G., editors, Fracture Mechanics Testing Methods for Polymers, Adhesives and Composites -ESIS Publ. 28, Elsevier Sci., Oxford, 2001, pp. 177-195. 9. Arkhireyeva A, Hashemi S, Polymer 2002; 43(2): 289-300. 10. Karger-Kocsis J, Czigany T, Polym. Eng. Sci. 2000; 40(8): 1809-1815. 11. Lu SX, Cebe P, J. Appl. Polym. Sci. 1996; 61(3): 473-483. 12. Chen LP, Yee AF, Moskala EJ, Macromolecules 1999; 3.2(18): 5944-5955.
How to Eliminate Buckling in the Essential Work of Fracture Measurement with Very Thin Plastic Films H. B. Chen, S. L. Liu and J. S. Wu Materials Research Group, Department of Mechanical Engineering, The Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong
ABSTRACT When the Essential Work of Fracture (EWF) method is used to evaluate the fracture toughness of ductile thin polymer films, buckling phenomenon is very often observed, which may violate the conditions for data validity. In some cases, buckling is so severe that to perform a valid EWF test is virtually impossible. In this work, we propose an experimental set-up using U-shaped fixture to eliminate the buckling problem in thin film EWF tests with double-edge notched specimen (DENT). The influences of the U-clamp on the yielding, plastic zone development, crack initiation and propagation behaviors of the thin film samples were examined by experiments as well as finite element analysis. The results demonstrate that the use of the newly designed U-clamp has little effect on the fracture behavior of the tested thin polymer films. Therefore, it is an ideal set-up for the EWF measurements with very thin films when buckling is a problem.
INTRODUCTION Essential work of fracture (EWF) method becomes quite popular recently in the fracture toughness characterization of ductile polymer materials [1-8]. This method is particularly useful when the toughness of plastic thin films is under concern. For thin ductile polymer films, due to extensive plastic deformation associated with crack propagation in a toughness test, neither linear elastic fracture mechanics (LEFM) nor J-integral analysis can be applied, because a valid measurement of fracture toughness by the two methods must be conducted under plane-strain condition to ensure small scale plastic deformation at the running crack tip. To maintain the plane-strain condition at a given testing temperature and strain rate, the size, mainly the thickness, of the specimens must be larger than a certain value that is determined primarily by the yield strength of the material being tested as well as specimen geometry. For ductile polymer materials at room temperature, the thickness requirement for a valid LEFM or J-integral test is rather difficult to meet. When fracture toughness of plastic film is required, a valid LEFM or J-integral test of the film is virtually impossible. Thus, the EWF method is an alternative methodology for such an application and being practiced increasingly in the plastic film industry and other industries, for example paper and textile industries. When EWF method is employed in the film toughness tests, a rigid and flat metal clamp is usually adopted to hold the film samples that have a double edge notched " Correspondence Author, Tel: (852) 2358 7200; Fax: (852) 2358 1543; E-mail: [email protected]
Eliminate Buckling in the Essential Work of Fracture Measurement
417
tensile (DENT) geometry. Previous work has proven that the flat clamp works very well as long as the thickness of the film is relatively large, for example, 200 /jm or larger. However, when the thickness of the film is smaller, it is often observed that use of the flat clamp may introduce film buckling during loading, which certainly has effect on the stress distribution and deformation behavior of the material in both the fracture processing zone and plastic deformation zone, leading to measurement errors. An example of the above-mentioned film buckling in the EWF test is shown in Figure 1, which is a HDPE film of about IQ/jm in thickness. The only effort to eliminate the buckling found in literature review was done by Mai and his co-workers [1]. The authors used a semi-circular metal holder to depress the buckling in the tests of a paper sample, hi other published work related to plastic film tests [7-8], the buckling phenomenon was not reported. In the present work, we report the results of our recent effort using a simple Ushaped clamp to eliminate the buckling in EWF tests of very thin plastic films. The effects of the constraint from the U-shaped clamp on the measurement of the specific essential work of fracture and specific non-essential work of fracture were examined experimentally and numerically by final element analysis.
• •-• £
-A
FIGURE 1 The buckling phenomenon in the EWF test
EXPERIMENTAL The materials used were high density polyethylene (HDPE) blown films with a thickness of 12.5 /Mn and isotactic polypropylene (iPP) extruded films with a thickness of 400 /jm . The double edge notched tensile specimens (DENT) were employed for the essential work of fracture tests with different ligament length ranging from 5 mm to 25 mm. The width of the specimen (W) was 50 mm and the length between two clamps is 60 mm. Initial notches were made with fresh razor blades and the ligament lengths were measured with a traveling microscope (Topcon, TMM-130 Z). All the fracture tests were performed on a universal testing machine (Sintech 10/D) with a crosshead speed of 10 mm/min at ambient temperature. ANSYS was used for numerical simulation. The model used was inelastic, rate independent and isotropic hardening mises plasticity. Three stages, i.e. elastic deformation, crack-tip yielded and full ligament yielded were chosen. RESULTS AND DISCUSSION To eliminate film buckling during thin film EWF test, a U-shaped fixture is used in the present work. As illustrated in Figure 2, buckling was not observed when the Ushaped fixture was applied, because the two legs of the U-clamp provided additional lateral constraint to hold the otherwise free edges of the specimen. The entire fracture
Eliminate Buckling in the Essential Work of Fracture Measurement
418
of the thin film took place in a typical and stable way, i.e. crack blunting, initiation and propagation. Figure 3 (a) gives the load-displacement curves of the HDPE blown film obtained using DENT geometry and U-shaped clamp. The geometric similarity of the curves indicates that the tests satisfy the prerequisite of the essential work of fracture approach [9]. The specific essential work and specific non-essential work of fracture are obtained by plotting the specific total fracture work against the ligament length as shown in Figure 3 (b). The linearity coefficient is high and the results are listed in Table 1. It seems that use of the U-shaped fixture may be a suitable measure for elimination of sample buckling in thin film EWF tests.
FIGURE 2 The fracture process of HDPE film with U-shaped fixture
HDPE film DENT specimen U-shape Clamp
HDPEfilm DENT specimen
5 10 15 20 Ligament length [mm]
Displacement [mm]
FIGURE 3 The load-displacement curves of HDPE film (a); Plot of wf against 1 (b) TABLE I The fracture parameters of HDPE film and iPP film with two types of fixture Materials
Fixture
we (kJ/m2)
HDPE iPP
U-shaped Flat U-shaped
70 57 54
^
(MJ/m3) 17.8 9.6 9.8
On the other hand, one may question that since the two legs of the U-shaped fixture impose additional lateral constraint to the specimen, the lateral constraint must have influences on the stress state in the ligament and affect the fracture process and the fracture parameters, particularly the specific essential work of fracture. To investigate this influence, an isotactic polypropylene (iPP) film with a large thickness was tested using both a flat and a U-shaped fixture. The iPP film does not have buckling problem using flat clamp due to its large thickness, as shown in Figure 4 (a). The load-displacement curves obtained in the EWF tests with different fixture geometries are drawn in Figure 5 (a). The shape of the curves is in fact identical, particularly in the region of crack initiation and ligament yielding. The sudden loaddrop corresponds to the full ligament yielding, followed with the crack propagation.
Eliminate Buckling in the Essential Work of Fracture Measurement
419
The similarity of the entire fracture process of the specimen with the two clamps can also be seen in Figure 4 (a) and (b). As a result, the specific essential work and specific non-essential work obtained with two different fixtures are same, refer to Figure 5 (b). This experimental evidence indicates that the clamp geometry has little effects on the measurement of EWF parameters.
(b) FIGURE 4 The fracture process of iPP film with (a) flat fixture and (b) U-shaped fixture 300. Ligament length = 25mm - Flat Clamp U-shape Clamp
i-PP
200-
.i
100
'
* ^
Flat Clamp
*~~^
U-Shape Clamp
& 0j - 3002001005
10
15
Displacement [mm]
05 - 1 0 15 20 Ligament length [mm]
FIGURE 5 The load-displacement curves of iPP with two fixtures (a); Plot of wf against 1 (b)
To confirm the findings from the experimental work, finite element analysis of the two fixtures were performed. The stress distribution and plastic energy dissipation of the specimen at various stages, including elastic deformation, crack-tip yielded and full-ligament yielded, were simulated and calculated numerically. The ligament length used for the simulation is 10 mm and the center of the ligament is set as the origin. Figure 6 (a) and Figure 7 (a) demonstrate the stress distribution along and around the ligament at the elastic deformation stage, respectively. It is clearly that at this stage, the stress distribution ahead of the crack tip and that around the ligament are slightly different with different fixtures due to the different clamp geometries. In the stage of crack-tip yielded as shown in Figures 6 (b) and Figure 7 (b), the same phenomenon is observed but the difference of the stress distribution becomes smaller. Since the fracture parameters of the EWF approach is energy related, the plastic energy dissipated ahead of the crack tip and around the ligament is more interesting and important. Figure 8 (a) gives a picture of the energy contours around the crack tip, which shows that the plastic work distribution around the crack tip is also very similar
420
Eliminate Buckling in the Essential Work of Fracture Measurement
for the U-shaped and flat fixtures, which indicates that the geometry of the clamp does not affect the plastic energy dissipation in the ligament region. Further, in the full ligament yielded stage, as shown in Figures 6 (c) and Figure 7 (c), the full ligament is yielded with a certain width in the loading direction. According to the EWF theory, the specific essential work of fracture is composed with the energy for yielding, necking and breaking the process zone, as expressed with following equation [4]. w=d\
ads+
a(A,)dA,
(1)
where (cr,£) are the true stress/strain, s~n and en are the true and engineering necking strains., a and A( are the stress and crack tip opening displacement within the fracture process zone. 5IC is the mode I critical value of A,; d is the width of the fracture process zone, which is in the order of the specimen thickness. The first item is the plastic work to yielding and necking and the second one refers to the fracture term of the neck. Clearly, the second fracture energy is related to the fracture mechanisms when tearing the neck, which should be less affected by the clamp geometry. On the other hand, some parameters would influence the first terms, including the size of the necked area, the opening displacement of the crack tip (CTOD). From the finite element analysis, the CTOD at the full ligament yielding stage is 0.81 mm for the U-shaped fixture and 0.82 mm for the flat one. Obviously, the discrepancy is negligible. Compared the pictures in Figure 7 (c), the width of the fully-yielded region are also identical for both fixtures. Thus, one can expect that the plastic work to yield and neck the ligament should be comparable for both fixtures. The energy dissipation around the ligament at this stage is shown in Figure 8 (b), which does not show any difference. Therefore, the finite element analysis results confirmed that though the geometry of the fixture influences the stress distribution ahead of the crack tip and around the ligament, the energy dissipation for fracture the materials are not affected. CONCLUSIONS A U-shaped fixture is employed to eliminate the buckling problem when very thin films are tested using the essential work of fracture method. The geometric influence of the U-shaped fixture on the fracture process is examined experimentally and by finite element analysis. The results indicate that the U-shaped clamp does not affect the fracture process and the fracture parameters. Reliable EWF parameters can be easily obtained using this U-clamp without introducing noticeable error. Therefore, the U-shaped clamp designed in this work is an ideal setup for the EWF measurements with very thin films. DENT specimen Liagment iength: 10 rr U-shape Clamp Rat Clamp
DENT specimen Liagment length: 10 mm U-shape Clamp — Flat Clamp
r
r |
DENT specimen Liagmeni length: 10 mm ——— U-shape Clamp Flat Clamp
10. C
>„ Distance [mm]
10
15
Distance [mm]
20 Distance [mm]
FIGURE 6 The stress distribution along the ligament at (a) elastic deformaiton stage; (b) crack-tip yielded stage; (c) full ligament yielded stage
Eliminate Buckling in the Essential Work of Fracture Measurement
421
# (a)
£*
"""I*
(b)
FIGURE 7 The stress distribution around the ligament at (a) elastic deformaiton stage; (b) crack-tip yielded stage; (c) full ligament yielded stage (left: flat fixture; right: U-shaped fixture)
FIGURE 8 The plastic energy around the ligament (a) crack-tip yielded stage; (b) full ligament yielded
REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9.
Mai YW and Cotterell B, Eng. Fract. Mech. 1985; 21(1): 123-128. Mai YW and Cotterell B, Int. J. Fract. 1986; 30(2): R37-R40. Mai YW, Cotterell B, Int. J. Fract. 1986; 32(5): 105-125. Mai YW, Int. J. Mech. Sci. 1993; 35(12): 995-1005. Wu JS, Mai YW and Cotterell B, J. Mater. Sci. 1993; 28(12): 3373-3384. Wu JS and Mai YW, Polym. Eng. Sci. 1996; 36(18): 2275-2288. Karger-Kocsis J, Czigany T, Polymer 1996; 37(12): 2433-2438. Hashemi S, Polym. Eng. Sci. 2000; 40(1): 132-138. Clutton, E. in Moore, D. R.; Pavan, A.; Williams, J. G., editors, Fracture Mechanics Testing Methods for Polymers, Adhesives and Composites -ESIS Publ. 28, Elsevier Sci., Oxford, 2001, pp. 177-195.
Fracture Behaviour of Sandwich Laminates Reinforced by Short-Glass Fibres Akbar Afaghi Khatibi* Department of Mechanical & Manufacturing Engineering University of Melbourne, Australia
ABSTRACT The main aim of this work was to develop new sandwich laminates using glass fibre/polyester facings with low density polyurethane foam reinforced by short glass fibres. Hand lay-up and casting techniques were used to manufacture test specimens with different characteristic parameters. Several experiments were then conducted in order to characterise the mechanical properties of sandwich laminates. It was found that reinforcing core material by short glass fibres improves the mechanical properties of sandwich laminates. However, the extension of this improvement depends not only on the length and shape of the short glass-fibre but also the weight percentage of the reinforcement. In addition, it was concluded that the curing temperature plays a significant role on the core-reinforcement alignment and its microstructure. Specimens cured at lower temperature (ambient) exhibited improved fracture properties compared with those of cured at an oven.
INTRODUCTION Composite sandwich panels consist of two thin face sheets or skins bonded to a thick and lightweight core. The faces are typically composite laminates or metals, while the core could be cellular foam, metallic and non-metallic honeycombs, balsa wood or trusses. The concept of these sandwich laminates is very suitable for lightweight structures with high in-plane and flexural stiffness. In compare with traditional stiffened panels, sandwich laminates offer many advantages such as high flexural rigidity and strength, ease of manufacture, improved stability and ease of repair [1]. There are a large number of papers and publications on the behaviour of sandwich structures. The basic principles of sandwich construction and reviews of analytical and computational methods can be found in references [2, 3, 4]. The structural performance of sandwich laminates depends not only on the properties of skins, but also on those of the core, the interface bonding between the core and the skins, and the geometrical dimensions of the components. Cellular foams are increasingly being used as core materials in conjunction with high strength skins, to produce strong, stiff and lightweight sandwich structures for aerospace and marine applications. Due to their higher impact resistance and energy absorbing capability, cellular foams are being also used extensively in automobile applications. The * Correspondence Author, Department of Mechanical & Manufacturing Engineering, The University of Melbourne, VIC 3010 Australia, facsimile: +61(0)393478784, email: [email protected]
Sandwich Laminates Reinforced by Short Glass Fibres
423
mechanical behaviour of foam depends on the structure of the cell and the density of foam. The focus of this work was to investigate the fracture behaviour of sandwich laminates constructed with and/or without short-fibre-reinforced core. The impact and flexural behaviour of sandwich laminates with short-fibre-reinforced core is characterised and compared by those with un-reinforced core. The effects of corereinforcement length and curing temperature were studied in detail. MATERIALS AND EXPERIMENTAL PROCEDURE Sandwich panels were manufactured from 300 mm by 300 mm glassfibre/polyester skins and polyurethane core. Hand lay-up and casting techniques were used to manufacture test specimens with different characteristic parameters such as short-fibre volume fraction, short-fibre length, and etc. Two individual wet layers of glass-fibre/polyester were placed on the mould's internal walls and premixed agents of polyurethane foam (Polyol and Isocyanate), with or without reinforcement were then cast into the mould cavity. Two types of short glass fibre were used as reinforcement for the foam, namely milled and chopped fibres. The length of milled and chopped short glass fibres was 0.8 mm and 6 mm, respectively. Curing of skins and core occurred simultaneously under ambient (18°C - 20°C) and/or oven (85°C) temperature. No adhesive was used between skins and the core. The completed sandwich panels were cut into different coupon sizes, using a diamond saw. A "XYYZ" notation was used to categorise specimens, where X: Curing temperature, R for ambient or O for oven YY: weight percentage of short-glass fibre reinforcement in the core Z: type of core reinforcement, M for milled or C for chopped short glass fibre For example R05C refers to a sandwich panel cured at the room temperature with its core has been reinforced by 5% (weight) of chopped short-glass fibres. The mechanical characterisation tests were conducted to determine the compression strength (ASTM C365-00), bending moduli and strength (ASTM C39300 and D790-96a) and impact strength of sandwich specimens. All compression and flexural 4-point bendmg tests were performed on MTS universal testing machine with a constant crosshead rate of 0.5 mm/min and 6 mm/min, respectively at ambient temperature. The load and displacement data were recorded through a computer data acquisition system. To characterise the impact strength of sandwich panels Charpy test was conducted using a drop-down pendulum. At least four specimens were tested for each individual case.
RESULTS AND DISCUSSION Effect of Fibre Length Typical load-displacement curves for sandwich panels under four-point bending tests are shown in Figure 1. For all fibre weight ratios studied in this work, a linear (elastic) behaviour is followed by a plateau regime where the load required to crash the sandwich remains nearly constant. In this regime, some foam cell walls are compressed until they buckle, while others are stretched until they crack [5]. When additional load is applied, cell walls are compressed against neighbouring cell walls and the stiffness of the material increases as it is compressed into the lock-up regime.
Sandwich Laminates Reinforced by Short Glass Fibres
424
15%
0
10
20
30
40
50
0
Displacement [mm]
10
20
25%]
30
40
50
Displacement [mm]
(b) (a) FIGURE 1 Effect of core-reinforcement weight percentage on load-displacement curves under four-point-bending: sandwich laminates reinforced by (a) chopped- and (b) milled-glass fibre.
The level of plateau value, however, depends on the core-reinforcement length. It can be seen that the reinforcement of the core with chopped-glass fibres (6 mm in length) had significant effect on the plateau value and increased it by up to 35%. Contrary to this, adding milled-glass fibres with only 0.6 mm length decreases this value by 30%. The failure mode was also different for laminates reinforced by chopped- and milledglass fibres. Extensive delamination between core and skin was observed for the later. The effect of core-reinforcement-fibre length on flexural strength and modulus of specimens cured at room temperature is shown in Figures 2a and 2b, respectively. Although adding 5% reinforcement to the core decreases both bending strength and modulus to some extent, however, increasing the reinforcement weight ratio to 15% and/or 25% improves both mechanical properties. This phenomenon is more 0 -— Chopped — -• —
Milled
14
r
y12
11! 1. °
^
^ ^
^
0 - — Chopped — •• — Milled
r I
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S. - "
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3 X
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a 4
1
2
6
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1 ' ' ' 0 •
10
t • ' • • I ' • ' '
15
20
Fibre Weiglh %
0 •
10
15
20
Fibre Weight %
(a) FIGURE 2 Effect of core-reinforcement weight percentage on (a) flexural strength and (b) bending modulus for sandwich laminates reinforced by chopped- and/or milled-glass fibre.
Sandwich Laminates Reinforced by Short Glass Fibres
425
significant with chopped-short-glass fibres with 6 mm length, hi this case, an increase up to 23% in flexural strength and 43% in bending modulus was observed. Reinforcing the core with milled-short-glass fibres with 0.6 mm length did not contribute to the flexural strength of sandwich panels and had an inverse effect, as shown in Figure 2a. The positive effect of milled fibres on bending modulus was observed only for specimens with 25% reinforcement. The effect of reinforcement length on impact strength of sandwich panels cured at room temperature is depicted in Figure 3a. For the laminates reinforced by choppedglass fibres an increase up to 15% was observed in impact strength. However, reinforcement by milled-glass fibres did not contribute to any improvement in impact behaviour. Furthermore, improvements at compressive strength were observed for reinforcement ratios of 15 and 25%, as shown in Figure 3b. Effect of Curing Temperature In order to investigate the effect of curing temperature on mechanical properties of sandwich laminates specimens were manufactured using two different curing temperature, namely ambient (18°C - 20°C) and oven at 85°C. Experimental results, as reported in Table I, indicate that curing temperature plays a significant role on the engineering properties of sandwich laminates. As it can be seen from Figure 4, all specimens cured at room temperature exhibit higher bending modulus and flexural strength compared with those of cured at higher temperature. This increase was up to 100% for bending modulus and 65% for flexural strength, as shown in Figure 4. These improvements in mechanical properties can be contributed to the microstracture of sandwich laminates. Since the microstructure of the reinforced-foam depends on the curing temperature, it's observed that specimens cured at high temperatures have got more porosities than those cured at room temperature. Although the manufacturing time was longer for specimens cured at room temperature but much more uniform structure was achieved in these specimens.
• Chopped QMilled
„
• Chopped DMilled
„
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:
.£.:£
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:
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-§1 -X
3,T
3-
s
a.
1 0.50
5
15
Fibre Weight %
(a)
5
15
Fibre Weighty.
(b)
FIGURE 3 Effect of core-reinforcement length on (a) impact and (b) compressive strength of sandwich laminates.
426
Sandwich Laminates Reinforced by Short Glass Fibres — • - — Room
—
m
—
O v e n
f
14-
i1 12-
2 ^ ^
i
c 10 3)
! 5
8-
< Q)
i.
4
2 0 -
10
15
1 •'
10
20
Fibre Weight %
15
'• i
'
20
Fibre Weight %
FIGURE 4 Effect of curing temperature on bending modulus and flexural strength.
TABLE I Experimental data
Sample R00 R05S R15S R25S R05M R15M R25M OOO O05S O15S 025 S O05M 015M O25M
Flexural Strength [MPa] Mean A 0.38 11.08 10.00 0.46 11.96 0.45 13.68 0.66 0.36 8.81 8.73 0.58 0.41 10.08 9.99 0.49 0.26 7.69 7.19 0.55 0.52 8.75 7.20 0.07 7.67 0.27 6.25 0.38
Bending Modulus [MPa] Mean A 83.54 618.91 601.13 37.58 95.39 738.78 885.70 68.90 541.23 61.16 604.54 69.79 827.52 52.89 54.20 550.08 364.56 29.55 369.12 36.80 414.64 45.38 398.24 27.45 478.97 57.86 51.26 553.79
Impact Strength [kJ/m2] Mean A 44.85 4.20 43.33 23.64 53.03 5.25 51.21 10.86 3.64 46.67 44.09 5.76 37.58 4.64 44.09 5.76 47.12 7.77 47.73 4.78 45.91 3.44 49.55 2.12 46.67 3.64 33.94 4.85
A: Standard deviation
CONCLUSIONS The effect of core-reinforcement in sandwich laminates was investigated. The core was reinforced by using milled- and chopped-glass fibres with 0.6 and 6 mm length, respectively. After conducting extensive experiments it was found that the length of core-reinforcement plays a significant role in fracture behaviour of sandwich laminates. The sandwich specimens with their core reinforced by chopped-glass fibres, exhibited 23% and 46% increase in flexural strength and bending modulus, respectively, compared with those of specimens without any core reinforcement. Furthermore, it was concluded that curing temperature is also affecting the engineering properties of the sandwich laminates. Specimens cured at lower temperature (ambient) showed higher fracture properties.
Sandwich Laminates Reinforced by Short Glass Fibres
427
REFERENCES 1. 2. 3. 4. 5.
Saporito J. 1989. "Sandwich structures on Aerospatiale helicopters" in Proc. 34* Int. SAMPE Symp and Exhibition, Reno, Nevada, pp. 2506-13. Zenkert D. 1995. "An introduction to sandwich construction" London: Engineering Materials Advisory Services. Noor AK, Burton WS, Bert CW. 1996. "Computational models for sandwich panels and shells" Applied Mechanics Reviews; 49: 15-199. Reddy JN. 1997. "Mechanics of laminated composite plates: theory and analysis" Boca Raton, FL: CRC Press. Neilsen MK, Krieg RD, Schreyer HL. 1993. "A constitutive Theory for Rigid Polyurethane Foam" in: MD-Vol 46 Use of Plastics and Plastic Composites: Materials and Mechanics Issues. ASME, New Orleans, Louisiana, pp. 181-194.
Analytical and Numerical Simulations of Plastic Zone at Crack Tip in Anisotropic Solids 'Hong-Xin Liu, 2Zhi-Ming Ye* ^ept.of Mechanics, 2Dept.of Civil Engineering, Shanghai University 99 Shangda Road, Shanghai, 200436, P.R.China 3
Hong-Yuan Liu Centre for Advanced Materials Technology (CAMT) School of Aerospace, Mechanical and Mechatronic Engineering, University of Sydney, Sydney, NSW 2006, Australia 3
ABSTRACT This paper presents analytical and numerical studies on fracture behavour of anisotropic materials. A theoretical model was developed to characterize the plastic zone size and shape at crack tip in anisotropic solids. Several cases of anisotropic materials will be discussed by using uni-axial stress and bi-axial assumptions. Additionally, numerical results of finite element analysis are applied to examine the theoretical models. The method developed by this work is expected to provide a useful tool towards a better description of the crack-tip field in those materials.
INTRODUCTION Composites, whether fibre reinforced polymer, ceramic, metal, or steel reinforced concrete, are often considered as orthotropic or anisotropic materials [1]. It has been widely recognized that crack propagation in such type of materials should be appropriately governed by mixed mode models [2]. Since the early studies the stress and displacement fields of crack tip by Sih and Liebowitz [3] and Wu [4], considerable attention has been given to this problem in ideally brittle isotropic materials. However, there was little research which focused on the mixed-mode crack propagation of orthotropic or anisotropic materials. Development on those problems were made by Saouma et al (1987) [5], Ye & Ayari (1994, 1995) [6, 7], in which the classical fracture theories were extended to anisotropic solid cases. But, one important characteristics shape and size of the plastic zone at crack tip in anisotropic solids was not showed in literatures. Based on the earlier work on the characterization of plastic zone by Ye (1995/6) [8], this paper presents analytical and numerical estimations of fracture plastic zone size and shape at crack tip in anisotropic solids. Some models of anisotropic materials will be discussed by using uniaxial stress and biaxial assumptions. For uniaxial stress assumption, three models will be presented for softening models. For biaxial stress * Correspondence Author: Fax: 86-21-66134021, email: zmve(«!yc.shu.edu.cn
Simulations of Plastic Zone at Crack Tip
429
assumption, Hill's yield criterion (see Ref. [1]) is adapted to seek the shapes of plastic zone. A finite element technique was also applied to verify the theoretical model.
ANALYTICAL AND NUMERICAL SIMULATIONS ON CRACK TIP FIELD hi this section, instead of the single component, ay, a biaxial state of stress around the crack tip will be considered. As such, the near crack tip stress field is substituted into the expression of a yield function, which is appropriate to anisotropic solids. Then the yield radius can be solved as a function of the polar angle 6 and the ratio Ku I Kj = m . This approach is very similar to the uniaxial Irwin's first order approximation. The only difference is that a surface, as plastic zone ahead of the crack tip, should be sought to determine the shape of the plastic zone using one of the appropriate yield surfaces to anisotropic solids. For this purpose, an approximate general yield function is taken as the form of following quadratic function: F{ay -azy+
G{az -ax}r2x + H{CTX -ay}
+ 2Lz2y2 + 2MT2X + 2Nr2xy =1
(1)
where. F, G, ..., N are the constants of materials. Equation (1) was utilized by Hill (1948) and was applied, in Hill (1950), to a number of technological problems. Also, the yield function can be expressed by the principal stress. First, we note that, in general, when the reference axes are principal axes, the shear stress components vanish and Eq. (1) can be written in the form of F(a2 -aj+
G(<73 -
(2)
If X, Y and Z are the tensile strengths in the principal directions, the Eq. (2) predicts 0)2=l
(3)
or G + H = l/X2
(4)
H+F = l/Y2
(5)
F+G = l/Z2
(6)
Similarly,
The principal stress field at the crack tip can be obtained. For plane problem, the principal stresses are
430
Simulations of Plastic Zone at Crack Tip
and the following expressions could be obtained
m
-FIy-mFIlyJ
+4^
+
mFIIJ (8)
Plane Stress State Here, we consider a case in plane stress state firstly. In this case, the stresses are in the conditions: az = %zx = ryz = 0, in which, az is one of the principal stresses, of + a2 - [2R /(l + R)\j,a2 = Y2
(9)
where, R = 2{z IY)2 -1. Substitute the principal stresses given by Eq. (8) into Eq. (9), then we can get the following expression, which presents the boundary of the plastic zone, as a function of 8, that is
^
^
{
^
(10)
in which
+ mFm + Fiy
+ >»FIIy
F.-rnF, ryy+4{Fby+>r
F,J
Plane Strain State In the same way, we have
r = r(9) =
AnY2
'+
2
(12)
here,
r n=4A 2 2
(13a,b,c)
r i =A 2 + (l-2v)A 1 ' and k = HY2. Parametric Study Three assumptions are used in the following analyses: i) The crack is aligned in direction 1 and assumed to correspond to one of the two major planes of elastic symmetry (corresponding to an ortho tropic case); ii) The crack tip is subjected to a mixed mode loading, I-II mode;
Simulations of Plastic Zone at Crack Tip
431
iii) To simplify the numerical calculation, we assume a polar variation of the toughness of the form:
*± = Ef
(14)
^
(15)
and a modulus G12 given by G12=
E1 + E2 +2vl2E2
The characteristic equation is given by [6,7] s4+(l + El/E2)s2+El/E2=0
(16)
which would yield s = ±i if El = E2. If we assume n
K m = — K,n— , n = •E.
(17a,b,c)
Dx = cos 8 + n sin 9 and 0< w< 10 and 0.1<w<10, m = 0 represent a pure mode I case, m = \0 represents an approxamte pure mode II case (numerically this assumption is very close to similarly pure mode II loading), and m-\, represents a mixed mode I-II case. A large number of engineering materials, e.g. roller concrete for dams, etc, was observed in conjunction with their tabulation of elastic properties with fifteen different anisotropic parameters [1-7] and should be considered as under mixed mode I-II.
NUMERICAL EXAMPLES OF PLASTIC ZONE SHAPES Numerical examples of this model are shown in Fig. 1 in which the shapes of plastic zone for different values of the ratio Kn I Kl and different material parameters, were obtained under plane stress conditions with Hill's yield criterion. A finite element technique for 2-D problem was applied to verify the estimated plastic zone shape. Here, the quarter point singular element model proposed by Barsoum in [9] and Hill's yield model were also adapted to seek the boundary line between elastic and plastic zones. Similarly, the parameters of models were the same as the ones of previous analysis, i.e. the orthotropic cases. The numerical simulations of plastic zone shapes at crack tip in orthotropic solid were shown in Figs. 2(a) and 2(b). It was found that there were similar characteristics between analytical and numerical estimations. It is of interest to notice that those kinds of plastic zone characteristics carried out the effects of fracture toughness measurements experimentally in the condition of the linear-elastic fracture field.
Simulations of Plastic Zone at Crack Tip
432 G
-
-
n-IO
\
A
B-O.l 10
i Crack
5
2 V
2
'f\
/m=IO
1
-5
Craot'
H. /
•
ft'
V, 1
4
10
-
6
-15
-10
IS
-5
-15
(a)
- 1 0 - 5
0
5
10
15
(b)
FIGURE 1 Numerical simulations on the shape of plastic zone at crack tip by present analytical model in which (a) n=10 and (b) n=0.1, respectively.
(a)
(b)
FIGURE 2. Numerical simulations on the shape of plastic zone at crack tip by finite element analysis, in which (a) n=10 and (b) n=0.1, respectively.
ACKNOWLEDGMENTS The financial support of Sciences Fund of Shanghai Education Committee for Scholars, is gratefully acknowledged. REFERENCES [1] H. Liebowitz, Fracture, An advanced treatise, Vol. II, Academic Press, New York & London, (1968). [2] F. Erdogan and G.C. Sih, J. Bos. Engng., 85, 519-527, (1963). [3] G.C. Sih, Int. J. Fracture Mech., 10, 305, (1974). [4] E.M. Wu, Composite Materials Workshop (Edited by Tsai, Halpin and Pageno), 20-43, Technonic Press, Stanford, CT (1968). [5] V. E. Saouma, MX. Ayari & D. A. Leavell, Engng. Fracture Mech., 27, 2, 171-189, (1987). [6] Zhiming Ye & M.L. Ayari, Engineering Fracture Mechanics, 49, 6, 797-808, (1994). [7] M.L. Ayari, & Zhiming Ye, Engineering Fracture Mechanics, 52, 3, 389-400, (1995). [8] Zhiming Ye, International Journal of Fracture, 74, 1, R3-R10, (1995/6). [9] R.S. Barsoum, Int. J. Num. Meth. Eng., 10, 25-38, (1976), 11, 85-98, (1977).
Application of Essential Work of Fracture Methodology to Polymer Fracture Kai Duan, Xiaozhi Hu School of Mechanical Engineering University of Western Australia Perth, Australia Yiu-Wing Mai Center for Advanced Materials Technology School of Aerospace, Mechanical and Mechatronic Engineering University of Sydney, Australia
ABSTRACT The applicability and limitation of the essential work of fracture model originally proposed for double-notched polymer and metal specimens with full ligament yielding prior to failure are studied using two sets of ABS polymer results measured with threepoint-bend specimens without full ligament yielding. The model is then extended and related to a simple fracture mechanics model on the local fracture energy distribution, which is originally developed for quasi-brittle fracture of concrete-like materials. Both models lead to the conclusion that the height of the crack-tip plastic zone controls the fracture toughness of materials, and the specific fracture energy dissipation along a crack path.
INTRODUCTION The essential work of fracture (EWF) model [e.g. 1,2] has been successfully used to analyze the specific fracture energy of double-notched polymer and metal specimens with full ligament yielding prior to failure. Recently, EWF has also been used to the plane strain fracture of ABS three-point-bend (3-p-b) specimens [3] that clearly do not satisfy the full ligament yielding condition prior to the final failure. In this paper, we are going to discuss the applicability and limitation of EFW, and show why EFW can still be used even if the full ligament yielding is not satisfied. The key argument is that the specific fracture energy Gf dealt with by EWF can always be determined experimentally regardless the ligament condition. SPECIFIC FRACTURE ENERGY Gf Interestingly, the quasi-brittle fracture of concrete-like materials is also frequently characterized by the specific fracture energy Gf as used for yield failure of polymers and metals. RILEM has set up a standard for Gf measurements of concrete [4]. Similar to the case of EWF for polymers and metals, a stable load (P) and load-point displacement •"Corresponding author, Fax: 61-8-9380-1024, Email: [email protected]
434
Application of Essential Work of Fracture Methodology to Polymer Fracture
(S) curve is required so that G/ can be evaluated from the total energy consumption over the initial ligament area.
where B is the specimen thickness, W is the width and a is the initial crack (or notch) length. In the case of a double-notched specimen, the total width (2W) and the total crack length from two notches (2a), as commonly denoted, should be used. Clearly, the specific fracture energy Gf as used by RTLEM and EWF is only an average fracture energy measurement, which is equivalent to assuming a constant fracture energy distribution over the entire fracture area. Such a simplified assumption has to be limited to special material and specimen conditions. To extend the applicability of the specific fracture energy G/ adopted by RILEM and EWF, a local fracture energy distribution concept has been proposed [5,6]. The local specific fracture energy gf is used to describe the energy dissipation along the crack path, over the fracture area of B-(W-a). Both G/and g/are related according the energy conservation principle. 1
W-a
If the local fracture energy distribution gyis indeed constant over the crack path, 0 < x < W-a, as assumed, then G/=gf= constant, and the RILEM definition which is also used by EWF is valid. Clearly, the local specific fracture energy concept extends the applicability of the RILEM definition and EWF. EWF: THE RELATIONSHIP BETWEEN G/AND LIGAMENT A typical double-notch specimen used by EWF is shown in Figure l(a). For the deep notch geometry, a circular plastic zone with the radius of (W-a) prior to fracture is adequate. EWF shows that the following linear relationship exists for polymers and metals. Gf = go + constant -(W-a)
where go is the essential work of fracture corresponding to zero plastic zone size. The non-essential work of fracture, gp, is related to the plastic zone size, which can be evaluated from the volume of the plastic zone for a constant plastic work density pp. _ 8p
(thickness • length • height | Pp
{
thickness-length (
J plasticzone
B-(2W-2a)-(2W-2a)]
= pn • constant p I
LA
-
B-(2W-2a)
v
v
= p • (constant • height) ^P
y
5
= constant -(W — a)
-plastic zone
...
l
) , t. '
' plastic zone
(4) '
K
Application of Essential Work of Fracture Methodology to Polymer Fracture
(a)
435
(b)
(a) Full yielding due to deep-notch influence (b) Full yielding due to specimen back-face influence
FIGURE 1 (a) Common EWF specimen showing the influence of deep double notches on the plastic zone and then Gf, and (b) deep single notched EWF specimen showing the influence of specimen back-face on the plastic zone and then Gf.
As shown by equations (3) and (4), the linear relationship between Gf and ligament 2-{W-a) actually proves that Gf is directly related to the crack-tip plastic zone height measured by 2-{W-a). The yield condition shown in Figure l(a) can also be satisfied by a single edge notched specimen either under direct tension or bending (e.g. 3-p-b) as illustrated in Figure l(b), where the full ligament length is given by (W-a) and equations (3) and (4) are still valid. Obviously, the full ligament yield can only be achieved for a very deep notch or crack. In this case, the crack-tip condition can also be considered under the strong influence of the specimen back-face boundary. When the boundary is far away from the crack tip, full ligament yield is not possible. However, it has been shown that EWF could still be used to ABS 3-p-b specimens without full ligament yield [3], which shows EWF can be extended to cases without full ligament yield. BOUNDARY EFFECT MODEL AND LOCAL ENERGY DISTRIBUTION Recognition of the boundary influence from Figure l(b) is important. The classic EWF can be considered modeling the specimen back boundary influence, a case dealt with frequently for quasi-brittle fracture of concrete-like materials. Similar to Gf of polymers and metals modeled by EWF, Gf of quasi-brittle materials like concrete is also found to be ligament and specimen size dependent. The fracture process zone (FPZ) in front of a crack tip in a quasi-brittle material like concrete is similar to a crack-tip plastic zone in a ductile polymer or metal. If a concrete specimen has a deep notch or crack as shown in Figure l(b), FPZ covers the whole ligament showing the strongest back boundary influence. If a crack tip is far away from the specimen back-face boundary, a fully developed FPZ without any back-face boundary influence is expected. The RILEM Gf definition does not require the condition that FPZ has to cover the entire ligament area. A simple boundary effect model has recently been developed [7-9], based on the local fracture energy concept proposed by Hu and his colleagues [5,6]. The full ligament region in a specimen with a single edge notch or crack has been separated into the inner and boundary zones illustrated in Figure 2(b). In the inner zone, the crack-tip FPZ is far away from the specimen back boundary, and can thus remains constant or shows no boundary effect. In the boundary zone, development of the crack-tip FPZ is restricted by
436
Application of Essential Work of Fracture Methodology to Polymer Fracture
the ligament as FPZ is too close to the specimen back-face boundary. This is akin to the full ligament yield in a polymer or metal specimen modeled by EWF. (a)
W-a Inner Zone
; Boundary Zone, a^
(b)
11'/
I-IV.
FPZ
W-a FIGURE 2 Separation of inner and boundary zones by a/* in a specimen of width W and crack a. (a) Corresponding bi-linear local energy gf distribution in comparison with the RILEM Gf as the average fracture energy, (b) Variation of FPZ and its height hFpz in the inner and boundary zones.
If a linear function is assumed for the local specific fracture energy gf as shown in Figure 2(a), it can be obtained from equation (2) that: (W-a) 2a\
W-a
•a'i
2(W-a)
W-a>a]
where GF is the maximum stable specific fracture energy in the inner zone. For a large specimen with a crack-tip away from all the specimen boundaries, GF is identical to the critical strain energy release rate G/C. The transitional ligament length a* is used to separate the inner and boundary zones as illustrated in Figure 2. Clearly, in the boundary zone where {W-a) < ai, equation (5) is identical to EWF or equation (3). Therefore, the linear relationship between Gf and ligament (W-a) as proven by EWF implies a linear local fracture energy distribution over the ligament area. ANALYSIS OF ABS 3-p-b RESULTS The specific fracture energy Gf of ABS-740 was measured using 3-p-b specimens [3]. The span is 56 mm, depth Wis 14 mm, and thickness B = A and 7 mm respectively. Two testing temperatures were 20 and 80 °C. The 20 °C results were measured using only the specimens with thickness B = l mm, and are shown in Figure 3(a). Even after excluding the two solid points that were questionable as discussed by the original authors, the relationship between Gf and (W-a) is clearly not always linear. Applying equation (5) to the results, it is found that g0 =
Application of Essential Work of Fracture Methodology to Polymer Fracture
437
3.35 N/mm, GF = 20.6 N/mm, and the transitional ligament length a* separating the inner and boundary zones is 5.8 mm. The curve from equation (5) is also provided. It should be noted the saturated specific fracture energy GF is higher than the experimental Gf values.
T = 80 °C B = 4mm 5
W-a (mm)
10
W-a (mm)
FIGURE 3 The comparison of the Gf predicted using Eq. (5) with experimental data [3]. The solid and dashed curves in (b) and (c) are obtained using different g0 values and an identical g0 value as listed in Table 1.
The 80 °C results were measured using the specimens with thickness of 4 and 7 mm, and are shown in Figures 3(b) and 3(c). Again, the relationship between G/and (W-a) is clearly not linear for the results in Figure 3(b). Two slightly different approaches are adopted in the present study. First, the two sets of experimental results with B = 4 and 7 mm can be used separately to determined their own go and GF values. Second, the same go can be assumed for both sets of experimental results if both specimens with B = 4 and 7 mm satisfy either the plane stress or strain condition at the same time. The results from equation (5) are listed in Table 1. The saturated GF is almost identical for both approaches for a given thickness of either 4 or 7 mm. The essential work of fracture go estimated appears to be thickness dependent if we assume the specimens with B = 4 and 7 mm are influenced by the plane stress condition. A higher go for the specimens with thickness B = A mm is consistent with the well-known plane stress fracture toughness behavior. The thickness dependence of GF is also consistent with the explanation. The single go assumed to be applicable to both specimens of B = 4 and 7 mm is 5.96 N/mm, between the two separate go values of 4.97 and 6.48 N/mm. The curves from equation (5) are plotted in Figures 3(b) and 3(c) for the two different approaches.
438
Application of Essential Work of Fracture Methodology to Polymer Fracture TABLE I 80 °C results from Equation (5) Identical g0
Different go 5 (mm) go (N/mm) GF(N/mm) d[ (mm)
7 4.97 13.80 3.50
4 6.48 15.12 7.82
7
4 5.96
14.06 4.40
15.11 7.27
DISCUSSIONS AND CONCLUDING REMARKS The non-linear Gf measurements of ABS polymer following the EWF methodology have been explained by introducing the concept of local fracture energy gf distribution, which extends the applicability of EWF. As a result, the full ligament yield in a polymer specimen prior to final failure is no longer necessary. A linear Gf and ligament (W-a) relation described by EWF implies a linear local fracture energy gf distribution in the specimen back-face boundary region, which is directly related to the plastic zone height at the crack tip. The conclusion that the crack-tip plastic zone height controls the fracture energy dissipation is significant, as the same linear Gf and ligament (W-a) relation can also be taken as the Gf and plastic zone height relation. This conclusion has led to a simple fracture mechanics model [10] recently proposed for the adhesive thickness effect on fracture toughness of adhesive joints, which is a case where the crack-tip plastic zone height is identical to the adhesive thickness. ACKNOWLEDGEMENTS The financial support from the Australian Research Council (ARC) through a Discovery Projects grant is acknowledged. REFERENCES 1.
Cotterell, B. & Reddell, J.K. 1977. "The Essential Work of Plane Stress Ductile Fracture," Int. J. Fract, 13: 267-277. 2. Atkins, A.G. & Mai, Y.W. 1985. Elastic and Plastic Fracture: Metals, Polymers, Ceramics, Composites, Biological Materials. Ellis Horwood Ltd., Chichester. 3. Luna, P., Bernal, C , Cisilino, A., Ftontini, P., Cotterell, B. and Mai, Y. -W. 2003. "The Application of the Essential Work of Fracture Methodology to the Plane Strain Fracture of ABS 3-Point Bend Specimens," Polymer, 44: 1145-1150. 4. RILEM TC-50 FMC, 1985. "Determination of the Fracture Energy of Mortar and Concrete by Means ofThree-Point Bend Tests on Notched Beams," Mater. Struct, 18:287-90. 5. Hu, X. Z. 1990. Fracture Process Zone and Strain Softening in Cementitious Materials. ETH Building Materials Reports No.l, ETH Switzerland. (AEDIFICATIO Publishers, 1995). 6. Hu X.Z, Wittmann F.H., 1992. "Fracture Energy and Fracture Process Zone," Mater. Struct. 25: 319326. 7. Duan, K., Hu, X.Z., Wittmann, F.H. 2002. "Explanation of Size Effect in Concrete Fracture Using Non-Uniform Energy Distribution," Mater. Struct., 35:326-331. 8. Duan, K., Hu, X.Z., Wittmann, F.H. 2003. "Boundary Effect on Concrete Fracture and Non-Constant Fracture Energy Distribution," Eng. Fract. Meek, 70:2257-2268. 9. Duan, K., Hu, X.Z., Wittmann, F.H., 2003. "Thickness Effect on Fracture Energy of Cementitious Materials," Cem. Concr. Res., 33(4):499-507. 10. Duan, K., Hu, X.Z., Mai, Y.W. 2003. "Substrate Constraint and Adhesive Thickness Effects on Fracture Toughness of Adhesive Joints", J. Adhesion Science and Technology, in press.
Three-Dimensional Micromechanics Analysis of Strain Energy Release Rate Distribution along Delamination Crack Front in FRP Hiroshi Tanaka and Yoshikazu Nakai Department of Mechanical Engineering, Kobe University, Japan
ABSTRACT The effect of fiber/matrix interfaces on the distribution of local strain energy release rates along crack front was studied by using a three-dimensional inhomogeneous model of a unidirectional FRP. For a crack with a straight crack-front line perpendicular to fibers, the local strain energy release rate along the crack front takes a maximum value at the crack-front point closest to the fiber/matrix interface. This result suggests that a crack with a straight front line starts to grow at the nearest crack-front point to interfaces and the crack growth in the region far away from interfaces follows behind.
INTRODUCTION Crack growth along fibers is one of the most prevalent failure mechanism for fiber-reinforced plastics (FRP). Most of researches on crack growth in FRP were on the basis of the macromechanics where FRPs were regarded as homogeneous orthotropic materials. However, to analyze damage processes in FRPs, a micromechanical analysis of the local stress state around crack tip is important. For cracked FRP plates, two-dimensional analyses by periodically layered models [1-2] and three-dimensional analyses by using a model containing cylindrical fibers [3-4] have been carried out by several researchers, but little attempt has been made to investigate the three-dimensional elastic stress state around crack tip. hi the present study, the elastic stress analysis of continuous fiber-reinforced plastics containing a crack parallel to fibers was conducted by using a three-dimensional inhomogeneous FRP model, and the effect of fiber/matrix interfaces on the distribution of the local strain energy release rate was discussed. ANALYSIS Problem Statement The three-dimensional elastic analysis of a unidirectional FRP plate with a uniform thickness as shown in Figure 1 was conducted. Figure l(a) shows a mode I problem for a center-cracked plate with a width of 2PF=4mm subjected to tensile stress, a. Figure l(b) shows a mode II problem for an edge-cracked plate with a width of W=2mm where the *Corresponding author, Department of Mechanical Engineering, Kobe University, 1-1, Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan, Fax: +81-78-803-6107 e-mail: [email protected]
Analysis of Strain Energy Release Rate Distribution
440 a
r tT 111111
'7, V ~ t ' «?I^* •'
o
u
o
o
o
c;
(;
z
Crack \
Crack
a=2mm
<
a=1mm
Fiber direction
W=2mm
<
(a) Mode I problem
1
>
Fiber direction
Umim 2W=4mm
A
>
(b) Mode II problem
FIGURE 1 Mode I and mode II problems
lower end is fixed and the upper end is subjected to uniform tangential displacement, w, as shown in the figure. The crack has a length of a=lmm (a/W=0.5) and is parallel to the fiber direction (z-direction) for both mode I and II problems. Inhomogeneous FRP Model We consider an inhomogeneous FRP model as shown in Figure 2(a) where circular cylindrical fibers are arranged in a square array with a pitch of £>=9.14um. The fiber diameter is d=8\xm and the fiber volume fraction is 60%. For all analyses in the present study, the crack plane is parallel to fibers and the crack-front line is perpendicular to the fiber axis, that is, z=constant. For a homogeneous orthotropic plate, the strain distribution along crackfrontis nearly uniform except near the plate surfaces. Therefore, in view of symmetry, an interior region with a thickness of D/2 containing only half of each fiber as shown in Figure 2(b) was analyzed under plane strain condition. The inhomogeneous FRP region contains every two fibers in the upper and lower sides of the crack plane. This region containing the crack tip has a length of 0.4 W in the fiber direction and is surrounded by homogeneous FRP as
Matrix
A Inho Tiogeneous FRF
x=DI2
(a) Arrangement of fibers (b) Inhomogeneous FRP (c) Model for analysis FIGURE 2 Arrangement of fibers in inhomogeneous FRP model
Analysis of Strain Energy Release Rate Distribution
441
illustrated in Figure 2(c). The height of the cracked matrix layer, t, is defined as shown in Figure 2(b). When tl{D-d)=\, t is equal to the height of other matrix layers. Finite Element Analysis The finite element analysis was carried out by the MARC software. For mode I loading, the right half of the FRP plate shown in Figure l(a) was modeled because of symmetry. The finite element model used is composed of 8000-10000 quadrilateral solid elements for both mode I and IT problems. The strain energy release rate was calculated from the modified crack closure integral method [5]. The matrix corresponds to isotropic epoxy with the Young's modulus of £'m=3.5GPa and the Poisson's Ratio of vm=0.35. The fibers are transversely isotropic graphite with the elastic constants of £3=295GPa, £i=17.5GPa, G3i=15GPa, v3i=0.3 and vi2=0.5. The elastic constants of homogeneous FRP were determined from the relationship between mean stresses and mean strains calculated by using the inhomogeneous FRP model without cracks. RESULTS AND DISCUSSION Distribution of Local Strain Energy Release Rate Figure 3 shows the distribution of the local strain energy release rate along crack front for tl{D-d)=\, where the crack is placed on the midplane between adjacent fibers. The abscissa is the x-coordinate of points on the crack front defined as illustrated in this figure. In the case of homogeneous FRP, the local strain energy release rate is constant along crack front. On the other hand, in the case of inhomogeneous FRP, the local strain energy release rate takes a maximum value, GmaX) at the crack-front point closest to the
^°- 2 F
^0.8
Model C,7 D 0.6
x=o
i
CD
x=DI2
0)
0.4
cp P
Homogeneous FRP 0.2
"8
I
i
)
/ x=0
\ ro
I
Mode II
V
0.1
Homogeneous FRP
u
x=DI2
'
/tetoaxtn
Inhomogeneous FRP~
e=0 f/(D-d) = 1.0 II 0.0 0.2 0.4 0.0
-a I 0.6
(D N
I
0.8
1.0
Location along crack front, x/(D/2)
Inhomogeneous FRP e=0 t /(D-d) = 1.0 II I I
0.0 0.0
0.2
0.4
0.6
0.8
1.0
Location along crack front, xl(DI2)
(a) Mode I (b) Mode H FIGURE 3 Distribution of strain energy release rate along crackfront
Analysis of Strain Energy Release Rate Distribution
442 Large 6
K—\ //* 1
X
Fatigue crack
Small G
-Large G
-•>
Crack-
\( \ (a) Distribution of strain energy release rate for cracks with straight front
(b) Front shape of a real fatigue crack observed on fracture surface (mode II).
FIGURE 4 Front shape of real crack
fiber/matrix interface (x=Q) and decreases as x increases away from fibers for both mode I and II cracks. This result suggests that a crack with a straight front line as illustrated in Figure 4(a) starts to grow at the nearest crack-front point to interfaces and the crack growth in the region far away from interfaces follows behind. Therefore, a real crack has a bow-shaped front line as shown in Figure 4(b). Effect of Height of Cracked Matrix Layer Figure 5 shows the ratio of the maximum energy release rate along crack front Gmax (at to the minimum rate Gm;n (atx=D/2) as a function of the height of the cracked matrix layer, t/(D-d). The value of Gmax/Gmm decreases with the increase of the height of the cracked matrix layer and the strain energy release rate along crack front is nearly uniform for t/(D-d)>7, that is, t>d (the height of the cracked matrix layer is more than the fiber diameter).
JC=O)
3.0
1
1
1
D
1
o Mode 1
2.5
•
Mode II
on
2.0 1.5 -
-
B
-
CP
Q
1.0 0.5 0.0 0
-
o
9
CftlQjO O_
V, = 60% e=0 1
1
I
1
2
4
6
8
10
Normalized height of cracked matrix phase, t /(D-d) FIGURE 5 Effect of matrix-phase height on Gmax IGmm .
Analysis of Strain Energy Release Rate Distribution
443
Effect of Crack Eccentricity A three-dimensional analysis of an eccentric crack away from the midplane between adjacent fibers was also conducted. An eccentric crack may be under a mixed-mode state microscopically, even if it is under macroscopically pure mode I or II condition. Figure 6(a) shows the shape of the eccentric crack in the section perpendicular to the fiber axis. For 2elt<\, the eccentric crack is a plane crack, while for 2elt>\, a part of the eccentric
0.8
1
1 2e/( = 0 2e/t = 0.613 2e/t = 2.065 -
o
CD
•
0.6>», 0.4 -
x=DI2
8
0.2 ~tl(D-d)= 1.0 Macroscopic
2e/t < 1
1
0.0 0.0
2e/f > 1
mode 11
1
0.2
0.4
I
I
0.6
0.8
1.0
Location along crack front, xl{D/2)
(a) Definition of e
(b) Distribution of total strain energy release rate FIGURE 6 Distribution of total strain energy release rate along front of eccentric cracks
2.0
tl{D-d) = 1.0
2.0 Macroscopic mode I 2e/f=0.613
cf
Macroscopic mode I 2e/t= 2.065
1.5
c|
1.5 Interface
Matrix
I.OmDDDDDDDDDDDDDDO CD
CD D
qo = 1S 0.5
o
0.0
0.2
0.4
C3,/GT
d
O G,,/GT
1 0.5
•
CD
0.6
6,,,/G,
0.8 1.0
Location along crack front, xl(DI2)
G,,/GT 0.0' 0.0
0.2
0.4
0.6
0.8 1.0
Location along crack front, xl{DI2)
(a)2e/< = 0.613 (b) 7e/t = 2.065 FIGURE 7 Change of rrode ratio along front of eccentric crack
444
Analysis of Strain Energy Release Rate Distribution
crack is an interface crack and the remaining portion is a matrix crack. Figure 6(b) shows the distribution of the total strain energy release rate, Gj, along the front of the eccentric crack under macroscopically mode I condition. For 2e/tl, the value of Gj increases locally near the boundary between the interface and matrix region. Figure 7 shows the mode I, II and III components of the strain energy release rate for eccentric cracks under macroscopically mode I condition. For 2e/t<\, there are little mode II and mode III components at the front of eccentric cracks. For 2e/t>\, the mode II and III components are generated in the neighborhood of the boundary between the interface and matrix region. CONCLUSIONS (1) For a crack with a front line perpendicular to the fiber axis, the local strain energy release rate takes a maximum value at the crack-front point closest to the fiber/matrix interface and decreases with increasing distance from fibers under both mode I and II loading. (2) For an eccentric crack, a part of which is an interface crack, the mode II and III components of the strain energy release rate are generated in the neighborhood of the boundary between the interface and matrix region, even if the crack is under pure mode I condition macroscopically. REFERENCES 1. 2. 3.
4. 5.
Kimachi, H., H. Tanaka and K. Tanaka. 1999. "Transition from Small to Large Interlaminar Cracks in Fiber-Reinforced Laminated Composites," JSME Int. Journal, Series A, 42(4):537-545. Jha, M. and P. G. Charalambides. 1998. "Crack-Tip Micro Mechanical Fields in Layered Elastic Composites: Crack Parallel to the Interfaces," Int. J. Solids Struct., 35(1-2):149-179. Crews, J. H., Jr., K. N. Shivakumar and I. S. Raju. 1992. "A Fibre-Resin Micromechanics Analysis of the Delamination Front in a Double Cantilever Beam Specimen," in Phase Interaction in Composite Materials, A. Paipetis and G. C. Papanicolaou, eds. Oxon: Omega Scientific, pp. 396-405. Dubois, F. and R. Keunings. 1997. "DCB Testing of Thermoplastic Composites: A Non-Linear Micro-Macro Numerical Analysis," Comp. Sci. Tech., 57:437-450. Rybicki, E. F. and M. F. Kanninen. 1977. "A Finite Element Calculation of Stress Intensity Factors by a Modified Crack Closure Integral," Eng. Fract. Meek, 9:931-938.
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour during Mode I Fracture in Glass Fibre Composites S. Feih*, B.F. S0rensen Materials Research Department, Ris0 National Laboratory, Denmark
ABSTRACT The mode I fracture toughness of glass fibre reinforced composites is studied by measuring the effect of fibre cross-over bridging in DCB specimens under pure bending moment. Bridging laws were obtained by simultaneous measurements of the crack growth resistance and the end opening of the notch end. For a given composite system, the constants of the bridging law depend on the interfacial properties of the fibre/ matrix interphase. A micromechanical model is used for relating the microscale parameters, such as the interfacial fracture energy, to the macroscopic bridging law. The microscale parameters are determined from investigations in the environmental scanning electron microscope.
INTRODUCTION Interfacial properties of glass fibre composites are controlled by the sizing, which is applied to the glass fibres during manufacture. For the same matrix system, a change of sizing results in changes of these properties, thereby influencing the mechanical properties such as strength and fracture toughness. The concept of strength is used for characterising crack initiation in composite design, while fracture toughness determines crack growth and damage development, hi this article, the influence of the interfacial properties on the crack growth parallel to the fibres during mode I fracture is investigated. PRINCIPLE OF MEASURING BRIDGING LAWS The approach for the measurements of bridging laws is based on the application of the path independent J integral [1], and has been used recently to determine the bridging characteristics of unidirectional carbon fibre/ epoxy composites [2] and glass fibre composites [3]. A symmetric DCB specimen is loaded with pure bending moments M (FIGURE 1). This specimen is one of the few practical specimen geometries, for which the global J integral (i.e. the integral evaluated around the external boundaries of the specimen) can be determined analytically [1]: M b H^3 E n 2
(
1
)
'Corresponding Author, Materials Research Department, Ris0 National Laboratory, P.O. Box 49, 4000 Roskilde, Denmark, Tel: 0045 4677 5787 / Fax: 0045 4677 5758, E-mail: [email protected]
446
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour
En is the Young's modulus referring to the material directions, V13 and v3i are the major and minor Poisson's ratio, b is the width and H the beam height.
2H
M' FIGURE 1 DCB specimen with pure bending moment
Now consider the specimen having a crack with bridging fibres across the crack faces near the tip. The closure stress a (x2-direction) can be assumed to depend only on the local crack opening 8, i.e. the crack grows in pure mode I. The bridging law a = a(8) is then taken as identical at each point along the bridging zone. Since fibres will fail when loaded sufficiently, we assume the existence of a characteristic crack opening So, beyond which the closure traction vanishes. Shrinking the path of the J integral to the crack faces and around the crack tip [4] gives p,
(2)
where JtiP is the J integral evaluated around the crack tip (during cracking Jtip is equal to the fracture energy of the tip, Jo). The integral is the energy dissipation in the bridging zone and 5* is the end-opening of the bridging zone at the notch root. The bridging law can be determined by differentiating equation (2) [4].
Thus, by recording JR and the end opening of the bridging zone 8*, the bridging law can be determined. This approach models the bridging zone as a discrete mechanism on its own. Contrary to crack growth resistance curves (R-curves), the bridging law can be considered a material property and does not depend on specimen size [4], EXPERIMENTAL METHODS Composite specifications We investigated two commercial E-glass fibre systems with the same fibre diameters (~l7\im ± 2|xm), but different silane-based sizings. Sizing A is described as multi-purpose compatible, while sizing B is epoxy compatible. A detailed chemical analysis of the two fibre sizings, which clearly showed differences regarding the surface groups, can be found in [5]. The two resin types consist of a bisphenol Abased epoxy resin and an orthophthalic polyester resin. An in-house developed resin transfer moulding technique was applied for the composite manufacture. The epoxy
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour
447
resin was cured at 120°C for six hours, and the polyester resin was cured at 50°C for 24 hours. The nominal fibre volume fraction was 55%. Crack bridging tests The specimen width b was 5 mm with a beam height of H=8 mm (FIGURE 1). The length of the specimen was 145 mm. The notch, cut with a 0.7mm diamond saw for a length of 36 mm, was parallel to the fibre direction and perpendicular to the plane of the plate. The subsequent crack growth was therefore intralaminar. At least 5 specimens of each fibre/ matrix type were tested. Extensometers were mounted at each face of the specimens just at the end of the notch to record 6 as a function of the applied bending moment. The crosshead displacement was kept at 2 mm/min, which corresponds to 0.15mm/min for the end opening rate d8*/dt (t denotes time). EXPERIMENTAL RESULTS With increasing applied moment, crack propagation took place. Fibre cross-over bridging developed in the zone between the notch and the crack tip. FIGURE 2 shows the bridging fibre ligaments for the different systems at the end of the test. With increasing opening, the bridging fibres eventually broke at the end of the notch for the epoxy systems. This point represented the start of the steady state cracking, where the bridging length remained approximately the same, and the bridging zone moved forward with the crack tip advancing into the specimen. The behaviour is nearly identical for the other epoxy composite. For the polyester resin systems, crack bridging was considerably more extensive.
(a) sizing A/ epoxy
(b) sizing B/ epoxy
(c) sizing A/ polyester
(d) sizing B/ polyester
FIGURE 2 Crack bridging behaviour of composite systems
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour
448
JR is calculated according to equation (1). Assuming that the unidirectional composite is transversely isotropic, the following elastic composite data were applied for equation (1) as previously measured: EnjepOxy= 41.5 GPa, E33= 9.2 GPa, En, polyester = 42 GPa, E33, pOiyester= 10 GPa and vi3=0.3 (assumption). The function 1/2
for8*<8 n
<(§*)= Jo
(4)
was found to fit all experimental data curves well, resulting in curve fits for the crack growth resistance JR as shown in FIGURE 3(a). Jo is the initial value of the experimental curve and equal to the fracture energy of the tip during crack growth, while AJSS, which is equal to (Jss-Jo), is the increase in crack growth resistance. S0rensen and Jacobsen [2] found that the same function fit the data of carbon fibre composite systems well. 6000 -•—A/ epoxy -"- B / epoxy —*-A/polyester ~»--B/ polyester
I 2
4000
E 1
2000
f
—•—A:/ epoxy -•- Bi/ epoxy -*-A'l polyester --•—Bi/polyester
£5
o
2 4 6 Crack opening [mm]
CO
^•^—f-"*—•0
8
MM*—ft—m-
2 4 6 Crack opening [mm]
(a)
(b)
FIGURE 3 Comparison of (a) crack growth resistance and (b) resulting crack bridging laws
The experimental values for the bridging laws are given in TABLE I. The starting value Jo indicates the point of crack growth initiation and can easily be determined during the experiment. The highest value of 355 J/m2 was observed for the sizing B/ epoxy system. The crack initiation value is significantly lower for the sizing B/ polyester system with 115 J/m2, which also relates to a significantly lower transverse strength of not more than half the transverse strength of the other composites [3]. TABLE I Experimental bridging law parameters for the different fibre/matrix systems Composite system sizing A/ epoxy sizing B/ epoxy sizing A/ polyester sizing B/ polyester
Jo [J/m2] 300±40 355±15 170±20 115±45
AJSS [J/m2l 4000±1000 3700±500 -3800 >4100
So [mm] 2.0±0.2 2.0±0.2 -5.5 >5.0
X [kPa m1'2] 44.7 41.4 25.6 29.0
The end opening value 5o at the onset of steady-state cracking was determined to be 2 mm for the epoxy systems. For the sizing B/ polyester system, steady-state cracking could not be determined with the present specimens, as the fibres continued to bridge
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour
449
the whole length of the crack after the maximum measurable end opening of 5 mm was obtained. Since no upper bound was found for AJSS, this bridging behaviour was termed 'infinite toughening'. Differentiating equation (4) according to (3) results in the bridging law
The bridging laws for the different fibre systems are compared in FIGURE 3(b). The bridging law can be considered a material property [6,7] and is in an accessible form for implementation in finite element codes with spring elements or cohesive elements. MICROMECHANICAL DISCUSSION Smaller DCB specimens (H=4 mm, b=5 mm) were loaded in a similar fashion within the environmental scanning electron microscope to study the crack development. FIGURE 4 shows the difference between two systems.
(a) sizing A/ epoxy
ISOum — C ' l OOum (b) sizing B/ polyester FIGURE 4: Micromechanical differences in fibre bridging for strong (a) and weak (b) interphase
For the strong composite, moderate fibre bridging is observed, where the ligaments mostly consist of around four fibres. These bridges tend to break at higher loads. For the weak composite, on the other hand, extensive bridging can be seen. With increasing crack front, the bridging ligaments separate and multiple crack fronts develop. Like for previous SEM results [2,7], the model in FIGURE 5 appears to provide a reasonable description of fibre bridging. The bridging ligaments are considered as short beams of rectangular section, capable of deforming in shear and bending. During loading, they peel away by overcoming an interfacial fracture energy, Fj. For single fibre bridging, this value is the fibre/ matrix interfacial fracture energy, while it must also include some fracture energy of the matrix itself if multiple-fibre ligament bridging is present.
450
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour
FIGURE 5 Cantilever beam used for micromechanical modelling of ligament bridging
The displacement relationship is derived in [7]. Neglecting shear deformation, the crack bridging stress can be related to 5 as [2] _1.373N(El) l/4 (wr i ) 3/ ~
(6)
gl/2
The bridging stress is a function of the number of bridging ligaments per unit area N (#/area), the ligament modulus E, width w and thickness 2t (resulting in a second moment of area I), and the interfacial fracture energy IV The micromechanical bridging law has a similar form as the measured experimental bridging law. Comparison of macro-equation (5) and micro-equation (6) leads to AJS • = 1313N{EljH{wT f"=X. i
(7)
The material parameter A, is constant for each composite system (see TABLE I). TABLE II summarises the micromechanical parameters. From the micrographs in FIGURE 4, the parameters 2t and n can be determined, where n is the number of ligaments for a given length. The width w of the ligament is assumed, and the number of ligaments per unit area N is extrapolated with the values of w and n by presuming evenly distributed ligament density. TABLE II Micromechanical parameters and predicted interfacial fracture energy Ligament parameters Modulus E [GPa] Ligament width w [\un] Ligament height 2t [|im] Number of bridging ligaments n [#/mm] Number of bridging ligaments N [#/mz] Interfacial fracture energy Fi [J/m2]
Sizing A / epoxy 41.5 -100 100 2/2 1E7 690
Sizing B / Polyester 42 -100 150 (before separation) 5/4 1.25E7 190
The interfacial fracture energy Fj is calculated from equation (7). The values are rather large with 690 J/m2 and 190 J/m2, as the literature reports values of around 100 J/m2 [8]. However, TABLE assumes that the surface observations from FIGURE 4 represent the internal bridging state. 3D tomography is currently undertaken to estimate the number of bridging ligaments in more detail. The micromechanical
Influence of Fibre/Matrix Interphase on Crack Bridging Behaviour
451
model, however, results in a reasonable difference of the interfacial fracture energy of the two composite systems. CONCLUSIONS The article emphasises that the characteristics of the interphase between fibre and matrix have a strong impact on the fracture toughness of a given composite material. Bridging laws were derived for four different composite systems from DCB specimens with mode I crack growth parallel to the fibres. These bridging laws can be considered material parameters and can easily be implemented in finite element codes. The article furthermore investigates micromechanical parameters during the development of bridging ligaments by studying in-situ micrographs. The interfacial fracture energy is linked to the ligament geometry. It is shown that a sufficiently small interfacial fracture energy can then lead to 'infinite toughening', where no upper bound can be found for the crack growth resistance as fibres continue to peel away from the composite material without fracture.
REFERENCES 1. Rice, J. R. A path independent integral and the approximate analysis of strain concentration by notches and cracks. Journal of applied mechanics. 1968, 35, 379-386. 2. S0rensen, B. F. and Jacobsen, T. K. Large-scale bridging in composites: R-curves and bridging laws. Composites: Part A. 1998, 29A, 1443-1451. 3. Feih, S., Wei, J., Kingshott, P. K., and S0rensen, B. F. The influence of fibre sizing on strength and fracture toughness of glass fibre reinforced composites. Composites: Part A. 2003, submitted. 4. Suo, Z., Bao, G., and Fan, B. Delamination R-curve phenomena due to damage. Journal of Mechanics and Physics in Solids. 1992, 40(1), 1-16. 5. Wei, J., Feih, S., and Kingshott, P. K. 2003, to be submitted 6. S0rensen, B. F. and Jacobsen, T. K. Crack growth in composites: Applicability of R-curves and bridging laws. Plastics, Rubber and Composites. 2000, 29(3), 119-133. 7. Spearing, S. M. and Evans, A. G. The role of fibre bridging in the delamination resistance of fiber-reinforced composites. Acta Metallica Materials. 1992, 40(9), 2191-2199. 8. Kim, B. W. and Nairn, J. A. Observation of fiber fracture and interfacial debonding phenomena. Journal of composite materials. 2002, 36(15), 1825-1858.
Behavior of Brittle Reinforced Composites Fracture at Elevated Temperatures Ashraf T. Mohamed* Professor, Production and Design Department, Faculty of Engineering, Minia University, Minia 61111, Egypt ABSTRACT Monolithic carbon, carbon/carbon composites, discontinuous fiber carbon/carbon composites, continuous fiber carbon/carbon composites and three different surface treatments silicon carbide/alumina composites has been tested at temperature ranges from 20°C to 1650°C. The tested specimen results are compared at various specimens orientations using two notch shapes. Two-dimensional three-point-bend SENB specimens, with both chevron-and straight-notch configurations were used to evaluate the resistance to crack initiation and crack propagation, in different orientations with respect to the reinforcement. The effect of temperature, elastic properties, weight loss by oxidation on the fracture process variables is carried out and investigated. INTRODUCTION Metal matrix composites are a new class of materials which find several industrial applications and form a new generation of materials. They are difficult to machine mechanically due to the presence of a hard ceramic phase. Shirakashi and Obikawa [1], discussed the transition condition of the machining mechanism from a brittle mode to a gentle one from the view-point of the size effect of brittle fracture using FEM simulation. Quan and Ye [2], concluded that the residual stress maybe released due to structural defects at the surface of composites reinforced by coarse SiC particles, for composites reinforced by fine particles there is a tendency for compressive residual stress in the surface. Cutting with a larger removal rate increases the possibility for tensile residual stress in the machined surface layer. The fracture toughness of the composites were much lower than that of the unreinforced alloy. Mohamed et al. [3] investigated the effect of hard reinforcements on the Al composites, also Mohamed et al. [4-6] developed a model to describe the densification mechanisms in isostatic pressing of the aluminium composites, discussed the effect of particle size on the composites properties and illustrated the relation between the elastic constants and the particle deformation of these composites. Oleszak [7], focused on the influence of consolidation methods and parameters on the density and final microstructures (crystallite size). Sima et al. [8], performed the MA process with Al-matrix powders reinforced by the hybrid mixture: SiC + Graphite in a high-energy ball mill in argon atmosphere, the influence of the graphite particles on the sintering response of the hybrid composite powders is discussed. Besterci [9], prepared dispersion strengthened aluminium compacts with dispersed ceramic particles by powder metallurgy. Carbon transformation to carbide AI4C3 is characterized. Over the recent years, there has been an increasing interest in using fiberreinforced composite (FRC) materials because of their superior properties such as high strength, low weight and high corrosion resistance [10]. Development of Al • Corresponding author. Email: [email protected]
Behavior of Brittle Reinforced Composites Fracture at Elevated Temperatures
453
alloys has led to materials which can challenge many other engineering materials in terms of specific strength. To compare failure events in different types of brittle materials, this research addresses two composite types, carbon fiber/carbon matrix composites with both continuous and discontinuous fibers, and a series of silicon carbide whiskers/alumina matrix composites differing by the nature of whisker/matrix interfacial film. The discontinuous fiber carbon/carbon material will be fully characterized in terms of fracture parameters. The fracture characterization includes measurements of the plane strain fracture toughness (Kic) and computations of the crack growth resistance curves (R-curves). The influence of temperature, elastic properties, weight loss by oxidation on the fracture process is investigated. EXPERIMENTAL PROCEDURES Materials A monophase commercial polycrystalline graphite material has been used to determine its fracture properties. The average grain size of 5 to 10 urn and the density was 1.795 g/cm3. The material was received in the form of plates [7]. The discontinuous fiber carbon/carbon composite material was developed for use in aircraft brake components. The 6-7|am diameter fibers are pyrolyzed from a polyacrylonitrile (PAN) precursor. Their outer surfaces have ridges running parallel to the fiber axes with 1.54 g/cm3 density and a total porosity of 16%. The fiber volume fraction is 40%. The two-dimensional woven continuous fiber carbon/carbon composite (ACC4) has a density of 1.68 g/cm3, and the fiber volume fraction is 45%. Three types (A, B and C) plates with 10 mm thickness of silicon carbide whisker reinforced alumina matrix composites were examined, they comprise of 25% of SiC in volume in the form of high aspect ratio whiskers. The density of A12O3 composites is 3.77g/cm3. Type A and B materials differ only by the surface chemistry of the whiskers. Type C material, the whisker/matrix interface chemistry was less controlled than for type A material. Type A whiskers material were subjected tocleaning heat treatment and chemical treatment, which removed the surface carbon layer and left a surface with siliceous elements. The type B whiskers remained coated with 10A thick film of carbon residues that promotes whisker pullout during fracture by lowering the frictional stresses. Fracture Tests The Young's modulus, fracture toughness, strength values, as well as crack growth resistance curves have been obtained for various specimen orientations, up to 1650 °C. Fracture testing was carried out on a screw-driven, displacement-controlled load frame having a room temperature compliance of 0.03 |im/Kg, with a 10000 kgf load capacity. A 200 Kg self-identifying load cell was used for all tests, which allowed simple calibration and balancing. Modulus of Elasticity (E) and Modulus of Rupture (MOR). For a measured load, P, and a displacement, u, both Young's modulus, E, and strength (modulus of rupture), Op, are; u = (PL3 / 48 El) (1) E = (P/u) (L3 / 4BW3), and (2)
454
Behavior of Brittle Reinforced Composites Fracture at Elevated Temperatures CTF = (3/2) * (Pmax * L) / (BW2).
(3)
R-Curves and Fracture Toughness. The calculated stress intensity factor K is equal to the crack growth resistance parameter KR when the load Pj reaches its maximum, Pmax, the critical fracture toughness is obtained by; Kic = P max Y ac ,/BVW. (4) Where Yact is the geometry correction factor obtained through the fracture parameters calculation sequence at the point where Pmax occurs. In this last case, since the R curve analysis starts at Pmax , the Kic data point is also the first point of the KR curve [7]. RESULTS AND DISCUSSIONS Moduli of Elasticity and Rupture Figure 1 shows the temperature effect on the elastic modulus of the monolithic carbon and alumina, Kobe C/C, ACC4, AlaCVSiC (type A). The essential role of the carbon fiber reinforcement in the improvement of elastic properties will be shown to be 4 to 6 times greater by fiber addition. They are representative of the range of stiffness of the carbon matrix phases in the carbon/carbon composites. The monolithic alumina and A^C^/SiC show a gradual decrease of elastic modulus with temperature up to 1000 °C and a rapid decrement at higher temperatures due to the silica-based grain boundary phase and the material softening. The composite elastic modulus trend is higher due to its higher strength. Figure 2 shows that the L-T (the first letter refers to the specimens length direction normal to the crack plane, and the second letter indicates the crack propagation direction) and T-L orientations tests consistently outperform their respective L-S and T-S orientations, by approximately 20%. This difference shows that the in-plane (LT) isotropy is not experimentally verified. This unexpected anisotropy will also be confirmed by a similar trend observed for the toughness. The L-T and T-L orientations are stiffer and stronger than their respective L-S and T-S orientations, in consistent with the composite laminar nature. The elastic properties follow the same trend as the strength data shown in Figures 3 and 4. The observed decrease of the elastic modulus and strength with increasing temperature is inconsistent with the mechanical behaviour of carbon materials, which indicate stiffening and strengthening at high temperatures [6]. This is attributed to weight loss by oxidation. Moreover, oxidation has been reported to degrade the material in a 150 |jm thick surface layer. This results in increasing the maximum flaw size and decreasing MOR strength values. Oxidation of The Carbon/Carbon Composite. As shown in Fig. 5, the minimum relative weight loss remains near 13% for a maximum argon flow of 18cf/h. This graph evidences the beneficial influence of an inert atmosphere to avoid degradation of carbon/carbon materials. For maximum thermal protection of the furnace, the minimum final weight loss has been to be 4.5%. This value is high compared to 0.5% weight loss measured under vacuum, but is nevertheless representative of realistic environmental service conditions. This level of oxidation must be taken into account to compensate mechanical properties deterioration.
Behavior of Brittle Reinforced Composites Fracture at Elevated Temperatures
455
Load/Displacement (LPD) Relation Fig. 6 shows the LPD of monolithic graphite for L-S and L-T orientation at different temperatures. The curves are remarkably unchanged over this range of test temperatures as opposed to the case of monolithic alumina and AI2O3 composites shown in Figs 7 and 8. This suggests that the temperature-independent mechanical behaviour of graphite over this range result from stable interfacial characteristics not available from the glassy intergranular phase of alumina. For Kobe C/C composite, the load-point-displacement (LPD) results for typical chevron-notch fracture tests of both L-T and L-S orientations are presented respectively in Fig. 9 from 20 to 1650°C. The L-S and T-S curves are characterized by frequent load drops which correspond to run-arrest crack propagation, which is also consistent with the fracture surface appearance. These load drops are associated with the massive fiber groups failure as crack advances through the layered structure. Deviation from linearity of LPD curve observed prior to Pmax, accentuated for L-S specimens attributed to matrix cracking. This results in increasing subcritical crack growth experienced by the L-S over that of L-T specimens. A comparison of the composites load-displacement plots obtained at 1400°C are shown in Fig. 8, type A supports much more load than the two other types. The behavior of type A, consistent throughout the entire tests compared to type B and C. A slightly higher softening temperature of the type A glassy interface, enhancing the friction at the whisker/matrix interface be the cause for such improvement. Crack Growth Resistance (KR). The fracture surface energy, GR, VS. dimensionless crack length for monolithic graphite and cobe C/C are shown in Fig. 10. The slopes of each of the L-S curves exceed those of the respective L-T orientation specimens by a factor of about two. This fracture behaviour is consistent with the relatively large area under the corresponding LPD curves, and reflects the increased energy consumed by local delamination, greater fiber pullout, and more extensive matrix damage associated with this crack orientation. Critical Stress Intensity (Kic) and Notch Shape Effect. Fig. 11 presents the K K data as a function of test temperature for the L-T and L-S orientations. The toughness of this material is lightly rising with temperature, the difference between the L-S and L-T orientations signifies that the crack encounters more resistance to propagate through the thickness of the material, in the compaction direction (S). Fig. 12 presents the variations of KIC data with temperature, for each of the specimen notch configurations tested in both the L-T and T-L orientations. The chevron-notch "Kic" values fall between 8.0 and 11.6 MpaVm, and increase slightly with slightly with increasing test temperature. The Kic values for both notch types of the L-T orientation specimen are 10 to 20% higher than the corresponding T-L values, and the L-S KIC values consistently exceed those of the T-S orientation. CONCLUSIONS 1. The fracture behavior of monolithic graphite, carbon/carbon composites, monolithic alumina (AI2O3) and three SiC whisker-reinforced alumina composites (A^Oa/SiCw) has been carried out successfully at the temperature range of 20°C to 1400°C. 2. In all AI2O3 /SiCw composites, it was found that the whiskers and test temperature enhance both the fracture toughness and crack growth resistance compared to the monolithic A12O3.
456
Behavior of Brittle Reinforced Composites Fracture at Elevated Temperatures
3. The whisker surface treatment has a remarkable effect on the composite properties. 4. The notch shape has a prominent effect on the composite fracture toughness and the crack growth resistance. The chevron notch effect is better than the straight notch. 5. The Kobe C/C composite exhibited an increase stress intensity factor with crack length, demonstrating the existence of commutative toughening mechanisms. REFERENCES 1.
Shirakashi, T. and T. Obika. 2003. "Feasibility of gentle mode machining of brittle materials and its condition," J. of Mat. Processing Technology., 138/1-3: 522-526. 2. Quan, Y. and B. Ye. 2003. "The effect of machining on the surface properties of SiC/Al Composites, "_J. of Mat. Processing Technology., 138/1-3: 464-467. 3. Ashraf, T.M., Y.M. Ismaiel, T.M. Salem and K.A. Khaliel. 1995. "An Investigation Into The Production of Al/Fe and Al/SiC Composites Using The Compaction Technique," The 4th AlAzhar Univ. Eng. Int. Conf, Nasr City, Cairo., December 16 - 19, 1995. pp. 155-166. 4. Chen, Y.C., T.M. Ashraf, H. Rahman and K. Salama. 1998. "Powder Densification Mechanism of Metal Matrix Composite Materials," The Fifth International Conference on Composite Engineering ICCE/5, Nevada, USA, July 5-11, 1998. pp. 791-792. 5. Ashraf, T.M., M.H. Rahman, Y.C. Chen and K. Salama. 1998. "Relationship Between Elastic Constants and Particle Deformation in Metal Matrix Composites," Review of Progress in Quantitative NDE,, Snowbird, Utah, USA. July 19-24, 1998. pp. 20-29. 6. Rahman, M.H., A. T. Mohamed, Y.C. Chen and K. Salama. 1998. "Ultrasonic Velocity Measurements Applied to Process Control of Metal Matrix Composites Densification," Review of Progress in Quantitative NDE, Snowbird. Utah, USA. July 19-24, 1998. pp. 40-49. 7. Oleszak, D. 2003. "Intermetallic Matrix Composites Reinforced with Alumina Prepared by Reactive Milling and Consolidation of The Powders,"_The 4th Int. Conf. on Mechanochemistry and Mechanical Alloying (INCOME 2003). Braunschweig, Germany. 7-11 Sept., 2003. p. 43. 8. Sima,G., O.Gingu and M. Mangra. 2003. "Sintering Response of the Mechanically Alloyed Hybride Composite Powders Al/SiC+Graphite," The 4th Int. Conf. on Mechanochemistry and Mechanical Alloying (INCOME 2003). Braunschweig, Germany. 7-11 Sep.,2003. p. 133. 9. Besterci, M. 2003. "Kinetics of Mechanical Alloying, Microstracture and Properties of A1-A14C3 System," The Fourth International Conference on Mechanochemistry and Mechanical Alloying (INCOME 2003). Braunschweig, Germany. 7-11 September, 2003. p. 73. 10. Ashraf, T.M. 2000. pp. 714-720. "The Reinforcement Surface Treatment Influence on The Fracture Bending of The Ceramic Composites" "I", Proceedings of The ACUN-2, Int. Conference: Composites in The Transportation Industry, Sydney, Australia, pp. 714-720. 450 400
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Behavior of Brittle Reinforced Composites Fracture at Elevated Temperatures
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Part IX
Impact
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Non-woven Fabric Reinforced Cellular Textile Composites with Improved Energy Absorption Capacity S.W. Lam1*, X.M. Tao ', and T.X. Yu 2 "^Institute of Textiles and Clothing, The Hong Kong Polytechnic University, Hong Kong 2 Department of Mechanical Engineering, The Hong Kong University of Science and Technology, Hong Kong
ABSTRACT Flat-topped grid-dome cellular composites made of non-woven PET fabric reinforcement with polypropylene (PP) matrix were subjected to quasi-static axial compression and impact conditions. The mechanism of deformation and the energy absorption characteristics of the cells were studied. Based on the observations of the cell deformation mode, analytical expressions were formulated to find the mean peak value and thus the energy absorption capacity of the cellular structure. The results obtained are in good agreement with the experimental results.
INTRODUCTION Textile materials to be designed specifically to form three-dimensional structure may absorb large amounts of energy with light-weight. Tao and Yu [1-3] investigated a range of cellular textile composite structures in terms of energy absorption behavior under both quasi-static compression and impact conditions, including circular and square tubular knitted, multi-layer 3D woven, non-woven spun sponded and grid-domed cells projected from knitted fabric. They have identified that the grid-domed cellular structure possesses the highest specific energy absorbing capacity among all the cell configurations, which is also greater than that of polyester foams of identical density, hi their studies, knitted fabrics were used to fabricate the cellular textile composites due to its excellent drapability with acceptable mechanical properties [4]. Replacement of the fabric reinforcement by non-woven fabric has shown the improved performance on the energy absorption capacity under dynamic response with more beneficial during manufacturing [5]. hi the present study, flat-topped grid-dome composite cells made of PET non-woven fabric reinforced in PP matrix were subjected to quasi-static axial compression and impact conditions. By observing the deformation mode during the compression process, an analytical model is proposed to predict the energy absorption capacity of the flat-topped grid dome cellular composites with isotropic reinforcement.
Lam S.W., Institute of Textiles and Clothing, The Hong Kong Polytechnic University, Fax: (852) 2773 1432, Email: [email protected]
Non-woven Fabric Reinforced Cellular Textile Composites
462 EXPERIMENTAL
Specimens and Experiments The cellular composites comprised a commercial PET non-woven fabric and polypropylene films were fabricated by compression molding. The number of non-woven fabric layers and PP matrix films for molding the composite depends on the fibre volume fraction required. Fabrication was detailed described in [5]. Figure 1 shows the dimension details of the cellular structure. Grid-dome cellular samples made of pure PP material, having the same dimension as described in the compression-molded samples, were prepared by injection molding. The quasi-static compression test was performed on the cellular composites and the pure PP cellular samples using the MTS Universal Material Tester with a crosshead speed of 5 mm/min. Each specimen containing four conical cells was used the test. The deformation mechanism of the cellular composites was observed on a single cell only. The impact tests were conducted on a Dynatup Drop Weight Impact Tester (Model GRC8250). The mass of a drop weight (6.61 kg) included a plate striker of 120 mm X 120 mm X 12 mm, which was normal to the plane of the samples. The selected impact velocity was 6.0 m/s by adjusting the height of the drop weight and the air pressure of the pneumatic assist. Specimens were put on the supporting base of the testers and were impacted by a flat steel plate. 18mm
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Centre distance: 23 mm
FIGURE 1
Schematic geometry of the grid-dome sample
RESULTS AND DISCUSSION Quasi-static Compression and Impact Tests Typical load-displacement curves of the cellular samples (ranged from 0 to 0.38 fibre volume fractions) under axial compression and impact conditions are shown in Fig. 2. With the increase of the fibre volume fraction in non-woven PET samples, the energy absorption capacity reduces by approximately 30 % at 38 % fibre volume under quasi-static compression. However, it is shown that pure PP matrix is brittle under impact. Increase in fibre volume fractions in non-woven composites has shown the improvement on the material ductility and a significant reduction on the peak load.
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Observation on the Cell Deformation It is observed that both the isotropic pure PP and the non-woven PET/PP cellular samples deformed in the same pattern as a ring on the cell walls, which is different from the previous study by Xue et al [6] on the cellular composites with knitted fabric reinforcement that deform into a two-lobe diamond pattern. Figure 3 shows the deformation process: (1) the flat top was bent inwards during the large deformation process; (2) the flat-topped conical shell plastically collapsed inwards to form a ring pattern; (3) circumferential hinge lines were observed when the loading plate was removed.
ft* FIGURE 3 Deformation process of a cell made of pure PP material under quasi-static compression at a loading speed of 5 mm/min.
Prediction of the Energy Absorption Capacity Figure 4 shows a flat-topped grid-dome cell of semi-apical angle (/) , cell height L, diameters D and d, collapsed inwards during axial compression. The assumptions are made for our model: (1) the cell wall collapses internally with a circular plastic hinge between the top and bottom; (2) the top circle remains unchanged during deformation; (3) the effect of the cell top deformation is negligible; (4) the values of xi and X2, the length variables referring to Fig. 4, are the same as those measured from the experiment.
Non-woven Fabric Reinforced Cellular Textile Composites
464
FIGURE 4
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cos {fi - ) dp
(1 (2
x2 cos(6> + 0) The internal plastic dissipation is done by bending along plastic hinge lines and by stretching of material between them. The plastic dissipation for bending {Wb) at the circular plastic hinges at points A, B and C of the cell wall as shown in Fig. 4, is =j= [d + 2{ + ) i ^ ( f)~ixi +* 2 )cos0] V3 2 where Y is the mean yield stress of the cellular structure, t is the cell wall thickness, d is the diameter of the cell top. While the plastic dissipation for stretching of plate {Wm) between the plastic hinges is Wm = ^ [ x 1 2 ( l + sin^) + x 2 2 ( l - s i n ^ ) ] As the total internal dissipation is Wb
(3;
(4;
w=wb+wm The corresponding mean post-buckling load is
V3 To verify the theoretical model, two sets of samples, i.e. the pure PP and non-woven PET/PP samples were made possessing the same cell parameters: semi-apical angle=16°, cell height Z=15mm, Z>=10mm, cf=18mm, while little difference on the cell wall thickness measured were £pp=1.15mm and />jw=1.0mm,
(5)
(6)
Non-woven Fabric Reinforced Cellular Textile Composites
465
respectively. The mean peak load and the energy absorption capacity predicted by the theoretical model are obtained and compared with those obtained from experiments, as summarized in Table I. The deviation comes up with 5.5% for the prediction on the PP samples, but only 2% on the non-woven PET/PP samples. The difference between the predicted and the experimental results may be attributed to the negligence of the deformation of the cell top, the non-uniformity of the non-woven fabric reinforced composites and the experimental measure errors on the deformation mode. TABLE I Sample PP FV3
Measured and predicted energy absorption capacity for a single . Buckling load (KN) Mean Maximum peak P (kNmm 2 ) load (,Pmax) Theor. Exp. 0.03365 1.310 1.130 1.071 0.670 0.02338 0.957 0.684
cell until collapse Energy absorption capacity (J) Exp. Theor. 11.78 12.43 7.52 7.37
CONCLUSION The cellular composites with non-woven PET fabric reinforcement in polypropylene matrix behave differently under quasi-static compression and impact conditions. A theoretical model is presented and it is able to predict the mean peak load and energy absorbing capacity of a cell during plastic collapse. The theoretical predictions for pure material or non-woven reinforced composite are all in good agreement with the experimental results, so it could provide a basis for the effective design of similar material systems.
ACKNOWLEDGMENT Miss Lam would like to acknowledge the postgraduate scholarship from The Hong Kong Polytechnic University Research Grants. REFERENCES 1. 2. 3. 4.
5. 6.
Yu T.X., Tao X.M., and Xue P. The energy-absorbing capacity of grid-domed textile composites. Composites Science and Technology. 2000; 60: 785-800. Tao X.M., Yu T.X., Ngan K.M., and Ko F.K. Energy absorption of cellular textile composite under quasi-static compression. In: Proceedings of ICCE-4. Hawaii, USA, July, 1997. p.981-2. Yu T.X., Tao X.M., and Wu K.Q. Energy absorption of cellular textile composite under impact. In: Proceedings of ICCE-4. Hawaii, USA, July, 1997. p.1099-100. Ramakrishna S., Hamada H., Cuong N.K., and Maekawa Z. Mechanical properties of knitted fabric reinforced thermoplastic composites. In: Proceedings of ICCM-10. Whistler, Canada, 1995. p.245-252. Lam S.W., Tao X.M., and Yu T.X. Comparison of different thermoplastic cellular textile composites on their energy absorption capacity, Composites Science and Technology, in press. Xue P., Yu T.X., and Tao X.M. Flat-topped conical shell under axial compression. International Journal of Mechanical Sciences. 2001; 43(9): 2125-2145.
Energy Absorption Properties of Braided Composite Tubes Masanori Okano, Kenichi Sugimoto, Asami Nakai* and Hiroyuki Hamada Kyoto Institute of Technology, Japan
ABSTRACT In this paper, the influence of material properties with respect to the middle-end-fiber inserted into braided composite tube on the energy absorption characteristic was investigated. The static compression tests by using three types of braided composite tube were carried out and crushing mechanisms based on precise cross-sectional observation of crush zone were discussed. It is considered that the energy absorption capability depends on the rupture elongation of the middle-end-fiber. Because the fiber is broken easily in the case of the fiber with small rupture elongation, it is considered that the energy absorbed by bending of fronds is very low. Thus, the energy required for fiber fracture is low and the energy absorption properties become low because of the low bending energy.
INTRODUCTION An important aspect of the crushing performance of a material is its specific energy absorption value which is much greater for polymeric composites than for conventional metallic materials. Many researches have studied the energy absorption characteristics of polymer composite materials [1-3]. It was clear that crushing mechanism and specific energy absorption of composite tubes depend on hoop-to-axial ratios for a fiber arrangement. Textiles such as weaving, knitting and braiding, have often been used as reinforcements of composite materials. Figure 1 shows a schematic of a triaxial braided structure. Multiple yarns are intertwined on a mandrel to form tubular shape. The triaxial braiding consists of three types of fiber orientation, 0°, +6° and -6°. In particular, the braiding has the characteristic that fibers are oriented continuously. Braiding yarns make braiding angles (±0°) with axis of the braided fabric. 0° yarns named middle-end-fiber can be inserted into braided fabric. It is easy to vary mechanical properties in the hoop direction and in the axial direction by arranging braiding angle and types of fibers. In previous study, it was not proven how the energy absorption capability was affected by middle-end-fiber. Hence this necessitates development of a design methodology of braided composites. In this paper, it was investigated how the energy absorption characteristic was influenced by the material properties of the middle-end-fiber. Hence the static test by using various braided composite tube were carried out and crushing mechanisms based on precise cross-sectional observation of crush zone were discussed. * corresponding author: Gosyo-kaidoucyo, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, JAPAN FAX: +81-75-724-7800 E-mail: [email protected]
Energy Absorption Properties of Braided Composite Tubes
467
Braiding angle
-e . +e
Braiding fiber
Middle-end-fiber
Longitudinal direction
Trsnswse direction
FIGURE 1 Schematic illustration of circular braided fabric
MATERIALS AND EXPERIMENTAL METHOD In this study, three types of the fiber; T700, T1000 and XN60 were chosen as the middle-end-fiber. Table 1 shows the material properties of T700, T1000 and XN60. Here, T1000 fiber is called the high strength fiber in which the tensile strength has higher than T700 fiber and XN60 fiber is called the high modulus fiber in which the tensile modulus has higher than T700 fiber. At first, the three-point bending test was performed to clarify bending properties of three types of the fiber. Three types of the specimen were fabricated by using only T700, T1000 and XN60 respectively. Epoxy resin was employed as matrix. The specimens for the bending test were cut along the longitudinal direction of the fiber. Geometry of the specimen was 2.0mm in thickness and 15mm in width. A span length was 80mm. The tests were performed by INSTRON testing machine at a cross-head speed of 2.0mm/min. Secondarily, three types of braided composite tubes were manufactured by inserting T700, T1000 and XN60 into braided tubes as the middle-end-fiber. Table 2 lists the specifications of the fabricated tubes. The type of braided yarn in all the tubes was carbon fiber, T700. Epoxy resin was employed as matrix similarly. Filaments of fiber bundles for the middle-end-fiber were adjusted to achieve the minimum differences in percentage of total fiber volume fraction of 0° yarn in each tube. Laminated structures were used to achieve the required thickness. Two braiding angles were used, which were 60° for the innermost layer and 30° for other layers. The fiber volume fraction was approximately 50% in each tube. The inside diameter was 50mm and the thickness was approximately 3.2mm. The height of specimen for static test was 100mm. In order initiate progressive crushing, 45° chamfer was made at either end of the specimens. The compression tests were performed by using INSTRON testing machine at a constant cross-head speed of 5.0mm/min.
468
Energy Absorption Properties of Braided Composite Tubes TABLE I. Material properties of the T700, T1000 and XN60 fiber
Type of fiber Tensile strength [MPa] Tensile modulus [GPa] Elongation [%]
T700|T1000|XN60 4900 6370 3530 230 294 590 2.1 2.2 0.6
TABLE II. Specification of the braided composite tubes Name of specimen Number of ply
Normal High strength High modulus 8 8 8 30° T700 T700
30°
30°
T700 T1000
T700 XN60
Fiber volume fraction of total middle-end-fiber [%]
22.9
24.3
24.3
Inside diameter [mm] Outside diameter [mm] Thickness [mm]
50.0 56.5 3.25
50.0 56.6 3.29
50.0 56.4 3.18
Layer
Braiding angle Braided yarn Middle-end-fiber
BENDING TEST Figure 2 shows the results of the load-deflection curves and Table 3 shows the results of the bending strength and bending modulus for each specimen. From the 1-d curves, it was shown that the maximum load of T700 fiber and T1000 fiber was higher than that of XN60. And also, the bending strength of T700 fiber and T1000 fiber were about 2.5 times as high as that of XN60 fiber. In respect to bending modulus, XN60 fiber showed the highest value of all specimens. On the other hand, comparing the T700 fiber with T1000 fiber, there was no almost difference of the bending strength between T700 fiber and T1000 fiber. CRUSHING TEST Typical load-displacement curves obtained from static testing of three tubes are shown in Figure 3. For the normal specimen and the high strength specimen, two curves showed a similar tendency. Initially, the load decreased rapidly drastically after the rapid increases of the loads. After the gradual increase of the load, the load kept a high value. However, for the high modulus specimen, the value of the load was very lower than that of two others. The results of mean crush load and specific energy absorption value, or Es value of each specimen are given in Table 4. The values of the loads of normal specimen and high strength specimen were almost same value. On the other hand, the value of the mean crush load of high modulus specimen was very lower than that of two others. Es values of normal and high strength specimens showed almost same and 1.5 times as high as that of high modulus specimen.
Energy Absorption Properties of Braided Composite Tubes i
469
.\J
T700 T1000 XN60
0.8 _ 0.6 0.4 -
TABLE III Results of bending strength and bending modulus
A y\
/ y^
0.2
5 10 Deflection [mm]
15
Type of Bending strength Bending modulus specimen fGPal [MPal T700 98 1368 130 T1000 1287 XN60 255 539
FIGURE 2 Load-deflection curves in bending test
100 - The high strength specimen
TABLE IV Results of mean crush load and specific energy absorption value
The normal specimen
igh modulus specimen
Type of specimen
20
10 20 30 Displacement [mm]
40
normal high strength high modulus
Specific energy mean crush load absorption value P[kN] Es [kJ/kRl 71.7 60.8 60.2 71.8 47.6 38.3
FIGURE 3 Load-displacement curves in static test
In order to investigate the crushing mechanism, detailed photographs and schematic illustrations of cross sections cut through the crush zones parallel to the axis of each specimen are shown in Figure 4 and Figure 5 respectively. For the normal specimen, the fronds spread inwards and outwards with central crack and many fragments were observed. A debris wedge was seen between fronds. For the high strength specimen, the fronds spread out toward inner and outer side with central crack similarly and many fragments were observed. A debris wedge was observed between fronds. For the high modulus specimen, the fronds spread out toward both sides with central crack. With respect to the central crack, the length of the central crack of the normal specimen was almost the same as that of the high strength specimen. However, the central crack of the high modulus specimen was shorter than those of two others and the curvature of fronds and the fragment were also small compared with those of two others. A clear debris wedge was not seen.
470
Energy Absorption Properties of Braided Composite Tubes
ENERGY ABSORPTION DURING CRUSHING The total energy (UT) absorbed during crushing is given by equation (1). UT=Uff(
Ubend ( Uic))+ Usf+ Ufr + others
(1)
where Uic is the energy required for longitudinal cracking of the pipe wall, USf is the energy absorbed by the splitting of fronds into beams, Ubend is the energy absorbed by bending of fronds, Uff is the energy required for fiber fracture and Ujr is the energy associated with frictional heating. In addition to these five main mechanisms, there are other fracture processes, such as splitting of the pipe wall into fronds along the circumference of the pipe, which contribute to the overall energy absorption. And Uff( Ubend ( Uic)) means that Ubend is function of C//c and Uff is function of UbendIf the crack which propagates in initial stage is short, the energy absorbed by bending of fronds is high. Subsequently, many fiber fractures are generated because of the increase in bending energy for the spreading of fronds. On the contrary, if the crack which propagates in initial stage is long, the bending energy of the. fronds is low. Therefore, less fiber fracture is generated due to the low bending energy. As it is considered that the energy Uff required for fiber fracture contribute to the total absorbed energy UT greatly, it had better increase the energy Uff. The Es value of the high modulus specimen was the lowest of all the specimens in static test. It is considered that the Es value might be related to rupture elongation. The elongation of the XN60 fiber was smallest of all specimens. If the rupture elongation is small, the fiber would be broken immediately without bearing of the axial load. Hence, it is considered that the energy Ubend absorbed by bending of fronds was low. Although the fiber fracture was generated, the energy Uff required for fiber fracture might be low.
(a) The normal (b) The high strength (c) The high modulus FIGURE 4 Detailed photographs of cross section of crush zone in static test
Wedge
' /Central i \ crack 1 .fragment
\r (a) The normal (b) The high strength (c) The high modulus FIGURE 5 Schematic illustration of cross section of crush zone in static test
Energy Absorption Properties of Braided Composite Tubes
471
CONCLUSIONS In this paper, it was investigated how the energy absorption characteristics were influenced by using three types of the braided composite tube with different middle-end-fiber. The specific energy absorption value of the high modulus was lowest of all specimens. The influence of the middle-end-fiber on energy absorption properties depends on the rupture elongation of the fiber. In the case of the small rupture elongation such as the XN60 fiber, it is considered that the energy Ubend absorbed by bending of fronds is very low. Because the fiber would be broken currently without bearing the axial load in the initial stage, considering the result of three-point bending test. Thus, it is considered that although the fiber fracture is generated, the energy U// required for fiber fracture is low. REFERENCES 1. P. H. Thornton, "Energy Absorption in Composite Structures", J. COMPOSITE MATERIALS, Vol.13, 1979, pp247-263 2. H. Hamada, S. Ramakrishna and H. Satoh, "Crushing mechanism of carbon fibre/PEEK composites tubes", COMPOSITES, Vol.26, Numberl 1, 1995, pp749-755 3. H. HAMADA, J. C. COPPOLA, D. HULL, Z. MAEKAWA and H. SATO, "Comparison of energy absorption of carbon/epoxy and carbon/PEEK composites tubes", COMPOSITES, Vol.23, Number4, 1992, pp245-252
Characterization of Damage Resistance and Damage Tolerance of Composite Materials Zhen Shen*, Shengchun Yang Aircraft Strength Research Institute of China, P. R. China Shaoyun Fu Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, P. R. China Lin Ye Centre for Advanced Materials Technology, School of Aerospace, Mechanical & Mechatronic Engineering. The University of Sydney, Australia
ABSTRACT A lot of experimental data showed that CAI was an ambiguous physical quantity, and could not to guide development of material systems and selection of materials during structural design. The research by authors showed that the damage resistance behavior and damage tolerance behavior of composite systems are corresponding to the design requirements of durability (against impact) and damage tolerance of composite structures, respectively. They can be characterized using the maximum contact force of the static contact force ~ dent depth curve, i ^ x and the threshold of the dent depth ~ compression failure strain curve, CAIT (Compression failure strain After Impact Threshold), respectively.
INTRODUCTION Aircraft integrity requirements usually include static strength, stiffness, durability and damage tolerance requirements. In order to meet these requirements it is necessary to establish corresponding material properties for material scientists to develop new materials and for structural designers to predict structure performance. There have been available material properties for metallic structures. In comparison with metallic structures composite structures have some peculiar contents in durability and damage tolerance requirements. The main difference is impact resistance and impact damage tolerance. ASTM D6264-98 [1] stated that the damage resistance is quantified in terms of a critical contact force associated with a single event or sequence of events to cause a specific size and type of damage in the specimen. But it is not so clear to definite a physical quantity characterizing damage resistance behavior in the standard. Recently MIL-HDBK-17-1F [2] stated that CAI obtained by NASA test standard or SACMA SRM 2R-94 method could be accepted as the
'Corresponding author, P O Box 86, Xi'an 710065, P R China, fax:+86-29-8214765, email: shenzhen@pub .xaonline. com
Damage Resistance and Damage Tolerance
473
characterization of damage tolerance behavior of composites. But a lot of research has showed that CAI was an ambiguous physical quantity. Authors have ever proposed that the threshold of impact damage failure curves by the impact under compression method could be assigned as the compressive impact damage tolerance allowable of composite laminates. In fact this value had been considered as the characterization of damage tolerance behavior of composite laminates. So far the research on the characterization of damage resistance and damage tolerance of composite materials is still under progression. In the paper Authors proposed two new physical quantities to characterize them based on our experimental study. SELECTION OF DAMAGE PARAMETER OF COMPOSITE LAMINATES Whichever of damage resistance and damage tolerance need to choose a suitable damage parameter to describe damage state before choosing the suitable physical quantity to characterize them. The available commonly-used damage parameters include damage area, damage width, and dent depth. All of the three parameters can be the alternative damage parameter used in measurement of damage resistance and damage tolerance behavior. According to the physical meaning of damage resistance (i.e. damage size for a given impact force), the most measurable impact force is impact energy. Fig 1 shows the relationships between impact energy and different damage geometrical quantities for two composite systems with different toughness. Among them E (impact energy) ~ 8 (dent depth) curves distinguish mostly the difference in toughness even though all of these curves could reflect their difference. Fig 2 shows the relationship between E (impact energy) and 5 (dent depth) for 7 composite systems. The rank of damage resistance of these composite systems is obvious. Composite system A and B belong to brittle composites and the others belong to toughened composites. The appropriate damage parameter should meet the following requirements: • For the same impact event (or impact force) the response of composite systems with different toughness (or damage resistance) should be significantly different; • It should be consistent with the parameter describing the damage state in the damage resistance and damage tolerance requirements of the aircraft structure design specification; • The damage parameter should be easily measurable. According the criterion stated above the dent depth is chosen as the damage parameter used in characterization of damage resistance and damage tolerance behavior of composite systems. PHYSICAL QUANTITY CHARACTERING DAMAGE RESISTANCE The available research has shown that impact damage can be produced by the quasi-static indentation (QSI) method instead of the drop-weight method. Fig.3 shows the contact force ~ dent depth curves for two different carbon/modified BMI by QSI method. The conclusion is nearly the same as that obtained from the drop-weight method, hi comparison with the drop-weight method QSI method can obtain the more obvious knee point and is much simpler. Actually, there exists the maximum contact force at the knee point. Repeatability of the contact force ~ dent depth curves of the same composite system is quite good. The definition of damage resistance in ASTM D 6264 is: in structures and structural materials, a measure of the relationship between
474
Damage Resistance and Damage Tolerance
the force, energy, or other parameter(s) associated with an event or sequence of events and the resulting damage size and type. According to this definition the maximum contact force Fmm at the knee point of the dent depth ~ contact force curve of the typical composite laminates is assigned as the physical quantity characterizing the damage resistance behavior of the composite system in this paper. It reflects the maximum capability of resin matrix and fibers near the surface in this composite system as a whole to withstand foreign object impact.Table 1 gives out the Fmax and CAI values for 4 different composite systems. It could be found that the order of both of Fmax and CAI is the same. It means that Fmax can characterize the damage resistance behavior of composite systems instead of CAI. 35
600 | to E
30
J.25 I 20
-400
S £300 00
I
1200
100
> Carbon/Brittle Epoxy
- V
10h > Carbon/Brittle Epoxy
5 0
5 10 15 Impact energy, J
20
0
0
5 10 15 Impact energy, J
20
0
5 10 15 Impact energy, J
20
• • Carbon/Toughened Epoxy • * • • •
Impact energy, J
FIGURE 1 The relationship between impact energy and different damage parameters for carbon/epoxy
3.0
•
2.5 g 2.0 • 1.5
4 Carbon/modified BMIA • Carbon/modified BMI B O Carbon/toughened BMI C ^ Cartran/toughened BMI D O Carbon/toughened BMI E A Carbon/toughened BMI F X Carbon/toughened Epoxy G A
A 1.0 0.5
AD
&
O
a
A m
A
°
0.0 20
40
60
80
100
120
140
Impact Energy, J
FIGURE 2 Impact energy ~ dent depth curves for 7 composite systems
Damage Resistance and Damage Tolerance
475
TABLE I F max and CAI for 4 composite systems Fmax[kN/mml 1.09 1.12 0.98 2.75
Material system Carbon/Modified BMIA Carbon/Modified BMI B Carbon/Brittle Epoxy Carbon/Toughened Epoxy
CAIfMPa] 171 177 151 >200
PHYSICAL QUANTITY CHARACTERING DAMAGE TOLERANCE Fig.4 shows the typical impact damage failure curve of composite laminates (including compression after impact and impact under compression). It is well-known that there exists a horizontal part, e.g. a threshold for all of the impact damage failure curves. The key issue of the damage tolerance requirement of composite structures is that the structure with impact damage meets the specified residual strength and the initial impact damage size assumption is that damage from a 25.4mm diameter hemispherical impactor with that kinetic energy required to cause a dent 2.5mm deep. All of test data show that the compressive failure strain approaches its threshold as long as the dent depth is deeper than 1.0mm. Based on the test data and the damage tolerance requirement of composite structures the CAIT ( Compression After Impact Threshold ) of the impact damage failure curve of a composite system with a specified lay-up under the specified impact condition is used as the physical quantity characterizing the damage tolerance behavior of the composite system. The quantity represents the damage tolerance of the structures with assumed initial defect/damage CONCLUSIONS • The maximum contact force F max obtained from the typical laminates by QSI method can be used as characteristics of the damage resistance behavior of a composite system. • The CAIT (Compression After Impact Threshold) can be used as characteristics of the damage tolerance behavior of a composite system. • In order to characterize damage resistance and damage tolerance behavior of a composite system the effect of a variety of parameters on Fnmx and CAIT should be investigated theoretically and experimentally so that the test standards on Fmiix and CAIT can be established.
Carbon/Modified BMI A
Carbon/Modified EMI B
»
i
F-2 F-3
H-2
\ •
-
a
-
F-5
-
M
'H-4
W
- - —H-5 :•:•:•:•:•:•:•:•:•:•:•:•:•:•:•:].]. g
0.0
0.2
0.4
0.6
0.8
1.0
Contact force, fcN/mm
Contact force, kN/mm
FIGURE 3 Repeatability of test data of contact force -dent depth for multi-specimens
Damage Resistance and Damage Tolerance
476
Impact energy or dent depth
FIGURE .4 Typical impact damage failure curve of composite laminates
ACKNOWLEDGEMENTS Authors would like to thank their colleagues in ASRIC: Liu J S and Chen P H for their contribution in experimental work and helpful discussion. Also authors are grateful to the National Key Laboratory Fund (00JS49. 3. 1.HK53O1) and Aeronautical Science Fund of China (ASFC)( 01B23001) for their financial support. REFERENCES ASTM Standard D6264-98. Standard Test Method for Measuring the Damage Resistance of a Fiber-Reinforced Polymer-Matrix Composite to a Concentrated Quasi-Static Indentation Force. 1998. Department of Defense. MIL-HDBK-17F Composite Materials Handbook. Vol 1. Polymer Matrix Composites Guideline for Characterization of Structural Materials. 17 June 2002
Simplified Prediction Method of Impact Response on Composite Laminates Sung Joon Kim and In Hee Hwang Korea Aerospace Research Institute, Korea
ABSTRACT A new method for simple prediction of the impact response on composite laminates subjected to low-velocity impact is proposed. The present method is based on mode analysis. The simplified prediction method can be efficiently applied to isotropic or orthotrpoic plates with unknown contact laws as well as composite laminates with no restraint on the material properties and geometrical shape. Predicted impact response using the present method is compared with the numerical ones from the impact response analysis using contact law. And in this paper, to investigate the effect of embedding directional damping material, the low-velociy impact response analysis was performed using the present method. Embedding viscoelastic-damping materials into composites can greatly increase the damping properties of composite structures.
INTRODUCTION Low-Velocity impact problems in composite structures have been a hot issue because damage due to the low-velocity impact might be left undetected and become potentially dangerous. Numerous analytical methods have been developed for solving this impact problem in composite laminates [1]. To determine the contact force from the impact response analysis an experimental indentation law or the modified Hertzian contact law proposed by Yang and sun [2]. The dynamic response analyses using this contact law have provided many numerical results on the impact response. However, these analyses using the finite element method on the impact response of the laminate have been known to require long computation time. Shivakumar et al. did not use the finite element method to analyze the impact response of the laminate but used the spring-mass model to efficiently predict the impact force history [3]. In their study the contact energy due to local indentation as well as transverse shear energy and bending energy of plate are considered, and they reported that the contact energy can be neglected in the impact by relatively low velocity foreign object on a flexible or thin plate. However, their study was restricted to circular laminates with transversely isotropic material properties. Choi et al. proposed the simple prediction method of impact force history on composite laminates subjected to low-velocity impact [4], They neglected the contact energy as it has been in other research [5]. The impact duration is computed from the eigenvalue analysis of lumped mass system in which the mass of an impactor is lumped with the plates, and the impulse-momentum conservation law is used with the concept of the spring-mass model. However, they considered only the first mode of lumped system. They did not consider the higher mode of impact response, m the present study, we propose a new method for Correspongding Author, P. O. BOX 113 YUSUNG TAEJON 305-600 KOREA, 82(42)860-2009, [email protected]
478
Simplified Prediction Method of Impact Response
simple prediction of impact response on composite laminates subjected to low-velocity impact. The impact response is computed from several eigenvalues of lumped mass system. Usually viscoelastic-damping materials behave isotropically so that their damping properties are the same in all directions. In these days, there is a desire to develop viscoelastic-damping materials that behave orthotropically so that damping properties vary with material orientation. These orthotropic damping materials can be made by embedding rows of thin wires within the viscoelastic materials [6]. These wires add significant directional stiffness to the damping materials, where the stiffness variation with wire orientation follows classical lamination theory, m this paper, the loss factor of composite laminate was evaluated based on Ni and Adams' theory [7]. SIMPLE PREDICTION ON IMPACT RESPONSE Impact Force Histories The impact duration determined from eigenvalue analysis may be more accurate than that from a direct analysis of spring-mass model, as shown in Ref. 3 where the effect of the mass of the plate were simplified with the concept of the effective plate mass in the spring-mass model analysis. The contact force history may be assumed to be a sine function as in Eq. (l)-(4). mi.sin^
T
-^f
i = \,-,n
i = 2,-,n
(1)
(2)
Where Fmi is the function of impactor mass, initial velocity and eigenvalues in spring-mass model. And 7} is period of each mode in spring-mass model. Neglecting thermal and acoustic dissipation as well as energy loss due to impact damage and residual vibration of the laminate after impact, the mechanical energy of the impact is conservative. Therefore, we may let the rebound velocity of the impact be equal to the impact velocity. Applying the impulse-momentum conservation to the impact history of Eq. (1). IT
(3)
Where mj is mass of impactor. Tf is period of impact force history, v is impact velocity of impactor. The approximate impact force history can be written be as 2m,v > T, sin ' *-• ' T.
Simplified Prediction Method of Impact Response
479
Impact Response Neglecting the gravity, the acceleration and velocity of impactor can be computed using the equations (5)-(6)
(5)
Mi
(6)
T{
To investigate the vibration characteristics of impact system, the lumped mass system in which the mass of the impactor is lumped with the laminate was solved using the finite element method. The size of laminate to be analyzed is 10x10x0.1 cm and stacking sequence is [0]8 and the material properties of a lamina are shown in Table 1. The boundary condition of plate has four edges clamped. In Figure 1, the simplified impact force histories from Eq. (1) is shown. The contact duration and impact force histories agree well with those from the impact response analysis using contact law. TABLE I Material properties of lamina used for analysis
Item
Ei (GPa)
E2 (GPa)
V
Gl2 (GPa)
(10-3)
(io-3)
AS4 Graphite/Acrylic (Damping Material)
156.0
24.8
0.30
8.1
27.7
1860.0 1310.0 1597.0
AS4 Graphite/Epoxy
122.2
17.9
0.27
6.2
1.84
8.58
(10-3)
9.48
kg/m3
1509.0
Mass ratio (M,/Mp) = 35.0 Impact velocity = 5.0 m/sec
0.0
1.0
2.0
3.0
4.0
5.0
6.0
7.0
8.0
9.0
Time (msec) FIGURE 1 Impact force histories using the contact law and present simplified results
480
Simplified Prediction Method of Impact Response
Damped Impact Force Histories The damped contact force history may be assumed to be a sine function as in Eq. (7).
i = l,---,n Where 7} is period. £. is damping ratio. Ando,. is angular natural frequency of each mode in spring-mass model. The Loss Factor of Composite Laminates In this paper, The overall damping loss factor(^ov) is expressed as fallows. AW
(8)
2KW
Where AW is the dissipated energy and W is the stored energy during a cycle. The strain energy dissipation can be divided into five parts as fallows. The overall damping loss factor for composite laminates embedding directional damping material is analyzed as fallows. The stacking sequence of composite laminates is presented in Figure 2.
Casel Angle
Case 2
Case 3
Mart Angle Mat'l Angle Mat'l [1]
0.0
[1]
0.0
[2]
0.0
[1]
[2]
0.0
[1]
[1] [2]
0.0
Damping Material
0.0 0.0
0.0
[2]
Wires at angle 6
[1]
0.0
[2]
0.0
[2]
Damping material
0.0 0.0
[1]
0.0
[2]
0.0
[2]
[1] [1]
0.0 0.0
[2]
Composite
0.0 0.0
[1]
0.0 0.0
[2] [2]
0.0
[1]
0.0
[1]
0.0
[2]
0.0
Composite
[1]: AS4 Graphite/Epoxy, [2] : AS4 Graphite/Acrylic FIGURE 2 Stacking sequence of composite laminate embedding directional damping Material
Damped Impact Force Histories A comparison of impact force histories with and without damping is shown in Figure 3 ~ 4.
Simplified Prediction Method of Impact Response
481
1400.0 Undamped S
1200.0
,
- - - • Damped
J3
b
r
b
ct Force (
g - 1000.0
400.0 200.0
\
J
\
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* 0.0
1.0
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3.0
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6.0
7.0
8.0
Time (msec) FIGURE 3 Impact Force Histories for Casel
9.0
0.0
1.0
2.0
3.0
4.0
5.0
6.0
7.0
8.0
9.0
Time (msec) FIGURE 4 Impact Force Histories for Case3
Conclusion In this paper, a new method for simple prediction of the impact response on composite laminates subjected to low-velocity impact is proposed. This method is based on mode analysis for lumped mass system. The impact duration is computed from the eigenvalue of the lumped mass system, and the impulse-momentum conservation law is used with the concept of the spring-mass model to predict the impact force history. The approximate impact force histories using the present method agree well with the numerical ones from finite element analysis. And to investigate the effect of embedding directional damping material, the low-velociy impact response analysis was performed using the present method. Embedding viscoelastic-damping materials into composites can greatly increase the damping properties of composite structures. The present analysis results show that directional damping material has a great influence on vibration and damping characteristic of composite laminate. Reference 1. Abrate, S., "Impact on Laminated Composite Materials," Applied Mechanics Review, Vol. 44, No. 4 , 1991, pp. 155-190 2. Yang, S. H., and Sun, C. T., "Indentation Law for Composite Material Laminates," Composite Materials : Testing and Design, 6* Conference, American Society for Testing and Materials, ASTM STP 787, Philadelphia, PA, 1982, pp. 425-449 3. Shivakumar, K. N., and Elber, W., "Prediction of Impact Force and Duration Due to Low-Velocity Impact on Circular Composite Laminates," Journal of Applied Mechanics, Vol. 52, Sept. 1985, pp. 674-680. 4. Choi, I. H., and Hong, C. S., "New Approach for Simple Prediction of Impact "AIAA Journal, Vol. 32, No. 10, October 1994, pp. 2067-2072 5. Tan, T. M., and Sun, C. T., "Use of Statistical Indentation Laws in the Impact Analysis of Laminated Composite Plates," Journal of Applied Mechanics, Vol. 52, March 1985, pp. 6-12 6. Biggerstaff, J. M. and Kosmatka, J. B., "Shear Measurements of Viscoelastic Damping Materials Embeded in Composite Plates," SPIE Proceedings, Vol. 3672,1999, pp. 82-92 7. Ni, R. G. and Adams, R. D., "The Damping and Dynamic Moduli of Symmetric Laminated Composite Beams-Theoretical and Experimental Results," Journal of Composite Materials, Vol. 18,1984, pp. 104-121.
Indentation Responses and Damage in Kaolin/CelluloseFibre Epoxy Nanocomposites S. Vaihola, W. Vilaiphand, A. Lopez, I.M. Low* Materials Research Group, Department of Applied Physics, Curtin University of Technology, GPO Box U1987, Perth, WA 6845, Australia
ABSTRACT The nature and degree of indentation responses as well as the deformationmicrofracture damage in the vicinity and below the Vickers contacts in epoxy composites reinforced with cellulose-fibre (CF) and nano-sized kaolin have been studied. The hardness of the nanocomposite is load-independent but is time-dependent as a result of both viscoelastic deformation and extensive microscale damage. A pronounced shear deformation within the CF/epoxy matrix is observed during indentation, indicating microscale quasi-plasticity which can be associated with interfacial sliding, interfacial debonding, and microcracking. However, no contactinduced cracks are observed and the extent of micro-damage distributed within the shear-compression zone around and below the contacts is profoundly suppressed as the thickness of the harder kaolin/epoxy layer increases.
INTRODUCTION There is currently a great interest in polymer-clay nanocomposites as a result of the pioneering work by researchers at Toyota on nylon-6/clay nanocomposites which have demonstrated an improvement in both physical and mechanical properties [1,2]. Because of the nanoscale structure, polymer-clay nanocomposites possess unique properties which include an improvement in mechanical (modulus, strength, toughness), thermal (thermal stability, decomposition, flammability, coefficient of thermal expansion), and physical (permeability, optical, dielectric, shrinkage) properties [3-7], Nanocomposites have been demonstrated with many polymers of different polarities including polystyrene, polycaprolactone, poly(ethylene oxide), poly(butylene terephthalate), polymethylmethacrylate, polyamide, polyimide, polyester, polyether, epoxy, polysiloxane, and polyurethane. Similarly, cellulose and other natural fibres are increasingly being used as reinforcements for enhancing the strength and fracture resistance of polymeric matrices because of their low density, low cost, renewability and recyclability as well as excellent mechanical characteristics that include flexibility, high specific strength and high specific modulus [8-13]. These unique properties are particularly desirable in applications as composite materials for automobiles, armour, sports, and marine industries. Here we describe a novel approach to design nano-hybrid eco-composites, in which micro structural elements are tailored to provide both nano- and fibre-dispersed * Corresponding author. Email: [email protected]
Kaolin/Cellulose-Fibre Epoxy Nanocomposites
483
compositions and generate different modes of strengthening and toughening. The basic idea is to produce an outer epoxy layer dispersed with nano-sized kaolin for strength and wear resistance, and with underlayers of cellulose-fibre reinforced epoxy for toughness and damage tolerance. EXPERIMENTAL PROCEDURE Commercial grade nano-sized kaolin and cellulose-fibre preforms derived from wood were used to fabricate kaolin-cellulose fibre-reinforced epoxy hybrid nanocomposites. Softwood aspen (Pinus radiata) mats in the form of bleached chemithermomechanical pulb (CTMP) were used as reinforcing fibre preforms. Samples were be prepared by casting an epoxy mixture in a greased silicone rubber mould filled with kaolin and cellulose-fibre. Initially, the mould will be filled with a thin layer mixture (0.3-1.0 mm) of kaolin/epoxy. Three sheets of previously epoxy soaked CTMP fibre-mat were then laid down. The fully-soaked samples were cured overnight at room temperature. Figure 1 shows the typical surface and crosssectional microstructures of the samples.
(b) (a) FIGURE 1 Typical microstructures of a sample showing the (a) cross-section and (b) cellulose-fibre layer. (Magnification: lOOx)
Samples for indentation tests were resin-mounted and polished with diamond paste down to 1 \xm with a Struers Pedemat auto-polisher. The Vickers hardness measurements were performed with a Zwick microhardness tester. The lengths of the diagonal (2a) were used to calculate the hardness, determined here as: Hv = P/2a2
(1)
where P is the load used. The variation of hardness as a function of load was performed over the range 10-100 N at an indentation time of 20 seconds. The effect of indentation time (0-720 min) on the variation of hardness at 30 N load was studied to ascertain the viscoelastic nature of this material. The time-dependent strain, e (/), due to creep was calculated from the difference in diagonal lengths (d) between the initial (t0) and continuous specified (t) loading times:
e(t)={d(t)-d(to)}/d(to)
(2)
484
Kaolin/Cellulose-Fibre Epoxy Nanocomposites
Information of subsurface damage during Vickers indentations was also obtained using a bonded-interface specimen configuration [7,10]. This test allows the nature and degree of damage accumulation beneath the indenter to be revealed. Polished surfaces of two half-specimens were glued face-to-face with a thin layer of adhesive under moderate clamping pressure. The top surface perpendicular to the bonded interface was polished for the indentation tests. The test to examine the suburface damage was also performed with a Zwick tester at P = 100 N. The two halves of the indented specimens were then separated by dissolving the glue in acetone, cleaned, and examined using an optical microscope. Details of damaged surface topography at higher magnifications were examined using scanning electron microscopy. RESULTS AND DISCUSSION The size of Vickers indents in both CF/epoxy and kaolin/epoxy layers increased with an increase in the load. Fig. 2 shows the typical indents in both layer types. However, no radial cracks were observed on the surface of the individual layers, even at the maximum load used. The absence of these cracks can be ascribed to both low hardness (Hv) and high critical load (Pc) to initiate cracks (15), where Pc is proportional to (KIC4/HV3). An extensive damage due to interfacial-shear debonding and damage was seen in the CF/epoxy layer but not in kaolin/epoxy layer. +*».
(a)
(b)
FIGURE 2 Typical indentation impressions in the (a) kaolin/epoxy and (b) CF-epoxy layer. (Magnification: lOOx)
Fig. 3 shows the hardness profile of a nanocomposite in cross-section. The higher hardness of the kaolin/epoxy (KE) and CF/epoxy (CFE) layers due to reinforcement by kaolin and CF is evident. Figure 4 shows the variation of hardness as a function of load for KE layer. There is clearly a modest display of load-dependent hardness in the KE layer. In contrast, this phenomenon was not observed for the CFE layer. The amorphous nature of epoxy and the fine dispersion of cellulose-fibres can account for the absence of load-dependent hardness in this system. This loadindependent hardness characteristic can be attributed to a grain-size effect (16,17) or the absence of fibre agglomeration. In contrast, agglomeration of kaolin particles can be readily seen in the KE layer. At small loads, the contact dimension (2a) of Vickers impression is comparable with the size of large agglomerated kaolin and the hardness measures properties similar to those of kaolin; when 2a becomes much larger than the average kaolin size at high loads, the hardness measures the "bulk"
Kaolin/Cellulose-Fibre Epoxy Nanocomposites
485
properties, with more kaolin/epoxy interfaces oriented for deformation by plasticshear and viscoelastic flow. It follows that this phenomenon will disappear in the KE layer if the fine kaolin particles can be uniformly dispersed within the epoxy matrix without formation of large agglomerates. The viscoelastic deformation of KE layer during indentation is clearly revealed in Fig. 5 which shows the creep strain as function of loading time. Over a period of 1 h, strain due to creep has increased by -30% but it leveled off after that. This suggests that during loading, the size of the indent increased with time as a result of viscoelastic flow and relaxation processes. As will be shown later, microdamage in the CFE layer due to prolonged indentation may also contribute significantly to the creep process.
-5-0.5-1 o_
o
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o
-a
o
2-0.4-
"0.2-
£ 0.3-
o
Hv (GPa)
0.6
1
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£0.1CFE
Layer type
> o3
2
4
6
8
10
12
Load (kg)
FIGURE 3 Hardness of the various layers within the nanocomposite.
FIGURE 4 Variation of hardness versus load.
Examination of sub-surface damages in the CFE system revealed a hemispherical shape deformation zone directly below the indenter. The size of the deformed zone and the associated extent of damage increased with load and time. However, there were no radial or lateral cracks formed (Fig 6). A closer examination of the damaged zone reveals an extensive debonding along the CF/epoxy interfaces (Fig. 7). In contrast, no debonding along the kaolin/epoxy was observed. It was further observed the degree of micro-damage within the CFE layer became more extensive as the thickness of the KE layer decreased from 1.0 mm to 0.3 mm. Thus, a thicker and harder KE layer has the capacity to shield the CFE underlayer from the undesirable micro-damage and creep. It is postulated that the pronounced and expanding sub-surface damage due to debonding at the CF/epoxy interfaces may also contribute to the indentation creep process observed in the CFE composite. The presence of CF fillers has acted as sites of stress-concentration and shear-deformation. In effect, the presence of these fillers in large amount has modified the intrinsic viscoelastic property of epoxy resin, rendering it more susceptible to shear-induced deformation at the CF-matrix interfaces. This mode of shear-deformation may impart an improvement in fracture resistance to the otherwise brittle epoxy resin.
Kaolin/Cellulose-Fibre Epoxy Nanocomposites
486
30 •
•ffi
20,
10
O
FIGURE 5 Creep strain of the kaolin /epoxy layer at 30 N.
FIGURE 6 Scanning electron micrograph showing the sub-surface damage at 100 N load
• k
FIGURE 7 A closer view of the sub-surface damage in the CFE layer.
FIGURE 8 Near absence of interfacial damage in the kaolin (k)/epoxy layer.
The study of subsurface damage has clearly revealed the existence of microcracks which are not apparent on the indent surface. The capacity of a thick and harder KE layer in providing shielding against excessive micro-damage in the CFE underlayer is also obvious. However, the mechanism for the apparent absence of any interfacial damage in the KE layer is puzzling and remains unclear. It is postulated that the elastic and thermal expansion mismatch in this layer may be favourable to minimize the formation of any undesirable residual stresses which might cause interfacial debonding. The presence of a KE layer is also expected to impart strengthening to the CF reinforced epoxy composite by virtue of nano-kaolin dispersion in the matrix. Contact damages show characteristics of quasi-plasticity in the CFE underlayer; namely large scale compression-shear deformation and absence of macrocrack systems but presence of extensive microdamage due to interfacial debonding. The deformation is accommodated by the buckling of CF and plastic shear at the CFepoxy interfaces which prevent the nucleation of subcritical voids or microcracks. The damage is observed to initiate in the subsurface region of high compressionshear beneath the contact instead of in the surface region of weak tension outside the contact. The primary stage of damage involves extensive sliding between CF/epoxy interfaces resulting in surface uplift, debonding, and interfacial microcracking.
Kaolin/Cellulose-Fibre Epoxy Nanocomposites
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Microcracks are facilitated by the presence of a large thermal expansion mismatch and initiated as a result of this sliding process which generates intense stresses. As previous eluded, the expansion or growth of these defects during prolonged contact loading may also account for the observed creep. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12.
13.
14. 15. 16. 17.
Kojima, Y., et al. 1993. "Mechanical Properties of Nylon 6-Clay Hybrid," J. Mater. Res., 8(12): 1185-1190. Usuki, A., et al. 1993. "Synthesis of Nylon 6-Clay Hybrid," J. Mater. Res., 8(12) 1179-1184. Park, J.H. and S.C. Jana. 2003. "The Relationship Between Nano- and Micro-Structures and Mechanical Properties in PMMA-epoxy-Nanoclay Composites," Polymer, 44(7) 2091-2098. Isik, I., U. Yilmazer and G. Bayram. 2003. "Impact Modified Epoxy/Montmorillonite Nanocomposites: Synthesis and Characterization," Polymer, 44 (12) 6371-6378. Ma, J., J. Xu, J-H. Ren, Z-Z Yu and Y-W Mai. 2003. "A New Approach to Polymer/Montmorillonite Nanocomposites," Polymer, 44(10) 4619-46-30. Kornmann, X., H. Lindberg & L. A. Berglund. 2001. "Synthesis of Epoxy-Clay Nanocomposites: Influence of the Nature of the Clay on Structure," Polymer, 42(5): 1303-1308. Fu, X. and S. Qutubuddin. 2000. "Synthesis of Polystyrene-Clay Nanocomposites," Mater. Lett. 42(1): 12-18. Bledzki, A.K. and J. Gassan, 1999. "Composites Reinforced with Cellulose-Based Fibres," Prog. Polym. Sci., 24(1): 221-228. G. Marsh, 2003. "Next Step for Automotive Materials," Materials Today 6(3) 36-41. Low, I.M., P. Schmidt and J. Lane, 1995. "Synthesis and Properties of Cellulose-Fibre/Epoxy Laminates,"/. Mater. Sci. Lett. 14 (1): 170-173. Low, I.M., P. Schmidt, J. Lane and M. McGrath, 1994. "Properties of Rubber-Modified Cellulose-Fibre/Epoxy Laminates," J. Appl. Polym. Sci. 54 (10): 2191-2194. Rowles, M., D. Lawrence, I.M. Low, P. Schmidt and J. Lane. 1999. "Indentation Responses and Micromechanisms of Failure in Cellulose Fibre/Mylar/Epoxy Laminates," Proc. Int. Workshop on Fracture Mechanics & Advanced Engineering Materials, (Eds. L. Ye & Y.W. Mai), 8-10 Dec. 1999, Sydney University, pp.343-50. Lawrence, D., G. Paglia and I.M. Low, 2000. "Indentation Responses and Damage of Polymeric Composites," Proc. Structural Integrity and Fracture 2000, (Ed. G. Heness), 29-30 June 2000, UTS,pp.ll9-127. Low, I.M. 1998. "A Modified Bonded-Interface Technique with Improved Features for Studying Indentation Damage of Materials. J. Aust. Ceram. Soc. 34 (1) 120-126. Lawn, B.R. 1993. Fracture of Brittle Solids, Cambridge University Press, Cambridge. Low, I.M., S.K. Lee, M. Barsaum and B.R. Lawn. 1998. "Contact Hertzian Response of Ti3SiC2 Ceramics." J. Am. Ceram. Soc. 81(1) 225-228. Low, I.M. 1998. "Vickers Contact Damage of Micro-layered Ti3SiC2." J. Europ. Ceram. Soc, 18(10)709-713.
Impact Performance of 3D Interlock Textile Composites J-H Byun , M-K Um and B-S Hwang Composite Materials Lab Korea Institute of Machinery & Materials, Korea S-W Song Department of Materials and Engineering Pukyong National University, Korea
ABSTRACT Impact tests of 2D and 3D textile composites have been carried out in order to identify the superiority of 3D composites. For 2D composites, the plain woven and the 8-harness satin woven composites of different fiber bundle size have been considered. For 3D composites, orthogonal woven preforms of different density and type of through-thickness fibers have been studied. To assess the damage after the impact loading, specimens were subjected to C-scan nondestructive inspection. Compression after impact (CAT) tests were also conducted in order to evaluate residual compressive strength. Under the impact energy of 15J the visible damage was small on the impacted side of the 3D woven composites, whereas the same impact energy caused perforation in 2D woven composites. Thus, the impact performance of 3D woven composites is superior to 2D woven materials, although the direct comparison of quantitative characteristics was not successful in this study.
INTRODUCTION The prepreg laminated composite has been widely used in various composites industry. However, laminated composites are liable to fatal damage under impact load due to the fact that they have no reinforcement in the thickness direction [1]. To overcome the inherent weakness and to widen its application to primary structural parts, three dimensional (3D) textile reinforcements have drawn much interests [2-4]. 3D fibrous preforms can be made by various ways such as stitching, needle-punching, 3D braiding and 3D weaving [5]. The needle-punching has been often used in the fabrication of preforms for carbon/carbon composites such as non-structural parts. The 3D braiding provides tubular type of axi-symmetric shapes. For the planar shape of preforms 3D weaving process is prefered. In the 3D weaving, yarns are interlaced in a manner similar to 2D woven structures, except that warp yarns may penetrate more than one layer of weft (fill) yarns. Many variations in the basic geometry of interlock preforms are feasible, depending on the number of layers interlaced, the pattern of repeat, and the presence of in-laid (stuffer) yarns. In this paper, impact performance of 2D and 3D textile composites has been characterized. For 2D composites, the plain woven and 8-harness satin woven composites Corresponding author, 66 Sangnam-dong, Changwon, Kyungnam, South Korea +82-55-280-3883, [email protected]
Impact Performance of 3D Interlock Textile Composites
489
of different fiber bundle size have been considered. For 3D composites, orthogonal woven preforms of different density and type of through-thickness fibers have been studied. The orthogonal preform has 3D orthogonally (x-y-z) arrangement of fibers. To assess the damage after the impact loading, specimens were subjected to C-scan nondestructive inspection. Compression after impact (CAT) were also conducted in order to evaluate residual compressive strength. EXPERIMENTAL Specimen Preparation Figure 1 shows schematic of 3D woven composites. Staffers and fillers are unidirectional carbon fiber bundles of 12K, and weavers for the through-thickness fibers are of smaller bundle size. Depending upon the density and the fiber type of weavers, three kinds of preforms have been fabricated: 3K carbon weavers of single density (SWC), 3K carbon weavers of double density (DWC) and Kevlar weavers of single density (SWK). Figure 2 shows SWC and DWC. For 2D fabric composites, 6K carbon fiber plain weaves (P6K), 3K carbon plain weaves (P3K) and 3K carbon 8-harness satin weaves (S3K) were used. All the specimens were fabricated by vacuum assisted resin transfer molding process. The epoxy resin and hardener were Kukdo Chemical KBR1729 and KBH1089, respectively. The dimension of the fabricated plate was 320x215x2.5mm. Plates were cut by 150x100mm according to SACMA SRM 2R-94 test specification [6]. The preforms information and the fiber volume fractions are summarized in Table 1. Warp weaver
> . ••
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=
iniinn B _ • _ *—*—»-^i • • •
t=t=c^jL: i ; : ; ; FIGURE 1 Unit cell of orthogonal woven Preform.
3D Woven 2D Woven
SWC DWC SWK P6K P3K S3K
C12K C12K C12K C6K C3K C3K
(Note) C : carbon fiber ; K : Kevlar fiber.
« »
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FIGURE 2 Surface pattern of SWC and DWC.
TABLE I Specifications of composite specimens
Stuffer (Warp)
i
Filler (Fill) C12K C12K C 12K C6K C3K C3K
Weaver C3K C3K K29 None None None
Volume Fraction 52% 54% 51% 54% 54% 54%
490
Impact Performance of 3D Interlock Textile Composites
Impact Test Samples were subjected to low speed drop weight impact test to examine damage resistance performance. Impact test setup is shown in Fig. 3. The energy levels imposed to the specimens were controlled by adjusting the height of the impactor of fixed weight. The impact energy was kept low to prevent perforation. The impactor weighs 3.605 kg and has a hemispheric tip with a diameter of 15.88mm. The specimen were placed in the test fixture as specified in SACMA and constrained by rubber tip clamps at every corner. During the falling and rebounding, the timing flag passes the timing gate which is placed just above the test specimen, and the impactor velocity is detected from the traveling time passing the timing gate. When the impactor contact with the specimen, the load cell in the impactor reads the impact force change. With the impact load data, the energy imposed to the specimens can be calculated.
Load cell and lf coo lai rts r
impactor lip lest specimen FIGURE 3 Drop weight impact test system.
FIGURE 4 SACMA CAI test.
Compression after Impact Test The compression after impact (CAI) test, which measures compressive strength of the impacted composite specimen was performed to examine the material's strength after exposition to an impact load [7]. The specimens were installed in the SACMA CAI test fixture, and four sides of the specimen were constrained carefully in order to prevent undesirable buckling or local crushing at the bottom. Fig. 4 shows CAI test fixture. The tests were performed at a cross-head speed of lmm/min. RESULTS AND DISCUSSION The impact energy of 15J has been applied on 3D woven composites, and the visible damage was small on the impacted side of the sample. For the case of 2D woven composites, however, the same impact energy caused perforation as shown in Fig. 5. It can be shown that the impact performance of 3D woven composites is superior to 2D woven materials.
Impact Performance of 3D Interlock Textile Composites
491
(a) (b) FIGURE 5 Damage comparison under impact energy of 15J: (a) 3D woven composite; (b) 2D woven composite.
Due to the perforation, impact energy of 7J has been applied for the case of 2D woven composites. Utilizing the different impact energy for these two cases has failed in comparing the impact performance between the 2D and 3D woven composites, quantitatively. Figure 6 shows the load-energy curves of 2D woven fabric laminated composites (P6K) and 3D woven composites (SWC). 3D woven composites reached at its maximum load without sudden load drop. However, 2D woven composites show drastic load drops, which is due to the delamination.
F6K
Load & Energy Histories
SWC
Load & Energy Histories
25006000 2000
/ 4000
1500-
/ 1000
/
/
\
2000
/ / 500
n
1/ t''
.
.
.
\
—
Load Energy
hi
n
Load Energy
\
6 "nm2[ms]
(a) 2D, P6K
"nme[ms]
(b) 3D, SWC
FIGURE 6 Load and energy histories of 2D and 3D textile composites
Table 2 summarizes the results of the impact test, C-scan, and the CAI strength of 2D and 3D woven composites. 2D woven fabric laminated composites show higher energy absorption rate than that of 3D woven fabric reinforced composites due to delamination. Absorbed energy of the 3D woven fabric reinforced composites shows that the specimen of double density weaver absorbed higher energy than the single density weaver. This is because the double density weaver has more resin rich area between stuffer and filler yarns. Among the 2D woven fabric laminated composites, 6K plain weave fabric composites (F6K) absorbed higher energy than the 3K plain weave fabric composites (P3K) because of the larger fiber bundle size. Between the same 3K fabric composites, the 8 harness satin showed higher energy absorption. This is due to the fact that satin
492
Impact Performance of 3D Interlock Textile Composites
weaves have larger area of unidirectional fibers. TABLE II Summary of impact test, C-scan, and CAI test results Impact Energy (J)
Absorbed Energy (J)
Damage Size (mm2)
Residual Comp. Strength (MPa)
3D Woven
SWC DWC SWK
14.8 14.9 14.8
6.0 6.9 5.7
512.7 762.2 454.0
172.3 184.6 164.3
2D Woven
P6K P3K S3K
7.0 7.0 7.1
4.4 2.8 3.0
381.7 197.5 250.2
150.7 172.0 175.4
C-scan results of each specimen are shown in Fig. 7. The damage areas indicate the pile-up images of the damage in the thickness direction. On the surface of the 3D woven fabric reinforced composites, there were small visible damages. However, the internal damage of the 3D woven composites are considerably large. The more the sample absorb impact energy, the bigger the damage size is.
(a) SWC
(d) P6K
(b) DWC
(c) SWF
(e) P3K
(f) S3K
FIGURE 7 C-scanned images of impacted panels.
Residual compressive strengths of the specimens subjected to the impact test were evaluated. Among the 3D woven fabric reinforced composites double density carbon weaver (DWC) specimen showed higher residual compressive strength than single weaver (SWC) composites in spite of its bigger damage area. This is because most of the damage is in the matrix rich area, and higher number of weavers contributed the increased compressive strength. Comparing SWC with SWK, Kevlar weaver composites showed smaller residual compressive strength due to the weakness of Kevlar fibers in the compressive load.
Impact Performance of 3D Interlock Textile Composites
493
Among 2D woven fabric laminated composites, 6K carbon plain woven composite (P6K) showed highest impact damage area and lowest residual compressive strength as can be expected. For the same fiber bundle size, the 8-harness satin (S3K) specimen showed bigger damage area, but has higher residual compressive strength than 3K carbon plain weave composite (P3K). This is due to the fact that satin weaves have more unidirectional fibers that contribute to the improvement of compressive strength. CONCLUSION (1) Under the impact energy of 15J the visible damage was small on the impacted side of the 3D woven composites, whereas the same impact energy caused perforation in 2D woven composites. Thus, the impact performance of 3D woven composites is superior to 2D woven materials. (2) Among the 3D woven fabric reinforced composites, double-density weaver specimen absorbed highest energy and the damage size was the largest. The specimens with Kevlar weavers absorbed lower energy and showed smaller damage size than the specimens of carbon weavers. (3) Among the 2D woven fabric laminated composites, 3K carbon plain weave composites showed smaller damage area than 6K carbon plain weave composite. For the same fiber bundle size, 8-harness satin specimens showed bigger damage area, but has higher residual compressive strength than plain woven composites.
ACKNOWLEDGEMENT This research was supported by a grant from the Center for Advanced Materials Processing (CAMP) of the 21st Century Frontier R&D Program and National Research Laboratory funded by the Ministry of Science and Technology, Republic of Korea. REFERENCES 1 2 3 4 5 6 7
Gao SL, Kim JK. Cooling rate influences in carbon fiber/PEEK composites. Part III: impact damage performance; Composites 2001;32:775-785. Tan P, Tong L, Steven GP, Ishikawa T. Behavior of 3D orthogonal woven CFRP. Part I. Experimental Investigation Composites Part A 2000;31:259-271. Callus PJ, Mouritz AP, Bannister MK, Leong KH. Tensile properties and failure Mechanisms of 3D woven GRP composites. Composites Part A 1999;30:1277-1287. Kuo WS, Fang J. Processing and characterization of 3D woven and braided thermoplastic composites. Composites Science and Technology 2000;60:643-656. Byun JH, Chou TW. Mechanics of Textile Composites. In: Kelly A, Zweben C, editors. Comprehensive Composite Materials. Amsterdam: Elsevier; 2000; chapter 22. SACMA, SACMA Recommended Test Method for CAI Properties of Oriented Fiber-Resin Composites; SRM 2R-94. Ishikawa T, Sugimoto S, Matsusima M, Hayashi Y. Some experimental findings in compression-after- impact (CAI) tests of CF/ PEEK(APC-2) and conventional CF/Epoxy flat plates. Composites Science and Technology 1995:55;349-363.
The Ballistic Impact Behavior of Composites Reinforced by Biaxial Weft Knitted UHMWPE Fabrics Zi-qing Liang Beijing institute of aeronautic material, Beijing 100095, China Guan-xiong Qiu Tianjin polytechnic university, Tianjin 300160, China Xiao-su Yi Beijing institute of aeronautic material, Beijing 100095, China
ABSTRACT Ultra-high Molecular Weight Polyethylene (UHMWPE) fiber is a kind of high-tech fiber proved to be the best bulletproof fiber by far. Because of a good ability of deformation Biaxial Weft Knitted (BWK) fabrics is a possible candidate for some molded bulletproof products such as helmets. The ballistic impact Behavior of Biaxial Weft Knitted UHMWPE composites has been investigated in this paper. It was found that ballistic performances were influenced by the pressing pressure strongly. The composites were manufactured under pressure of IMpa, 2Mpa, 5Mpa, respectively, which results in different matrix contents and ballistic performance. Those samples with higher matrix contents were penetrated by the '51' lead-core bullet fired by the '54' handgun, whereas a sample with lower matrix content arrested the bullet effectively. The ballistic impact responses of penetrated and non-penetrated composites were analyzed comparatively. Both in penetrated and non-penetrated composites, the main failure mode of fiber is cut-out by shear, especially for the penetrated samples, in which there seem to exist a change of failure modes from shear fracture to tensile rupture along the thickness of the target. But for the non-penetrated composites, tensile rupture can be observed only in those layers where the bullets were stopped. Most fibers in the following layers behave in an elastic manner although a 'back bulge' would come into being under ballistic impact. The difference of the delamination in the tow kinds of samples were studied also. Because of the peculiar fabric construction, some special phenomena were observed in the research such as yarn slippage and the fragments of the bonding coils. INTRODUCTION As a novel reinforcement material of bulletproof composites, UHMWPE fiber is a kind of high-tech fiber proved to be the best bulletproof fiber by far [1]. It has been applied in soft bulletproof vests, helmets, insert panels and composite armors successfully till now. hi the process of manufacturing this kind of bulletproof products, the pre-impregnated non-woven or woven fabrics would be laid perpendicular to each other and then pressed on the hot-pressing machine. Especially for some deep-pressed * Correspondence Author, P.O.BOX 81-3, Beijing 100095, Fax:0086-10-62458002, email: zqliang [email protected]
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products such as helmets, these fabrics must be cut into a special with several petals, which will be lapped one after another later. Thus many overlapped seams appear in the final products. The overlapped seams and the potential wrinkles in the helmets would decrease the bulletproof performance. Furthermore, the construction of UHMWPE macromolecule is uniform. There is no side chain and polar group on the main chain. This results in a weak interface bonding between fiber and matrix. The composites will delaminate easily under ballistic impact. The delamination, which will be discussed later, influences the bulletproof performance seriously. Biaxial fabrics were developed in the latest several decades. The load responding speed is faster than that of traditional woven fabrics. Jiang[2] studied the formation of Multi-axial warp fabrics by semi-sphere pressing experiment. He found that the deformation of fabrics depends on the number of lining yarn systems strongly. Those fabrics with fewer lining yarn systems formed well in the pressing process. Compared with warp knitted fabrics, weft knitted fabrics have a better ability of deformation. The lining yarns would slide and twist easily so that the fabrics need not be cut out with petals and the decrease of bulletproof performance due to overlapped seam can be avoid. Another advantage of biaxial weft knitted fabrics is that the bonding coils can limit the slide of lining yarns in a reasonable extent and improve the delamination of composites under ballistic impact. The ballistic impact behavior of Biaxial Weft Knitted UHMWPE composites was studied in this paper. EXPERIMENT MATERIALS The lining warp and lining weft are UHMWPE fibers supplied by Sinotex investment & development co,. LTD, China.(Specification: 400den/60f;Tensile strength: 2.8Gpa;Tensile modular: 81Gpa;Elongation: 3%.) The bonding yarns are high tensile strength polyester filaments with the fineness of 135 denier. Because UHMWPE fiber has a low melt point, the cure temperature of resin should be below 130°C. Herein unsaturated polyester was chosen to be the matrix. SPECIFICATION OF BWK FABRIC The Biaxial Weft Knitted fabrics (see Figure 1) were made by a lining warp and weft-knitting machine, which was developed by the Composites research institute of Tianjin Polytechnic University, China. The lining warp is UHMWPE fiber with 3200den and the lining weft with 1200den. The density of lining yarn is 23.6 warps/lOcm and 80+80 wefts/lOcm. The areal density of fabric is about 340g/m2.
FIGURE1 Morphology of BWK UHMWPE fabric
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The fabrics were cut into pieces with the sizes of 20cmx20cm, and then treated with acetone to remove the remaining spin solvent. The initiator and promoter were put into the unsaturated polyester which was stirred after mixing. The prepared resin was coated on the fabrics by manual. Because there is a sandwich construction with one lining warp layer and two lining weft layers in the fabric, these pieces of fabric were laid perpendicular to each other. The preimpragnated fabrics were put on the hotpress and molded at required temperature and pressure. Figure 2 is the photograph of BWK UHMWPE-Reinforced Composites.
(a) (top view) (b) (side view) FIGURE 2 Photograph of BWK UHMWPE-reinforced composites
A "54"handgun and "51" bullets were used in the research. The distance from the gun to the target is 5 meters, which was regarded as the most dangerous distance for a target to be penetrated by this kind of handgun. The shot angle is zero degree. THE BALLISTIC IMPACT BEHAVIOR OF COMPOSITES REINFORCED BY BWK UHMWPE FABRICS The Ballistic Performances of the Composites Reinforced by Bwk Uhmwpe Fabrics In the research three different pressures were used to manufacture the composite target. It was found that ballistic performances were influenced by the pressing pressure strongly. The composites were manufactured under pressure of IMpa, 2Mpa, 5Mpa, respectively, which results in different matrix contents and ballistic performance (see table 1). Those targets with higher matrix contents were penetrated, whereas the target with lower matrix content arrested the bullet effectively, even each target has the same 20 layers of BWK UHMWPE fabrics. The possible reason is that higher matrix contents lead the fibers apt to be failure by shear (see figure3). TABLE I The targets parameters and ballistic results
Target no. 1 2 3
Molding pressure IMpa 2Mpa 5Mpa
Matrix content 40.5% 28.4% 20.0%
Areal density 2
11.43kg/m 9.5kg/m^ 8.5kg/m2
Target thickness 13.02mm 10.96mm 9.78mm
Ballistic results penetrated penetrated Non-penetrated
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FIGURE 3 Section of a penetrated target
The Ballistic Impact Response of Composites Reinforced by BWK UHMWPE Fabrics The ballistic impact response of composites reinforced by BWK UHMWPE fabrics was examined comprehensively. The failure mode of fiber was found to exhibit cutout of a sheared plug. Because of the ovoid shape of the lead-core bullet, the crater aperture is smaller than the diameter of the bullet, and most fibers were pushed aside. A small annulate wrinkle can be observed around the striking point (see Figure 4). The stress wave initiated by ballistic impact spread in the laminate. The longitudinal wave is a kind of compressive wave and the transverse wave is a shearing wave. The former spreads faster than the later. But the transverse wave is main factor on interface debonding. After ballistic impact, a white area similar to rhombus appears on the laminate (see Figure 5). The reason for this phenomenon is that the laminate has different modulus at different direction. The modulus along the filaments is much higher than those at other direction. Another possible reason is that the shock wave will transmit and reflect when arriving at a interface between fiber and fiber or fiber and matrix. Its strength will lower down due to reflection. Along the direction of off-axle, the attenuation of shock wave will be more obviously than that at the direction of axle.
FIGURE 4 The shearing failure of composites under ballistic impact
FIGURE 5 The similar rhombus white area formed by shock wave
Under ballistic impact, some target materials moved with the bullet along the thickness of laminate. A peeling force arose before these materials were sheared. Due to the peeling force, the composite delaminated. The delamination was different with the process of penetration. At the area where the bullet was stopped, the delamination extended to the edge of the laminate (Fig. 6). But for the penetrated panel, there is no obvious delamination can be observed (see Fig. 3).
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The bullet was arrestedhere
FIGURE 6 Delamination of the target. The right side of the black line is the delamination in the target. The white arrow shows the penetration direction.
In fact, a reasonable delamination is helpful for the laminate to arrest the bullet. One, the delamination needs energy. The more important is that when delamination happened, the filaments can embrace the bullet at a certain angle. This is the key for the fibers to utilize its high strength and high modulus. A strong interface bonding will restrain the delamination and the fibers in the laminate tend to be sheared rather than to be stretched. On the contrary, a weak interface bonding will make the fibers slide along the surface of the bullet under ballistic impact, which followed by a unacceptable damage to the bulletproof performance. When the bullet hit the laminate, a unrecoverable deformation occurred to the bullet. The bullet arrested by the laminate looks like a mushroom. From this phenomenon, it can be inferred that the contacting area between bullet and laminate enlarged during the entire penetration. More and more fibers involved in the bullet resistance. The increase of load-bearing fibers combined with the delamination made the energy-absorbing mode changed. At first, most fibers were rupture by shear. With the penetration going on, a 'back bulge' came into being (Fig.7), which is regarded as a evidence of fiber experiencing a tensile load.
FIGURE 7 "Back bulge" of the I.II LV
FIGURE 8 The broken and slid yarns
FIGURE 9 The cracked bonding coils
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The tangential component of anti-penetration force made some filaments on the 'back bulge' slide down to the slope (Fig. 8). A few bonding coils were drawn to break. Those UHMWPE filaments broken by tensile released the deformational energy. They rebounded roughly so that the bonding coils were cracked apart (Fig.9). CONCLUSIONS To meet the bulletproof demand, the area density of composites must be up to a certain range decided by protective level and reinforcement construction. The areal density of the laminate used in the research is about 8.5 kg/m2. Matrix contents is approximately 20%. The ballistic impact response of Biaxial Weft Knitted fabrics reinforced composites was studied in this paper. It was found that the response is familiar with those composites reinforced by other constructional fabrics. However, some special phenomenons were observed in the research. REFERENCES [1], Cunniff, P.M., An Analysis of the System Effects in Woven Fabrics Under Ballistic Impact, Textile, Res. J. [J], Vol.62, No. 9, 509-516(1992). [2], Jiang Ya-ming, Study on the Mechanical and Forming Properties of Multi-axial Warp Knitting Fabrics, Dissertation for Doctor Degree, Tianjin Polytechnic University,(1999). [3]. Lee, B.L., Song, J.W., Ward, J.E., Failure of Spectra Polyethylene Fiber-Reinforced Composites under Ballistic Impact Loading, Journal of Composite Materials [J],Vol.28,No.l3,p p. 1202-1226(1994).
Low Speed Impact Behavior of Aluminum Honeycomb Sandwich Panel Jung-Il Song1*, Sung-In Bae1, Mun-Sik Han2, Kyung-Chun Ham3 Department of Mechanical Engineering, Changwon National University 9 Sarim-dong, Changwon, Kyongnam, 641-773, South Korea 2 Department Mechanical&Automotive Engineering, Keimyung University 1000 Sindang-dong, Dalseo-gu, Daegu 704-701, South Korea 3 Department of Machine Design Information System, Pnha Technical College 253 Yonghyun-dong, Nam-gu, Inchon, 402-752, South Korea 1
ABSTRACT Impact behaviors of Aluminum Honeycombs Sandwich Panel (AHSP) by drop weight test were investigated in this study. Two types of specimens with 1/2" and 1/4" cell size were tested by two impactors with the weight of 5.25kgf and 11.9kgf respectively. Transient, contact and elastic-plastic analyses were performed by finite element method. Impact behavior of AHSP about impact sites appeared nearly the same in low impact energy, but it was different in high impact energy. Face was the strongest about impact and short-edge was the weakest. The damaged area of AHSP was enlarged with the increase of impactor weight that is corresponding to impact energy. After 3-point bending test, fracture modes of AHSP were analyzed with AE counts, lower face sheet was fractured in the long-edge direction first, and then separation between face sheet and core happened. In the short-edge direction after core wrinkled, lower face sheet was torn, impact behavior by FE analysis were increased localized damage in high velocity because the faster velocity of the impact was, the smaller the stress of core was. Consequently, impactor weight had an effect on widely damaged area, while the impact velocity gave rise to localized damaged area.
INTRODUCTION Aluminum honeycomb sandwich panels (AHSP) have been widely used in the fields of aerospace, defense, automotive, railway, marine, communication and sport industry for the merits of light weight, high strength and high stiffness. But AHSP shows it's vulnerable before impact force. McGowan et al.[l] represented that manufacturing defect would happen to AHSP caused by careless impact. This damage almost didn't mark on the face sheet externally but it would cause strength reduction internally. It was also stated that the conditions and degrees of impact damage were variable according to the test methods such as drop weight impact test and air-gun test etc. Santosa et al.[2] compared the impact strength between the honeycomb cell and foam. They found that the aluminum honeycomb could own better impact behavior than aluminum foam under unidirectional loading and a combination load of compressive and bending. Reddy et al.[3]analyzed the impact conformation with the experiential equation derived. Papka et al.[4] evaluated the * Corresponding author, Visiting Professor, Biomedical Engineering Department, The University of Memphis , TN 38152 ,USA, E-mail; [email protected], Fax; 901-678-5281
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damage mechanism after impacting by optical analysis and ultrasonic c-scan. Kim et al.[5] found that test frequency is lower than resonance frequency of honeycomb structure by using mechanical impedance method in spite of various ways of finding the debonding honeycomb structure. Kim et al.[6] calculated the elastic modulus, shear modulus, Poisson's ratio, compressive bending strength, shear bending strength and flexibility of the sort of cell. In his research triangular and star cell was weak compressive bending strength and shear bending strength. But it had high flexibility. hi our previous work the variable fracture mode was found corresponding to the increase of impact energy. Goldsmith et al.[7] checked buckling pattern of core and analyzed small elastic energy after AHSP, aluminum core and flex core were impacted. These studies promoted the research of composite honeycomb sandwich panel. But the study of aluminum honeycomb sandwich panel was subject to be developed with consideration of the effect of impact position, weight and velocity. In this study a typical impact fracture mode was evaluated. The analysis of the impact energy caused during the damage of impacted specimens was also stated. Fracture modes of AHSP were analyzed with AE counts according to 3-point bending test. Impact damage area was observed with ultrasonic c-scan. Nonlinear impact analysis is carried Ansys5.5. EXPERIMENTAL METHOD AND FEM ANALYSIS Materials of Specimens Impact behaviors of Aluminum Honeycombs Sandwich Panel (AHSP) by drop weight test are investigated in this part. AHSPs with hexagonal-cell shape are fabricated by A 3003H14 sheet. Bondex is used for adhesive. Mechanical properties of the Aluminum plate (A3003H14) and tup (SS400) are listed in table. 1. Two types of specimens with 1/2" and 1/4" size cell are tested by two impactors with the weight of 5.25kgf and 11.9kgf respectively. Dimension of impact specimen is 100mmxl00mmx6mm. Thickness of upper face sheet is lmm and that of lower face sheet is 0.5mm. The height of core is 4.5mm and thickness of it is 0.0762mm. TABLE I Mechanical Properties of Aluminum Plate (A 3003H14) and tup (SS400)
ou a u (MPa) oys (MPa) e(%) £(GPa) p (g/cm3) A 3003H14 185 150 16 69 2.73 SS400 400 210 235 20 7.85 Experimental Method and FEM Analysis The 3-point bending lest is executed to check the impact mode by using MTS. during the 3-point bending lest, AE signal was analyzed about fracture mode by displacement controls. As shown in Fig. 1, Dynatup GRC8250 drop tower is driven by Instron to finish the impact test, impact behaviors of AHSP are examined according to the parameter changes such as the weight or initial position of the impactor. In Fig. 2, the spherical tup with the diameter of 12.7mm (1/2") is used for impact. AHSP is fixed at the center of the clamp with a 75mm diameter hole. For considering the effect of weight 5.25kgf and 11.9kgf impactors are used with the considering the sum of crosshead and tup weight. Impact sites are chosen at face, long-edge, short-edge and point in order to observe, the impact effects of face sheet and core. AHSP is impacted corresponding to the impact energy of 10J, 19J, 32J and 43J respectively.
502
Aluminium Honeycomb Sandwich Panel
The impact process is simulated numerically using a finite element model by Ansys 5.5 with nonlinear FE code. The meshed model for 1/4 symmetric condition is all constrained except for y direction. AHSP is full constrained because of the fixture of clamp. In contact analysis, the contact pairs are formed by target and contact surface, the upper face sheet of chosen for AHSP Target surface, and the external area of tup is closen for contact surface. Yielding stress and tangent modulus of tup and AHSP are inputted for elastic-plastic analysis. The tup with the weight of 11.9kgf and 5.25kgf contacts AHSP with the initial velocity of v0 = -Jlgh . The commercial program Ansys 5.5 is applied to analyze the relation between the time, stress of face sheet and core and impact energy.
A:face , B: long-edge, C: short-edge, D : point L)long-edge direction, S) short-edge direction FIGURE 1 Specimen fixture of drop weight tester Fig. 2 Impact position and bending direction
EXPERIMENTAL RESULTS AND DISCUSSION Static and Dynamic Behavior According to the AE signals, in the short-edge direction wrinkle of core emitted the low signal at 0-1.5sec. Then several burst signals engenders and debonding is starting at inner face sheet from 1.5~3.5sec. Because of friction between upper and lower face sheet, continuous burst signal appeared at 3.5-5.5sec. Lower face sheet began tearing at 5.5~7.5sec. In the long-edge direction burst signal appeared because of fracture of lower face sheet at 0~1.5sec. Large signal occurred to core tear at 1.5-3.5sec Fig. 2 shows torn specimen observed after impact by naked eye, (a) 34J in face, (b) 21J in long-edge, (c) short-edge, (d) point, damaged at 19J. Thefracturemode of AHSP under stronger impact force is indicated in Fig.2 at the site of face, long-edge, point, and short-edge, respectively
(a)
(b)
(c)
(d)
FIGURE 2 Visible Damage at upper site
(a)
(b)
(c) "
(d)
FIGURE 3 Typical fracture mode
Results in Fig. 3 express the typical fracture modes of honeycomb specimen that is damaged by impact position. After initial tear happens to the point or edge of core at the impact energy of 43J, face sheet begins to be depression as shown Fig.3(a). In 43J penetration happens 6 adjacency cores transmit impact load adequately from the face
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Which doesn't tear the face sheet under 10J, 19J, 32J. Fig. 3 (b) and (c) display the damaged specimen of long edge, short edge each in 32J. Fracture mode develops. Core cuts into face sheet when the limit load level is exceeded at the edges and tile fracture is transmitted by linked 4 edges. This certifies that the fracture of edge is the reason of final penetration, furthermore, long edge appears to be stronger under impact than short edge for 4 long edges are linked by 4 short edges. Fig.3(d) illustrates the impact mode at point under impact energy 32J. Embayment and buckling occur in face sheet similarly with Fig.3(b) and (c). While the support load at point exceed the limit, tear happens to face sheet along 3 edges by pinning of the core. Impact load data report that the curve related in hysteresis or impact load-time displays similar tendency to impact load-deflection curve. When U.9kgf impact three is applied to AHSP by 1/2" cell, impulsive load appears increasing tendency with the increases of impact energy (Fig. 4). Result of impact load expressed large difference under 32J, 43 J which is illustrated in Fig.4(a), (b). The impact energy of 10J and 19J cannot give great damage to AHSP. But under 32J and 43J the impact loads create considerable crash at face, long-edge, and point and short edge. After delivering enough shear force by adjacency core face sheet of lower part suffered high impact force from rebounding of the core damage. Buckling occurs to edge and point because of the shear force and upper-part or lower-part face sheet tears by this buckling. 5.5
face long-edge
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Time (msec)
(a) 32J (b) 43J FIGURE 4 Impact load of 1/2" AHSP cell corresponding to 11.9kgf impactor
The curves with impact load of 11.9kgf and 5.25kgf are almost similar behavior. The cell size is 1/2". The values of impact load of 5.25kgf and 11.9kgf in equal 1/2" specimen appear to have the similar tendency. But because of the unequal weight and different impact height, the impact is imposed for the increased final speed. For 11.9kgf impact load the speed reaching to maximum impact load is 8.5m/sec for 10J, 8m/sec for 19J, 4~8m/sec for 32J, 4~6m/sec for 43J. For 5.25kgf impact load the impact speed of is 5.5m/sec, 4~6m/sec, 3~5m/sec for 10J, 19J, 32J, 43J respectively, which is much faster than the first case. It invokes larger strain energy and produce bigger damage area. We know the impact energy is the function of speed. But from the data above we can find that the weight is more dominant element of impact behavior than speed. Absorbed Energy The maximum absorption energy is marked as Ea in the absorbed energy curve, which leads to the damage of AHSP. The amount of absorbed energy dedicated to the damage is marked as El, and the remaining elastic energy is marked as Ee. Fig. 5 is the graph of absorption, energy obtained by 32 J impact energy toward 1/2" cell's honeycomb panel with impact tup of 11.9kgf and 5.25kgf, respectively. The elastic
Aluminium Honeycomb Sandwich Panel
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energy of face and long-edge is shown in Fig. 5(a) under 11.9kgf impact damage. In Fig.5 (b) elastic energy curves of face, long-edge as well as point are illustrated under 5.25kgf. It can be clearly observed that weight has an obvious effect on the impact damage, that is, heavier weight will produce larger damage.
:
face long-edge short-edge point
/
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20
22
24
long-edga short-edge point
20
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£4
25
(a)11.9kgf (b)5.25kgf FIGURE 5 Absorbed energy of 1/2"AHSP cell corresponding to 32J
Whole absorption energy curves display similar results regardless of impact position in 10,19J. The impact resistance is increasing by the order of face, long edge, point and short edge in 32, 43J, which can be observed in the cases of existence and nonexistence of elastic energy. The short edge elastic energy appears less than 11.9kgf. This means that the impact energy that the short edge can suffer is lower than 11.9kgf. Ultrasonic c-scan is known as a useful method to observe damage face size after impact. From this figure we can find that the afloat area of 11.9kgf impact force with 32J impact energy in 1/2" cell size's specimen is larger than that of 5.25kgf. This means that heavy impact tup creates big damage face about the same impact energy, which explains that impact experiment data and c-scan image agree well. Finite Elements Analysis Nonlinear analysis about each impact energy that use impact tup of 11.9kgf and 5.25kgf about 1/2" cell is performed by finite element method. From these results we could obtain Von Misses stress of the case of 11.9kgf impact force and 32J impact energy in 1/2" cell specimen. Maximum stress 133.8MPa happens to the face sheet that tup is touched. The maximum in the core is about 58.1Mpa. When impact acts to the face, large stress impose on the edge and joints of edge and the stress is transmitted by contiguity core. 0.12
- o
0.11 0.10 -•-Time • °
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(msec)
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Impact Energy (J)
(a)5.25kgt
(b)11.9kgt
FIGURE 6 Stress and time of impact energy by 5.25kgf and 11.9kgf impactor
5
Aluminium Honeycomb Sandwich Panel
505
In Fig. 6, with the increase of impact energy, the maximum stress happens in face sheet. The stress transmitted through the core is decrescent. While the impact speed quickens, stress concentration is happened locally at impact position before damage is transmitted. Comparing Fig. 6 (a) and (b), stress of the core is larger in the case of 11.9kgf than that of 5.25kgf under the same impact energy. This analysis data also agree with the experimental results and c-scan image. Furthermore, the impact tup of 5.25kgf of the faster speed generates yielding stress into face sheet with shorter time. CONCLUSIONS Damage mode at 3-points bending test using AE count is analyzed. By the result, the tear of lower-part face sheet happens while preserve bending forces were applied at the core early in the short-edge direction. After lower-part face sheet of long-edge tears, separation of core and face sheet occur. Therefore, Short edges in the honeycomb structure receive more bending forces. Impact behaviors for various AHSP's positions are similar under low impact energy. However, in high impact energy it is different by the positions such as AHSP's face, long-edge, point and short-edge, Face is strongest to suffer the impact. And thickness is also an important factor to prevent tear of upper-part and lower-part face sheet. Under the same impact energy, heavy impact tup needs more time to reach the maximum impact load than light impact tup. The strain energy is much larger for heavy tup. The wider damage area is engendered which is confirmed by c-scan image. This means that low-speed impact is dominated by the effect of weight. According to finite element analysis of impact behavior, if the speed is the faster, the time that reaches the maximum stress is shortened by increasing the speed. Impact damage increases locally, which explains that the speed is the main variable to generate localized damage. ACKNOWLEDGEMENT This work was supported by grant from the Basic Research Program of the Changwon National University 2001.
REFERENCES 1.
2. 3.
4. 5. 6. 7.
David M. McGowan and Damodar R. Ambur.,"Damage Characteristic and Residual Strength of Composite Sandwich Panels Impacted with and without a Compression Loading", Materials Conference and Exhibit and AIAA/ASME/AHS Adaptive Structures Forum - PART 1, pp. 713-723, 1998 S. Santosa and T. Wierzbicki.,"Crash behavior of box columns filled with aluminum honeycomb or foam", Computers & Structures, Vol. 68, pp.343-367, 1998 T. Y. Reddy, H. M. Wen, S. R. Reid and P. D. Soden., "Penetration and Perforation of Composite Sandwich Panels by Hemispherical and Conical Projectiles," Journal of Pressure Vessel Technology, Vol. 120, pp. 186-194,1998 S. D. Papka, S. Kyriakides and S. Kyriakides., "Experiments and Full-Scale Numerical Simulations of In-Plane Crushing of a Honebcomb," Elsevier Science, Vol. 46, pp. 2765-2776, 1997 M. K. Lim, S. C. Low, L. Jiang and K. M. Liew "Dynamic Characteristics of Disbonds in Honeycomb Structures," Engineering Structures, Vol. 17, pp. 27-38, 1995 7. Beomkeun Kim, Richard M. Christensen.,"Basic two-dimensional core types for sandwich structures,"International Journal of Mechanical Science, Vol. 42, pp. 657-679, 2000 14. Werner Goldsmith and Jerome L. Sackman.,"An Experimental Study of Energy Absorption in Impact on Sandwich plates'lnternational Journal of Impact Engineering, Vol. 12, No.2, pp. 241-262, 1992
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PartX
Industrial Applications
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Thermomechanical Analysis of Water Aged Pultruded Composites Salwan Al-Assafi Composite Materials Research A Division of Pultron Composites Ltd, Gisborne, New Zealand
ABSTRACT Water absorption behaviour of pultruded fibre reinforced plastic (FRP) composites has been investigated in this study. Three resin systems were evaluated in distilled water and salt-water environments. The effect of water absorption on dynamic mechanical properties of the composite was analysed. Results indicate that rate of water absorption was the lowest for the vinylester and the highest for the polyester composite. It was also shown that the vinylester composite reached equilibrium faster than the other composites. Results also showed that changes in storage modulus and loss tangent subsequent to aging varied depending on type of matrix resin.
INTRODUCTION Demand has been growing in the construction industry for alternatives to steel, particularly in harsh environments where corrosion is a major concern. FRP composites can provide the required corrosion resistance, in addition to other advantageous properties such as high specific strength and low thermal and electrical conductivity. However, questions still remain on durability and performance of composites in various environments. Dynamic mechanical thermal analysis has been used in a number of studies to investigate performance and evaluate properties of matrix and fiber/matrix interface under various conditions [1-8]. Chin et al. investigated effects of water and salt solution on polyester and vinylester unreinforced matrix resins. An increase in glass transition temperature (Tg) was detected for both polyester and vinylester and it was attributed to hydrolysis and subsequent dissolution of low molecular weight segments. However, the study found vinylester to be more resistant to hydrolysis than polyester due to the difference in the position of the ester functional groups. Ester groups in vinylester are terminal and shielded by methyl groups, while in polyester they are positioned along the main chain, making them more vulnerable to hydrolysis reaction. Fraga et al. employed dynamic mechanical measurement to study water absorption effects on hand-lay-up polyester and vinylester composites [4]. Results of the study showed after immersion in 40°C water and subsequent drying, neat polyester resin samples exhibited lower loss tangent peak than that for the vinylester neat resin sample. That was attributed to the extraction of monomer. Results also indicated the * Corresponding author, P.O. Box 323, Gisborne, New Zealand. Fax: +64 6 867 8542. email: [email protected]
510
Water Aged Pultruded Composites Secondary Bonding
Tg for polyester matrix increases, while the width of loss tangent peak decreases, due to lower molecular weight distribution. Vinylester neat matrix showed similar behavior, where Tg increases and the width of loss tangent peak decreases, though to a lesser degree compared to the polyester. This study investigates short-term water absorption behaviour of polyester, vinylester and polyurethane pultruded composites. Changes in thermomechanical properties as a result of exposure to elevated temperature distilled water and salt solution are investigated. The results of this study can help in understanding effects of aqueous environments on performance of pultrusions with various resin systems and can assist in the selection of proper characterisation methods for the evaluation of aged composites. EXPERIMENTAL PROCEDURE Samples with a rectangular 19mm x 5mm cross-section were supplied by Pultron Composites Ltd. The samples were produced using the pultrusion process utilising three resin types; vinylester, polyester and polyurethane. E-Glass unidirectional ravings were used as reinforcement for all samples. The same glass volume fraction was used for all samples. All samples were cut to a length of 31mm and then conditioned for 24 hours at 50°C then weighed using an electronic scale with 0.1 mg accuracy to establish dry weight. A set of samples was then immersed in 60°C distilled water. Another set was immersed in a 60cC solution composed of 0.6 mol/L NaCl in distilled water. Samples were kept in the solutions for up to 17 days. Periodically samples were taken out, wiped with a dry cloth and weighed to determine weight gain. The measurement of dynamic mechanical properties was carried out on (5mm x 0.85mm x 31mm) strips in a Rheometric Scientific (New Jersey, USA) DMTA V using a 28mm span three-point bend configuration. The strips were cut from the edge of the 19mm x 5mm specimens. All samples were heated at 3°C/min from 30°C to 300cC and cycled at a frequency of 1 Hz. RESULTS AND DISCUSSION The weight gain for the vinylester, polyester and polyurethane FRP composites in water and salt solution is shown in Figures 1 and 2 respectively, hi both figures, vinylester samples reached equilibrium prior to the end of the trial. Polyester and polyurethane samples continued absorbing water and did not reach equilibrium within the duration of the test. This can be attributed to possible microcracking or crazing which commonly takes place during accelerated aging tests carried out at elevated temperatures2. It is evident that the rate and the final level of weight gain for vinylester are significantly lower than those for polyester and polyurethane. It is also shown in Figures 1 and 2 that the final levels of weight gain are higher for samples immersed in distilled water compared to those immersed in salt solution. This is likely to be a result of sorption retardation due to the presence of salt ions.
Water Aged Pultruded Composites Secondary Bonding
511
0.600 -i 0.500 -
d 0.400 • Vinylester • Polyester A Polyurethane
W 0.300 •
+•«
U)
*
•
'I 0.200 0.100 -
0.000 -T0
.•
•••
100
200
300
400
500
Time (hr) FIGURE 1 Weight gain for vinylester, polyester and polyurethane composite samples immersed in 60°C distilled water.
0.600
n
0.500
d 0.400 c "(5 O 0.300 O)
0.200 0.100 -
M•
•
• Vinylester • Polyester A Polyurethane
•
0.000 0
100
200
300
400
500
Time (hr) FIGURE 2 Weight gain for vinylester, polyester and polyurethane composite samples immersed in 60°C salt solution.
Water Aged Pultruded Composites Secondary Bonding
512 0.07
"Control * 17 days
0.01
50
100
150
200
250
300
350
Temperature (C)
FIGURE 3 Loss tangent plot for the polyurethane control sample and the re-dried distilled water aged sample.
0.07
0.06
"Control •17 days
50
100
150
200
250
300
350
Temperature (C)
FIGURE 4 Loss tangent plot for the vinylester control sample and the re-dried distilled water aged sample.
Water Aged Pultruded Composites Secondary Bonding
513
0.06
0.04
"Control •17 days
0.03
0.02
100
150
200
250
300
350
Temperature (C)
FIGURE 5 Loss tangent plot for the polyester control sample and the re-dried distilled water aged sample.
Dynamic mechanical thermal analysis can provide useful information on changes to the matrix and fibre / matrix interface that are taking place during aging. As shown by Fraga[4], the width of tan 8 peak can give clues on molecular weight distribution of the matrix. Figures 3-5 depict tan 8 plots for the polyurethane, vinylester and polyurethane pultruded samples. It is evident that polyurethane and vinylester samples did not show signs of changes in molecular weight distribution. On the other hand, a significant reduction in the width of tan 8 was observed for the polyester samples (Figure 5). This can be attributed to lower molecular weight distribution caused by monomer extraction or post cure [4], This also resulted in a shift of the tan 8 peak to a higher temperature, indicating a higher Tg for the aged sample. Monitoring the storage modulus (E') during aging can assist in detecting changes in the performance of a composite. As temperature is increased and the sample reaches the glass transition region, E' drops from glass-state level to rubberstate level. A study of E' in the rubber-state can give useful information on polymer molecular structure. High rubber-state E' values correspond to high crosslinking density and low molecular weight between crosslinks [4]. As shown in Figure 6, vinylester and polyurethane composites exhibited no rise in E' in the rubber-state after immersion in distilled water and salt solution for 17 days. On the other hand, polyester samples showed an increase in rubber-state E', which could be attributed to post-cure or monomer extraction.
Water Aged Pultruded Composites Secondary Bonding
514
10000
FIGURE 6 Rubber -state storage modulus for control samples and re-dried distilled water aged samples. All values were recorded at 290°C.
CONCLUSIONS Results presented in this study point to the importance of selecting proper material system for composites employed in wet environments. Sorption tests showed vinylester pultruded composites with the least weight gain in both distilled water and salt solution compared to polyester and polyurethane pultruded composites. Dynamic mechanical analysis of aged samples indicated a drop in molecular weight distribution and an increase in storage modulus of aged polyester samples, possibly due to monomer extraction and post cure. REFERENCES l.J. W. Chin, K. A. Aouadi, M. R. Haight, W. L. Hughes, and T. Nguyen, "Effects of Water, Salt Solution and Simulated Concrete Pore Solution on the Properties of Composite Matrix Resin Used in Civil Engineering Applications", Polymer Composites, vol. 22, no. 22, pp. 282-298, April 2001. 2. S. Zhang, W. Chu and V. M. Karbhari, "Investigation of Environmental Effects on Pultruded EGlass/Vinyl ester Composites", Proc. ACUN-3 "Technology Convergence in Composites Applications", pp. 201-207, NSW, Sydney, Australia, 2001. 3.S. Guionnet and J. C. Seferis, "Water Absorption of Model Phenolic Resin Systems for Composite Applications", vol. 34, no. 3, July 2002. 4. A. N. Fraga, V. A. Alvarez, A. Vazquez and O. De La Osa, "Relationship Between Dynamic Mechanical Properties and Water Absorption of Unsaturated Polyester and Vinyl Ester Glass Fiber Composites", Journal of Composite Materials, 37 (17) 1553 (2003). 5. A. Pegoretti, C. D. Volpe, M. Detassis, C. Migliaresi, and H. D. Wagner, "Thermomechanical .Behaviour of Interfacial Region in Carbon Fibre/Epoxy Composites", Composites: Part A, 27 1067 (1996). 6. S. Keusch and R. Haessler, "Influence of Surface Treatment of Glass Fibres on the Dynamic Mechanical Properties of Epoxy Resin Composites", Composites: Part A, 30 997 (1999). 7. A. Afaghi-Khatibi and Y. Mai, "Characterisation of Fibre/Matrix Interfacial Degradation under Cyclic Fatigue Loading Using Dynamic Mechanical Analysis", Composites: Part A, 33 1585 (2002). 8.V. A. Alvarez, M. E. Valdez, A. Vazquez, "Dynamic Mechanical Properties and Interphase Fiber/Matrix Evaluation of Unidirectional Glass Fiber/Epoxy Composites", Polymer Testing, 22 611 (2003).
Secondary Bonding in the Construction of Large Marine Composite Structures Gary J. Simpson* and Peter J. Burchill Maritime Platforms Division, Defence Science and Technology Organisation, Australia
ABSTRACT An investigation of secondary bond performance of composite systems used in the construction of large marine structures is described. Simple surface preparations were evaluated and materials and techniques that could enhance the strength of the structure and improve through life reliability were investigated. The phenomenon of fibre bridging and the effect it has on the fracture resistance of composite systems is discussed. Simple modifications to the composite systems are suggested that can improve the strength of the secondary bond to beyond that of the original. INTRODUCTION A composite laminate once cured is known as the primary laminate, any subsequent lamination to the primary laminate is known as secondary bonding. If all the constituents are the same as those used for the production of the primary laminate, then the secondary bond will generally prove to be weaker than the primary bond. Glass reinforced polymer (GRP) composites are increasingly being used in the manufacture of large marine structures. The logistics of more complex and extensive construction with composite materials will require wider use of secondary bonding through delayed lay-ups and joining. If the growth in the size of vessels made from composite materials continues at the present rate [1], confidence in being able to achieve effective and reliable secondary bonding will be essential. The through life operational conditions that marine composite structures could experience include damage from shock, impact, fatigue and long-term environmental exposure. For all of these scenarios the use of secondary bonding could be necessary if repair to the damaged composite is required. In addition, it is likely that if fatigue damage repair is required, then the secondary bond would require improved bond strength beyond that of the primary bond since it was the primary bond that can be seen as having failed. In this study, the method used to determine secondary bonding effectiveness is mode I fracture toughness, as measured by the Double Cantilever Beam test (DCB). DCB is a widely used method of evaluating the effectiveness of a composite to resist delamination in terms of interlaminar fracture energies for Mode I (tension failure). Characterisation of the fracture energies, which are seen to propagate these interlaminar cracks, is achieved through linear elastic fracture mechanics (LEFM).
* Corresponding author, Maritime Platforms, DSTO, PO Box 4331, Melbourne, Victoria, Australia, 3001, Australia. 9626 8409, [email protected]
516
Secondary Bonding in the Construction of Large Marine Composite Structures
This allows deduction of the energy release rate (Gi) for the crack growth and hence a measure of fracture toughness. The polyester/E-glass composite chosen for this study is commonly used in marine construction. The secondary bonding systems used were selected to give a reasonable range of the many toughening techniques [2] available rather than for the development of any definitive repair system for this particular marine composite system. EXPERIMENTAL The marine resin used is an unsaturated isophthalic polyester. The fibre reinforcement is a heavy (1400 grams per m2) woven silane sized E-glass roving. The weft fibre is "spun", meaning it is hirsute, which appears to help fracture resistance by increasing the contribution of fibre bridging. Initially the effect of surface preparation on secondary bonding was examined. These secondary bonding surfaces were lightly hand sanded (using A80 grit sand paper), heavily sanded (using a power tool), left unsanded (control), or had a peel ply applied to the wet resin surface. The peel ply is a widely used non-coated polyester available from Advanced Composites®. The most effective surface preparation was then used to prepare secondary bonding surfaces, for the lamination of the toughening systems. A number of the secondary bonding systems used are based on Derekane® 8084. Derekane® 8084 is a widely used vinyl ester that has been internally modified with carboxyl-terminated acrylonitrile-butadiene copolymer (CTBN) to give greater toughness. It is used here as a secondary bonding resin by itself (VE Control) and also blended with both 5% VTBN X33 (VE Toughened A) and 5% Core-Shell rubber (VE Toughened B). VTBN X33 is a vinyl terminated acrylonitrile-butadiene copolymer produced by B. E. Goodrich®, from a group known as reactive liquid rubber. Core-Shell rubber (CSR) can be used as an alternative to toughening with liquid rubbers. CSR's generally have a rubber core, poly (butadiene) in this case, with a more rigid polymer shell, poly (alkyl methacrylate) in this case. The CSR used here was made by Rohm and Haas®. The other systems studied were a toughened version of the original polyester resin, using CSR toughening at 5% (PE Toughened) and the use of a scrim or interweave (PE Interweave). Scrim materials are low cost, continuos filament, reinforcing fabrics, used here as an interply in the interphase region of composite materials. The scrim used here is called Colback®, produced by ColBond®, which is a very thin open weave made from bicomponent polymer filament. The scrim is used with the original marine composite system. All laminates were manufactured using a hand lay-up technique and cured using a peroxide catalyst at room temperature. There was no post-cure. The initial primary bonding sample was prepared as a 4-ply composite. For secondary bonding, 2-ply primary laminates were fabricated. There was a 60-day gap between the initial 2-ply lamination and subsequent secondary bonding to mimic the time gaps between laminations that occur during construction. A teflon ply was inserted, during the primary lamination at the central interphase or, onto the base laminate at the beginning of the secondary lamination. This insert extended 50 mm into the specimen to act as a pre-test crack debond (Ao). For testing, the data analysis method used required specimen thickness (B) to be measured, while load (P), displacement (d), compliance (C) and crack length (a) were measured during the test. These values were subjected to analysis by computer
Secondary Bonding in the Construction of Large Marine Composite Structures
517
spreadsheets to derive a value for Gi. The resulting Gi value has been found by also taking into account the various inconsistencies that can occur with this sort of testing. Hashemi [3] proposed various corrections, as detailed in equation 1. Gi = (F/N)3Pd/2B(a+Zh)
(1)
The value X^ is added to the crack length to correct for the deformation of the beam due to rotation. Correction F allows for the apparent shortening of the beams due to displacement of the beam arms. Corrections N involves minor adjustments made due to stiffening of the specimen by the end blocks. Various methods have been published on the derivation of mode I fracture energies, though from the methods used [3,4,5], very little variation in the final Gi value was observed. RESULTS AND DISCUSSION Effect of Surface Preparation on Secondary Bonding. The following plot details the effect different surface preparations had on the composite system.
1.0
T
Model Fracture Toughness (kJ/m) 0.5-
0.0
Primary bond
No Sand
Light Sand
Heavy Sand
Peel Ply
FIGURE 1 Effect of surface preparation on the Mode 1 fracture toughness of bonded laminates.
The results show a small but significant decrease in secondary bond performance from the best of the series of simple surface treatments when compared to the primary bond. The worst performance was found to be from the use of the peel ply. The weakness appears to be due to the larger resin rich interphase area that occurs with the use of a peel ply. This provided a thicker plane of matrix resin, with relatively poor cohesive forces, through which the crack could propagate. Sanding provided an improvement, though the statistical difference between light hand sanding and a heavy grind using an abrasive power tool did not appear to be significant. For the secondary bonding lay-ups, a medium (80gm) sand paper was used to lightly abrade the bonding surfaces. This was mainly for simplicity than for any advantage in secondary bond strength. No peel ply or chemical surface treatment was used. When comparing the primary and secondary bonding performance of this particular polyester/E-glass marine composite, fibre bridging is an important factor. Fibre bridging has been a widely reported [6,7,8] phenomenon from the early
518
Secondary Bonding in the Construction of Large Marine Composite Structures
seventies and is known to cause an increase in fracture toughness in the form of higher tensile loads needed to propagate the crack front between two plies of the reinforcement. Clumps of fibre strands are attached to either side of the interlaminar crack, mechanically resisting crack growth, as seen in Figure 2. This mechanism will be observed, at least to some extent, in any composite system where the plies of the reinforcement are intertwined or compressed together during the manufacturing process. This intertwining is known as "nesting" and is mainly and most significantly observed with unidirectional reinforcements. The mechanism is also seen [9] to increase crack propagating loads in bi-directional woven reinforcements. While not as extensive as observed in unidirectional composites, it is known to enhance resistance to cracking in woven reinforcements to a significant degree.
.«*,Trw>i Sg
^*~ill^iiiI^^Tif E Ti^'^ l ^ t '''^f ^ '
«»*£?• 15»ii.m rff^jyi ^~ifti •%^'V ^A.
FIGURE 2 Fibre bridging mechanism that increases fiacture resistance in less tougher matrix resins
The spun weft fibre in the reinforcement appears to increase the occurrence of fibre bridging, thus increasing the interlaminar crack resistance. Therefore the subsequent decrease in fracture toughness, normally observed in secondary bonding, is more apparent in this case given the absence of the enhanced fibre bridging in the secondary bond. Delayed lay-up, which occurs in the manufacture of thicker structures, can cause inherent weaknesses due to thicker interply regions. Partial cure of the surface, caused by an overnight stop to the lay-up, will however provide a degree of molecular cross-linking on resumption of the lamination the following day. Given the dependence on fibre bridging that this and other polyester composite system appear to rely on for interlaminar strength, a partly cured resin barrier that result from staged lay-ups prevents the fibres from intertwining causing a potentially weaker final laminate. Furthermore, the absence of fibre bridging during secondary bonding, when laminating critical structural joints or connections, suggests toughened resin systems are vital for obtaining satisfactory structural integrity. Effect of Toughened Composite Systems on Secondary Bonding. The test data obtained for the toughened secondary bonding methods is shown in Figure 3. Major improvements in delamination resistance, above that of both the primary and secondary bond of the original composite, were found for all of the toughening techniques studied. The technique of blending butadiene elastomeric materials has been widely used to toughen epoxy [2] and vinyl ester matrix resins [9].
Secondary Bonding in the Construction of Large Marine Composite Structures
519
The particular blend used is Derekane® 8084 with VTBN, at a 5% loading (VE Toughened A). A previous study [9] has shown this blend to provide much tougher room temperature curing matrix resins with enhanced cohesive and adhesive properties. Similarly, the use of CSR required a blending technique using a highspeed shear stirrer to fully mix the core shell with both resins (PE and VE Toughened B). The immiscibility of various toughening mechanisms with matrix resins is a problem [2] with this sort of technique, though the systems used here are known to be stable for long periods after mixing. 2.0 -r
1.5 --
Mode I Fracture Toughness (kJ/m)
1.0 - •
0.5--
0.0 Primary PE Bond
PE Bond (no sand)
PE Bond (lightsand)
Tough'd PE
PE Interweave
VE Control
TouglVdVE B
Tough'dVE A
FIGURE 3 DCB testing of Primary and secondary bonding systems.
For the toughened secondary bonding systems the observed increased fracture resistance is due to the improved adhesive and cohesive properties of the toughened systems. The failure mechanism of the toughened secondary bond was observed to be more complex than for the failure of the primary bond. The surfaces of the failed secondary bond showed one face mostly devoid of any residual resin, while the other face had a mixture of the primary and secondary bonding resins. An explanation for this is that tough secondary bonding resins adhere much more strongly to the remaining primary resin than the primary resin could adhere to the glass fibre surface. This failure was observed for all of the toughening blends including the VE Control. The tougher the system used, as seen by the Gi result (Figure 3), the more marked this mode of failure would be. The PE Interweave gave a good Gi value considering the matrix resin was the standard polyester. The fracture surfaces showed fibre from the scrim matt on either face, indicating the scrim had a fibre bridging type effect on the crack propagation. The effect would be enhanced given the pliable polymeric materials used in the interweave. This was unexpected as there was residual polyester interphase, unaffected by the interweave scrim, that could have failed at lower loads. There is no obvious explanation as to why the crack would propagate through the tougher scrim interweave region. It appears a value of around 2 kJ/m2 is a maximum achievable limit in secondary bond fracture toughness. This is an acceptable result as it provides a large improvement in mode I fracture toughness when compared to both the primary and conventional secondary bond in the polyester/E-glass composite studied.
520
Secondary Bonding in the Construction of Large Marine Composite Structures
Manufacture of large marine structures using GRP will mean the cost of the two components of the composite will be a large part of the total cost of the structure and in many cases the major reason for the use, or not, of these materials. The use of polyester matrix resins is common, mainly due its low cost compared to other resins such as vinyl esters and epoxies. However the strategic use of the more expensive materials would enhance overall structure integrity and reliability for only minor increases in overall costs. An example of where effective choice of secondary bonding materials could give critical and significant improvement is in the construction of large composite ocean-going vessels. It has been shown [10] that the most likely damage site for heavy impact or shock to such a ship would be in the bulkhead to hull connection. These joints in composite construction generally use an overlaminate method to give the joint strength. Through necessity a large degree of secondary bonding occurs in the various designs of these critical joints. Strategic application of these toughened, more expensive materials could see large increases in initial strength and long-term durability. Improved secondary bonding using the toughened systems studied here would also aid significantly the performance of repairs such as the Scarf repair. CONCLUSION The work detailed in this report shows that secondary bonding problems can be overcome by strategic use of more costly materials in the manufacturing process that would increase resistance to fatigue, impact and shock damage and allow subsequent repairs to be much more effective. When using a secondary bond the inclusion of a toughened system for the first two plies onto a lightly sanded and cleaned surface would enhance the strength and through life reliability of a composite structure. The use of the polyester interweave was also found to be surprisingly effective in improving secondary bond fracture toughness REFERENCES 1. Mouritz A. P., E. Gellert, P. Burchill and K. Challis. "Review of Advanced Composites for Naval Ships and Submarines," Composite Structures, 53 (2001) 21-41, Elseiver Science. 2. Hourston, D. J. and S. Lane, "Rubber Toughened Engineering Plastics," Chapters 8, pp 24359, Chapman and Hall, London, 1994, A.A Collyer ed. 3. Hashemi S., A.J Kinloch and J.G Williams. Proc R Soc Lond, 1990, A427. 4. Carlson L. A. and J B Pipes, "Experimental Techniques in Composite Materials," Elseiver Publications, Chapter 8, 1992. 5. Gdoutos E. E., K. Pilakoutas and C.A. Rodopolous. "Failure Analysis of Industrial Composite Materials," Chapter 4, V. Kostopolous, pp 152-174. McGraw-Hill 2000. 6. Begley J. A. and J. D. Landes. "The J Integral as a Fracture Criterion," Fracture Toughness, Proceedings of the 1971 National Symposium on Fracture Mechanics, Part II, ASTM STP 514, American Society of Testing and Materials, 1972, pp 1-20. 7. Davies, P. and M. L. Benezeggagh. "Interlaminar Mode I Fracture Testing in Applications of Fracture Mechanics in Composites," Composites Materials Series, (K Fredrich ed.), Elsevier Science, Vol 6, pp 81-112. 8. Kardomateas G. A., R. L. Carlson and C. H. Ferrie. "A Micromechanical Model for the Fibre Bridging of Macro-Cracks in Composite Plates," AMD-Vol 196, "Failure Mechanics in Advanced Polymeric Materials," ASME 1994. 9. Simpson G. J., P. J. Burchill and P. J. Pearce. "Tougher Vinyl Ester Resins and their Fibre Glass Composites," Feb 1995 20th Australian Polymer Symposium. 10. Smith C. S., "Design of Marine Structures in Composite Materials," pp 283, Elsevier Science, England, 1990.
Surface Analysis of "Class A" Polymer Composite Substrates for the Automotive Industry P.J. Schubel*, L.T. Harper, T.A. Turner, N.A. Warrior, CD. Rudd University of Nottingham, U.K. K.N. Kendall Aston Martin Lagonda, U.K.
ABSTRACT This work looks at quantifying the level of surface finish needed on a polymer substrate to obtain an acceptable painted finish on a highly visible body panel for use in the automotive sector. A range of materials were investigated with stylus profilometry, light reflectivity and subjective assessment. Results were statistically analysed to produce limits for acceptable surface quality on a bare polymer substrate.
INTRODUCTION The term 'Class A' has been widely used as a classification of surface quality for automotive exterior body panels, however there has been limited work to establish a threshold for identifying a Class A surface. Generally, it is believed that a substrate made of composite material represents a class A surface if its optical appearance is identical to an adjacent steel panel. The market, type segment and brand all influence the definition for a Class A standard [1]. The requirements of a composite body panel for the prestigious automotive sector is generally higher in all aspects compared to mass production vehicles. Emphasis is placed on producing a lightweight panel with a high level of dimensional stability and good surface quality. Polymer matrix fibre composite materials exhibit designer specified mechanical properties and low density, however surface quality is largely dependent on material type, stacking sequence, cure process and mould surface quality. Composite substrates potentially exhibit a range of surface defects which can be attributed to characteristics of manufacture, the application of high gloss coatings (Clearcoat) or a combination of both these factors (see Figure 1). Composite manufacture using liquid moulding may potentially produce porosity and fibre readout as a prevailing surface defect [1]. Porosity occurs as air is entrapped in the surface layers during processing. This can cause an elevation of the coating or destroy the coating layer, creating pinholes due to baking temperatures. Fibre readout becomes more pronounced as the deviation of fibre and resin shrinkage increases during processing as a result of temperature changes. This problem is more evident in thermoplastic processes due to the large temperature drop and high coefficients of linear thermal expansion (CLTE). ""Correspondence Author, ITRC Building, University of Nottingham, University Park, Nottingham, NG7 2RD, England. [email protected]
522
"Class A " Polymer Composite Substrates for the Automotive Industry
Neitzel [1] used surface profilometry to obtain arithmetic mean (Ra) values for a selection of composite surfaces. He observed that glass mat reinforced thermoplastic (GMT) and long fibre reinforced thermoplastic (LFRT) show single filaments, resulting in relatively higher surface roughness. In comparison SMC and RTM both yielded significant improvements in surface quality due to lower CLTE. Laser topography was conducted on both bare and coated (40 urn thick) substrates. Results showed a distinct decrease in surface roughness created by the fabric architecture on the coated substrate. Neitzel concluded that fibre readout and textile induced waviness were considered to be the dominant defects. Wenger [2] and Dickson [3] both used contact stylus profiling to categorise the surface roughness of polymer composite components. These related papers both looked at the effects of tool material, autoclave pressure and fabric lay-up. Wenger stated that the most appropriate parameters for characterising the surface of a composite plaque are Ra, skewness (Rsk) and kurtosis (Rk). The studies were based on an 8-harness satin weave carbon prepreg, moulded on two steel tools of differing hardness. Ra and Rt measurements improved with increased autoclave pressure and skewness increased up to a moulding pressure of 400 kPa but then decreased at higher pressures. Dickson also suggested that there is no immediate difference in surface quality for plain weave and 8 harness satin weave. Halden [4] used a range of amplitudes to categorise the surface of automotive steel body panels and their associated effects on paint quality. He concluded that there was no correlation when comparing the Ra values of steel surfaces to the relative surface tension. Halden [4] also concluded that peak count (Pc) has poor correlation with paint appearance and noted that variation in peak height is one of the critical parameters for paint appearance. Although there have been numerous investigations on automotive related surface quality, studies on the acceptable surface quality limit of a bare polymer substrate are rare. The presented work covers a range of polymer substrates for surface characterization, first by stylus profiling before paint treatment and second by laser diode reflectivity (Wavescan DOI) and subjective assessment after painting. The results are analysed collectively to obtain a quantitative limit for the acceptable surface quality of a bare composite substrate.
Coating
Substrate
Disturbance of coating flow Enclosure of dust particles Colour conformity Roughness, gloss Surface cracking Porosity (coating elevation, blisters, pinholes) Fibre readout, waviness FIGURE 1: Allocation of surface defects on coated substrates [1]
"Class A " Polymer Composite Substrates for the Automotive Industry
523
MATERIALS/ PROCESS The materials used in the study are detailed in Table I, with steel and aluminium being included as reference samples. All mould surfaces were measured to have an Ra of 0.07 um. TABLE I Constituents used in surface quality trials Material
Sample ID Steel Al PD9551E
Twintex
HexMC Sprint
Areal Fibre Mass (gsm)
Resin Type
Mould Process
Scott Bader (resin) Sotira (fibre)
Random mat
3025
RTM
Twintex® commingled Eglass HexMC" carbon
Saint-Gobain Vetrotex
2x2 twill
Ortho UP, 30wt% PVAc, 30wt% CaCO3 Polypropylene
Hexcel
50x8mm strips
Random mat
Sprint" CBS ST85
SP Systems
6
2x2 twill
600
ST86/ S2
Compres sion moulding RFI
ACG
3
2x2 twill 4x4 twill
199 280
VTS263
RFI
SP Systems SP Systems SP Systems/ Hexcel Hexcel (resin) Sotira (fibre) Scott Bader (resin) C. Cramer & CO. Scott Bader (resin) C. Cramer & CO. Scott Bader (resin) C. Cramer & CO. Scott Bader (resin) C. Cramer & CO. Scott Bader (resin) C. Cramer & CO. Scott Bader (resin) C. Cramer & CO. Scott Bader (resin) C. Cramer & CO. Scott Bader (resin) C. Cramer & CO. Hexcel (resin) C. Cramer & CO. Hexcel (resin) C. Cramer & CO. Hexcel (resin) C. Cramer & CO. Hexcel (resin) C. Cramer & CO.
6 12 6
2x2 twill 2x2 twill 2x2 twill Random mat
600 600 300 3025
ST85 ST85 DLS 1554-2 DLS 1648 (epoxy) RT2557 (polyester) RT2557 (polyester) RT2557 (polyester) RT2557 (polyester) PD9749 (vinyl ester) PD9749 (vinyl ester) PD9749 (vinyl ester) PD9749 (vinyl ester) DLS 1648 (epoxy) DLS 1648 (epoxy) DLS 1648 (epoxy) DLS 1648 (epoxy)
RFI RFI LRI RTM
UncoatedFeP04 (0.7 mm) Aluminium6016 (1.2 mm) E-glass preform + E-glass surface veil
3k UP 6k UP
Style 428 carbon
RC300 RC303T RC300LRI 1648E Veil UP
Tow Size (K)
Weave Style
SF95 surfacing film (glass) VTS263 backing layer ZPREG263 surface layer RC300T carbon RC3O3T carbon RC300 carbon LRI E-glass preform + E-glass surface veil Oxidised PAN veil Style 452 carbon Style 452 carbon
Zpreg
Manufacturer
12k UP
Style 424 carbon
VeilVE 3k VE
Oxidised PAN veil Style 452 carbon Style 452 carbon
6k VE
Style 428 carbon
12k VE
Style 424 carbon
Veil EP 3k EP
Oxidised PAN veil Style 452 carbon Style 452 carbon
6k EP
Style 428 carbon
12k EP
Style 424 carbon
Alcan
Continuous 3 3
2x2 twill 2x2 twill
80 200 200
6
2x2 twill
285
12
2x2 twill
660
Continuous 3 3
2x2 twill 2x2 twill
80 200 200
6
2x2 twill
285
12
2x2 twill
660
Continuous 3 3
2x2 twill 2x2 twill
80 200 200
6
2x2 twill
285
12
2x2 twill
660
RFI
RTM RTM RTM RTM RTM RTM RTM RTM RTM RTM RTM RTM
RFI - Resin Film Infusion LRI - Liquid Resin Infusion RTM - Resin Transfer Moulding
Paint Process Half of each test plaque (300 x 210 mm) was painted in an automotive paint process with no excessive abrasion on the surface. The panel was degreased with a degreasing agent, keyed using a 3M® fine grade sanding sponge then degreased again. Two coats of high build primer were sprayed to obtain a film build of 65 um. This was then baked at 80 °C for 20 mins. Once cooled, the surface was lightly sanded with P400 paper and a sealing primer was applied and baked, followed by a light sanding with P400 paper. Two
524
"Class A " Polymer Composite Substrates for the Automotive Industry
coats of solid, dark base paint and two coats of Clearcoat were applied, producing an average total film build of 160 urn. Each Clearcoat was baked at 80 °C for 20 mins. Surface Characterisation Surface roughness was recorded on bare substrates using stylus profiling. A Mitutoyo Surftest SV622 profiler with 5 um stylus and auto drive unit was used to measure an evaluation length of 12.5 mm at a speed of 0.5 mm/s and pitch of 0.8 um. An 'R' profile was applied with a Gaussian filter and cut-off length of 0.8mm to exclude surface waviness. Five traces in both x and y directions were systematically taken from various locations on the sample to obtain an average reading. The surface waviness of the painted substrates was measured using a BYK Gardner Wavescan DOI with built-in laser diode light source and optical camera. A minimum of three scans in the x and y direction was taken over a scan length of 100 mm to obtain an average value. Visual assessment of the substrates was conducted to categorise painted surface quality and relate human perception to machine sensitivity. 15 subjects were used to assess the panels under florescent light to determine the visibility of the defects on the painted surface as a direct result of the patterns seen on the bare substrate. RESULTS & DISCUSSION Subjective visual assessment rated the dedicated body paneling systems (PD9551E and semi pre-pregs), RTM moulded epoxy substrates and the reference steel and aluminium substrates to show no visible defects on the painted surface. Commingled Eglass polypropylene was determined to have the most visible defects on the painted surface, with strong fibre readout caused by high CLTE. Figures 2 and 3 show the samples grouped into three categories in accordance with results obtained from subjective assessment i.e. No visible defects, Visible defects, Highly visible defects. Combined Ford (CF), shortwave (SW) and longwave (LW) readings obtained using a Wavescan DOI (Figure 2), show general trends that match subjective assessment. Linear trendlines fitted to CF, SW and LW results show that substrates classed with having no visible defects are generally within tolerance ranges specified by the original equipment manufacture automotive paint standards for non flattened/polished finishes. Surface roughness measurements were recorded for Ra, Rz, RzDIN, Rq, Ku and Sk. The surface roughness measurements for the bare substrates were analysed using normal (Gaussian) distribution and confidence intervals. The Kurtosis and Skewness of the bare substrates showed no correlation to the resulting paint surface quality, with Rz, RzDIN and Rq showing major discrepancies (results not presented). The arithmetic mean (Ra) of the bare polymer substrate surfaces (Figure 3) best depict the painted surface quality trends measured using Wavescan DOI. Figures 4a,b and c show the normal distribution for the grouped surface roughness data of the bare substrates seen in Figure 3. In each case a normal distribution was assumed and the standard error approximately equalled the standard deviation. Table II shows the resulting 95 % confidence intervals calculated for each of the three categories. From the results it was possible to set a range for acceptable and non-acceptable surface quality for Class A bare polymer substrates. A bare polymer substrate with a Class A surface finish was found to have an Ra equal or less than 0.16 um. Visible defects in the painted surface would be seen on bare substrates above an Ra of 0.16 um and highly visible paint defects would be expected on bare substrates above an Ra of 0.54 um.
"Class A " Polymer Composite Substrates for the Automotive Industry
525
The calculated lower limit of Ra (0.16 um) is comparable to the measured Ra of an aluminium body panel, however a steel body panel measures approximately 1 um Ra. The discrepancy can be attributed to the fine amorphous structure of the steel substrate, which is easily masked under the paint process to produce an acceptable painted surface finish.
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"Class A " Polymer Composite Substrates for the Automotive Industry
526
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CONCLUSIONS Results show that Wavescan DOI reproduces the human visual perception of an acceptable painted polymer substrate with reasonable accuracy. Assessing surface roughness parameters in relation to Wavescan DOI and subjective assessment results, show that the arithmetic mean (Ra) best represents the expected paint quality from the bare substrate. For the materials presented, it has been shown that an acceptable painted automotive finish is obtainable on a bare polymer substrate below or equal to an Ra of 0.16 um. However, each material has its own unique surface pattern, which adversely affects the final painted substrate. The use of instrumented devices is a useful tool for predicting surface quality, however human visual assessment is still a necessary component in assessing painted Class A polymer substrates. REFERENCES 1. Neitzel, M., et al., Surface quality characterisation of textile-reinforced thermoplastics. Polymer composite, 2000.21(4): p. 630-635. 2. Wenger W., et al., The surface-finish characteristics of composite components. Mat proc tech, 1992. 33: p. 439-452. 3. Dickson G.R. and Mcllhagger R., Assessing the surface finish ofpolymer composite components. J. Mach. Tools Manufact., 1992. 32: p. 51-56. 4. Halden M., Characterisation of steel sheet surfaces in order to predict surface appearance after painting. IBEC, 1997: p. 115-120.
Injection Molding of Silk Composite from Industrial Fiber Waste Teruo Kimura*, Tomohiro Suzuki Kyoto Institute of Technology, Advanced Fibro Science, Japan Seiji Hatta Kyoto Municipal Industrial Research Institute, Japan
ABSTRACT This paper presents a study on injection molding of silk composite from industrial fiber waste. The cut waste of silk textile was pre-treated by opener and card machines and mixed with PP fiber. The sliver-type silk/PP mixture was fed into the injection molding machine directly. As a result, the silk fiber reinforced PP composites were obtained. The mechanical properties of composites were measured and discussed. It is concluded here that the silk waste is good for the reinforcement of composite. The results suggest that the injection molding method described herein shows promise for contributing toward the material recycling of cut waste of silk textile. INTRODUCTION In recent years, the textile industry has taken a growing interest in developing system for recycling waste fibers which result from the process of manufacturing products with the goals of protecting the environment and saving energy. For example, the large amounts of cut wastes of silk textile are discharged from the necktie manufacture factory. However, most of these waste products are destroyed by fire or buried underground. Meanwhile, in the field of composite materials, recent attention has been shifting from glass and carbon fibers to natural fibers because of their renewable nature, low cost, low density and low energy consumption. Application of the cellulosic fibers such as jute, flax and hemp to the reinforcement of composites has been discussed in many papers[ 1-4]. Few papers, however, can be seen about the protein fiber as a reinforcement of composites. Under these circumstances, the present paper discusses the recyclability of cur waste of silk(protein fiber) textile as a reinforcement of fiber reinforced composite. SILK FIBER WASTE Figure 1 shows the cut wastes of silk textile which are discharged from the necktie manufacture factory. As can be seen in the figure, the silk fabrics were dyed in many colors. In this paper, such silk waste was used for the reinforcement. The tensile strength and modulus of silk fiber are about 500MPa and lOGPa, respectively.
* Corresponding author, Matsugasaki, Sakyo-ku [email protected]
,Kyoto 606-8585, Japan, +81-75-724-7863, Email:
528
Injection Molding of Silk Composite from Industrial Fiber Waste
FIGURE 1 Silkfiberwaste
PRE-MOLDING OF SILK/PP SLIVER The cut waste of silk textile was pre-treated by opener and card machines and mixed with PP fiber as shown in Fig.2. Namely, the PP fiber was used as a matrix material of composites.
FIGURE 2 Mixing of silk and PPfibersby using card machine
Figure 3 shows the well-mixed silk/PP sliver. The silk length is about 10 mm in the sliver. The volume fraction of silk fibers was adjusted by regulating the mixing ratio of silk and PP fibers. As the silk fiber waste used in this research was not intended for recycling, PP(density of 0.91g/cm3, graft denaturation rate of 0.30wt%) denaturated with anhydro-maleic acid was used as adhesive resin with silk fibers and non-extended fibers were fabricated using mono-filament solvent yarning device in order to facilitate supplying to the molding machine, as discussed later.
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Figure 4 shows anhydromaleic acid denatured PP fibers (called g-PP hereafter) wound by a bobbin.
Injection Molding of Silk Composite from Industrial Fiber Waste
529
FIGURE 4 Anhydromaleic acid denaturedPP fibers
INJECTION MOLDING METHOD AND MECHANICAL TESTS For molding of silk fiber reinforced PP composite materials, the injection molding method was used. In this case, sliver-type silk/PP mixture was fed into the injection machine directly without forming pellets. With this method, simultaneous supply of woven g-PP is possible. Although g-PP can be supplied in the pellet shape, the supply can be stabilized by yarning. Figure 5 shows an overview of the molding machine used (manufactured by Toyo Machinery & Metal CaLtd., Plaster Ti-30G).
FIGURE 5 Injection molding method
The molding temperature 190deg. was determined as the melting point of PP fiber. The molds were tensile testing specimens whose size followed the JIS K 7133 standard. The specimens for bending and impact tests were cot from the molded specimens. The tensile and bending properties were measured at an ambient temperature using INSTRON (model 4206) according to JIS K7113 and JIS K 7171 standards, respectively. Moreover, impact test was done on an Izod impact tester (model DG-IB) according to JIS K 7110. The specimen dimensions are 80x30x 10 mm. Five samples were tested in each set. RESULTS AND DISCUSSION The sliver of silk/PP fibers used was bitten by the screws of the injection machine by being lightly pushed into the outlet of the machine at the start of molding and automatic continuous molding was possible thereafter. Figure 6 shows the molded tensile test piece. The specimen turned black because of the dyed silk fibers.
Injection Molding of Silk Composite from Industrial Fiber Waste
530
FIGURE 6 Molded test specimen
Figure 7 shows the SEM observations of cross-section of molded specimen without g-PP. The good dispersion of silk fibers can be seen in this figure.
FIGURE 7 SEM observation of cross section (V, =23%)
Figures 8(a) and (b) also show the SEM observation of interface between silk fiber and PP matrix for the specimens with/without g-PP. The lack of adhesion can be seen for the specimen without g-PP. However, the good adhesion can be achieved for the specimen with g-PP.
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(b)with g-PP
FIGURE 8 SEM observation of interface between silk and PP matrix
Attention is now focused on the tensile properties of the molded composites. Figure 9(a) and (b) shows the relation between the volume fraction of silk fiber and the tensile strength and modulus of the composites, respectively.
Injection Molding of Silk Composite from Industrial Fiber Waste 60
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The lozenges in the figure are the result without using g-PP. As is seen from these figures, the strength and modulus were improved along with the increase of the volume fraction of silk fiber. Especially, the fairly large strength and modulus can be obtained for the composites with using g-PP. It is believed that such property improvement is due to the improvement of adhesion between the matrix and silk fibers by g-PP as is seen from the cross section photo in Fig.8. Figures 10 (a) and (b) show the bending strength and modulus, respectively. It is cleared from the figures that the bending properties also improved along the increase of the volume fraction of silk fiber.
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The impact value for matrix and composite materials can be seen in Fig. 11. It is seen from the figure that the impact value becomes larger for the larger volume fraction of silk fiber. However, the value for the specimens with g-PP takes a lower value than that for the specimen without g-pp. This fact suggests that the lack of adhesion between silk fiber and matrix is advantage for the impact energy absorption.
Injection Molding of Silk Composite from Industrial Fiber Waste
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CONCLUSIONS The present paper discussed the recyclability of cur waste of silk (protein fiber) textile as a reinforcement of fiber reinforced composite. The molding method in which the cut waste of silk fabrics was pre-treated by opener and card machine as raw material of injection molding was proposed. As a result, it is concluded that the silk wastes used are the good reinforcement of composites. The molding method of composite materials described in the present paper shows promise as a contribution towards the recycling of cut waste silk fabrics generated in the process of manufacturing.
REFERENCES 1. 2. 3. 4.
X.chen, Q.Guo and YMi. 1998. "Bamboo Fiber-Reinforced Polypropylene Composite: A Study of the Mechanical Properties", J.ofApplied Polymer Science, 69:1891-1899. MAvella, L.Casale, RDeU'erba, B.Focher, E.Martusceffi and A.Marzetti. 1998. "Broom Fibers as Reinforcing Materials for Polypropylene-Based Composites", J.ofApplied Polymer Science, 68:1077-1089. Norma EJVIarcovich, Maria M.Reboredo and M.LArangurea 1998. "Mechanical Properties of Woodflour Unsaturated Polyester Composites",J.of Applied Polymer Science, 70:2121-2131. Michael P.Wolcott, S.Yin and Timothy GRials. 2000. "Using Dynamic Mechanical Spectroscopy to Monitor the Crystallization of PP/MAPP Blendin thePresence of Wood",Composite Interface^:3-12.
Test of Full Scale Integrally Stiffened Composite Spoiler Adrian Rispler* Hawker de Havilland, Australia
ABSTRACT An integrally stiffened composite spoiler for a large civil aircraft has been designed, manufactured and tested. The spoiler is a spar and rib dominated design with six hinges and a single central actuator. This paper describes the analysis of the spoiler test set-up and the correlation between the predicted and actual stiffness of a spoiler for a typical large airliner. The aims of this test program were fourfold. Firstly to carry out an assessment of the spoiler's structural strength. Secondly to evaluate the overall stiffness and buckling characteristics of the spoiler. Thirdly to validate the theoretically predicted strength and deformation characteristics from numerical analysis with the actual test results. The correlation of the model allows for the validation of additional technical requirements such as aerodynamic smoothness by means of analysis only. Finally, to validate the manufacturing methodology employed. Three tests were conducted at ambient temperature using the same test article, hi all tests, an enforced displacement proportional to the limit load condition was applied to the spoiler to replicate the wing bending component. The set-up represents the most critical spoiler deployment position. The first test subjected the spoiler below Limit Load and was carried out in order to establish the buckling performance of the spoiler. The second test went up to 1.0 Limit Load with the final test conducted up to 1.5 Limit Load (DUL). Strain and displacement results were recorded throughout the duration of the tests to allow for the correlation of experimental results with the finite element analysis predictions. The test was deemed to be successful as FAR and specific performance requirements were all met. The onset of buckling as well as strain trends for most of the strain gauges showed good correlation between prediction and test results.
INTRODUCTION A co-cured carbon fibre composite control surface demonstrator has been designed, manufactured and tested [1],[2]. The spoiler, shown in Figure 1, is 2.5 metre in span and 1.2 metres in chord is based on a design study for a large civil aircraft. The spoiler is a spar and rib dominated design with six hinges, two of which are nonfunctional and only come into play if one of the functional hinges fail. The spoiler has a single central actuator. Three structural tests were carried out on the same test article. The set-up represents the most critical spoiler deployment position. These tests were conducted from zero Limit Load (DLL) up to design ultimate load (DUL) as described below for the critical deployed configuration: * Corresponding author, Hawker de Havilland, PO Box 30, Bankstown, NSW 2200, Fax (02) 9772-8301, email: [email protected]
534
Full Scale Integrally Stiffened Composite Spoiler
1. 0.8 LL (To ascertain buckling requirements, ie no buckling up to 0.8LL) 2. 1.0 LL (Limit Load case) 3. 1.5 LL (Ultimate Load case) Closing Ribs ^
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The loads applied to the structure consist of aerodynamic as well as wing bending loads. Wing bending loads are applied through enforced displacements at Hinge 1 and Hinge 6 fittings. Aerodynamic loads are applied by the use of hydraulic rams, whose loads are then dispersed through the whiffletree into the spoiler by means of pivoted links and foam pads. This paper describes the analysis of the spoiler under test conditions and correlation of test results with finite element analysis predictions of displacements and strain gage readings for the ultimate load case. EXPERIMENTAL SET-UP Testing was carried out under ambient conditions and the test article was tested at room temperature dry conditions. The test was carried out at the bi-axial test facilities of the University of New South Wales, Solids Laboratory. A schematic of the test article with installed hinges and actuators and the upper and lower whiffletree is shown in Figure 2. Figure 3 shows a front view, looking on the spoiler upper skin, of the actual test set-up. Three tests were conducted using the same test article. In all tests, an enforced displacement proportional to the limit load condition was applied to the spoiler to replicate the wing bending component. Strain and displacement results were recorded throughout the duration of the tests to allow for the correlation of experimental results with the finite element analysis predictions.
Full Scale Integrally Stiffened Composite Spoiler
535
Aerodynamic loads are applied by the use of three hydraulic rams, whose loads are then dispersed through whiffletrees U p p e r Whiffletree
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536
Full Scale Integrally Stiffened Composite Spoiler
Each hydraulic ram or actuator feeds two articulated form-boards. The load distribution employed during the test replicates the critical load case. The form-boards apply a quasi-uniform spanwise distribution and trapezoidal chordwise distribution. The whiffletree is composed of 6 upper/lower form-boards, which are placed at rib locations. The spoiler is loaded through the upper skin by the foam pads attached to the form-boards through segmented pivoted links. The two-segmented pivoted links per form-board ensure the load is distributed along the full chord top skin. This arrangement is required to accommodate both the pre-stressed shape of the spoiler and its deformed shape under load due to wing bending and chordwise bending under the simulated air load. FINITE ELEMENT ANALYSIS PATRAN/NASTRAN finite element modelling and analysis were employed in all cases to calculate stresses, eigenvalues and deflections of the spoiler under the aerodynamic pressure provided as shown on Figure 4 and under the test load cases to simulate the aerodynamic loading. The model consisted of 4083 Nodes, 4511 CQUAD4 elements, 17 CTRIA3 elements, 216 CHEXA elements, 37 RBAR elements and 2 RROD elements. For the test case (deployed position), the pressure distribution was applied at pivoted links /form-board positions. As each of these foam-padded links was connected to form-boards by means of single pins and spherical bearings; it was assumed that the load was distributed along the full length of each articulated link. The loads to be transferred at each link were calculated from equilibrium equations at each section and area of each link to yield a pressure load. This pressure load was calculated for each link and divided by the load percentage and applied on the QUALM elements where contact existed between foam padded link and top skin of spoiler. Wing bending was super-imposed with the pressure load. The actuator jack position was rotated accordingly for the deployed position. Boundary conditions and pressure loading as employed for the test case (DHL) is shown in Figure 4. SPCs were used to constrain hinge points at Hinges 3 and 4 in the x, y and z directions. MPCs were used to represent the links at Hinges 1 and 6, and for the connection between the actuator hinges and the actuator point. A further SPC was applied at the actuator point in the x, y and z directions. Induced wing bending effects, at 1.0 DLL, were simulated by enforced displacement of 7mm in the upward direction at the link nodes at Hinges 1 and 6. SPCs were also applied at these enforced displacement points to constrain movement in the chordwise direction. These enforced displacements were factored according to the load case being analysed, i.e. for 1.5LL analysis; a factor of 1.5 was applied to the enforced displacement values. When analysing the spoiler to represent the deployed test position, the MPC connecting the centreline between the actuator hinges and the main actuator point was rotated to represent the deployed position about the actuator centreline, hence moving the main actuator point. The enforced displacements at Hinges 1 and 6 were also split into chordwise and out of plane components. Further MPCs were included in the deployed case to connect the hinge fittings to the bottom skin in to prevent the elements moving through each other (in this case there is a pressure between the fittings and bottom skin).
Full Scale Integrally Stiffened Composite Spoiler
537
TEST RESULTS The correlation is applicable for the 1.5LL test and analysis carried out for the critical spoiler deployed position.
efo FIGURE 4 Test pressure loading and boundary conditions
All the available results from the data acquisition system are compared against their finite element prediction by means of graphically representing their discrete values at 10% intervals for each test. Visually no buckling could be detected, although the back to back strain gages show panel instability between 1.0 LL and 1.1 LL (Figures 5,6). There is a marked change in slope occurring almost simultaneously at the outboard and inboard sections (where strain gages were positioned) at 1.1 LL. This lead to the belief that although the onset of buckling occurred at approximately 1.0 LL, the panels where the strain gages were installed undergo post-buckling behaviour at values above 1.1 LL. This can be clearly seen by the diverging plots of back to back strain gauges above 1.1 LL.
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538
Full Scale Integrally Stiffened Composite Spoiler
The front spar close to the actuator location was identified as a critical region and a strain gauge was placed there to monitor the maximum strain. Figure 7 depicts the correlation between predicted and actual critical strain showing that the finite element analysis accurately predicted the strain in this region. Finally, Figure 8 shows the measured strain on the actuator link compared to the predicted one. This strain was monitored to ensure that the test item was subjected to the correct hinge moment. 300.0
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CONCLUSIONS The test was considered to be successful as the design ultimate load (DUL) was slightly exceeded and this load was maintained for over 5 minutes as measurements were recorded. FAR Part 25 Sub-Part C, Sec. 25.305 Strength and deformation (b) requires that "The structure must be able to support ultimate loads without failure for at least 3 seconds". Furthermore, the same directives stipulate that "(a) the structure must be able to support limit loads without detrimental permanent deformation. At any load up to limit loads, the deformation may not interfere with safe operation". No permanent deformation was seen after unloading once the limit load test was completed. This was further corroborated during the third and final test up to 1.5 LL by looking for hysteresis effects on the strain and deflection plots. Therefore regulatory requirements were all met. Furthermore and after unloading of the structure, NDI indicated no failure or delamination between the co-moulded bottom skin and the substructure (ribs & spars). Buckling was not seen to occur under 1.0 LL whereas the technical requirements specified that no buckling should occur up to 0.8 LL. Critical strains correlated well to predicted values. However, actual maximum tip displacement was underestimated by approximately 25 %. ACKNOWLEDGEMENTS The author would like to thank the RMIT Start Grant Team and UNSW staff for their help during the set-up and testing of the spoiler at University of New South Wales. The efforts of Mr Michael Marelli (CRC-ACS) in manufacturing the test rig components well within schedule and budget are greatly appreciated. Thanks are also extended to Dr Ben Qi (CRC-ACS) and Dr Roger Li (UNSW) for their help in setting up the Data Acquisition System. REFERENCES 1. 2.
Rispler, A.R., Raju, J., 2002. "Design and Analysis of a Composite Spoiler", Report No. 180-RSM20002, Issue No. 1, Hawker de Havilland Internal report. Rispler, A.R., Raju, J., Varbola, M., McMahon, C , 2002. "Spoiler Test Analysis and Correlation", Report No. 180-RSM20-003, Issue No. 1, Hawker de Havilland Internal report.
Study on the Polypropylene(PP) Fiber/Cement Mortar Workability Hui Zhang, Liming Zou, Jianhua Ni, Yimin Wang* State Key Laboratory for Chemical Fibers and Polymer Materials Donghua University, Shanghai, 200051, P. R. China
ABSTRACT The ways to measure polypropylene fiber cement mortar workability are simply discussed in this article. By measuring the flowing extent, the effects of length and content of polypropylene fiber, the ratio of water to cement, mineral additive and the ratio of cement to sand are discussed in this paper. The results show that: 1) the longer polypropylene fiber length and the larger the content, the lower the flow extent of cement mortar; 2) with the increase of the ratio of water to cement, the flow extent is also increased; 3) as the decrease of the ratio of cement to sand, the flow extent of polypropylene fiber cement mortar will be increased; 4). for mineral additive, the addition of fly ash can improve the flow extent of polypropylene fiber cement mortar, while the silica fume can reduce slightly the flow extent of polypropylene fiber cement mortar.
INTRODUCTION The workability of cement mortar is a comprehensive technical target and significant in practice construction, that is because it has something with its mechanical performance such as strength and its efficacy in actual application [1]. However, it's very difficult to find a practical and effective way to predict the workability of cement mortar. Since the workability of cement mortar is markedly affected by flow extent, the general way is to measure its flow extent, and according to the acquired results it is determined whether the cement mortar is fit for practice performance requirement. There are many ways to measure the flow extent, which could be classified into two types: one is to put some external force on cement mortar, generated transmutation value is commended to be the scale of flow extent, and the other is to make cement mortar absorb certain energy to generate transmutation, absorption energy value is the scale of flow extent. The tests include flow cone method and vibrating method or mortar thickness method etc. Polypropylene fiber has many special features such as easy processing, good chemical resistance, high-energy absorption, 100% wet strength retention and low density [2]. Polypropylene fiber has been used as secondly reinforcement in cement material for over thirty years [3] and the studies are still active in ACBM (Advanced Cement * Corresponding author, Donghua University, Tel: 86-21-62379785, Fax: 86-21-62379309, E-mail address: [email protected]
540
Polypropylene(PP) Fiber/Cement Mortar Workability
Based Materials ) , American Northwestern University, American Concrete Institute[4-5] and some Japanese research institutes, Tongji University [6-7] and Donghua University of China etc. [2,8]. Polypropylene fiber can greatly improve cement materials performances such as anti-crack property, toughness [9], impact resistance [10] and permeability [11]. This paper makes use of vibrating method testing flow extent to evaluate the workability of polypropylene fiber cement mortar. EXPERIMENTAL Materials Materials used in this experiments include: 1) Jiaxin 325# common silicate cement produced by Taiwan Jiaxin Cement Group; 2) tap water; 3)mineral additives produced by Shanghai Fulai Zaoxing Material Corporation; 4)standard sand; 5)polypropylene fiber produced by Zhangjiagang Polypropylene Fiber Factory, the features are presented in Table I. Table I The features of polypropylene fiber
Polypropylene fiber Density /g/cm 3 Tensile strength / Mpa Elastic modulus / Gpa Melting point/ °C Wet strength retention / % Acid and alkali resistance
Features 091 400 8.3 160—170 100 very good
Measurements Rationed cement, sand and fiber are mixed in a container, stirred for 5 seconds, and then tap water was fed in slowly, stirred for another 3 minutes. The mixed mortar is fed promptly into the cone for measuring flow extent at two layers. The first layer of mortar is about 2/3-cone height, uniformly pressed, and then the second layer of mortar is put on it, 20mm higher than the cone height, uniformly pressed again. The cone is taken out; the sample is vibrated for 30 times at the speed of once per second. The max diffuse diameter and its upright diameter with the calipers is measured, the flow extent (mm) of cement mortar is attained. The operation must be finished in 5 minutes [12]. RESULTS AND DISCUSSIONS The effects of PP fiber length and content on the cement mortar flow extent The length and content of polypropylene fiber added are two of the most important parameters influencing the properties of cement mortar. The following figures show the effects on the polypropylene fiber cement mortar flow extent. In Figure la, it is noted that with the increase of the length of polypropylene fiber, the fiber crimp in the mortar increases, conglutination of fiber and mortar is higher, and the viscosity of polypropylene fiber cement mortar is therefore enlarged. It leads
Polypropylene(PP) Fiber/Cement Mortar Workability
541
to the decrease of flow extent of polypropylene fiber cement mortar; In Figure lb, it is noted that with the increase of the content of polypropylene fiber, the number of PP fiber is more, the viscosity of polypropylene fiber cement mortar is enlarged and the flow extent of polypropylene fiber cement mortar also goes down.
195-,
220-
190E 200-
— 185|
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120 0.0
150 5cm
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15cm
0.3
19cm
0.6
0.9
1.2
1.5
1.8
21
3
PPfiberccntent( kg'm )
FPfiberlergth
FIGURE 1 (a) The effect of PP fiber length on flow extent, (b) The effect of PP fiber content on flow extent
The effects of the ratio of water to cement on the cement mortar flow extent The ratio of water to cement is the most important factor affecting the strength of cement material. Figure 2 shows the relation of flow extent and the ratio of water to cement.
2001 190•§ ISO's' 170-
I 16°-
| 150o) 140o 130120 0.40
0.45
0.50
0.55
0.60
the ratio of water to cement
FIGURE 2 The effect of ratio of water to cement on the PP fiber cement mortar flow extent
Polypropylene(PP) Fiber/Cement Mortar Workability
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From Figure 2, it is noted that the PP fiber cement mortar flow extent goes down with the decrease of the ratio of water to cement. When the ratio of water to cement goes down to 0.4, PP fiber can't be distributed uniformly and conglobations would be happened in the matrix, which cause stress partly concentrated. The sample surface has much disfigurement and is difficult to mold. Adjusting the ratio of water to cement, which making PP fiber distribute uniformly in the matrix, can therefore control PP fiber cement mortar flow extent. Thus, it is possible to get the predicted mechanical properties of polypropylene fiber cement composites. The effects of the ratio of cement to sand on the cement mortar flow extent
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1.0:2.5
1.0:2.0
1.0:1.5
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the ratio of cement to sand
FIGURE 3 The effect of ratio of cement to sand on the flow extent of PP fiber cement mortar
The ratio of cement to sand is also a very important parameter. Figure 3 shows the relation of flow extent and the ratio of cement to sand. From Figure 3, it is noted that the PP fiber cement mortar flow extent increases slowly with the decline of the ratio of cement to sand. That is because when the amount of sand increases, the viscosity of mortar matrix material will go down, resulting in the increase of polypropylene fiber cement mortar flow extent. The effects of the mineral additive on the cement mortar flow extent There are two functions to add appropriate content of mineral additive. One is to make use of the high fines property of mineral additive, making PP fiber distributed uniformly in the matrix; the other is to improve the compactness of the matrix by adding the mineral additive and modify the interphase behavior of polypropylene fiber and cement matrix, enhancing the strength of the composite.
Polypropylene(PP) Fiber/Cement Mortar Workability
120 0.0
2.5
5.0
543
7.5 10.0 12.5 15.0 17.5 20.0
the quantity of mineral additive( %)
FIGURE 4 The effect of the mineral additives on the PP fiber cement mortar flow extent
In this experiment, two kinds of mineral additives are used: silica fume (SF) and fly ash (FA). The effects of the mineral materials on the PP fiber cement mortar flow extent are shown in Figure 4. From Figure 4, it is noted that the mortar flow extent slightly goes down with the adding of silica fume. The adding of silica fume can fill the vacant space of cement, sand and fibers, with the improvement of compactness of the mortar, the mortar flow extent goes down; whereas when fly ash is added, two things have to be considered [13]. From physical aspect, granule fly ash can act as a lubricator and from chemical aspect, the hydration reaction rate of fly ash is slower comparing to the cement, consequently, the absorption of the water is reduced, which making the whole structure slack, and it can improve the cement mortar flow property. CONCLUSIONS The longer the polypropylene fiber length and the larger the fiber content, the lower the cement mortar flow extent. With the increase of ratio of water to cement, the flow extent is also increased; As the decrease of the ratio of cement to sand, the flow extent of polypropylene fiber cement mortar will be increased. For mineral additive, the addition of fly ash can improve the flow extent of polypropylene fiber cement mortar, while silica fume can reduce slightly the flow extent of polypropylene fiber cement mortar. REFERENCES 1. 2. 3. 4.
Li Wei-wen, Leng Fa-guang, Qi Yun, Xing Feng.2001. "Research and Experiment on Workability of Concrete Incorporated with Cemfiber," Concrete, No.9: 54-58 He Yuan, Liao Xian-ting, Wang Yi-min.1998. "The Application of Polypropylene Stable in Cement Concrete'" Synthetic Technology and Application, 13(4): 36-39 L.Tu, D.Kruger, J.B. Wagener and P.A.B. Carstens.1998, "Surface Modified Polypropylene Fibers for Use in Concrete," Magazine of Concrete, 50(3), 209-217 Ziad Bayasi, Marc Mclntyre.2002. "Application of Fibrillated Polypropylene Fibers for Restraint of Plastic Shrinkage Cracking in Silica Fume Concrete", ACI Materials Journal, 99(4): 337-344
544 5. 6.
7. 8.
9. 10.
11. 12. 13.
Polypropylene(PP) Fiber/Cement Mortar Workability
P. S. Ravanbakhas.1998. "Control of Plastic Shrinkage Cracking with Specialty Cellulose fibers," ACI Materials Journal, 95(4), 429-435 Ma Yi-ping, Tan Mu-hua.2000. "Effects of Polypropylene Fibers on the Physical and Mechanical Properties of Cement Based Composites( I )-Plastic Shrinkage Cracking Resistance," Journal of Building Materials, 3(1): 48-52 Ma Yi-ping, Tan Mu-hua, Wu Ke-ru. 2001, "The Effects of PP Fiber Geometry on Cement Mortar Plastic Shrinkage Cracking Resistance," China Concrete and Cement Products, No.2, 38-40 Liao Xian-ting, He Yuan, Yang Xu-gang, Wang Yi-min.2000, "Interfacial Behavior of PP Fiber Reinforced Cement Composite ( II ) -SEM Observation and Morphological Study on Fracture Surface," Journal of Building Materials, 3(1): 64-67 Victor C. Li & Mohamed M..1996, "Toughening in Cement Based Composites," Cement & Concrete Composites, 18(4): 239-249 A.M.Alhozaimy, P.Soroushian & F. Mirza. 1996. "Mechanical Properties of Polypropylene Fiber Reinforced Concrete and the Effects of Pozzolanic Materials," Cement & Concrete Composites, 18(2): 85-92 Zhu Jiang.2001. "Water Resistance Mechanism of Polypropylene Fiber Concrete (Mortar) and its Application Technique," Architecture Technology, 32(7): 456 Shi Hui-sheng.1999. "Inorganic Nonmetal Materials Experiment," Tongji University Publisher Wu Cheng-zhen.1999. "Influences of Cements and Reduction-Water Agents on Performances of Cement Mortar," Journal of Nanjing University of Chemical Technology, 21(5): 40-41
Hybrid Composites for Engineering Application Faiz Ahmad*, M. Ridzuan A. Latif Mechanical Engineering Dept, Universiti Teknologi PETRONAS 31750 TRONOH, Perak Darul Ridzuan, Malaysia. Harris Nisar Dept. of Aerospace Engineering, College of Aeronautical Eng. PAF Academy, Risalpur, NWFP, Pakistan.
ABSTRACT Composite materials have extensive engineering application where strength to weight ratio, low cost and ease of fabrication are required. Hybrid composites provide combination of properties such as tensile modulus, compressive strength and impact strength which can not be realized in composite materials. Results presented in this paper relate to the development of glass, kevlar49 and carbon woven fibres (WF) reinforced polyester and epoxy based hybrid composites. In our study, a range of composites containing various volume fractions of woven fabric were manufactured by hand lay-up technique and tested mechanically. The results have shown linear increase in tensile strength with an increase in volume fraction fabric for both polyester and epoxy based composites. Hybrid composites have shown up to more than 100% increase in modulus of polyester composites while glass fabric reinforced polyester composites showed high tensile properties.
INTRODUCTION Application of composite materials is increasing due to their lightweight, high modulus and tensile properties. Favourable consideration is given to composite materials over the conventional materials due to ease in fabrication and high strength to weight ratio [1]. The development of glass fibre reinforced composites started in 1940's has revolutionized the materials world. Presently, composite materials have found extensive applications particularly in aviation industry [2], sports, naval [3] and automobiles [4]. The development of hybrid composites [5-6, 12] has led to the application where combination of properties such as tensile strength, tensile modulus [7-8] and impact is required [9-13]. This paper presents results of an experimental work based on woven glass Kevlar and carbon fabric (WF) reinforced polyester and epoxy composites.
* Corresponding author. Mechanical Engineering Dept., Universiti Teknologi.PETRONAS 31750 TRONOH, Perak Darul Ridzuan, Malaysia
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546 MATERIALS
Matrix Materials Polyester and epoxy resin were used as matrix materials for the composites. Polyester resin (civicl99) and hardener (norpol catalyst No. 1)*. Polyester resin was cured at room temperature and curing time was varied between 2 to 4 hrs. Epoxy with hardener for the composites fabricated were cured at 50°C and curing time was varied between 4 to 6 hrs. Fibrous Materials Three types of materials were used as the reinforcement: S-glass woven fabric (WF), Kevlar49 woven fabric and carbon fabric (woven fabric). The properties of matrices and fibres are listed in Table l(a) and (b) respectively.
(a) Resin
Polyesterl99 Epoxy
Tensile strength (MPa) 41.8 83.6
TABLE I (a) Resin and (b) Fibre Properties (b) Modulus (GPa) 2.09 3.83
Fibres
Carbon Glass Kevlar49
Tensile strength (MPa) 4500 2600 2900
Modulus (GPa) 251 73 125
EXPERIMENTAL WORK The following procedure was adopted for manufacture of polymer composites samples of 8X8 inch square plate. This size was selected to manufacture a minimum four test bars for testing mechanical properties of the composite samples. Mould surface was cleaned to remove impurities and was coated with wax for easy removal of the sample. Polyester and hardener was homogenized in the ratio of 100:1. In the case of epoxy based composites the ratio of hardener to epoxy was kept at 9:10. Mixture of polyester was uniformly coated on the mould surface already coated with wax to get an excellent exterior surface finish of the composite. The desired size of fabric was spread on the resin or epoxy and another coat was applied with the help of brush. Similar procedure was repeated to produce multiple layered composites containing various volume fractions of fibres. Finally the samples were left for curing as per requirement. Polyester based composites were named as P-type composites and epoxy based composites were named as E-type composites. P-type Composites The following were produced to study various effects on the P-type composites. P-type composites containing glass (WF) 15, 30, 45, 60% volume fraction were produced to study the effect of increase in volume fraction and directionality of fibres on modulus and tensile strength of composites. A composite reinforced with glass fibre mat, non-woven fabric (NWF) containing 15, 30, 45, 60% volume was produced to compare the effects of volume fraction of fibres on modulus and tensile properties of composites. P-type composites containing 15, 30,45% volume fraction of Kevlar49 (WF) reinforced polyester composites.
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E-type Composites Composites containing 15, 30 and 45% volume fraction of glass (WF) were produced. Composites containing 15, 30, 45% volume of Kevlar 49 (WF) were produced. Three composites were selected due to limited quantity of kevlar49 available. Hybrid Composites Hybrid composites based on polyester and epoxy were called as P-type hybrid and E-type hybrid composites. P-type Hybrid Composites Three types of hybrid composites were produced according to the following stacking sequence: (i) Four alternate layers of glass fibres (WF) and Kevlar 49 (WF) reinforced polyester; (ii) Two layers of glass (WF) and two layers of Kevlar 49 (WF) were reinforced polyester; and (iii) One layer of glass (WF) and one layer of Kevlar 49 (WF) were reinforced in polyester. E-type Hybrid Composites As for the E-type hybrid composites, the following were manufactured: (i) Four alternate layers of glass (WF) and carbon (WF) reinforced epoxy; and (ii) Two layers of glass (WF), one layer of Kevlar (WF) and one layer of carbon (WF) were reinforced in epoxy. Mechanical Testing Tensile Properties Samples of composite material were prepared according to ASTM and test was carried out on computerized Universal testing machine model manufactured in Italy. The results of load vs. strain plot were recorded for each sample and stress was calculated for each composite and hybrid composite samples. RESULTS AND DISCUSSION P-type Composites Figure 1 shows the effect of fibre volume fractions on stress for glass (WF), glass (NWF) and Kevlar (WF) based composites. Stress values found for glass (WF)/ Polyester composites were considerably higher when compared with the stress values for glass (NWF) / polyester composites. Lower values of tensile stress were considered due to randomly oriented fibres in glass (NWF) composite. Results showed that tensile properties of Kevlar 49(WF) composite also increases with volume fraction and this was related to the higher tensile properties of Kevlar 49 compared to glass (WF) and glass (NWF) based composites. The effect of increase in volume fraction of glass (WF) on tensile modulus of Ptype composites is illustrated in Figure 2. It is evident from Figure 2 that tensile modulus of composites is increased with an increase in volume fraction of glass (WF) and this increase is approximately 100% increase within 15 to 30% volume fraction. Further increase in this fibre volume fraction showed approximately 25% increase in tensile modulus of this composite. This was related to isotropic properties of glass (WF) in composite. Similarly, results of glass (NWF) reinforced composites are also
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shown in Figure 2. Uniform increase in tensile modulus up to 45% volume fraction of glass (NWF) and at 60% volume fraction approximately 100% increase in tensile modulus was observed in accordance with earlier results [7]. It was considered due to anisotropic characteristic of glass (NWF). Kevlar (WF) based composites exhibited higher tensile modulus due to higher properties of Kevlar. 30
1
20 4
a Glass(WF)
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0Glass(WF)
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150 i
100
s
50 15
30
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30
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Fibre Vol (%)
Fibre Vol (%)
FIGURE 1 Fibre volume fraction vs. strength of P-type composites.
FIGURE 2 Fibre volume fraction vs. modulus o f p . t y p e composites.
E-type Composites Figure 3 shows the affect of fibre volume fraction on stress of glass (WF) and Kevlar (WF) reinforced epoxy composites. Results showed a considerable increase in stress data for Kevlar based composites. The properties were relatively lower and were considered due to poor bonding between fibres and matrix. Figure 4 represents fibre volume fraction vs. modulus of glass (WF) and Kevlar (WF) based epoxy composites. Results showed that higher tensile modulus of Kevlar-based composites can be achieved with Kevlar (WF) compared to glass (WF) composites.
30
45
Fibre Vol (%)
FIGURE 3 Fibre volume fraction vs. stress of E-type composites.
30
45
Fibre Vol (%)
FIGURE 4 Fibre volume fraction vs. modulus of E-type composites.
P-type Hybrid Composites P-type hybrid composites containing four alternate layers of Kevlar (WF) and glass (WF) were manufactured and their properties were compared with P-type composites as illustrated in Figure 5. Results showed that hybrid composites have higher tensile properties compared to other composites in the P-type category. Higher properties of hybrid composites were due to kevlar (WF) and glass (WF) reinforced in
Hybrid Composites for Engineering Application
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polyester. A comparison of modulus between hybrid and other composites is illustrated in Figure 6. Results showed that hybrid composite have higher strain compared to other composites, thus resulting lower modulus values. 30 -r a Glass (WF) ED Kevlar (WF) • Glass (NWF) &20
Q Glass (WF) Glass (NWF) DIKevlar(WF) D Hybrid (WF)
300 — 200
t
2 100 -
15
30
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60
Fibre Vol (%)
FIGURE 5 Comparison of strength of P-type and hybrid composites
FIGURE 6 Comparison of "modulus of P-type and hybrid composites
E-type Hybrid Composites Results of E-type hybrid composites are shown in Figure 7. Hybrid composite consisted of four alternate layers of Kevlar (WF) and carbon (WF) reinforced in epoxy. Three sets of composites were prepared due to limited quantity carbon (WF) available. Hybrid composite containing high modulus carbon (WF) showed high strength and high modulus as illustrated in Figure 8. A comparison of properties of composites prepared and tested is given in Table 2, which summarise the results of both E-type and P-type hybrid composites. TABLE II Properties of hybrid composites compared with P-and E-type composites. Hybrid Composites Lay-up
Multilayered Composites
Tensile Strength (% Modulus increase (% increase or or decrease) decrease)
Kevlar (WF) / Glass (WF) / Kevlar (WF) / Glass( (WF) (P-type hybrid)
4 Layers Kevlar (WF) 4 Layers Glass (NWF) Polyester (P-type)
18% decrease 41% increase
20% decrease 11% increase
Kevlar / Kevlar / Glass (WF)/ Glass (WF) (P-type hybrid) Glass (WF) / Kevlar (P-type hybrid)
4 Layers Kevlar 4 Layers Glass (NWF) Polyester (P-type) 2 Layers Glass (WF) 2 Layers Kevlar Polyester (P-type) 4 Layers Glass (WF) 4 Layers Kevlar Epoxy(E-type).
3% decrease 79% increase
10% increase 22% increase
97% increase 14% increase
123% increase 43% increase
16% increase 72% increase
7% increase 67% increase
58% increase 7% increase
31% increase 87% increase
Glass (WF) / carbon (WF) / Glass (WF) / carbon(WF) (E-type hybrid)
Glass (WF) / carbon / Kevlar / 4 Layers Kevlar Glass(WF) 4 Layers Glass (WF) (E-type hybrid) Epoxy (E-type)
CONCLUSIONS Results showed that tensile strength and modulus of composites are dependent on volume fraction of fibres. The results have shown linear increase in tensile strength with an increase in volume fraction fabric for both polyester and epoxy based
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composites. Hybrid composites have shown up to more than 100% increase in modulus of polyester composites while other hybrid composites have also shown significant improvement in both tensile strength and modulus, signifying that they are suitable and most appropriate for certain engineering applications. It is hoped that future work would include some impact and fatigue studies to further strengthen the suitability of the 'hybrids' for engineering application where a combination of strength and impact resistance is necessary. 300 -, 40 0 Glass (WF)
1200 £150 2 100 50 0
HI Kevlar (WF)
S.30"
• Hybrid (WF)
| 20
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30
a Glass (WF) ED Kevlar (WF)
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I10 45
Fibre Vol (%)
FIGURE 7 Comparison of strength of E-type and hybrid composites.
30
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FIGURE 8 Comparison of modulus of E-type and hybrid composites.
ACKNOWLEDGEMENT We would like to acknowledge Fibre Tech. Lahore and Pakistan Aeronautical Complex, Kamra for their support in terms of supplying research materials. REFERENCES 1. 2. 3.
4.
5. 6. 7.
8.
9.
10. 11. 12. 13.
Ahmad, F. and M. J. Bevis. ISAM-97 P: 32 Islamabad Pakistan Georgi, H. 1979. "Damping Effects in Aerospace Structures," AGARD Conference Proceedings No. 277 , 1979. Davey, A. E. 1994. "GRPC Minesweeper: Pre-production Test Structure with Box Core Sandwich Construction," in Handbook of Polymer Composites for Engineers, Woodhead Publishing Ltd., pp.304. Crivelli-Visconti, I., A. Langella, L. Nele G. Delia Valle. 1990. "Improvement on Composite Connecting Rod Design" presented at the 4Th ECCM, September 25-28, 1990. Stuttgart, Germany, pp.837. Adams, D. F. and A. K. Miller. 1975. "An Analysis of Impact Behavior of Hybrid Composite Materials," Materials Sci. & Eng., 19, pp. 245-260. Summerscales, J. and D. Short. 1978. "Carbon Fibre and Glass Fibre Hybrid Reinforced Plastics," Composites, 9(3): 157-166. Fowser, S., D. Wilson, T. Chou and R. Pipes. June 1986. "Influence of Constituent Properties and Geometric Form on the Behavior of Woven Fabric Reinforced Composites," Progress Report for NASA, Grant No: NAG-1-378. Mohamed, M. H. Z. and L. C. Dickinson. "Manufacture of Multilayer Woven Preforms" in ASME Advanced Composites and Processing Technology, MD-Vol.5 Book No. 00484 , pp. 8189. Beaumont, R. P. W., A. P. G. Reiwald and C. Zweben. 1974. "Methods for Improving The Impact Resistance of Composite Materials" in Foreign Object Impact Behavior of Composites, ASTM STP 568, ASTM, PA., pp. 138-158. Toland, R. H. 1974. "Instrumented Impact Testing of Composite Materials" ASTM STP 563, Philadelphia, PA, pp. 133-145. Toland, R. H. 1978. "Failure Modes in Impact Behavior of Composite Panels," J. Test. & Eval, 6(3):202-210. Broutman, L.J and P. K. Malik. Nov 1974. "Impact Behavior of Hybrid Composites" AFOSR TR-75-0472. YANG, Y. H. 1988. "Aramid Fibre" in Fibre reinforcement for composite materials: Composite Materials Series 2, H.R. Bunsell, ed. Elsevier press.
Development of a Knowledge Warehouse for Intelligent Risk Mapping and Assessment System S. Savci * Hawker de Havilland - Boeing, Australia B. Kayis Mechanical & Manufacturing Engineering, University of New South Wales, Australia
ABSTRACT An Intelligent Risk Mapping and Assessment System is an application of knowledge engineering that involves a combination of case-based reasoning approaches aimed at managing risks. To manage risks, the knowledge' of the different tasks constituting product design, development and delivery must be captured, organised and information on the causes of risks that have a threshold effect on time, cost and performance must be available. The efficiency and reliability of design processes can be improved if risk is taken into account at each phase of design, development and delivery. The System aims to reflect several decision-making factors and criteria to build a conceptually complete model comprised of fundamental engineering knowledge as well as "know-how" from general principles, generic knowledge, specific knowledge and case based reasoning. Forward and backward reasoning methods, along with an informal knowledge association method for building dynamic associations between a starting risk and other risks, based on keyword search have been used to ensure a reliable, accessible and updateable information. This paper primarily details the reasoning and methodology used to populate the Knowledge Warehouse module of the Risk Management and Assessment System which not only will support the decision-making process of the user but also aid the knowledge retrieving, storing, sharing and updating process of manufacturing organizations. This risk assessment tool has been targeted for project manager level education with emphasis on advanced composite manufacturing technology.
INTRODUCTION There are several factors that influence the level of sophistication of a risk mapping and assessment system, namely the scope of the project, the size of the company, the inter-dependency of tasks, multi-site locations of project partners, the type of business and finally the provision for on-going capture of information, what is commonly referred to as intelligence. Over the past several years there have been numerous studies on risk management, but none which address all the aforementioned criteria. Hence a collaborative research between various research institutions and Hawker de Havilland Aerospace was formed for the development of an Intelligent Risk Mapping and * Corresponding author, Hawker de Havilland - Boeing, 361 Milperra Road, Bankstown, NSW, 2200, Australia, Tel: 97728558, Fax: 9772 8482, email: [email protected]
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Knowledge Warehouse for Intelligent Risk Mapping and Assessment
Assessment System anomalously referred to as IRMAS™. The system is based on the Australian/New Zealand Standard on Risk Management [1]. It provides the basis for identifying, analysing, processing, mitigating and monitoring risks. Furthermore, since the nature of advanced composite structures requires complex technologies as well as concurrent engineering, the system needs to accommodate another dimension of complexity in managing the risk. IRMAS™ aims to cater for a highly technologically demanding field of composite manufacturing. Additionally, it provides a systematic engineering approach to risk management of concurrent product and process development. The knowledge warehouse which interacts with a collaborative environment is built to identify several factors that had an impact on other projects' success and/or failures. The contributions from a collaborative environment can take many forms such as the knowledge distributed over space, time, processes and people. A holistic picture gathered from lessons learnt, case studies, best practices, generic engineering standards and procedures would enhance the validity of IRMAS™ The essence of using knowledge warehouse is to sufficiently identify and detail several critical success factors. Thus, the knowledge warehouse emerges as an appropriate choice of resource to be used for identifying, assessing, monitoring and mitigating risks resulting in measurable benefits. Techniques to support evaluation of case, scenario based systems in a collaborative environment remain as an active topic of research [2, 3, 4, 5, 6 and 7]. It is evident from the review of the literature that the key challenge is to go beyond common assumptions such as "increased collaboration will make a positive contribution to organisational performance" to understand how IRMAS™ features will be used to support the decision-making process of the managers and contribute to projects' unique objectives. IRMAS™ is composed of six modules namely; context establishment, risk identification, risk assessment, risk mitigation, knowledge warehouse and decision support systems. It has been compiled as a web-based portal in Java which also facilitates effective communication between non-geographically co-located project partners. CONTEXT ESTABLISHMENT The risk management system is a model essentially comprising a generic representation of design build (or simply build to print) activities with the aid of cause and effect functions. Causal diagram representation of the inter-relationships between various tasks was used in order to flush out all possible risk items for a manufacturing environment from conceptual design through to delivery. Additionally it simplifies the definition of the risk paths to be used later in the risk assessment component. Every organisation has an inherit culture whereby the influences can be observed throughout the majority of the company. These factors determine the systematic problems which essentially do not change from one project to another. Therefore the initial module for the intelligent risk mapping and assessment system establishes the overall risk profile by assigning a weighting to the infrastructure of the system. The contextual component primarily sets the scene for the organizational nature of the company such as the project objective and management style or company culture. RISK IDENTIFICATION Risk identification focuses on product, project and process specific risks. The tool being developed here takes a more holistic approach to project management than conventional
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techniques. Functional heads such as quality assurance, design, tooling, manufacturing, business development, Research and Development are involved as early as the first phase (i.e. conceptual design) thereby promoting higher levels of communication between various departments and hence reducing theory driven risks. Additionally the data capturing process is based on quantitative analysis of the specific risks with the aim of maximising objectivity and minimising subjectivity. More specifically, the magnitude of the risks identified is a product of its consequence and its likelihood where a 5 point, exponentially increasing scale was employed as the example in Table I illustrates for establishing how the milestones were derived. Furthermore, the questions are structured aimed at optimising success factors. For instance the co-location of team members will dictate the success factor for the location risk category as would logistics with suppliers and customers. TABLE I: An example of quantitative identification of risk likelihood and consequence Likelihood 1. In-house expertise and include reserve time 2. Quantitative based duration (bottom-up) 3. Expert judgement (consultants) 4. Parametric/ simulation technique 5. Analogous methodology (top-down)
Consequence 1. Schedule contingency plan 100% valid 2. Up to 90% valid 3. Up to 70% valid 4. Up to 50% valid 5. Up to 30% valid
Each phase was defined by sub-activities and specific risk items classified by 8 risk types namely schedule, technical, external, organizational, communication, location, resource and financial. The complexities and risks associated with composite technology are primarily covered under technical and resource related risks. For instance technical specification completeness comprises product specification completeness, process specification completeness, level of "know-how". More specifically, it encompasses product performance, design and functional requirements. Additionally technical specification completeness covers quality assurance specifications, understanding of technological area/platform familiarity, process completeness, technical support, material familiarity and regulatory requirements. Plus the resource requirement completeness investigates material, people, equipment and facility related requirements. Furthermore, personnel skills and training requirements are addressed as well as equipment performance, reliability, capacity familiarity and compatibility. The risk identification stage can potentially be extremely large and cumbersome due to the expanse of the scope. For instance major activities such as maintenance, Occupational Health & Safety, design, manufacturing and product life cycle issues have been included. Therefore, customer and supplier profiles were constructed with the aim of increasing inherit intelligence and promoting the user friendly aspect. Similar analysis techniques to the product, project and process risks were used in capturing information on the reliability, expertise, capability, capacity and compatibility of customer and supplier profiles. RISK ASSESSMENT All identified risks with their assigned magnitudes are processed through the risk paths given by the interactions between other risk items. The consequences of the risks are computed using the Analytical Hierarchy Process (AHP) [8] concept while the likelihood of the risks adopts Bayesian Belief Network (BBN) [9] Both techniques will process the risks through the defined paths, capturing concurrency between tasks as well
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Knowledge Warehouse for Intelligent Risk Mapping and Assessment
as further reducing user related subjectivity. Risk assessment not only provides an automated and reliable mathematical cross reference in calculating the risk magnitude but it is sufficiently flexible to allow the user to also provide a manual assessment of the identified risks. The system thereby is capable of increasing its level of intelligence by building onto the knowledge base via this interactive network.
RISK MITIGATION The risk mitigation module will prioritise the assessed risks and weave an avenue for alternate mitigation strategies. A collaborative environment interacting with the knowledge warehouse may be accessed using a search and retrieval tool. The priority for the mitigation actions will be dictated by the risk magnitude and the threshold value required for that specific risk item. A search facility was developed for access to various components of the knowledge warehouse including case studies, lessons learnt, best practices and generic engineering standards and procedures. Furthermore, other selection criteria governing the mitigation plan will be via associated costs and available resources. Finally, the risk mitigation implemented will feed back into the knowledge warehouse as a "lessons learnt" thereby increasing its intelligence database. RESULTS AND DISCUSSION A comprehensive risk management tool has been developed with a contingency for multi-site concurrent engineering projects. The software systematically integrates an organisation's procedures to identify and assess risks for a scope entailing conceptual design through to product life cycle customer service. The knowledge warehouse collates information captured from generic engineering know-how, lessons learnt (in-depth internal expertise), case studies (internal and external case based knowledge), best practices (external benchmarking) and engineering standards (e.g. Australian/New Zealand Risk Management Standard). The access to such a wealth of knowledge means that the tool is not a mere risk tracking mechanism but potentially a boost forward for the company's success from years of experience from previous projects. Similarly there is a provision for the update of "know-how" which is especially required for dynamic technological areas such as composite manufacturing applications. In other words, it is critical that the intelligence is updated to reflect the current knowledge warehouse if the organisation is to maintain a competitive edge in the market forum. Figure 1 gives a snap shot of the process flow of information within the intelligent risk management and assessment system.
Knowledge Warehouse for Intelligent Risk Mapping and Assessment
Context Establishment
KNOWLEDGE WAREHOUSE
Engineering standards
organizational risks Risk Identification Analytical Hierarchy Process
risk consequence
product, process, project risks Risk Assessment
Belief Bayesian Network
risk likelihood
555
Case studies
Best practices
Lessons learnt
risk magnitude Risk Mitigation
Collaborative Environment
FIGURE 1: Snap shot of Intelligent Risk Mapping and Assessment System
More specifically, the information from the knowledge warehouse may be derived based on criteria such as risk event drivers, resource constraints, type of business activity (e.g. aerospace, automotive etc), project type (design build or build to print) and risk item specifics. The software will automatically access the mitigation strategies associated with the generic risk item identified, however the applicability of the information source needs to be examined before the risk mitigation can be imported into the current project. Hence keyword search facility for various fields was adopted for simplicity and convenience. The knowledge warehouse not only provides the knowledge warehouse for managing the risks but it is additionally a useful tool for educating project managers on the technical aspects of manufacturing without the danger of micromanaging the project. CONCLUSION This study discusses the modules constituting an intelligent risk mapping and assessment system IRMAS™ which also supports concurrent engineering. IRMAS™ is a virtual workbench built as a web-based portal in Java to facilitate multi-site locations. The tool is modelled on the Australian New Zealand risk management standard and it achieves the incorporation of success factors into the management of risks with emphasis on the manufacture of advanced composite structures. This paper serves two purposes, firstly it outlines an intelligent risk mapping and assessment system and it also serves as an educational tool for the purpose of transferring knowledge. In particular, the education of managers has been outlined through a collaborative environment with the use of the knowledge warehouse. The knowledge warehouse captures the wealth of experiences from various sources such as generic engineering "know-how", specific case based knowledge and best practices. Finally, the knowledge warehouse provides the relationship between risk items, risk event drivers and mitigation strategies. In
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Knowledge Warehouse for Intelligent Risk Mapping and Assessment
conclusion, IRMAS™ is capable of integrated product design/development taking a wider holistic perspective in the transfer of knowledge and the management of risks. REFERENCES 1 Anon., "Australian/New Zealand Standard - Risk Management", AS/NZS 4360,1999. 2 Ackerman, M. The Intellectual challenge of Computer Supported Co-operative work: The Gap Between Social requirements And Technical Feasibility. Human Computer Interaction, 15, 179-203,2000 3 Baeza-Yates, R. and Pino, J. A., A First Step to Formally Evaluate Collaborative Work. Proceedings of the International Conference on Supporting Group work: The Integration Challenge, Phoenix, AZ, 56-60, November, 1997 4 Carroll, J.M., Making Use: Scenario-Based design of Human Computer Interactions, Cambridge, MA, The MIT Press, 2000 5 Ross, S., Ramage, M., and Rogers, Y., Participatory Evaluation through Redesign and Analysis, Interacting with Computers, 7 (4); 335-360, 1995 6 Rosson, M.B., Carroll, J.M., Usability Engineering: Scenario- Based Development of Human-Computer Interaction. San Fransisco: Morgan Kaufmann, 2002 7 Stiemerling, O., Cremers, A. B., The Use of Cooperation Scenarios in the Design and Evaluation of a CSCW System. IEEE Transaction on Software Engineering, 24(12), 1171-1181,1998 8 Saaty, T.L., "Decision Making for Leaders - The Analytical Hierarchy Process for Decisions in a Complex World", Ed. 3, RWS Publications, USA, 2001. 9 Press, SJ "Bayesian Statistics: Principles, Models and Applications", John Wiley & Sons Inc., USA, 1989.
Opportunities for Nanocomposites in the Oil & Gas Industry Russell Varley1'* and K. H. Leong2 'CSIRO Molecular Science, Bag 10, Clayton South, VIC 3169, Australia. 2 PETRONAS Research & Scientific Services Sdn Bhd (PRSS), Lot 3288 & 3289, Off Jalan Ayer Itam, Kawasan Institusi Bangi, 43000 Kajang, Selangor Darul Ehsan, Malaysia.
ABSTRACT The use of advanced and more efficient materials are increasingly critical to the oil and gas industry as it strives towards enhanced recovery in marginal and deepwater exploration and production activities. Composites have proved to be extremely advantageous in selected niche applications in the industry, and in recent years they have been identified as an enabling technology for even more demanding requirements, particularly in the upstream sector. However composites still exhibit limitations in certain properties including toughness and fire performance that are impeding the expanded application of the material within the industry. Potentially, the answer to some of these weaknesses could lie, at least in part, with nanocomposite technology.
INTRODUCTION The 21 st century continues to witness an ever increasing need for improved materials which demonstrate significant property enhancements over and above those which already are available. Fibre reinforced polymer (FRP) composite materials are well placed to meet many of these needs due to their excellent strength and stiffness to weight ratios, corrosion resistance and fatigue properties, whilst affording design flexibility. Unfortunately, composites have some serious limitations, including impact properties, cost and fire performance that have inhibited their adoption for more applications and by a wider scope of industries. A new class of materials known as nanocomposites has been shown to have the potential to address these issues, and more, and this has attracted significant interest from the scientific community and industry alike. A nanocomposite is broadly defined as the dispersion of an additive into a matrix where at least the dimension of the additive is of the order of nanometres (10~9). Due to the high aspect ratio of these nano-additives, nanocomposites have the potential to significantly enhance mechanical and physical properties of polymer matrices with minimal impact on cost and processability. This paper reviews some of these enhancements in properties and how they could present opportunities to increase the level of acceptance and application of polymeric based composites in the oil and gas (O&G) industry in its continuing effort to cut costs and to improve operational * corresponding author. Tel: +61 3 9545 2196 Fax : +61 3 9545 2517 Email: [email protected]
558
Opportunities for Nanocomposites in the Oil & Gas Industry
efficiency and safety. In particular, emphasis will be given to the upstream business where the viability of many deepwater and marginal field developments are increasingly dependent on new technologies to remain competitive. Opportunities for downstream businesses of the O&G industry will also be discussed.
NANOCOMPOSITE TECHNOLOGY The most common type of nanocomposites studied today are materials based upon naturally occurring polymeric layered silicate clays which are formed by the intercalation of a polymer into the gallery of the clay. Another additive being actively studied currently is the use of nanofibers such as carbon nano-fibres, nano-tubes or whiskers. These two groups of materials each have their own unique challenges associated with the optimisation of the dispersion within the polymer matrix which is considered to be critical to optimising the transfer of the unique properties of the nano-material to the nanocomposite material. Nanocomposite Formation - Polymeric Layered Silicates Polymeric layered silicates (PLS) consist of stacked layers of lnm thick octahedral silicate layers separated by approximately 10A, as shown in Figure 1. This class of nanocomposite is widely studied due to their availability and their wellknown intercalation chemistry. The use of polymeric layered silicates has been shown to improve mechanical properties, such as moduli, toughness, strength, and heat resistance, while decreasing their gas permeability and flammability in a wide variety of thermoplastic and thermosetting polymer matrices at low additive levels [14]. The fundamental principle of the nanocomposite formation involves migration of the polymer into the interlayer galleries of the layered silicate and pushing apart or swelling the silicate layers. When the polymer is mixed intimately with the clay and the distance between the layers is increased, the clay is said to be intercalated. If the distance between the layers increases such that the layers become completely and randomly dispersed within the polymer matrix, the silicate is said to be exfoliated. Kornmann et al. [5] report that the polymerisation of the epoxy resin is the indirect driving force for exfoliation due to changing polarity of the polymer as the molecular weight increases. Pinnavaia et al. [6] reported that controlling the intragallery polymerisation of the epoxy resin was critical to achieving exfoliation. It was reported that when the intragallery polymerisation was faster or equal to that of the bulk epoxy resin, an exfoliated morphology was achieved. The delicate balance required to achieve the optimum balance of polymerisation between the intragallery cure and the bulk resin is demonstrated by Becker et al. [7] who achieved improved exfoliation at higher cure temperatures and hence higher cure rates. Nanocomposite Formation - Carbon Nano-fibre/nano-tubes The use of carbon nano-tubes or nano-fibers, as shown in Figure 2, holds much promise due to the very extraordinary mechanical properties of the fibres. Their dispersion in polymer matrices is made difficult due to the high degree of entanglement of the fibres. This is a result of the attractive molecular forces such as Van der Waals and the high aspect ratio of the fibres. The dispersion of carbon nanofibers in polymer matrices has been widely investigated using either mechanical or chemical methods. Mechanical methods have focussed upon various ultrasonic and milling techniques [8]. These techniques tend to work well because they reduce the
Opportunities for Nanocomposites in the Oil & Gas Industry
559
length of the fibres, reducing entanglements but also producing large amounts of amorphous carbon, and reducing the benefit of the nano-reinforcement. O
oxygen
©
hydroxyl aluminium and • magnesium o " " silicon
FIGURE 1. Schematic diagram showing the general structure of a polymeric layered silicates (PLS).
l-'ltiLRL 2. LxaiiipL ul i;pu.dl Loibuu Nanofibres commercially available
Chemical methods used to improve dispersion involves activating the surface of the carbon with reactive functional groups enhancing the ability of the nano-fibre/nanotube to transfer its properties to the polymer matrix. This is often performed via an acid treatment method in combination with thermal oxidation or decomposition and tends to significantly reduce the mechanical properties of the nano-tubes. A promising method is to use surfactants which have far less negative impact upon the properties of the carbon nano-fibre/nano-tubes while promoting optimum dispersion. OPPORTUNITIES It has been reported that nano-reinforcements are able to concurrently improve strength, modulus and toughness of neat resins while having minimal impact upon other properties such as Tg and processability [7,9]. Becker et al. [10] demonstrate this for a range of high performance epoxy resin systems which exhibit large improvements in toughness (up to -200%) and modulus (up to 20%). Becker and his colleagues [7] further show the potential of nano-clays to toughen FRP composite materials via a supplementary reinforcement mechanism. Figure 3 illustrates that apart from modulus and strength, the flexural strain-to-failure also increases significantly for a 5wt% clay modified epoxy resin system. More modest improvements are achieved for coefficient of thermal expansion (CTE) and the char yield while Tg is only marginally compromised, but is still around 170°C. These improvements in properties are encouraging since the O&G industry are increasingly turning to composite materials as solutions for not only corrosion problems, but for weight reduction issues so that its superior strength and stiffness to weight ratios are important considerations. This is particularly so as the quest for oil and gas moves towards more demanding conditions, such as deepwater exploration and production. One of the more pressing challenges facing composites development is the need for improved fire performance, preferably with little or no effect upon mechanical and other physical properties, weight, processability as well as cost. Nano-clay and nano-fibre reinforcement has been shown to have great promise in this area. While the most promising improvement in fire performance have been achieved through the addition of nano-clays to thermoplastics such as nylons and polystyrenes, others have also shown that nano-clays are able to significantly improve the fire performance of thermosetting materials. Gillman et al. [12] showed that for a 6wt% addition of a silicate additive approximately a 40% improvement in the peak heat
560
Opportunities for Nanocomposites in the Oil & Gas Industry
release rate was achieved for different epoxy resin systems. For vinyl ester resin systems, a slightly more modest improvement was observed. This improvement was attributed to the clay improving the stability of the char layer and preventing combustible products escaping the condensed phase. However, other studies [13] have found that the addition of clay has little effect upon the fire properties and that the incorporation of phosphorous or silicone based species into the epoxy backbone are far more advantageous. It is expected therefore that a combined approach to fire improvement is expected to provide the solutions required for the oil and gas industries for new materials in this area. 160 -, 135.6
140-
&120-I 0
8 0
-
1 60-
58.4
52.1
S 40 S. 20 -I
21.3
-10.9
0 -20
J
FIGURE 3. Changes in properties for a high performance epoxy resin system due to nano-reinforcement [11].
Magnesium hydroxide nano-particles have been shown to perform better than a corresponding micro-particle for an ethylene vinyl acetate (EVA) composite for peak heat release rate, and carbon monoxide and carbon dioxide emissions, see Figure 4. Whilst the time to ignition is shorter for the microcomposite, the nanocomposite also shows an improvement, and in both cases the degradation temperature and level of smoke emission are improved as well. Other results have revealed the potential use of carbon nanotubes as fire retardants. Kashiwagi et al. [15] found up to a 32% improvement in heat release rate in polypropylene using only 2 vol% of additive. They explained the improvement being a result of an improvement in the mechanical integrity of the protective layer acting as a thermal insulation layer and a barrier for degradation products to the gaseous phase. Another possibility with nano-reinforcement is a significant enhancement of barrier properties. In the O&G industry pressure vessels are used in abundance at a variety of pressure ratings from quite low to extremely high. High pressure vessels are used, for example, in liquid nitrogen gas storage cylinders (downstream) and accumulator bottles (upstream) where operating pressures in the region of 3 OOOpsi are not uncommon. Where polymeric liners are used, sufficient barrier properties are needed to ensure efficient pressure containment. The use of FRP composite materials over metals for pressure vessels is driven by weight savings, as well as corrosion resistance and fatigue performance. The main drawback however is the poor impact properties, which can be significantly lower than metals. The application of
Opportunities for Nanocomposites in the Oil & Gas Industry
561
nanocomposite techniques to this area has considerable potential due to the dual benefit of being able to improve both toughness and barrier properties concurrently. The low level of addition of additive is also advantageous in that it would have minimal effect upon the processing conditions. This is an important consideration for the fabrication of pressure vessels as they are predominantly made via a filament winding process, which is a process that has tight requirements with respect to resin viscosity and reactivity. As we move into the hydrogen era it is anticipated that barrier requirements will be even higher and nanocomposites could well play an important role towards meeting those ever demanding requirements. 140 @Micro5wt% MgOH3
120 -
115
HNano5wt% MgOH3
100 -
Ia.
80
0)
60 -
n c o
40 -
a
20
+•*
57 48 27 15
19
0 Time to ignition
Peak heat release rate
CO release CO2 release
FIGURE 4. Some indicative values of enhanced flammability : comparison between nano- and micro-reinforcement [14].
CHALLENGES For the concept of nano-structure composite materials to be taken to the product development stage the dispersion of these additives needs to be achieved in a manner which is cost effective, reproducible and scalable for manufacturing conditions. When using nano-clays, the chemistry of the organo cation and the processing conditions are critical to the compatibility and dispersion within the polymer matrix. Optimising these factors within a reactive matrix while also ensuring that the fibre matrix adhesion remains unaffected will require a processing and chemical based solutions approach. When using carbon nano-fibres there are significant processing challenges in producing scalable and optimised nanodispersions with no deleterious effects upon the mechanical properties. This suggests that the commonly used approaches such as acid etching and ball milling/ultrasonication may not be sufficient and will require an innovative approach. In addition to technical issues, there is also an urgent need to increase the general awareness and appreciation of "oil men" and "diehard metallurgist" for the potential and abilities of nanocomposites and FRP composite materials. Mathematical models and other techniques with enhanced predictive capabilities, coupled with accelerated testing are needed to address the skepticism of potential users for long-term behaviour thus improving the acceptability of the "new" materials. It is noteworthy that better simulation procedures also contribute towards reducing the cost of certification which is an important element in the viability of adoption of new materials and structures.
562
Opportunities for Nanocomposites in the Oil & Gas Industry
Nevertheless, significant amount of testing is still required to generate a database of properties that will demonstrate the efficacy of composites for O&G operators.
CONCLUDING REMARKS There is evidence, albeit limited at this stage, that nanocomposites has significant potential for the oil and gas industry. They have been demonstrated to enhance fire performance, toughness, barrier properties, strength and stiffness, amongst others, of neat resins that could ultimately be use in advanced FRP composites in the form of matrices. The concept of nano-reinforcement presents an opportunity to improve matrix-dominated properties of FRP composite materials with little cost and weight penalty since they are typically required only in small quantities for a correspondingly large improvement in property or performance. However, enhanced effort in R&D that includes field trials is needed before the potential benefits of nanocomposites and the use of nano-reinforcement in advanced FRP composite materials can be fully realised. The ability to control a uniform dispersion of the nano-particles and the chemical interactions between them and the resin and possibly other additives, plus a full understanding of how the enhanced properties are transferred to an FRP composite material shall be key to engineering the optimum nanocomposite and nano-based advanced FRP composite material. Other issues standing in the way of ultimately seeing the materials in actual applications are not dissimilar to those faced by other new materials - scepticism, cost of qualification and certification, lack of database of properties and experience, etc. - and should be addressed through enhanced capability and effort in testing and modelling, and sound design principles.
REFERENCES 1. 2. 3. 4. 5. 6.
Lan, T. & Pinnavaia, TJ, Chem. Mater., 6, 2216 (1994). Giannelis, E.P., Advanced Materials, 8, 29 (1996). Xu, W.B., Bao, S.P. & He, P.S., J. Appl. Polym. Sci., 84, 842 (2002). Alexandra, M. & Dubois, P., Mat. Sci. Eng., 28, 1 (2000). Kommann, X., Lindberg, H. & Berglund, L.A., Polymer, 42, 1303 (2001). Pinnavaia, TJ. & Beall, T.G., (Eds.), Polymer Clay Nanocomposites 1st Ed., Wiley Series in Polymer Science, Chichester (2000).
7. 8. 9. 10. 11.
Becker, O., Cheng, Y-B., Varley, R.J. & Simon, G.P., Macromolecules, 36, 1616 (2003). Hilding, J., Grulke, E., Zhang, G. & Lockwood, F., J. Disp. Sci. Tech., 24, 1 (2003) Choi, M.H., Chung, IJ. & Lee, J.D., Chem. Mater., 12, 2977 (2000). Becker, O., Varley, R.J. & Simon, Q., Polymer, 43,4365 (2002). Chiefari, J., Gadd, G., Gilbert, E., Kozielski, K., Varley RJ. and Thomson S. manuscript in preparation. Gillman J.W., Appl. Clay Sci., 15, 31 (1999). Hussain, M., Varley RJ., Cheng, Y.B. and Simon G.P., J. Appl. Polym. Sci., 91, 1233 (2004) Okubo, N., Okumura, H. & Okoshi, M., (Proc Conf.) 8th Japan International SAMPE Symposium, Eds. Takeda, etal, SAMPE, 1, 55 (2003). Kashiwagi T., Morgan A., Antonucci J., Harris R., Grulke E., Hilding J. and Douglas J.,, Thermal Degradation and Flammability Properties of Nanocomposites, (Proc Conf.) Nancomposites 2002, September 23-25, 2002, San Diego, USA
12. 13. 14. 15.
Part XI
Interface
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Interfacial Properties of Polypropylene Fibre-Matrix Composites S. Houshyar, R. A. Shanks*, A. Hodzic** Applied Chemistry, RMIT University, GPO Box 2476V, Melbourne, 3001, Australia
ABSTRACT A novel composite consisting of polypropylene fibres (PP) in a random poly (propylene-co-ethylene) (PPE) has been prepared and its properties evaluated. The matrix and fibre components retained their separate melting temperatures. The melting temperature of the polypropylene fibres increased after formation of the composites. The compression moulding of the composites at a temperature below the melting temperature of the fibres caused annealing of the fibre crystals. The mechanical properties of the all PP composites were measured and it was found that by incorporation of long PP fibres into a PPE matrix the flexural and tensile modulus increased. The adhesion between the PPE matrix and PP fibres in the PP composite was characterized using a micro-bond test inspired by the fibre pull out technique. The results show that the adhesion was remarkably increased when polypropylene fibres were substituted for glass fibres in a polypropylene matrix. Nevertheless the thermal processing conditions of the composite materials cause a large reduction in the mechanical behavior of the reinforcement. INTRODUCTION There is a demand for plastics, which requires enhanced performance above which can be achieved with an un-reinforced polymer. Thus, there is much interest in the production of fibre composites in which are oriented polymeric fibres, yarn or woven fabric combined with a lower melting temperature polymer, from the same semicrystalline polymer [1,2]. However, a composite consists of two chemically distinct constituents, which are widely used. Many composites are focused on glass fibres as a dispersed or reinforced phase, are combined with polypropylene. These are used in transport as well as in construction industries [3]. The fibre composite has improved mechanical, thermal and structural properties in comparison with the un-reinforced polymer. In most cases, the density and impact rupture is increased but at present, recycability and low-density composites are of interest in a number of industries especially in the automotive sector [1,4]. Recent research is based on the enhancement of the properties of a base polymer by development of a very high degree of preferred molecular orientation. The composite, which has good stiffness and modulus properties, can be produced by using suitable techniques, but there are problems with recycling and interfacial bonding if the two phases consist of two different polymers [1,2]. This gap in composites can be filled by using the same semi-crystalline polymer in the matrix and reinforcement. A number of techniques has been reported in the * Correspondence Author, Applied Chemistry, RMIT University, GPO Box 2476V, Melbourne, 3001, Australia, Tel and fax: +61 3 9925 2122, [email protected] ** Current address: School of Engineering, James Cook University, Townsville, Australia
566
Interfacial Properties of Polypropylene Fibre-Matrix Composites
literature for production of these composites [2]. Although the majority of publications are on single polymer composites with polyethylene, Loos was the first to investigate the production of PP single fibres, embed in a block of PP matrix [4]. Subsequent work by Poldervaart and Kitayama extended this technique to making unidirectional PP-PP composites using film lamination [5,6]. Other techniques for producing single polymer composites include hot compaction. In the hot compaction method, a major issue is melting of the reinforcement during preparation of the composite, which can reduce mechanical properties of the composite. Recent research has explored the improvement of the sandwich technique for production of single polymer composites. Initial studies showed that the reinforcement of the composite was completely in the matrix, without melting, by using suitable conditions of temperature and pressure [7]. The present work is aimed at preparing all PP composites, which unites the advantages of both PP fibres and PPE matrix, that is a composite material in which both the reinforcement and matrix material are made of PP with significant interfacial interaction between reinforcement and matrix. EXPERIMENTAL The materials employed in this investigation were random poly(propylene-coethylene) matrix (PPE) (density, p = 0.905 gem"3 , MFI = 0.8 dg/min, melting temperature = 147.5 °C, ~ 5 % ethylene) and PP fibres (diameters = 50 urn, tensile strength = 250-350 MPa, tensile modulus = 4.7 GPa and length = 2-3 cm). The fibres were obtained from Melded Fabrics Pty Ltd and the PPE from Basell Australia Pty Ltd. According to differential scanning calorimetry results, the melting temperature of the PPE film and PP fibres was 147 and 165 °C respectively, so that 152-157 °C was selected as the moulding temperature range. A heated press was used. Long PP fibres were distributed randomly on top of a PPE film (with ~ 0.2-0.4 mm thickness) and placed between two Teflon sheets, then pressed at 152 -157 °C for 5-7 minutes. After that, an 11-14 kPa pressure was applied for 8-10 minutes. The fibre volume content of the PP-PPE composites was 50 %. To provide a uniform composite, three layers of composite were laminated together. The composite, fibres and polymers were thermally analyzed using a differential scanning calorimetry (DSC, Perkin-Elmer Pyrisl). Samples of about 3 mg were placed in sealed 10 uL aluminum pans. A constant nitrogen flow of 40 mL/min was used to purge the instrument. The samples were held at 30 °C for 2 min, then heated from 30 to 180 °C at a rate of 10 °C/min, held at 180 °C for 2 min, cooled to 30 °C at the same rate and held for 2 min. Tc was measured from the peak of the exothermic during cooling. The second heating cycles provided results that were more consistent for (Tm) measured from the peak value of the endotherm. For clarity of presentation, successive curves have been shifted by 5 units in Figure 1. The tensile properties of each composite was determined using the average of five specimens for each composite with an Instron Universal Testing machine (Model 4065), following the ASTM standard D 3039-93, with 50 mm/min crosshead speed. Standard tensile specimen shapes with dimensions 57 x 5.9 mm and a gauge length of 57 mm were used. The flexural properties of the composites were measured with a Perkin-Elmer DMA7e in three-point bend mode at 25 °C. The static force was scanned from 100 mN to 8000 mN at 100 mN/min and the samples were cut from the sheets, with dimensions 1x12x5 mm. Specimen for single-filament tests were fabricated by mean of film laminating and process as shown in Figure 2. In this case the geometry of the micro-drop was modified by making cubic matrix samples,
Interfacial Properties of Polypropylene Fibre-Matrix Composites
567
as shown in Figure 2. The strip of matrix was divided into three individual specimens, with one of the two free ends of the roving being cut off in each case.
25 -
5" 13
|
* > •
^
15 -
I ...
12
TemperatureCC)
(a)
Temperature(°C)
(b)
FIGURE 1 DSC (a) and melting (b) crystallization of PP-PPE-composite
The interfacial properties of each composite were determined using the average of ten specimens for all PP composite with a Rheometric DMTA IV. The long fibre end of the specimen was first pulled through the hole in the disc (while observed under a stereo microscope) until the face of disc contacts the matrix cube and is then clamped to the lower tensile fixture.
FIGURE 2 Schematic representation of sample preparation preliminary to the debonding test
In order to prevent slippage of the fibre gripped in the fixture, a thin folded piece of paper was adhered to the fibre end with instant adhesive and placed in the fixture, directly before the experiment was carried out. The experiments were carried out with 100 urn aperture hole diameter. The average gauge length was 6 mm and a forcedisplacement curve was recorded at a pulling speed of 0.001 /s. Prior to the microbond test, the images of the specimen were recorded using a Nikon Labophot 2 optical microscope, which was connected to a digital camera. The images of the specimen after the microbond and tensile test were recorded using an FEI Quantum 200 Scanning Electron Microscopy (SEM) in a low-voltage mode (LVSEM). RESULT AND DISCUSSION Figure l(a) shows that in all PP composites the peak at approximately 150 °C corresponded to the melting of spherulites in the matrix. The second endothermic peak at approximately 165 °C, whose size was determined by fibre volume fraction, was the melting endotherm of the fibres. The distinct melting temperatures of the matrix and fibres confirm that the PP in the matrix and fibres remained as separate phases in the composites. A significant increase of about 1.5-2.0 °C in the melting temperature of the matrix was observed in the composites compared with the pure
568
Interfacial Properties of Polypropylene Fibre-Matrix Composites
matrix PP, Figure l(a). The compression molding of the composites has enabled the matrix to crystallise with nucleation from the fibres. The combined crystallinity of matrix and fibres was greater than that of the separate matrix PPE. This may be attributed to an increased crystallinity in the matrix due to the presence of a transcrystalline interphase in the matrix, or perfection of the matrix crystals after the moulding heat treatment. Figure 1 (b) shows that the crystallisation peak of all composites is slightly shifted to a higher temperature compared with that of pure coPP. This can be explained by the assumption that PP fibres act as a nucleating agent for the matrix, which would increase both the crystallization nucleation and the number of spherulites nucleated in the matrix phase [1,2,6]. Note the PP fibre crystallised separately from the matrix, since there was insufficient time for intermixing of the two components. Figure 3(a) shows characteristics typical of a ductile material, with a maximum in the stress-strain curve, which corresponds to the initiation of necking (yielding). A load drop and subsequent levelling of the stressstrain curve was observed, which corresponds to the initiation of de-bonding of fibre from the matrix in the composites.
PP-PPE composite
U)
20 •
w
e
S5 S t r a i n (% )
10 H 1
2
3
4
5
6
Strain (%) (a) (b) FIGURE 3 Stress- strain curve for all PP composites (a) tensile (b) Flexural mode
It is clear that the addition of fibre reduced the strain to failure of the matrix sharply. This is attributed to the fact that stress concentration at the fibre ends leads to matrix cracking, which ultimately leads to failure when the surrounding matrix and fibre can no longer support the increased load caused by the local failure [8]. The tensile modulus of the composite shows a high value, which is 6 times higher than the matrix, due to the restriction of matrix movement and the effectiveness of the reinforcement. In Figure 4 there is a small amount of fibre pull-out from the matrix. In this case, there exists a tearing of the matrix as well as fibre tensile or shear failure modes. There is considerable fibre rupture during the tensile event that seems to be the dominating failure mechanism.
FIGURE 4 Scanning electron microscopy of fractured sample after tensile fracture
Interfacial Properties of Polypropylene Fibre-Matrix Composites
569
The microbond test described was carried out with as-received polypropylene fibre embedded in PPE matrix. The system with all PP, PP fibres and PPE matrix, is known to develop physico-chemical interaction between two phases. The maximum debonding forces as a function of embedded length are shown in Figure 5. The results display that the load which is necessary for interface debondment for all PP composites are high and greater in comparison with the results for a glass-PP system for a given embedded length, from a literature survey [10]. This can be attributed to the fact that if the interfacial bonding between fibre and matrix is weak, the fibre can be easily separated from the matrix when a load is applied.
300
400
500
600
700
600
Embeded Length (microm)
FIGURE 5 Variation of the debonding force of the embedded length for all PP composite
In this case there are no advantages of high strength and stiffness of the fibre. However, if the interfacial bond is too strong between the two phases, the fibre cannot de-bond from the matrix when the fibre is broken by application of a load [6,8]. When a filament is broken, de-bonding to some extent disperses the possibly concentrated stress, and a crack is developed, which results in matrix failure. Figure 6 and Table 1 show the variation of interfacial shear stress (IFSS) as a function of embedded length and type of fibre when a load is applied along the fibre direction. The load will be transferred through interfacial bonding due to its high modulus and low elongation. If the tensile force exceeds the strength of a single fibre, the fibre is fractured and the broken fibre undergoes continuous fragmentation due to the action of interfacial shear stress remaining at the interface and becomes shorter by a specified value. TABLE I Comparison between debonded force and IFSS of all PP composite and glass-PP composite
Sample All PP composite Glass-PP composite Glass-PP composite
Agent for fibre treatment
Designation
-
Cl C2 C3
r-amino-propyltriethoxysilane
IFSS (MPa) 5.18 2.75 2.83
However, if the force is equal to or less than the strength of the fibres; this results in less shorter broken fibres or longer IFSS. An all PP composite has greater IFFS than glass-PP composite. It can be seen from our experiments that the maximum value of IFSS is 5.2 MPa, while the tensile strength of the PPE matrix is about 78 MPa. Hence, normally PPE cannot be stretched to break by only 5.2 MPa at the stress of the broken end of the fibre. However the stress is extended into the matrix when the fibre is suddenly broken similar to an impact test.
570
Interfacial Properties of Polypropylene Fibre-Matrix Composites
300
400
500
600
700
800
Embeded Length (microm)
FIGURE 6 Experimental results and fitting of the average shear stress as a function of the embedded length for all PP composite
CONCLUSION This study revealed a strong nucleation ability of the fibres on matrix crystallization. An increase of melting temperature of the matrix with introduction of the fibres was observed. Incorporation of the fibres gave a considerable increase of the tensile, flexural modulus and strength, due to the efficient reinforcement imparted by the fibre. The adhesion of matrix and fibre has been characterized by using a micro-bond test, essentially a pull out technique. IFSS showed a significant increase for all PP systems, 5.2 MPa, whereas IFSS is about 2.9 MPa for glass-PP system, which leads to the good mechanical properties. This demonstrates the use of PP fibres in all-PP composite application. ACKNOWLEDGEMENTS Financial support of an International Postgraduate Research Scholarship (IPRS) is acknowledged. REFERENCES 1. PJ. Hine, I. M. Ward, N. D. Jordan, R. Olley, D. C. Bassett. 2003. "The hot compaction behavior of woven oriented polypropylene fibres and tapes. I. Mechanical properties," Polymer, 44, 1117-1131. 2. PJ. Hine, I. M. Ward, N. D. Jordan, R. Olley. 2001. "A comparison of the hot-compaction behaviour of oriented high-modulus, polyethylene fibres and tapes," Journal of Macromolecular Science and Physics, 5, 959-989. 3. Z. Xiaodong, L. Qunfang,D. Gance. 2002. "Studies on mechanical properties of discontinuous glass fibre/continuous glass mat/polypropylene composite," Polymers & Polymer Composites, 10, 299-306. 4. J. Loos, T. Schimanski. 2001. "Morphological investigations of polypropylene single-fibre reinforced polypropylene model composites," Polymer, 42, 3827-3834. 5. T. Kitayama, K. Ishikura, T. Fukui, H. Hamada. 2000. "Interfacial properties of PP/PP composites," Science and Engineering of Composite Materials, 9, 67-73. 6. S. Houshyar S, R. A. Shanks. 2003. "Morphology, thermal and mechanical properties of polypropylene fibre-matrix composites," Macromolecular Materials and Engineering, 288, 599. 7. H. Fujimatsu, Y. Ishikawa, H. Usami, Y. Nasu, K. Kajiwara. 2002. ""Formation of adhesive phae onto high strength and modulus PE fibre by PE solution treatment for making PE fibre-reinforced PE composite," Composite Interface, 9, 157-169. 8. A. Zheng, H. Wang, X. Zhu. 2002. " Studies on the interface of glass fibre-reinforced polypropylene composite", Composite Interface, 9(4) 319-333.
Surface Grafting of Nano-SiC with Glycidyl Methacrylate in Emulsion and Its Effect on the Tribological Performance of Epoxy Composites Min Zhi RONG*, Ying LUO, Ming Qiu ZHANG Materials Science Institute, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education of China, Zhongshan University, Guangzhou 510275, P. R. China Bernd WETZEL, Klaus FRIEDRICH Institute for Composite Materials (IVW), University of Kaiserslautern, D-67663 Kaiserslautern, German
ABSTRACT To improve the tribological performance of nano-SiC particles filled epoxy composites, surface modification of the fillers is necessary. By means of soapless emulsion polymerization method, graft polymerization of glycidyl methacrylate (GMA) onto the surface of alkyl nano-SiC was carried out. The monomer, polyglycidyl methacrylate (PGMA) is chemically attached to the nanoparticles by the double bonds introduced during the pretreatment with a coupling agent. By analyzing the reaction mechanism, the emulsion polymerization loci were found to be situated at the SiC surface. Besides, the factors affecting the grafting yielding of PGMA on the particles were investigated, including monomer concentration, initiator consumption, reaction temperature, reaction time, etc. Accordingly, an optimum grafting reaction condition was determined. It was shown that the grafted nanoparticles exhibit greatly improved dispersibility in good solvent for the grafting polymer. The primary studies about the tribological performance of epoxy composite showed a positive effect of grafted nano-SiC as expected.
INTRODUCTION hi recent years, there is an increasing trend of utilizing nano-sized powders in various aspects, such as toughening of plastics [1] and tribological performance enhancement of polymers [2]. ha all these applications, establishment of modification technique for the nanoparticles' surface is highly desired to improve dispersibility of the powders in polymer matrices and to tailor the interface interaction. Grafting polymer onto the surface of inorganic particles is a field of great interests. Most of the works were carried out for micron and sub-micron particles in solutions via various chemical processes, including radical, anionic and cationic polymerizations [3]. Besides, a few reports have been devoted to the grafting of polymers onto the particulate surfaces in emulsion rather than in solution [4]. It was suggested that emulsion * Correspondence Author, Dr. Min Zhi RONG, Materials Science Institute, Zhongshan University, Guangzhou 510275, P. R. China. Tel/Fax: +86-20-84114008, E-mail: [email protected]
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Surface Grafting of Nano-SiC with Glycidyl Methacrylate in Emulsion
polymerization offers strong potential advantages for modifying the surface of nano-sized particles. This is because the grafting polymers tend to cover the particles so long as suitable reaction conditions are available, for example, in the presence of functionalized particles or using small amount of surfactant. From both theoretical and engineering points of view, however, the grafting reaction mechanism involved has not been elucidated with satisfaction so far, and most of the grafting polymers attached to the particles do not possess any reactive group that can be used to chemically link the particles to the matrix. In our previous studies [1, 2], the necessity of nanoparticles surface modification in improving the wear resistance of epoxy based nanocomposites was illuminated. To further bring the positive effects of nanoparticles into play in the very area, the authors of the present work plan to introduce grafting polymers containing reactive groups onto nanoparticles so as to build up chemical bonding at the filler/matrix interface during the subsequent composites manufacturing. That is, a fine adjustment of the interfacial interaction in the subsequent composites can be completed by controlling the amount and species of the reactive groups. EXPERIMENTAL Materials The nano-sized SiC particles supplied by Hua-Tai Co. Ltd., China, were in their a-phase, with a specific surface area of 15.2 m2/g and an averaged diameter of 61nm, respectively. A KH570 silane coupling agent (g-methacryloxypropyl trimethoxy silane, provided by Liao Ning Gaizhou Chemical Industry Co. Ltd., China), was employed to introduce the reactive double bonds on the surface of the nanoparticles. Since the ultimate aim of the present work lies in the introduction of grafting polymers on SiC nanoparticles via the methacryloxy groups, a monolayer coverage of silane or a relative thin attachment of KH570 should be beneficial to the subsequent grafting polymerization and the linkage between the particles and the grafting polymers. Therefore, the silane treated SiC nanoparticles containing 1.24wt% KH570 was used in the following grafting reaction. All the materials are commercial products and were used without further purification except GMA monomer, which was distilled under low pressure prior to the grafting polymerization. Emulsion Graft Polymerization The typical graft polymerization experiments were carried out using a four-neck flask (ca. 250cc) fitted with a stirrer. A desired amount of SiC-KH570 and 70ml ammonia were charged into the flask. Then the non-ionic surfactant was incorporated with a dosage lower than the critical micelle concentration (CMC). Having been ultrasonically agitated for 30min, the above mixture was stirred for additional 5.5h under argon atmosphere. The reaction temperature was increased up to 60°C and then the initiator (potassium persulfate) was added. After 35min, the graft polymerization was started when the monomer was filled by drip-feeding. The reaction had to proceed for a period of time (usually 16h), and was stopped by ice cooling. After the graft polymerization, the resultant suspension was filtered, washed and extracted with methanol for 8h to remove the residual monomer. The dried mixture was extracted with acetone for 5 Oh to isolate the polymer-grafted SiC (SiC-g-PGMA) from the absorbed polymers. Then the grafted nanoparticles were dried under vacuum at 50°C. Some of them were transferred to a Shimadzu TA-50 thermogravimeter (TGA) to determine the percent grafting (yg).
Surface Grafting of Nano-SiC with Glycidyl Methacrylate in Emulsion
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Monomer conversion (7C) and grafting efficiency (ye) were calculated according to Ref. [3]. Dispersibility Characterization and Wear Tests The dispersibility of the grafted nanoparticles was characterized by the time dependence of the weight of SiC-g-PGMA suspending in acetone. Unlubricated sliding wear tests were carried out on a pin-on-ring apparatus under a constant velocity of 0.4m/s and pressure of 3MPa, respectively. The carbon steel ring had a diameter of 40mm and an initial surface roughness of 0.1mm. The specimens for wear tests were machined with a geometry of 6 x 10 xl7 mm3, resulting in an apparent contact area of about 5xl0mm2. Prior to wear testing, all the samples were pre-worn to average surface conditions and reduce the running-in period. The actual steady-state test period was set to 3hr. RESULTS AND DISCUSSION Mechanism of the Grafting Polymerization The locus of polymerization is now of prime concern. Normally, the micelles are favored as the reaction sites because of (i) larger surface area of the micelles than that of the droplets by over two orders of magnitude, and (ii) higher monomer concentration (similar to bulk monomer concentration) compared to that in solution. In the presence of nanoparticles, their surfaces become more favorable reaction sites when they have been modified by silane. If the nanoparticles were uniformly dispersed, they possess quite large surface areas (the concentration of the particles is 1013 per milliliter). Besides, the double bonds on the particles surfaces can take part in the initiation reaction to form particulate nucleation. This process is believed to be easier than the formation of polymer particles by micellar nucleation. More importantly, the amount of the introduced monomers remains low at any time and may be fully adsorbed onto the surfaces of SiC nanoparticles due to their hydrophobic surface feature. TABLE I Effect of pre-dispersion time with stirring on the grafting reaction of PGMA (Each reaction was carried out at 60°C for 16h, and the surfactant concentration is 0.0001 mol/L)
Monomer Initiator Weight of Nano-SiC Concentration Concentration [mol/L] [mol/L] [g] 2
0.2
0.003
Pre-dispersion time [h] 7 5 3
Tc [%1
7g
[%1
[%1
64.12 46.07 50.37 30.67 17.24 59.11 13.14 8.03 64.26
The aforesaid analysis receives supporting evidences from Table I. The longer dispersion time for the particles in solution before reaction has a significant effect on the improvement of monomer conversion and percent grafting. Such an improvement can be reasonably related to the increase of the number of the isolated particles with a rise in the dispersion time. The rate of polymerization, Rp, at the stage when only polymer particles exist (free of micelles), is generally given by the following expression [5]:
Surface Grafting of Nano-SiC with Glycidyl Methacrylate in Emulsion
574
*,=
XtfNEk [M]
(1)
where N denotes the particles concentration, n the average number of radicals per particle, and NA the Avogadro number. Evidently, the increase of Nwith longer dispersion time should result in the increase of Rp, and js and yc as well. Effect of Reaction Conditions on the Grafting Polymerization Grafting kinetics of GMA polymerization onto silane modified SiC nanoparticles have been studied. As shown in Fig.l monomer conversion and percent grafting increase with time initially and then level off at about 6h. On the other hand, the grafting efficiency shows the highest value at the beginning of the reaction, and decreases with increasing time. These phenomena imply that the grafting of GMA onto the surface of SiC prefers to take place at the beginning of the reaction. The succeeding polymerization is mainly controlled by the homopolymerization of GMA, because of the blocking effect of the grafting polymers on the subsequent grafting reaction. That is, the surface double bonds cannot be initiated at the latter stage of polymerization as the growing polymer radicals and/or grafting polymer chains block the diffusion of radicals to the particles' surfaces. This is understandable when considering that the grafting PGMA chains must be very close to the particles surfaces in an emulsion system. Besides, the possible hydrogen bonding between SiC and PGMA is also favorable for encapsulation of the polymer around the particles.
100
E 80 A-
_A
a
a
—•— Monomer conversio —O— Percent grafting —A— Grafting efficiency
n |
60
—D— Monomer conversion —0— Percent grafting — A - Grafting efficiency I
.
I
,
10
i
15
.
i
.
i
.
20
Reaction Time [h]
FIGURE 1 Grafting kinetics of PGMA onto silane modified nano-SiC.
0.10
0.15
0.20
0.25
0.30
Monomer concentration [mol/L]
FIGURE 2 Effect of monomer concentration on the grafting polymerization of GMA onto nano-SiC.
Fig.2 shows that the higher monomer concentration, the higher percent grafting and monomer conversion. The values of grafting efficiency exhibit a peak-like dependence on monomer concentration. These results can be attributed to the fact that the polymerization rate increases with monomer concentration. It is consistent with the general law of emulsion polymerization [ 5 ]. With respect to the influence of initiator concentration, it is seen from Fig.3 that with a rise in initiator concentration all the grafting parameters show a significant increase at the beginning. Then, jc and yg keep almost unchanged or decrease slightly, while 7, shows a slight increase at higher initiator concentration. It is known that higher initiator concentration would lead to higher initiation rate, and hence more double bonds on the
Surface Grafting of Nano-SiC with Glycidyl Methacrylate in Emulsion
575
particles' surfaces can be initiated. This accounts for that yc, yg and ye increase evidently with a small rise in initiator concentration at low concentration level. However, a further increase of initiator concentration hardly affects the reaction due to the blocking effect as mentioned above. The decreasing trend of grafting efficiency at higher initiator concentration can be ascribed to the faster bimolecular termination caused by the entry of a second radical into the polymer particles. The effect of reaction temperature on yc, yg and ye is illustrated in Fig.4. Clearly, the proper reaction temperature range should be between 60 and 80°C. When the temperature is lower than 60°C, the rate of radical generation is very slow, resulting in low yc, yg and ye. On the other hand, the initiating rate may be very fast at a temperature higher than 80°C, leading to substantial exhaustion of initiator at the beginning of the reaction and hence low yc, yg and ye. Comparatively, the reaction at 80°C can lead to higher yc, yg and ye than that at 60°C because the overall rate of polymerization increases with increasing temperature. It is similar to the effect of reaction temperature on homogeneous polymerization. A rise in reaction temperature raises the reaction rate by increasing both Kp and N (see Eq.(l)). The increase in N is factually due to the increased rate of radical generation at high temperature.
£,
80
«
I
—D— Monomer conversion —O— Percent grafting —A— Grafting efficiency 0.003
0.006
0.009
0.012
Initiator concentration [mol/L]
FIGURE 3 Effect of initiator concentration on the grafting polymerization of GMA onto nano-SiC.
Reaction temperature [°C]
FIGURE 4 Effect of reaction temperature on the grafting polymerization of GMA onto nano-SiC.
Effect of Grafted Particles on the Dispersibility and Wear Resistance To check the effect of surface treatment qualitatively, the dispersibility of PGMA grafted SiC in acetone was compared with that of the untreated nano-SiC (Fig.5). The results clearly show a remarkable improvement of dispersibility of the former particles originating from the surface grafting. Untreated nano-SiC completely precipitates after a few hours. On the contrary, SiC-g-PGMA gives a stable colloidal dispersion in the solvent. In addition, the grafted SiC nanoparticles with higher percent grafting tend to be less stable than that with smaller amount of the grafting polymers, indicating that excessive grafting polymer chains interfere with the dispersion of SiC nanoparticles due to molecule entanglement. The sliding wear properties of the composites rilled with untreated nano-SiC are shown in Fig.6 as a function of particle content. It is evident that the nano-SiC particles can significantly reduced the wear rate of the composites even at very low filler loading (about 0.3 vol.%). Beyond this value, the wear rate tends to keep unchanged with arisein the fraction of the nanoparticles. On the contrary, the frictional coefficient of the
576
Surface Grafting of Nano-SiC with Glycidyl Methacrylate in Emulsion
composites reduced gradually with the addition of particles, which does not correspond to their filler content dependences of wear rate. Above phenomena, reveal an existing of a special mechanism for nanoparticles filled composites, which may relate with the role of particles as a roller. In case of grafted particles, it was found that the grafted SiC (1.18 vol.%) filled epoxy composites also exhibit improved ws and u, values (0.41 and 2.8x 106 mm/Nm) in comparison with untreated SiC/epoxy composites (0.44 and 5.6xlO6 mrn/Nm) at rather lower percentage grafting (about 10 %). However, at a higher % (40%), both cos and u. values become increasing. The grafting polymer should enhance the interface interaction, but also be detrimental to the particle dispersion by entanglement between the particles. This may explain why the tribological performance tends to decrease at higher yg.
- D - SiC-g-GMA (Tg=52.33%) - O - SiC-g-GMA (y g =27.56%) — A - Untreated SiC
20
30
Time [h]
FIGURE 5 Dispersibility of untreated nano-SiC and SiC-g-PGMA in acetone at room temperature.
1
2
3
4
5
Content of SiC [vol%]
FIGURE 6 Frictional coefficient, jx, and specific wear rate, a>s of neat epoxy and its composites filled with untreated nano-SiC
ACKNOWLEDGEMENTS The financial support by the Volkswagen-Stiftung, Federal Republic of Germany (Grant No.1776645), for the cooperation between the German and Chinese institutes on this subject is gratefully acknowledged. Further thanks are due to the Natural Science Foundation of China (Grant: 50273047) and the Team Project of the Natural Science Foundation of Guangdong, China (Grant: 20003038) for supporting some parts of the chemical works involved in this project. REFERENCES 1.
2.
3. 4. 5.
Zhang, M. Q., Rong, M. Z., Friedrich, K. 2003. "Processing and properties of Non-layered nanoparticle reinforced thermoplastic composites,"In Handbook of Organic-Inorganic Hybrid Materials and Nanocomposites, Volume 2: Nanocomposites; Nalwa, H. S., Ed.; California: American Science Publishers, Chapter 3, pp. 113-150. Rong, M. Z., Zhang, M. Q., Shi, G., Ji, Q. L. Wetzel, B., Friedrich, K. 2003. "Graft polymerization onto inorganic nanoparticles and its effect on tribological performance improvement of polymer composites," Tribol. Int., 36: 697-707. Rong, M. Z., Ji, Q. L., Zhang, M. Q., Friedrich, K. 2002. "Graft polymerization of vinyl monomers onto nanosized alumina particles," Eur Polym J, 38: 1573-1582. Espiard Ph., Guyot A. 1995. "Poly (ethyl acrylate) latexes encapsulating nanoparticles of silica: 2. Grafting process onto silica," Polymer, 36: 4391-4395. Odian, G. 1991. Principle of Polymerization, John Wiley & Sons: New York, pp.335-353.
Influence of Matrix Type and Processing Conditions on the Morphology of the Interface and the Interfacial Adhesion of PE/PE Composites Mahmood Masoomi \ S. Reza Ghaffarian^and N. Mohammadi1 1) Polymer Engineering Department, Amir Kabir University of Technology, Tehran, Iran
ABSTRACT Four different types of polyethylene, high density (HDPE), linear medium density (MDPE), linear low density (LLDPE) and low density (LDPE) have been used to prepare composites with ultra high molecular weight polyethylene (UHMWPE) fibers. PE/PE micro composites were prepared from the above materials and the crystalline morphology of the fiber and matrices interfaces were studied by a polarizing microscope. The interfacial shear strength (IFSS) of UHMWPE fiber with PE matrices was determined by micro bond pull-out method. Thermal behavior of the matrices, the fiber and the prepared hot pressed composites were investigated by differential scanning calorimeter (DSC) analysis. All above specimens were cooled by using two processing conditions, i.e. isothermal crystallization (ISO) and ice water quenching (IWQ). The microscopic images showed a big difference between those samples prepared by HDPE matrix and other matrices that cooled by ISO methods. The ISO cooled sample with HDPE matrix contained a regular transcrystallinity (Tc) region. The intensity of the T c layer in the IWQ cooled samples with LDPE and LLDPE matrix was very poor, hi the micro composites prepared by MDPE and LLDPE as matrix and cooled by ISO method, sever irregular T c region was appeared. The DSC studies revealed that only HDPE had a crystallization condition similar to the melted fibers. The preliminary microbond test results indicated that the IFSS of the ISO cooled samples decreased relative to the IWQ cooled samples.
INTRODUCTION The PE/PE composites are an important group of homopolymer composites possessing interesting and some unique properties. Some of these properties are: toughness, Impact resistance, chemical resistance, lightness, abrasion resistance, weld ability, hydrophobicity, low dielectric properties, acceptable biocompatibility and possible application in cryogenic temperature. Like other composites, interface adhesion is the most influential factor, which affects the mechanical properties of PE/PE composites. Interface adhesion is closely related to interface morphology. This later parameter is itself influenced by processing condition and materials properties. So a good knowledge of the interface morphology and the effects of processing condition and material properties on it is a key factor in controlling the interface * Corresponding author, Polymer Engineering Department, Amirkabir University of Technology, Tehran, Iran, sr_ghaffarian(S).aut.ac.ir.
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Influence of Matrix Type and Processing Conditions
adhesion. The most common morphology in the interface of thermoplastic composites is transcrstallinity (Tc). For the first time, He and Porter [1] observed Tc layer in the interface of HDPE- PE fiber composite. They claimed that T c layer consist of an inner and outer zone. Ishida and Bussi [2] proposed a model to study the Tc growth in the PE/PE composite, by modifying the theory of heterogeneous nucleation. In another work, Teishev and Marom [3] studied the effect of Tc growth on the transverse mechanical properties of HDPE-PE fiber composite. They claimed the Tc growth resulted in a 50% decrease of the transverse tensile strength and strain to failure. Stern et al. [4] found a Tc interface on the fiber surface. They indicated that Tc growth had not effect on tensile strength and modulus of PE/PE composites. This researcher in another work investigated the effect of cooling rate on the crystals morphology of the interface. Also, they extended a model for microstructure of Tc layer by X-ray diffraction. An important and influential factor on the formation and structure of T c region is the type of PE which is used as matrix in the PE/PE composite. With regard to this fact that in the processing and manufacturing of PE-PE composite a surface melting is occurring on the PE fibers, the type of PE, as matrix, can play an important role in the structural morphology of the interface, of these composites. In this article the formation and structure of Tc region when four different types of PEs are used as the matrix have been investigated. Moreover the influence of T c region on the interface adhesion, in the presence of different types of PE as the matrix was studied. EXPERIMENTAL Materials The UHMWPE fiber used in this study was Dyneema SK60 (DSM High Performance Fibers BV). The PE matrix materials were high density polyethylene (HDPE) copolymer grade with narrow molecular weight distribution, trade name of Rigidex HD 5218EA (BP Solvay), linear medium density polyethylene (MDPE), trade name of Rigidex HD 3840UA (BP Solvay), linear low density polyethylene (LLDPE) copolymer grade with narrow molecular weight distribution, trade name of M500026 (Sabic corporation) and low density polyethylene (LDPE), trade name of MG70 (Qapco). Methods Micro-composite samples containing different types of matrix were prepared and analyzed with a Leica polarizing microscope which was equipped with a hot stage crystallization unit and connected to a photo camera. Samples were prepared by laying separately a few monofilaments between two matrix films with 100 |xm thickness and placing the assemblage on a microscope slide, topped with a cover glass, and then placed in the hot stage. The temperature of samples were increased to 137 °C and held for 15 min, thereafter either quenched in the ice water (IWQ) or cooled at constant rate of 1 °C/min to the isothermal crystallization temperature (ICT) and held for 60 min in this temperature, then cooled to the ambient temperature (ISO). The isothermal crystallization temperature for each matrix is different which should be determined e.g. with DSC analysis. To measure the interfacial strength between the fiber and different types of matrices, samples were prepared according to the following procedure. A matrix
Influence of Matrix Type and Processing Conditions
579
ribbon was carefully cut out of a film of that matrix (typically 100 um thick, 500 urn wide and 20 mm long). The matrix ribbon was placed on the middle of a microscope slide. Then a few equally spaced monofilaments were placed on the ribbon in a way that the fibers axes were normal to the ribbon longer side. Finally another matrix ribbon was carefully placed on top of the previous ribbon to sandwich the filaments. The whole assembly was then positioned within the hot stage and the same thermal program as mentioned above was exerted on it. The matrix ribbon was then cut from the middle of the space between the monofilaments; the obtained specimens then were used to determine the IFSS of fiber-matrix by means of pull out test. The test was preformed according to the procedure described by BIRO et al. [5]. In this experiment some length of a monofilament was embedded in a matrix droplet. The upper surface of the droplet was holed against two jaws of a caliper that was mounted on the crosshead of a Zwick tensile machine (type 146460) in a way that the fiber located freely between the jaws. The machine was equipped with a 10 Newton load cell. The crosshead speed was 0.5 mm/min. For thermal analysis, the samples were prepared by molding them in a hot press. The mold pressure was adjusted on 5-7 bar and the molding temperature was controlled with the accuracy of ± 1°C during molding cycle. At the end of molding the mold containing the specimen cooled with two methods: quenching in a mixture of ice and water (IWQ) and isothermal at crystallization temperature for 1 hour (ISO). To investigate the thermal analysis of the prepared composites, a differential scanning calorimeter (DSC) was used. To study the melting and crystallization processes, the DSC analysis was performed in heating and cooling mode. The samples heating and cooling rate was 5 °C /min for all the DSC tests. RESULTS AND DISCUSION One of the criteria in choosing the PEs as matrix was their flow-ability. This parameter is important in the wetting of the fibers. Melt flow index (MFI) is a parameter that quantitatively can express the flow-ability of PEs. Since the processing temperature of PE/PE composites are less than 140 °C, in order to have a proper view of the flow-ability of matrices, the MFI of PEs were also obtained around this processing temperature. TABLE I Physical and rheologieal properties of raw materials. Raw materials UHMWPE Fiber HDPE Matrix MDPE Matrix LLDPE Matrix LDPE Matrix
Density (gr/cm3) 0.975 0.952 0.938 0.926 0.922
Melting peak °C 147, 156 130 126.5 124 104
Crystallization peak °C 117.3 117.7 114.8 109.6 90
ICT °C 121 120.1 116.8 113.8 95
MFI(2.160kg) 190°C 138°C 18 7 4 1.6 50 16 70 9
The DSC curves for UHMWPE fiber and matrices were prepared in order to carefully determine the processing temperature of PE/PE composites. Table 1 shows some of the obtained physical and rheologieal results for the UHMWPE fiber and matrices which were used to select the processing conditions. Melting of UHMWPE fiber in DSC begins at around 127 °C which is due to melting of the low molecular
Influence of Matrix Type and Processing Conditions
580
mass macromolecules present on the periphery of the fibers [6]. The main melting peak, at 147.3 °C, appears with a shoulder at 155.8 °C. Figure 1 and 2 show the DSC curves of the composites produced from four different type of PE as matrix and cooled by ISO and IWQ methods, respectively, hi heating rout of all curves two peaks appeared which the lower one corresponds to the melting of matrix and the other is related to melting of fibers, hi curves la and 2a which belong to a HDPE matrix type composite, only a sharp exothermic peak was seen in cooling, while in other curves two exothermic peaks or a broad peak have been appeared. So it can be deduced that only for the HDPE composite the possibility of co-crystallization of the fiber and matrix in the interface could be conceivable.
100 Temperature 'C FIGURE 1 DSC thermograms of PE/PE composites that cooled by ISO method, a) HDPE, b) MDPE, c) LLDPE and d) LDPE .
100 Temperature °C
200
FIGURE 2 DSC thermograms of PE/PE composites that cooled by IWQ method, a) HDPE, b) MDPE, c) LLDPE and d) LDPE .
Figures 3 and 4 show the microscopic images of composites with HDPE and MDPE matrices that have been cooled by ISO and IWQ methods. The HDPE matrix composite that cooled by ISO method, Figure 3a, have an interface with a uniform thickness which contains of needle like compacted crystals that have been propagated vertically from the surface of fiber. For this system those parts of matrix in the vicinity of the Tc layer have lower crystallinity relative to the bulk of matrix. The MDPE composite which was cooled by ISO method, Figure 4a, have thicker Tc layer compared to other specimens. For this specimen the structure of crystals in the interface is similar to that of the bulk of matrix, but more compacted. Moreover the
Influence of Matrix Type and Processing Conditions
581
compaction intensity of the crystals within the Tc layer along the fiber is variable and in some of, its region reaches the compaction state of the bulk of matrix.
FIGURE 3 Optical micrographs of micro-composite with HDPE matrix (a) ISO and (b) IWQ cooled.
I. FIGURE 4 Optical micrographs of micro-composite with MDPE matrix (a) ISO and (b) IWQ cooled.
Figures 3b and 4b show micrographs of composites with HDPE and MDPE matrix, respectively, that have been cooled by IWQ method. The Tc layer in these samples has variable thickness and the thickness in some region even is near zero. The structure of Tc crystals is the same as the bulk of matrix in both composites. When the composite with LLDPE matrix was cooled by ISO method, a thin Tc layer with variable thickness was appeared. In the IWQ cooled composite with LLDPE matrix, and the composites with LDPE matrix that were cooled by ISO or IWQ methods, no significant Tc layer were observed. Therefore according to these results the Tc layer only appears in the composites with HDPE and MDPE matrix with any processing condition. But for LLDPE matrix the Tc layer was present only in the ISO cooling method. So, both the type of matrix and the cooling process show strong influence on the morphology of the interface in the PE/PE composites. The IFSS, x , can be calculated by using the following equation: Where Fmax is maximum force that was measured from the pull out curve, d is the fiber diameter and L is the embedded fiber length which was determined by an optical microscope. The average IFSS, T , was determined either by the average of 15 to 20 measured values or by evaluating the slop of a best fit linear regression line from plots of Fmax versus embedded area [5]. The maximum value of the IFSS, r max , is
582
Influence of Matrix Type and Processing Conditions
determined when the embedded length reduced to zero [7]. r m a x can be determined by extrapolating the line, which is obtained from plots of r versus the embedded area, to a zero embedded area. Table 2 shows the T and T max of different samples. As can be seen from these results the HDPE and MDPE composites have higher T max with respect to LLDPE specimen. This can be related to the better compatibility between HDPE and MDPE and PE fibers in co-crystallization process at the interface. TABLE II The results of pull out test
r max (Mpa) T (Mpa)
HDPE Composite ISO IWQ 12 9.7 6.2 5.1
MDPE Composite IWQ ISO 14.9 11.1 6.2 7.2
LLDPE Composite ISO IWQ 6.6 5.1 5 4.5
The ISO-cooled HDPE sample showed lower interfacial adhesion in comparison to the ISO-cooled MDPE composite which could be as a result of the needle-like structure of the Tc layer. CONCLUSION Morphology of the Tc layer in PE/PE composites was found to be sensitive to the type of matrix and processing condition. Sample containing HDPE which is cooled by ISO method in contrast to other specimens showed a highly uniform Tc with needlelike structure, which was different from the crystal structures of its bulk. For LDPE composite no obvious Tc layer was observed under the applied cooling methods. The pull out test revealed that the ISO-cooled MDPE composite had the highest IFSS. hi the MDPE composite, the IFSS of ISO-cooled samples was higher than IWQ-cooled samples while in the HDPE composite the results was vice versa. This difference can be related to different Tc structure of HDPE matrix with MDPE matrix. REFERENCES 1.
He, T. and R. S. Porter. 1988. "Melt transcrystallization of polyethylene on high modulus polyethylene fibers," J. of Applied Polymer Science, 35:1945-1953. 2. Ishida, H. and P. Bussi. 1991. "Surface-Induced crystallization in ultra high modulus polyethylene fiber reinforced polyethylene composites," Macromolecules, 24: 3569-3577. 3. Teishev, T. and G. Marom. 1995. "The effect of transcrystallinity on the transverse mechanical properties of single-polymer polyethylene composites," J. of Applied Polymer Science, 56:959966. 4. Stern, T., A. Teishev and G. Marom. 1997. "Composites of polyethylene reinforced with chopped polyethylene fibers: Effect of transcrystalline interface," composites science and technology, 57: 1009-1015. 5. Biro, D. A., P. Mclean and Y. Deslandes. 1991. "Application of microbond technique: characterization of carbon fiber-epoxy interfaces," Polymer Engineering and Science, 37(17):1250-1256. 6. Hsieh Y. and J. Ju. 1994. "Melting behavior of ultra-high modulus and molecular weight polyethylene (UHMWPE) fibers," Journal of Applied polymer Science, 53:347-354. 7. Devaux, E. and C. Caze. 1999. "Composites of ultra-high-molecular-weight polyethylene fibers in a low-density polyethylene matrix II. Fiber/matrix adhesion," Composites Science and technology, 59:879-882.
Filler-Elastomer Interactions: Effect of Ozone Treatment on Adhesion Characteristics of Carbon Black/Rubber Composites Soo-Jin Park , Hwa-Young Lee, Jae-Rock Lee Advance Materials Division, Korea Research Institute of Chemical Technology, P.O. Box 107, Yusong, Taejon 305-600, Korea Byung-Gak Min Department of Polymer Engineering, Chungju National University, Chungju, 380-702 Chungbuk, Korea
ABSTRACT hi this work, the changes in surface and adhesion characteristics of carbon black/rubber compoundings treated by ozone technique are investigated in different treatment times. The surface properties of carbon blacks are studied by contact angle measurement and their adhesion characteristics are determined by crosslinking density and tearing energy (Gmc) of the composites. As a result, it is found that the increasing of the ozone treatment time leads to an increase of the introduction of oxygen-containing functional groups onto carbon black surfaces and to an increase of the polar component (/sSP) of surface free energy (/$), resulting in improving the crosslink density and tearing energy (Gmc) of the composites. The results can be explained by the fact that the polar functional groups of carbon black surfaces by the treatment lead to an increase of the adhesion at interfaces between carbon blacks and polar rubber matrix.
INTRODUCTION Commercial applications of elastomers often require the use of particulate fillers to obtain the desired reinforcement. In the rubber industry, carbon blacks are one of the most important reinforcing filler used to impart specific properties to filler compounds [1,2]. The reinforcement of elastomers by particulate fillers has been studied in depth in numerous investigations, and it is generally accepted that this phenomenon is, to a large extent, dependent on the physical interactions between the filler and rubber matrix, which can determine the degree of adhesion at interfaces. Generally, it is dependent on the active functional groups, surface energy, and energetically different crystallite faces of the filler surfaces [2-4]. Various methods have been used to modify the surface properties of the carbon blacks, such as liquid or gas oxidation, chemical, electrochemical, plasma treatment, and ozone treatment [5,6]. Among them, ozone treatment, one of the most commonly processes used in industry, is used to introduce the oxygen-containing functional groups on carbon black "Correspondence Author. Advanced Materials Division, Korea Research Institute of Chemical Technology, P. O. Box 107, Yusong, Taejon 305-600, South Korea Fax: +82-42-861-4151. E-mail: [email protected]
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surfaces [7,8]. Many authors have reported that ozone treatment of carbon blacks enhances the reinforcement of polar rubber, such as acrylonitrile butadiene rubber (NBR). Chemical reactivity of the polar rubber-carbon blacks is attributed to the presence of oxygen-containing functional groups, including phenol, quinone, carboxyl, and lactone [9]. The main objectives of the present work are to investigate the influence of ozone treatment on surface properties and adhesion characteristics of the carbon black/acrylonitrile butadiene rubber composites. EXPERIMENTS Materials and sample preparation Carbon blacks (N220 noted in ASTM destination) were obtained from Korea Carbon Black Co. and NBR was prepared by Kumho Petrochem. Co., South Korea. The ozone treatment for the carbon blacks were carried out using a ozone generator (LAB 2B, Korea Ozonia Co.) with pure oxygen gas. The ozone concentration was fixed at 30 mg/£ and the treatment time was varied within 0, 10, 30, 60, and 120 min, namely OCB-0, OCB-10, OCB-30, OCB-60, and OCB-120. Prior to measuring the mechanical properties of the composites, the filled rubbers were cured at 1.5 MPa pressure and 160 °C temperature for 60 min. The compounding formulations were reported in Table 1. TABLE I Compounding formulations J- .L Ingredients a
xmr. NBR
Carbon ,, , black
Zinc ., oxide
Loading 100 30 5 (phr) a ./V-Oxydiethylene-2-benzothiazole sulfenamide.
Steanc ., acid 2
. , , = Accelerator 1
„ m Sulfur 2
Measurements Contact angles were measured using the sessile drop method and about 5 /A of wetting liquid was used for each measurement at 20 °C. The test liquids were deionized water and diiodomethane and more than five drops were tested for each of the untreated and ozone-treated carbon black surfaces studied. The degree of swelling was measured according to ASTM D366-82 and calculated using the relation [10,11] (1) where, m0 and m were the masses of the sample before and after swelling (measured using an electric balance of sensitivity 10"5g), respectively. The solvent used in this work was toluene (molar volume 107 cmVmol; cohesive energy density 37.2 (J/citf)05). The tearing energy (Gmc), one of the critical strain energy release rate (Gc), was characterized by trouser beam tests for the mechanical interfacial properties of rubber compounds. Rectangular specimens about 70 X 50 X 2 mm3 thick
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were cut from a sheet that was manufactured by a two-roll mill technique. All tests were conducted at a crosshead speed of 2 mm/min. RESULTS AND DISCUSSION Contact angle and surface free energy Early on, Fowkes introduced the concept of the surface free energy of a solid. The surface free energy as expressed by the sum two components: a dispersive component, "f, attributable to London attraction, and a specific (or polar) component, "f, owing to all other types of polar interactions (Debye, Keesom, hydrogen bonding, and other weakly polar effects) [12,13] 7L
=
7i
+ 7LSF
(2)
where y is surface free energy and superscripts L and SP refer to the London dispersive and specific components, respectively. Figure 1 shows the results of surface free energies of the ozone-treated carbon blacks. The polar component of surface free energy is largely increased with increasing the ozone treatment time, resulting in improvement of the total surface free energy. The results can be explained that the ozone treatment of the carbon black surfaces produces carbon radicals from the hydrocarbon backbone, followed by the formation of unstable hydro peroxides to produce various oxygen functional groups i.e., carboxyl, hydroxyl, lactone, and carbonyl groups by reaction with additional oxygen.
FIGURE 1 Surface free energy of the carbon blacks treated by ozone gas
Crosslink density of carbon black/rubber composites The crosslinking density, Ve per unit volume on a perfect network, is given by the equation [10,11] V =
Mr
(3)
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where, pp is the polymer density, NA Avogadro's number, and Mc the average molecular weight of the polymer between crosslinks. Using Eq. (3), the crosslink density, Ve and the degrees of swelling, Q are calculated for the carbon black/rubber composites, as shown in Table 2. As results, the crosslink density is slightly increased and the swelling behavior of the composites is significantly decreased compared to that of untreated one. These results can be expected to diminish the reinforcing ability or network chain density of the composites TABLE II Crosslink density and degree of swelling of the carbon black/rubber composites
Specimen FeX1019 (m"3)
OCB-0/ NBR 4.52 158.5
OCB-10/ NBR 7.63 116.4
OCB-30/ NBR 8.71 107.6
OCB-60/ NBR 9.34 103.1
OCB-120/ NBR 8.87 106.6
Mechanical interfacial properties of carbon black/rubber composites According to Kraus, the degree of adhesion between the filler surface and the rubber can be assessed from the swelling behavior of the sample in a solvent. Therefore, the importance of tearing energy, Gmc; a s a criterion of the interfacial adhesion relationship can be considered. The tearing energy can be considered to be an interfacial behavior of the constitutive elements of a material. The tearing energies (Gmc) are measured by a trouser beam test and are calculated using equation [14]
mc
t
(4)
where F is the applied force and t the width of the tear path after tearing is completed.
OCB-0 OCB-10 OCB-30 OCB-60 OCB-120
FIGURE 2 Tearing energy (Gmc) of the carbon black/rubber composites
Figure 2 shows the tearing energy (Gmc) of the carbon black/rubber composites. As shown on Figure 2, the tearing energies (Gmc) of the composites made from ozone
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treatments are largely increased with increasing the ozone treatment time. It reveals that the polar rubber, such as acrylonitrile butadiene rubber (NBR), shows a high intermolecular interaction with oxygen-containing functional groups of the carbon blacks, resulting in improving the tearing energy (Gmc) of the carbon black/rubber composites. CONCLUSION In this work, the rubber composites filled with the carbon blacks modified by ozone treatments are studied in terms of surface free energetics, crosslink density, and tearing energy (Gmc) for predicting and understanding the mechanical interfacial properties of the composites. The experimental results show that the surface treatment leads to an increase of polar component of surface free energy, and crosslink density, resulting in improving the tearing energy of the carbon black/rubber composites. It is then considered that the ozone treatment of carbon blacks is one of the useful methods in enhancing the degree of adhesion at interfaces between carbon blacks and polar rubber matrix in a composite system. REFERENCES 1. 2.
3. 4. 5. 6. 7. 8.
9.
10. 11. 12. 13. 14.
Donnet, J. B., Bansal, R. C, and Wang, M. J. 1993. Carbon Black Science and Technoogy. 2nd ed. New York: Marcel Dekker. Park, S. J. and Kim, J. S. 2000. "Roles of Chemically Modified Carbon Black Surfaces in Enhancing Interfacial Adhesion between Carbon Black and Rubber in a Composite System," J. Colloid Interface Set, 232:311-316. Frysz, A. and Chung D. D. L. 1997. "Improving the Electrochemical Behavior of Carbon Black and Carbon Filaments by Oxidation," Carbon, 35:1111-1127. Lin, J. H., Chen. H. W., Wang. K. T., and Liaw F. H. 1998. "A Novel Method for Grafting Polymers on Carbon Blacks," J. Mater. Chem., 8:2169-2173. Champman, B. 1980. Glow Discharge Processes. New York: Wiley, pp. 139-173. Donnet, J. B., Park, S. J., and Brendle, M. 1992. "The Effect of Microwave Plasma Treatment on the Surface Energy of Graphite as Measured by Inverse Gas Chromatography," Carbon, 30:263-268. Fu, X., Lu, W., and Chung, D. D. L. 1998. "Ozone Treatment of Carbon Fiber for Reinforcing Cement," Carbon, 36:1337-1345. Rivera-Utrilla, J. and Sanchez-Polo, M. 2002. "The Role of Dispersive and Electrostatic Interactions in the Aqueous Phase Adsorption of Naphthalenesulphonic Acids on Ozone-treated Activated Carbons," Carbon, 40:2685-2691. Park, S. J., Cho, K. S., and Ryu, S. K. 2003. "Filler-Elastomer Interactions: Influence of Oxygen Plasma Treatment on Surface and Mechanical Properties of Carbon Black/Rubber Composites," Carbon, 41:1437-1442. Flory, P. J. 1950. "Statistical Mechanics of Swelling of Network Structures," /. Chem. Phys., 18:108. Gwaily, S. E., Badawy, M. M., Hassan, H. H., and Madani, M. 2003. "Influence of Thermal Aging on Crosslinking Density of Boron Carbide/Natural Rubber Composites," Polym. Testing, 22:3. Fowkes, F. M. 1962. "Determination of Interfacial Tensions, Contact Angles, and Dispersion Forces in Surfaces by Assuming Additivity of Intermolecular Interactions in Surfaces," J. Phys. Chem., 66:382. Israelachivili, J. 1992. Intermolecular and Surface Forces. 2nd ed. London: Academic Press. Griffith, A. A. 1921. "The Phenomena of Rupture and Flow in Solids," Phil. Trans. R. Soc. London, A. 221:163.
Interface End Theory and Fragmentation Test Xing Ji*, Ying Dai Key Laboratory of Solid Mechanics of MOE, Tongji University, Shanghai, China Lin Ye, Yiu-Wing Mai Centre of Advanced Materials Technology (CAJVIT), School of Aerospace, Mechanical and Mechatronic Engineering J07, The University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT Fiber fragmentation test is one of the micro-mechanical test methods to measure the interfacial shear strength in fiber composites. Its result exhibits large discrepancy with those of other three tests (fiber pull-out, micro-indentation and micro-debond tests). It's noticed that there are two questions in the fragmentation test. First, if stress singularity exists at the interface end due to the fiber breaks; second, if de-bonding occurs at the interface end as the critical length is achieved. An axisymmetric model of interface end is used to analyze the stress singularity. With the aid of an asymptotic procedure and variable separation, a characteristic equation is derived to determine the eigen-value of stress singularity. The relation of stress singularity index and Dundurs parameters is presented. It is found that the fragmentation test has the most serious stress singularity at the interface end when compared to the stress singularity indices of these four test methods. This means that the result obtained from the fragmentation test is not exactly the interface shear strength (IFSS), and is not comparable to those determined from the other three methods. The question whether de-bonding at the interface end commences when the critical length is reached is also discussed.
INTRODUCTION Due to their outstanding properties of high strength, high toughness and lightweight, fiber composites have been used for decades as structural materials in aerospace applications and many other fields. Although the mechanical properties of the composites are mostly governed by the properties of the reinforcing fibers and the matrix materials, the interfacial shear strength (IFSS) between fiber and matrix is also a critical factor. Thus, the experimental determination of IFSS has received intensive research interests in the past three decades. The test methods of IFSS may be divided into two categories: macroscopic and microscopic. Macroscopic tests (such as three-point bending) are used to measure the IFSS indirectly. Microscopic test are aimed to measure directly and quantitatively the IFSS. There are four microscopic (single fiber composite) test methods, which have been developed to measure the IFSS: fragmentation test [1], micro-indentation test [2], * Corresponding author, Department of Engineering Mechanics and Technology, Tongji University, Shanghai 200092, China. Fax: +86-21-6598-3267. E-mail address: iixmgl(o>,shl63.net
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pullout test [3] and micro-debond test [4]. In these tests, the specimens with different geometry are used, and a shear force is effectively applied to the fiber-matrix interface. When interfacial de-bonding occurs, IFSS is calculated based on the ultimate shear load and the de-bonded area of the interface. Even though the principle of the test methods seems simple, and many improvements have been made in technique, the results from the four tests often show large discrepancies [5]. Recently, the stress singularities near the interface ends in the pullout, microindentation and micro-debond specimens have been investigated by using the method of asymptotic expansion approach [6]. Due to the differences in their geometry at the interface ends [7], the stress singularity indices of these three specimens are different, even though fiber and matrix materials are the same. Based on the elastic properties of carbon fiber and epoxy matrix given in Ref. [5], the stress singularity values were calculated and compared [7]. Apparently, the stress singularity indices near interface ends can be used to assess the reliability of the test methods. If a stress singularity exists near the interface end, the IFSS result is suspect. If the stress singularity is free from the interface end, the result is not disturbed by the singular stress field, and hence, the test method is acceptable. For completeness, the singularity analysis of the interface end in fragmentation test is given in this paper. A characteristic determinant is derived for the fragmentation test, and the relation between the stress singularity index and Dundurs parameters is obtained. Again, by using the elastic properties of carbon fiber and epoxy matrix in [5], the value of the stress singularity index near interface end for the fragmentation test is calculated and compared with those of the other three tests in Ref. [7]. It is found that the fragmentation test has the most serious stress singularity at the interface end. This means the result from the fragmentation test is not a true IFSS, and is not comparable to those derived from the other three methods. The question if de-bonding occurs at the interface end when the critical length is reached is also discussed. FRAGMENTATION TEST A brief description of the fragmentation test is needed to illuminate the issues in the test method and analysis. As shown in Figure 1, a single fiber is embedded in a tensile specimen of matrix material, and a tensile load is applied to the specimen end, which is transmitted to the fiber via interfacial shear stress. As the stress in the fiber reaches its tensile strength, the fiber breaks. The number of breaks increases with the increase of the applied load, until the number of fiber breaks becomes saturated. Then, the length of each fragment is measured and the average length is called the critical length. Kelly proposed a simple formula to determine the interfacial shear strength with the shear lag theory, T=
FIGURE 1.
Single fiber fragmentation test
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It's noticed that there are two problems in the fragmentation test. First, whether the stress singularity exists at the interface end due to the broken fiber; second, whether debonding occurs at the interface end as the critical length is achieved. STRESS SINGULARITY ANALYSIS NEAR INTERFACE END Usually, the thickness and width of the specimen for fragmentation test are 2 and 4 mm, respectively, and the diameter of the fiber is 0.01~0.001mm. Compared to the diameter of the fiber, the matrix can be considered as an infinite medium, and the load as axisymmetically distributed around the fiber. So an axisymmetric interface end model, shown in Figure 2, is adopted to simulate the single fiber fragmentation test. The fracture in the fiber may be considered as a crack whose tip touches the interface at o, and o is the interface end.
Fiber
Matrix s—Interface
Crack -
A o Fiber
|o\ p j \ Interface End I Matrix
FIGURE 2. Axisymmetric model of fiber fragmentation
Assume that when the number of the fiber breaks is saturated, neither the fiber crack spreads inside the matrix, nor the fiber-matrix interface de-bonding occurs. In practice, there will be a competition between these two processes following a fibre break. This problem has been addressed and analysed by Liu et al [8] and interested readers may refer to this work. In Figure 2, Rf is fiber radius, O-pz is cylindrical coordinates referred to the fiber axis, and o-r6 is polar coordinates referred to the interface end. The cracked surface (z = 0, 0 < p ^ #/) is free from stresses, and the deformation of the matrix is symmetric referred to z = 0, Rf ^p <°°. Along the interface, the stresses and the displacements satisfy the continuity conditions. Assume fiber and matrix are isotropic. hi axisymmetric problems, the governing elastic equations are: dp2 A Ay, =(
p8p
dz2
+ + j) and y/ [9]. For easy representation of the boundary and continuity conditions, components of stress and displacement could be transformed from cylindrical coordinates O-p z to polar coordinates o-rO, whose origin o is at the interface end, Figure 2. Thus the boundary conditions are:
Interface End Theory and Fragmentation Test
= 0,
= 0,
a.
2
up(r,0-) = up(r,0+), ap(r,0') = ap (r ,0+ ),
2
u,(rfi-)
=0
= 0,
uz
2
591
2
=uz{rfi+)
o ^ (r ,0") = a„ (r,0+ )
Eq. (1) should also be transformed to polar coordinates (r, 6) to maintain the consistency of the functions and variances in the analysis. Then, for the condition: — <1, an asymptotic expansion is applied to the transformed equations. If only Rf the stress singularity near the interface end is of interest, the first order asymptotic equation is accurate enough and easy to be solved with method of variable separation. Substituting the solution into the boundary conditions, Eq. (2), homogeneous linear algebraic equations with eight unknown constants are obtained. According to non-zero solutions condition of homogeneous linear algebraic equations, the coefficients of these unknown constants must satisfy the coefficient determinant, simplified below: 2(1 - P)\ (a - P)X7 + (1 + /?)sin2 — I - (1 + a) = 0
(3)
where, X is the eigen value of the determinant, a and p are Dundurs parameters [6]. The stress singularity index Xs (XS=X— 1) of interface end can be obtained from the eigen value X, solved from Eq. (3). The stress singularity index Xs of interface end in fragmentation test only depends on Dundurs parameters a and p. The variation of Xs with a and p is shown in Figure 3. The stress singularity index Xs of interface end equals -1/2, if Dundurs parameters a and /? satisfy: a + p = 0. It means that in this case, the stress singularity index Xs is equivalent to the stress singularity index of a crack tip in a homogeneous medium. For most fiber-epoxy composites, their Dundurs parameters, a and p, are located in the left region of the line: cc+ p = 0 in Figure 3. Therefore, in fragmentation test of fiber-epoxy composites, the stress singularity of interface end is stronger than -1/2. This implies that the stress singularity near the interface end of the fragmentation test will never disappear for any combination of fiber and matrix system. Using the method of singular integral equation, Wang [10, 11] studied the problems of a crack perpendicular to the interface of fiber and matrix. It is equivalent to the case of fragmentation test when the crack in the fiber spreads to the interface in his consideration [10]. If the cracks in fiber and matrix both extend to the interface, this is the case of push-in test [11]. In [10, 11] the solutions are derived analytically. For the problem on solving stress singularity index, the analytical solutions and the asymptotic solutions adopted in the present paper and Ref. [7] give the same results. DISCUSSIONS By using the mechanical properties of fiber and matrix given in [5], the stress singularity index near the interface end of the fragmentation test was calculated, and compared with those of micro-debond, micro-indentation and pullout tests [7], shown in Table 1. The stress singularity indices of micro-debond, micro-indentation, pullout
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and fragmentation tests are -0.0002 (wedge angle of resin droplet = 40°), -0.3283, -0.3383 and -0.9290, respectively. Theus, among these four tests, the stress singularity near the interface end of fragmentation test is the strongest one. If the wedge angle of the resin droplet is less than 40°, the stress singularity index near the interface end of the micro-debond test is negligible. Because it is almost free from the disturbance of stress singularity, the results from the micro-de-bond test are most reliable. The specimen used in micro-indentation test is unidirectional composite. The matrix surrounding the indented fiber is strengthened by the neighboring fibers. The stress singularity index near interface end may not be -0.3283. As = -0.3283 is derived from the single fiber model of the micro-indentation test [7]. A further study for the micro-indentation test using composite specimen is needed. It is noticed that the stress singularity near interface end of fragmentation and pullout test [7] never disappears for any combination of fiber and matrix system. The experimental IFSS results from these two tests geometries are always suspect due to the existence of the strong stress singularity at the interface end.
FIGURE 3.
Eigen-value diagram at interface end of fiber fragmentation test
TABLE I Eigenvalue and stress singularity index of specimen in four tests Test Method Pullout Micro-debond (6=60°) (6=40°) Micro-indentation Fragmentation
P
a -0.9857
-0.1949
-0.9857
-0.1949
-0.9857 -0.9857
-0.1949 -0.1949
X 0.6613 0.8786 0.9998 0.6717 0.0710
-0.3387 -0.1214 -0.0002 -0.3283 -0.9290
Another issue of fragmentation test is whether interface de-bonding occurs when the critical length of the fragments is achieved. After the fiber has broken into fragments, fiber cracks will form. There are four cases to be considered. (1) Fiber crack ends at the interface, and does not extend into the matrix. Interface is intact. Stress singularity near the interface end exists, and the stress singularity index equals -0.9290. (2) Fiber crack penetrates through the interface, and spread into the matrix. Interface remains intact. Stress singularity near the interface end exists, and the stress singularity index equals -0.3283, because this is just the case of single fiber model of micro-indentation test.
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(3) Fiber crack ends at the interface, and does not extend into the matrix. Interface de-bonding occurs. The interface de-bonding is influenced by the stress singularity near the interface end, and the stress singularity index is -0.9290. (4) Fiber crack penetrates through the interface, and spread into the matrix. Interface de-bonding takes place. The interface de-bonding is affected by the stress singularity near the interface end, and the stress singularity index is -0.3283. For cases (1) and (2), the IFSS obtained from fragmentation test is suspect, since the interface does not de-bond. For cases (3) and (4), the IFSS evaluated from the fragmentation test is also dubious. This is because interface de-bonding is influenced by the stress singularity near the interface end. ACKNOWLEDGEMENTS Financial supports from the Natural Science Foundation of China (No. 10372072), the Science and Technology Foundation of Tongji University are much appreciated. XJ was Visiting Professor at the CAMT, University of Sydney, supported by the Australian Research Council (ARC) projects when parts of this work were completed. YWM wishes to thank the ARC for the award of an Australian Federation Fellowship tenable at the University of Sydney. REFERENCES I. Kelly, A. and W. R. Tyson. 1965. "Tensile Properties of Fiber-Reinforced Metal: Copper- Tungsten and Copper-Molybdenum," J. Mech. Phys. Solids, 13: 329-350. 2.Favre, J. P. and M. C. Merrine. 1981. " Characterization of Fiber/Resin Bonding in Composites Using a Pull-out test," Int. J. Adhesion Adhesives, 1:311-316 3. Mandell, J.F., J. H. Chen and F. J. McGarry. 1980. "A Microdebonding Test for in situ Assessment of Fiber/Matrix Bond Strength in Composite Materials," Int. J. Adhesives, 1: 40-44. 4. Miller, B., P. Muri and L. Rebenfeld. 1987. "A Microbond Method for Determination of the Shear Strength of a Fiber/Resin Interface," Compo. Sci. Technol., 28: 17-32. 5. Pitkethly, M. J., et al. 1993. "A Round Robin Programme on Interfacial Test Methods," Compo. Sci. Technol., 48: 205-214. 6. Zheng, B. L. and X. Ji. 2002. "Stress Singularity Analyses of Interface Ends in Micro-Mechanics tests," Compo. Sci. Technol., 62: 355-365 7. Ji, X., Y. Dai, B. L. Zheng, L. Ye and Y.-W. Mai. 2003. "Interface End Theory and Re-Evaluation in Interfacial Test Methods," Accepted by Composite Interface. 8. HY Liu, Y-W Mai, L Ye and LM Zhou, "Stress transfer in the fibre fragmentation test: Part III. Effect of matrix cracking and interface debonding", J Mater Sci. Vol 32, 1997, pp 633-641 9.Y. Dai, and X. Ji. 1994. "The Stress Singularity of Axisymmetric Cylindrical Interface Crack," Shanghai Journal of Mechanics, 15(3): 29-39. 10. Wang, Q., X. Ji and Y. G. Wang. 1996. "3D Axisymmetric Analysis of a Cracked Fiber in a Transversely Isotropic Elastic Medium," Mech. Research Communication, 23(2): 171-174. II. Wang, Q., X. Ji and Y. G. Wang. 1998. "Stress singularity near the end of a cylindrical interface and the linear elasticity of push-in tests," Science in China (Series E), 41(5): 471-481.
Stress Singularity Analysis of Interface End and Specimen Design for Fiber Pullout Test Ying Dai*, Xing Ji Key Laboratory of Solid Mechanics of MOE, Tongji University, Shanghai 200092, China Lin Ye, Yiu-Wing Mai Centre of Advanced Materials Technology (CAMT), School of Aerospace, Mechanical and Mechatronic Engineering J07, The University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT Since stress singularity was found at the interface end in current specimen of pullout test, interface shear strength (IFSS) obtained from the tests loses its rationality [2]. But a useful conclusion [2] is that when the wedge angle of the matrix is less than a critical angle, the singularity of stress field at the interface end of the specimen in micro-debond test nearly disappears. Following this conclusion, a conic specimen shown in Figure 1 is presented, in which the wedge angle of the specimen is designed to be less than a critical angle in order to prevent the singular stress field occurred at the interface end. The conic specimen is designed for pullout test to avoid disadvantages inherent in the micro-debond test [3]. An axisymmetric model of fiber/matrix system with arbitrary wedge angles at the interface end is used for the determination of critical wedge angle. With the aid of asymptotic analysis and variable separation, eigenvalue, A,, could be determined by a characteristic determinant. For a given fiber-matrix system, a curve representing the relationship between the stress singularity index and wedge angle could be obtained by solving the characteristic determinant. We define the critical wedge angle, 6cr, as that for a singularity index of-0.005. The design of a conic pullout specimen is also discussed. INTRODUCTION Since fiber-matrix interface plays a main function of stress transfer from the matrix to the fiber in composite materials, the mechanical performance of many fiber composites depends greatly on the properties of the interface. Study on interface properties has been a major driving force to develop various experimental techniques to assess the interface bond quality. The fiber pullout, micro-indentation, microdebond and fragmentation tests are widely used methods to measure the interfacial shear strength (IFSS). Unfortunately, there always exist large discrepancies among the experimental results of these four test methods [1]. Xing Ji et al [2] re-evaluated these Corresponding author. Key Laboratory of Solid Mechanics of MOE, Department of Engineering Mechanics and Technology, Tongji University, Shanghai 200092, China. Fax: +86-21-6598-3267. Email address: [email protected]
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595
four test methods based on the interface end theory. Singular stress fields were found at the interface ends in all four specimen geometries. This result makes the interface shear strength (IFSS) obtained from the tests loses its credibility. But when the wedge angle of the matrix is less than a critical angle, the singularity of stress field at the interface end of the specimen in micro-debond test disappears [2]. Following this conclusion, a conic pullout specimen shown in Figure 1 is presented, in which the wedge angle of the specimen is designed less than a critical angle to prevent the singular stress field occurred at the interface end. The conic pullout specimen is designed to take advantage of the micro-debond test [2], and to avoid dis-advantages inherent in the micro-debond test [3]. An axisymmetric model of fiber-matrix system with arbitrary wedge angles at the interface end is used for determination of critical wedge angle. With the aid of asymptotic expansion and variable separation techniques [4], eigen-value, X, which has the relation of stress singularity index, Xs, as Xs=X-\, were determined by a characteristic determinant. The contours of eign-value via Durndurs parameters with wedge angles 90° and 60° are shown in Figure 3. It is found that the eign-value contours shift to the right as the wedge angle decreases from 90° to 60°. The relation of stress singularity index and wedge angle of three fiber-matrix systems (listed in Ref [2] ) is presented in Figure 4. It can be seen that the stress singularity index approaches zero as the wedge angle of matrix approaches zero. Hence, for a given fiber-matrix system, there exists a critical wedge angle, below which the stress singularity equals -0.005. Since Xs= -0.005 is a very small singularity and can be ignored in practice, we can define a critical wedge angle, 9cr, with stress singularity index -0.005. Thus, a conic specimen for pullout test with non-singularity at the interface end could be designed. SINGULARITY ANALYSIS OF INTERFACE END An axisymmetric model shown in Figure 1 is used here to investigate the stress singularity at the interface end. O-pz is a set of cylindrical coordinates referred to the fiber axis, and o-rO is a set of polar coordinates referred to the interface end. a and b are wedge angles from interface to the free surface of fiber and matrix, respectively. The test methods can be identified by different combinations of the wedge angles a and b, Viz., (a=n, b=7d2); {a=7d2, b=7tl2) and (CF^K, b<7tl2) corresponding to the
pullout, micro-indentation and micro-debond tests, respectively. In axisymmetric problems, the governing elastic equations are expressed by Papkovich-Neuber functions cp and y/, dp2 d2 dp2
p dp Id p dp
dz2 d2 dz2
Stress Singularity Analysis of Interface End
596
1
Fiber Matrix
Holder
FIGURE 1. Sketch of conic pullout specimen FIGURE 2. Axisymmetric model of interface end
where g> and y/ are harmonic functions. The displacement and stress components can be expressed in terms of
« 1 , and neglecting R
f
higher order terms, the basic governing equations of the first order are:
dr2
r dr
d1y/l
1 dt//1
~drr
+
^~dr~
r2 862 +
-=0
1 d^V, _
(2)
^2~ d62 ~
The solutions of
(3)
+ sin2 X(n + b)-X2 sin2 b = where, a and /? are Dundurs' parameters; eigen-value X is related to the interface stress singularity index, Xs, as Xs=X-\ (4) Fig. 3 shows the eigen-values of pullout specimens with a wedge angle of 90° (plane matrix surface) and 60° (conic matrix surface). It's found that the oscillation region, in which the eigen-values are complex, is shrinking with the reduction of wedge angle of the matrix, and contours of eign-values also shift towards the right corner as the wedge angle is decreased.
Stress Singularity Analysis of Interface End
597
SPECIMEN DESIGN FOR FIBER PULLOUT TEST Tracking the characteristics of eign-value distribution shown in Fig. 3, the value of stress singularity index with different wedge angle of the fiber-matrix systems (listed in Ref [2]) were calculated and shown in Fig. 4. Fig. 4(b) is an enlarged drawing of Fig. 4(a). It can be seen that the stress singularity index approaches zero as the wedge angle of matrix approaches zero. It is noticed that there exists a "critical wedge angle" for a given fiber-matrix combination, below which the singularity index is less than 0.005. Since Xs= -0.005 is a very small singularity and can be neglected in practice, we consider a specimen as non-singular if its wedge angle is less than the critical wedge angle 6cr. For each fiber-matrix combination, a curve representing the relation between stress singularity index and wedge angle can be obtained by solving Eq. (3), and the critical wedge angle can be determined. A conic specimen with nonsingularity at the interface end for pullout test can be designed under the condition that the wedge angle of matrix is less than the critical angle. However, in practice, if the stiffness of the fiber is not very much higher than the matrix, for example, combinations of Courtaulds XAS/Aluminium and Courtaulds XAS/ Ceramic (Ref [2]), the critical wedge angle is very small (around 1.3° and 0.32°), Fig. 4(b). In these cases, there would be difficulties at least in specimen manufacture and application of the applied loads. So a non-singular conic geometry is appropriate to fiber reinforced plastic composites, but is not suitable for those fiber-matrix combinations with a small stiffness ratio.
•0.5 J-
FIGURE 3(a). Eigenvalue diagram of specimen (wedge angle of matrix: 8 = 90°).
598
Stress Singularity Analysis of Interface End
0.5
[—.55 I [-.52
xr =
P
r-5
1{
Hi*
0.15
xt =
Comp] Eigen-
0.1
X=Xr+i 0.05
,=0 1.0
•0.5
FIGURE 3(b). Eigenvalue diagram of specimen (wedge angle of matrix: 0 = 60°).
X s=-0. 005
Carbon fiber/epoxy resin - » - a=-0.9857 P=-0.1949 Carbon fiber/aluminum - * - a=-0.5394 P=-0.W54 Carbon fiber/AI2O3
•a
Carbon fiber/epoxy re a=-0.98S7 =-0.1949 Carbon fiber/aluminum - A - <x=-0.5394 =-0.1054
Carbon fiber/AI,O,
I 20 30 40
50 60
70 SO
90 100 110
10
Degree of Wedge angle
20
30
Degree of Wedge angle
FIGURE 4. (a) Variation of stress singularity index at interface end with wedge angle of matrix; (b) Critical wedge angle of conic pullout specimen
CONCLUSION An axisymmetric model of fiber-matrix system with arbitrary wedge angles at the interface end is used to determine the critical wedge angle. With the aid of asymptotic expansion and variable separation methods [4], eigenvalue, X, which has the relation of stress singularity index, Xs, as Xs=X-l, were determined by solving a characteristic determinant. The value of stress singularity index with different wedge angle of the fiber/matrix combination systems (listed in Ref [2]) were calculated and shown in
Stress Singularity Analysis of Interface End
599
Figure 4. It can be seen that the stress singularity index approaches zero as the wedge angle of matrix approaches zero. It's noticed that there exists a "critical wedge angle" for a given fiber-matrix combination, below which the singularity index at interface end is less than -0.005. We consider a conic pullout specimen as a non-singular specimen if the wedge angle of the matrix is less than the critical wedge angle, 6cr. Therefore, a conic specimen with non-singularity at the interface end for pullout test can be designed. But in practice, if the stiffness of the fiber is not much higher than that of the matrix, the critical wedge angle can be very small. This will present difficulties for preparation of specimens and methods of loading. So non-singular conic specimen is a suitable geometry for testing fiber reinforced plastic composites, but is not appropriate to other fiber-matrix combinations with small stiffness ratios.
ACKNOWLEDGEMENTS Financial supports from the Natural Science Foundation of China (No, 10372072), the Science and Technology Foundation of Tongji University are much appreciated. XJ was Visiting Professor at the CAMT, University of Sydney, supported by the Australian Research Council (ARC) projects when parts of this work were completed. YWM thanks the ARC for the award of an Australian Federation Fellowship tenable at the University of Sydney. REFERENCES 1. 2. 3. 4.
Pitkethly, M. J., et al. 1993. "A Round Robin Programme on Interfacial Test Methods," Comp. Sci. Technol., 48:205-214. Ji, X., Y. Dai, B. L. Zheng, L. Ye and Y.-W. Mai. 2003. "Interface End Theory and Re-Evaluation in Interfacial Test Methods," Accepted by Composite Interface. Kim, J. K. and Y.-W. Mai. 1998. "Engineered Interfaces in Fiber-Reinforced Composites," Elsevier, Oxford. Dai Y. and X. Ji. 1995. "Elastic Analysis of a Cylindrical Interface Crack," ACTA Mechanica Solida Sinica, 8: 569-573
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Part XII
Joint
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Evaluation of Strength of SiC/SiC Composite Joint Using New Interface Potential Hisashi Serizawa*, Hidekazu Murakawa Joining and Welding Research Institute, Osaka University, Japan Charles A. Lewinsohn Ceramatec Inc., 2425 South 900 West, Salt Lake City, Utah 84119, USA
ABSTRACT In order to examine mode-I & II type fracture behavior of ceramic joints, the interface element was proposed as one of the simple models which represent the mechanism of failure in an explicit manner. It was applied to the analyses of four point bending test and asymmetrical four point bending test for SiC/SiC composite specimen joined by ARCJoinT™. By using a new type interface potential, which is a coupled function of opening and shear deformations, both the bending and asymmetrical bending tests were simulated. From the comparison with the experiments, the surface energy at the interface between the joint and composite was estimated to be about 30 N/m regardless of the fracture mode.
INTRODUCTION Silicon carbide-based fiber reinforced silicon carbide composites (SiC/SiC composites) are promising candidate materials for high heat flux components because of their potential of low-activation, low-afterheat and their high-temperature properties [1-4]. For fabricating large or complex shaped parts of SiC/SiC composites, practical methods for joining simple geometrical shapes are essential. As a result of R & D efforts, an affordable, robust ceramic joining technology (ARCJoinT™) has been developed as one of the most suitable methods for joining SiC/SiC composites among various types of joining between ceramic composites [5]. To establish useful design databases, the mechanical properties of joints must be accurately measured and quantitatively characterized, where the bending and shear strength ofjoints are most basic and important mechanical properties. Therefore, the types of fracture behavior for each test configuration have to be precisely studied to measure those properties. To describe deformation and fracture behavior more precisely, a new and simple computer simulation method has been developed [6-13]. The method treats the fracture phenomena as the formation of new surface during crack opening and propagation. Based on the fact that surface energy must be supplied for the formation of new surface, a potential function representing the density of surface energy is introduced to the finite element method (FEM) using cohesive elements [6] or interface elements [7-13]. So, in this research, to examine mode-I & II types of fracture behavior in SiC/SiC composite * Corresponding Author: 11-1 Mihogaoka, Ibaraki, Osaka 567-0047, Japan; Fax: +81-6879-8645; E-mail: [email protected]
604
Evaluation of Strength of SiC/SiC Composite Joint y
Crack tip
i
A A
B B
C
c
.1 D
(a) Before Crack Propagation
0.5 (b) During Crack Propagation
FIGURE l(a) Representation of crack growth using interface element
10
J.5
2.0
Opening Displacement 6 / r 0
FIGURE l(b) Relation between crack opening displacement and bonding stress
joint, the four point bending test and the asymmetrical four point bending test [14-17] were analyzed by using the interface element. INTERFACE POTENTIAL Essentially, the interface element is the distributed nonlinear spring existing between surfaces forming the interface or the potential crack surfaces as shown by Figure 1(A). The relation between the opening of the interface 8 and the bonding stress cris shown in Figure 1(B). When the opening S is small, the bonding between two surfaces is maintained. As the opening 8 increases, the bonding stress a increases till it becomes the maximum value acr at the opening 8cr. With further increase of 8, the bonding strength is rapidly lost and the surfaces are completely separated. Such interaction between the surfaces can be described by the interface potential. There are rather wide choices for such potential. The authors employed the Lennard-Jones type potential because it explicitly involves the surface energy y which is necessary to form new surfaces. Thus, the surface potential per unit surface area (j> can be defined by the following equation.
(1)
where, constants y, ro, and N are the surface energy per unit area, the scale parameter and the shape parameter of the potential function. From the derivative of ^ with respect to the opening displacement S, the maximum bonding stress, <jcr, is obtained as follows when the opening displacement is 8cr.
cr
=
(2)
By arranging such interface elements along the crack propagation path as shown in Figure 1(A), the growth of the crack under the applied load can be analyzed in a natural manner.
Evaluation of Strength of SiC/SiC Composite Joint
605
(a) Four Point Bending Test ~™ Load: P
(b) Asymmetrical Four Point Bending Test
FIGURE 2 Schematic illustration of bending and asymmetrical bending tests
hi this case, the decision on the crack growth based on the comparison between the driving force and the resistance as in the conventional methods is not necessary. As results of our previous researches using the interface elements, it was found that the failure mode and the stability limit depend on the combination of the deformability of the ordinary element in FEM and the mechanical properties of the interface element controlled by the surface energy yand the scale parameter r0 in Equation (1); furthermore, the fracture strength in the failure problems of various structures might be quantitatively predicted by selecting an appropriate value for the scale parameter [12,13]. MODEL FOR ANALYSIS SiC/SiC composite specimens joined by ARCJoinT™ were selected as the ceramic joint for this study. Figure 2 shows schematic illustrations of the four point bending and asymmetrical four point bending tests. L\ and L2 are the inner and outer span lengths, respectively. According to our previous experimental results for 501 x 4* x 4h mm3, L\ and L2 were chosen to be 20 and 40 mm for the bending test and 12 and 44 mm for the asymmetrical bending tests, respectively [5,15,16]. The thickness of the joint was set to 100 \xm, for a typical example of ARCJoinT™ [5]. Young's moduli and Poisson's ratios of SiC/SiC composite and the joint were assumed to be 300 GPa, 393 GPa, 0.3 and 0.19, respectively. Although the mechanical properties of SiC/SiC composites should be anisotropic, the properties were assumed to be isotropic since the difference between the properties of the composite and the joint material is significantly larger than those due to the composite anisotropy. Because of the brittleness of the ceramic materials, the FEM calculations were conducted assuming linear elastic behavior in two-dimensional plain strain. The interface elements were arranged along both the interfaces between SiC/SiC composite and the joint. hi order to examine the mode-I & II fracture behavior, the mechanical properties of the interface element need to be defined for both the opening and the shear modes since the mode of the failure is mixed mode, hi this research, the interface potential
606
Evaluation of Strength of SiC/SiC Composite Joint
Experimental Result
10
10
Experimental Result
10 10 10 10 10 Scale Parameter r0 (y.m)
FIGURE 3(a) Effect of scale parameter and surface energy on bending strength of SiC/SiC composite joint
10 10 10 10 Scale Parameter ro
10
10
10
FIGURE 3(b) Effect of scale parameter and surface energy on shear strength of SiC/SiC composite joint
(4)
(5)
Where a second term of Equation (3) was introduced to prevent overlapping in the opening direction and K was a constant having a large value. The bending strength of the composite joint was experimentally measured to be about 75 MPa, which is different from the shear strength obtained (about 30 MPa) [5,15,16], and it means that an effect of the interaction between the opening and the shear deformations seems not to be equal. The parameter A in Equation (4), however, was assumed to be 1.0 because the fracture in the bending or the asymmetrical bending test would be controlled by only the opening or shear deformation at the joint interface, respectively. Then, by changing the scale parameter r0 and the surface energy /, both the bending and the asymmetrical bending tests were analyzed by using the finite element method with the interface element. The parameters r0 and 2^were varied from 0.1 nm to 100 um and from 3.0 x 10"5 to 300 N/m, respectively. The shape parameter N was assumed to be 4 according to our previous researches [12,13]. CALCULATION RESULTS AND DISCUSSIONS The effects of scale parameter and the surface energy on the bending and shear strength of joint were summarized into Figures 3(A) and 3(B), respectively. The experimental results are also shown in these figures. From the similarity of the interface element to the ordinary element, the predicted joint strength can be rearranged to a single curve [8,13]. As one example of a single curve, the predicted shear strength TJ can be re-plotted as shown in Figure 4 where zcr was a maximum shear strength at the interface calculated from Equation (4). From this figure, the single curve was considered to be divided into three parts. From our previous research [12,13], it was found that the results in the middle part could be quantitatively compared with the experimental results, which were indicated by dotted lines in Figures 3(A) and 3(B).
Evaluation of Strength of SiC/SiC Composite Joint
607
10" 10" 10w 10" 10" 10* 16' 10" 10' 10" 10"
r o 2 /V FIGURE 4 Influence of r^/yon failure process in asymmetrical bending test
10
Asymmetrical Bending Test,.-"'
ir Point Bending test
10
10
10
10
10
10
10
Surface Energy 2 7 (N/m)
FIGURE 5 Relationship between scale parameter and surface energy of interface element
Figure 5 shows the relationships between the surface energy and the scale parameter, where the predicted strength agreed with the experimental results. From the above discussions, a valid combination between 2y and r0 would be limited in the gray area shown in this figure. Especially, from the view point that the surface energy for the opening and shear deformations should be same, a most suitable surface energy of the interface was considered to be 30 N/m, which is as same as the fracture energy of porous SiC made by chemical vapor infiltration process [18]. Since the slopes of two lines in Figure 5 was almost same, it was found that the correlation between the opening and shear deformations would have a fixed link, that means the parameter^ in Equation (4) can be decided to be a fixed value regardless of the fracture mode. That is, the fracture behavior of mode-I & II might have a strong relationship. Moreover, from these results, this proposed method with the new interface potential was considered to have a great potential as a tool to study the failure problems whosefracturetype was a mixture of mode-I & II. CONCLUSIONS The interface element was proposed as one of the simple models which represent the mechanism of failure in an explicit manner. It was applied to the analyses of the fracture strengths SiC/SiC composite specimen jointed by ARCJoinT™ under the four point bending and the asymmetrical four point bending tests. The conclusions can be summarized as follows.
608
Evaluation of Strength of SiC/SiC Composite Joint
1. By using a new type interface potential, which is a coupled function of the opening and shear deformations, both the bending and asymmetrical bending tests were simulated. 2. From the comparison with the bending and shear strengths experimentally obtained, the surface energy at the interface between the joint and composite was estimated to be about 30 N/m regardless of the fracture mode. 3. The proposed method was considered to have a great potential as a tool to study the failure problems whose fracture type was a mixture of mode-I & II. REFERENCES 1. 2.
3.
4. 5. 6. 7. 8.
9. 10. 11. 12. 13.
14. 15.
16.
17. 18.
Jones, R.H. and C. H. Henager, Jr. 1994. "High-Temperature Properties of SiC/SiC for Fusion Applications," J. Nucl. Mater, 212-215:830-834. Jones, R.H., C. A. Lewinsohn, G. E. Youngblood and A. Kohyama. 1999. "Properties of Advanced Fibers for SiC/SiC Composite Applications in Fusion Energy Systems," Key Engineering Materials, 164-165:405-408. Serizawa, H., C. A. Lewinsohn, G. E. Youngblood, R. H. Jones, D. E. Johnston and A. Kohyama. 1999. "High-Temperature Properties and Creep Resistance of Near-Stoichiometric SiC Fibers," Ceram. Eng. Sci. Proc, 20 [4]:443-450. Kohyama, A. and Y. Katoh. 2002. "Overview of Crest-Ace Program for SiC/SiC Ceramic Composites ' and Their Energy System Applications," Ceram. Trans., 144:3-18. Singh, M. 1999. "Design, Fabrication and Characterization of High Temperature Joints in Ceramic Composites," Key Engineering Materials, 164-165:415-419. Needleman, A. 1990. "An Analysis of Decohesion Along An Imperfect Interface," Int. J. Fracture, 42:21-40. Wu, Z.Q., H. Serizawa and H. Murakawa. 1999. "New Computer Simulation Method for Evaluation of Crack Growth Using Lennard-Jones Type Potential Function," Key Engineering Materials, 166:25-32. Murakawa, H., H. Serizawa and Z. Q. Wu. 1999. "Computational Analysis of Crack Growth in Composite Materials Using Lennard-Jones Type Potential Function," Ceram. Eng. Set. Proc, 20 [3]:309-316. Serizawa, H., M. Ando, C. A. Lewinsohn and H. Murakawa. 2000. "New Evaluation Method of Crack Growth in SiC/SiC Composites Using Interface Elements," /. Nad. Mater., 283-287:579-583. Serizawa, H., M. Ando, C. A. Lewinsohn and H. Murakawa. 2000. "Computational Analysis of Creep Fracture Deformation in SiC/SiC Composites," J. Ncul. Mater, 289:16-22. Serizawa, H., C. A. Lewinsohn and H. Murakawa. 2002. "Effects of Scarf Angle on Stress Singularity and Strength of Ceramic Joints," Ceram. Eng. Set Proc, 23 [3]:825-832. Serizawa, H., H. Murakawa and C. A. Lewinsohn. 2002. "Modeling of Fracture Strength of SiC/SiC Composite Joints by Using Interface Elements," Ceram. Trans., 144:335-342. Murakawa, H., H. Serizawa, K. Miyamoto, I. Oda. 2003. "Strength of Joint Between Dissimilar Elastic Materials," Proc. 2003 Int. Conf. Computational & Experimental Engineering & Sciences (ICCES '03), 6:(CD-ROM). Unal, 0., I. E. Anderson and S. I. Maghsoodi. 1997. "A Test Method to Measure Shear Strength of Ceramic Joints at High Temperatures," J. Am. Ceram. Soc., 80 [5]:1281-1284. Lewinsohn, C.A., M. Singh, T. Shibayama, T. Hinoki, M. Ando, Y. Katoh and A. Kohyama. 2000. "Joining of Silicon Carbide Composites for Fusion Energy Applications," J. Nucl. Mater., 283-287:1258-1261. Lewinsohn, C.A., R. H. Jones, M. Singh, T. Nozawa. M. Kotani, Y. Katoh and A. Kohyama. 2001. "Silicon Carbide Based Joining Materials for Fusion Energy and Other High-Temperature, Structural Applications," Ceram. Eng. Sci. Proc, 22 [4]:621-625. Serizawa, H., C. A. Lewinsohn and H. Murakawa. 2001. "FEM Analysis of Experimental Measurement Technique for Mechanical Strength of Ceramic Joints," Ceram. Eng. Sci. Proc, 22 [4]:635-642. Bordia, R.K., D. H. Roach and S. M. Salamone. 1995. "Crack Growth Resistance of CVI Processed Ceramic Matrix Composites," Proc. lOthlnt. Conf. Comp. Mater., IV:711-718.
Static and Fatigue Analysis of Double-Bolted-Joints for Gr/Epoxy after Thermal Cyclic Loading Ming-Chuen Yip and Rui-youg Li Chih-han Yang2 Department of Power Mechanical Engineering, National Tsing-Hua University Hsinchu, Taiwan, R. O. C.
ABSTRACT The strength and fatigue life of [0/45/90/-45]2s Gr/Epoxy double bolted joints subjected to thermal-cycle loading has been investigated experimentally in this study. The fatigue tests were performed by the Instron-1322 servohydraulic testing system; four kinds of stress levels under tension-tension loading withfrequencyof 5 Hz were tested. It is found that the static strength after thermal-cycles has a little increase, but the fatigue life has different results in high and low stress levels. Two bolts and nuts disposed for different ways created three cases. The stress distribution of these three kinds of two-bolted joints of graphite-epoxy laminates were determined experimentally by using the method of photoelasticity, the differing extent of defects caused by the three different cases have been determined, the stress around the hole edge and across the net-section are presented. One of the three cases had the ability to transfer load uniformly, which caused small influence on the gross section of bolt configuration, thus the static and fatigue strengths are better than other two cases. Thermal cyclic loading are performed at -5O°C~5O°C with 145 min/cycle, after 150 thermal cycles, the static and fatigue strength of the fastened components were tested to compared with the original specimens. INTRODUCTION Composite materials have better mechanical properties than the metallic materials for its high strength, high stiffness, lightweight, and material's performance to be designed by need, etc. Therefore, it is usually adopted to replace metal and widely used in the components for aviation, medicine and living industry. Since composites are widely used in many mechanical components, the joint strength problem has been treated as an important factor because it will result in different fracture modes following the design conditions of clamping torque of bolt, bolt diameter, bolt gap, etc. The key factors for affecting these fracture modes are discontinued stress distribution and stress concentration around boltholes. These stress concentration areas would form the multi-axes stress/strain situation when construction took single-axis loading and reduced static and fatigue strength of the composites. Therefore, it would be influence the advantage application of composites. The construction of an airplane will take different thermal cyclic loading following the various conditions of plane taking-off, flight, and landing. However, composite materials are combined with at least two kinds of material, which has different thermal expansion * Corresponding author, Email: [email protected]
610
Static and Fatigue Analysis of Double-Bolted-Joints for Gr/Epoxy
coefficients, and then thermal loading may cause debonding, microcrack and degradation of matrix. To protect the possible of construction fracture and huge damage for a plane during flight, it is important to investigate the strength reduced resulted due to thermal cyclic loading effect. EXPERIMENT PROCEDURE Static and fatigue strength of bolted-joints of [0/45/90/-45]2s quasi-isotropic graphite/epoxy laminates are taken into experimentally investigated, the testing are considered thermal cyclic loading effect, the experimental design for this study is illustrated in figure 1. Original Specimen (1) Static tension test The specimen was cut in the size of 19.1mmx207mm based on static strength experiment requirement, which is specified in ASTM D3479-76 [1] and Instron-1322 testing system. The control mode was displacement controlled with crosshead speed of O.Olmm/s to satisfy the quasi-static assumption, the ultimate strength of material <Jo is obtained. These value are use to be the reference data for choosing the maximum stress of axial fatigue test. (2) Axial tension fatigue test The tests were preformed by Instron-1322 testing system with the sinusoidal waveform. The control mode was load controlled with a load ratio of R = 0.1 and frequency of 5 Hz. Four stress levels are selected to be tested. The fatigue life curve of materials can be obtained. Double-Bolted-Joint Specimen The clamping torque of bolt is applied of 6 Kgf-cm in static strength test and conducted ultimate tensile strength (UTS) for the reference in fatigue test. The specimen size are cut of wld = 6, eld = 3 and t = 2mm, where w is the width of specimen, d is the bolt diameter, e is the distance from the center of hole to the end of plate, and t is the thickness of specimen, it is based on the requirement as specified in ASTM D5961/D5961 M-96 [2]. (1) Static tension test The operating mode of static tension test is the same of original specimen, which was selected to obtain the bearing strength a\, of the component, where Ot, = PI td, in which P is the applied load. The bearing strength was used as the reference value for the fatigue test of the components. (2) Axial tension fatigue test Four stress levels of O\, are selected as applied stress on specimen respectively for performing the fatigue tests at least 3 effect data for each loading condition are preformed, the fatigue life curve of the components can be obtained. (3) Static tension and fatigue tests after thermal cyclic loading
Static and Fatigue Analysis of Double-Bolted-Joints for Gr/Epoxy
611
The temperature range for thermal cyclic loading was -50 • -50 • , the temperature rate was 5 n/min and humidity is free controlled, it takes approximate 145 minutes for each cycle, 150 thermal cycles are preformed for each specimen before the static and fatigue test. After specimen subjected to thermal cycles, the test method are of the same as stated in the pervious section. (•r/kpo\y 620Ori'.'iii.il Sp.'
600580-
• P
S. 560-1 540•
520-
Epoxy
500480Siatii.
SI.UK .uid l.iimuu i
1000
10000
100000
Number of cycles (Nf)
FIGURE 1 Experiment flow chart
FIGURE 2 Relations of loading stresses and number of fatigue cycles for Gr/epoxy
RESULTS AND DISCUSSIONS Mechanical Property Analysis for Original Specimen (l)Static tension test Seven specimens of [0/+45/90/-45]2S Gr/Epoxy are selected arbitrary for static tension test and the average static strength was obtained of 881.88 MPa for Gr/Epoxy. This value was adopted as the reference basis of UTS(oo) in the axial tension fatigue test. (2)Tension-tension fatigue test The relations of applied stress and number of cycles to failure for Gr/Epoxy are shown in figure 2, it is seen the approximate linear relationship is obtained in the semi-log scale plot [3]. During low stress level test, the fatigue life and stiffness loss for specimens were mainly caused by damage of matrix. Fracture mode was starting from delamination of outside area of specimen, it was then gradually extending to the center. When the net area of specimen couldn't bear the fatigue loading, it caused the stiffness reduced rapidly up to failure. Following the stress level increase, the leading role of damage from matrix would be changed to fiber gradually. Due to defect of non-plane shape of specimen edge, the damage of specimen started from this defect and the fiber will break. Finally, the specimen would be fractured because it couldn't subject the fatigue loading. The fracture situation resulted from high stress level was similar to static strength test and the specimen
612
Static and Fatigue Analysis of Double-Bolted-Joints for Gr/Epoxy
life was controlled by its defects. During this condition, stiffness loss was instable and would cause larger distribution areas for fracture cycles. Mechanical Property Analysis for Double-Bolted-Joint Specimen (1) Static tension test Three kinds of configurations for double-bolted-joint components are shown in figure 3. The average static bearing stress of Case 1 was 986.02 MPa, which are resulted from static tension test of 7 specimens. Case fCase 1
Case 2 Case 3 m bolt head O nut
™ bolt head ° nut
FIGURE 3 Three kinds of bolt-jointed modes for EB2 FIGURE 4 Stress concentrated in area II for Case 1 subjected to torsion of 6 kgf-cm
By using the method of SAM to inspect the specimen, it is obtained the results indicated that the double bolt-jointed mode produced un-balanced loading in the joints of composite plates and resulted in different damage situations in bearing face. This paper performed further investigation regarding the effect of different joint moduli on the construction strength and found the best bolt-jointed mode for improving static bearing stress and fatigue life for three kinds of bolt-jointed modes. It was discovered that static strength of configuration for second jointed mode was highest when arbitrarily selected five specimens for static axial tension test. It is indicated the trend for different bolt-jointed modes by the method of PSM-1 photoelasticity [4] with the specimen subjected to 3 KN loading: A. Adding a clamping torque on each bolt in Case 1 and investigated the stress distribution situation. The stress concentrated in Area I evidently when the component subjected to 0.5 Kgf-cm torque and seemed no effect in Area II. Figure 4 indicated that it disclosed the loading effect when torsion was increased to 6 Kgf-cm. It proved that side-supporting force affected the difference of stress transmission. Therefore, the static bearing stress was higher when bolt subjected to higher torque. B. Figure 5 shows the stress distribution in Case 2, it was evident that the stress distribution was more uniform than that of Case 1, i.e. loadings acting on bolts of Areas I & II were almost symmetrical. This caused 2.3% increase of strength than in Case 1. Furthermore, there was no bolt broken in Case II when reached to the specified limited of displacement for 5 mm, in which one bolt was broken in Case 1 among two sets out of five specimens before the displacement reaching to 5mm. C. Figure 6 shows the stress distribution for Case 3, it shows that stress distribution was also uniform, but stress was concentrated in Area I evidently when compared to Case 2. This was resulted from difference of clipping force between bolt and nut, which caused 3.5% decrease in static strength when compare to Case 2.
Static and Fatigue Analysis of Double-Bolted-Joints for Gr/Epoxy
613
When the clamping torque is added on the specimen before test, the side supporting forces provided by bolt head or nut was the same [5,6]. When subjecting to loading for a period of time, the fractured pieces pressed upwardly and downwardly. The upward fractured pieces caused tighter contact between bolt head and construction due to obstacle . •
,
'-r.-rfi- - -r
bolt head nut
bolt head nut
FIGURE S Stress distribution for Case 2 bolt subjected to torsion of 6 kgf-cm
FIGURE 6 Stress distribution for Case 3 bolt subjected to torsion of 6 kgf-cm
of bolt head. The downward fractured pieces provided nut with loosing force, which caused larger clearance existence between nut and construction and made more sliding damage on the bolt. Therefore, it caused more severe damage on the contact face with nut when fracture happened. It was evident that the elliptic damage area resulted from nut was larger than the bolt head. Because the clipping force for nut was looser, it would not produce stress concentrated situation in AreaDeven if stress was over-restrained when Case 2 subjected to loading. Therefore, the bolt-jointed mode in Case 2 was the best configuration in this test. Overall, the shear area for double-bolted-joint components was larger than that of single-bolted-joint components, which was investigated, in the pervious study [7]. Hence, both of static strength and fatigue life for the former construction were higher than the latter one. In addition, the bearing displacement decreased when number of bolts increased and then reached to a stable value rapidly. The static strength of double-bolted-joint components for these 3 cases is shown in figure 7. (2) Axial tension fatigue test Axial tension fatigue test for the component of Case 2 are performed, the testing condition are state in the pervious section, the S-N curve for the components is shown in 104010201000-
T
980960-
I-
9409201000
900 Casel
Qise3
TEB2
FIGURE 7 Static bearing strength under four different Cases
10000
100000
Number of cycles (logNf)
FIGURE 8 Compare with EB2 and TEB2 for S-Nf curve
614
Static and Fatigue Analysis of Double-Bolted-Joints for Gr/Epoxy
figure 8 and denote by EB2. It is seen that the slightly bilinear relation for the applied stress and the failure cycles is obtained. Mechanical Property Analysis of Double-Bolted-Joint Components after Thermal Cyclic loading (1) Static tension test The average static bearing stress of double-bolted-joint component was 997 MPa, which are obtained from arbitrarily 7 specimens of configuration of Case 2, the result is also shown infigure7 and denote by TEB2. The static bearing strength was 1.1% increase than that of specimen without thermal cycles. (2) Axial tension fatigue test Axial tension fatigue test for the component of Case 2 with 150 thermal cycles are performed, the testing condition are state in the pervious section, and the S-N curve for the components is also shown in figure 8 and denote by TEB2. It is seen that the bilinear relation for the applied stress and the failure cycles is also obtained, for higher stress level, the fatigue life decrease rapidly because the materials are more brittle when it is subjected to thermal cycles. CONCLUSIONS Due to the experimental results, the following conclusions can be commented: (l)The static strength of bolted components is increased when the clamping torque of bolts are applied. (2)The stress distribution for the bolted components was better for the configuration of Case 2. (3)The S-N curve for bolted components are obtained as the bilinear relation in semi-log scale for both with and without thermal-cyclic effect. (4)After thermal-cyclic loading, the materials changed more brittle, the fatigue life for higher stress level decrease more rapidly. REFERENCES [1] "Standard Test Method for Tension-Tension Fatigue of Oriented Fiber, Resin Matrix Composites," ASTM D3479-76, 1982. [2] ASTM standard D 5961/D 5961 M-96. Standard test method for bearing response of polymer matrix composite laminate, 1996. [3] W. Hwnag and K. S. Han, "Fatigue of Composites Fatigue Modulus Concept and Life Prediction," Journal of Composite Materials, Vol. 20, 1986, pp.154-165. [4] M. W. Hyer and D. J. Liu, "Stress in Pin-Loaded Orthotropic Plates: Photoelastic Results," Journal of Composite Material, Vol. 19, No. 2, 1985. [5] T. Ireman, T. Ranvik and I. Eriksson, "On Damage Development in Mechanically Fastened Composite Laminates," Composite structure, Vol. 49, 2000, pp.151-171. [6] E. Persson and I. Eriksson, "Fatigue of Multiple-row Bolted Joints in Carbon/Epoxy Laminates: Ranking of Factors Affecting Strength and Fatigue life," International Journal of Fatigue, Vol. 21, 1999, pp. 337-353. [7] M.C. Yip, R.Y Li, "Static and Fatigue Analysis of Single-Bolted-Joint Components for Gr/Epoxy and Gr/PEEK After Thermal Loading," Proceeding of 20 National Conference in Mechanical Engineering, Taipei, Taiwan, R.O.C., Dec. 2003.
Tensile Strength and Fatigue Properties of Z-Pinned Composite Lap Joints P. Chang, A.P. Mouritz* School of Aerospace, Mechanical & Manufacturing Engineering, RMIT University, GPO Box 2476V, Melbourne, Victoria, 3001, Australia B.N. Cox Rockwell Scientific Co LLC, 1049 Camino Dos Rios, Thousand Oaks, CA 91360, USA
ABSTRACT The effect of z-pinning on the tensile strength, fatigue life and failure mechanisms of single lap joints is experimentally investigated. Under tensile loading, the tensile load to initiate delamination cracking in the adhesive bond-line to a lap joint can be reduced slightly by z-pinning, however the ultimate failure strength and elongation limit are improved by z-pins bridging the bond-line. Z-pinning is also highly effective in extending the tensile fatigue life of lap joints by the crack bridging mechanism. Transitions in the failure mechanisms were observed from joint debonding in the absence of pins to pull-out and/or shear failure of pins or tensile failure of the laminate, depending on the volume content and diameter of the z-pins. It is shown that under certain z-pinning conditions, bond-line delamination of the joint can be suppressed and the failure mechanism is changed to rupture of the composite laminate. INTRODUCTION A long-standing concern with adhesively bonded joints made using fibrereinforced polymer composite is catastrophic failure of the bond-line due to overloading, environmental degradation or fatigue. A novel approach to improve the ultimate strength of joints is the placement of reinforcing fibres or rods in the throughthickness direction using stitching or z-pinning. Stitching can increase the ultimate strength and fatigue performance of composite joints by a crack bridging mechanism that transfers the applied stress across the joint region [1-4]. Likewise, Freitas et al. [5] and Rugg et al. [6,7] demonstrated that z-pinning can improve the ultimate strength of lap joints by a crack bridging mechanism. However, the ability of zpinning to improve the fatigue endurance of composite joints is not known. This paper investigates the improvement to the tensile strength and fatigue life of single lap joints by z-pinning. The effects of the amount and size of z-pins on the strengthening and fatigue mechanisms of carbon/epoxy composite joints is experimentally investigated. The z-pinning conditions needed to maximise the loadcapacity and fatigue endurance of lap joints is determined.
* Corresponding author: Email: [email protected]
616
Properties of Z-Pinned Composite Lap Joints
MATERIALS & EXPERIMENTAL TECHNIQUES Manufacture of Lap Joints Single lap joints were made using woven carbon/epoxy prepreg (Fiberdux 914) supplied by Hexcel. The lap joint dimensions are given in figure I. Prior to curing, the joints were z-pinned through the overlap region using pultruded carbon/bismaleimide Z-Fibers™ produced by Aztex Inc. The influence of z-pin content on the failure strength and fatigue life was investigated by reinforcing the lap joint with 0.28 mm diameter pins to volume contents of 0%, 0.5%, 2.0% and 4.0%. The effect of z-pin size was examined by reinforcing the joints using 0.28 mm or 0.51 mm diameter pins to a volume content of 2.0%. The percentage area of the bonded overlap region containing z-pins is the same value as the volume content of z-pins. The z-pins were inserted in the through-thickness direction using a hand-held ultrasonically actuated horn in a process described by Freitas et al. [8]. During insertion of the z-pins and subsequent consolidation of the lap joints during curing a large number of z-pins became misaligned. The offset angle from the orthogonal (through-thickness) direction for the 0.28 mm and 0.51 diameter z-pins was measured to be 13.8±4.2° and 23.4±4.5°, respectively. After z-pinning, the lap joints were consolidated in an autoclave at an overpressure of 500 kPa and temperature of 115°C for one hour and then 750 kPa and 180°C for two hours. z-pinning
A-
•4. 85mm
60mm
30mm
60mm
85mm
FIGURE 1 Dimensions of lap joint specimens.
Mechanical Testing of Lap Joints The bond-line delamination strength, ultimate strength and elongation limit of the lap joints was determined under axial tensile loading at a crosshead speed of 1 mm/min. The fatigue life of the joints was measured under repeated tension-tension loading using a cyclic sinusoidal waveform with a stress (R) ratio of 0.6 and loading frequency of 5 Hz. The number of load cycles to failure was taken to be when the joint could no longer carry the peak fatigue stress. RESULTS & DISCUSSION Tensile Properties of Z-Pinned Lap Joints Typical tensile stress-displacement curves for the lap joint with and without z-pins are shown in figure II. The curve for the unpinned joint increases linearly up to failure, which occurs by rapid (unstable) delamination fracture of the adhesive bondline. The curve for the z-pinned joint also increases linearly until a small load drop is experienced at a stress slightly lower than the failure stress of the unpinned joint. Cracking along the adhesive bond-line occurs at this stress, however the z-pins remain undamaged and bridge the crack that transfers load across the fracture surfaces. The crack bridging action of the z-pins provides the joint with increased strength and elongation until the ultimate strength is reached.
Properties of Z-Pinned Composite Lap Joints
617
Table I shows the effect of z-pin content on the tensile properties of the lap joint. The bond-line strength values refer to the stress required to initiate delamination cracking in the adhesive bond-line, and this was found to decrease progressively with increasing z-pin content. However, while unstable crack growth occurred in the unpinned joint that caused complete failure, the crack was arrested after growing for a short distance (<5 mm) in the lap joints with z-pin contents of 2% and 4%. Delamination growth in the order of 2-5 mm is required before z-pins become effective in raising the critical shear stress for crack propagation by a crack bridging mechanism, at which point further crack growth was suppressed in the joint specimens. Increasing the z-pin content also resulted in a large improvement to the ultimate strength and elongation limit of the lap joint. This is because the z-pins are able to support increased loading by the crack bridging mechanism. The relatively modest z-pin content of 2% provided the highest improvement in ultimate strength (41%) and elongation limit (56%). 20 r
ultimate failure stress—^
Pinned Joint. 15 Unpinned J o i n t s ' '
£ 10
55
bond-line failure stress
0.00
0.25
0.50
0.75
1.00
1.25
1.50
Displacement (mm)
FIGURE 2 Stress-displacement curves for an unpinned and z-pinned lap joint. The z-pinned joint was reinforced with the thin pins to a volume content of 2%. TABLE I Effect of z-pin content on the tensile properties of the lap joints. The joints were reinforced with 0.28 mm diameter z-pins. (Numbers in brackets indicate the percentage change in properties). Maximum Ultimate Strength Z-pin Content Bond-line Failure Mode Strength Elongation 0.87 mm 0% 13.2 MPa Bond-line failure 13.2 MPa 0.97 mm (+11%) 0.5% 12.7 MPa (-4%) 14.2 MPa (+8%) Bond-line failure 2.0% 18.7 MPa (+41%) 1.35 mm (+56%) 11.5 MPa (-13%) Laminate failure 4.0% 10.3 MPa (-22%) 16.2 MPa (+23%) 1.15 mm (+33%) Laminate failure
It was found that increasing the z-pin content altered the failure mechanism. As mentioned, the unpinned joint failed by unstable crack propagation along the adhesive bond-line. The joint with 0.5% z-pins also failed along the bond-line, however the zpins were able to withstand increased loading by crack bridging until they failed by shear rupture at the fracture surface (figure Ilia). The joints with 2% and 4% z-pins suppressed the growth of a long bond-line crack, and failed within the first few rows of z-pins in the laminate (figure Illb). The transition in the failure mode from the adhesive bond-line to the laminate accounts for the increased strength in these zpinned joints. However, while both of these joints failed in the laminate, the ultimate strength and elongation limit of the joint with 2% z-pins was higher. Freitas et al. [8] found that the tensile strength of carbon/epoxy laminate is degraded with increasing zpin content due to an increased incidence of distortion and crimping to the load-
Properties of Z-Pinned Composite Lap Joints
618
bearing fibres by the z-pins. It is therefore believed the ultimate strength of the joint decreased when the z-pin content was raised from 2% to 4% because of increased damage to the fibres by the pins. The effect of z-pin size on the tensile properties of the lap joint is shown in table II. It is seen the ultimate strength and elongation limit is greatly improved for both zpin sizes. The size of the z-pins also had a major influence on the failure mechanism. As mentioned, at a volume content of 2% the thin z-pins suppressed large-scale cracking along the bond-line, and this caused the joint to fail in the laminate (figure Hlb). However, complete delamination failure of the bond-line occurred in the joint reinforced with the thicker z-pins, eventhough the volume content of pins was the same. This resulted in the formation of a large-scale bridging zone across the fracture surfaces until the z-pins failed by transverse (shear) rupture and pull-out, as shown in figure IV. The difference in the failure mechanisms for the joints reinforced with thin or thick z-pins is probably due to the influence of pin size on delamination toughness. Cartie and Partridge [9] determined the mode II interlaminar fracture toughness properties of a carbon/epoxy composite reinforced with the same thin and thick z-pins used in this study. Cartie and Partridge found that the shear load required for crack growth was about 50% higher when thin z-pins were used instead of thick pins. The number of thin pins within the joint area is over three times higher than the thick pins to achieve the same volume content. It is believed the higher number of pins allows the applied stress to be distributed more evenly over the joint, and this raised the interlaminar fracture toughness and thereby the ultimate strength of the joint.
(a)
(b) FIGURE 3 Side-views of the overlap region of lap joints containing the thin z-pins that failed in the (a) bond-line at the low pin content (0.5 vol%) and (b) laminate at the intermediate (2.0 vol%) and high (4.0 vol%) pin contents. TABLE II Effect of z-pin size on the tensile properties of the lap joints. The joints were reinforced with 2 vol% of pins. (Numbers in brackets indicate the percentage change in properties). Z-pin Diameter Bond-line Ultimate Strength Maximum Failure Mode Elongation Strength 13.2 MPa 0.87 mm Bond-line failure 0mm 13.2 MPa 18.7 MPa (+41%) 1.35 mm (+56%) Laminate failure 0.28 mm 11.5MPa(-13%) 17.8 MPa (+35%) 0.51mm 14.4 MPa (+9%) 1.20 mm (+39%) Bond-line failure
*
.,i..
'
t'
FIGURE 4 Side-view and top-view of the fracture surface of the joint reinforced with thick z-pins. The pins failed by pull-out and transverse rupture.
Properties of Z-Pinned Composite Lap Joints
619
Fatigue Properties of Z-Pinned Lap Joints The effect of volume content and size of z-pins on the fatigue life (S-N) curve for the lap joint is shown in figure V, and it is seen that z-pinning can provide a large improvement to the fatigue endurance. As with static tensile loading, it was found that the greatest improvement in fatigue performance was achieved using the thin z-pins to a volume content of 2%.
• •--•o--——O"— *
0% z-pins o.5% z-pins 2.0% z-pins 4.0% z-pins
10
100
1000
10000
100000 1000000
Cycles to Failure (a)
as 0= 15
I
5
•--•a— •
No z-pins 0.28 mm z-pins 0.51 mm z-pins
10
100
I0
1
1000
10000
100000 1000000
Cycles to Failure (b)
FIGURE 5 Effect of (a) volume content and (b) diameter of z-pins on the S-N curve of the joint.
The joint without z-pins failed under fatigue loading by delamination cracking at the adhesive bond-line. Likewise, the joint failed along the bond-line when reinforced with 0.5% thin z-pins or 2.0% thick z-pins. In these joints the delamination crack grew slowly along the bond-line during fatigue loading. This led to the development of a crack bridging zone that transferred the applied fatigue stress across the delaminated surfaces, and this mechanism is responsible for the increased fatigue life. The z-pins in these lap joints eventually failed by fatigue-induced pull-out or transverse rupture. Two different fatigue failure mechanisms were observed for the joint reinforced with 2.0% thin z-pins; these being delamination cracking of the adhesive bond-line or
620
Properties of Z-Pinned Composite Lap Joints
rupture of the laminate. This suggests that the fatigue properties of the overlap region and laminate are virtually identical in this joint, resulting in the two failure mechanisms. Only the lap joint with 4% z-pins did not fail at the bond-line, and instead failure always occurred by fatigue-induced rupture of the laminate. It is believed that an excessive amount of fibre distortion caused by the high amount of zpins reduced the fatigue life of the laminate below the endurance limit of the overlap. CONCLUSIONS The through-thickness reinforcement of single lap joints using z-pins is an effective method for improving the ultimate tensile strength and fatigue endurance. While it was found that z-pinning can reduce the tensile stress to initiate delamination cracking at the adhesive bond-line to a lap joint, the z-pins can greatly improve the ultimate strength, elongation limit and fatigue life by a crack bridging mechanism. The tensile properties and failure mechanisms of the joint are dependent on the volume content of z-pins. The properties can be improved greatly by increasing the volume content of z-pins. However, the optimum amount of z-pins was determined to be between 2% and 4%, which increases the ultimate strength and peak fatigue stress limit by about 40% because complete failure of the bond-line was suppressed and the joint failed in the laminate. ACKNOWLEDGMENTS This research was performed with financial support provided by the Australian Research Council (Grant No. DP0211709). PC thanks the CRC for Advanced Composite Structures Ltd. for the provision of a top-up scholarship. BNC was also supported by the U.S. Dept. of Energy, Grant No. DE-FG03-97ER45667. REFERENCES 1.
Sawyer, J.W. 1985. "Effect of Stitching on the Strength of Bonded Composite Single Lap Joints", J. AIAA, 23:1744-1748. 2. Lee, C , and D. Liu. 1990. "Tensile Strength of Stitching Joint in Woven Glass Fabrics", J. Eng. Mat. Tech., 112:125-130. 3. Tong, L. J.K. Jain, K.H. Leong, D. Kelly, and I. Herszberg. 1998. "Failure of Transversely Stitched RTM Lap Joints", Comp. Sci & Tech., 58:221-227. 4. Tong, L., K. Cleaves, T. Kruckenburg, and G.P. Stevens. 1998. "Strength of RTM Single Lap Joints with Transverse Stitching", Key Eng. Mats., 137:195-202. 5. Freitas, C , T. Fusco, T. Campbell, J. Harris, and S. Rosenberg. 1996. "Z-fibre Technology and Products for Enhancing Composite Design", in Proceedings of the 83th AGRAD Conference, Paper 17. 6. Rugg, K.L., B.N. Cox, K.E. Ward, and G.O. Sherrick. 1998. "Damage Mechanisms for Angled Through-Thickness Rod Reinforcement in Carbon-Epoxy Laminates", Comp., 29A:1603-1613. 7. Rugg, K.L., B.N. Cox, and R. Massabo. 2002. "Mixed Mode Delamination of Polymer Composite Laminates Reinforced Through the Thickness by Z-Fibers", Comp., 33A: 177-190. 8. Freitas, G., C. Magee, P. Dardzinski, and T. Fusco. 1994. "Fiber Insertion Process for Improved Damage Tolerance in Aircraft Laminates", J. Adv. Mats., 25:36-43. 9. Cartie, D.D.R., and I. Partridge. 1999. "Delamination Behaviour of Z-Pinned Laminates", Proc. 2"dESIS TC4 Conf, 13-15 Sept., Les Diablerets.
The Effect of Thickness on Joint Property of Mechanical Joint with Washer and Torque Akihiro Ochi, Kenichi Sugimoto, Asami Nakai and Hiroyuki Hamada Kyoto Institute of Technology, Japan
ABSTRACT In this study, the effect of thickness, fastening torque and washer on joint property of mechanical joint were investigated. Three types of laminate thickness were fabricated by hand-lay-up technique and three fastening conditions were used, one was without any washers and torque, another was that the washers were used onto both side of specimen with significantly low torque of 0.1N- m and the other was that the washers were used onto both side of specimen with high torque of 5N- m. In case of thin specimen without washer and torque, the large out-plane deformation was generated. On the other hand, in case of using washer and torque of O.lNm, slant cracks caused by shear fracture were generated overall. Also, in the case of using washer and torque of 5N-m, delamination and transverse crack occurred overall. INTRODUCTION The most of structures possess the joint part in which mechanical joint is often used because mechanical joint is more reliable and useful than the other joint methods. In case of mechanical joint, the circular hole is required in order to put the fastener such as bolt and rivet in, so that the strength of joint part should decrease due to the stress concentration. When composite material is applied into the large structure, the thickness has to become large. Stress distribution of thick composite is possible to change compared with that of thin composite, and mechanical behavior may be changed. Hence, to understand the effect of thickness on mechanical property is much important. The fracture aspect of mechanical joint is mainly classified into Net-Tension, Shear-Out, Bearing failure and so on. In case of a small width, Net-Tension failure occurs, instead, Shear-Out failure occurs when end distance is small. The joint with the large width and end distance fails in Bearing failure which shows more ductile manner than the others and the highest failure load. Therefore, the design of mechanical joint failed in Bearing is desired. Also it is well known that the failure behavior was changed and failure load was increased by applying washer and fastening torque [1-3]. However, the effect of laminate thickness on the characteristic of mechanical joint with washer and fastening torque has not been clarified well. In this study, the effect of laminate thickness on joint property of mechanical joint with washer and fastening torque was investigated. Three fastening conditions were applied to investigate the effects of washer and fastening torque on mechanical property and failure mechanism. Matsugasaki, Sakyo-ku, Kyoto , Japan, 606-8585, FAX: +81-75-724-7800; A. Ochi: ochi03(g,ipc.kit,ac,jp. K. Sugimoto: ksugiO2(a>ipc.kit.ac.ip, A. Nakai: [email protected]: And H. Hamada: [email protected]
622
Effect of Thickness on Joint Property
EXPERIMENTAL METHOD Materials and Specimen The 0°/90° multi-axial warp knitted fabric was used as reinforcements. The schematic diagram of 0°/90° multi-axial warp knitted fabric is shown in Figure 1. Multi-axial warp knitted fabric allows the placement of warp, weft, and off-axis materials directly into the fabric structure. The composites with the multi-axial warp knitted fabric can possess higher mechanical properties, because of no crimp of reinforcement. Moreover, not only the unidirectional fiber bundles, but also chopped strand mat can be combined. Multi-axial warp knitted fabric has the ability to combine multiple layers of oriented yarn in a single structure. This reduces the cost with omission of the stacking process. The unsaturated polyester resin (RIGOLAC, 150HRBQTNA, Showa High polymer Co., Ltd, Japan) was used as matrix resin. The specification of specimen is shown in Table 1. The composite laminates with 2.8, 5.5 and 11 .Omm, thickness in which number of plies were 4, 8 and 16 respectively, were fabricated by hand-lay up method. The joint specimens were cut into 36.0mm width and 200.0mm length on each laminates. The circular hole with 12.0mm diameter was drilled at the center in width direction and 36.0mm distance from edge of the specimen. The d/t was the value divided by thickness; t into hole diameter; d. The d/t was increased with increase in the hole diameter or decrease in the thickness.
0-direction
90-direction
FIGURE 1 0790° multi-axial warp knitted fabric.
TABLE I Specification of specimen. Number of ply thickness, t (mm) Hole diameter, d (mm) d/t
4 2.8 4.36
8 5.5 12.0 2.18
16 11.0 1.09
TABLE II Fastening condition. Number of ply No washer, no torque O.INg torque Washer 5 . 0 N 8 torque
4 4NW 4LT 4HT
8 8NW 8LT 8HT
16 16NW 16LT 16HT
Joint Test The Double lap joint was used to joint test. In this study, three fastening conditions were used, one was without any washers and torque on each specimens (i.e. 4NW, 8NW and 16NW respectively), another was that the washers were used onto both side of specimen with significantly low torque; O.lN-m on each specimens (i.e. 4LT, 8LT and 16LT respectively) and the other was that the washers were used onto both side of specimen with high torque; 5N-m on each specimens (i.e. 4HT, 8HT and 16HT respectively). The fastening condition is shown in Table 2. The inner and outer diameters of washer were 12.7mm and 25.9mm respectively and thickness of washer was 2.2mm. The joint test was performed by using INSTRON testing machine (Type 4206) with lmm/min. cross-head speed at room temperature.
Effect of Thickness on Joint Property
623
RESULT AND DISCUSSION Joint Test Fracture aspects of NW, LT and HT specimens are shown in Figure 2, 3 and 4 respectively. The joint testing was stopped at first peak stress which was corresponding to the circle on the joint stress-displacement curves as shown in Figure 5. iilniT
Bearing failure
(a)
(b)
Hearing failure ;
' ' '(V
FIGURE 2 Fracture aspect of (a) 4NW-200MPa (b) 8NW-270MPa and (c) 16NW-300MPa.
Bearing failure
UL';
hiiluri'
Bearing failure
Q (a)
(b)
(c)
FIGURE 3 Fracture aspect of (a) 4LT-230MPa, (b) 8LT-340MPa and (c) 16LT-330MPa. [ Sticur-Oiil failure
Shear-Out failure
O (a)
(b)
(c)
FIGURE 4 Fracture aspect of (a) 4HT-230MPa, (b) 8HT-340MPa and (c) 16HT-330MPa.
In NW specimen (see Figure 2) and LT specimen (see Figure 3), Bearing failure was observed at loaded part. On the other hand, in HT specimen (see Figure4), Shear-Out failure was dominant. Therefore, the load was normalized by the cross section. The joint stress was the value divided by hole diameter and thickness into the load. The joint stress-displacement curves obtained from joint test of NW specimen, LT specimen and HT specimen are shown in Figure 5. Regarding NW specimen, the stress increased linearly and decreased drastically after peak stress. The tendency of joint stress-displacement behavior in LT specimen was same as that in NW specimen until first peak stress. After first peak stress, 4LT specimen showed that the initial peak stress is
624
Effect of Thickness on Joint Property
followed by other peak stresses. 8LT and 16LT specimen kept almost constant stress after maximum stress. In HT specimen, the stress increased linearly until the first peak stress. The stress increased until the final failure in 4HT specimen, and the stress gradually decreased in 8HT and 16HT specimen. Experimental results of each specimen are summarized in Table 3. In 8LT, 16LT, 8HT and 16HT specimen, the a j is almost the same value. The a j of 4LT and 4HT was higher by 7.5% than that of 4NW specimen. 8LT and 8HT specimen showed higher a j by 25% than 8NW specimen. The a j of 16 LT and 16HT was higher by about 12% than that of 16NW specimen. From these results, increase ratio of joint strength in 8 plies specimen was the highest among three types of laminate thickness. Relationship between joint strength and d/t is shown in Figure 6. In the case of NW specimen, a j was decreased gradually with increase in d/t. UJ of LT and HT specimen at d/t of 2.18 and 1.09 was almost the same value, however, a j decreased at d/t of 4.36.
2
4 6 Displacement (mm)
10
(a) 500
500 400 300
-"—16LT
200
8LT -m
100 0
//,
2
4LT
. , . j
10
4 6 Displacement (mm)
2
4 6 8 Displacement (mm)
10
(c)
(b)
FIGURE 5 Joint stress-displacement curve of (a) no washer, (b) torque 0.1 and (c) torque 5
TABLE III Experimental results.
4NW 8NW 16NW 4LT 8LT 16LT 4HT 8HT 16HT
Thickness, t (mm) 2.8 5.5 11.0 2.8 5.5 11.0 2.8 5.5 11.0
d/t 4.36 2.18 1.09 4.36 2.18 1.09 4.36 2.18 1.09
First peak load, P (fcN) Joint strength, a i (MPa) 7.13 216.1 18.01 272.9 38.78 293.8 232.2 10.86 22.57 341.9 327.8 43.27 232.2 10.79 341.5 22.54 330.8 43.66
Effect of Thickness on Joint Property
625
400
I no washer A torque 0.1 -O— torque 5
^300
'200 c 'o
100, 0
1
2
3
4
5
FIGURE 6 Relationship between joint strength and d/t.
Cross Sectional Observation In order to confirm the effects of thickness and torque on failure mechanism, cross sectional observation was performed. Optical micrograph of cross section inNW, LT and HT specimens are shown in Figure 7, 8 and 9 respectively. The observed position was indicated Figure 7, 8 and 9. Regarding NW specimen, out-plane deformation, large delamination and shear fracture were dominant. The large delamination was generated at outer layer and inner layer in 4NW specimen. Delamination at inner layer was generated from crossing point of shearfractures.The slant crack caused by shearfractureoccurred from outer layer to inner layer. Also, large out-plane deformation was generated. In the case of 16NW specimen, large delamination was observed at outer layer. Shear fracture occurred from inner layer to outer layer. Out-plane deformation was generated at outer layer. Regarding LT specimen, out-plane deformation was restrained and shear fracture and delamination were dominant. For 4LT specimen, delamination occurred at outer layer and slant crack caused by shear fracture was generated overall. Delammation was propagated from the end of slant crack. In 16LT specimen, delamination occurred at outer layer. Two types of shear fracture were seen. One was generated from outer layer to inner layer. The other was generated from inner layer to outer layer. Two slant cracks were propagated in almost parallel. Because HT specimen showed shear-out failure, the cross section offracturepart (see Figure 9) was observed. Delamination and transverse crack occurred. In both 4HT and 16HT specimens, delamination was generated at inner layer and transverse crack was generated at overall. CONCLUSION In this study, joint strength and fracture aspect of composite joint with and without washer under two fastening torque were investigated. Joint strength was improved by using washer and torque. The out-plane deformation was restrained by using washer even though remarkably low fastening torque. Also, the failure aspect was changed by increase in the torque.
Effect of Thickness on Joint Property
626 Drlumination
Slant crack I
(b)
(a)
FIGURE 7 Optical micrograph of cross section in (a) 4NW-200MPa and (b) 16NW-300MPa.
i[o^
Ik'lainiiialiiiii \
v.
| IK'iiiiiiin.iliiiii Maul
I
T W;
\\
/
(a)
(b)
FIGURE 8 Optical micrograph of cross section in (a) 4LT-230MPa and (b) 16LT-330MPa.
[ lh-l:iniiinaiiiin
!
i_!_raii%U'rM'
; ..J
aiiMiTM-vi-.H-k
' I »'•«•'•"•«" l>»''
Di'liiiiiiiiiiiinii i
1 (a)
(b)
FIGURE 9 Optical micrograph of cross section in (a) 4HT-230MPa and (b) 16HT-330MPa.
REFERENCES 1. 2. 3.
Y.Yan, W.-D.Wen, F.-K. Chang andP. Shuprykevich. 1999. "Experimental study of clamping effects on the tensile strength of composite plate with a bolt-filled hole" Composite, Part A, 30: 1215-1229. T,A,Collings. 1977. "The strength of bolted joints in multi-directional CFRP laminates" Composite, 8: 43-54 G.Kretsis and F.L.Matthews. 1985. 'The strength of bolted joints in glass fibre/epoxy laminates" Composites, 16: 92-105
Part XIII
Metal Matrix Composites
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Micromechanical Modelling Of Hybrid Metal Matrix Composites Prem E. J. Babu, S. Savithri *, U.T.S. Pillai* and B.C. Pai Metal Processing Division, # Computational Modelling and Simulation Section, Regional Research Laboratory (CSIR), Thiruvananthapuram - 695 019, India.
ABSTRACT A micromechanical model based on generalised method of cells (GMC) is employed to predict the effective behaviour of hybrid metal matrix composite systems (HMMCs). A quantitative analysis is done to study the effect of two reinforcements on the effective elastic properties of HMMCs. The HMMC taken for the study is Al/SiCp/CBNp (CBN = Cubic Boron Nitride) system. The predicted effective properties of the HMMC are compared with those of the corresponding mono composites. INTRODUCTION Over the past several years, developments in the processing of metal matrix composites (MMCs) have provided new and exciting opportunities for tailoring the properties of these composites to specific applications. For example, the addition of ceramic reinforcements such as A12O3, SiC, B4C, CBN, etc in the metallic materials increases the strength and stiffness of the base matrix, and finds increasing applications in automobile and aerospace industries. Eventhough these composites are capable of giving better strength properties than the base matrix, typical components like automobile piston or other parts that are in sliding contact, such as guideways have to exhibit good strength as well as better wear resistant properties. This type of typical synergistic responses cannot be achieved with mono composites (composites having single reinforcement). These limitations have fostered a renewed interest for multi systems of particle/fiber reinforced metal matrix composites, so called hybrid metal matrix composites (HMMCs). Exploitation of these composite systems to a reliable design requires an accurate characterization of properties especially the elastic properties. Since the experimental characterization involves time and expenditure, micromechanical models are normally used to predict these properties. A number of micromechanical models have been extensively used since 1960s for predicting the macroscopic behaviour and effective properties of mono composites. An extensive account of the characteristics and capabilities of these models can be found in ref. [1]. Among the various micromechanical models, the generalised method of cells [2] has emerged as an attractive tool to predict the mechanical behaviour of mono MMCs. One of the most attractive features of this GMC is its capability to give accurate macroscopic responses using a relatively small number of subcells, thereby requiring very little computational effort [3]. Moreover the capability of the GMC for * Corresponding author, Ph: +91-471-2515251, Fax: +91-471-2491712, E-mail: [email protected]
630
Micromechanical Modelling of Hybrid Metal Matrix Composites
predicting the effective properties of a variety of composites such as unidirectional MMCs [4], intermetallic MMCs [5] and the particulate MMCs [6,7] are well proven. Hence, in this work, an attempt has been made to explore the capabilities of GMC to predict the effective properties of hybrid MMCs having two particulate reinforcements. The work is primarily focussed in predicting the variation of effective properties in HMMCs when different types of reinforcements are added in a base metallic matrix. The effects of varying volume proportions of the two particles on the effective properties of a HMMC having a total particle volume of 20% are also discussed. GENERALISED METHOD OF CELLS The micromechanics model chosen for this work is the generalised method of cells (GMC) proposed by Aboudi [2], to predict the responses of triply periodic microstructures. It uses a repeating unit cell, also called repeating volume element (RVE), divided into rectangular parallelepiped subcells to characterize the microstructure. Periodic boundary conditions are enforced on the unit cell and, under the assumption of perfect bonding, displacements are assumed continuous across subcell boundaries. The requirements for equilibrium are satisfied by also requiring the continuity of tractions across these micro-level boundaries. The homogenization process in GMC then connects the material microstructure to an equivalent homogeneous material through a set of continuum level equations, which result from the continuity conditions and effective properties are predicted in an average sense. GMC is thus capable of calculating the effective elastic and shear moduli as well as Poisson ratios for the assumed microstructure, based on the known effective properties of the individual phases. The representative unit cell of a composite material with a triply periodic structure is shown in figure 1. It consists of Nax Npx Nr subcells in a, /3 and y directions as shown in figure 1, where each subcell can have different material properties: a = l...Na P = l...Np and y = l...Nr. Some subcells are identified as reinforcement and some as matrix subcells depending upon the concentration of the reinforcement. The volume of each subcell is da hp l7, where a, /? and y are running indices: in the xi, X2 and Xi directions respectively. The volume of the repeating volume element is dhl where
d=~£da, a=l
/! = £/*» p=l
and / = 2 X .
A local system of coordinates
y=l
(xl(a), x2(t>>, x3), as shown in figure 1, are introduced, whose origins are located in the center of each subcell (afty), and are oriented parallel to the global coordinate system (xj, X2, X3). As the average behaviour of the composite is sought, a first order theory in which the displacements uf'"' in the subcells are expanded linearly in terms of the distances from the center of each subcell is considered. Thus the first order expansion of the displacements «,-, i =1, 2, 3 in each subcell (afiy) is represented as
uf1 = wf(x) + xiaiSff +x2hT +x31wfr f=l, 2, 3
(1)
1
where, w^" are the displacement components at the centre point of the subcell, and(|)"(il',x"PY ,i|/,a(iTare the unknown micro variables that characterize the linear dependence of the displacements w(aPTon the local coordinates of the subcell.
Micromechanical Modelling of Hybrid Metal Matrix Composites
RVE
631
/ \/ / / / / / / /
FIGURE 1 A repeating unit cell having triple periodicity
The effective average strains in the composite is then expressed as (2) «=/ p=i y=i
where the subcell strains are (3)
The average stress in the composite is determined in a similar fashion as in equation (2). The next step is to impose the continuity of displacements and tractions at the interfaces. If T is the interface between two subcells, assuming displacement continuity on an average basis over the interfaces in xi direction yield,
I JK
xf=da/2
=0
(4)
Similar type of equations will be obtained for the other directions also. The final set of displacement continuity equations is expressed in the matrix form as A c — 1 ~c Aabs - J &
r
(^ (3)
Additionally, tractions must be continuous across subcell interfaces as <jff = cr"fr, \p + l p < N p <j"fr = a"fr and <j"fr = a"fY where p = < , in which p may represent a or p or y. Imposing the continuity of tractions at the subcell interfaces gives a set of equations, which are represented in matrix form as AM es = 0 (6) The overall elastic constitutive law is obtained by combining equations (5) and (6) as \0\
Ass = K s , where A =
and K =
. Solving for the subcell strains yields
ss=As, (aPr)
where A = A~'K. Thus e
(7)
=A
(aPr>
e and hence
A(uPr)
j g c a u e c j a s m e mechanical concentration tensor. Finally the effective mechanical law for the composite is established a =B x s
(9)
632
Micromechanical Modelling of Hybrid Metal Matrix Composites
where the effective elastic stiffness tensor, B , is given by B* = — j r f; x dahpirc
(10)
Once the stiffness matrix B* is obtained, the compliance matrix S* can be found out by inverting the B* matrix. From the compliance matrix, the effective elastic properties of the composite can be obtained. To illustrate the periodic HMMC system, a representative cubic unit cell is taken and is equally divided into 5 x 5 x 5 subcells. Hence each and every cell will have 0.8% of total volume. In the 125 subcells, the numbers of subcells for the reinforcements are determined based on their volume percent. The subcell positions for the phases are randomly chosen in the unit cell.
SAMPLE MATERIAL SYSTEM Since well known experimental results for the variation in effective elastic properties for bi-particle reinforced HMMCs are not available in the literature, a hypothetical HMMC (Al/SiCp/CBNp hybrid MMC) has been taken for the purpose. The effective properties assigned for the Al and SiC for this study are taken from ref. [8] and the values for CBN is taken from ref. [9] and are shown in table 1. TABLE I Material Properties
Material Elastic modulus E, (GPa) Poisson ratio
Aluminium [8] 70 0.33
SiCp [8] 450 0.17
CBN [9] 915 0.1187
RESULTS AND DISCUSSIONS The capability of the GMC for predicting the effective properties of a variety of composites such as unidirectional MMCs [4], intermetallic MMCs [5], and the particulate MMCs [6, 7] are well proven in the literature. However, for stronger evidence in the case of particulate reinforced mono MMCs, results are generated using GMC model for the effective properties of a 2024 Al alloy - SiCp composite and the experimental [10] as well as the predicted values are shown in table II. TABLE II Effective properties for an Al/SiC p mono composite
Experimental Vs Predicted Values 2% SiC composite 10% SiC composite
Effective Properties Poisson Ratio Young's Modulus (GPa) Experimental [10] Predicted Experimental [10] Predicted 77.22 0.330 77.35 0.331 88.03
87.16
0.325
0.322
Figure II (a) and (b) compares the Young's modulus and Poisson ratio respectively of the Al/(MgO).(1.25Al2C>3). spinel mono composite as predicted by GMC model, Rule of Mixtures (ROM) and experimental values [11]. From the above comparisons, the efficiency of the GMC model in predicting the effective properties of mono MMCs is well proven, hi view of the fact that HMMCs are more attractive than mono MMCs, an attempt has been made to explore the capabilities of GMC in predicting their effective properties. It should be noted that, the new results presented in this
Micromechanical Modelling of Hybrid Metal Matrix Composites
633
section are intended to display the theory's unique capabilities as opposed to addressing a practical structural design problem. As of now no experimental results on HMMCs are available to validate this model, future work is planned to validate when it becomes available.
(a) ...» - ROM prediction —•- - Experimental value Model Prediction Ill
- ROM prediction - Experimental Values Model Prediction
Particle volume fraction V((GPa)
Particle volume fraction V,(%)
FIGURE 2 Comparison of effective properties for Al/Spinel composite
• S i - Al/SiC composite -••g— Al/CBN composite ^ AlfSiCJCBN HMMC (Ratio SiC:CBN = 50:50) 3
(a)
g
> D2D
Total particle volume fraction in the composite,
6D:iD
iDSD
2BSD
Q:1DD
SiC : CBN volume proportion
FIGURE 3 (a) Comparison of effective properties for HMMC and the mono composites (b) Effect of varying volume proportions of SiC:CBN for a 20% HMMC
Figure III (a) presents the effective elastic modulus of the HMMC as well as mono composites Al/SiC and Al/CBN. The vol.% of the particles in HMMC reported here is the sum of the vol.% of the two particles, SiC and CBN, and they are in 50:50 ratio. It can be seen from the figure that, the modulus of HMMC lies in between the modulus of Al/SiC and Al/CBN mono composite for all volume of particles studied. However, upto 25 vol.%, not much improvement is noticed in the elastic modulus of HMMC, and the values are closer to the values of Al/SiC composite. At higher vol.%, the modulus of HMMC gets increased and approach towards the modulus values of Al/CBN composite. The results also clearly show that the behaviour of HMMCs is significantly different from those of mono composites. The modulus valus of HMMC with 20% (SiC and CBN) in varying proportions is shown in figure III (b). It can be clearly seen from the figure that the increase in modulus values is not linear and represents the typical composite behaviour. The proposed GMC formulation is thus found to be extremely useful in predicting the effective properties of the HMMCs.
634
Micromechanical Modelling of Hybrid Metal Matrix Composites
However, a clear-cut inference is not possible with this single result. Analysing more systems with experimental validation is indeed the focus of the future studies. CONCLUSIONS Generalised Method of Cells (GMC) micromechanical model developed for predicting the effective properties of bi-particle reinforced HMMCs has been presented. The applicability and validity of this model has been checked for Al/SiCp/CBN hybrid MMC system. Comparison of effective properties shows that the behaviour of HMMCs might significantly differ from those of the corresponding mono composites. The predictions of the effective properties of HMMCs thus form a base for analysing their overall behaviour in a macro-scale. REFERENCES 1. 2. 3.
4. 5.
6.
7.
8. 9. 10. 11.
Aboudi J. 1991. Mechanics of Composite Materials: a unified micromechanical approach, New York, Elsevier. Aboudi J. 1995. "Micromechanical analysis of thermo-inelastic multiphase short fiber composites", Comp. Engng, 5(7): 839-850. Wilt T.E., 1995. "On the finite element implementation of the generalized method of cells micromechanics constitutive model", Technical Report NASA-CR-195451, National Aeronautics and Space Administration, Lewis Research Center, USA. Salzar R.S., Pindera M.-J., Barton F.W. 1996. "Elastic/plastic analysis of layered metal matrix composite cylinders. Part I. Theory"., J. Pressure Vessel Technol., 118(1), 13-20. Baxter S.C., Pindera M.-J. 1999. "Stress and plastic strain fields during constrained and unconstrained fabrication cool down of fiber reinforced IMCs", J. Compos. Engng. 33(4), 351376. Prem E. J. Babu, Savithri S., Pillai U.T.S. and Pai B.C., 2002. "Role of particles on the elasticplastic behaviour of metal matrix composites", Proc. of the Conf. on Light Metals and Composites for Strategic and Societal Needs (LMCSSN'02), eds. Pillai R.M., Pai. B.C , Trivandrum, 239-244. Prem E. J. Babu, Savithri S., Pillai U.T.S. and Pai B.C., 2003. "3D micromechanical model for predicting the thermo-elastic behaviour of particulate reinforced aluminium matrix composites", Proc. of the Int. Conf. on Aluminium (INCAL '03), eds. Subramanian S., Sastry D.H., New Delhi, 315-321. Ge D., Gu M., 2001, "Mechanical properties of hybrid reinforced aluminium based composites", Materials Lett., 49, 334-339. Teter D.M., 1998, "Computational Alchemy: The search for new superhard materials", Materials Research Society Bulletin, 23, 22. Geni M. and Kikuchi M., 1998, "Damage analysis of aluminum matrix composite considering nonuniform distribution of SiC particles", Acta. Mater, 46, 3125-33. Gustafson T.W., Panda P.C., Song G. and Raj R., 1997, "Influence of microstructural scale on plastic flow behavior of metal matrix composites", Acta mater. , 45, 1633-43.
Formation of Nanostructured Magnesium Composite Reinforced by in-situ TiC L. Lu*, M. Gupta and K.W. Tay Department of Mechanical Engineering The National University of Singapore Singapore 117576, Singapore
ABSTRACT Nanostructured magnesium composite reinforced by in-situ TiC was synthesized via mechanical milling of the elemental magnesium, aluminium, titanium and graphite powders at room temperature. Formation of in-situ TiC was observed after 20 hours of mechanical activation. However, full reaction between Ti and C could not be achieved through single mechanical activation. The residual Ti and C were found to react upon sintering at relatively low temperature in comparison with nonmechanically activated powder. Mechanical properties and microstructure were characterized showing a tremendous improvement in terms of tensile strength but on the cost of ductility.
INTRODUCTION Mg has a low density of 1740kg/m3, which is approximately 35% lighter than that of Al alloys and 65% lighter than that of Ti alloys. It has a relatively high strength-toweight ratio and high specific stiffness, good elastic modulus and conductivity as well as high damping capacity [1]. However, mechanical properties of Mg alloys are in general poor in comparison with other light-weight alloys. The relatively poor mechanical properties can be improved by grain refinement and by incorporation of ex-situ reinforcements [25] . Another possible processing technique is in-situ reaction which is often used in liquid phase processing in which at least two elements react each other forming in-situ reinforcement. Since in-situ reinforcements are formed insitu, they are stable with their matrix. In addition to in-situ reaction in liquid phase, it has also been explored in solid phases [69] . Following Hwang's work[101 where an in-situ TiC Mg composite was formed and compression properties were investigated, this research intents to investigate formation of in-situ TiC via mechanical alloying and sintering, and tensile properties of the in-situ composites. EXPERIMENTAL PROCEDURES Elemental powders of Mg, Ti, Al, and C of purity > 98% were used. The nominal compositions of Mg5wt%Al with addition of Ti and C were prepared. A Fritsch planetary ball mill operated at 200 rpm was employed. Forty 15 mm diameter steel * Corresponding Authot: Fax (65) 6779 1459; E-mail [email protected]
Formation of Nanostructured Magnesium Composite
636
balls were used with a ball-to-powder weight ratio of about 20:1. 2wt.% of stearic acid was added to the powder mixture as a process control agent to prevent agglomeration and excessive cold welding of the powders. Prior to mechanical alloying, the powder mixtures were sealed in milling vials with 99.9% pure argon gas inside. After mixing and mechanical alloying, the powders were cold-compacted into rods of 35 mm diameter and about 35 mm length which was then sintered at 500°C for two hours. Extrusion of the sintered compacts with an extrusion ratio of 25:1 was carried out at 400 °C using graphite as lubricant. The characterization of the mechanically alloyed and unmilled powders and rods was carried out using the Shimadzu Lab-XRD-6000 x-ray diffractometer with Cu Ka radiation operating at 40 kV and 30mA, with a scan speed of 2°C/ min. Tensile tests in accordance with ASTM test standard E8M-96 were also performed to evaluate the mechanical properties of the composites. The tensile tests were conducted on round tension test specimens of diameter of 5 mm and gauge length of 25 mm. An automated servohydraulic Instron 8500 machine with a strain rate of 3.3 x lO'V 1 was employed. RESULTS AND DISCUSSION Fig. 1 shows XRD spectra of the original blended powder mixture and the powders after different durations of mechanical alloying. Clearly four elements of Mg, Ti, Al and graphite are shown in the mixture of unmilled powder. After 10 hours of mechanical milling, a potential phase of Al^Mgn appears while graphite diffraction disappears. After 20 hours of mechanical alloying, two new peaks identified to be (111) and (200) TiC diffractions appear indicating formation of in-situ TiC during mechanical alloying. Although in-situ TiC was found, reaction was not completed in this stage judged from retained Ti. To avoid contamination of iron from milling tools, no further milling was carried out while the powders before and after milling were cold-compacted and sintered at 500°C. Powders
40
50
60
70
Diffraction angle (29? FIGURE 1
XRD spectra of powder mixtures after different duration of milling.
Formation of Nanostructured Magnesium Composite
637
Two very different diffraction spectra can be seen from Fig. 2, one of which is the sintered and extruded rod made form unmilled powder and another one made from mechanically alloyed powder. Though TiC diffraction of the unmilled specimen is shown after sintering at 500°C, the intensity of TiC is low implying small amount of TiC formed during sintering. Furthermore, there still exists Ti diffraction. This observation is not surprising since the sintering temperature is low and graphite may also be separated from Ti. For milled specimens, strong diffraction of TiC can be seen although there also exists Ti. The in-situ reaction after sintering is more completed than that after mechanical alloying.
Extruded • • 0 ^
*
J,
Mg Ti Al12Mg17 TiC
(c) 20 h milling 0 •
•
"A
i
•
1
L___JLJ iy^
>AAV~-,
A_^jJU
(b) 10 h milling
<> • "A
•
#
(a) Original
i
A i
i
30
\ j; • ;J\J i
i
40
i
i
i
i
i
50
i
i
i
1
1
1
60
1
1
1
70
Diffraction angle (29? FIGURE 2
XRD spectra of extruded rods.
Grain sizes of Mg powder were dramatically reduced to 29 and 28 nm for 5 and 10 vol %TiC after 10 hours of milling as listed in Table I. The sizes of grain do not change much after 20 hours. The grain sizes are not stable upon sintering. For example, for 5% TiC composites, grain size increases to 153 nm and 87 nm respectively for 10 and 20 hours mechanically alloyed specimens. It is noted that grain size is much stable for longer milled specimen. The stability of longer milled specimen is attributed to final distribution of Ti and TiC which pin the movement of grain boundaries during sintering. The same trend for 10%TiC is also observed. Mechanical properties of the composites are given in Table II. The tensile properties of the unmilled composites are seen to slightly increase with the increase in the volume of Ti and C. Though it is not possible to form large amount of TiC in the unmilled composites but the addition of Ti and C particles in the matrix generally increase the yield strength and tensile strength. It is also found that elongation of the specimen with 10vol%TiC is higher presumably due to incorporating ductile Ti element. Both yield and ultimate tensile strengths of mechanically alloyed composites are found to be almost doubled in comparison with their unmilled counterparts. The increase in strengths are attribute to formation of TiC formed during mechanical
Formation of Nanostructured Magnesium Composite
638
alloying and subsequent sintering, smaller grain size and homogeneous distribution of reinforcement. However, the increase in strength is at the cost of ductility. TABLE I
Duration 0 10
Mg5%Al/5vol%TiC
Mg5%Al/10vol%TiC
TABLE II
Mg-Al-5%volTiC Mg-Al-10%volTiC Mg-Al-5%volTiC Mg-Al-5%volTiC
Crystalline size
Duration (hour) 0 0 10 20
Crystalline Size (nm) Powder Extruded Rod 541 653 29 153
20
24
87
0
541
620
10
28
138
20
17
77
Mechanical Properties UTS (MPa) 234 265 426 460
0.2%ay (MPa) 174 198 426 460
Elongation (%) 1.29 2.32 0.10 0.09
CONCLUSIONS In-situ TiC can partially be formed via mechanical alloying and subsequent sintering at 500°C. Full formation of TiC is not possible. Grain sizes of mechanically alloyed composites are less then 30 nm while increase to over 130 nm and 70 nm, respectively for 5vol% and 10vol% TiC. Extremely high strengths of mechanically alloyed composites have been obtained but their ductility is low. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10.
W.Kai, J.M. Yang and W.C. Harrigan, Scripta. Metall., Vol. 23 (1989), 1277. J.V. Foltz and W. C. Harrigan, Proceedings of the PM in Aerospace and Defense Technologies Symposium, Tampa, FL, USA, MPIF, Ed. F.H. Froes. (1991), 123. M.R. Krishnadev, R. Angers, C.G. Krishnadas Nair and G. Huard, JOM, 8 (1993), 52. V. Laurent, P. Jarry, G. Regazzoni and D. Apelian, J. Mater. Sci., 27 (1992), 4447. A. Matin, L. Lu and M.Gupta, Scripta Mater., Vol. 45 (2001), 479. H.J. Brinkman, J. Duszczy and L. Katgerman, Scripta Mater., Vol. 37 (1997), 293. P.C. Maity, S.C. Panigrahi and P.N. Chakrabory, Scripta Mater., Vol. 28 (1993), 549. C.F. Feng and L. Froyen, Scripta Mater., Vol. 36 (1998), 109. L. Lu, M.O. Lai, Y.Su, H.L. Teo and C.F. Feng, Scripta Mater., Vol. 45 (2001), 1017. S. Hwang, C. Nishimura and P.G. McCormick, Scripta Mater., Vol. 44 (2001), 2457.
Preparation of Mg-based Hydrogen Storage Nano-composite by Reaction Ball Milling Y.Q. Hua'b*, C. Yanb, H.F. Zhanga, L. Yeb, Z.Q. Hua Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang, 110016, China
a
b
Centre for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering, J07, The University of Sydney, NSW 2006, Australia
ABSTRACT 7.5 composite was successfully prepared by reactive mechanical alloying (RBM). The hydrogen storage capacity and absorption kinetic were investigated. The phase structure and micro structure were evaluated using X-ray diffraction, SEM and TEM. The effects of initial hydrogen pressure and milling time on absorption kinetics and impurities in the composite were investigated. The analysis of Avrami exponent indicates that the formation of hydrides is a three-dimensional growth mechanism with a reduced nucleation rate with time, which is controlled by the diffusion of hydrogen atoms.
INTRODUCTION In recent years, production of nanocrystalline metal hydride [1, 2], especially Mgbased, by mechanically activated gas-solid reactions has been reported. Although several investigations have been dedicated to the formation of Mg hydride via milling [3-6], there are few studies on the kinetics themselves and how the supplied mechanical energy affects the reaction rate. Furthermore, for mass production of Mgbased hydrogen storage composites via ball milling, a problem needs to be solved is the possible contamination resulting from the milling tools (vessel and balls) and/or from milling atmosphere. hi this work, the hydrogenation kinetics was investigated to understand the possible mechanisms that govern the mechanically activated reaction. The structural evolution and its dependence on gas pressure was examined. The results may provide useful information for further development of hydrogen storage nano-composites. EXPERIMENTAL PROCEDURE Synthesis of Hydrides .5 (bcc structure) alloy was used as catalyst due to its good hydriding properties and high hydrogen storage capacity. Ti37.sV25Cr37.5 powder (30wt. %) was mixed with Mg (purity>99%, 100 mesh) and then mechanically milled in a ' Corresponding author. E-mail: [email protected]
640
Mg-based Hydrogen Storage Nano-composite
SPEX8000 machine. A cylindrical stainless steel vial was used and the ball to powder ratio was 20:1. The vial was sealed by an O-ring and connected to a gas reservoir under different initial pressure of 0.5, 0.8, 1.0, 1.2 MPa. The total volume of the system was 260 cm3 and about 2.7 g material could be produced. The milling duration was 5 h. Evaluation of Absorption Kinetics During the milling, the change of hydrogen pressure due to hydrogen absorption by the sample was continuously monitored using a pressure transducer. The method proposed by Bab et al [7] was adopted to evaluate the absorption kinetics. During the reaction ball milling (RBM), the weight of hydrogen absorbed as a function of milling time, can be evaluated as, WH%=(100mHAPV)/(MRT)%,
(1)
where mH is the atomic mass of hydrogen, AP is the change of pressure, V is the volume of the system, M is the initial powder mass, R is the gas constant and T is the temperature. Characterization At different milling duration, small amount of powder was taken out of the vial and the structural evolution was examined using a Rigaku X-ray diffractometer equipped with a graphite monochromator with Cu kot radiation. The composition of the milled powders was also determined by chemical analysis. The microstructures were observed using SEM (PHILIPS XL 30CP) equipped with an energy dispersive X-ray analysis system (EDS) and TEM (PHILIPS EM420). RESULTS Hydrogen Absorption The time dependence of the hydrogen absorption during the milling is shown in Fig. 1. An amount of hydrogen, about 1.05wt % is absorbed quickly in the initial 10 min. nte nt, wt.
A - Mg A - pMgH •
o - bcc phase $ - Fe
-TMSZ
•Cs - hydrides of Ti37 5v25Cr37 s A
/
4
8 c 3 8> o
tI
DDDpmi
AA A
0
A
A
/
J
p jTff
2
-
1 0
* A 0 ,
-
J 0
2000 4000 6000 8000 1000012000140001600018000
Milling time, s
FIGURE 1 Hydrogen content as a function of milling time for Mg+Ti37.5V25Cr37.5 alloy in hydrogen atmosphere.
20
50
60
70
80
2-Theta
FIGURE 2 X-ray diffraction patterns of mixture of Mg and Ti37.5V25Cr37.5 in a hydrogen atmosphere after (a) 1 h, (b) 2 h, (c) 3 h and (d) 5 h of milling.
Mg-based Hydrogen Storage Nano-composite
641
The hydrogen absorption is slowed down in the following 1 h. The hydrogen content increases rapidly during the period of 1 h to 3 h, and a saturated value of 6.39 wt. % is finally achieved. The capacity of hydrogen absorption of Ti37.5V2sCr37 5 alloy during the milling was also investigated separately. About 3.52 wt. % hydrogen was absorbed after 10 min milling, but no appreciated hydrogen was absorbed after 10 min. Therefore, it was considered that in the initial 10 min the hydrogen was mainly absorbed by the Ti37.5V25Cr37.5 alloy but the absorption of the rest of hydrogen was attributed to the Mg for the mixture of Mg and Ti37.5V25Cr37.5. Considering the theoretical capacity of hydrogen absorption of Mg, it is clear that Mg particles are transformed into hydrides completely under the catalysis effect of Ti37.5V25G"37.5 alloy and the mechanical energy. Phase Structure and Crystallite Size The XRD spectra as a function of milling time for the Mg-Ti37.5V25Cr37 5 under hydrogen atmosphere are shown in Fig. 2. Tetragonal P-MgH2 and hydrides of Ti37.jV25Cr37.5 are generated after 1 h milling. The relative intensity of Mg decreases and the peaks broaden drastically after 2 h milling. The reduction of relative intensity of Mg is attributed to hydriding and grain refinement. After 5 h milling, XRD patterns of Mg almost disappear and nano-sized P-MgFk and hydrides of Ti37.5V2sCr37 5 become the principal components of the composite. The patterns of Fe can be observed after 5 h milling, indicating that iron contamination may occur after long time milling. A minimum crystal size of P-MgH2 during milling exists and has been estimated as about 10 nm using the Scherer's equation. Fig. 3 shows the change of the crystal size of P-MgH2. The crystallite size decreases rapidly to about 20 nm after 1-2 h milling. Then, the size is kept stable, about 10 nm. Fig. 4 shows a SEM image of the composite particles after 5h milling. EDS analysis indicated that there is a concentration of Ti, V and Cr in the bright phases (white dots). It is reasonable to assume these bright phases as Ti37.5V25Cr37.5, which are dispersed uniformly on the surfaces of Mg particles. The formation of this ideal microstructure can be attributed to the continuous cold welding and fracture during the ball milling. The microstructure and phase composition of the composite were also examined using TEM analysis, shown in Fig. 5. The bright field image shows that the grain size of Mg is about 10 nm. This is in agreement with the XRD analysis. 50
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.
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FIGURE 3 Crystalline size of MgH2 as a function of milling time.
FIGURE 4 Scanning electron micrograph of the Mg- T137 5V25Cr37 5 composite after 5h milling.
642
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Milling time, s FIGURE 5 TEM image of the MgTi37.5V25Cr37.5 particle.
FIGURE 6 Iron and oxygen content of the milled samples as a function of milling time under l.OMPa hydrogen pressure.
Impurity Analysis Due to the structure of the mill, tiny amount of iron (from the steel balls and vial) and oxygen (from the atmosphere) may be incorporated into the milled powder. It was found that the intake of iron increased steadily but the content of oxygen changed a little with the milling time, as shown in Fig. 6. Interestingly, the content of Fe is higher under a higher hydrogen pressure, shown in Fig. 7.
Hydrogen pressure, MPa
FIGURE 7 Iron content after 5 h milling as a function of hydrogen pressure.
Milling time,!
FIGURE 8 Hydrogen content as a function of milling time for Mg+Ti37.5V25Cr37 5 alloy under different hydrogen pressure.
DISCUSSION Effects of Milling Conditions To understand the effect of hydrogen pressure during milling on the absorption kinetics, different initial pressure (0.8, 1.0, 1.2 MPa) was used. The results are shown in Fig. 8. No significant difference in hydrogen absorption rate can be observed within this pressure range. This may be due to the existence of shortly lived surface-active areas created by the contact of milling balls with powder surfaces and followed relaxation [8]. Above a critical pressure, the time interval between collisions of gas molecules with surface atoms is shorter than this relaxation time, hi this case, the
Mg-based Hydrogen Storage Nano-composite
643
absorption kinetics will be governed by the surface properties rather than gas pressure [7]. hi Figure 6, Fe element is observed in the powder due to the wear of the vial and milling balls. The increase of Fe is accelerated with milling time. This is due to the increased wear of vial and balls caused by the generation of MgH2 that has a higher hardness than the elemental powders. It is still not clear why the Fe content increases with the hydrogen pressure, as shown in Figure 7. The oxygen content in the powder is stable (Fig. 6). The possible reasons are good sealing and the reductive atmosphere created by hydrogen. Mechanism and Kinetics of Hydrogenation Based on the Johnson-Mehl-Avrami equation [9], the Avrami exponent (n) can be evaluated on the assumption that all Mg is in the form of hydride. Fig. 9 shows the relationship between reaction volume fraction and milling time where the hydrogen absorbed by Ti37.5V25Cr37.5 alloy (about 1.05 wt. %) is ignored.
0
2000 4000 6000 8000 10000 12000 14000 16000 18000 Milling time, s
FIGURE 9 Reaction fraction as a function of milling time.
0.0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9 1.0
Reaction fraction (x)
FIGURE 10 Variation of local Avrami exponent (n) with reaction fractions.
Also, it is assumed that no hydrogen is absorbed by Mg in the initial 10 min. hi principle, Avrami exponent is closely associated with nucleation and growth mechanisms [10]. Corresponding to 0-0.9 of the reaction fraction, the value of Avrami exponent (n) is in the range of 1.5-2.3, shown in Figure 10. This implies that the formation of hydrides phases is a three-dimensional growth mechanism with a reduced nucleation rate with time, which is controlled by the diffusion of hydrogen atoms. During the ball milling, the catalytic phases, i.e. Ti37.5V2sCr37.5 alloy, can be distributed uniformly on the surface of Mg particles due to continuous stirring and cold welding. By providing the diffusion passageway for hydrogen atoms and degrading the dissociation energy of hydrogen molecules breaking into atoms, Ti37.5V25Cr37.5 can accelerate the hydriding process of magnesium particles. In addition, ball milling is a nonequilibrium process that can create a specific state on the surface of the materials. A large surface-to-volume ratio and a significant amount of defects and imperfections can enhance the accessibility of a material for hydrogen penetration. As a result, the addition of T137.5V25Cr37.5 alloy and the mechanical force upgrade the diffusion capacity of hydrogen atoms, which is regarded as the key step for the hydriding process.
644
Mg-based Hydrogen Storage Nano-composite
CONCLUDING REMARKS composite was successfully prepared by reactive mechanical alloying (RBM). The grain size can be reduced to about 10 nm after 5 h ball milling. The composite has high hydrogen storage capacity and exhibits excellent absorption kinetic. The hydrogen absorption is not sensitive to the initial hydrogen pressure in the range of 0.8-1.2 MPa. The analysis of Avrami exponent indicates that the formation of hydrides phases is a three-dimensional growth mechanism with a reduced nucleation rate with time, which is controlled by the diffusion of hydrogen atom. Increase of milling time and hydrogen pressure results in a high Fe content in the composites. ACKNOWLEDGEMENTS This work was carried out under the financial support of National High Technical Research Development Program of China (No. 2001AA331010) and National Key Basic Research and Development Program of China (No.G2000067201). The authors also acknowledge the support of a Sydney University Sesqui R & D grant. REFERENCES 1. J. L. Bobet, B. Chevalier, M.Y. Song, B. Darriet, and J. Etourneau. 2002. J. Alloys Compels., 336: 292. 2. P. Wang, H. F. Zhang, B. Z. Ding, and Z. Q. Hu. 2000. J. Alloys Compds., 313:209. 3. F. C. Gennari, F. J. Castro, and G. Urretavizcaya.2001. J. Alloys Compds., 321:46. 4. P. Wang, A. M. Wang, B. Z. Ding, and Z. Q. Hu. 2000. J. Alloys Compds., 334:2243. 5. P. Wang, A. M. Wang, H. F. Zhang, B. Z. Ding, and Z. Q. Hu.2000. J. Alloys Compds., 313:218. 6. Y. Q. Hu, H. F. Zhang, A. M. Wang, B. Z. Ding, and Z. Q. Hu. 2003. J. Alloys Compds., 354:296. 7. M. A. Bab, L. Mendoza-ze' Us and L. C. Damonte. 2001. Ada mater. 49:4205^1213. 8. A.N. Streletskii, O.S. Morozova, A.B. Borunov, and P.J. Butyagin. 1996. Mater. Sci. Forum, 225227:539. 9. M. Avrami. 1941. /. Chem. Phys., 9:177. 10. J. W. Christian. 1965. The Theory of Transformation in Metals and Alloys, Pergamon Press. Oxford, p. 489.
A Tin-based Composite Solder Reinforced by Nano-sized Particulates and its Soldering Ability
1
X. P. Zhang1*, Y. W. Shi2, L. Ye1 and Y. W. Mai1 Center for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering, the University of Sydney, NSW 2006, Australia 2 School of Materials Science and Engineering, Beijing Polytechnic University, Beijing 100022, China
ABSTRACT Traditional tin-lead based solders used for packaging have recently met some serious challenges. These mainly include the increasing global concern on the environment and health, which requires to reduce or completely eliminate the use of toxic lead in most products, and the increased functionality and miniaturisation of modern optoelectronic and photonic components where the operational temperatures and stresses increase the demands of mechanical and electric properties on soldered interconnection and joints, hi this work, a tin-based composite solder reinforced by nano-sized metallic particulates was developed, and its soldering process performance, mechanical properties of the soldered joints were characterized with a comparison to a traditional tin-lead based solder. The results show that the soldering process performance of the nano-composite solder is comparable to that of the traditional 63Sn-37Pb eutectic solder, and its soldered joints are superior to the latter in creep resistance and shear strength.
INTRODUCTION Recently, traditional tin-lead eutectic systematic solders meet some serious challenges which are mainly: 1) increasing global concern on the environment and health, which is bringing regulatory and consumer pressure on the electronic and communication industry in developed countries to reduce or completely eliminate the use of toxic lead in most products; and 2) the increased functionality and miniaturisation of modern products, in particular for electronic components, optoelectronics and photonic packaging systems, where operational temperatures and stresses increase the demands of mechanical property, size and geometry stability, and other service performances on soldered joints [1-8]. Especially, there is a day-by-day enlarging contradiction between the continuously expanding consumption of the soldering materials in microelectronic/ optoelectronic/photonic packaging field where the traditional Sn-Pb family is still predominant, and the increasing global concern on the environment and health, which requires to eliminate the use of toxic lead. Therefore, the research in replacing conventional Pb-contained solders has long drawn more attention, not only from the science and engineering community, but also from the public. From technical point of view, for solders, lead (Pb) is a major constituent of traditional solders Correspondence author. Tel: 61-2-93517146; fax: 61-2-93517060; Email:[email protected]
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Composite Solder Reinforced by Nano-sized Particulates
which have very good soldering process performance and satisfied properties of the soldered joints or connections. However, toxicity is the main reason for Pb to be eliminated from many applications. The possibility of removing the constituent Pb from tin-lead based solders, has highlighted a whole series of questions associated with professional knowledge and technical expertise, as well as dissemination of existing information, materials availability, soldering technology and equipment, implementation of any new technology, added costs and competitiveness etc [4, 6, 7]. Besides the requirement for excellent mechanical properties of the soldered interconnections, the excellent processing performance of the solders is also acutely demanded. As known, Sn-Ag and Sn-Sb alloy systems are the most likely candidates for the substitution of SnPb solders. To improve the processing performance of the lead-free solders, some surface-active elements have been considered, for example, Ag, Bi, and In, which have been employed as the promising constituent alloys in lead-free solders in some recent researches [9-13]. Currently in optoelectronics and photonics packaging, Au-based solders (such as a binary eutectic solder 80Au-20Sn, with a melting-point of 278 °C) are widely employed to solder the joints or interconnections to ensure the dimensional stability (or alignment) of the devices or systems [13]. With offering excellent creep resistance, however, the high soldering temperatures of these solders can deteriorate the properties of optical fibers and other optoelectronic or photonic components besides the high cost of Au-based solders. Lead-free nano-sized particulate reinforced solders have been expected to meet above requirements, in particular the expected anti-creep property which is critical and essential for optoelectronics and photonics devices due to an acute demand of high size stability. This work aims at developing a tin-based creep-resistant composite solder reinforced by nano-sized metallic particulates, and comparing its soldering process performance, mechanical properties of the soldered joints with a traditional tin-lead eutectic solder. SOLDERS DEVELOPMENT AND ESTIMATION The base alloy of the solder is tin-lead powder (with the average size of 43 |J,m), but with a less Pb content. The f.c.c. metal nano-sized particulates (Cu or Ag powders, with a nominal size of 25-35 nm) were mixed with the alloy solder with a volume fraction of 2-4%. The mixed powders (matrix alloy powder and nano-particulate) were then mixed with the flux to form a paste solder. The paste may be cold compressed to form different shapes. The melting-point of the nano-composite solder was measured as 183-188 °C. Wetting Performance of Solder The wetting ability of a solder on a substrate is very important for its soldering process. In general, a satisfactory wetting of a solder on the substrate results in a good flowing and joint-gap-filling capacity (i.e., capillarity capacity), and consequently the soldered joints would have satisfactory formation and integrity as well as the mechanical properties [14]. The wetting ability was estimated by a standard method [15], that is, by measuring the wetting area of a given weight solder on a square copper plate with the side length of 40 mm and a thickness of 0.2 mm. The wetting tests were carried out in a furnace in open-air condition at different temperatures and dwell times. The wetting area of the solder on copper plate was measured by a planimeter. Mechanical Property Tests Mechanical property tests include: shear strength and creep lifetime (or creep
Composite Solder Reinforced by Nano-sized Particulates
647
resistance) of the soldered joints. The joint specimen used for shear strength test consisted of two identical copper plates. Each plate had a geometry of 80 x 25 x 1.5 (length x width x thickness, mm). Two plates were soldered with an overlapping length 10 mm and a joint gap 0.10 mm. The joint specimens were soldered at a temperature of 230 °C with a dwell time 5 min in a furnace. Mechanical tests were performed using an Instron 5567 test machine with a loading speed of 0.5 mm/min at room temperature. The dog-bone miniature samples were used to evaluate creep resistance of the solders as shown Figurel (the soldered joint is in the middle). The creep tests were conducted in the Dynamic Mechanical Analyzer (DMA 2980 model) with the following testing parameters: testing temperature = 20 °C, and a constant tensile stress =12 MPa.
FIGURE 1 The dog-bone joint specimen (copper) used for creep property test
RESULTS AND DISCUSSIONS Wetting Performance of the Solders The wetting tests were conducted at four temperatures, 200, 215, 230 and 245 °C, respectively. The typical observation of the wetting specimens for the nano-composite and 63Sn-37Pb solders are shown in Figure 2. The measured wetting areas increase with the soldering temperature increasing as illustrated in Figure 3. In Figures 2 and 3, it can be seen that the wetting performance of the nano-composite solder is comparable to the 63Sn-37Pb solder, being slightly lower by less than 5% in terms of wetting area.
(a) Nano-composite solder
(b) 63Sn-37Pb solder
FIGURE 2 Wetting morphologies of the nano-composite and 63Sn-37Pb solders (230°C, dwell time 20S)
Composite Solder Reinforced by Nano-sized Particulates
648 140
-Nano-composite solder -Sn-Pb solder
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100
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80
60 180
200
220
240
260
Temperature [°C] FIGURE 3 The results of wetting areas versus soldering temperature for both solders
Strength of the Soldered Joints A comparison of shear strength of the joints soldered by both the nano-composite and 63Sn-37Pb solders is shown in Table 1. Clearly, the joints soldered by the nanocomposite solder have higher shear strength than the 63Sn-37Pb solder by an increase of -30%. This manifests that nano-sized particulates do enhance the tin-lead based solder by the mechanisms of fining grain size and precipitate dispersion alloy strengthening. TABLE I Comparisons of mechanical properties of the joints by two solders Mechanical properties of the joints Shear strength of joints (MPa)
Nano-composite solder
63Sn-37Pb solder
40
30
Creep life of the joints — time to joint failure (average, hour)
368
Relative creep lifetime (over the 63Sn-37Pb)
52
The grain size has a significant influence on solder strength. As known, for most metals, the yield strength, uy, increases monotonically with a decrease in grain size (or average grain diameter), D, as expressed by Hall-Petch Equation [16]: •D
(1)
where G0 is friction stress opposing dislocation motion, and k a material dependent constant (also called unpinning constant, measuring the extent to which dislocations are piled up at barriers). The gain size for the nano-particulate reinforced composite solder is about 102 [im, and 146 urn for the 63Sn-37Pb eutectic solder which has a typical cast microstructure. In addition to the fined grain size effect in the nano-composite solder, the nano-sized particulate reinforcements with a uniform dispersion also provide effective impediment to grain boundary sliding and dislocation movement. These all result in an increase in strength of the nano-composite solder.
Composite Solder Reinforced by Nano-sized Particulates
649
Creep Property of the Soldered Joints A comparison of the creep property of the joints soldered by both the nanocomposite and 63Sn-37Pb solders is also shown in Table 1. It is clear that the joints soldered by the nano-composite solder have much longer creep lifetime than 63Sn-37Pb solder, i.e., more than 50 times longer than the latter. After creep failure/fracture, the fractographies of the joints were observed by an SEM, typically shown in Figure 4. It can be seen that a progressive shear deformation occurred as the main creep fracture mechanism. Essentially, creep is a slow rate plastic deformation in materials, and the plastic deformation in materials occurs actually by sliding blocks of the crystal over another along the crystallographic slip planes. The slip is the result of the dislocation motion, which in turn is because of the lattice imperfection of the material. The nano-composite solder provides better creep resistance without sacrificing ductility. The mechanism of enhancing creep resistance of the solder joints is that the fine (i.e. nano-sized) particulates with a uniform dispersion can provide effective resistance by impeding the grain boundary sliding and dislocation movement. Moreover, the nano-size particulate reinforcements would stabilize the solder microstructure during service, in particular for joints serviced in the thermo-mechanical coupling condition. As the above mentioned, for polycrystalline materials, one important factor influencing their mechanical properties, such as yield strength and fatigue performance as well as anti-creep property, is the grain size. These effects would rather be the effects of grain boundaries. The grain size is normally defined by the average grain diameter D within a random area, and the ratio of grain-boundary surface S to the volume V is related to this average diameter/) [16], and expressed by following:
£--?-
(2)
(2) V ~D Clearly, a decrease in grain size results in an increase in the left hand side of Eq.(2), that is, an increase in specific grain boundary surface. This actually means an increased impediment to dislocation motion and grain boundary sliding. The nanoparticulate reinforced composite solder has a smaller grain size than 63Sn-37Pb solder (by less than 43%), correspondingly, it is superior to the latter in creep resistance. It should be indicated that this study is a preliminary attempt at developing nanocomposite solders with excellent creep property and satisfactory processing performance. The optimization on solder fabrication processes and solder composition design, as well as an in-depth characterization of solders properties, are still needed.
I •
(a) Nano-composite solder joint
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(b) 63Sn-37Pb solder joint
FIGURE 4 Fractographies of soldered joints after creep failure/fracture
is
650
Composite Solder Reinforced by Nano-sized Particulates
CONCLUSIONS 1. A tin-based composite solder reinforced by nano-sized metallic particulates has been developed, which has a comparative processing performance with the traditional 63Sn-37Pb eutectic solder, in terms of wetting ability or fluidity. 2. The nano-sized particulate reinforced composite solder is superior to the 63Sn37Pb eutectic solder in creep resistance and joint shear strength. 3. For the nano-sized particulate reinforced composite solder, the mechanism of enhancing creep property of the solder is that the uniformly dispersed fine particulates provide effective impediment to the dislocation movement and grain boundary sliding.
ACKNOWLEDGEMENT Authors wish to thank Prof. Lutz Dorn and Dr. Shiva Shrestha in Institute of Materials Technology at Technical University Berlin, Germany, for their help in materials preparation and experiment. REFERENCES 1. 2. 3.
4. 5. 6. 7. 8.
9.
10. 11. 12.
13.
14. 15. 16.
Plumbridge, W. J. 1996. "Solders in electronics," Journal of Materials Science, 31:2501-2514. Shangguan, D. and Gao, G.1997. "Lead-free and no-clean soldering for automotive electronics," Soldering and Surface Mount Technology, 26: 5-8. Hua, F. and Glazer, J. 1997. "Lead-free solders for electronic assembly, Design and Reliability of Solder Interconnections", Mahidhara, R. K., Frear, D. R., Sastry, S.M.L., Murty, K. L., Liaw, P. K. and Winterbottom, W., Eds., The Minerals, Metals and Materials Society, Pennsylvania, USA, 65-73. Richards, B. P., Levoguer C. L., Hunt, C. P., Nimmo, K., Peters, S. and Cusack, P.1999. "Lead-free soldering-an analysis of the current status of lead-free soldering," Rept, Dept. Trade & Industry, 1-80. Bradley, E. and Hranisavljevic, J. 2001. "Characterization of the melting and wetting of Sn-Ag-X solders," IEEE Transactions on Electronic Packaging Manufacturing, 24 (4): 255-260. Chen, Z. G., Shi, Y. W. and Xia, Z. D.2002. "Study on the microstrucutre of a lead-free solder alloy Sn-Ag-Cu-RE and its soldered joints," Journal of Electronic Materials, 31(10): 1122-1128. Tu, K. N., Gusak, A. M. and Li, M. 2003. "Physics and materials challenges for lead-free solders," Journal of Applied Physics, .93: 1335-1353. Dorn, L., Herbert, F. und S. Shrestha. 2000. "Pb-free solders under the laser beam," Proceedings of System Integration in Micro Electronics, Exhibition & Conference, Nuernberg, Germany, 27-29 July 2000,349-357. Habu, K., Takeda, N., Watanabe, H., Ooki, H., Abe, J., Saito, T., Taniguchi, Y. and Takayama, K. 1998. "Novel Lead-Free Solder Alloys for Electronic Assembly," Proceedings of Conference on Comprehensive Approach for the Recycling and Eco-efficiency of Electronics (CARE) — Innovation'98, Vienna, Austria, 16-19 November 1998, 125-128. Bath, J., Handwerker, C. and Bradley, E. 2000. "Research update: Lead-free solder alternatives," Circuits Assembly, May 2000, 31-40. Bradley, E. and Hranisavljevic, J. 2001. "Characterization of the melting and wetting of Sn-Ag-X solders," IEEE Transactions on Electronics Packaging Manufacturing, 24 (4): 255-260. Zhang, X. P., Wang, H. and Shi, Y.W. 2003. "Influence of minute amount of elements Bi, Ag and In on surface tension and soldering process performance of tin-lead based solders," Journal of Materials Science: Materials in Electronics, 15 (in press). Shi, Y.W. 2000. "Creep-fatigue resistant solder for optoelectronic materials joining," China-European Union Workshop on Materials Strategies for the New Millenium, Beijing, China, 8 December 2000, 39-43. Lancaster, J. F., 1980. Metallurgy of Welding, 3rd Ed., George Allen & Unwin Ltd., London, 87-93. GB11364-89. 1989. "The standard test method on wettability estimation of solders," the National Standard of China. Dieter, G. E. 1986. Mechanical metallurgy. New York: McGraw-Hill, 3rd Ed.
Suitability of Metal Composite Suspensions for Injection Moulding Faiz Ahmad* Mechanical Engineering Dept., Universiti Teknologi Petronas 31750 TRONOH, Perak, Malaysia
ABSTRACT Flow properties of metal composite suspensions have significant impact on the fibre orientation during mould filling. Flow properties are strongly influenced by fillers concentration. The results presented in this paper relate to the flow properties of a composite suspension of aluminium powder and glass fibres compounded into a sacrificial polymeric binder. A range of aluminium mixes and composites were investigated over a wide shear rate range experienced during the Injection Moulding process. Aluminium composite suspensions were prepared by replacing glass fibres for aluminium powder .An optimum level of fibre content without deteriorating viscosity of the mix is determined. The effect of moulding temperature on the flow behaviour of aluminium composite mixes was also investigated.
INTRODUCTION Favorable strength to weight ratio of aluminium composites results into many applications in automotive and defence industries [1]. The orientation of fibres maximizes the mechanical properties [5]. Conventional techniques [2-4] to control the orientation of fibres are limited thereby cannot produce complex geometry components of metal matrix composites containing fibres [7]. Mechanical properties of aluminium and its alloys can be enhanced by controlling fibre orientations in preferred directions [5]. Powder Injection Moulding is a potential processing technique [6] for fabrication of complex shape components of metal matrix composites containing aligned fibres [7]. For the injection moulding process exerting a shear rate range 100-3500 Sec ~', viscosity number in the 100-1000PaS would be expected. Higher viscosity suspension can also be injection moulded and this depends on the capacity of the moulding machine and geometry of the part [12]. In order to study the rheological properties of aluminium composites [9], prior study incorporated the use of sacrificial polyner binder into aluminium compounds. Chong's equation [11] was used to optimize the volume fraction of aluminium in composites. Any change in viscosity of aluminium compounds with increasing volume fraction of powder in the mix was compared with theoretical viscosity number [8-10, 13, 18, 19 & 21]. The flow characteristics of aluminium mixes and composites were evaluated using empirical power equation [12].
* Corresponding Author, Email: [email protected]
652
Suitability of Metal Composite Suspensions for Injection Moulding
This led the use of fibres instead of powder for composite mixes. In our study, a critical volume fraction of fibres in aluminium compound was determined. An interaction between powder-fibre and their arrangement was corroborated with the work presented by Thomas and Milewski [16-17]. The effects of temperature on the viscosity of aluminium composites were determined and interpreted with the help of published results [15]. EXPERIMENTAL MATERIALS SEM photograph of argon atomized aluminium powder of grade-CPA supplied by Aluminium Co.West Midland England is shown in Figure-1 and its particle size distribution was 8-45 um. Particle shape of this powder is spheroidal and hence it is expected to offer appreciable resistance to the flow of mixes.
TABLE I: Compositions of aluminium mixes Compound Powder vol % NF60 60 NF65 65 NF70 70 NF75 75 FC1 58.5 FC2 55.25 FC3 52
Powder Fibre wt.% vol. % 81.6 84.6 86.2 89.9 76.5 6.5* 72.46 9.75* 68.2 13.0*
Binder vol.% 40 35 30 25 35 35 35
:
Glass fibre 20 fiai diamtere & 5.0 mm long, p: 2.55 gm/cc, supplied by Pilkington,UK NF- mix contains no fibres and FC mixes are with fibres.
The polymeric binder system selected for incorporation of fibres consist of polypropylene -23.45 vol.%, microcrystalline wax -7.7 vol.% and strearic acid -3.85 vol.% as flow aid in finally selected composite mix in our study. The binder volume fraction was 35 percent and remaining 65 percent was powder and fibres volume loading. All test mixes shown in Table 1 were prepared using co-rotating twin screw extruder model Betol TS 40. The temperature profile between nozzle and feed zone was set at 210 "C-190-180-170 °C .The speed of screws was held constant at 60 rpm throughout the compounding trials. Two groups of test mixes presented in Table 1 were utilized throughout research study. EXPERIMENTAL PROCEDURES
FIGURE 1 SHM micrograph ol" aluminium powder X1000
While performing injection moulding experiment at 215 °C, Davenport Capillary rheometer was used to measure the flow characteristics. A schematic diagram of Davenport Capillary Rheometer is shown in Figure2. In order to collect the data for the shear rate range of 100-3500 Sec"1, a die of dimensions 1.5 mm diameter and 35 mm long was fitted to the bottom of the barrel and allowed to heat the barrel to the test temperature 215° C.
Suitability of Metal Composite Suspensions for Injection Moulding
653
The barrel was filled with test material and slightly pressed with piston and allowed for approximately 10-15 minutes to attain equilibrium temperature throughout the batch. No back flow was ensured to piston then extruded the test batch. Dynisco pressure transducer, PT 422-10M-6118 was used to monitor the pressure drop across the die. Power driven rheometer piston can be operated at various speeds ranging from 5mm/min to 250mm/min to achieve shear rate between 71 Sec" to 3500 Sec"1. However, shear rate 143 Sec"1 was selected for analysis considering a stable flow rate through the capillary die. Pressure drop across the die was calculated for viscosity of the mixes. Volumetric flow rate was calculated using following formula: barrel Q :n R2V Where,R= radius of the piston=9.525 mm, V= speed of piston (mm/min). presure Shear rate was calculated from the transducer capillary following relationship; die y: 4Q/7I r3, retaining where r: radius of die (mm). Viscosity collar was calculated and log(viscosity) vs log (shear rate) were plotted and slop n-1 was calculated to find out flow index to determine the flow index for FIGURE 2: Schematic arrangement of each composite mix. Davenport Capillary Rheometer (DCR) used in study.
RESULTS AND DISCUSSION Confirmation of Volume Loading The volume fractions of ingredients in the mixes were crosschecked before further work was carried out. The concentration of the binder was determined by removing it in an oven at 500°C. The volume fraction of aluminium powders were measured using weight-volume relationship at various stages of the experiment and listed in Table 2. The data indicated that it was maintained within ± 0.45% during compounding. TABLE II: Volume % of Aluminum powder in Test Mixes at various stages Compound NF60 NF65 NF70 NF75 FC1
FC2 FC3
compounding (% Wt) 81.61 84.33 87.29 89.75 84.40 84.21 86.01
Rheometer (%wt) 81.52 84.11 87.01 89.62 84.31 84.23 85.99
mounding(%wt)
powder (%vol)
81.52 84.67 86.99 89.50 84.35 84.19 85.12
59.81 64.53 69.46 74.61 64.58* 64.65* 65.16*
' Volume loading required in all compositions at all stage was 65%
654
Suitability of Metal Composite Suspensions for Injection Moulding
Flow Properties of Aluminium Compounds The volumetric flow data for test mixes in the shear rate range of 100-3500 Sec "' was collected using rheometer. All the test mixes were used to generate data and flow characteristics was evaluated using an empirical power law equation used for Newtonian fluids [18]:
JJ =K.7 n " 1
(1)
where, rj = viscosity of fluid PaS, y = shear rate Sec l' ,K= constant and n= flow index. When the value of flow index; n< 1, occurs when fluid is Pseudoplastic where viscosity decreases with an increase in shear rate, and n > 1 indicates dilatant type of flow where viscosity is not affected by the shear rate. The shear rate viscosity data of aluminium compounds is illustrated in Figure-3 shows that viscosity of test mixes increases steadily up with the concentration of powder. Mix "NF75" did not have desired flow properties and hence dropped from further studies. The flow index was evaluated using equation 1 and it varies in the range of 0.6-0.7.
• Binder
10000
ANF60
1000
• NF65
100 10-
XNF70
•••••••
• NF75
1
1000
2000
3000
4000
Shear Rate (1/sec)
FIGURE 3: Viscosity shear rate results of aluminium compounds at 215 °C
Relative Viscosity of Aluminium Powder Compounds The relative increase in viscosity of test mixes was calculated by dividing the available viscosity results of aluminium mix by binder -18 PaS, which is, determined at a shear rate 143 Sec" . Figure 4 indicates the plot of relative viscosity number v/s volume percentage of aluminium powder. Equation 2 [12] is used for the calculation of relative viscosity; Vr = r]m I Vb (2) where ??r = relative increase in viscosity, r/m = viscosity of metal powder and rjb = viscosity of polymeric binder. Using Chong's equation [11], it was noticed that the relative viscosity of mix NF70 corresponds to the theoretical relative viscosity number calculated at powder volume fraction 0.705. The powder under investigation showed a maximum volume fraction 0.76,while Chong's equation was valid up to 0.74. This was attributed to a wide range of particles (8-45 micrometers) in aluminum powder. The presence of large particles provide ample voids to be occupied by small ones. This criterion was used by Chong et.al and it fits our case. Brodnyan [13] and Chong et.al [14] used equation for mono sized powder particles for predicting the viscosity, therefore, these are not applicable in our case.
Suitability of Metal Composite Suspensions for Injection Moulding
655
Flow Behaviour of Aluminium Composite Mixes Viscosity shear rate results for composite mixes are shown in Figure 5. It illustrate that the viscosity of FC1 and FC2 increased by 20% and 40% respectively compared to the viscosity of NF65 without fibre at the shear rate of 143 Sec -1 . This increase in viscosity is due to the substitution of glass fibres by aluminum powder. However, composite FC3 did not 90 ~~ ————— —£• show a proportional increase in A Experimental data viscosity. Re-alignment of fibres and M 70 their breakage take place during the 8 60 • Chong's theoretical flow of viscous mass through narrow 50 o 40 channels of moulding dies. This factor 5 30 • directly affects the viscosity of the mix. Heavy loading of fibres in FC3, &• 10 •i B 0 • • • • • resulted into higher breakage of fibres, 0 20 40 60 80 which maintained favorable aspect ratio. Due to this reason, the viscosity Metal Powder (%vol) of FC3 did not increase in proportion to its fibre contents. Steadman [12], FIGURE 4 Relative increase in viscosity vs Brodnyan[13] Chung & Cohan [14] powder volume fractio had made similar observations. r
£ L
Determination of Critical Volume loading of Fibres in Aluminium Composite Mixes The truly relative increase in viscosity of FC1, FC2 & FC3 at a shear rate of 143 sec "' v/s fibre percentage is plotted in Figure 6 .It is noticed that relative viscosity of mixes increased up to an optimum value of 13 volume % fibre additions and then tapered off. Milewiski [17] and Starr[16] had studied filled particle packing model. Milewiski [17] studied a model consisting of 27 vol.% powder and balance fibre. The later is 5.5 times more than FC3 mix and hence too remote fitted our study. Starr, s study involved the use of long fibres and particle, and, indicated randomly oriented long fibres provide ample free space for small particles. Composite mixes contained 5 mm long fibres with an aspect ratio of 250. During compounding and palletizing, fibre lengths in FC1, FC2 and FC3 mixes reduced to 1.7,1.65 and 1.5 mm respectively. The reduced fibre length resulted in increased volume of fibres causing a decrease in the packing density. Due to heavy loading, the fibre length reduced the most in FC3 and resulted into lower aspect ratio. This number was critical and further reduction of aspect ratio did not increase the viscosity. Several empirical equations [13,18] were used for predicting the viscosity of fibre containing suspensions, but these equations did not include the metal powder as ingredient and hence not applicable directly to the current study. Temperature Effects on Viscosity of Composite Mixes The rheometry experiments showed that melt temperature within the die was little degree below the set temperature of 215°C. This occurred because the mix absorbed the heat produced due to shearing of melt. Gibson and William [15] had worked with the mix containing - CaCO3 and glass fibre in resin, and, they also did not observe
656
Suitability of Metal Composite Suspensions for Injection Moulding
any increase in the melt temperature. Our test mixes contained aluminium, hence heat generated due to mixing was quickly dissipated to the surroundings. Effect of temperature on the viscosity on FC2 mix was tested at 200-225 °C and results are shown in figure-7. Slight increase in viscosity and melt temperature indices with rise in temperature is observed. Activation energy as a function of temperature was also evaluated using Arrhenius equation: E = A.e(~ ' where, A = constant, R= Universal gas constant, E= Activation energy and T= temperature, K. The viscosity data at a shear rate of 143 Sec"1 was plotted against the reciprocal of test temperatures 200 °C, 215 ° C, 225 °C and is illustrated in figure 8.
FIGURE 5 Viscosity shear rate results of composite mixes at 215 °C
FIGURE 6 Relative increase in viscosity of composite mixes vs fibre volume fraction
It is in agreement with data plotted in Figure -7. The activation energy was found to be dependent up on viscosity of composite melt as per Mohn and Evans[19] and Billiet[20]. The viscosity results of metal composites suspension illustrated in Figure7 showed that temperature had very little effect on the flow properties of the mixes because an appreciable amount of heat was absorbed by aluminium powder. 10000
1200 _ 1000
S. 800 £
600 400 200 0
10 100
1000
10000
Shear Rate (1/sec)
FIGURE 7 Viscosity-shear rate relationship for composite mix FC2 at 200-225 °C
0.0019
0.002
0.0021
0.0022
Temperature (1/K)
FIGURE 8 Viscosity vs temperature results of composite mixes.
CONCLUSIONS With the help of rheological properties of metal composite mixes, an optimum mix containing 65 vol.% aluminium powder-35 vol.% binder was developed. Composite blend of aluminium powder with 13 vol.% fibre was found to be critical. Reduction in fibre length during processing did not increase its viscosity and blend
Suitability of Metal Composite Suspensions for Injection Moulding
657
was successfully injection moulded. The aspect ratio of fibre used for composite mix and its alignment in the matrix affected the viscosity of composites. The flow characteristics of composite mixes at 200-225 °C were found to have little temperature effects. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20. 21.
Metal Matrix Composites: Emerging Tech No.20 publisher, Insight Englewood Inc. N J USA Berghezan,A Sep. 1972, 200 Girot,A,G MJ. Quenisset and R.Naslain: composite Sci &Tech.30(1987),155 Clyne,T.W and M.G.Bader : 5th ICCM, W.C Harriganged San Diego, (1985), 745 Homeny, J L.V Wallace and K.F.Mattison, Ceramic Bulletin,66 (1987) German,R.M Mat.Sci & Engg. 107A (1989), 107 Ahmad,F and MJ.Bevis: Advanced materials. ISAM-95 Islamabad, Pakistani 1995,279 Mutsudy,B.C Ind. Res.& Dev. July (1983),76 Ahmad, F and MJ.Bevis Advanced materials,ISAM-97, pp27-31 Islamabad, Pakistan Eiler.H Kollied97, (1941) ,313 Chong, J.S E.B. Christiansen and A.D Baer, appl. Polym.sci. 15 (1971),369 Evan J.R.G, and S. Steadman J.Mat.Sci 25 (1990), 1833 Brodnyan J.G: Trans.Soc. Rheology iii (1959),61 Chung,B and C. Cohan Polym. Engg. & Sci 25 (1985) ,16 Gibson, A.G. andG.A Williamson: Polym. Engg. & Sci. 25 (1985), 965 Thomas Starr, L: Ceramic bulletin 65 (1986)12930 Milewski, J.V: 29th, Am. Tech. Conf. (1974) ,1 Kitano,T ,T Tataoka and T. shirota: Research Institute of Polymer & Textile, ibarabi (JPN) Edirisinghe,MJ and J.R.G Evans: J.Mat.Sci 22 (1987) ,269 Billiet,R: Powder Met. 41 (1985) ,723 Paven suri,Sundar V. atre, R.M German, Jupiter P.de Souza , Materials Science and Engineering A 356 (2003) 337-344
Effect of Intermetallic Volume Fraction on the Mechanical Properties of Intermetallic/Metal Micro-laminated Composites Hee Yeoun Kim, Soon Hyung Hong 373-1 Kusong-dong, Yusong-gu, Daejeon 305-701, KAIST, Korea Dong Seok Chung 110, Chungang-dong, Changwon, 641-030, Changwon Polytechnic College, Korea Manabu Enoki 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Univ. of Tokyo, Japan
ABSTRACT The effects of intermetallic volume fraction on the mechanical properties of micro-laminated NiAl/Ni composites have been investigated. Two types of intermetallic/metal micro-laminated composites having various intermetallic volume fractions were fabricated through reaction synthesis using element foils. The difference of microstructure caused two types of micro-laminated composites had reverse dependence of tensile strength on intermetallic volume fraction. From the relationship between characteristic multiple crack spacing normalized by intermetallic thickness during tensile loading and relative strength of each phase, it was concluded that the reverse tensile behavior of micro-laminated composites were brought from different fracture strength of brittle intermetallic phase. The fracture toughness results by the SENB (Single Edge Notched Beam Bending) test showed R-curve behavior with upward curvature based on LSB (Large Scale Bridging) condition. Bridging stress based on LSB condition was estimated to 250~300MPa that was about three times of yield strength of unconstrained pure Ni foils. Transformation offracturemodesfrommultiple cracking to single cracking when the intermetallic volume fraction increased was explained by combined model of shear lag and LEFM(Linear Elastic Fracture Mechanics). The stress field changes according to intermetallic volume fraction were analyzed by FEM and these results were in good agreements with experimental results.
INTRODUCTION The intermetallic/metal laminated composites were suggested by various researchers to improve the brittleness of intermetallic at ambient temperature.[l] These composites offer an attractive combination of mechanical properties distinct from the separate constituent phases, e.g. high toughness of the metal coupled with low density, high oxidation resistance and high strength at elevated temperature of the intermetallic.
* Corresponding author, Prof., Dept. of Mat. Sci., KAIST, 373-1 Kusung-dong Yusung-gu Daejeon Korea, Fax: +82-42-869-3310, E-mail: [email protected]
Intermetallic/Metal Micro-laminated Composites
659
Reaction synthesis has been used for the fabrication of intermetallic/metal laminated composites and had many advantages such as near-net shaping, crucible-less processing of materials with high melting point, microscopic compositional homogeneity and low cost compared with conventional processing using melting and casting methods. It has been successfully manufactured by alternatively stacking commercial elemental foils such as Ni, Ti, Nb, Fe, and Al.[2] Generally, microstractures obtained by reaction synthesis have composition gradient along the direction perpendicular to stacking and these anisotropic and heterogeneous microstructure can highly affect the mechanical properties of intermetallic/metal micro-laminated composites. There are little published experimental data and theoretical approach on mechanical behavior of intermetallic/metal micro-laminated composites due to the difficulty of strength measurement and composition gradient of intermetallic layer. In this study we examined tensile properties and R-curve behavior of NiAl/Ni micro-laminated composites. Intermetallic fracture strength was deduced from the analysis of multiple cracking behavior during tensile loading of micro-laminated composites. Fracture toughness improvement due to the bridging of ductile metal layer was examined quantitatively based on LSB model. Fracture mode transition from multiple cracking to single cracking according to intermetallic volume fraction in NiAl/Ni micro-laminated system was experimentally investigated and explained by combined model of LEFM and shear lag. The stress field change around crack tip bringing in fracture mode transition was analyzed by FEM using SENB specimen geometries as a function of intermetallic volume fraction. EXPERIMENTAL Two types of micro-laminated composites using commercially pure(99.0% min.) Ni and Al foils were fabricated. One was made by using various Al thicknesses with constant Ni thickness(lOOnm) and the other was made by using various Ni thicknesses with constant Al thickness(lOnm). These foils were alternatively stacked and heat-treated by three thermomechanical steps.(diffusion bonding; reaction synthesis; post-heat treatment) The volume fraction of each phases in laminated composites were analyzed by image analyzer through optical microscope. By EDS and XRD to identify crystal structure and chemical composition of each constituent on the microstructure analysis, lOO/anNi specimens had the phase sequences of Ni3Al/Nio.5gAlo.42/Nio.9Ali.i/Nio.58Alo.42/Ni3Al and lOjumAl had the phase sequences of Ni3Al/Nio.58Alo.42/Ni3Al. Quantitative analysis of acquired micro-laminated composites is summarized in Table I. Tensile test specimens were machined from the heat-treated micro-laminated composites with dimension of 5x5x50(WxTxL, mm) by electrodischarge wire cutter. Lateral sides of micro-laminated composites were mirror-surface polished by 0.25/an diamond paste to investigate multiple cracking during tensile loading. Tension tests were performed in Instron 5583 static testing machine with loading speed of 0. lmm/min. Strain was measured by extensometer with the gage length of 10mm. Fractured surface of each specimens were examined by SEM. Specimens for fracture toughness tests had dimension of 4x4x30(WxTxL, mm). Every sides of crack arrester direction were mirror polished by 0.25//m diamond paste. Notch was introduced by diamond blade with thickness of 100/im in the crack arrester direction of micro-laminated composites and the crack root radius was about 10~50/^m. R-curve tests were performed with manually loaded 3-point bend tester in the SEM(Hitachi). Crack length was directly measured during loading. FEM analysis using quadratic SENB geometry was conducted by ANS YS program.
Intermetallic/Metal Micro-laminated Composites
660
TABLE I Summarized results of irdcrostructures of micro-laminated composites Initial Thickness(^m) Ni 100 20 50 75
Intermetallic Volume Fraction
Al 100 50 25
Main Phases
0.55 0.45 0.35 0.63 0.34 0.27
10
N10.9AI1.1 Nio.58Alo.42
Ni3Al Nio.5gAlo.42
Ni 3 Al
RESULTS AND DISCUSSION Tensile Properties When the intermetallic volume fraction increases as shown in Figure 1, tensile strength of two types varies inversely each other due to the difference of intermetallic strength. This could be explained by the characteristic multiple cracking during tensile loading of micro-laminated composites as shown in Figure 2(a). Generally speaking, shear-lag condition is satisfied at the interface of ductile metal and brittle intermetallic and normalized multiple cracking distances are represented as follows;[3] _ -v 3
IR
(1)
2 CT()
tlM
where lR,tiM><7iM>CTo ^e average multiple cracking distance, intermetallic thickness, intermetallic fracture strength and unconstrained yield strength of metal. Knowing the experimentally measured normalized multiple cracking distance and unconstrained yield strength of Ni foils, normalized multiple cracking distances were plotted on theoretical curve(Figure 2(b)) and intermetallic fracture strengths were calculated to 160~210MPa for type 1 and 360~560MPa for type 2. Other researcher's results were also displayed for comparison. Therefore intermetallic fracture strength of type 2 was higher than two times of type 1 and this must have changed tensile behavior of micro-laminated composites according to intermetallic volume fraction.
j , Ni/10pmAI - a- E.L.(%), 100>imNi/AI - O - E.L(%), Ni/10nmAI a - -Q,.
I
10 ro
(/) 300
0.3
0.4
0.5
0.6
Volume Fraction of Intermetallic
FIGURE 1 Tensile strength and elongation of intermetallic/metal micro-laminated composite
Intermetallic/Metal Micro-laminated Composites
661
Cal. by Hwu and Derby Al/Alumina, tm/tc=6.0 Cu/Alumina, tm/tc=6.0 Ni/Alumina, tm/tc=2.3 1Q0,imNi/AI Nr/10umAI
3: '- ' 0.0
0.2
0.4
0.6
0.8
1.0
"Ai
FIGURE 2 (a) Lateral view of tensile tested specimen showing multiple crack and (b) relationship between normalized multiple cracking distance and ratio of intermetallic to unconstrained metal yield strength.
Fracture Properties R-curve Behavior In Figure 3(a), R-curve behaviors of intermetallic/metal micro-laminated composites show upward curvature whish is typical in LSB condition. From these experimental observations, it is apparent that the source of the R-curve toughness in the micro-laminates is associated principally with the crack-tip shielding that results from the bridging of intact Ni layers in the wake of the crack. Quantitatively, the contributes to the toughness due to crack bridging can be obtained by LSB model as follows;[4]
(2)
AK = 2[G(x,a,w)o(x)dx h
where o(x) is the traction as a function of distance x behind the crack tip, G(x, a, w) is the weight function, a is crack length from edge, and b is crack length from edge at the crack initiation. o(x) is related to the constrained flow stress of the metal reinforcement and the assumption of constant traction function appears to be reasonable. [4] Using the crack-initiation toughness of Ko and geometric weight function, G(x,a,w), the bridging stresses are calculated as 250~300MPa which is about three times of unconstrained yield strength of metal.(90MPa)
• \
-
A A
" 8*8 "
Aa(mm)
0 A
• \
Cal. 100nmNi/AI Ni/10jimAI Al/Alumina Cu/Alumina Ni/Alumlna
j Multiple Cracking | 2v
A
9
s
A
IT——
H
i
8_
J Macr scopic Cracking |
Vim
FIGURE 3 (a) R-curve behaviors and (b) fracture mode changes of intermetallic/metal micro-laminated composites
Intermetallic/Metal Micro-laminated Composites
662
SOjimNlBOiiinNW
\
Normalized distance from crack plane(x/tj
Normalized distance from crack plane(z/tj
FIGURE 4 Calculated (a) c x and (b) a z around crack tip by FEM.
Fracture Mode Fracture modes of micro-laminates are transformed from the multiple cracking to the macroscopic cracking depending on the intermetallic volume fraction. As supported by Hwu and Derby's results, crack-tip stress and crack-wake stress will depend on the thickness ratio of intermetallic and metal and determine the fracture mode.[3] Figure 3(b) represents the results of experimental fracture mode plotted on the fracture map calculated by combined model of shear lag and LEFM. Experimental fracture mode follows well the predicted fracture mode. The stress field around crack tip was analyzed by FEM. From the elastic stress field displayed in Figure 4, ox and oz at the metal layer in front of crack tip were investigated. In case of 10jMnNi/20/zmNiAl specimen, az along the distance normalized by intermetallic thickness is nearly constant and a x is the highest than the others at crack tip. This stress condition will make single fracture easily. Li other words, other two specimens have peak o x at shorter normalized distance from the crack plane and lower ax at crack tip than that of 10//mNi/20janNiAl specimen and these will make multiple cracking dominant. As a result, FEM results were well matched with analytical results given as Figure 3(b). CONCLUSION Microstructures of two types of micro-laminated composites fabricated by reaction synthesis showed the composition gradient and different volume fraction depending on initial foil thickness ratio. This different microstructure led to the reversed tensile strength behavior according to intermetallic volume fraction. Multiple cracking during tensile loading of micro-laminated composites could be related to the shear-lag condition satisfied at the intermetallic/metal interface and the tensile strength behavior was explained very well. R-curve test results showed increasing fracture toughness rather than the monolithic intermetallic and the bridging traction based on LSB model was estimated to be 250~300MPa. Fracture mode transition from single to multiple fracture in intermetallic/metal micro-laminated composites were successfully explained by combined model of LEFM and shear lag model and also FEM analysis. REFERENCES 1. 2. 3. 4.
K. S. Kumar and G. Bao 1994. "Intermetallic-matrix Composites: An Overview", Composites Set & Tech., 52:127-150. D. E. Alman, J. C. Rawers and J. A. Hawk 1995. "Microstructural and Failure Characteristics of Metal-Intermetallic Layered Sheet Composites", Metall. Mater. Trans. A,26A(3):589-599. K. L. Hwu and B. Derby 1999. "Fracture of Metal/Ceramic Laminates-I. Transition from Single to Multiple Cracking", Acta. Metall. Mater., 47(2):529-543. D. R. Bloyer, K. T. V. Rao and R. O. Ritchie 1996, "Fracture Toughness and R-curve Behavior of Laminated Brittle-matrix Composites", MatSci. & Eng. A, 216:80-90.
Part XIV
Nanocomposites
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Fracture Behaviour of Nano-composite Ceramics Ai Kah Soh*, Dai-Ning Fang Department of Mechanical Engineering, The University of Hong Kong, Hong Kong Department of Engineering Mechanics, Tsinghua University, Beijing 100084, P. R. China Zhao-Xu Dong Department of Aeronautical and Astronautical Engineering, Purdue University, USA
ABSTRACT In this paper, the toughening mechanisms of zirconia ceramics with dispersed silicon carbide nano-particles is studied and a model, which accounts for three toughening effects, i.e., nano-particle clustering, crack pinning, and transgranular fracture, is developed to predict the overall toughness of nano-composite ceramics. The theoretical prediction, based on the combination of the three effects of nanoparticles, is in agreement with the experimental data.
INTRODUCTION Since nano-composite ceramics were first made inl980's, the experiments carried out by many researchers, e.g., Tian et al. (1998), have shown that the ceramic matrix can be significantly toughened by dispersing nanometer sized particles in it to form nano-composite ceramics. The toughening mechanisms of such process have attracted the interest of many researchers. The most valuable theoretical work on examination of toughening mechanisms was done by Tan and Yang (1998) who highlighted three toughening mechanisms, which were (a) switching from intergranular to transgranular fracture; (b) fracture surface roughening by zigzag crack path; and (c) shielding by clinched rough surfaces near the crack tip. In this paper, the toughening mechanisms of zirconia ceramics with dispersed silicon carbide nano-particles is studied and a model, which accounts for three toughening effects, i.e., nano-particle clustering, crack pinning, and transgranular fracture, is developed to predict the overall toughness of nanocomposite ceramics. EXPERIMENT The nano-composite ceramics with zirconia (ZrOa) matrix and silicon carbide nano-particles were fabricated by the coagulation casting approach (Izaki et al., 1988). The Young's modulus and Poission's ratio of the zirconia matrix are £m=400GPa and vm = 0.25, respectively, and the corresponding values of the nano-
* Corresponding author. Department of Mechanical Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong, fax: (852) 28585415 and email: [email protected].
666
Fracture Behaviour of Nano-composite Ceramics
SiC particles are £p=440GPa and vp = 0.17. The zirconia ceramic, which consists of 0% nano-particle, and the nano-composite ceramics with 2%, 5%, 10%, 20% volume fraction of nano-particles were produced at the sintering temperatures of 1600°C, 1650°C, 1700°C, 1750°C, and 1800°C, respectively. The average size of the SiC nano-particle and the zirconia matrix grain were 60 nanometers (run) and 3 um, respectively. The strength of the nano-composites with different volume fractions of nano-particles was measured using three-point-bending specimens with length 36mm, height 4mm and thickness 4.0mm. The fracture toughness was obtained from the indentation test, which has been accepted as a standard test for toughness measurement of brittle materials (Lawn et al. 1980). Figure 1 shows the average bending strength of the nano-composite with respect to the volume fraction of the dispersed nano-particles. Note that each experimental point represents the average measured value of nine specimens. Figure 2 demonstrates the toughness of nano-composites with respect to the volume fraction of the dispersed nano-particles. It can be seen from the experimental data in Figs.l and 2 that both the strength and toughness increase with increasing of volume fraction of nano-particles. However, the strength reaches its highest value at ^=10%. Figure 3 shows the TEM images of ZrCVnano-SiC composite ceramics. Figure 3(a) clearly illustrates the clustering of nano-particles within the grains; Fig. 3(b) clearly shows the inter/intra distributions of nano-particles; and Fig. 3(c) reveals crack pinning due to nano-particles. The microscopy observations reveal the following basic facts: (1) The matrix grains can be refined by adding nano-particles, which leads to the increase of fracture strength and toughness. (2) The transgranular cracking increases with increasing volume fraction of nanoparticles. (3) Clustering of nano-particles does exist and it affects both the strength and toughness of nano-composite ceramics. Such clustering increases with increasing volume fraction of nano-particles. (4) The nano-particles may be dispersed in three different patterns, i.e., the inter/intra-pattern with nano-particles distributed both within the grains and along the grain boundaries; the intra-pattern with nano-particles distributed within the grains; and the inter-pattern with nano-particles distributed along the grain boundaries (Tan and Yang, 1998). Based on experimental results, Sawaguchi et al. (1991) pointed out that the inter/intra-pattern possesses the highest toughness while the intra-pattern the lowest. (5) Crack propagation may be pinned by the nano-particles near the crack tip. The experimental results of Hwang et al. (1997) showed that crack pinning might give rise to pull-out of nano-particles. This was because when a crack growth was pinned by a nano-particle, the crack cannot penetrate through the nanoparticle by breaking it. ANALYSIS Based on the above experimental measurement and observation, three major toughening mechanisms are identified for theoretical modeling. The overall toughness of the Z,O2/nano-SiC ceramics with different volume fractions of nanoparticles will be calculated and compared with the experiments.
Fracture Behaviour of Nano-composite Ceramics
667
Effects of Nano-Particle Clustering Assume that the nano-particles with an average size, dp , are randomly distributed. The random distribution can be produced in the following manner. At the initial state, the two-dimensional coordinates (*,•,>",•) for each nano-particle with radius, r{ = rp, is introduced into the representative element by a randomizer, as shown in Figs. 4(a). After randomly distributing the nano-particles, an approach is adopted to statistically record the clustering. Upon completion of this clustering process, a new random distribution is formed, as shown in Fig. 4(b). For each and every step of the statistical clustering process, two parameters, which are important to the toughening analysis to be carried out later, are to be recorded. One is the volume fraction, VJ , of the clustered nano-particles, which is given by V"f = nN" I N""al, where N" is the number of the clustered nano-particles, each of which consists of n original nano-particles. It is obvious that Vf =^V"
. The other
n
is the probability of crack pinning, pn, which defines the chance that a crack is impeded by a nano-particle and, thus, cannot pass through the nano-particle. The probability is defined as pn = l/n 2 . If n = 1, there is no clustering, i.e. pn = 1, which means that the crack cannot pass through the nano-particle. The larger the value n, the smaller is the probability pn. In other words, the larger the size of the clustered particle, the more defects it contains and, thus, the easier it is for the crack to pass through the clustered particle. Therefore, pn reflects the effect of nano-particle clustering. Effects of Crack Pinning of Nano-Particles When a main crack is pinned by a nano-particle, the latter may be pulled out from the matrix since the crack cannot penetrate directly through the nano-particle. By adopting Toya's (1972) approach, it can be shown that the "pull-out" stress and stressintensity-factor are as follows:
(1)
0.593278 where
in which
1+
(3)
T=—, w = —, and the parameters k, N ^ In and v are given in Toya's paper (1972), /u1, v, are the shear modulus and Poisson's ratio of the matrix, respectively, and // 2 , v2 are the corresponding values of the nano-particle. It is obvious that crack pinning gives rise to toughening because K{ = 3 - 4 V J , K2 = 3 - 4 V 2 ,
668
Fracture Behaviour of Nano-composite Ceramics
higher stress intensity factor, Kmno , leading to "pull-out" of the nano-particle. Indeed, the numerical calculation indicates that Knan0 is much larger than that of the matrix ceramics. Transgranular Fracture Induced by Nano-particles For nano-composite ceramics, the probability of having transgranular fracture may be estimated based on the area percentage occupied by nano-particles along a strip covering the grain boundary. Assuming that the nano-particles distribute homogeneously inside the matrix grain and along the grain boundary strip, the area percentage Vf can be determined. Since the probability of having transgranular fracture for the ceramic grains without nano-particles is /"" = 1 - /'"', where /'"' is the probability of having intergranular fracture, an increased portion of transgranular fracture induced by nano-particles is f""Vf. Thus, due to the presence of nanoparticles, the probability of transgranular fracture is increased to /"" + f""Vf . Obviously, the probability for nano-composite ceramics to have intergranular fracture is / " " ( 1 - F / ) . By considering the mechanism of transgranular fracture, the overall toughness of the nano-composite ceramic can be expressed as J = (/"" + fiMvf
)jf
+ /'"' (1 - Vf )•//"'
(4)
4
where
J '=
cos (/'"^/4)J -J~A1 1 - / ' " ' + / ' " ' cos4 (fmtnl 4)
(5)
:
j} = / i i v ; m + ( i - / m t ) j ; " s
(7)
Since the fracture resistance of the grain boundary is lower than that of the matrix, the higher the probability of transgranular fracture induced by nano-particles, the tougher the nano-composite ceramics is. Toughening of Nano-Composite Ceramics The three effects of nano-particles on the toughness of nano-composite ceramics discussed above can be combined to obtain a general formula for calculating the overall toughness of such ceramics. Thus, the critical stress intensity factors for intergranular fracture, K'"1, and transgranular fracture, K'"s, are given by
{v;PnKmm + {i-Pn Y;K{2) )
(8)
n
T
={i-vf
)K;;
+ Y^nfPnKnan0 + (1 - Pn Y;K{2) )
(9)
where subcript 1 and 2 denote the matrix and nano-particle, respectively. Thus, KQ) and K{2) axe the critical stress intensity factors of the matrix ceramic and nanoparticle
materials,
respectively.
Note
that
K'^ = ^E^J™ /(l - vf)
and
Fracture Behaviour of Nano-composite Ceramics
669
The overall toughness of nano-composite ceramics can be calculated by combining equations (4), (8) and (9) as follows: (10) Figure 2 shows that the solid curve, which was plotted using equation (10), for the ZrCVnano-SiC composite ceramics agrees with the corresponding experimental data represented by the solid circles. The theoretical prediction indicates that the toughness reaches its maximum value when the volume fraction of the nanoparticles equals 25%. Figure 5 shows the effects of the property ratios between the matrix ceramic and nano-particle, i.e., E2IEi and KQIKQ), where E denotes Young's modulus, on the overall toughness of nano-composite ceramics. Note that in the calculations, the size of the nano-particle was assumed to be 60 nm in average diameter, and that of the matrix grain was 3 (im in average diameter. It can be clearly seen from Fig. 5 that the toughness ratio of the matrix ceramics to nanoparticle has more significant influence on the overall toughness of nano-composite ceramics as compared with that of the ratio between Young's moduli. CONCLUSIONS Three effects of nano-particles on the mentioned toughness, namely, nanoparticle clustering, crack pinning and transgranular fracture, are identified from both the experimental and analytical studies. The theoretical prediction, based on the combination of the three effects of nano-particles, is in agreement with the experimental data. It is important to note that the toughness ratio between the matrix ceramic and nano-particle has more significant influence on the overall toughness of nano-composite ceramics, as compared with that of the ratio between Young's moduli. Acknowledgement. Support from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. HKU 7086/02E) and the National Science Foundation of China under grants #19891180 and #59772017 is acknowledged. REFERENCES 1.
2. 3. 4. 5. 6. 7.
Hwang, K.T., C.S.Kim, K.H. Auh, D.S. Cheong and K. Niihara. 1997. "Influence of SiC Particle Size and Drying Method on Mechanical Properties and Microstructure of Si3Ni4/SiC Nanocomposite," Materials Letters, 132:251-257. Izaki, K., K. Hakkei and K. Ando. 1988. infrastructure Processing for Advanced Ceramics. New York, John Willey & Sons, pp. 981-990 Lawn, B.R., A.G. Evans and D.B. Marshall. 1980. "Elastic/Plastic Indentation Damage in Ceramics: The Median/Radial Crack System," J. Am. Ceram.Soc, 62:574-581. Sawaguchi, A., K. Toda and K. Niihara. 1991. Mechanical and Electrical Properties of NanoComposites,'V. Am. Ceram. Soc, 74:1142-44. Tan, H.L. and W. Yang. 1998. "Toughening Mechanisms of Nano-Composite Ceramics," Mechanics of Materials, 30:111-123. Tian, W., Y. Zhou and W.L. Zhou. 1998. "SiC Nanoparticle Reinforced Si3N4 Matrix Composites,"/ Mat. Sci., 33:797-802. Toya, M. 1972. "A Crack along the Interface of a Circular Inclusion Embedded in an Infinite Solid,"/ Meek Phys. Solids, 22:325-348.
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Theoretical curve - - • — Experimental data
0.2
0.2
0.3
0.3
0.4
0.5
0.6
Volume fraction, V t
Volume fraction, V t
FIGURE 1 Three-point-bending strength of the ZfCVnano-SiC ceramics with different volume fractions of nano-particles.
FIGURE 2 Fracture toughness of the ZAi/nano-SiC ceramics with different volume fractions of nano-particles.
• —
•
.
*
•
(a)
(b)
(c)
FIGURE 3 TEM images of ZrO2/nano-SiC composie ceramics: (a) clustering of nano-particles within the grains; (b) inter/intra distributions of nano-particles; (c) crack pinning of nano-particles
(a) original random distribution
(d) distribution after clustering operation
FIGURE 4 Nano-particle clustering operations for 30% volume fraction
1,4-
1.3-
dm=3 u.m d =60 nm
vs (b) 0.00
0.05
0.10
0.15
0.20
Volume fraction, V,
0.25
0.3'
0.00
0.05
0.10
0.15
0.20
0.25
0.30
Volune fraction, V,
FIGURE 5 Effects of property ratios between the matrix ceramic and nano-particle on the overall toughness of nano-composite ceramics: (a) Young's modulus; (b) toughness
Structure-property Relationships of Polymer Nanocomposites Filled with Mechanochemically Grafted Nanoparticles Wen Hong RUAN1'2, Ming Qiu ZHANG2*, Min Zhi RONG2 'Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Zhongshan University, Guangzhou 510275, P. R. China 2
Materials Science Institute, Zhongshan University, Guangzhou 510275, P. R. China Klaus FRIEDRICH Institute for Composite Materials (IV W), University of Kaiserslautern, D-67663 Kaiserslautern, Germany
ABSTRACT Nanocomposites of ethylene-propylene block copolymer filled with nanosilica pre-treated through ball milling aided graft polymerization are prepared by conventional compounding technique. Mechanical performance of the nanocomposites and morphological changes induced by the addition of the nanoparticles are investigated. It is confirmed that the polymer chains are chemically bonded to the particles during the mechanochemical grafting in the ball mill. Morphology observations reveal that strong interfacial interaction between the grafting polymer and the matrix is critical to bring reinforcing effect of the nanoparticles into play. Owing to the enhanced interfacial interaction, grafted nanoparticles ehxibit nucleating effect and improve crystallinity of the polymer matrix. In addition, the particles also have toughening effect on the amorphous polypropylene phase due to the entanglement between the grafting polymer and the matrix. The insufficient interaction between the nanoparticles and rubber phase of the copolymer matrix actually introduces restraints. As a result, the tensile strength of nanocomposites can be significantly increased at low loading of the treated nanoparticles. The decrement of notched Charpy impact strength is insignificant in comparison to that of conventional micron-scale inorganic particles filled composites. The technical route proposed in the current work is thus proved to be feasible for fabricating polymer composites with inorganic nanoparticles.
INTRODUCTION Polymer based nanocomposites in which inorganic nanoparticles dispersed in organic polymer matrices have attracted material scientists' attention owing to their unique properties resulting from the nano-scale microstructure. However, a homogeneous dispersion of nanoparticles is very difficult because nanoparticles with high surface energy are easy to agglomerate. Researches proposed the approaches of in-situ polymerization of monomers in the presence of nanoparticles [1] and intercalation polymerization techniques [2]. The methods with the requirements of complex processing procedures, special conditions and high cost are limited to laboratory scale. By examining * Correspondence Author: Prof. Ming Qiu ZHANG. Materials Science Institute, Zhongshan University, Guangzhou 510275, P. R. China. Fax: +86-20-84036576. E-mail: [email protected]
672
Structure-property Relationships of Polymer Nanocomposites
the current technical level and the feasibility of the available processing methods, it can be inferred that melt blending nanoparticles with polymer is the most optimum compounding technique in the case of mass production of nanocomposites with low cost. To give play to the non-layered inorganic nanoparticles, modification of nanoparticle agglomerates becomes the focus of a new research initiative of our group. Irradiation grafting polymerization method was used to modify nanoparticles and then the grafted particles were mechanically mixed with polymer as usual [3]. Double percolation mechanism of stress volumes was proposed to explain the special effects generated by the low loading grafted nanoparticles [4]. To develop a more industrial route, in the work presented here nano-silica are treated by ball milling in the presence of butyl acrylate monomer. It is expected that mechanochemically initiated in-situ grafting polymerization of the monomer onto the nanoparticles would take place. Then the modified nanoparticles are melt compounded with ethylene-propylene block copolymer. Stucture-property relationships of the nanocomposites are discussed in detail to understand the role of the treated nanoparticles and the feasibility of the method suggested above. EXPERIMENTAL Ethylene-propylene block copolymer EPS30R® (Melt flow index=1.9g/10min) was supplied by Qilu Petrochemical Industrial Co., China. Precipitated silica(average primary particle size=10nm, specific surface area=640m2/g) was selected as the filler. Commercial butyl acrylate and isobutyronitrile were used as monomer and initiator. The nanoparticles were preheated at 140°C under vacuum for 5h. Then, a mixture of monomer/nanoparticles and a certain amount of initiator was ground by a planetary ball miller under atmosphere at room temperature. The concentrations of the monomer and the initiator, incorporation manner of the components, as well as milling conditions, were changed in order to study their influences on the reaction processes. The weight increase in nano-SiCh due to the presence of the grafting poly(butyl acrylate) was determined by a Netzsch TG 209 thermogravimetre (TG) under N2 atmosphere. By using a Bruker Equinox 55 Fourier transform infrared spectroscope (FTIR), the chemical structures of the nanoparticles were characterized. The nanoparticles were compounded directly with EPS30R matrix in the mixer of Haake Rheocord 300p torque rheometer at 60rpm, 180°C for lOmin. The standard bars were prepared by a Y-350 vertical injection molding machine. Tensile testing was conducted on a Hounsfield H10K-S universal testing machine at a crosshead speed of 50mm/min. According to ISO 179-2, notched Charpy impact strength was determined by an API advanced pendulum impact at a rate of 3.8m/s. The fractured surfaces were studied by a JEOL-5400 scanning electron microscope (SEM). Non-isothermal melting and crystallization behaviors of the materials were examined by a TA MDSC2910 differential scanning calorimetry (DSC). Both the heating and cooling rates were 10°C/min. RESULTS AND DISCUSSION FTIR spectra of untreated and treated nano-silica (in which the homopolymer had already been extracted) are shown in Figurel. In comparison with the spectrum of SiCh as-received, the absorption peak at 1717cm"1 in the spectrum of treated sample indicates the existence of carbonyl group, proving that polybutyl acrylate (PBA) has been chemically bonded to the surface of nano-silica during grinding processes. Results of weighing and thermogravimetric analysis of the samples also suggest that the method of
Structure-property Relationships of Polymer Nanocomposites
673
in-situ grafting polymerization in mechanochemical environment works. The PBA grafted nano-silica (denotes as SiCVg-PBA) with conversion of 20.85% and percent grafting of 5.96% is chosen for preparing the composites studied hereinafter.
o c E c
3600 3200 2800 2400 2000 1600 1200 800 400 Wavenumber [cm1] FIGURE 1 FTIR spectra of SiO2 as-received and grafted SiO2
O-SQ/EPS30R • - SiO,-g-PB/VEPS30R 30l— 0.0
0.5
1.0
1.5
2.0
Z5
SO, FIGURE 2 Tensile strength of EPS30R based nanocomposites as a function of nano-SiO2 volume fraction
Figure 2 shows the tensile strength of the PP block polymer based nanocomposites as a function of silica content. It can be seen that tensile strength of SiO2-g-PBA/EPS30R is improved much more greatly than that of the untreated case. Apart from providing mechanical stress for the mechanochemical reaction, the main roles of milling are homogenization of the reaction mixture and disintegration of the severely agglomerated nanoparticles. As a result, the following effects can be obtained: (i) Agglomerates of the pretreated nanoparticles would become smaller and much stronger because they turn into a nano-composite microstructure consisting of the primary particles and the grafted, homopolymerized secondary polymer; (ii) An increase in hydrophobicity of the nanoparticles due to the grafting polymers would be beneficial for the filler/matrix compatibility; (iii) The filler/matrix interaction would be enhanced by interdiffusion and entanglement between the grafting polymer and the polymer matrix. In general, tensile strength of a particulate composite is reduced with filler content following a power law in the case of poorfiller/matrixbonding [5]. The results given in Figure 2 demonstrate that
674
Structure-property Relationships of Polymer Nanocomposites
the reinforcing effect of nanoparticles on the polymer can be realized so long as the particles are grafted and properly dispersed in the matrix polymer. For better understanding the reinforcing mechanism of the nanoparticles, Table 1 shows the DSC studies of non-isothermal crystallization and melting behaviour of the matrix and its nanocomposites. The experimental data demonstrate that both untreated and PBA-grafted SiO2 particles exert nucleating effect on the crystallization of the matrix polymer. The crystallinity increases significantly when SiO2-g-PBA particles are incorporated, reflecting that nano-silica grafted by ball milling has enhanced interfacial adhesion and more uniform particles dispersion than the untreated particles. TABLE I Non-isothermal crystallization and melting data of EPS30R nanocomposites Tm(°C) Samples EPS30R 166.1 165.3 SiO2/EPS30Ra 166.9 SiO2-g-PBA/EPS30Rb 'Content of SiO2: 1.30vol% bContentofSiO2: 1.36vol%
Tc(°C)
110.0 117.2 127.9
1.0
AT(°C) 54.3 48.9 39.0
Xc(%)
31.2 33.2 47.0
1.5
SiO2 [vd%]
FIGURE 3 Notched Charpy impact strength of nanocomposites as a function of nano-Si02 volume fraction
Figure 3 illustrates notched Charpy impact strength of EPS30R based composites as a function of nano-silica content. The addition of the nano-fillers indeed introduces mechanical restraints and reduces deformation ability of rubber phases of block copolymer, causing reduction in impact strength of the composites consequently. Nevertheless, compared to the untreated case, it can be stated here that mechanical loading seems to be more effectively transferred from the matrix to the modified particles owing to the interfacial bonding effect of the grafting polymer PBA, which might result in an interdiffusion and entanglement between the molecules of the grafting polymers and the matrix. The decrement of the impact toughness of SiO2-g-PB A/EPS30R composites is about 26% as compared to the value of unfilled matrix. Recalling that the impact strength is decreased by 46% in micro-sized calcium carbonate filled EPS30R [6], 46% in talc filled propylene-ethylene block copolymer [7], and 58% in glass spheres filled propylene-ethylene block copolymer [7], respectively, conclusion can be drawn that the decrement of grafted nanoparticles filled EPR30S is insignificant in comparison to the conventional micron-scale inorganic particles filled composites.
Structure-property Relationships of Polymer Nanocomposites
•<*
675
:•.>,-.. •l
•
'•
•*b'"
(a) FIGURE 4 SEM micrographs of tensile fractured surface of (a) neat EPS30R and (b) SiO2-g-PBA/EPS30R (content of SiO2=l .36vol%)
V.-
(a)
(b)
(c)
FIGURE 5 SEM micrographs of notched Charpy impact fractured surface of (a) neat EPS30R and (b)~(c) SiOrg-PBA/EPS30R (content of SiO2=1.36vol%).
SEM micrograph of the tensile fractured surfaces of unfilled EPS30R has an uneven appearance full of relatively smooth bumps (Figure 4(a)), indicating that resistance of the polymer to crack propagation is still weak. The fracture surface of the nanocomposite incorporating PBA-grafted nanoparticles is full of extensive matrix fibrils (Figure 4(b)), showing a clear evidence of plastic stretching of the matrix ligaments. During the tensile procedure, the modified nanoparticles act as stress concentrators and the yielding process of the matrix propagates through the ligaments between the dispersed particles when interfacial interaction is strong enough. In accordance with the model describing double
676
Structure-property Relationships of Polymer Nanocomposites
percolation of yielded zones [4], the appearance of extensive fibrils would result from the superposition of stress volumes around the nanoparticles. Therefore, it can be proved that the grafting polymers on the nanoparticles enhance the fillers dispersion and interfacial interaction, and thus dissipate more energy through matrix stretching, which might account for the measured reinforcing effects on SiO2-g-PBA/EPS30R composites. Figure 5 illustrates fracture surface micrographs of the specimens tested by notched Charpy impact measurements. Neat EPS30R (Figure 5 (a)) shows ductile fracture surface similar to other ethylene-propylene block copolymer. The micrographs of SiO2-g-PBA/EPS30R composites show distinct features. A number of concentric matrix circles around particle-like object can be found (Figure 5(b)). High magnification picture taken from the particle-like object (Figure 5(c)) demonstrates that it indeed is a cluster of microfibrils, which might be composed of stretched matrix and modified nanoparticle agglomerates. These microfibrils actually introduce restraints to the rubber phases of the matrix polymer, and act as stress concentrators inducing multiple crazing and plastic deformation of the matrix. Once debonding of the modified nanoparticle agglomerates occurs, the shear stress is locally relieved and the deformation circles form due to a gradual contraction of the matrix. In consideration of the results of impact testing (Figure 3), it might be deduced that the toughening effect of modified nanoparticles is somewhat shielded by a reduction in matrix deformability due to the restraints to the rubber phase. CONCLUSIONS This work shows that tensile performance of ethylene-propylene block copolymer can be improved at low loading of nano-silica, that is pre-treated by ball milling initiated graft polymerization and incorporated into the matrix polymer using conventional compounding technique. The technical route proposed in the current work is proved to be feasible for fabricating polymer composites with inorganic nanoparticles. The interfacial characteristics between the grafted nanoparticles and the polymer matrix can be tailored by changing the species of the grafting monomers and the ball milling conditions. Further studies should be made to identify the mechanochemical mechanism of the ball milling process and to improve the interaction between the nanoparticles and the rubber phase of the block copolymer to achieve greater toughening effects. ACKNOWLEDGEMENTS The authors are grateful to the support of the Deutsche Forschungsgemeinschaft (DFG FR675/40-1) for the cooperation between the German and Chinese institutes on the topic of nanocomposites. Further thanks are due to the Team Project of the Natural Science Foundation of Guangdong, China (Grant: 20003038). REFERENCES 1. 2. 3. 4. 5. 6. 7.
NOVAK, B. M. 1993. Adv. Mater., 5:422-433. GIANNELIS, E. P. 1996. Adv. Mater., 8:29-35. ZHANG, M. Q., M. Z. RONG, H. M. ZENG, S. SCHMITT, B. WETZEL and K. FRIEDRICH. 2001. J. Appl. Polym. Sc. 80:2218-2227. RONG, M. Z., M. Q. ZHANG, Y. X. ZHENG, H. M. ZENG and K. FRIEDRICH. 2001. Polyme, 42:3301-3304. JANCAR, J., A. DIANSELMO and A. T. DIBENEDETTO. 1992. Polym. Eng. Set, 32:1394-1399. ZUO, S. W., W. H. RUAN and J. W. SHEN. 2001. Qilu Petrochem. Technol, 29(3):183-186 [in Chinese]. BRAMUZZO, M., A. SAVADORI and D. BACCI. 1985. Polym. Compos. 6:1-8.
A Numerical Model for Evaluating Elastic Properties of Carbon Nanotube Reinforced Composites Ning Hu*, Hisao Fukunaga and Masaki Kameyama Department of Aeronautics and Space Engineering, Tohoku University, Aobayama 01, Aoba-ku, Sendai 980-8579, Japan
ABSTRACT In this paper, a numerical model is set up for a representative volume element (RVE) to evaluate the macroscopic elastic properties of carbon nanotube reinforced composites. This RVE contains a carbon nanotube, a transition layer between the nanotube and polymer matrix and an outer polymer matrix body. First, based on the force field theory of molecular mechanics and computational structural mechanics, an equivalent beam model is constructed for the carbon nanotube. Second, the molecular mechanics computations have been performed to obtain the various properties of the transition layer at the level of atoms. Moreover, an efficient 3 dimensional (3D) 8-noded brick finite element is employed to model the transition layer and the outer polymer matrix. The macroscopic behaviors of the RVE can then be evaluated using the proposed finite element model.
INTRODUCTION The exceptional mechanical and thermal properties plus their low density and high aspect ratio, exhibited by carbon nanotubes, make them an ideal candidate for composite reinforcement [1]. Although there are quite a lot of researches dealing with the elastic properties of the carbon nanotube through various means, the investigations about the mechanical properties of carbon nanotube reinforced composites have been rarely reported [2]. In this paper, as shown in Figure 1, a cylindrical RVE is set up, which consists of three components, i.e., a nanotube, a transition layer between the nanotube and the polymer matrix, and an outer polymer matrix. First, for modeling the nanotube, we build up a 3D beam model based on the molecular force field in molecular mechanics and the computational structural mechanics. The explicit relationships between the material properties of the equivalent beam element and the molecular force field constants are obtained. Second, to describe the interaction between the nanotube and the outer polymer matrix at the level of atoms, the molecular mechanics computations have been performed. An efficient 3D 8-noded brick element proposed by the present authors [3] is employed to model this layer and the outer polymer matrix. Therefore, the elastic deformation of the RVE under various loading conditions can be predicted using a finite element model. Finally, the macroscopic elastic properties of nanotube reinforced composites have been investigated using this RVE.
* Corresponding Author, Department of Aeronautics and Space Engineering, Tohoku University, Aobayama 01, Aoba-ku, Sendai 980-8579, Japan, Fax: 81-22-217-4109, Email: [email protected]
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Elastic Properties of Carbon Nanotube Reinforced Composites
MODELING OF NANOTUBE First, consider C-C bonds in a unit cell of nanotube in Figure 2, the potential function of molecular mechanics force field among atoms can be expressed as [4] (i) dihedrals Bonded interactions
atoms atoms Non-boned interactions
where Vs=KsAR2/2 is the bond stretch potential summed over all bonds, Va=KgA.(?/2 the bond angle bending potential summed over all angles, Vt the torsion potential 3D element for matrix Beam model for nanotube
3D element for transition layer FIGURE 1 RVE model
FIGURE 2 Unit cell of nanotube
due to dihedrals torsion, Vv the van der Waals potential summed over all atoms, and Ve the electrostatic interactions, respectively. To predict the Young's modulus of nanotube, an equivalent beam model is created. The strain energy of a beam element of length R can be expressed as: -EAe2dx + t-ElK2dx+ 2 * 2
t-GJAco2c *2
(2)
where e, /cand Aa> are the stretching strain, curvature and torsional angle of beam. From Eqns (1) and (2), after a complex derivation procedure, we can finally identify
36Kg(KsR2-Kg)
R
(3)
Here, we take Ks=&05.5 nN/nm, ^e=1.438 nN'nm and Fffl=14.5 kcal/mol, which are
Elastic Properties of Carbon Nanotube Reinforced Composites
679
consistent with the values in various references [4]. The capability of this beam model is verified for single walled carbon nanotubes with a fixed end and the applied tension and torsion loads at another free end. A typical beam model of a zigzag nanotube (15,0) is shown in Figure 3. The results of the Young's and shear moduli for nanotubes of thickness of 0.34 nm are demonstrated in Figure 4. From it, it can be seen that the Young's and shear moduli of both kinds of nanotubes are very close to the experimental values for graphite sheet, i.e., 1.06 TPa and 0.433 TPa. The present Young's and shear moduli of nanotube are both in the very good agreement with the many previous theoretical predictions and experimental results [5].
• Armchair (E) —#— Armchair (G) —D— Zigzag (E) - O - Zigzag (G) Graphite (E) • • • • Graphite (G)
1.6
1.2
0.8
Z 0.0 '— 0.4
0.8
1.2
1.6
2.0
2.4
Nanotube Diameter (nm) FIGURE 3 A zigzag nanotube
FIGURE 4 Young's and shear moduli of nanotube
f F,
o
FIGURE 5 MM model of nanotube polymer chain
FIGURE 6 Shear modulus of transition layer
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Elastic Properties of Carbon Nanotube Reinforced Composites
ANALYSIS OF TRANSITION LAYER Here, one key task is to understand the interactions between the nanotube and the matrix, i.e. the transition layer. We perform the molecular mechanics computation by selecting a chain of Polystyrene [(-CH2CHC6H6-) „] with 24 benzene rings and a (6,6) armchair nanotube. A many-body bond-order potential was used to describe the intramolecular interactions between the nanotubes and polymer chains. The final equilibrium configuration is shown in Figure 5, where the polymer chain surrounds the nanotube in a regular, structured and stable way. The average equilibrium distance between H atoms on polymer and C atoms on nanotube is 0.415 nm. hi our computations, no formation of chemical bonds has been identified. To further investigate the properties of translation layer, a molecular dynamics computation has been performed to simulate the nanotube pull-out process under 300 K with the time step of 0.1 femtosecond. The polymer is fixed in the computation. All non-bonded interactions within the polyethylene matrix and between the nanotube and the matrix are modeled with Lennard-Jones 6-12 potentials. Using the displacement of nanotube at various time steps, we can identify the shear modulus of transition layer in the meaning of average as shown in Figure 6. The identified stable shear modulus range from 4.2 GPa to 50 GPa, which decreases nonlinearly as the shear deformation increases.
PREDICTION OF MATERIAL PROPERTIES OF COMPOSITES After determining the properties of nanotube and transition layer, the material properties of the nanotube reinforced composites can be predicted. We consider the case of polymer matrix reinforced with many unidirectional short nanotubes. A (6,6) armchair single wall nanotubes is considered. In the model of Figure 7, for the Polystyrene polymer matrix, its Young's modulus Em and Poisson ratio vm are set as 3.0 GPa and 0.33. The macroscopic composites can be thought of as transversely isotropic materials with four material constants, i.e., Ez, Ex, vxy and vzx, which can be obtained using three loading cases as shown in [2]. First, for the various Young's modulus of transition layer ET, Ez of composites is shown in Figure 8. When ET is from 3 GPa to 50 GPa, the effect of transition layer is obvious, however, from 50 GPa to 100 GPa, its effect becomes weak. The influence of Lm on Ez is shown in Figure 9. It reveals that with the decrease of Lm, i.e, increase of nanotube length, Ez increases remarkably. Our results are consistent with previous experimental ones, e.g., Qian et al. [6] have found that with only the addition of 0.5% multi-wall nanotubes by weight (0.5-1.0% by volume fraction), the elastic stiffness achieved between 36% and 42% increase.
Elastic Properties of Carbon Nanotube Reinforced Composites
681
FIGURE 7 Tension loading case for cylindrical RVE
1.6 -E/E m (E T =3GPa) -E z /E m (E T =20GPa
lodulus
1.5 1.4
<5 -d
1.3
~EJEJET=50GPa) -Ez/Em(ET=100GPa)
N
forn
1.2 1.1 1.0
0.5
1.0
1.5 2.0 2.5 3.0 Volume Fraction (%)
3.5
4.0
FIGURE 8 Effect of stiffness of transition layer
1.8 1.7 1.6 -a o
1.5
2
1.4
"(3 O
Z
1.3
- Lm=1 nm (Es/Em, £,=50 GPa) - Lm=2 nm (E/E m , Er=50 GPa) - Lm=4 nm (E/E m , ET=50 GPa) - Lm=5 nm (E/E m , ET=50 GPa) - Experimental (Ec/Em, CSan et al.)
^T
1.2 1.1 1.0 0.0
0.5
1.0
1.5
2.0
2.5
Volume Fraction (%) FIGURE 9 Effect of nanotube length
3.0
682
Elastic Properties of Carbon Nanotube Reinforced Composites
CONCLUSIONS The elastic properties of carbon nanotube reinforced composites are predicted using a numerical model for RVE. The following conclusions can be drawn: (1) No chemical bonds are formed between the nanotube and polymer in the molecular mechanics computations. The shear modulus of transition layer decreases nonlinearly as the shear strain increases. The stable value ranges from 4.2 GPa~50 GPa; (2) When £Yis lower than 50 GPa, the effect of stiffness of transition layer is significant on Ez. However, further increase of £Y has little effect; (3) Increase of nanotube length leads to higher reinforcement in the nanotube length direction. When the volume fraction ranges from 0.48 % to 2.75 %, depending on the stiffness of transition layer and nanotube length, the reinforcement in the length direction can be achieved from 10 % to 80 %.
REFERENCES 1. Tostenson, E.T., Z.F. Ren, and T.W. Chou. 2001. "Advances in the science and technology of carbon nanotubes and their composites: a review," Compos. Sci. Tech. 61(2): 1899-1912. 2. Liu, YJ. and X.L. Chen. 2003. "Evaluations of the effective material properties of carbon nanotube-based composites using a nanoscale representative volume element," Mech. of Mater. 35: 69-81. 3. Cao, Y.P., N. Hu, J. Lu, H. Fukunaga and Z.H. Yao. 2002. "A 3D brick element based on Hu-Washizu variational principle for mesh distorsion," Int. J. Numer. Meth. in Engrg. 53: 2529-2548. 4. Cornell, W.D., P. Cieplak, C.I. Bayly, I.R. Gould, K.M. Jr. Merz, D.M. Ferguson, D.C. Spellmeyer, T. Fox, J.W. Caldwell and P.A. Kollman. 1995. "A second generation force field for the simulation of proteins, nucleic acids, and organic molecules,"/ Am. Chem. Soc. 117: 5179 -5197. 5. Popov, V.N., V.E. Van Doran and M. Balkanski. 2000. "Elastic properties of single-walled carbon nanotubes," Phys. Rev. B 61: 3078-3084. 6. Qian, D., E.C. Dickey, R. Andews and T. Rantell. 2000. "Load transfer and deformation mechanisms in carbon nanotube-polystyrene composites," Appl. Phys. Lett. 76: 2868-70.
Interfacial Bonding Strength between Carbon Nanotubes and Epoxy Resin Matrix: Experimental and Computational Studies Ben Wang*, Zhiyong Liang, Jihua Gou, Tiehu Jiang and Chuck Zhang Florida Advanced Center for Composite Technologies College of Engineering, Florida A&M University-Florida State University 2525 Pottsdamer Street, FL, 32310, U.S.A. Leslie Kramer Lockheed Martin Missiles and Fire Control-Orlando 5600 Sand Lake Road, Orlando, FL 32819-8907, U.S.A.
ABSTRACT Since the discovery of carbon nanotubes, many researchers have been fascinated by their intrinsic mechanical, thermal and electrical properties. The potential for using carbon nanotubes as reinforcements to created composites of superior strength has been a focus of numerous research projects. Attempts to produce nanocomposites have seen limited success, due to the nanotubes' small diameters, extremely large surface areas and unique chemical characteristics creating intensive molecular interactions between nanotubes, epoxy and curing agents. Achieving good tube/resin wetting and strong interfacial bonding in SWNT/epoxy composites is crucial for realizing the full potential of nanocomposites. In this study, molecular dynamics (MD) simulations revealed the molecular interactions between single-walled carbon nanotubes (SWNTs) and Epon 862 resin/EPICURE W curing agent molecules before polymerization. The research involved investigating the possibility of filling Epon 862 resin molecules into an open ended (10,10) SWNT. In addition, a three-dimensional cross-link model of the cured resin was established for the MD simulation of a single carbon nanotube pullout to predict the interfacial bonding of the resultant composites. The simulation results indicated that both Epon 862 and EPI-CURE W curing agent molecules have attractive interactions with the nanotubes, and their molecules have a tendency to stretch and wrap around the nanotube surfaces. The simulations indicated that good wetting could be expected between nanotubes and the Epon 862 matrix. The molecular interaction energy during single nanotube pullout from resin cross-link network was calculated in the MD simulation, and the interfacial shear strength between nanotubes and the Epon 862 matrix was estimated. The MD simulation results are in agreement with our preliminary experimental observations. INTRODUCTION SWNTs have demonstrated remarkable characteristics, such as novel electronic properties, exceptionally high strength and axial Young's modulus of lTPa. Coupled * Corresponding author, 2525 Pottsdamer Street, Tallahassee, FL 32310-6046fax: 850-410-6377, email: [email protected]
684
Interfacial Bonding Strength
with their defect-free molecular structures, they are considered by many as the ideal reinforcements for next generation of high performance composites, capable of producing new materials with revolutionary properties for use in wide variety of applications [1-3]. Attempts to produce nanocomposites have seen limited success, due to the nanotubes' small diameters, extremely large surface areas and unique chemical characteristics creating intensive molecular interactions between nanotubes, epoxy and curing agent during material processing and difficult to forming chemical bonding between tubes and resin matrix. Achieving good tube/resin wetting and strong interfacial bonding in SWNT/epoxy composites is crucial for realizing the potential of nanocomposites [4-9]. In this study, molecular dynamics (MD) simulations were conducted to reveal the molecular interactions between single-walled carbon nanotubes (SWNTs) and Epon 862 resin/EPI-CURE W curing agent molecules before polymerization. The research involved investigating the possibility of filling Epon 862 resin molecules into an open ended (10,10) SWNT. In addition, a three-dimensional cross-link model of the cured resin was established and used for MD simulation of a single carbon nanotube pullout to predict the interfacial bonding of the resultant composites. The experimental observations of the interfacial bonding of the composites were also provided and compared to the MD simulation results. In the research, MD simulations were carried out on a SGI-Octane2 workstation using Materials Studio, a commercial software package developed by Accelrys, Inc. The condensed phase optimization molecular potentials for atomistic simulation studies (COMPASS) module in the Materials Studio software was used to conduct force field computations [10,11]. All calculations were carried out at the initial temperature of 300 K, using NVT ensembles constant number of particles, constant volume and constant temperature. SWNTs-reinforced Epon 862/DETDA resin matrix composites were fabricated using a buckypaper/resin infiltration process developed by the authors [14]. The SWNTs used in this study were BuckyPearls™, purified SWNTs from Carbon Nanotechnologies, Inc. (CNI), Houston, TX. The dynamic mechanical properties of the resultant nanocomposites were tested using dynamic mechanical analyzer (DMA). SEM and AFM analysis revealed the interfacial bonding in the composites. INTERACTIONS BETWEEN SWNT AND EPON 862 MOLECULE Snapshots of the MD simulations of the interactions between (10,10) SWNT and Epon 862 molecule are shown in Figure 1. Initially, the chain of Epon 862 resin molecule was twisted under a minimum energy status. One end of the chain was put near the nanotube's wall, while the other end was placed away from the nanotube. The simulation shows that during the initial 16ps, the molecular chain of the Epon 862 resin stretched and moved toward the nanotube. All atoms in the resin molecule gradually moved towards the nanotube's wall. After a long equilibration period of lOOps, the resin molecule chain eventually tended to spirally wrap on the surface of the nanotube. The nanotube maintained its overall shape, although some distortion of its cross section occurred during the interaction. As shown in Figure 1, two aromatic rings of the molecule fmally orientated to align their ring plane parallel to the SWNT surface, which is called it-stacking effect. The negative interaction energy of the MD simulation indicates that the EPON 862 epoxy resin molecule moved towards the nanotube's surface due to an attractive force. The interaction energy of the SWNT and the EPON 862 epoxy resin molecules decreased by 25 kcal/mol based on the MD simulation result.
Interfacial Bonding Strength
685
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INTERACTIONS BETWEEN SWNT AND DETDA The MD simulations of the interactions between SWNT and DETDA molecules were conducted using the same procedure. The MD simulation results are provided in Figure 2. The DETDA molecule also tried to orient its aromatic ring plane to face the SWNT surface and move closer to the SWNT to achieve a low potential energy status, which indicated that the DETDA molecule also had an attractive interaction with the SWNT.
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EPON 862 RESIN MOLECULE FILLING SWNT Since SWNTs are hollow, MD simulations were conducted to demonstrate the possibility of Epon 862 resin molecule filling into the open end of SWNTs. Two possible configurations of the resin molecule filling into SWNT were observed. The MD simulation snapshots shown in Figure 3 demonstrate that the molecule could be filled into the SWNT regardless if the molecule conformation was initially perpendicular or parallel to the tube open end. Filling resin matrix molecules into SWNTs is a possible way to form mechanical locking or connections between chopped nanotubes and resin cross-linked networks, and creating more functional groups at open ends for enhancing interfacial bonding in nanotube-reinforced composites.
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Parallel filling
FIGURE 3 Filling Epon 862 molecule into a (10,10) SWNT
SINGLE SWNT PULLOUT AND INTERFACIAL BONDING To theoretically predict the interfacial bonding strength of the SWNT/epoxy composite, a molecular model of a single SWNT/cured Epon 862/DETDA matrix was established, as shown in Figure 4. In the model, the matrix density around the SWNT tube was 1.2 g/cm3 and the model dimensions were 50A x 50A x 100A, having a total of 21,288 atoms. No chemical bonding between the tube and resin matrix was included in the model. In this study, a simplified and fast computational pullout approach was applied to obtain the interaction energy change during the SWNT pullout by directly calculating the system potential energy at different stages, as shown in Figure 5. The system potential energy increase was monitored during the tube pullout. At the initial stage (before tube pullout), the potential energy of the composite was 152,665 kcal/mol. After the completion of the tube pullout (AZ = 110 A), the potential energy increased to 154,951 kcal/mol. The increase of the potential energy is mainly due to the creation of a new surface and the molecular interaction changes between the tube and resin matrix in the material system. Furthermore, the increase of the potential energy can be used to estimate the interfacial shear strength between the tube and the resin matrix [12]. The estimated interfacial shear strength of the SWNT/epoxy composite is about 75 MPa, which is about 20%~80% higher than that of most carbon fiber reinforced composites [13]. Such high interfacial shear strength could be attributed to large surface area/volume ratio of well-dispersed individual SWNTs embedded in the resin matrix in the computation model.
Interfacial Bonding Strength
687
EXPERIMENTAL OBSERVATIONS SWNT-reinforced Epon 862/DETDA resin matrix composites with a high SWNT loading (25w/w%-47w/w%) was fabricated using a SWNT buckypapers/resin infiltration process. The DMA analysis of the nanocomposites of 31.1wt% tube loading is shown in Figure 6.
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FIGURE 4 Molecular model of single (10,10) SWNT/Epon 862 nanocomposite
AZ = 75 A
AZ = 25 A
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FIGURE 5 Snapshots of single (10,10) SWNT pullout from Epon 862/DETDA matrix
Compared to the neat Epon 862 resin, more than 480% increase of the storage modulus was achieved, which indicates effective interfacial bonding and load transfer in the resultant nanocomposites (w-lOc). In Figure 7, AFM observation of the cross-section of the nanocomposites shows that the surface of SWNTs or their ropes are well covered by the Epon 862 resin matrix. A good interfacial bonding between the SWNT rope and Epon 862 matrix is demonstrated in Figure 8, which shows some epoxy resin still firmly adhered on the surface of the tube ropes after it was pulled out of the resin matrix at the facture cross-section. These observations show that Epon 862/DETDA resin has a tendency of forming good bonding with SWNTs, agreeing with MD simulation results. CONCLUSION The MD simulation results show that the molecules of Epon 862 resin and DETDA will change their molecular conformation and try to align their aromatic ring parallel to the surface of (10,10) SWNT due to 7t-stacking effect. As a result, these molecules will
Interfacial Bonding Strength stretch and wrap on the surface of the SWNT. Good tube/resin wetting and bonding can be expected. The simulations also show Epon resin molecules can be filled into the SWNT due to their molecular interactions. The interfacial shear strength could be as high as 75MPa for a single SWNT pullout from the cured resin matrix in the SWNT/Epon 862 resin nanocomposites due to van der Waals interactions. The nanostmctural observations show relatively good wetting and bonding between SWNT and Epon 862 resin system, preliminarily in agreement with MD simulation results.
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FIGURE 6 480% increase of the storage modulus of the nanocomposites
FIGURE 7 AFM observation of SWNT/resin wetting
ACKNOWLEDGEMENTS This research is sponsored by Air Force Research Laboratory (Grant #: F0863001-1-0010), NSFIUCRC Program (Award #: 0224612), IUCRC members, and Florida State University Cornerstone Research Program. FIGURE 8 Good SWNT/resin bonding
REFERENCES 1.
9. 10. 11. 12. 13. 14.
Cooper, C.A., Young, RJ. and Halsall, M. 2001.Composites Part A: Applied Science and Manufacturing, 32, 401 -411. Thostenson, E.T., RenZF, and Chou, T.W. 2001 .Composites Science and Technology, 61,1899-1912. Lau, K.T. and Hui, D. 2002. Composites Part B, 33, 263-177. Schadler, L.S., Giannaris, S.C. and Ajayan, P.M. 1997. Applied Physics Letter, 73(26)- 3842-3844 1998. Ajayan, P.M., Progress Crystal Growth and Characterization, 34: 37-51. Dujardin, E., Ebbesen, T.W., Hiura, H. and Tanigaki, K. 1994. Science, 265: 1850-1852. Ajayan, P.M., Schadler, L.S., and Giannaris, C , and Rubio, A. 2000. Advanced Materials, 12(10): 750-753. Jin, Z.X., Pramoda, K.P., Xu, G.Q, and Goh, S.H. 2001 .ChemicalPhysics Letters, 337: 43-47. Lozano, K., Rios, J. andBarrera, E.V., Journal of Applied Polymer Science, 80: 1162-1172 2001. Materials Studio, User's Manual, Version 1.2. 2001. Accelrys, Inc., San Diego, CA. Sun, H. 1994. Journal of Computational Chemistry, 15 (7), 752. Liao, K. and Li, S. 2001. Applied Physics Letters, 79 (25), 4225. DiBenedetto, A.T. 1991.Composites Science and Technology, 42, 103. Gou, J., Liang, Z., Zhang, C , Wang, B. and Kramer, L.. 2002. Proceedings ofTEXCOMP 6.
Epoxy-clay Nanocomposites: Morphology, Moisture Absorption Behavior and Thermo-mechanical Properties Chugang HU and Jang-Kyo KIM Department of Mechanical Engineering, Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong Sharmin BARI Materials Science and Engineering Program, Hong Kong University of Science & Technology, Clear Water Bay, Hong Kong
ABSTRACT: The morphology and moisture barrier characteristics are studied of epoxy-based nanocomposites reinforced with layered silicates. Two different types of organoclay, including the octadecylamine modified montmorillonite (I30P) and the quaternary alkylamine modified montmorillonite (KH-MT), were studied. The X-ray diffraction (XRD) and transmission electron microscopy (TEM) indicated the formation of intercalated nanocomposite for the KH-MT system, while intercalated/ordered-exfoliated nanocomposite for BOP system. The moisture absorption behaviour was different for different organoclays: the moisture absorption rate was similar for the neat polymer and the KH-MT system, which could be fitted to the Fick's second law. The moisture absorption rate of the I30P system was much lower than the two systems, which was predicted using a non-Fickian model based on the ID Langmuirian solution. The deviation from the Fickian diffusion for the latter system is associated with exfoliated morphology and more uniform dispersion of clay particles, which altered the diffusion path of water molecules in the nanocomposite. The moisture diffusivity of nanocomposites in general decreased with increasing clay content, the reduction being more pronounced for the I30P system. Moisture-induced thermomechanical properties changes for these two nanocomposites were studied as well.
INTRODUCTION Polymer-clay nanocomposites are considered a new class of advanced organic-inorganic materials. The nanoclay consists of nanoscale silicate sheets and other mineral oxides and possesses unique capabilities valuable to the nanocomposites, which cannot be found in conventional micrometer-scale particulate reinforcements. Apart from improved mechanical properties [1], the excellent barrier capability arising from the extremely high aspect ratio of nanoclay plates is one of the most attractive properties of nanoclay composites that have only started to be used in practical applications. The barrier characteristics are manifested in terms of reduced
* Correspondence Author: Clear Water Bay, Kowloon, Hong Kong; E-mail: [email protected]; Fax: 23581543.
690
Epoxy-clay Nanocomposites
permeability of moisture, gases and solvents, improved chemical resistance, reduced swelling by solvents compared to neat polymers [1-2]. This paper studied barrier properties of clay-epoxy nanocomposites for applications as adhesive, coating, moulding compound and matrix for fiber reinforced composites in the electronic packaging and infrastructure industries. The moisture absorption and diffusion behavior is investigated of the nanocomposite containing different types of clay and clay contents. Special emphasis is placed on the influences of moisture on the changes in thermomechanical properties, such as glass transition temperature, Tg, and coefficient of thermal expansion (CTE). THEORY OF MOISTURE DIFFUSION IN POLYMERIC MATERIALS The moisture absorption is most often represented with a Fickian model with solution for one-dimension case shown in equation (1) [3], where Mt is percentage weight gain, D is diffusivity and t is diffusion time. M
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A more versatile model used for composite materials for the relative moisture uptake can be expressed using the one-dimensional Langmuirian solution [4] having two exponential terms as shown in equation (2), where a and ft are constants. EXPERIMENTAL Materials and Sample Preparation The resin system used throughout this work consists of a diglycidyl ether of bisphenol A (DGEBA) epoxy (Epon828, supplied by Shell Corp.), and 1,3-phenylenediamine (mPDA, supplied by Aldrich) amine curing agent. Two organically treated clay, namely, KH-MT-TJ2 (Quaternary alkylamine modified montmorillonite, described as KH-MT hereafter) and I.30P (Octadecylamine modified montmorillonite, described as BOP hereafter) were used as the reinforcement to prepare nanocomposites. Desired amount of epoxy was drawn into a breaker, which was heated to 75° C to lower the resin viscosity. Clay of 3 and 5wt% was added to resin, which was stirred with a mixer for 12 h. The mixture was outgassed in a vacuum oven, followed by addition of a stoichiometric amount of mPDA (14.5 wt% of Epon828) and mixing for another 3 min. The mixture was then cast into the flat mold that consisted of two matching aluminum plates and a Teflon dam of nominal thickness lmm, with an approximately square mould cavity. The mould was cured at 75°C for 3h, followed by postcure at 125°C for 3h. Characterization of Morphology, Moisture Diffusion and Thermomechanical Properties The degree of intercalation or exfoliation of the layered silicates and their interlayer distance were studied using an X-ray diffraction analyzer. The transmission
Epoxy-clay Nanocomposites
691
electron microscopy (TEM) was used to directly examine the morphology of the nanocomposites. The nanocomposite plates released from the mould were approximately square with nominal dimensions of 100 mm x 100 mm x 1 mm, which well follows the ASTM 5229 for moisture absorption test of composite materials. All specimens were dried in a vacuum oven at 90°C for 4 days. For the moisture absorption test, specimens were hygrothermally treated in an environmental chamber at 85°C and 85% RH. The linear expansion of specimens in the thickness direction with and without moisture exposure was measured using a thermo-mechanical analyzer (TMA, SDTA840). The coefficients of thermal expansion (CTEs) were determined at temperatures below and above Tg. The loss modulus and the corresponding glass transition temperature, Tg, after moisture absorption were studied using a dynamic mechanical analyzer (DMA, 7 Perkin Elmer) at temperatures between 30°C and 200°C. RESULTS AND DISSCUSSION Morphology The degree of silicate layer separation was studied using the XRD spectra and TEM (see Figures 1). A negligible increase in interlayer distance (from 3.21nm to 3.3pnm) was observed for the KH-MT filled nanocomposites. TEM micrograph confirmed the formation of intercalated nanocomposite for the KH-MT system, whereas intercalated/ordered-exfoliated nanocomposite were formed for the I30P system [5], 1.96 nm
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Moisture Absorption Behavior Figure 2(a-e) shows the plots of percentage weight gains as a function of root time per specimen thickness, t1/2/h, for specimens with varying clay contents. Also superimposed in these figures are the prediction curves based on Equations (1) and (2), respectively for the KH-MT and I30P systems. For the KH-MT system, the weight gain increased linearly with t1/2 /h, followed by saturation, whose phenomenon was fitted to the Fickian model. In contrast, the experimental data deviated significantly from the prediction if the same Fickian model was used for the I30P system. This means that a non-Fickian model described in Equation (2) was needed to fit the abnormal moisture absorption curve. It is noted that the KH-MT and neat epoxy systems were fully saturated with moisture within 20 days, whereas the BOP system could not be saturated even after 25 days.
692
Epoxy-clay Nanocomposites
The different moisture absorption behaviours shown by different types of organoclay are attributed to the degree of exfoliation and dispersion of clay particles. The well-dispersed BOP clay particles provided a better barrier property, significantly delaying the moisture saturation. However, the KH-MT clay hardly exfoliated, preventing the curing agent from permeation into the gallery and thus creating locally amine-rich regions external to the clay galleries. The presence of excessive amine groups that are of polar functionality may absorb more moisture than the stoichiometric one. Another possible reason for the rapid moisture saturation in the KH-MT system is that the water molecules tended to gather around the clay particles especially when the particles are poorly bonded to the matrix. The diffusivity data for the KH-MT and BOP systems calculated based on the Fick's second law or the non-Fickian solution, respectively, are presented in Fig. 2(f). The diffusivity in general decreased with increasing clay content, the reduction being far more prominent for the BOP system than the KH-MT system. A remarkable 42% reduction in diffusivity compared to the neat epoxy resin was achieved with only 5wt% clay content for the BOP system, whereas a 24% reduction was recorded for the KH-MT system for the same condition. 3
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(c) (f) FIGURE 2 Plots of weight gain, Mt, vs square root time (sec) per specimen thickness (mm), t"2/h, for (a) neat epoxy; (b) and (c) nanocomposites systems containing 3 and 5 wt% KH-MT; (d) and (e) nanocomposites containing 3 and 5 wt% BOP, respectively, (f) diffusivity as a function of clay content for nanocomposites containing different type of clay.
Epoxy-clay Nanocomposites
693
Effects of Moisture on Thermomechanical Properties The changes in loss modulus with temperature for the nanocomposite with 5wt% BOP clay with varying moisture contents are shown in Figure 3(a). It is clearly seen that the loss peak shifted to a low temperature and the curve broadened with increasing moisture content. The shift of loss peak is the consequence of plasticization of epoxy by moisture. The variations of glass transition temperature, Tg, that correspond to the peak values obtained from the loss modulus curves are plotted as a function of moisture content for three different systems in Figure 3(b). The Tg decreased linearly with increasing moisture content for all materials studied. The 13 OP filled nanocomposite showed much higher Tg values than the KH-MT system or the neat epoxy over the whole moisture content studied. There were virtually no improvements of Tg by adding KH-MT clay into epoxy, nor was KH-MT clay effective in mitigating the plasticizing effect of moisture.
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(a) (b) (c) FIGURE 4 Comparisons of CTE values obtained before and after moisture absorption as a function of clay content for the BOP/mPDA system: (a) below T& (b) above Tg and (c) relative thickness change, AH/H, as a function of temperature change obtained from TMA for the BOP nanocomposites before and after moisture exposure.
The CTE values determined below and above Tg for BOP/mPDA system are presented in Figure 4. The CTE decreased consistently with increasing clay content for all conditions studied. The reduction of CTE at temperatures above Tg was particularly pronounced. It appears that the intercalated/exfoliated silicate layers constrained the chain mobility of the polymer in the nanocomposite, reducing the
694
Epoxy-clay Nanocomposites
thermal expansion with increasing clay content. The CTE values obtained below Tg after moisture absorption were higher than the dry samples. The absorbed water molecules can form hydrogen bonds with hydroxyl groups in polymer chains, which may interrupt the initial bonds between polymer chains. This results in higher mobility of polymer chains at elevated temperatures, giving rise to a higher free volume change and a higher CTE. When temperature is increased toward the Tg of the wet composite, the moisture evaporates, leading to a rapid expansion of free volume in polymers (see the abrupt peaks in Figure 4(c)). When temperature is further increased beyond the Tg, the majority of moisture has already evaporated and the expansion of free volume becomes limited. This may be responsible for the lower CTE values than the dry samples above Tg. CONCLUSION The morphology, moisture barrier characteristics and the thermo-mechanical properties affected by moisture absorption were studied for epoxy-based nanocomposites containing organoclays. I30P system can form intercalated/ordered-exfoliated nanocomposite with d-spacing larger than 8nm, while the intercalated nanocomposite were synthesized for KH-MT system with the final interlayer distance of 3.39nm after cure. The well dispersed clay particles in the I30P system provided a better moisture barrier property than the KH-MT system or neat epoxy. The Ficldan equation was used to predict the moisture diffusion through the KH-MT and neat epoxy systems, whereas the non-linear Fickian equation based on the ID Langmuirian solution should be used to fit the experimental data for the 13OP system. The glass transition temperature, Tg, decreased linearly with increasing moisture content for all materials studied. The BOP system showed consistently higher Tg values than the KH-MT system or the neat epoxy in the range of moisture content studied. After moisture exposure, the CTE below Tg is higher than dry case, but the reverse is true for CTE above Tg. ACKNOWLEDGEMENTS This work has been supported by the Research Grants Council of the Hong Kong Special Administrative Region (Project No. HKUST 6184/03E) and Direct Research Grant (DAG 02/03.EG31). The technical supports by the Advanced Engineering Material Facilities and Materials Characterization and Preparation Facilities, HKUST are also acknowledged. REFERENCES 1. T. J. Piimavaia and G. W. Beall. 2000. "Polymer-clay nanocomposites." 2. Lan T, and Pinnavaia TJ. 1994. "Clay-reinforced epoxy nanocomposites," Chem. Mater., 6(12): 2216-2219. 3. Crank J. 1956. "The Mathematics of Diffusion," Clarendon Press, Oxford, UK. 4. Gurtin ME and Yatomi C. 1979. "On a model for two phase diffusion in composite materials," J. Compos. Mater., 13: 126-130. 5. HU C.G., KIM J.K. and LI Robert K.Y.. "Effects of Clay Type and Curing Agent on Mechanical and Thermal Properties of Epoxy-layered Silicate Nanocomposites," ACCM-4, 6th-9th July, 2004.
Study on Fabrication and Properties of Nano-alumina Particles Reinforced Thermosetting Matrix Composites Yihua Cui1*, Jie Tao1, Dingzhu Wo1 College of Material Science and Technology, Nanjing University of Aeronautics &Astronautics, Nanjing, P.R.China
ABSTRACT In this research work, nano-alumina particles were treated in advance by KH-570 and ND-204 silane coupler and dispersed into unsaturated polyester by mechanical mixing with the help of ultrasonic wave. The micro structure of the prepared nanocomposites was observed by TEM and the properties of the nanocomposites including barcol hardness, viscosity, flexural strength and impact toughness were tested and analyzed. The fracture surface of the nanocomposites was observed and studied by SEM. The results show that by ultrasonic dispersion, the nano-alumina particles may be uniformly decentralized into unsaturated polyester resins. With the incorporation of nano-alumina particles, the viscosity of the liquid mixture increases a little. Compared with neat resin, bacol hardness of the cured resin was enhanced as a function of particles volume fraction. The flexural and impact strength of prepared nanocomposites are also notably enhanced if the content of nanoparticles is not more than a certain range. The fracture surfaces of nanocomposites are notably different from the polymer matrix. The adhesion between the nanoparticles and polymer play an important role in the fracture toughness of nanocomposites. INTRODUCTION Developments on material performance depend on the ability to synthesize new materials that exhibit enhanced properties including mechanical strength, stiffness, impact resistance, wear resistance, durability, etc. The incorporation of inorganic particulate fillers has been proved to be an effective way for improvement of the mechanical properties, and in particular the mechanical properties of polymeric materials. Thermosetting polymer such as unsaturated polyesters, epoxy resins and phenol resins, exhibit many useful characteristics including mechanical, electrical, and chemical properties because of their high degree of cross-linking between individual polymeric chains and have been used extensively as matrix materials for many high-performance parts in the aeronautics, automobile, and electrics industry. However, thermosetting polymeric materials are poor inhibitors of crack initiation and propagation. Recently, it has been demonstrated that addition of nanometer-sized fillers can be used to significantly enhance the mechanical properties of thermosetting polymer [1-4]. * Corresponding Author, Box 1006, 29 Yudao Street, College of Material Science and Technology, NUAA, 210016, Nanjing, P.R.China, Fax:0086-25-4895378 E-Mail: [email protected]
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Nano-alumina Particles Reinforced Thermosetting Matrix Composites
To successfully fabricate nanocomposites, it is very important to be able to thoroughly and uniformly decentralize the nanoparticles in the matrix and to maximize the interaction between the nanoparticles and polymer matrix. However, nanoparticles easily tend to form agglomerates or clusters which containing numerous nanoparticles. Several techniques have been used to fabricate nanocomposites: sol-gel, hot pressing and melt interaction [5-8]. Mechanical mixing is a relatively simple method to make nanocomposites. By this process, thermosetting resins and nanoparticles are mixed together, cast into a mold, and polymerized [9,10]. In this research work, nano-alumina particles were treated in advance by KH-570 and ND-204 silane coupler and dispersed into'unsaturated polyester with the help of ultrasonic wave. The micro structure of the prepared nanocomposites was observed by TEM. The properties of the nano-alumina reinforced nanocomposites including barcol hardness, viscosity, flexural strength and impact toughness. The fracture surface of the nanocomposites was observed and studied by SEM. EXPERIMENTAL PROCEDURE Thermosetting polymer nanocomposites were fabricated by incorporating alumina (AI2O3) particles (provided by Nanjing Haitai Nanomaterials Co., Ltd) with average diameter of 60-80 nm into unsaturated polyester resin (P65-901, Jinlin DSM Rein Co., Ltd). Two kinds of silane coupler named by KH-570 and ND-204 were used to treat the nano-alumina particles. The content of coupler is about 0.5-5 wt% of nano-alumina. An appropriate amount of KH-570 or ND-204 silane was diluted by alcohol-water solution (alcohol/water=9/l in volume ratio) and the pH value of above was adjusted by glacial acetic acid to 3.5-5.5. Keep the solution being stirred for 1.5-2 hours. The amount of silane was determined based on its wetting surface and the effective surface area of the particles to provide complete coverage. Nano-alumina particles were added to above solution at varying volume percentages (0%, 1%, 3%, 5%, 7%) and mechanically mixed in a glass beaker for approximately 10 min. The mixture was placed in a vacuum chamber at 50-100 Pa for 5 min to remove trapped air bubbles generated during the mechanically mixing process. After the deaeration process, this was followed by further dispersion through ultrasonication using a KQ-2200 Sonic Disruptor. The ultrasonic probe amplitude was fixed, and disruption was carried out for 30 min in the pulsing mode (5 s on, 10s off) to prevent undesirable heating of the polyester resin. This mixture was then again placed in a vacuum chamber at 50-100 Pa for 15 min to remove trapped air. The viscosity of each mixture was tested by NDJ-2 rotatory viscosimeter. Then methl ethyl ketone peroxide and cobalt octoate (obtained from Zhejiang Huangyan Jiaokang Chemical Co., Ltd) added respectively at 1.0%, 0.5% by weight of polyester was used as the catalyst and the accelerator to initiate polymerization under ambient conditions in specially prepared molds made of two sheets of glass to yield 8-mm-thick cast sheets of the composite. These sheets were postcured at 55°C for 3h followed by 65 °C for 4h in a forced convection oven, which yield completely cross-linked material free of any residual stresses. The specimens were machined into the desired size for property testing. Transmission electron microscopy (TEM) was used to analyze the dispersion of nanoparticles in the matrix. The bacol hardness, flexural strength and fracture toughness of prepared samples were tested according to corresponding standard.
Nano-alumina Particles Reinforced Thermosetting Matrix Composites
697
RESULTS AND DISCUSSION
(a) X 20000
(b) X 20000
FIGURE 1 Dispersion of nano-alumina particles in the matrix (a - ND-204, b -KH-570)
TEM micrographs of specimens with nanoparticles being treated respectively by ND-204 and KH-570 are shown in Fig. 1. As can be seen from the picture, the fabrication procedure in this work may be used to produce nanocomposites with good particle dispersion, particularly in specimens being treated by ND-204 coupler. Although it is clear that there were many and somewhat large agglomerates present in the specimens, but the vast majority of these agglomerates were still in the nanometer size range. KH-570 and ND-204 are two different kinds of silane coupler. This organofunctional silane acts as a chemical bridge between the inorganic nano-alumina particles and the organic polyester matrix and leads to strong particle-matrix adhesion. The effect of incorporation of nanoparticles on the technological properties of resins is very necessary to be studied. Fig. 2(a) shows the relationship between the viscosity of polyester resins and the volume fraction of nanoparticles. The addition of the nano-alumina particles resulted in enhanced viscosity of polyester resins. There wasn't a great range of viscosity variation when the volume fraction of nano-alumina particle was less than 3%. On the contrary, the viscosity of polyester resin increased 2 times of neat resin as the volume fraction of the particles was increased to 7%. This may be explained by the fact that there were more and larger agglomerates present in the resins when the volume fraction of nano-alumina particle was more than 3%. When the nano-particles were treated by ND-204 coupler, the enhanced viscosity value was less than that by KH-570, which implied a better chemical resemblance between polymer chains and treated nano-particles in the former than in the later.
1500
3%
5%
7%
Particle volume fraction
Particle volume fraction
(a) (b) FIGURE 2 Variation of viscosity and bacol hardness, as a function of particle volume fraction
Nano-alumina Particles Reinforced Thermosetting Matrix Composites
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Fig. 2(b) plots the variation of bacol hardness of nanocomposites, as a function of the volume fraction, for the cases of KH-570 treated and ND-204 treated nano-alumina particles. As shown in this figure, the addition of nano-alumina particles resulted in a little increase in bacol hardness of nanocomposite when the volume fraction of nano-alumina particles was less than 5%. ND-204 coupler showed better effect than KH-570 coupler to raise the hardness of nanocomposites. When the volume fraction of nano-alumina particles was more than 5%, the hardness of nanocomposites decreased to some extent, this may also be caused by worse dispersion of nano-particles.
0%
1%
3%
5%
7%
particle volume fraction
1%
3%
5% 7% Particle volume fraction
(a) (b) FIGURE 3 Flexural strength and impact toughness of nanocomposites, as a function of particle volume fraction
There was a notable increase in flexural strength of nanocomposites with incorporation of nano-alumina particles. The flexural strength of nanocomposite will increase when the volume fraction of nanoparticles was not more than 3%, and ND-204 coupler has better effect than KH-570 coupler. When the volume fraction of nano-alumina particles was more than 7%, the flexural strength of nanocomposites was even less than matrix (Fig. 3(a)). Fig. 3(b) showed the relationship between the impact toughness of nanocomposites and particle volume fraction. It is clear that the addition of the nano-particles had a great effect on fracture toughness of nanocomposites. Even at small amount of 3%, increases in toughness of 67% for ND-204 and 59% for KH-570, were observed when compared with the neat polyester. At 7 vol.%, though the toughness of nanocomposites was approximately the same of the matrix, this was because specimens containing 1% and 3 % alumina particles possessed better particle dispersion with only a little agglomeration. On the other hand, for specimens containing 5 % and 7 % alumina particles, more agglomerations were present. If the particulates are weak, crack may pass through the particles, known as trans-particulate fracture. On the other hand, if they are strong enough, particulates can inhibit crack initiation and propagation if there exists a strong bond between the fillers and the matrix. Agglomerations, on the other hand, can behave as crack initiation sites, lowering the fracture toughness of nanocomposites. Previous research work [11] demonstrated that both micrometer- and nanometer-sized particles can lead to significant increase in fracture toughness, even at very small volume fractions and well-dispersed particles that are strongly bonded to the polyester matrix promote crack front trapping as the primary extrinsic toughening mechanism and thus lead to an increase in fracture toughness.
Nano-alumina Particles Reinforced Thermosetting Matrix Composites
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iv-.v rat* SAW*** JE
• •:
' •
(a) (b) FIGURE 4 Fracture surface of matrix and nanocomposites
Fig. 4(a) and (b) are respectively the impact fracture surface of matrix and nanocomposites. As can be seen from the figure, the fracture surface of the neat polyester specimen is relatively smooth, indicating that minimal energy was required to fracture the specimen and a weak resistance to crack propagation. On the other hand, the surfaces of the specimens embedded with nanoparticles depict rougher features such as out-of-plane flaking and thumbnail-type markings that require additional energy to be formed. Meanwhile, the particle interface was clean or only a thin layer of residual polyester was left which implied the nano-alumina particles were poorly bonded to the polyester matrix and debonded easily during the fracture process. This lack of particles-matrix adhesion implied the particles were unable to promote crack trapping and thus could not promote enhancements in the fracture toughness. Moreover, the poorly bonded particles acted as defects in the composites, thereby lowering the resistance to crack growth and thus leading to deterioration in the fracture toughness [2]. To make nanocomposites with high mechanical strength fracture toughness, a strong particle-matrix interface is very necessary to obtain. CONCLUSIONS The procedure described in this paper can be successfully used to make polymer matrix nanocomposites. Incorporation of nano-alumina particles will affect the viscosity, hardness, flexural strength and impact toughness of polymer resin, the effectiveness of which depend on the volume fraction of nanoparticles and the type of coupler. The fracture surfaces of nanocomposites are notably different from the polymer matrix. The adhesion between the nanoparticles and polymer play a role in the fracture toughness of nanocomposites.
REFERRENCES 1.
2. 3. 4.
R. P. Singh, and M. Zhang. 2001. "Fracture of a Brittle Polymer Reinforced with Micron and Nanometer Sized metal and Ceramic Particles," Symposium on Multi-Physical Length Scale Modeling Simulation and Design of Materials and Systems, 2001 Mechanics and Materials conference, San Diego, CA, June 2001. Victor M. F. Evora, Arun Shukla. 2003. "Fabrication, characterization and dynamic behavior of polyester/TiO2 nanocomposites," Materials Science and Engineering, A. 361(1-2): 358-366 I. Crivellivisconti, A. Langella, M. Durante. 2001. "The wear Behavior of composite materials with epoxy matrix filled with hard powder," Applied Composite Materials, (8): 179-189 Bernd Wetzel, Frank Haupert, M. Q. Zhang. 2003. "Epoxy nanocomposites with high mechanical
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and tribological performance," Composite Science and Technology, (63): 2055-2067 M. C. Cheung, H. L. W. Chan, Q. F. Zhou, C. L. Choy. 1999. "Characterization of barium titanate ceramic/ceramic, nanocomposite films prepared by a sol-gel process," Nanostructure Materials, (11): 837 6. J. Zhao, L. C. Stearns, M. P. harmer, H. M. Chan, G.A. Miller. 1993. "Mechanical Behavior of Alumina-Silicon Carbide 'Nanocomposites'," J. Am. Ceram. Soc, (76): 503 7. C. C. Anya. 1999. "Microstructural nature of strengthening and toughening in Al2O3-SiC (p) nanocomposites," J. Material Science, (34): 5557 8. Asma Yasmin, Jandro L. Abot, Isaac M. Daniel. 2003. "Processing of clay/epoxy nanocomposites by shear mixing," Scripta Materialia, (49): 81-86 9. R.P. Singh, M. Zhang, D. Chan. 2002. "Toughening of a Brittle Thermosetting Polymer: Effects of Reinforcement Particle Size and Volume Fraction," J. Material Science, (37): 781-788 10. C. B. Ng, B. J. Ash, L. S. Schadler. 2001. "A study of the mechanical and permeability properties of nano- and micro-TiO 2 filled epoxy composites," Advanced Composites Letters, 10(3): 101-111 11. A. J. Kinloch, A. C. Taylor. 2003. "Mechanical and fracture properties of epoxy/inorganic microand nano-composites," J. materials Science Letters, (22): 1439-1441 5.
Investigating High Strain Rate Responses of Nylon 6/ Clay Nanocomposites Jen Chieh Huang and Jia-Lin Tsai* Department of Mechanical Engineering National Chiao Tung University Hsinchu, Taiwan 300, R.O.C
ABSTRACT This research aims to investigate the high strain rate responses of nylon 6/clay nanocomposites. High strain rate experiments were conducted on both nylon 6 nanocomposites with 5 wt% loading of the organoclay and nylon 6 resins using an aluminum Split Hopkinson Pressure Bar (SHPB). hi order to extract the reliable stress and strain relation in the small strain ranges on the nanocomposites with the characteristics of low mechanical impedance, a pulse shaper technology were employed in the SHPB tests. Experimental observations demonstrate that at high strain rates, the supplement of 5 wt% organoclay in the nylon 6 can enhance the Young's modulus up to 25%. This increment is greater than that obtained at low strain rates.
INTRODUCTION With the latest development of nanotechnology, composites reinforced with nanoclay platelets have been of great interest to many researchers [1]. The nanoclay platelet is an ultra thin (1 nm) silicate film with lateral dimensions up to 1 ju m. Without special processing, the platelets are held together by the weak ionic bond into clay tactoids. Through the ion exchange process, the sodium ions attracted on the surfaces of the platelets were replaced with organic cations which can improve the interfacial adhesion between the polymer and the platelet. After an appropriate process, the aggregated platelets can be exfoliated and dispersed uniformly in the polymer. Depending on the degree of the exfoliation, there are three categories of nanocomposites generated, i.e., tactoid intercalated and exfoliated [2]. Toyota research center carried out a pioneering work on synthesizing the nylon 6/clay nanocomposites by means of polymerization process. The increments of tensile strength, modulus and heat distortion temperature relative to pure resin were reported in their studies [3-5]. Cho et al [6] demonstrated the preparation of nylon 6/organoclay nanocomposites via direct melt compounding approach using a conventional twin screw extruder. The mechanical properties and morphology of these nanocomposites were examined and compared to those made by an in situ polymerization process. They concluded that the organoclay was better exfoliated into nylon 6 matrix when compounded using the twin screw extruder rather than the single screw extruder. The similar process for the fabrication of nanocomposites using a twin screw extruder was employed by Liu et al [7]. It was indicated that the nanocomposites
Jia-Lin Tsai, Department of Mechanical Engineering National Chiao Tung University Hsinchu, Taiwan 300, Fax:886-3-5720634, Email: [email protected]
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High Strain Rate Responses of Nylon 6/Clay Nanocomposites
are superior to Nylon 6 in terms of strength and modulus. In view of the foregoing, most of efforts were made to synthesize the nanocomposites as well as to conduct quasi-static tests for the investigation of the material properties. It is well known that polymer materials are sensitive to strain rate and thus, the nanoclay/nylon 6 nanocomposites may also be rate dependent. The high strain responses of polymeric materials were characterized by Chen et al [8] using the aluminum split Hopkinson pressure bar (SHPB). A variety of polymers at different strain rates were examined by Walley et al [9]. However, few literatures concerning the dynamic response of organoclay nanocomposites were reported, hi this study, the dynamic responses of neat nylon 6 and nylon 6/clay were investigated using SHPB. In order to attain more accurate stress-strain curves, the pulse shaper technique was employed in SHPB tests. Based on the experimental data, the Young's modulus of the materials at high strain rates was evaluated and the results were compared with those measured from quasi-static tests. SPECIMEN PREPARATION AND CHARACTERIZATION The neat nylon 6 (RTP 200A) and nylon 6/clay nanocomposites (RTP 299AX) used were commercially available from RTP Company USA. The organoclay (5.0 wt.%) was dispersed into nylon 6 via melt compounding process to form nanocomposite pellets [10]. The pellets were then injection molded into cylindrical specimens with 10 mm long and 10 mm in diameter for the compression tests. The barrel temperature and the mold temperature were set at 235 °C, and 75 °C. An injection pressure of 3.2MPa and holding pressure of 4.8MPa was used. hi order to reduce the contact friction between the specimen and the loading fixture, all specimens were polished using a lapping machine with 25um aluminum oxide powder, hi this manner, the specimens with smooth and parallel loading surfaces were achieved. Before the tests were conducted, all specimens were kept in a vacuum oven at temperature 50 °C to prevent from the moisture effect.
(a) 100, 000 X
(b) 50,000 X
FIGURE 1 TEM micrographs of nylon 6/clay nanocomposites
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The morphology of nylon 6/clay nanocomposites was investigated using a JEOL JEM-200CX transmission electron microscope (TEM). The 100 nm thick sample was cut from the specimens along the axial direction using a microtome at cryogenic conditions. Figure 1 reveals TEM micrographs of nylon 6/clay nanocomposites at 100,000 and 50,000 magnifications, respectively. It is shown that a large number of the mixed intercalated/tactoids structures still exist, whereas only fewer layers of platelets tend to exfoliate. As a result, the organoclay is not well exfoliated in the current nanocomposite specimens.
EXPERIMENT High Strain Rate Tests High strain rate experiments were conducted on nylon 6 and nylon 6/clay nanocomposites using a Split Hopkinson Pressure Bar (SHPB) which is an effective but costless apparatus for determining the dynamic stress and strain relation [8]. The schematic of SHPB is shown in Figure 2. During the test, the specimen was sandwiched between the incident bar and the transmission bar and, based on the one dimension wave theory, the stress and strain histories of the specimens can be calculated from the signals obtained from gages A and B, respectively using Hopkinson bar formula [11]. In the present study, the strain response of the specimen was also measured using strain gage directly mounted on the specimen. Figure 3 shows the comparison of the strain histories for the nylon 6/clay nanocomposite specimen obtained using the Hopkinson bar formula and the strain gage on the specimen, respectively. It is evident that the strain history calculated based on the Hopkinson bar theory deviates from that directly measured on the specimen. Consequently, the respective stress and strain relation obtained were also different, hi this study, the strain rate measured directly from the specimen was used and the average strain rates for nylon 6 were about 400/s. It is noted that since the mechanical impedances for nylon 6 and nylon 6/clay nanocomposites are lower, aluminum SHPB were employed in the test to enhance the intensity of the strain gage signals. Moreover, pulse shaper technique was utilized to facilitate the homogeneous deformation of the specimens and as a result, the reliable stress and strain curves in small strain ranges were obtained [12,13]. hi this study, a 5mm thick nylon 6 disk was selected as a pulse shaper for SHPB tests
Pulse shaper
\| Striker bar
Gage A
Specimen I Gage B
• Incident bar
1 l ^
D
Transmission bar
FIGURE 2 The split Hopkinson pressure bar apparatus
Throw-off bar
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High Strain Rate Responses of Nylon 6/Clay Nanocomposites 0.03
— SHPB Formula — Gage 0.02
c
I V) 0.01
0
20
40
60
80
100
US FIGURE 3 The comparison of the strain histories for the nylon 6/clay nanocomposite specimen
Low Strain Rate Tests In order to have consistency, the specimens used for high strain rate test were employed for low strain rate tests. In addition, the same end loading condition as shown in Figure 4 was applied on the specimens. A self-adjusting device was used to eliminate potential bending moments and also to ensure the specimen to be in full contact with the loading surfaces. During the tests, the stress was obtained from the load cell and the corresponding strain was measured from strain gages mounted on the specimens. The stress and strain history for each test was recorded using LabVIEW. It is noted that at least two specimens were tested in each case to conform the experimental results.
Specimen Hardened steel Self-adjusting device
rurr
Applied displacement FIGURE 4 A self-adjusting device for low strain rate tests.
RESULTS AND DISCUSSION The dynamic stress and strain curves for nylon 6/clay nanocomposites and nylon 6 were shown in Figure 5. The values of the Young's modulus were extracted from the curves and the results were summarized in Table 1. In the same manner, the Young's modulus obtained from quasi-static compression tests was also enclosed in Table 1 for
High Strain Rate Responses of Nylon 6/Clay Nanocomposites
705
comparison. It was shown that, at high strain rate, the increment of Young's modulus for nylon 6 with the inclusion of clay is about 25%. However, only about 10% increment of Young's modulus was achieved for nylon 6 at low strain rates, which is quite lower than the results reported in the literatures [6,7]. This discrepancy may be attributed to the poor exfoliation and dispersion of the nanoclay into nylon 6. From TEM observation, it was illustrated that lots of clay platelets are still conglomerated together and thus, the effect of the nanoclay is not significant. Moreover, by looking closely at the Young's modulus of nylon 6 measured at different strain rates, it was found that the values are almost the same, which imply that nylon 6 is rate independent in the linear range. However, it is quite surprising that for nylon 6/clay nanocomposites with 5% nanoclay present, little rate sensitivity was observed.
0
0.005
0.01 Strain
0.015
0.02
FIGURE 5 Stress-strain curves of neat nylon 6 and nylon 6/clay nanocomposites at high strain rate.
TABLE I Young's modulus of nylon 6 and nylon 6/clay nanocomposites under two different strain rates
Material Nylon 6 Nylon 6/clay Enhancement
Dynamic (~400/s) 3.13GPa 3.90GPa 24.6%
Quasi-static (0.0001/s) 3.10GPa 3.39GPa 9.4%
SUMMARY High strain responses of nylon 6/clay nanocomposites were investigated using aluminum SHPB together with pulse shaper technology. The initial fluctuation in the dynamic stress strain curve was effectively reduced and as a result, the Young's modulus at high strain rate was obtained with accuracy. Based on the experimental results, it was indicated the effect of nanoclay on the stiffness enhancement for nylon 6 is more appreciable at higher strain rate rather than that at low strain rates. ACKNOWLEDGEMENTS This research was supported by the National Science Council, Taiwan under the contract No. NSC 91-2212-E-009-053 to National Chiao Tung University.
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High Strain Rate Responses of Nylon 6/Clay Nanocomposites
REFERENCES 1. 2.
3. 4.
5.
6. 7. 8. 9.
10. 11. 12. 13.
Pinnavaia, T.J. and Beall, G.W. (2000), Polymer-Clay Nanocomposites, John Wiley & Sons Ltd, New York. Dennis, H.R., Hunter, D.L., Chang, D., Kim, S., White, J.L. Cho, J.W. Paul, D.R. 2001 "Effect of Melt Processing Conditions on the Extent of Exfoliation in Organoclay-Based Nanocomposites," Polymer, Vol. 42, pp. 9513-9522. Usuki, A., Kojima, Y., Kawasumi, M., Okada, A., Fukushima, Y., Kurauchi, T., Kamigaito, O., 1993 "Synthesis of Nylon 6-Clay Hybrid," Journal ofMaterials Research, Vol. 8, No. 5, pp. 1179-1184. Kojima, Y., Usuki, A., Kawasumi, M., Okada, A., Kurauchi, T., Kamigaito, O., Kaji, K., 1994 "Fine Structure of Nylon 6-Clay Hybrid," Journal of Polymer Science: Part B: Polymer Physics, Vol. 32, pp. 625-630. Usuki, A., Koiwai, A., Kojima, Y., Kawasumi, M., Okada, A., Kurauchi, T., Kamigaito, O., 1995 "Interaction of Nylon 6-Clay Surface and Mechanical Properties of Nylon 6-Clay Hybrid," Journal of Applied Polymer Science, Vol. 55, pp. 119-123. Cho, J.W. and Paul, D.R., 2001 "Nylon 6 Nanocomposites by Melt Compounding," Polymer, Vol. 42, pp. 1083-1094. Liu, L. Qi, Z., Zhu, X. 1999 " Studies on Nylon 6/ Clay Nanocomposites by Melt-Intercalation Process" Journal of Applied Polymer Science, Vol. 71, PP. 1133-1138. Chen, W., Lu, F., Cheng, M. 2002 "Tension and Compression Tests of Two Polymers under Quasi-Static and Dynamic Loading" Polymer Testing, Vol. 21, pp. 113-121. Walley, S. M., Field, J. E., Pope, P. H., Safford, N. A., 1989 "A Study of the Rapid Deformation Behavior of a Range of Polymer," Philosophical transactions of the Royal Society of London A, Vol. 328, pp. 1-33. RTP® material data sheet. Graff, K.F., 1975. Wave Motion in Elastic Solids. Dover Publications, New York. Ninan, L., Tsai, J., Sun, C. T., 2001. "Use of split Hopkinson pressure bar for testing off-axis composites''', International Journal of"Impact Engineering, Vol. 25, pp. 291-313. Chen, W., Song, B., Frew, DJ. and Forrestal, M.J. 2003 "Dynamic Small Strain Measurement of a Metal Specimen with a Split Hopkinson Pressure bar" Experimental Mechanics, Vol. 43, No. 1 pp. 20-23.
Mechanical Properties of Si02/Epoxy Nanocomposites at Cryogenic Temperature C. J. Huanga'b, S. Y. Fua*' Y. H. Zhanga'b and L. F. Lia a. Cryogenic Materials Laboratory, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100080,China b. Graduate School of the Chinese Academy of Science, Beijing 100039, China
ABSTRACT Organic-inorganic hybrids were prepared using diglycidyl ether of bisphenol-F (DGEBF) type epoxy and tetraethylorthosilicate (TEOS) via the sol-gel process. The mechanical properties of the composites were studied at cryogenic temperature (77K). Results showed that the tensile strength, elongation at break and impact strength were enhanced by the addition of silica particles. The ashes of the composites were collected after burning off the matrix resin and the silica nano-particles were observed by TEM. The fracture surface was examined by scanning electron microscopy (SEM). The dependence of the mechanical properties of the nanocomposites at cryogenic temperature was discussed on the silica content. INTRODUCTION Epoxy resins played an important role in cryogenic engineering such as cryostat, superconducting magnets. However, cured epoxy resins were characterized by poor resistance to crack propagation. High mechanical properties are always desired for cryogenic application [1,2]. Recently, organic/inorganic hybrid materials have been investigated as promising materials with good mechanical properties. An approach to preparation of organic/inorganic hybrid materials is rigid particle addition [3-5]. Inorganic fillers are widely adopted for epoxy resins to improve strength and toughness. The mechanical properties of the inorganic-organic hybrid materials are determined by the following parameters such as particle size, filler volume fraction, properties of the filler and the matrix. The variation of some of these parameters leads to improved toughness and strength synchronously. Sol-gel process is a recommendable method for preparing inorganic-organic hybrid materials [6-8]. One of the advantages of the sol-gel process over directly dispersing nano-particles into organic matrix is easier to obtain homogeneous and transparent nanocomposites.
In the present study, epoxy-based organic/inorganic hybrid composites were prepared using the bisphenol-F type epoxy resin (DGEBF) and tetraethylorthosilicate (TEOS) as the organic and inorganic sources, respectively. The inorganic phase was incorporated into epoxy resin by sol-gel process. The tensile and impact properties of
' Corresponding author. Tel: +86-10-62659040, 80669735; Fax: +86-10-62564049,62659040; E-mail address: svfu(i2jcl.cry0.ac.cn
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SiO2/Epoxy Nanocomposites at Cryogenic Temperature
the silica/epoxy hybrids were investigated in detail. The fracture surfaces of tensile and impact samples were studied by scanning electron microscope (SEM). EXPERIMENTAL WORK Materials The materials used in this study were diglycidyl ether of bisphenol F (YDF-175,Kukdo chemical Ind. Co., Korea) as epoxy matrix, and polypropylene glycol diglycidyl ether (PPGDE) (PG-207, Kukdo Chemical Ind. Co., Korea) as plasticizer and Diethyl toluene diamine (DETD) (ETHACURE-100, Albemarle Co., USA) as hardener, and tetraethylorthosilicate (TEOS) (A.R. Beijng Chemical Co., China)as a precursor, and Ammonia solution (A.R, Beijing Chemical Co.) as a catalyst and Acetone (A.R. Beijing Chemical Co., China) as solvent. Specimen preparation The epoxy resin/silica nanocomposites were prepared via the following steps. Firstly, epoxy resin, ammonia and acetone were mixed and stirred (tagging solution A). At the same time, acetone and TEOS in a volume ratio of 10:2, were mixed and stirred for 2-3 min (tagging solution B). Then the two solutions (A and B) were mixed and stirred for 2-4 hours at ambient temperature. Secondly, the mixture was degassed in order to get rid of the more acetone, ammonia and H2O. Then, the plasticizer and the curing agent were addedto the above mixture. The resulting mixture was stirred for about 20min at ambient temperature. The mixture was impregnated into the preheated mould in an oven. Then the samples were gelled at 78 C for 24h and post-cured at 135°C for 12h. The tensile samples were prepared according to the recommendation of ASTM D638-96. The impact specimens were prepared according to GB/T2571-95, the same as ISO-179-92 [9]. Figurel shows the geometry of the impact specimen. After curing process, all the tensile and impact specimens were ground and polished. Then the specimens were stored in a drying oven for mechanical testing.
FIGURE 1 Geometry of the impact specimen
Microscopy Silica/epoxy hybrid materials were burned in an electric muffle furnace for 2~3 hours at 620°C. The ashes were collected after burning off the epoxy matrix and the silica nano-particles (Figs.2 and 3) were observed by transmission electron microscope (TEM, JEM-200CX). The fracture surfaces were examined by scanning electron microscopy (SEM, Hitachi S-450). Before SEM observation, the fracture surfaces were cleaned with alcohol and coated with a thin gold layer to improve image quality.
SiO2/Epoxy Nanocomposites at Cryogenic Temperature
FIGURE 2 TEM of silica particles from 2 wt% Silica/epoxy hybrid materials
0
1
2
3
4
Silica Content (wt%)
FIGURE 4 Effect of silica content on the tensile strenth
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FIGURE 3 TEM of silica particles from Silica/epoxy hybid materials
1 2 3 Silica Content (wt%)
FIGURE 5 Effect of silica content on elongation at break
Mechanical testing The stress-strain curve was obtained using an axial extensometer coupled to a Reger mechanical tester with a lOkN load cell and a crosshead speed of 2 mm/min. The tensile testing was performed at both room temperature (RT) and liquid nitrogen temperature (LNT). Impact energy (IE) was measured according to GB/T2571-1995. Testing was carried out on a Reger impact tester type machine equipped with a hammer of 7.35 J. Five samples from each formulation were tested. Average IE values along with the standard deviations were reported. The IS is calculated as follows: (kJ/m2) (1) (w-a)t where Ai is the impact energy, A2 denotes the residual energy (in kilojoules) ,w is the specimen width, a, is the notch length and t denotes the specimens thickness. IE =
RESULTS AND DISCUSSION Tensile properties The effect of silica content on the tensile properties of the epoxy is illustrated in Figure 4 and Figure 5. At ambient temperature, a slight enhancement of the strength was observed when the silica content was 2 wt%, accompanied by a dramatic increase in the strain at break. A slight reduction in the strength and significant in crease in elongation at break were observed by addition of 4 wt% silica content. At cryogenic temperature, the strength was significantly improved by the addition of silica particles.
SiO2/Epoxy Nanocomposites at Cryogenic Temperature
710 Impact energy
The impact energy at ambient and cryogenic temperature of epoxy matrix and hybrid materials with different contents of silica is showed in Figure 6. When the silica content is 2 wt%, the impact energy has an increase. However, when the silica content is 4 wt%, a decrease in impact strength was observed. Addition of silica particles reduced the fraction of the matrix, and rigid silica particles were hard to deform. On the other hand, the silica-matrix interfaces debonding would absorb impact energy. So a small increase in impact energy was obstained. When the silica content was 4 wt%, some agglomerations of silica particles would take place. The agglomeration caused macrocracks (see Fig. 7) and acted as a stress concentrator which lead to decrease in the EE.
Silica Content (wt%)
FIGURE 6 Effect of silica content on impact energy
FIGURE 7 Macrocracks caused by particles agglomerations
Fractography Figure 8 showed the SEM photograph of impact samples of neat epoxy. Fine lines that emanated mainly from the crack-initiation region was observed. Similar results have been
FIGURE 8 Micrograph of fracture surfaces of neat epoxy at ambient temperature
SiO2/Epoxy Nanocomposites at Cryogenic Temperature
FIGURE 9 Micrograph of fracture surfaces of neat epoxy at cryogenic temperature
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FIGURE 10 Micrograph of fracture surface of 2 wt% silica/epoxy hybrid materials at 77K
reported elsewhere [3]. The smooth surface indicated that the epoxy matrix fractured in a brittle mode. The surface of impact samples of epoxy samples at cryogenic temperature was much smoother (see Fig.9) indicating a more brittle behavior. Figure 10 showed the micrographs of impact samples of silica/epoxy hybrids. Many curving lines were observed which indicated the silica-epoxy adhesion diverting the crack propagation. So an increase in toughness was obtained. When more silica particles were added, agglomeration of silica particles (see Fig. 7) might be responsible for the decreaseof impact energy (see Fig.6). CONCLUSIONS Addition of appropriate silica nano-particles via sol-gel process can improve tensile strength, elongation at break and impact strength at both ambient and cryogenic temperature. At cryogenic temperature, the addition of silica nano-particles dramatically increased the strength. While elongation at break was obviously improved at ambient temperature. ACKNOWLEDGEMENTS This work is funded by the Hundred Talents Program of CAS; Key Research Program of Beijing City Science and Technology Committee (No H020420020230); National High TechnicalResearch and Development Program of China (No 2002AA306171). REFERENCES 1. M. Hara, H. Okubo. "Electrical insulation characteristics of superconducting power apparatus," Cryogenics. 38:1083-1093. 2. S. Usami, H. Ejima, T. Suzuki, et al. "Cryogenic small-flaw strength and creep deformation of epoxy resins," Cryogenics. 39:729-738. 3. S. Fellahi, N. Chikui, M. Bakar. "Modification of epoxy resin with kaolin as a toughening agent," Journal ofApplied Ploymer Science. 82:861-878. 4. T. Iida. "Fracture toughness of spherical silica-filled epoxy adhesives," International Journal ofAdhesion & Adhesives. 21: 389-396. 5. D. A. Norman, R. E. Robertson. "Rigid-particle toughening of glassy polymers," Polymer. 44:2351-2362. 6. Chin-Lung Chiang, Chen-Chi M.Ma. "Synthesis, characterization and thermal properties of novel epoxy resin containing silicon and phosphorus nanocomposites by sol-gel method," European Polymer Journal. 38:2219-2224. 7. M. Ochi, R. Takahashi, A. Terauchi. "Phase structure and mechanical and adhesion properties of epoxy/silica hybrids," Polymer. 42:5151-5158. 8. Q. Hu, E. Marand. "In situ formation of nanosized TiO2 domains within
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poly(amide-imide)by a sol-gel process," Polymer. 40:4833-4843. 9. S. Y. Fu, B. Lauke. "Fracture resistance of unfilled and calcite-particle-filled ABS composites reinforced by short glass fibers (SGF) under impact load," Composites. 29A:631-641.
Mechanical Properties and Fracture Performance of Nanoclay-reinforced Polypropylene Modified with Maleic Anhydride Shing-Chung Wong* Department of Mechanical Engineering and Applied Mechanics, North Dakota State University, Fargo, ND 58105, USA Ling Chen, Tianxi Liu and Chaobin He Institute of Materials Research and Engineering 3 Research Link Singapore 639798, Singapore Xuehong Lu School of Materials Engineering Nanyang Technological University Singapore 639798, Singapore
ABSTRACT It is unclear fracture performance can benefit from well exfoliated clays at nanoscale in polymer matrices. The size and length scales of nanoclay particles do not offer crack bridging, deflection, debonding or cavitation mechanisms. However, our investigations using continuum fracture mechanics and small-angle X-ray scattering (SAXS) in nanoclay-reinforced polypropylene demonstrated increases in plastic zone size proportional to the increases in fracture toughness and the relative invariant measured from SAXS. Our results reinforced the notion that it is plausible for nanoscale reinforcements to play a toughening role in addition to strengthening and stiffening contributions. The correlation between the toughness increase and the matrix plastic deformation was evident. INTRODUCTION Development of polymeric nanocomposites has received extensive attention in recent years. Much effort is centered on exfoliating the nanoclay particles in polymer matrices in order to optimize the performance of the nanocomposites so obtained [14]. The attractive properties arising from well exfoliated nanofillers can be exemplified as follows: (1) when nanoscale fillers are finely dispersed in the matrix, the tremendous surface area developed could contribute to polymer chain confinement effects which could lead to higher glass transition temperature, stiffness and strength; (2) nanoscale fillers provide an extraordinarily zigzagging, tortuous diffusion path that leads to enhanced barrier performance for gas, moisture and oxygen transmissions; and (3) nanoscale fillers can also enhance the controlled electrical and thermal conductivities to finely tune insulating, dielectric and semi-conductive * Corresponding author. Prof. S.-C. Wong. Fax:(701)231-8913. Email: [email protected]
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Nanoclay-reinforced Polypropylene modified with Maleic Anhydride
properties. Advantage (3) is not directly related to layered silicates type nanocomposites. However, enhancement in strength and stiffness for exfoliated clays is well documented in the literature [1-4]. The improvement in barrier properties in the nanocomposites derived from layered silicates, or smectite clays, has been well studied in recent years [5-8]. Little is understood on the toughening effect arising from nanoclay reinforcements. Should nanocomposites be designed such that nanoclays be uniformly and fully exfoliated or be intercalated, or should they be a mixture of both, in order to optimize fracture toughness? To date, there is no evidence that a simple answer exists to this question for a wide variety of nanocomposite matrices. A fully exfoliated nanocomposite does not lend itself to toughening applications in view of length scale and size arguments. Nanoparticles are too small to provide crack bridging, deflections, debonding or cavitation mechanisms. Therefore, intercalated structures, or microscale inclusions, potentially can give rise to mechanisms such as cavitation, which relieves triaxial tension and promotes localized deformation near the crack tip. However, it is plausible that the increase in particle surface area can contribute to enhanced plasticity of polymers provided that the interfaces are sufficiently strong [9]. As a result, the plastic deformation is expected to increase with decreasing scale of reinforcement. Such an argument favors nanosized tougheners over larger tougheners. This paper addresses the effect of nanoclay reinforcement on the fracture toughness of maleated polypropylene, an engineering polymer that can be fabricated cost-effectively. The toughness will be evaluated in terms of the plastic zone size and microdeformation using small-angle X-ray scattering (SAXS). EXPERIMENTAL WORK The matrix materials studied were maleic anhydride modified polypropylene (Bynel 50E561) from Du Pont (Singapore) Pte. Ltd. The organoclay (Nanomer 1.3IPS onium ion modified montmorillonite clay), which was modified with octadecylamine, was supplied from Nanocor me, USA. Maleic anhydride modified polypropylene (MAPP) and organoclay were melt compounded in a co-rotating intermeshing twin screw extruder (Leistritz Micro 18 L/D=30). The compounding temperature was 210°C to produce the masterbatch containing 50 wt% clay, followed by recompounding with fresh maleated PP to obtain clay filled polypropylene with desired loading levels. The blended samples were reextruded to achieve more uniform dispersion. Materials were injection molded into 3.5 mm-thick dumbbell specimens and 6.17 mm-thick single-edge notch-bend (SENB) specimens for fracture tests. All materials were dried in a vacuum oven prior to compounding and injection molding. Tensile tests were conducted according to ASTM D638 using an Instron Model 5567 equipped with an extensometer. The crosshead speed was kept constant at 5 mmmin"1 at ambient temperature. At least five specimens of each composition were tested. The stress-strain curves in Fig. 1 show considerable post-yield deformation and, therefore, elastic-plastic parameter, J, was adopted. The J-R curves for the specimens were determined using deeply notched three-point bend specimens (SIW = 4, L = 55mm, W= 12.50mm, B = 6.17 mm). Pre-cracks were made by inserting a fresh razor blade into the machined slot. Multiple specimen technique was used to measure the /-integral fracture toughness. The amount of stable crack growth, Aa, was measured from the fracture surface using an optical microscope (Olympus BH-UMA)
Nanoclay-reinforced Polypropylene modified with Maleic Anhydride
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attached with a micrometer eyepiece. Stable crack growth and a large stress-whitened zone were observed for all specimens. Crosshead speed was 5 mmmin" and tests were conducted at room temperature. /« was determined from
r -2U J *~lb
m ()
where U is the area under the load vs load point-displacement curve and b = W-a is the ligament length and a the initial crack size. The data for the //{-curve were best fitted to a linear regression line and the intersection between the regression line and a 0.2 mm offset line, which is parallel to the blunting line, was used for evaluation of the initiation value of /. All Jc values except for the one at 10 wt% clay loading did not satisfy the full plane strain conditions. As a result, the fracture toughness can only be compared at the given thickness (6.17 mm). To evaluate the deformation mechanisms in the nanocomposites, a small angle Xray diffractometer (NanoStar) with wavelength, X,(CuKa)=1.5418A, was used to probe the craze morphology. The undeformed and unaxially loaded sections for small angle X-ray scattering (SAXS) study were cut from tensile specimens that were subjected to 0 and 100% tensile strain, respectively. For 40 wt% clay filled MAPP which fractured at the strain of about 10%, the section containing fracture surface was cut out. All other samples did not break at 100% in tensile strain. Sections were scanned by SAXS for 2 h at voltage of 40 kV and current of 30 mA. After subtracting background signals, scattering intensity I(q) and corresponding wave vector q were collected from both equatorial and meridional scatterings. In addition, I{q) was normalized by specimen thickness for relative invariant calculation. RESULTS AND DISCUSSION Tensile Properties First, it is clear the nanoclays can effectively reinforce the PP matrix, despite the increases in tensile strength and modulus are considered as gentle in comparison to other nanoclay reinforced systems such as the type derived from polar nylon matrices [1,2]. Figure 2 shows the tensile strength and modulus nanoclay reinforced PP as a function of the clay content. An increase of 57% in tensile modulus is achieved at a loading of 2.5 wt% clay and a sixfold increase is observed at 50wt% clay. The tensile strength increases by twofold at 50 wt% of clay. Such improvements in mechanical strength, coupled with sustainable fracture toughness, can broaden the high performance applications for engineering PP. Fracture Toughness Figure 3 is a plot of the /-integral fracture toughness of maleated PP as a function of clay loading. Note that the values shown are plane stress toughness, except for 10 wt% clay composition, at 6.17 mm in thickness. The toughness is compared at the same thickness and increases more than fourfold at 2.5 wt% clay loading. That is, at a small clay loading, the reinforced PP exhibits concomitant strengthening (Fig. 2) and toughening. This result is significant because it confirms that the nanoclays enhance the strength for polymer matrix and, simultaneously, enhance the constitutive parameters including localized yield stress, ay, and yield stress, sy, in an elastic-plastic field such as one governed by the well-known HRR stress-strain field [10]:
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Nanoclay-reinforced Polypropylene modified with Maleic Anhydride
(2)
where, J = J-integral toughness K = stress intensity factor; v= Poisson's ratio; /„ = numerical constant depending on the stress-strain relation; R is a constant.
-10wt% - 7.5 wt% -5wt% - 2.5 wt% -0wt%
5
10
20
15
Strain (%)
FIGURE 1 Tensile stress-strain curves of clay filled MAPP 3.5
«
1
3-
2
-5-
s
I 1.5
1 13
0.5 0
0
10
20
30
40
50
Clay Content wt%
0
10
20
30
40
50
Clay Content wt%
(a) (b) FIGURE 2 Tensile properties vs. clay content (a) Yield strength; (b) Modulus.
It is clear ay derived from exfoliated clay in the crack tip deformation zone would contribute to the toughness, J, of a matrix. The actual fracture mechanisms need to be critically examined. At present, a plot of the J-integral fracture toughness and the plastic deformation zone scaling factor around the crack tip gives good linearity as shown in Fig. 4. The linearity is indicative of the fracture process zone governed by the similar type of singularity function of Eq. 2. Small-angle X-ray Scattering (SAXS) Prior study [11] using TEM examination of the crack-tip region shows that the clay particles do not debond extensively from the polymer matrix. This is expected as
Nanoclay-reinforced Polypropylene modified with Maleic Anhydride
717
the particle size is too small to promote stress concentration. More details in clay morphology are given elsewhere [12]. Instead, small angle X-ray scattering (SAXS) confirms the extent of plastic deformation, which is proportional to each of the nanocomposite toughness and thus crack-tip deformation zone in Fig. 4.
Plastic Zone Size Scaling Factor
Clay Content (wt%)
FIGURE 3 /-integral fracture toughness vs. clay zone size
FIGURE 4 Fracture toughness vs. plastic loading
For undeformed sample, there is no oreintation signature (Fig. 5a). Fig. 5b is the SAXS signature for 2.5 wt% deformed sample. A strong streak pattern on the equator is observed in addition to the two-bar pattern on the meridian. The pronounced equatorial scattering is attributed to scattering from fibrils of the crazes or the ligaments of microvoids in between the polymers. The results suggest that the presence of dispersed clay particles facilitates the formation of crazes and microvoids in maleated PP matrix. To quantify the concentration of craze, invariant analysis [13] is used in this study. The relative invariant, Qr, can be calculated according to
(3)
l where I(q) is the scattering intensity from crazes at wave vector q and q ~ — sin 6
(4)
inwhichg is Bragg's angle and the wavelength X=1.5418A. Table 1 summarizes the results from the invariant analysis. Clearly, Qr is the highest at 2.5 wt% clay loading. This is consistent with the fracture toughness and crack-tip deformation zone we characterized using large-scale mechanical testing techniques, Figs. 3 and 4. As a result, both large-scale fracture and uniaxially loaded SAXS techniques point us to the fact that concomitant strengthening and toughening are plasuible for nanoclay-filled PP modified with maleic anhydride. TABLE I Comparison of SAXS relative invariant for MAPP reinforced with different clay loading levels Clay loading (wt%) 0 Qr
2.5
5
10
0.026 0.083 0.067 ° - 0 4 2
FIGURE 5 Comparison of SAXS patterns for 2.5 wt% reinforced (a) undeformed and (b) deformed samples
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Nanoclay-reinforced Polypropylene modified with Maleic Anhydride
CONCLUSIONS Interesting results on concomitant strengthening, stiffening and toughening were reported in 2.5 wt% nanoclay reinforced maleated PP. At 2.5 wt% clay loading, the J-integral toughness was the highest and the tensile modulus considerably increased when compared to unreinforced maleated PP. Our results reinforced the notion that it is plausible for nanoscale reinforcements to play a toughening role in addition to strengthening and stiffening contributions. The correlation between the toughness increase and the matrix plastic deformation was evident. The matrix crazing and microvoid formation were carefully examined using highly sensitive SAXS techniques. The concentration of craze-like deformation was quantified using invariant analysis whereby the equatorial scattering was most pronounced in 2.5 wt% clay sample. Further increase in nanoscale reinforcements dramatically reduced the scattering and thus the matrix plasticity. ACKNOWLEDGEMENTS The authors thank Nanyang Technological University and the Institute of Materials Research & Engineering for the support of this work. One of us (SCW) acknowledges the support of NSF SGER Grant# CMS 0335390 administered by the Mechanics and Materials Program. REFERENCES 1. 2. 3. 4.
Cho, J.W. and Paul, D.R., Polymer, 42, 1083-1094 (2001) Fornes, T.D., Yoon, P.J., Keskkula, H. and Paul, D.R., Polymer, 42, 9929-9940 (2001) Yoon, P J., Hunter, D.L. and Paul, D.R., Polymer, 44, 5323-5339 (2003) Manias, E., Touny, A., Wu, L., Strawhecker, K., Lu, B., Chung, T. C , Chem Mater, 13, 3516-3523 (2001) 5. Alexandra M. and Dubois P., Mater Sci Eng R 28 (2000) 1-59. 6. Usuki A., Kojima Y., Kawasumi M., Okada A., Fukushima Y., Kurauchi T. and Kamigaito O., J Mater Res 8 (1993) 1179-1183. 7. Theng B.K.G., The Chemistry of Clay-Organic Reactions, Wiley, New York, 1974 8. Lagaly G., Appl Clay Sci 15 (1999) 1-9. 9. Nair, S. V., Goettler, L. A., Lysek, B.A., PolymEng Sci, 42, 1872-1882 (2002) lO.Hutchinson, J. W., Trans of the ASME 1983, 50, 1042-1051 11. Chen, L., Wong, S.C. and Pisharath, S., J. Appl. Polym. Sci. 88, 3298-3305 (2003) 12. Chen, L., Wong, S.C, Liu, T.X., Lu, X.H. and He, C.B., "Deformation mechanisms of nanoclayreinforced polypropylene modified with maleic anhydride" submitted to Journal of Polymer Science Part B: Polymer Physics September, 2003 13. He, C , Donald, A.M. and Butler, M.F., Macromolecules, 31, 158-164 (1998)
Nanoclay Reinforced UV Curable High-barrier Coatings Fawn M. Uhl1, Siva Prashanth Davuluri2, Shing-Chung Wong2'*, Dean C. Webster3 1
Center for Nanoscale Science and Engineering department of Mechanical Engineering and Applied Mechanics 3 Department of Polymers and Coatings North Dakota State University Fargo, ND 58105, USA
ABSTRACT Recent advances in functional nanocomposites have created new frontiers in research for radiation-curable organic coatings making use of nanocomposite technology. Such UV curable systems would enable the widespread use of nanocomposites in microfabrication. Little is understood on incorporating organomodified clays in UV curable polymers. UV curable films were reinforced with organically modified montmorillonite (MMT). The organically modified MMT were prepared by an ion exchange process in which sodium ions were replaced by alkyl ammonium ions. Acrylate films were reinforced with organoclays, which serve as reinforcements and barrier fillers in the polymer matrix. The microstructures were characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). Physical properties were examined by real time infrared spectroscopy (RTIR), differential scanning calorimetry (DSC), photoDSC, dynamic mechanical thermal analysis (DMTA), Instron, and pendulum hardness. Preliminary results showed that aliphatic urethane acrylate nanocomposite coatings exhibited an intercalated structure and enhanced properties. 10 to 20 percent increase in tensile strength and a 25 to 50 percent increase in Young's Modulus were observed. Decreased cure time to a tack free film and a slight increase in conversion as seen by RTIR were interestingly reported, suggesting the presence of nanoclays can improve the cure speed of acrylate coatings. Thermal stability was also enhanced. Potential applications of UV curable materials exist in the electronics industry where it is desirable to have coatings with good flexibility, dimensional stability, chemical resistance, thermal stability, transparency, and fast cure. This work demonstrated coatings with nanoscale reinforcements are ideal in such applications.
INTRODUCTION Organomodified clay-type nanocomposites have been shown to exhibit enhanced properties such as mechanical, thermal, barrier, solvent resistance, etc [1-5]. In general, one of several methods is utilized to form nanocomposites and these include * Corresponding author: Shing-Chung Wong, Department of Mechanical Engineering and Applied Mechanics, North Dakota State University, Fargo, ND 58105, Tel: +1(701)231-8840 Fax:+l(701)2318913 Email: [email protected]
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Nanoclay Reinforced UV Curable High-barrier Coatings
solution blending, in situ polymerization, or melt blending. These techniques are generally done by a thermal method. For microelectronic and MEMS applications, however, radiation curing is highly desired and thermal curing is not an efficient route for microfabrication. Little work has been done in the area of UV curable clay nanocomposites. Decker et al showed by x-ray diffraction that clay nanocomposites could be prepared with UV curable formulations [6]. UV curing is of critical importance for rapid cure, solvent free systems, application versatility, low energy requirements, and low temperature operation [7,8]. It is ideal to be able to produce UV curable firms made of nanocomposites, which offer higher glass transition temperatures, barrier properties, low shrinkage, flexibility, and increased mechanical properties. The focus of this paper is on UV curable formulations of various clays in a urethane acrylate. An examination of structure and properties will be presented.
EXPERIMENTAL Materials Montmorillonite K10 (MMT), cetyltrimethylammonium bromide (CTMA) and [(2-acryloyloxy)ethyl](4-benzoylbenzyl)dimethylammonium bromide (AEBBDMA) were obtained from Aldrich. Nanomer clay was obtained from Nanocor Inc. 15A Cloisite and Na+ Cloisite were obtained from Southern Clay. CN929, a trifunctional urethane acrylate oligomer, and SR454, an ethoxylated (3) trimethylolpropane triacrylate, were obtained from Sartomer. The photoinitiator Darocur 1173, 2hydroxy-2-methyl-l-phenylpropane-l-one, was obtained from Ciba Specialty Chemicals. Characterization UV curing of samples was performed using a Dymax light source with a 200 EC silver lamp (UV-A, 365 nm). The intensity was 35 mW/cm2. X-ray powder diffraction (XRD) data were collected using a Phillips PW3040 X'pert-MPD Multipurpose Diffractometer in Bragg-Brentano geometry (CuK« radiation). Qualitative variable slit data were collected over 2°-40° 20, using a step size of 0.02 and a run time of Is/step. Ultrathin samples were cut using a diamond knife and RMC MTXL ultramicrotome. The thin sections were then placed on 400 mesh copper grids and photographed using a JEOL 100cx-II Transmission Electron Microscope (TEM) operating at 80kV. Photo-infrared was performed using the Nicolet Spectrometer and a UV optic fiber mounted in a sample chamber. Light source is a 100 watt DC mercury vapor short-arc lamp. This setup monitors the conversion as reaction proceeds, which is known as the real time infrared spectrometry (RTIR). Scans were taken over a 60 s period at 1 scan/s and UV source was adjusted to be approximately 35 mW/cm2. Differential scanning calorimetry (DSC) was performed on a TA Instruments Q1000 series calorimeter. Samples were subjected to a heat, cool, heat cycle from -20 °C to 200 °C at a ramp rate of 20 °C/min. Glass transition temperatures (Tg) were reported from the 2nd heat cycle at the midpoint. Dynamic mechanical thermal analysis (DMTA) was performed using a Rheometnc Scientific 3E apparatus in the rectangular tension/compression geometry. Tg was obtained from the maximum peak in the tan delta curves and crosslink densities were calculated from the storage modulus (E') values in the linear portion at
Nanoclay Reinforced UV Curable High-barrier Coatings least 50 °C greater than the Tg. following equation: [9]
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Crosslink density can be calculated from the
E = 3veRT
(1)
where ve is the crosslink density. Sample sizes for test were (3 x5 x (0.05 to 0.09)) mm3. The analysis was carried from -50 to 200 °C at a frequency of 10 rad/s and ramp rate of 5 °C/min. Tensile properties were measured using an Instron 5542 and 5 specimens were taken for each sample to obtain an average value. Film Preparation Film formulations employed in this study were 50:50 mixture of CN929:SR454. CN929 is a trifunctional aliphatic polyester urethane acrylate oligomer. SR454 is ethoxylated trimethylolpropane triacrylate. The clay loadings in these systems were 1, 3, and 5 wt%. Mixture was stirred for 24 h followed by sonication for 8 h. The 4 wt% of the initiator Darocur 1173 was added and the mixture was stirred overnight. RESULTS AND DISCUSSION In order to prepare nanocomposites the clays are typically modified with an organo-ammonium salt. Clays and organomodifiers used thus far are: (1). Bentonite modified with CTMA Bromide, AEBBDMA bromide; (2). Montmorillonite modified with CTMA Bromide, AEBBDMA bromide and a combination of the two; (3). Commercial MMTs - Nanomer (from Nanocor Inc.), 15A Cloisite (Southern Clay), Na+ Cloisite (Southern Clay). We also prepared formulations using unmodified montmorillonite (MMT) and bentonite. The choice of modifier CTMA bromide was considered based on the reports from other researchers and can serve as a control sample while the AEBBDMA bromide was chosen due to its acrylate functionality and the portion that is similar to benzophenone photoinitiator. Both features make it attractive for use in our formulations. Structures of nanoreinforced films were evaluated by XRD and TEM. We observed intercalated structures regardless of the content or type of clay used. Figure 1 shows a TEM of 3 wt % AEBBDMA MMT formulation and the layered structure is observed indicating intercalation with a
FIGURE 1. TEM of 3 wt % AEBBDMA MMT.
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Nanoclay Reinforced UV Curable High-barrier Coatings
Cure refers to the crosslinking of a polymer to produce a three dimensional network. Polymerization occurs in three steps [15]: (1) a change in the refractive index, (2) a change in tackiness, and (3) the formation of a tack-free crosslinked system. Figure 2 shows the effect of the nanoclay on the curing rate of the polymer films, hi general, the cure time decreases as the clay content increases.
FIGURE 2. Cure time for various clay-urethane acrylate formulations.
In general an increase in Tg is observed (exceptions are unmodified bentonite and MMT). These data suggest that clay may be effectively restricting polymer chain motion. Figure 3 shows that the Southern Clay formulations (both 15A and Na+ Cloisite) show a significant increase in Tg (13 - 30% increase), relative to the unmodified urethane acrylate. The 3 wt % loading of the AEBBDMA bentonite, 3 and 5 wt % CTMA MMT, and 3 wt % AEBBDMA MMT also show significant increases. The Nanomer clay formulations show a relationship to the amount of clay present, that is, as the clay content increases so does Tg.
FIGURE 3. Tg of clay-urethane acrylate formulations as a function of clay content.
An increase in Young's modulus on the stress-strain behavior for samples containing clay relative to the unmodified film (exception is the samples with MMT) is seen in Figure 4. Tensile strength is shown in Figure 5. From these figures we can see that in most cases there is an increase in mechanical properties. Exceptions include the MMT formulations and the ones containing 1 wt% Nanomer and 1 and 3 wt% CTMA bentonite. It is understood that filler particles reduce the molecular mobility of polymer chains resulting in a less flexible material with a higher tensile strength and Young's modulus. However, the increase in tensile strength is less dramatic than that for tensile modulus.
Nanoclay Reinforced UV Curable High-barrier Coatings
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FIGURE 4. Young's modulus for the various urethane acrylate films.
FIGURE 5. Tensile strength as a function of clay concentration in urethane acrylate formulations.
CONCLUSIONS XRD and TEM data showed that intercalated structures of these UV curable formulations were formed. An increase in glass transition temperatures for the nanocomposites relative to the unmodified coating was also observed suggesting that the clay is restricting the motions of the polymers within the clay layers. Claypolymer nanocomposites typically exhibit an increase in mechanical properties. In the work shown here increases in mechanical properties for these UV curable formulations were observed. Young's modulus was increased more dramatically as compared to that of tensile strength. This work illustrates our pioneering efforts in preparing UV curable nanoclay-polymer films and shows promise for future microelectronic and MEMS applications. ACKNOWLEDGMENTS The authors thank the Center for Nanoscale Science and Engineering (CNSE) and the Defense Microelectronics Activity (DMEA), contract number DMEA-90-02-C0224, for support of this research. One of us (SCW) acknowledges the support of NSF SGER Grant# CMS 0335390 on nanocomposites administered by the Mechanics and Materials Program.
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REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11.
12.
13. 14. 15.
M. Alexandre, P. Dubois, Mater Sci. Eng. R28, 1 (2000). M. Ogawa, K. Kuroda, Bull. Chem. Soc. Jpn. 70, 2593 (1997). W. J. Wang, W.-K. Chin, J. Polym. Sci. PartB: Polym. Physics 40, 1690 (2002). M. Tortora, G. Gorrasi, V. Vittoria, G. Galli, S. Ritrovati, E. Chiellini, Polymer. 43, 6147 (2002). J. Wu, M. M. Lerner, Chem. Mater. 5, 835 (1993). C. Decker, K. Zahouily, L. Keller, S. Benfarhi, T. Bendaikha, J. Baron, J. Mater. Sci. 37, 4831 (2002). P. Jackson, Paint and Resin Times 1, 26 (2002). J. P. Fouassier, Photoinitiation, Photopolymerization, and Photocuring Fundamentals and Applications (Hanser Publishers, New York, 1995), pp. 246. Z. W. Jr Wicks, Jones, F. N., Pappas, S. P., Organic Coatings (John Wiley & Sons, New York, ed. 2, 1999), pp. 71. F. M. Uhl, S. P. Davuluri, S.-C. Wong, D. C. Webster, manuscript in preparation (2003). F. M. Uhl, B. R. Hinderliter, S. P. Davuluri, S. G. Croll, S.-C. Wong, D. C. Webster, "UV Curable Polymers with Organically Modified Clay as Nanoreinforcemnt" submitted to MRS proceedings (2003). F. M. Uhl, S. P. Davuluri, S.-C. Wong, D. C. Webster, "Polymer Films Possessing Nanoreinforcemnt via Organically Modified Layered Silicate", submitted to Chemistry of Materials, November, 2003. F. M. Uhl, S. P. Davuluri, S.-C. Wong, D. C. Webster, "Structure-Polymer Relationships of UV Curable Nanoclay Films ", submitted to Polymer, November, 2003. F. M. Uhl, S. P. Davuluri, S.-C. Wong, D. C. Webster, "UV Curable-Polymer Clay Composites: Structure and Properties" manuscript in preparation (2003). J. P. Fouassier, Photoinitiation, Photopolymerization, and Photocuring Fundamentals and Applications (Hanser Publishers, New York, 1995), pp. 164-174.
A Comprehensive Study on Intercalation and Exfoliation of Epoxy/Clay Nanocomposites Jia Liu, Jingshen Wu Department of Mechanical Engineering The Hong Kong University of Science and Technology, Hong Kong
ABSTRACT In this work, a series of epoxy/montmorillonite (MMT) nanocomposites were synthesized. As a general procedure, organo-modified clay of 1,3 or 5 wt% loadings was thoroughly mixed with epoxy resin diglycidylether of bisphenol A (DGEBA), at 80°C for lh. After that, a stoichiometric amount of curing agent was added and the mixture was then degassed, molded and cured at 80°C for 2h and 160°C for another 2h. The nanocomposites samples were analyzed by X-ray diffraction (XRD) and transmission electron microscopy (TEM), in order to characterize the nanoscale dispersion and intergallery spacing of nanoclay. Following the above general procedure, the intercalation and partial exfoliation of epoxy/MMT nanocomposites were easily achieved, with the intergallery spacing of 32-41A in average. hi order to realize exfoliation, various processing conditions were tried in laboratory, e.g., extending the mixing time to 24h, elevating the mixing temperature to 200°C, or shearing the mixture with strong agitation, etc. However, these efforts seemed useless in expanding clay intergallery spacing. Higher initial curing temperature was also tried. For those samples with 1 and 3 wt% clay loadings cured at 160°C and 5 wt% at 200°C, the [001] diffraction peak of the clay disappeared from the XRD patterns, which indicated that the exfoliation was achieved. Other characterization methods have been applied to the above nanocomposites. Further investigation is currently continuing in progress. INTRODUCTION Polymer-based nanocomposites are a new class of high performance materials consisting of nanometer scale inorganic particles or fillers dispersed in an organic polymer matrix [1]. Such nanocomposites will have superior specific strength and stiffness, and good barrier and fire-retardant properties, even with only a small weight fraction of the nano-fillers [2]. During the past decade, polymer nanocomposites containing clays have been intensively investigated, in both academic and industrial fields [3]. Owing to its ultrathin lamella-like structure and high aspect ratio, clay endows the polymer matrix a pronounced improvement in properties. A lot of researchers have been working in this area since Toyota first time reported the potential application of polymer/nanoclay composites in 1980s [4-6].
* Correspondence author. Address: Department of Mechanical Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong. Fax: +852-23581543. Email: [email protected]
726
Intercalation and Exfoliation of Epoxy/Clay Nanocomposites
Epoxy/clay nanocomposites, for example, have drawn great attention of many researchers [7-13]. It is generally accepted that the intercalation or especially the exfoliation of clay layers plays a most important role on the resulting nanocomposites properties. Clay modification method, curing agent type, processing condition, curing profile, and other factors, may all influence the dispersion of clay in epoxy matrix. In this work, we prepared epoxy/clay nanocomposites with different clay types and loadings. Some fundamental characterizations were applied to" the samples. We also studied the intercalation and exfoliation of clay in nanocomposites, by changing various processing and curing conditions. EXPERIMENTAL Materials Epoxy resin EPIKOTE 828, the diglycidyl ether of bisphenol A (DGEBA), used in this study was a commercial product and produced from Resolution Performance Products. 4,4'-Methylene dianiline (MDA), used as a curing agent, was purchased from Aldrich. The nanoclay Cloisite 30B, was a montmorillonite (MMT) modified with a bis-2-hydroxyethyl methyl tallow ammonium cation, which was provided by Southern Clay Products. Preparation of Epoxy/MMT Nanocomposites All the chemicals and clays were predried in vacuum oven over 24h. The epoxy resin was added into a beaker and heated to 75°C until its viscosity got lowered. Then, a certain amount of nanoclay corresponding to 0, 1, 3, or 5 wt% was introduced and kept stirring for lh at 75°C. The epoxy/MMT mixture was sonicated at 75°C for 5min. Subsequently, a stoichiometric amount of curing agent (27 phr for MDA) was added and kept stirring for another lOmin. The mixture was then degassed in a vacuum oven at 75°C for 7-8min. Finally, the mixture was cast into Teflon and Al molds and cured by a certain curing profile, i.e., first precured at 80°C for 2h and postcured at 160°C for another 2h. Various processing conditions were tried in laboratory, e.g., extending the mixing time to 24h, elevating the mixing temperature to 200°C, or shearing the mixture with strong agitation, etc. For comparison, unmodified pristine clay was also used in sample preparation. Characterization To detect the dispersion of fillers, the nanocomposites samples were cut and polished to around 40um in thickness and observed under an optical microscope (OM) in transmission mode. The ultrathin sections of 70-80nm were prepared by an ultracut and observed with PHILIPS CM20 transmission electron microscope (TEM) operated at an acceleration voltage of 120kV. The intelgallery space of layered clay in the nanocomposites samples was detected by means of X-ray diffraction (XRD). XRD patterns were recorded by monitoring the diffraction angle 26 from 2° to 10° on PHILIPS PW 1830 using Cu Ka radiation with a wavelength of 1.54A. The scanning speed and step size used were 0.003°/sec and 0.05°, respectively. To determine the coefficient of thermal expansion (CTE), thermal mechanical analysis (TMA) was conducted on METTLER TOLEDO TMA/SDTA 840 from 50°C to 240°C at a heating rate of 10°C/min and a load of 0.1N. Besides, moisture absorption testing was taken in ETAC humidity chamber at 85°C and 85%RH for totally 168h, data being collected per 24h.
Intercalation and Exfoliation of Epoxy/Clay Nanocomposites
727
RESULTS AND DISCUSSION Morphology of Epoxy/MMT Nanocomposites Figure 1 shows the OM images of epoxy/MMT nanocomposites. In Figure 1 (a), the agglomeration (l-50um in length) of pristine clay is easily found even at a relatively small magnification, although the macroscopic dispersion is quite homogeneous. This agglomeration, however, can not be observed in epoxy/organo-modified clay nanocomposites, as shown in Figure 1 (b).
(b)
(a)
FIGURE 1 Optical microscope images of epoxy/MMT nanocomposites using (a) pristine clay and (b) organo-modified clay
It is well known that clay has a lamella-like structure and the intelgallery space of clay layers can be detected by means of XRD. As shown in Figure 2, the intelgallery space of pristine clay is 12.19A, while it is enlarged to 17.48A after organo-modification. In the epoxy/organo-modified clay nanocomposites, this intelgallery space is further enlarged up to more than 40A. 5.05° 17.48A
2000-
7.25° 11.7A
2
3
4
5
6
7
8
9
10
Degrees 2-Theta
FIGURE 2 XRD patterns of (a) pristine clay, (b) organo-modified clay and (c) epoxy/organo-modified clay nanocomposite with 5 wt% clay loading
728
Intercalation and Exfoliation of Epoxy/Clay Nanocomposites
The XRD results can be confirmed by the TEM observations. As shown in Figure 3 (a), in epoxy/organo-modified clay nanocomposite, the intercalation of clay has been achieved, with intelgallery space of around 40A in average. Generally the clay layers are still of parallel arrangement. The disorder and extremely large intelgallery space of clay, however, are also apparently observed in this sample, which indicates a partial exfoliation. For comparison, the TEM image of epoxy/pristine clay nanocomposite is shown in Figure 3 (b). The clay layers are closely packed together and the intelgallery spaces between layers are very small and even hard to distinguish.
FIGURE 3 TEM images of epoxy/MMT nanocomposites using (a) organo-modified clay and (b) pristine clay, both with 5 wt%clay loading
Thermal-Mechanical Properties of Epoxy/MMT Nanocomposites Upon TMA testing results, the comparison of CTEs of nanocomposites with different clay loadings, is displayed in Table I. It is clear that the CTEs of nanocomposites at temperatures above Tg decrease consistently with increasing clay loadings, although this phenomenon is not observed at temperatures below Tg. TABLE ICTE data of epoxy/organo-modified clay nanocomposites Specimen (clay wt%) 0 1 3 5
CTE below Te (ppm/K) 64.34 67.50 62.45 65.56
CTE above Tg (ppm/K) 190.81 188.31 183.74 179.94
Intercalation and Exfoliation of Epoxy/Clay Nanocomposites
729
Moisture Absorption of Epoxy/MMT Nanocomposites Moisture absorption testing of nanocomposites with different clay loadings was conducted in ETAC humidity chamber at 85°C and 85%RH for totally 168h. Figure 4 shows their moisture absorption ratios every 24h. From the results, the moisture absorption ratio of epoxy is lowered down with the addition of clay, especially for the one with 1 and 3 wt% clay loadings. It is also interesting that the moisture absorption ratio increases with increasing clay loading. This phenomenon is just the opposite of our expectation and might be due to the voids in the nanocomposites specimens.
24
48
72
96
120
144
168
Time (Hours) FIGURE 4 Mositure absorption ratios of epoxy/organo-modified clay nanocomposites with clay loadings of (a) 0, (b) 1 wt%, (c) 3 wt% and (d) 5 wt%
Influence of Processing and Curing Conditions m order to realize exfoliation, various processing conditions were tried in laboratory, e.g., extending the mixing time to 24h, elevating the mixing temperature to 200°C, or shearing the mixture with strong agitation, etc. However, the nanocomposites undergoing those processes showed almost no enlargement of the clay intergallery spacing. From the comparative results, processing conditions could do little in clay exfoliation. Moreover, higher initial curing temperatures were also tried. The XRD patterns of epoxy/organo-modified clay nanocomposites with various curing temperatures from 120°C to 200°C are illustrated in Figure 5. For those samples with 1 and 3 wt% clay loadings cured at 160°C, the [001] diffraction peak of the clay disappeared from the XRD patterns, which indicated that the complete exfoliation was achieved. But for the sample with 5 wt% clay loading, the curing temperatures at 120°C to 160°C would not realize the exfoliation, until the curing temperature was elevated up to 200°C. CONCLUSIONS Epoxy (DGEBA)-based nanocomposites containing organo-modified clay (MMT) with different loadings of 1, 3 and 5 wt%, were synthesized in our laboratory. Upon XRD and TEM results, the intercalation and partial exfoliation of clay in those nanocomposites were easily achieved by means of a general procedure, with the intergallery spacing of 32-41A in average. By the comparison with epoxy/pristine clay composites, the
730
Intercalation and Exfoliation of Epoxy/Clay Nanocomposites
organo-modification made clay much easier to be dispersed in matrix without agglomeration. Through our investigation, the efforts by changing various processing conditions seemed useless in expanding clay intergallery spacing, e.g., extending the mixing time to 24h, elevating the mixing temperature to 200°C, or shearing with strong agitation, etc. The initial curing temperature, however, was found to have a great influence on the clay dispersion. Higher curing temperatures facilitated the complete exfoliation. For the nanocomposites samples with 1 and 3 wt% clay loadings cured at 160°C and 5 wt% cured at 200°C, the [001] diffraction peak of clay disappeared from XRD patterns, which indicated that the exfoliation was achieved.
14000130001200011000100009000800070006000500040003000200010000 5
6
7
Degrees 2-Theta
FIGURE 5 XRD patterns of epoxy/organo-modified clay nanocomposites (a) containing 1 wt% clay and cured at 160°C, (b) containing 3 wt% clay and cured at 160°C, (c) containing 5 wt% clay and cured at 120°C, (d) containing 5 wt% clay and cured at 160°C and (e) containing 5 wt% clay and cured at 200°C
REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13.
Alexandra, M. and Dubois, P. Materials Science and Engineering 2000,28,1. Biswas, M. and Ray, S. S. Advances in Polymer Science 2001,155, 167. Kato, M. and Usuki, A. in 'Polymer-Clay Nanocomposites' (Ed. T. J. Pinnavaia and G. W. Beall), Wiley, New York, 2001, chap. 5, p. 97. Okada, A. et al, Polym. Prepr., 1987, 28,447. Usuki, A. et al., J. Mater. Res. 1993, 8, 1174. Usuki, A. et al., J. Mater. Res. 1993,8,1179. Wang, Z., Massam, J. and Pinnavaia, T. J. in 'Polymer-Clay Nanocomposites' (Ed. T. J. Pinnavaia and G. W. Beall), Wiley, New York, 2001, chap. 7, p. 127. Lan, T. and Pinnavaia, T. J. Chem. Mater. 1994, 6, 2216. Lan, T., Kaviratna, P. D. and Pinnavaia, T. J. Chem. Mater. 1995, 7, 2144. Kommann, X., Lindberg, H. and Berglund, L. A. Polymer 2001, 42,4493. Messersmith, P. B. and Giannelis, E. P. Chem. Mater. 1994, 6, 1719. Kommann, X., Lindberg, H. and Berglund, L. A. Polymer 2001, 42, 1303. Becker, O., Cheng, Y. B., Varley, R. J. and Simon, G. P. Macromolecules 2003, 36, 1616.
Hydrogen Bonding, Mechanical and Physical Property, and Surface Morphology of Waterborne Polyurethane / Clay Nanocomposite Chen-Chi M. Ma , Hsu-Chiang Kuan, Wen-Ping Chuang and Hsun-Yu Su Department of Chemical Engineering, National Tsing Hua University, Taiwan, R.O.C
ABSTRACT A novel clay / waterborne polyurethane (WPU) nanocomposite was synthesized from polyurethane and saponite organoclay. The hydrogen bonding was characterized using Fourier transform infrared (FT-IR). Results implied that hydrogen bonding increased drastically with organo-clay content. Mechanical and wear property studies revealed that introducing clay into WPU polymer enhance Young's modulus(from 55.67 MPa increased to 126.14 MPa), maximum stress (from 3.97 MPa to 7.61 MPa)and elongation at break (from 27.7% to 58.7%) of the nanocomposite by two times, while the wear loss is only one third of neat WPU. Atomic Force Microscopy (AFM) microphotograph showed that the surface of clay / waterborne polyurethane nanocomposite was smoother when adding clay in WPU. Average roughness (Ra) decreased from 0.999 to 0.197
INTRODUCTION During the past decade, polymer nanocomposites with layered silicates(clays) have been intensively investigated and commercialized for their novel physical properties including mechanical properties (modulus, strength, fracture toughness, and surface hardness),[l-3] barrier property,[4-6] flammability resistance,[7] and solvent(or water) uptake,[8,9] compared to the unmodified resin or conventional polymer composite with inorganic fillers. Pn order to achieve equivalent physical properties, a conventional polymer composite would have to be mixed with more than 30-40 vol % of inorganic fillers such as talc, mica, silica and carbon black, while nanocomposite only need adding 1 run thick layered silicate well-dispersed in a nanoscale (exfoliation) . Clay as an inorganic nano-filler in a polymer nanocomposite also has advantages of processability, cost, and clarity[7]. Combination of waterborne polyurethane and clay can not only improve the properties of polyurethane but also protect the environment due to the solvent free and less toxicity. This study presents the synthesis of nanocomposites from waterborne polyurethane and layered clay. Waterborne polyurethane disperses in water solution; hence, hydrophilic clay would be dispersed more stable in waterborne polyurethane than in solvent-based polyurethane. Several characterizations and properties of nanocomposite were also discussed. Corresponding Author, National Tsing Hua University, Department Of Chemical Engineering, Hsinchu, TAIWAN 300, R.O.C. ; TEL: 886-3-5713058,FAX: 886-3-5715408 ; Email:[email protected]
732
Waterborne Polyurethane/Clay Nanocomposite
EXPERIMENTAL Materials Clay (Na+- Saponite) was obtained from Katamine Co., Tokyo (Japan). Swelling agent l,3-bis(3-aminopropyl)-l,l,3,3-tetramethyl-disiloxane was purchased from Tokyo Chemical Industry Co., Ltd, Tokyo Japan. The 3-isocyanatemethyl-3,5,5-trimethyl-cyclohexylisocyanate (IPDI), Neopentylglycol (NPG), and Dimethylol-propionic acid (DMPA) were purchased from Lancaster Company, Esatgate, White Lund Morecambe, England. Polycaprolactone (PCL) with molecular weight 550 - 830 ^ 1000 were obtained from Aldrich Chemical Company. Milwaukee, WI, U.S.A. Triethylamine (TEA) and Ethylenediamine (EDA) were supplied by Lancaster Company Fairfield, OH, U.S.A. Synthesis of Clay / Waterborne Polyurethane The acetone solvent was distilled over P2O5 and stored in the presence of 4 A molecular sieve to keep it dry. A 500-ml round bottom, 4-necked separable glass reactor with a mechanical stirrer, thermometer, and condenser, was used in preparation of nanocomposite. Reaction was conducted in a N2 atmosphere at constant temperature. The organoclay (0,1,2,4 phr (p_art per hundred parts of resin)) and PCL were mixed and dried in the reactor at 120°C for lh. A stoichiomitric mixture of IPDI, NPG, TMP, DMPA and acetone was fed into the reactor at 60 °C for 6 h. The NCO-terminated prepolymer was obtained. TEA was added and stirred 30 min for neutralization. Then, the EDA/H2O solution was added and carefully controlled by syringe pump. Acetone was removed by a rotary evaporator under reducing pressure, the nanocomposite WPU was obtained. The product was a stable PU anionomer dispersion with 35wt % solid content.
RESULTS AND DISCUSSION Transmission electron microscopy (TEM) microphotograph TEM provided further evidence of the nano-scale dispersion of clay / waterborne polyurethane nanocomposite, as presented in Figurel. hi the TEM cross sectional view of 4phr clay/WPU nanocomposite, the silicate layers were parallel to the surface of the films, and were dispersed in waterborne polyurethane. The distance between the silicate layers of organoclay in PU ranged from 4 to 10 nm. Hydrogen bonding of clay / waterborne polyurethane nanocomposite The structures of the clay / waterborne polyurethane nanocomposite coatings were analyzed by FT-IR. If C=O group formed hydrogen bonding with N-H group, C=O stretching of urethane would appear at 1710 cm"1, if no hydrogen bonding existed, it appeared at 1737 cm"1. Hydrogen bonding index (R) can be calculated by equation 1[8]. n
_
_
HH
cc
^^
F F bonded °° bonded bonded bonded C F ^ free e free
=
^ ^ C
bmdei
HS = 1 - HH
A A
_
-^ 11710 -^ A ^ 1737
= — — + C
free
(2)
R + 1 (3)
Waterborne Polyurethane/Clay Nanocomposite
t
733
A
FIGURE 1 TEM microphotograph of soft segment molecular weight 550 WPU/clay nanocomposite with 4phr clay (x450,000)
Cbonded : concentration of hydrogen bonding C=O, Cfree : concentration of non hydrogen bonding C=O* ^bonded : extinct coefficient of C=O hydrogen bonding effect , efree : extinct coefficient of C=O hydrogen bonding effect ; Generally speaking , value of bmiei £
is between lto 1.2 and assumed to be 1 in this study. Hydrogen bonding between
free
hard segment and hard segment (HH) or between hard segment and soft segment(HS) can be determined by equations 2 and 3. Form TABLE 1, it confirms that hydrogen bonding index increases 20% ( from 1.0 to 1.2 ) with the increasing of organoclay content. TEM indicates that clay/WPU is intercalated nanocomposite. The molecular motion of WPU polymer is restricted in layer structure of clay and reduces the inter- and intra-molecular hydrogen bonding. On the other hand, the OH group on the clay would form hydrogen bonding between clay and PU. Besides C=O group, the hard segment also possesses N-H group, hence, the hard segment has more hydrogen bonding with clay than that of soft segment. HH would increase faster than HS, consequently, HH was increased and HS was decreased with the increasing of clay content. Absorption peak of N-H functional group shifted around 36 cm"1 to lower wavenumber, which confirms the increasing of hydrogen bonding. Mechanical property of clay / waterborne polyurethane nanocomposite Figure 2 illustrates the mechanical property Young's modulus% maximum stress and elongation at break of WPU/clay nanocomposite with soft segment molecular weight 1250 and with different clay contents. The young's modulus raised from 55.67 MPa to 74 MPa and 126.14 MPa with 0.5phr and 4phr clay content respectively. Maximum stress increase form 3.97 MPa to 4.34 MPa and 7.61 MPa when adding 0.5phr and 4phr organoclay respectively. Unlike traditional composites, those results showed the more the clay added the better the elongation property for WPU/clay nanocomposite. The elongation at break of the WPU/clay nanocomposite increased 61.37% (from 27.7% to 44.7% ) when 0.5phr clay added, and raised 106% (from 22.7% to 57.2%) when 4 phr clay was added. Swelled clay can be regarded as a cross- linking center of polyurethane polymer via swelling agent, consequently, not only toughness but also elongation of nanomaterials would be enhanced.
734
Waterborne Polyurethane/Clay Nanocomposite TABLE I Hydrogen bonding index (R), Hard segment-Hard segment hydrogen bonding (HH) and Hard segment-Soft segment hydrogen bonding (HS) of waterborne polyurethane/clay nanocomposite with different organoclay contents
Clay contents
R
HH (%)
HS (%)
NH (cm"1)
Ophr
1.019
50.46
49.54
3341.74
0.5 phr
1.204
54.64
45.36
3323.7
lphr
1.308
56.68
43.32
3314.61
2phr
1.458
59.32
40.68
3305.43
4 phr
1.468
59.48
40.51
3305.32
^—Young's modulus
140
'-** Max. stress
120 100 80 60
55
40 20
3.97
4.34
4.95
6.23
0 1
2 content of clay (phr)
3
FIGURE 2 Young's modulus and maximum stress of WPU/clay nanocomposite with soft segment molecular weight 1250 and with different clay contents
Surface morphology of clay / waterborne polyurethane nanocomposite A series of AFM (Atomic force microscopy) 3D topography - average roughness (Ra) - root mean square roughness (RMS) and maximum height (Rmax) were illustrated in TABLE 2. Surface roughness would be diminished obviously initially beginning and started to raise after 2phr clay added, that is, the surface of nanocomposite film would be smoothened by addition of clay. When nanocomposite is prepared, the surface starts to shrink due to solvent vaporization. Introducing clay into WPU would restrict the shrinkage of polymer surface; hence, the roughness of nanocomposite would be reduced. Clay starts to aggregate when 2 phr clay was added and increasing the surface roughness of the nanocomposite.
Waterborne Polyurethane/Clay Nanocomposite
735
TABLE II Average roughness (Ra), root mean square roughness (RMS),maximum height roughness (Rmax) values ofWPU/clay nanocomposite with soft segment molecular weight 1250 and with different clay contents
Average roughness (Ra) value (nm)
Root mean square roughness (RMS) value (nm)
Maximum height roughness (Rmax) value (nm)
0
0.999
1.284
8.723
0.5
0.699
0.927
6.915
1
0.199
0.250
2.128
2
0.197
0.247
2.017
4
0.572
0.719
5.603
CONCLUSIONS A novel Clay / Waterborne Polyurethane (WPU) nanocomposite has been synthesized by polyurethane and organoclay. TEM analysis showed that clay still remains its layer structure in the Clay / Waterborne Polyurethane (WPU) nanocomposite, i.e., this nanomaterial is an intercalated nanocomposite. FT-IR showd that hydrogen bonding increased drastically by adding organo-clay. Hydrogen bonding index increases 20% ( from 1.0 to 1.2) with the increasing of organoclay content.Mechanical and wear property revealed that introducing clay into WPU polymer can enhance Young's modulus(from 55.67 MPa increased to 126.14 MPa), maximum stress(from 3.97 MPato 7.61 MPa) and elongation at break(from 27.7% to 58.7%) by two times and wear loss is only one third of neat WPU. AFM microphotograph showed that the surface of clay / waterborne polyurethane nanocomposite was smother when adding clay in WPU; Average roughness (Ra) decreased from 0.999 to 0.197 . ACKNOWLEDGEMENTS The authors would like to acknowledge the National Science Council, Taiwan, Republic of China, for the financially supporting this research under the contract No. : NSC 91-2216-E-007-020. REFERENCES (1) Okada, A.; Kawasumi, M.; Usuki, A.; Kojima, Y.; Kurauchi, T.; Kumigato, O. Mater. Res. Soc. Symp. Proc 1990, 171, 45 (2)1 Kojima, Y.; Usuki, A.; Kawasumi, M.; Okada, A.; Fukushima, Y.; Kurauchi, T.; Kamigaito, O.; J. Mater. Res 1993,8, 1185 (3) Giannelis,E. P. JOM1992,44, 28 (4) Yano, K.; Usuki, A.; Okada, A.; Kurauchi, T.; Kamigaito, O.; J. Polym. Set, A: Polym. Chem. 1993,31, 2493 (5) Yano, K.; Usuki, A.; Okada, A.; J. Polym. Set, A: Polym. Chem. 1997, 35, 2289 (6) Lan, T.; Kaviratna, P. D.; Pinnavaia, T. J. Cham. Mater. 1994, 6, 573 (7) Gilman, J. W.; Kashiwagi, T.; Lichtenhan, J. D. J. Appl. Clay. Sci 1999, 15, 31 (8) Emel Yilgor, Ersin Yurtsever, Iskender Yilgor, Polymer, 2002,43,6561
Thermal, Mechanical and Electrical Properties of Multiwall Carbon Nanotube / Waterborne Polyurethane Nanocomposite Hsu-Chiang Kuan and Chen-Chi M. Ma* Department of Chemical Engineering, National Tsing Hua University, Taiwan, R.O.C
ABSTRACT A novel nanocomposite consists of multiwall carbon nanotube / waterborne polyurethane nanocomposite has been successfully prepared. The effects of dispersion agent on thermal, mechanical and electrical properties of nanocomposite were investigated. Thermogravimetric analyzer (TGA) was used to study the thermal properties of carbon nanotube / waterborne polyurethane. Thermal properties of nanocomposite showed that adding carbon nanotube improve the thermal degradation properties by 25 "C (from 273 °C to 298 °C) when carbon nanotube content was 2phr. Thermal conductivity of nanocomposite was increased from 0.21 W/mk to 0.26 W/mk when the carbon nanotube content was Ophr to 2phr. Mechanical property tests showed that adding multiwall carbon nanotube improve the tensile properties significantly (679% in tensile modulus and 882% in tensile strength). Surface electrical resistance of nanocomposite decreased from 3.20E+14 (Q/cm2) to 7.99E+08(G/cm2) while the carbon nanotube content was Ophr to 4phr.
INTRODUCTION Polyurethane (PU) is one of the most interesting classes of synthetic elastomers with unique properties. Hence, more attention has been attracted to the synthesis, morphology, chemical and mechanical properties of this materials. [1-2] The linear structure of segmented PU is in the form of (A-B)n. The soft-segment part B is normally a polyester or polyether (PE) macrogel of molecular weight between 1,000 and 3,000, and the hard-segment part A is consisted of a low-molecular weight diol or diamine reacted with diisocyanate. Owing to the difference in the chemical structure of the soft and the hard segment, soft or hard segment form microdomains by mutual attractions involving intermolecular hydrogen bonding [1]. There has been a great interest in development of nanotube-based polymer composite. In addition to the exceptional mechanical properties associated with carbon nanotube (CNT), CNT possesses superior thermal and electrical properties: thermally stability up to 2800°C in vacuum, thermal conductivity about twice as high as diamond, electric-current-carrying capacity is 1000 times higher than copper wires [3-5]. In this study, carbon nanotube/waterborne polyurethane nanocomposite was prepared. The effect of dispersion agent has been investigated. Thermal - mechanical and electrical properties of nanocomposite have been characterized when the carbon nanotube
Correponding author, National Tsing Hua University, Department Of Chemical Engineering, Hsinchu, Taiwan 300, R.O.C. ; TEL: 886-3-5713058,FAX: 886-3-5715408 ; e-mail:[email protected]
Multiwall Carbon Nanotube/Waterborne Polyurethane Nanocomposite
737
content is from 0 to 4 phr. The effects of dispersion agent on those physical properties were also investigated in this study. EXPERIMENTAL Materials Carbon nanotube was obtained from Nanotech Port Company, Shenzhen, China. (The diameter of CNT is 40-60nm, length is 0.5-40 // m, and specific surface area is 40-3000 m2/g). The 3-isocyanatemethyl-3,5,5-trimethyl-cyclohexylisocyanate (IPDI), Neopentylglycol (NPG), and Dimethylol-propionic acid (DMPA) were purchased from Lancaster Company, Esatgate, White Lund Morecambe, England. Polycaprolactone (PCL) was obtained from Aldrich Chemical Company. Milwaukee, WI, U.S.A. Triethylamine (TEA) and Ethylenediamine (EDA) were supplied by Lancaster Company Fairfield, OH, U.S.A. n-Hexadecyl)trimethylammomum bromide was purchased from Lancaster Company, Esatgate, White Lund Morecambe, England. Synthesis of CNT / Waterborne Polyurethane Composite The acetone solvent was distilled over P2O5 and starred in the presence of 4 A molecular sieve to keep it dry. A 500-ml round bottom, 4-necked glass reactor with a mechanical stirrer, thermometer, and condenser, was used in the preparation of nanocomposite. Reaction was conducted in a N2 atmosphere at constant temperature. PCL was dried in the reactor at 120°C for lh. A stoichiomitric mixture of IPDI, NPG, TMP, DMPA and acetone was fed into the reactor at 60 °C for 6 h. The NCO-terminated prepolymer was obtained. TEA was added and stirred 30 min for neutralization. Then, the EDA/H2O solution was added and carefully controlled by syringe pump. The multiwall carbon nanotube (0,1,2,4 phr (part per hundred parts of resin)) and surfactant (n-Hexadecyl)trimethylammonium bromide) was added, then dispersed in an high-shear mixer. A rotary evaporator under reducing pressure removed acetone, then the carbon nanotube/waterborne polyurethane was obtained. The product was a stable PU anionomer dispersion with a 35wt% solid content.
RESULTS AND DISCUSSION Microphotograph of multiwall carbon nanotube used in this study Figure 1 show that the multiwall carbon nanotube used in this study. The furnace-grown carbon nanotube was prepared by fluidized bed method. From the HR-SEM microphotograph shows random, curled structure and possesses high aspect ratio. Surface resistance of carbon nanotube/waterborne polyurethane nanocomposite Figure 2 presents the data of surface resistivity of carbon nanotube/waterborne polyurethane nanocomposite. From figure, one can find that the surface resistivities decrease with the increasing of carbon nanotube content. The surface resistivities of nanomaterials with 4 phr of carbon nanotube with and without surfactant decreased from 3.2xlO14 fi/cm2 to 8.98xlO12 0/cm2 and 9.4*109 fl/cm2, respectively. The gradually increase of CNT in waterborne polyurethane is suitable for forming a conductive network
738
Multiwall Carbon Nanotube/Waterborne Polyurethane Nanocomposite
in materials. Since carbon nanotube possesses high aspect ratio, it is easier to form a conductive network in polyurethane resin and thus causes lower surface resistivity. According to the results of Zhou et al. [6], the intensity of surface electrons for aspect ratio of whisker is 10, which is 400 times higher than that of general spherical particles. The conspicuous charge concentrating effect may cause higher conductivity. Results also showed that nanocomposite with surfactant treatment exhibit better electrical conductivity (curve B versus curve A of Figure 2).
*••:.,.
,'-"
. . * ^ '
:
% ^ '
H
FIGURE 1 HR-SEM Photograph of carbon nanotube used in this study
1E14
-= \
1E13
1
1E12
•=
1E11
-,
1E10
-=
—•—(A)Without Surfactant —•—(B)With Surfactant
\
\
1E9,
0
1
2
3
4
CNT Content(phr)
FIGURE 2 Surface Resistance of carbon nanotube/waterborne polyurethane nanocomposite with or without surfactant treatment
Thermal conductivity of carbon nanotube / waterborne polyurethane nanocomposite : Thermal conductivity of carbon nanotube/waterborne polyurethane nanocomposite was shown in Figure 3. From the figure one can see that thermal conductivity of nanocomposite increased with the increasing carbon nanotube content. When 1 phr CNT was added to polyurethane resin, thermal conductivity increased from 0.151W/mk to 0.216W/mk.
Multiwall Carbon Nanotube/Waterborne Polyurethane Nanocomposite
739
Alumium Metal
>
0.30-
£ 0.2 -Carbon Nanotube
1
2
3
CNT Content (phr)
FIGURE 3 Thermal Conductivity of carbon nanotube/waterborne polyurethane nanocomposite with various filler content
Thermal degradation properties Figure 4 presents that 10% weight loss temperatures of carbon nanotube/waterborne polyurethane nanocomposite (molecular weight of soft segment was 1250) with various CNT contents. Results indicated that adding carbon nanotube will increase the temperature of thermal degradation, however, it reduces the molecule weight of waterborne polyurethane when it polymerized. These two effects competed each other. Consequently, the thermal degradation temperature increased initially and then decreased. Tensile Properties Figure 5 indicates the tensile properties of carbon nanotube/waterborne polyurethane nanocomposite. Adding carbon nanotube to the waterborne polyurethane will enhance the initial tensile modulus of the composites. The tensile stress of carbon nanotube/waterborne polyurethane nanocomposite with 4phr CNT increased from 0.29MPa to 2.56 MPa (882%). The tensile modulus of carbon nanotube/waterborne polyurethane nanocomposite with 4phr CNT increased from 6.11MPa to 41.94MPa (679%). The dispersion agent plays an important role in strengthening the composites by effectively transferring the stress between the CNT and the polyurethane matrix.
740
Multiwall Carbon Nanotube/Waterborne Polyurethane Nanocomposite
1 phr without DP 2 phr without DP 1 phr with DP 2 phr with DP
1.0-
0.8-
g. 0.4-
s? 0.2-
0.0-
0
100
200
300
400
500
600
700
Temperature(°c) FIGURE 4 Thermal degradation temperature of WPU/CNT NanoComposite with different CNT contents
3.0-
2.5-
2.0-
1.5-
1.0-
0.5-
A
Without Dispersion Agent — — W i t h Dispersion Agent
nnCNT Content (phr)
(a)
CNT Content (phr)
5(b)
'
FIGURE 5(a) Tensile modulus and tensile stress 5(b) of multiwall carbon nanotube / waterborne polyurethane NanoComposite with different CNT contents
CONCLUSIONS Multiwall carbon nanotube / polyurethane nanocomposite has been prepared successfully. Thermal properties show that adding carbon nanotube would improve the thermal degradation properties by 25°C(from 273°C to298°C) when carbon nanotube content was 2phr. Thermal conductivity of nanocomposite was increased from 0.21 W/mk to 0.26 W/mk when the carbon nanotube content was 2phr. Surface electrical resistance of nanocomposite decreased six order from 3.20E+14 (12/cm2) to 7.99E+08(Q/cm2) when the carbon nanotube content was 4phr. Mechanical property tests showed that adding multiwall carbon nanotube would improve the tensile modulus by 679% and tensile strength by 882% .
Multiwall Carbon Nanotube/Waterborne Polyurethane Nanocomposite
741
REFERENCES 1. 2. 3.
4. 5.
6.
PenczekP, FrischKC, Szczepaniak B, Rudnik E Jpolym Sci Chem, 31, 1211(1993) (a)Dearlove T. J, et al JPolym. Sci 1977, 21, 1499 (b) Tang W , Frries R. J., Macknight W. J., Eisenbach CD Macromolecules 1994, 55, 153 Erik T. Thostenson, Zhifeng Ren, Tsu-Wei Chou, "Advances in the science and technology of carbon nanotubes and their composites: a review, composites science and technology, vol.61, pl899-1912(2001) Haggenmueller R, Gommans HH, Rinzler AG, Fischer JE, Winey KI. Aligned single-wall carbon nanotubes composites by melt processing methods. Chemical Physics Letters 2000;330(3-4): 219-25. Gommans HH, Alldredge JW, Tashiro H, Park J, Magnuson J, Rinzler AG. Fibers of aligned single-walled carbon nanotubes: polarized raman spectroscopy. Journal of Applied Physics 2000; 88(5):2509-14. Zuowan Zhou, Longsheng Chu, Wenming Tang, Lixia Gu, "Studies on the antistatic mechanism of tetrapod-shaped zinc oxide whisker", Journal of Electrostatics 57 (2003) p347
Preparation and Properties of Toughened Novolac Type Phenolic /SiO2 Flame Retardant Nanocomposite Chen-Chi M. Ma , Hsin Tai Department of Chemical Engineering, National Tsing-Hua University, Taiwan, R.O.C Chin-Lung Chiang Department of Industrial Safety and Health, Hung-Kuang University, Taiwan, R.O.C Hsu-Chiang Kuan Department of Chemical Engineering, National Tsing-Hua University, Taiwan, R.O.C Jen-Chang Yang Chemical System Research Division, Chung-Shan Institute of Science, Taiwan, R.O.C Chia-WenHsu Department of Chemical Engineering, National Tsing-Hua University, Taiwan, R.O.C
ABSTRACT In this study, Polydimethylsiloxanes (hydroxyl group terminated, PDMS) are utilized to toughen 3-Glycidoxypropyltrimethoxysilane (GPTS) modified novolac type phenolic resin / S1O2 organic/inorganic nanocomposite material (P80T20G10 system) via sol-gel method. Furtheremore, due to the incompatibility of polydimethylsiloxane and P80T20G10 system, the coupling agent GPTS, was used to modify PDMS and the properties were investigated. It was found that the Td5 (Temperature of 5% weight loss) of P80T20G10 system condensed with GPTS modified PDMS (GPTS-PDMS toughened P80T20G10 system) increased from 381 °C to 390 °C. From mechanical property measurement, it can be seen that the impact strength of GPTS-PDMS toughened P80T20G10 system increased from 8.4kJ/m2 to 10.8 kJ/m2. The flexural strength increased from 77.2 MPa to 85.1 MPa. The L. 0.1. values of all nanocomposite reached 35-38 and the U. L. value is 94V-0. INTRODUCTION Nano technologies have been developed rapidly for the past decade [1]. The materials prepared by nano-technologies usually possess unique physical and chemical properties such as excellent electrical properties, mechanical properties, thermal properties and flame retardance, etc. Recently, the novolac type phenolic resin blended with inorganic compound exhibits significant improvement on thermal properties and mechanical properties of the nanocomposite material. However the nanocomposite material is still brittle. There are two main reasons for using polydimethylsiloxane Corresponding Author, National Tsing Hua University, Department Of Chemical Engineering, Hsinchu, Taiwan300, R.O.C. ; TEL: 886-3-5713058,FAX: 886-3-5715408 ; [email protected]
Toughened Novolac Type Phenolic /SiO2 Flame Retardant Nanocomposite
743
(PDMS) as the toughening agent. The first reason is utilizing the flexibility of the PDMS, incorporating silicon rubber to inorganic structure to toughen resin [2-8], The other reason is using the excellent thermal property of PDMS, since the silicon rubber can be used up to 350°C even as high as 400°C • Furthermore, sol-gel process is a promising method to syntheses organic / inorganic composite materials. This study is intended to toughen the phenolic resin by utilizing modified polysiloxane. The properties of hybrid nanocomposites will be investigated.
EXPERIMENTAL Materials The phenolic resin used is a novolac type (PF1120HH), which was received from the Chang-Chun Plastics Co., Taiwan. The coupling agent: 3-Glycidoxypropyltrimethylenesiane (GPTS) was purchased from Acros Organics Co., New Jersey, U.S.A. Hexamethylene Tetramine (Hexamine) was used as curing agent, which was also received from Acros Organics Co., New Jersey, U.S.A. Preperation of Modified-Phenolic resin with modified PDMS The preparation of the hybrid materials involved two mixing parts, i.e. solution A and solution B. Solution A is the modified phenolic resin that was prepared as the following steps. Neat novolac type phenolic resin is dissolved in solvent, tetrahydrofuran (THF), and the solid content was kept at 50% or 10 phr (i.e., based on 100 parts of phenolic resin) 3-Glycidoxypropyltrimethoxysilane (GPTS) is used as coupling agent to modify phenolic resin. GPTS is added slowly to the solution of phenolic resin and TFfF, and stirs the mixture at 70°C for 20-24 hours. The GPTS modified phenolic resin is obtained through the ring-opening reaction of GPTS with hydroxyl groups in phenolic resin. The GPTS modified phenolic resin / THF solution is called as solution A. Solution B is prepared as the precursor of toughening agent. 3-Glycidoxypropyltrimethoxysilane (GPTS) was used as the coupling agents, respectively, which cap the two ends of PDMS. The coupling agents was heated at 80°C and stirred for 24 h. When the coupling agent was reacted completely with the hydroxyl groups, the ends of PDMS, the solution of the modified PDMS is called as solution B. According to the equivalent of the hydroxyl group of alkoxide group of the GPTS in solution A, the equal equivalent water was added in order to hydrolyze the alkoxide group. On the other side, different contents of PDMS (lphr, 3phr, 5phr, 7phr and 9phr, based on the amount of phenolic resin) are incorporated with 20wt% TEOS, based on phenolic resin, four times moles of TEOS, 50% vol. of THF and five drops of hydrochloric acid to lower the PH value to below 3. The mixture is called as solution C. When the hydrolysis reaction in solution C is completed, solution A and solution C were mixed to form the nanocomposite material toughened with PDMS. After solution A and solution C were mixed, the mixture was put in a vacuum oven to remove 60wt% of solvent, then casting. There are three main steps in curing process. The first step is the aging step, the sample was aged at room temperature for 2~3 days, the second step is drying, the sample was dried at the rate of 5°C per 4h in the oven from 25 °C to 80°C. Then the samples were heated in a vacuum oven at the rate of 15CC for 4hr
744
Toughened Novolac Type Phenolic /SiO2 Flame Retardant Nanocomposite
from 80°C to 230°C, and cured isothermally at the temperature of 130°C, 180°C and 200 °C for 8 hours respectively for curing and post curing. RESULTS AND DISCUSSION Characterization of GPTS modified PDMS Figure 1 shows the FT-IR spectra of the reaction between novolac type phenolic resin and 3-Glycidoxypropyltrimethoxysilane (GPTS). The Figure displays the change of the characteristic peak of epoxy group of GPTS at 914cm"1. Due to the ring-opening reaction of GPTS, the peak of 914 cm"1 disappeared and the bending red-shift of C-H out of plane was moved to 889 cm"1. Result confirms that the novolac type phenolic resin has reacted with GPTS at various times. Hydroxy group (SOOO-SeOOcm"1)
Epoxy group (9] 4cm1')
OHin^
' ™ j ^ ^ c ring deformat ring defOTmaliG
(3312im )
"~s"^-''~~ A _/
\,
T=initial
y
j^r
\~{
~^\_s^~~\
T=5 hr
f~~
T=9hr
1/1
r
'\J
T=final '
-
-^-i
lljf -
Si-O-C sir (1000-12
4000
3000
2000
Wavenumber (cm1)
BO (stretchin|) 1100cm'1
FIGURE 1 FT-IR spectrum of GPTS modified Phenolic resin at Different reaction times. (a)initial, (b)t=6hr, (c)t=20hr, (d)final.
4000
3500
3000
2500
2000
1500
1000
500
Wavenumber(cm' 1 )
FIGURE 2 FT-IR spectra of GPTS-PDMS at different reaction times. (a)initial, (b)t=lhr, (c)t=5hr, (d)t=9hr, (e)final.
Figure 2 shows the FT-IR spectra of the reaction between polydimethylsiloxane (PDMS) and 3-Glycidoxypropyltrimethoxysilane (GPTS). The characteristic peak of OH group in PDMS appears at 3312cm"1. The symmetric ring deformation band appears at 855cm"1 and the asymmetric ring deformation band appears at 890cm"1. Structure characterization of 29Si NMR spectra Figure 3 shows the solid-state 29Si NMR spectra of P80T20G10 system with the different contents o f ( l , 3 , 5, 7, 9phr, based on the amount of phenolic resin) GPTS-PDMS. Results reveal that Q4, T3 are the major microstructures in the modified PDMS with phenolic resin nanocomposite, i.e., the network structure is toughened by modified PDMS. Thermal Properties and Flame Retardance The TGA curves are ranging from room temperature to 800°C in N2 atmosphere. Table 1 summarized char yield, Td5 and Tdio (the temperature of degradation at which the weight loss is 5% and 10%) of all contents of the coupling agent for PDMS / P80T20G10
Toughened Novolac Type Phenolic /SiO2 Flame Retardant Nanocomposite
745
system. The degradation temperature of GPTS-PDMS / P80T20G10 system (Td5 is 369.4 °C and Tdiois 447.2°C) is lower than that of only P80T20G10 system (Td5 is 381°C and Tdiois 448°C). This was due to the bond energy of Si-C (275 kJ/mol) in PDMS is lower than the bond energy of C-C (348 kJ/mol). The L. O. I. testing values of all matrix toughened by modified PDMS are ranging from 32 to 38 and 37 for P80T20G10 system. For most matrices which have less toughened by modified PDMS are classified as the 94V-0 in U. L. testing and the same as P80T20G10 system.
-65.7 ppm (T3) -58.8 ppm
. i ^
p p m m_nQ45
^ X ^
p p m (Q<)
TABLE I Characteristic peaks of NMR
.
GPTS PDMS Tl -51 Ql Q2 -91 T2 -58 -19.8D -21.6 Q3 -101 T3 -65 Q4 -110 TEOS
-19.8--21.6 ppm (D)
GPTS-PDMS Content '"/•«-»'"« 9phr
7phr
200
100
0
-100
-200
-300
ppm
FIGURE 3 29Si-NMR spectra with different contents of GPTS-PDMS / P80T20G10 system
TABLE II 5% > 10% weight loss and Char Yield of composite materials (GPTS modified phenolic resin + TEOS 20wt%) blended with different contents of modified PDMS
Temperature of Temperature of 5% weight loss( 10% weight lossfC) °C)
Char Yield (wt%)
L.O.I. testing
U.L. testing
448
63.1
37
94V-0
366
438
63.3
37
94V-0
3
370
451
66.5
38
94V-0
5
368
444
66.0
36
94V-0
7
353
439
65.4
35
94V-0
9
390
464
69.1
35
94V-0
sample
ph r
GPTS-phenoIic resin nanocomposite
0
381
1 GPTS-PDMS Content (phr)
746
Toughened Novolac Type Phenolic /SiO2 Flame Retardant Nanocomposite
Mechanical Properties Table 3 summarizes the mechanical properties of the toughed P80T20G10 system. P80T20G10 system, condensing with GPTS modified PDMS, shows good impact strength increased from 8.19 kJ/m2 to 9.84 kJ/m2. This may due to GPTS-PDMS can well-distributed in network of phenolic resin nanocomposite. The flexural strength and modulus of GPTS-PDMS toughened P80T20G10 system increased with the GPTS modified PDMS content. Toughness was usually discussed by the area under the curve of stress versus strain. Therefore, it is found that when the content of GPTS modified PDMS equaled to 5phr, the matrix performed the highest toughness property. TABLE III Mechanical Properties of different content of GPTS-PDMS toughened P80T20G10 system
P80T20G10 system lphr 3phr GPTS-PDMS 5phr (phr) 7phr 9phr
Impact Notched Unnotched (ft-lbf/in) (ft-lbf/in) 1.60 3.79 2.01 78.5 81.3 2.07 2.00 87.1 2.08 85.2 2.11 93.3
Flexural strength modulus (MPa) (103xMPa) 77.2 3.9 78.5 5.2 81.3 4.6 87.1 4.9 85.2 5.2 93.3 6.3
Toughness Toughness (103xkJ/m3) 100.9 105.3 128.1 135.9 125.0 106.7
CONCLUSIONS Polydimethylsiloxanes (hydroxyl group terminated) toughen 3-Glycidoxypropyltrimethoxysilane (GPTS) modified novolac type phenolic resin / SiC>2 organic/inorganic nanocomposite materials (P80T20G10 system) via sol-gel method have been prepared. From thermal property study, the degradation temperature of GPTS-PDMS / P80T20G10 system (Td5 is 369.4°C and Tdi0 is 447.2°C) is lower than that of only P80T20G10 system (Td5 is 381°C and Td)Ois 448°C). GPTS-PDMS modified P80T20G10 system was investigated that the toughness property has been successfully improved. Impact strength increased from 8.19 kJ/m2 to 9.84 kJ/m2. The flexural strength and modulus of GPTS-PDMS toughened P80T20G10 system increased with the GPTS modified PDMS content. The matrix performed the highest toughness property when the content of GPTS modified PDMS is 5phr, Moreover, the L. O. I. and U. L. values are 35-38 and 94V-0, respectively. REFERENCES C. L. Chiang, C. C. M. Ma, D. L. Wu, H. C. Kuan, "Preparation, Characterization, and Properties of Novolac-Type Phenolic/Si02 Hybrid Organic-Inorganic Nanocomposite Materials by Sol-Gel Method", Journal of Polymer Science: Part A: Polymer Chemistry, Vol. 41, p905-913, 2003 K. H. Schimmel, G. Heinrich, "Influence of the molecular weight distribution of network chains on the mechanical properties of polymer networks", Colloid and Polymer Science, v269, nlO, pl003-1012, 1991. Ulibarri, Tamara A. Bates, Susan E., Black, Eric P., Schaefer, Dale W., Beaucage, W. Greg, Lee, Michael K., Moore, Pat A., Burns, Gary T., "Solvent effects on silica domain growth in silica/siloxane
Toughened Novolac Type Phenolic /SiO2 Flame Retardant Nanocomposite
4.
5.
6.
7. 8.
747
composite materials", International SAMPE Technical Conference 27 Oct 9-12 1995, p560-567, 1995. Hyeon-Lee, Jingyu, Guo, Ling, Beaucage, Gregory, Macip-Boulis, M. Antonieta, Yang, Arthur J.M., " Morphological development in PDMS/TEOS hybrid materials", Journal of Polymer Science, Part B: Polymer Physics, v34, nl7, John Wiley & Sons Inc. p3073-3080, Dec 1996. Hyeon-Lee, Jingyu, Guo, Ling, Beaucage, Gregory, Macip-Boulis, M. Antonieta, Yang, Arthur J.M., "Morphological development in PDMS/TEOS hybrid materials", Journal ofPolymer Science, Part B: Polymer Physics, v34, nl7, John Wiley & Sons Inc., p 3073-3080, Dec 1996. Mackenzie, D. John, Bescher, P. Eric, "Structures, properties and potential applications of ormosils", Journal of Sol-Gel Science and Technology, vl3, nl-3, p 371-377, Kluwer Academic Publishers, 1998. Ling Guo, H. L. Jingyu, Gregory Beaucage, "Structure analysis of poly(dimethylsiloxane) modified silica xerogels", Journal of Non-crystalline Solids, 243, p61-69,1999. B. Zhu, D. E. Katsoulis, J. R. Keryk, F. J. McGarry, "Toughening of a polysilsesquioxane network by homogeneous incorporation of polydimethylsiloxane segments", Polymer, 41, 20, p 7559-7573, Elsevier Science Ltd., 2000.
Synthesis, Thermal Properties and Flame Retardance of Novel Phenolic Resin/Silica Nanocomposites Chin-Lung Chiang Department of Industrial Safety and Health, Hung-Kuang University, Taiwan, R.O.C Chen-Chi M.Ma*, Hsu-Chiang Kuan Department of Chemical Engineering, National Tsing-Hua University, Taiwan, R.O.C Hey Rey Chang2 Department of Industrial Safety and Health, Hung-Kuang University, Taiwan, R.O.C Shiu-Chun Lu3 Department of Chemical Engineering, Ming Hsin University of Science and Technology, Taiwan, R.O.C
ABSTRACT The novel phenolic/silica hybrid ceramers were synthesized by sol-gel process. FTIR and 29Si NMR were used to characterize the structure of the hybrids. Results revealed that Q4, Q3, T3 are the major environments, i.e., it formed network structure. The thermal properties were investigated by thermogravimetric analysis (TGA). The char yields of the hybrids increase with increasing TEOS content. Tas (the temperature of degradation at which weight loss is 5%) of the hybrid containing 20% TEOS content was 290°C. As the TEOS content increases to 80%, Td5 of the hybrid raises to 312°C. TEOS inorganic components enhance the thermal stability of hybrids. Limiting oxygen index (L.O.I.) and UL-94 test reveals that the hybrid ceramer possesses excellent flame retardance.
INTRODUCTION The organic-inorganic hybrid materials are new types of composites have attracted much interest in recent years. Of the several kinds of inorganic components, metal oxides such as silica[l,2],alumina[3,4]and titania[5-8]are the most preferred in hybrid materials since they are readily prepared in-situ by the sol-gel process using the corresponding organic metal alkoxide. Especially, silicon alkoxide and silica are perhaps the most widely used for this purpose since the sol-gel reaction of silicon alkoxide is both mild and easily controlled. The fabricated materials possess the advantages of both organic polymers and inorganic ceramics. These materials are termed "Ceramers" by Wilkes[9]or "Oimosils" by Schmidt[10].Several polymers have been investigated as the organic phase of the hybrids such as polyimides[ 11,12] ,polybutadiene and polydimethylsiloxane[13],and so on. Corresponding Author, National Tsing Hua University, Department Of Chemical Engineering, Hsinehu, Taiwan 300 , R.O.C. ; TEL: 886-3-5713058,FAX: 886-3-5715408 ; Email:[email protected]
Novel Phenolic Resin/Silica Nanocomposites
749
The sol-gel process [14 -21]has provided promising opportunities for the preparation of variety of organic-inorganic hybrid materials at the molecular level. The in-situ development of a three-dimensional cross-linked inorganic network structure using an organic precursor such as an alkoxide, M(0R)4, can be carried out within the polymer matrix. The sol-gel method was utilized to improve the flame retardance and thermal stability.[22-27] In this study, coupling agent was utilized to form the covalent bonding between organic and inorganic phases, which will promote the miscibility of hybrid creamers. FTIR and 29Si NMR were used to identify the structures of the hybrid ceramers. The thermal properties were investigated by thermogravimetric analysis (TGA). The flame retardancy of hybrid ceramers was determined by limiting oxygen index (L.O.I.) test and UL-94 vertical test.
EXPERIMENTAL Materials Phenol and formaldehyde monomers are supplied by the Union Chemical Works Ltd, Taiwan. The novalac-type phenolic resin was synthesized in this laboratory. Hexamethylenetetramine (hexamine) was a purified industry grade reagent obtained from Chu-Chung Resin Co., Taiwan, R.O.C. The concentrated sulfuric acid used guaranteed reagent, which was obtained from the Osaka Chemical Co.,Osaka, Japan. Isocyanatopropyltriethoxysilane was purchased from United Chemical Technologies Inc.,PA, U.S.A. Tetraethoxysilan (TEOS) was supplied from Acros Organics Co.,PA, U.S.A.. Tetrahydrofuran is reagent grade supplied by Echo Chemical Co. Ltd., Taiwan, R.O.C. Preparation of Hybrid Ceramers Preparation of the hybrid ceramer involved mixing of two solutions, A and B. Solution A consisted of modified phenolic resin and THF. The modified phenolic resin was synthesized as follows: 4g 3-isocyanatopropyltriethoxysilane (equivalent weight 247g) was added into lOg phenolic resin ( equivalent weight 90g ) at 60 °C, then it was stirred for 4 hours until the characteristic peak of NCO group disappeared. Solution B contains H2O /HC1 /TEOS with a molar ratio of 9:0.63:1. HC1 was used as the catalyst for hydrolysis. DGEBA type epoxy (equivalent weight 180g) was poured into the mixture of solution A and B. DGEBA type epoxy was used as curing agent of the modified phenolic resin. 3-Isocyanatopropyltriethoxysilane/ phenolic resin / epoxy with the equivalent ratio is 0.3:1:1. The mixture was stirred until the solution became clear. The solution was cast into aluminum dishes to gel at room temperature. The wet gel was aged at room temperature for 48 hours, then dried at 80°C for 24 hours. The samples was put in a vacuum oven at 150°C for 24 hours. RESULTS AND DISCUSSION 3-1 Characterization Figure 1 shows the FT-IR spectra of the reaction between novalac phenolic and 3-isocyanatopropyltriethoxysilane. The figure displays the change of the characteristic peak of NCO group of 3-isocyanatopropyltriethoxysilane at 2270cm"1. Result reveals that
Novel Phenolic Resin/Silica Nanocomposites
750
novalac type phenolic resin has reacted with 3-isocyanatopropyltriethoxysilane at various times.
CH-l FIGURE 1FT-IR spectra of the reaction between nocalac phenolic resin and 3-isocyanatopropyltriethoxysilane, reaction time (a) initial reaction (b) 4 hr (c) 8 hr (d) 12 hr
Figure 2 shows the curve of solid-state 29Si NMR spectra of phenolic nanocomposite. Condensed siloxane species for TEOS in which a silicon atom mono-, di, tri, tetra-substituted siloxane bonds are designated as Q1, Q2, Q3, Q4, respectively. The chemical shifts —91, -101, -109 ppm of Q2, Q3, Q4, respectively, are in good agreement with the literature data[28]. For 3-isocyanatopropyltriethoxysilanes with mono-, di-, tri-, tetra-substituted siloxane bonds are designated as T1, T2, T3. The chemical shifts -56, -65 ppm of T2, T3, respectively, conform the literature values[29]. Results revealed that Q4, Q3, T3 are the major environments, i.e., it formed network structure. 5.00E+008 -,
phenolic hybrid ceramer
4.00E+008 -
-20
-40
-60
-SO
-100
-120
-140
FIGURE 2 The curve of solid-state 29Si NMR spectra of phenolic hybrid creamer
Novel Phenolic Resin/Silica Nanocomposites
751
3-2 Thermal properties of hybrids Figure 3 shows the TGA curves of the hybrids for different TEOS compositions from room temperature to 800°C in the N2 atmosphere. The char yields of the hybrids increase with increasing TEOS content. Increasing char formation can reduce the production of combustible gases, decreases the exothermicity during the pyrolysis reaction and inhibits the thermal conductivity of the burning materials[30]. As the TEOS content increases, the rates of degradation will be slower. The inorganic components can retard the degradation of the hybrids. The char yield has been correlated to the flame retardance[31]. 20% 100-
90 80 70 6050-
40 g> '(13
30-
5
2010-
0
Temperature) C) FIGURE 3 TGA curves of phenolic resin/silica hybrid creamer
3-3 L.O.I .and UL-94 test The flame retardant properties of the obtained hybrids were examined by measuring the L.O.I, of the hybrids. From Table 1, a significant increase in L.O.I, (from 32 to 43) was observed when TEOS was utilized in the phenolic resins. This indicates that incorporating silicon shows a significant effect on promoting the flame retardance of phenolic resins. This result is coincident with the char yield data. Moreover, the UL-94 test was also applied to probe the flame retardance of the hybrids and to rank them into an industrial expression. The results of UL-94 test are also shown in Table 1. From this Table, the neat phenolic resin may be classified into the UL-94 V-l. The hybrids containing 20 % TEOS content can be classified as UL-94 V-0 grade. The phenolic hybrids with good flame retardancy(L.O.I. : 32 ~ 43, UL94 V-0 grade) and excellent thermal stability (Tg is above 300°C) are considered to be sufficient for the applications as green flame retardant materials.
CONCLUSIONS A novel phenolic/silica hybrid ceramer synthesized by sol-gel process has been demonstrated. FTIR and 29Si NMR were used to characterize the structure of the hybrids. Results revealed that Q4, Q3, T3 are the major environments,i.e..,it formed the network structure. TGA data were investigated by thermogravimetric analysis (TGA). The neat phenolic resin may be classified into the UL-94 V-l. The hybrids containing 20 % TEOS
752
Novel Phenolic Resin/Silica Nanocomposites
content can be classified as UL-94 V-0 grade.TEOS inorganic components enhance the heat stability of hybrids. L.O.I.(32->43) and UL-94 V test results reveal that the hybrid ceramer possesses excellent flame retardance. TABLE I The UL-94 and L.O.I, test results of Novolac type phenolic/TEOS hybrids TEOS content(wt%)
Flaming drops
Cotton ignited
UL-94 standard
L.O.I.
Neat phenolic
N/A*
N/A
94V-1
32
20
N/A
N/A
94V-0
35
40
N/A
N/A
94V-0
37
60
N/A
N/A
94V-0
40
80
N/A
N/A
94V-0
43
*N/A:Not Available
REFERENCES 1. 2. 3. 4. 5. 6. 7. 8.
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14. 15. 16. 17. 18.
M. W. Ellsworth and B. M. Novak, " Mutually Inorganic-Organic Networks, New Routes into Nonshrinking Sol-Gel Composites Materials" J. Am. Chem. Soc. 113, 2756, 1991. B. M. Novak, " Silicon oxide coating on anodized aluminium by the sol-gel process and its evaluation'Mrfv. Maten 5, 422, 1993. J. E. Mark and S. B. Wang, "Reinforcement from alumina type Fillers precipitated into an elastomer"_Po/yw. Bull. 20, 443, 1988. F. Suzuki, K. Onozato, and Y. Kurokawa, "A Formation of Compatible Poly (vinyl Alcohol) / Alumina Gel Composite and Its Properties"/ Appl. Polym. Sci., 39, 371, 1990. S. B. Wang and J. E. Mark, "Crystallinity of Cellulose, as determined by CP/MAS NMR and XRD msXho£\Polym. Bull 17, 231, 1987. S J. Clarson and J. E. Mark, "Reinforcement of elastomeric poly(methylphenylisiloxane by the in-situ precipitation of titania)"Po(ym. CommunL30, 275, 1989. K. A. Mauritz and C. K. Jones, "A Formation of Compatible Poly (vinyl Alcohol)/Alumina Gel Composites and Its Properties" J. Appl. Polym. Sci. 39, 371, 1990. M. Nandi, J. A. Conklin, L. Salvati Jr and A. Sen, "Phosphonate modified titanium alkoxides: Intermediates in the sol-gel processing of novel titania/phosphonate inorganic-organic hybrids" Chem. Mater. 3, 201, 1991. GL.Wilkes, B.Orler and H.H.Huang, " Ceramers : Hybrid Materials Incorporating Polymeric/ Oligomeric Species with Inorganic Glasses by a Sol-Gel Process" Polym.Bull._ 14, 557(1985). H.Schmidt, "New Type of Non-crystalline Solids Between Inorganic and Organic Materials" J.Non-crystal.Solids 73, 681, 1985. A.Kioul and L.Mascia, "Compatibility of polyimide-silicate ceramers induced by alkoxysilane silane coupling agents"J.Non-crystal.Solids 175, 169, 1994. L.Mascia, Z.Zhang and S.J.Shaw, "Carbon fibre composites based on polyimide/silica ceramers: aspects of strucure-properties relationship" Composites Part A 27, 1211, 1996. F.Surivet, T.M.Lam, J.P.Pascault and C.Mai, "Organic-Inorganic Hybrid Materials. 2. Compared Structure of Polydimethylsiloxane and Hydrogenated Polybutadiene Based Ceramers"Macromo/. 25, 5742, 1992. Mark JE. "Novel Reinforcement Techniques for Elastomevs"J.Appl.Polym.Sci.Appl.Polym.Symp. 50:273, 1992. Mark JE. "Physical Properties of Sol-Gel Coating"J. Inorg.Organomet Polym. 1:431 , 1993 Schmidt H. "Transparent Inorganic/Organic Copolymer by Sol-Gel Process" J Sol-Gel Sci. Technol. 1:217, 1994. Betrabet SC, Wilkes GL. "Inorganic-Organic Copposites, including some examples Involing Polyamides and Polyimides'V. Inorg. Organomet Polym^4:343, 1994 Schmidt H, Kasemann R, Burkhart T, Wangner G, Arpac E, Geiter E. "Interphase Bonding in
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Organic / Inorganic Hybrid Mterials using Amino phenyl trimethoxy silane" ASC Symp Ser on Hybrid Organic-Inorganic Composites 585:331, 1995 Mascia L. "Effect of composition and cross-Link Function"Marcromolecules, Polvm. Sci"". 3:61(1995) Gaw K, Suzuki H, Kakimoto M,Imai Y. "Molecular Design of Sol-Gel Derived Hybrid Organic/Inorganic Nanocomposites" JPhotopolym. Sci. TechnoL 8:307, 1995 Kita H, Saiki H, Tanaka K, Okamoto K. "The Sol-Gel Process as a Basic Technology for Nanopaticles Dispersed Inorganic- Organic Composites'^/Photopolym. Sci. TechnoL%-3\i, 1995 Chin-Lung Chiang and Chen-Chi M.Ma, "Synthesis,Characterization and Properties of Novel
Ladder-like Polysilsesquioxanes containing Phosphorus " Journal of Polymer Science : Part A : Polymer Chemistry, 41, 9, pl371-1379, 2003 23. Chin-Lung Chiang, Chen-Chi M.Ma, Dai-Lin Wu and Hsu-Chiang Kuan, "Preparation, Characterization and Properties of Novolac Type Phenolic / SiO2 Hybrid Organic/Inorganic
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Nano-Composite Materials by Sol-Gel Method " Journal of Polymer Science : Part A : Polymer Chemistry, Vol 41,7,p905-913, 2003 Chin-Lung Chiang and Chen-Chi M.Ma, "Thermal-Oxidative Degradation of Novel Epoxy Containing Silicon and Phosphorous Nanocomposites" European Polymer Journal, 39/4, p825-830, 2003 Chin-Lung Chiang and Chen-Chi M.Ma, "Synthesis, Characterization and Thermal Properties of Novel Epoxy Containing Silicon and Phosphorous Nanocomposites by Sol—Gel Method" European Polymer Journal, Vol 38/ll,p2219-2224, 2002 Chin-Lung Chiang, Feng-Yih Wang, Chen-Chi M.Ma, and Hey-Ray Chang, "Flame Retardance and Thermal Degradation of Novel Epoxy Containing Silicon and Phosphorous Hybrid Ceramer by Sol-Gel Method" Journal ofPolymer Degradation and Stability, Vol77/2,pp273-278, 2002 Chin-Lung Chiang and Chen-Chi M.Ma, "Synthesis, Characterization and Thermal Properties of Novel Phenolic Resin/Silica Hybrid Ceramer" Journal of Polymer Degradation and Stability (accepted), 2003 C.J.Brinker, G.W. Scherer, Sol-Gel Science, The Physics and Chemistry of Sol-Gel Processing, Academic Press,_San Diego, 1990 Joseph R, Zhang S, Ford W. "Structure and Dynamics of a Colloidal Silica-Poly (methyl methacrylate) Composite by 13C and 29Si MAS NMR Sepctroscopy"_Macromoiecules, 29:1305, 1996 Pearce EM, Liepins R. "Hybrid Nanocomposite Materials-Between Inorganic Glasses and Organic Polymers'\&ivz>o» Health Perspect_U:69, 1975 KrevelenDW. "Some Basic Aspects of Flame Resistance of Polymeric Materials"_/>o/'_ymer 16:615, 1975
On the Enhancement of the Creep Resistance of Polymer by Inorganic Nanoparticles Zhong Zhang , Jing-Lei Yang, Klaus Friedrich Institute for Composite Materials University of Kaiserslautern, 67663 Kaiserslautern, Germany
ABSTRACT In the present study, one of the unique improvements in polymer nanocomposites has been detected. Only with a very low volume fraction of inorganic nanoparticles, the creep resistance of thermoplastic could be significantly improved. 21nm-TiO2/PA6,6 nanocomposites were compounded using a twin-screw-extruder. The final specimens were formed using an injection-moulding machine. Static tension and tensile creep tests were carried out at room and an elevated temperature (50°C). It was found out that the nanoparticles contributed to a remarkable reduction of the creep rate under various constant loads at both temperature levels. It is assumed that the nanoparticles restrict the slippage, reorientation and motion of polymer chains. In this way, they influence the stress transfer on a nanoscale, which finally results in these improvements.
INTRODUCTION To incorporate micron-size inorganic particles into a polymer matrix is a well-known method for improving the modulus of such composites. However, a reduction in the ductility of the material may take place. Furthermore, either by diminishing the particle size or by enhancing the particle volume fraction, the flexural strength and even the tensile strength can be enhanced. On the other hand, the fracture toughness and modulus remain fairly independent of the particle size [1], even when going down to the nanoscale [2-4]. Recently, researchers demonstrated that inorganic nanoparticles could be of benefit for an increased tensile elongation [5,6]. Many researchers also reported about an increase of the glass transition temperature (Tg) of polymers by the addition of various nanoparticles, which may be due to a good bonding between the nanoparticles and the polymers, thus restricting the motion of the polymer chains [7,8]. However, the potential of property improvements of structural polymer nanocomposites is still not fully explored. Creep is a time-dependent plastic deformation, which takes place under stresses lower than the yielding stress of materials. Recently, it was reported by Tanelke et al. [9] that nano-sized carbonitride dispersions could significantly improve the creep strength of steel at high temperatures. Relatively poor creep resistance and dimensional stability of thermoplastics are generally a deficiency, impairing the service life and safety, which is a barrier for their further expansion of application, e.g. in the automotive industry or in biomedical applications. To overcome this problem, it is shown in the present work, that even a very low volume content of 21nm-TiO2 particles in a Polyamide 6,6 (PA6,6 or * Correspondence Author, fax: +49-631-2017196, email: [email protected].
Creep Resistance of Polymer by Inorganic Nanoparticles
755
nylon6,6) matrix can remarkably improve the creep behaviour of this thermoplastic polymer under various creep loads at both room and elevated temperature. The influence of particle size and volume fraction on the property improvement was also investigated, but these results will be reported in a later paper, lvol.% TiO2/PA6,6 (3.4% by weight) exhibited best performances in all the static and creep investigations, which will be concentrated in the present paper.
EXPERIMENTAL Materials: A commercial Polyamide 6,6 (DuPont, Zytel 110) was considered as a matrix material. TiC>2 particles (a white, dry powder of Degussa P25) were applied as fillers with a density of 4 g/cm3 and a diameter of 21 run. The volume content was in the range of 1% (3.4% by weight). Extrusion: Nanocomposites were compounded using a Bersdoff twin-screwextruder (screw diameter=25 mm, screw aspect ratio L/D=44). Compounding was carried out at a barrel temperature of 292°C, a screw speed of 150 rpm, and a finial extrusion rate of 9 kg/hour. PA6,6 was dried in a vacuum oven at 70°C for a minimum of 24 hours before extrusion. Other processing parameters were also optimised in order to achieve a fine nanoparticle distribution in the matrix. In order to precisely control the filler content of nanoparticles, commercial K-Tron weightcontrolled feeders were applied. After cooling by water bath, the extruder blanks were cut as granules with a length in a range of 3 to 5 mm for further injection moulding. Injection Moulding: The composites were finally manufactured using an Arburg All-rounder injection moulding machine for various specimen sharps, according to different moulds, e.g. dog-bone tensile specimens (160x10x4 mm3, according to the German standard of DIN-ISO-527) for tensile and creep tests. The barrel temperature of the injection moulding machine was selected to be 295°C. The injection pressure was kept constant at 500 bars, the mould temperature was fixed at 70°C, and a constant injection speed of 80 ccm/s was applied for all specimens. Uniaxial Tension: A Zwick universal testing machine was applied for monotonic uniaxial tensile testing. Both a 250kN load cell and a strain gauge extensometer were equipped for measuring the tensile modulus and strength. Dog-bone tensile specimens were applied with a dimension of 160x10x4 mm3. A span length of 50 mm was considered. The crosshead speed was kept constant at 2 mm/min for room temperature and 5mm/min for elevated temperature measurements. A temperature chamber was used for elevated temperature measurements. At least four specimens of each composition were tested, and the average values were reported. Uniaxial Tensile Creep: Uniaxial tensile creep tests were preformed by a Creep Rupture Test Machine with double lever system (Coesfeld GmbH, model 2002). Ten specimens can be measured simultaneously in a testing chamber. Before testing, the desired constant load for each measurement unit was calibrated by using a force transducer. Then the samples were fixed into the clamps. For the elevated temperature measurement, the chamber was preheated to 50°C for at least 48 hours before loading was applied to the specimens in order to reach a steady temperature condition. A span length of 30 mm was marked on each specimen, and the elongation was monitored by a video camera which was equipped with a recorder and a computer image analysis system during the whole period of creep testing. The creep modulus was calculated by the ratio of the initial stress level to the measured creep stain. The measurement procedure was performed based on ASTM 2990-01 [10].
756
Creep Resistance of Polymer by Inorganic Nanoparticles 80
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Elongation [%] FIGURE 1 Transmission Electron Microscopy of a 2vol.% 21nm TiO2/PA6,6 specimen after injection moulding.
FIGURE 2 Tensile stress-strain curves of neat PA6,6 and lvol.% 21nm TiO2/PA6,6 composites at room temperature and 50°C.
RESULTS AND DISCUSSIONS Transmission Electron Microscopy (TEM) was applied to investigate the nanocomposites, and a relatively satisfactory dispersion of the nanoparticles, with a large amount of single particles, can be observed in Fig. 1. Glass transition temperatures of these materials were measured by a Dynamical Mechanical ThermoAhalysis (DMTA) approach, especially by evaluating the damping peaks. Two damping peaks at about -53°C and 75°C were observed for the neat PA6,6, which correspond to the primary- and the secondary- glass transitions, respectively. The results showed that the 21nm-TiO2 particles shifted both damping peaks to higher temperatures. It is a general believe that the primary-glass-transition depends on the motions of fully flexible molecular chains, and the secondary-glass-transition relies on the motions within a molecular chain. Both transitions are native characteristics of polymers, which are hard to be modified by traditional reinforcing approaches. However, in the present case, the 21nm-TiO2 particles contributed to a more than 5degree increase of the primary- and secondary- glass transition temperatures of PA6,6, respectively. The tensile stress versus strain curves of neat PA6,6 and 1% TiO2/PA6,6 nanocomposite are given in Fig. 2. After a linear dependence of stress on strain at room temperature, the tensile behaviour of the neat PA6,6 was characterised by a yielding point at about 70 MPa, from where a uniform plastic deformation along the specimen length took place. Necking happened at about 23% of elongation, at which the tensile stress dropped down by about 10%, before final failure occurred at a strain of ca. 35%. No obvious necking was detected for nanocomposite. lvol.% of nanoparticles resulted in about the same elongation to failure, but with a slight reduction of the yielding stress and the ultimate tensile strength (UTS). Series investigations were also preformed at elevated temperatures, e.g. at 50°C. A comparison of the tensile stress versus strain curves of the neat PA6,6 and the nanocomposite at this temperature is given additionally in Fig. 2. Both modulus and UTS were increased at elevated temperature once only lvol.% of nanoparticles was incorporated. On the other hand, the elongation at necking was slightly reduced.
Creep Resistance of Polymer by Inorganic Nanoparticles 80
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Tensile Creep at Room Temperature Creep Load: 80% of Static UTS
Tensile Creep at Room Temperature Creep Load: 80% of Static UTS
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Time [hour] FIGURE 3 Tensile creep strain vs. test duration-curves under 80% of the static UTS at room temperature. Constant creep stresses: 60MPa for the neat PA6,6, and 59MPa for the nanocomposite.
10
100
1000
Time [hour] FIGURE 4 Tensile creep modulus vs. test duration-curves under 80% of the static UTS at room temperature.
In addition to the static tests, creep measurements were carried out at room temperature, in which the creep stress was selected as 80% of the static UTS for each material, i.e. 60MPa for the neat PA6,6 and 59MPa for the nanocomposite, respectively. In general, a creep strain versus time curve can be considered as four stages (as shown in Fig. 3): (i) initial rapid elongation, (ii) primary creep, (iii) secondary creep, and (iv) tertiary creep [10]. The initial rapid elongation is due to the elastic and plastic deformation of the polymer specimen once the constant load is applied; this stage is independent of time. In the primary creep stage, the creep rate starts at a relatively high value, but decreases rapidly with time, which may due to the slippage and reorientation of polymer chains under persistent stress. After a certain period, the creep rate reaches a steady-state value in the secondary creep stage, in which normally the duration is relatively long. Finally, the material falls into the tertiary creep stage, where the creep rate increases rapidly and final creep fracture occurs. Neat PA6,6 exhibited a relatively long creep life (more than 600 hours), but at a high creep strain under this load level, as shown in Fig. 3. On the other hand, lvol.% 21nm TiC>2 particles significantly reduced the creep strain of PA6,6 over all the three creep stages, although the final creep life was not very much different from that of the neat polymer under the present testing conditions. Considering the most important creep stages separately, the nanocomposite (in spite of a slightly lower modulus and yield stress in the static tensile test) exhibited a much lower initial creep rate at the transition between the initial and the primary creep stage in comparison to the neat PA6,6. This resulted in the fact, that the creep strain boundaries for the secondary creep stage of the lvol.%TiO2/PA6,6 nanocomposite were at around 14% and 34%, respectively. Both were much smaller than those of the neat PA6,6, amounting to 22% and 62%, respectively. Therefore, the steady-state creep rate of the nanocomposite was about 3xl0"5 [hour"1] in the secondary stage, which was much lower than that of 6.5xlO"5 [hour"1] for the neat polymer. It is the authors' point of view that, in practice, the reduction of the creep strain is even more important for polymers than the
758
Creep Resistance of Polymer by Inorganic Nanoparticles 40
neat PA6.6 at 90% static UTS
30
1vol.%21nm 1vol.%21nmat 81% static UTS
10 Tensile Creep at Room Temperature . Creep Load: 90% of Static UTS i
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Time [hour] FIGURE 5 Tensile creep strain vs. test duration-curves under 90% of the static UTS at room temperature. Constant creep stresses: 68MPa for the neat PA6,6, and 66MPa for the nanocomposite.
200
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800
1200
1600
Time [hour] FIGURE 6 Tensile creep strain vs. test duration-curves under various load levels at 50°C. Constant creep stresses: 50MPa (90% of UTS at 50°C) or 43MPa (78% of UTS at 50°C) for neat PA6,6, and 46MPa (81% of UTS at 50°C) for nanocomposite.
extension of the creep life, since the former relates to the dimensional stability of the materials. The dimensional stability normally is defined as the ability of a material to maintain its size and shape under various temperatures and stresses. The curves of creep modulus versus time in Fig. 4 release further details of the deformation process. Under 80% of the static UTS, the nanocomposite possessed a much shorter primary creep stage of only about 2 hours, whereas 5 to 6 hours were measured for the neat PA6,6. Within these time periods, a very intense modulus reduction occurred for the neat PA6,6, whereas this decrease was much smaller for the 21nm particle filled PA6,6 system. In other words, the incorporation of smaller nanoparticles led to a much higher creep modulus in the whole range compared to neat PA6,6. This means, the load-bearing capability and the dimensional stability for the PA6,6 polymer under creep load were definitely improved by only lvol.% TiO2 nanoparticles. Enhancing the creep load to 90% UTS definitely accelerated the creep process, as shown in Fig. 5. A very high initial creep rate occurred for neat the PA6,6 in the primary creep stage, which was followed by a relatively short secondary creep stage with a steady-state creep rate, being clearly highly than that at the lower load level. A transition to the tertiary creep stage took already place after a creep duration of 80 hours only. The incorporation of nanoparticles remarkably reduced the initial creep rate in the primary creep stage. This ended up in a lower steady state creep rate within the secondary creep stage. As a result, the total creep strain was on a significantly lower level under this high creep load situation. Simultaneously, the creep life was also extended up to about 160 hours. The creep modulus results confirmed this effect as well. Creep curves of the neat PA6,6 and the nanocomposites, measured at 50°C, are plotted in Fig. 6. The unfilled matrix was measured at two constant stresses, i.e. 50MPa (*90% of UTS measured at 50°C) and 43MPa (78% of UTS at 50°C), respectively. The higher loading level resulted in a very high initial rapid elongation and a primary creep stage up to about 100 hours. The steady-state secondary creep
Creep Resistance of Polymer by Inorganic Nanoparticles
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stage lasted more than 1200 hours, thereafter, a rapid increase of the creep rate occurred in the tertiary creep stage, until the polymer fell into creep failure. A similar dependence of creep strain on time was measured for the neat polymer when loaded at 78% of UTS at 50°C, but as expected this took place at a much lower creep strain level. The best performance was, however, found for the TiO2/PA6,6 nanocomposite, which showed a much better creep resistance even at a high load situation, i.e. 46MPa (81% of UTS at 50°C). The creep modulus results confirmed again that the loadbearing capability was improved at the elevated temperature by the incorporation of nanoparticles. CONCLUSIONS lvol.% 21nm-TiO2 particles contributed to a significant improvement of the creep resistance of PA6,6 at both room and elevated temperature. The creep strain was remarkably reduced in all cases, and the creep life was extended at higher creep loading conditions (90% UTS). Nanoparticles may restrict the slippage, reorientation and motion of polymer chains. In this way, they influence the stress transfer, which finally results in these improvements. This result should lead to improved grades of creep resistant polymer nanocomposites for engineering applications. ACKNOWLEDGEMENTS Z Zhang is grateful to the Alexander von Humboldt Foundation for his Sofja Kovalevskaja Award, financed by the German Federal Ministry of Education and Research (BMBF) within the German Government's "ZIP" program for investment in the future. The authors appreciate Prof. MQ Zhang, Zhongshan University of China, who kindly provided the TEM pictures. Additional thanks are due to Dr. GJ Xian and Mr. H Zhang for their assistance of composite compounding. REFERENCES 1.
Moloney, A.C., H.H. Kausch, T. Kaiser, and H.R. Beer. 1987. "Parameters determining the strength and toughness of participate filled epoxide resins," Journal ofMaterials Science, 22:381-393. 2. Ng, C.B., L.S. Schadler, and R.W. Siegel. 1999. "Synthesis and mechanical properties of TiO2-epoxy nanocomposites," Nanostructured Materials, 12:507-510. 3. Ng, C.B., BJ. Ash, L.S. Schadler, and R.W. Siegel. 2001. "A study of the mechanical and permeability properties of nano- and micron-TiO2 filled epoxy composites," Advanced Composites Letters, 10:101-111. 4. Ou, Y., F. Yang, and Z. Yu. 1998. "A new conception on the toughness of nylon 6/silica nanocomposite prepared via in situ polymerization," Journal of Polymer Science, Part B, 36:789-795. 5. Zhang, M.Q., M.Z. Rong, Y.X. Zheng, H.M. Zeng, R. Walter, and K. Friedrich. 2001. "Structureproperties relationships of irradiation grafted nano-inorganic particle filled polypropylene composites," Polymer, 42:167-183. 6. Ash, B.J., D.F. Rogers, C.J. Wiegand, L.S. Schadler, R.W. Siegel, B.C. Benicewicz, and T. Apple. 2002. "Mechanical properties of Al2O3/Polymethylmethacrylate nanocomposites," Polymer Composites, 23(6):1014-1025. 7. Fornes, T.D., D.R. Paul. 2003. "Crystallization behavior of nylon 6 nanocomposites," Polymer, 44:3945-3961. 8. Sumita, M., H, Tsukihi, K. Miyasaka, and K. Ishikawa. 1984. "PP composites filled with ultrafrne particles," Journal of Applied Polymer Science, 29:1523-1530. 9. Tanelke, M., F. Abe, and K. Sawada. July 2003. "Creep-strengthening of steel at high temperatures using nano-sized carbonitride dispersions," Nature, 424:294-296. 10. "Standard Test Methods for Tensile, Compressive, and Flexural Creep and Creep Rupture of Plastics", [ASTM D2990-01] West Conshohocken, PA, ASTM International, 2001.
The Stress Transfer in a Single-Walled Carbon Nanotube-Reinforced Epoxy K. Q. Xiao and L. C. Zhang* School of Aerospace, Mechanical and Mechatronic Engineering The University of Sydney, NSW 2006, Australia
ABSTRACT This paper investigates the effects of tube length and diameter on the distributions of tensile stress and interfacial shear stress of a single-walled carbon nanotube in epoxy matrix. It was found that, according to the extended Cox model, a carbon nanotube has a greater stress transfer efficiency than a solid fibre, providing flexibility for toughness and tensile strength optimization.
INTRODUCTION The low density of defects and high strength of the carbon-carbon sp2 bond give carbon nanotubes (CNT) the highest axial strength and modulus among all existing whiskers. Recent theoretical calculations and direct experimental measurements showed that the elastic modulus of a CNT is in the range of 1-5 TPa [1-3], which is significantly higher than that of a carbon fibre from 0.1 to 0.8 TPa [4]. Such superior mechanical properties make CNTs a promising reinforcing material. If CNTs can have a large interfacial bonding strength with a matrix material, a great load transfer ability can be achieved, because a strong bonding allows shear stress to build up without causing interfacial failure. Some studies on a number of CNT-reinforced polymer composites have discussed the CNT-matrix interfacial bonding strength. For example, Wager and coworkers [5-8] claimed that a strong CNT-polymer adhesion and a high interfacial bonding strength in a CNT/polyurethane system [6] could be possibly attributed to a "2+2" cycloaddition reaction between the tube and the polymer. By extending the traditional Kelly-Tyson model [9], Wagner [5] suggested that the interfacial bonding strength in a CNT composite might be higher than that in a fibre-reinforced composite, although this model is unable to demonstrate the distribution of the tensile and interfacial shear stresses along a tube under an external loading. Liao and Li [10] used molecular mechanics to simulate a pull-out process in a Single-Walled Nanotube (SWNT)/polystyrene system and reported that the interfacial bond strength could be up to 160 MPa even without considering the chemical bonding between the tube and matrix. Qian and coworkers [11-12] found a significant load transfer ability of CNTs under tension. Recent work [13-14] on the direct experimental measurement of bonding strength also showed remarkably high adhesion between a mulit-walled nanotube (MWNT) or a SWNT and polymer. However, in a transmission electron microscopy study of an aligned nanotube/epoxy Corresponding author, School of Aerospace, Mechanical and Mechatronic Engineering, The University of Sydney, NSW 2006, Australia, Fax 61-2-93513760; Email [email protected]
Stress Transfer in a Single-Walled Carbon Nanotube-Reinforced Epoxy
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composite, Ajayan et al. [15] indicated that the interfacial bonding between a MWNT and epoxy matrix was weak. Schadler et al. [16], using Raman spectroscopy, also concluded that the interfacial bonding was very weak when a MWNT/epoxy composite was under tension. Some investigations also showed that interfacial bonding strength increased either with increasing the nanotubes' wall thickness [17] or with the formation of cross-links [18]. Previous investigations have mainly focused on the interfacial bonding strength. However, the dimensions of a nanotube can also influence its load transfer ability. To obtain a deeper understanding, the present study will use a modified Cox model to investigate the effects of length and diameter of a single-walled nanotube (SWNT) in an epoxy matrix on the load transfer properties. STRESS TRANSFER Modeling
FIGURE 1 Schematic representation of a single SWNT composite cylinder under applied strain e. It is assumed that no epoxy is filled inside the nanotube
The Cox model [19-20] for a solid fibre, assuming a perfect interfacial bonding, can be extended to a hollow SWNT shown in Fig. 1. This gives rise to the following formulae for calculating the tube's tensile stress, at, and interfacial shear stress, T, along the longitudinal axis of the SWNT:
cosh pL/2 27ir2
(l)
cosh J3L/ 2 At\n(R/r2)
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Stress Transfer in a Single-Walled Carbon Nanotube-Reinforced Epoxy
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maximum value should be smaller than the theoretical diameter of a carbon atom if the equilibrium of a tube cross-section is considered [22]. For convenience, in this work, two wall thickness values, «=0.34nm and ?=0.142 nm (carbon atom covalent diameter [23]) are used to examine the thickness effect. Stress Distribution O.OB ~
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In this section, stress distribution in a single SWNT composite cylinder will be discussed when the SWNT changes its geometric size. The distribution of the shear and tensile stresses along a tube of diameter <5f=2r2=2nm is shown in Fig. 2. The shear stress has its maximum value, Ttmax, at the two tube ends and is zero at the middle. Tensile stress starts to build up at the two ends of the nanotube and reaches its maximum, Gtmax, at the middle. Increasing L increases atmax and when L=500nm atmax becomes uniform and reaches nearly Ete. Thus to have an effective reinforcement, L must be sufficiently long to make full use of the high tensile strength of a CNT. The above variations of the shear and tensile stresses along the nanotube axis indicate that the interfacial bonding failure between a CNT and its surrounding matrix must start from the tube's two ends. If the bonding strength is good enough, then the breaking of the nanotube should be at the middle of the tube. U.I 0.08 ' O
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•
-0.04 L=100nm
•0.06
L=1500nm
*
-0.08 -n 1 0.4
0.6 Distance [X/L]
FIGURE 3 Effects of tube diameter d and wall thickness t on the interfacial shear stress (left: L=100nm and right: L=1500nm)
Stress Transfer in a Single-Walled Carbon Nanotube-Reinforced Epoxy
763
Figs. 3 and 4 show the effects of diameter and wall thickness of a nanotube on the distributions of the stresses. It is seen that an increase in d leads to a decrease in Ttmax and atmax- On the other hand, variation of t has a mixed influence. Increasing t increases load transfer and decreases tensile stress. However, it increases interfacial shear stress simultaneously. The effects of d and t become more obvious when the tube length is small. It
a d/t=1/0.34 o d/t=3/0.34 « d/t=3/0.142
12
IE 10
L=100nfn
D
Tensil
A d/t=1/0.34 ° d/t=3/0.34 °d/t=3/0.142
°
L=1500nm
0.5 Distance [X/L]
FIGURE 4
0.5 Distance [WL]
Effects of tube diameter d and wall thickness t on the tensile stress (left: L=100nm and right: L=1500nm)
Stress Transfer Efficiency The ratio of atmax to Ttmax, 8, characterizes the efficiency of transferring shear stress into tensile stress through a tube-matrix interface. Fig. 5 shows the variation of 5 with the tube length L, diameter d and wall thicknesses t. Clearly, 5 increases with L and approaches its saturation value 8S when L becomes infinite. It is also seen that a larger d or a smaller t (smaller tlr2) can greatly raise 8S. 300 250 U
fficiei
r-
200
1
150
s
100
to
50
c
tres
to
4
D o ° o o o o o o o o o o • o o ° o o o o o o o o o o o o o o o o
0.2 0.4 SWNT length [urn]
FIGURE 5
0.6
Effects of tube diameter and wall thickness on the stress transfer efficiency: +, d—\via and *=0.142nm; • , rf=2nm and 7=0.142nm; •, rf=3nm and i=0.142nm; o, rf=lnm and i=0.34nm; O , rf=2nm and Z=0.34nm; o, rf=3nm and (=0.34nm.
764
Stress Transfer in a Single-Walled Carbon Nanotube-Reinforced Epoxy
The effect of a tube's structure and Young's modulus on the stress transfer efficiency is shown in Fig. 6. When ^/r2=constant and n=0 (corresponding to a solid fibre), 8S becomes independent of the radius r2, according to Eqs. (1) to (3). Assuming that a tube has carbon fibre's modulus (E=230GPa), when its structure changes from a solid one to a hollow one (fif=3nm, £=0.142nm), 8S increases from 49.5 to 117 (see curves x and -). Keeping its hollow structure unchanged but changing its modulus to its real value (1.2TPa), 8S increases from 117 to 267 (see curves - and • ) . This shows that 69% of the difference in 8S is caused by the value of Young's modulus and 31% is induced by the structural change from solid to hollow. For another nanotube with d=lnm and ?=0.34nm, calculation indicates that the contribution from tube hollow structure is only about 2% (see curves X, A and o). It seems that the contribution of the hollow structure increases with decreasing tfo. Since the real wall thickness t of a nanotube can be smaller than its atomic diameter (0.142 nm) [22], the structural effect of a CNT on the 8S of a CNT-reinforced nanocomposite can be considerable.
0.2 SWNT length [n
0.4
FIGURE 6 Effects of a tube's structure and Young's modulus on the stress transfer efficiency: •, =3nm and f=0.142nm; o, d=lnm and J=0.34nm; and with Young's modulus assumed to be 230GPa for,-, rf=3nmand/=0.142nm; A , rf=lnm and Z=0.34nm, a n d X , rf=lnmandr;=0 ( S =thatof a carbon fibre).
Because the bonding between inner and outer tubes of a multi-walled nanotube is weak [24-25], inter-wall sliding may occur. Thus, a MWNT may be approximately treated as a SWNT in a composite system. The above discussion indicates that a MWNT should have a larger 8S than that of a SWNT since the outer diameter of the former is usually 10 times larger. The large stress transfer efficiency of a CNT-reinforced composite indicates that the improvement of its toughness can be achieved at a less loss of its tensile strength, and vice versa, by tailoring the interfacial bonding strength. Its large 8 also allows to obtain a high tensile stress at a relatively low shear stress level to reduce the possibility of matrix failure. These cannot be achieved by the usual fibre-reinforced composite [20]. CONCLUSIONS The Cox model was modified and applied to assess the load transfer of CNTreinforced composites. It was found that a larger SWNT wall thickness leads to a
Stress Transfer in a Single-Walled Carbon Nanotube-Reinforced Epoxy
765
decrease in tensile stress and an increase in shear stress. The stress transfer efficiency 8 of a CNT-reinforced composite is much higher than that of its carbon fibrereinforced counterpart, caused by the high Young's modulus and hollow structure of CNTs. This provides the flexibility of property optimization in terms of tensile strength and toughness of a CNT-reinforced composite. ACKNOWLEDGEMENT The authors thank their colleague Dr H. Y. Liu for fruitful discussion. This work is financially supported by Australia Research Council (ARC) through a Discovery Grant. REFERENCES 1. Treacy, M. M., T. W. Ebbesen, and J. M. Gibson. 1996. Nature, 381:678. 2. Wong, E. W., P. E. Sheehan, and C. M. Lieber. 1997. Science, 277:1971. 3. Zhang, P., Y. Huang, P. H. Geubelle, P. A. Klein, and K. C. Hwang. 2002. International Journal of Solids and Structures, 39:3893. 4. Peebles, L. H. 1995. Carbon Fibres: Formation, Structure and Properties. CRC Press, Boca Raton. 5. Wagner, H. D. 2002. Chemical Phys. Lett., 361:57. 6 Wagner, H. D., O. Lourie, Y. Feldman, and R. Tenne. 1998. Appl. Phys. Lett., 72:188. 7. Wagner, H. D., and O. Lourie. 1998. Appl. Phys. Lett., 73:3527. 8. Lourie, O., and H. D. Wagner. 1999. Compos. Sci. Technol., 59:975. 9. Kelly, A, and W. R. Tyson. 1965. J. Mech. Phys. Solids, 13:329. lO.Liao, K, and S. Li. 2001. Appl. Phys. Lett., 79:4225. 11. Qian, D., E. C. Dickey, R. Andrews, and T. Rantell. 2000. Appl. Phys. Lett., 76:2868. 12.Qian, D., and E. C. Dickey. 2001. J. Microscopy, 204:39. 13. Barber, A. H., S. R. Cohen, and H. D. Wagner. 2003. Appl. Phys. Lett., 82:4140. 14. Cooper, C. A., S. R. Cohen, A. H. Barber, and H. D. Wagner. 2002. Appl. Phys. Lett., 81:3873. 15,Ajayan, P. M., O. Stephan, C. Colliex, andD. Trauth. 1994. Science, 265:1212. 16. Schadler, L. S., S. C. Giannaris, and P. M. Ajayan. 1999. Appl. Phys. Lett., 73:3842. 17.Lau, K. T. 2003. Chemical Phys. Lett., 370:399. 18. Frankland, S. J. V, A. Caglar, D. W. Brenner, and M. Griebel. 2002. J Phys ChemB, 106:3046. 19. Cox, H. L. 1952. Brit. J. Appl. Phys., 3:72. 20. Kelly, A., N. H. MacMillan. 1986. Strong Solids (Third edn.). Clarendon Press, Oxford, pp. 258. 21,Delmotte, J. P. S., and ARubio. 2002. Carbon, 40:1729. 22. Vodenitcharova, T., and L. C. Zhang. 2003. Physical Review B, 68:165401. 23. Aylward, G. H., and T. J. V. Findlay. 1974. SI Chemical Data. John Wiley and Sons, pp. 10. 24. Yu, M. F., O. Lourie, M. J. Dyer, K. Moloni, T. F. Kelly, and R. S. Ruoff. 2000. Science, 287:637. 25. Yu, M. F., B. S. Files, S. Arepalli, and R. S. Ruoff. 2000. Phys. Rev. Lett., 84:5552.
A Study on Mechanical Properties of MWNT/PMMA Nanocomposites Hyun-Chul Kim1, Sang-Eui Lee2, Chun-Gon Kim2 and Jung-Ju Lee*1 Division of Mechanical Engineering, Department of Mechanical Engineering, KAIST, Korea 2 Division of Aerospace Engineering, Department of Mechanical Engineering, KAIST, 1
Korea
ABSTRACT Multi-walled carbon nanotube (MWNT) / poly (methyl methacrylate) composites were fabricated with the variation of the nanotube - concentration through film casting. It was confirmed that the nanotubes were well dispersed in PMMA according to SEM images. To investigate the mechanical properties of the MWNT / PMMA nanocomposites, tensile tests were performed varying the MWNT - concentrations. As the MWNT concentration increased from 0 to 0.15 wt%, MWNT / PMMA nanocomposites were improved by about 20% in the tensile strength and by about 32% in the tensile modulus. Because MWNTs in MWNT / PMMA nanocomposites were assumed to be randomly oriented, the tensile modulus of the nanocomposite was evaluated through the Tsai-Pagano equation which has been applied to short fiber composites for estimating their modulus. However, the estimated results were not in agreement with the experimental results from tensile tests. It is attributed to two reasons. First, MWNTs in this research were not stretched straightly but entangled ones. That is, MWNT could not be assumed to be a short fiber. Second, the concentration of MWNT is too small to be compared with that of the short fiber composites. INTRODUCTION Carbon nanotubes (CNTs) are the most remarkable materials that have ever been discovered. Since the discovery of carbon nanotubes by Iijima in 1991 [1], carbon nanotubes are called as 'materials for 21th century' due to their superior electrical and mechanical properties. They are noticed by many scientists and engineers, and accepted as the core of nano science. At this writing their competition in price is poor, but it has been continuously studied to cut down expenses through mass production. If these efforts come in reality, it will become to apply carbon nanotubes to structural materials as composites. Poly(methyl methacrylate) (PMMA) is a kind of thermoplastics and selected as a matrix material of composites because of its good variable-climate-resisting property and transparency. * Correspondence Author : Division of Mechanical Engineering, Department of Mechanical Engineering, ME3073, KAIST, 373-1 Guseong-dong, Yuseong-gu, Daejeon, 305-701, South Korea, Tel: (82-42) 869-3033, Fax : (82-42) 869-3210, E-mail: [email protected]
A Study on Mechanical Properties of MWNT/PMMA Nanocomposites
767
There are many technical requests desired to make nanocomposites using CNT and PMMA. To apply superior properties of CNT to composites, it is important to disperse CNTs in matrix materials uniformly and intensify the coherence at the interfaces of CNTs and matrix materials. Several dispersion methods such as melt blending [2], in-situ polymerization [3], solution mixing [4] have been proposed. The objectives of this paper are to manufacture CNT/PMMA nanocomposites and to improve their mechanical properties. Multiwalled nanotues (MWNTs) are purchased at Iljin nanotech Co., Ltd. Tensile test is performed to measure the changes of mechanical properties. We exploit scanning electron microscope (SEM) to observe the MWNT dispersions. FABRICATION OF CNT/PMMA NANOCOMPOSITES Dispersion Equipment and Solvent Selection It is the preceding procedure to disperse nanoparticles in the matrix material to improve the properties of nanocomposites. We performed sonication to disperse CNTs into polymers. First, CNTs were dispersed in a solvent using the sonicator. Then PMMA were dissolved and mixed with the above suspension by the homogeizer. The homogenizer is a stirring equipment that has very high rpm of several ten thousands. It helps PMMA to be well dissolved in a solvent. After above processes, we put the CNT/PMMA/solvent suspension into an oven to vaporize the solvent for 2 days and we can obtain CNT/PMMA nanocomposites. The solvent which we have selected to dissolve PMMA is acetone. Change of Dispersion State with the PMMA Concentrations of PMMA/Acetone Solution It takes about 2 days to cure the CNT/PMMA nanocomposites and it is important to maintain the dispersion state of the CNT/PMMA/acetone suspension during that time. We compared the dispersion-maintaining period of several PMMA/acetone concentrations, 10 wt%, 20 wt%, 27 wt%. The results are showed in FIGURE 1. When the concentration is 10 wt%, much CNTs are precipitated after 2 days. The suspension containing 20 wt% of PMMA showed precipitations at the 3rd day. But when the concentration of the suspension was 27 wt%, CNT particles were well dispersed in the suspension after 3 days. From these observations, it can be inferred that the dispersion state will be maintained well in more than 20% concentration of the PMMA/acetone. Curing of CNT/PMMA Nanocomposites CNT/PMMA composites were fabricated by film casting process, in which acetone in PMMA/acetone suspension was evaporated. The maximum temperature is 50 °C because the evaporation point of acetone is 56 °C. When we maintained the maximum temperature during about 15 hours, we could obtain the composites of good quality. To prevent the plate from the distortion caused by the effect of the thermal residual stresses from the composites, we turned over the plate and repeated the identical curing cycle.
768
A Study on Mechanical Properties of MWNT/PMMA Nanocomposites
PMMA: acetone =
2 days later
PMMA: acetone - 1 : 4
3 days later
^ Obvious precipitation after 2 days
PMMA : acetone = 27 : 73
1 days later
-' Precipitation was conformed after 3 days
*' Stable dispersion was maintained after 3 days
FIGURE 1 Comparison of dispersion states by PMMA concentration of PMMA/acetone solution
Observation of the Dispersion Degree of CNT/PMMA Nanocomposites We confirmed the dispersion state of CNTs in CNT/PMMA nanocomposites by SEM. The specimen was cut to 30 mm x 5 mm x 1 mm and putted into liquid nitrogen for 5 minutes. We picked up the specimen with nippers and broke it. The SEM images shown in FIGURE 2 shows the fractured section. FIGURE 2-(a) shows the configuration of the section and FIGURE 2-(b) shows a zoomed image of the left side box that particles are gathered. FIGURE 2-(a) shows that aggregated CNTs were dispersed at intervals of 10 ~ 20 \m. CNTs were not dispersed well in nano scale, but PMMA were well distributed among CNTs. So we presume that CNT can contribute to increase the strength of PMMA. MECHANICAL TEST OF CNT/PMMA NANOCOMPOSITES CNT/PMMA nanocomposites can be considered as a kind of reinforced plastics, so tensile test was executed according to ASTM D638. Tensile Properties Estimation of CNT/PMMA Nanocomposites Prior to the tensile test of CNT/PMMA nanocomposites, the elastic modulus was estimated by assuming that CNT is a kind of short fiber. We assumed that CNT belongs to the randomly oriented discontinuous fiber and that CNT/PMMA can be a isotropic material if CNT was randomly distributed and well dispersed in PMMA.
(a) Fractured section (b) Zoomed image of the left side box FIGURE 2 SEM image of the fractured surface of CNT/PMMA nanocomposites
A Study on Mechanical Properties of MWNT/PMMA Nanocomposites
769
Tsai and Pagano [5] developed the following approximate expressions: E1
E1
~
8
i
1
/"I "\
E*
„ O
2
V J
where E = averaged Young's modulus for randomly oriented fiber composite, Ex, E2 are induced from the Halpin-Tsai equation which are:
where
r, = ^ f
uJk)
(2)
d
where , = | ^ ( ^ 2 )
(3)
£, is the curve-fitting parameter, which is a measure of the strengthened degree of the matrix by the fiber. In case that E, is twice the aspect Ratio in Eqs. (2) and 2 in Eqs. (3), the approximation has the closest value. The elastic modulus of MWNT was assumed to be 0.3 TPa as Cooper et al. published [6]. That of PMMA was about 1.67 GPa from experiment. The aspect ratio of MWNT is about 3000 according to the information given by Iljin nanotech Co., Ltd. So from Eqs. (2), £ is 6000. The density of MWNT was about 0.13 g/cnf and that of PMMA was about 1.19 g/cnf. TABLE I shows that the elastic modulus E varies with the mass concentration of MWNT. Also, because the CNT/PMMA nanocomposites can be considered as isotropic material, the Poisson's ratio and the shear modulus can be calculated according to the following equations, Eqs. (4) and (5) : (4) (5)
-v) TABLE I Estimation of elastic modulus by Tsai-Pagano equation
Weight % of CNT
,
£(GPa)
0.000
0.0
1.554
0.025
2.283 xl0~ 3
1.808
0.050
3
2.061
0.075
3
6.819 xlO~
2.313
0.100
9.071 xl0~ 3
2.564
0.150
J
v
4.556 xlO"
13.54 xl0~
3.062
770
A Study on Mechanical Properties of MWNT/PMMA Nanocomposites TABLE II Tensile test results of CNT/PMMA nano- composites (a) Tensile strength of CNT/PMMA (unit: MPa) 0.0 0.025 0.05 0.10 20.181 18.697 20.878 18.847 19.917 18.657 20.683 17.978 18.160 20.727 20.095 21.541 18.739 20.266 21.879 19.151 19.404 19.772 18.631 21.447 19.057 19.832 20.448 19.793 0.9204 0.7560 1.1075 1.6119
0.15 24.763 22.047 23.292 21.393 22.874 1.4855
(b) Tensile modulus of CNT/PMMA (unit :GPa) Weight % of CNT 0.0 0.025 0.05 0.10 Testl 1.693 1.898 2.046 2.022 Test 2 1.832 2.374 1.745 1.729 Test 3 1.544 1.804 2.179 2.123 1.741 Test 4 1.546 1.804 1.945 Test 5 1.795 1.825 1.240 1.651 1.9186 Average 1.5536 1.7772 2.0578 Deviation 0.1860 0.1966 0.0926 0.2076
0.15 2.134 2.114 1.991 2.016 2.0638 0.0708
Weight % of CNT Testl Test 2 Test 3 Test 4 Test 5 Average Deviation
3.4 3.2 3.0 2.8
? 2.6
—A— Tsai-Pagano Equation ' Experiment
C3
r 2.4
1.6 1.4 0.2:
ff : : : : : • : : : : : : : 1 0.025
0.050
0.075
0.100
0.125
0.150
weight % of CNT
FIGURE 3 Comparison of theoretical estimation and test results.
Tensile Test of CNT/PMMA Nanocomposites The amount of CNT is remarkably fewer than that of PMMA in CMT/PMMA nanocomposites, so the mass ratio of CNT means (the mass of CNT) / (the mass of PMMA). The tensile test is performed according to the CNT mass ratios 0.0 wt%, 0.025 wt%, 0.05 wt%, 0.10 wt%, and 0.15 wt%, respectively. For each CNT mass ratio, 5 specimens were tested and averaged to calculate the tensile strength and the Young's modulus. The longitudinal and transverse strains were measured at the same time to calculate Poisson's ratio and the shear modulus. The tensile test results are written down in TABLE II. FIGURE 3 shows the comparison of elastic modulus between the experimental
A Study on Mechanical Properties of MWNT/PMMA Nanocomposites
771
results and the theoretical approximations by Tsai-Pagano equation. The tensile strength and the elastic modulus of CNT/PMMA nanocomposites were increased in comparison with those of the pure PMMA. As CNT is added, the properties were increased, but there were no clear variation according to the mass ratios of CNT. The Poisson's ratio was about 0.165 and was aknist unchanged as CNTs were added. So it could be mentioned that the Poisson's ratio was constant and the shear modulus behavior was similar with the elastic modulus calculated in the Eqs. (5). CONCLUSION The tensile strength and the elastic modulus of the CNT/PMMA nanocomposites were improved in comparison with those of the pure PMMA. When the CNT mass ratio was 0.15 wt%, tensile strength was increased about 20.0 % and elastic modulus was increased about 32.8%. There was a remarkable distinction between the experimental results and the theoretical ones in which CNT was assumed to be a randomly oriented short fiber. It is attributed to the fact that the architecture of CNT is not a common short fiber, but a thread-like aggregation. That's why it is not reliable to assume that CNT is a short fiber. The properties of CNT itself, although, have been studied by many researchers, those keep in uncertainty.
REFERENCES 1. 2.
3.
4.
5. 6.
S. Iijima, "Helical Microtubules of Graphitic Carbon," Nature, Vol. 354, No. 6348, pp. 56-58, 1991 Z. Jin, K. P. Pramoda, G. Xu, S. H. Goh, "Dynamic Mechanical Behavior of Melt-Processed Multi-Walled Carbon Nanotube/Poly(Methyl Methacrylate) Composites," Chemical Physics Letters, Vol. 337, No. 1/3, pp. 43-47, 2001 Z. Jia, Z. Wang, C. Xu, J. Liang, B. Wei, D. Wu, S. Zhu, "Study on Poly(Methyl Methacrylate)/Carbon Nanotube Composites," Materials Science and Engineering : A, Vol. 271, No. 1/2, pp. 395-400, 1999 C. Stephan, T. P. Nguyen, M. Lamy de la Chapelle, S. Lefrant, C. Journet, P. Bernier, "Characterization of Singlewalled Carbon Nanotubes-PMMA Composites," Synthetic Metals, Vol. 108, No. 2, pp. 139-149,2000 R. F. Gibson, Principles of Composite Material Mechanics, McGraw-Hill, 1994 C. A. Cooper, R. J. Young, M. Halsall, "Investigation into the deformation of carbon nanotubes and their composites through the use of Raman spectroscopy," Composites : Part A, Vol. 32, No. 3/4, pp. 401-411,2001
Fabrication and Microstructure of Si3N4-TiCnano Composites Jun Zhao , Xinping Huanga, Xing Ai, Zhijie Lil School of Mechanical Engineering, Shandong University, Jinan 250061, P. R. China "Department of Engineering, Laiyang Agricultural College, Laiyang 265200, P. R. China
ABSTRACT ceramic matrix composites toughened with TiC-nanoparticles were fabricated by using hot pressing technique with AI2O3 and Y2O3 as sintering aids. The effects of TiC-nanoparticles and hot pressing temperature on the densification and mechanical properties of Si3N4-TiCnan0 composites were investigated. The experimental results showed that optimum mechanical properties could be achieved for S13N4-3OV0I. % TiCnano composite sintered at 1750°C for 60min, under 30MPa pressure in N2, with the fiexural strength, fracture toughness and hardness being 850MPa, 6.7MPa-m1/2 and 16.5GPa respectively. The microstructure and phase composition of the material were characterized with scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). It was found that a-phase Si3N4 grains were completely transformed into P-phase S13N4 grains with high aspect ratio. Both intraand intergranular TiC-nano particles were present. Dislocations, sub grain boundaries as well as twin crystal resulting from thermal expansion mismatch were observed in grains.
INTRODUCTION Silicon Nitride (Si3N4) ceramics are currently the premier ceramic materials for high stress, high temperature applications such as gas turbines, turbochargers, engine valves as well as cutting inserts as a result of their higher strength, thermal conductivity, lower thermal expansion coefficient and resultingly their higher thermal shock resistance. However, the characteristics of S13N4 ceramics limiting their applications are their relatively lower hardness, wear resistance andfracturetoughness. Many efforts have been directed towards improving the mechanical properties of Si3N4 by controlling the microstructure or by making various types of composites [1-5]: designing microstructures with elongated grains which act as bridges, between crack faces just behind the crack tip; incorporating fibers or whiskers which bridge the crack faces; incorporating secondary phase particles which deflect the crack making it travel a more tortuous path. hi the present work, Si3N4 ceramic matrix composites toughened with TiC-nanoparticles were fabricated by using hot pressing technique with AI2O3 and Y2O3 as sintering aids. The effects of TiC-nanoparticles and hot pressing temperature on the densification and mechanical properties of Si3N4-TiCnano composites were investigated. The microstructure and phase composition of the material were characterized with * Correspondence Author, 73 Jingshi Road, Jinan, 250061, P. R. China, fax: +86-531-8392618. E-mail address: [email protected] (J. Zhao)
Fabrication and Microstructure of Si3N4-TiCnano Composites
773
scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD), which were correlated to the analysis of thermal expansion mismatch induced residual microstresses and mechanical properties. EXPERIMENTAL PROCEDURES Materials The starting materials were a-SisN4 powders with average grain size of approximately 0.5 |im, purity 99.5%, and TiC nanoparticles with average grain size of 140 nm, purity 99.8%. The a-Si3N4-TiCnano powders were mixed and dispersed ultrasonically in absolute alcohol, with 2wt% of AI2O3 and 3wt% of Y2O3 used as sintering aids. The mixtures were ball-milled for 24h. The slurries were subsequently dried in vacuum. The sieved powder mixtures were loaded in a cylindrical graphite die with an inner diameter of 42 mm. The specimens were then sintered by hot pressing inflowingN2 at temperatures in the range of 1650°C~1850°C for lh under a fixed uniaxial pressure of 30MPa. Characterization Sintered compacts were cut and machined into bend bars with dimensions of 3 mmx4 mmx36 mm for strength measurements. All specimen surfaces were ground flat to a 10 |am finish. Flexural strength was measured using a three-point bend fixture with a 30 mm span width at a loading crosshead rate of 0.5 mm/min. An indentation method (BVI) was used to determine the fracture toughness [6]. The density of each specimen was measured by the Archimedes method. A minimum number of five specimens was tested for each experimental condition. XRD (Rigaku D/max- IIB) was used to record the XRD patterns of the different composites. Microstructures of samples were analyzed by SEM (Hitachi S-570) and TEM (Hitachi H-800) equipped with the energy spectrum. RESULTS AND DISCUSSION Mechanical Properties The effects of TiCnano content on the mechanical properties of SisNVTiCano composites hot pressed at 1750°C for 60min were investigated and the results revealed that the composite containing 30vol.% TiC nanoparticles exhibited the highest flexural strength, toughness and Vicker's hardness. The relative density, flexural strength, fracture toughness and Vicker's hardness of Si3N4/30vol.% TiCnano composites hot pressed at temperatures in the range of 1650°C ~1850°C for 60min are shown in FIGURE 1 respectively. It can be seen clearly from FIGURE la that the density increased markedly at temperatures in the range of 1650°C ~1750°C and decreased thereafter. It is well known that the phase transformation and densification of Si3N4 ceramics during the liquid sintering process is controlled by the viscosity of the liquid phase to a great extent. The viscosity of the liquid phase decreases with the increase in sintering temperature, leading to the liquid capillary action which promotes the rearrangement of the particles. Then the enhanced reactivity of the liquid with the solid results in phase transformation and densification through a rapid dissolution-transport-reprecipitation process which is believed to be responsible for the sharp increase in density in the temperature range of 1650°C~1750°C. No crystalline
774
Fabrication and Microstructure of Si3N4-TiCnano Composites
phases other than P-Si3N4 and TiC were identified by XRD analysis for specimen hot pressed at 175CTC, see FIGURE 2. 100
900 r
r
850 800
53 98 •o o * 97
3 &
750 700
1600 1650 1700 1750 1800 1850 1900
1600 1650 1700 1750 1800 1850 1900
Hot pressing temperature /°C
Hot pressing temperature /°C
(b) Flexural strength
(a) Relative density 17
7.0 r 6.5
O 16
J3
w
I
4.0 1600 1650 1700 1750 1800 1850 1900
13
1600 1650 1700 1750 1800 1850 1900
Hot pressing temperature /°C
Hot pressing temperature /°C
(c) Fracture toughness (d) Vicker's hardness FIGURE 1 Properties of Si3N4-30vol.%TiCnlmo composites versus hot pressing temperaturte
2.00K
i
CPS
i
i
10
20
30
40
50
60
70
29 FIGURE 2 XRD pattern of Si3N4-30vol.% TiCnano composite hot pressed at 1750°C: A, TiC; O, p-Si3N4
The mechanical properties of the specimen such as flexural strength, hardness and fracture toughness are closely correlated with the variations in density and microstructure.
Fabrication and Microstructure of Si3N4-TiCnano Composites
775
As can be seen clearly from the experiments, the highest values of flexural strength, fracture toughness and Vicker's hardness of the specimen are all achieved at the sintering temperature of 1750°C (FIGURES lb, c and d). The sharp increase in density in the temperature range of 1650 °C-1750 °C is deemed to be the essential cause for this phenomenon. When the hot pressing temperature was increased up to 1850°C, Si3N4 grains were thermally decomposed and the reactions between S13N4 and oxide additives were accelerated, leading to the decrease in S13N4 content and the increase in glassy phase content, as well as the formation of pores and probably the abnormal growth of S13N4 grains. Microstructural Characterizations FIGURE 3 shows a fracture surface of the Si3N4/TiCtlano specimen hot pressed at 1750 °C. The specimen exhibited a well densified structure and small grain size, and the fracture surface was characterized mainly by a mixed mode of intergranular and transgranular fracture. The TEM observation of Si3N4/TiCnano specimen sintered at 1750 °C revealed clearly that larger TiC nanoparticles were located at grain boundaries, while the smaller ones were trapped inside the P-Si3N4 grains (FIGURE 4). The sub grain boundaries formed around the TiC nanoparticles were observed inside the P-Si3N4 grains, which is assumed to cause some grain refinement. All these microstructural characteristics contributed to the optimum properties of the composite. Twin crystals of were also observed, as shown in FIGURE 5.
FIGURE 3 SEM morphology of Fracture surface
FIGURE 4 Intragranular and intergranular TiC
The 'nanosize' strengthening and toughening mechanisms remains controversial especially for S13N4 ceramic matrix composites (am), furthermore, the difference between thermal expansion coefficient of Si3N4 and the secondary phase is in the opposite sense as in the AI2O3 ceramic matrix composites (afc
776
Fabrication and Microstructure of Si3N4-TiCnano Composites
radial and tangential directions, respectively, of the S13N4 matrix around the nanoparticle, and the stresses inside the nanoparticle are hydrostatic tensile. FIGURE 6 shows a intragranular microcrack inside a Si3N4 grain, propagating along the tangential direction of TiC nanoparticle, which implied that the toughening mechanisms in the composite could be microcracking toughening, crack deflection, and crack impedance by the periodic compressive stress in the Si3N4 matrix.
FIGURE 5 Twin crystal of Si3N4
FIGURE 6 Intragranular microcrcking
CONCLUSIONS The densification behavior, microstructural evolution and mechanical properties of Si3N4/TiCnano composite containing AI2O3 and Y2O3 as sintering aids were investigated. The experimental results showed that optimum mechanical properties could be achieved for Si3N4-30vol. % TiCnano composite sintered at 1750 °C for 60min, under 30MPa pressure in N2. The microstructure of the composite was characterized by fine, elongated P-S13N4 grains, with larger TiC nanoparticles located at grain boundaries, while the smaller ones trapped inside the P-Si3N4 grains. The toughening mechanisms in the composite was believed to be microcracking toughening, crack deflection, and crack impedance by the periodic compressive stress in the S13N4 matrix.
ACKNOWLEDGEMENTS This work was supported by the National Natural Science Foundation of China (50105011) and the Foundation for the Author of National Excellent Doctoral Dissertation of P. R. China (200231) as well as the SRF for ROCS (2002 [247]), SEM.
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REFERENCES 1.
Chu, C. -Y., J. P. Singh, and J. L. Routbort. 1993. "High-Temperature Failure Mechanisms of Hot-Pressed Si3N4 and S^N^Si^-Whisker-Reinforced Composites," J. Am. Ceram. Soc, 76(5): 1349-1353. 2. Baris, D., S. P. Tremblay, and M. Fiset. 1993. "Silicon Carbide Platelet-Reinforced Silicon Nitride Composites," J. Mater. Set, 28: 5486-5494. 3. Huang, J. L., M. T. Lee, H. H. Lu, D. F. Lii. 1996. "Microstructure, Fracture Behavior and Mechanical Properties of TiN/Si3N4 Composites," Mater. Chem. &Phys., 45: 203-210. 4. Stemitzke, M. 1997. "Review: Structural Ceramic Nanocomposites," J. Eurp. Ceram. Soc, 17(9): 1061-1082. 5. Park, H., H. Kim, K. Niihara. 1998. "Microstructure and High-Temperature Strength of Si3N4-SiC Nanocomposite," J. Eurp. Ceram. Soc, 18(7): 907-914. 6. Mikio, F. 1985. "Physical Properties and Cutting Performance of Silicon Nitride Ceramics," Wear, 102: 195-210. 7. Seising, J. 1961. "Internal stresses in ceramics," J. Am. Ceram. Soc, 44: 419.
Synthesis, Thermal and Wear Properties of Waterborne Polyurethane / Polysilicic Acid Nanocomposite Hsun-Yu Su1, Chen-Chi M. Ma1*, Hsu-Chiang Kuan1 and C. P. Wang2 department of Chemical Engineering, 2 Department of materials science and engineering National Tsing Hua University HsinChu, Taiwan, 300, R.O.C
ABSTRACT A unique nanocomposite consists of polysilicic acid nanoparticles (PSA) / waterborne polyurethane (WPU) has been prepared. The PSA nanoparticles size distribution was measured by dynamic light scattering method. The nanocomposites were investigated by Fourier-Transform Infrared spectrophotometer (FT-IR). Si-mapping technique was used to observe the dispersion of PSA in the polymer matrix. The morphology studies showed that PSA nanoparticles was well dispersed in waterborne polyurethane matrix within a nano-scale(50 nm). When PSA content was over 20 wt%, phase separation may occur. The wear index was the lowest when the PSA content was 15 wt%. Thermogravimetric analysis (TGA) results showed that adding PSA nanoparticles would increase the thermal degradation temperature by about 25 °C when the content of polysilicic acid nanoparticles was 20 wt.%. INTRODUCTION In the past decade, the synthesis and characterization of inorganic-organic hybrid materials by the sol-gel process have received great attention[l-3]. For example, flexible polymers with high modulus, along with the high themal stability and good optical properties of inorganic glasses can be prepared. The properties of the inorganic-organic hybrid materials are dependent on the nature and relative content of the constitutive inorganic and organic components[4-7]. The basic sol-gel process involves the hydrolysis and polycondensation reactions of metal or silicon alkoxide, e.g. Si(OEt)4 or Si(OMe)4, which are governed by the value of pH, solvent, catalyst and temperature[8]. Polyurethane (PU) is globally used on a large scale for adhesive, coating, and cast applications due to its high toughness, high impact strength, and so on. However, the environment protection trend was led by government regulations such as the Clean Air Act in the United State. Therefore, the development for waterborne polyurethane is very critical. The drawbacks of traditional sol-gel process are that tedious preparation procedure and difficulty to control the reaction. The phase separation between inorganic and organic components will take place and will deteriorate the properties of the materials. This article presents that the polysilicic acid nanoparticles which contain many silanol groups on the surface of the particle which could be directly incorporated with the SiOEt groups in the waterborne polyurethane (WPU). Therefore the polymer with silane * Corresponding author, National Tsing Hua University, Department Of Chemical Engineering, Hsinchu, TAIWAN 30034, R.O.C. ; TEL: 886-3-5713058, FAX: 886-3-5715408 ; Email:[email protected]
Waterborne Polyurethane/Polysilicic Acid Nanocomposite
779
group in the chains is necessary. When the solvent and water were removed, the nanocomposites were obtained. The thermal and wear properties of hybrid materials with various ratios of WPU/PSA were studied. EXPERIMENTAL Preparation of Polysilicic Acid Nanoparticles 30g sodium metasilicate(Na2SiO3* 9H2O) dissolved in 100 ml water and then added the solution into 2.5N 100ml hydrochloric acid solution with stirring at 0°Cin 10 min. Then 100ml THF and 60g NaCl were added into the solution subsequently. After stirring vigorously for 15 min, the reaction mixture was allowed to stand for 10 min. The organic layer (THF layer) was separated and dried with 30g of anhydrous sodium sulfate. The size of the PSA particles in THF solution was investigated by dynamic light scattering (DLS) measurement. Preparation of WPU / PSA Hybrid Materials The prepolymer was prepared by reacting 0.025mol PCL and 0. lmol IPDI with acetone at 70°C for 12 hr. Then 0.0125mol DS-200 (contain sulfonic acid group)was added and stirred at 70°C for 5 hr. 0.0375mol NPG was added into the polymer solution at 70°C for 3 hr. The solution of 0.025mol coupling agent in 50ml DI water was dropped into the polymer solution by micro-tube pump. Then the preparation of WPU was completed. PSA-THF solution was added into the WPU solution according to the different content including 0,5,10,15,20 wt%. The mixture was stirred at room temperature for lhr. Films of hybrid materials with uniform thickness were then obtained by removing THF and excess H2O in vacuum at 100°C after the mixing. Fourier Transform Infrared Spectroscopy FT-IR spectra of the hybrid creamers were recorded between 4000 and 400 cm"1 on a Nicolet Avatar 320 FT-IR spectrometer. A minimum of 32 scans was signal averaged with a resolution of 2 cm"1 at the 4000-400 cm4 range. Dynamic Light Scattering (DLS) Measurement The DLS measurement for particle size distribution of PSA was performed with a Malvern series 4700 apparatus (Malvern Instrument, Worcestershire UK). A 2W argon-ion laser operating at a power of 500mW with a wavelength of 514.5nm was used as the light source, which was focused on the sample cell within the temperature 25.0 ±0.1°C, and with the scattering angle at 90°. Morphological Properties The morphology of the fracture surface of the nanocomposite was examined by a scanning electron microscope (HITACHI-S4700 , S570,Tokyo, Japan). Si Mapping Technology The distribution of Si atoms in the nanocomposites was obtained by SEM EDX mapping (HITACHI-S4700, S570, Tokyo, Japan). The white points in the photographs denote Si atoms.
780
Waterborne Polyurethane/Polysilicic Acid Nanocomposite
Wear Index Measurement The nanocomposite membranes tailored to circle with 10 cm in diameter were put on the PT-3050 (Perfect Instrument Co. Ltd., Taichung, Taiwan) grindstone machine. The samples were taken to measure the weight loss after 500 and 1000 rounds. The wear index can be obtained by the following equation: 1
c Where I is wear index, Wi is original weight, W2 is the weight after grinding, C is wear cycles Thermogravimetric Analysis The nanocomposite was themally degraded by thermogravimetric analyzer (Du-Pont-951) from room temperature to 800°C with a heating rate of 20°C/min in N2 atmosphere. The measurements were taken using 7-10 mg samples. Weight-loss/temperature curves were recorded. RESULTS AND DISCUSSION Particle Size of PSA The particle size of PSA prepared by hydrolysis and condensation of sodium metasilicate in 2.5N HC1 solution was measured by the DLS measurement. Figurel indicated that the particle size distribution of PSA range from 3-25nm, and the average size is 9nm in THF solution at steady state. PSA particle can well dispersed in THF solution in a nano scale, so it is more easily to disperse it in waterborne polyurethane prepolymer to form the nanocomposite with the conventional stirring machine. Characterization of PSA and WPU by FT-IR Spectra Figure 2 shows the -OH group characteristic absorption peak was broad at 3200cm"1 It indicated that hydroxyl group was attached on the surface of PSA nanoparticle. Figure 3 displays the WPU has reacted with coupling agent from the appearance of urea of C=O stretching at 1650cm"1. Additionally, Figure 3 shows an asymmetric stretching of S=O at 1150cm-1. The S=O absorption peak revealed that sulfonic acid emulsifier agent was grafted to the polymer chain.
D h(n m )
FIGURE 1. The particle size distribution of PSA in THF solution at steady state
Waterborne Polyurethane/Polysilicic Acid Nanocomposite
781
Stretching of o
W.1mu.b.r[or.'|
FIGURE 2. FT-IR spectra of PSA nanoparticle
Wavenumber (cm"')
FIGURE 3. FT-IR spectra of WPU
3. Morphological properties SEM observed the morphology of the fractured surfaces, and mapping technique was used to elucidate the distribution of PSA nanoparticles in the hybrid matrix. Figure 4 shows particles with 15wt.% content in the polymer matrix was dispersed well, and the particle size was about 50nm. Figure 6 indicates the aggregation of PSA nanoparticles occurred when the content was over 20wt.%. The white dots represented the PSA nanoparticles as shown in Figure 5 and Figure 7.
FIGURE 4. SEM of WPU/15% PSA nanoparticles
FIGURE 6. SEM of WPU/20% PSA nanoparticles
FIGURE 5. Si mapping of WPU/15%PSA nanoparticles
FIGURE 7. Si mapping of WPU/20%PSA nanoparticles
Wear Index Figure 8 and Figure 9 show the wear index decreased with the increasing of the particles contents below 15wt.% under 500 and 1000 wear cycles. The wear index was proportional to the reciprocal of wear-resistance. From SEM result it reveals the particles were well dispersed in the polymer matrix. It indicated the nanocomposites exhibit good miscibility between organic and inorganic phases. There was strong interaction existed
782
Waterborne Polyurethane/Polysilicic Acid Nanocomposite
between the two phases. The wear-resistance of nanocomposites was the best with 15wt.% PSA nanoparticle content.
5
10
15
20
PSA contents (%) FIGURE 8 Wear index of WPU/PSA nanocomposites under 500 wear cycles
5
10
15
20
PSA contents (%) FIGURE 9 Wear index of WPU/PSA nanocomposites under 1000 wear cycles
Thermogravimetric analysis (TGA) The inorganic PSA nanoparticles have higher thermal stability. Figure 9 shows that more PSA nanoparticles added in the polymer matrix would increase the thermal degradation temperature of the hybrid materials. It was found that the char yield of nanocomposites was increased with PSA nanoparticles content. PSA nanoparticles possesses better thermal stability than waterborne polyurethane. If the PSA nanoparticles were well dispersed in polyurethane matrix, it can enhance the thermal stability of nanoparticles, the organic-inorganic hybrid will exhibit higher thermal degradation temperature.
Waterborne Polyurethane/Polysilicic Acid Nanocomposite
783
100- A-pure -B-5 wt.% C-10 wt.% -D-15wt.% E-20 wt.%
80-
60-
CD
3 20-
200
400
600
800
temperature (°C)
FIGURE 10 TGA results of WPU/PSA hybrid with different contents
CONCLUSIONS In this study, novel WPU/PSA nanocomposites have been prepared successfully. Through this modified sol-gel process, the drawbacks of the traditional sol-gel process, and tedious manufacturing procedure were precluded. From SEM result it revealed when the PSA nanoparticles content is below 20wt.%, which will dispersed well in the polymer matrix. The wear indices of WPU with different PSA contents show the same tendency under 500 and 1000 wear cycles. The WPU with 15wt% PSA content possesses the best wear-resistance property under 500 and 1000 wear cycles. The thermal degradation temperature was increased by 25°C when the content of PSA nanoparticles was 20 wt.%. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8.
Wikes GL,Huang HH, Glaser RH. In: Silicon-based polymer science, Advances in chemistry series 224. Washington, DC: American Chemical Society; 1990. p. 207-26 Philip G, Schmidt H. J Non-Cryst. Solids 1984;63:283. Mark JE, Jiang C, Tang MY. Macromolecules 1984;17:2616. J. D. Mackenzie, YJ. Chung, J. Non-Cryst. Solids 147 (1992) 271. Y. G. Hsu, F.J. Lin, J. Appl. Polym. Sci. 75 (2000) 275. A. B. Nrennan, G. L. Wikes, Polymer 332 (1991) 733. D. Tan, P. Dubois, R. Jerome, J. Polym. Sci. Polym. Chem. Ed. 35 (1997) 2295. Brinker CJ, Scherer GW. Sol-gel science, the physics and chemistry of sol-gel processing. San Diego: Academic Press; 1990.
Preparation and Properties of Epoxy-Bridged PolyorganosiloxanesNanoComposite Tzong-Ming Lee, Chen-Chi M. Ma*, Chia-Wen Hsu Department of Chemical Engineering, National Tsing-Hua University, Taiwan, R.O.C Chin-Lung Chiang Department of Industrial Safety and Health Hung-Kuang University, Taiwan, R.O.C
ABSTRACT Novel epoxy-bridged polyorganosiloxanes nano-composites are preparaed by reacting various kinds of aminoalkoxysilanes with DGEBA typel epoxy resin. The reactivities of Mono-alkoxyaminosilane (APTES)' di-alkoxyaminosilane (APMDS) > and Tri-alkoxyaminosilane (APDES) with epoxy resin are compared in this study by FTIR spectrum. It is found that the absorption peak of epoxide group at 913cm"1 disappears after reaction. The epoxy-bridged polyorganosiloxanes precursors synthesized in this study are cured at 150°C. Various kinds of curing catalysts such as dibutyltindilaurate (DBTDL), tetrabutylamonium (NH4OH) hydroxide, are mixed with epoxy-bridged polyorganosiloxanes precursors; respectively. Si-29 NMR is used to detect the structural changes of final cured structure. The cured nanocomposites with catalysts exhibit better thermal stability than cured nanocomposite without catalyst. The Tds (temperature of 5% degradation) of TGA analysis on Epoxy-APTES Bridged Polyorganosiloxane (BPOS) without catalyst, with DBTDL and with NH4OH are 270°C, 323°C and 338°C, respectively. The char yields are 18.91%, 50.73%, and 44.87%, respectively.
INTRODUCTION Epoxy Resin is challenged in recent years by the newly emerging request from the fast booming of electronic information products and electronic optical devices. [1] There have been a great number of research works in studying the effect of polyorganosiloxane on the enhancement of thermal, optical, and mechanical properties of epoxy resin [2-11]. The most popular synthetic route to form a polyorganosiloxane-epoxy hybrid system is to prepare a polyhedral oligomeric polysilsesquioxanes (POSS) from the sol-gel process of TEOS followed by the incorporation of epoxide group on the polyhedral terminal site. The hybrid system can be crosslinked with various kinds of curing agent to form a organic-inorganic polyorganosiloxane-epoxy hybrid network [12]. The sol-gel process to synthesize Corresponding author, National Tsing Hua University, Department Of Chemical Engineering, Hsinchu, Taiwan 30034, R.O.C. ; TEL: 886-3-5713058,FAX: 886-3-5715408 ; [email protected]
Epoxy-Bridged Polyorganosiloxanes NanoComposite
785
POSS structure is deeply depending on the condition and catalyst used during synthesis process and the purity of POSS. In order to improve the drawbacks in forming polyorganosiloxane-epoxy hybrid system from POSS structure, novel epoxy-bridged polyorganosiloxanes precusors are synthesized by reacting various kinds of aminoalkoxysilanes with di-functional epoxy resins in this study. Different types of catalysts and terminated alkoxy-silanes have been added to the precursor systems to study their effects on the final network structures and thermal mechanical properties. EXPERIMENTAL Materials The diglycidyl ether of bisphenol A (DGEBA) epoxy used in this study was supplied by Nan Ya Plastic Co.Ltd., Taiwan. The 3-Aminopropyltriethoxysilane (APTES, Z-6011) was purchased from Dow Corning Co., Ltd., Midland, Michigan, U.S.A.. 3-Aminopropylmthyldiethoxysilane (APMDS) was obtained from TCI, Tokyo Chemical Industry Co., Ltd, Tokyo, Japan. 3-Aminopropyldimthylethoxysilane (APDES) is provided by Gelest Inc., East, Morrisville, PA, U.S.A. Dibutyltindilaurate and Tetrabutylamonium hydroxide obtained from TCI, Japan is used as catalysts for the curing of epoxy-bridged polyorganosiloxanes precursors. Synthetic Process Preparation of epoxy-bridged polyorganosiloxanes precursors Excess amounts of APTES, APMDS, or APDES are added; respectively, to a 100 ml of single necked flask with DGEBA epoxy with a molar ratio of 1:2 (nEp0Xy : nanimosiiane). The reaction mixture is then mixed with a magnetic stirrer under room temperature. The reaction time is around 4-5 hours. The reaction scheme of these three types of precursors are shown as scheme 1. Scheme 1
o
o
™3
f'
H^CH—R-CK-\H2
+
2
HjN-fcH,-)-!!!—OEt
or
O E t
Epoxy Resin
or
2
|
'
> EtO
OEt I , > ? i ~(-H 2 c)
H.N-fcHj-^-Si—OEt
°Et 3-Aminopropylmethyldiethoxysilane
3-Aminopropyltriethoxysilane CH3 | U N — { C H A — *>i OEt ( '1 | CH3
2
H N
OH OH OEt 2 I I Hj H / \ I C—CH—R—CH—c N-^CH,-j— Si—
H
OEt
OEt
3-Aminopropydimethylethoxysilane CH3
OH
APTES modified Epoxy resin OH
CH3
W ^ H I ' ' ^ S O - OE, |
3
I
or
f*
, H * ?" ? H * H,
U ' APMDS modified Epoxy resin
J*
Ete-SMH2c)-N-C^CH-R-CH-c-N-{CH2)-Si-OEt
U
APDES modified Epoxy resin
786
Epoxy-Bridged Polyorganosiloxanes NanoComposite
Formation of organic-inorganic polyorganosiloxanes
network
from
reactive
epoxy-bridged
The precusors are cured directly at 150°C or with the addition of curing catalyst such as Dibutyltindilaurate (DBTDL) or Tetrabutylamonium hydroxide; respectively to observe the curing behaviors and final structures of the cured organic-inorganic network. Organic-inorganic networks are epoxy-APTES bridged polyorganosiloxane (Epoxy-APTES BPOS), epoxy-APMDS bridged polyorganosiloxane (Epoxy-APMDS BPOS), and epoxy-APDES bridged polyorganosiloxane (Epoxy-APDES BPOS), respectively. Thermal Analysis Thermgravimetric Analyzer, TGA The hybride materials of about 10 mg are placed in the furnace chamber of TGA(TA 2000, TA Instruments, Inc, U.S.A.) and heated to 800°C under nitrogen with a heating rate of 20°C/min to compare the thermal degradation temperatures and char yields of Epoxy-Bridged Polyorganosiloxanes nanocomposite Thermomechanical analyzer, TMA Cured organic-inorganic hybrid films with 2.0cm x 0.3cm are hanged under 0.05N of tension force in heating chambers of TMA (TA 2940, TA Instruments, Inc. U.S.A.) and heated to 200°C under nitrogen with a heating rate of 10°C/min to observe Tgs and coefficient of thermal expansions (CTE) of Epoxy-Bridged Polyorganosiloxanes nanocomposite. RESULTS AND DISCUSSION Analysis of reactive precursor with FTIR The reaction between excess amount of aminosilanes and epoxy group will form an alkoxy silane terminated reactive precursors as shown in scheme 2. As can be seen in Figure 1, which the epoxy groups of 913cm"1 in FTIR spectrum decrease with the increasing of reaction time and finally disappear after 5 hours of reaction time. The absorption peak of amino groups at 3500cm"1 in FTIR is shifted to 3200cm"1 which shows that amino group has reacted with epoxy group to form hydroxy group. Scheme 2 H 2 C—CH
R
CH—CH2
+
2 H2N
R1
Si—("OR" ) (CH 3 )
n-1-3
II "• OH O - ("RO ) Si ' 3-n n
R'
N
C—CH
OH R—CH— c -
N
R1
Si
ft>R")(CH3) n 3-n
n-1-3
Epoxy-Bridged Polyorganosiloxanes NanoComposite
787
j or -OH
epoxy group
32OOcm"1 -35OOcm'1
3000
913 cm" 1 0 hr
2000
wavenumber (cm'1)
FIGURE 1 FTIR Spectra of Synthesis of Epoxy and APTES at Different Times
Determination of organic-inorganic hybrid network with 29Si Solid State NMR In Epoxy-APTES BPOS cured network, it is found that the spectrum of 29Si Solid State NMR of cured network with catalyst shows obvious difference with that of cured network without catalyst as shown in Figure 2. T1 shift disappears after the addition of DBTDL and NH 4 0H.
-59.916ppm -46.104ppm (T1)
2
(T ) .
4
-66.143ppm
3
(T )
No cat
DBTDL NH4OH 300
200
100
0
-100
-200
-300
-400
ppm
FIGURE 2 29Si NMR Spectra of Epoxy-APTES BPOS with no catalyst, DBTDL and NH 4 0H
Thermal Analysis of organic-inorganic hybrid network TGA analysis of cured network In Epoxy-APTES BPOS cured network, it is found that the addition of catalyst, DBTDL and NH 4 0H, will promote the thermal stability of cured network. The Td5s of Epoxy-APTES BPOS with no catalyst, with DBTDL and with NH4OH are 270°C, 323 °C and 338°C, respectively. The Tds of cured network with catalyst shows 50°C higher than that of cured network without catalyst as shown in Figure 3. The char
788
Epoxy-Bridged Polyorganosiloxanes NanoComposite
yields are 18.91%, 50.73%, and 44.87%, respectively. The char yields of cured network with catalysts are higher than that of cured network without catalyst. The addition of catalyst will enhance the thermal stability of cured hybrid structure.
100-
DBTDL NH4OH
No cat.
200
100
200
300
400
500
600
700
800
Temperature (°C)
FIGURE 3 TGA Curves of Epoxy-APTES Bridged Polyorganosiloxane with no catalyst, DBTDL, and NH4OH
TMA analysis of cured network As shown in Figure 4, the Tgs of Epoxy-APTES BPOS, Epoxy-APMDS BPOS, and Epoxy-APEDS BPOS with no catalyst are 88°C, 1H°C, and 86°C respectively. The cured network from difunctional reactive alkoxysilane possesses a higher Tg than that from trifunctional reactive alkoxysilane. The cured network from monofunctional reactive alkoxysilane shows the lowest Tg among the three different cured network systems. The cured network from trifunctional reactive alkoxysilane might have less crosslinking extent than that from difunctional reactive alkoxysilane due the stereo hindrance during curing process. 40003500?
3000-
-
2500-
1 Epoxy-APDES BPOS
01 J 2000" 1500-
y
0 1000|
500-
5
0-
i
/
Epoxy-APMDS BPOS Epoxy+APTES POS 0
50
100
150
200
Temperature (°C)
FIGURE 4 TMA Curves of Epoxy-APTES, Epoxy-APMDS and Epoxy-APDES Bridged Polyorganosiloxane with no catalyst
Epoxy-Bridged Polyorganosiloxanes NanoComposite
789
CONCLUSIONS A novel convenient synthetic method to form polyorganosiloxane-epoxy nano hybrid composite structure is demonstrated in this study. New epoxy-bridged polyorganosiloxanes precusors are synthesized by reacting various kinds of aminoalkoxysilanes with DGEBA typel epoxy resin in this study. The addition of catalysts to the reactive epoxy-bridged polyorganosiloxanes shows significant effect in increasing the thermal stability of cured organic-inorganic network therefrom. It is found that cured network from difunctional reactive epoxy-bridged polyorganosiloxanes exhibits the highest Tg (111°C verse 88°C and 86°C) among the three kinds of cured networks of epoxy-bridged polyorganosiloxanes. REFERENCES 1.
2. 3. 4. 5. 6. 7. 8. 9.
10.
11. 12.
G L. Wilkes, B. Drier, H. H. Huang, "Ceramers - Hybrid Materials Incorporating Polymeric Oligomeric Species into Inorganic Glasses Utilizing a Sol-Gel Approach", Abstracts of Papers of the American Chemical Society, 1985, 190, 109 R. H. Baney, M. Itoh, A.Sakakibara, T. Suzuki, "Silsesquioxanes ", Chem. Rev 1995; 95, 1409 A. Provatas and J. G Matisons, "Porosity in hexylene-bridged polysilsesquioxanes. Effects of monomer concentration", TRIP 1997; 5, 10 M. Tanimura, Handbook of silicon materials. Tokyo: Dow Corning Toray Silicon; 1993, 299 L. H. Brown, Treatise: Silicones in protective coatings, vol. 1, Part 3. New York: Marcel Dekker; 1972, 539 J. D. Lichtenhan, "Aryl-bridged polysilsesquioxanes. A new class of microporous materials", Comments Inorg Chem 1995; 17, 115 F. K. Chi "Carbon Containing Monolithic Glasses via the Sol-Gel Process", Ceram. Engng. Sci Procl983;4,704 A. S. Gozdz, "Dialkylene Carbonate-Bridged Polysilsesquioxanes. Hybrid Organic-Inorganic Sol-Gels with a Thermally Labile Bridging Group", Polym. Adv. Technol., 1994; 5, 70 Chin-Lung Chiang, Chen-Chi M. Ma, "Synthesis, characterization and thermal properties of novel epoxy containing silicon and phosphorus nanocomposites by sol-gel method", European Polymer Journal, 2002, 38, 2219-2224 Chin-Lung Chiang, Feng-Yih Wanga, Chen-Chi M. Ma, Hey-Rey Changb, "Flame retardance and thermal degradation of new epoxy containing silicon and phosphorous hybrid creamers prepared by the sol-gel method", Polymer Degradation and Stability, 2002, 77, 273-278 S. Ananda Kumar, T. S. N. Sankara Narayanan, "Thermal properties of siliconized epoxy interpenetrating coatings", Progress in Organic Coatings, 2002, 45, 323-330 Jiwon Choi, Jason Harcup, Albert F. Yee, Quan Zhu, and Richard M. Laine, "Organic/Inorganic Hybrid Composites from Cubic Silsesquioxanes", 11422 J. Am. Chem. Soc, 2001, 123, 46
Moisture Absorption and Hygrothermal Aging of Organomontmorillonite Reinforced Polyamide 6/Polypropylene Nanocomposites W.S.Chow1, Z.A. Mohd Ishak1* School of Materials and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, Seri Ampangan 14300 Nibong Tebal, Penang, Malaysia J. Karger-Kocsis2 Institute for Composite Materials Ltd, University of Kaiserslautern, P.O. Box 3049, D-67663 Kaiserslautern, Germany
2
ABSTRACT A study of hygrothermal aging in terms of moisture absorption by uncompatiblized organo-montmorillonite reinforced polyamide 6/polypropylene (PA6/PP=70/30) and maleated polypropylene (MAHgPP) compatibilized PA6/PP/organoclay nanocomposites was undertaken. Hygrothermal aging was investigated by immersion of specimens in distilled water at 60 °C. Tensile test was performed to study the retention-ability of the hygrothermal aged specimens. The morphology of PA6/PP nanocomposites was assessed by a scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The kinetic of water absorption of the PA6/PP nanocomposites conforms to Fickian's Law behaviours, which the initial moisture absorption follow a linear relationship between Mt and f^2, following by saturation by immersion time. It was found that the equilibrium moisture content (Mm) and the diffusion coefficient (D) are dependent on the organo-montmorillonite loading, and MAHgPP concentration. Both the tensile modulus and strength of the PA6/PP nanocomposites deteriorated after exposed to hygrothermal aging. MAHgPP act as a good compatibilizer for PA6/PP/organomontmorillonite nanocomposites, traced to its higher retention-ability in modulus and strength (at the wet-state and upon re-drying of the specimens), lower Mn and D and reduced water permeability of the nanocomposites.
INTRODUCTION Hygrothermal aging refers to the process in which the deterioration of the mechanical performance and integrity of composite materials results from the combined action of moisture and temperature. Several hygrothermal aging studies have been carried out on polymer composites. Most of these studies have mainly been concerned either with thermoplastics matrix-based such as on nylon 6.6 [1], poly(butylene terephthalate) [2-3] or thermoset matrix-based composites such as " Corresponding author, School of Materials and Mineral Resources Engineering , Engineering Campus, Universiti Sains Malaysia, Seri Ampangan 14300 Nibong Tebal, Penang, Malaysia. Fax: +604 5941011 E-mail: [email protected]
Organo-montmorillonite Reinforced Polyamide 6/Polypropylene
791
epoxy [4], bismaleimide [5], vinylester [6], and polyimide [7]. However, there are still very limited publications on the hygrothermal aging of nanocomposites. In the present study, an attempt has been made to enhance the water resistance and mechanical performance of PA6/PP by using organo-motmorillonite (act as reinforcing agent and impermeable silicate layers) and MAHgPP (act as compatiblizer to improve the interfacial bonding between PA6, PP and organo-montmorillonite). The main aim is to investigate the roles of intercalant in organo-montmorillonite and MAHgPP with regard to water uptake and subsequently to illustrate how water absorption influences the tensile behaviour of PA6/PP nanocomposites. EXPERIMENTAL Materials, Specimen Preparation and Characterization PA6/PP/organo-montmorillonite blends were extrusion compounded and injection moulded as described in our earlier papers [8-9]. Tensile tests have been made on Instron-5582 machine at 23 °C, according to ASTM D638, at a crosshead speed of 50 mm/min. The fracture surface of selected PA6/PP based nanocomposites was inspected in a scanning electron microscope (SEM; Leica Cambrige Ltd. model S 360). Transimission electron microscopy (TEM) measurements were carried out with LEO 912 Omega transmission electron microscope. The designation of the materials tested is given in Table 1. TABLE I Designation of materials Designation PA6/PP PA6/PP/2TC PA6/PP/4TC PA6/PP/6TC PA6/PP/8TC PA6/PP/10TC PA6/PP/5M/4TC PA6/PP/10M/4TC
Composition PA6/PP PA6/PP/organc-montmorillonite PA6/PP/organo-montmorillonite PA6/PP/organo-montmorillonite PA6/PP/organc-montmorillonite PA6/PP/organo-montmorillonite PA6/PP/MAHgPP/organo-montmorillonite PA6/PP/MAHgPP/organo-montmorillonite
Parts 70/30 70/30/2 70/30/4 70/30/6 70/30/8 70/30/10 70/30/5/4 70/30/10/4
Kinetics of Moisture Absorption Specimens were dried at 80 °C in a vacuum oven until a constant weight was attained prior to immersion in hot water in a thermostated stainless steel water bath at 60 °C. The percentage gain at any time /, Mt as a result of moisture absorption, was determined by: Mt(%) = (Ww - Wd) I Wd x 100
where Wd and Ww denote, respectively, weight of dry material (the initial weight of materials prior to exposure to the hygrothermal aging) and weight of materials after exposure to hygrothermal aging. The percentage equilibrium or maximum moisture absorption, Mm, was calculated as an average value of several consecutive measurements that shows no appreciable additional absorption. The weight gain resulting from moisture absorption can be expressed in terms of two parameters, the diffusion coefficient or diffusivity, D, and the maximum moisture content, Mm, as:
Mm
Organo-montmorillonite Reinforced Polyamide 6/Polypropylene
792
where h is the thickness of the sample.
RESULTS AND DISCUSSION Figure 1 shows the percentage moisture absorption M, of PA6/PP/organomontmorillonite as a function of t1/2 at an immersion temperature of 60 °C. The initial linear relationship between Mt and t112 is observed in each case, followed by saturation. This indicates that Fickian behaviour was observed. The Mt and D values are summarised in Table 2. 9.00 XT
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D A
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1000
1500 1
2000
2500
3000
3500
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t V ) FIGURE 1 Effect of organo-montmorillonite loading and compatibilizer (MAHgPP) on the moisture uptake of PA6/PP blends during hygrothermal aging at 60 °C (HTA60)
It is interesting to note that both Mt and D values of organo-montmorillonite filled PA6/PP nanocomposite, are higher than that of neat PA6/PP blends. This is contrary to the data reported for either short carbon reinforced polyamide 6 [1] or short glass fibres reinforced poly(butylene terephthalate) [3]. The higher Mt and D values may be attributed to hydrophilic nature of octadeylamine groups which acts as intercalant in the organo-montmorillonite. It is known that the organomontmorillonite used in this study contained about 30 wt% octadecylamine intercalant [8-9]. Thus when the silicate layers are exfoliated/intercalated, some of the intercalant group in the organo-montmorillonite will be available for interaction with the water molecules. There is a strong possibility for the intercalant to interact with water molecules forming hydrogen bonding. However, increasing the organo-montmorillonite decreased both Mt and D values. This may be attributed to the possibility of agglomeration of clay at a higher loading of organo-montmorillonite, which could hinder the moisture penetration into the nanocomposites. This is supported by the evidence obtained from TEM analysis shown in Figure 2. There is also a possibility that the poor interfacial bonding between PA6/PP and organo-montmorillonite may also influence the nature of the moisture uptake. In the fibre-reinforced composites, for instance, the interfacial
Organo-montmorillonite Reinforced Polyamide 6/Polypropylene
793
damage was observed to be one of the main factors responsible for the enhancement of moisture penetration into the composites [3].
agglomeration
FIGURE 2: TEM picture\aken from the PA6/PP/organoclay (70/30/4 parts) nanocomposites
From Table 2 it can be seen that both Mt and D values are reduced remarkably in the presence of MAHgPP. Both values are even lower than that of neat PA6/PP blends. This provides a clear indication that the resistance to moisture uptake have been enhanced via compatibilization. The amide-amine reaction that occurred between the MAH group of the compatibilizer and octadecylamine group of the clay is believed to have resulted in a significant improvement of the interfacial adhesion between PA6, PP and organo-motmorillonite, and subsequently reduced the diffusion rate. The possible chemical interaction between PA6, PP, organophilic modified montmorillonite and MAHgPP was earlier proposed by Chow et al. [9]. TABLE II The effect of clay and MAHgPP on diffusivity (D) and equilibrium moisture content (Mm) of PA6/PP/organo-montmorillonite nanocomposites
PA6/PP PA6/PP/2TC PA6/PP/4TC PA6/PP/6TC PA6/PP/8TC PA6/PP/10TC PA6/PP/5M/4TC PA6/PP/10M/4TC
HTA M m (%) 6.82 8.53 8.25 8.01 7.57 7.07 5.60 5.34
60 °C D(x10 1 0 m 2 /s) 1.70 3.39 2.97 2.75 2.16 1.94 1.60 1.09
Table 3 shows the tensile properties of PA6/PP blend and composites in as received (AR), hygrothermal aging (HA) and re-dried (RD) states, respectively. The effect of organo-montmorillonite loading on the tensile properties of PA6/PP has been discussed earlier [8]. From Table 3 it can be seen that both tensile strength and Emodulus of organo-montmorillonite reinforced PA6/PP decreased after being subjected to hygrothermal aging at 60 °C. The low percentage retention-ability in tensile strength (about 55%) indicates that hygrothermal aging has caused a dramatic reduction in the strength of the nanocomposites. This may probably arise as a result of the combined effect of plasticization of the PA6/PP matrix (as evidenced by the increase in the elongation at break of the composites in the wet states), as well as the degradation of the polymer-organo-montmorillonite interface. Upon redrying, the
794
Organo-montmorillonite Reinforced Polyamide 6/Polypropylene
strength of the nanocomposites is not fully recovered, as in the case of neat PA6/PP. The differences in the percentage recovery between PA6/PP and its nanocomposites lie in the fact that, in the latter, the action of water may have resulted in the partial disruption of the bonds between the organo-montmorillonite and matrix and the formation of additional micro cavities, which would be filled with water. Upon drying, these cavities will act as stress concentrators, which can then initiate matrix cracking, leading to reductions in both stiffness and strength of the composites. Note that the incorporation of MAHgPP compatibilizer into PA6/PP nanocomposites has increased the retention-ability of the composites upon subjected to hygrothermal aging (c.f. Table 3). The percentage retention of tensile strength is much higher i.e. almost 90% as compared to about only 55% for the uncompatibilized nanocomposites. Upon redrying, the percentage recovery of as high as 93% of tensile strength has been recorded for the PA6/PP nanocomposites compatibilized with 10wt% MAHgPP. This may indicate that the interaction of the water molecules with PA6/PP matrix is physically in nature, and water is merely act as a plasticizer. The excellent recoverability of MAHgPP compatibilized PA6/PP/organo-montmorillonite may be attributed to the improvement of interfacial adhesion between PA6 and PP by the addition of MAHgPP. TABLE III Tensile properties of PA6/PP nanocomposites in AR, HA and RD states
Materials PA6/PP
PA6/PP/2TC
Mechanical Properties Control (AR) 1.87 E-modulus (GPa) 32.10 Tensile strength (MPa) 22.82 Elongation at break (%)
E-modulus (GPa) Tensile strength (MPa) Elongation at break (%) PA6/PP/4TC E-modulus (GPa) Tensile strength (MPa) Elongation at break (%) PA6/PP/6TC E-modulus (GPa) Tensile strength (MPa) Elongation at break (%) PA6/PP/8TC E-modulus (GPa) Tensile strength (MPa) Elongation at break (%) PA6/PP/10TC E-modulus (GPa) Tensile strength (MPa) Elongation at break (%) PA6/PP/5M/4TC E-modulus (GPa) Tensile strength (MPa) Elongation at break (%) PA6/PP/10M/4TC E-modulus (GPa) Tensile strength (MPa) Elongation at break (%)
1.90 36.43 14.90 2.11 37.98 4.16 2.20 36.44 2.56 2.32 31.04 1.87 2.38 29.19 1.52 2.38 49.64 4.79 2.30 48.45 5.26
Hygrothermal aging 60 °C Wet (HA) . Redried(RD) 1.51 (80.7) 26.25(81.8) 18.40(80.6)
1.68(89.8) 27.10(84.4) 19.63(86.0)
1.49 (78.4) 21.90(60.1) 15.80(106.0) 1.61 (76.3) 20.70 (54.5) 5.16(124.0) 1.67(75.9) 19.85(54.5) 3.50(136.7) 1.75(75.4) 17.45(56.2) 2.70(144.4) 1.86(78.2) 16.23(55.6) 2.40(157.9)
1.63(85.8) 26.50 (72.7) 14.89(99.9) 1.87(88.6) 24.80 (62.3) 4.15(99.8) 1.93 (87.7) 23.20 (63.6) 2.54 (99.2) 2.02(87.1) 19.40(62.5) 1.85(98.9) 2.11 (88.7) 18.70(64.1) 1.50(98.7) 2.20 (92.4) 44.23(89.1) 4.78 (99.8) 2.08 (90.4) 45.10(93.1) 5.25 (99.8)
2.10(88.2) 42.65 (85.9) 7.80(162.8) 2.00 (86.9) 43.01 (88.8) 9.40(187.7)
Figure 3 shows the SEM micrograph of uncompatibilized and MAHgPP compatibilized PA6/PP/organo-montmorillonite nanocomposites after subjected to
Organo-montmorillonite Reinforced Polyamide 6/Polypropylene
795
hygrothermal aging at 60 °C, respectively. Irregular and large PP particles and poor interaction between PA6 and PP (shown by the micro-void or gap) was shown in uncompatibilized PA6/PP nanocomposites. In contrast, fibrillated morphology and smaller PP particle shown in the MAHgPP compatibilized PA6/PP/organomontmorillonite nanocomposites owning to the increased of the interfacial bonding of PA6 and PP in the presence of MAHgPP. The fibrillated morphology manifested by the increased of the elongation at break of the composites (c.f. Table 3).
microvotd
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FIGURE 3 SEM micrograph taken from the fracture surface of uncompatibilized PA6/PP/organoclay (a) and MAHgPP compatibilized PA6/PP/organoclay (b) nanocomposite in HA states
CONCLUSIONS The kinetic of water absorption of the PA6/PP nanocomposites conforms to Fickian's Law behaviours. Both the tensile modulus and strength of the PA6/PP nanocomposites deteriorated after being exposed to hygrothermal aging. The presence of MAHgPP has not only enhanced the resistance of the nanocomposites against direct water immersion but has also improved the resistance of the composites against hygrothermal attack. REFERENCES l.Mohd Ishak, Z. A. and Berry, J. P. 1994. "Hygrothermal aging studies of short carbon fiber reinforced nylon 6.6," J. Appl Polym. Sci., 51(13):2145-2155. 2. Mohd Ishak, Z. A., Ariffm, A., and Senawi, R. 2001."Effects of hygrothermal aging and a silane coupling agent on the tensile properties of injection molded short glass fiber reinforced poly(butylenes terephthalate) composites," Eur. Polym. J., 37(8):1635-1647. 3.Mohd Ishak, Z. A., Ishiaku, U. S., and Karger-Kocsis, J. 2000. "Hygrothermal aging and fracture behavior of short-glass-fiber-reinforced rubber-toughened poly(butylene terephthalate) composites", Comp. Sci. Tech., 60(6):803-815. 4.Guo, Baochun., Jia, Demin., Fu, Weiwen., and Qiu, Qinghua. 2003 "Hygrothermal stability of dicyanate-novolac epoxy resin blends, "Polym. Degrad. Stab, " 79(3):521-528. 5.Bao, Li-Rong., F. Yee, Albert., and Y. -C. Lee, Charles. 2001. "Moisture absorption and hygrothermal aging in a bismaleimide resin", Polymer, 42(17):7327-7333. 6.Karbhari, V. M., Rivera, J., and Zhang, J. 2002. "Low-temperature hygrothermal degradation of ambient cured E-glass/vinylester composites," J. Appl. Polym. Sci., 86(9):2255-2260. 7. Han, Man-Hee and A Nairn, John. 2003. "Hygrothermal aging of polyimide matrix composite laminates", Comp. Part A: Appl. Sci. Manufacturing, 34(10):979-986. 8. Chow, W.S., Mohd Ishak, Z.A., Ishiaku, U.S., Karger-Kocsis, J., and Apostolov, A.A. 2004 "The Effect of Organoclay on the Mechanical properties and Morphology of Injection-Molded Polyamide 6/Polypropylene Nanocomposites," J. Appl. Polym. Sci., 91(1),175-189. 9. Chow, W.S., Mohd Ishak, Z.A., Karger-Kocsis, J., Apostolov, A.A., and Ishiaku, U.S. 2003. "Compatibilizing effect of maleated polypropylene on the mechanical properties and morphology of injection molded polyamide 6/polypropylene/organoclay nanocomposites," Polymer, 44(24):74277440
Geopolymer Reinforced Polyethylene Nanocomposites X.W.Yuaif, A.J. Easteal and D. Bhattacharyya3' Centre for Advanced Composite Materials department of Mechanical Engineering b Department of Chemistry The University of Auckland, Private Bag 92019, Auckland, New Zealand
ABSTRACT Rotational moulding has significant advantages over other methods such as injection moulding and blow moulding for the production of large hollow plastic parts but at the same time it is limited by its dependence on the use of polyethylene (PE) as the base resin. Polyethylene is suited for rotomoulding because of its thermal stability, low cost and the low melting point. However, its low mechanical strength and stiffness must be improved to meet product requirements. Rotational moulding of fibre and/or inorganic powder reinforced polyethylene has proved to be difficult to achieve due to segregation of plastic powder and the reinforcements. In this paper, it is proposed to develop a novel hybrid organic/inorganic resin, in effect a 'precomposite', which will generate a microcrystalline reinforcing phase during the rotomoulding heating phase to achieve better distribution of reinforcement within the polymer matrix. For this investigation, a formulation of inorganic mixture of "Geopolymer" is developed to form a microcrystalline phase under injection moulding with the same heating conditions as those of rotomoulding. The mixing of "Geopolymer" with polyethylene powder is achieved in such a way that the inorganic component is uniformly dispersed in the resin while rotomoulding takes place. The preliminary results show an improvement in mechanical properties of Geopolymer-PE composites. Scanning Electron Microscopy clearly shows the existence of an acicular crystalline structure in nano-scale dimension on the fracture surface of geopolymerPE composites, which is an interesting finding. This micro-/nano-crystalline phase acts as fibre-like reinforcement that is believed to give the improvement of mechanical properties.
INTRODUCTION Rotational moulding ('rotomoulding') is used to produce seamless, stress-free, hollow plastic parts that can be large and structurally complex [1]. This process involves charging a metal mould with powdered polymer, dominantly polyethylene, then heating the mould while it is slowly rotated about two perpendicular axes so that the polymer melts to form coating on the inside of the mould. Rotation continues as the mould is cooled, until the plastic part is sufficiently rigid to be removed. The Corresponding author, Director of Centre for Advanced Composite Materials (CACM), Head of Department of Mechanical Engineering, School of Engineering, University of Auckland, Private Bag 92019, Auckland, New Zealand; Phone: +64-9-3737599 Ext. 88149; Fax: +64-9-3737479; E-mail: [email protected]
Geopolymer Reinforced Polyethylene Nanocomposites
797
rotational moulding industry has achieved a growth rate of more than 10% per annum over the last decade, and the process technology has developed to the extent that a very large variety of parts/products can be made [2,3]. While rotational moulding has significant advantage over other methods such as injection moulding and blow moulding for production of plastic parts, it has the limitation of dependence (to the extent of about 90% of the market) on use of PE as the base resin. Polyethylene is a low cost resin that is thermally stable and hence is well suited to the fairly long cycle times required for rotomoulding. Furthermore, it has a low melting point compared to those of many resins allowing it to be processed at a relatively low temperature. However, its mechanical properties, in particular strength and stiffness, are inferior to those of most other plastics. Substitution of other base resins with superior mechanical properties instead of PE is not a viable option due to the requirement for high thermal stability of the resin during moulding. Consequently, the method that is currently used for enhancing the stiffness of rotomoulding is to increase the wall thickness of the product. A better solution to the problem of the low strength and stiffness of PE is to enhance the mechanical properties of the base resin by using fibres and/or particulates as reinforcing elements. Rotational moulding of fibre and/or inorganic powder reinforced polyethylene has also been an elusive goal due to the segregation of plastic powder and the reinforcing phase. Research has been carried out to improve the incorporation of the reinforcement and polyethylene matrix in order to improve the mechanical properties of the final products. However, the uniformity of the reinforcement distribution has proved extremely difficult to achieve [2,4]. Crawford has noted that successful fibre reinforcement of rotomoulded polyethylene parts is a challenge of great industrial significance [2]. This paper describes a novel concept of in situ formation of a reinforcing phase which is analogous with the production of a glass ceramic, in which heat treatment of an initially homogeneous inorganic glass containing a nucleating agent such as TiCh produces a material which is typically about 98% microcrystalline, with an amorphous phase providing a very thin layer of adhesive at the grain boundaries. This morphology, coupled with microcrystalline phases with zero (or even negative) coefficients of expansion gives glass ceramics their remarkable strength, resistance to thermal and mechanical shock and other qualities [5]. Inorganic geopolymers have emerged as promising materials in various fields for their better properties with respect to ceramics and cement-based materials [6]. Their physical properties make them viable alternatives for many conventional cements and plastics, and their synthesis at a low temperature is energy-efficient and more environmentally friendly [7]. Geopolymers are similar to zeolites in chemical composition but they reveal an amorphous microstructure [8]. In 1972, Joseph Davidovits developed a kind of mineral polymer material with amorphous to semicrystalline three-dimensional alumino-silicate structure. This inorganic polymer material was first named "Polysialate"; but later Davidovits coined another term "geopolymer" in his US patent [9] to stand for this family of inorganic polymers. Nowadays, the term "geopolymer" (mineral polymers resulting from geochemistry) has already been widely accepted. Geopolymerisation involves a chemical reaction between various alumino-silicate oxides with silicates under highly alkaline conditions, yielding polymeric Si-O-Al-0 bonds [8]. These polymers possess excellent mechanical properties, fire and acid resistance [8,10]. The techniques of making geopolymers have been well reported [9,11,12]. hi this study, we have developed a novel mineral polymer compound of silicoaluminate mixture, mixed together with polyethylene powder, then heated up to
798
Geopolymer Reinforced Polyethylene Nanocomposites
150°C to form a hybrid organic/inorganic resin. Some preliminary results on the mechanical properties are reported and scanning electron microscopy (SEM) is used to analyse the fracture surfaces of the composites. EXPERIMENTAL DETAILS Low density Polyethylene (LDPE) Alkatuff™ 711UV was supplied as a dry white powder by Oenos Pty Ltd. It has a relatively low melting point (130°C) and low melt flow index (3.5 g/10 min at 190°C), and is used for rotational and injection moulding processes. A petroleum wax modifier, Epolene™ C-17, manufactured by Eastman Chemicals (USA) was used as a compatibiliser. Sodium silicate, wollastonite (calcium silicate), metakaolin and solid NaOH particles that were used in this study were supplied by Coatings and Resins International Ltd, New Zealand. Dry powders of geopolymer mixture, e.g. wollastonite, metakaolin and NaOH were mixed manually for about 3 minutes; then polyethylene powder and a small amount of water were mixed with the geopolymer mixture in a mechanical processor for 5 minutes. The mixture of organic and inorganic powders was subjected to different pre-treatments before injection moulding to make the composite test samples. The pre-treatments included using maleated polyethylene (MAPE) as a coupling agent to improve the adhesion between inorganic powders and polymer matrix; preheating the mixture of powders in an oven for various times; and thermal/mechanical mixing in a Brabender melt blender for various times at speed of 60 rpm at 140°C. Samples from the Brabender were granulated before injection moulding. The heating conditions in injection moulding were the same as those used later in rotational mouldings. The tensile strength and modulus of the composite samples were measured according to ASTM standard D638. The tests were performed on a computer controlled Instron 5567 universal testing machine with an extensometer gauge length of 50 mm and a test speed of 50 mm/min. At least five specimens for each sample were tested to confirm the repeatability. Tensile fracture surfaces of the composite samples were vacuum coated by evaporation with platinum (Pt), and then analysed using a scanning electron microscope, Philips XL 30 FEG, operated at 5 KV. RESULTS AND DISCUSSION Fig. 1 shows that the tensile strengths and moduli of geopolymer-polyethylene composites improve by adding 5-20 mass% geopolymer. Tensile moduli show a more significant improvement - the higher the proportion of added geopolymer, the greater is the improvement of tensile modulus. However, the tensile strength decreases when the geopolymer content exceeds 20 mass%. Higher temperature in oven preheating shows a positive effect on tensile properties, Fig. 2. However, MAPE has not functioned as expected to improve the tensile strength and modulus, Fig. 3. Moreover, adding 2-5 mass% MAPE decreases the modulus remarkably, Fig. 3.
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Geopolymer Reinforced Polyethylene Nanocomposites
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Percentage of GE (%) FIGURE 1. Tensile strength and tensile secant modulus at 0.2% strain of different percentage geopolymer (GE) at mass fraction. 18.0 2 1 % increase
H 40% GE
—i
oven 90 °C
no oven dried
FIGURE 2. Tensile strength at different oven drying temperature.
Tensile strength Tensile modulus
0
5
10
Percentage of MAPE (%)
FIGURE 3. Tensile strength and tensile secant modulus at 0.2% strain of different mass% MAPE composites.
Geopolymer Reinforced Polyethylene Nanocomposites
800
Mechanical/thermal mixing of GE-PE composites with a Brabender slightly improves the mechanical properties, but more extended mixing gives no additional improvement, Fig. 4. Although XRD has not yet provided clear identification of the ceramic phases formed in the composites, SEM analysis has clearly shown the existence of an acicular crystalline structure in nano-scale dimension on the fracture surface of geopolymer-PE composites, which is an interesting finding, Fig. 5. This micro-/nanocrystalline phase acts as fibre-like reinforcement that is believed to give the improvement of mechanical properties. However, the crystalline phase is not uniformly distributed throughout the matrix, Fig. 6, causing the tensile strengths of geopolymer composites not improving as expected. Further work will focus on how to form this crystalline phase uniformly. 15.0 14.9
S
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FIGURE 5. SEM micrograph of fracture surface of GE-PE composites with the crystalline structure.
Geopolymer Reinforced Polyethylene Nanocomposites
801
..*.,"..
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J FIGURE 6. SEM micrograph of fracture surface of GE-PE composites.
CONCLUSIONS The preliminary results obtained so far have shown the potential of geopolymer for enhancing the mechanical properties of linear low-density polyethylene. SEM analysis has identified the micro-/nano-crtytalline structure formed in the composites, which acts as fibre-like reinforcement and is expected to enhance the mechanical properties when it is uniformly distributed in the geopolymer reinforced polyethylene composites. ACKNOWLEDGEMENTS This project was supported by the Vice-Chancellor's University Development Fund of the University of Auckland. The authors are thankful to Mr Oliver Lott for his contribution to this project. REFERENCES 1. 2.
3.
4. 5. 6.
Crawford, R.J., Rotational moulding ofplastics (second edition). 1996: Research Studies Press LTD. Crawford, R J. and A. Robert. Reinforcement of Rotomoulded Plastic Parts - A Challenge, in The Third Asian-Australasian Conference on Composite Materials (ACCM-3). 2002. Auckland, New Zealand. Cramez, M.C., M.J. Oliveira, and RJ. Crawford, Optimisation of rotational moulding of polyethylene by predicting antioxidant consumption. Polymer Degradation and Stability, 2002. 75: p. 321-327. Ward, J., et al., Rotational Molding of Flax Fibre Reinforced Thermoplastics, in Paper No: MBSK 02-209, An ASAE Meeting Presentation, 2002. Holloway, D.G., The Physical Properties of Glass. The Wykeham Science Series, ed. N. Mott and E. Cavendish. 1973, London: Wyheham Publications Ltd. Zhang, S., K. Gong, and J. Lu, Novel modification methodfor inorganic geopolymer by using water soluble organic polymers. Materials Letters, 2003. Article In Press (Available on line at www.sciencedirect.com).
802 7.
8. 9.
10. 11.
12.
Geopolymer Reinforced Polyethylene Nanocomposites Barbosa, V.F.F. and K.J.D. MacKenzie, Thermal behaviour of inorganic geopolymers and composites derived from sodium polysialate. Materials Research Bulletin, 2003. 38: p. 319331. Xu, H. and J.S.J.V. Deventer, The geopolymerisation of alumino-silicate minerals. International Journal of Mineral Processing (Int. J. Miner. Process.), 2000. 59: p. 247-266. Davidovits, J., Synthetic menieral polymer compound of the silicoaluminates family and preparation process, in USPTO Patent Full-Text And Image Database. 1984, United States Patent 4,472,199: USA. Ke, Y.C. and P. Stroeve, Polymer-Inorganic Nanocomposite Materials. 2003, Beijing, China: Beijing Chemical Industry Publisher (China). Iwahiro, T,, Y. Nakamura, and R.K. Ikeda, Crystallization behavior and characteristics of mullites formed from alumina-silica gels prepared by the geopolymer technique in acidic conditions. Journal of European Ceramic Society, 2001. 21: p. 2515-2519. Davidovits, J., Mineral polymers and methods of making them, in USPTO PATENT FULLTEXT IMAGE DATABASE. 1982, United States Patent 4,349,386: USA.
Part XV
Processing
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Understanding the Thermoforming Issues of Carbon Fibre Reinforced Polyphenylene Sulphide [PPS] Composite Meng Hou1* and Lin Ye2 'Cooperative Research Centre for Advanced Composite Structures Ltd 361 Milperra Road, Bankstown, NSW, 2200, Australia 2
School of Aerospace, Mechanical & Mechatronic Engineering University of Sydney, NSW, 2006, Australia
ABSTRACT This paper presents the recent research results in understanding the processing parameters of rubber stamp forming of CF/PPS. Processing conditions such as mould temperature, consolidation pressure and forming time were investigated to determine their effect on the forming of CF/PPS composites. The effect of forming conditions on the spring-in phenomena, deconsolidation of CF/PPS and the morphological property of PPS matrix were studied. CF/PPS composite quality was assessed using micrographs of sectioned specimens and mechanical characterisation. The temperature profile of CF/PPS during stamp forming was monitored and simulated using finite element analysis. INTRODUCTION
FIGURE 1: Thermoplastic component made of CF/PPS
Thermoplastic composites have a number of advantages over traditional thermosetting composites in aeronautical application which could lead to cost reduction. Rapid transformation of advanced thermoplastic composites into finished parts is vital to the acceptance of these materials by industry. Thermoforming is one such fabrication method. In order to develop an Australian capability for design and production of cost-effective advanced thermoplastic composite aircraft structures, a project of design and manufacturing of a demonstrator thermoplastic composite Correspondence author, Fax: +61 2 9772 8482, Email: [email protected]
806
Carbon Fibre Reinforced Polyphenylene Sulphide Composite
component (Figure 1) was undertaken in a research program within the Cooperative Research Centre for Advanced Composite Structures (CRC-ACS), which included researchers from the University of Sydney and Hawker de Havilland. Rubber stamp forming and thermal welding techniques were used to manufacturing the demonstrator. This paper presents the recent research results in understanding the effect of processing parameters of rubber stamp forming on the mechanical and morphological properties of CF/PPS composite. EXPERIMENTAL Material Cetex Carbon fabric [plain weave and 5H satin] reinforced PPS pre-consolidated laminates and CF Fabric/PPS semipreg supplied by Ten Cate Advanced Composite, The Netherlands, were used in the study. The pre-consolidated laminates had a stacking sequence of [±45, 0/90, ±45, 0/90]s and had a resin content of about 50% by volume. The semipreg was made of 5H satin fabric sandwiched between two PPS films. The fibres were not impregnated but only slightly fused to the PPS film, which was quenched to an amorphous state to provide an improved drapability. Laminates [0/90]g with embedded thermocouples were made in-house using the semipreg. The semipregs were placed between two aluminium platens and UPLEX films were introduced between the composites and aluminium platens for easy de-moulding. The materials were then consolidated in hot press and the moulding conditions were adopted from Ref [ 1 ]. Forming Facility
n Daylight 1 70mm
Heated Metal Tool
^^^^^^.^
Hot-plate Preheating
FIGURE 2: Forming facility
The experimental set up used in this study is shown in Figure 2. The hydraulic press (TYSCY 5092) has two working strokes, i.e. opening/closing and compression stroke and can build up a maximum load of 10 kN in opening/closing stroke and 500 kN in compression stroke, respectively; further, it allows opening and closing velocities of 70 mm/s and a compression stroke rate between 1 and 3 mm/s, respectively. The characteristic of the press is that it allows the mould to be rapidly closed on the preheated laminate panel in the opening/closing stroke to a specific pressure and then close more slowly in the compression stroke to build up high pressure during forming and dwell to promote consolidation of material in the mould. A specially designed die-set was installed in the press. Metal and rubber [rubber block or rubber cavity] were fixed onto the die-set as the forming tools. The metal tool was equipped with electric heating elements and could be heated up to 200 °C. A hot plate
Carbon Fibre Reinforced Polyphenylene Sulphide Composite
807
was used to pre-heat the CF/PPS laminate. The typical forming procedure involves: (a) heating the pre-consolidated laminate panel to a temperature above the melting temperature of PPS matrix between two hot plates without any external pressure; (b) quickly transferring the hot laminate panel into the forming system (transfer times are of the order of a few seconds to prevent significant cooling); and (c) forming the hot laminate panel into the final part, in which the press is so adjusted that a high closing speed is used to close the mould in the opening/closing stroke, and when a specified pressure was reached, the press was changed to its compression stroke, in which the mould was closed slowly but a high pressure could be built up. Characterisation Characterisations of mechanical properties as a function of the processing conditions were carried out using flexure (three-point bending) tests. The span was 48 mm; the width and length of the specimen were 25 mm and 60 mm, respectively. The crosshead speed was set to 1.2 mm/min. The flexure elastic modulus and flexure strength were determined according to ASTM D-790. At least five specimens for each processing condition were tested at ambient temperature. DSC and DMA were used to investigate the morphological property and deconsolidation behaviour of PPS matrix, respectively. In addition, reconsolidation and crystallite structure were examined using light microscopy and polarized light microscopy. RESULTS & DISCUSSION Deconsolidation The major problem encountered was the de-consolidation of the laminate during heat-up. It was found that the degree of de-consolidation was dependent on the structure of the reinforcement (Figure 3) and the optimum processing conditions had to be adjusted accordingly. It was found that higher pressures; higher speed and higher pre-heating temperature were needed to form 5H satin CF/PPS than plain weave CF/PPS. As an example, Figure 4 shows the voids formed on the metal tool surface (due to a quick cooling) could be eliminated by an applying high stamping pressure. 1
30
Q
25
|
10 0
100
200 300 Temperature [°C]
400
FIGURE 3: Deconsolidation of CF fabric/PPS laminate
Spring-in Due to high processing temperatures, the residual stresses in thermoplastic composites are inevitable. The most common residual stress effect encountered in manufacturing composites is a reduction in the enclosed angle in channel or angle
808
Carbon Fibre Reinforced Polyphenylene Sulphide Composite
components [2]. This reduction in enclosed angle is referred to as spring-in. The spring-in phenomenon was investigated at an early stage of the project in order to provide necessary information for tool design. Based on the experimental results an allowance angle was set up in tooling system to compensate for part spring-in. Figure 5 shows the effect of different holding time on spring-in angle of 5 H satin CF/PPS. It can be seen that the spring-in angle was a function of forming time and was minimised to 0.5 degree when the holding time was 30s or more.
FIGURE 4: Re-consolidation of 5H satin CF/PPS 5H Salin CF/PPS 1.0 0.8
W
"i
i—
I
0.2
S
t"
„ 5
10
20
30
i 40
50
Holding Time [ s ]
FIGURE 5: Spring-in angle of 5H satin CF/PPS
Temperature Profile during Stamp Forming The temperature profile of CF/PPS during forming was monitored using in-house made laminates with embedded thermocouples, which were placed in different locations as well as through the thickness of the laminate. Different temperatures have been used for the metal tool, while the rubber side was kept at room temperature. It was found that the metal tool had a predominate influence on the cooling of CF/PPS. Because of the good insulation properties of rubber, the contact between the rubber mould and the hot laminate does not lead to excessive cooling of the laminate. A 2DFEM heat transfer model was also generated to simulate the cooling-down temperature profile (Figure 6). The temperature profiles provided valuable information on the thermal history, degree of crystallinity and the morphological property of PPS matrix.
Carbon Fibre Reinforced Polyphenylene Sulphide Composite
|
Rubbe = 25 °C
100
\
h
•
E
t
\V— """"" 200
^k
^
Metal To
809
I
I ol = 170 °
FEM
~^%fe^
150
FIGURE 6: Cooling-down temperature profile of CF/PPS laminates
Morphological Property of PPS Experimental results showed that different tool temperatures result in different cooling histories of PPS matrix and hence generated various degrees of crystallinity [Figure 7]. The amount of crystals formed depended on the energy absorbed during cooling. By cooling slowly (higher tool temperature) maximum crystallinisation occurred. cooling rate: 11.6°C/s
i
As Received Film
8.7°C/s
1
20.1
24.6
ToolT 130 QC
ToolT 170 °C
Temperature [ °c ]
FIGURE 7: Different tool temperatures resulted in different degree of crystallinity of PPS matrix
The image of PPS crystal spherulite was investigated using polarised light microscopy. Amorphous PPS film (obtained from the CF/PP semipreg) was stamp formed under the same processing conditions as the CF/PPS laminates. Figure 8 shows the spherulitic structures formed by different tool temperatures. In general, high tool temperatures resulted in slow cooling rates and large sizes of crystal spherulite. To ensure optimal performance of PPS composites after processing, maximum crystallinity is usually desired. However, larger crystals will cause extensive resin volume shrinkage and can generate micro-cracks in the PPS composite. For this reason, processing conditions need to be carefully controlled in such a way that a high degree of crystallinity as well as small crystals can be obtained.
130
[°C]
150 [ ° C ]
•HT: "
170,
Size of Spherulite
Tool Temperature Cooling Rate
FIGURE 8: PPS Crystal structures formed by different tool temperatures
190 [ ° C ]
810
Carbon Fibre Reinforced Polyphenylene Sulphide Composite
Mechanical Performance of Stamp Formed CF/PPS Different from matched metal die forming, in rubber forming one of the rigid metal dies was replaced with a flexible rubber block. The rigid metal die determined the final shape of the component and gave a good surface quality on the contacting side of the product, while the rubber produced a homogeneous pressure distribution. Figure 9 shows the effect of forming pressure on the flexural properties of CF/PPS laminates. It was found good quality of CF/PPS composites could be obtained in the pressure range from 2 to 5 MPa and the rubber tool needed to be constrained within a solid metal frame to prevent extensive deformation of the rubber. Large deformation of the rubber would delay the time needed to build up the maximum pressure and generate voids in the composite.
2
3
4
2
5
Fonring Ftessue [ ^/P^ ] *s (Graved CF/PFS
3
4
5
FoTTingRessjre[MRa] Rmedwithlvtetal Rare
Fonredwittai Matal Frams
FIGURE 9: Flexural properties of formed CF/PPS laminate
CONCLUSIONS The project has focused upon providing deep understanding of processing conditions of rubber stamp forming of the CF/PPS composites. Processing conditions such as mould temperature, consolidation pressure and forming time were investigated to determine their effect on the forming, morphological, consolidation and mechanical performance of carbon fibre reinforced PPS composites. Generic aircraft rib components were manufactured to investigate the forming behaviour of the material and to demonstrate the rubber stamp forming concept. A sound scientific basis for understanding what happens during the processing and how that stage affects the service performance of the structure has been established. The outcome of this project will benefit the ongoing technology development program of CRC-ACS. REFERENCE CETEX®- PPS Guide Lines, Ten Cate Advanced Composites, Nijverdal, The Netherlands. 2000 [ITD4401.01] Jain, L. K., Hou, M., Ye, L. and Mai, Y. W., "Spring-in study of the aileron rib manufactured from advanced thermoplastic composite", Composites Part A: Applied Science and Manufacturing, Vol. 29, issue 8, 1998, p. 973-979
A Numerical Approach to Analyze the Curing Process of Railroad Composite Brake Shoe Akbar ShojaeiI'3'*and Farhang Abbasi '3 'Chemical and Petroleum Engineering Department, Sharif University of Technology, Tehran, Iran 2 Chemical Engineering Department, Sahand University of Technology, Tabriz, Iran 'Manufacturing and Production Group, Railway Research Center, Tehran, Iran
ABSTRACT In the present article, the cure process of the railroad composite friction materials in the compression molding process is studied. Numerical simulation is used to analyze the process and a series of parametric studies are performed to reveal the effect of process parameters and material variables. The results show that the cure process and also the braking performance are governed by the thermophysical properties of the friction compound formulation, which are in turn dominated by the compound ingredients. It is suggested that such information can be used in designing of compound formulation to achieve a friction material with good frictional and processing properties.
INTRODUCTION The conventional cast iron brake blocks are increasingly being replaced by the newly developed composite friction materials in the railroad industry. Numerous economical and technical advantages of composite friction materials compared with the cast iron ones are the major motivation for this replacement [1]. The replacement may be performed either by changing the braking system of the rail vehicle or by direct replacement for cast iron brake blocks. The manufacturing of composite brake block is an important issue, influencing the production rate and part quality. Compression molding is a major processing technique used to fabricate the composite brake block [2]. Prediction of cure process inside the mold will provide good information to obtain a proper processing condition. On the other hand, since a large variety of compound formulations with a wide range of physical properties can be developed and used, analysis of in-mold cure provides important information regarding the designing of both compound formulation and processing conditions. The present study is devoted to explore the effect of processing and material parameters on fast and uniform cure process of composite railroad brake shoe and the connection of dominant parameters to the braking performance of the brake shoe. First, heat and conversion balance equations governing the cure process are presented and the cure kinetics of the polymer matrix.used in the friction compound is modeled. Corresponding author. Chemical and Petroleum Engineering Department, Sharif University of Technology, Tehran 11365-9465, Iran. Fax: +98-21-6022853. Email: [email protected]
812
Curing Process of Composite Railroad Brake Shoe
For the sake of simplicity, one-dimensional cure process is considered and the governing equations are solved by the explicit finite difference method. Based on this approach, a series of parametric studies are presented, indicating the influence of important process and material parameters on the cure process. THEORY The models used in this study are based on some assumptions including: 1) No flow during compression process, 2) well-mixed and homogeneous compound implying uniform physical properties and uniform heat of reaction, 3) onedimensional heat flow and 4) isothermal mold wall. These assumptions have been justified in the analysis of compression molding process [3]. The energy and mass balance equations The temperature and conversion profiles inside the cavity can be predicted by energy and mass balance equations, respectively. According to earlier mentioned assumptions, energy balance is one-dimensional transient heat conduction equation with internal heat generation term which is expressed as [4]: 1 dT o" dt
82T dz2
„ „ da ' r dt
(1)
and mass balance equation becomes:
— = f(a,T) dt
(2)
where a and k are thermal diffusivity (a = kjpCp ) and thermal conductivity of the composite, respectively, a is the conversion, T is the absolute temperature and f(a,T) is a function of a and T representing the reaction kinetics of the reactive components and may be given based on either empirical or mechanistic models. Hr and Vr represent the total heat of reaction and the volume fraction of reactive components in final compound, respectively. Cure kinetics modeling Since mechanism of thermosets curing reaction is generally complex, the reaction kinetics is actually modeled based on empirical approach. A variety of empirical models are available, among them, the generalized expression given by Kamal and Sourour [5] has found large applications. This model can be expressed as: of
(3)
where m and n are model constants and kj and fo are temperature-dependent reaction rate constants having Arrhenius temperature dependence as: (4)
Curing Process of Composite Railroad Brake Shoe
813
In Eq. (4), A is the pre-exponential factor, E is the activation energy and R is the universal gas constant (R= 8.314 J mol"1 K"1). Eq. (3) has been successfully used to model the cure kinetics of both resin and rubber compounds [5-7]. It has been observed that for rubber compounds, there is a period in the vulcanization of rubber compound during which chemical reaction does not take place and the reaction rate is zero. This period which is called induction time, occurs at the start of vulcanization. Induction time for a given rubber compound depends on temperature according to Arrhenius-type temperature relation as: (5)
where /,- is the isothermal induction time and t0 and r 0 are model constants which are obtained based on kinetic study under isothermal conditions. For nonisothermal process, induction time may be estimated by [7]:
',(*•)
where tt{T) represents temperature-dependent induction time given by Eq. (5) and t is a dimensionless parameter. According to Eq. (6), when the value of t reaches one, upper limit of the integral, namely t, becomes the nonisothermal induction time. The temperature and conversion distributions inside the mold can be predicted by solving Eqs. (l)-(2), simultaneously, with the aid of appropriate initial and boundary conditions, i.e. mold wall temperature is Tw and the Initial temperature is T}. MODEL PARAMETERS Many components are involved in a specific friction material compound so that each component has a special function in the final product. Here all of these components are categorized into two major groups, comprising: 1) reactive components or polymer matrix and 2) nonreactive components which may be friction modifiers, reinforcements, fillers and other additives [8]. A vast number of raw materials are available which can be used in friction materials formulation, so that frictional performance as well as physical properties of the product are significantly governed by the raw materials used in the final compound. Consequently, commercially available railroad friction material developed by companies have a wide range of physical properties. Table 1 shows the range of physical properties of commercially available brake shoes. The most important polymer matrix used in the railroad friction materials is a combination of SBR (styrene butadiene rubber) and phenolic resin. The kinetic behavior of a pure SBR compound has been reported in literature. However, there is no kinetic data for the combination of SBR and phenolic resin. This subject is our current research and the results will be published in the future. The kinetics parameters used in the present article, which are given for a pure SBR compound, are taken from Ref. [7] and are as: A,=0 s\ A2=352 s'\ Ej=0 J/gmol, £>=3.62xlO4 J/gmol, m=0.6, n=\, Hr=2xl07 J/m3, ;0=5.786><10"12 s and r 0 =1.28xl0 4 °K.
Curing Process of Composite Railroad Brake Shoe
814
TABLE I The range of physical properties of composite railroad brake shoes [9-11]
Quantity
Value
P (kg/m 3 ) ff(m2/s)
1700-3200 xl0-7~3.7xl 0.5-8.5
k (W/m.°C) RESULTS AND DISCUSSION
Based on the physical properties and kinetics data for railroad friction materials given in previous section, a parametric study is performed to explore the effect of processing parameters such as mold wall temperature and compound preheating and also materials variables such as thermal conductivity and thermal diffusivity on the cure process. The mold thickness considered in the analysis is 4.2 cm which is a practical value for a railroad brake shoe. Simulation is performed for four different molding conditions including: easel: Tw = 170°C and Tt = 25°C, case2: Tw = 170 °C and Ti = 100°C and case3: Tw =150°C and Tt = 100cC. In cases 1 to 3, thermophysical properties of friction material are: p=1700 kg/m3, <7=0.52xl0~r m2/s and k= 0.75 W/m.°C. The variables in case 4 are: Tw =150°C and 7} = 100°C, p=3\5O kg/m3, 0=2.98x10"" m7s and k= 7 W/m.°C. In all cases Fr=0.25.
150
IS
]
I 1
~~~~
a. 60
-
/
1=0 sec 1=300 sec 1=600 sec 1=900 sec 1= 1200 sec
I I I
I 1
I
" X
0.2
0.4
0.6
0.8
Z/H
FIGURE 1 Temperature and state of cure (S.O.C) distributions (easel)
Figures 1-4 show the temperature and conversion (state of cure) distributions through the thickness of the mold for different molding conditions. As seen in the figures, when the temperature increases in a specified location inside the mold, reaction rate increases and consequently the state of cure (S.O.C) or conversion enhances. In all cases, temperature inside the mold does not exceed the mold wall temperature. This means that the heat released due to chemical reaction does not predominately contribute in enhancement of temperature. This is because of low heat of reaction of rubber compound compared to the conversional resins such as epoxy and polyester which is normally greater than 200 J/g [5,6]. Therefore temperature and state of cure as well as in-mold cure time are governed by thermophysical properties of the friction compound and molding strategies. In molding strategies, one can decrease the molding time by increasing the mold wall temperature and preheating the
Curing Process of Composite Railroad Brake Shoe
815
initial charge. Due to some economical and practical considerations, it is not advisable to increase the mold wall temperature to a very high level. Also one must be careful to avoid the curing of the friction compound during the preheating process.
0.8
0.2
FIGURE 2 Temperature and state of cure (S.O.C) distributions (case2)
160
\
^^
0.9
140
0.8 120 100 O 80
6 0.5
0 sec 300 sec 600 sec 900 sec 1200 sec t= 1600 sec
60 40
0.7 0.6
"0.4 0.3 0.2
20
0.1 n 0.2
0.4
0.6
- - - 1= 0 sec 1= 300 sec - - - .1=600 sec 1= 900 sec - " 't= 1200 sec 1= 1500 sec
i\ \A, v 0.2
Z/H
>
I
/
y
0.4
Z/H
/
'
0.6
/
/ 0.8
FIGURE 3 Temperature and state of cure (S.O.C) distributions (case3)
160 140 0.8
•tioo
0.6 |
at
5 80
- - -
re
1=0 sec
0.2
0.2
0.2
0.4
aH
I
0.4
- - - .t= 600 sec 1=900 sec - - - .t= 1200 sec 1=1500 sec
I 40
• • - l=0sec — — 1 = 300 sec - - - .|=600sec 1= 900 sec — — 1 = 1 2 0 0 sec t= 1500 sec
0.6
0.8
1
0.4
0.6
Z/H
FIGURE 4 Temperature and state of cure (S.O.C) distributions (case4)
0.8
816
Curing Process of Composite Railroad Brake Shoe
Other important parameters which can have a dominant effect on cure time are the thermophysical properties including thermal diffusivity and thermal conductivity of the friction material compound. These parameters are directly related to resin compound formulation. Our previous work has shown that frictional performance of a friction material is controlled by high thermal conductivity and thermal diffusivity together with low compression modulus of the final product [12]. Thermophysical properties are governed by nonreactive components but the compression modulus is mainly dictated by reactive component, namely rubber component. Since the reaction rate does not affect the cure process, increasing volume fraction of rubber component in the formulation does not significantly influence the cure process, except that it may decrease the thermal conductivities of the final formulation. This study reveals that designing a friction material formulation with high thermal conductivity and thermal diffusivity ensures good performance of the products and appropriate molding process. CONCLUSION The cure process of the composite frictional material in the compression molding process was analyzed based on the numerical simulation. The numerical studies revealed that for a friction material compound; although the mold wall temperature and preheating of the compound may affect the in-mold cure time, the physical properties of the composite brake shoe, in particular thermal conductivity and thermal diffusivity, have a significant effect on both the cure time and uniformity of the cure inside the mold. On the other hand, according to our previous results, high thermal diffusivity together with low compression modulus leads to high performance of the braking. Since these properties are directly dominated by the individual components involved in the friction compound formulation, the results presented in this paper help the designer to select compound materials in such a way both good performance and efficient molding process are achieved. REFERENCES 1. 2.
3. 4. 5. 6. 7. 8. 9. 10. 11.
12.
Gibson, P. A. 1996. "Composition Friction Materials for the Replacement of Cast Iron Railway Blocks," IMechE seminar publication in Railway traction and braking, 75-85. Dong, F., F. D. Blum, L. R. Dharani. 2000. "Effects of Moulding Pressure on the Mechanical and Friction Properties of a Semi-metallic Friction Material," Polymer & Polymer Composites, 8(3):151-156. Lee, L. J. 1981. "Curing of Compression Molded Sheet Molding Compound," Polymer Engineering and Science, 21(8):483-492. Holman, J. P. 1997. Heat transfer, Me Graw-Hill Book Company. Kamal, M. R. and S. Sourour. 1973. "Kinetics and Thermal Characterization of Thermoset Cure," Polymer Engineering and Science, 13(l):59-64 Loos, A. C. and G. S. Springer. 1983. "Curing of Epoxy Matrix Composites," Journal of Composite Materials, 17:135-169. Isayev, A. I. and J. S. Deng. 1988. Nonisothermal Vulcanization of Rubber Compounds," Rubber Chemistry and Technology, 61:340-361. Bijwe, J. 1997. "Composites as Friction Materials: Recent Developments in Non-asbestos Fiber Reinforced Friction Materials-A Review," Polymer Composites, 18: 378-396. "Technical Specification of Friction Materials of Railway Product," Feredo Company. "Technical Specification of L Brake Blocks," Futuris Brakes International. Mercer, C. I. 1987. Medium Friction Non-Metallic Composition Brake Shoes as Direct Replacement for Cast Iron Brake Shoes on Rolling Stock," Proceedings of Institution of Mechanical Engineers, 2O1(D1) :11-20. Abbasi, F., A. Shojaei and A. Katbab. 2001. "Thermal Interaction between Polymer-Based Composite Friction Materials and Counterfaces," J. Applied Polymer Science, 81:364-369.
Possibility of Fabricating Mixed a/p Sialon Ceramics as Composite Materials B .S .B .Karanaratne* Department of Physics, University of Peradeniya, Peradeniya, Sri Lanka.
ABSTRACT Possibility of fabricating composite ceramics based on mixtures of the two sialon phases a/p was studied. Sialons are 'ceramic alloys' of SisN4 and the two sialon phases a and p are formed by substituting Al for Si and O for N in the network of S1N4 tetrahedra based on a and p S13N4. Furthermore, the formation of a-sialon requires addition of suitable cations to the initial composition. These cations were added in the form of an oxide or as a glass composition to the other raw materials. This initial composition and the sintering procedure were carefully controlled in order to achieve the required a:p phase ratios. The phase ratios and the chemical composition of the sintered samples were experimentally verified by X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive X— ray Analysis (EDS). A range of sialon ceramics with different cations and different a/p phase ratios was prepared. Mechanical properties such as fracture toughness (Kic) and hardness were measured to assess the performance of a/p composite samples. SEM observations revealed that the main feature of the micro structure was the presence of elongated needle shaped p grains in the matrix of equiaxed a- sialon grains. Fracture toughness measurements showed that the fracture toughness (Kic) increased with the increasing amount of the elongated needle shaped P grains. This general trend was observed for all the sialon samples containing different cations. It was also observed that the aspect ratio of p grains was an important parameter in achieving high fracture toughness. The mixed a/p sialon ceramics can behave as composite materials in which the needle shaped P grains can provide the toughness by mechanisms of crack bridging, pull-out and crack deflection. INTRODUCTION Excellent mechanical and thermal properties of silicon nitride based ceramics make them very attractive in high temperature engineering applications. Si3N4 has two hexagonal crystal forms, a andp [1]. A wide range of solid solutions with the a /p silicon nitride structures is well recognised under the name of a/p Si-Al-O-N (sialons). Sialons exhibit a number of interesting features. The most important property of sialons in relation to the ceramic technology is the sinterability and many of them are sinterable up to the theoretical density. The solid solution of P-Si3N4, in * Corresponding Author, Email: [email protected]
Fabricating Mixed a/p Sialon Ceramics
818
which Si and N are substituted by Al and O, respectively, is known in the literature as P-sialon [2] and is expressed by the general formula Si6-Z Alz Oz Ns-Z , where, Z is the Al substitution level and 0< Z <4.2. oc-Si3N4 forms a more limited solid solution, a-sialon, which results from a similar substitution to p sialon but its stability requires the addition of metal cations (M= Ca, Y and selected rare earth elements) which partially occupy two large interstitial sites in the unit cell [3]. The metal cation should be just large enough to occupy the interstitial volume and the suitable ionic radius is about 1 A. The a-sialon is expressed by the general formula, 12-(m+u)
On N16.n
where v is the valency of the metal cation M. Therefore, unlike in the case of Psialon the phase field of the a-sialon is represented by a plane. Densification of both a and P sialons occurs via liquid phase sintering, which requires a metal oxide additive as the basis for an oxynitride sintering liquid. However, in the case of a-sialon, additive metal cations can be accommodated in the a-sialon structure and hence offer the possibility of producing a single phase material via transient liquid sintering, a and p phases are totally compatible and composites of them can be prepared with different a:P ratios by sintering appropriate oxidenitride powders. The Janecke prism [4] has been used to describe the composition of the five component constitutes in three dimensions. In the present work a series of a/p sialon ceramics with different cations was synthesised to give different a:P ratios by controlling the initial composition and composite properties of these ceramics were studied. EXPERIMENTAL a-Si3N4 (UBE grade SN 10E), A1N (Starck C), A12O3 (Alcoa), SiO2(99.9% purity ,BDH-Merck) rare earth oxides (99.9% purity, Aldrick Chemical Company) and CaCC>3(99.9% purity ,BDH-Merck) were used as the starting powders. The interstitial cations for the a-sialon were added in the form of a glass or as an oxide. The glass compositions were selected to give a low melting clear glass. TABLE I A typical set of composition of the a/p sialon ceramics (in wt % ). Cations were added as glass or as an oxide. M
m
n
Si3N4
A1N
M-Glass
Y Y Ca Ca Yb Yb Yb Yb
1.5 1.5 1.5 1.0 1.5 1.5 1.0 2.0
0.75 0.75 0.75 2.0 0.75 0.75 2.0 1.0
69.1964 56.3944 58.5260 78.4662 61.1192 67.4915 65.1212 72.2050
19.1010 26.0590 26.6050 14.8313 21.0190 18.0585 19.1338 14.3450
11.7026 17.5466 14.8690 6.7025 17.8618
M Oxide
14.4500 15.7450 13.4500
Expected
a:P 50:50 75:25 75:25 50:50 75:25 95:5 95:5 50:50
The rare earth oxide powders were calcined at 1000 C for several hours and determined the amount of moisture and CO2 content (water pick-up) before using.
Fabricating Mixed a/p Sialon Ceramics
819
This was in a range of 0.2 to 0.5 % for different rare earth oxides and was taken into account when the rare earth oxides were weighed for making glass. The oxide powders were stored in desiccators containing silica gel. The powders for the glass compositions were mixed thoroughly and then melted in a platinum crucible at 1575°C for about two hours. The melted glass was poured into deionised water. The dried glass was crushed and milled in a rotating polyethylene bottle in iso-propyl alcohol with sialon balls as the milling media. The precursor charge was 50 grams and the milling time was 72 hours. The milled wet glass powder was sieved through 38 |^m grid and then dried. The constitution of the a/p sialon phases was predicted by balancing of compositions using a computer programme. The composition of the a phase was defined by choosing suitable m and n values and then the metal oxide (or glass) addition was calculated in order to obtain the desired proportion of a phase. Having subtracted the total Si, Al, O, N and the cation M required to form the defined a content, the residue was assumed to form p and the necessary equivalence of O and Al adjusted in the initial mixture via A1N. The programme output defines p composition (Z value) and component mixture (ALN, Si3N4 and glass) necessary to form the chosen a composition and content. A typical set of data is given in Table I. The composition and the proportions of the a and P phases formed in the resulting materials were confirmed by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray analysis (EDS) and by X- ray Diffraction (XRD). The appropriate amounts of nitride powders and the glass powder (Table I) were milled and sieved in a similar way as described above. The wet powder was dried quickly in a flat glass dish to avoid preferential sedimentation of the powders. A portion of the dried powder was iso-statically pressed (150 MPa) and pressureless sintered for 4 hours at 1775°C in a sialon-lined graphite crucible in a carbon resistance furnace under one atmospheric pressure of pure nitrogen. The furnace was de-gassed at 1150°C for 2 hours prior to back filling with nitrogen to one atmosphere. The other portion was hot pressed ( 30 MPa) in a BN coated graphite die at 1750° C for 2 hours in and ambient atmosphere, using a RF induction heating furnace. The heating rate was 10°C per minute. The densiflcation was monitored by means of a transducer and the pressure was gradually increased. The temperature, pressure and the transducer movement were recorded in a computer. Both the pressureless and hot pressed samples were allowed to cool slowly with the cooling of the furnace. Densities of the samples were determined using Archimedes' principle. X-ray Diffractometry was conducted on the bulk-cut polished samples as well as on the powdered samples using Cu-Ka radiation and Si as an internal standard. The a:p ratio in the sample was determined based on the technique used by Ekstrom et al.[5] from the X-ray intensities of 102 and 210 for a phase and 101 and 210 for p phase. The sintered ceramics were cut into discs about 2 mm thick using a high speed diamond saw. The cut samples were polished by standard diamond polishing techniques. For scanning electron microscopy (SEM), the polished samples were carbon coated to avoid electric charging and were examined in a SEM equipped with an EDS analyser. An 'Instron Testing Machine' with a Vickers diamond indenter was used for measuring hardness (HV10) and indentation fracture toughness (Kic) for selected samples. Indentation fracture toughness was calculated assuming a value of 300 GPa for Young's modules using the method described by Anstis et al.[6].
Fabricating Mixed a/p Sialon Ceramics
820 RESULTS AND DISCUSSION
The density measurements showed that the materials sintered (pressureless) with glass addition were of high density. However, some of the materials prepared with metal oxides in order to obtain high a content were porous. All the hot-pressed samples were fully densified and no porosity was observed in the SEM. The XRD studies showed (Fig.l) that the crystalline phases in the materials were a and P and the ratio of a:p was very similar to that predicted by the compositional programme. Similar observations were made in the SEM in relation to the a:P ratio. The back scattered electron mode in the SEM showed very clearly the difference between different phases present in the microstructure due to atomic number contrast (Fig.l). Therefore in micrographs obtained with back scattering mode, the brighter areas contain more of the heavy elements than the darker areas. Needle shaped Psialon grains, which contain no metallic cations appeared black relative to the asialon grains and to the residual glass phase. The amount of the glass phase was small (about 5%) and appeared white due to high content of metal cations present in this phase relative to the other phases. The EDS analysis of a, p grains and residual glass confirmed this observation. The actual compositions obtained by EDS for a and p phases were subsequently used in the compositional programme to redefine the a and p phases and hence to reduce the amount of undesirable residual glass phase in the final product for further improvement of properties. The residual glass present in these ceramics degrades the intrinsic properties of these ceramics. Preliminary experiments on indentation on selected samples showed that the hardness increases in proportion to the amount of cc-sialon present and the fracture toughness (Kic) increases with the increasing amount of the needle shaped P- grains present (Table II). TABLE II The hardness and the fracture toughness (K[C) values of some selected samples Predicted a: (3 ratio 95:05 75:25 50:50
XRD
a:P ratio 96:04 80:20 57:43
Hardness (GPa) 19-22 18-20 17-19
(MPa m1'2) 3.2-3.7 3.6-4.0 3,9-4.3
This general trend was observed for all the ceramics containing different cations. The values given for hardness and Kic in the Table II are the extreme values obtained for different test pieces and these values are comparable with those reported in literature [7,8]. It is important to note that the aspect ratio of p grains is the important parameter in achieving high Kic values. For anisotropic growth of p grains it is required to have a large amount of liquid at the sintering temperature. However, the presence of glass in the final microstructure will reduce hardness and degrade the high temperature properties. The higher aspect ratio would cause more crack deflection and branching, thereby consuming more fracture energy and hence toughening the composite. Besides crack deflection and branching, crack bridging by elongated P grains as well as grain pull out can also occur. Therefore mixed a/p
821
Fabricating Mixed a/p Sialon Ceramics
(a)
(a) O
300 i
"B
o
2? 3001
0 •
1 1
200- • 100-
102|
f 1 ¥
I^— -\ JU^
.25
30
II
5-
I
i
§ £
PI *J HA, 40
(b)
(c)
FIGURE 1 (i) XRD patterns and (ii) SEM Back scattering micrographs showing a/p phase ratios of siaion ceramics having predicted ratios {a} 95:05 {h» 75:25 and (c) 50:50. The a:P ratio in the sample was dettmiincd from the X-ray intensities of 102 and 210 fora phaseand 101 and 210 tor (3 phase. Elongated (5-sialon grains, which contain no metallic catkins, appear black in SBM back scattering micrographs, relative to the a-sialon grains and to the.residual glass phase( appear white),
sialon ceramic can behave as a composite (a phase as the matrix) in which the needle shaped (3 grains can provide the toughness by mechanisms as shown in the figure 2.
822
Fabricating Mixed a/p Sialon Ceramics
FIGURE 2 Toughening mechanisms in a/p sialon composites
CONCLUSIONS The microstructure of these ceramics was affected by the initial composition as anticipated and this subsequently had an influence on mechanical properties. The presence of an increased amount of elongated P-grains in a/p sialon composites results in higher strength and fracture toughness, whereas the presence of an increased amount of equiaxed oc-sialon grains contributes to higher hardness. The possibility of adjusting the cc:p phase ratio of a/p sialon composites by changing the initial composition opens a method of tailoring the microstructure and hence a means of optimising hardness, toughness and strength of these ceramics. ACKNOWLEDGEMENTS I am grateful to Professor M. H. Lewis and Dr. R. J Lumby, University of Warwick, U.K. for their helpful advice and useful input during this work. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8.
Jack,K. H. 1976. "Review: SiAlONs related nitrogen ceramics," J. Mat. Sci. 11: 1135-1158. Jack, K. H. and W. I. Wilson. 1977. "Ceramics based on the Si-Al-O-N and Related systems," Nature 238: 28-29. Hampshire, S ., H. K. Park, D. P. Thompson, and K. H. Jack. 1978. "oc-Sialon ceramics," Nature 274: 880-882. L. J . Gaukler, H. L. Lukas, G. Petzow ,and J. Am. Ceram. 1975. "Contribution to the Phase Diagram Si3N4-AlN-Al2O3-SiO2," Soc. 58: 346-351. Ekstrom, T., P.O. Kail, M. N. Nygred and P.O. Olsson. 1988. "Mixed a-and p1- (Si-Al-O-N) Materials with Yttria and Neodymia Additions," Matter. Sci .Eng .Al05/106: 161-165. Anstis, G. R., P. Chantukul, B. R. Lawn, D. B. Marshall, and J. Am. Ceram. 1981. "A Critical Evaluation techniques for measuring Fracture Toughness," Soc. 64 : 533-538. Mandal,H., and Hoffmann M. J. 2000." Hard and Tough a- SLA1ON Ceramics,"Maferiafc Science Forum. 325-326:219-224. Thompson,D. P., and H.Mandal. 2001. "New Heat Treatment Methods for the Optimization and Improvement of SiAlON Ceramics," J.Mater.Science. 35 : 6285-6292.
High Quality and Low Cost Manufacture of Potassium Titanate Whiskers Xiaohua LU*, Chang LIU, Ming HE, Zhuhong YANG, Ningzhong BAO & Xin FENG Nanjing University of Technology, P. R. China
ABSTRACT Potassium titanate whisker (PTW) is an advance material. The method of the large scale manufacturing PTW is a bottleneck in the application of this material. Hydration of the sinter is the key step of the PTW synthesis. In the present work, ionic exchange equilibrium and mass balance in the hydration are integrated to establish a predictive model describing the conditions of the hydration process. The results show that the aimed product can be controlled mainly by pH during hydration. The amount of water (Vo) is reduced to 1/10 comparing with the literature. The pH and water volume are both controlled easily in a large scale production. INTRODUCTION Potassium titanate whisker K2O-6TiO2 (PTW) is a kind of high performance material in micron scale [1-2]. One of the key steps of its large scale application is to develop a method to manufacture PTW with high quality and low cost. Generally, the preparation process of PTW is consisting of calcinations, hydration and heat-treatment. The conditions in the process have to be optimized to reduce the manufacture cost, of which the hydration process is a key step. A large numbers of studies about the hydration process have been reported [3-6]. However, many factors, such as the value of pH, the amount of water, the concentration of the ions in aqueous phase and the reaction time, affect the hydration process. And a large amount of water such as lOOml/g is often needed in these studies, which results into the high cost of preparation and environmental problem. Many attempts have been made to describe the ionic exchange equilibrium in hydration process in our previous work [7-8]. In this paper, ionic exchange equilibrium and mass balance in the hydration are integrated to establish a predictive model describing the conditions of the hydration process.
THEORY ha the hydration process, HC1 solution is added continuously in constant pH to enhance the K+/H+ exchange. There are five intermediate solid phases appearing in the process [4], and the equilibrium constant for each reaction Ki (i=l, 2, 3, 4) are 1.16xlO6, 4.83xlO8, 7.47xlO10 and 5.42xlOn respectively [4]. With the solid liquid * Corresponding Author, College of Chemical engineering, Nanjing University of Technology, Nanjing 210009, China. Tel:0086-25-83588063, Fax: 0086-25-83588063, Email: [email protected]
824
Manufacture of Potassium Titanate Whiskers
equilibrium stage theory [9], the ionic exchange equilibrium and mass balance can be integrated as follows:
mr
U
— — ^ V n -0.001 + mK + mH - C, — V U
°
2
x j=2
-w^-K,-0.001 = 0
M 0 -4-
Where a gram of sinter is added into Vg volume of water (ml/g), mKo is the concentration of potassium ion in the solution, mCw is the concentration of chlorine ion in the solution, Ci is the concentration of HCl solution, Mo is the molecular weight of the sinter, no is the TiC^/IvO mole ratio in the sinter, nix is the concentration of potassium ion in the equilibrium solution, mu is the concentration of hydrogen ion in the equilibrium solution, yH and yM are the activity coefficients of hydrogen ion and potassium ion in the equilibrium solution. kw is ionization constant of water. Bj is the stoichiometric coefficient of potassium atom in the molecular formula of intermediate phase j (j=l, 2, 3,4). There is only one unknown variable mx in equation (1). Solving the equation the value of mK can be derived. And then the value of the TiO2/K2O mole ratio R in the products and the gross volume of water F^can be deduce. RESULTS AND DISCUSSION With this model, the effects of a variety of factors including the concentration of HCl {Ci), the composition of sinter (no), the volume of water (Vo) and pH on the hydration process are investigated when R is controlled to 6 for preparing PTW to minimize the gross volume of water (Vt). Effect of the Concentration of HCl on the Gross Volume of Water Figure 1 shows that the gross volume of water (Vt) is decreased with the increase of the concentration of HCl (Ci) under the conditions of «o=4 and (/o=lOOml/g. The higher the concentration of HCl is, the fewer the gross volume of water is. However, the framework of the solid may be destroyed when the concentration of HCl solution is higher than 0.1M [6]. Therefore, the optimal concentration of HCl is 0.1M. Effect of the Composition of Sinter on the Gross Volume of Water Figure 2 shows that the gross volume of water (Vt) is decreased with the increase of the composition of sinter (no) under the conditions of Cy=0.1M and Fo=lOOml/g. It means that the sinter contains some K2O when «o<4, and more amount of HCl solution is needed to enhance the process. Effect of the Initial Volume of Water on the Gross Volume of Water Figure 3 shows that the gross volume of water (Vt) is decreased with the increase
Manufacture of Potassium Titanate Whiskers
825
of the initial volume of water (Vg) under the conditions of «o=4 and C;=0.1M. Therefore, the minimum gross volume of water is 26.1ml/g when the initial volume of water is lOml/g which is the smallest value that can satisfy the demand of stirring. Effect of pH on the Gross Volume of Water Figure 4 presents some pH and the initial volume of water for preparation of PTW at «0=4 and C/=0.1M. It is clear that the decrease of pH slightly will result into the decrease of the gross volume of water rapidly. Therefore, the minimum gross volume of water can be approached atpH=9.3 and Vo=lOm\/g when the composition of sinter no is 4 and the concentration of HC1 solution is 0.1M.
140
100
)
0.4
0.8
cum FIGURE 2 The effect of n0 on V,:
FIGURE 1 The effect of C, on V,:
C,=Q.\, F0=100ml/g
no=4, F0=100ml/g 120
120
100 80 E
60 40 20 0 0
20
40
60
80
100
120
V0(ml/g) FIGURE 3 The effect of Vo on V,: »0=4, C;=0.1M
FIGURE 4 The effect ofpH on V,\ no=4, C,=0.1M
The Verify for the Optimal Condition The hydration process is operated under the condition pH=9.3 and F0=10ml/g.
826
Manufacture of Potassium Titanate Whiskers
When the equilibrium is approached, the solids are filtered and calcinated at 800 °C. Figure 5 shows the X-ray powder diffraction patterns of the solids after the calcinations. It is clear that the products are almost pure PTW. The SEM of products (Figure 6) also shows that the whisker morphology is unchanged.
7* ///Jr.'-'if 10
20
30
40
50
60!
2 theta FIGURE 5 XRD patterns of products • : ?TW,pH=9.3,
F0=10ml/g
FIGURE 6 SEM of products pH=9.3, F0=10ml/g
CONCLUSIONS Ionic exchange equilibrium and mass balance in the hydration are integrated to establish a predictive model describing the conditions of the hydration process. The results show that the aimed product can be controlled mainly by pH during hydration. The amount of water (Vo) is reduced to 1/10 comparing with the literature. The optimal condition for preparation of PTW is pH=9.3 and Vo=lOmVg. The pH and water volume are both controlled easily in a large scale. ACKNOWLEDGMENTS Authors appreciate the Outstanding Youth Fund of National Natural Science Foundation of P. R. China (29925616) and National High-tech Research Development Program(863 Program: 2003AA333010) and Natural Science Foundation of P.R. China (20246002, 20236010).
REFERENCES 1. 2. 3. 4. 5.
Lu, J. Z., and X. H. Lu. 2001. "Elastic Interlayer Toughening of Potassium Titanate Whiskers-Nylon66 Composites and Their Fractal Research," /. Appl. Polym. Set., 82(2):368-374. Clearfield, A. 1988. "Role of Ion Exchange in Solid-State Chemistry," Chem. Rev., 88(1): 125-148. Izawa, H., S. Kikkawa, and M. Koizumi. 1982. "Ion Exchange and Dehydration of Layered Titanates, Na2Ti3O7andK2Ti4O9," J. Phys. Chem., 86(25):5023-5026. Sasaki, T., M. Watanabe, Y. Komatsu, and Y. Fujiki. 1985. "Layered hydrous titanium dioxide: potassium ion exchange and structural characterization," Inorg. Chem., 24(14):2265-2271. Harada, H., Y. Kudoh, Y. Inoue, and H. Shima. 1995. "Synthesis and evaluation of potassium hexatitanate fibers with negligible leachability," J. Ceram. Soc. Jpn., 103(2): 155-161.
Manufacture of Potassium Titanate Whiskers
827
Lee, C. T., MH. Urn, H. Kumazawa. 2000. "Synthesis of titanate derivatives using ion-exchange reaction,"/ Am. Ceram. Soc, 83(5): 1098-1102. Bao, N. Z., X. H. Lu, X. Y. Ji, X. Feng, and J. W. Xie. 2002. "Thermodynamic modeling and expertimental verification for ion-exchange synthesis of K2O.6TiO2 and TiO2 fibers from K2O.4TiO2," Fluid Phase Equilibria, 193,(1-2): 229-243. He, M , X. Feng, X. H. Lu, X. Y. Ji, C. Liu, N. Z. Bao and J. W. Xie. 2003. "The application of Ion-exchange Model for the Synthesis of Derivatives of K2Ti4O9 fiber," J. Chem. Eng. Jpn., 36 (10): 1259-1262. Ji, X. Y , X. Feng, X. H. Lu, L. Z. Zhang, Y. R. Wang, and J. Shi. 2002. "A Generalized Method for the Solid-Liquid Equilibrium Stage and Its Application in Process Simulation," Ind. Eng. Chem. Res., 41(8):2040-2046.
What Darcy Really Meant - the Truth on Permeability Georg Bechtold Deutsche Forschungsgemeinschaft, 53175 Bonn, Germany
ABSTRACT This paper points up a common misunderstanding in the fields of liquid composite moulding. If during an injection process of a fibre architecture the fibre volume content is increased, e.g. by applying transverse load or by shearing the textile fibre architecture, the flow permeability is influenced. However the direction of this influence is controversial. At first, the relevant equations are presented and their application is explained. Then, a simple injection case is calculated and the result is interpreted. After that, flow through a sheared fibre bed is regarded. It is finally concluded that an increase in fibre volume content usually decreases the apparent permeability. However, for sheared fibre beds and low fibre volume contents, the shearing increases apparent permeability.
INTRODUCTION Most production processes of composite materials require filling of fibre bundles by liquid matrix. Simulations of such fill processes are usually based on the continuity equation and on Darcy's law. Darcy's law was originally deduced from liquids flowing through sand beds and it has the mathematical characteristics of a typical transport equation with material constant viscosity and geometrical constant permeability. The permeability is strongly dependent on the fibre volume content. It is obvious that at increasing fibre volume content (e.g. by compression of the fibre architecture; relevant for many composite material processing methods), the resistance against flow increases. However, also the open cross section for the fluid decreases, resulting (assuming the fluid to be incompressible) in a higher flow speed, if the inlet pressure remains constant. Question now is, does the increase of fibre volume content increases or decreases the apparent permeability? THEORETICAL BACKGROUND Darcy's law was first presented in 1860 [1] and it correlates the "flow resistance", the pressure and the flow speed of a liquid through a porous medium. It has the form of a common transport equation:
* Corresponding Author, Deutsche Forschungsgemeinschaft. Kennedyallee 40, 53175 Bonn, Germany, fax ++49 228 885 2777, [email protected]
What Darcy Really Meant - the Truth on Permeability
829
with q being the flow rate (i.e. the volumetric flow divided by the cross section of the porous medium perpendicular to the flow), t] the viscosity of the medium, p the pressure, x the direction of flow and K the permeability of the porous medium. A common source of misunderstanding is q. It is often confused with the apparent flow speed, i.e. the velocity v/of the flow front seen from a position perpendicular to the porous medium. However it can be easily converted by the Dupuit-Forchheimer equation [2], taking into account the free flow space by introducing (in the case of fibre beds) the fibre volume content <§7V: (2) It is obvious, that the permeability K depends on the fibre volume content. Furthermore, at a constant fibre volume content, it makes a difference if few large diameter fibres or many small diameter fibres are present. These interrelations are included in the Kozeny-Carman equation (clear deduction in [3]):
with TF the fibre radius and KQK the so-called Carman-Kozeny constant. From a physical point of view, in fact KQK is not constant but depends on many other parameters [4]. However for applications in engineering problems, for unidirectional fibre beds KCK is usually taken to be 10 for flow perpendicular to the fibre direction and to be 0.5 in the parallel case [5]. Such, it becomes clear that the permeability becomes a tensor and the flow rate a vector, if three-dimensional non-isotropic cases are considered [2]. For the purpose of this paper however, an easy one-dimensional mathematical model is sufficient. UNIDIRECTIONAL MOULD FILLING WITH CONSTANT PRESSURE As an illustrating example, injection of a flat mould with a linear gating is regarded, see Figure 1. The pressure at the resin inlet is kept constant. The flow front position is abbreviated as x/. For incompressible media, the equation of continuity yields
Let Pi be the injection pressure. The pressure at the flow front equals to 0. Equation (4) can then be integrated and yields X
xf
What Darcy Really Meant - the Truth on Permeability
830
Flow front position Resin inlet fibre bed Wet
FIGURE 1 Linear injection with flow in one direction
Darcy's equation combined with the Dupuit-Forchheimer assumption yields the following equation for the velocity of the flow front: K
dp
dt
(6)
dp can be obtained by equation (5), leading to the position of the flow front dx depending on time:
x
(t)=
Pit
(7)
-Pi
(8)
and such K
vAt) =
After inserting the Kozeny-Carman equation in (8), for v(t) results r2P r
Fri
with y =
(9)
— . In other words, the flow front velocity only depends on the time
and on y, as any other magnitudes are constant, y is now derived after the fibre volume content, eventually leading to dy
1
(10)
What Darcy Really Meant - the Truth on Permeability
831
This expression is smaller than 0 for any £,Fv. Therefore, with increasing fibre volume content, v/ decreases, as y in equation (9) decreases. Coming back to equation (1), at a constant dp/dx, q has also a lower value, and that means that K, let's call it the apparent permeability in that case, also has decreased compared to the uncompressed state.
PRACTICAL EXAMPLE: FLOW THROUGH SHEARED TISSUE In this section, the flow through a sheared fibre bed should be described. Starting point is a 0°/90° tissue with the same quantity of fibres in both directions. This tissue is then sheared to 0°/45°. Such a process is quite common in textile composite processes and is shown in Figure 2.
Shearing
FIGURE 2 Fibre architecture before and after shearing by 45°
During the shearing process, the fibre volume content and also the Carman-Kozeny constant change: Epv is increased to 42 fyv. KCK is more difficult to explain. As mentioned above, KQK is 10 in the 90° case and 0.5 for 0°. For angles in between both values, a sinusoidal curve as shown in Figure 3 below is assumed. The curve can be described by the equation Kr.
(11)
K CK <9)
0.5
FIGURE 3 KCK dependent on fibre angle q>
This results inKQK45° = 5.25 and KQK22.50 = 1 -9.
832
What Darcy Really Meant - the Truth on Permeability
Following Advani [6], KCK is the arithmetic mean of KCK of the single layers. In Table 1, some possibilities of flow through unsheared and sheared tissue and the resulting KCKS are shown. Assumed is that both main directions of fibres do have the same number of layers. Besides the first unsheared case, most relevant is the last case, because the flow will take the path with the lowest resistance, which corresponds to an effective layup of ±22.5°. Resulting KQK is then 1.9. TABLE I KCK values for different flow cases Flow Case
KCK *^CK9tf
'-^Ci
^-5.25
2
^-2.875
K
CK
2
^ = 7.625
KCK =
+K•CK225°
-1.9
With the presented data, the change of flow speed v* of the sheared tissue related to the one before shearing can be calculated quite simply by the aid of equation (9): the flow speed after shearing is divided by the flow speed before shearing. Results are shown in Figure 4. It can be seen that at low fibre volume contents, after shearing, the effect of decreasing KCK overbalances the increase in E,Fv and at higher fibre volume content, the increase of §?v due to shearing dominates. > 1.2
o 0) a
1
(0
I
0.8
o
0.4
Q>
0.2
o03
o
0.6
0.1
0.2
0.3
0.4
0.5
Original Fibre Volume Content 4FV FIGURE 4 KCK dependent on fibre angle cp
0.6
What Darcy Really Meant - the Truth on Permeability
833
CONCLUSIONS The parameter "permeability" is often diffuse. A common dispute is, how a compression of a fibre bed influences permeability. One position is, that decreasing fibre interspace increases flow speed and therefore the apparent permeability, the other position is that decreasing fibre interspace increases the flow resistance and therefore decreases permeability, hi this paper, the following assumptions were made: injection pressure is always constant, the Kozeny-Carman expression is valid to determine permeability, the Kozeny-Carman constant has a value of 10 at flow perpendicular and a value of 0.5 at flow parallel to the fibres, at flow oblique to the fibres, the value of the Kozeny-Carman constant follows a sinusoidal curve, layups with layers result in a simple arithmetic mean value of the layer's Kozeny-Carman constants, - the total height of unsheared and sheared layup is constant. These assumptions lead to the following "truth": Increasing the fibre volume content leads to a decrease in flow speed and therefore a decrease in apparent permeability. Shearing of a 0°/90° fibre layup to 0°/45° leads to increased flow speed and apparent permeability if the original fibre volume content was below about 25% and leads to decreased flow speed and apparent permeability at higher initial fibre contents. This conference paper serves as a basis for a more detailed journal paper, comparing this completely theoretical discussion with experimental results. REFERENCES 1. 2. 3. 4. 5.
6.
Darcy, H., 1856, Les Fontaines Publiques cle la Ville de Dijon. Dalmont. Scheidegger, A.E. 1974. The Physics of Flow Through Porous Media. University of Toronto Press. Astrom, B.T., R.B. Pipes and S.G. Advani. 1992. "On Flow Through Aligned Fiber Beds and its Application to Composites Processing," Journal of Composite Materials, 26 (9):1351 — 1373. Bechtold, G. and L. Ye. 2003. "Influence of Fibre Distribution on the Transverse Flow Permeability in Fibre Bundles," Composite Science and Technology, 63 (14):2069-2079. Lam, R.C. and J.L. Kardos. 1991. "The Permeability and Compressibility of Aligned and Cross-plied Carbon Fiber Beds During Processing of Composites," Polymer Engineering and Science, 31(14):1064- 1070. Advani, S.G. 1994. Flow and Rheology in Polymer Composites Manufacturing. Elsevier.
Study on Re-pull Force in Pultrusion Processes— I. Experimental Observations Cherryn Smith , Brent Johnstone Research and Development Hawker de Havilland Pty Ltd, 361 Milperra Rd, Bankstown, NSW 2200, Australia Meng Lu, Lin Ye, Yiu Wing Mai CAMT, School of Aerospace, Mechanical and Mechatronic Engineering (J07) The University of Sydney, NSW 2006, Australia
ABSTRACT This paper presents experimental observations of re-pull force which was assessed in conjunction with the validation of a numerical model to predict pull-forces in the pultrusion process. The re-pull force was measured after a previously pultruded composite component was placed into a pultrusion die and re-pulled, with a period of delay of several days. Five re-pull experiments were conducted on the same composite component, under similar heating conditions. It was observed that the re-pull force, which was quite large during the first run, gradually decreased with each re-pull. The heat of reaction for the composite was also found after each experiment, providing information on the degree of cure at each re-pull stage. INTRODUCTION Pultrusion is an automated process for manufacturing continuous fibre-reinforced components with constant cross-section. It is probably one of the most efficient composite processes, and has been demonstrated to be the manufacturing method with the lowest cost in comparison to others for the components in question. In the pultrusion of composite components, there are several critical factors, including material preform in-feed, material forming, resin impregnation, temperature profile of die-heating, as well as the pull forces required during processing, etc, that control the quality and success of the products [1-3]. Particularly, of these issues, controlling the build-up of pull forces and understanding the relevant mechanisms are of major concern to all pultraders. This is because reducing the pull forces allows the use of smaller, less costly manufacturing equipment, and reduces damage and distortion to the pultruded products. Pull force is an easily measured (and almost always monitored) processing parameter that can also be used to quantify other aspects of processing when a corresponding relationship has been established. Pull force can therefore be used as a process indicator and parameterisation can also extend its usefulness into quantifying other non-measurable processing changes. Previous studies demonstrated that the pull force is highly dependent on the state of the matrix and the pressure profile inside the die [4-7]. Briefly, according to the state of the resin, there may exist four basic zones characterising the major internal regions in the *Correspondence Author, Research and development, Hawker de Haviland Pty Ltd, 361 Milperra Rd, Bankstown, NSW2200, Australia; E-mail: [email protected]
Re-pull Force in Pultrusion Processes -I. Experimental Observations
835
die. These are 1) tapered section zone (if any); 2) expansion zone; 3) gelation/postgelation zone; and 4) release zone. Previous models have all stated that in the gelation/post-gelation region, primary contributions to the pull force disappear. After this point, the effect of shrinkage overwhelms that of thermal expansion, and the pultruded component detaches from the die wall (the release zone). This results in no further contribution to the pull force. During experimental validation of a computational model designed to predict pull force in the pultrusion process, it was found that there may still exist contributions to the pull force in the release zone. The aim of this paper is to show that the pull force predictions based on the above-mentioned analysis may not always be correct. The results presented in this paper indicate that, when a composite component is placed into the pultrusion die and re-pulled after it has already been pultruded, significant re-pull force may still be observed, which is against the theoretical predictions as addressed above. EXPERIMENT Pultrusion Process Figure 1 illustrates a schematic representation of the pultrusion process. A pultrusion machine normally consists of creels for feeding dry fibres, preform fixtures for fiber alignment, a resin injection die which is integral with the main die (another method of resin delivery is the resin tank as shown in Figure 1), a main heated forming die for consolidation and curing, synchronized pulling mechanisms for pulling the cured composite component and a cut-off saw to cut parts to the desired length. During processing, continuous layers of mat and roving are passed from creels and pulled simultaneously through the preform fixtures that align and contour them to the desired shape. If the resin tank method is being employed, the fibres are drenched in resin before entering the preform fixtures. However, for this set of experiments the direct resin injection method is used. The preformed fibres are then pulled through the injection die where they are impregnated with resin. The fibres and uncured resin (either from resin bath or direct injection into a pre-die) then pass through the heated die, are consolidated and cured to the final cross-section of the composite component. Resistance of pulling force
pulling force
FIGURE 1 Illustration of the pultrusion process
The heat from the die wall initiates an exothermic chemical reaction in the resin, therefore causing the matrix to cure and increase in viscosity. The cured component is extracted at a uniform speed from the die by a set of pullers. The finished component exiting the die is a solid and well-formed product.
836
Re-pull Force in Pultrusion Processes - I . Experimental Observations
Re-pull Experiment During a pultrusion process the pull force can be measured using on-line transducers. Three sorts of transducers were used in these experiments: a load pin, rear gripper and front gripper. The specimen was a carbon fiber/epoxy resin composite component, with a high fiber volume fraction. The part was initially pultruded in a simple slat die, 4mm thick and 77 mm wide. Figure 2 gives the measurement of the pull force during the initial pultrusion. Note that only the results measured by the rear and front grippers have been included in the figure, the result recorded by the load pin has been removed for an easy to read graph. It should be noted that on exit from the die, the composite slat is a solid product, though not fully cured.
— • Rear Gripper o
Front gripper
a. To o
"3> c a>
0.00
0.20
0.40
0.60
0.80
1.00
1.20
1.40
1.60
Time (hours) FIGURE 2 Measurement of pull force during the initial pultrusion process
After the initial pultrusion, and after a certain period of time, the partially cured slat was placed into the die and "pultruded" again (re-pulled through a heated die). The die temperature profile, pull speed and other pultrusion parameters remained the same as in the initial pultrusion. Figure 3 illustrates results of the first re-pull experiment. The average re-pull force measured was around 85% of the initial pull force. Note, the pull force starts to decrease from time=0.8 hours. This was due to the end of the composite slat entering the die, and therefore reducing the contributions to the pull force. Also, for the initial period of time the pull force was higher. This was because the beginning of the slat was left sitting in the die during heat-up, thereby altering the state of the matrix. It follows that until this initial section was pulled from the die, the results are not indicative of the experiment as a whole.
Re-pull Force in Pultrusion Processes -I. Experimental Observations
837
— Rear gripper
2o
— • Front gripper
c
o
a c V
Vc o
0.00
0.20
0.60
0.40
0.80
1.00
1.40
1.20
1.60
Time (hours) FIGURE 3 Measurement of re-pull force during the first re-pull experiment
This experiment was repeated five times. The composite slat, which now had a higher degree of cure, was again re-pulled through the heated die. As before, the same temperature profile, pull speed and other pultrusion parameters remained. It was found that after repeating the experiment several times, with the same composite slat and the same experimental conditions, the re-pull force decreased. Figure 4 shows the results of the sixth re-pull of the composite slat. It can be seen from this figure that the average re-pull force had decreased to about 30% of the initial pull force. — - Rear gripper — Front gripper
Q.
75
o 'at
c a
:u
—t— V_,
U M'T 0.00
0.20
0.40
0.60
0.80
a
fS , I
1.20
1.40
u
J L 1.00
1.60
Time (hours) FIGURE 4 Measurement of re-pull force during the sixth re-pull experiment
Figure 5 shows the variation in pull force from each re-pull experiment. It can be seen from the experimental data, that from the 3rd re-pull, the pull force stabilised and maintained approximately 30% of the initial pull force. It should be noted here that the pultrusion machine used in these experiments registered a "free" pull force of approximately 20% of the initial pull force. Therefore, each result had incorporated this free pull force.
Re-pull Force in Pultrusion Processes - I . Experimental Observations
838
LU initial pull force
.LFOR
o
§§§
B
HI
I• •I
_i
Q. <
NON-DIIWENSIOf
85%
11
40%
11
§§§| IrajsfHH
—^Sl—
0
1
2
30%
—mil— 3
30%
30%
30%
4
5
6
I 11
RUN SEQUENCE OF RE-PULL EXPERIMENTS FIGURE 5 Variation of re-pull force
Further investigation revealed that the variation of re-pull force was closely correlated with the evolution of degree-of-cure. After the initial pultrusion, and after each re-pull, a sample was taken from the slat and the residual enthalpy of reaction was found. Figure 6 shows the enthalpy of reaction during each re-pull experiment. Since the enthalpy of reaction is inversely proportional to the degree-of-cure, the result shown in Figure 6 implies that a low degree of cure (higher enthalpy of reaction) will result in a higher pull force being produced. From the 3rd re-pull the composite slat was fully cured (zero enthalpy of reaction) and, correspondingly, the re-pull force was stabilised.
O
I <
h z <
o55 2tc z
Ul
S
9 z o
1
2
3
4
5
RUN SEQUENCE OF RE-PULL EXPERIMENTS FIGURE 6 Enthalpy of reaction
Re-pull Force in Pultrusion Processes -I. Experimental Observations
839
CONCLUDING REMARKS The occurrence of a re-pull force shown in the experiment presented in this paper was not well explored in earlier theories. This effect is probably more prevalent with epoxy resins which generally have slower reactions and less shrinkage in comparison to the more widely practiced pultrusion of polyester and vinyl-ester resin systems. Thus, a new mechanism needs to be incorporated into the computational models of pultrusion processes so that the pull force can be more accurately estimated. The mechanism behind the re-pull force will be addressed in part 2 of this present study. Pull force during the initial pultrusion can vary widely due to the number of process interactions involved. However, during re-pull the number of interactions is greatly decreased, so there can be some confidence in the repeatability along the length of the slat in comparison with the initial pultrusion. Only one re-pull trial has been carried out to date and therefore, these results have not yet been repeated and verified. More work needs to be undertaken to fully understand the origin and mechanism of this re-pull force. In context with the numerical model, there needs to be some understanding of the interactions between the gelation/post-gelation zone; and release zone in order to produce a model which accurately predicts the many interactions and contributions to the pull force during the pultrusion process. ACKNOWLEDGEMENTS This work is supported by ARC Linkage SPIRT project. The authors are grateful for this support. REFERENCES 1. 2.
Gutoski, T.G. 1997. Advanced Composites Manufacturing, John Wiley & Sons Inc., New York. Sumerak, J.E. 1997. "The Pultrusion Process for Continous Automated Manufacture of Engineered Composite Profiles," in Composites Engineering Handbook, P.K.Mallick, ed. M.Dkker, New York. 3. Fanucci, J.P., S.Nolet and S.McCarthy. 1997. "Pultrusion of Composites," in Advanced Composites Manufacturing, T.G.Gutowski, ed. John Wiley & Sons Inc., New York. 4. Moschiar, S. M., M. M. Reboredo, H. Larrondo, and A. Vazquez. 1996. "Pultrusion of Epoxy Matrix Composites: Pulling force Model and Thermal Stress Analysis," Polymer Composites, Vol. 17, pp.478-485. 5. Suratno, B. R. L. Ye, and Y. W. Mai. 1998. "Simulation of Temperature And Curing Profiles in Pultruded Composite Rods," Composites Science and Technology, Vol. 58, pp. 191-197. 6. Chachad, Y.R., A.Roux and J.G.Vaughan. 1995. 'Three-dimensional Characterisation of Pultruded Fibreglass-Epoxy Composite Materials," Journal of Reinforced Plastics and Composites, Vol. 14, pp.495-512. 7. Z. Ding, L. Xu, S. Li, and L. J. Lee. 2003. "Experimental and Theoretical Analysis of Pulling Force in Pultrusion and Resin Injection Pultrusion (RTP) - Part II: Modelling and Simulation," Journal of Composite Materials, Vol. 37, No. 3, pp. 195-216.
Study on Re-pull Force in Pultrusion Processes— II. Theoretical Analysis Meng Lu , Lin Ye, Yiu Wing Mai CAMT, School of Aerospace, Mechanical and Mechatronic Engineering (J07) The University of Sydney, NSW 2006 Australia Cherryn Smith, Brent Johnstone Research and Development, Hawker de Havilland Pty Ltd 361 Milperra Rd, Bankstown, NSW 2200, Australia
ABSTRACT An attempt is made in this paper to give a qualitative interpretation to the experimental observations of the re-pull force which has been presented in Part I. A mechanistic model is established which assumes that a pultruded composite component, which is not fully cured, will experience a creeping expansion due to the de-compaction of fiber reinforcement in the release zone. It is shown that such expansion, under certain conditions, may overwhelm the effect of resin shrinkage, and cause a considerable contribution to the pull force. Thus, the model established in this paper is expected to characterize, at least partially, the relevant mechanisms behind the pull force. INTRODUCTION hi Part I of this study it was demonstrated that, when a composite component is placed into a heated pultrusion die and re-pulled, after it has already been pultruded, a considerable re-pull force may be observed [1]. This result is against what earlier theories predicted [2-6]. According to these theories, a pultruded composite component may have four different states in the interior of the die that can be defined by four regions. These are 1) tapered section zone (if any); 2) expansion zone; 3) gelation/postgelation zone; and 4) release zone. Based on these theories, the primary contribution to the pull-force is friction, up to and including the gelation/post-gelation zone. In the release zone, resin shrinkage occurs and the surface of the component being pultruded separates from the die wall, resulting in no further contribution to the pull-force. Clearly, these models are not able to account for the phenomenon of re-pull force. The occurrence of a re-pull force suggests that its influence may have to be taken into consideration when the temperature profile is varied to pursue a more efficient process. Such temperature distributions could lead to a significant increase in pull force and therefore require larger pull equipment. Thus, it is important to understand its mechanism when optimization of processing conditions is pursued. The present paper attempts to establish a mechanistic model to interpret the experimental observation of re-pull force presented in Part I. Regarding the deformation of the composite component being pultruded. Earlier theories merely consider two •"Correspondence Author, CAMT, School of AMME (J07), The University of Sydney, NSW2006, Australia; Fax: 61-2-9351 3760, E-mail: [email protected]
Re-pull Force in Pultrusion Processes - II. Theoretical Analysis
841
effects, namely, the thermal expansion due to the heating of the die and resin shrinkage due to the increase in degree-of-cure. The model established in this paper adds a third effect—the creeping expansion due to the residual stresses in the compacted fiber reinforcement in a partially-cured resin. It is shown that, with the introduction of such an effect, the re-pull force can, though only qualitatively at this stage, be characterized. THEORETICAL CONSIDERATION OF RE-PULL FORCE Internal Profile for Initial Pultrusion As demonstrated in previous studies [2-6], when a composite component is first pultruded, four major regions can be defined. These are: (i) the taper section region; (ii) the expansion region; (iii) the gelation/post-gelation region; and (iv) the release region. After the resin is injected into the die (either before or after the taper section), it will first experience thermal expansion as the die is heated. On the other hand however, with the increase in degree-of-cure, the resin also gradually shrinks. Thus, the total deformation of the composite component is subjected to two competing effects—thermal expansion and shrinkage. When the degree-of-cure is below a certain value (this value may differ for different resins), the thermal expansion of the resin is larger than the shrinkage. Therefore, it produces pressure on the wall of die and results in friction that resists the pulling of the component. However, after further increase in the degree-of-cure, the resin will continue to shrink and finally the effect of shrinkage overwhelms that of thermal expansion. Then, according to previous theories, the composite component enters the release zone, where the surface of composite starts to separate from the die wall. The friction disappears, resulting in no further contributions to the pull-force. Unlike the earlier studies in which only thermal expansion and shrinkage effects are considered, an additional deformation mechanism is introduced here. Without it, the observation of re-pull force would be difficult to interpret. This deformation is caused by the creeping behavior of the resin under the de-compaction of the fiber reinforcement. This originates from the relaxation of the residual stresses that were caused by consolidation of the fibers. Internal Profile in Re-pull Operations In comparison with the aforementioned configuration for the initial pultrusion process, the internal profile during a re-pull does not have the gellation/post-gellation zone, as the resin is now in a solid state inside the die. Thus, all the effects associated with backflow, viscous drag, and compaction of fibres in the taper section do not exist. Instead, the main concern is now focused on the dry friction between the surface of the composite component and the die wall. As the composite is still only partially cured at this stage, resin shrinkage is still taking place. This allows the creeping expansion to occur, incurring a pressure on the die wall. The pull force produced by this effect is dependant on the degree of cure and the internal stresses developed within the composite. Creeping Expansion Model A simple slat die during a re-pull is considered here. Since, in typical slat configurations, the thickness dimension is considerably smaller than the width, we may as a first order approximation merely consider the variation in deformation of the slat in thickness. In this way, we can establish a simple one-dimensional model.
842
Re-pull Force in Pultrusion Processes - II. Theoretical Analysis
Suppose after the initial pultrusion, the composite slat is not fully cured. Then it can be dealt with as a viscoelastic medium which may be described by the Kelvin constitutive law a = Es + t]s (1) where a denotes stress and s is strain, while E and r\ are Young's modulus and viscous coefficient of the resin, respectively; s = dsjdt is the strain rate. To obtain the average deformation in thickness and load, we invoke the concept of representative volume element, which is schematically illustrated in Figure 1. Let, Ar and Vr be the surface and volume of the representative volume element, respectively, and Vr = Vmatrlx © Vflbre, in which Fmflfra is the volume occupied by the matrix while Vf,t,reis the volume occupied by fibres. Thus, under the traction of an external force F and the de-compaction force f\decom, the total deformation of the slat in thickness can be expressed by F + Lecom=fV+L(2) Then, we have
F/A,
(3)
Jv =
along with the model shown in Figure 1 and Eq. (2). Let the external force F vanish in the following analysis, since here what we are concerned with is \hefree deformation of the slat subject to the traction of de-compaction pressure p
F
/,
fe
FIGURE 1 Illustration of a representative volume element and an equivalent model
Note that
Letting e = — [£•(.*:, ^)iv denote the volume average strain and using Eq. (4), Eq. (3) can be reduced to (5)
Re-pull Force in Pultrusion Processes - II. Theoretical Analysis
843
Here, juf = Vflbre jVr denotes the volume fraction of the fiber, hi the one-dimensional case nf =L{ jL, where Lf denotes the effective thickness of the fiber reinforcement and L is the current thickness of the slat. Note that Lf remains unchanged as the compressibility of the fiber is ignored. The relationship between the average strains, and the fiber volume fraction juf, can be obtained in the following way. Let Lc denote the reference thickness, which corresponds to the fiber volume fraction fif , while juf is the critical fiber volume fraction below which the fiber reinforcement is unable to carry substantial load. Then,
e = (L-Lc)/Lc and
Since Lc /L = (L/Lc)'' = (L/Lc -1 +1)'1 =(e +1)~', one finds ff, (7) fc The viscous coefficient rjm of the resin is strongly dependent on temperature Tand the degree-of-cure, a, which may be expressed with [4,7] rim=Voexp{AlT + Ba) (8) where rjg, A and B are material constants. Young's modulusEm, of the resin should also be related to temperature and the degree-of-cure a . Unfortunately, the relationship among E, a and T is not available and therefore we have to take an assumed form in this study. Suppose that the dependence of E on T and a follows a similar law as the viscous coefficient r\m, namely, Em=Eoexp[C/T + D{a-ao)] (9) where, Eg, C and D are material constants, and a0 is the initial degree-of-cure with which the resin commences to possess elasticity. That is, E
= Eo.
Regarding the dependence of E on T, unlike the resin viscosity, which is extremely sensitive to variations of temperature, it is relatively weak and therefore we may approximately take C « 0 . Then, leti?| _ = Ea, where Ex is the ultimate Young's modulus of the resin corresponding to a = 1, the material constant D, can readily be obtained by D = (amax - ag )ln Ex
jE0.
The evolution law of degree-of-cure has different forms and we choose the following form [6]
*SL dt
JA<\
{ RT
-ay
(10)
where kg, AE and n are material constants, and R is the universal gas constant. The relationship between p ^ ^ and /j.f can be obtained in terms of consolidation experiments [7], and for many fiber reinforcements an empirical expression P., =-Paexp\uf - ur)lcA (11) can approximately be used. Here,/>o and cv are material constants with po usually being 1 atmosphere pressure.
844
Re-pull Force in Pultrusion Processes - II. Theoretical Analysis
We can readily obtain the relationship between p\ and strain £ by virtue of Eqs. (7) and (11). Given the variation of temperature with time, one is now allowed to evaluate the dependence of strain on time using Eqs. (5) and (7)-(l 1). For this purpose, suppose that the degree-of-cure of the resin, after the initial pultrusion, has reached up to 100-Z%. Suppose that the pultruded slat is placed in a room temperature environment for a certain period of time and then is placed again into a heated die for re-pulling: Note that under the conditions that the pulling speed, vpun, is steady and the influence of exothermal reaction of resin is neglected, we may shift t to / with t = l/vpilll, where / represents the distance to the entrance of the die. Then, each representative volume element of the slat is equivalently experiencing such a thermal history described below, shown in Figure 2.
T=T0forl
-tJ-t -t,)-t -t2)-t
+ fr-iT, -T0)/{tl + [T2 -{T2 -Tj)/(t2 + [T3 -{T3 -T2)/(t3
-to)-to] -t,)-t,] -t2)-t2]
for t0 < t < t,; for t, < t
r2
1.6T0
T
JON-D MENSIONAL H T E M P ERATURE
1.5T0
I
\
1 t2
O.E+00
1.E+03
2.E+03
tsj 3.E+0:
u
1x10 3 4.E+03
2x10 3
'i
3x10 3
TIME [s]
TIME[S]
FIGURE 2 Equivalent temperature history that each material element experiences
FIGURE 3 Variation of creeping strain with time
Using generic parameter values (many of them are obtained from [3]-[8]), the computational result for £ is illustrated in Figure 3. It can be seen from this figure that the slat commences to have creeping expansion immediately after the initial pultrusion process. This deformation, as evaluated later, may indeed become a source for yielding a significantly large re-pull force. In fact, after the dependence of strain e(t) on time t is obtained, we can evaluate the resultant friction force. Note that in doing so, the transformation l=vpuii t is again used. Thus, the pressure exerted on the wall of die can be written as P(l) = Ec {{l - nf [e{l)}\k(T{l) -To)- 7a(lj\+e{l)\ (11) ignoring the viscous effect. Here, Ec is the effective modulus of the composite slat (laminate), k is the thermal expansion coefficient of the resin, and y is the shrinkage coefficient of the resin, whose values are given above.
Re-pull Force in Pultrusion Processes - II. Theoretical Analysis
845
Accordingly, the re-pull force can be evaluated by F = 2w \$P(l)dl
(12)
where w is the width of the composite slat, LD is the length of the die, and £ is the friction coefficient between the die wall and the composite slat. Using relevant parameters to the experimental conditions, the re-pull force in terms of Eq. (12) yields a value 20% greater than the experimental value of the initial pull force. Using the procedure addressed above and taking the last ultimate values of the strain and degree-of-cure as the initial values of the next run, one is then able to evaluate the re-pull force in the second run. Repeating the same procedure, we can continue to evaluate the re-pull force in the third, forth, as well as any following re-pull runs. However, the computations based upon this procedure indicate that the degree-of-cure will quickly reach up to unity during the first re-pull, and the re-pull forces would vanish in all following re-pull operations. This result does not agree with the experimental observations reported in Part 1, and further work is needed to find why the model fails to predict those results. CONCLUDING REMARKS The model presented in this paper predicts that there may be considerable expansion strain occurring within a partially cured slat after the gelation zone, and therefore proposed a possible mechanism to account for the experimental observation of re-pull force. However, the prediction is very sensitive to the material properties regarding the dependence of viscosity and elasticity of the resin on the degree-of-cure, which, unfortunately are often not accurate for the highly cured case and even not available. ACKNOWLEDGEMENTS This work is supported by ARC Spirt Linkage program. The authors are grateful to this support. REFERENCES 1. 2. 3. 4.
5. 6.
7.
8.
Smith, C , B. Johnstone, M. Lu, L. Ye, and M.Y. Mai. "Study on Re-pull Force in Pultrusion Processes—Part 1. Experimental Observation," to be presented in ACCM-4, July 6-9,2004 Sumerak, J.E. 1997. "The Pultrusion Process for Continous Automated Manufacture of Engineered Composite Profiles," in Composites Engineering Handbook, P.K.Mallick, ed. M.Dkker, New York. Fanucci, J.P., S.Nolet and S.McCarthy. 1997. "Pultrusion of Composites," in Advanced Composites Manufacturing, T.G.Gutowski, ed. John Wiley & Sons Inc., New York. Moschiar, S. M., M. M. Reboredo, H. Larrondo, and A. Vazquez. 1996. "Pultrusion of Epoxy Matrix Composites: Pulling force Model and Thermal Stress Analysis," Polymer Composites, Vol. 17, pp.478-485. Suratno, B. R. L. Ye, and Y. W. Mai. 1998. "Simulation of Temperature And Curing Profiles in Pultruded Composite Rods," Composites Science and Technology, Vol. 58, pp.191-197. Chachad, Y.R., A.Roux and J.G.Vaughan. 1995. "Three-dimensional Characterisation of Pultruded Fibreglass-Epoxy Composite Materials," Journal of Reinforced Plastics and Composites, Vol. 14, pp.495-512. Z. Ding, L. Xu, S. Li, and L. J. Lee. 2003. "Experimental and Theoretical Analysis of Pulling Force in Pultrusion and Resin Injection Pultrusion (RIP) — Part II: Modelling and Simulation," Journal of Composite Materials, Vol. 37, No. 3, pp. 195-216. Gutoski, T.G. 1997. Advanced Composites Manufacturing, John Wiley & Sons Inc., New York.
Influence of Foaming Temperature and Time on the Hardness of Cellular Al-Si-Cu-Mg Alloys MD Anwarul Hasan and Amkee Kim* Department of Mechanical Engineering, Kongju National University, Korea Hyo-Jin Lee Department of Building Service Engineering, Hanbat National University, Korea Seong-Seock Cho School of Materials Engineering, Chungnam National University, Korea
ABSTRACT Micro Vickers hardness was measured on the cell wall of Al-Si-Cu-Mg alloy foams having different compositions and subjected to different foaming temperature and period of time during production. The powder metallurgical route was utilized to obtain aluminium alloy foam. Al-5%Si-4%Cu-4%Mg-l%TiH2 alloy precursor showed higher hardness value than Al-3%Si-2%Cu-2%Mg-l%TiH2 alloy because of higher alloying element. The hardness value was increased with the increase of foaming period of time at all foaming temperatures while foams having same composition but higher foaming temperature showed higher hardness value regardless of material. These might be due to the fine eutectic grain size effect. Local hardness of foams at a-Al grain boundaries and junctions of multiple grains were found to be higher than that inside the a-Al grains. Higher hardness value of eutectic phase and accumulation of eutectic phase near grain boundaries are responsible for this higher hardness value at a-Al grain boundaries.
INTRODUCTION Multi functionality is a key factor for modern engineering materials, metal foams fulfill this requirement by offering a combination of attractive properties such as super light weight, good impact absorption, outstanding sound isolation and high damping properties for attenuation of electromagnetic waves [1]. Recent development and improvements of the powder metallurgical method of aluminum foam production as well as continued fall of relative cost of metallic powders have given rise to renewed interest in the aluminum foam [2]. Some detailed explanations of the powder metallurgy method of foam production are available elsewhere in literatures [3-5]. From the viewpoint of application, mechanical properties of Al-foam are of paramount importance. Works of Ashby, Gibson and Banhart have shown that mechanical properties such as compressive strength are associated with the density of foam [6,7]. Duarte, Weig and Banhart have shown that density of Al-foam is determined by parameters such as alloy composition, the type of foaming agent and its content, the "•Correspondence Author, Department of Mechanical Engineering, Kongju National University, 182 Shinkwan-dong, Kongju Chungnam, 314-701 Korea. Fax: +82-41-854-1449. E-mail: [email protected]
Hardness of Cellular Al-Si-Cu-Mg Alloys
847
heating rate, the mould material as well as shape, and the type of furnace [8]. Thus above parameters as well as the properties and quality of alloy powder, the morphology and distribution of foaming agent, homogeneity of mixture, compaction pressure and time, and the temperature control during foaming process affect the density and hence mechanical properties of produced Al-foam [8,9]. However foams having same composition and same density may have different cell morphology and different micro level properties of cell wall due to different manufacturing parameters which may affect the global mechanical properties of foam. Since the understanding of global properties are based on a hierarchical micro-meso-macro concept of analysis, the micro level analysis must be prior to others. In this paper the influence of foaming temperature and foaming time duration on the microstructure and hardness of aluminum alloy foam with two different compositions has been investigated. Al-Si-Cu-Mg alloy was chosen for its extensive industrial application and well-investigated foaming behavior. EXPERIMENT Materials and Specimen The aluminum alloy powders of the chemical composition of Al-3wt%Si-2wt%Cu -2wt%Mg (322 alloy) and Al-5wt%Si-4wt%Cu-4wt%Mg (544 alloy) were produced by centrifugal atomization [10]. The particle size of alloy powders ranges from 150 urn to 900 |jm, and the shape of alloy powders is ligament. 99%wtAl-Si-Cu-Mg alloy powders and l%wtTiH2 particles were mixed in a rotating V-mixer with a velocity of 300 rpm for 30 minutes. The mixtures were then consolidated by cold compaction at a pressure of 4 MPa and hot extruded into a rod precursor of 12 mm diameter at a temperature of 430 °C with an extrusion ratio of 20:1 by a uni-axial extrusion machine. Foaming of the extruded precursor was performed by heating them in a pre-heated furnace. The pre-set foaming temperature was varied between 650 °C and 800 °C. The foamable precursors without a mould were kept inside the furnace for different period of time at 650 °C, 700 °C, 750 °C and 800 °C respectively. The foaming process was terminated by simply removing the samples with different period of time from the furnace. Specimens of 5 mm thickness for the hardness measurement were cut off from each sample and were mounted into thermo-set epoxy resin of 20 mm diameter x 10 mm thickness. One face of the mounted specimens was polished to mirror surface. Experimental Method Vickers hardness under a test load of 0.98 N and a loading time of 15 seconds was measured at various locations in the precursors as well as cell wall of foam specimens. Such a test load was chosen so that an indentation covers several grains and so a measured value may be considered as a global property of the foam. The spots for measurement were first determined at equal steps along an approximate straight line starting from the center of the specimen toward the skin as shown in figure 1. When the spot did not lie on metal matrix, the next available suitable spot was used. Measurement was taken on at least 10 points for each specimen. ASTM testing standard for micro Vickers hardness requires a minimum distance of 2.5 times the diagonal of indentation from the center of the indentation to the edge of cell wall and a minimum indentation center to center distance of 3 times the diagonal of the indentation. The cell walls in most cases were thick enough to fulfill this standard. In cases, when the wall was not thick enough to fulfill the standard
848
Hardness of Cellular Al-Si-Cu-Mg Alloys •
9085-
•
•
•
8075-
T
T
70v 6560-
• •
322 alloy precursor 544 alloy precursor
5550Distance from Center{mm)
FIGURE 1 Micro Vickers indentation marks on the foam cell wall
FIGURE 2 Hardness of 322 and 544 alloy precursors
requirement, indentations were checked for possible asymmetries and only data from the symmetric indentations were taken to evaluate the hardness. RESULTS AND DISCUSSION Micro Vickers hardness of the 544 and 322 alloy precursors are shown in figure 2. The 544 alloy precursor showed considerably higher hardness value than 322 alloy. This is attributed to the higher content of alloying element in 544 alloy than in 322 alloy, which in other term can be regarded as solution hardening or phase hardening, i.e. the presence of Mg2Si, AI2CU and Si in greater proportion in 544 alloy than in 322 alloy. The chemical composition of the alloys infers that the microstructure contains some size factor compounds such as Mg2Si and AI2CU because of a substantial difference in size between the component atoms [11]. hi 544 alloy the amount of these compounds are higher than that in 322 alloy. Since Si content of the Al-Si system determines the fraction of the a-Al phase, higher content of Si decreases the fraction of the solid a-Al phase [10] and thus increases fraction of eutectic phase. Thus the higher content of Mg2Si, Al2Cu and Si results in the higher fraction of eutectic phase which in turn increases the hardness value. Hardness values of the precursors as well as those of the foam cell walls show significant scatter. The scatter in precursor is apparently originated from heterogeneous distribution of T1H2 particles and the size difference of dispersed T1H2 particles in the alloy matrix, hi both of the precursors the hardness tends to increase from the center of the specimen toward the skin. This would be because after hot extrusion, the cooling rate near the free surface was higher than that of inside, hi foam cell walls scattering in hardness could have several possible reasons: (i) Local heterogeneities in the cell wall due to the specific nature of the material containing oxide inclusions, micro pores etc. (ii) micro structural differences between areas within a grain caused by incomplete homogenization after foaming, (iii) different quenching rates due to non-uniform thermal conductivity in the heterogeneous foam. Average Vickers hardness values of 322 and 544 alloy foam cell walls with foaming time are shown in figures 3(a) and (b) respectively. In the figures, remarkable increase in hardness value is observed with increase of period of time for foaming at a temperature. This is due to the fact that allowing longer period of foaming time in a pre-heated furnace increases the foaming material temperature, hi the range between solidus line and liquidus line, higher temperature increases the liquidfraction.Since the cooling is non equilibrium
Hardness of Cellular Al-Si-Cu-Mg Alloys
5
6
7
8
9
10
11
12
13
14
15
849
3.0
3.5
4.0
4.5
Foaming Titne(min)
5.0
6.0
55
6,5
7.0
7.5
8.0
Foaming Time(min)
(a) (b) FIGURE 3 Foaming time versus Vickers hardness graph for (a) 322 alloy and (b) 544 alloy
4 '€ 40-
/ • • * T
650 °C 700 °C 750 °C BOO °C
'
/
'
/
/ • • T *
/
/ 1.5
5.0
5.5
6.0
6.5
7.0
650 C C 700 °C 750 °C 800 °C 7.5
Foaming Time (min)
(a) (b) FIGURE 4 Results of image analysis from (a) 322 alloy and (b) 544 alloy, showing pore fraction growth with temperature and time
cooling, higher fraction of liquid leads to the formation of higher amount of eutectic phase on solidification (some non equilibrium eutectic phase is formed) and gives higher hardness value. Initially the rate of increase of hardness is very high. However, it decreases gradually until a maximum plateau hardness value is reached. The deceleration of hardness with the foaming period of time may be explained from the phase diagram of Al with Cu, Mg and Si. Since the slop of liquidus line in the phase diagrams is negative and the longer foaming period of time allows the temperature of foam to become closer to the liquidus line, the rate of increase of eutectic phase by increase of liquid fraction decreases, which in turn slows down the increase rate of hardness. Finally when the temperature reaches the liquidus line due to the enough foaming period of time, 100% of the alloy is converted into liquid. Hence further foaming period of time does not increase the proportion of eutectic phase and thus the hardness reaches a plateau value. The increase rate of hardness with foaming period of time is higher at high foaming temperature. This is due to the high heating rate in high temperature furnace and increased diffusion coefficient. Figure 4(a) and (b) represents the evolution of the pore fraction with respect to the foaming period of time in 322 and 544 alloys by the image analysis. Figure 5 represents the hardness of foams with same pore fraction at different foaming temperatures based on figure 4.
Hardness of Cellular Al-Si-Cu-Mg Alloys
850
660
700
720
740
760
Foaming Temperaiure( ° C )
FIGURE 5 Hardness of similar density foams obtained at different foaming temperatures
FIGURE 6 Microstructureofcellwallof322 alloy for 6 min. at 750 °C
The variations in hardness of foams having same density but obtained at different foaming temperatures are very small, which implies that the hardness values of foams with same pore fraction, i.e. same density, obtained at different foaming temperatures are almost same. This is in accordance with findings of Ashby and Banhart that density is the main parameter affecting mechanical properties of Al foam. Besides, longer foaming time periods at low temperatures were able to produce same density foams as ones obtained from shorter foaming time at higher foaming temperature. Moreover these foams showed same hardness value, which means that they have same property. Thus it may be concluded that the time-temperature-superposition concept of G. Wisanrrakkit and J.K. Gilham is true for the hardness of Al-foam. Figure 6 shows a typical microstructure of cell wall of alloy indicating that the cell walls of alloy consist of as-Al phase and eutectic phase. The eutectic phase was found at the grain boundaries and at the junctions of multiple grains, and it contains some Mg2Si, AI2CU, excessive Si particles etc. The presence of these compounds in the eutectic phase is assumed to be the cause of higher hardness value at grain edges and boundaries. CONCLUSIONS Al-Si-Cu-Mg alloy foams were produced using powder metallurgy method. Microstructures were investigated by the digital microscope, image analysis, SEM and EDX mapping. Effect of foaming temperature and foaming time on microstructure and micro hardness was studied. The results are summarized as follows: (1) Al-5%Si-4%Cu-4%Mg-l%TiH2 alloy precursor and foams have higher hardness values than Al-3%Si-2%Cu-2%Mg-l%TiH2 alloy precursor and foams due to higher alloying element effect. (2) At any foaming temperature (in the experimental range) initially the hardness value increases sharply with increase in foaming time because of higher fraction of eutectic phase effect, the increase rate then decreases gradually and finally the hardness reaches a plateau value because the temperature of the foaming alloy reaches the liquidus line. (3) Local hardness near grain boundaries and grain edges were higher than that inside the grains. (4) Similar density foams obtained from same precursor but at different foaming temperature and time showed similar hardness value.
Hardness of Cellular Al-Si-Cu-Mg Alloys
851
ACKNOWLEDGEMENT The authors wish to acknowledge the financial support of the Korea Science and Engineering Foundation by grant No. R01-2002-000-00093-0(2002) from its basic research program. REFERENCES 1.
H. Fusheng and Z. Zhengang, 1999, "The Mechanical Behavior of Foamed Aluminum," J. Mater. Sci., 34:291-299. 2. D. Lehmhus and j . Banhart, 2003, "Properties of Heat-treated Aluminum foams," Mater. Sci. and Eng. A00: 1-13. 3. J. Banhart, 2000, "Manufacturing Routes For Metallic Foams," J. Metal, 52: 22-27. 4. F. Baumgartner, I. Duarte and J. Banhart, 2000, "Industrialization of Power Compact Foaming Prosess," Adv. Eng. Mater. 2: 168-174. 5. I. Duarte and J. Banhart, 2000, "A Study of Aluminum Foam Formation-Kinetics and Microstructure," Acta Mater. 48: 2349-2362. 6. M. F. Ashby, A. G. Evans, N. A. Fleck, L. J. Gibson, J. W. Huchinson and H. N. G. Wadley, 2000, Metal Foams-A Design Guide, Butterworth Heinemann, Boston. 7. J. Banhart and J. Baumeister, 1998, "Deformation Characteristics of Metal Foams," J. Mater. Sci. 33: 1431-1440. 8. I. Duarte, P. Weig, J. Banhart, 1999, Foaming Kinetics of Aluminum Alloys, Metal Foams and Porous Metal Structures, Verlarg MIT publishing, pp. 97-104. 9. F. Simancik, N. Minarikova, S. Culak, Kocacik, 1999, Foaming Kinetics of Aluminum Alloys, Metal Foams and Porous Metal Structures, Verlarg MIT publishing, pp. 105-108. 10. Lee, H. J., Eom, S. H., Song, Y. K. and Cho, S. S. 2003. "The Effects of Aluminum Powder Content and Cold Rolling on The Foaming Behaviors of xAlp/A15Si4Cu4Mg/0.8TiH2 Composites," Material Science and Technology, 19(6): 819-825. 11. R. A.Higgins, 1998, The Properties of Engineering Materials, Viva Books, New Delhi, pp. 153-154.
Forming Characteristics of Aluminium and Glass-Reinforced Thermoplastic Fibre-Metal Laminates Luke Mosse*, Paul Compston, Shankar Kalyanasundaram, Michael Cardew-Hall Department of Engineering, FEIT, Australian National University, Canberra, Australia Wesley Cantwell Department of Engineering, University of Liverpool, L69 3GH, UK
ABSTRACT This study investigates the effects of tooling temperature and blankholder force on the formability of glass-fibre reinforced polypropylene and aluminium Fibre-Metal Laminates (FML). Comparisons between FMLs and monolithic aluminium reveal that FMLs can possess better formability characteristics than aluminium. FMLs demonstrated one third of the springback and one quarter of the channel base curvature of the equivalent aluminium form and surface strains were observed to be considerably lower on bend regions. Finally, it was found that interfacial delamination caused by the stamping process can be eliminated by appropriate choice of blankholder force and process temperature. INTRODUCTION Sandwich structures often consist of alternating thin layers of metal and fibre reinforced polymer-matrix composite or polymers. These hybrid material systems have the potential to tailor the overall mechanical properties of the sandwich structure based on the properties of the constituents. Fibre Metal Laminates (FML) and conventional composite materials have demonstrated success in their usage in low volume aerospace and defence applications. There has been limited use of these hybrid material systems in the high volume industries such as construction, automotive and consumer goods because of long production times. Stamping provides a means of making sheet products at rates ten to hundreds of times faster than any existing fabrication processes for these material systems. The combination of two distinctly different materials in FMLs provides an interesting challenge when applying stamp-forming methods. Much work has been done in developing understanding of the springback phenomenon in metal stamping while investigations into composite forming have revealed spring-in effects and many issues relating to damage and fibre dislocation. Darrow and Smith [1] studied the effects of part thickness, fibre orientation, fibre volume fraction gradients and mould stretching due to thermal expansion differences between the mould and specimen, for carbonepoxy composites. They found that thinner composite specimens demonstrated significantly higher levels of spring-in than thicker specimens and the effects of mould stretching and fibre volume fraction on spring-in were more pronounced for thinner specimens. They also found that fibre orientation has a significant effect on spring-in * Correspondsing author, Department of Engineering, Engineering Building 32, North Road, Australian National University, Acton, ACT, 0200, Australia, Fax: +61 2 6125 0506, [email protected]
Aluminium and Glass-Reinforced Thermoplastic Fibre-Metal Laminates
853
values and this effect varied with specimen thickness. Jain and Mai [2] developed a mechanics based model of anisotropic cylindrical shells for determining spring-in due to resin shrinkage and moisture gradients and verified the model with experimental results. Both methods showed a dependence on the through thickness temperature distribution on the degree of spring-in. Jain, et al. [3] investigated a variety of factors on the degree of spring-in in unidirectional and plain weave carbon epoxy composites. They found that spring-in remained constant for all values of specimen radius to thickness ratios; spring-in decreased with increasing tool angle and spring-in was not affected by lay-up sequence for symmetric lay-ups. Jain et al. [4] applied the findings in [3] to compensate for spring-in effects in the manufacture of an aileron rib from carbon fibre/polyetherimide composite. By determining the degree of spring-in that would result from the necessary processing temperature it was possible to compensate for the spring-in in the tool design. Hou [5] investigated the effect of blank-holder forces on fibre strain and fibre dislocation during stamping of glass fibre and polyetherimide composites. It was found that there is a significant difference in the strain distributions over the dome surface due to fibre orientation and that blank-holder force is a dominant factor in reduction of wrinkling. Polymer-metal laminates used for sound damping purposes consist of alternating layers of metal and un-reinforced polymer. Kim and Thomson [6] found that high forming speed increased the transverse stiffness of the laminate and the degree of spring back and forming at elevated temperatures decreased the rigidity but improved the springback characteristics. Kim and Thomson also studied the laminate separation behaviour of polymer-metal laminates [7] using a combination of four-point bending and tensile tests. They showed that the mode of failure was dependent on the proximity of a free edge and that tensile failure of the adhesive occurred by a void growth mechanism. A synergy of material properties gives FMLs superior mechanical properties to their constituent materials. Similarly, synergies between the forming characteristics of composites and metals in FMLs could result in an increase in formability for the system. Mosse et al. [8] studied the effects of pre-heat temperature and blankholder force on the formability of steel based FMLs. It was shown that it is necessary to pre-heat the FML to the melting temperature of the polymer matrix in order to achieve good formability. Furthermore, it was revealed that the constituent materials in the FML have significantly different load-unload characteristics yet a good quality channel could still be produced. This paper applies an open die, channel-forming test to investigate the effects of tooling temperature, blankholder force and punch and die radii on the formability of aluminium and glass-fibre reinforced polypropylene FMLs. Formability is assessed in terms of the springback of the channel wall, delamination and deflection of the base of the channel. EXPERIMENTAL METHOD FMLs were made in a 2/1, aluminium/composite configuration. The outer layers were 0.5 mm thick 5005 H34 aluminium. The inner layer of the FML consisted of two layers of a commingled 2:2 twill weave glass-fibre/polypropylene composite prepreg (Twintex, Vetrotex) of 745 gsm. The composite was pre-consolidated by heating to 185°C and applying IMPa of pressure. The FMLs were produced by arranging the aluminium and composite layers in a mould, (FIGURE ) A hot-melt polypropylene adhesive (Gluco), recommended for bonding polypropylene and metal, was placed at the bi-material interface. The aluminium surface was prepared with a simple solvent (isopropanol) wipe. The mould was placed in a hot press and heated to 155°C. A thermocouple was used to monitor the temperature inside the mould. At 155°C, a
854
Aluminium and Glass-Reinforced Thermoplastic Fibre-Metal Laminates
pressure of IMpa was applied then the mould was immediately water-cooled. Laminate thickness of 2.25mm was achieved. For channel forming, the laminates were sectioned into 20 x 150 mm strips. Plain aluminium samples were prepared using 2mm thick 5005 H34 aluminium sheet.
20mm 150mm 0. 5mm 5005 Aluminium
c ompos i ie
0 . 0 5 m m p o I y p r o p y ] e oe adhesive
FIGURE 1 Fibre-metal laminate construction
An Enerpac 30Ton press with a 700bar 20 Series pump was used for channel forming. The blankholder rig was integral with the punch and was pneumatically controlled so that the blankholder force would be applied immediately before the sample was punched. The pneumatic pressure was controlled with a SMC solenoid valve controlled on a PC by Lab View. The die consisted of two inserts that could be positioned on the die plate in order to set the desired tool gap. A 3mm tool gap and punch and die radii of 3mm, 5mm and 7mm were used. FMLs were pre-heated to 160°C in the hot-press and the die and blankholder were heated using PID temperature controllers. Channels were formed at tooling temperatures of 80°C and 120°C and blankholder forces of lkN, 3.5kN and 6kN. The formed channels were held in the press for 30 seconds after the stamping was complete before being removed. By varying the temperatures of the blankholder and die, some control of the cooling rate of the FML can be achieved. The tool temperatures should be sufficiently low such that the FML is dimensionally stable when it is removed from the press but high enough to allow the polymer to flow during forming. Three measures were used to assess the quality of the stamped FML (FIGURE 2): (i) the deviation in channel wall angle (A0), referred to as springback, (ii) the curvature of the base of the channel determined from the maximum displacement of the channel base from the bottom of the punch, (iii) delamination severity quantified by measurement of the increase in channel side-wall thickness.
W o 1 I th i c k n e s s increase due lo de i ami nat i on
FIGURE 2 FML channel quality measures
Aluminium and Glass-Reinforced Thermoplastic Fibre-Metal Laminates
855
RESULTS AND DISCUSSION Tool Temperature and Blankholder Force The influence of blankholder force and die and blankholder temperature on springback in channel-formed FMLs is shown in FIGURE 3. For both 80°C and 120°C tool temperatures there is a trend for springback to increase with blankholder force. At the lowest blankholder setting (lkN) and 80°C tooling temperature, springback levels are close to zero. Comparison with plain aluminium shows significantly lower levels of springback for all levels of blankholder force and temperatures.
-80-gtoolTerrp -120SStoolTerrp - Aluninium
3.5 Blankholder Force (kN)
FIGURE 3 Effect of tooling temperature and blankholder force on springback in aluminium-Twintex FML and aluminium
Conversely, FIGURE 4 shows that increasing the blankholder force decreases the occurrence of inter-layer delamination. This is supported by visual inspection of the side-wall region of the channel sections (FIGURE 5). These results suggest that it is likely that forming at higher temperatures would result in a more robust process for a range of blankholder force values.
0.2 n 0.15 0.1 -
i
-120-StoolTerrp
1
3.5 Blankholder Force (kN)
FIGURE 4 Effect of tooling temperature and blankholder force on side-wall delamination in aluminiumTwintex FML
856
Aluminium and Glass-Reinforced Thermoplastic Fibre-Metal Laminates
1
J .1
FIGURE 5 Side-wall of FML. Left- delamination visible, right- no delaminations
FIGURE 6 illustrates the effect of blankholder force and tooling temperature on the curvature of the base of the channels. Decreasing levels of curvature in FMLs are apparent for increased blankholder force whereas curvature tends to increase for aluminium. This indicates that increasing blankholder force improves the conformity of the stamped part to the punch shape without the presence of a normal reaction force that would be provided by a closed die. Inspection of the laminate edge in the base of the channel reveals noticeably more interfacial delamination in all FMLs stamped with low blankholder force.
V 0.005 "L 0.0045| 0.004 •=•0.0035— • — H * tad Temp
2 0.003B 0.0025> 0.002
—•—120ft tod Temp —A— Aluminium
3 0.0015 u 0.001 S 0.0O05 3.5 Blankholder Force (kN)
FIGURE 6 Effect of tooling temperature and blankholder force on channel base curvature
Small Radii Stamping Stamping flat panels with small radii tooling tends to generate higher strains in the bend region than stamping with larger radii. It also increases the degree of work hardening due to the bending and unbending in the side-wall of a channel section. Channels were stamped using 3mm punch and die radii at the blankholder forces found to be optimal for 7mm radii channels at the two tool temperatures, that is, 3.5kN at 120°C and 6kN at 80°C. Both conditions produced similar levels of springback (approximately 0.5°). However the channels stamped at 80°C had close to zero delamination while channels stamped at 120°C had a 1.3mm wall thickness increase. This was consistent with visual inspection of the side-wall.
Aluminium and Glass-Reinforced Thermoplastic Fibre-Metal Laminates
857
Channel Surface Strain Deformation of a circular grid etched onto the blank provides major and minor strain information for the stamped form. FIGURE 7 shows the deformed circles on a bend region for plain aluminium and FML. Based on qualitative evidence, it is clear that the surface strains on a stamped aluminium part are considerably higher than the strains on the surface of the outer metal laminate layer on an equivalent FML part.
FIGURE 7 Circular grid on bend region of channel. Aluminium-left, FML-right
CONCLUSION It has been shown that good formability of glass-fibre reinforced thermoplastic and aluminium FMLs can be achieved with appropriate choice of process conditions. Comparisons between FML and aluminium channel sections reveal that significantly less shape error and lower strain levels can be achieved with the FML system. This would be beneficial to manufacturers because springback compensation is a major part of the die try-out stage in stamp forming operations. Future investigations will focus on the variation of adhesive and composite material behaviours with temperature and the effects of punch feed rate and hold time. REFERENCES 1.
Darrow D.A. 2002. "Isolating components of processing induced warpage in laminated composites," Journal of Composite Materials, 36(21):2407-2419 2. Jain L.K., Mai Y-W. 1997. "Stresses and deformations induced during manufacturing. Part 1: Theoretical analysis of composite cylinders and shells," Journal of Composite Materials, 31(7):672695 3. Jain L.K., Lutton B.G., Mai Y-W., Patton R. 1997. "Stresses and deformations induced during manufacturing. Part II: A study of the spring-in phenomenon," Journal of Composite Materials, 31(7):696-719 4. Jain L.K., Hou M., Ye L., Mai Y-W. 1997. "Spring-in study of the aileron rib manufactured from advanced thermoplastic composite," Composites Part A, 29(8):973-979 5. Hou M. 1996. "Stamp forming of fabric-reinforced thermoplastic composites," Polymer Composites, 17(4):596-647 6. Kim J.K., Thomson P.F. 1990. "Forming Behaviour of Sheet Steel Laminate," Journal of Materials Processing Technology, 22:44-64 7. Kim J.K., Thomson P.F. 1990. "Separation Behaviour of Sheet Steel Laminate During Forming," Journal of Materials Processing Technology, 22:47-161 8. Mosse L., Cantwell W.J., Cardew-Hall M.J., Compston P., Kalyanasundaram S. 2003. "Stamping Analysis of Steel-Composite Laminates", in International Conference on Manufacturing Excellence. Melbourne
Compaction of Single Layer Plain Weave Fabric Preform Zuo-Rong Chen, Lin Ye*, and Teresa Kruckenberg Centre for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering (J07), The University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT A micromechanical model was developed to investigate the compaction behavior of single layer plain weave fabric preform. The compaction model consisted of two submodels: the micro-deformation model of yarn cross-section compacting, and the macro-deformation model of yarn bending. Accordingly, to distinguish the two different deformation mechanisms, the stress in fabric preforms was decomposed into two parts: one was related to the yarn cross-section deformation and compaction in microscopic level, and the other was related to the yarn bending deformation in macroscopic level. Thus, the compaction behavior of single layer plain weave fabric preform was determined by the two different deformation mechanisms. With this micromechanical model, the effect of micro structure of a single layer plain weave fabric on its compaction behavior was investigated. INTRODUCTION Various techniques for manufacturing processes of advanced polymer composites involve the compression of resin-impregnated or dry fibre/textile preforms. The major role of compression is to achieve consolidation of fiber/textile materials, to obtain the desired high fiber volume fraction in the finished part, generally between 0.5 and 0.7. During these processes, transverse compression of the preform results in changes of local micro-geometry such as the inter-fibre spacing, porosity and pore dimensions, and hence the fiber volume fraction. This has significant effects on the processability by altering the permeability of the preform, and on the quality and mechanical properties of the final product. The compaction behavior of fabric preforms has been increasingly seen as an important parameter of definition of these processes [1]. It appears that it was van Wyk in 1946 [2] who first developed the idea that the transverse elastic behavior of a bundle of fibers is controlled by a fiber bending mechanism. Since then, a larger amount of research has been devoted to the investigation of compressibility of various fibre/textile preforms [3-11]. hi this paper, a micromechanical compaction model was proposed to investigate the elastic compression behavior of single layer plain weave fabric preforms. Each fibre in the yarn was treated as an elastic curve beam, which waveform flattened during the compaction process. The yarn cross-sectional shape deformed and simultaneously its cross-sectional area changed. Thus, the elastic compression of a single layer plain weave fabric preform during compaction was attributed to two different levels of * Corresponding author. Tel.: +61-2-9351-4798; fax: +61-2-9351-3760. E-mail address: [email protected] (L. Ye)
Compaction of Single Layer Plain Weave Fabric Preform
859
deformation mechanisms: the yarn cross-section deformation and compaction, and the yarn bending deformation companied by its waveform flattening. The former was accounted for in terms of the compaction model for fibre bundle, and the later was governed by beam bending theory, which was closely dependent on the configuration of the fabric perform. THE MICROMECHANICAL COMPACTION MODEL Fig. 1 shows a unit cell of a single layer plain weave fabric preform with an initial thickness, h0. The yarn is assumed have a cross section of elliptical shape with the initial minor axis and major axis, 2a0, and, 2b0, respectively. When compressed, the yarn is flattened, and the yarn itself is compacted and deformed [see Fig. 2(b)]. Then the thickness, h, reduces as the applied compressive force increases. Thus, both the yarn flattening and compaction contribute to the compaction of a single layer woven fabric preform. These two different deformation mechanisms were accounted for by the yarn macro bending model and yarn micro compaction model, respectively.
FIGURE 1. One-quarter of 3-D unit cell of a plain weave fabric preform.
Yarn Macro Bending Model Considering the symmetry and similarity of the four yarns, it is sufficient to investigate only one yarn shown in Fig. 2. As shown in Fig. 3, each fibre in the yarn is treated as an elastic curve beam subjected to the lateral actions of the external load, p, and the internal load, q, both them are assumed to distribute uniformly over the fibre. The compaction and deformation of the yarn cross-section is determined by the internal load, q , while the macro bending deformation due to yarn waveform flattening is attributed to the net load, p - q. Each fibre is assumed to have a circle cross-section with a diameter of dQ, and its waveform is described by (
(
)
)
/
(1)
860
Compaction of Single Layer Plain Weave Fabric Preform
(a) before compaction
(b) after compaction
FIGURE 2. Yarn configurations of plain weave fabric preform.
FIGURE 3. Fibre macro bending deformation.
The symmetry requires that the two end cross-sections of the fibre do not rotate during the process of compaction. This leads to the following boundary conditions (2)
Using the beam theory in the mechanics of materials, the deflection of the fibre at the end x = L can be obtained as
{clL)*]/\2EI,
(3)
where El denotes the bending stiffness of the fibre. Yarn Deformation and Compaction Model As shown in Fig. 4, the initial configuration of the yarn cross-sectional shape is assumed elliptic. When compressed, the central part of the yarn cross section will first carry load, thus deform and be compacted first. While the two side parts of the yarn cross section will deform due to the action of squeeze out, but no compaction happens in these area because the fibres in these two parts do not carry any load. So the deformed cross section is assumed to consist of a central rectangular part and two
Compaction of Single Layer Plain Weave Fabric Preform
861
semi-elliptic side parts. The fibre volume fraction of the compacted central part is vf, while those of the two side parts remain v0. Then the fibre continuity requires 7ta0bQv0 =Ka(b-c)vo+
Aacv
(4)
FIGURE 4. Yarn micro compaction model.
It has been shown that compared with the deformation of the thickness, the deformation of the yam width due to the compressive load, q, generally is very small. Then it can be assumed that the semi major axis, b , keeps constant during compression = bn.
(5)
The fact that the deformation of the yarn cross-section mainly takes place in its thickness direction also leads to the following relation (6)
av = anvn.
Substituting Eq. (5) and Eq. (6) into Eq. (4), we have
c/bo=(l-a/ao)(4/x-a/aoy\
{vo/va
(7)
Eq. (7) describes the deformation of the yam cross-section shape. The compressive load, q, is determined by q = 2abc.
(8)
where <Jb, the bulk compressive stress, is determined by the deformation behaviour of yarn [4], The deformation compatibility requires yx=L=a-aQ.
(9)
862
Compaction of Single Layer Plain Weave Fabric Preform
Substituting Eq. (8) and Eq. (9) into Eq. (3), we obtain the load carried by a single fiber
P=
(a-4)a0L
ax(c-bo)[l-2(c/L)2+(c/L)3]
+ 2a,c,
(10)
where a = L*/l2EI. During the process of compaction, only fibres in the central part of the yarn carry the external load. The number of the effective fibres that carry load, ne, is determined by ne _ 4acv _ 4 c N nanbnvn n bn '
(11)
where N is the total number of fibres in a yarn. Then the external compressive force, P, exerted on one yarn can be given as
P=£pcdne.
(12)
As shown in Fig. 2, there are two complete yarn segments in the unit cell, thus the external force applied on the unit cell is •^WOVHl = 2 ^
=
CnominalL ,
(13)
where <Xnominal is the nominal stress acting on the unit cell. The thickness reduction of the single layer plain weave fabric preform is
= ho-h = 4(ao-a),
(14)
Eqs. (13)-(14) describe the elastic compression behaviour of a single layer plain weave fabric preform. L= 2.0 mm va/v0= 1.5 L= 1.5 mm va/vD= 1.8 L= 2.0 mm Wv o = 1.8
0.2
0.4 0.6 Pressure [MPa]
0.8
FIGURE 5. Pressure-thickness curve.
1.0
Compaction of Single Layer Plain Weave Fabric Preform
863
PARAMETRIC INVESTIGATION Fig. 5 shows the pressure-thickness curve for a plain weave fabric. It can be seen that the compaction behaviour of plain weave fabric is very sensitive to the fibre packing state of yarn, va/v0. The fibre packing state of yarn affects the compaction behaviour of woven fabric preforms in two ways. One is that the yarn itself becomes more difficult to compress as the initial fibre packing ratio, v0, increases or va/v0 decreases. The other is that it consequently makes the macro bending deformation of yarn more difficult. Actually, a smaller initial fibre packing ratio of yarn means more room for yarn to compact, and hence easier for preform to be compressed. As the macro geometric parameter, L, increases, the micro compaction behaviour of yarn does not change, but the macro bending deformation of yarn becomes easier, which makes the fabric preforms easier to compress. CONCLUDING REMARKS A micromechanical model, which consists of the micro-deformation model of yarn cross-section compacting, and the macro-deformation model of yarn bending, was developed. Parametric investigation showed that both the macro-bending stiffness of the fibre and the initial fibre packing ratio of the yarn evidently affect the compaction of the fabric preform. ACKNOWLEDGEMENT The authors are grateful to the Australian Research Council (ARC) for its financial support to this project. REFERENCES [I] Robitaille F, Gauvin R. 1998. "Compaction of textile reinforcements for composites manufacturing. I: Review of experimental results," Polymer Composites, 19(2): 198-216. [2] van Wyk CM. 1946. "Note on the compressibility of wool," The Journal of the Textile Institute, 37:T285-T292. [3] Gutowski TG. 1985. "A Resin Flow/Fiber Deformation Model for Composites," Sampe QuarterlySociety for the Advancement of Material and Process Engineering, 16(4):58-64. [4] Cai Z, Gutowski T. 1992, "The 3-D Deformation-Behavior of a Lubricated Fiber Bundle," Journal of Composite Materials, 26(8): 1207-1237. [5] Pearce N, Summerscales J. 1995. "The compressibility of a reinforcement fabric," Composites Manufacturing, 6(1): 15-21. [6] Matsudaira M, Qin H. 1995. "Features and Mechanical Parameters of a Fabrics Compressional Property," Journal of the Textile Institute, 86(3):476-486. [7] Toll S, Manson J-AE. 1995. "Elastic compression of a fiber network," Journal of Applied Mechanics, Transactions ASME, 62(l):223-226. [8] Hu J, Newton A. 1997. "Low-load lateral-compression behaviour of woven fabrics," Journalofthe Textile Institute, 88(3):242-254. [9] Saunders RA, Lekakou C, Bader MG. 1998. "Compression and microstructure of fibre plain woven cloths in the processing of polymer composites," Composites Part a-Applied Science and Manufacturing, 29(4):443-454. [10] Chen BX, Chou TW. 1999. "Compaction of woven-fabric preforms in liquid composite molding processes: single-layer deformation," Composites Science and Technology, 59(10):15191526. [II] Kruckenberg T, Ye L, Paton R. "Nesting and deformation in the compaction of plain-weave woven fabrics," presented at the 14th International Conference on Composite Materials (ICCM-14), San Diego, California, USA, July 14-18, 2003.
A Study on the Control Strategy to Minimize Voids in Resin Transfer Mold Filling Process Yun-Hee Park, Doh Hoon Lee, Woo II Lee School of Mechanical and Aerospace Engineering Seoul National University, Seoul, 151-742, Korea Moon Koo Kang School of Electrical Engineering and Computer Science Seoul National University, 151-742, Korea
ABSTRACT hi case of Resin Transfer Molding(RTM) process, "race-track" effects and non-uniform fiber volume fraction may cause undesirable resin flow pattern and thus result in dry spots, which affect the mechanical properties of the finished parts, hi this study, a real time RTM control strategy to prevent these unfavorable effects is proposed. The control strategy consists of two "stages" depending on the extent the resin front has reached. Through numerical simulations and experiments, the validity of the proposed scheme is demonstrated. The results show that the proposed scheme is effective in reducing the void formation during RTM mold filling.
INTRODUCTION Resin Transfer Molding (RTM) process is being used to manufacture a variety of composite structures ranging from simple plates to large, complex structures. For products with a complex geometry, complete wet-out of the preform may become difficult for various reasons, hi many cases, poor design of the mold and the process is responsible for unsuccessful mold filling. Mold and process design can be improved using available numerical tools. These simulation tools aid in determining proper locations of injection ports and vents. However, there are other factors that need to be considered in the practical situation. For example, when the preform is installed into the mold, there may exist thin gap along the edge causing the "race-track" effect during mold filling. In other cases, the preform may be nipped or folded at some location to cause a very dense inclusion around which a dry spot may be formed. Due to the nature of the problem, these situations cannot be predicted a priori. hi this study, a control strategy is proposed to prevent the flaws originating from the uncertainty during the process, hi RTM, these uncertainties can be interpreted as the uncertainty in the permeability. Along the "race-track," permeability is abnormally low while in the folded region the fiber volume fraction becomes doubled and the permeability increases by orders of magnitude, hi order to find the rales to cope with these unexpected situations, computer simulations are performed for a given geometry to Corresponding Author, School of Mechanical and Aerospace Eng., Seoul Nat'l Univ., Seoul, 151-742, Korea, FAX : ++82-2-883-0179, E-mail: [email protected]
Strategy to Minimize Voids in Resin Transfer Mold Filling Process Known Permeability (Numerical)
865
Unknown Permeability (Actual)
Low Permeability
\ High Permeabiiil ji
^•N Sensors
( a ) initial Setup
(b) Mold Filling
(c) Preform Permeability
FIGURE 1 First Stage Control
evaluate the effect of non-uniformity in the preform permeability on the resin flow. In RTM mold filling process, numbers and locations of the inlet gates and vents are fixed from the mold design. Control may be achieved with the existing injection gates through manipulating the injection pressure at each gate. This control (the First Stage Control) can be effective only in the initial stage of the mold filling since the far-reached resin front becomes more difficult to manipulate. In order to gain control during the more advanced phase of the mold filling, auxiliary gates and vents may have to be employed. In the Second Stage Control, the resin front can better be controlled by modulating the pressure of the auxiliary injection gates which are closer to the resin front. Based upon the aforementioned idea along with the data from numerical simulations, a control strategy is devised to prevent the formation of dry spots. Experiments are carried out to verify the validity of the control scheme. The results show that the proposed scheme is effective in reducing the void formation during RTM mold filling CONTROL STRATEGY Control of the resin front is achieved by two different "stages" depending on the extent the resin front has reached. The First Stage Control If there is no uncertainty in the permeability, flow pattern deviating from the predicted pattern means that there are unexpected changes in permeability. These unexpected variations can be caused by, for example, the "race-track" effect or sudden increase in the fiber volume fraction due to folding. Once numerical prediction is available for the ideal situation, the flow can be regulated and corrected by comparing actual flow front with the numerically data. For example, if the actual flow front is ahead of that of the predicted front, it means that there are certain zones with higher permeability than intended. In order to put it under control, the inlet pressure has to be turned down. Based upon this reasoning, control scheme is proposed as illustrated in Figure 1. As shown in the figure, sensors are located along the predicted flow front. These sensors can detected the arrival of the resin front at the sensor location. As the resin front passes over the locations, the sensors send a signal to the computer and the times are
866
Strategy to Minimize Voids in Resin Transfer Mold Filling Process >
Oil comparison lilll I'll " l i r e
Output
Actual fill time
Output
\iiiuil lillinj;
(a) Control Setup
(c) Flow Front without Control
(b) Permeability Calculation Zone
(b) Flow Front with Control
FIGURE 2 First Stage Control - Setup and Results
recorded. By comparing the numerically predicted time at the sensor location, the deviation of the actual permeability from the ideal value can be estimated. According to the permeability information thus obtained, inlet pressure can be regulated to reduce the discrepancy in the resin front location. Numerical prediction is modified according to the permeability value obtained from the measurement. Numerical experiments are done using a simulation code based on the Control Volume Finite Element Method (CVFEM). To emulate the actual mold filling process, a random distribution in the variation of permeability is given throughout the mold. Figure 2 shows the result of the first stage control. The flow front pattern was regulated to more desirable pattern. The Second Stage Control In the later stage of resin injection, the resin front becomes far from the original injection gate(s). Numerical results indicate that the sensitivity of the resin front on the inlet pressure change becomes minimal. At this stage, much better control can be achieved by using additional gates and vents located closer to the resin front. These auxiliary gates and vents can be engaged only when anomaly has been detected.
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In many practical cases, the locations of dry spots are qualitatively predictable to a certain extent. Dry spots tend to from near the vents or in the vicinity of the high permeability region. In this stage, sensors have to be located in the region where dry spots are expected. If the sensors ever recognize the formation of dry spots, the auxiliary gates /vents are engaged. Numerical simulations are also performed to verify the second stage control strategy for the geometry shown in Figure 3. hi this case, permeability along the mold wall is abnormally high due to the "race-track" effect. The flow therefore reaches the vent along the race-track faster than through the perform creating a large air entrapment near the lower left corner (Figure 3b). Based on the simulation, sensors and gates are installed in the area of high risk. Once the control is in effect, the sensors recognize the formation of the dry spot at the early stage and, consequently, the auxiliary gates were opened to eliminate the dry spot (Figure 3c). EXPERIMENT To evaluate the validity of the proposed scheme, experiments were performed. The experimental setup is illustrated in Figure 4. The geometry of the mold used in the experiment is shown in Figure 3. A photo-sensor (an infrared LED and a photo detector packaged in a single housing, SG-2BC by Kodenshi) was flush mounted on the mold surface. The principle of the sensor operation is demonstrated in Figure 5. Before the resin front arrives, the dry fibers scatter the infrared emission from the LED and much of the infrared is reflected back to the sensor to yield a high output voltage. When the resin front reaches the sensor, as the refractive indices of the fiber and resin matches closely, more infrared emission is transmitted forward reducing the amount of reflected energy.
FIGURE 4 Experimental Equipments
Strategy to Minimize Voids in Resin Transfer Mold Filling Process
(a) Before Flow Front Passes
(b) After Flow Front Passes FIGURE 5 Principle of Flow Font Detecting
RESULTS Using the setup as illustrated in Figure 4, experiments were performed to verify the control rules. The results are shown in Figure 6. The flow front unexpectedly reaches the vent by race tracking and air is trapped(Figure 6 a- ©). Even though more resin is injected, the trapped air could not be ejected(Figure 6 a- ©, ©, ©)• To eliminate the dry spot in this stage, it is necessary to employ auxiliary gates. When trapped air is detected(Figure 6 b- (D), auxiliary gates are opened to eliminate the dry spot(Figure 6 b- (2), ©, ©)•
(a) Without control
(b) With Control
FIGURE 6 Dry Spot Control
Strategy to Minimize Voids in Resin Transfer Mold Filling Process
869
CONCLUSION A real time control strategy to minimize voids in RTM mold filling process was proposed. The strategy consists of two stages. One is for the region in which the control is effective with only preset inlet gates and vents, the other is for the region where the control requires auxiliary gates and vents. Numerical code was developed to verify the effectiveness of the strategy. In order to demonstrate the validity of the approach, experiments were performed. According to the numerical simulations and experiments the control strategy was found to be effective in minimizing voids during RTM mold filling process. REFERENCES 1. 2. 3. 4.
5.
6. 7.
Moon Koo Kang, Jae Joon Jung, Woo and II Lee, 2000. "Analysis of resin transfer moulding process with controlled multiple gates resin injection,", Composites: Part ^,31:407-422. S. Bickerton, Suresh G. Advani, 1999, "Characterization and modeling of race-tracking in liquid composite molding process," Composite Science and Tech nology 59:2215-2229 Moon Koo Kang, 1997, "A Numerical and experimental study on mold filling and void formation during resin transfer molding," Seoul National University, Ph.D thesis S. Bickerton, E.M. Sozer, P.J. Graham, 2000, S.G. Advani, "Fabric structure and mold curvature effects on perform permeability and mold filling in the RTM process, Part I. Experiments," Composite Part A, pp. 423-438. S. Bickerton, E.M. Sozer, PJ. Graham, 2000, S.G. Advani, "Fabric structure and mold curvature effects on perform permeability and mold filling in the RTM process, Part n. Predictions and Comparison with experiments "Composite Part A, pp. 439~ 458. C.W.Hirt and B.D. Nichols, "Volume of Fluid (VOF) Method for the Dynamics of Free Boundaries," J. of Computational Physics 39, pp.201-225,1981. C.L.Tucker," Fundamentals of Computer Modeling for Polymer Processing," Hanser Publishers, Oxford University Press, New York, 1989.
Fabrication Process and Characterization of Conductive Composite for PEFC Bipolar Plates S.I. Heo, J.C. Yun, Y.C. Yang and K.S. Han* Department of Mechanical Engineering, Pohang University of Science and Technology, San 31 Hyoja-dong, Nam-gu, Pohang 790-784, Korea
ABSTRACT Carbon reinforced conductive polymer composites were fabricated by the compression molding technique. Conductive fillers (graphite powder, carbon black and carbon fiber) were mixed with an epoxy resin to impart electrical property in composites. The ratio of graphite powder/carbon black/carbon fiber as well as filler/resin was varied to investigate electrical property of cured conductive composites. In this study, carbon/graphite filled conductive polymer composites with high filler loadings (>60wt.%) were manufactured to accomplish high electrical conductivity (>100S/cm). Graphite powder was the main filler to increase electrical conductivity of composites by direct physical contact between graphite powders. While high filler loadings are needed to attain good electrical property, the material becomes brittle. So carbon fiber was added to compensate weakened mechanical properties. Carbon black was dispersed in the epoxy resin to obtain the additional increase of conductivity by using very low percolation threshold. The electrical conductivity of composites was controlled with varying the amount of graphite powder, carbon black, and carbon fiber. The optimum molding pressure according to filler was proposed experimentally. And the behavior of carbon black in conductive composites with high filler loadings was proved through analyses of manufacturing condition.
INTRODUCTION As early as 1839, Sir William Grove discovered that it might be possible to generate electricity by reversing the electrolysis of water. Since then, the research of fuel cell is being performed constantly. Lately, a number of manufacturers including major automobile makers and various governments have supported ongoing research into the development of fuel cell for use in vehicles and other applications. There are various types of fuel cells, which as a rule can be classified according to the kind of electrolytes used. Polymer electrolyte fuel cells (PEFCs) are under widespread development to produce electrical power for a variety of stationary and transportation applications. To date, the bipolar plate remains the most problematic and costly component of PEFCs [1,2]. The bipolar plates have to achieve many functions in the fuel cell stack. Main functions are: (1) distribution of fuel and oxidant within cell, (2) facilitation of water management within cell, (3) separation of the individual cells in the stack, and (4) conduction of current from cell to cell [3]. Carbon/graphite filled conductive polymer Corresponding Author, Department of Mechanical Engineering, Pohang University of Science and Technology, San31 Hyoja-dong, Nam-gu, Pohang, 790-784, KOREA, fax: +82-54-279-2845, [email protected]
Conductive Composite for PEFC Bipolar Plates
871
composites are expected to satisfy these requirements. Many researches of conductive filler reinforced polymer composites have already performed vigorously. Various fillers (graphite particle, carbon fiber, carbon black and carbon nanotube) are used to impart electrical property in insulating polymer [4-8]. Generally, these researches are focused on low filler loadings: nano particle (60wt.%) is required to attain high conductivity above lOOS/cm. But existing researches are confined case studies and not systematic [1,10-13]. The aims of the present work are to fabricate high conductive composites and to prove the electrical property according to types offillersby systematic approach. EXPERIMENT The thermosetting resin used in this study is epoxy resin, YD-128, based on bisphenol-A. Hardener and accelerator are D-230 and KH-30, respectively. These were obtained from Kukdo Chemical Co., Korea. These components (epoxy, hardener and accelerator) were mixed in the ratio of 70:23:7. Before mixing with hardener, epoxy was heated at 70°C to reduce the initial viscosity. And then fillers were added to the epoxy resin compound by using high shear mixing technique. Conductive fillers used are listed in Table 1. Graphite/carbon fillers were selected for bipolar plates since they have high electrical conductivity, high mechanical strength and immunity to corrosion [14]. Graphite powder was a main filler to increase electrical conductivity of composites. Carbon fiber and carbon black were added to investigate the effect of variousfillers,hi the case of carbon black, it was dispersed in the epoxy resin by using ultrasonic bath. Afterwards the hardener and the accelerator were mixed to carbon black/epoxy resin compound by conventional stirring. Conductive filler/epoxy compound was compression molded at 120°C for 10 min. And molding pressure was varied from 100 to 3000psi according to fillers. The mold was 80 x 80 x 2 (mm) flat type. The microstructure analysis and the density measurement of cured composites were performed to investigate the manufacturing condition. The density of composites is measured by Archimedes's principle. Bulk electrical conductivity was measured by a four-point probe technique. Samples were cut to size of 60 x 20(mm) using a bandsaw and painted with conductive silver paste on four regions to be contacted with probe. And heat treatment was conducted at 50°C for 2 h. The current between -20 and 20mA was applied through the two outermost probes by 220 Programmable Current Source (KEITHLEY) and the resulting voltage across the two innermost probes was measured by 196 System DMM (KEITHLEY). TABLE I Types of fillers Filler Graphite powder
Manufacturer GX- 25, Carbonix Co.
Carbon fiber
M-102S,Kreca
Carbon black
HIBLACL 40B2, Korea Carbon Black
Size 25 [j.m diameter: 18 fj.m length: 200 jum
23 nm
872
Conductive Composite for PEFC Bipolar Plates
RESULTS AND DISCUSSION Graphite Powder/Epoxy Composites The microstructure of cured composites was illustrated in Figure 1. The ratio of graphite powder to epoxy was fixed to 4:1 because the conductivity of composites was small to apply to fuel cells below that ratio. With increasing the molding pressure during the curing cycle, the level of compaction between graphite powders was increased. And the level was not changed above lOOOpsi. Figure 2 shows this aspect was reconfirmed at the result of density measurement. These results obtained from manufacturing condition indicate that the compaction of composites was almost finished at molding pressure, lOOOpsi. Figure 3 represents bulk electrical conductivity with varying the molding pressure. The conductivity of composites was rapidly increased till lOOOpsi and then the rate of increase was reduced gradually. At 1500psi, the conductivity reached nearly 180S/cm. hi the case of graphite powder/epoxy composites, the optimum molding pressure for electrical conductivity was determined on 1000~1500psi. Effect of Carbon Fiber When carbon fiber was blended with graphite and epoxy, the optimum molding pressure was changed. The total ratio of fillers to epoxy was fixed to 4:1. Figure 2 shows the density of composites containing carbon fiber was lower than that of composites used graphite powder only at lOOOpsi. This phenomenon was caused for lack of compaction betweenfillers.With increasing the molding pressure, the compaction between fillers was processed more and more. At 2000psi, the density of composites containing carbon fiber 10wt.% of the total system, increased to that of composites containing graphite powder only. The conductivity was also increased to the high value about 170S/cm.
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Conductive Composite for PEFC Bipolar Plates
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hi the case of carbon fiber 20wt.% of the total system, the density and the conductivity of composites were increased slightly as molding pressure was increased as shown in Figure 2 and Figure 3. Figure 4(b) presents the answer. While the compaction between graphite powders was processed sufficiently at 2000psi, the compaction between graphite powder and carbon fiber was still far from perfect. It is the difference between Figure 4(a) and Figure 4(b). So far, it was just reported that the addition of carbon fiber deteriorated the conductivity of high loading filler conductive composites without any explanations [11]. But this result suggests that the increase of molding pressure can significantly improve the conductivity of material containing carbon fiber. Therefore some additional mixing step between graphite powder and carbon fiber is expected to increase of conductivity at high loading ratio of carbon fiber. Effect of Carbon Black Carbon black was filled into epoxy resin in the range of 0.6 to 5wt.% of total graphite/epoxy resin system (3 to 25wt.% of epoxy resin system). Figure 5 shows the microstructure before and after adding carbon black, hi Figure 5(a), the shape of graphite powders was so distinct. But in the case of carbon black 5wt.%, graphite powders were covered with epoxy resin as shown in Figure 5(b). This may obstruct compaction and slightly increase the spacing between graphite powders. This interpretation could be supported by the result of density measurement in Figure 6. At carbon black 5wt.%, the density of material decreased to 1.85g/cm3. This value is near to the density of molding pressure, 700psi, for graphite powder/epoxy composites. These results practically induced the decrease of conductivity of cured material as shown in Figure 7. With increasing the contents of carbon black, the conductivity of composites was decreased gradually.
(a) No carbon black
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FIGURE 5, Microstructure before/after adding carbon black (molding pressure: 15OOpsi)
874
Conductive Composite for PEFC Bipolar Plates
0
1 2 3 CB contents(wt.%)
4
FIGURE 6 Density of graphite powder/carbon black/epoxy composites
0
1 2 3 CB content (wt.%)
4
FIGURE 7 Conductivity of graphite powder/ carbon black/epoxy composites
These phenomena were occurred because the adding of carbon black (nano particle) in the epoxy resin extremely increased the viscosity of the resin. It is known that the viscosity of polymer resin was increased as contents of micro/nano fillers were increased [15,16]. Especially, carbon black causes high viscosity of the polymer resin due to its high surface area [11]. Since high viscosity caused by carbon black disturbed the direct contact between graphite powders, the conductivity of graphite powder/carbon black/epoxy composites was decreased. Therefore, the addition of carbon black has a reverse effect on conductivity of composites with high filler loadings in spite of its high conductivity in itself.
CONCLUSIONS hi this study, carbon reinforced conductive polymer composites were fabricated successfully. And the electrical conductivity was investigated under various conditions. The conclusions are summarized as follows: 1. In the case of graphite powder/epoxy composites, the optimum molding pressure for electrical conductivity was determined on 1000-1500psi. 2. The improvement of conductivity of composites containing carbon fiber was possible through increasing the molding pressure up to 2000psi. And some additional mixing step between fillers is expected to the increase of conductivity at high contents of carbon fiber. 3. The addition of carbon black deteriorated the electrical conductivity of composites with high filler loadings.
ACKNOWLEDGMENTS This work was supported by Hyundai Motor Company & Kia Motors Corporation.
Conductive Composite for PEFC Bipolar Plates
875
REFERENCES 1. 2. 3. 4. 5.
6.
7.
8. 9. 10. 11. 12. 13. 14. 15. 16.
Deanna N. Busick and Mahlon S. Wilson. 1999. "Low-cost composite material for PEFC bipolar plates, " Fuel cells Bulletin, 2(5): 6-8. Isa Bar-On, Randy Kirchain and Richard Roth. 2002. "Technical cost analysis for PEM fuel cells," Journal of Power Sources, 109: 71-75. Viral Mehta and Joyce Smith Cooper. 2003. "Review and analysis of PEM fuel cell design and manufacturing," Journal of Power Sources, 114: 32-53. Wenge Zheng and Shing-Chung Wong. 2003. "Electrical conductivity and dielectric properties of PMMA/ expaned graphite composites," Composites Science and Technology, 63: 225-235. R. Taipalus, T. Harmia, M. Q. Zhang and K. Friedrich. 2001. 'The electrical conductivity of carbon-fibre-reinforced polypropylene/polyaniline complex- blends: experimental characterisation and modeling," Composites Science and Technology, 61: 801-814. J. Sandier, M. S. P. Shaffer, T. Prasse, W. Bauhofer, K. Schulte and A. H. Windle. 1999. "Development of a dispersion process for carbon nanotubes in an epoxy matrix and the resulting electrical properties," Polymer, 40: 5967-5971. L. Flandin, T. Prasse, R. Schueler, K. Schulte, W. Bauhofer and J. -Y. Cavaille. 1999. "Anomalous percolation transition in carbon-black-epoxy composite materials," Physical Review B, 59(22): 349-355. Ryszard Wycisk, Ryszard Pozniak and Aleksy Pasternak. 2002. "Conductive polymer materials with low filler content," Journal of Electrostatics, 56: 55-66 Mark Weber and Musa R. Kamal. 1997. "Estimation of volume Resistivity of Electrically Conductive Composites," Polymer Composites,18(6): 711-725. Richard H. J. Blunk, Daniel J. Lisi, Yeong-Eun Yoo and Charles L. Tucker III. 2003. "Enhanced Conductivity of Fuel Cell Plates through Controlled Fiber Orientation," AIChE Journal, 49(1): 18-29. Mahlon S. Wilson and Deanna N. Busick. 2001. US patent 6,248,467. Kazuo Saito, Atsushi Hagiwara and Takashi Maki. 2002. US patent 6,397,901. Hitoshi Yamada, Kazuki Morimoto, Katsuya Kusuno, Shuichiro Wada and Kazuo Nishimoto. 2002. US patent 6,500,893. Mukesh K. Bisaria, Peter Andrin, Mohamed Abdou and Yuqi Cai. 2002. US patent 6,379,795. Petra Potschke, T. D. Fornes and D. R. Paul. 2002. "Rheological behavior of multiwalled carbon nanotube/polycarbonate composites," Polymer, 43: 3247-3255. Anqiang Zhang, Lianshi Wang and Yiyu Zhou. 2003. "A study on rheological properties of carbon black extended powdered SBR using a torque rheometer," Polymer Testing, 22: 133-141.
Si02/Sulfonated PEEK Doped with Dodecatunstophosphoric Acid Hybrid Materials — Preparation and Properties Han-Lang Wu, Chen-Chi M. Ma* Department of Chemical Engineering, National Tsing-Hua University, Taiwan, R.O.C
ABSTRACT A novel organic/inorganic proton conducting composite membrane based on sulfonated poly (ether ether ketone)(sPEEK) for utilizing in the polymer electrolyte has been prepared. The composite membrane was modified with dodecatunstophosphoric acid (PWA) and colloidal silica (SiCh). Results show that the longer the sulfonation time, the higher the proton conductivity. However, it may cause over swelling. The modification with PWA shows increasing in the proton conductivity, however, when PWA content is over 40phr, phase separation may occur. PWA leaking problem was found in membrane durability testing, but the modification with SiC>2 will reduce the degree of PWA leaking and the swelling of membrane. The degree of methanol crossover was also investigated in this study. Comparing to Nafion® membrane, sPEEK/PWA organic/inorganic composite membrane possesses almost the same proton conductivity of 0.05 S/cm at room temperature, but has the lower methanol permeability (2*10"7cm2/s). Consequently, the sPEEK/PWA organic/inorganic composite membrane may be suitable for the application of direct methanol fuel cell (DMFC).
INTRODUCTION For several energy conversion devices, fuel cells have high efficiency and low emission of pollutants thus attract high interests. Among several kinds of fuel cells, proton exchange membrane fuel cells (PEMFCs) attain the requirements for automobile and portable devices have increasing interests. In PEMFC system, two kinds of fuel, hydrogen and methanol, are used to process chemical reaction and generate electricity [1-3]. Usually, fuels for PEMFC system are hydrogen and for the use of methanol as fuels in PEMFC system has another term called direct methanol fuel cell (DMFC). Proton conducting membranes in hydrogen fuels PEMFC system are designed to have high ion conductivity and good thermal stability. However, in DMFC system, the methanol cross over the proton conducting membrane led to reduce fuel cells efficiency and decrease the cathode performance, hence the methanol cross-over problem is very important in DMFC. The composite membrane in this paper is not only for PEMFC but also for direct methanol fuel cells DMFC [1-6]. hi this study, composite membranes were prepared from the sulfonation of PEEK, i.e. sulfonated poly (ether ether ketone) (sPEEK), and inorganic materials. * Corresponding author, National Tsing Hua University, Department Of Chemical Engineering, Hsinchu, Taiwan 30034, R.O.C. ; TEL: 886-3-5713058,FAX: 886-3-5715408 ; e-mail:[email protected]
SiO2/Sulfonated PEEK
877
Proton conductivity can be improved via the sulfonation of PEEK and doped with inorganic acids. The more the degree of sulfonation, the higher the ion conductivity attains [1]. However, the higher degree of sulfonation may increase the swelling of polymer in water or methanol. The inorganic acid used in this study was dodecatunstophosphoric acid (PWA). In order to modify the membrane properties; SiO2 was added in polymer matrices to reduce the degree of swelling, that is, the lower water uptake and improve the thermal stability. Furthermore, SiO2 hybrids decrease the degree of inorganic solid acids leaking from the polymer matrices [5]. SiO2 hybrids in sPEEK play a role in reducing methanol cross-over. This paper reports the electrical and thermal properties of SiO2/PWA/sPEEK composite membranes. The SiCVPWA/sPEEK composite membranes are promising materials for the proton conducting membrane in both PEMFC and DMFC systems.
EXPERIMENTAL Polymer modification PEEK (polyoxy-l,4-phenyleneoxy-l,4-phenylene-carbonyl-l,4-phenylene) to be sulfonated is the PEEK 450G from Victrex®. It is randomly sulfonated with sulfuric acid and used without further purification. The sulfonation of PEEK is according to the following procedure: 20g of polymer was dried for more than 12h in an oven at 80°C and then dissolved in 200g of concentrated sulfuric acid (>95%) and stirred in a water bath at 40°C for a given time between 6-8h to achieve the desired conversion. Then, the polymer solution was gradually precipitated into a large excess of ice-bath water and washed with distilled water until the pH is nearly 7. The polymer was then dried in an oven at 80°C for 1 day. Preparation of composite membranes The sPEEK polymer solution was prepared by dissolving (10 wt %) in 1-methyl2-pyrrolidinone (NMP). The appropriate weight of solid acids and colloidal silica (SiO2) were added to this solution. Solid acids were obtained from Nalgene chemicals. Colloidal silica was obtained from Du Pont Co. U.S.A. The solution was heated to evaporate most of the solvent and was cast on a glass plate. The cast membranes were dried 4h in an oven at 60°C and then at 100°C for 8h.
CHARACTERIZATION AND PROPERTY MEASUREMENTS Scanning Electronic Microscopy (SEM) Surface morphology of SiO2/PWA/sPEEK composite membranes were investigated by Scanning Electron Microscope (JEOL JSM 840A, Japan). The fracture surfaces were sputter coated with gold prior to scanning. The distributions of Si atoms in the hybrid creamers were obtained from SEM EDX mapping. The white points in the figures denote the Si atoms [7-8].
878
SiO2/Sulfonated PEEK
Conductivity Conductivity of composite membrane was measured by AC impedance method using an electrochemical interface solartron (SI 1260) at room temperature. The sample was place between two platinum electrodes in an open cell. The membrane was soaked in 60 °C water for lh before conductivity testing. The conductivity was calculated from the following equation: a = L/RA, where L is the membrane thickness, A the surface area of the electrodes and R is the resistance derived from the SI 1260 [2]. Water uptake The sample was dried in an oven 90°C for 8h and weighted. Then immersed the sample in distilled water and heated at various temperatures for 2h. The water uptake was calculated using this equation, (Wwet - Wdiy)/Wdry*100% [9]. Methanol permeability The methanol permeability across the membrane was measured at room temperature, using two cells with 19.6cm2 cross area. 40wt% methanol and pure water 40ml for each were placed in two sides. The amount of permeate was determined by the refractive index, comparing to methanol concentration calibrate curve[10].
RESULTS AND DISCUSSION Morphological Properties The morphology of the fractured surfaces was investigated by SEM (Scanning Electronic Microscopy), the mapping technique was utilized to elucidate the distribution of silica and the separation of microphase in the hybrid matrix. Fig. 1 shows that the polymer matrix is porous comparing to Fig. 3. Si mapping of SiCVsPEEK hybrids was shown in Fig. 2 and Fig. 4. In these figures, the white dots represent the silicon atoms. In Fig. 2, particles were uniformly dispersed throughout the polymer matrix. From Fig. 4, one can find the aggregation of particles occurred in the polymer matrix. This result shows sPEEK with 20phr SiC>2 hybrids exhibit good miscibility between organic and inorganic phases.
eoOnra F I G U R E 1 SEM of sPEEK with 20phr SiO 2
I
F I G U R E 2 Si mapping of sPEEK with 20phr SiO 2
SiO2/Sulfonated PEEK
879
#
>
(
•
FIGURE 3 SEM of sPEEK with 80phr SiO2
FIGURE 4 Si mapping of sPEEK with 80phr SiO2
Conductivity Prior to conductivity measurements all the membrane samples were immersed in water for hydration. As can be seen from Table 1, the increasing of SiC>2 contents does not decrease the conductivity significantly; on the contrary, the conductivity of SiCVsPEEK membrane increases slightly when the SiC>2 content increases from Ophr to 80phr. The conductivity of sPEEK membranes depends on parameters such as degree of sulfonation and connected hydrophilic channels [3]. Hence, supposing the sPEEK incorporates with SiC>2 inducing the good connectivity of hydrolytic channels and improves the conductivity. TABLE I Conductivity of SiO2/sPEEK hybrid with different silica content sample sPEEK 20phr SiO2 60phr SiO2 80phr SiO2
film thickness (/an) 217 127 176 180
Resistance(O) 268 125 134 125
5 10 20 PWA content (phr)
Conductivity (S/cm) 1.03E-02 1.29E-02 1.67E-02 1.83E-02
60
FIGURE 5 Conductivity of lOphr SiO2/sPEEK hybrids with different PWA contents.
880
SiO2/Sulfonated PEEK " original " 3 days in 60°C water
0.07
0.06 0.05 0.04 0.03 0.02 0.01 0.00
" original - 3 days in 60°C water
0.05 0.04 0.03 0.02 0.01 0
3
10
20
3
40
10
20
40
PWA content (phr)
PWA content (phr) FIGURE 6 Conductivity of sPEEK with different PWA content
FIGURE 7 Conductivity of lOphr SiO2/sPEEK with different PWA content
In Figure 5, SiO2/sPEEK hybrids doping with solid acid, PWA, resulting in a 3-5 times increases in conductivity. However, when PWA content is over 40phr, phase separation may occur. At low solid acid contents, increasing PWA causes larger cluster of SiO2/PWA and decrease the channel connectivity thus the lower conductivity [5]. Furthermore, the SiO2 prevents solid acids leaking from the polymer matrix. According to Figure 6 and Figure 7, Figure 6 shows the significant decrease in conductivity after soaking the membrane in 60°C for 3days then that sPEEK/PWA with SiO2. Water uptake
I 60 ^
no silica
• 20phr silica
60phr silica
• 80phr silica
40 30
30
40
40 60 Temperature (°C)
70
FIGURE 8 Water uptake of SiO2/sPEEK hybrid with different silica contents
Water uptake presents the degree of hydrophilicity of the membrane. Generally speaking, the presence of water is known to facilitate proton transfer and enhance the conductivity of the membrane. However, higher water uptake led the over swelling of the membrane and decreased the thermal stability. As shown in Figure 8, the water uptake of SiO2/sPEEK hybrids ranges between 40-75 wt%. The apparent trend was not found in this result, it indicates that the effect of SiO2 on sPEEK polymer swelling in water is significant [8]. Methanol permeability The methanol permeability of 40 wt% methanol through the membranes was investigated as a function of time. Comparing Figure 8 with Table 2, the sPEEK with
SiO2/Sulfonated PEEK
881
20 phr SiO2 contents has the lowest methanol permeability and the lowest water uptake, a correlation between two properties may be existed. TABLE II methanol permeability of SiO2/sPEEK hybrid with different silica contents
^ sPEEK 20phr SiO2 60phrSiO2 80phr SiO2
methanol permeability (107cm2/s) 3.799 2.936 4.404 3.523
CONCLUSIONS hi this study, SiO2/PWA/sPEEK hybrids have been prepared. Results show that solid acids PWA can enhance the conductivity; however, when PWA content is over 40phr, phase separation may occur. SiO2 inorganic components have the lower water uptake (i.e. 45%) than the pure sPEEK which is 70%. From conductivity durability test, the addition of SiO2 in PWA/sPEEK has only 10% decrease in conductivity comparing to the PWA/sPEEK hybrids. It shows that SiO2 prevents solid acids leaking from polymer matrix. The sPEEK with 20phr SiO2 contents has the lowest methanol permeability which is 2.936*10"7 cm2/s. REFERENCES 1.
S.MJ. Zaidi, S.D. Mikhailenko, G.P. Robertson, M.D. Guiver, S.Kaliaguine. 2000. "Proton Conducting Composite Membranes from Polyether Ether Ketone and Heteropolyacids for Fuel Cell Applications," J. Membrane Science, 173:17-34. 2. Jae-Hyuk Chang, Jong Hyeok Park, Gu-Gon Park, Chang-Soo Kim, O. Ok Park. 2003. "Proton Conducting Composite Membranes Derived from Sulfonated Hydrocarbon and Inorganic Materials," J. Membrane Science, 124:18-25. 3. K.D. Kreuer. 2001. "on the Development of Proton Conducting Polymer Membranes for Hydrogen and Methanol Fuel Cells," J. Membrane Science, 185:29-39. 4. S. D. Mikhailenko, S.MJ. Zaidi, S. Kaliaguine. 2000. "Electrical Properties of Sulfonated Polyether Ether Ketone/Polyetherimide Blend Membranes Doped with Inorganic Acids," J. Polymer Science: PartB: Polymer Physics, 38:1386-1395. 5. I. Honma, Y. Takeda, J.M. Bae. 1999. "Protonic Conducting Properties of Sol-gel Derived Organic/Inorganic Nanocomposite Membranes Doped with Acidic Functional Molecules," Solid State Ionics, 120:255-264. 6. G. Alberti, M. Casciola, L. Massinelli, B. Bauer. 2001. "Polymeric Proton Conducting Membranes for Medium Temperature Feul Cells (110-160°C)," J. Membrane Science, 185:73-81. 7. Chin-Lung Chiang and Chen-Chi M. Ma. 2003. "Synthesis, Characterization, and Thermal Properties of Novel Phenolic Resin/Silica Nanocomposites" ICCM-14 (International Conference on Composite Materials). 8. F.G. Wilhelm, I.G.M. Punt, N.F.A. van der Vegt, H. Strathmann, M. Wessling. 2002. "Cation Permeable Membranes from Blends of Sulfonated Poly(ether ether ketone) and Poly(ether sulfone)," J. Membrane Science, 199:167-176 9. Hsu-Chiang Kuan and Chen-Chi M. Ma. 2003. "Morpholical and Mechanical Properties of Colloid Silica/Waterborne Polyurethane Nanocomposite" ICCM-14 (International Conference on Composite Materials). 10. MX. Ponce, L. Prado, B. Ruffmann, K.Richau, R. Mohr, S.P. Nunes. 2003. "Reduction of Methanol Permeability in Polyetherketone-Heteropolyacid Membranes," J. Membrane Science, 217:5-15
Thermoplastic Composite Access Cover Manufactured by Co-Consolidation after Thermoforming Stiffers Kejian Wang* and Xiao-Su Yi National Key Laboratory of Advanced Composites (LAC) Beijing Institute of Aeronautical Materials (BIAM), Beijing 100095, P.R.C.
ABSTRACT This paper reported an integrated manufacturing process of one thermoplastic composite airplane access cover with L-shaped stiffers of poly(ether ether ketone)(PEEK) matrix carbon fiber reinforced composites. The used flexible prepreg fabric was cowoven with carbon fiber and PEEK fiber. It was found that the stiffer margins were not well consolidated by directly press forming after laying up the designed number of fabric in mold though the cross round part was smoothly consolidated. However, a matched-die press thermoforming from the preformed blank solved the problem while the cross round part was easily delaminated. The L-shaped stiffers were then fixed in upper molds with their lower surface close to the multiple fabric for cover flat part and finally bonded to such post-formed part during consolidation. In fact, the stiffers were melted again but their shape was remained because there was less enough flow under small pressure in them. Therefore, the process referred to co-consolidation. This way overcame the common problems by direct welding. The bad stickability of the dry prepreg for curved part was not met in thermoforming. The fabrication cost could drop dramatically in large volume production. In all, thermoforming and co-consolidation were perspective in fabricating aerospace composites 3-D structural parts.
INTRODUCTION Advanced thermoplastic composites are increasingly considered for structural application in aerospace with such attractive features as better toughness/damage tolerance, weight reduction and recyclability. The greater promise can be realized only if rapid, cost effective, large scale manufacturing techniques are developed11'21. The relative technical issues and theoretical basics have been under discussion. The novel suitable processing methods include thermoforming^3'41, fusion bonding^51 and integrating consolidation. Exploited were many complex thermoplastic aircraft parts as Fokker's main under carriage door, Lockheed's forward fuselage demonstration article. Beijing Institute of Aeronautical Materials has also fabricated skins, access cover and so on. This paper was to carry out simple application research of one airplane access cover with L-shaped stiffers of poly(ether ether ketone)(PEEK) matrix carbon fiber reinforced composites using the novel techniques. * Correspondence Author, Kejian Wang, Beijing 81-3, 100095, Fax: +86-10-62458002, kejian.wang@ biam.ac.cn
Thermoplastic Composite Access Cover
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MATERIALS AND PREPREG The used carbon fiber was AS4c-3K by Hercules Inc., original PEEK resin was produced by Jilin University. PEEK was first spinned into fine fiber in our laboratory, and then co-woven with carbonfiberto prepareflexibleprepreg (Figure 1,2). The area density and the carbon fiber volume percentage (60%) of the prepreg should be controlled so that the thickness of each ply in consolidated laminate was 0.125mm.
PEEK Fibre
Carbon Fibre
nun
FIGURE 1 Sketch of co-weaving PEEK fiber with carbon fiber
FIGURE 2 PEEK fiber and the plain co-woven prepreg
PREPARING BLANK COMPOSITE AND ITS PROPERTIES
FIGURE 3 C-scannmg for unidirectional blank of CF Vol60% AS4c/PEEK composite
The blank composite was press formed. The process parameters were optimized in a large number of experiments until the void percentage was lower than 0.5%. The properties were tested together with analyzing structural quality using C-scanning and
884
Thermoplastic Composite Access Cover
microscopy. The final optimized unidirectional composite blank of CF Vol60% AS4c/PEEK was checked as in Figure 3 by C-scanning and in Figure 4 by Microscopy. They showed that the composite blank was textured. Table 1 listed the high mechanical properties of resultant blanks. The 130°C or 150°C Flexural Strengths were as high as 1280MPa, the 150°C Short Beam Shear Strength was 57 MPa, and 90°C water absorption is less than 0.2%. The high temperature mechanical properties and moisture resistance showed that the prepared compoMic siilisfial liv iiuioi-uuliaii sub-structural part demand.
"I
FIGURE 4 Microstructure of unidirectional blank of CF Vol60% AS4c/PEEK composite TABLE I Mechanical properties of unidirectional AS4c/PEEK Properties
Value
Tensile Strength
(MPa)
1920
Tensile Modulus
(GPa)
149
Compression Strength
(MPa)
1300
Compression Modulus
(GPa)
141
Flexural Strength
(MPa)
1990
Flexural Modulus
(GPa)
130
130°C Flexural Strength
(MPa)
1280
150°C Flexural Strength
(MPa)
1000
Short Beam Shear Strength
(MPa)
92
150°C Short Beam Shear Strength
(MPa)
57
90°C water absorption
< 0.2%
FORMING L-SHAPED STIFFERS The flexible prepreg was directly laid up in one set of L-shaped stiffer mold. The layup sequence was [±45°]4S or [907-457+4570°]2S, the final thickness of stiffer was 2±0.05mm. The optimized process parameters were designed in press forming. It was found that of the right angle region and the neighboring straight side region of the bend were smooth, the inner radius and the outer radius of the right angle were as the same as those of the designed mold. However, the carbonfiberin the straight side margins was not even wetted by resin at all, which forced us to cut the margins. The stiffers were shown in Figure 5. Figure 6 of C-scanning implied its bad consolidation. The situation was not improved when changing prepreg layup and process parameters.
Thermoplastic Composite Access Cover
885
FIGURE 5 The L-shaped stiffers formed in press directly from prepreg
FIGURE 6 C-scanning for one side of L-shaped staffer press formed directly from prepreg
In direct press forming from prepreg, two straight stiffer sides were, in mold, at 45° relative to the vertical direction along which the press applied pressure onto the mold, i.e., the pressure on round angle was sufficient while it was not enough on the sides. Besides, the stickability of the dry prepreg was bad, so the accurate positioning the plies was difficult in mold, but this problem was not serous in forming flat blank. Thirdly, the production efficiency was lower because each small stiffer experienced the same process procedure. These might be solved by thermoforming technique^ \
'i
FIGURE 7 The thermoformed stiffers and the corresponding C-scanning
Wide flat blanks were fabricated ahead, then they could be press thermoformed in a matched-die into stiffers after being cut narrow. The narrow blank was moved into the L-shaped mold for thermoforming at 140°C -340°C when they were heated up to 340°C-380°C in one oven. To realize the quick forming in one press with compression speed at constant lOmm/sec, the blanks were heated to 380°C so as to allow the ply slippage and to avoid fiber breakage in deformation. The forming pressure was limited below 2MPa. The inner thickness of mold was 2±0.05mm to fill the final formed stiffers. It was successful to fabricated the stiffers from the layup of [±45°]4S or [907-457 +4570°]2s. The qualified wide blanks (Figure 3) could indeed transformed into good stiffers as shown in Figure 7. The straight sides were smooth while some carbon fibers in the outer round angle were broken while the inner fibers were buckling under quick
886
Thermoplastic Composite Access Cover
compression, this was worse when the round radius were too small. To ensure the reasonable superplastic deformation when heated laminate, the stamping velocity should be lower. FUSION BONDING There are many bonding methods. However, most have not been applicable in large-scale industry. For instance, the lap strength was up to 28MPa in our resistance welding. But connecting area was not consistent, which resulted in the distorted or twisted assemble. Therefore, bulk fusion bonding was chosen to fix the stiffers on the flat blank. The specific fixing tooling was used to position the stiffers on the flat blank. They were heated under press to 360°C at 2MPa for 30 minutes. Then they were cooled to demold. They were closely bonded together, their original geometry was well kept and the connecting rounds were smooth as shown in Figure 8.
FIGURE 8 The stiffer, the wide flat blank and their assemble by bulk fusion bonding
CO-CONSOLIDATION The compression direction in the foregoing bulk fusion bonding was the same as for pressing the flat blank when formed. Consequently, such two steps could be integrated into one. i.e., the compression for bonding could be fulfilled when press forming the flat blank. We called this technique as co-consolidation. In mold design, the upper male die was divided three elements, between which vertical sides of two stiffer were fixed when they were connected through screws. The bottom surface of the straight sides of two fixed stiffers were in one plane with the bottom surface of the assembled upper male die elements to act as one large 'male die'. The female die was of one element, i.e., it was similar to the one to formed the flat balnk. The prepreg plies for flat part were laid up in this female die. After the 'male die'.and the female die were matched to close mold, the mold could be treated in the optimized process procedures. In addition, the demolding process was reverse. In forming, the flat prepreg plies were heated to consolidate. At the same time, the horizontal sides of stiffers melted to bonding the flat ply set under certain pressure while the geometry of vertical sides were kept under less pressure. The consolidation of the flat blank and its bonding with stiffers occurred almost simultaneously. The margins of the demolded assemble were cut in terms of the design dimensions. The final demonstration article was shown in Figure 10. The positioning of stiffers was accurate, the bonding strength was high, and their connecting interfaces were smooth
Thermoplastic Composite Access Cover
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and of no clearance. It seemed that this way overcame two problems by direct welding: insufficient bonding strength and the resultant buckled or distorted joining surface. The further improving research has been carried out[7]. The major steps include the original materials, prepreg, elements and their integration as well as machining into final dimensions. Material researchers not only focused the high quality prepreg and optimized process parameters, but also advised the designer to adjust the product structure for simplifying the forming process.
FIGURE 9 The access cover demonstration article
CONCLUSIONS (D The L-shaped stiffers were prepared either in direct press forming from prepreg or in thermoforming the pre-consolidated blanks. The latter method was more cost-effective with higher product quality. The bad stickability of the dry prepreg for single curved part was not met in thermoforming. ©Both fusion welding and consolidation were successful in manufacuting part with stiffers.The latter method was more cost-effective. In all, thermoforming and co-consolidation offered strong potential especially in large volume production of aerospace 3-D composite structural parts. Our access cover demonstration article almost satisfied the final product design requirement. REFERENCES 1. Gutowski T.G., 1997. Advanced composites manufacturing, John Wiley&Sons, Inc. 2. Cogswell, F.N., The processing science of thermoplastic structural composites, International Polym.Process, 1,1987:157-165 3. Okine, R.K., Analysis of forming parts from thermoplastic matrix composite sheet materials, J. Thermoplastic Compos. Mater., 2, 1989:50-76 4. DUTTA A., M NIEMEYER and M CAKMAK, Thermoforming of advanced thermoplastic composites. Polymer Composites, 12(4),1991:257-272 5. Ageorgesa C , L. Ye,and M. Hou, Advances in fusion bonding techniques for joining thermoplastic matrix composites: a review, Composites: part A, 32, 2001:839-857 6. Harper R.C., Thermoforming of thermoplastic matrix composites,part II, SAMPE J., 28,1992:9-17 7. Kejian Wang, 2003, Study on advanced thermoplastic resin matrix composites — Maufacturing, applications and theoretical analyses. Postdoctoral report, Beijng Institute of Aeronautical Materials.
Dome Forming of Triaxial Non-Crimp Fabrics H. Kong, A.P. Mouritz* School of Aerospace, Mechanical & Manufacturing Engineering, RMIT University, GPO Box 2476V, Melbourne, Victoria 3001, Australia R. Paton Cooperative Research Centre for Advanced Composite Structures Ltd., 226 Lorimer Street, Fishermans Bend, Victoria 3207, Australia
ABSTRACT The influence of stitches on the deformation properties and mechanisms of triaxial non-crimp fabrics during dome forming is experimentally investigated. The dome forming properties are improved by minimising the line-tension on the stitches because this lowers the resistance against tow sliding, which is identified as an important deformation mechanism. Lowering the stitch tension also reduces the forming loads and amount of tow crimp damage to the fabric. Stitch location also affects the amount of tow crimping. Stitches located to the sides, rather than through, the tows provide less resistance to tow sliding and thereby cause less fabric damage. The number of stitches in the fabric was found not to affect the forming properties.
INTRODUCTION Polymer matrix composites reinforced with multiaxial non-crimp fabrics can be cost-effectively fabricated into complex, near net-shape components for primary aircraft structures. Multiaxial non-crimp fabrics consist of multiple layers of reinforcement yarns stacked in different orientations that are stitched by warp knitting into a single layer. The unique fibre architecture makes it possible to deform noncrimp fabrics to high strains during manufacture because of an ability of the fibre tows to slide and rotate without crimping, warping or buckling [1], whereas these defects often form when using prepregs and conventional woven fabrics. The high formability of non-crimp fabrics allows composite components to be fabricated with complex shapes. Despite the potential for non-crimp fabrics in highly curved composite structures, the deformation mechanisms of these fabrics during forming into a curved component are not well understood. This paper investigates the deformation mechanisms and forming limits of triaxial non-crimp fabrics when deformed into a curved section. The influences of the linetension, density and location of the stitches on the deformation behaviour of triaxial non-crimp fabrics is experimentally investigated using a dome forming test that simulates diaphragm forming. This study of the deformation properties enables the optimum design of the architecture of non-crimp triaxial fabrics to be determined. * Corresponding author, School of Aerospace, Mechanical & Manufacturing Engineering, RMIT University, GPO Box 2476V, Melbourne, Victoria 3001, Australia
Dome Forming of Triaxial Non-Crimp Fabrics
889
MATERIALS & EXPERIMENTAL TECHNIQUES Triaxial Non-Crimp Fabrics Six varieties of E-glass triaxial non-crimp fabric were custom-made using a Liba warp knitting machine by Colan Australia for this study. The architecture of the fabrics is summarised in tables 1-3, and a fuller description is given by Kong et al. [1]. The fabrics were stitched in a warp knitting process using 140 um diameter polyester filament in a tricot pattern. The areal density (760 g/m2) and ply lay-up pattern [0/+45/-45] of the fabrics is the same, and the only known difference is the condition of the stitches. The influence of stitch tension on dome forming was examined using three fabrics warp knitted with a low, intermediate or high line tension on the thread (table 1). These fabrics had the same stitch density (4.5 stitches/cm2). During production it is possible to adjust the tension exerted on the stitch thread, however the amount of tension cannot be easily measured. For this reason, the actual line-tension on the stitches at the low, intermediate and high levels is not known, and therefore the distinction between the fabrics is qualitative. The effect of stitch density on the forming properties was investigated using fabrics stitched to a low (4 stitches/cm2), intermediate (4.5 stitches/cm2) or high (5.6 stitches/cm2) density (table 2). The line tension on the stitch thread was at the intermediate level for each fabric. In addition to stitch density and stitch line-tension, the effect of stitch location on the forming properties of triaxial non-crimp fabric was investigated. The fabrics manufactured by Colan Australia had the stitches located between the glass tows. Triaxial Fabric II was compared to an E-glass triaxial fabric produced by Cotech (UK) that had a high proportion of the stitches passing through, rather than to the sides, of the tows (table 3). It must be noted that the areal weight of the Colan fabric (760 g/cm2) was higher than that for the Cotech fabric (583 g/cm2), and therefore a direct comparison is difficult. Table I Specifications of triaxial fabrics with different stitch line-tension. Fabric Type
Supplier
Triaxial I Triaxial II Triaxial III
Colan Colan Colan
Stitch Density (stitch/cm2) 4.5 4.5 4.5
Stitch Tension
Fabric Weight (g/m2)
Low Intermediate High
760 760 760
Table II Specifications of triaxial fabrics with different stitch densities. Fabric Type
Supplier
Triaxial IV Triaxial II Triaxial V
Colan Colan Colan
Stitch Density (stitch/cm2) 4.0 4.5 5.6
Stitch Tension
Fabric Weight (g/m)
Intermediate Intermediate Intermediate
760 760 760
Table III Specifications of triaxial fabrics with different stitch locations. Fabric Type
Supplier
Triaxial II Triaxial VI
Colan Cotech
Stitch Density (stitch/cm2) 4.5
Stitch Tension
Fabric Weight (g/m2)
Intermediate Not known
760 583
890
Dome Forming of Triaxial Non-Crimp Fabrics
Dome Forming Test A standard test method does not exist for determining the curved forming characteristics of fabrics. However, several research groups use a dome forming test to study the forming characteristics of composite textile fabrics, and this technique was used to study the non-crimp fabrics [eg.2]. The test as used here involves pressing a 150 mm<|) hemispherical plunger into the fabric under controlled loading at a crosshead speed of 30 mm/min to a maximum displacement of 75 mm. The test is shown in Figure 1. The fabric specimens were circular with a diameter of 340 mm, which is large enough to eliminate the influence of edge effects on the forming behaviour. The specimen edges were sandwiched between two aluminium clamping rings, and a vacuum bag was used to apply a uniform clamping pressure of ~1 atmosphere. A series of concentric circles were drawn on the lower 0° face of the fabric to determine the local apparent fabric strains during forming (figure lb).
(a) (b) FIGURE 1 (a) Dome forming test, (b) Deformed fabric specimen.
RESULTS & DISCUSSION The dome forming loads for the three triaxial fabrics with different stitch linetension values are compared in figure 2. The displacement is the distance the dome is pressed into the fabric: the maximum distance for the test is 75 mm. The forming loads for the fabrics with intermediate and high stitch line tension are similar. However, the loads for the fabric with the low stitch tension are slightly lower when the displacement exceeds -45 mm. This reveals that minimising the stitch tension can reduce the forming resistance of triaxial fabrics. After the triaxial fabrics were deformed to the maximum displacement, the apparent strain along the 90° (weft) and ±45° (bias) directions was measured from the increased spacing between the concentric circular lines drawn on the specimen 0° face before testing (as shown in figure lb). The apparent fabric strain in these directions is not constant, but varies with dome angle (9) from the dome apex (9 = 0°) to the boundary (9 = 90°). Figure 3 shows the local apparent strain in the 90° and ±45° directions with dome angle for the triaxial fabrics with different stitch line tension. The apparent strain increases rapidly from the dome apex to the boundary. The strain in the 90° direction was the same for the three fabrics. However, the apparent strains in the ±45° directions of the fabric with the low stitch line tension were considerably higher than the strains in this direction in the other fabrics. This suggests that the low
Dome Forming of Triaxial Non-Crimp Fabrics
891
stitch tension allows the ±45° tows to slide more easily. An examination of the fabrics confirmed sliding of these tows through the stitch loops during dome forming. Kong et al. [1] recently found that reducing the stitch tension also lowers the forming resistance by enhancing tow sliding under bias extension loading. 4000 r - High stitch tension - Intermediate stitch tension • Low stitch tension
3000
2000
1000
0
25
50
Displacement (mm)
FIGURE 2 Load-displacement curves for the triaxial fabrics with different stitch line-tension.
Figure 3 also shows that the apparent strains in the 90° and ±45° directions were similar from the dome apex up to 9 « 40°. However, at dome angles 40° to 90° (ie. the dome boundary), it is seen in figure 3 that the apparent strain in the 90° and ±45° directions are different. This difference is greatest for the fabrics with the intermediate or high stitch line-tension. Between dome angles of 40° and 90° there is significant crimping of some of the fibre tows, as shown in figure 4, although the damage is less in the fabric with the low stitch tension because the tows can slide more easily under the stitch loops.
0.5 — • — High stitch tension --•a---
0.5 r—•— High stitch tension ••a—- Intermediate stitch tension -w— Low stitch tension
Intermediate stitch tension
—ca— Low stitch tension
0.4
0.4 c 'ro
c 'ro
55
55
0.3
E o
0.3
D)
c 0.2
0.2
0.1
0.1
0.0
0.0
0
30 60 Dome Angle (degrees)
90
"0
30 60 Dome Angle (degrees)
90
(a) (b) FIGURE 3 Variation in local dome forming strains in the (a) 90° and (b) ±45° directions in the triaxial fabrics with different stitch line-tension.
Dome Forming of Triaxial Non-Crimp Fabrics
892
0.8
•*
*!
r
0.6 •2
i
I 0.4 b 5 0.2-
o.oLLow
Intermediate High Stitch-Line Tension
(a) (b) FIGURE 4 (a) Tow crimping in triaxial fabric, (b) Effect of stitch line-tension on linear forming ratio.
The stitch line-tension was also found to influence the 'dome forming ratio', Rf, of the fabrics. This is defined as the arc length measured from the dome apex to where crimping occurs in the fabric normalised agamst the total dome length from the apex to boundary. This ratio is a measure of the local deformation that can be accommodated by the fabric without tow crimping. The effect of stitch tension on the dome forming ratio measured in the 90° direction is shown in figure 4b. The forming ratio increases when the stitch tension is reduced, further demonstrating that lowering the stitch tension significantly improves the formability of triaxial fabrics. The influences of the density and location of the stitches on the load-displacement curves of the triaxial fabrics is shown in figure 5. It is seen that the stitch density has little affect on the forming load. It was also observed that the stitch density did not influence the local strains or the linear forming ratio of the fabric. The forming load of the fabric was also not significantly affected by the location of the stitches. Figure 5b shows that the load-displacement curves are similar. However, tow crimping was observed to be more severe in the fabric with stitches through the tows, because the stitches impede the sliding action of the tows. The reader is reminded that comparison of behaviour of these two fabrics is difficult. 4000
- High stitch density - Intermediate stitch density Low stitch density
3000
2000
g> 2000 •
1000 -
0
0
25
50
Displacement (mm)
75
0
25
50
75
Displacement (mm)
(a) (b) FIGURE 5 The effect of (a) stitch density and (b) stitch location on the load-displacement curves for the triaxial fabrics.
Dome Forming of Triaxial Non-Crimp Fabrics
893
CONCLUSION Triaxial non-crimp fabrics have good forming properties when deformed into a double-curved shape due to the tow sliding mechanism. However, the stitches affect the forming behaviour by influencing the resistance to tow sliding. Lowering the line tension exerted on the stitches increases the ease by which tows can slide, and this reduces the resistance against forming, increases the linear forming ratio, and minimises the severity of crimp. The amount of crimp can also be reduced by locating the stitches to the sides, rather than through the centre, of the tows. While stitch tension affects the forming properties of triaxial fabrics, the areal density of the stitches appears to have little influence. ACKNOWLEDGEMENTS Helen Kong thanks RMIT University and the CRC for Advanced Composite Structures (CRC-ACS) for provision of scholarships. The authors thank Colan Australia for fabricating the triaxial fabrics. The work presented in this paper is part of a research task on Composites Forming in the CRC for Advanced Composite Structures Ltd.
REFERENCES 1. 2.
Kong, H., A.P. Mouritz, and R. Paton. 2004. "Tensile Extension Properties and Deformation Mechanisms of Multiaxial Non-Crimp Fabrics', Comp. Struct, (in press). Zhong, C , J.Z. Yu, and F.K. Ko. 1994. "Formability of Textile Preforms for Composite Applications. Part 2: Evaluation Experiments and Modelling. Comp. Man, Vol 5: 123-132.
In situ Microfibrillar Reinforced Composites of PET/PC Genhai G. Liang KCPC, Chemistry School, The University of Sydney, Australia Allan J. Easteal Chemistry Department, The University of Auckland, New Zealand
ABSTRACT Microfibrillar reinforced composite (MFC) is a new kind of in situ composite, found by Evstatiev and Fakirov in 1992 [1]. This MFC was made by the zoneannealing method from PET/Nylon-6 binary blend, or PET/Nylon-6/PBT ternary blend, in which oriented PET fibres act as reinforcement, and crystalline polymer, Nylon or Nylon/PBT, as matrix. In the present study an amorphous polymer, PC, was used to replace the crystalline polymer to act as matrix, with PET fibres as reinforcing phase, to form microfibrillar reinforced amorphous polymer composite. The composite was made by an improved drawing-annealing method, i.e., amorphous PET/PC blend films were drawn using tension of ca. 15 MPa at ambient temperature, to 300% extension, then the drawn films were subjected to isothermal annealing with the ends fixed, at 160°C for 10 hours in vacuum. The properties were investigated by optical microscopy, XRD, SEM and DSC, and the MFC structure and formation were confirmed. It is found that there are some fibres aligned with the stretching direction in a transparent matrix, and the MFC film becomes non-transparent with increase of the annealing time. XRD shows that in the MFC there is a crystalline phase which is attributed to PET fibres. From DSC, the degree of crystallinity of the PET fibres was evaluated as 46.7% from the heat of fusion. From the etched MFC samples it is found that the oriented PET fibres are preserved in the composites. The formation of MFC is believed to proceed by formation of the PET and PC fibres in the cold-drawing stage; the amount of the PET fibres increases and the PC fibres revert to amorphous polymer in the annealing stage. We conclude that the cold drawing/annealing process leads to a new type of MFC in which the reinforcing phase is highly oriented PET, and amorphous PC (plus amorphous PET) acts as the matrix.
INTRODUCTION Traditional composite material is made up of the reinforcing material and the matrix, between which there is a definite interface. The interface is formed in the composite forming process in which the reinforcing material is always in the solid * Corresponding author, Key Centre for Polymer Colloids, Chemistry School, The University of Sydney, Sydney NSW 2006, Australia, Fax: +61 2 9351 8651, Email: [email protected]
In situ Microfibrillar Reinforced Composites of PET/PC
895
state but the matrix is initially liquid and finally in the solid state. As a result the interface is the weakest place in the composites due to the immiscibility of the matrix and the reinforcement. Since the invention of modern composite materials, many techniques have been developed to improve the strength of the interface, but due to the inherent structure of the composites, the interface problem is one of the principal issues to be resolved. Microfibrillar reinforced composite (MFC) is an in situ composite material, in which crystalline micro-fibres of thermoplastic polymers act as the reinforcing elements and the amorphous parts of the polymers as the matrix, and the polymers, as usual, are initially blended. MFC is manufactured using the zone-annealing method: a film of polymer blend is drawn to about 400% extension at above 80°C, then is subjected to isothermal annealing with the ends of the film fixed, at 220°C for up to 25 hours in vacuum [1]. Because in a molecular chain some chain segments stretch under applied force to form the microfibres, and some segments coil to form the amorphous phase, there are no weak interfaces between the reinforcement and the matrix. The results showed that MFC had excellent mechanical properties; its tensile strength and Young's modulus were similar to the glass-fibre-reinforced (25-40% glass fibres) engineering plastic nylon-66 [2]. So far all MFCs have been made from the crystalline polymers blends, such as polyethylene terephthalate (PET), Nylon-6 and polybutylene terephthalate (PBT), but the crystalline polymers tend to phase separate in the process of crystallisation, which may cause reduction of the strength due to the existence of internal stress in the sample [3]. Some improvement has been achieved by means of blending of the miscible polymers, but the results do not meet expectations. In this paper we use a crystalline polymer, PET, and an amorphous polymer, polycarbonate (PC), to blend together to form a non-phase-separated MFC. In this composite the PET microfibre acts as the reinforcement, and the amorphous polymer, PC, together with amorphous PET, as the matrix.
EXPERIMENT Raw Materials Polyethylene terephthalate (PET) was a product of Nexus Co.. Polycarbonate (PC), labelled Makrolon 2658, was an injection moulding grade for food contact applications made by Bayer. Titanium terabutoxide (TTBO) was laboratory reagent grade material, used as a transesterification catalyst in these experiments. Manufacture of MFC The MFC was obtained according to the principle of the method of drawingannealing under the following conditions: A mixture of PET powder and PC powder, in equal proportions by weight, made using solution/precipitation method [4], together with 0.013% of catalyst TTBO, was melted and efficiently mixed at 280°C for 2 minutes, then cooled to form a single phase solid blend of PET and PC. The sample was weighed and put into a circular cup with an aluminium foil cover pre-coated with Teflon™ spray, then inserted in a Graseby Specac P/N 15800 high temperature constant thickness film maker. Films were made at 250°C at a pressure of 2 tonnes, for 1 minute, then the cover with the film was immediately immersed in a
896
In situ Microfibrillar Reinforced Composites of PET/PC
quenching bath of liquid nitrogen. Finally, the cup and its cover were removed, giving films with thickness 70 um, and diameter 29 mm. This amorphous PET/PC blend film was drawn using tension of ca. 15 MPa at ambient temperature, to about 300% extension. Subsequently the drawn samples were subjected to isothermal annealing with ends fixed, at 160 °C for 10 hours in a vacuum oven. Thus microfibrillar reinforced composite of PET/PC was prepared with PET microfibres as the reinforcement and PC and the amorphous part of the PET as the matrix. Test Conditions Differential scanning calorimetry (DSC) was carried out using a Polymer Laboratories model 12000 instrument, and the degree of crystallinity of the MFC was calculated from the heat of fusion of the film. Samples for scanning electronic microscopy (SEM) were made as follows. The MFC specimens were put into hot tetrachloroethane for about 10 min, in order to remove the PC phase from the surface, then dried samples were coated with a layer of gold. SEM analysis was performed using a Philips SEM 505 instrument. X-ray Diffraction (XRD) was done on a Philips X-ray diffractometer by scanning the samples at 1.05° (29) min"1.
EXPERIMENTAL RESULTS AND DISCUSSION Using optical microscopy it was found that the untreated PET/PC/TTBO (50/50/0.013) blend film was transparent, and hence amorphous. After drawing, the blend film became slightly opaque, some fibres aligned with the stretching direction were found, and the fibre and the matrix could be discriminated clearly. This observation indicates that the drawn film begins to crystallise to form fibres under the applied tension, and the fibre is different material from the matrix. This drawn film was further treated by annealing, after which the film was nontransparent and whitened. Relatively large fibres were visible, and a very small transparent part between the fibres was discernible. It can be deduced that the annealed film has more and larger crystalline regions whose higher degree of crystallinity makes it more different from the matrix in refractive index, causing the film to be opaque. The transparent part should be the amorphous matrix, PC, and part of the PET. XRD spectra showed that in the blended film samples both before and after colddrawing, no Bragg reflections were apparent. However after drawing and annealing, Bragg reflections were clearly visible, as shown in Fig. 1. The 28 values correspond to crystallites with dimensions (A) 3.42x3.88x5.08 (axbxc).
In situ Microfibrillar Reinforced Composites of PET/PC
897
ouu -
5.08 A
250 •
1
A
200 •
3.88 ?
A
I" 150 •e
3.42 0
.Jr
100
,
A
\L>
50
h A rW
'
Vl ^**Vlrf>fti*UILjLLi-i
0 15
10
20
25
30
35
Diffraction angle / 28
FIGURE 1. XRD spectrum of the PET/PC/TTBO (50/50/0.013) blend film after drawing then annealing.
When the blend film is quenched from the molten state, the molecular chains are frozen in the random coil condition, so it is an amorphous polymer. After the quenched film is drawn, its molecular chains will uncoil and align partially along the draw direction. The chains should crystallise and have a certain degree of crystalhnity, but the degree of crystallinity will not be high because below the glass transition temperature (Tg) of the PET phase the molecular chains do not have sufficient energy and free volume to rotate freely. This low degree of crystallinity was not detected with XRD. When the film was annealed at 160°C, between Tg and the melting temperature (Tm) of the PET phase, the molecular chains have sufficient energy and free volume to crystallise rapidly, so that the degree of crystallinity is high. In this process the films ends were fixed, which prevents the stretched molecular chains from re-coiling. Consequently, with XRD this crystalline character was detected, with unit cell dimensions is similar to those of single crystal PET, indicating that the crystallinity is attributable to the PET phase of the blend film.
50% i 45% 40% 35% •
30% 25% • 20% •
15% 10% 5% 0%
I
|
Untreated film
Draw n film
Annealed film
FIGURE 2. The degree of crystallinity of the PET/PC/TTBO (50/50/0.013) blend film at different stages, as determined by DSC.
898
In situ Microfibrillar Reinforced Composites of PET/PC
With XRD, quantitative measurement of the degree of crystallinity is more difficult than with DSC. With DSC it was found that the heat of fusion was largest in the annealed film, and the degree of crystallinity was the highest (46.7%). In the drawn film the PET phase had 31.0% crystallinity. The untreated film had near zero enthalpy of fusion and hence very small crystallinity. These results are shown in Fig.2.
•
\Sj-*
• •
.
'
i
i
" _
•__
" t'J'i.
*;•
\
* *,
\ * "
• if
v
FIGURE 3. SEM micrograph of MFC of PET/PC (x 388).
As shown in the SEM micrograph, in this MFC the microfibre diameter was less than 1 urn. It can be deduced that the microfibres are crystalline PET, and amorphous PET and the PC phase (the removed parts) make up the matrix. The above experiments confirmed that the drawn and annealed blend films have formed microfibrillar reinforced composites (MFC), in which the PET fibre acts as the reinforcement, and both the PC phase and amorphous PET phase as the matrix. This is another kind of MFC, i.e., with amorphous polymer as the matrix, that is different from the MFCs which have been found previously, where the matrix is a crystalline polymer. The MFC forming process can be divided into following steps. Firstly, in the blend of PET/PC the molecular chains are random and coiled. The blend film is drawn by a tensile force, and when the stress reaches the film's yield strength, it begins to show necking. In the neck area, the molecular chains uncoil and align in the direction of the force, and the unidirectional chains start to crystallise. When the neck part reaches the whole area of the film, the film attains maximum strain, and cannot be extended any further without breaking. For the PET phase, the extension can reach about 400% [5], but for PC it is only about 100% [6]. Consequently, in this film the PET phase must be continuous and the PC phase non-continuous. Finally, after annealing, because of high temperature, the molecular chain has more energy, while the free space is also greater due to thermal expansion, which causes more extended molecular chains to align and to crystallise. As a result the
In situ Microfibrillar Reinforced Composites of PET/PC
899
degree of crystallinity becomes higher and the number of fibres increases. For the PC phase, the molecular chain segments will rotate freely due to the annealing temperature being above Tg of PC, and the chains will re-coil to return to the amorphous state in some degree. On the other hand, the PET molecular chains will not find it easy to re-coil because chain stretching was maintained continuously with a tensile force. A schematic diagram of the proposed molecular chain development is given in Fig.4. PET microfibres
Polymer blending
After drawing
After annealing
FIGURE 4. Schematic of molecular chains in the PET/PC blend at different stages.
CONCLUSIONS From the above experimental results, the conclusion can be drawn that by means of drawing and annealing, a new kind of microfibrillar reinforced composite has been found, in which the PET fibre acts as the reinforcement, and both the amorphous polymer, PC, and amorphous PET, as the matrix. The PET microfibres are unidirectional, with diameter less than one micrometer. As the blend of PET and PC shows a single glass transition temperature in the DSC [7], the blend is evidently a single phase so that the phase separation problem does not occur in this MFC.
REFERENCES 1. 2. 3. 4. 5. 6. 7.
Evstatiev, M. and Fakirov, S., 1992, Polymer, 33, pp. 877-880 Fakirov, S. Evstatiev, M. and Schultz, M , 1993, Polymer, 34, pp.4669-4679 Evstatiev, M. and Fakirov, S., 1994, Polym. Networks Blends, 4(1), pp. 25-31 Liang, G. and Easteal, A. 2001, World Chemistry Congress, 1-7 July 2001, Brisbane Australia, pp. OA 34 Mark, H. F. and Kroschwitz, J. I., 1988 "Encyclopedia of Polymer and Engineering", 4, WileyInterscience, New York, pp. 487-489. Mark, H. F. and Kroschwitz J. I., 1988 "Encyclopedia of Polymer and Engineering", 11, WileyInterscience, New York, pp. 658. Liang G. and Easteal A., 1998. World Polymer Congress, 12-17 July 1998, Gold Coast, Australia, pp. 531
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Part XVI
Smart Composites
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EPR and Magnetic Susceptibility Studies on the Structure and Polaron Dynamics on V2O5-, MoO3- and CuOContaining Glasses B. B. Das*, R. Ambika; S. Ageetha; P. Vimala Department of Chemistry, Pondicherry University, Pondicherry 605014, India
ABSTRACT EPR lineshapes studies on O.7V2O5-O.3P2O5 (SI), 0.7MoO3-0.2B2O3 (S2), O.5M0O3-O.2SD2O3-O.3K2O (S3), and 0.05CuO-0.7B2O3-0.25Li2O (S4) glasses were performed at various temperatures. The trends in g-values of gj < gi in the cases of SI, S2 and gx < gy in S3 and S4 show that the paramagnetic ions formed in the matrices are vanadyl, VO2+, molybdenyl, MoO3+, Mo5+ and Cu2+, respectively in highly distorted octahedra of oxygens having C4V symmetry. The values of the small polaron exchange integrals calculated from the magnetic susceptibility data at 300 K are found to be 0.04, 0.012, 0.004, and 0.028 eV for SI, S2, S3, and S4, respectively. However, exchange integrals calculated from the non-linear fit of the magnetic susceptibility versus temperature plots of S3 and S4 in the range 4.2-300 K are found to be 0.001 eV in both the glasses.
INTRODUCTION Glasses containing V2O5II], MoO3[2] and CuO[3] exhibit semiconducting property due to the thermally excited hopping of the small polaron [4-6] from a lower valent state(Mo5+) to a higher valent state(Mo6+) of the metal atom, for example, in the case of MoO3-containing glasses. These lower valent states of V4+(3d'), Mo5+(4d1), and Cu2+(3d9) ions are formed in the matrix due to reduction during the melting process, and the ions are interesting paramagnetic probes for studying the local structures of these glasses by electron paramagnetic resonance (EPR) spectroscopy. Furthermore, the temperature dependent small polaron hopping has a marked effect on the nature of the EPR lineshapes[7] in the glasses, m this paper, we report our EPR and magnetic susceptibility studies on 0.7V2O5-0.3P2O5(Sl), 0.7MoO3-0.2B2O3(S2), 0.5MoO30.2Sb2O3-0.3K2O(S3), and 0.05CuO-0.7B2O3-0.25Li2O (S4) glasses and discuss the EPR lineshapes modulation due to the exchange of the small polaron.
EXPERIMENTALS The glasses were prepared by solid state reactions using reagent grade chemicals.
* Correspondence author; Department of Chemistry, Pondicherry University, Pondicherry (India); Fax: 91-413-2655211/2655265; e-mail:[email protected]
605014
904 Structure and Polaron Dynamics on V2O5-, MoO3- and CuO- Containing Glasses The glassy phase was ascertained by XRD patterns which show a broad peak at the lower diffraction angles. The chemical analysis was performed using standard oxidation and reduction method. The magnetic susceptibilities of the samples at room temperature were measured using an EG and G Vibrating Sample Magnetometer (VSM). While the magnetic susceptibilities of the sample S3 and S4 in the range 4.2300 K were registered with a SQUID magnetometer (Quantum Design) in a magnetic field of 3000 G. The X-band EPR lineshape of V2O5-containing glass (SI) at 4 K was recorded in a Varian EPR spectrometer, while for rest of the glasses at 77 K a JEOL JES-TE110 EPR spectrometer system was used. In both of the above cases, a 100 kHz magnetic field modulation was used. The magnetic field calibration has been made with respect to the resonance line of the DPPH (gDppH=2.00354) [8] in the case of glass SI and with respect to tempol (gtempor 2.0032) for rest of the glasses. RESULTS AND DISCUSSION Figure 1 shows our observed and computer simulated EPR lineshapes of glasses O.7V2O5-O.3P2O5 (SI), 0.8 M0O3-O.2B2O3 (S2), 0.5MoO3-0.2Sb2O3-0.3K2O (S3), and 0.05CuO-0.7B2O3-0.25Li2O (S4). All the lineshapes are axially symmetric with 16-line feature 51V(I=7/2) nuclei (SI), 22-line feature of two magnetically equivalent 97 95 Mo (1=5/2) nuclei (S2 and S3), and 4-parallel lines with unresolved perpendicular lines of 63Cu (1=3/2) nuclei (S4). Using the axially symmetric spin Hamiltonian as under, A±(SJX+Syly),
(1)
we simulated the lineshapes using the Bruker EPR lineshapes simulation program Simfonia. The spin Hamiltonian parameters obtained from simulation are presented in Table 1. TABLE I Spin Hamiltonian parameters obtained from simulation of O.7V2O5-O.3P2O5 (SI), 0.7MoO 3 -0.2B 2 O 3 (S2), 0.5MoO3-0.2Sb2O3 -0.3K2O (S3) and 0.05CuO-0.7B2O3-0.25Li2O (S4) glasses at 4, 77, 300 K.
Glass No.
9 II 300K
S1
1.959®
S2
1.940
A|,(x10 -W)
9, 77K
77K
300K
77K
300K
*
1.987®
*
156.6
-
1.935
1.974
1.975
150.0
141.9
Ax(x10*W1) 300K 53.8
77K -
35.5
34.5
S3
1.998
1.986
1.973
1.970
171.0
130.0
63.0
50.0
S4
2.223
2.388
2.035
2.055
70.0
121.0
49.0
42.0
g|l and gx values are at 4 K; * Lineshape is isotropic at 77 K(gj so =1.963).
Structure and Polaron Dynamics on V2O5-, MoO3- and CuO- Containing Glasses
905
tto,} t t h fk rIs t ! Bnft,, t iis,,»h• n a
2000
3175
4350
MAGNETIC FIELD (G)
FIGURE 1 (a) Experimental (b) computer simulated lineshapes of 0.7V2O5-0.3P2O5(Sl), 0.8MoO3-0.2B2O3 (S2), 0.5MoO3-0.2Sb2O3-0.3K2O (S3), and 0.05CuO0.7B2O3-0.25Li2O(S4) glasses at various temperatures.
The trend in the g-values of gn < g± in the cases of SI and S2 shows that the ,2+ paramagnetic ions formed in the glassy matrices are vanadyl, VO , molybdenyl, 3+ MoO ,
906 Structure and Polaron Dynamics on V2O5-, MoO3- and CuO- Containing Glasses respectively, whereas, in the cases of S3 and S4, the trend in the g-values of g±< gy shows that the paramagnetic ions formed are Mo5+ and Cu2+, respectively. In all of the above cases, the metal ion is in a distorted octahedron of six oxygens atoms having C4V symmetry. The octahedral units are [CNMO4/2-O1/2] (M=V, Mo) in the cases of glasses SI and S2, whereas, the units are [Oi/2-MO4/2-Oi/2](M= Mo, Cu) in the cases of glasses S3 and S4 where the axial M - 0 bonds are unequal. Our room temperature IR spectral studies reported earlier also show that the stretching modes of V=O [9] occurs at 1015 cm'1 in the case of glass SI, and that of Mo=O [10] at 991 cm"1 for glasses S2 and S3, respectively. The molecular orbital calculations performed on the above glasses with the above spin Hamiltonian parameters using the relations [2,11] for C4V symmetry show that in all the glasses the octahedral units are highly squeezed. The values of the small polaron exchange mtegrals calculated from the magnetic susceptibility data at 300 K are found to be 0.04, 0.012, 0.004, and 0.028 eV for SI, S2, S3, and S4, respectively. However, in Figure 2 we show the magnetic susceptibility, % versus temperature ,T (K) in the range 4.2-300 K of S3 and S4. The plots are fitted with the following equation:
X=
(2)
+ TIP, T+A
where c is the Curie constant, A is the Weiss constant, and TIP is the temperature independent paramagnetism term. The obtained parameters are shown in Table 2. All the parameters are found to be similar in the cases of both the glasses. The exchange integrals calculated from the Weiss constants using the relations [12] in the range 4.2-300 K are found to be 0.001 eV in both the glasses. The difference with the values of exchange integrals at room temperature is attributed to the difference in the range of temperature for measurements. 1.0x10
5.0x10"
50
100
150
250
300
T(K) FIGURE 2 Magnetic susceptibility, % versus Temperature, T(K), plots of glasses 0.5MoO3 - 0.2Sb2O3-0.3K2O (S3) and 0.05CuO-0.7B2O3-0.25Li2O(S4) in the range 4.2-300K
Structure and Polaron Dynamics on V2O5-, MoO3- and CuO- Containing Glasses
907
TABLE II. Curie constant c, Weiss constant, A, and temperature independent paramagnetism, TIP, and small polaron exchange integral of glasses 0.5MoO30.2Sb2O3-0.3K2O (S3) and 0.05CuO-0.7B2O3- 0.25Li2O (S4). Glass Mo.
Curie constant c (emu-K/gG)
A(K)
TIP (emu/gG)
Exchange integral (eV)
Weiss constant
S3
5.072x10"3
4.718
1.66X10"4
0.001
S4
3
4.727
1.66x10""
0.001
5.058x10"
CONCLUSION From our EPR lineshapes studies on the above glasses at various temperatures the following are our major conclusions. The trend in the g-values of gj < gx in the cases of SI and S2 shows that are drawn as follows: the paramagnetic ions formed in the matrices are vanadyl, VO2+, and molybdenyl, MoO3+ ions, respectively, whereas the trend g± < gy in S3 and S4 shows that the paramagnetic ions formed in the matrices are Mo5+ and Cu2+ ions, respectively. The paramagnetic ions are in highly distorted octahedra of oxygens having C4v symmetry. The exchange integrals calculated from the non-linear fit of the magnetic susceptibility versus temperature plots of S3 and S4 in the range 4.2-300 K are found to be 0.001 eV in both the glasses.
ACKNOWLEDGEMENTS We thank Prof. C. Michel for providing us with the magnetic susceptibility data in the temperature range 4.2-77 K. REFERENCES 1. Sayer, M., and A. Mansingh. 1972. "Transport properties of semiconducting phosphate glasses," Phys. Rev., B6: 4629-4643. 2. Baugher, J., and S. Parke. 1972. "E. S. R. and opical studies of Mo5+ ions in phosphate glasses," in Amorphous Materials, R. W. Doughlas, and B. Ellis, eds. New York: Wiley, pp. 399-408. 3. Duran, A., Jurado J., and Navarro J. F. 1986. 'Electrical properties of copper phosphate glasses I. DC electrical behaviour," J. Non-Cryst. Solids, 79: 333-351. 4. Schimid, A. P. 1968. "Evidence for the small polaron as the charge carriers in glasses containing transition metal oxides" J. Appl. Phys., 39: 3140-3149. 5. Bosman, A. J., and H. J. Van Daal, 1970. "Small-polaron versus band conduction in some transitionmetal oxides," Adv. Phys., 19: 1-117. 6. Rao, C. N. R., and Gopalakrishnan, J. 1986. New directions in solid state chemistry, Cambridge University Press, Cambridge, p. 268. 7. Raghunathan, P., andB. B. Das. 1989. "EPR lineshape studies on low-temperature vanadium 3d1 polaron dynamics in the 70V2O5-30P2O5 binary glass," Chem. Phys. Letts., 160: 627-631. 8. Hocking, M. B., and S. M. Mater. 1972. "Electron paramagnetic resonance examination of aqueous anthrasemiquinone radical anion," J. Mag. Reson., 47:187-199. 9. Dimitriev, Y., V. Dimitrov, M. Arnaudov, and D. Topalov. 1983. "IR- spectral study of vanadate vitreous systems,"/ Non-Cryst. Solids, 57:147-156. 10. Muthupari, S., and K. J. Rao. 1996. "Thermal and infrared spectroscopic studies of binary MO3P2O5 and ternary Na2O-MO3-P2O5 (M= Mo or W) glasses," J. Phys. Chem. Solids, 57: 553-561. 11. Lin, W. C. 1979. "Electron Spin Resonance and Electronic Structure of Metalloporphyrins," in The Porphyrin, vol. IV, D. Dolphin, eds. New York: Academic Press, pp 335-377. 12. Poole, Jr. C. P. 1967. Elecrtron Spin Resonance, Interscience, New York, p. 20.
Increase of High Burst Pressure in CFRP Vessels Reinforced by SMA Fibers Goichi Ben* and Kazuhiro Sakata Nihon University, Japan
ABSTRACT CFRP pressure vessels are now widely using in compressed natural gas vehicles (CNGV) and have a possibility to be employed in fuel cell vehicles (FCV) for storing of highly compressed Hydrogen, hi order to increase a driving distance in CNGV and FCV, lighter vessels proofed against a higher pressure are required. When pressure vessels are received internal pressure, the tensile circumferential stress at the inner radius should be decreased in order to increase their burst strength. This paper presents a method how to increase the burst strength of CFRP pressure vessels. For increasing the burst strength of CFRP pressure vessels, the shape memory alloy (SMA) fiber memorized a compressive stress is wound around the outer surface of cylindrical part of the CFRP pressure vessel. When the CFRP pressure vessel is received the internal pressure, its tensile circumferential stress can be reduced by the compressive stress of the SMA fiber and the experimental results of increasing the burst strength are shown. Furthermore, the experimental results are compared with numerical ones obtained by FEM and their good accordance is presented in this paper.
INTRODUCTION The use of CFRP in aerospace structures has significantly increased in the recent years due to its distinct advantages, namely high specific strength and modulus, corrosion resistance and other properties. CFRPs are also now widely used in pressure vessels of compressed natural gas vehicles (CNGV) [1],[2] and they have a possibility to be employed in fuel cell vehicles (FCV) for storing of highly compressed Hydrogen. In order to increase a driving distance in CNGV and FCV, lighter vessels proofed against a higher pressure are required. When pressure vessels are received internal pressure, the tensile circumferential stress at the inner radius should be decreased in order to increase their burst strength. Otherwise, SMA is being now utilized as one of candidate actuators in smart composite structures [3]. When the SMA is heated under the temperature of Austenite finished point, its shape returns to the memorized shape and its strength and modulus changes depend on the environmental temperature. For increasing the burst strength of CFRP pressure vessels, the SMA fiber memorized a compressive stress is wound * Corresponding Author, 1-2-1, Izumicho, Narashiono, Chiba 275-8575 Japan Fax No. +81-47-474-2349, Mail address; [email protected]
High Burst Pressure in CFRP Vessels Reinforced by SMA Fibers
909
around the outer surface of cylindrical part of the CFRP pressure vessel. When the CFRP pressure vessel is received the internal pressure, its tensile circumferential stress can be reduced by the compressive stress of the SMA fiber. This paper presents a method how to increase the burst strength of CFRP pressure vessels and the experimental results of increasing the burst strength are shown. Furthermore, the experimental results are compared with numerical ones obtained by FEM and their good accordance was presented in this paper. EXPERIMENTS Specimens The dimensions of CFRP pressure vessel used in the experiment were a total length of 385mm (cylindrical part length of 280mm), an outer diameter of 98.8mm and a thickness of 4.15mm. The CFRP vessel having an Al liner was covered with GFRP for the impact safety and then its lamination sequence from the center was the Al linear, CFRP and GFRP layers. The SMA (Ti-Ni alloy) fiber having 1.0mm diameter was wounded around the steel cylinder whose diameter was 0.5% or 2.0% smaller than the outer diameter of pressure vessel. Then, the wounded SMA wire was heated under 480°C for 1 hour and it was cooled by water in order to memorize the ring shape having the diameter of cylinders. The Young's modulus SMA fiber with a ring shape was determined by the following equation after tensile test under 20°C (Martensite state) and 80°C (Austenite state). E = Pna2/(ud4)
(1)
In which, P,a,u and d were a tensile load, a radius of ring, a displacement and a diameter of SMA, respectively. The results of Young's modulus were 43.8GPa (Martensite) and 88.4GPa (Austenite), respectively. The CFRP pressure vessel was closely wounded around its cylindrical part by the SMA fibers in the Martensite state. Figure 1 shows the CFRP vessel wounded with the SMA fiber.
FIGURE 1 CFRP Pressure Vessel Wound with SMA Wire
Internal Pressure Test An internal pressure test was executed in a heat chamber and the temperature of SMA fibers was measured by thermo-couples. After the temperature of SMA fibers reached to one of Austenite finished point, the internal pressure was loaded by using water pressure until the level of 20MPa and the circumferential and axial strains on 7 locations were measured as shown in Figure 2. Figure 3 shows the relation of
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High Burst Pressure in CFRP Vessels Reinforced by SMA Fibers
circumferential strain at the 4ch to the internal pressure. In which, the symbols of A and • present the strains of CFRP pressure vessels wounded SMA fibers under the temperature of 20°C (Martensite state) and the temperature of 80°C (Austenite state), respectively. In this case, the SMA fiber was memorized the 2% of compressive strain. Otherwise, the symbol of • shows the strain of specimen not winding the SMA. The three slopes of pressure to strain were agreed well with each other and the two (A and •) of them showed the same results. Namely, the Martensite state of SMA fibers does not any effect on the relation of pressure to strain. Otherwise, the result of Austenite showed the effect of reinforcement by the SMA fibers and presented the initial compressive strain of 1454 ii due to the SMA fiber under the no pressure.
1
T"1
• A
Jit' FIGURE 2 Strain Gages Positions
FIGURE 3 Relation of Internal Pressure to circumferential Strain
Burst Test A burst test was followed after the internal pressure test and this test was carried out by a guideline of the High Pressure Gas Safety Institute of Japan. In the guideline, the pressure speed is 2.0MPa/sec and then the pressure of 72.54MPa (minimum burst pressure of this vessel) is kept for one hour and the pressure loading continues until the burst of vessel. The burst pressure of CFRP vessel without SMA fibers was 81.54MPa and the burst pressure of CFRP vessel wounded SMA fibers of 0.5% compressive strain was 102.3MPa. This value was 25.5% larger than one without SMA fibers and it broke at near the center of vessel (Figure 4). Otherwise, the burst pressure of vessel in the case of 2% strain was 99.94MPa and it was the 21.3% of increase. Although the SMA fiber was memorized the larger compressive strain, the burst pressure was smaller than one of the 0.5% strain This vessel broke at near the end of cylindrical part as shown in Figure 5 and the stress distribution at this region was supposed to be complicated, especially depend on the winding method of SMA fibers.
High Burst Pressure in CFRP Vessels Reinforced by SMA Fibers
FIGURE 4 Specimen after Burst (Compressive Strain 0.5%)
911
FIGURE 5 Specimen after Burst (Compressive Strain 2%)
FEMANLYSES Modeling hi order to compare with the results of internal pressure test, numerical analyses were executed by the FEM code (ANSYS ver.7.0). This problem was treated as a 2-dimensional axi-symmetric problem under the elastic-plastic state. The pressure vessel was divided by the plane element (element type of PLANE 182) and the compressive strain of SMA fiber was modeled by the thermal expansion coefficient and the negative temperature, hi Tablel, mechanical properties of CFRP, GFRP, Al and SMA fiber are listed. The CFRP, GFRP layers and the SMA fiber were supposed to remain in an elastic state until the burst but the Al linear was supposed to change from the elastic state to the plastic one. In the plastic state, Young's modules was determined by the slope of the line connecting the stress of 321.1MPa (a yield stress corresponding to 0.2% strain) and the stress of 338MPa (corresponding to 2% strain). Before the pressure loading, an autofrettage which meant to give the pressure of 35.9MPa and to return to zero pressure, was carried out in the experiment and then the compressive stress in the Al linear and the tensile stress in the CFRP layer remained. TABLE I Material Properties Aluminum Liner CFRP
GFRP
SMA Fiber
Young's Modulus (GPa) Poisson's Ratio Modulus of Elasticity Longitudinal (GPa) Transverse (GPa) Shear (GPa) Poisson's Ratio Longitudinal Transverse Modulus of Elasticity Longitudinal (GPa) Transverse (GPa) Shear (GPa) Poisson's Ratio Longitudinal Transverse Young's Modulus (GPa) Poisson's Ratio
68.6 0.3 125 7.8 4.4 0.345 0.0196 45.1 12.7 4.71 0.26 0.0732 88.35 0.3
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High Burst Pressure in CFRP Vessels Reinforced by SMA Fibers
Comparisons with Experiment In Figure 6, the numerical result of CFRP vessel with the SMA finer memorized 2% compressive strain is compared with the experimental one. Since the numerical strains of the circumferential and the axial directions at the location 4 did not consider the residual tensile strain owing to the autofrettage effect and the thermal expansion of CFRP owing to the application of heat until the Austenite finished point, they were somewhat smaller than experimental ones. However the numerical method developed here can be used to examine the behavior of CFRP pressure vessel reinforced by the SMA fiber.
FEM Axis FEM C ircum efelence A Exp Axis @ Exp C icum eference
-2000
0
2000
4000
6000
8000
10000
12000
Stoh (II )
FIGURE 6 Comparison of FEM and Experimental Value
Stress ratios of CFRP and Al linear hi order to examine the effect of compression by the SMA fibers to the Al linear, the numerical results of the CFRP vessels with and without SMA fibers are shown for the Al linear in Figure 7 and for the CFRP in Figure 8.
- -
No SMA SMA2% 01 uste
^ "*
1
lie)
-* - '
—
_ 40
50
•
60
70
8
FIGURE 7 Relation of Circumferential Stress to Internal Pressure (Aluminum Liner)
High Burst Pressure in CFRP Vessels Reinforced by SMA Fibers
913
No SMA SMA 2> lAustente)
10 -500
20
30
40
50
60
70
L
ktemolPressun UPa)
FIGURE 8 Relation of Circumferential Stress to Internal Pressure (CFRP Layer)
In this case, the residual stresses in the Al linear and the CFRP layer owing to the autofrettage effect were taken into consideration. The compressive stress acted at the Al linear in the initial stage and it approached to a constant value of tensile strength (350.4MPa) and then the stress of CFRP layer increased. This increase of stress became smaller owing to the SMA fibers. CONCLUSIONS 1) The burst strength of CFRP pressure vessels reinforced by the SMA fiber memorized compressive strain increased over 20% to ones not reinforced by the SMA fiber. 2) This increase of burst strength depended on a degree of compressive strain in SMA fibers and a method of winding the SMA fibers around the CFRP pressure vessel. 3) The numerical results by FEM were well agreed with the experimental ones and this numerical result can be employed to examine the design of CFRP pressure vessel reinforced by the SMA fiber. This research was supported by the Ministry of Education, Culture, Sports, Science and Technology in Japan as a Grand-Aid-for Scientific Research (C)(term of project 2001- 2003) and we express our thanks to Dr. T. Takehana (the High Pressure Gas Institute of Japan) and Dr. A.Kitano (Toray Co.) for their regards in the experiment. REFERENCES 1.
G. Ben and A. Moroi, 1998. "Burst Strength of CFRP FW Cylinders Having Damage", Proc. of 1st ACCM 641/1-641/4.
2.
T. Takehana, 2000. "A Study on Design and Safety Evaluation of FRP Composite Vessels", Doctor-Thesis of Tokyo Metropolitan University.
3.
H. Yoshida, K. Heshiki and G. Ben, 1998. "Bi-Directional Temperature Response and Responsive Power on Shape Memory Composite with Embedded Ti-Ni Alloy as Effectors", Proc. of 13th Technical Conference on Composite Materials, ASC, pp. 1181-1186.
Monitoring the Strain in the CFRP Laminates and CFRP/Concrete Structures Keiji Ogi Department of Materials Science and Engineering, Ehime University, Japan Yoshihiro Takao Research Institute for Applied Mechanics, Kyushu University, Japan
ABSTRACT This paper presents monitoring the strain in carbon fiber reinforced plastic (CFRP) laminates and CFRP/concrete structures by means of pizeoresistance properties of CFRP. First, the piezoresistance behavior in a CFRP unidirectional laminate under mechanical loading was characterized. A two-dimensional model was proposed using a DC circuit equivalent to an electric resistance network in the CFRP laminate to predict the resistance change due to tensile loading. The surface resistivity and the initial gage factor are expressed as a function of the off-axis angle in the model. Secondly, the strain in the concrete/CFRP structures was monitored using the piezoresistance behavior of the CFRP in order to verify the validity of the electric strain monitoring method. The resistance change together with the mechanical strain was measured in the CFRP laminate adhesively bonded to concrete under three-point flexural loading.
INTRODUCTION Carbon fibre reinforced plastics (CFRP) have been used as light-weight structural materials since they exhibit excellent performance in the mechanical properties such as elastic modulus and strength. Another notable function of this material is electric conductivity. Taking advantage of this property, it is expected that structural health monitoring is performed through the detection of the change in electric resistance or potential [ 1 -7]. Electric resistance is supposed to be changed by mechanical strain as well as damage accumulation. A lot of work has been conducted on the micromechnanical modeling of piezoelectric fibre composites [8-10], However, there are few mathematical models on piezoresistance of CFRP laminates although a constitutive model describing the relation between the mechanical strain and piezoconductivity has been proposed based on a lamination theory [11]. Recently, Park et al.[4] proposed a model to describe the change in electric resistance in the fibre direction taking account of fibre breakage due to tensile strain. However, the piezoresistance behavior in the off-axis and transverse directions has not been theoretically investigated in the literature. In the present paper, at first, the piezoresistance behavior in a CFRP unidirectional laminate under mechanical loading was characterized. A two-dimensional model was proposed using a DC circuit equivalent to an electric resistance network in the CFRP laminate to predict the resistance change due to tensile loading. The surface resistivity and Correspong Author, Ehime University, 3, Bunkyocho, Matsuyama, Ehime 790-8577, Japan Fax: +81-89-927-9811, Email:[email protected]
Monitoring Strain in CFRP Laminates and CFRP/Concrete Structures
915
the initial gage factor are expressed as a function of the off-axis angle in the model. Secondly, the strain in the concrete/CFRP structures was monitored by means of the piezoresistance behavior of the CFRP in order to verify the validity of the electric strain monitoring method. The resistance change together with the mechanical strain was measured in the CFRP laminate adhesively bonded to concrete under three-point flexural loading. PIEZORESISTANCE MODEL Here a piezoresistance model based on constitutive equations [12] is summarized. The gage factor of the off-axis specimen is derived as % (g\ Cu +Cu S12 /Sn +c]6Sl6/2Sn | t S12 s
A°
where Ztj and Stj denote off-axis piezoresistivity and compliance given in the literature [12] and /?n° denotes surface resistivity given by Pn P22 n2//3u°+m2//322° £() = l-exp(-atan* 6>J (3) in which m = cos 6 , « = sin 0 and 0 denotes the off-axis angle and a and b are empirically determined constants. Next, it is assumed that the resistance in the unidirectional laminate is equivalent to a DC circuit consisting of electrical unit cells with an H-shape [12]. Each unit cell is decomposed into four resistance elements R with the length of 812 in the fibre direction and a resistance element r in the transverse direction. A cell group consists of N unit cells connected in parallel and M cell groups are connected in series to form a whole DC circuit. In the present model the initial surface resistivity and piezoresistivity are given by Pn
(4) c
cu=c(ax-\)RQ, p
^21
(a,+lX+r 0 ' 1 Z.
— —
cl2=cR0, '
p C
22
c
{a2i -\)rQ1 -RQ
— _J
~
(5)
c
where c, a{, a2, RQ and r0denotes material properties empirically determined using initial surface resistivity and gage factors of 0-degree and 90-degree specimens.. EXPERIMENTAL Piezoresistance behavior of CFRP laminates Unidirectional laminates of a carbon fibre reinforced epoxy (T800H/#3631) with the thickness of 1.1 mm were employed for tensile tests. Coupon specimens were cut out from the laminates at angles of 0-, 10-, 45- and 90-degrees with respect to the fibre direction. The electrodes made of silver conductive paste were formed on the surface of the specimens. The four-terminal method was adopted to avoid the effect of contact resistance at the electrode. The quasi-static and loading/unloading tensile tests were conducted with the use of an electrohydraulic testing machine at a constant loading speed of 49 N/s for the 0-degree, 9.8 N/s for the 10-degree and 4.9 N/s for the 45- and 90-degree specimens. The
916
Monitoring Strain in CFRP Laminates and CFRP/Concrete Structures
electric resistance change together with the axial strain was measured for each specimen during loading. The initial surface resistivity J3U° and the initial gage factor Kn were calculated for the off-axis angle 8 of 0, 10,45 and 90 degrees. Piezoresistance behavior of CFRP/concrete structures Figure 1 shows a CFRP/concrete sample used in the study. A unidirectional CFRP laminate 1 mm thick was bonded on concrete (160 mm *40 mm * 40 mm) with epoxy adhesive. The four-terminal electrodes were formed on the surface of the CFRP plate in the same way as above. A strain gage was bonded on the center of the CFRP plate to measure the maximum strain in the CFRP plate. Three-point flexural tests with a span L of 100 mm were performed at a crosshead speed of 0.3 mm/min such that tensile stress was applied to the CFRP plate. The electric resistance change together with the strain was measured. Loading/unloading tensile tests were also conducted in the same way. The maximum tensile strain in the CFRP plate £™x are related with the maximum tensile stress in the CFRP and concrete cr™*, o-™* as E
_ {h + h l
pj I A
(7) w
where P and h denote load and the distance from the CFRP surface to the neutral axis, respectively, the subscripts 1,2 and 3 represent concrete, adhesive layer and CFRP, respectively, and EjIt and h{ denote flexural rigidity and thickness of each material.
160
FIGURE 1 Geometry of a CFRP/concrete sample.
RESULTS AND DISCUSSION Figure 2 shows the relative resistance change-strain curves together with the longitudinal stress-strain curves for the on-axis (0- and 90-degree) and off-axis (10- and 45-degree) specimens. The relative resistance change in the on-axis specimens (Fig. 2 (a) and (d)) increases almost linearly within the low strain less than 0.15 %, and the slope increases gradually at the large strain, hi the 10-degree specimen (Fig. 2 (b)), the resistance change increases linearly at low strains and decreases gradually and becomes the minus value. In the 45-degree specimen (Fig. 2 (c)), the resistance exhibits the
Monitoring Strain in CFRP Laminates and CFRP/Concrete Structures
917
Strain 00
(a) 1
tress (MPa
too
" delR/RO
20
- /
0
iJ
/ / Stress -
1
1
Strain (») (C)
FIGURE 2 Stress-strain and electric resistance change ratio-strain curves for (a) 0-, (b) 10-, (c) 45- and (d) 90-deg specimens under monotonic tensile loading.
20
40
60
80
100
Off-axis angle (deg) FIGURE 3 Measured and predicted initial gage factor vs. off-axis angle.
distinctive four-stage behavior, namely, (i) primary linear (-0.15 %), (ii) secondary linear (0.15-0.4 %), (iii) plateau (0.4-1.0 %) and (iv) final increase region (1.0 %~). Figure 3 shows measured and predicted initial gage factors as a function of the off-axis angle, where round plots stand for experimental results. Peaks in the predicted curves are observed at around 12 degrees and the experimental data agrees well with the predictions. Figure 4 shows the maximum stress in concrete calculate using eq. (6) and resistance change in the CFRP plate plotted against the maximum strain in the CFRP laminate measured with the strain gage. A straight line is the predicted stress based on the linear beam theory. The sample fractured at flexural stress of 16 MPa which is much larger than flexural strength of concrete. The resistance change decreased almost linearly with
918
Monitoring Strain in CFRP Laminates and CFRP/Concrete Structures
increasing strain. The reason for this negative gage factor is presumably ascribed to thickness effect. Part of electric current flows in the direction of thickness which decreases with tensile stress. The resistance in the thickness direction is much larger than that in the length direction. As a result, the total resistance decreases with tensile stress. Another reason for the negative gage factor is the gage length which is equal to the distance between electrodes. Short gage length and thin laminate should employed in order to obtain an accurate positive gage factor [13]. However, relative long gage length is required to monitor the strain in large CFRP/concrete structures. This problem must be solved to facilitate practical technique using the electric method. Figure 5 shows the maximum stress in concrete and resistance change in the CFRP plate plotted against the maximum strain in the CFRP laminate. The resistance change-strain curve exhibits approximate linearity within small applied stress while nonlinearity and hysteresis are observed for loading/unloading at large stress. It is found that stress and strain in concrete can be monitored by measuring the CFRP bonded on concrete in linear region where electric resistance shows good correlation with strain. Naturally, similar nonlinear behavior is observed in CFRP laminates themselves [14]. This is another problem to be solved for accurate monitoring the strain. 25
200
400
600
800
1000
-0.6 1200
Maximum strain in CFRP
FIGURE 4 Stress-strain and resistance change-strain curves in the monotonic flexural test.
Monitoring Strain in CFRP Laminates and CFRP/Concrete Structures
0
919
200 400 600 800 1000 Maximum strain in CFRP (« i )
FIGURE 5 Stress-strain and resistance change-strain curves in the loading/unloading flexural test.
CONCLUDING REMARK An attempt is made to monitor the strain in CFRP laminates and CFRP/concrete structures by means of pizeoresistance properties of CFRP. It is possible to monitor the strain by measuring electric resistance change as far as piezoresistance response is almost linear. Negative gage factors must be predicted theoretically based on a piezoresistance model in order to apply the electric method to structural healthmonitoring. REFERENCES 1. 2. 3. 4. 5. 6.
7. 8. 9.
10. 11. 12. 13.
14.
Shulte, K. and Ch. Baron. 1989. "Load and failure analyses of CFRP laminates by means of electrical resistivity measurements," Comp. Sc. Tech., 36: 63-76.. Shulte, K. 2001. "Sensing with carbon fibers in polymer composites," Materials Science for the 21" Century, Invited Papers: 286-295. Song, D.-Y., J.-B. Park and N. Takeda. 2000. "Failure behavior and electrical property of CFRP and C¥G¥KP," Key Engineering Materials, 183-187: 1129-1134. Park, J.-B., T. Okabe, N. Takeda and WA Curtin. 2002. "Electromechanical modeling of unidirectional CFRP composites under tensile loading condition," Composites Part A, 33: 67-275. Arby J. C , S. Bochard, A. Chateauminois, M. Salvia and G. Giraud. 1999. "In situ detection of damage in CFRP laminates by electrical resistance measurements," Comp. Sci. Tech., 59: 925-935. Todoroki, A., M. Tanaka and Y. Shimamura. 2002. "Measurement of orthotropic electric conductance of CFRP laminates and analysis of the effect on delamination monitoring with an electric resistance change method," Comp. Sci. Tech., 62: 619-628. Todoroki A., Y. Tanaka and Y. Shimamura. 2002. "Delamination monitoring of graphite/epoxy laminated composite plate of electric resistance change method," Comp. Sci. Tech., 62: 1151-1160. Poizat, C. and M. Sester. 1999. "Effective properties of composites with embedded piezoelectric fibres," Computational Mater. Sci., 16: 89-97. Steinhausen, R., T. Hauke, W. Seifert, H. Beig, W. Wateka.S. Seifert, D. Sporn, S. Starke and A. Schonecker. 1999. "Finescaled piezoelectric 1-3 composites: properties and modeling," J. European Ceram. Soc, 19: 1289-1293. Jiang, C. P., Z. H. Tong and Y. K. Cheung. 2001. "A generalized self-consistent method for piezoelectric fiber reinforced composites under antiplane shear," Mechanics ofMaterials, 33: 295-308. Xiao, J., Y. Li and W. X. Fan. 1999. "A laminate theory of piezoresistance for composite laminates," Comp. Sc. Tech., 59: 1369-1373. Ogi, K. and Y. Takao. 2003. "Characterization of piezoresistance behavior in a CFRP unidirectional laminate," submitted to Comp Sci Tech. Todoroki, A., J. Yoshida and Y. Shimamura. 2003. "Piezoresistance measurement of CFRP for reliable gage factor," presented at International Conference on Advanced Technology on Experimental Mechanics 2003, Nagoya, Japan, September, 2003. Ogi. K. and Y. Takao. 2003."Effects of loading history on electric resistance in CFRP unidirectional composites," J. Japan Soc. Comp. Mater., 29: 217-225 (in Japanese).
Free Vibration of Perforated Aluminum Plates Reinforced with Bonded Composite Patches Jalil Rezaeepazhand* and Hadi Sabouri Department of Mechanical Engineering Ferdowsi University of Mashhad, P.O. Box: 91775-1111 Mashhad, Iran.
ABSTRACT The use of advanced laminated composite materials for repair and strengthening of existing structures has emerged as a promising technology in aerospace, mechanical and civil engineering. Performance level and life span of existing structural elements can be increased by repair and strengthening of these structural elements using advanced composite materials. The performance of damaged metallic plates reinforced with fiber-reinforced polymer composite materials (composite patch) are presented in this study. Numerical studies using commercial finite element software were conducted to investigate the effects of variation in patch geometries and lamination parameters on free vibration responses of repaired plates. A quantitative measure for the effectiveness of the composite patches is taken to be the relative change in natural frequencies of the reinforced plates compare to those of the un-reinforced one. The results presented herein indicated that, for vibration response of a repaired metallic plate with central cutout, a set of laminated composite patches with different number of plies and stacking sequences can be found which improve vibration frequency of damaged plates. INTRODUCTION Thin panels and shells of various constructions find wide uses as primary structural elements in simple and complex structural configurations. In recent years, the increasing need for lightweight efficient structures has led the structural engineer to the field of structural optimization and simultaneously to the use of advanced composites. Such composites are attractive because of their high stiffness and/or strength to weight ratios. Different cutout shapes in structural elements are needed to provide access to other parts of the structure and to reduce the weight of the system. In the other hand, structural elements are at the risk of being damaged during their service life. In this case, usually, the damage area/material is removed by cutting a circular or elliptical shape cutout and then the cutout area is repaired using patches. There are different types of bonded repairs. One of the most practical and easy to apply type of patches is adhesively bonded external patches made of composite materials. In the cases which, cutout is a part of initial design of the structures, composite external patches can be applied to reinforced and strengthening the cutout
' Corresponding Author, Email: [email protected]
Perforated Aluminum Plates Reinforced with Bonded Composite Patches
921
area. These types of patches must have a cutout area similar to the one in the structure. The enormous design flexibility of advanced composites is obtained because of the large number of design parameters .The correct and effective use of advanced composite materials requires complex analyses in order to achieve good understanding of the system response characteristics to external causes. With a view to better understanding the applicability of composites patches in repair and strengthening of existing structures, a numerical investigation was undertaken to assess the feasibility of their use. This type of investigation can save considerable expense and time, and provide the necessary information on behavior of repaired systems. The procedure consists of systematically observing the effect of each parameter. In this study application of external patches for repair and strengthening of metallic plates with circular central cut out is presented. Particular emphasis is placed on the case of free vibration of square aluminum flat plates. In the present studies, the material behavior is assumed to be linearly elastic. Furthermore, it is assumed that the plate and patches are without imperfections and the adhesive layer perfectly bonded between the base plate and composite patches. LITERATURE REVIEW Some studies concerning the use of external patches in repair of structures have been conducted in the past. Baker and Jones[l] presented most of the worked on developing the adhesively bonded repairs up to 1988. Most of this development has been made by Aeronautical Research Laboratory(ARL) in Australia. Chue and Liu[2] investigated the effect of stacking sequences of laminated composite patch for a plate with an inclined central cracked under biaxial loads. Pai et al.[3] investigated the effect of debonding on dynamic response and buckling of cracked aluminum plates repaired with a composite laminate. Wang and Pidaparti[4] investigated analytically and experimentally the static and fatigue response of cracked aluminum specimen with and without bonded patches. Boron/epoxy laminates were used as composite patches. Schubbe and Mall [5] investigated fatigue cracked growth based on a three layer two dimensional plate element to model cracked plate, adhesive layer and composite patches. Based on these studies, for cracked structures, the adhesively bonded composite patches reduce the stress intensity factor and extend the fatigue life. Engels and Becker[6] represented a closed-form solution for analysis a laminated plate with an elliptical cutout repaired by elliptical patches. Chai[7] presented finite element and some experimental results on the free vibration of symmetric composite plates with central hole. Huang and Sakiyama[8] are proposed an approximate method for analyzing the free vibration of rectangular plates with different cutouts. Few works has reported in retrofit and changing vibration response of perforated panels or shells. This study investigates problems associated with the performance of damaged metallic plates reinforced with fiber-reinforced polymer composite materials (composite patch). A square aluminum plate with a central circular cutout is considered as a damaged structural element. Numerical studies using commercial finite element code, Ansys, were conducted to investigate the effects of variation in patch geometries and lamination parameters on free vibration responses of repaired plates.
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Perforated Aluminum Plates Reinforced with Bonded Composite Patches
MATERIALS AND METHODS The base plate is a square aluminum plate. The dimensions of the plate are 200x200xlmm. A circular hole of radius 20 mm at center of plate is considered as a cutout. The vibration analysis is performed for six different type of patches: strengthening of perfect plate with un-symmetric(single side) (Fig. l-a) and symmetric(double sides) patches(Fig. l-b) - repair of perforated plate with unsymmetric(Fig. 1-c) and symmetric(Fig. l-d) patches and strengthening of perforated plate with un-symmetric(Fig. 1-e) and symmetric(Fig. l-f) composite patches.
& idl s efl-n
*- i
| 4 - II "
b
d
f
FIGURE 1: Six different cases of repair and strengthening of perfect and perforated plates.
Boron/epoxy and graphite/epoxy have been the main composite materials used to bond to metallic structures using epoxy based adhesive, hi this study, a square, 100x100 mm, Boron/Epoxy (B5.6/5505) laminate was considered as composite patches. The adhesive layer thickness is 0.15 mm. The thickness of each layer of composite patch is o.2 mm. The material properties used in this analysis are shown in Table 1. TABLE I : Material properties. Epoxy
Al2024-T6 E = 70.02 GPa v = 0.32 p = 2700 kg/m3
E = 2.55 GPa V = 0.32 3 P = 1200 kg/m
Boron/Epoxy B5.6/5505 E[ = 201 GPa E 2 = E 3 1 =21.7GPa G,2 = 5.4 GPa v12 = 0.32 p = 2100 kg/m3
FINITE ELEMENT MODELS With the availability of powerful finite element software, vibration responses of square plates with external patches are analysis with the aid of Ansys finite element
Perforated Aluminum Plates Reinforced with Bonded Composite Patches
1.05 -
923
10.95-
1 -
a. u." 0.95' «
•
•
•
»
• • - • •• • • »
•• •
•
0.85 -
1—f~J»—i—T—m
0.8 -
0.9 C
22.5
45
67.5
e
— (9) -•-(0/9) —(9/- )) —(B/-6/9) ^ N = 5 - ^ N = 7
FIGURE 2: Strengthening of perfect plate with composite patches (single side).
22.5
[
90 ["•-(9)
45 B
67.5
90
- (0/0)
FIGURE 3: Strengthening of perfect plate with composite patches (double side).
software. A finite element model is created for each case. Shell93 elements were chosen for aluminum plates. The shell91 layered element is used to model the adhesive layer and composite patches. Both elements have 8 nodes with 6 DOF at each node. For each case mesh sensitivity is investigated and acceptable mesh is chosen. The analytical frequency of the perfect plate, 771.16 rad/s, is compared to the results obtained from Ansys. For perfect and perforated plates the finite element solution are 763.60 rad/s and 752.47 rad/s respectively.
RESULTS AND DISCUSSION Vibration of six different cases of repaired plates are investigated. The varying laminate parameters such as, number of plies, fiber angles, and stacking sequences could allow the designer to modify the vibration response of damaged plates. For this reason, the following lay ups are used in this study. Nl-( 6), N2-(0/ d), N3-( 6 I 6), N5-[(±^2/ 6], and N7-[(±#3/ 6], For each case different fiber angles are considered. To demonstrate the effect of composite patches on the frequency response of repaired plates the frequency of the perfect plate is compared to those of repaired one. Frequency Ratio(FR), is defined as the ratio of frequency of a repaired plate to the frequency of perfect plate. Both frequencies are calculated using finite element models. The results for these cases are presented here. Strengthening of Perfect Plate with Composite Patches Figures 2 and 3 present frequency ratios(FR) for perfect plates strengthening with composite patches. As shown in these figures, for both symmetric and un-symmetric patches, FR is changed with variation of fiber orientation. For un-symmetric patches(Fig 2), the FR values can be grater than unit. But for symmetric patches the FR is less than unit, hi the other words, for the same number of plies and stacking sequences, un-symmetric patches have grater influence on vibration response of plates, hi both cases when fiber angle is equal 45, FR reaches its maximum values and graphs are symmetric with respect to this angle.
Perforated Aluminum Plates Reinforced with Bonded Composite Patches
924
1.1 1 -
~«—•—•—»—«
£0.9 —•—«—•-•-"•-] 0.8
J
0.85 0
22.5
45
67.5
90
e -•-(6)
FIGURE 4: Repair of perforated plate with composite patches (single side). 1.2 -
-MO/8) — (B/-B) — (9/-9/B) -»-N=5
-^N=7
FIGURE 5: Repair of perforated plate with composite patches (double side).
F.R.
;
0.9 -
•
^
»"^
'
0.8 C
22.5
45
67.5
90
e — (6 ) • -(0/9) -*-(8/-9) ^ ^ (6/-9/8) -«-N=5 ^-N=7
FIGURE 6: Strengthening of perforated plate with composite patches (single side).
FIGURE 7: Strengthening of perforated plate with composite patches (double side).
Repair of Perforated Plate with Composite Patches hi these cases, a plate with a circular cutout is repaired using one side and double side patches. Figures 4 and 5 present frequency ratios(FR) for repaired plates, hi these cases, variation of FR with respect to fiber angle are different than those of perfect plates(Fig.2&3). As it shows, when 8 increases, the FR increases up to some values of 8 and then it decrease or remain constant. As the number of plies increases, higher values of FR can be achieved. Strengtheuing of Perforated Plate with Composite Patches hi order to strengthening a perforated plate, a patch with the same cutout area as the base plate is used to reinforced the cutout area, hi these cases figure 6 and 7, for lower values of 8, the FR is almost constant. For 25<6 <60, the FR values increase sharply. Similar to lower values of 8, FR is insensitive to the higher values of 6 . CONCLUSIONS AND RECOMMENDATIONS The main goal of repair/strengthening with composite patches is to restore the damaged structures to its original performance condition and change the load carrying capacity or vibration response of existing structure. The use of advanced composite materials for changing the vibration response of repaired and strengthened aluminum
Perforated Aluminum Plates Reinforced with Bonded Composite Patches
925
plates has been studied. Numerical results show that vibration frequencies of perforated plates can be significantly change by using composite patches. Vibration responses of aluminum plates with variety of composite patches were evaluated in order to investigate the effective of composite patches properties, materials and geometries, in changing the frequency response of repaired systems. Then acceptable intervals and limitations for these parameters are presented, m each case, a set of composites patches that accurately satisfy the design criteria was introduced. The results presented herein indicate that, for vibration response of a perforated plate, a set of laminated composite patches can be found which change the frequency of repaired plates. Some recommendations for future research include a) the extension of the present work to general cutout configurations, b) study of the effect of boundary conditions, and c) initiation of an experimental program for validation.
REFERENCES 1. Baker, A.A., Jones, R., "Bonded Repair of Aircraft Structures", Martinus Nijhoff Publishers, 1988. 2. Chue, C. and Liu, J., "The effects of laminated composite patch with different stacking sequence on bonded repair", Composite Engineering, Vol. 5,pp.223-230, 1995. 3. Pai, P.F., Naghshineh-Pour, A.H., Schulz, MJ. and Chung, J., "Dynamic characteristics and buckling strength of composite-repaired aluminum plates", Finite Element in Analysis and Design, Vol. 28, pp.55-275, 1998. 4. Wang, Q. Y. and Pidaparti, R.M., "Static characteristics and Fatigue behavior of composite-repaired aluminum plates", Composite Structures, Vol. 56, pp. 151-155, 2002. 5,Schubbe, J.J and Mall, S., "Modeling of cracked thick metallic structure with bonded composite patch repair using three-layer technique", Composite Structures, Vol. 45, pp. 185-193, 1999. 6. Engels, H and Becker, W, "Close-form analysis of external patch repair of laminates", Composite Structures, Vol. 56, pp.259-268, 2002. 7. Chai, B. G., "Free vibration of laminated plates with a central circular hole", Composite Structures, Vol. 35, pp. 357-368, 1996. 8. Huang, M. and Sakiyama, T, "Free vibration analysis of rectangular plates with variously shapeholes", Journal of Sound and Vibration, Vol. 226, pp. 769-786,1999. 9.Rezaeepazhand, J and Sabouri, H., "Vibration analysis of perforated metallic plates repaired with composite patches", Proceeding of the Is' Iranian Conference on Strengthening & Retrofitting of Structures 16-18 May 2002, Tehran, Iran. 10. Rezaeepazhand, and Sabouri, H., "Vibration behavior of panels repaired or strengthened by composite materials ", Proceeding of the Is' Iranian Thin-Walled Structure Conferences 26-27 Feb. 2003, Urmia, Iran.
Design Method for SMA Super Hybrid Composite Materials Boming ZHANG , Shunli LI, Zhanjun WU and Shanyi DU Center for Composite Materials, Harbin Institute of Technology, Harbin 150001, P.R. China Qinfen LI Harbin Engineering University, Harbin, 150001, China
ABSTRACT The shape memory alloy (SMA) hybrid compotes material has been paid attention to due to its outstanding conventional performance and unique ability of large rang active deformation. This paper mentions the system design method on this new kind of smart material. This method gives consideration to conventional mechanical performance and capability of active deformation. The main design parameter has been choused the SMA volume fraction for SMA spate, ribbon and wire. The request of driving power has been reduced and respond speed has been raised by increasing SMA resistance. This design method has been proved by using finite element method design and analyses. INTRODUCTION Shape memory alloy (SMA) are a class of materials that exhibit a martensitic transformation when cooled from the higher-temperature austenitic state'-1'. A SMA can be easily deformed in the low temperature martensitic condition and can be returned to its original configuration by heating the reverse transformation temperature range, i.e. the shape memory effect(SME). After trained, the SMA can be returned to its original configuration in free state, the recovery stress to constraint can be produced in constraint state[ I According to the above principle, a new class of applications was developed when Rogers and Robertshaw introduced the idea of embedding SMA actuators in a composite laminate for structural control. A structure of this type has been termed a shape memory alloy hybrid composite (SMAHC)[3'. SMA actuators are bonded within the composite matrix and the boundaries of the structure serve also as mechanical restraints for actuators. The structure bending, the structure active control, adaptively stiffening, and other functions can be completed when SMA actuators are heated by current. The work presented in this study focuses on the SMAHC beam bending. SMAHC BEAM STRUCTURE AND DESIGN CONTENT OF FINITE ELEMENT SMAHC Beam Structure NiTi layer was embedded between first 0° layer and -45° layer of sixteen layers lamination in the order of (45707-4570°). hi Figurel, black is NiTi layer. The matrix * Correspondence Author, Tel: (86)451-86414323; Fax:(86)451-86414323; E-mail address: [email protected]
SMA Super Hybrid Composite Materials
927
material (carbon/epoxy or glass/epoxy) serves as mechanical restraints. After heated by current, recovery stress will be produce. Constitute deformation of bending and compress was produced because the composite lamination was put on off-centered loads. Beam compress deformation can be neglected here. The beam dimension is 200x20x2(mm) and thickness is 0.125mm per layer in Figurel.
20
FIGURE 1 Schematic of SMAHC beam structure
The matrix material is glass/epoxy (carbon/epoxy), and its volume fraction is 50% (61.5%). The material properties of glass/epoxy (carbon/epoxy) are shown in Table 1(2). TABLE I Material properties of glass/epoxy Elastic constant of material
Coefficient of thermal expansion
Ex=30GPa Ey=l0G?a Gv=5GPa vw=0.22 21.1"C ax =5.22xKr < 7"C ay = 10.80x10^/"C 65.6'C ax =6.80xKr 6 /"C ay = 24.28x 10^/°C 150"C a , =7.63xl0" 6 /°C ay = 26.28 xlO"6/°C
TABLE II Material properties of carbon/epoxy Elastic constant of material
Es=\W.\G?s. £,,=8.92GPa GJ3,=4.97GPa vw=0.37
Coefficient of thermal expansion
a^-O^xltrVC
aj,=29xl0"
6
/°C
Four phase transformation temperatures are Ms = 17 °C ., Mf = 0 °C -. As = 45 'C and Af = 60 "C P1. Plate, ribbon and wire of NiTi were embedded in composite matrix respectively. The structure of NiTi plate is shown in Figure2. The volume fraction of NiTi is 90% in this layer and the volume fraction of NiTi is 5.3% in the component. If wideness of the trough is decreased to 0.2mm and wideness of NiTiribbonis 3mm, the volume fraction of NiTi will be 95% in this layer and the volume fraction of NiTi will be 5.6% in the component, hi order to improve response speed, if wideness of the trough is decreased to 0.1mm and wideness of NiTiribbonis 0.2mm, the volume fraction of NiTi will be 67% in this layer and volume fraction of NiTi will be 3.9% in the component. Therefore, the response speed and the volume faction of NiTi must be considered. Recovery force was be ensured, cross section will be as small as possible so that resistance of NiTi will be increase and response speed will be improve. The volume fraction of NiTi is 59% in this
928
SMA Super Hybrid Composite Materials
layer and the volume fraction of NiTi is 3.5% in the NiTi ribbon component. The volume fraction of NiTi is 5% in this layer and the volume fraction of NiTi is 0.3% in the NiTi wire component.
200
FIGURE 2 Schematic of NiTi plate's structure
Recovery Stress and Young's Modulus of NiTi Recovery stress and Young's modulus of NiTi are shown in Table 3 [3l TABLE III Recovery stress and Young's modulus of NiTi Temperature [JC] 21.1 60.0 82.2 104.4 126.7 143.3 148.9
Recovery stress [ Mpa]
Young's modulus [ Gpa]
0 217.9 372.0 448.2 478.8 487.3 490.7
27.17 42.61 64.19 65.78 70.81 69.29 68.74
Content of Finite Element Design for SMAHC Beam Bending The content of finite element design for SMAHC beam bending is shown in Table4. Results of Finite Element Design for SMAHC Beam Bending Using finite element program, SMAHC beam structure is analyzed. The calculative results are shown in Table 4 when NiTi is heated to 150"C. Table 4 shows the bending angle of NiTi plate beam is the biggest and the bending angle of NiTi wire beam is the smallest for the same matrix. And also shows the bending angle of glass/epoxy matrix is bigger than that of carbon/epoxy matrix for the same form of NiTi. According to lamination theory, the changes ratio of SMAHC's engineering constant is shown in table 5 "+" means increase "-" means reduce„ TABLE IV Calculative results of SMAHC beam (degree)
Carbon/epoxy matrix
Glass/epoxy matrix
Plate
3.29
5.12
Ribbon
2.55
3.14
Wire
0.23
0.28
Form of NiTi
SMA Super Hybrid Composite Materials
929
TABLE V Percent of increased or reduced of SMAHC engineering constant (%)
Carbon/epoxy SMAHC 150"C/20t:
Glass/epoxy SMAHC 150°C/20t:
Form of NiTi
Plate
Ribbon
Wire
Plate
Ribbon
Wire
Longitudinal elastic
+2.8A2.5
-0.5/-3.5
-4.9A5.2
+22.2/+5.1
+13.1/+1. 8
-2.2/-4.1
-5.4A5.4
-5.4A5.4
-5.4A5.4
-4A/-4A
-4.4A4.4
-4.4A4.4
-4.5A4.5
-4.57-4.5
-4.5A4.5
-4.47-4.4
-4.4/-4.4
-4.47-4.4
modulus Transverse elastic modulus Shear elastic modulus
Table 5 shows that transverse elastic modulus and shear elastic modulus of lamination are reduced for carbon/epoxy or glass/epoxy, longitudinal elastic modulus is bigger when NiTi is 150°C than when NiTi is 20°C. The changes ratio of SMAHC's density is shown in table 6, "+" means increase "-"means reduce. TABLE VI Percent of increased or reduced in SMAHC density (%)
Carbon/epoxy SMAHC
Glass/epoxy SMAHC
Form of NiTi
Plate
Ribbon
Wire
Plate
Ribbon
Wire
Density
+16.5
+10.8
-0.6
+12.4
+7.7
-1.1
Table 6 shows the density of SMAHC component is increased except wire NiTi. If SMAHC servers as a aerial material, the increase of density should be considered. The NiTi wire with the diameter of 0.5mm is heated from 21 °C to 65'C in 2.88s, and the NiTi with diameter of 0.2mm is heated from 21°C to 65 "C in 0.072s[4]. In order to predict response time of NiTi, NiTi 300x$0.5mm is tested using thermal sensitive resistance method, and this NiTi wire is heated from 21 °C to 65 °C in 5s. The volumefractionof NiTi in component vs. bending angle curve is shown in Figure3. Figure3 shows the volume fraction of NiTi in component is the bigger, the beading angle is the bigger.
930
SMA Super Hybrid Composite Materials
volume fraction (%)
FIGURE 3 Volume fraction of NiTi in component vs. bending angle curve
CONCLUSION l)Plate NiTi, ribbon NiTi and wire NiTi are applied for the SMAHC lamination of the same structure dimension, the volume fraction of NiTi in plate NiTi component is the biggest and the volume fraction of NiTi in wire NiTi component is the smallest. If some special making method is applied and the wideness of trough and ribbon is decreased, not only the volume fraction but also resistance of NiTi will be increase, so the response speed will be improved. 2) Calculative results show that beam bending angle of spate NiTi is the most and beam bending angle of wire NiTi is the smallest for the same matrix material, i.e. the volume fraction of NiTi is the bigger, the beam bending angle is the bigger; beam of glass/epoxy matrix bending angle is bigger than beam of carbon/epoxy matrix bending angle. 3) The stiffness of component is changed after laying up NiTi, longitudinal elastic modulus is bigger when NiTi is 150 D than when NiTi is 20 D, transverse elastic modulus and shear elastic modulus of component are decreased. 4)The density of component is changed after laying up NiTi, and the density of SMAHC lamination is bigger than composite without NiTi because the density of NiTi is bigger that of composite. REFERENCES 1 2 3 4 5
Zhao liancheng, Cai wei, Zheng yufeng.2002. Shape memory effect and superelasticity. National defence industry press.China Wang zheng, Wu jiansheng, and Xu ying. 1997. "Experimental research on smart composite embedded with shape memory alloy wires". Journal of Shanghai Jiaotong University > 31 (4) : 104—107 Travis L Turner, Cynthia L Lach, and Roberto J Cano.2001. "Fabrication and characterization of SMA hybrid composites". SPIE Vol.4333:24~35 He cunfu.1999. "Method of improving the work frequencies of shape memory alloy wire actuator". Acta Materiae Composite Sinica,China,20(2):148~151 Ya Xu, Kazuhiro Otsuka, Nopbuyuki Toyama, hitoshi Yoshida, Byung K Jang, Hideki Nagai, Ryutaro Oishi ,and Teruo Kishi. 2000. "Fabrication of TiNi/CFRP smart composite using cold drawn NiTi wires". SPJE Vol.4699:564~574
Control of Crack Closure in Shape Memory Alloy TiNi Fiber Embedded CFRP Composite Materials Akira Shimamoto Department of Mechanical Engineering, Saitama Institute of Technology, Japan Cheong-Cheon Lee Graduate School of Engineering, Saitama Institute of Technology, Japan
ABSTRACT In this work, the TiNi fiber embedded Carbon Fiber Reinforced Plastic (CFRP) composite materials were developed. Various levels of prestrain e = 0,1, 3, and 5% were applied to the embedded TiNi fiber and angles of CFRP layer 0 and 90°. The thin layer of photoelastic material was coated on the surface of the specimen, and then the specimens were processed with a pre-crack on one side. Tensile tests under constant load were carried out for the specimens made of this composite. The reduction effect of the stress concentration, enhancement of mechanical properties and resistance of deformation of the TiNi fiber reinforced CFRP composite materials were investigated, and action of the crack closure due to the shape memory effect was studied by using the reflection photoelasticity method. Stress intensity factor K value was determined by using reflection photoelasticity to examine the crack closure effect of the TiNi fiber reinforced CFRP composite materials. The results show that the crack closure effect improved greatly. Decreasing stress intensity factor K value suggests the shape memory effect and thermal expansion of the matrix caused by temperature increasing improve the fracture resistance effect. It was confirmed that the effect of crack closure is attributed to the compressive stress field in the matrix due to shrinkage of the TiNi fibers above austenitic finishing temperature {Aj). INTRODUCTION Research and development for improving the mechanical property of composite materials, reducing material degradation of machines and making long life structures become important as the safety design requirement for an industrial material increases. Thus, the development of the material systems with the artificial defense such as intelligent materials is indispensable. There are several researches about the intelligent composite systems that actively control the damage and fracture. For example, Rogers et al. [1] reported the possibility of controlling the stress intensity factor at the crack tip by using the current-carrying shrinkage phenomenon of shape memory alloy (SMA) TiNi wires that were implanted in the notch bottom. However, a systematic research for this proposal has not been performed yet. We previously proposed the composite design concept that used the * Corresponding author, [email protected]
1690 Fusaiji,
Okabe, Saitama, 369-0293, Japan, +81-48-585-6717,
Crack Closure in Shape Memory Alloy TiNi Fiber embedded CFRP
932
high temperature side reinforcement. By embedding the shape memory TiNi fibers in the matrix, we use its high temperature side reverse transformation to generate the compressive stress in the matrix [2-6]. hi this study, we examined the stress reducing effect above the reverse transformation temperature (Aj). We used the TiNi fiber reinforced / CFRP composite that we developed as the specimen. We calculated K\ value (fracture toughness) in the vicinity of notch tip by the reflection photoelasticity. SPECIMEN We used shape memory alloy Ti50.2Ni49.8 (at %) fiber with 0.4mm a diameter. The TiNi fiber had maintained for 2 minutes at atmospheric 470°C, and using the ice water quenching heat-treatment. We measured the reverse transformation temperature of SMA Ti50.2Ni49.8 (at %) Ni fiber embedded in the matrix with a differential scanning calorimeter (Shimadzu DSC-60), as shown in Figure 1. Transformation temperatures of TiNi fiber are martensitic starting temperature Ms=45.0°C, martensitic finishing temperature Mf =36.0°C, austenitic starting temperature AS=42.4°C, and austenitic finishing temperature A/ =50.7°C. Figure 2 shows the stress-strain curve of the Ti50.2Ni49.8 (at %) fiber according to the temperature change. It suggests that the modulus of longitudinal elasticity rises as the ambient temperature increases. The crack closure measurement specimen is TiNi fiber reinforced CFRP composite that authors made. Figure 3 and table I show the geometry of the specimen and the mechanical properties of CFRP [7]. CFRP (P3052S-17, 8131 TORECA, Toray Co. Ltd.) used for the matrix is has fiber weights 175g/m2 and resin content 33Wt%. We produced 4 different kinds of the specimen that differentiated by its prestrain values. We set the prestrain as 0,1,3 and 5% respectively, hi order to produce the specimen, we fixed TiNi fibers (2 or 3 fibers) by a tensile prestrain device. Then, we put the fibers between two prepregs. Each prepreg has 10 accumulated layers. The angle of TiNi fiber and prepreg were 0° and 90° respectively. After that, we put pressure on the specimen, and gradually changed temperature. The volumefractionsof the TiNi fibers embedded in the matrix are 0.45% and 0.68%, respectively. Because CFRP is opaque, we attached the coating sheet of 3mm in thickness (PS-IA, VISHAY Measurement Group, hie.) to the surface of the specimen by using adhesive (PC-1, VISHAY Measurement Group, Inc.). We created the edge crack in the specimen to 4.5mm in length, 0.3mm in width and 60° in the crack tip angle with the milling cutter. 0.2 , 600 » 0.1
, 500
\ 0.0
400
20°C 40°C • • • • 60°C 80°C 100°C
Ti-50.2at%Ni
300
I
-0.1 200 -0.2
-0.3
100 0 0
10
20
30
40
50
60
70
80
90
Temperature [°C]
FIGURE 1 Transformation temperature measurement by Differential scanning calorimeter
0
1
2
3
4
5
6
7
8
9
10
Strain [%]
FIGURE 2 Stress-strain curves of TiNi fiber at different temperatures
Crack Closure in Shape Memory Alloy TiNi Fiber embedded CFRP
933
Pack Length : 4 5 m n
§
Coaling Material (PS-1)
Adhesive (PC-1)
-l|.
1 8
Layer A n ^ e
J 200
\' V V Vicinity of Crack-tip
Layer An^e=9(f
FIGURE 3 Dimension of SMA Ti Ni CFRP composite TABLE I Mechanical properties of carbon fiber TORECA Tensile strength Tensile modulus Rupture elongation Compressive strength Bending strength Bending modulus Interlaminar shearing strength Poisson's ratio
[MPa] [GPa] [%] [MPa] [MPa] [GPa] [MPa]
2550 (0°) 137 (0°) 1.8(0°) 1520(0°) 1670(0°) 123 (0°) 88 (0°) 0.34 (0°)
67. (90°) 8.8 (90°) 0.8 (90°)
EXPERIMENTAL METHOD The testers used for this experiment is Tensiron/RTM-IT tensile device with an isothermal bath, and a reflection photoelastic device. We caused the stress concentration at the crack tip so that the 5 or 6th photoelastic fringe order appeared. Subsequently, we heated the entire specimen in eight stepes in the isothermal bath. The stages of ambient temperature are 20, 30, 40, 50, 60, 70, 80, and 90°C. By this way we caused the shape memory reverse transformation above the Af temperature. The changes in K\ value at the crack tip due to the heating shrinkage of the TiNi fiber is observed from the change of photoelastic fringe pattern at the crack tip region. We sequencialy take a pictuare of the photoelastic fringe pattern with CCD(charge-coupled device) camera. They are analyzed by a personal computer according to the temperatute change. One problem with this method is that the photoelastic fringe order decrases as the compressive force is generated above the reverse transformation temperature (A/). This may cause the inaccurate measure of the stress intensity factor. To solve this problem, we employ the technique of fringe doubling and sharpening was employed [8-10]. For calculating the stress intensity factor K\ value from the photoelastic fringe patterns, we measure the distance rm and the angle 6mfromthe crack tip to the furthest point on the fringe (figure 4). Then, we plug the values in Eq. 1.
K,=-
at sin #
1+
2tan(3c9m/2) 1+ 3tan6>
(1)
Where n is the fringe order, t is the specimen thickness, and a is a photoelastic sensibility, respectively. To minimize the error, we use the range of 6m where 73.5°<4n<134°. For the same reason, we calculate Ki values from 2 or 3fringeloops [4]. Then, we estimate the mean K\ value from them. We calculate a that is a photoelastic
934
Crack Closure in Shape Memory Alloy TiNi Fiber embedded CFRP
sensibility from Eq. 2. We substitute a and t that is thickness of the coating sheet into Eq. 1 to calculate the stress intensity factor by the photoelastic coating method
hi Eq. 2, X is the light wavelength (white light, 0.577jim), AT is a strain optical coefficient, E is the Young's modulus, and v is Poisson's ratio according to the coating sheet, respectively. Table II shows mechanical and optical properties of coating sheet TABLE II Mechanical and optical properties of PS-1A Strain optical coefficient
K
0.15
Elongation
e
[%]
5
Young's modulus
E
[GPa]
2.5
Poisson's ratio
V
Maximum usable temperature
Crack tip
0.38 [°C]
150
a (Crack size) FIGURE 4 Photoelastic fringe pattern schematically developed in front of a crack size a
RESULTS AND DISCUSSIONS Figures 5 and 6 show the examples of the photoelastic fringe pattern of the specimens (TiNi fiber prestrain and layer angle) at each ambient temperature level under the constant load 3364 N and 196 N(stress 60MPa, 3.5MPa respectively), and the image processing of doubling and sharpening, respectively. Along with the rise of the ambient temperature in the isothermal bath, the distance rm from the crack tip to the apogee of the each isochromatic fringe loop decreases rapidly over austenitic finishing temperature 50.7°C. The stress at the crack tip vicinity decreases as the TiNi fiber prestrain increases. This is due to the different thermal expansion coefficients between the carbon fiber of CFRP matrix and TiNi fiber. Next, we investigate the relationship between the ambient temperature in the isothermal bath and stress intensity factor K\ value for TiNi fiber with prestrain 0,1,3, and 5%, and layer angle 0° and 90°, respectively. Figure 7 and 8 show the results. Figure 7 (a) shows that Kj values decrease 21.8% at 20 °C, 29.3% at 30 °C, 40.1 % at 40 °C, 49.4% at 50 °C and 86.2% at 60 °C when TiNi fiber volume fraction 1^=0.45% and the prestrain amount 5% comparing to only CFRP matrix. Similarly, K{ values decrease 43.8% at 20°C, 51.3% at 30°C, 61.2% at 40°C and 86.5% at 50°C when TiNi fiber volume fraction Vf =0.68% and the prestrain amount 5%. Figure 7 (b) shows that Ki values decrease 70.2% at 20 °C, 84.6% at 30 °C, 87.4% at 40 °C, and 93.0% at 50°C when TiNi fiber volume fraction J^=0.68% and the prestrain amount 5% comparing to 0%. In case of Vf =0.45% and CFRP with the layer angle 90°, the specimens were ruptured under a constant load 198 N. Unfortunately, we cannot evaluate K\ values when ambient temperature becomes above 60 °C since photoelastic fringes around the crack tip vicinity decrease rapidly. This indicates that the stress at the crack tip vicinity decreases due to the shape recovery of the TiNi fiber at 50.7 °C that is the reverse transformation temperature of the TiNi fiber. Figure 8 shows the relationship between stress intensity factor K\ and the prestrain. Stress intensity factor K\ value decreases as the prestrain increases. From figure 8 (a), in the case Vf =0.45% and temperature 60 °C, the K\ value decreases 27.4% as the prestrain increase 0 to 5%. Similarly, the K\ value decreases 62.4% when Vf=Q.6&%
Crack Closure in Shape Memory Alloy TiNi Fiber embedded CFRP
935
and 50 °C. From figure 8 (b), in the case F/-=0.68% and temperature 50 °C, the Ki value decreases 83.2% as the prestrain increase 0 to 5%. Above results suggest that our proposed intelligent composite material can contribute to establish long lasted, safety improved structures and machines. 20°C
30°C
40°C
50°C
60°C
(c) 5% (0°)
(d) 0% (90°)
(e) 5% (90°)
FIGURE 5 Fringe patterns of different temperature at the prestrain and layer angle (Vf= 0.68, Dark field)
mi
(c) Sharpening
(d) Doubling and sharpening
Min.
I..HII l i i M n h t
and doubling fringe
FIGURE 6 Image processing of isochromatic fringe doubling and sharpening (CFRP, 20°C) -i
•
1—
Theory K/K0=1.4332 K0=0.60MPaTtl1'2
•
- " - 0% - • - 1 % - * - 3% —•—5%
•
\ 20
30
40
50
60
20
30
40
Temperature, [°C]
(a) Angle 0° (Volume fraction Vf = 0.45 and 0.68%)
50
60
Temperature, [°C]
(b) Angle 90° (Volume fraction V,= 0.68%)
FIGURE 7 Relation between Kt value ratios and temperature
936
Crack Closure in Shape Memory Alloy TiNi Fiber embedded CFRP
0
1
2
3
4
5
Prestrain, s [KJ (a) Angle 0° (Volume fraction V, = 0.45 and 0.68%)
1
2
3
4
5
Prestrain, s [%] (b) Angle 90° (Volume fraction V,= 0.68%)
FIGURE 8 Relation between Kf value ratios and prestrain
CONCULUSIONS We examined the effectiveness of our proposed TiNi fiber/CFRP composite that has self-reinforcement behavior at high temperature side. The following conclusions can be drawn. (1) We confirmed the fracture resistance improvement. The stress intensity factor decreases along with the rise of the ambient temperature in the isothermal bath for all specimens. (2) The stress intensity factor K\ value decreases as the amount of the prestrain increases. Also, it is evidenced that an increase in the volume of the TiNi fiber results in a decrease in K\. (3) There is a strength improvement by the angle of CFRP layer direction. ACKNOWLEDGMENT This work was supported by High-Tech Research Center of Saitama Institute of Technology. REFERENCES 1.
Rogers, C. A., Liang, C. and Lee, S. 1991. "Active Damage Control of Hybrid Material Systems Using Induced Strain Actuator", Proc. 32tnd, Struct. Dynmc. and Math. Conf., pp. 1190-1197. 2. Yamada, Y., Taya, M. and Watanabe, R. 1993. "Strengthening of Metal Matrix Composite by Shape Memory Effect", Mat!. Trans., JIM, 34-3, pp. 254-260. 3. Taya, M., Yamada, Y., Furuya, Y., Watanabe, R., Shibata, S. and Mori, S., 1993. "Strengthening the Mechanism of TiNi Shape Memory Fiber/Al Matrix Composite", Proc. Smart Math., SPIE 1916, Varadan, V. K. ed, pp. 373-383. 4. Shimamoto, A., Furuya,Y. and Taya, M., 1995. "Active Control of Crack-tip Stress Intensity by Contraction of Shape Memory TiNi Fibers Embedded in Epoxy Matrix Composite", Proc. of the International Symposium on Microsystems, Intelligent Materials and Robots, pp. 463-466 5. Shimamoto, A. and Taya, M., 1997. "Crack closure acts use the shrinkage effect of shape memory TiNi fiber embedded/epoxy matrix composite", JSME Journal, Vol. 63-605 A, pp. 26-31 6. Shimamoto, A., Furuya, Y. and Taya, M., 1999. "Reduction in Ki by Shape Memory Effect in a TiNi Shape-Memory Fiber-Reinforced Epoxy matrix Composite", JSME Journal, pp. 96-100 7. Composite data ofTORECA, TORAY Co. Ltd. , 8. Baek, T.H. and Lee, J.C., 1994. "Development of Image Processing Technique for Photoelastic Fringe Analysis ", KSME Journal, Vol. 18-10, pp. 2577-2584 9. Han, B. and Wang, L., 1993, "Isochromatic Fringe Sharpening and Multiplication", Proc. of the 1993 SEM 50th Anniversary Spring Conf. on Exp. Mech., SEM, pp. 1206-1209. 10. Baek, T. H. and Kim, M. S., 1993. "The Study of Accuracy Improvement Technique for Stress Analysis in Photoelasticity through Digital Image Processing", Proc. of the 1993 SEM 50th Anniversary Spring Conf. on Exp. Mech., SEM, pp. 674-681. 11. Coating material data ofPhotolastic Division, VISHAY Measurement Group, Inc.
Influence of Stress Induced Birefringence on FBG Sensors Embedded in CFRP Laminates Tadahito Mizutani*, Nobuo Takeda Department of Advanced Energy, Graduate School of Frontier Sciences, The University of Tokyo, Japan Takafumi Nishi, Ryohei Tsuji, and Yoji Okabe Department of Aeronautics and Astronautics, School of Engineering, The University of Tokyo, Japan
ABSTRACT In previous research, the authors studied detection of transverse cracks in CFRP laminates using small-diameter fiber Bragg grating (FBG) sensors. FBG sensors were embedded in cross-ply or quasi-isotropic laminates, and tensile tests were carried out. As transverse cracks occurred, a reflection spectrum of FBG sensors was deformed due to a non-uniform axial strain distribution near transverse cracks. The spectrum width defined by FWQM (full width at quarter maximum) showed a good correlation with the crack density. However, calculated FWQM were slightly different from the measured one. One of the reasons is the presence of birefringence effect on embedded FBG sensors. When FBG sensors are embedded in the CFRP laminates, the sensors are subjected to an asymmetric residual stresses. The refractive index changes due to the photoelastic effects. Consequently, birefringence effect occurs and induces a split of the reflection spectrum, hi this research, these effects were considered theoretically. Reflection spectrum was calculated by solving coupled-mode equations of x-polarization and y-polarization, respectively. Calculated results were compared with the previous analysis in which the birefringence effect was not considered. As a result, the theoretical calculation considering the birefringence effect showed a better correspondence with the experimental results.
INTRODUCTION For the evaluation of the material integrity and the enhancement of the structural performance, smart health monitoring technologies for composites have been developed in recent years. In previous research, the authors studied detection of transverse cracks in CFRP laminates using small-diameter fiber Bragg grating (FBG) sensors [1, 2]. A unique embedment technique using the small-diameter optical fiber enabled us to detect the microscopic damage in CFRP with a high sensitivity. When FBG sensors are bonded to the laminate, laminate strain would be transferred only to the axial direction of the FBG sensor. The transferred axial strain affects sen* Corresponding Author, Takeda Laboratory, Department of Aeronautics and Astronautics, School of Engineering, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan, TEL/FAX: +81-3-5841-6642, E-mail Address: [email protected]
938
Stress Induced Birefringence on FBG Sensors
sor properties, such as the refractive index (photoelastic effects) and the grating period. Consequently, the center wavelength of reflected light from FBG sensors shifts corresponding to the strain. On the other hand, when FBG sensors are embedded in the laminate with our technique, transverse strain, which is applied perpendicular to the axial direction, is also applied to the FBG sensor. Especially a non-axisymmetric strain induces birefringence effect, and therefore the reflection spectra from the FBG sensors are deformed [3, 4]. In the case of cross-ply or quasi-isotropic laminates, the birefringence effect would be induced due to the thermal residual stress. In our previous research in the damage detection in composites, only the non-uniform axial strain was considered in the theoretical calculation of the reflection spectra. Since the birefringence effect was not considered, the calculated reflection spectra were slightly different from the measured ones. Consequently, in this research, we present the theoretical extension to integrate the birefringence effect into the previous method. THEORETICAL BACKGROUND The FBG sensor is one of optical fiber sensors, and fabricated to have periodic refractive index change in the core of an optical fiber. The reflection spectra from FBG sensors can be calculated by use of coupled-mode theory [5, 6, 7]. Although coupled-mode equations have closed form solutions under specific conditions, generally, it is difficult to solve these equations directly. Thus, transfer matrix formalism is often applied to these equations, whereby the grating is divided into discrete uniform sections [8]. hi this section, a simple extension of these techniques to integrate the birefringence effect is discussed. Coupled-mode Theory for the Fiber Bragg Grating FBG sensors are fabricated in single-mode fibers. Using the weakly guiding approximation, we need to consider only LPoi mode. In this case, mode coupling occurs between the counterpropagating LPOi modes. One is the LPOi mode propagating along the +z-axis with a propagation constant p. The other is also LPOi mode, but propagates along the -z-axis with -/?. The coupling of these two modes is formulated by using a coupled-mode equations and described as follows [8],
dz ^ dz
• = i>cB(z)exp[-2iApz], = -itcA(z)exp[2iA/3z],
where A(z) and B(z) are the slowly varying amplitudes of LPoi mode traveling in the -z and +z directions (the electric fields can be expressed as EJz, t) = A(z) exp[i(at + fiz)] and Eb{z, t) = B(z)exp[i(cot - fiz)], respectively), K is the coupling coefficient between the two modes and A/? is the differential propagation constant associated with detuning from the Bragg condition. For a smusoidally modulated refractive index with the form, n(z) = «eff + An cos(27tz/A), Kris given as follows [7],
where e, is the transverse modal field of LPOi mode, «efr is the refractive index of the
Stress Induced Birefringence on FBG Sensors
939
core, An indicates the refractive index modulation depth of gratings, and A is the grating period. Finally, A/3 is defined as, (3)
A where A is the wavelength of laser. Transfer Matrix Method for the Non-uniform FBG
When K and A/3 are constant, which means that the grating parameters such as neff, An, and A are constant, Eqs. (1) can be solved easily by using the change of variables, a(z) = A(z) exp[z/?z] and b(z) = B(z) exp[-i/3z],
ru b(0)
Tula(L) T22\[b(L)j
(4)
where Tn = T22 = \
cosh[(pL]-i^-sinh[
R:
> A/?)
(5)
T =T* =-i — si 9 cp = (K2 - A/32)112, L is the grating length and /?o is the propagation constant at the Bragg wavelength. However, for the non-uniform gratings, Eqs. (1) cannot be solved analytically. Thus, we divide discretely the non-uniform gratings into a total of N uniform grating segments. Each segment has own grating parameters (nett, An, and A) determined by the grating structure, applied strain and temperature. Consequently T matrix of rth segment [Ti\ {i = 1, 2,... , N) in Eq. (4) is calculated, and the total grating is expressed as the following equation, (6)
b(L)\ Stress Induced Birefringence Effect
When the FBG sensors are embedded in the composites, the grating parameters are affected by strain and temperature. In our previous research, the small-diameter FBG sensor was embedded in CFRP cross-ply laminate as shown in Fig. 1 [1]. The changes of grating parameters, «eff and A, subjected to tri-axial strain (ex, Sy, e^ and y^) and the temperature change (AT) are expressed as follows,
*"'
2
5n=Pn«z +On + A 2 K - 1 — — ^ 5 '" 2 = (s2+agAT)A,
AT + Ai •AJ-^
- A2
, (7) (8) (9)
Stress Induced Birefringence on FBG Sensors
940
where sh = {ex + Sy)/2, ^max = [{sx - Sy)2 + yXy2]V2- P\i and/»i2 are strain-optic coefficients, dneff/dT is the thermo-optic coefficient, and ag is the thermal expansion coefficient of the optical fiber. Subscripts, p and q, denote the directions of the optical axes of the optical fiber shown in Fig. 2. 52 ).im
,
Small-diameter
al Fiber i^j / Optical Fil 0 plv;
cross-section of x-y plane Bragg Gratings x,y, z: coordinate system of the laminate ~p,~q : directions of the optical axes of the sensor in the plane perpendicular to the z axis.
CFRP Laminate
FIGURE 1 Location of the small-diameter FBG sensor embedded in the CFRP cross-ply laminate.
FIGURE 2 Definition of the coordinate system of the sensor,
Eqs. (7-8) show the birefringence effect on the FBG sensors. When fmax has a non-zero value, np and nq have different values. Consequently, LP^ mode, which propagates with the propagation constant f5p associated with np, and LP0' mode with the different propagation constant J3q from fip, appears in the core. Since the mutual coupling of these modes is very small, only the coupling in each mode (between forward and backward propagating waves) is considered in this paper. T matrix associated with LPg'j mode, [Tp], and that with LP*, mode, [Tg], can be expressed by using Eq. (6), for jp-polarization bp(0)
bp(L)
(10)
for g-polarization (11) where a(z)p and b(z)p are the amplitude parameters associated with the LP^, mode, and a(z)q and b{z\ are that associated with the LP0?, mode. Finally, the reflection spectrum considering the birefringence effect can be obtained by superposition of LP* and LP*, modes. DISCUSSION It was impossible to include the birefringence effect into the calculation using the previous analysis that considers only the axial strain [1, 2]. In this section, the reflection spectrum including the birefringence effect was calculated theoretically, and compared with the measured one. At first, the thermal residual strain components applied to the small-diameter FBG sensor was calculated using FEM analysis with ABAQUS code. For the simplification, all material properties used in the analysis were assumed to be elastic. Figure 3 shows
Stress Induced Birefringence on FBG Sensors
941
a 3D finite element model of CFRP cross-ply laminate [02/902]s which include an embedded small-diameter optical fiber. FBG sensors, which were fabricated in the core of the small-diameter optical fiber, were embedded in the 0° ply on the border of 90° ply. The mechanical properties of CFRP T800H/3631 and small-diameter optical fiber used in this calculation were quoted from the reference [2]. All components of the strain tensor in the CFRP laminate are assumed to be zero at the manufacturmg temperature of 185°C, and the thermal residual strains at the room temperature of 25°C were calculated in FEM analysis. Figure 4 shows the contour plot of ez component in the z-symmetric plane. Calculated residual strain components of the glass, sx, sy, EZ and yxy were -393JUS, 309 jus, -478 /us and -50 jus, respectively.
+2.77e-03 " +2.06e-03 +1.35e-03 +6.47e-04 |- -5.96e-05 -7.67e-Q4 -1.47e-03 -2.18e-03 (- -2.89e-03 -3.59e-03 f -4.30e-03 -5.01e-03 -5.72e-03
FIGURE 3 3D finite element modeling of the CFRP cross-ply laminate with the em- FIGURE 4 Contour plot of the calculated thermal bedded small-diameter optical fiber. residual strain in z-symmetric plane.
Next, changes of the refractive index and the grating period were calculated using Eqs. (7-9). Optical constants of the small-diameter optical fiber used in these equations were also quoted from the reference [2], and the temperature change, AT, was assumed to be zero. Then the reflection spectrum including the birefringence effect was calculated using the transfer matrix method expressed by the Eqs. (10) and (11). A calculated initial reflection spectrum of the small-diameter FBG sensor was shown in Fig. 5, which was determined to be fitted to the measured spectrum. Since a single-mode small-diameter optical fiber was used, there was no birefringence before the embedment. However, the influence of the birefringence effect was apparently appeared after the cure process as shown in Fig. 6. This calculated result shows a good correspondence with the measured one. In the near future, 3D finite element model will be modified to include transverse cracks. Then the spectrum deformation due to the generation of transverse cracks will be calculated with high accuracy. CONCLUSIONS In this research, the influence of birefringence effect on the embedded FBG sensors was considered, hi our previous research, transfer matrix method, which solves coupled-mode equations discretely, was used to calculate the reflection spectrum. The theoretical extension to the stress induced birefringence was presented in this research. The reflection spectrum considering the birefringence effect can be obtained by calculating the transfer matrix of each polarization. When small-diameter FBG sensors were embedded in the CFRP cross-ply laminate,
Stress Induced Birefringence on FBG Sensors
942
1.0 0.8 -
'£ 0.6 C 0.4 -
£
0.2 0.0
1549.5
1550.0
1550.5
1549.0
Wavelength (nm)
1550.0
1550.0 [analysis] 1550.5
[experiment]
Wavelength (nm)
analysis experiment o FIGURE 5 Reflection spectra from the small-diameter FBG sensor before the embedment in the CFRP laminate.
1549.5
analysis (include birefringence effects) analysis (only axial strain) experiment
FIGURE 6 Reflection spectra after the cure process. These spectra (except for the broken line) were deformed due to the birefringence effect..
the non-axisymmetric thermal residual strains were applied to the sensors. These non-axisymmetric strains were calculated using '3D FEM analysis. Then, the reflection spectrum including the birefringence effect was calculated. As a result, the calculated result showed a good correspondence with the measured one. REFERENCES 1. Y. Okabe, T. Mizutani, S. Yashiro, and N. Takeda. 2002. "Detection of microscopic damages in composite laminates with embedded small-diameter fiber Bragg grating sensors," Compos. Sci. Techno!., 62(7-8):951-958. 2. T. Mizutani, Y. Okabe, and N. Takeda. 2003. "Quantitative evaluation of transverse cracks in carbon fiber reinforced plastic quasi-isotropic laminates with embedded small-diameter fiber Bragg grating sensors," Smart. Mater. Struct., 12(6):898-903. 3. R. Gafsi and M. A. El-Sherif. 2000. "Analysis of Induced-Birefringence Effects on Fiber Bragg Gratings," Opt. Fiber Techno!., 6(3):299-323. 4. Y. Okabe, S. Yashiro, R. Tsuji, T. Mizutani, and N. Takeda. 2002. "Effect of thermal residual stress on the reflection spectrum from fiber Bragg grating sensors embedded in CFRP laminates," Compos. Part A, 33(7):991-999. 5. T. Erdogan. 1997. "Fiber Grating Spectra," J. Lightwave Techno!., 15(8):1277-1293. 6. Y. J. Rao and D. A. Jachson. 2000. "Principles of Fiber-Optic Interferometry," in Optical Fiber Sensor Technology, K. T. V. Grattan and B. T. Meggitt, eds. Kluwer Academic Publishers, pp. 185-186. 7. A. Othonos and K. Kalli. 1999. Fiber Bragg Gratings, Fundamentals and Applications in Telecommunications and Sensing. Artech House, Inc., pp. 191-205. 8. S. Huang, M. LeBlanc, M. M. Ohn, and R. M. Measures. 1995. "Bragg intragrating structural sensing," Appl. Optics, 34(22):5003-5009. 9. R. J. V. Steenkikiste and G. S. Springer. 1997. Strain and Temperature Measurement with FIBER OPTIC SENSORS. Technomic Publishing Company, Inc., pp. 112-119.
Magnetoelectric Properties of Piezoelectric and Magnetostrictive Composites with 2-2 and 3-1 Connectivity Haitao Huang and Li Min Zhou* Department of Mechanical Engineering, The Hong Kong Polytechnic University Hung Horn, Kowloon, Hong Kong
ABSTRACT The past few years have seen several attempts to make laminate composites consist of piezoelectric and magnetostrictive layers to achieve Magnetoelectric (ME) coefficients higher enough for real applications. However, all the efforts are limited to composites with the 2-2 and 3-0 connectivity. In general, the ME field coefficient is much higher in laminate structure with the 2-2 connectivity. In this article, we propose a new type of ferroelectromagnetic (FEM) composite with the 3-1 connectivity, that is, the piezoelectric fibers preferentially aligned and uniformly distributed in a magnetostrictive matrix. The ME properties of this type of composite are theoretically studied and compared to that of the 2-2 laminate composite. Our theoretical calculation shows that the 3-1 composite has higher ME field coefficient than the 2-2 one. The advantages and disadvantages of the composites with the 2-2 and 3-1 connectivity are discussed.
INTRODUCTION FEM material is a material, which has both the ferroelectric and ferromagnetic properties. With the coexistence of the electric and magnetic order, a "magnetoelectric" (ME) effect can be realized, e.g., an electric field can be induced by a magnetic field and vice versa. Due to the coupling between electric and magnetic order, the FEM material is expected to have many potential applications, such as, magnetic field sensing devices, leak detectors for microwave ovens, current measurement of high-power electric transmission system, new data-storage media, spintronic devices, new actuators, etc. However, single-phase FEM materials are rarely been found or synthesized [1]. The reason is that most of the ferromagnetic oxides contain the center of symmetry and do not allow an electric polarization, whereas most of the ferroelectric oxides consist of transition-metal ions without the d electrons, which are essential for magnetism. For magnetic oxides with certain dorbital occupancies, a Jahn-Teller structural distortion is likely to happen [2, 3], which overrides the tendency for an off-center displacement leading to ferroelectricity. Moreover, the single-phase FEM materials have low ME coefficients and need to be used under low temperatures, which prohibit the use of these materials in practical applications [4]. Recently, exceptionally high ME effect are found in laminate composites of piezoelectric and magnetostrictive materials [4-6] and particulate composite [7-9]. * Corresponding author. Fax: (852) 2365 4703; Email: [email protected]
944
Magnetoelectric Properties of Piezoelectric and Magnetostrictive Composites
All of these composites have either the 2-2 or the 3-0 connectivity. In general, the ME voltage coefficient is higher in laminate structure with the 2-2 connectivity. Up to now, little work has been reported on the FEM composite with a 3-1 connectivity. In this article, we study the ME properties of this kind of FEM composite theoretically. The piezoelectric fibers are assumed to be preferentially aligned and uniformly distributed in a magnetostrictive matrix. The calculated magnetoelectric properties of the 3-1 composite are compared to that of the 2-2 laminate composite. THEORY 2-2 Composite Generally, an applicable 2-2 FEM composite has a three-layer structure as shown in Fig.l (a). The piezoelectric layer is bonded by two magnetostrictive layers on the top and bottom surfaces, respectively. Suppose the external magnetic field and the magnetic bias field being both along the thickness direction of the magnetostrictive layer. Due to magnetostriction, the magnetic layer will shrink by A/o if there is no constraint on the magnetic layer. However, since the magnetostrictive and piezoelectric layers are well bonded, both layers will be strained in such a way that the total internal force becomes zero. The final length of each layer is identical after the expansion of the magnetic layer by A/2 and the shrinkage of the piezoelectric layer by A/i. According to Virkar et a/.'s calculation [10] using simple beam theory, the stresses in the piezoelectric layer is given by, -2ElE2d2M0
...
where Eh a, dh and o; (i=l, 2) represent the elastic modulus, Poisson's ratio, thickness and stress of the respective layer, respectively. The subscript 1 and 2 stand for the piezoelectric and magnetic layers, respectively. For simplicity, only symmetric case is considered, i.e., the top and bottom layers are of the same thickness. The Poisson's ratio is assumed to be the same for both piezoelectric and magnetic layers. Since A/o=/o^3iH3 (i/31 being the magnetostrictive constant), the ME field coefficient of the 2-2 composite can be calculated, =SE
2E1E2v2g3ld31
=
(2)
where V\=d\/(d\+2d2) and V2=d2l{d\+2d2) are the volume fractions of the respective piezoelectric and magnetostrictive materials while gi\ is the piezoelectric voltage constant. A/2/2 1 i
!1
T 1A 1 i
i 1
h-
A/,/2 (a)
FIGURE 1 Schematic of deformations introduced in (a) laminated 2-2 composite structure and (b) 3-1 composite structure. The strains in the respective layers are exaggerated for clarity.
Magnetoelectric Properties of Piezoelectric and Magnetostrictive Composites
945
3-1 Composite For the 3-1 composite, we consider a simplified case, that is, the piezoelectric fiber with a radius of Ri is surrounded concentrically by a magnetostrictive tube with an outer radius of R2. Figurel (b) shows the schematic of radial changes introduced in the 3-1 composite structure with a cylindrical symmetry. For convenience, a cylindrical coordination will be used in the following calculation. It is assumed that the external magnetic field and the magnetic bias field are both along the axis of symmetry. Due to magnetostrictive effect, the inner radius of the magnetic tube is expected to shrink by ARo if there is no constraint. However, the resistance of shrinkage from the piezoelectric fiber pushes the inner wall of the magnetic tube outward by AR2. Accordingly, the piezoelectric fiber suffers a uniform compressive stress along the radial direction and its radius shrinks by ARj. Similarly, along the axial direction (z direction), the magnetostrictive effect causes the magnetic tube to expand by AZ0 if without any constraint. Under constraint, the tube is shortened by AZ2 and the fiber is elongated by AZi. Since the fiber and tube is well bonded at the interface and no relative gliding exists, the deformation along the radial and axial directions should satisfy the following boundary condition, ARo=ARi-AR2
AZ0=AZi-AZ2
(3)
For simplicity, it is supposed that the material is isotropic and the deformation is homogeneous, that is, no bending or twisting exists. The stress and strain tensor can be rigorously solved from the following equilibrium equation of deformation [11] if gravity is neglected, 2(l -
f3
2a(d3l+ad33) \E (1 2 \ E E)]\ + v2E2 (1 + a\Ex + (1 - 2a\v,Ex + v2E2)] The ME field coefficient of the 3-1 composite then becomes, +7 + 7(1
#33^33
,
(}
v2E2)
AvEEH
2(g 3 , +^33X^3. + ^ 3 3 )
where J33 is the magnetostrictive constant, g3i and g33 the piezoelectric voltage constants. RESULTS AND DISCUSSIONS The ME field coefficient m2-2 of the 2-2 composite as a function of the volume fraction vi of the piezoelectric material is plotted in Fig. 2. Here and in all
946
Magnetoelectric Properties of Piezoelectric and Magnetostrictive Composites
calculations in the following, we assume the Poisson ratio to be equal to 1/3. hi Fig.2(a), the elastic modulus of the piezoelectric material is kept constant while that of the magnetic material varies from 0.5£i to 2E\. On the contrary, Fig. 2(b) shows the ME coefficient under various elastic modulus (O.5.E2 to 2E2) of the piezoelectric material while that of the magnetic material is kept constant. It can be seen from both figures that, generally, the ME coefficient decreases with increasing volume fraction of the piezoelectric material. This can be understood since the ME voltage is produced due to the piezoelectric effect under the stress generated by the magnetic material. Therefore, for practical applications, it is desirable to use a small volume fraction of the piezoelectric material in order to maintain a high ME coefficient. It can also be found from Fig. 2 that, under the same volume fraction, the higher the elastic modulus the higher the ME coefficient. It can be further concluded that, for small volume fraction of the piezoelectric material, the increase in the elastic modulus of the magnetic material does not has significant effect in increasing the ME coefficient. The more efficient method to achieve a high ME coefficient is to use a high modulus piezoelectric material rather than a high modulus magnetic material. For the 3-1 composite, in order to study the effect of elastic modulus on the ME coefficient it is necessary to simplify the form of Eq. (7). By introducing the piezoelectric voltage constant ratio g=galg3\, the magnetostrictive constant ratio ^,\ and the elastic modulus ratio e=EilE\, Eq. (7) can be reduced to, gd v,+ (l-v,)e
m,, =
(8)
Generally, for piezoelectric material like PZT, the piezoelectric voltage constant ratio g is within the range of-2—3 [12]. The magnetostrictive constant ratio such as the Terfenol-D is also within the range of -2—3 [13]. For the study of the elastic modulus effect, we choose g=-2.5 and rf—2.5. The results are shown in Fig.3 for different elastic moduli of the piezoelectric and magnetic materials, respectively. It can be found that the elastic modulus has the similar effect in the 3-1 composite as it has shown in the 2-2 composite. It is interesting to compare the ME voltage coefficients in the 2-2 and 3-1 composites. For simplicity, we define a reduced elastic modulus
3.0
(a)
2.5
% 2'° S 1.0
05.
\
^
\
^
0.5
on 0.4
0.6
0.8
V,
FIGURE 2 ME field coefficient of the 2-2 composite as a function of the volume fraction of the piezoelectric material under (a) various elastic modulus (E2) of the magnetic material while the elastic modulus (Ei) of the piezoelectric material is kept constant. Their modulus ratio E2IEX is indicated beside each curve; and (b) various elastic modulus (Ei) of the piezoelectric material while the elastic modulus (£2) of the magnetic material is kept constant. Their modulus ratio E\IEt is indicated beside each curve.
Magnetoelectric Properties of Piezoelectric and Magnetostrictive Composites
947
FIGURE 3 ME field coefficient of the 3-1 composite as a function of the volume fraction of the piezoelectric material under (a) various elastic modulus (E2) of the magnetic material. The elastic modulus (£i) of the piezoelectric material is kept constant. Their modulus ratio E2/Ei is indicated beside each curve, and (b) various elastic modulus (E{) of the piezoelectric material. The elastic modulus (E2) of the magnetic material is kept constant. Their modulus ratio Et/E2 is indicated beside each curve.
(9) The ME field coefficient ratio m of the 3-1 to 2-2 composite structure is, ^ (10) m=m^2 i 18 + 6e The ME coefficient ratio m versus reduced elastic modulus under different piezoelectric voltage constant ratio g is plotted in Fig. 4. The magnetostrictive constant ratio d is fixed as -2. It can be seen that in all the cases the ME field coefficient of the 3-1 composite is higher than that of the 2-2 composite. It can also be found that the higher the piezoelectric voltage constant ratio g is, the higher the ME coefficient ratio m will be. Similarly, the higher the magnetostrictive constant ratio d is, the higher the ME coefficient ratio m will be. As can be seen from Fig. 4, the ME coefficient ratio is insensitive to the reduced modulus which implies that it is insensitive to the both the volume fraction of the piezoelectric material and the elastic modulus. Therefore it can be concluded that generally the 3-1 composite has a higher ME field coefficient than the 2-2 composite irrespective of the component materials and their volume ratio. 2.8 2.6
g=-4
2.4
S=-3.5
2.2 g=-3
2.0
g=-2.5 g=-2
0.0
0.5
1.0
1.5
2.0
2.5
reduced modulus FIGURE 4 The ME field coefficient ratio m of the 3-1 to 2-2 composite as a function of the reduced elastic modulus under different piezoelectric voltage constant ratio g. The magnetostrictive constant ratio d is fixed as -2.
948
Magnetoelectric Properties of Piezoelectric and Magnetostrictive Composites
A careful examination of Eq. (10) shows that the first term on the right side is due to longitudinal stress generated by the magnetostriction along the magnetic field direction. Since g and d are usually within the range of -2 to - 3 , the first term is always greater than 1. The second term on the right side of Eq. (10) is due to the transverse stress generated by the magnetostriction in the plane perpendicular to the magnetic field direction. The magnitude of the second term is almost negligible as compared to that of the first one. Even for some exceptionally highly anisotropic material such as the piezoelectric ceramics supplied by Sensor Technology Limited, Canada, where the g value can be as large as -6—17 [14], the magnitude of the second term is still small as compared to that of the first one. Generally, the longitudinal stress is more effective in generating the piezoelectric voltage since g-33 is normally larger than g^. The 3-1 composite structure makes use of this longitudinal stress to generate higher piezoelectric voltage than in the 2-2 structure. However, the 2-2 structure has the merit of easy production. The 3-1 structure adds the difficulty in the processing. Another drawback of the 3-1 structure is that the magnetic material normally has too high an electrical conductivity which will greatly lower the charge accumulated due to the piezoelectric effect and thus lower the ME voltage. There are ways to eliminate these problems. For example, one can coat the piezoelectric fiber with an insulating layer but the processing becomes even more complicated. Another way is to use an insulating magnetic material or composite as the matrix for the 3-1 structure. Especially for highly anisotrpic (very large g value) piezoelectric material, the 3-1 composite structure is still worthwhile trying since it has a much larger ME voltage coefficient than the 2-2 structure does. CONCLUSIONS Several conclusions can be drawn from the theoretical calculation. In order to get a high ME voltage coefficient, a small volume fraction of the piezoelectric material should be used. A high elastic modulus piezoelectric material is more effective in increasing the ME coefficient than a high modulus magnetic material. The 3-1 composite structure generally has a higher ME voltage coefficient than the 2-2 structure especially when the piezoelectric material used has a large g33/g3i ratio. REFERENCES 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14.
T.Kimura, S.Kawamoto, I.Yamada, M.Azuma, M.Takano and Y.Tokura, Phys.Rev.B 67, 180401 (2003) N.A.Hill, J.Phys.Chem.B 104, 6694 (2000) N.A.HM, Annu.Rev.Mater.Res. 32, 1 (2002) J.Ryu, S.Priya, K.Uchino and H.-E.Kim, J.Electroceramics. 8, 107 (2002) G.Srinivasan, V.M.Laletsin, R.Hayes, N.Puddubnaya, E.T.Rasmussen and D. J.Fekel, Solid State Commun. 124, 373 (2002) G.Srinivasan, E.T.Rasmussen, J.Gallegos and R.Srinivasan, Phys.Rev.B 64, 214408 (2001) C.W.Nan, M.Li, X.Feng and S.Yu, Appl.Phys.Lett. 78, 2527 (2001) J.van den Boomgaard, A.MJ.G.Van Run and J.Van Suchetelene, Ferroelectrics 10, 295 (1976) J.Ryu, A.V.Carazo, K.Uchino and H.-E.Kim, J.Electroceramics. 7, 17 (2001) A.V.Virkar, J.L.Huang and R.A.Cutler, J.Am.Ceram.Soc. 70, 164 (1987) L.D.Landau, Theory of Elasticity (third edition), Chapter 1, Pergamon Press, Oxford, 1986 M.J.Haun, Z.Q.Zhuang, E.Furman, S.J.Jang and L.E.Cross, Ferroelectrics 99, 45 (1989) A.B.Flatau, M.J.Dapino and F.T.Calkins, Comprehensive Composite Materials (Elsevier, Amsterdam, 2000) Vol.5, p.563 http://www.sensortech.ca/bm900.html as of Feb.4, 2004
Shape Memory Effect on Interfacial Strength of SMA-reinforced Composites Chi-kin Poon and Li Min Zhou Department of Mechanical Engineering, the Hong Kong Polytechnic University Hung Horn, Kowloon, Hong Kong
ABSTRACT Shape memory alloys (SMAs), when in the form of wires or short fibers, can be embedded into a host material to form SMA-composites for satisfying a wide variety of engineering requirements. Recovery action of SMA inclusions induced by elevated temperature can change the modal properties and hence the mechanical responses of the whole composite structure. However there is a lack of experimental findings on the interfacial behavior of this 'novel' material system, which governs the mechanical limitation of composite structures. Therefore, the principal aim of this paper is to study the shape memory effect (SME) on interfacial strength of SMA composites and validate the previously developed theoretical model for the prediction of interfacial debond using the SMA wire pullout test. The embedded wires were subjected to electrical resistive heating for SME generation inside the epoxy matrix cylinder. Stress-displacement results were obtained and the debonding processes were closely monitored and recorded by using a high-resolution digital video camera. Results for different actuation temperatures were analyzed systematically and compared with the theoretical solutions of partial debond stresses under SMA actuation. The generally good agreement between experimental findings and theoretical results convinced the application of the new developed model for the prediction of interfacial strength, which is crucial for fully utilizing the SME inside a composite without destroying the interface during actuation.
INTRODUCTION A great deal of effort was expanded over the past decade in developing the applications of shape memory alloys in composite materials. Numerous designs and fabrication processes of composite structures with SMA inclusions have been proposed by different research groups [1-3]. Using the concepts of active control, structure acoustic control [4] or shape control [5] can be accomplished with SMA reinforced composites utilizing a novel technique termed 'Active Modal Modification' [6]. As an example, the modal response of a structure can be modified by heating the embedded SMA wires to change the modulus of elasticity or even the yield strength of the whole structure. However, successes of those active controls or modal modifications rely on excellent interfacial properties between wire and matrix. Effectiveness of stress transfer from actuated wire to matrix is definitely restricted by their interfacial strength. Therefore, it is crucial to clarify the influence of SME on the interfacial behavior for the further development of SMA composites. * Corresponding author. Fax: (852) 2365 4703; Email: [email protected]
950
Shape Memory Effect on Interfacial Strength
This paper focuses on the interfacial behavior of NiTi SMA reinforced epoxy matrix composite. Experimental setup and fabrication of specimens are described in section 2. For simplicity, actuation temperature is limited from 20°C to 60°C to avoid the interfacial debond to occur at embedded ends due to over-actuation. In section 3, pullout test results and influence of SME as well as wire embedded length on interfacial debond are discussed and systematically analyzed. EXPERIMENT In order to increase the reliability and stability of SMA wires that were used to make SMA composite, a thermal-mechanical cycle treatment was firstly performed until no variation in stress-strain characteristic was observed. Material properties of SMAmatrix cylinders employed in this study are summarized in Table I. The NiTi wires were elongated to 4% residual strain and then embedded into the epoxy matrix cylinder during the lay up process. Wire's ends were fixed to guarantee the alignment inside cylinder and prevent it from any shape change during the curing process of epoxy matrix. Total twenty specimens were fabricated; dimensions and the corresponding quantities are listed in Table n. One specimen of each dimension was employed as basic sample so as to identify the influences of SME in the pullout tests. Experimental setup for the SMA-wire pullout test is schematically illustrated in Fig. 1. Both debonding process and pullout test data (including force, displacement and time) were captured by using the high resolution digital video camera and MTS Tytron250 micro-force testing machine respectively. The embedded SMA wires were firstly heated to 20°C, 40°C or 60°C and then the pullout test started under the constant actuation temperature. Loading end of the wire was clamped on load cell and the cylinder was slowly pulled away from loading end at 0.5mm/min. Temperature on wire had been continuously monitored and only ±1°C was found during the test. From the plots of pullout test data, both the maximum debond stress, <x/ and initial factional stress, Cfr can be obtained directly. However, the initial deobnd stress, of is relatively difficult to be identified from the plot. The two major reasons including the risk of over-actuation and stress-induced martensitic transformation (SIM) occurred during the test. Over-actuation is able to initiate interfacial debond at free end instead of loading end [7]. In the other words, even though af can be clearly identified, it is not necessary to represent the normal debonding behavior with interfacial crack propagation from loading end to embedded end. On the other hand, SIM yields sudden slope change of stress-displacement curve. The initial debond, which is normally identified by sudden slope change, may be covered up by the SIM. Therefore, in this paper, data obtained TABLE I Material properties of constituents a(mm)
b(mm)
sp(%)
EL(%)
EA(GPa)
EM(GPa)
Em(GPa)
CA(MPa/0C)
CM(MPa/°C)
0.2
5
4
8
38
19.2
2.12
28
20
ascr(MPa) CTfcr(MPa) AS(°C) 120
200
38
A,(0C)
MS(°C)
Mf(oC)
75
33
18
6(MPa/°C) T0(°C) 0.55
20
•y,.
y
0.33
0.35
TABLE n Dimensions and quantities of specimens Wiredia (mm) 0.40
Embedded Length L (mm) 5 30
2 o
0
o
20°C/40 Cx2/60 Cx2 20 C/40°Cx2/60°Cx2
20°C/40°Cx2/60 °Cx2
50 o
20 "C/40 Cx2/60°Cx2
Shape Memory Effect on Interfacial Strength
951
Video capturing ofdebonding process
Pullout test data acquisition
K-type Thermal couple DC power supply FIGURE 1 Experimental setup for SMA-wire pullout test
pullout test were compared with the captured debonded length, / and its propagation so as to estimate the initial debond stresses. As an example, if the debonding length observed in video is 5mm from loading end and the corresponding time frame was 50sec at the instant, the value of applied stress, ap/l) can be traced back from the pullout test data for the same time frame. Depending on sizes of specimens and the transparency of the matrix cylinder, two to five sets of Op/l) and / were obtained for each pullout test for further analysis. DATA ANALYSIS All the pullout test results showed the similar responses toward the influence of SMA actuations. Therefore, only the plots of typical results for SMA-epoxy matrix cylinders with embedded length L = 30mm are shown in Fig. 2 for illustration purpose. Obviously, the higher the actuation temperature, the higher the maximum debond stress can be attained. The recovery stress in the opposite direction of the applied load moderates the interfacial shear at loading end - the potential crack tip. As a result, higher applied load is required to initiate interfacial debond in the actuated SMA composites. It should be noted that a 'minor' improvement of maximum debond stress can also be observed at 40°C, which is supposed immediately higher than austenitic transformation start temperature, Tfo. The recovery stress for T < T* should be increased linearly with temperature under a strain-constrained condition and it is generally governed by a thermal coefficient of expansion, 9. Therefore it is not surprised for having improvement of maximum debond stress in such low actuation temperature. As discussed previously, relations between apd(l) and / at different actuation temperatures can be obtained by using the digital video capturing system. Again, due to the similar results obtained for specimens in different dimensions, only the plots for wire embedded length L = 30mm are illustrated in Fig. 3. All the pullout test results are compared with the previously developed theoretical solution of partial debond stress [8], 2naGi =
+Q2ascrpd
+L2(
(1)
where G,- represents the fracture toughness determined from SMA-wire pullout test. Q {1=1,2,3) are functions of material constants, geometric factors of the constituents and actuation temperature. Z,- (z = 1,2,3) are the functions arising from SMA actuation.
Shape Memory Effect on Interfacial Strength
952
0.00
0.50
1.00
1.50
2.00
Displacement (mm)
FIGURE 2 Typical pullout test results for SMA-epoxy matrix cylinders subjected to different actuation temperatures.
Predictions of partial debond stress,
500 !
%
•••-
• - • • • • •
"
"
|
•is
° ^ < h—•
*=
\v
• * » o A o
402C Theory 60°C Theory 20QC Exp. 40°C Exp. 60QC Exp. IDS at 20=C IDS at 40DC IDS at 60eC
0
10
20 30 Debonded length (mm)
FIGURE 3 Comparisons between theoretical solutions and pullout test results of partial debond stress, <rpli against debonding length, /. (IDS: Initial debond stress)
Shape Memory Effect on Interfacial Strength
953
600 550 •5- 500 Q.
15
n O
20
Theory L=5mm Theory L=30m m Theory L=50mm L=2mm L=5mm L=30mm L=50mm
25
30
35
40
45
50
55
60
65
Temperature (°C) FIGURE 4 Influence of SMA actuation on the initial debond stresses.
Since the data presented in Fig. 4a are all obtained from video capturing system, due to the small dimensions and unclear matrix cylinder of several specimens, some of the initial debond stresses could not be clearly captured during the pullout tests. Considering the results for specimens with embedded length 5mm, one may notice that the initial and the maximum debond stresses for 60°C are lower than the cases of 40°C. This observation is contradicted to the outstanding improvement of debond stresses for 60°C as found in all other available results or even the theoretical predictions. Referring to captured videos, for this particular case, it was found that the interfacial debond initiated at free end instead of loading end as shown in Fig. 5. It is probably the problem of overactuation on SMA wire. When the wire has been heated to a relatively high temperature (T > 60°C), interfacial shear at loading end was moderated. However the shear stress components at free end arising from recovery action and applied load were acting in the same direction. In the other words, the resultant interfacial shear became higher and eventually damaged the interface. CONCLUSIONS The previously developed theoretical model of partial debond stress, aptj on actuated SMA-composites has been validated by using a hybrid-experimental method in this study. Except the conventional type of fiber-pullout test, a digital video capturing system was also employed to identify the direction of debond propagation and partial debonded length during the pullout tests. This newly proposed experimental method is particularly useful to capture captioned information, which can never be obtained from the traditional wire pullout test. Pullout test results confirm that both the initial and maximum debond stresses are improved with actuation temperature increase and the results obtained from video monitoring system are able to present the relationship between partial debond stress and the corresponding debonding length (Figure 3). It is also found that the initial debond stress under the same actuation temperature increases with wire embedded length. The problem of 'free-end debond', which is arising from over-actuation of the embedded wire, is observed and discussed for the decrease of debond stress in actuated condition.
954
Shape Memory Effect on Interfacial Strength
FIGURE 5 Interfacial debond occurred at free end instead of loading end.
ACKNOWLEDGEMENTS The authors acknowledge the financial support by The Hong Kong Polytechnic University Research Grants (H-2H38, G-T673 and A-PD79). REFERENCES 1. 2.
3. 4. 5. 6. 7. 8.
Rogers, C. A., Liang C. and Jia J., 1991, "Structural Modification of Simply-supported Laminated Plates Using Embedded Shape Memory Alloy Fibers", Comput. Struct. 38, pp. 569-580 Bidaux J. E., Bernet N., Sarwa C , Manson J. A. E. and Gotthardt R., 1995, "Vibration Frequency Control of a Polymer Beam Using Embedded Shape-Memory-Alloy Fibres", J. Physique IV, 5 pp. 1177-1182 Hamada K., Lee J. H., Mizuuchi K., Taya M. and Inoue K., 1997, "Mechanical Properties of Smart Metal Matrix Composite by Shape Memory Effects", Mater. Res. Soc. Symp. Proc. 459, pp. 143-148 S. Saadat, M. Noori, H. Davoodi, Z. Hou, Y. Suzuki and A. Masuda, 2001. "Using NiTi SMA Tendons for Vibration Control of Coastal Structures," Smart Mater., 10: 695-704 D. C. Lagoudas and I. G. Tadjbakhsh, 1992, "Active Flexible Rods with Embedded SMA Fibers," Smart Mater. Struct. 1: 162-167 C. A. Rogers, C. Liang and J. Jia, 1989. "Behavior of SMA Reinforced Composites Plates Part I," Proceedings of the 3(fh Structures, Structural Dynamics and Materials Conference, Mobile, AL Poon C. K., Zhou L. M. and Yam L. H., 2003, "Size Effect on the Optimum Actuation Condition for SMA-composites", presented at ICCS-12 in Melbourne, Australia, Nov 2003 Poon C. K. , Zhou L. M. and Yam L. H, 2003, "Prediction of Interfacial Debond for Smart Composites", Presented at MM2003, Dec 8-12, 2003.
Part XVII
Structural Health Monitoring
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Modified Acoustic Emission Generated in a Full-Scale Aircraft Wing Subjected to Simulated Flight Loading Christophe A. Paget, Kathryn Atherton and Eddie O'Brien Airbus UK, Experimental Mechanics Group, Building 09H-D1, Dept. ESUSZ, New Filton House Filton, Bristol, BS99 7 AR / UK
ABSTRACT In previous studies, systems based on modified acoustic emission (MAE) showed outstanding results in monitoring damage on aeronautical structures, locating all damages measured by conventional NDT. The present investigation focuses on the characteristics of those modified acoustic emissions generated by fatigue cracks and fretting. The structure being studied was a full-scale metal aircraft wing subjected to simulated flight loading. The structural damage assessment system, called BALRUE, measured the waveform characteristics of the MAE-bursts, as well as the burst rate and location. The investigation highlighted the major differences between a crack and fretting, in terms of burst characteristics. This allows the damage types to be distinguished in metal structures. It also permits improvements of the crack growth rate measurement, separating modified acoustic emission due to crack propagation from that due to fretting generated by the two crack surfaces during loading.
INTRODUCTION Structural damage assessment has become one of the key technologies for aeronautics over the last 5 years, mostly due to the increased use of composite structures from weight saving challenges [1,2]. At Airbus, a research team from the Experimental Mechanics group collaborated with Lloyd's Register EMEA and Ultra Electronics Ltd to develop a structural damage assessment system called BALRUE [3]. The primary goals of Airbus were to design a system able to continuously monitor structural damage anywhere in the aircraft without prior knowledge of damage location, identify the damage type and use small sensors so as not to impede NDT from being carried out. The system shall also be capable of being retrofitted to in-service aircraft, recovering damage data even after the extreme case of damage assessment system failure and ultimately reducing work of the maintenance team whilst maintaining the same safety standards. Amongst all available techniques, clearly one of the techniques that fulfils all aforementioned requirements is modified acoustic emission (MAE) [4]. This technique differs from conventional acoustic emission by its extensive data filtering and compression features.
* Corresponding Author, Airbus UK Ltd, Bldg 09H-D1, New Filton House, Filton, Bristol BS99 7AR, UK, Phone: +44 117 936 4636, Fax: +44 117 936 5903, Email: [email protected]
Modified Acoustic Emission Generated in a Full-Scale Aircraft Wing
958
For about 6 years, Airbus and Lloyd's Register have been using the modified acoustic emission systems internally, providing outstanding results. Numerous trials on metallic structures proved the ability of the system to reliably locate the damage and monitor crack growth in metals. The present investigation focuses on differentiating the damage type in metallic structures. It is important for the maintenance team to know if there are cracks or even fretting occurring in the structure. Although, the need of crack detection is obvious, it is equally important to know where fretting occurs, since fretting can be a precursor to rivet failure or rotating bolts. The paper discusses the results obtained by monitoring a full-scale fatigue test. The monitoring of the structure lasted over 13 months, although only the first two-months of data is discussed here. The paper shall first discuss the fundamentals of modified acoustic emission, as well as describe the specimen and setup. It also shall discuss the results and draw conclusions.
FUNDAMENTALS Damage, such as fretting, delamination or cracking, generates mechanical waves throughout the structure. The waves are further converted into an electrical signal by the use of a sensor, or more particularly a piezoelectric ceramic element made of soft lead zirconate titanate (PZT) bonded onto a ceramic shoe. The electrical signal is preamplified and filtered at the material natural frequency. It may be expected that fretting and cracking in metallic structures could be differentiated by the burst duration, as further highlighted in this investigation. The burst corresponds to the high amplitude portion of the signal generated by the damage itself, as shown in Figure 1. The figure shows the envelope of theoretical acoustic emission related to fretting and cracking. RT and BD stand for rise time and burst duration, respectively. The fretting may be described as an event of "long" duration as opposed to a crack that would be described as a "short" duration. Therefore, the burst duration was considered herein as the main feature closely related to the damage type in metals. Similarly to the burst duration, the rise time may be used to determine the damage type. Both burst duration and rise time shall be investigated.
Amplitude
Amplitude Fretting
FIGURE 1 Theoretical acoustic emission signal from crack (left) and fretting (right)
In some cases, the burst duration can be dependent on the propagation distance, which increases the problem difficulty. The phenomenon is due to the dispersive nature of the waves. The use of relatively low frequency filters (at material natural frequency) provide the user with two Lamb wave modes, in the case of, for instance, 5mm-thick aluminium structures with 300kHz sensors and 300kHz band-pass preamplifier/filter. The expected group velocities are 5km/s and 3km/s for So and Ao modes, respectively, as shown in the dispersion curves of Figure 2.
Modified Acoustic Emission Generated in a Full-Scale Aircraft Wing
0
0.4
0.8 1,2 Frequency (MHz)
1.6
959
2.0
FIGURE 2 Dispersion curves for a 5mm-thick aluminium material
In general, when the distance from the AE source to the sensor is large, the Somode is greatly attenuated due in part to its dispersive nature. In some cases the Somode amplitude falls below the detection threshold, allowing only the A0-mode to be measured by the system. The Ao-mode, as shown in Figure 2, is not a dispersive mode and subsequently the corresponding burst duration is likely to be independent of the propagation distance. The data analysis becomes thus more straightforward and the damage type easy to distinguish. When the sensors are closer to each other, the preponderant signal being collected is the S0-mode. At 300kHz in 5mm-thick aluminium, the So-mode is dispersive and the corresponding burst durations may be dependent on the propagation distance, making the damage type more difficult to identify from the acoustic emission response. However, problems related to So-mode dispersion could be overcome as the distance between source and sensor is determined by the structural damage assessment system BALRUE. Knowing the relationship between burst-duration and propagation-distance for So-mode would allow the system to recover the burst duration at source and therefore deduce the damage type. By using a Hsu-Nielsen source during installation of the structural damage assessment system, the user should be able to establish which mode shall be collected by the system. A Hsu-Nielsen source generates an approximately 13dB higher amplitude signal than a real crack in metal. The user should then allow a 13dB margin when setting up the system, namely the "amplitude detection threshold", well known to acoustic emission system users. The user should then be able to impose which mode will be collected by the system. As a rule of thumb, the installation engineer should make sure that the sensor separation distance is such that mainly A0-mode can be detected by the structural damage assessment system, subsequently simplifying the problem. There is also the case where the first hit sensor collected So-mode and the second Aomode. This case can easily be detected as the respective amplitudes would not follow the expected amplitude attenuation curve of the material used.
SPECIMEN DESCRIPTION AND TEST SETUP The specimen used for this investigation is a full-scale metallic wing based on the A340-600 aircraft wing, excluding the flaps, slats and trailing edges as well as the fittings (hydraulics and cabling).
960
Modified Acoustic Emission Generated in a Full-Scale Aircraft Wing
The structural damage assessment system monitored three areas, as shown in Figure 3. The first area was bordered by rib 3, rib 10, the rear spar and the centre spar, monitoring both upper and lower skins. The other monitored areas were the landing gear rib 6 and the vicinity of the inboard pylon.
Monitored areas„
FIGURE 3 Specimen description. Upper and lower skins monitored
The monitored portions of the wing contained both cracks and fretting at the time of the BALRUE system installation, since this was performed after nearly 2.5 lifetimes of simulated fatigue cycling on the specimen. Simulated cracks were created at random location in the structure using a Hsu-Nielsen source (breaking a 0.5mmdiameter pencil lead), in order to verify the detection, location and reliability of the system. The specimen was loaded in fatigue, following a standard simulated flight spectrum of 50 000 simulated flight cycles, at 110% load. The structural damage assessment system was installed at cycle number 22 000, and monitored the specific regions of the structure for 28 000 cycles, lasting over a year. The sensors were surface-bonded to the structure using silicone paste. Preamplifiers with 40dB gain were used to transfer the acoustic emission signal through 75m-long coaxial cable with minimum signal loss. The coaxial cables were further connected to the structural damage assessment system for data recording, filtering and processing. The system was then calibrated against the CEN standards (Hsu-Nielsen source) throughout the entire monitored structure, to determine the experimental group velocity and attenuation curves of the generated modes.
RESULTS In-house analysis software was used to process the MAE data collected by the BALRUE system. Acoustic emissions propagate throughout the entire structure, providing mainly two types of information related to early- and mature-stage damage. This would generally be recognised by an acoustic emission density of "medium" and "high" level, respectively. The results were analysed focusing only on the average value of both rise-time and burst-duration data. The standard deviation of the rise-time and burst-duration data was also processed to insure the reliability of the averaged results.
Modified Acoustic Emission Generated in a Full-Scale Aircraft Wing
961
Over 15 zones of high acoustic emission activity are analysed herein. Figures 4 and 6 show examples of average burst duration and rise time for a MAE source. The present analysis has clearly identified two burst-duration ranges, to first varying between 1.5ms and 2.3ms, and the second range between 2.3ms and 5.1ms. The burst duration ranges were associated with cracks and fretting, respectively. The standard deviation for the burst duration results was relatively low, about 0.3ms and 0.5ms, respectively. The investigation has also found two rise time ranges: 30|j,s to 50(is and 200(j,s to 650|^s, for cases of cracking and fretting, respectively. The standard deviation for the cracking and fretting cases was about 6|as and 27|as, respectively. ! I11 IK;
75Ot?
701IH
65m
Damage A \
i - 70UCI
509!
/ Damage B '
liU'O "400 X-coordinates (mm)
1'
Damage A\
1
4* !
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;
1 65f.H'l o lei?
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1<<75
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* Damage B
2S00 " .. 3400 X-coordinates (mm)
55S
4
M
F I G U R E 4 Average burst duration (left) and rise time (right) between sensors 6, 12, 14; Z-axis in ms
Rib 6
Rib 8
.DamageA/
Damage B
FIGURE 5 AE density (left) and their location on the structure (right) between sensors 6, 12 and 14
These results were qualitatively expected since fretting is a phenomenon occurring over a far longer time interval than a crack. The present investigation therefore provides a way to not only identify what type of damage is being monitored, but it also allows fretting information, generated by the rubbing surfaces of a crack, to be separated from the crack information itself. The latter is a form of data filtering, allowing more automatic crack growth rate measurement. Further work on this topic shall be carried out at Airbus shortly. Across the entire monitored areas, all MAE with high density had consistent burst duration and rise time data with each damage type. Figure 5 shows the location of two areas of high MAE on the specimen, as an example. They correspond to two reported points of damage, designated by A and B, both fretting and recorded as rotating fasteners.
Modified Acoustic Emission Generated in a Full-Scale Aircraft Wing
962
^4
1 Hi 96L® 1
Damage,
Damage,
\ 1 920|
92m
• t?
881$ X-coordinates (mm)
"4
X-coordinates (mm)
•
FIGURE 6 Example of average burst duration (left) and rise time (right) near sensor 9; Z-axis in ms
CONCLUSIONS The present investigation was focused on differentiating damage types in metallic structures using the structural damage assessment system (BALRUE) developed partly by Airbus. The system is based on modified acoustic emission, allowing high data filtering, and further facilitating the determination of the damage type. The results showed the possibility of distinguishing fretting from cracking by the use of burst duration or rise time provided by the BALRUE system. Indeed, both the average burst duration and rise time demonstrated a marked difference in both damage types. This characteristic also permits improvements in crack growth rate measurements by extracting neighbouring fretting data from the growing crack during modified acoustic emission processing.
REFERENCES 1.
2.
3.
4.
C. A. Paget, "Active Health Monitoring of Composites by Embedded Piezoceramic Transducers," Doctoral Thesis, Report 2001-25, Department of Aeronautics, The Royal Institute of Technology, Sweden, Dec. 2001 B. Beral and H. Speckmann, "Structure Health Monitoring (SHM) for Aircraft Structures: A Challenge for System Developers and Aircraft Manufacturers," Proc. Of the 4th International Workshop on Structural Health Monitoring, Stanford University, CA, USA, pp. 12-29, Sep. 2003 Ultra Electronics, Controls Division, 417 Bridport Road, Greenford, Middlesex UB6 8UE, UK, (www.balrue.co.uk), Structural Damage Assessment System for all typical applications (including intrinsically safe and airborne) C. A. Paget, K. Atherton and E. O'Brien, "Triangulation Algorithm for Damage Location in Aeronautical Composite Structures," Proc. Of the 4th International Workshop on Structural Health Monitoring, Stanford University, CA, USA, pp. 363-370, Sep. 2003
In-situ Health Monitoring of Filament Wound Pressure Tanks using Embedded FBG Sensors Dong-Hoon Kang, Cheol-Ung Kim, Sang-Wuk Park, Chang-Sun Hong and Chun-Gon Kim Division of Aerospace Engineering, KAIST, Korea
ABSTRACT In this research, in-situ structural health monitoring of filament wound pressure tanks were conducted during water-pressurizing test using embedded fiber Bragg grating (FBG) sensors. We need to monitor inner strains during working in order to verify the health condition of pressure tanks more accurately because finite element analyses on filament wound pressure tanks usually show large differences between inner and outer strains. Fiber optic sensors, especially FBG sensors can be easily embedded into the composite structures contrary to conventional electric strain gages (ESGs). In addition, many FBG sensors can be multiplexed in single optical fiber using wavelength division multiplexing (WDM) techniques. We fabricated a standard testing and evaluation bottle (STEB) with embedded FBG sensors and performed water-pressurizing test. In order to increase the survivability of FBG sensor during cure, we suggested a novel fabrication process for embedding FBG sensors into a filament wound pressure tank, which includes a new protecting technique of sensor heads, the grating parts. From the experimental results, it was demonstrated that FBG sensors can be successfully adapted to filament wound pressure tanks by embedding.
INTRODUCTION Recently, the use of filament wound pressure tanks is increasingly prevalent because of high specific strength and specific stiffness over their metal counterparts, as well as excellent corrosion and fatigue resistance. The main applications of filament wound pressure tanks are fuel tanks, pressure tanks and motor cases of aerospace structures. A filament wound pressure tank, a kind of composite structure, has the complexity in damage mechanisms and failure modes. Most of the conventional damage assessment and nondestructive inspection methods are time-consuming and are often difficult to implement on hard-to-reach-parts of the structure. For these reasons, a built-in assessment system must be developed to monitor the structural integrity of critical components constantly. Fiber optic sensors (FOSs) have shown a potential to serve as real time health monitoring of the structures. They can be easily embedded or attached to the structures and are not affected by the electro-magnetic field. Also, they have not only the flexibility in the selection of the sensor size but also high sensitiveness. Recently, fiber optic sensors have been introduced to composite structures [1-2]. FBG sensors based on WDM technology are attracting considerable research interest and appear to be ideally suitable Correspondence Author : Division of Aerospace Engineering, KAIST, 373-1 Guseong-dong, Yuseong-gu, Daejeon, 305-701, Republic of Korea. Tel: (82-42) 869-3719, Fax: (82-42) 869-3710, Email: [email protected]
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In-situ Health Monitoring of Filament Wound Pressure Tanks
for structural health monitoring of smart composite structures. FBG sensors are easily multiplexed and have many advantages such as linear response, absolute measurement, etc. Among many researches on filament wound pressure tanks, only a few were performed using FBG sensors. Foedinger, et al.[3] measured the temperature and strains during cure and studied ingress/egress method for STEB using FBG sensors. Lo, et al.[4] measured the unbalanced strain from the wavelength difference of a pair of FBG sensors during the water-pressurizing test. Degrieck, et al.[5] embedded a FBG sensor between the hoop layers and measured the internal pressure of the tank through the water-pressurizing test from the wavelength shift of a FBG sensor. Kang, et al.[6] attached 32 FBG sensors on the filament wound pressure tank as 4 channels and measured the strains through water-pressurizing test. From the above literatures, we can find out that only a few FBG sensors were used when embedding sensors into the pressure tank and relatively a large number of FBG sensors were used when attaching sensors on the surface. In this paper, the strains of a filament wound pressure tank were monitored using a number of embedded FBG sensors in real time; 14 FBG sensors were embedded into the dome and cylinder part of the pressure tank. The strains measured by FBG sensors were compared with those measured by ESGs and calculated by FEM analyses. FABRICATION OF FILAMENT WOUND PRESSURE TANKS Fabrication of FBG sensor lines There are many fabrication methods of FBG sensors. Among the methods, the fabrication method using a phase-mask is very popular, nowadays. In this research, multiple FBG sensors were fabricated in a single optical fiber in order to increase the accuracy of sensor position and to decrease the strength degradation of optical fiber caused by arc-fusion splicing between optical fiber segments. For the fabrication of a FBG sensor, photo-sensitive optical fiber (Fibercore Ltd.), phase-mask (IBSEN Co.) and excimer laser (MPB Co.) with the wavelength of 248 nm were used. Four FBG sensor lines were fabricated in total. Before embedding FBG sensor lines into filament wound pressure tanks, the grating parts were protected using arcylate recoating and adhesive film in order to increase the survivability of FBG sensors during the fabrication process. Figure 1 shows the FBG sensor line protected with arcylate recoating and adhesive film.
FIGURE 1 FBG sensor line protected with arcylate recoating and adhesive film
Fabrication of filament wound pressure tank The equipments for the filament winding are composed of a tension controller which regulates the fiber tension, a resin bath, a fiber roll and a control panel which commands the winding pattern, winding speed and etc. Before the main winding of the tank, rubber winding was conducted on an aluminum mandrel. The rubber liner made by rubber winding is necessary for the prevention of a water leakage during the use of fabricated pressure tank. The pressure tank consists of a front dome, an aft dome, a cylinder and a skirt for joining with other structures. This tank was fabricated by the wet winding process using a 4-axis filament winding machine controlled by a computer. The winding tension was
In-situ Health Monitoring of Filament Wound Pressure Tanks
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1.5kg/end and the bandwidth of hoop and helical layer was 10.0, 10.5(mm) for 5-ends, respectively. The cylinder part includes a 3-body helical layers and 5-body hoop layers so that the sequence is (±27.5)3/905 denoting from inner to outer layers. Figure 2 shows the embedded sensor lines during the fabrication process.
(c) cylinder : axis direction
(d) cylinder : hoop direction
FIGURE 2 Embedded FBG sensor lines during the fabrication
The channel 1(CH1) and channel 2(CH2), each has 4 FBG sensors, were embedded between the layer 1 and 2 at aft dome and the layer 2 and 3 at front dome, respectively. The channel 3(CH3) and channel 4(CH4), each has 3 FBG sensors, were embedded between the layer 5 and 6 in the axial direction and the layer 6 and 7 in the hoop direction at cylinder part, respectively. Since most of the loading applied to a pressure tank is sustained by reinforcing fibers, it is important to measure the strains along the fiber direction. Hence, all FBG sensors were aligned to fiber directions of the pressure tank except 3 sensors of CH3 embedded in perpendicular to the reinforcing fiber direction at the cylindrical part. After embedding each sensor line, embedding positions of FBG sensors were measured accurately using a laser pointer. The filament wound pressure tank with embedded FBG sensor lines were cured under rotating condition in the curing cycle ; 80oC(lhr)->120°C(lhr)-^150°C(3hr) in an oven. EXPERIMENTAL APPARATUS AND METHOD Just after the fabrication process of the pressure tank, 11 of 14 sensors survived. Three sensors of CH3 failed during the cure. Figure 3 shows the positions of embedded FBG sensors and ESGs attached on the surface. 'F' means FBG sensor and 'E' means ESG. The figure following 'F' means the channel number. As shown in Figure 3, 11 FBG sensors and 8 ESGs were embedded in and attached on the filament wound pressure tank, respectively. Figure 4 depicts the experimental setup for the strain monitoring of a filament wound pressure tank during hydrostatic pressurization. The strain measurement was performed at intervals of 100 psi up to 500 psi(3.448 MPa). The strain data from the FBG sensors, ESGs, and a pressure transducer were acquired and processed by a computer in real time.
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In-situ Health Monitoring of Filament Wound Pressure Tanks
On the domes, 4 ESGs were attached on the surface at the same locations of embedded FBG sensors, aligned to the helical winding direction. On the cylinder, also, 4 ESGs were attached in the hoop winding direction, i.e., the circumferential direction of cylinder.
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FIGURE 3 The positions of FBG sensors and electric strain gages in STEB
FIGURE 4 Experimental setup and schematic diagram
The signals of the FBG sensors, strain gauges and a pressure transducer were acquired simultaneously by computers, processed and displayed by a signal-processing program written in Lab VIEW® software. The specifications of used FBG sensor system are shown in Table 1. TABLE I Specifications of FBG interrogator
LS-7000 FBG Interrogator (FiberPro Co.) Wavelength range Average output power Resolution Measurement speed # of channels Temperature range
35 nm (1530- 1565 ran) 3mW <2pm 200 Hz 8 10~40°C
FINITE ELEMENT MODELING Finite element analyses on STEB were done by a commercial code, ABAQUS. In this research, the 3-D layered solid element was utilized and the boundary condition was considered as cyclic symmetric. Figure 5 shows the detailed FEA model of STEB realized
In-situ Health Monitoring of Filament Wound Pressure Tanks
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by a commercial code, PATRAN, and the material properties of T700/Epoxy used in the analysis were as follows. Ei = 134.6 GPa, E2 = 7.65 GPa, Gi2 = 3.68 GPa, v i2 = 0.3 a f = 2290 MPa, o t = 31.8 MPa, S = 75.8 MPa 10 elements in the cylinder part
Cycle symmetry Z-ans symmetry
30 elements in the dome part
6 elements through the thickne
Displacement Fixed in X and V directions
FIGURE 5 The FEA model of STEB
The modified Hashin's failure criterion was selected and applied to progressive failure analysis. For the purpose of failure analysis, a subroutine, USDFLD of ABAQUS ver 6.3 was coded to define the change of mechanical properties due to failure. RESULTS AND DISCUSSIONS Figure 6 shows the strain results measured by FBGs, ESGs and FEA simultaneously at 500 psi. The results from FBG sensors were compared with those from ESGs which were attached at the same longitudinal locations with FBG sensors. Both strain results were also compared with those of FEM analyses, which were indicated as lines in Figure 6. 0.28 T •'I
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i
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400
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In-situ Health Monitoring of Filament Wound Pressure Tanks
The strain measured by each FBG sensor showed a good linearity with the increase of pressure. Considering only the FEA results, helical layers of front dome and aft dome showed a large difference in strains between inner and outer layers. However, there was little difference in strains between inner and outer layers at cylinder part. hi Figure 6, the strains measured by FBGs and ESGs were similar at hoop layers of cylinder part and also showed good agreement with the FEA results while the results from FBGs and ESGs at both domes showed a large difference with each other. The differences in strains measured by FBG sensors and ESGs may be occurred by a mismatch of attaching angles and locations between them. Also, these differences may be caused by . the slippage of an embedded FBG sensor line during the curing process due to resin flow. FBG sensors can measure the strain at the positions where the measurement is impossible with ESGs, for example, between the layers of dome and cylinder. And, this is very important advantage of FBG sensors, especially in filament wound pressure tank because it has a severe change in strains between layers of dome part. CONCLUSIONS FBG sensors totaled 14 were embedded into the domes and cylinder parts of a filament wound pressure tank in order to measure the strains in real time during hydrostatic pressurization. FBG sensors, 11 out of 14, survived through the whole fabrication processes. When embedding multiplexed sensor lines into a filament wound pressure tank, some fabrication steps with sensor line protection were introduced to increase the survivability of FBG sensors. From the experiment, the strain data from FBG sensors showed close agreement with the data from ESGs and the results were also verified by the finite element analyses. Thus, it was successfully demonstrated that the FBG sensors could be useful for the strain monitoring of filament wound structures that require a large number of sensor arrays. ACKNOWLEDGEMENTS The authors would like to thank to the Agency for Defense Development for assistance in research funds.
REFERENCES 1. 2.
3.
4.
5.
6.
H. K. Kang, J. W. Park, C. Y. Ryu, C. S. Hong, and C. G. Kim. 2000. "Development of fibre optic ingress/egress methods for smart composite structures," Smart Materials and Structures, 9(2): 149-156. J. W. Park, C. Y. Ryu, H. K. Kang, and C. S. Hong. 2000. "Detection of buckling and crack growth in the delaminated composites using fiber optic sensor," Journal of Composite Materials, 34(19): 1602-1623. R. C. Foedinger, D. L. Rea, J. S. Sirkis, C. S. Baldwin, J. R. Troll, R. Grande, C. S. Davis, and T. L. VanDiver. 1999. "Embedded fiber optic sensor arrays for structural health monitoring of filament wound composite pressure vessels," Proc. OfSPIE, 3670: 289-301. Y. L. Lo, P. H. Sung, H. J. Wang, and L. W. Chen. 2000. "Pressure vessel wall thinning detection using multiple pairs of fiber Bragg gratings for unbalanced strain measurements," Journal of Nondestructive Evaluation, 19(3): 105-113. J. Degrieck, W. De Waele, P. Verleysen. 2001. "Monitoring of fibre reinforced composites with embedded optical fibre Bragg sensors, with application to filament wound pressure vessels," NDT&E International, 34: 289-296. H. K. Kang, J. S. Park, D. H. Kang, C. U. Kim, C. S. Hong, and C. G. Kim. 2002. "Strain Monitoring of Filament Wound Composite Tank Using Fiber Bragg Grating Sensors," Smart Materials and Structures, 11(6): 848-853.
An Approach towards Predicting the Evolution of Fire Damage for Marine Composites Z. Mathys*, C. P. Gardiner, P.J. Burchill Maritime Platforms Division, Defence Science and Technology Organisation, Australia
ABSTRACT This paper describes a preliminary investigation into the mass loss that occurs from styrenic composites and castings exposed to various heat flux intensities using cone calorimetry and a fuel fire of controlled duration. Some simple relationships have been determined for the combustion of resin and the ability to predict the mass loss rate for both castings and composites at different heat fluxes if the mass loss at one heat flux is known. The study also investigates the relationship between mass loss and the corresponding level of damage after exposure to a fuel fire and controlled heat fluxes in a cone calorimeter. It was found that the damage depth of styrenic composites is linearly related to mass loss and that the damage depth can be predicted if the resin volume fraction of the composite is known. This analysis enables the level of thermally-induced charring of a composite structure to be predicted with a minimal quantity of experimental data. Conversely, given a measure of the damage depth, the average fire intensity and the residual structural properties of a burnt composite panel can be estimated. An example case study of a representative bulkhead to deckhead structure of the Royal Australian Navy Huon Class minehunter coastal vessel is demonstrated.
INTRODUCTION Glass reinforced polymer (GRP) composites are increasingly being introduced in many marine, building and transport applications, both as light weight structural and non-structural components, due to their increasing cost effectiveness, corrosion and chemical resistance, and high specific mechanical properties. However, a limitation with the use of composite materials is their susceptibility to combustion and fire damage because of their organic matrix component. The flammability of composites has been studied extensively and has been attributed to the poor fire reaction properties of the polymer matrix including short ignition times, high peak and total heat release rates, smoke density and toxic gas emissions [1-4]. Another factor limiting the use of GRP is the reduction in stiffness and strength that may be experienced both during and after a fire event. For example, it has been shown that the strength of a burnt composite is dependant on the depth of thermally induced fire damage [5-8]. However, the relationship between the burning process and the damage observed has not been determined. This paper describes a preliminary investigation into the * Corresponding author, DSTO, PSL, P.O. Box 4331, Melbourne, Victoria, Australia 3001, 03 9626 8448, [email protected]
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Predicting the Evolution of Fire Damage for Marine Composites
mass loss that occurs from cone calorimetry and exposure to a fuel fire. The relationship between mass loss and various heat flux intensities of several styrenic thermoset GRP composites are studied and the corresponding level of damage is investigated. EXPERIMENTAL Several composite panels with various resins systems were manufactured using a hand-layup technique and were cured either with an autoclave or at room temperature. The autoclaved composites were manufactured using a woven roving fabric (600 g/m2) with various matrix resins. These include a Crystic® 3-491PS orthophthalic polyester, Derakane® vinyl ester 411 and 8084 matrix resins. The resin castings were cured under the same temperature conditions as their composites. The room temperature cured specimens were manufactured using 1400 g/m2 woven E-glass fabric with an isophthalic polyester matrix resin, Synolite 0288-T-l. Autoclaved and hand layup composite specimens were tested according to the ASTM standard [9] in a horizontal orientation using a Stanton Redcroft cone calorimeter at heat fluxes (cone irradiances) of 35, 50 and 75 kW/m2. The isophthalic polyester composite specimens were also placed horizontal to the heat source in the cone calorimeter and exposed to heat fluxes of 25, 35, 50, 75 and 100 kW/m2 for selected exposure times. The ignition times were noted for all the composites and the mass loss of the composite was measured independently of the calorimeter's balance and the depth of charring revealed by sectioning. Fire tests were also performed on larger isophthalic polyester glass reinforced composite panels (1.35 x 0.55 m) by burning over a kerosene fuel fire for various times up to 15 minutes. After cooling to room temperature the panels were trimmed and the mass loss was determined as well as the depth of charring. A larger-scale test representative of a bulkhead to deck structure of a Minehunter coastal vessel was conducted. The bulkhead (1.2 x 2 m) and deckhead (1.2 x 1 m) structure consisted of a isophthalic polyester glass reinforced composite and was instrumented with a grid of K-type thermocouples and exposed to a kerosene fuel fire for 10 minutes. RESULT AND DISCUSSION Fire Damage The fire damage of the isophthalic polyester composites was examined after exposure to a radiant heater in the cone calorimeter and a fuel fire. A cross-section through-the-thickness of samples exposed to both conditions revealed three easily distinguishible zones. The zones include a char layer consisting of glass and residue from combustion of the resin, a discoloured zone with no visually obvious material loss, and undamaged material. The depth of charring and discolouration is dependent on the intensity and duration of the fire and may be expected to be related to the level of mass loss. Heat Flux and Mass Loss The mass loss rate curves at different heat fluxes have a similar characteristic profile. This similar characteristic profile allows the mass loss data to be translated from one heat flux to another due to their linear relationship. Figure 1 shows the
Predicting the Evolution of Fire Damage for Marine Composites
971
linear relationship of mass loss of a polyester casting and vinylester laminate at different heat fluxes up to a mass loss of 40 and 60 % respectively. Figure 1 implies that the slope is a measure of the relative rates at the different heat fluxes for a given level of reaction or depletion of resin. Therefore the relative rates using the above observation have been determined against the reciprocal of the (Heat Flux)1'4 for various resins and their composites, Figure 2. Then recalling the StefanBoltzmann equation it may be expected that the relative rates of mass loss be directly proportional to the temperature of the heat source. While there is appreciable scatter in the data, it is evident that the decomposition in the neat resins and their composites have a similar activation energy. The linearity of the plot in Figure 2 indicates that this kinetic process is defined and driven by the energy of the heat source. This was found to be valid up to mass losses of 30-40%.
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FIGURE 1. Comparison of the times to reach a specified mass loss for isophthalic polyester resin, consumption to 40% and for Vinylester 8084 composite, consumption to 60%
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FIGURE 2. Arrhenius plot for all the materials. Rates relative to a flux of 35kW/m2, and the temperature scale defined as (Heat Flux)1'4.
Thus for all the materials studied the relative mass loss can be estimated from the expression: +C
(1)
In which F is the incident flux in kW/m2 and kF/k35 is the relative mass loss, with B =-4.90 and C = 2.01. Hence, if the behaviour in terms of mass loss of a material with time at a flux of 35 kW/m2 is known, then the resulting factor from this equation can be used to predict the mass loss at another heat flux. However, the ignition time at the new heat flux needs to be determined to generate the mass loss curve. The ignition time can be viewed as a measure of the surface temperature of the material. That is, when the temperature is sufficiently high so that the rate of decomposition can support continued combustion. This implies a relationship between heat flux and ignition time. It was found that the product Ftjg1/2 (where F = heat flux and tig = ignition time) was constant for the various styrenic resins and composites. This ignition factor (FtjgI/2) has been found to be constant for a given material and can be used to determine the ignition time at any heat flux. Hence using equation (1) and the ignition factor a profile of mass loss with time can be determined for a given material and desired heat flux. Figure 3 shows the
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Predicting the Evolution of Fire Damage for Marine Composites
experimental results at 35 kW/m2 and 75 kW/m2 for the polyester GRP composite. The graph also shows that the data for the composite at 35 kW/m2 can predict the mass loss at a flux of 75 kW/m2 by the use of equation (1) and the ignition factor. All resin-composite data sets at the three fluxes showed a similar correspondence. • * •
Mass oss data at 35 kW/m2 Mass oss data at 75 kW/m2 2 Calcu ated 75 kw/mJ using the 35 kW/m data E nd eqn 1)
Time (5)
FIGURE 3. Shift of the mass loss for the polyester GRP composite at 35 kW/m2 to that at 75 kW/m2.
Physical Damage and Mass Loss The relationship between mass loss and the level of physical damage was studied at various heat intensities and exposure times for the isophthalic GRP composite exposed to both the radiant heater in the cone calorimeter and the fuel fire test for selected times. Upon burning, pyrolysis of the resin matrix occurs and a char layer is formed as described above. The char thickness of the samples was measured and the results have been plotted against mass loss, Figure 4. This shows that a linear trend exists between char thickness and mass loss for samples exposed to a fuel fire and a range of heat fluxes using a radiant heater. Hence mass loss and char thickness will have a similar dependence with respect to heat flux and time. The data points for the fuel fire have the same linear trend but have a lower mass loss than those exposed to the radiant heater for a given char thickness. This is due to differences in the test configuration. Nevertheless, the difference between the two data sets is small and it is proposed that a consistent trend exists between char thickness and mass loss for samples exposed to both a fuel fire and a radiant heater for a range of heat fluxes. The char thickness, dc, can be related to the mass loss per unit area (M) as follows; (2) where: Vr - volume fraction of resin (= 0.659) pr - density of resin (~ 1300 kg/m3) d - original thickness of sample a - average density of resin beyond the char front relative to the density of resin P - average density of residue relative to the density of resin. Equation (2) assumes a step change in density between the charred region and the uncharred region beyond the char front. The actual change in density will follow a smoother transition. The production of volatile gases may cause some mass loss
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Predicting the Evolution of Fire Damage for Marine Composites
beyond the char front such that a is slightly less than 1.0. Similarly, the char layer may not be completely degraded and the average relative density, /?, will be greater than zero. For /?, an approximate average density for the char region was measured and found to be 6.5 %, (ie ji = 0.065). The relative density beyond the char front, a, is assumed to vary with mass loss as follows; (3)
a = 1 - k.M where: 0
The solid line in Figure 4 was calculated using equation (2) and (3) with (5 = 0.065 and k adjusted to obtain the best fit to the measured data such that k = 2.57* 10"4 m2/kg. From this it became evident that the change in a was small in magnitude, and hence the change in density beyond the char front, in the discoloured region, due to the generation of volatiles is extremely small. The preceeding analysis is useful for predicting the level of thermally-induced charring of a composite structure with a minimal quantity of experimental data. Using experimental mass loss data at one heat flux, a simulated set of mass loss data can be generated for any other desired heat flux. Then using equation (2), with the constants determined above, the corresponding char thickness can be determined. Figure 5 shows calculated curves of char thickness for isophthalic composites exposed at 50, 75 and 100 kW/m2 determined from mass loss data measured at 35 kW/m2. The calculated curves provide a reasonable representation of the limited measured data.
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100 kW/m2 measured 100 kW/m2 calculated
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FIGURE 4. Char thickness versus mass loss for samples exposed to a fuel fire and a radiant heater. The solid line was calculated using equation (2)
300
400
500
Post-Ignition Time (seconds)
FIGURE 5. Char thickness calculated for 50, 75 and 100 kW/m2 determined from mass loss data measured at 35 kW/m2.
Estimation of char thickness is useful for predicting the residual structural properties of a burnt composite panel. It has been shown [4-6] that the residual tensile and flexural strength and stiffness of burnt composite coupons and plates can be approximated using simple models based on the char thickness of the specimen. The analysis also facilitates the estimation of the intensity of a fire that has burnt a composite structure. The first step is to measure the average char depth. From this the average mass loss per unit area can be determined using equation (2). Then, if the
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Predicting the Evolution of Fire Damage for Marine Composites
duration of the fire is known the mean heat flux can be determined using equation (1). For example, the maximum char thickness on the bulkhead of the bulkhead-deckhead structure was approximately 5.2 mm after 600 s exposure. The mass loss was therefore 3.66 kg/m2 (Vf = 0.40). The bulkhead initially ignited at 40 s and thus the average mass loss rate was 6.54xlO"3 kg/m2s. Using equation (1) with k35 = 7.0*10"3 kg/m2s, the mean heat flux is calculated to be 30.9 kW/m2. However, the average time to ignition over the region of maximum char thickness was longer than 40 seconds due to the time required for the flame to spread to this area. Hence the mass loss over the 10 minutes would be reduced and a higher incident heat flux would be expected for this depth of char. It has been estimated that the ignition at this maximum char thickness occurred at approximately 100 s. Therefore the estimated mean heat flux is 38.6 kW/m2. CONCLUSIONS Some simple relationships have been determined for the combustion of resin and depth of damage for several styrenic thermoset resins and their fibre glass composites. The time of exposure from ignition determines the mass loss and the extent of damage. While the time dependence of the mass loss rate is a complicated and undetermined function, it has been possible to show that the rates at different heat fluxes are linearly related. Thus, knowing the relationship of mass loss with time for a given flux enables the time dependence of mass loss at a different flux to be predicted. While the same approach cannot be used for depth of damage, it has been shown that this depth is proportional to mass loss. Hence damage depth can be predicted knowing the resin volume fraction of the composite. In addition, it has been shown that the average incident fire intensity on a composite structure exposed to a kerosene fuel fire can be estimated from a measure of the damage depth and the exposure time. These experiments have also confirmed that the damage and mass loss as a result of exposure to a fuel fire can be considered the same as that arising from exposure to a radiant heat source. Further experimental work is planned to further refine and validate the analysis described. REFERENCES 1.
Scudamore MJ. Fire performance studies on glass-reinforced plastic laminates. Fire and Materials 1994;18:313-325. 2. Sorathia U, Rollhauser CM, Allen Hughes W. Improved fire safety of composites for naval applications. Fire and Materials 1992; 16:119-125. 3. Brown JR, Mathys Z. Reinforcement and matrix effects on the combustion properties of glass reinforced polymer composites. Composites (PartA) 1997;28:675-681 4. Hume J., Assessing the fire performance characteristics of GRP composites, Proc. Int. SAMPESymp., 1992, 7, 11. 5. Pering GA, Farrell PV, Springer GS. Degradation of tensile and shear properties of composites exposed to fire and high temperature. Journal of Composite Materials 1980, 14, 54-66. 6. Mouritz AP, Mathys Z. Post-fire mechancial properties of marine polymer composites. Composite Structures 2000, 47, 643-653. 7. Gardiner CP, Mathys Z, Mouritz AP. Post-fire structural properties of burnt GRP plates. Marine Structures (submitted). 8. Sorathia U, Beck C, and Dapp T. Residual strength of composites during and after fire exposure. Journal of Fire Sciences, 1993,11, 255-270. 9. ASTM E1353-92, Standard test method for heat and visible smoke release rates for materials and products using an oxygen consumption calorimeter. (American Society for Testing and Materials, Philadelphia, PA, (1990).
A Bayesian Artificial Neural Network Method to Characterise Laminar Defects using Dynamic Measurements Heung Fai Lam Department of Building and Construction, City University of Hong Kong Martin Veidt* Division of Mechanical Engineering, University of Queensland Sritawat Kitipornchai Department of Building and Construction, City University of Hong Kong
ABSTRACT This paper reports on the development of an artificial neural network (ANN) method to detect laminar defects following the pattern matching approach utilizing dynamic measurement. Although structural health monitoring (SHM) using ANN has attracted much attention in the last decade, the problem of how to select the optimal class of ANN models has not been investigated in great depth. It turns out that the lack of a rigorous ANN design methodology is one of the main reasons for the delay in the successful application of the promising technique in SHM. In this paper, a Bayesian method is applied in the selection of the optimal class of ANN models for a given set of input/target training data. The ANN design method is demonstrated for the case of the detection and characterisation of laminar defects in carbon fibre-reinforced beams using flexural vibration data for beams with and without non-symmetric delamination damage.
INTRODUCTION The potential advantages of fibre-reinforced composites are well recognised for a large number of applications. The fact that the materials still do not play the dominant role in structural applications as they could, can be partly explained by their cost. Another important reason is the potential of the material to experience barely visible damage during service and/or manufacturing. Hence, much effort has been made in the last two decades to develop structural health monitoring (SHM) techniques for fibre-reinforced composites. Recently, SHM and damage detection using Artificial Neural Network (ANN) have attracted much attention, e.g. [7, 8, 9]. However, the issue of ANN design is usually not addressed in the area of ANN-based damage detection. In general, the design of ANN involves (1) the design of neurons, that is the selection of activation (also called transfer) functions; (2) the design of ANN architecture (the synaptic interconnections and arrangement of neurons); and (3) the training or learning rules for updating the connecting weights and biases. Although the ANN architecture has significant effects on both the training of ANN and the performance of the trained ANN the literature shows that normally very little attention is given to step (2) of the ANN design process. It is common * Correspondence Author, Mechanical Engineering, University of Queensland, Brisbane, Qld 4072; phone: (07) 3365 3621, fax: (07) 3365 4799; e-mail: [email protected]
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Characterise Laminar Defects using Dynamic Measurements
practice to use only one single hidden layer. As a result, the designer only needs to decide on the number of hidden nodes. Some ad hoc guidelines and rules of thumb can be used to estimate the number of hidden nodes, e.g. [3]. However, those guidelines and rules are valid only for some special cases and are highly depending on the designer's judgment. The lack of a systematic, practical and rigorous ANN design methodology is one of the main reasons for the delay in the successful application of the promising technique in SHM. This paper investigates the application of the Bayesian ANN class selection method [4] in the design of ANN for the detection and characterisation of laminar defects following the pattern matching approach. Numerical examples for carbon fibre-reinforced beams applying Timoshenko beam theory are employed to demonstrate the methodology. METHODOLOGY This section starts with a short description of the application of Timoshenko beam theory [0,2] to calculate the dynamic behaviour of damaged fibre-reinforced beams. This is followed by the ANN-based damage detection method using the pattern matching approach utilizing measured natural frequencies and mode shapes. Then, the formulation of the Bayesian ANN model class selection method [4] is given.
a
-^f-
examination
m o d e sha
7
P e evaluation locations
FIGURE 1 Sketch of the carbon fibre-reinforced beam specimen
Timoshenko Beam Model The vibration behaviour of the (damaged) beam is characterised using a three segments Timoshenko beam model as illustrated in Figure 1, with segments 1 and 3 representing the undamaged sections of the beam and segment 2 the delamination region. The equations of motion of Timoshenko beam theory are expressed in terms of the lateral displacement w and the angle of rotation 0 [2],
where K" denotes a shear correction factor, G is the shear modulus, p is the mass density, A is the cross section area, E is the Young's modulus and / is the second moment of area. The free vibration solution is found using the method of separation of variables, which yields fundamental solutions for the lateral displacement Wk and angle of rotation 6(t amplitude functions in the three segments (£=1,2,3) of the following form
Characterise Laminar Defects using Dynamic Measurements
977 u
smalk/3k
(3)
sinau/3k + muAu cosa2kj3k (4) u,.. .,A^k are constants, and aik, efek, mik, «2k and/i are functions of the sample's fundamental material and geometry parameters. Explicit values of these parameters are given for example in [0]. Formulating the boundary conditions at the free ends and the kinetic and kinematic continuity conditions between the three segments results in a system of twelve homogeneous, coupled, transcendental equations for the mode shape coefficients An,..., A42. These equations enable the determination of the natural frequencies of the beam as the roots of the determinant of the 12 x 12 coefficient matrix and the mode shapes as the corresponding eigenvectors. With the above formulation, the delamination (damage) can be parameterised by the delamination location a and width c as indicated in Figure 1. Damage Detection by the Pattern Matching Approach Experimentally, the natural frequencies and the corresponding mode shapes can be measured. The measured pattern is defined as
J
(5)
where w\ and $„_,- for z = 1toNs are the measured eigenvalue and eigenvector of the z'-th selected mode and Ns is the total number of selected modes. It must be pointed out that <j)m\ in equation (5) is not necessarily the mode shape of mode 1 but the 1-st selected mode. The selection of modes to be included in the damage detection process depends on several factors [5], such as the sensitivity of a mode to the damage and the accuracy of the measured mode. With a computer model, the eigenvalues and eigenvectors of the undamaged structure and the structure under different damage cases can be calculated. The calculated patterns for different damage cases are
M-M.s.(k)
A^,(4...,A^»f for*=ltoK
(6)
where k is the damage case number; and K is the total number of damage cases to be considered. The basic idea of the pattern matching approach is to match the measured pattern in equation (5) to the K calculated patterns in equation (6) one by one. The damage case corresponding to the calculated pattern, which is best fitted to the measured one, is the most possible damage case. This approach has many advantages. For example, no matrix condensation and modal expansion techniques are required to fit the measured mode shapes to the theoretically calculated ones. These treatments are essential for many existing model updating based damage detection methods. Furthermore, it is possible to select the type of patterns such that the method can be applicable in the absence of measured system input, which is very difficult if not impossible to obtain in field tests. One problem of the pattern matching approach is that it is difficult to find a systematic and intelligent way to match the measured pattern with all the calculated patterns. Traditional computers are fast in algorithmic computational tasks and precise arithmetic
978
Characterise Laminar Defects using Dynamic Measurements
operations. However, they are inefficient at tasks, such as pattern matching and classification, and function approximation and optimisation [6]. The proposed damage detection method takes the advantage of ANN in overcoming this difficulty. Artificial Neural Network (ANN) was not specifically developed for the purpose of structural damage detection, but its pattern recognising and generalisation capabilities make it very suitable to be employed as a tool for structural damage detection following the pattern matching approach. Instead of matching the measured pattern to the calculated ones, the proposed method uses the calculated patterns and the corresponding damage cases, which are represented by different values of a and c as defined in Figure 1, as the input/target pairs to train an ANN. According to the generalisation property, the trained ANN is able to approximate the values of a and c (the damage) when the measured pattern is applied as network input. ANN Class Selection Method In this paper, the Bayesian ANN design method in reference [4] is employed as a means to select the "best" class of ANN models. Figure 2 shows a typical multi-layer feed forward ANN. In the figure, «/ and no are the numbers of nodes at the input and output layers, respectively; NH is the number of hidden layers; «,• is the number of nodes at they-th hidden layer; and x and y are the input and output of the ANN, respectively. The value of nj and no depends on x and y, and therefore, the class of ANN models is decided by NH and nj fory = 1 to NH.
Input Layer
1-st Hidden Layer
Afo-th Hidden Layer
Output Layer
Ntf Hidden Layers
FIGURE 2 The structure of ANNs to be considered in this study
Let D denote the set of input/target data for ANN training. The goal is to use D to select the most plausible class of ANN models out of NM given classes of models Mj, for/ = 1 to NM- Here different classes of ANN models have different number of hidden layers and different numbers of nodes in the hidden layers. The probability of a class of models conditional on the set of input/target training data can be obtained by using the Bayes' Theorem as follows {D\M.,U)P{MJ\U)
(7)
Characterise Laminar Defects using Dynamic Measurements
979
It is clear that the class of models to be used is the one who maximizes this probability. Referring to reference [4], the value of the probability in equation (7) is dominated by the term/>(£) | Mj, U) =p(D | Mj), and it can be approximated as
(8)
where Nj is the number of ANN parameters (weights and biases) of the ANN model class Mf, Qj is a vector of all ANN parameters of M/, 6;. is the most probable (or optimal) set of ANN parameters; and Hy.(9y) is the Hessian matrix of the function -ln|/>(:D|8J.,Af;)p\f)j \Mj)\ evaluated at the optimal parameter Qj. Owing to the limited space in this paper, please refer to reference [4] for the detail formulation of ( ) ( )
NUMERICAL EXAMPLE A simple carbon fibre-reinforced beam as shown in Figure 1 is employed as an example to demonstrate the procedures of the ANN design and damage detection methods. The dimension of the sample is L = 250 mm and t = 2 mm. The density, Young's modulus and shear modulus of the beam are 1650 kg/m3,135 MPa and 5.6 MPa, respectively. In order to simulate the measured pattern, time domain ambient lateral responses of the beam at 0, 50, 100, 150, 200 and 250 mm from the left end are calculated using the Timoshenko beam model. White noise whose amplitude equals to 5% of the root mean square of the calculated time domain responses is added to simulate the effect of measurement noise. The natural frequencies and mode shapes of the undamaged and damaged beams can then be obtained based on existing modal identification techniques. Damage is simulated by delamination of the beam at a = 90 mm with delamination width c = 15.5 mm. The measured pattern for this damage is calculated using equation (5). Only the first two modes are employed in the damage detection process. Based on the Timoshenko beam model, the changes in natural frequencies and mode shapes due to different damage cases can be easily calculated. The calculated patterns corresponding to delamination location a from 25 mm to 225 mm with step size 12.5 mm and delamination width c from 2.5 mm to 25 mm with step size 2.5 mm are generated, and treated as input/target training pairs. For demonstration purpose, a single hidden layer feed forward ANN with sigmoid and pure linear as activation functions for neurons at the hidden and output layers, respectively, is employed. Note that the real damage case {a = 90 mm and c = 15.5 mm) is not included in the training data. Five classes of ANN models with reasonable number of hidden nodes (from 6 to 10) are considered. The Bayesian ANN model class selection method in reference [4] is used to select the optimal class of models from these 5 classes. The probability p(Mj \ D, U) in equation (7) for all 5 cases is calculated. For easier comparison, normalised probabilities are summarized in Table I. The table shows that the ANN model class with 8 hidden nodes («i = 8) has the highest relative probability, and therefore is selected in this study.
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Characterise Laminar Defects using Dynamic Measurements TABLE I. Relative probabilities of different classes of ANN models
n\ 6 7 8 9 10
Relative probability 6.1 x lO"148 9.5 x 10"23
1 4.6 x 10'18 S 9 v 1 IT 44
o.z x iu
After training, the measured pattern is fitted into the input of the ANN, and the output of the trained ANN is a = 89.8 mm and c = 15.525 mm, which are close to the simulated damage case. The ANN has no difficulty in identifying both the delamination location and width. CONCLUSION An ANN-based method is developed to characterise laminar defects following the pattern matching approach utilizing dynamic measurements. In order to provide a rigorous ANN design method, a Bayesian method is employed in the selection of the optimal class of ANN models. The ANN class selection method can be used to quantify the optimality of different classes of ANN models based on the ANN training data. For example, it can be used to tell how "good" is a class of ANN models with 1 hidden layer of 10 nodes when compared to another class of ANN models with 2 hidden layers of 5 nodes in each hidden layer. Furthermore, it is a general method that can be applied in the training of ANN in different fields (e.g., function approximation). The method is rigorous, and no ad hoc assumptions are made in its development, hi other words, the judgment of the designer is not crucial in the method. ACKNOWLEDGEMENT This research work was supported by the CityU Strategic Research Grant (7001521) of City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong. REFERENCES 1. 2. 3. 4.
5. 6. 7. 8. 9.
Chang, C.C. and L.W. Chen, 2003, "Vibration Damage Detection of a Timoshenko Beam by Spatial Wavelet Based Approach", Applied Acoustics, 64:1217-1240. Doyle, J.F., 1997, "Wave Propagation in Structures", Springer, New York. Kermanshahi, Bahman, 1999, "Design and Application of Neural Networks", Shokodo, Tokyo. Lam, H. F. and K. V. Yuen, 2003, "Design of Artificial Neural Networks for Structural Health Monitoring", Proceedings of the first international conference on structural health monitoring and intelligent infrastructure, 13-15 November 2003, Tokyo, Japan, Volume 1, pp. 611-618. Lam, H. F., 1994, "Detection of Damage Location Based on Sensitivity and Experimental Modal Analysis", MPhil Thesis, Department of Civil Engineering, Hong Kong Polytechnic University. Lin, Chin Teng and C. S. George Lee, 1996, "Neural Fuzzy Systems: A Neuro-Fuzzy Synergism to Intelligent Systems", Prentice Hall PTR, Upper Saddle River, NJ 07458. Ni, Y.Q., B. S. Wong, and J. M. Ko, 2002, "Constructing Input Vectors to Neural Networks for Structural Damage Identification", Smart Materials and Structures, 11:825-833. Tsou P. and M.-H. Herman Shen, 1994, "Structural Damage Detection and Identification Using Neural Networks", AIAA Journal, 32(1): 176-183. Wu, X., J. Ghaboussi, and Jr. J. H. Barrett, 1992, "Use of Neural Networks in Detection of Structure Damage", Engineering Structures, 42(4): 649-659.
A Damage Detection Technique of Composite Laminates with Embedded FBG Sensors Won-Seok Kim, Sang-Hoon Kim, and Jung-Ju Lee Department of Mechanical Engineering, Korea Advanced Institute of Science and Technology, Korea
ABSTRACT hi this paper, a new real-time damage detection method for composite laminates through the use of embedded FBG sensors is presented. This method monitors the ply stress states of a laminate and compares them with failure criteria. The ply stress state of each ply of the composite laminate can be obtained by embedding three FBG sensors in the laminate based on the classical lamination theory. Experimental results show that laminates experience fracture when the ply stress states are over the boundaries of failure criteria, hi this method, critical damage can be detected by the ply stress state which are close to the boundary of the failure criteria.
INTRODUCTION Damage detection of structures is considered to be very important for securing safety, determining economical replacement time, and improvement of manufacturing and operating conditions by analyzing the cause of damage. The structural health monitoring (SFDV1) concept has many advantages compared with classical NDT/NDE methods, primarily because the classical techniques of NDT/NDE are not suitable for in situ implementation. One of the most popular ways to solve this problem is to embed an optical fiber sensor network in the structure under analysis. For the composite laminates in particular, embedding optical fiber sensors can be executed without much difficulty and without material degradation. Fiber Bragg grating (FBG) sensors are considered to have the following competitive advantages over other fiber optic sensors [1,2]: (a) absolute measurement of strain; (b) linear sensor output corresponding to strain; (c) ease of multiplexing; (d) inherent high strength; and (e) potential for automated production with resulting low-cost, hi the present study, we embedded FBG sensors in graphite/epoxy composite laminates and detected critical damage initiation and growth before the laminates failure. DAMAGE DETECTION METHODS Generally designers calculate and analysis the ply stress states in the early stages of design and compare them with failure criteria. However, in the method proposed here, this process can be executed continuously during service time. This approach will help avoid catastrophic structure failures and inform operators of damage accumulated during the * Corresponding author, 373-1, Guseong-dong, Yuseong-gu, Daejeon 305-701, South KOREA, Fax : (82-42)869-3210, E-mail: [email protected]
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Damage Detection Technique of Composite Laminates
Embedded optical fibers parallel to carbon fibers
FIGURE 1 [0B / 30, / - 30n ]s laminate with three optical fibers embedded
working time. The algorithm to calculate the ply stress states of each ply of the laminate is as follows. Generally there are six unknowns, e°t £\ r", K t K t K to describe the deformation of the composite laminate [3]. If the bending load and deformation is negligible, K « 0, we can calculate all the stress and strain states of the plies with three laminate coordinate strains e °, e" r° . Because ply coordinate strains and laminate coordinate strains are convertible, we only need to know three independent strain components in a laminate. Three FBG sensors were embedded in a laminate whose stacking sequence was [O4/3O4/-3O4],,. FBG sensor inscribed optical fibers were .embedded parallel to carbon fibers so as not to reduce the durability of the sensors [4]. Figure 1 shows a schematic diagram of the embedded optical fiber sensors in a laminate. With three embedded FBG sensors, we can obtain three ply strains, f,0,,?,30,^30. Then we transform them into laminate coordinate strains with a strain transformation matrix
(1)
hi this case, eq.l should be modified to fit obtained carbon fiber direction strains, as given in eq.2. cos20 sin20 cosOsinO 2 cos 30 sin230 cos30sin30 cos2-30 sin2-30 cos-30sin-30
(2)
Each time we obtain the laminate coordinate strains, we can update ply coordinate stress of each ply with the following two sequences. The First step is to calculate the stress state of the laminate using the reduced stiffiiess matrix |~g~]. Then we can transform the stress state into ply coordinate stress for each ply using the stress transformation matrix [TJ , in the same manner as the strain transformation.
Damage Detection Technique of Composite Laminates -FBGstrain1(30°) - FBGstrain2(-30°) - FBGstrain3(0°) - ESGstrain
3.0-1 2.5-
0° Fiber Breakai at 1.44% strain
2.0strain gauge saturation at 1.40% strain
1.5-
0
983
100 120 140 160 180 200 220
20 40 60
time (sec) FIGURE 2 Strain increase during tension test
EXPERIMENTAL RESULTS Tension tests were performed under the static and fatigue loading conditions. FBG sensor embedded graphite/epoxy composites were fabricated according to ASTM-D3039 specifications. Figure 2 shows typical strain increase during a tension test. A conventional strain gauge was also attached to the surface along the 0° ply fiber direction to verify and compare FBG strain signals. As we can see, the signals of strain gauge and the embedded FBG sensor in the 0° ply show a good agreement. However, about 1% strain in both the strain gauge and the FBG sensor, strain signals do not linearly increase according to increasing displacement. This phenomenon is due to numerous fiber breakages in the 0° ply. The strain gauge signal was saturated at 1.4% strain. While the embedded FBG sensor was broken at 1.44% strain. Meanwhile the FBG sensors that were embedded in the 30° plies did not break, even after specimen failure. They showed abrupt strain drop at the failure point. Thus embedded FBG sensors in graphite/epoxy laminates can be used to monitor critical strain and stress conditions of a laminate Figure 3 shows the ply stress states tracing program. FBG sensor output was obtained with an ADC board at a rate of lOHz. Using the explained algorithm, the strains were then calculated into ply stresses, continuously updating the current stress states. We can monitor the stress states of 0°, 30°, -30° plies by plotting them on Gi-02 and Oi-Oe planes.
•».•
IV-U
1
•>
FIGURE 3 Ply stress states tracing program
984
Damage Detection Technique of Composite Laminates —Theoretical Failure Points Experiment 1 Experiment 2 Experiment 3
-•• * •
Theoretical Failure Points Experiment 1 Experiment 2 Experiment 3
a, (MPa)
-1500
-1000
500
-500
1000
1500! 2000 ° , ( M P a >
-150-200-
FIGURE 4 Laminate failure stress states compared with failure criteria
Graphically we can monitor whether the stress states are within failure criteria. The Tasi-Wu failure criterion was also compared by updating its index continuously. Figure 4 shows final fracture stress states of the laminate specimen. Theoretically [0/±30]s specimen should fail due to the strength of shear stress, <J6(=Ti2). Experimental results showed that Oe first exceeded failure criteria, but the specimen did not fail immediately after a^'s contacting the boundary. Stress states were far beyond the boundary of failure criteria at the specimen's failure point. Experiment 2 displayed an exception because the 0° ply embedded FBG sensor was broken before the specimen's failure. This large gap between real failure stress states and failure criteria resulted from the difference between the ply failure and the laminate failure. Although the 30° ply inside of the laminate failed, the laminate still sustains the load. Another contribution comes from composites' stiffness reduction. As the damage grows during the high load condition, stiffness gradually decreases; however we cannot measure the exact current stiffness. Hence the calculated stress states with initial undamaged stiffness are larger than the real stress states. As shown in eq.4 the calculated stress is enlarged as much as dividing D in eq.3. This effect is more clear in fatigue load condition that will be shown next.
1.6-
FBGslrain1(0°) Abnormal strain increase due to material damage • - „
1.4-
FBGstrain2(30°) FBGstraln3(-30°)
1.2-
0.8-
il
0.6-
•j^H abrupt strain decrease M M /'' due to 30° ply failure
is
0.40.2- Wflljflf||||»|||||j||i||j||B 0.03
200
400
600 800
1000
1200
cycle
FIGURE 5 Strain change under a fatigue load of
1400
Damage Detection Technique of Composite Laminates
985
—•— first cycle strain of 0° ply — T — first cycle strain of 30° ply —•— maximum strain of 0° ply —T— maximum strain of 30° ply
102
103
10*
10s
10'
Number of cycles to failure
FIGURE 6 Maximum strains of first and final cycle obtained from 4 fatigue experiments
E,
E1 : instantaneous modulus
(3)
(4)
aaa : actual stress Thus we can use the failure criteria as an over stress alarm boundary and trace the ply stress states during structure's service time in order to avoid catastrophic structural failures and critical over-stress conditions. Fatigue load was also applied to the same specimen. Four experiments were performed in the load control mode with Prrm=0-9Pms, 0.8POTS, 0JPms, 0-6Pms and a stress ratio of 0.1. Figure 5 shows the results of a fatigue test when pmax = 0.8PUTS. Because the fatigue test was performed in the load control mode, as the cycle increased the maximum strain values also gradually increased. After 1,000 cycles of sine wave load, there is an abrupt strain increase in the 0° ply FBG sensor. This abrupt strain increase resulted from delamination
~ strain gauge peak strain — FBG sensor peak strain
I
1.2-
0.60.4-
Strain gauge fatigue life 20,500 cycle
Abrupt strain increase due to delamination
FBG sensor fatigue life upto 100,000 cycle clear signal over 66,000 cycle
0.20.0 0
1x104 2x10" 3x10" 4x10 4 5x10 4 6x10 4 7x10 4
number of cycle
FIGURE 7 Maximum strain change of FBG and strain gauge
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Damage Detection Technique of Composite Laminates
that was induced by 30° ply failure at 800 cycle. FBG sensors embedded in 30° ply showed the abrupt strain drop at 800 and 1,200 cycles. This strain drop indicates 30° ply failure. Like the static tension test, 30° ply embedded FBG sensors did not break even after specimen failure, and they continually sent a strain signal. Figure 6 shows the strain increase of the FBG sensors embedded in 0° and 30° plies during fatigue load. The final cycle strains are clearly larger than the first cycle strains, but there is no trend in the final cycle strains. However, we can use the ply stress state tracing method with the adapted failure criterion to specified fatigue life. Figure 7 shows maximum strains of the 0° ply embedded FBG and surface attached electric strain gauge sensors during tension fatigue test. These results were obtained when Ptmx = 0.6PUTS. In this experiment both the strain gauge and FBG sensors failed before specimen failure. The specimen had infinite life cycle; we stopped the experiment at 1,000,000 cycles. The embedded FBG sensor strain is higher than that of the surface attached strain gauge. FBG sensor has longer fatigue life than the strain gauge. The FBG sensor survived until 100,000 cycles and a clear signal could be obtained until 66,000 cycles. During this period FBG sensors detected delamination by abrupt strain increase. CONCLUSION hi this paper real-time ply stress states tracing technique was proposed and performed by embedding 3 FBG sensors in a composite laminate. The FBG sensor's capability to measure critical strain was also evaluated. The following important conclusions were obtained. • The embedded FBG sensor in the 0° ply can not survive until laminate failure, but its maximum strain is sufficient to give alarm of accumulated damage, (maximum measurable strain : about 1.2%). • The Embedded FBG sensor can effectively detect 30° laminate failure under both static and dynamic load conditions. • Under a static tension load, the composite laminate failed far beyond the failure criteria. Hence proposed ply stress tracing method can be used to give notice of damage before structure's failure. • Accumulated damage in the composite laminates during fatigue load induces strain increase but the increased amount until failure does not show any specific trend. • The 0° ply embedded FBG sensor has longer fatigue life than the conventional strain gauge. The FBG sensor provided a clear signal up to 66,000 cycles under high strain condition of 0.6%. REFERENCES 1. 2. 3. 4.
S. M. Melle, K. Liu, and R. M. Measures. 1993. "Practical Fiber-optic Bragg grating strain gauge s y s t e m , " ^ / . Opt., Vol. 32(19). pp. 3601-3609. R. M. Measures. 1998. PreFace of special issue, Smart Mater. Struct. Vol. 7(2). pp. 1 Dae Gil Lee, and Nam Pyo Suh. 2004. Axiomatic Design and Fabrication of Composite Structures. Oxford Press Tae Seong Jang, Jung Ju Lee, Dong Chun Lee, and Jeung Soo Huh. 1999. "The mechanical behavior of optical fiber sensor embedded within the composite laminate," Journal of Materials Science, Vol. 34. pp. 5853-5860.
Damage Detection in Composites Using Fiber Bragg Grating Sensors as Ultrasonic Receivers Yoji Okabe , Hisao Tamaue, Junichiro Kuwahara, and Nobuo Takeda Graduate School of Frontier Sciences, The University of Tokyo, Japan
ABSTRACT Taking advantage of the sensitivity of ultrasonic waves to internal damages in composite laminates, the authors are constructing a new damage detection system, hi this system, a piezo-ceramic actuator generates an ultrasonic wave at a surface of a CFRP laminate. After the wave propagates in the laminate, the transmitted wave is received by a fiber Bragg grating (FBG) sensor embedded in the laminate. As preliminary researches, the optimum gauge length of the FBG sensor to detect ultrasonic waves was determined through the theoretical calculation of the reflection spectrum. Then, the feasibility of the damage detection using the Lamb waves was confirmed by theoretical simulation of the wave propagation in the CFRP laminates.
INTRODUCTION For the weight saving of airplanes, carbon fiber reinforced plastic (CFRP) laminates are being used for the primary structures of the airplanes. However, the maintenance cost of the structures increases because of the complicated fracture process of the CFRP laminates. A new technological innovation to reduce the maintenance cost is a health monitoring system. As one of the systems, the authors are developing a new damage detection system using ultrasonic waves. Since the propagation properties of the ultrasonic waves depend on the mechanical properties of the laminates [1], the waveform of the ultrasonic waves propagating in the composite plates changes when damages occur in the propagation path [2]. In this system, a piezo-ceramic actuator generates an ultrasonic wave at a surface of a CFRP laminate. After the wave propagates in the laminate, the transmitted wave is received by a fiber Bragg grating (FBG) sensor embedded in the laminate. The use of the optical fiber sensor has some advantages, such as the easiness of the embedment and the immunity to electromagnetic interference. Currently, a high-speed demodulator of the FBG sensor to detect ultrasonic waves is being developed in collaboration with Hitachi Cable Ltd. When the FBG sensor is applied to the ultrasonic detection, the gauge length of the FBG should be much smaller than the wavelength of the ultrasonic waves [3]. Thus, in order to determine the optimum gauge length, the relationship between the gauge length and the wavelength was investigated through the theoretical calculation of the reflection spectrum of the FBG.
* Corresponding Author, Takeda Lab., Komaba Open Laboratories, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, JAPAN, FAX: +81-3-5452-5211, E-mail: [email protected]
Damage Detection Using Fiber Bragg Grating Sensors Digital Oscilloscope Amplifier
Function Generator
High-Speed FBG Demodulator
Piezo-Ceramio
CFRP Laminate FIGURE 1 Damage detection system using a piezo-ceramic actuator and an FBG sensor embedded in a CFRP laminate.
Then, the feasibility of the damage detection using the Lamb waves was confirmed by theoretical simulation of the wave propagation in the CFRP laminates.
DAMAGE DETECTION SYSTEM Figure 1 shows the damage detection system that the authors are attempting to construct. The piezo-ceramic generates elastic waves, and the waves propagate in the CFRP laminate as Lamb waves in this case. After that, the embedded FBG sensor detects the transmitted waves. Since the internal damages in the propagation path, such as delamination and matrix cracks, affect the waveform of the Lamb waves, the appearance of the damages in the laminate will be identified from the change in the waveform. The schematic of the high-speed FBG demodulator is shown in Fig. 2. A broadband light is emitted from the light source and propagates into the FBG sensor. Then, the
Circulator
r
(B)
Amplifier (A)
Wavelength Filter
-•-
Photo Detector
Output
(C)
Reflection Spectrum
Wavelength
Wavelength
Wavelength
(A)
(B)
(C)
FIGURE 2 Schematic of the high-speed FBG demodulator.
Damage Detection Using Fiber Bragg Grating Sensors
989
reflection light from the FBG is transmitted through the wavelength filter, and the optical power is modulated to PI and P2 depending on the center wavelength of the reflection light. The optical powers are detected by the photodetecters, and the center wavelength, which is proportional to the strain applied to the FBG sensor, is calculated from the powers PI and P2. Since this system converts the wavelength into the optical powers directly without mechanical moving parts, the strain change will be measured fast enough to detect the Lamb waves. DETERMINATION OF THE GAUGE LENGTH OF FBG SENSORS When the FBG sensors are applied for the detection of ultrasonic waves, the relation between the gauge length of the FBG sensors and the wavelength of the ultrasonic waves is important, since FBG sensors are also sensitive to non-uniform strain in the grating region [4]. When the FBG sensor is under non-uniform strain, the reflection spectrum of the FBG is deformed because various wavelength components return from the FBG depending on the strain distribution. Hence, the relationship between the gauge length of the FBG L and the ultrasonic wavelength X was investigated through the theoretical simulation of the reflection spectrum. The distribution of strain s in the direction of z generated by an ultrasonic wave (longitudinal wave) with the wavelength of X and the angular frequency co in a solid can be expressed by the following equation [3]
£mcos\—z-a>t
(1)
A
where em is the amplitude of the strain. From this strain, the distributions of the grating period and the average refractive index of the FBG sensor embedded in the direction of z in the solid can be calculated. Then the reflection spectrum is simulated using a couple mode theory and a transfer matrix method from the distributions [5]. According to this procedure, the reflection spectrum of an FBG, whose gauge length L was assumed to be 10mm, was calculated at various wavelengths X. First, when the X is smaller than the L, the sensor is affected by the whole strain range of 2sm, so that the reflection spectrum becomes very broad as shown in Fig. 3. Furthermore, since the average strain is almost steady, the center wavelength of the spectrum hardly shifts. Hence it is difficult to detect the ultrasonic wave from the wavelength shift of the spectrum. Secondly, Fig. 4 shows the spectrum change at the X of
1.57 1.56 Time (t/T)
0^54
1 00
'
Wavelength (\im)
FIGURE 3 Reflection spectra of the FBG sensor receiving the ultrasonic wave of X = 5mm.
Damage Detection Using Fiber Bragg Grating Sensors
990 1.0
f 5 1 °1
--53 0 10 05 Time (t/T) 0 T.54
Wavelength (urn)
FIGURE 4 Reflection spectra of the FBG sensor receiving the ultrasonic wave of X = 30mm.
30mm. When the X is larger than the L, the average strain changes depending on time. However, since the spectrum is broad because of the non-uniformity of the strain, the waveform of the ultrasonic wave reconstructed from the shift of the reflection spectrum is slightly different from the actual waveform. Thirdly, Fig. 5 shows the spectrum change at the X of 70mm. When the X is sufficiently larger than the L, the strain distribution in the FBG becomes close to uniform and the average strain changes largely. Thus, since the spectrum becomes narrow and the average strain changes largely, the ultrasonic wave can be detected. From the simulation results, it was found that the gauge length of the FBG sensor should be shorter than 1/7 of the ultrasonic wavelength. FEASIBILITY OF THE DAMAGE DETECTION USING LAMB WAVES Then, the feasibility of the damage detection using the Lamb waves was confirmed by theoretical simulation of the wave propagation in the CFRP laminates. This simulation was conducted using the solver "PZ Flex" developed by Weidlinger Associates, Inc., which is a time domain finite element program for solving the coupled mechanicalpiezoelectric-acoustic equations. Figure 6 shows the calculation model for the analysis of the wave propagation. The CFRP laminate is cross-ply [02/902]s, whose dimensions are 100mm x 100mm x lmm. The mechanical properties of T700S/2500 (Toray Industries) were used for the calculation. A piezo-ceramic was adhered on the surface of the laminate, and a sensing point was located 50mm awayfromthe piezo-ceramic. The calculation was conducted for
Time (t/T)
o T.54
"
Wavelength (|xm)
FIGURE 5 Reflection spectra of the FBG sensor receiving the ultrasonic wave of X = 70mm.
Damage Detection Using Fiber Bragg Grating Sensors Piezo-Ceramic
Delamination 50mm
0° 90° 0°
991 Sensi
"9Point
/
Transverse Cracks FIGURE 6 Calculation model for the analysis of the wave propagation.
three types of laminates: a laminate without damage, a laminate that had a delamination of 10mm in length at the upper 0790° interface, and a laminate that had three transverse cracks in the 90° ply at intervals of 5mm. These damages were assumed to penetrate the width of the laminate. A 300kHz Ricker wavelet was used for the input signal to the piezo-ceramic as shown in Fig. 7(a). Figure 7(b) shows the waveform received at the sensing point in the case that the laminate had no damage, hi the waveform, two modes of the Lamb waves appeared. The faster wave with the velocity of 5.0km/sec is So mode, and the slower one of 1.3km is Ao mode. On the other hand, Fig. 8 shows the received waveforms in the case that there were damages in the laminate. When the laminate had a delamination, a new mode appeared between the So and the Ao modes. The new mode might be caused by the propagation of the Ao mode in the upper part [02] within the delaminated area. When three transverse cracks appeared in the laminate, the amplitude of the Ao mode was decreased. These simulation results indicate that the damages in CFRP laminates can be detected from the change in the waveform of the Lamb waves propagated in the laminates. CONCLUSIONS The authors conducted preliminary researches for the construction of the new damage detection system for CFRP laminates using a piezo-ceramic actuator and an FBG sensor. First, the optimum gauge length of the FBG sensor to detect ultrasonic waves was
.... (a)
YV
7 7
20
40
60
40
60
Time (us)
1.0 £
0.6
1 0.2 -1.0
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FIGURE 7 Waveforms calculated in the case of no damage: (a) an input waveform to the piezo-ceramic and (b) the waveform received at the sensing point.
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20
40
60
40 Time (|is)
60
Time (us) 0.4 CD
3 0.0 w
1-0.4 -0.8
20
FIGURE 8 Received waveforms calculated in the case that there ware damages in the laminate: (a) a delamination and (b) three transverse cracks.
investigated through the theoretical simulation of the reflection spectrum. As a result, it was found that the gauge length should be shorter than 1/7 of the ultrasonic wavelength. Secondly, the feasibility of the damage detection using the Lamb waves was examined by theoretical simulation of the wave propagation in the CFRP laminates. The simulation results indicated that the occurrence of the delamination or the transverse cracks can be identified from the change in the waveform of the Lamb waves propagated in the laminates. REFERENCES 1. 2.
3.
4. 5.
Nayfeh, A. H. 1995. Wave Propagation in Layered Anisotropic Media. Elsevier. Kessler, S. S., S. M. Spearing, and M. J. Atalla. 2002. "In-Situ Damage Detection of Composites Structures Using Lamb Wave Methods," presented at the First European Workshop on Structural Health Monitoring, July 10-12, 2002. Coppola, G., A. Minardo, A. Cusano, G. Breglio, G. Zeni, A. Cutolo, A. Calabro, M. Giordano, and L. Nicolais. 2001. "Analysis of Feasibility on the Use of Fiber Bragg Grating Sensors as Ultrasound Detectors," presented at Smart Structures and Materials 2001: Sensory Phenomena and Measurement Instrumentation for Smart Structures and Materials, Proceedings ofSPIE Vol. 4328, March 4-8, 2001. Huang, S., M. M. Ohn, M. LeBlanc, and R. M. Measures. 1998. "Continuous Arbitrary Strain Profile Measurements with Fiber Bragg Gratings," Smart Mater. Struct, 7(2): 248-256. Othonos, A. and K. Kalli. 1999. Fiber Bragg Gratings: Fundamentals and Applications in Telecommunications and Sensing. Artech House, pp. 189-222.
Inverse Analysis for Damage Identification in CFRP Laminates with Embedded FBG Sensors Shigeki Yashiro1*, Tomonaga Okabe2, Nobuo Takeda1 Graduate School of Frontier Sciences, The University of Tokyo, Japan c/o Takeda Lab., Komaba Open Laboratories, The University of Tokyo, Japan 2 Department of Aeronautics and Space Engineering, Tohoku University, Japan 1
ABSTRACT A method is proposed to identify the various damage state in a composite laminate using an embedded fiber Bragg grating (FBG) sensor. Numerical analysis to calculate a reflection spectrum of an FBG sensor is directly linked to a damage analysis based on layer-wise finite element method, hi this damage analysis, cohesive elements are arranged at interfaces where cracks or delaminations may occur to represent extension of these damages. Then solving the inverse problem of the relationship between the damage state and the reflection spectrum, we estimate the positions and the sizes of various types of damages in a composite laminate. This inverse analysis is applied to the experimental results of a tensile test for a double-edge-notched CFRP cross-ply laminate with an embedded FBG sensor. Minimizing errors between the reflection spectrum measured in the experiment and the temporarily-estimated one, it is found that the estimated damage state corresponds well with the one observed in the experiment. INTRODUCTION Structural health monitoring recently attracts many attentions to enhance structural integrity or validity. Furthermore, many attempts to detect internal damages have been conducted using various types of optical fiber sensors [1]. Above all, fiber Bragg grating (FBG) sensors have more advantages such as high accuracy and multiplexing capability. FBG sensors are normally used as strain or temperature sensors using the peak shift of the reflected light from the gage section (typically 5-10 mm long) where periodic gratings (typically 0.5 \xm in spacing) are inscribed. A recent study to detect transverse cracks by FBG sensors [2] proved that FBG sensors have high sensitivity to non-uniform strain distributions due to the internal damages. In a composite structure, stress concentrated sections induce complicated damages such as splittings, ply cracks and delaminations. The complicated damage state cannot be monitored only by measuring the average strain around the region. We suggest that the reflection spectrum of the FBG sensor, which has the information of strain distribution, is useful to monitor the damage state. Therefore, this study proposes a new approach to identify the damage state in a composite laminate by embedded FBG sensors. A mathematical programming technique is applied to analyze the relationship between the damage state and the reflection spectrum. Then, we estimate the damage state in a double-edge-notched cross-ply laminate from the reflection spectrum of the embedded FBG sensor. * Correspondence Author, 4-6-1 Komaba, Meguro-ku, Tokyo, 153-8904, JAPAN, TEL/FAX: +81-3-5452-5257, E-mail: [email protected]
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EXPERIMENTAL Setup A quasi-static tensile test was conducted for a double-edge-notched (DEN) cross-ply laminate with an embedded FBG sensor. CFRP T800H/3631 (Toray Industries, Inc.) was used in this research, and the stacking configuration was [02/902]s. The optical fiber was embedded in a 0° layer in contact with 90° plies, and one end of the FBG sensor was positioned with care near a notch tip. After the specimen fabrication, the coupon specimen was notched by a fine cutter. The FBG sensor (NTT-AT Co.) was coated with polyimide resin whose outside diameter was 150 |am. Gage length of the sensor was 10 mm. The dimensions of the DEN specimen are shown in Figure 1. The reflection spectrum was measured using an optical spectrum analyzer (AQ6317, Ando Electric Co., Ltd.) while the load was held at the constant. Then, the damage state of the specimen was observed by soft X-ray radiography. Results Figure 2 shows the observed damage state of the DEN specimen. The initial damages were small splittings in 0° plies and transverse cracks in 90° plies both from the notch tips (Figure 2(a)). As the load increased, the splittings extended and more transverse cracks occurred. Also 0/90 interfaces were delaminated in elliptical shape at the notch tip as shown in Figure 2(b). Figure 3 shows the measured reflection spectrum. These spectra correspond to the damage states shown in Figure 2. The initial reflection spectrum had narrow spectrum width (0.2 nm in full width at half maximum). When initial splittings and transverse cracks occurred, the reflection spectrum became broadband and had some peaks (Figure 3(a)). Then the ply interfaces were delaminated at the vicinity of notch tips, the shape of the spectrum distorted drastically (Figure 3(b)): a rather high peak appeared in the spectrum in the longer wavelength which was not visible in the lower strain level. Our previous study [2] pointed out that spectrum shapes changed due to the non-uniform strain distribution along the FBG sensor. This non-uniform strain distribution occurred both by the stress concentration of the notch tip and by various damages near the sensor. 170 100
(FBG sensor)
21 .5
\
50
11.0
t
><|> 0.15 (Optical fiber) j 4.0 Unit: mm
FIGURE 1 Dimension of the double-edge notched (DEN) specimen. The stacking configuration was cross-ply [02/902]s, and an FBG sensor was embedded in a 0° ply in contact with 90° plies. The position of the FBG sensor was 1.8 mm apart from the notch tip.
Damage Identification in CFRP Laminates with Embedded FBG Sensors
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10 mm (a) 0.35 % strain
(b) 0.45 % strain
FIGURE 2 Typical damage extension of the DEN specimen. Initial damages were small splittings and transverse cracks. Delaminations appeared at the notch tips as the load increased.
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FIGURE 3 Reflection spectra of the embedded FBG sensor at the damage state shown in Figure 2. Black lines are spectra measured in the experiment, and gray lines are optimized ones by the analysis. The spectrum shape changed when damages occurred and extended.
ANALYSIS Finite Element Model We use layer-wise finite element analysis to obtain the strain field in the composite laminate. The finite element mesh used in this analysis is shown in Figure 4 considering the symmetry of the model. A whole model is separated to two finite element layers which represent 0° plies and 90° plies. The Mindlin plate elements are used for these layers to consider the out-of-plane deformation. An optical fiber is also built into the 0° layer as the line elements. Material properties of CFRP are listed in Table 1. In this analysis, three types of damages (i.e. splittings, transverse cracks and delaminations) are considered based on the experiment. Cohesive elements [3] are used to represent these damages and also in-process damages in the damage analysis. These elements are implemented at the region where damages may occur. Splittings are expressed by cohesive elements in the 0° layer, which are placed from the notch tip along tensile direction. Other cohesive elements for transverse cracks are introduced in the 90° layer at intervals of saturated crack spacing in the transverse direction. Furthermore cohesive elements are placed to link the two layers and also to represent delaminations. Calculation of the Reflection Spectrum Once the strain distribution of the embedded optical fiber is obtained by the finite element analysis, the reflection spectrum of the FBG sensor can be calculated solving Maxwell's equations. The grating period and the change of effective refractive index in the FBG sensor are easily related to the longitudinal strain [4]. Then the reflection spectrum
Damage Identification in CFRP Laminates with Embedded FBG Sensors
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Optical fiber (line element) Y=6.3 X
Cohesive element for splitting Y=4.5
0° layer
10.5 15 Notch tip Y=4.5 Notch
4-node Mindlin plate element 90° layer 0
Cohesive elements for transverse cracks
FIGURE 4 Layer-wise finite element model of the cross-ply laminate with an embedded optical fiber considering the symmetry of the model. The optical fiber is introduced by line elements.
TABLE I Material properties of CFRP T800H/3631 used in the analysis. Longitudinal Young's modulus (GPa) Transverse Young's modul us (GPa) I n-plane shear modul us (GPa) Out-of-plane shear modulus (GPa) In-plane Poisson's ratio Out-of-plane Poisson's ratio Longitudinal thermal expansion coefficient (x 1Cr6/K) Transverse thermal expansion coefficient (x 1a 6 IK)
148 9.57 4.50 3.5 0.356 0.49 -0.6 36.0
can be calculated by transfer matrix method [5] using these non-uniform strain profiles along the embedded FBG sensor. Optical properties of the FBG sensor used in the analysis are listed in Table 2. Damage Identification Technique We applied a mathematical programming technique to identify the damage state of the composite laminate, reproducing the measured reflection spectrum analytically. Figure 5 shows the definition of the design variables xt (i = 1,..., 7) to represent the damage state. The design variables contain the damage process zone, where the cohesive elements are weakening but are not perfectly broken. The variables for the splitting are defined as the length from the notch tip. We assume that the delaminations occur in the elliptical shape, and the delaminations are expressed by the lengths of major and minor axes of the ellipse. TABLE II Parameters of the optical fiber and the FBG sensor to calculate the reflection spectrum. Gage length (mm) Initial center wavelength (nm) Initial refractive index of the core Strain-optic coefficient p ^ Strain-optic coefficient p 12
10 1549.40 1.4490 0.113 0.252
Damage Identification in CFRP Laminates with Embedded FBG Sensors 1
Perfectly damaged zone
997
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FIGURE 5 Definition of the design variables to express the damage state of the DEN specimen. There are two assumptions; delaminations occur in elliptical shape, and transverse cracks are equally spaced.
Also, the transverse cracks are assumed to have equally spacing and to penetrate through the model width. Then, the number of occurred cracks and the length along the transverse direction are adopted to the design variables. Each variable is estimated minimizing the following performance function mathematically. (1) This performance function means the sum of errors between the measured spectrum and the temporarily estimated one. In this method, the reflection spectrum is expressed by Fourier series to quantitatively evaluate the relationship between wavelength and intensity with limited parameters, hi equation (1), the variables x, aj and a- mean design variables, y'-th Fourier coefficient of the experimental spectrum, and 7-th Fourier coefficient of temporarily estimated one, respectively. Fourier coefficients under the 20th order are evaluated, because lower orders can represent the spectrum shape approximately. Also, lower coefficients have more weight multiplying B-spline function. The performance function is minimized by the steepest descent method. It should be noted that this analysis requires a direct linkage between the damage analysis and the calculation of the reflection spectrum. ANALYTICAL RESULTS AND DISCUSSION The damage state of the DEN specimen is identified from the measured reflection spectrum. The reflection spectra shown in Figure 3 (black lines) are given as the inputs of the inverse problem. The spectra optimized in the mathematical programming are also shown in Figure 3 (gray lines) with the experimental results. The estimated damage states are listed in Table 3 with the experimental results. In this table, the estimation has some range, because we believe that the actual damage size will fall within the range from perfectly damaged zone to damage process zone. The estimated results at initial damage state (Table 3(a)) are less reliable particularly about splittings and delaminations. These damages are small and far from the embedded FBG sensor at lower strain. Therefore the reflection spectrum has smaller effects of splittings and delaminations. On the other hand, the estimation at higher strain level (Table 3(b)) is improved because all damages extend sufficiently to affect the reflection spectrum. Consequently, it is found that the position of the embedded FBG sensor is very important to obtain accuracy of the estimation.
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Damage Identification in CFRP Laminates with Embedded FBG Sensors
TABLE III Results of the damage identification with the experimental results. Analytical results have ranges which correspond to the perfectly damaged zone and damage process zone.
Splitting Domination
praxis Minor axis Transverse crack
(a) 0.35 % strain
(b) 0.45 % strain
Experiment
Experiment
Analysis
7.4
7.8-9.1 3.4-7.8 0.9-2.0 4 cracks
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More studies are required to improve the accuracy of the damage identification mainly in the finite element model and the definition of design variables. The present model cannot express the various crack spacing and shape of delaminations observed in the experiment. We will address these problems in the near future. CONCLUSIONS A method is proposed to identify the damage state of a composite laminate by an embedded FBG sensor. Quasi-static tensile test was conducted for the DEN cross-ply laminate with an embedded FBG sensor near the notch tip. Complicated damage state of the DEN specimen was well estimated by solving the inverse problem of the relationship between the damage state and the reflection spectrum from the FBG sensor. This technique can be easily applied to other stress concentrations such as circular holes. ACKNOWLEDGEMENT One of the authors S. Y. was supported through the 21st Century COE Program, "Mechanical System Innovation," by the Ministry of Education, Culture, Sports, Science and Technology. REFERENCES 1. 2. 3. 4. 5.
Zhou G. and Sim L. M. 2002. "Damage detection and assessment in fiber-reinforced composite structures with embedded fibre optic sensors-review," Smart Mater. Struct, 11:925-939. Okabe Y., Yashiro S., Kosaka T. and Takeda N. 2000. "Detection of transverse cracks in CFRP composites using embedded fiber Bragg grating sensors," Smart Mater. Struct., 9:832-838. P. H. Geubelle and J. S. Baylor. 1998. "Impact-induced delamination of composites: a 2D simulation," Composites B, 29B:589-602. R. J. Van Steenkiste and G. S. Springer. 1997. Strain and temperature measurement with fiber optic sensors. TECHNOMIC Publication, pp. 162-171. S. Huang, M. LeBlanc, M. M. Ohn and R. M. Measures. 1995. "Bragg integrating structural sensing," Appl. Opt., 34(22):5003-5009.
Parameterised Modelling Technique & Its Application to Artificial Neural Network-based Structural Health Monitoring Nao Huang, Lin Ye* & Zhongqing Su Laboratory of Smart Materials and Structures (LSMS) Centre for Advanced Materials Technology (CAMT) School of Aerospace, Mechanical and Mechatronic Engineering The University of Sydney, NSW 2006, Australia
ABSTRACT A Parameterised Modelling Technique (PMT) for composite structures was developed on PATRAN® PCL platform. Such a method is able to offer end users a friendly environment to build FEM models for complicated engineering systems while with minimum human efforts and cost. This technique was then validated by selected case study, in which quasi-isotropic CF/EP composite laminates containing delamination with various locations, interlaminar positions and geometric identities were automatically and successively modelled in terms of provided parameters (laminate geometric characteristics, materials properties, delamination location/shape/size/orientation, mesh density, constraint conditions, etc.). An interface was also programmed to conduct dynamic FEM simulation based on developed models using ABAQUS/EXPLICT FEM code. In the selected case study, the proposed approach was also employed to develop an artificial neural network-based structural delamination detection system. It was observed that computational effort and expenditure have been exponentially decreased via such a technique.
INTRODUCTION Modern commercial Finite Element Analysis (FEA) software can offer powerful, accurate, reliable implementation for most structural digital simulations. However, under most circumstances, these software programs can only provide single modelling interface for a specified geometry. When geometric parameters change, the whole system has to be re-modelled. Such a procedure is tremendously heavy and repetitive. This concern becomes more serious when the parameter varies frequently and/or there are many parameters need to be changed. Motivated by this, a Parameterised Modelling Technique (PMT) was developed in this study on commercial FEM platform PATRAN®, to efficiently establish complicated FEM models for different composite structures. As an industry's leading finite element modeller, MSC/PATRAN® provides a developing environment, Patran Command Language (PCL), to customise specific applications, perform variational modelling, and integrate self-developed programs * Corresponding author: Email: [email protected]. Fax: +61-2-9351-3760
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into commercial ones[l]. Consequently, PCL is adopted to develop the parameterised program. Such a technique was then validated by building up a Damage Parameters Database (DPD) for selected composite structures to fulfil the online structural health monitoring. PROBLEM DESCRIPTIONS Parameters Consider a quasi-isotropic CF/EP composite laminate with rectangular shape suffering from an elliptic delamination, as shown in Figure 1. The whole laminate is artificially quartered, counterclockwise denoted by Zone-1, Zone-2, Zone-3 and Zone4 from the bottom-left quadrant, respectively.
P8 : Zone-4
r:
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FIGURE 1 Composite laminate with a delamination
To build up a database, different laminate dimension, layer numbers, materials properties, boundary conditions are of concern. And delaminations with various location, interlaminar position, shape, size, and orientation were then taken into account. PZT disk attached on each laminate and numbered from PI to P9 as shown in Figure 1, were also considered under different location, geometry, and intensity of applied electrical field. Additionally, FEM mesh density, element category, load cases were also included in the parameters that should be specified. Summarily, all the parameters to be considered in this case are briefly listed in Table 1. User Interface Used in conjunction with PATRAN, PCL is able to provide a Graphic User Interface (GUI) for end users to monitor the finite element meshing procedures. The
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process can be supervised by users to guarantee the meshing procedures fully satisfy their requirements. To facilitate and simplify input file preparation for analyser ABAQUS/EXPLICIT®, a seamless interface needs to be designed, with which the users can directly acquire input data file for ABAQUS/EXPLICIT® by simply providing their parameters which are different from default values[2]. TABLE I Parameters to be considered laminate
Delamination
PZT actuators/sensors
Geometric length, width, thickness locations, length of semiparameters per layer, number of major axes and semi-minor positions, radii layers axes, height of delamination FEM seed density, element category parameters load cases load function, position exerting on the specimen boundary conditions material properties element properties Modelling Considerations Previous study [3, 4] has demonstrated that propagation characteristics of Lamb wave, generated by PZT actuators and collected by PZT sensor, are highly sensitive to the existence of structural damage. Without losing generality, a delamination was considered to occur in Zone-1. FEM mesh should be particularly densified in this area to gain the satisfactory precision, where each laminar was individually modelled and there are more than 10 FEM nodes existing along wavelength. The other three quadrants, i.e. Zone-2, 3, 4, to be modelled for geometric consecution but not virtually contribute to the identification, are simplified by choosing consolidated single layer elements. Under such a circumstance, degrees of freedom (DoF) are incompatible at conterminous edges between Zone-1 and the other three zones. Multi-point constraints (MPC) technique is invoked to harmonise different DoF. As explained in Figure 2, MPC constrains each DoF at nodes p and q to be interpolated linearly from DoF at nodes a and b, whose linear relation is represented by scale of shadow. Such a measure makes it possible to connect models with different mesh density while without eliminating any DoF [2]. SOFTWARE REALISATION Design Before coding, the streamline and structure of the program was designed to decompose the programming procedure [5]. Based on above-mentioned requirements, a top-down function-oriented design was adopted to programme the software. Similar to general FEM modelling process, the programme is composed of the following procedures:
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FIGURE 2 MPC technique
(1) Geometric modelling; (2) Meshing and generating the finite elements; (3) Input material properties and element properties; (4) Create boundary conditions; (5) Create load cases and exert on the FEM nodes or elements; (6) Output the generated data. whose flow diagram is shown in Figure 3. VALIDATION AND VERIFICATION Recently, Neural Network-based methods have emerged rapidly in the research field of Structural Online Health Monitoring [3, 4, 6, 7]. As a predictive system modelled after the structure of the human brain, Artificial Neural Network (ANN) methods are performing successfully in various areas ranging from providing insights of human brain to solving problems in engineering, science, economics and fmance[8]. One of the main characters of ANN is its learning mechanism. After being trained by a number of data, including both input data and output data, ANN is able to predict the behaviour of a system, which is usually considered as a black box, as well as the output by giving a specific input. Damages such as cracks, holes or delamination usually result in deterioration of the whole structure system. The properties and the parameters of a structural system such as stiffness, strength, natural frequencies, and mechanical wave propagation properties are different in light of the properties of the damages. The properties of damages which are the inputs of the structural system, as well as the mechanical parameters of the structure which are the outputs of the system, which can be extracted from the measured experimental data, are used to train the ANN for the identification of the system. To embark on the study on delamination behaviour in CF/EP composite laminate, a Damage Parameters Database (DPD) for training the ANN is constructed. To this end, enormous training data, both system input data such as the depth, length, width, shape of delamination and system output data, say, wave propagation properties in this case are required. Taking consideration of the extraordinary cost of experiments and the tedious and time-consuming work of manual modelling, a program using PMT is developed to meet the requirements of database construction. To make sure the validation of the programme, many cases with different parameters are tested. The results proved that the programme meets the expectations
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of the software users. The input files for ABAQUS satisfy the specification and format requirements of ABAQUS when the parameters are in reasonable ranges. Get parameters
Geometric modelling parameters
Meshing and Generating FEM nodes and elements Boundary conditions
Choose other parameters from databases and apply them on the generated FEM model
Material properties Element properties
Format and output the data according to the specification of ABACUS
FIGURE 3 Data flow diagrams 1 T
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Parameterised Modelling Technique
The diagnostic results for the delamination detection from the ANN, which was trained by DPD, are shown in Figure 4, which illustrates that an accurate prediction for presence, location, geometry and orientation of delamination in CF/EP composite laminates has been achieved with the maximum estimation error falling into an acceptable range. MAINTAINABILITY AND FURTHER CONSIDERATION Although this programme was developed for the purpose of the specific problem, it can be employed in many other researches by simply changing specific parameters. As a result, attention should be paid on the maintainability and adaptability to facilitate further uses and development. For this purpose, a naming system was developed and many comments were inserted to improve readability of the programme. Documentation was also built to make the programme procedures understandable for successive programmers. To widen the utility of the proposed technique, further development can be considered on the following aspects: (1) Adding parameters. There are some other parameters that can be taken into account, such as shape of the laminate, number of delamination, form of defects, etc. (2) Interface improvement. File input has been employed in this programme. On the other hand, interactive input method through PATRAN GUI can be added to make the input more intuitive. (3) Library construction. A library which stores material properties and load cases needs to be built when dealing with more structures. CONCLUSIONS The developed PMT is able to greatly reduce human efforts on FEM modelling and analysis, so as to considerably enhance the versatility and efficiency of proposed method, making structural health monitoring for complicated structures feasible and exact. To build DPD with the aid of PMT, other than manual method which costs approximately 16 working hours to model each structure, will save over 93% modelling time by running only 50 minutes and furthermore, in the most of the other 7% running time, users can also leave it unattended. Additionally, human error during the modelling process can be avoided. Finally, further development to make the programme broader use was facilitated. REFERENCES l.MSC Software, (2001). PatranUser's Manual, Ver. 2001. 2.Hibbitt, Karlsson & Sorensen Inc., (2003). ABAQUS User's Manual, Ver. 6.2.4. 3.Su, Z. and L. Ye. 2004. Lamb wave propagation-based damage identification for quasi-isotropic CF/EP composite laminates using artificial neural algorithm, Part I: methodology and database development, Journal of Intelligent Material Systems and Structures. 4. Su, Z. and L. Ye. 2004. Lamb wave propagation-based damage identification for quasi-isotropic CF/EP composite laminates using artificial neural algorithm, Part II: implementation and validation, accepted by Journal of Intelligent Material Systems and Structures. 5. Sommerville, I. 1996. Software engineering. Addison-Wesley Pub. Co.. 6. Doebling, S.W., C.R. Farrar, M.B. Prime, and D.W. Shevitz, Damage Identification and Health Monitoring of Structural and Mechanical Systems from Changes in Their Vibration Characteristics: A Literature Review. 1996, Los Alamos National Laboratory: New Mexico, p. 127. 7.Marwala, T. 2001. Probabilistic Fault Identification Using Vibration Data and Neural Networks, Mecham'ea/ Systems and Signal Processing, 15(6): p. 1109-1128. 8. Mehrotra, K., S. Ranka, and C.K. Mohan. 1997. Elements of artificial neural networks. MIT Press.
Information Fusion in Distributed Sensor Network for Structural Damage Detection Xiaoming Wang* and Greg Foliente CSBR.0 Manufacturing and Infrastructure Technology, Commonwealth Scientific and Industrial Research Organisation, Graham Road, Highett, Melbourne VIC 3190, Australia Zhongqing Su and Lin Ye Centre of Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering, The University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT Distributed sensor networks are becoming a critical technical driver in the application of structural health monitoring for large-scale structures such as commercial aircrafts since it greatly increases the reliability and robustness of monitoring systems. One of the key technical issues in the implementation of distributed sensor network is the application of an information fusion that enables integration of data from all sensors for the assessment of structural conditions. In this paper, we demonstrate the feasibility of combining a distributed sensor network and a two-level information fusion technique to damage detection in composite structures.
INTRODUCTION Fighting for dominance in commercial aviation industry, Boeing is putting a lot of hope on its new 7E7 dreamliner, which is claimed to be 20% more fuel efficient by applying new generation of engines, composite materials, advanced electrical systems, better aerodynamics and structural health monitoring (Talbot, 2003). That would be the first commercial aircraft equipped with an advanced distributed sensor network to monitor the integrity of its structural system, such as fuselage and wings, continuously and autonomously. In competition, Airbus is also considering the integration of structural health monitoring into its future Airbus fleet (Beral and Speckmann, 2003). Structural health monitoring was also introduced in a new maintenance policy by the US Department of Defence (DoD), known as 'Condition-Based Maintenance Plus (CBM+)', to reduce the cost in maintenance by a schedule-based approach (Derriso et al, 2003). Basically, structural health monitoring is a technique to use sensors, which may or not be attached on/embedded in structures, to collect the information of structural mechanical or physical behaviours continuously or periodically for the diagnosis and prognosis of structural integrity and performance. The recent development of multi* Corresponding author, Email: [email protected].
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sensor network greatly enhances the feasibility of applying structural health monitoring into large-scale structures such as aircrafts. The advantages of using a multi-sensor network include its ability to combine all kind of information sources that can be the same type or completely different, and also its enhanced awareness of targets with superior system reliability and robustness (Xiong and Svensson, 2002). One of key issues in a multiple sensor network is information fusion, which deals with the establishment of algorithms for data cleansing, feature extraction and information integration on consideration of the data from all sensors. This paper demonstrates the feasibility of applying a distributed sensor network and a two-level information fusion technique for damage detection in composite structures. The information considered is associated with the "Digital Damage Fingerprint' (DDF) studied by Su and Ye (2002). Its representative data are essentially extracted from spectrographic features of fundamental Lamb modes over the time-frequency space, and has proved to be sensitive to the damage that existed in the composite materials during their propagation.
SENSING SCHEME AND INFORMATION FUSION IN DISTRIBUTED SENSOR NETWORK For a structural component, a number of piezoelectric sensors may be mounted on the plate as shown in Figure 1. Each sensor can be active capable of sending interrogating stress waves to others and requesting their responses, while it can also be a part of passive sensors to respond to each request from active sensors. Bearing this in mind, the distributed sensors network in Figure 1 may be a sub-network of a large-scale sensor network.
Level 2 Sensor 4 Sensor 5
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FIGURE 1 Distributed sensor network
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—
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FIGURE 2 Information fusion scheme
Following the request by each sensor to others in the network, they establish their own knowledge or information on the state of structural health. Fusion of the information from all sensors leads to an overall assessment of structural damages. As shown in Figure 2, there are two level of information fusion for damage assessment in this case, with one combining responses from passive sensors at requests of an active sensor and another consolidating the combined information from each sensor when it
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is taking an active duty. Since the assessment is based on a multi-sensor network with redundant paths for information acquisition, disruption due to the malfunction or failure of any sensor is reduced to minimum. As a consequence, it may provide a more reliable and robust structural damage assessment. To illustrate the sensing scheme and information fusion for distributed sensor network, nine sensors are attached on a composite plate as a sensing network in Figure 1. The plate is divided into four areas, scanned separately by the sensor network to assess structural damage. As an example, the shadow area at the rightupper side will be assessed. Starting with level one information fusion in the network, sensor 9 initiates the interrogation of sensors 4, 5 and 2, simultaneously, by producing a Lamb stress wave, followed by sensors 8, 5 and 6 sending requests to sensors 6 and 3, sensor 5, and sensors 8 and 7, respectively. As shown in Figure 2, the information fusion at level two is then subsequently conducted for damage assessment. Like all others, sensor 9 can be an active sensor at the first stage, then it can also be a passive sensor later. There have been some algorithms available for information fusion. One of the simplest is the use of voting scheme as a decision is made according to the voting index, (1) where N is the total locations where a damage assessment is conducted, «,- is the total number of sensors/information sources used to assess the 2-th location (z'=l, ..., N), Yy is the decision made by the z-th sensors in relation to the j-th location. Typically, it equals one for a positive decision and zero for a negative decision, wy in the equation represents the voting weight of the z-th sensor on they-th location. Equation 1 is here applied for information fusion both at levels one and two, shown in Figure 2. The voting weight is assigned with the correlation coefficient between field-measured DDF and the DDF in a so-called knowledge database, which is about to be established by FEM modelling as discussed in the following section. After two levels of information fusion, the area with the voting index in equation 1 greater than an acceptable level would be considered most possibly to have damages.
KNOWLEDGE DATABASE BASED ON FEM MODELS The CF/EP quasi-isotropic [45/-45/0/90]s composite laminate (475 mm x 475 mm x 1.275mm), as shown in Figure 3, was investigated. Nine piezoelectric wafers with 6.9mm in diameter and 0.5mm in thickness, were bonded on one side of laminate surface. Up to 50 damage scenarios from early studies by Su and Ye (2003) were considered for the establishment of a preliminary knowledge database, where 3D finite element models for each individual presumed damage situation were created, employing S-node consolidated solid brick elements with effective anisotropic laminate elastic properties. One of them is paradigmatically shown in Figure 4. The fundamental Lamb waves, conditioned with 5-cycle sinusoidal toneburst at the central energy of 0.5MHz, were activated. Structural responses for wave propagation were simulated using ABAQUS/EXPLICIT® FEM code (Hibbitt, 2003).
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FIGURE 3 Composite laminate involving defective a hole impact damage
'-
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FIGURE 4 Ichnography of FEM model for the laminate shown in Figure 1
The signal was processed based on a wavelet transform to obtain DDF to simplify complicated signals without the loss of their fundamental characters. It generally consists of data cleansing and feature extraction. As an example, a sampled data via sensing path 5-9 is described in figure 5(a). After data cleansing and feature extraction, the final data of DDF is given by figure 5(b). The same approach was also applied to other sensing paths to construct a comprehensive set of DDF for presumed damage scenarios. These become the fundamental foundation of the knowledge database.
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FIGURE 5 Data cleansing and feature extraction in the time domain for sensing path 5-9.
EXPERIMENTAL VERIFICATION OF DAMAGE DETECTION A specimen of T650/F584 CF/EP [0/45/-45/90]s quasi-isotropic laminate was manufactured with an artificial through-hole defect introduced. Nine piezoelectric Lead Zirconate Titanate (PZT) wafers with 6.9 mm in diameter and 0.5mm in thickness were bonded on laminate as shown in Figure 1. By the use of a high-speed data acquisition system based on a VXI platform through IEEE-488 bus, the responses
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of all passive sensors to the interrogating stress wave emitted from an active sensor, as displayed in figure 2, were measured. Based on Equation 1, voting patterns for each sensing scheme were obtained as shown in figure 6, where the ellipse with dotted line indicated the size and location of an artificial hole damage. The solid curve in the figure represented the boundary of the voting index, beyond which it is the area with the index higher than 0.7 or the area with a high damage possibility based on the belief of sensors. Figure 6(a) displays the voting pattern from one sensing path 5-9, implying that the sensor 5 is an active sensor and the sensor 9 is a passive sensor. It is obvious that the pattern does not provide reasonable information matching the size and location of the damage. Figure 6(b) gives the voting pattern from sensing path 9-5. Figure 6(c) and 6(d) describes the patterns derived from the level one information fusion provided by the sensing paths of 9-5 and 9-2, and the paths of 9-5, 9-2 and 9-4, respectively, hi the figures, the index in the area without colour represents a lower value when the area is enclosed by a 'dark area', while it indicates a higher value when the area is enclosed by a 'bright area'. Results show an increasing improvement in the relevance of voting pattern to the size and location of the damage, with 'noise' being apparent in these figures. Therefore, it is important to select an appropriate fusion scheme to minimise interference from noise. The negative effect of noise can particularly be found in Figures 6(f) and 6(h), which describe no improvement on the relevance of the voting pattern to the damage although the level-one information fusion scheme was applied to add sensing paths 67 to 6-8 and 8-3 to 8-6. However, the application of the level two information fusion greatly improved the relevance of the voting pattern to the damage, as shown in Figure 7(a). This was based on all fused information obtained at level one, as shown in Figure 2. When negative effects of some sensing paths were excluded from the level 2 information fusion, some improvements can be seen in Figure 7(b).
CONCLUSION A distributed sensor network can provide flexibility in the design of structural health monitoring systems with considerable reliability and robustness through multiple sensing paths/levels and redundant information acquisition/fusion structures. The voting algorithm as one of the simplest techniques for information fusion was demonstrated here to establish voting patterns, from which structural damages can be identified. The technique of multi-level information fusion shows much promise. Appropriate selection of fusion algorithms and filtering of noise during data fusion are the keys to further improve the accuracy and efficiency of damage identification using distributed sensor networks.
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References Beral, B. and Speckmann, H. (2003). 'Structural health monitoring (SHM) for aircraft structures: A challenge for system developers and aircraft manufacturers'. In Proceedings of the 4 International Workshop on Structural Health Monitoring (edited by Fu-Kuo Chang), Stanford, USA. Derriso, M.M., Pratt, D.M., Homan, D.B., Schroeder, J.B. and Bortner, R.A. (2003). 'Integrated vehicle health management: the key to future aerospace systems'. In Proceedings of the 4 International Workshop on Structural Health Monitoring (edited by Fu-Kuo Chang), Stanford, USA. Hibbitt, Karlsson & Sorensen Inc. (2003). ABAQUS User's Manual, Ver. 6.2.4. Su, Z. and L. Ye. 2002. 'A damage identification technique for CF/EP composite laminates using distributed piezoelectric transducers', Composite Structures, 57:465-471. Su, Z. and L. Ye. 2003. 'Lamb wave propagation-based damage identification for quasi-isotropic composite laminates using artificial neural algorithm, part I: methodology and database development', accepted by Journal of Intelligent Material Systems and Structures. Talbot, D. (2003). 'Boeing's flight for survival', Technology Review, September, 2003: 35-44. Xiong, N. and Svensson, P. (2002). Multi-sensor management for information fusion: issues and approaches. Information Fusion, 3:163-186.
Remaining Life of FRP Rehabilitated Bridge Structures Luke S. Lee, Becki Atadero and Vistasp M. Karbhari* Department of Structural Engineering, MC-0085 University of California San Diego, La Jolla, CA 92093-0085, USA Charles Sikorsky California Department of Transportation, Sacramento, CA, USA
ABSTRACT A time dependent reliability approach is presented for estimation of remaining life of FRP rehabilitated structures incorporating field measured structural health monitoring data and laboratory durability results. An estimation of the remaining life of the structure is provided from time-superposition of the deterioration curves following progressive damage cases.
INTRODUCTION The combination of a deteriorating civil infrastructure and limitations on available resources necessitates maximizing or extending the service life of structures. Rehabilitation of civil structures using fiber reinforced polymer (FRP) composites is becoming a viable option to increase capacity and extend the service life of a structure; however, issues pertaining to quality control during manufacture and durability of FRP remain, especially as related to their capacity for sustained performance under extreme and changing environmental conditions under load. It is hence necessary to assess the effectiveness of a strengthening measure and monitor subsequent damage or degradation in the system. In the following an approach to remaining life estimation of FRP rehabilitated bridge structures using structural health monitoring data and material durability results is presented. OVERVIEW OF BRIDGE STRUCTURE The bridge structure, located on California Interstate 40 constructed in 1968, consists of two parallel structures each of which is a skewed, two lane bridge 225.9 m long. The superstructure consists of a cast-in-place reinforced-concrete deck and girder structural system with sixteen 12.8 m central spans and two shorter spans of 10.5 m at each abutment. The 15.6 cm thick deck spans transversely across six girders at 2.13 m centers. The bridge consists of 18 spans and five bays in each span. Frame 3 of the southern bridge component, denoted Frame S-3, is the primary substructure of interest. Bays within each span are identified 1 thru 5 from North to South, i.e. Location 9-3 is Span 9, Bay 3.
* Corresponding author, Department of Structural Engineering, University of California, San Diego, La Jolla, CA 92093-0085, USA, Fax: (858) 534-6373, Email: [email protected]
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A visual inspection of the bridge shows the development of transverse and longitudinal cracks on the soffit of the bridge deck potentially caused by increased traffic loads and steel reinforcement deficiencies. Transverse cracks are spaced at approximately 14 cm corresponding to the spacing of bottom transverse steel reinforcement. Longitudinal cracks are observed at 24.4 cm centers corresponding to bottom longitudinal steel reinforcement distributed in the deck slab. A global inspection of the structure was conducted using a vibration based damage detection procedure in order to identify stiffness losses in the structure. The global evaluation indicates that spans 8 and 9 contain damage whereas spans 10 and 11 do not. Therefore, flexural rehabilitation of the deck was conducted with the application of CFRP composites to spans 8 and 9 while spans 10 and 11 remain unstrengthened. DECK REHABILITATION The damage assessment revealed that development of transverse and subsequent longitudinal cracking is due to increased load demands on the bridge structure and the lack of steel reinforcement to accommodate increased loads. Utilizing computed steel reinforcement deficiencies; an equivalent CFRP design was determined. The number of strips corresponding to the deficiency of the #5 steel rebar was determined for both composite strips manufactured via wet lay-up and pultrusion techniques. The minimum requirement for the deck rehabilitation is prevention of punching shear failure. Locations 8-1, 9-1, and 9-4 were rehabilitated with pultruded CFRP composites for the punching shear load criterion. Locations 8-2, 8-3, 9-2, and 9-3 are rehabilitated considering the Permit truckload requirement, 106.8 KN, with wet lay-up CFRP in 8-3, 9-3 and pultruded CFRP in 8-2 and 9-2. Locations 8-5 and 9-5 were strengthened for the permit truckload with a nominal safety factor applied. SYSTEM LEVEL ASSESSMENT A global nondestructive damage assessment methodology as developed by Stubbs et al. [1] was employed to detect changes in modal strain energy in order to identify, locate, and quantify damage. A comparison of mode shapes before and after the CFRP rehabilitation provided an estimation of stiffness changes as listed in Table I. TABLE I Stiffness Changes in Spans 8 and 9 of Frame S-3
8-1 13.3
8-2 20.5
% Stiffness Change by Span-Bay Combination 8-3 8-4 8-5 9-1 9-2 9-3 19.5 -0.2 N/A 7.9 9.9 11.6
9-4 13.6
9-5 6.4
An average increase in stiffness of 17.8% is observed from the preliminary results for bays 1 thru 3 of span 8, while location 8-4 indicates relatively no change in stiffness since this bay is unrehabilitated for purposes of comparison and detection. In Span 9, an average stiffness increase of 9.9% is observed. The measured stiffness changes of the structure indicate that CFRP rehabilitation provided a measure of improvement to the stiffness of the structure. ESTIMATION OF REMAINING SERVICE LIFE In determining the remaining life of an FRP rehabilitated structure, a condition based monitoring approach is implemented which involves the following, 1) acceptance that
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damage is present or will occur, 2) an adequate method of inspection is available, and 3) adequate strength is retained in the damaged structure. Damage accumulation is measured in terms of a cumulative stiffness loss in the system correlated to a selected measure of performance. The reliability, beta, defined by system probability of failure is used as the indicator of performance for the system. For a single instance of time, the standard second moment equation is used to compute reliability, (5, of the structure. r m
r
m
f
(1)
where p, denotes reliability of the system; \x[ ] indicates mean value; a 2 [ ] is the variance; R, is resistance; S, is demand. Since rehabilitation designs vary, reliability of the system is defined with consideration only for specific rehabilitated bays. It is noted that in this preliminary investigation several simplifying assumptions are made, including: (1) All variables are normally distributed; (2) Load bias factors defined for girders are applied directly to slab load demand; (3) Flexural failure defined by steel yield is considered the governing failure mode. Other possible failure modes such as shear failure in the deck slab or debonding of FRP rehabilitation are not included; (4) Only FRP is assumed to degrade. Degradation of other materials is not included; (5) Cracking patterns indicate two-way slab behavior; therefore the load demands in the transverse direction of the slab are conservatively assumed to apply to the longitudinal direction of the slab, where less reinforcement is available; and (6) Demand on the structure, its bias factors and variability are assumed to remain unchanged with respect to time. Dead load moment is calculated by modeling a transverse segment of the slab as a simply supported beam with a continuity factor of 0.8 per California Department of Transportation Bridge Design Specifications (Caltrans BDS) section 3.24.3.1 [2], A dead load moment bias factor of 1.05 is included for cast-in-place concrete bridges, with coefficient of variance (COV) of 10% [3] MDL=XDLQ.%WDL'L2"""
(2)
where MDL, is dead load moment per 30.48 cm of slab or per foot of slab; XDL, dead load moment bias factor, 1.05; Lsiab, is the clear span of the slab, 1.85 m; WDL, dead load distributed load denned as wDL =ts:wc + surface ; ts, thickness of the slab, 15.56 cm; wc, normal weight concrete, 150 pcf; surface, surface material on the top of the deck, 25 psf. The resulting dead load moment is 0.535 kN-m per 30.48 cm of slab, or 1.76kN-m/m. Live load moment demands are calculated per eqn. 3-15 in the Caltrans BDS [2]. The formulation below is specified for the FPS unit system. The resulting live load moment is converted following the calculation. A live load bias factor of 1.2 and COV of 18% [3] are applied in addition to the dynamic load factor of 1.3 per Caltrans BDS [2]. A reduction factor of 0.85 is also included for a two lane highway bridge in the live load moment demand [3]. ^
\-PHS20
(3)
where MLL is the live load moment demand; Xiyn, dynamic load factor, 1.3; XLL, live load bias factor, 1.2; Lsiatl, is the clear span of the slab, 1.85 m (6.08 ft); PHS2O, design truck load of 71.2 kN (16 kips). The resulting live load moment is 23.38/W-m/m with 18% COV. The total moment demand and standard deviation are derived with the standard combinations,
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] (4) 'zJ (5) where |a[ ] indicates mean value; cr2[ ] is the variance; COV is ///<7. The resulting total mean moment is 25.59kN-m/m, with a resulting COV of 16.8%. Following rehabilitation the resulting moment resistance in the longitudinal direction of location 9-5 is 54.46 kN-m/m, with a COV of 14.2%. Utilizing equation (1) the reliability in location 9-5, pnMb =3.271. If all spans are rehabilitated using the CFRP design in location 9-5, the reliability result is applicable to the other bays of the bridge. The reliability of the system before CFRP rehabilitation, considering an undamaged slab is #, = 2.293 . Time-dependent reliability, J3(t), is developed by identifying and introducing timedependence to variables within the simple second moment reliability equation and the remaining service life of the system is determined by solving for time, t, at the target reliability of the structure (the target reliability for this evaluation is 1% probability of failure or p = 2.33). Degradation of the CFRP modulus is empirically modeled from accelerated aging tests of wet lay-up manufactured CFRP and is used to determine the forces contribution to section equilibrium changes resulting in a time dependent depth of neutral axis, c(t). The resulting time-dependent reliability formulation for the wet lay-up manufactured CFRP in location 9-5 of the Watson Wash Bridge can be summarized as M >®-Mr m = x (6)
where My(t) = Efv(t)Afipefip(h-d)
+ O.&5Xj:fc'b(o.85c(t))\d— . The change in reliability
with respect to time in location 9-5 is shown in Figure 1. The result indicates that in approximately 13 years, the reliability of the system degrades to 2.333 or a 1% probability of failure. P(t post ) =
Limit [(t)
(years)
FIGURE 1 Change in Performance of Location 9-5 after CFRP Rehabilitation
APPLICATION OF PROGRESSIVE DAMAGE SCENARIOS Demolition of the Watson Wash Bridge provided a unique opportunity to conduct destructive testing on specific rehabilitated locations of the bridge. Damage scenarios were applied to two locations of the structure, one of which was rehabilitated using wet lay-up manufactured CFRP in location 9-5 and the other a pultruded CFRP rehabilitation in location 8-1. Only location 9-5, with wet lay-up manufactured CFRP is considered as an example in this paper. The damage cases in location 9-5 are as follows with
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corresponding cumulative measured stiffness loss: (1) Removal of one longitudinal strip, -8.0%; (2) Removal of four transverse strips; (3) Punch out of bridge deck, -16.0%. Utilizing stiffness changes measured from a global NDE assessment, the reliability following each damage scenario is determined using the following simple beam relationship, M>(t) = E(t)l*y(t)
(7)
where My(t) is time dependent moment resistance of the system, E(t) is a time dependent system stiffness, I is the moment of inertia of the system and is assumed constant with respect to time, and ij>y (t) is time dependent yield curvature of a beam. Each damage scenario applied to the section of the bridge is considered a single instance in time at which damage severity, in terms of stiffness loss is measured. The measured percentage stiffness change is applied directly to the flexural stiffness to acquire an updated resistance measure of the system and ultimately a reliability estimate. It is assumed that yield curvature changes negligibly with damage and deterioration in the system. Table II shows results for Bay 5 Span 9 in terms of two theoretical reliabilities, namely before rehabilitation, tpre, and after rehabilitation, tpost with the estimated reliabilities after incorporating the measure stiffness losses of the system. TABLE II Instantaneous Reliabilities Pre-Rehab, tpre
2.293
Post-Rehab, tpost
3.271
Damage 1, ti
Damage 2, t2
Damage 3, t3
2.956
N/A
2.593
Introducing the time dependence to the reliability following each damage case an estimate of the change in reliability with respect to time is available incorporating measured stiffness loss within the system. Following each systems level inspection an update is provided for the system reliability relative to the baseline reliability; in this case the initial reliability or time zero of the structure is taken as the theoretical post-rehab reliability at time, tpost. The three damage cases are integrated together to provide a prediction of the remaining life of the system following the cumulative effect of three damage cases. As shown in Figure 2 for location 9-5, incorporating the three damage severity cases the structure is likely to have a 1% probability of failure in approximately 10.6 years.
P(tpost) = 3.
FIGURE 2 Remaining Life Estimate for Location 9-5
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For purposes of comparison, an evaluation using bias factors and variance for load and demand is also performed in accordance with [3] using a Monte Carlo simulation to estimate the initial reliability of slab after rehabilitation with CFRP. The reliability result is 4.80 for location 9-5 after rehabilitation in the longitudinal direction and considering a 75 year design period. Applying the stiffness loss measurements and FRP degradation model results in the following life degradation curves and life estimation for location 9-5 of the Watson Wash Bridge shown in FIGURE 3.
= 35 6 yrs
FIGURE 3 Remaining Life with Initial Reliability Using NCHRP Method
Utilizing the an initial reliability calculated in accordance with NCHRP guidelines and a Monte Carlo simulation, the time remaining before reaching a 1% probability of failure in the slab is 45.6 years. SUMMARY Prediction of the remaining service life of the structure requires an integration of a global NDE technique, with information regarding the durability of the composite materials used for application. An estimate of the remaining life of the system is in essence a design tool, which assists in characterizing the effect of FRP durability to a rehabilitation design. The destructive testing sequence to the rehabilitation on the Watson Wash Bridge serves as an experimental validation for the methodology and an initial implementation of quantifying the effect of FRP rehabilitation on a bridge structure. REFERENCES 1. Stubbs, N., S. Park, C. Sikorsky, and S. Choi. 2000. "A Global Non-destructive Damage Assessment Methodology for Civil Engineering Structures," IntlJ. ofSys. Set, 31(11):1361-1373. 2. California Department of Transportation, Bridge Design Specifications 3. Nowak, A.S. (1999) NCHRP Report 368, Calibration of LRFD Bridge Design Code. National Academy Press, Washington D.C.
Delamination Monitoring of CFRP Laminates Using Electrical Potential Method Masahito Ueda* Graduate student of Tokyo Institute of Technology, Japan Akira Todoroki, Yoshinobu Shimamura and Hideo Kobayashi Tokyo Institute of Technology, Department of Mechanical Sciences and Engineering, Japan
ABSTRACT Monitoring of delamination is indispensable for CFRP structures. It is, however, very difficult to detect a delamination visually. This demands a new structural health monitoring method. For aerospace structures, it is required to monitor a delamination before flight, and this means the monitoring system must detect the delamination without loading. In authors' previous studies, the delamination can be monitored with the electric resistance change method. The method provided excellent performance of estimations. The method, however, requires complicated electric circuits and uses a two-probe method: two-prove method includes effects of the electric resistance change at the electrodes. To resolve these problems, an electrical potential method is employed here. In the previous paper, the electrical potential method showed poor performance of estimations for delamination cracks located near the center of the specimen. The practical zigzag crack has large effect on the performance of estimation when the delamination locates at the center segment of the specimen. In the present paper, the problem is overcome by means of a new proposed concept of the electrical potential method. The method shows excellent performance of estimations on the basis of FEM analyses. INTRODUCTION Carbon Fiber Reinforced Plastic (CFRP) laminates is widely used in aerospace structures because of its superior mechanical properties. For the CFRP laminates, a delamination is easily induced by a slight impact. The delamination causes large reduction of strength and stiffness of the CFRP laminates, and it brings deterioration of structural reliability of the CFRP structure. Detection of a delamination of the CFRP laminates is a difficult task for visual inspection. The monitoring of a delamination is, therefore, indispensable for maintaining the reliability of the CFRP structures. Authors have already employed an electric resistance change method for identifications of a delamination. On the specimen surface, multiple electrodes were mounted by means of co-curing copper foil as electrodes to measure electric resistance changes between two-adjacent electrodes. The applicability of the method was investigated analytically and experimentally using the beam type specimen and plate-type specimen [1 to 4]. The data-normalization method provided significant improvement of performance of estimations [5]. The method, however, requires * Corresponding author, 2-12-1 O-okayama Meguro, Tokyo 152-8552, Japan. +81-3-5734-2809. [email protected]
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complicated electric circuits and uses a two-probe method: the two-prove method includes effects of the electric resistance change at the electrodes. The accuracy of estimation is severely affected by the condition of electrical contact at the electrodes. To resolve these problems, electrical potential method is adopted in the present paper. The electrical potential at the electrodes are measured by charging electric current from one electrode to another electrode made on the surface of the both ends of a beam specimen. The method is applied to beam type specimens and investigated using FEM analyses. The application of the method showed poor performance of estimations when practical cracks such as zigzag crack locate near the center of the specimen. If the practical zigzag cracks can be estimated using the response surfaces made from the analyses of the straight crack, this provides large reduction of computational cost. To solve this problem, non-symmetric charging is newly adopted and investigated by means of FEM analyses. ANALYTICAL METHOD Analytical Model In this study, FEM analyses are performed with the commercially available FEM code ANSYS. The specimen is a two-dimensional beam. The configuration of the specimen is 200 mm in length and lmm in thickness as shown in Figure 1. The stacking sequence of the specimen is [0/90]s. Seven electrodes are mounted on the one surface of the specimen with spacing of 30 mm. This is assumed that electrodes are mounted on the inside surface of structures. The width of each electrode is 5 mm. For cross-ply composites, the electric current flows not only to the longitudinal direction in the top surface ply, but also to the thickness direction throughout the specimen. Since electric current is impeded by an existence of a delamination, the electrical potential change is created in the specimen. The delamination can be detected by means of measuring the electrical potential change between electrodes. For FEM analyses, four-node elements are adopted and size of the element is 0.0625 mm in height and 0.25mm in width. The FEM calculations are performed using the electric conductance of ao=4.6OxlO3, CJ90 =4.83 and ut =1.030"^"'. This electric conductance was obtained from the experimental results of a CFRP laminate of fiber volume fraction Vf= 0.472 [6]. Solver of Problem A delamination in a CFRP laminate is identified using a response surface. Our previous studies demonstrate that quadratic polynomials provide high performance of estimation for this inverse problem.
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Location
FIGURE 1 Analytical model of CFRP laminate beam
Electric current is charged at an electrode and other electrode is set to be 0V. Electrical potentials between electrodes are calculated before and after a creation of a delamination. Electrical potential change ratios are calculated from the measured results. The electrical potential change ratios are normalized by the norm of the obtained electrical potential change vector [5]. Predictor variables of response surface are the normalized electrical potential change ratios and the norm. Response variables are delamination location and size. When a regression coefficient has low contribution to the regression, the coefficient is eliminated from the response surface to maximize the adjusted coefficient of multiple determination. Shapes of Delamination Three shapes of delamination are investigated in this paper: straight crack, Z-type crack and inverse Z-type crack (Figure 2). Straight crack is placed at the interlamina near the electrodes because large delamination is generally created at the opposite interlamina to the impacted surface. It is impossible to make response surfaces from the analyses of all types of the shape of delamination. If practical cracks such as the Z and inverse Z-type crack can be estimated using the response surfaces made from the analyses of the straight crack, this reduces huge computational cost. ESTIMATION RESULTS The electric current was charged at the end-electrode A and electrical potential was set to be 0V at another end-electrode G, i.e. the electric current flows throughout the specimen. FEM analyses were conducted for the cases of delamination sizes of 5, 7, 10, 15, 20, 25, 30, 35 and 40mm and of various delamination locations from -90mm to +90mm: the delamination was shifted by spacing of 5mm. FEM runs of 315 were performed. Response surfaces were made from the normalized electrical potential change ratios between the electrodes AD, BD, CD, DE, DF, DG. Figure 3 (a) and (b) show the estimation results of location and size of the straight crack. The adjusted coefficients of multiple determination are 0.999 and 0.925 respectively. The abscissa shows delamination location or size and ordinate shows estimation location or size. Diagonal line (solid line) in the figures means the exact estimations and dotted lines show the error of band of + 5mm. Figure 4 (a) and (b) show the estimation results of Z-type and inverse Z-type crack using the response surface made from the analyses of the straight crack. As shown in this figure, the scattered estimations of location exist near the center segment of the specimen. Several estimations of delamination size show very poor results. The large errors are also induced at the center segment of the specimen.
Delamination Monitoring of CFRP Laminates 0°-ply
Electrode
^P
1021 90°-ply
Impact
(a) Straight delamination (Without matrix crack)
(b) Z-type delamination (With matrix crack)
(c) Inverse Z-type delamination (With matrix crack)
FIGURE 2 Types of delamination crack shape
The electrical potential changes are strongly affected by the matrix crack when delamination locates at the center segment of the specimen. The electric current density to the thickness direction significantly decreases at the center segment. The contribution by the existence of matrix crack to the total electrical potential change is very high because the contribution by the straight delamination is small near the center segment. Then, the difference due to the matrix crack is magnified by the data-normalization. This creates large errors when Z-type or inverse Z-type crack is estimated by the response surface made from the analyses of straight cracks. The detail of this mechanism is shown in the reference [7] NEW MODIFIED METHOD The electrical potential method shows poor performance of estimations for practical crack near the center of the specimen, in other words, at the center segment of charged electrodes. On the other hand, the estimation shows excellent performance when delamination locates near the charged electrodes without the effect of matrix crack. For these symmetric electrical charging, electric current in the thickness direction almost vanishes near the center segment. In the present study, therefore, non-symmetric charging is adopted. Let's consider a 9-electrode specimen as shown in Figure 5. The distances between adjacent electrodes are 30mm. The total length of the specimen is 260 mm. The thickness and stacking sequence are the same as those of Figure 1. At first, electric current is charged between the electrode A and electrode G: G is set to be 0V. After that, electric current is charged between C and I. In the first case, it is expected that a delamination would be estimated with good performance inside the segments AC and EG. On the other hand, a delamination may be estimated with poor performance inside the segments CE. 100
-100 -100
0 Location [mm]
100
10
20
30
40
50
Size [mm]
(a) Estimated location (b) Estimated size FIGURE 3 Estimation results of straight crack using the response surface made from the straight crack
1022
Delamination Monitoring of CFRP Laminates
-100 -100
0
100
10
20
30
40 50
Size [mm]
Location [mm]
(a) Estimated location (b) Estimated size FIGURE 4 Estimation results of Z and inverse Z-type crack using the RS made from the straight crack 24C
10mm
30mm
i 30mm B
,
30mm
C
3
F
[
LULUL
| fc S
m
mm
30mm
V
G
H
. . M.
.
<
/ / 0°-ply (0.25mm) 90°-ply (0.5m m)
S ize
Location
•I
FIGURE 5 Analytical model of CFRP laminate beam with 9 electrodes
In the second case, the estimations in the segment CE and GI would show the good performance although the poor estimation may be created inside the segment EG. By combining the two cases, all cases may be expected to have a good performance. The rough estimation of location should be performed to obtain the information which response surface must be used, hi the first step, the delamination size is divided into 4 levels : level 1 is -130^x<-60, level 2 is -60^x<0, level 3 is 0 ^ x ^ 6 0 and level 4 is 60<x^ 130. If the estimated division is 1 or 3, former case (charged electrodes are A and G) should be used, and if the estimated division is 2 or 4, latter case (charged electrodes are C and I) should be used. Electric current of 50mA was charged at the end-electrode A and electrical potential was set to be 0V at electrode G. FEM analyses were conducted for the cases of delamination sizes of 5, 7,10,15,20,25,30,35 and 40mm and of delamination locations from -120mm to +120mm with spacing of 5mm. FEM runs of 427 were performed here. Electrical potential change ratios between the electrodes AD, BD, CD, DE, DF, DG are calculated. After this, electric current of 50mA was charged at the electrode C and electrical potential was set to be 0V at another end-electrode I. FEM analyses were conducted for the cases of delamination sizes of 5, 7,10,15,20,25, 30, 35 and 40mm and of delamination locations from -120mm to +120mm with spacing of 5mm. FEM runs of 427 were performed. The electrical potential change ratios between the electrodes CF, DF, EF, FG, FH, FI are calculated. Firstly, response surface for identification of division is made using these 12 normalized electric potential change ratios. Figure 6 shows estimation result of division of straight crack, Z-type crack and inverse Z-type crack. The results show, however, some miss-estimation between adjacent divisions. These errors occur at the boundary of adjacent division. Therefore, the estimation of location and size of delamination must have some tolerance for the segments of overlap. After the rough estimation, delamination location and size are estimated more accurately. A response surface for estimation of delamination that locate between electrodes AC and EG is made using the above calculated data (in case of charged
Delamination Monitoring of CFRP Laminates
1023
electrodes A and G) of delamination location from -120mm to -60mm and 0mm to +60mm. The predictor variables of the response surface are normalized electrical potential change ratios between the electrodes AD, BD, CD, DE, DF, DG. Similarly, a response surface for estimation of delamination that locate between electrodes CE and GI is made using the above calculated data (in case of charged electrodes C and I) of delamination location from -60mm to 0mm and +60mm to + 120mm. The predictor variables of the response surface are the normalized electrical potential change ratios between the electrodes CF, DF, EF, FG, FH, FI. Delaminations locate inside the segment AC and EG are estimated by the former response surface and delaminations locate inside the segment CE and GI are estimated by the latter response surface. Figure 7 (a) and (b) show the estimation results of location and size of straight crack, Z-type crack and inverse Z-type crack. The estimation shows excellent performance of estimations without dependency on delamination shapes. 5 >4
LLJ
0 0
1 2
3
4
5
Level FIGURE 6 Estimation result of size level
-150
-50
50
Location [mm]
0
10
20
30
40
50
Size [mm]
(a) Estimated location (b) Estimated size FIGURE 7 Estimation results of Z and inverse Z-type crack using the RS made from the straight crack
CONCLUSIONS Delamination is estimated by using the electrical potential method. The electrical potential method showed poor performance of estimation when delamination locates near the center of the charged electrodes. The zigzag shape caused by the matrix cracking has large effect on the performance of estimations when the delamination locates at the center segment of charged electrodes. In this paper, the problem is overcome by introducing the non-symmetric charging concept to the electrical potential method. The validity of this method has been shown by means of FEM analyses.
1024
Delamination Monitoring of CFRP Laminates
REFERENCES 1. 2. 3.
4.
5.
6.
7.
A. Todoroki and H. Suzuki. 2000: "Health monitoring of internal delamination cracks for graphite/epoxy by electric potential method," Applied Mechanics and Engineering, 5(1): 283-294. A. Todoroki and Y Tanaka. 2002. "Delamination identification of cross-ply graphite/epoxy composite beams using electric resistance change method," Composites Science and Technology, 62(5): 629-639. A. Todoroki, Y. Tanaka and Y. Shimamura. 2002. "Delamination monitoring of graphite/epoxy laminated composite plate of electric resistance change method," Composites Science and Technology, 62(9): 1151-1160. A. Todoroki, M. Tanaka, Y. Shimamura, H. Kobayashi. 2003. "Analysis of the Effect of the configuration of the delamination crack on delamination monitoring with electric resistance change method," Journal of the Japan Society for Composite Materials, 29(3): 113-119. A. Todoroki, M. Tanaka and Y. Shimamura. 2003. "High performance estimations of delamination of graphite/epoxy laminates with electric resistance change method," Composites Science and Technology, 63(13): 1911-1920. A. Todoroki, M. Tanaka and Y. Shimamura. 2002. "Measurement of orthotropic electric conductance of CFRP laminates and analysis of the effect on delamination monitoring with electric resistance change method," Composites Science and Technology, 62(5): 619-628. M. Ueda, A. Todoroki, Y. Shimamura, H. Kobayashi: Advanced Composite Materials, (to be published)
Damage Detection in Glare plate-like structures S.C. Rosalie and W.K. Chiu* Department of Mechanical Engineering, Monash University, Victoria 3800, Australia
ABSTRACT With the development of new technology and use of lightweight material such as composite laminates, new methods must be developed for in-situ structural health monitoring of these materials. In this paper, a numerical study of a new method for the detection of delamination present in Glare plate-like structures is introduced. The method is based on the change in the group velocity of Lamb waves with frequencythickness product as the determinant parameter for the detection of delamination. The generation of selective Lamb mode was numerically simulated using a finite element method and the finite element analysis was based on the transmitted signal. The numerical results were validated against analytical predictions and indicated good agreement. It was found that the method enabled the detection of delamination in the Glare specimens, showing an increase in group velocity when delamination occurs. INTRODUCTION Fibre reinforced metal laminates (FRMLs) consist of alternating metal sheets and fibre reinforced epoxy layers. FRMLs have been tested extensively in recent years to assess their mechanical properties in comparison to those of traditional isotropic materials. It was found that these hybrid materials offer some superior mechanical properties compared to more traditional materials. These properties enable them to be applied in fibre bridging, which impede crack propagation of the aluminium alloy layers under tensile cyclic loading, for instance. Also, significant weight savings can be achieved due to the specific strength and stiffness in the fibre direction of FRMLs compared to the normal aluminium alloys. One of these FRMLs is Glare, with its most common form constructed using aluminium with glass fibre reinforcing. The outer layer of aluminium protects the glass fibres against strength reduction from environmental and impact damage. A common phenomenon in composite laminates under cyclic loading is delamination. When delaminations occur, the strength of the composite material is greatly reduced, causing the material layers to act independently. These delaminations can have catastrophic consequences when they occur in load bearing structures. Therefore, the early detection of delaminations in critical applications, such as on aircraft fuselage, is vital in maintaining the structural integrity. There are many techniques available for detection of delaminations [4-11], however not all can be applied in practical situations. An attractive ultrasonic NDE method is the use of Lamb or plate waves. Numerous workers have investigated the use of Lamb waves for 'Corresponding Author: Department of Mechanical Engineering, PO Box 31, Monash University, Victoria 3800, Australia; Tel: +61 3 9905 5595 Fax: +61 3 9905 5595; E-mail: Wing. Kong. [email protected]. an:
1026
Damage Detection in Glare plate-like structures
the ultrasonic inspection of structural components in numerical and experimental studies [1-11]. The application of Lamb waves has long been acknowledged in the literature as a potential solution for large area scanning as they are able to travel relatively long distances, allowing the entire thickness of the material between transmitter and receiver to be interrogated [1,11]. Moulin et al. [9] undertook a numerical study of Lamb wave propagation using finite element methods in composite material. This analysis modelled the generation of Lamb waves using small surface-bonded or embedded piezoceramic transducers. These transducers were used in conjunction with a carbon reinforced epoxy [O32] composite of total thickness of 4mm. The results showed that their technique provided an accurate representation of the physical situation through comparison of the finite element model results to experimental data, and therefore that the method could be used to study the behaviour of Lamb waves generated from embedded transducers. Grondel et al. [7] used similar composite material and further investigated an optimal configuration of the surface or embedded transducers for selective mode generation, namely, the Ao mode. Both the theoretical and experimental investigations showed the possibility of designing transducers to make the damage sensitive Ao mode more dominant over the So mode in orthotropic composites. The selective Lamb mode technique outlined by Grondel et al. [7] was then shown to have a large sensitivity of the Ao mode to composite damage. Diaz V aides and Soutis [6] investigated the application of Lamb waves in detecting delamination in thick composite laminates. The paper discussed the use of various methods of producing anti-symmetric Lamb waves, and focused on interdigital transducers (IDTs). Tests were performed on narrow beam specimens made of aluminium and composite material. Using this technique, they were able to detect delamination as small as 100-mm2. Finally, they employed finite element analysis to model qualitatively the response of laminate plates to wave propagation and substantiate their experimental results. Even though, it can be seen that there has been much comprehensive research completed on the use of Lamb waves for flaw detection in composite materials, there has been no specific testing of their effectiveness in Glare. With Glare now being incorporated into the upper fuselage of Airbus aircraft; a very safety critical application, it is important to determine whether this material could eventually be used in a continuous health monitoring system within a smart structure. The aim of this investigation is to determine the applicability and effectiveness of Lamb waves for detection of delaminations in Glare.
BACKGROUND Lamb waves can propagate in the plane of a plate-like structure in two possible modes; symmetric mode, Sn, or asymmetric mode, An, with respect to the middle of the vertical plane of the plate, n being the order of the mode. The velocities of Lamb waves are functions of the product of the frequency of excitation and thickness of the plate. At any given frequency of excitation, there are several modes of Lamb waves present. Hence, the selection of the frequency-thickness product determines the Lamb modes present in the plate-like structure. It is possible to numerically excite certain modes at a preferred frequency by satisfying two conditions. Firstly, the frequency of excitation must be appropriate to excite the desired Lamb mode and secondly, the variation of excitation with z , the thickness of the plate-like structure at the excitation position (x = 0) must correspond
Damage Detection in Glare plate-like structures
1027
to the exact mode shape(s) of the Lamb mode(s) being excited [1]. The selection of the frequency-thickness product also determines the dispersion properties of Lamb waves propagating in the specimen being interrogated. Figure 1 shows a Dispersion curve of a 1.5-mm thick aluminium plate and a 4-mm thick Glare, generated from Disperse®, a program developed by Lowe (1992). The through thickness displacement components of the symmetric Lamb waves are obtained from the following equations: d
M,
[ cosh q z
2q s
cosh s z
-~-
—
=Ak\ ^ sinned
w, =-/
1
(1)
ks —ss svahssd
2k] k] + s] sinh std
^ sinh qsd
(2)
where M,and wsare the displacements in x and z directions, respectively, ft, is the wave number of the symmetric Lamb modes, qt = k] - k\, and s) = k] - k\. A similar set of equations can be obtained by changing the subscript s to a, and replacing sinh by cosh and vice versa [1,10].
,~*X'~ ,• '^
1
^
Aluminium AQ
Glare A. '^
2 3 Frequency-thickness (MHz-mm)
4
FIGURE 1 Dispersion plot for Lamb waves propagating in a 1.5-mm thick aluminium substrate and in a 4-mm thick single layered Glare
THEORY The method for detecting the presence of delamination in Glare formulated in this paper is as follows. As previously mentioned, the velocity of Lamb waves is a function of the product of frequency of excitation and thickness of specimen being excited. From figure 1, it can be seen that for a change in frequency in a region of constant thickness or a change in thickness at constant frequency, the group velocity will change. Based on this physical relationship, it was hypothesised that the group velocity of a fundamental Lamb mode increases when delamination occurs. This phenomenon will be demonstrated in this paper. However, there are other factors that need to be considered in this hypothesis. One of these factors is that their velocity is also highly dependent on the stiffness, or Young's modulus of the specimen [8]. In a
1028
Damage Detection in Glare plate-like structures
specimen with lower stiffness, the Lamb waves travel slower than in one with higher stiffness. This is clearly demonstrated in figure 1 where the presence of glass fibres causes the overall group velocity of Lamb waves to decrease in the Glare analytical model as compared to the group velocities in a 1.5-mm thick aluminium-5005. NUMERICAL STUDY Numerical Model Development A schematic of one of the Glare two-dimensional numerical models is shown in figure 2 and is not to scale. The Glare model was 200-mm long and 4-mm thick and consisted of a single alternating layer of aluminium substrate and uni-directional glass fibre reinforced epoxy matrix. The mesh density was such that there were 15 nodes per wavelength and 7 nodes in the thickness to describe the mode shape of the desired Lamb mode. The models were clamped at one end to simulate in-situ conditions, and were excited at x=0-mm using a 10-cycle sine wave tone burst input signal with centre frequency of 0.4-MHz (i.e., 1.6-MHz-mm in Glare) windowed by a Hanning function. The frequency was selected on the basis of an impulse analysis to determine the dominant frequencies of the Glare and the group velocity characteristic of the Lamb modes at the frequency chosen. This is further explained in the results and discussion. The signals were acquired at positions x = 60-mm and x = 140-mm. These corresponded to positions before and after the delamination region respectively. The delamination was 60-mm long and centrally located. The bulk properties of the aluminium strips and the glass fibre reinforced epoxy matrix are tabulated in table 1.
Unidirectional EGlass Fibre Reinforced Epoxy Matrix ~~
1.5-mmthfck Aluminium-5005
Delamination Region
FIGURE 2 Schematic of Glare Numerical model with delamination
TABLE I Mechanical Properties of Glare
Aluminium-5005 E [GPa] 71 i) 0.33 P [kgm3] 2700
GFR-Epoxy E n [GPa] 15.08 E22 [GPa] 8.92 Gi2 [GPa] 3.18 0.38 t>12 0.22 1>21 1532 P [kgm3]
Damage Detection in Glare plate-like structures
1029
Selective Mode Excitation Method In this paper, the study was focussed on simulating a surface contact method, which involves excitation of the fundamental So [12]. The frequency regime chosen for the current study ensured that only the fundamental modes could be present in the aluminium substrate whereas the highest order mode that could be present in the Glare model was the Ai mode. The fundamental So mode was selected because of the very large difference between its group velocity in the aluminium substrate and its group velocity in Glare at the frequency chosen. RESULTS AND DISCUSSION The results obtained from the numerical study were very promising. It was found that the group velocity of Lamb waves increased when delamination occurred in Glare. This is explained by analysing the time histories of propagating Lamb waves before, over and after the delamination in the damaged model and of the corresponding regions in the undamaged model. A two-dimensional Fast Fourier Transform was performed on the time histories of 128 nodes over each of the aforementioned regions. The contour plots are presented in figures 4(a) to 4(f). It was found that prior to the Lamb waves propagating over the delamination region, the Ai and So modes corresponding to those of the Glare analytical model were present in both the damaged and the undamaged model. The Ai mode in Glare was generated at the excitation even though the through thickness displacement corresponded to the mode shape of So in Glare. This phenomenon could not be explained and needs to be further investigated. When the Lamb waves travelled over the delamination, the Lamb modes present were the Ao and So modes corresponding to those of 1.5-mm thick aluminium analytical model, whereas in the undamaged model, the Lamb modes were unchanged. This phenomenon occurring in the damaged has the effect of an increase in the group velocity of the Lamb waves since the Lamb waves were travelling in thinner material, that is, at a frequency thickness of 0.6MHz-mm in Aluminium substrate. Figures 3 (a) and (b) show the increase in group velocity when delamination occurs and further confirms our experimental results [12].
10
20
30
40
50
60
70
Time(microsec)
10
20
30
40
50
60
70
50
Time(microsec}
(b) FIGURE 3 (a) Time history for transmitted signal at X = 60-m; (b) Time history for transmitted signal at x =140-mm
Past the delamination region, the propagating Lamb modes were those of So mode in the Glare and the So mode in the aluminium substrate. However, in the corresponding region in the undamaged model, the So mode travelling the Glare had a
1030
Damage Detection in Glare plate-like structures
low energy level whereas the So mode in the aluminium substrate has energy level comparable to that in the damaged model. There are two reasons for this phenomenon. Firstly, according to the Dispersion plot for So mode in Glare, it can be seen that at 1.6-MHz-mm, the Lamb mode is highly dispersive. Secondly, the group velocity of So in Glare is very low compared to that in the aluminium substrate. Hence, if the number of time steps were increased in the finite element analysis, this would have allowed the So mode in Glare to propagate a greater distance and hence, the energy level of So would have been higher. However, since only the transmitted signal was being analysed, the time gating was necessary. •-— Glare A. ^ GtoS Glare A, AIAO
2500
1
umber(
•O2000
i
h
>1000
500
f
Q.6 Frequency(MHz)
Frequency(MHz)
(a)
(b)
2500
— •
Glare A o Glares Glare A,
—
AIS0
I
2300
|2000
|2000
O •|1500
•91500
- — Glare A o ^ Glare SQ • Glare A, A1A,, __AIS0
1
c >1000
>1000
500
500
0
0.2
Frequency(MHz)
(c)
r.
0. 0.6 Frequency(MHz)
0.8
(d) - ^ Glare A o - — Glare So Glare A, ...... AlAj, — Also
Frequency(MHz)
Frequency(MHz)
(e)
(f)
FIGURE 4 Comparison of two-dimensional FFT analysis of numerical results compared to analytical results from Disperse 0 for the transmitted signal (a) before the delamination region in undamaged numerical model; (b) before the delamination region in damaged numerical model; (c) over the delamination region in undamaged numerical model; (d) over the delamination region in damaged numerical model; (e) after the delamination region in undamaged numerical model; (f) after the delamination region in damaged numerical model;
Damage Detection in Glare plate-like structures
1031
CONCLUSIONS This paper demonstrates the potential for the use of the change in group velocity of Lamb waves as a powerful tool for the detection of the presence of delamination in Glare. The numerical results presented in this paper have confirmed our experimental results [12]; That is, the group velocity of low orders Lamb modes increases when delamination occurs in Glare and that this is shown through a selective mode excitation and analysis. Further studies will include a numerical analysis of a threedimensional model with increasing delamination size in the Glare. REFERENCES l.AUeyne, D.N., and P. Cawley. 1991. "A two-dimensional Fourier transform method for the measurement of propagating multimode signals,"/ Acoust. Soc. Am., 89(3): 1159-1168. 2.AUeyne, D.N., and P. Cawley. 1992. "The interaction of Lamb Waves with Defects," lEEEJrans. Ultras. Ferroelectr. Freq. Control, 39:381-397. 3. Alleyne, D.N. and P. Cawley. 1994. "The Practical Excitation and Measurement of Lamb Waves using Piezoelectric Transducers," Review of Progress in Quantitative NDE, 13:181-188, edited by D.O. Thompson andD.E. Chimenti (Plenum Press). 4. Cawley, P. 1990. "Low Frequency NDT Techniques for the detection of Disbonds and Delamination", British Journal of NDT, 32(9):454-460. 5. Diaz Valdes, S. and C. Soutis. 2000. "Health monitoring of composites using Lamb waves generated by piezoelectric devices," Plastics, Rubber and Composites, 29(9):475-481. 6. Diaz Valdes, S. and C. Soutis. 2002. "Real-time non-destructive evaluation of fibre composite laminates using low-frequency Lamb waves,"/ Acoust. Soc. Am., lll(5):2026-2033. 7. Grondel, S., C. Paget, and K. Levin. 2002. "Design of optimal configuration for generating Ao Lamb mode in a composite plate using piezoceramic transducers," J. Acoust. Soc. Am., 112(l):84-90. 8,Kessler, S.S., S.M. Spearing, and C. Soutis. 2002. "Damage detection in composite materials using Lamb wave methods," Smart Materials and Structures, 11:269-278. 9.Moulin, E., J. Assaad, and C. Delebarre. 2000. "Modelling of Lamb waves generated by integrated transducers in composite plates using a coupled finite element- normal modes expansion method," J. Acoust. Soc. Am., 107(1): 87-94. 10. Viktorov, I. 1967. Rayleigh and Lamb Waves, Plenum Press, New York, U.S.A 11. Worlton, D.C. 1957. "Ultrasonic Testing with Lamb Waves", Non-Destructive Testing, 15:218-222. 12. Rosalie, S.C., M. Vaughan, A. Bremner, W.K. Chiu, (2003), "Variation in the group velocity of Lamb waves as a tool for the detection of delamination in Glare aluminium plate-like structures", presented at the 12th International Conference on Composite Structures November 17-19,2003.
Quantitative Nondestructive Evaluation in Composites Beam Using Piezoelectrics Young-Geun Choi, Zhongqing Su, Zuo-Rong Chen and Lin Ye Centre for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering J07, The University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT A quantitative prediction method for initial crack length in a carbon fibre/epoxy (CF/EP) composites beam using active piezoelectric transducers was established in this study. Wavelet Transform (WT)-based signal processing and identification technique in time-frequency domain was developed to facilitate the determination of damage presence and severity. Dynamic response of a CF/EP composites beam containing a continuously expanding crack, coupled with a pair of active piezoelectric disks, was examined under a narrowband excitation, and then applied with the proposed signal processing technique. INTRODUCTION Though serving as competitive candidates to meet current and future challenges imposed on aeronautical vehicles, carbonfibre/epoxycomposite structures still run a large risk of losing efficiency under occurrence of structural damage, which can potentially lead to catastrophic failure of the whole system if without timely detection. Quantitative nondestructive evaluation (QNDE) therefore plays an essential role in confident acceptance of composite materials and structures. Amongst them, the detection approaches based on the elastic wave propagation have been attracting more and more attentions from both researchers and engineers, regarded as one of the most promising solutions to the quantitative assessment of the structural deterioration and the prevention for catastrophic failure. On the other hand, signal processing is a key point to make an identification scheme applicable and understandable. Wang and Chang [1] discussed the damage detection technique based on the Lamb wave generated by ultrasonic transmitter, and Lemistre et al. [2] reported a structural defect identification method using piezoelectrics. The wavelet transform can also be used to detect the arrival times of the dispersive waves propagating in plates. There has been intense research activity in the application of wavelets in various fields of science and engineering [3-5], The present work aims at developing a practical and effective real-time damage identification technique for Carbon/Epoxy composite materials. For this purpose, a damage diagnosis system incorporated with a piezoelectric transducer, in correlation with an elastic wave propagation model, was developed. The validity of this system was then investigated by applying it to a composites beam bearing a transverse crack with an increasing length, simulating the damage growth. It is shown that the damage parameters, including the damage presence, location and its variable severity, can be identified promptly and accurately using this technique. * Corresponding author, Centre for Advanced Materials Technology, School of Aerospace, Mechanical and Mechatronic Engineering J07, The University of Sydney, Sydney, NSW 2006, Australia, +61-2-9351-3760, ve(S,aeromech.usvd.edu.au
Quantitative Nondestructive Evaluation in Composites Beam
1033
EXPERIMENTAL SETUP The composite materials used in this study were unidirectional carbon/epoxy laminates. The carbon fibers used were T300 fibers and the epoxy matrix was the CIBA 934. An active online damage diagnosis system was established in accordance with the identification principle, sketched in Figure 1. It consists of Signal Excitation Unit (SEU), Signal Acquisition Unit (SAU) and Central Control Unit (CCU). A transducer network was designed using Piezoelectric Lead Zirconate Titanate (PZT) wafers, 6.9mm in diameter and 0.5mm in thickness, which was surface-bonded on each laminate and controlled by the SEU and SAU.
asss H—(»-»
L _
I
Agilent
Amplifier Piezo Sys EPA-.
•ioA
H . Generator Switch
FIGURE 1 Configuration of diagnosis system based on VXI platform
In order to evaluate the effectiveness of the proposed model and identification scheme, the diagnosis system was then applied to a defective CF/EP cantilever beam (cross-section of 15mm x 1.16mm) as shown in figure 2. The beam has a small crack at edge which is perpendicular to the beam axis. The width of the crack is 0.39mm and its length varied from 0.343mm to 11.720mm gradually long.
1.16 250
FIGURE 2 Experiment setup (dimensions in mm)
NUMERICAL APPROACH Finite element analyses (FEA) were performed for the elastic wave propagation in a composites beam with a transverse crack using a three-dimensional model. As shown in figure 3, the PZT actuator and sensor were assumed to be completely adhered to the composites beam. The physical properties of the composites beam and the PZT actuator and sensor are listed in Table 1.
1034
Quantitative Nondestructive Evaluation in Composites Beam
TABLE I Geometry and physical properties of the materials used in this study Properties Geometry [mm] 3
PZT
Carbon/epoxy
0:6.9, hpzT: 0.5
250x15x1.16
Density, p [g/cm ]
7.80
1.52
Poisson 's ratio, v12
0.31
0.22
Young's modulus, Eu[GPa]
66.7
131
Young's modulus, E22[GPa] Young's modulus, E33[GPa]
103 86.2
103
Shear modulus, G,2, G,3, G23[GPa] Charge constant, d31 [m/Vj Charge constant, d33 [m/Vj
6.9 -IJOxia'2 450x10'12
A very fine mesh was employed in the crack region and the region where the PZT actuator and sensor adhere to the composites beam. The eight-node linear brick element was employed to model both the composites beam and the PZT actuator and sensor, and the total number of elements was. The end close to the PZT actuator was geometrically constrained to simulate the cantilever beam boundary condition. The input electrical signal in experiments was transformed into excitation force which was applied on the PZT actuator in FEA model. The analyses of elastic wave propagation process were carried out based on a dynamic explicit method by using a commercial finite element code ABAQUS/Explicit (Version 6.2). hi order to investigate the effect of crack length on the elastic wave propagation in the composites beam, various crack lengths were modeled, and the averaged stress of the PZT sensor was adopted as an indicator for assessment. The averaged stress of the PZT sensor was calculated, which was then processed by using Wavelet Transformation analysis. First, the analysis of the beam without crack was carried out for comparison. Then the beams of different crack lengths were analyzed and compared with that without crack. PZT Actuator
Crack
Composite I! MM
*" - - ^
P Z T Sensor
FIGURE 3 Geometry of the finite element model
RESULTS AND DISCUSSION Signal Analysis
Quantitative Nondestructive Evaluation in Composites Beam
1035
In figure 4, relationship plots of amplitude versus time for tests at different crack length are displayed. Containing the structural vibration components and diverse bandwidth noises, the acquired raw signals can hardly be used for the evaluation of damage detection. Daubechies function, *F (a, b), at level 8 (dblO) was chosen as the wavelet transform function and the Continuous Wavelet Transform (CWT) of a function f(t) is defined by [6,7]: Wf (a,b) =
(t) • -dt = (1) Va _ where a and b are the scale and time shifting (or translation) parameters, respectively. The wavelet transform Wf is the wavelet coefficient for the wavelet *P* (t) with dilation a and position b. The function *F (t) is termed as the mother (basic) wavelet serving to analyze an arbitrary sampled signal f(t). The *F *(t) denotes the complex conjugate of *F (t). If the transform is invertible, the inverse wavelet transform exists:
where a is positive and Cw is a constant that depends only on *F (t). The sampled signal f(t) passes through two complementary filters and can be analyzed into low frequency [Approximations (A's)] and high frequency [Details (D's)] signals. Wavelet transform provides how to analyze the vicinity of location using variable scale. The analytical results by the Discrete Wavelet Transform (DWT) at the 8th level for signals via PZT actuator-sensor shown in figure 4 is displayed and illustrated in figure 5. In this work, the damage degree regarded as a singularity involved in the signal, was determined using the CWT and DWT spectrographic analyses. The damage degree was calibrated upon the relation with the normalized energy. Spectrographic analyses based on the CWT and DWT techniques [8] were accordingly executed. A series of band filters with proposed threshold and different frequency scopes were designed and applied on the sampled signals to suppress the diverse interferences and effectively extract diagnostic components. Thus the interrogation on the sampled signals can be concentrated in a specific frequency scope.
i I ! |
0.0 -0.2 -0.4 -0.6 -0.8 -1.0 -1.2 66 Time [MS]
(a)
(b)
Quantitative Nondestructive Evaluation in Composites Beam
1036
(c)
(d)
FIGURE 4 Raw sampled signals via two piezoelectric transducers (a) Without-crack from experiment (b) crack of 3.12 mm from experiment (c) Without-crack from FEM (d) crack of 3.12 mm-asA from FEM
Meanwhile, in this work, the Sampling Point (SP) was hereafter introduced instead of the direct Time Point (TP) in CCU to expedite and facilitate the data processing procedure. The DWT analytical results at level 8 for without crack and 3.12mm cracks are displayed in Figure 5 for comparison. In the meantime, the 2D and 3D spectrographic analyses via CWT were performed.
1300
1400
Sampling Points
1200
1300 1400 Sampling Points
(a)
(b)
3.12 mm-Crack
1.0 0.8 0.6 0.4 0.2 0.0
-0.2 •0.4 -0.6 -0.8 -1.0 -1.3
A A
fI M A f I /1 / i
A / \
V
"
Sampling Points
(c)
A
I
^^-\/~\ j \ } \ I \ I \ I \ } \i l / l / \ / \ / \/
(d)
FIGURE 5 Detail at level 10 by DWT analysis for signals in Figure3 (a) Without-crack from experiment (b) crack of 3.12 mm from experiment (c) Without-crack from FEM (d) crack of J.72 mm-crack from FEM
Quantitative Nondestructive Evaluation in Composites Beam
1037
Damage Diagnosis The damage diagnostic results were achieved via the proposed identification scheme and the actual damage parameters are compared in Table II. TABLE II Diagnostic results and relative percentage errors for crack severity Damage Diagnosis [mm] Actual Damage Length [mm]
Calculated Value by Integration Method
Minimum Error of Prediction [ % ]
0341 1.016 1.780 3.120 4.613
0.320 1.051 1.741 3.152 4.646
6.70 3.44 2.19 1.02 0.72
CONCLUSIONS This paper showed that the wavelet transform to the experimental time-frequency domain analysis has been developed as a damage detection method for the beam structures. The Continuous Wavelet Transform (CWT) analysis and the Discrete Wavelet Transform (DWT) analysis are shown to a very effective method in damage detection of a unidirectional carbon/epoxy beam. An identification and monitoring scheme for structural damage has been developed in correlation with the excitation response analysis, and its validity was examined experimentally through a quantitative diagnosis for the size of damage with an increasing depth in a two-dimensional structural beam. REFERENCES 1. 2.
3. 4. 5.
6. 7. 8.
Wang, C. S. and Chang, F. K., 1999, Built-in diagnostics for impact damage identification of composite structures. In: Chang F. K., editor. Structural Health Monitoring. Lancaster: Technomic, pp. 612-621. Lemistre, M., Guoyon, R., Kaczmarek, H. and Balageas, D., 1999, Damage localization in composite plates using wavelet transform processing on Lamb wave signals. In: Chang F. K., editor. Structural Health Monitoring. Lancaster: Technomic, pp. 861-870. Chui, C. K., 1992, An introduction to wavelets, San Diego: Academic Press. Ruskai, M. B., Beylkin, G., Daubechies, I., Meyer, Y., Coifman, R. R., Mallat, S. and Raphael, L., Eds. 1992, Wavelets and Their Applications, Boston, MA: Jones and Bartlett. Jeong, H. J. and Jang, Y. S., 2000, Fracture source location in thin plates using the wavelet transform of dispersive waves, IEEE transactions on ultrasonics, ferroelectrics, and frequency control, 47,3, pp. 612-619. Chan, Y. T., 1995, Wavelet basics, Kluwer Academic Publishers, Boston, 1st Edition. Chui, C. K., 1997, Wavelets: A mathematical tool for signal analysis, SIAM, Philadelphia, 1st Edition. Boashash, B., Time-Frequency Signal Analysis, Methods and Applications. (Longman Cheshire Press, 1st edn, Melbourne, 1992).
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Part XVIII
Textile Composites
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Mechanical Properties of Textile Hybrid Composite Miyako Inoda1, Kenichi Sugimoto2, Asami Nakai2 and Hiroyuki Hamada2* 'Kyoto Institute of technology, Japan 2 Graduate school of Kyoto Institute of Technology Kyoto, 606-8585, Japan
ABSTRACT In order to fabricate thick composite laminates, the large number of stacking process is generally required. The thickness was easily increased by placing knitted fabric with bulky characteristic. Textile hybrid composite consisting of woven fabric, knitted fabric and braided fabric can be a new concept of textile composites. In this paper, the impact property of textile hybrid composites was investigated. Two woven fabrics were placed at outer layer, and one or two knitted fabric was placed at core layer, in textile hybrid composite. The energy for failure propagation in textile hybrid composite was higher, while in elastic energy calculated from elastic recovery was lower. The absorbed impact energy was higher compared with strain energy obtained from static bending test.
INTRODUCTION Textiles such as woven, knitted and braided fabric consist of continuous fiber, so that higher mechanical property can be obtained. Moreover the textile can be treated as the pre-form material, therefore complicated shape of structural components can be easily fabricated. The mechanical properties of knitted fabric composites are lower than woven and braided fabric composites due to its fiber loop configration, on the other hand, the knitted fabric has higher drapability than the others [1-3]. Moreover, knitted fabric is more bulky, so that large thickness of composite laminates can be obtained by a fewer number of layers compared with woven fabric composites. In general, in order to fabricate a thick composite, the number of plies is increased to the specified thickness. Also for taking into account of bending stiffness, the mat or forming materials have been inserted as a core component of sandwich plates. Similarly, a new thick composite with higher performance, which increases mechanical properties and decreases fabrication costs, can be achieved by combination of textiles. Textile hybrid composite consisting of woven fabric, knitted fabric and braided fabric can be a new concept of textile composites. The woven fabric and knitted fabric were placed at skin and core materials respectively. The thickness of plate can be increased easily by small stacking process. For example, 16 plies of woven fabrics were required to make 3mm thickness in case of only woven fabric composites laminates, on the contrary, hybrid composites with 3mm thickness could be fabricated by using 4 plies of woven fabrics and 2 plies of knitted fabrics. In this study, impact properties of textile hybrid composite laminates were * Corresponding author, Email: [email protected]
Mechanical Properties of Textile Hybrid Composite
1042
investigated. Two types of applied energy were used in order to investigate the relation between fracture aspects and impact load and energy. In addition, the energy absorption property was compared with static bending test. EXPERIMENTAL METHOD Materials As reinforcements, glass plain woven fabric (WE18E, Nitto Boseki Co., ltd.) and rib knitted fabric made of the glass fiber (DB450 1/2 44S Y23, Nippon Electric Glass Co., ltd.) were used. The schematic drawings and overviews of woven fabric and knitted fabric are shown in Fig. 1. Vinyl ester resin (RIPOXY R806, Showa high polymer Co., ltd.) was used as matrix. The schematic drawings of stacking sequence of the specimen are shown in Fig. 2. W14 with 2.49 mm thickness consisted of fourteen woven fabrics in which the directions of each fabric were same. In W2K1W2 with 2.95 mm thickness, two woven fabrics were placed at both outer layers and a knitted fabric was inserted at core layer. Similarly, W2K2W2 with 4.71 mm thickness was with two knitted fabrics at core layer. In both W2K1W2 and W2K1W2, the warp direction of woven fabric was corresponded to the wale direction of knitted fabric. All specimens were fabricated by hand-lay-up technique. Warp
Plane-woven fabric
Rib-knitted fabric
(a)
FIGURE 1 Schematic diagrams and overviews of (a) plane-woven fabric and (b) rib-knitted fabric. Woven fabric Knitted fabric
W14
(a)
W2K1W2
(b)
W2K2W2
(c)
FIGURE 2 Schematic diagrams of stacking sequence in textile hybrid composite laminates.
Mechanical Properties of Textile Hybrid Composite
1043
Impact test For impact test, the 100 mm squared specimen was cut from the molded plate by diamond saw. The drop weight impact test was performed by using INSTRON impact testing machine (Type 8510). The specimen was fixed in circular with 76 mm diameter , and the 5.0 kg weight striker which has spherical nose with 6.4 mm radius was dropt to the center of circular fixture. Two types of applied impact energy were used by changing the drop height. One was 5 J applied energy, and the other was 40 J in which the striker completely penetrated through the specimen.
RESULT AND DISCUSSION Figure 3 (a) indicates the load-deflection curves of each specimen at applied energy of 5 J. In all specimens, the deflection was decreased after the maximum load because the striker did not penetrate. In W2K1W2, the load dropped at maximum value and kept the almost constant value. On the other hand, W14, W2K2W2 did not show the drastic decrease at the maximum load as shown in W2K1W2. The fracture aspects in top and bottom sides are shown in Fig. 4. In all specimens, the dent caused by hit of the striker was observed at top sides, and the whitening caused by the delamination and radial crack were seen at bottom sides. At the top sides, W2K1W2 and W2K2W2 showed the buckling of weft fibers of woven fabric. The whitening at bottom side of the W14 and W2K2W2 was the circular region, on the other hand, that of W2K1W2 was elliptical region and fiber breakage in weft fiber of woven fabric was observed. From these pictures, the magnitude of the damage was different in each specimen. The degree of the damage in W14 seemed to be the lowest, and that in W2K1W2 seemed to be the highest. The initial peak load; Pm, elastic energy; UE and absorbed energy, Uab are summarized in Table 1. UE and Uab are defined as shown in Fig. 5(a). UE means the energy for elastic recovery after impact testing. In order to compare these specimens with different thickness, Pin, UE and Uab normalized by the laminate thickness are indicated in Table 1. W2K1W2 was lower Pin/t by 28 % and U^t by 41 % than W14 and was almost same as W2K2W2. Uab/t of W2K1W2 was almost same as that of W14, and that of W2K2W2 was the lowest. Impact energy 5J
Impact energy 40J
W2K2W2 W14
W2K1W2
6 Deflection (mm) (a)
0
10 15 Deflection (mm)
20
(b)
FIGURE 3 Relationship between impact load and deflection in (a) 5J and (b) 40J applied energy.
Mechanical Properties of Textile Hybrid Composite
1044
Top side
Bottom side
(a)
(b)
(c)
FIGURE 4 Fracture aspects in top side of (a) W14, (b) W2K1W2 and (c) W2K2W2 at 5J impact energy.
Deflection
(a)
Deflection
(b)
FIGURE 5 Definition of (a) elastic energy and absorbed impact enerty in 5 J applied energy and (b) energy for initial peak load and propagation energy in 40 J applied energy.
TABLE I Experimental results in 5J applied energy. Thickness Initial peak load Elastic energy Absorbed impact P l n / t energy, Uab (J) (kN/mm) U E (J) t (mm) Pin(kN) W14 2.487 2.19 2.03 3.34 0.88 0.64 W2K1W2 2.950 1.88 1.43 3.89 (T0.28) 0.63 W2K2W2 4.707 2.97 2.30 2.96 (T0.29)
UE/t U a b /t (J/mm) (J/mm) 0.82 1.34 0.48 1.32 T0.41) (T0.02) 0.49 0.63 T0.40) (TO.54)
T m eans decrem e n t com pared w irh W 14
Mechanical Properties of Textile Hybrid Composite
1045
Figure 3(b) indicates the load-deflection curves of each specimen at applied energy of 40 J. The load-deflection curves of W14 and W2K1W2 were the tooth like behavior until the maximum load. The circular mark in this figure was the initial peak load of each specimen. In W14, the initial peak load was corresponded to the maximum load, however, maximum load point appeared after the initial peak load in W2K1W2. W2K2W2 showed two large peak load in which the initial peak load was slightly higher than the second peak load. The fracture aspects in top sides are shown in Fig. 6. In W14, rectangular cave and rhombus whitening were observed. For both W2K1W2 and W2K2W2, the circular cave, whitening along the weft fiber of woven fabric and elliptical whitening were observed.
*:
(a)
(b)
f
(c)
FIGURE. 6 Fracture aspects in top side of (a) W14, (b) W2K1W2 and (c) W2K2W2 at 40J impact energy.
The experimental results obtained from impact test at applied energy of 40 J are summarized in Table 2. In this table, the initial peak load is correspond to the circular mark as shown in Fig. 3(b). The energy to initial peak load, Uin and propagation energy, Upro were defined as shown in Fig. 5(b). Similar to Table 1, normalized Pin, U n and Upr0 by the thickness are indicated in this table. Pjn/t of W2K1W2 and W2K2W2 were lower by 50 % and 44 % than that of W14 respecively. From 5 J to 40 J applied energy, Pin/t of W14 and W2K2W2 was increased, although that of W2K1W2 was not changed. As shown in Fig. 4, W2K1W2 had already showed the fiber breakage at bottom side even though 5 J applied energy, on the other hand, the fiber breakage did not occur in W14 and W2K2W2. Therefore, it was considered that the initial peak load related to the damage at bottom side. Regarding Uin/t and Upro/t, the decrease in Uin/t of W2K1W2 and W2K2W2 were much lower by 65 % and 49 % than that of W14 respectively, however, the degree of decrease in Upro/t of W2K1W2 and W2K2W2 were 22 % and 27 % than that of W14. As a result, Upro/Ura of W2K1W2 and W2K2W2 were much higher than that W14. The reason of this result was considered that higher impact energy was absorbed by high deformability of knitted fabric during the impact failure progression. Table 3 indicates the absorbed energy for final failure normalized by the thickness in static bending test at three types of loading direction. The absorbed energy of W2K1W2 in wale, course and 45 degree directions was lower by 68 %, 77 % and 66 % than that of W14 in warp, weft and 45degree directions respectively. For
1046
Mechanical Properties of Textile Hybrid Composite
comparison between impact and static test in W2K1W2, absorbed impact energy was greater than static absorbed energy. The reason of this result was considered that the impact damage included the delamination which was shown as whitening, while in static delamination was hard to be generate. Consequently, it was expected that the textile hybrid composite with knitted fabric was effective to the application which required both high impact performance and progressive failure. TABLE II Experimental results in 40 J applied energy. Thickness t (mm) 2.487
W14 W2K1W2
2.950
W2K2W2
4.707
Propagation P,n/t Um/t u p r o / t u pro /u in energy, Upr0 (J) (kN/mm) (J/mm) (J/mm) Uia (J) (-) 3.43 18.13 1.38 4.05 7.29 1.80 10.08 0.69 1.43 5.69 3.99 2.03 16.80 4.21 (•0.50) • 0 . 6 5 ) (•0.22) (A 1.22) 2.07 5.29 0.78 2.56 3.65 24.92 9.72 (•0.44) • 0 . 4 9 ) (•0.27) (A0.43) • and A m eans decrem ent and hcrem ent com pared w ith W 14 respectively
Initial peak load, P in (kN)
Energy to Pin
TABLE III Absorbed energy / thickness of static bending test.
Thickness Absorbed energy, Uab (J) t (mm) A 1.914 W14 2.50 E 2.005 45° 4.354 W 0.730 W2K1W2 C 2.95 0.545 45° 1.753 W 2.151 W2K2W2 C 4.71 1.234 45° 3.493 Sample
Increased ratio Uabft ofU ab (-) (J/mm) 0.766 1.00 0.802 1.00 1.742 1.00 0.247 (T0.68) 0.185 (T0.77) 0.594 (T0.66) 0.457 (T0.40) 0.262 (T0.67) 0.742 (T0.57)
CONCLUSION In this paper, the impact property of textile hybrid composites was investigated. Woven fabric and knitted fabric were placed to surface and core layers respectively. The absorbed impact energy was higher compared with absorbed energy obtained from static bending test. Textile hybrid composite with knitted fabric decreased fabrication process, and showed low energy for elastic deformation and higher energy for progressive fracture. Therefore it was possible that the textile hybrid composite was effective to the application which required both high impact performance and progressive failure. REFERENCES 1.
2.
3.
K.Sugimoto, T.Fukui, M.Inoda, A.Nakai and H.Hamada. 2003. "Mechanical Properties of Knitted Composite with Flexible Interphase,"presented at 8th Japan International SAMPE Symposium and Exhibition, November 1 8 - 2 1 , 2003. S.Ramakrishna, H.Hamada, and D.Hull. 1995. "The Effect of Knitted Fabric Structure on the Crushing Behaviour of Glass-Epoxy Composite Tubes," Impact and Dynamic Fracture of Polymers and Composites, 19, pp. 453-464. Y. Hirai, H. Hamada, and J. K. Kim. 1996. "Damage Modes in Impact Loading of Glass Woven Fabric Composites," Advanced Composites Letters, 5, 2, pp.59-63.
Effects of Fabrication and Processing Techniques of Aramid/Nylon Weft-Knitted Thermoplastic Composites on Tensile Behaviour Omar Khondker*, Tatsuro Fukui, Asami Nakai and Hiroyuki Hamada Advanced Fibro-Science, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan
ABSTRACT Preliminary investigations on the fabrication, processing and tensile behaviour of Aramid/Nylon weft-knitted thermoplastic composites were reported in this paper. An intermediate material called "micro-braided yarn" (MBY) was used to fabricate thermoplastic composites with textile reinforcements. Using a tubular braiding machine Aramid/Nylon66 (AF/PA66) micro-braided (MB) yarns were produced. These MB yarns were subsequently used to produce weft-knitted fabrics having lxl rib architecture. Three types of knitted composites were fabricated by combining microbraiding and compression molding techniques and mechanical tests were conducted to study their tensile behaviour. Tensile properties were also compared with those of Aramid/Epoxy and Aramid/Nylon film-stacked knitted composites. Cross-sectional observations on the selected AF/PA66 MB knitted specimens, by optical microscopy, have confirmed that molding condition at 290°C under the pressure of 2 MPa for 20 minutes could achieve better matrix fusion and improved state of resin impregnation. The overall changes in the mechanical properties were found to be broadly related to several factors such as, continuity in the reinforcing fibres within the preform structure, molding techniques, process-parameters, state of pre-tensioning prior to consolidation and to the fibre/matrix interfacial adhesion.
INTRODUCTION The presence of fibre/matrix interfaces strongly influences the overall mechanical properties of composites. Combination between inorganic fibres and organic matrices can produce high performance composites, such as CFRP and GFRP. However, dissimilar materials do not essentially provide good adhesion properties due to complete difference in nature. The concept of interface-less composites is mainly driven by the need to avoid physical deterioration due to interfacial problems and to achieve improved interfacial, thermal, mechanical, economical and eco-logical benefits. Composites consisting of the same material with a different reinforcement and matrix phase can reveal higher interfacial strength. These new breeds of materials can be defined as "oneunity" composites, which could exhibit little or no chemical mismatch in the adhesion properties, because of the active cohesive forces acting between the fibre/matrix * Correspondence Author, Advanced Fibro-Science, Kyoto Institute of Technology, Matsugasaki, Sakyoku, Kyoto 606-8585, Japan Phone: (81-75) 724 7844 Fax: (81-75) 724 7800 Email: [email protected]
Aramid/Nylon Weft-Knitted Thermoplastic Composites
1048
interfaces. Recent researchers have studied polyethylene (PE) and polypropylene (PP) materials [1-8] as single-polymer composites and have reported an improvement in the interfacial properties. Polyamide (PA) materials were also chosen to combine with aramid fibre in order to extend this family of "one-unity" composites [9-13]. hi this paper, a tubular braiding machine [14] was used to produce micro-braid yarn that has a unique combination of reinforcement and matrix phases. MBY can be treated as a single fibre bundle, so as to fabricate varieties of textile processed goods. Microbraiding technique offers minimum or no damage to the reinforcing fibre bundles, when compared to using commingled yarns. In this study, microbraid yarns were produced using continuous aramid fibre bundle as the straightly inserted axial fibre, and nylon 66 as the matrix fibre that was braided around the reinforcing aramid fibre. Weft-knitting technique was then used to produce narrow and wider fabrics having 1><1 rib architecture. Weft-knitting is a fast, continuous and extremely versatile transformation process for fibres which can produce structural preforms that provide required fibre orientations and through-thickness fibre reinforcement. Three types of AF/Nylon66 MB hybrid knitted composites (Knit 1, Knit 2 and Knit 3) were fabricated by compression moulding technique and tensile tests were conducted to study their tensile behaviours. Properties were also compared with those of Aramid/Nylon6 (AF/PA6) film-stacked (Knit 4) and Aramid/Epoxy (Knit 5) knitted composites [13]. EXPERIMENTAL Fabrication, Composite Processing and Tensile Test 8 spindles of nylon 66 fibres (PA66) were braided around 2 bundles of aramid fibres using a tubular braiding machine to produce continuous microbraid yarns (Figure 1). Micro-braid yarns were then used to produce lxl rib weft-knitted fabrics.
FIGURE 1 Fabrication process of microbraid yarns
FIGURE 3 Tension rig and consolidation setup for compression molding
FIGURE 2 Weft-knit architecture and 1 x 1 rib knitted continuous strip
FIGURE 4 Optical micrographs confirming better matrix fusion and resin impregnation
These fabrics were produced as continuous narrow strips with a nominal width of 2 cm (Figure 2) as well as wider cloths. These MB knitted strips were compression
Aramid/Nylon Weft-Knitted Thermoplastic Composites
1049
molded to produce two types of tensile specimens, namely Knit 1 and Knit 2. Knit 1 composite used a metallic frame as the tension rig (Figure 3) to which the narrow preform strip was attached before being placed in the pre-heated die for compression molding (Figure 3). The tension rig has a spring mechanism to enable adjustment of tension caused by thermal shrinkage. Knit 2 composite specimens were produced in the similar fashion without using the tension rig. Knit 3 composite specimens were compression molded from the wider knitted fabric having a nominal areal dimension of 27cmx27cm without applying any tension load to the preform. The processing condition for these Aramid/Nylon knitted composites was set at 290°C (molding temperature) under the pressure of 2 MPa for 20 minutes. The heated die was let to cool naturally under the pressure. Straight-sided tensile specimens (Knit 3) were cut from the compression molded composite panel. All tensile specimens with the nommal dimension of 180mmx20mmx lmm and fibre content of 47wt% have the loading axis parallel to the wale direction of the knitting axes. No fewer than four specimens were tested for each specimen type using an Instron Universal Testing Machine (Type 4206) under a nominal test speed of 5.0 mm/min, in accordance with ASTM D638. Tensile specimens were clamped over an area of 40mm><20mm at each end leaving a gauge length of 100mm. An open mesh emery sheet (Polynet sheet - 240 grit) was used in the gripped areas instead of aluminium end tabs. Grip pressure was pneumatically controlled. RESULTS AND DISCUSSION Optical micrographs of the polished cross-sections, as shown in Figure 4, provided evidences of complete matrix fusion, and better resin impregnation was confirmed that was indicated by the lack of microvoids between the fibre and the matrix. Typical tensile stress-strain curves are shown in Figure 5a. Composites with continuous preform structure (Knit 1 and Knit 2) have revealed superior tensile performance than all the other knit candidates. Knit 3, Knit 4 and Knit 5 have suffered discontinuities in the knitted preform structures and hence performed poorly with regard to load bearing and energy absorption capabilities. MB knitted specimens (Knit 1) having continuous and pre-tensioned preform structure prior to consolidation reaches the maximum peak load before final failure. Tensile strength, modulus and strain-to-failure values were graphically presented in Figuress 5b through 5d. Knit 1 composite exhibited the highest tensile strength than all the other knit types (Figure 5b). Knit 1 composite has shown superiority over Knit 2 composite in tensile strength (about 55% stronger). This indicates the fact that pretensioning of the knitted strip might have prevented the realization of possible thermal shrinkage within the preform structure and thereby enhancing and/or maintaining better fibre alignment in the loading direction. Knit 1 composite is more than 80% stronger than Knit 3, Knit 4 and Knit 5 composites when tensile strengths are compared. This was primarily attributed to the lack of continuity in the reinforcing fibre bundles within the knit structure due to the cut. On the other hand, modulus is predominantly controlled by the fibre content of the composites. As shown in Figure 5c, tensile moduli of Knit 1 and Knit 2 composites are almost comparable, with Knit 3 (cut-out specimens) only being marginally inferior due to the loss of fibre continuity or directionality resulting from the cut. Knit 4 (Film-stacked) and Knit 5 (thermosets) composite counterparts are also inferior in tensile moduli due to a notably smaller fibre content [13] as well as for the lack of fibre continuity in the knitted preform. It was remarkably noteworthy that tensile strain-to-failure (fracture strain) values (Figure 5d) obtained in the knitted composites with continuous preform structures (Knit 1 and Knit 2) are about 4 times higher than those of the cut-out specimens (Knit 3, Knit 4 and Knit 5). Knit 2 specimens, which did
Aramid/Nylon Weft-Knitted Thermoplastic Composites
1050
not undergo any pre-tension prior to consolidation have revealed higher strain-to-failure values (40% higher) than the pre-tensioned specimens (Knit 1). This was because of the added stretchability of the knits during tensile test. Typical fractured specimens are shown in Figure 6. Knit 3 composites showed normal tensile failure in a brittle manner with a clear split-out phenomenon, whereas both Knit 1 and Knit 2 MB knitted composites did not show any splitting because of the preform continuity that also has contributed to their notably higher strain-to-failure values.
2
b. 59
|:
I I
| AF/PA66 MB-Ktii I
AF/PA6S MB-Knil 1
2 0.3
I
"•»•
sStrai
'a
2.o-
I AF/FA66
AF/PA66
AF/PA06
AF/PA6
AF/Epoxy
AF/PA66 Mfl-Kni 3
AFWA6 AF/Iipoxy Fflm-Siacked Knit 5 CuI-uU
d.
3 0.4 3
a «»-
62
= 0.25
[Ml
11
AF/PAfifi AF/VA6S MB-Kniil MB-Knil 2 Conlauuus C:orlinuous Pre-[etisioiw^l Nott-leiiswned
am AF/PA66 MB-Kni 3 Cut-oul SpcciET^ns
0.055
0.03
AF/PA6 AF/^ioxy Film-Stacked Knit 5 Cut-out Knit 4 Cut-out Speciieiis Specimens
FIGURE 5 a. Typical tensile stress-strain characteristics, b. Tensile strength, c. Modulus, d. Strain-tofailure
Continuous, pre-tensioned Knitl
Continuous, without pre-tension, Knit 2
Cut-out specimen Knit 3
FIGURE 6 Fractured specimens
CONCLUSIONS lxl rib knitted strips were produced using Aramid/Nylon66 Microbraid yarns. 8 spindles of PA66 fibres were braided around 2 bundles of AF fibres to produce these continuous microbraid yarns. Microbraided knitted composites were fabricated using compression molding consolidation technique. Optical microscopy confirmed better resin impregnation into the fibre bundles. Knitted composites having continuous preform structure (Knit 1 and Knit 2) revealed superior tensile performance and excellent energy
Aramid/Nylon Weft-Knitted Thermoplastic Composites
1051
absorption capabilities as compared to other knit candidates. Application of pre-tension to the knitted preform might have prevented the realization of possible thermal shrinkage within the knit structure and thereby enhancing and/or maintaining better fibre alignment in the loading direction. Relatively inferior tensile properties were observed in the knitted composites that suffered lack of fibre continuity or directionality due to cut. Continuous knitted preform reinforced composites that experienced no pre-tension prior to consolidation revealed notably higher strain-to-failure values than the pre-tensioned specimens due to the added stretchability of the knits. Cut-out specimens showed a clear split-out fracture in a brittle manner. REFERENCES 1. Fukui, T., Tsujii, T., Nakai, A. and Hamada, H. 2002. "Fabrication and Mechanical Properties of Unidirectional PE/PE Composites", Journal of the Society of Material Science, 51:1323-1328. 2. Fukui, T., Inoda, M. and Hamada, H. 2001. "Fabrication and Mechanical Properties of PE/PE Knitted Fabric Composites", Journal ofJapan Society of Polymer Processing, 13:641-648. 3. Kitayama, T., Ishikura, K., Fukui, T. and Hamada, H. 2000. "Interfacial Properties of PP/PP Composites", Science and Engineering of Composite Materials, 9:67-73. 4. Stern, T., Teishev, A. and Marom, G. 1997. "Composites of Polyethylene Reinforced with Chopped Polyethylene Fibres: Effect of Transcrystalline Interphase", Composites Science and Technology, 57:1009-1015. 5. Stern, T. and Marom, G. 1997. "Origin, Morphology and crystallography of Transcrystallinity in Polyethylene-Based Single-Polymer Composites", Composites Part A, 28A:437-444. 6. Loos, J., Schimanski, T., Hofman, J., Peijs, T. and Lemsttra, PJ. 2001. "Morphological Investigations of Polypropylene Single-Fibre Reinforced Polypropylene Model Composites", Polymer, 42:3827-3834. 7. Hine, P.J., Ward, I.M., Jordan, N.D., Olley, R.H. and Bassett, D.C. 2003. "The Hot Compaction Behaviour of Woven Oriented Polypropylene Fibres and Tapes. I. Mechanical Properties", Polymer, 44:1117-1131. 8. Jordan, N.D., Bassett, D.C, Olley, R.H., Hine, P.J. and Ward, I.M. 2003. 'The Hot Compaction Behaviour of Woven Oriented Polypropylene Fibres and Tapes. II. Morphology of Cloths before and after Compaction", Polymer, 44:1133-1143. 9. Klein, N., Marom, G., Pagoretti, A., Migliaresi, C. 1995. "Determining the Role of Interfacial Transcrystallinity in Composite Materials by Dynamic Mechanical Thermal Analysis, Composites", Composites, 26:707-712. 10. Klein, N., Marom, G. and Wachtel, E. 1996. "Microstructure of Nylon 66 Transcrystalline Layers in Carbon and Aramid Fibre Reinforced Composites", Polymer, 37:5493-5498. 11. Nuriel, H., Klein, N. and Marom, G. 1999. "The Effect of the Transcrystalline Layer on the Mechanical Properties of Composite Materials in the Fibre Direction ", Composites Science and Technology, 59:1685-1690. 12. Nuriel, H., Kozlovich, N., Feldman, Y. and Marom, G. 2000. "The Direction Properties of Nylon 6,6/Aramid Fibre Microcomposites in the Presence of Transcrystallinity ", Composites Part A, 31:6978. 13. Khondker, O.A., Fukui, T., Inoda, M., Nakai, A. and Hamada, H. 2003. "Fabrication and Mechanical Properties of Aramid/Nylon Plain Knitted Composites", Submitted to Composites Part A. 14. Sakaguchi, M., Nakai, A., Hamada, H. and Takeda, N. 2000. "Mechanical properties of thermoplastic unidirectional composites using microbraiding technique", Composites Science and Technology, 60:717-722.
Modeling and Characterization of 3D Heterogeneous Tissue Scaffolds Z. Fang, B. Starly, A. Darling, W. Sun* Department of Mechanical Engineering and Mechanics Drexel University 3141 Chestnut Street Philadelphia, PA, 19104, U.S.A.
ABSTRACT This paper presents a computer-aided modeling and characterization approach for design and evaluation of mechanical properties and structural heterogeneity of 3D tissue scaffolds. An outline of a computer-aided tissue engineering approach for biomimetic design and freeform fabrication of 3D tissue scaffold, a procedure of computer-aided characterization and a computational algorithm for implementing asymptotic homogenization theory, and its application for predicting the effective mechanical properties of heterogeneous Poly-e-Caprolactone scaffold fabricated through a novel precision extruding deposition process are presented.
INTRODUCTION Three-dimensional (3D) tissue scaffolds play an important role in cell attachment, proliferation, and guidance of new tissue formation, hi theory, tissue scaffolds should be designed to have special characteristics in order to function as true tissue substitutes that satisfy the patient-specific biological, mechanical and geometrical requirements [1]. Research has shown that both mechanical and biological properties of porous scaffolds, as well as cell growth and migration processes are determined in part by the local microarchitecture of scaffold [2]. Ability to determine the mechanical properties and structural heterogeneity of the porous scaffolds with designed microarchitecture, particularly for load bearing bone and cartilage scaffolds is practically important for the scaffold intended tissue engineering applications. Available methods for characterization of mechanical properties of porous scaffolds and heterogeneous tissues were primarily based on using experimental approaches [3], finite element numerical calculation [4], or effective property modeling. For example, to characterize a heterogeneous bone tissue at different structural organization, an effective modeling approach was used to analogize bone tissue as a composite material with complex microstructure and use a representative volume element (RVE) and standard mechanical approach to calculate the apparent moduli of the heterogeneous and/or porous tissue structure [5]. In the RVE based approach, the predicted effective moduli are based on the averaged field theory and, * Correspondence Author: Dr. Wei Sun, Associate Professor, 215-895-5810; [email protected] Dept. of Mechanical Engineering, Drexel University, Philadelphia, PA 19104, USA.
3D Heterogeneous Tissue Scaffolds
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therefore, are sensitive to the size and applied boundary conditions of the selected RVE. To overcome the size and boundary effects, the asymptotic expansion homogenization theory, based on the assumptions that the structure is varying on multiple spatial scales due to existence of a spatially periodic microstructure, was developed and applied to the characterization of various bone tissues [6]. However, the utilization of the theory requires finite element implementation and the associated computational algorithm for the numerical calculation. So far, there is no computational algorithm available for scaffold characterization and general application to tissue engineering. The objective of this paper is to present our study on developing a computeraided characterization approach for applying asymptotic homogenization theory to evaluate the mechanical properties and structural heterogeneity of porous tissue scaffolds. The central of the characterization approach is the developed computational algorithm for finite element implementation of asymptotic homogenization theory. This computational algorithm enables the integration of design, fabrication, and characterization of tissue scaffold within one computer aided tissue engineering paradigm [7, 8] which provides quantitative parameters for scaffold design and application. DESIGN AND FABRICATION OF TISSUE SCAFFOLDS A computer-aided tissue engineering (CATE) approach for modeling, design and fabrication of tissue scaffolds has been utilized in this study. The CATE approach begins with acquisition of noninvasive image and the image processing of appropriate tissue region of interest, followed by a three-dimensional reconstruction of anatomical structure using enabling imaging reconstructive and reverse engineering techniques. The next step is to define tissue anatomic features and to characterize the tissue properties by qualitative computed tomography (QCT) method. A computer-aided design (CAD) technique is applied to design CAD based cellular unit cell models according to the defined tissue features. These cellular unit cells will serve as building blocks to construct final scaffolds. Based on the designed CAD geometrical configuration and the selected scaffolding materials, the computer-aided characterization approach is applied to determine the scaffold effective mechanical properties. The designed scaffold mechanical properties are compared to properties of the to-be-replaced tissue, and the unit cells with matching properties will be selected as candidate unit cell building blacks. The candidate unit cells will be further evaluated in terms of their internal architectures and the intended biological applications. With the help of CAD solid modeling and Boolean operation algebra, the final selected unit cells will be integrated to form the final tissue construct with specified internal architecture, structural properties, and external anatomic geometry to match that of the to-be-replaced tissue. Once the cellular tissue scaffold is designed, a process planning program will convert the designed scaffold architectures to layered deposition patterns for the freeform fabrication of cellular scaffold. In this study, a Precision Extruding Deposition (PED) system was used to freeform fabricate Poly e-Caprolactone (PCL, Sigma Aldrich Inc, Milwaukee, Wisconsin) cellular tissue scaffolds [9]. The following PED processing parameters were used for the scaffold fabrication: the processing liquefier temperature 90°C, the orifice diameter of the tip 0.25 mm, deposition velocity at 20mm/s, and the layer thickness at 0.254 mm. Two specific scaffold patterns were analyzed: 0°/90° and 0°/60°. The image and schematic of the scaffold layout patterns is shown in Figure 1.
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3D Heterogeneous Tissue Scaffolds
k — FILL GAP
*-
MM j r
M
Sitee mckrsess(Ss)
W M M M M M M M M * M M M M J 9 M M M M MT M M M *
(a)
(b)
m
# - - - a Read W;dtr. •'
•• •Ml
Layer Gap (LG)
:
* i
(d)
(c)
FIGURE 1: (a) scaffold image; (b) 0/90° layout pattern; (b) 0/60° layout pattern; (c) layout pattern definition
COMPUTER-AIDED CHARACTERIZATION AND ALGORITHM Based on the assumption of microstructural periodicity, the asymptotic homogenization theory uses the multi-scale asymptotic expansion technique to predict the effective mechanical properties of the heterogeneous material with periodic micro structure. For the sake of simplicity, only selected key equations in the theory are presented here. Detail of the formulation can be found in reference [10]. For example, the macro-level weak-form equilibrium equation can be written as HM(x)dv,(x)
dx.
dXj
'.dQ, .
(1)
in which, u\ are macro-level displacement, tt are traction acting on the boundary F1,., V,. is virtual displacement. E"kl, defined as the homogenized effective stiffness constants are calculated as
•/« ~~ y ic
jkl
(2)
*
where, function %** satisfies (3)
It can be seen that the expression of Eq. (3) is similar to a generalized displacement based finite element formulation. Therefore, the homogenized effective stiffness constants E"tt can be determined through a finite element implementation and numerical solution algorithm by solving %kJ in Eq. (3) and plugging in Eq. (2) for overall mechanical properties D" (a compact form of E"u). Thus Eq. (2) and Eq. (3) can be written in a discrete form as Ku< = / ; and
D? = -j- [{Di} -dfBu'W
i = 1,..,6
(4)
The outline of computational algorithm for the solution procedure is described as follows. For a designed cellular unit cell, the solution procedure starts from to convert a CAD based unit cell model into a finite element pre-process model, including the model discretization, mesh generation, and applying periodic boundary conditions and scaffold material properties. Then, the finite element implementation is
3D Heterogeneous Tissue Scaffolds
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carried out through our developed computational algorithm: 3DHOMOG. As shown in Figure 2, the solution algorithm begins with taking modeling information, such as the elements, nodes, material and boundary conditions derived from the FEM model, determine local stiffness matrices, and then resemble the global stiffness matrix used in the effective properties calculation. The global stiffness matrix only needs to be assembled once for all the case studies (6 cases in total for a three dimensional model). The local and global force vectors are calculated and assembled for each case. After the boundary conditions are imposed and the global stiffness matrix is input, the locallevel displacements for each given cases can be calculated using Gaussian elimination method. Then the overall effective mechanical properties can be determined and be used for the biomechanical compatibility study between the tissue and the scaffolds. Tissue feature pattern Biomimetic designed scaffold unit cell CAD model Preprocess for mesh, BC, material information _ I
,
Initialize stiffness matrix in unit cell domain CO
Introduce boundary condition
K = \tBTDBdY
o
o o CD
Store and retrieve stiffness matrix K for all 6 case calculation
Initialize force vector
Solve homogenization equation Ku' ={' for ff Compute effective mechanical properties i , . for each case
H
Output the effective mechanical properties for biomechanical compatibility study
FIGURE 2: Functional flowchart of computational algorithm: 3DHOMOG
APPLICATION FOR CHARACTERIZATION OF PCL SCAFFOLD The 8-node hexogen elements with a total node numbers of about 1500 were used in the finite element implementation algorithm for the numerical calculation. The cellular unit cell models and the corresponding meshing for both 0/90° layout pattern and 60° layout pattern are shown in Figure 3. Results of the prediction of the effective constants of the PCL scaffolds with the two different layout patterns are presented in Figure 4 and Figure 5, respectively.
3D Heterogeneous Tissue Scaffolds
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7 (a): with 0/90° layout pattern (b) with 0/60° layout pattern FIGURE 3: Unit cells and meshing The effect of the Fill Gap on the effective properties of the 0/90° layout pattern PCL scaffold is presented in Figure 4. For PCL scaffold unit cell with 0/90° layout pattern, there are 6 independent elastic constants Ex (Ey = Ex), E2, Gxy, Gxz (Gyz = Gxz), Hxy, and \ixz (|iyz = Uxz) due to its symmetry to x and y axis. It can be seen from Figure 4 that the increase of the fill gap in general results in a decrease of the modulus and Poisson ratio, particularly for the fill gap in the range between 0.42mm to 0.69mm. This can be explained that the increase in the fill gap will result in an increase in scaffold porosity, thus a decrease in the effective constants. However, the change of the out-of-plane Poisson ratios seems to be not as sensitive as the other constants.
FIGURE 4. Effect of the fill gap on the effective elastic constants (0/90°) •-D11 I-D12 k— D13 I-D16 *-D22 >-D23
0.51
0.69 Fill Gap (mm)
r~-D26 1-D33 —-D36 •-D44 1-D45 1-D55 I-D66
FIGURE 5: Effect of the fill gap on the effective elastic constants (0/60°)
The PCL scaffold unit cell with 0/60° layout pattern behaves as a typical anisotropic material with 13 independent elastic constants shown in Figure 5. The same trend can be observed that an increase of the fill gap in general will result in a decrease of the stiffness constants, particularly for D33. This is because that the increase in the fill gap will result in an increase in the scaffold porosity, thus a decrease in the effective constants, as shown in Figure 5.
3D Heterogeneous Tissue Scaffolds
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CONCLUSIONS AND DISCUSSIONS A computer-aided characterization approach for evaluation of mechanical properties and structural heterogeneity of porous tissue scaffolds was presented in this paper. The characterization approach was applied to predict the effective mechanical properties of Poly e-Caprolactone (PCL) tissue scaffolds manufactured through precision extruding process and to study the effect of the design and process parameters on the structural properties of the interested scaffolds. Results of the characterization show that the effective mechanical properties of the PCL scaffold are the function of the scaffolding materials, the orientation pattern, and the overall porosity of the structure. In general, the scaffold structures behave with anisotropic mechanical properties and the degree of the anisotropy is depending on the deposition layout pattern. ACKNOWLEDGEMENT The authors acknowledge the support from NSF-ENG-DMII-0219176 project to this research.
REFERENCES 1.
Hutmacher, D.W., "Scaffolds in tissue engineering bone and cartilage," Biomaterials, 21, 2000, pp. 2529-2543. 2. Hollister, S.J., Maddox, R.D. and Taboas, J.M., "Optimal design and fabrication of scaffolds to mimic tissue properties and satisfy biological constraints," Biomaterials 23, 2003, pp. 4095-4103, 2002. 3. Hing K, Best S, Bonfield W., "Characterization of porous hydroxyapatite," J. of Material Science: Materials in Medicine, 10, 1999, pp. 135 - 145. 4. Beaupif, G.S., Hayes, W.C., Finite element analysis of a three dimensional open celled model for trabecular bone. J. Biomech. Eng., 107, 1985, pp. 249-256. 5. Williams, J.L., Lewis, J.L., "Properties and an anisotropic model of cancellous bone from the proximal tibia epiphysis," J. Biomech. Eng., 104, 1982, pp. 50-56. 6. Hollister, S.J. and N. Kikuchi, "A comparison of homogenization and standard mechanics analyses for period porous composites", Computational Mechanics, 10, 1992, pp. 73-95. 7. Sun, W., Darling, A., Starly, B. and Nam, J., "Computer aided tissue engineering: Part I Overview, Scope and Challenges" J. of Biotechnology and Applied Chemistry, in press. 8. Sun, W., Starly, B. Darling, A. and Gomez, C , "Computer aided tissue engineering: Part II — Application to biomimetic modeling and design of tissue scaffolds" J. of Biotechnology and Applied Chemistry, in press. 9. Wang, F., Shor, L., Darling, A., Khalil, S., Sun, W., Giiceri, S. and Lau, A., "Fabrication and Characterization of Cellualr Poly-E-Caprolactone (PCL) Scaffolds," Proceedings of 14th Solid Freeform Fabrication Symposium, August 4-6, 2003, Austin, TX, U.S.A. 10. Z. Fang, W. Sun and J. Tzeng, "Asymptotic Homogenization and Finite Element Implementation for Electromagnetic Composite Conductor," J. Composite Materials, in review.
Continuative Fabrication and Mechanical Properties of Multi-axial Warp Knitted Thermoplastic Composites using Micro-braided Yarn Tsutomu Narita*, Asami Nakai, Hiroyuki Hamada Division of Advanced Fibro Science, Kyoto Institute of Technology, Goshokaido-cho, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan Iwao Komiya, Eisuke Fukui FUKUI FISHING NET CO, LTD, Iwanishi, Nakahara-cho, Toyohashi, Aichi, 441-3196, Japan
ABSTRACT In this study, multi-axial warp knitted thermoplastic composites were fabricated by our-developed Micro-braiding technique. Cross-sectional observation, tensile test and 3 point bending test were performed. The composite with good impregnation state was obtained under appropriate molding conditions, consequently high mechanical properties were achieved. The multi-axial warp knitted fabric composite without unimpregnated region had the equivalent mechanical properties with unidirectional composite laminates. Moreover, continuative fabrication method was developed, in which compression machine equipped with swing device in order to enhance the impregnation and to expel air. From these results, continuous fiber reinforced thermoplastic panel was realized by combining braiding and knitting technique.
INTRODUCTION FRP (Fiber Reinforced Plastic) is attractive in various fields, due to the lightweight and high strength. Especially, continuous fiber reinforced composites has been focused in automobile, sports, aerospace industries. For the matrix, thermoplastic resin has been required because of the excellent properties and wide selectivity. Moreover, in the automobile industry, recycling matter is one of the keys for selection of resin, and thermoplastic resin should be used. However, the main problem with using thermoplastic matrices for continuous fiber reinforced composites is the difficulty in impregnating the reinforcing fiber bundles with the high molten viscosity resin. This has led to the development of a number of different manufacturing techniques, such as Commingled Yarn and Powder Impregnated Yarn etc. An intermediate material for fabrication of continues fiber reinforced thermoplastic composites called "Micro-braided Yarn" was introduced in previous study. Micro-braided yarn is fabricated using tubular braiding machine as shown in Figure 1. In Micro-braided * Corresponding author, Division of Advanced Fibro Science, Kyoto Institute of Technology, Goshokaido-cho, Matsugasaki, Sakyo-ku, Kyoto, Japan 606-8585, FAX: +91-75-724-7800, Email: [email protected]
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yarn, the reinforcement fiber bundle is straightly inserted in the center ('axial fiber') and the matrix resin fiber bundles are braided around reinforcing fiber bundle as shown in Figure 2. Resin fiber is melted by heating with appropriate temperature and becomes matrix for FRP. Resin fibers could directly contact with reinforcing fiber, so that melted thermoplastic resin is easy to impregnate into reinforcing fiber. Moreover, Micro-braided yarn can be treated as a single fiber bundle, so that textile processed goods can be easily fabricated. In this study, as application of textile composites using Micro-braided yarn, multi-axial warp knitted thermoplastic composites were fabricated. Multi-axial warp knitted fabric is one of the textiles suitable for mass production. In order to investigate the mechanical properties of the multi-axial warp knitted thermoplastic composites, 3 point bending test, tensile test and microscopic observation were performed. Moreover, for the molding method, continuative fabrication method was discussed, in which compression machine equipped with swing device in order to enhance the impregnation and to expel air. For the development of continuative fabrication process, double compression molding and swing compression molding were examined.
EXPERIMENTS Materials and Specimen Preparation Multi-axial Warp Knitted Fabric Schematic drawing of multi-axial warp knitted fabric is shown in Figure 3. Multi-axial warp knitted fabric allows the placement of warp, weft, and off-axis materials directly into the fabric structure. The composites with the multi-axial warp knitted fabric can possess higher mechanical properties, because of no crimp of reinforcement. Moreover, not only the unidirectional fiber bundles, but also chopped strand mat can be combined. Multi-axial warp knitted fabric has the ability to combine multiple layers of oriented yarn in a single structure. This reduces the cost with omission of the stacking process. Materials Materials used in Micro-braided yarn were carbon fiber bundles (T300, 3000 filaments, TORAY Co., Ltd.) as reinforcement and PA6 resin fiber bundles as matrix resin. The fiber volume fraction and diameter of Micro braided yarn were about 37% and 0.6 mm respectively. In this study, the multi-axial warp knitted fabric with structure of [0° / + 45°/ 90° / -45°] was used and two layers of fabrics were pressed by compression molding machine. Double Compression Molding First, multi-axial warp knitted thermoplastics composites were fabricated using compression molding with the change of processing condition as shown in Table I. The molding process is composed of pre-molding process, molding process and cooling process. Pre-heating aims to reduce the viscosity of resin and induce to impregnate at next molding process. Preheating temperature was 260°C or 280°C. Pre-molding pressure was IMPa and pre-molding time was 5min. Immediately after the pre-molding, the molding pressure which was higher than pre-molding pressure was applied for molding time (20 or 40min.). The composites plate was gradually cooled to room temperature with molding pressure.
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Next, double compression molding was tried in order to improve the productivity by repeating short-time molding. For first compression, only preheating and pre-molding pressure were applied (specimen FC). For the second compression, specimen FC was used. Thus, molding pressure of 4MPa was applied without pre-heating and without pre-molding pressure (specimen SC). Swing Compression Molding Schematic drawing of swing compression molding method is shown in Figure 4. Multi-axial warp knitted thermoplastics composites were fabricated using swing compression molding with the change of compression speed as shown in Table II. Molding temperature was 280°C and swing holding time was 2min. After consolidation, the composites plate was gradually cooled to room temperature. Experimental Procedures Double Compression Molding Microscopic observation of the cross section perpendicular to 0° direction in molded plate specimens was performed with optical microscopy. 3-point bending test and tensile test were also performed using Instron Universal Testing Machine (Type 4206) at crosshead speed of lmm/min. The specimens for 3 point bending test and tensile test were cut along the 0° direction. Geometry of the specimens for bending test and tensile test were about 2.5mm in thickness, 30mm in width, and the span length was 43mm and 180mm, respectively. Swing Compression Molding Tensile test was performed using Instron Universal Testing Machine at crosshead speed of lmm/min. The specimens for tensile test was cut along the 0° direction. Geometry of the specimens for tensile test was about 2.5mm in thickness, 25mm in width, and the span length was 200mm. RESULTS AND DISCUSSIONS Double Compression Molding Figure 5 and 6 show cross-sectional photograph for specimen 260-40 and 280-40. In the case of molding temperature of 260°C, unimpregnated region and resin rich region were observed at the inside of fiber bundle. On the other hand, there is no unimpregnated region and the resin rich region became smaller with increase in molding temperature from 260°C to 280°C. Figure 7 shows the cross-sectional photograph for specimen FC, that is specimen before repeat compression. There is much unimpregnated region inside of fiber bundle. The results of SC are shown in Figure 8 and 9 with different molding time. No unimpregnated region can be observed both for molding time of lOmin. and 40min. Table III shows tensile and bending properties of each multi-axial warp knitted composites. Here, the theoretical elastic modulus was calculated by lamination theory on assumption that the multi-axial warp knitted composites could be regarded as laminated plate with unidirectional composite. The value, in which elastic modulus obtained by experiments (Eexp) was divided by theoretical value (Etheo), was also listed in table III. In the case of molding temperature of 260°C, all properties were almost same regardless of the molding time. However, the values were much lower than those of specimens molded at 280°C.
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The specimen FC with only preheating and pre-molding pressure had lowest value among all specimens. However, these values were improved by second compression. It is noteworthy that the Eexp/Etheo was almost 100% in case of specimen SC regardless of the molding time. This result means that repeat compression is effective molding method to improve the productivity with short-time molding. For example, specimen of 280-40 needs 45min. molding time, however, specimen of SCI0 needs only lOmin. at final molding. Also the obtained panel could be used as intermediate material for compression molding in which final products with complex shape and the complete impregnation might be achieved. Swing Compression Molding Table IV shows tensile properties of each multi-axial warp knitted composites. The Eexp/Etheo was almost the same value at each specimen. However, tensile strength was increased with increase in the compression speed. The flow speed of resin was increased with increase in the compression speed. Then, the air was expelled from the inside of multi-axial warp knitted composites with the flow of resin. As a result, it was conceivable that the tensile strength was increased because of the decrease of voids. CONCLUSIONS hi the double compression molding, from the results of cross-sectional observation, tensile test and 3 point bending test, the composite with good impregnation and mechanical properties was obtained by appropriate molding conditions. The multi-axial warp knitted fabric without unimpregnated region had the equivalent mechanical properties with unidirectional composite laminates. Moreover, it was confirmed that repeat compression molding improve the productivity with short-time molding, hi the swing compression molding, swing compression molding method was effective for air-release method. Based on these results, we have proposed new continuative fabrication method consists of double compression machine equipped with swing device. REFERENCES 1.
Masahide Sakaguchi, Asami Nakai, Hiroyuki Hamada and Nobuo Takeda, Mechanical Properties of Thermoplastic Unidirectional Composites using Micro-braiding Technique, Composite Science and Technology, 60(2000), pp.717-722.
TABLE I Molding Conditions of Double Compression Molding
260-0 260-20 260-40 280-40
Preheating Temperature (°Q 260 260 260 280
FC SC-10 SC-20 SC-40
280 280 280 280
Specimens name
Pre-Molding Pre-Molding Pressure Time (MPa) (min.) 1 5 1 5 1 5 1 5 1 -
5 -
Molding Temperature (°C) 260 260 280 _ 280 280 280
Molding Pressure (MPa) 4 4 4 _ 4 4 4
Molding Time (min.) 20 40 40 _ 10 20 40
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Multi-axial Warp Knitted Thermoplastic Composites TABLE II Molding Conditions of Swing Molding Specimens name Type A TypeB TypeC
Molding Temperature (°C) 280 280 280
Swing Holding Time (min.) 2 2 2
Compression Speed (mm/min.) 0.46 2.4 5
Molding Time (min.) 20 20 20
TABLE HI Mechanical Properties of Double Compression Molding Specimens name 260-0 260-20 260-40 280-40 FC SC-10 SC-20 SC-40
Vf Tensile Tensile Modulus Bending Bending Tensile (%) Modulus (GPa) Strength (MPa) Eexp/Etheo (%) Modulus (GPa) Strength (MPa) 36 33 282 79 50 596 34 34 47 510 261 83 34 30 53 560 290 73 45 61 38 371 93 j |_ 778 32 38 42 51
29 45 47 54
186 334 408 447
28 66 65 74
76 94 95 96
363 859 837 772
TABLE IV Mechanical Properties of Swing Molding Specimens name Type A TypeB TypeC
vf (%) 48 47 47
Tensile Strength (MPa) 364 383 400
Tensile Modulus (GPa) 38 37 38
Tensile Modulus Eexp/Etheo (%)
66 64 66
Reinforcement fib (Carbon fiber) Matrix resin fiber '(PA6 resin fiber)
^^
Characteristics of Micro braided yarn Micro braided yam can be treated as a single fiber bundle. Damage to reinforcement fiber bundle is small in making Micro braided yarn . •Various resin as matrix can be adopted.
FIGURE 1 Photograph of Tubular Braiding Machine
FIGURE 2 Schematic Diagram and Characteristic of Micro-braided Yarn
n n Materialj - y
y-j
n ^ ^
|
i M
Mold L
o tt. setting
|
—oh 1
Holding of (he o n e sjde
FIGURE 3 Schematic Diagram of Multi-axial Warp Knitted Fabric
1 11 1
41 L Compression molding
FIGURE 4 Schematic Drawing of Swing Compression Molding Method
Multi-axial Warp Knitted Thermoplastic Composites
1063
1
Kf-.Ul Mill I
i i t i n o i II II »mnile
II
1
id it i i ill r MtuMUe
p •>" In turn
I i ••uiuUe
i* ilin II n lili 11
1 IIK ii
Itimdle
il'.i Inuidle
•" tin M • iii .
bundle
I IIIII i 11 II iii I iii.nni bdiftttuoiiuber uuniiie
FIGURE 5 Cross-sectional Photograph of Multi-axial Warp Knitted PA6 Composites (Molding temperature of 260°, Molding pressure of 4MPa, Molding time of 40min.)
^...\-
?-• -"•'
FIGURE 6 Cross-sectional Photograph of Multi-axial Warp Knitted PA6 Composites (Molding temperature of 280°, Molding pressure of 4MPa, Molding time of 40min.)
„ _ , „ „ „ _, . , _, , „ FIGURE 8 Cross-sectional Photograph of .... . , „ , T, . . . . . . ° K , Multi-axial Warp r Knitted PA6 Composites . , . .r (After Second compression) . . , , ,,..,.,.,. . t (Molding ttemperature of 2 80 , Molding pressure of , , „ , , ,.• • , ft • N 4MPa, Molding time of 1lOmrn.)
FIGURE 7 Cross-sectional Photograph of Multi-axial Warp Knitted PA6 Composites (Molding temperature of 280°, Pre-Molding pressure of IMPa, Pre-Molding time of 5min.)
FIGURE 9 Cross-sectional Photograph of . . ... . . . . . „ - ^ j n A ^ o u Multi-axial Warp Knitted PA6 Composites ,.„ „ , • , (After Second compression) , ,,. ^5n«o ... (Molding temperature of 280 , Molding , „ ... . . . pressure of 4MPa, Molding F 6 time of 40mm.) y
Multi-Scale Analysis for Material Characterization of Textile Composites Jun Liang*, Kuisun Wang and Shanyi Du Center for Composites of Harbin Institute of Technology, Harbin 150001, P. R. China
ABSTRACT Multi-scale analysis using the asymptotic homogenization method is becoming a matter of concern for microstructural design and analysis of advanced hemerogeneous materials, hi this paper, the 3D textile composite material is simplified to minor period structure composites, and a unit cell is then built to enclose the characteristic periodic pattern in the textile composites. The predicted effective elastic moduli of textile composite materials through a combined approach of asymptotic homogenization method and the finite element method are obtained. The predicted elastic properties agreed quite well with the experimental values. Using the proposed approach, the material characterization of textile composites can be anticipated accurately and efficiently.
INTRODUCTION Textile composite materials have recently received considerable attention, due to their structural advantages of high specific-strength and high specific-stiffness as well as their improved resistance to impact. Besides their advantageous mechanical properties, textile composites are easy to handle and have excellent formability and hence are widely employed in aircraft, boat and defense industries. However, For the textile composite materials, as the heterogeneity, anisotropy and the geometrical structure complexity such as very small length of minor period structure exists, a problem lies essentially in the difficulty to understand the very complex stress distribution in the microstructure. The microscopic stress is rapidly changing in a small-scale length depending on the heterogeneity. Thus it is very difficult to calculate directly the stress and the displacement fields through the traditional FEM, since the difficult mesh partition and large quantities of the calculations. Multi-scale analysis for various advanced materials with microscopic heterogeneity has been one of the major topics in both computational mechanics and materials. Among some computational methods for the multi-scale analysis, the asymptotic homogenization method has been successfully applied to the composite materials. It is capable of dealing with complex microstructures in a periodic order, which may be too computationally intensive to be discretized into a conventional FEM model. This method was firstly developed by many applied mathematicians to solve linearly elastic problem and thermoelastic problem of heterogeneous media considering the microscopic properties (Lions, [1-2]; lene and leguillon, [3]; Marcin, [4]). In recent years, the many efforts have been devoted to the enhancement of the homogenization method to the estimation of * Corresponding Author, Center for Composites of Harbin Institute of Technology, China. Fax: +86-451-86414323. E-mail address: [email protected]
Material Characterization of Textile Composites
1065
effective material properties of composites. Dasgupta and Agarwa [5] predicted the orthotropic thermal conductivity of plain-weave fiber reinforced composites by the homogenization method. Liew et al. [6] formulated a periodic model to estimate the effect of porosity on the moduli of woven fabric composites and validated their model by experiments. Peng and Cao [7] predicted the effective nonlinear elastic moduli of textile composites through a combined approach of the homogenization method and the finite element formulation. In this paper, the predicted effective elastic moduli of textile composite materials through a combined approach of asymptotic homogenization method and the finite element method are presented. BASIC EQUATIONS OF MULTI-SCALE METHOD We assume that an elastic body Q as shown in Fig. 1 is an assembly of a periodic microscopic unit cell. The global coordinate x is related to the local coordinate £ as:
Z = e-Xx
(l)
where e is the ratio between the dimension of a unit cell and a structure body, which is a very small positive number( £- — , 0 < £ « 1 ) . 1-4
'•8
fc.
•_.:
??.
V
:'•••:
:*
"•
el
U
Unit cell
._.
FIGURE 1 The periodic structure and basic configuration
The important essential postulation in the Multi-Scale method is that the displacement field can be expressed as an asymptotic expansion[l]
uf (x) = uf (x, £) + eu) (x,
(2)
Noting that: |
where <j> is a general function. We have, for the strain tensor
(3)
Material Characterization of Textile Composites
1066
The elastic coefficients Cm are periodic functions of x and depend on£
(5)
Thus the stress can be expressed as
(6)
where
e"u(x,Z),
« = -1,0,1,-
(7)
Therefore, the elastic problem with a periodic microstructure is presented as
in
(8) on Q Substituting Eq.(2) in Eq. (8), and equaling the powers of s, we obtain
°(L1u2 +L2ul +L3u°)
(9)
where
L2(x)^^r ,(*) =
ox,
) — dx,' 3 dx,
{Cijkl *
(10)
Next, we equate to 0 the terms with the same order of s obtaining an infinite sequence of equations. The relations of zeroth, first and second order can be written as follows
Material Characterization of Textile Composites
1067
Z 1 (x) M o (x,^) = 0
(11.1)
l
Ll(x)u (x^) + L2{x)u°(x^)^0 2
Lx (x)u (x, £) + L2 (x)u' (x, %) + L3 (x)u ° (x, £) = / ( * )
(11.2) (11.3)
The displacements fields uf ,u],uf can be found form these equations recurrently if only x and E, are independent variables. Les us also note that the equation L^+P^O
(12)
with ut as a £ -lperiodic function, has a unique solution for[4] (13)
where \Q\ is the volume of the unit cell. Considering this fact and the statements Eq.(l 1.1) and (10) we may obtain that
u\x,?) = u\x)
(14)
i.e. u° is a function of x only, we can regard u° as the macroscopic displacement, while u), uj are the microscopic displacements. The physical meaning of Eq. (2) thus is that the real displacement ut is rapidly oscillating around u° due to the inhomogenity form the microscopic point of view u\,u),--- are the perturbing displacements according to the microstructure. Hence, the scale factor e is multiplied to the microscopic displacements. Thus substituting Eq.(14) in Eq. (11.2) yields (15) we obtain the solution by separating x and £, variables as follows - o
K,W) = -<(*,£)-^-+ «/(*) dx,
(16)
the last two equations (11.2) and (11.3) give the formulation for the £, -periodic functions
Nf(x,4) as
J_(C
SNZOcJl J_
what completes considerations on general homogenization method for linear elastostatic problems. Thus, Eq.(8) can be rewritten as follows
1068
Material Characterization of Textile Composites
u°(x) = >(*)
in
Q
on
Q
(18)
where Ciju is the homogenized elasticity tensor that is also symmetric defined by
^ w ~|g|l [C *
(19)
Jkl(
The microscopic stress can be analyzed by Eq.(18). This quantitative evaluation is essential for analyzing the damage and fracture of the composite materials NUMERICAL RESULTS BY FINITE ELEMENT ANALYSIS The E, -periodic function Nf (x, £,) is a weak solution for the following formulations
in Q
iimn
(20)
on Q
Let Eq.(22) left multiplied byN" (£), we can obtain
in Q (21)
on Q Using the divergence theorem on Eq.(21) with specific boundary conditions on a unit cell yields
= - ( - | - Nf on Q
A detailed finite element model was developed to model a unit cell of the textile carbon/carbon composites (Fig.2), the fiber bundle is shown in yellow, blue and red with its cross-section represented by a rectangular flat-plate. The matrix is shown in green.
Material Characterization of Textile Composites
1069
fiber FIGURE 2 FEM mesh of the 3D-textile composites
The elastic moduli of the constituent phases of the fiber yarn and matrix are assumed to be linear and isotropic, tensile modulus of the fiber yarn is 341.7GPa, poisson's ratio is 0.25; tensile modulus of the matrix is 2.73GPa, poisson's ratio is 0.35. The volume fraction of the fiber is 59.13% (Vfx =V& =1632%,V/Z =26.49%). The unit cell is discretized by 3D 10-node tetrahedral continuum elements. The homogenization method presented above demonstrates its accuracy and reliability in obtaining the equivalent elastic moduli of orthotropic textile composites. The predicted elastic constants for the composites are given in Table 1. TABLE I Predicted properties of the textile composites Property
Ex (GPa)
Ey (GPa)
Ez (GPa)
Gxz (GPa)
Gyz (GPa)
G^ (GPa)
Numerical 6969Q 69.690 59.590 69.690 39.823 89.823 4.915 4.915 4.915 4.915 Value Experimental 71.857 71857 76.060 5.516 5.813 Value Error 3.01% 3.01% 18.09% 10.90% 15.45%
6.829 6.829
lxy
%z
0.28
0.31
7.552 9.57%
REFERENCES 1 2 3 4 5 6 7
J. L. Lions, and G. Papanlcolaou. 1978. "Asymptotic analysis for periodic structure," North-Holland, Amsterdam. J. L. Lions. 1980. "Asymptotic expansions in perforated media with a periodic structure," The Rocky Mountian. J. Math. 10(l):125-140 Lene F., Leguillon D. 1982. "Homogenized constitutive law for a partially cohesive composite material," Int. J. Solid Struct. 18:443-458 Marcin Kaminski. 2000. "Homogenized properties of periodic n-component composites," Int. J. Eng. Sci. 38:405-427 Dasgupta A., Agarwal RK. 1992. "Orthotropic thermal conductivity of plain weave fabric composite using a homogenization technique," J. Compos. Mater. 26(18):2736-2758 Liaw PK., Yu N., Hsu DK., Miriyala N., Saini V., Snead LL. McHargue CJ., Lowden RA. 1995. "Moduli determination of continuous fiber ceramic composites," J. Nucl. Mater. 219:93-100 Xiongqi Peng, Jian Cao. 2002. "A dual homogenization and finite element approach for material characterization of textile composites," Composites. PartB, 33:45-56
Study on Damage Development of Woven Fabric Composites with Spread Tow Tetsusei KURASHIKI , Masara ZAKO, Yoshihiko HAYASHI Graduate school of Eng., Osaka University, JAPAN Ignass VERPOEST Katholieke Univ. Lueven, BELGIUM
ABSTRACT Woven architecture with spread tow may induce the improvement of resin impregnation, high strength by high volume fraction, etc. However, the mechanism of damage development of woven fabric composites with spread tow has not been completely investigated. To investigate the effect of spread tow on the damage development, the numerical results of the mechanical behavior have been described. We have developed a numerical simulation on damage development of woven fabric composites based on damage mechanics. From the numerical results of mechanical behaviors under tensile loading for woven fabric composites with/without spread tow, it is found that the location of occurrence and the type of propagation of transverse cracks are quite different due to the effect of spread tow. Furthermore, an effect of volumefractionin spread tow on the damage development has also been described. It has been recognized that the damage development inside lamina considering an effect of a spread tow, which has been never observed in experiments, can be predicted by the finite element analysis based on damage mechanics.
INTRODUCTION Woven fabric reinforced plastics have been applied widely in many structures, because they have some advantages like easy handling, high lateral strength, etc. A woven architecture with spread tow has been investigated. The architecture may induce the improvement of the resin impregnation, the high strength by high volume fraction. The mechanical behavior of woven fabric composites with spread tow is one of the very important properties to be investigated, however, the estimation of damage development is very difficult, because matrix cracks and delamination at the crossover points of fiber bundle may occur leading to complicated fracture modes in comparison with uni-directional fiber reinforced composites. If damages can be estimated with numerical simulation, it will become very useful tool for estimation of mechanical properties of woven fabric composites. We have developed a numerical simulation program on damage development of woven fabric composites based on damage mechanics [1,2]. A tensile test and fatigue test for a lamina of woven fabric composites withfri-siteobservation had been carried out [3], and an effect of a disorder of pile-up for woven fabric composites laminate * Corresponding author, Department of Manufacturing Science, Osaka University, 2-1, Yamadaoka, Suita, Osaka, 565-0871 JAPAN, fax: +81-6-6879-7570, e-mail: [email protected]
Damage Development of Woven Fabric Composites with Spread Tow
1071
on damage development had been investigated in a previous paper [4]. An effect of a spread tow on the damage development had not considered in that paper. Therefore, we have developed a numerical simulation program on damage development of woven fabric composites with spread tow based on damage mechanics. The failure behaviors for woven fabric composites with several types of spread tow under static tensile load have been analyzed with the developed program. In this paper, the numerical results of the damage states are described. SIMULATION METHOD OF DAMAGE DEVELOPMENT To make clear the different location of damages, we have developed a numerical simulation program for damage development of woven fabric composites based on damage mechanics. In the simulation, the modeling of anisotropic damage is very important. Woven fabric composites are treated as a heterogeneous body composed of fiber bundles and matrix. The isotropic damage model is applied for matrix, and anisotropic damage model is applied for the fiber bundle, respectively. The damage in fiber bundle consists of four modes shown in Fig.l [1,2]. Mode L is dominated by fiber breaking, the others are matrix cracking caused by different stress components. The occurrence of damage can be predicted by using Hoffman's criterion. The damage mode is judged by the maximum value among the corresponding stress-to-strength ratios in Table I. The constitutive equation can be obtained by the characterization of the damage mode. TABLE I Classification of damage mode Mode T<
ModeL
Maximum value
ModeL
x'xc a} ylyc
y,yC
Mode Z&ZL
Mode TZ
FIGURE 1 Anisotropic damage mode
Damaged pattern
V
" I AJ -|
ModeT&TL Mode Z&ZL Mode TZ
{a, v. stress, X, Y, S: strength) NUMERICAL RESULTS AND DISCUSSION Distribution of Volume Fraction inside a Fiber Bundle The volume fraction in a fiber bundle has been measured by the digital image processing and SEM. Figure 2(a) shows the observational result about cross section of the fiber bundle by SEM. From this figure, the volume fraction inside a fiber bundle can be calculated with an image process. In case of a woven FRP, volume fraction is distributed in a fiber bundle. The center parts have higher volume fraction 65.3% and edge parts have lower value of 58.3%. This tendency is almost same with the results of previous study [4], To estimate the woven architecture with/without spread tow on the damage development, finite element model was prepared as Fig.2(b) and the mechanical properties at each divided part of a bundle was calculated. A fiber bundle is treated as
1072
Damage Development of Woven Fabric Composites with Spread Tow
uni-directional fiber reinforced composites, and the mechanical properties can be calculated by the rule of mixture based on the obtained volume fractions.
i.u( inos •*'. linn nl .1 Illvi InuiilL1 IT. si \ l
sac**"
- , • -"- ••
9581 ^———- — d
| a1 b c
f
e
(b) Finite elements of a part of a fiber bundle FIGURE 2 Numerical model with a distribution of volume fraction inside a bundle
Comparison of Damage Development of Woven FRP with/without Spread Tow The mechanical behaviors of woven fabric composites with/without spread tow under on-axis tensile load had been analyzed by the developed simulation. Figures 3,4 show the finite element models. Two types of numerical model have been generated. One is the model of non-spread tow, which has 3.1mm width of a bundle and 0.73mm thickness. Another model has been generated by spreading the tow of 4.1mm width. The width of a bundle is 6. lmm, and the thickness of the composites is 0.36mm. Numerical models of the damage states are also shown in Figs.3, 4. To make clear the damage in the strand, the only strand parts are also indicated. The colored parts represent the damaged elements judged by Hoffman's criterion. In case of the numerical model for non-spread tow, the initial damage of transverse cracks (Mode T<) appears at the center of a weft bundle, however, no cracks occur at Tensile direction
ModeT
(a-l) Fiber bundles and matrix
(a-2) Only fiber bundles (a) £ = 0.66%
Matrix crack ModeT /
(b-1) Fiber bundles and matrix
-
'
ModeZL / (b-2) Only fiber bundles
FIGURE 3 Damaged states of woven FRP for non-spread tow
Damage Development of Woven Fabric Composites with Spread Tow
1073 M. J- T
(a-1) Fiber bundles and matrix
(a-2) Only fiber bundles (a) £=0.58% \\ ..k I
(b-1) Fiber bundles and matrix
(b-2) Only fiber bundles (b)e=1.25% FIGURE 4 Damaged states of woven FRP for spread tow 300 250
1? 200 ^
150
I <» 100
•
- Spread tow Non-spread tow o Occurrence of initial damage
50 0
0.0
0.5
1.0
1.5 2.0 2.5 3.0 3.5 Strain (%) FIGURE 5 Numerical results of stress-strain curves
the edge part as shown in Fig.3(a). After that, the damages has propagated and the Mode ZL, which is the damage mode caused by shearing stress at the warp bundles, appear at the strain 1.25% in Fig.3(b). On the other hand, numerical results for spread tow indicate that the initial failure appears at the center of a weft bundle as shown in Fig.4(a), and the transverse cracks develop in the edge parts of a weft bundle at the strain 1.25%, however, the Mode ZL doesn't appear in the warp bundles. From these results, it is revealed that the location of occurrence and propagation of damages are quite different due to the effect of a spread tow. Numerical results of relation between stress and strain are shown in Fig.5. The results show that a woven architecture for spread tow has high rigidity and strength as compared
1074
Damage Development of Woven Fabric Composites with Spread Tow
with the conventional architectures for non-spread tow. It is generally difficult to detect the strain level of the initial failure by the experiments, however, the strain of initial damage can be also evaluated conveniently with the proposed numerical simulation. An Effect of Fiber Volume Fraction in a Spread Tow on Damage Development Numerical results of the damage development indicate that the initial damages of transverse cracks have appeared at the center parts of a weft bundle with/without spread tow. We can guess that the reason why the phenomena occur is an effect of interfacial bonding force between a fiber and resin caused by the distribution of volume fraction inside a bundle. The center part of a weft bundle has high volume fraction, and the high volume fraction area induces the decrease of interfacial bonding force. Therefore, we propose a new woven architecture which has a low volume fraction in the center part of a fiber bundle. Figure 6 shows the distribution of the volume fraction at the area inside a fiber bundle as shown in Fig.2(b). Type (A) means the distribution of a specimen measured by the digital image processing and SEM as shown in Fig.2(a). Type (B) means the proposed distribution which the volume fraction in the center part of a fiber bundle is low. To estimate an effect of volume fraction inside a fiber bundle on the damage development, four types of numerical models with several thicknesses have been analyzed. Figure 7 shows the numerical results of the strain level when the initial failure (Mode T) appears, hi case of the numerical model for spread tow (0.36mm thickness) with the proposed distribution type (B), the initial transverse cracks appear at the edge parts of the weft bundles. The strain of initial failure of type (b) is larger than that of a numerical model with volume fraction type (A). The results have revealed that an effect of volume fraction inside a bundle can not be neglected for the estimation of damage development of woven fabric composites, and the control of the distribution has a possibility of high rigidity and strength as compared with the conventional architectures. 0.8
IQf
i Distribution type (A) / i— Distribution type (B)
&65p
m
0.6
a o 60'
I
OType(A) • Type(B)
•
o • o •
m
0.4
l
O
o •
—
50 FIGURE 6 Volume fraction inside a fiber bundle
0.2
0.8 0.6 0.7 Strain (%) FIGURE 7 Relation between strain level of an initial damage and thickness 0.4
0.5
CONCLUDING REMARKS The failure behaviors for woven fabric composites with/without spread tow under static tensile loading have been simulated with the developed program. The location of occurrence is quite different due to the effect of a woven architecture. It is recognized that the damage development inside a lamina considering an effect of a spread tow which had
Damage Development of Woven Fabric Composites with Spread Tow
1075
been never observed in experiments can be predicted, and the strain of initial damage can be also evaluated conveniently by the proposed simulation. Therefore, the proposed numerical method is very useful for the estimation of mechanical properties of woven fabric composites with spread tow. The numerical results show that an effect of the distribution of volume fraction inside a bundle can not be neglected for the estimation of damage development of woven fabric composites. In this paper, we propose a new woven architecture which has a low volume fraction in the center part of a fiber bundle. The numerical results derive that a woven architecture with the proposed distribution has good mechanical properties as compared with the conventional architectures.
REFERENCES 1. 2. 3.
4.
Zako, M., Uetsuji, Y., and Kurashiki, T. 2003. "Finite Element Analysis of Damaged Woven Fabric Composite Materials", Composites Science and Technology, Vol.63, pp.507-516. Zako, M., Takano, N., and Uetsuji, Y. 1996. "Prediction of Strength for Fibrous Composites based on Damage Mechanics", Proc. 3rd international symposium TEXCOMP, pp.7/1-7/9. Zako, M., Takano, N., Kurashiki, T., and Moriki, H. 2000, "Characterization of Low Cycle Fatigue for Woven Fabric Composites (Below the Freezing Point)", 2nd Asian-Australasian Conference on Composite Materials (ACCM-2), pp. 111-117. Kurashiki, T., Zako, M., and Verpoest, I. 2002, "An Effect of a Disorder of pile-up for Woven Fabric Composites on Damage Development", 3rd Asian-Australasian Conference on Composite Materials (ACCM-3), pp. 685-703.
Measurement of Material Damping Properties of Triaxial Woven Fabric Composites in Low-Pressure Condition Masara ZAKO , Tetsusei KURASHIKI, Yasumasa NAKANISHI Department of Manufacturing Science, Osaka University, Japan Kin'ya MATSUMOTO Faculty of Education, Mie University, Japan
ABSTRACT An effect of the air on the material damping of triaxial woven fabric (TWF) composites has been investigated. Two types of TWF composites, i.e., basic and bi-plain weave, are used as reinforcement. An excitation test of TWF composites is carried out in the atmosphere and in the low-pressure chamber, respectively. Comparing the both of experimental results, the effects of an atmosphere on the natural frequency and on the damping ratio have been discussed. As a result, it may be concluded that the aerodynamic force has a great influence on the damping properties and few influence on the natural frequencies.
INTRODUCTION TWF composites have been applied to the space structures and sports items like golf shafts etc. Though many researchers have reported the static characteristics of TWF composites [1,2] and the damping properties for only unidirectional fiber reinforced plastics [3], the damping properties for TWF have not been investigated. It is important for the structural design to reveal the damping properties of TWF composites, because the damping is the essential properties for the dynamic analysis of structure design. Especially, a comprehension of material damping properties of TWF composites is still lacking [4]. The vibration tests are often performed under atmospheric pressure. Aerodynamic resistance forces affect to the vibrating structures. As the internal friction of a vibrating material, we should take the work done by aerodynamic forces into consideration. It is very important for the structural design to understand the affect of aerodynamic forces on the material damping properties of TWF composites. The purpose of this study is to obtain the accuracy material damping properties of TWF composites. An excitation test of TWF composites are carried out in the atmosphere and in the low-pressure chamber. An effect of the air on the material damping has been investigated. Comparing the both of experimental results, the effects of an atmosphere on the natural frequency and damping ratio have been discussed.
* Correponsing author, Department of Manufacturing Science, Osaka University, 2-1 Yamada-oka, Suita, Osaka, 565-0871, Japan, fax:+81-6-6879-7563, E-mail: [email protected]
Material Damping Properties of Triaxial Woven Fabric Composites
1077
EXPERIMENT The specimens have been made of a triaxial woven fabric carbon fiber (T300) and polypropylene. Two types of TWF as shown in FIGURE 1 are used as reinforcement. The length and width of specimens are 220mm and 20.0mm, respectively. The longitudinal direction of specimen is shown in FIGURE 1. Table 1 shows the thickness and the density of specimens and the mechanical properties. hi order to reveal the effect of the air on the damping properties, the excitation tests have been carried out in the atmospheric pressure condition (760torr) and in the low-pressure chamber (0.4torr) at room temperature, respectively. FIGURE 2 is a schematic of the apparatus used. The exciting point is the center of the specimen. The forces of input and the acceleration of output have been measured by an impedance head. The natural frequency and the damping ratio have been obtained by modal analysis. o
I (a) Basic weave
(b) Bi-plain weave
FIGURE 1 Two types of triaxial woven fabric
Table I Mechanical properties Basic
Bi-plain
34.6 0.3 17.8 1410 0.71
43.9 0.3 27.5 1530 0.90
Young's modulus, GPa Poisson's ratio Fiber volume fraction, % Density, kg/m3 Thickness, mm
RP
Vacuum chamber CFRP specimen
Exciter Impedance head
Input signal FIGURE 2 Schematic of test apparatus
Material Damping Properties of Triaxial Woven Fabric Composites
1078
RESULT AND DISCUSSION FIGURE 3 shows the relation between the vibrational characteristics and the pressure in chamber. It has developed that the damping ratio depends on the pressure. In addition, it is recognized that the damping ratio decreases with the reduction of pressure at the range from 760torr to 1 .Otorr and it remains constant at below 1 .Otorr. The obtained the damping ratios for each natural frequency are shown in FIGURE 4. FIGURE 4(a) is the experimental results for the basic weave composites and FIGURE 4(b) is one for the bi-plain weave composites. The damping ratios in the low-pressure (0.4torr) are smaller than ones in the atmosphere. FIGURE 5 shows the experimental results of damping ratios of TWF composites in the low-pressure condition. Although the damping ratios for the basic weave composites and the bi-plain weave composites are almost same, the natural frequency of bi-plain weave is higher than one of basic weave, because the moduli of elasticity of bi-plain are higher than ones of basic woven fabric composites as shown in Tablel. Damping ratio decreases with increase of the fiber volumefraction,because the moduli of elasticity increase with the fiber volume fraction. However, the tendency of the experimental results is the opposite. It will be considered that the woven architecture has an influence on the damping ratio. 0.20
J
ooc
feo
Dampin 3 ratio, %
80
n-n—nnrm
<xx>—
I" "TO
0.15
0.10
0.05
—0— Basic weave
—O— Basic weave
—a— Bi-plain weave
n
101
102
10"
10 4
10 5
- D — Bi-plain weave 10 6
0.00
101
102
Pressure, Pa (a) Natural frequency
103 10" 105 Pressure, Pa (b) Damping ratio
106
FIGURE 3 Relation between pressure and vibration characteristics
0.4
0.4 —0-—0.4torr
—0—0.4torr - - -o- - - 760torr
0.3
- • o- • • 760torr 0.3 Q
0.2
0.2 •
o... 0.1
•
0.1
0.0 102 10 3 Frequency, Hz
(a) Basic weave
104
•
0.0 101
102 103 Frequency, Hz (b) Bi-plain weave
FIGURE 4 Relation between pressure and vibration characteristics
104
Material Damping Properties of Triaxial Woven Fabric Composites
1079
10°
.2
)10" 'Q.
I
— 0 — Basic weave . . -•• - - Bi-plain weave
104
10 2 10 3 Frequency, Hz
FIGURE 5
Comparison between vibration properties of basic weave and that of bi-plain weave
hi order to make clear the effect of the aerodynamic forces, the following equations are applied.
~ Co. o.4torr x 1 QQ /o. o.4torr
where, f^Qtm
[O /O ]
hOAton
and /o4torr are natural frequencies at atmosphere and at 0.4torr,
respectively. ^760torr and <^04tOTr are damping ratios at atmosphere and at 0.4torr. FIGURE 6 show the values of dy and dg for each natural frequency, respectively. Although the values of dj- for each natural frequency are lower than 1.0%, the ones of d{- for damping ratio are bigger than 30%. The differences of damping ratio have a maximum at 1st mode and they decrease with an increase the modal number. From these results, it is recognized that aerodynamic force has great influence on the damping ratio and cannot neglected.
1.0 08 0.6
O
O O
. D
D
D
O
-20
O
•
-40
D
0.4 O Basic weave
0.2
-60
O
D Bi-plain weave
u.o
O Basic weave a Bi-plain weave
-80 1st
4th 3rd Mode (a) Natural frequency 2nd
1st
2nd
3rd
Mode (b) Damping ratio
FIGURE 6 Relation between pressure and vibration characteristics
4th
1080
Material Damping Properties of Triaxial Woven Fabric Composites
CONCLUSION REMARKS The material damping properties of two types TWF composites have been obtained from the excitation tests at several pressure conditions. The damping ratio at low-pressure (0.4torr) is about a half the damping ratio at atmosphere. From these experimental results, it is revealed that the aerodynamic force has a great influence on the damping ratio and the test at below l.Otorr requires to obtain the real damping ratio. However, there is a little effect of the air on the natural frequency.
1. A. Fujita, H. Hamada, Z. Maekawa, Journal of Composite Materials, 27 (1993) 2. S.V. Hoa, et. al., Composites Science and Technology, 63 (2003) 3. R.D. Adams, Damping Properties Analysis of Composites, Composites (Engineered Materials Handbook Volume 1), 1984,pp.206-217 4. M. Zako, K. Matsumoto, Y. Nakanishi, N. Matsumoto, The Fourth joint CANADA-JAPAN workshop on composites, (2002)
CTE Model of 3D Orthogonal Textile Reinforced Aluminum Matrix Composites S-K Lee , J-H Byun Composite Materials Lab Korea Institute of Machinery & Materials, Korea S-H Hong Department of Materials Science and Engineering Korea Advanced Institute of Science and Technology, Korea
ABSTRACT The geometric model and the effective coefficient of thermal expansion (CTE) model have been proposed for three-dimensional orthogonal textile composites. The volume averaging of stiffness and compliance coupled with CTE of warp weaver, stuffer and filler yarns have been utilized in the homogenization. Composite samples were fabricated by vacuum assisted pressure infiltration method for the verification of the model. PAN-type carbon fibers and pure aluminum were used as reinforcements and matrices, respectively. CTE of the sample was measured by strain gages. Fairly good agreement has been observed between the model prediction and the test results for Oy. However, a large discrepancy exists in the case of c^.
INTRODUCTION In recent years, there has been increasing interests in textile reinforced composites due to the attractive capabilities for a variety of applications [1]. Coupled with the ability of tailored design for composite materials, the unique properties of textile reinforced metal matrix composites (MMCs) include increased through-thickness moduli and strength, fracture toughness, and damage tolerances. Due to the advantages of high temperature performance, superior dimensional stability, and cost-effective manufacturing, textile reinforced MMCs have high potential in the application of space structures or electro packaging parts. In this study, emphasis is placed on the prediction of thermal properties of three-dimensional (3D) orthogonal textile reinforced aluminum matrix composites. PAN-type carbon fibers and pure aluminum were utilized as reinforcements and matrices, respectively. Geometric model was established based upon the microstructures of the sample sections. Analytic models based on the unit cell and Selective Volume Averaging (SVA) technique have been developed to predict the coefficient of thermal expansion (CTE) of 3D orthogonal textile composites. In order to verify the model prediction, samples of 75mm diameter have been fabricated using pressure infiltration casting process and five specimens have been obtained for the determination of coefficient of thermal expansion. * Corresponding author, 66 Sangnam-dong, Changwon, Kyungnam, South Korea +82-55-280-3883, lsk6167(2Jkmail.kirnm.re.kr
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3D Orthogonal Textile Reinforced Aluminum Matrix Composites
GEOMETRIC MODEL The 3D orthogonal (ORT) woven preform consists of stuffer yarns (x-direction) and filler yarns (y-direction) and warp weavers (z-direction) which interlace stack of stuffer and filler yarns. Figure 1 (a) shows the unit cell of ORT composites. Figure 2 is the micrographs of cross-sections, which clearly demonstrate the interlocking nature of warp weaver yarn.
h
Filler yam
(a)
(b)
FIGURE 1 Schematic of unit cell. FIGURE 2 Cross-sectional micrographs: (a) y-z plane; (b) z-xplane.
The thermo-mechanical property of textile composites varies by geometrical structure and thermo-mechanical property of constituent materials. To establish a geometric model of ORT composites, the yarn cross-sections are considered rectangular shapes. Denoting the size of the unit cell in x, y, and z direction as ux, uy, and uz, respectively, they can be expressed as:
u =ws+ww ;
ur =.
uz=nts+(n-l)tf+wf
(1)
Here, w and t are the width and the thickness of the yam cross-section, and subscripts w, s, and/are warp weaver, stuffer, andfiller,respectively. The number of stuffer yam layers is indicated as n, and the volume and thefibervolume fraction of the unit cell are VuandVf, respectively. Within the unit cell volume (Vu) the total yarn volume (Vy) comprises the volumes of the warp weavers (Vyy,), the fillers (Vyf), and the staffers (Vys). With the definition of the yam packing ration (tc), which is the local fiber volume fraction of the yarn, the overall fiber volume fraction of composites can be obtained as follows. ;Vyf=2wftfuy(n Vu = uxuyuz
+ l) ; Vyw =
v =v y
y
+v
f yf
+v
[2nts+2(n-l)tf+nwf]tw Vf=KVyIVu
(2)
yw
CTE MODEL Averaging Scheme Since the unit cell was defined as the representative volume element, which is the same as the actual composite, homogenization of each yam elements in the unit cell can be applied based on the volume averaging. Figure 3 shows schematic of the sequential homogenization. Because the warp weavers, stuffer, and filler yams are arranged on a plane with specific fiber orientations, they are regarded as an independent element. In the first step, the warp weavers and the assemblage of stuffer and filler yarns are
3D Orthogonal Textile Reinforced Aluminum Matrix Composites
1083
homogenized, separately. Then, the blocks of the sniffer and the filler yarns are collected and homogenized. Finally, the unit cell consists of block I and block II as shown in Fig. 3 (a). In the homogenization process, proper assumption based upon the plain strain or the plain stress condition should be invoked.
X
>[
(a) (b) FIGURE 3 Averaging scheme under the mechanical and thermal loading: (a)three-element system for warp weaver, stuffer, and filler yarns are absorbed into two-element system: (b)warp weaver hybridization.
It is assumed that the strain or the stress of the assembled element due to temperature change is the same as the strain or stress of the individual element. When two elements are arranged in the serial connection, iso-stress condition can be assumed, and the effective coefficient of thermal expansion (CTE) multiplied by the effective compliance of the assembled element is the same as the sum of respective CTE multiplied by the compliance of individual elements. If two elements are connected in parallel, iso-stress condition can be assumed, and stiffness is involved. Serial connection: [Sre][a'!] = e
(3)
e
Parallel connection: [C ][a ] =
(4)
Here, the matrices S, C, and a denote the compliance, stiffness, and CTE, respectively. Volume Averaging of Compliance and Stiffness In obtaining the effective quantity of a warp weaver element, further simplification has been made. The curved part of the yarn is simplified as consisting of right-angled yarns as shown in Fig. 3(b). This assumption is justified because the fraction of warp weaver with respect to the whole ORT structure is normally less than 5%, and the portion of the curved part is even the less. From Eqn. (3) and (4), it is also necessary to calculate the compliance and the stiffness of the elements. Since yarns are fiber assemblage, they are considered as unidirectional composites, and the compliance matrix of a stuffer yarn, for example, is expressed as: l/Eu VnlEu
vu/En 0 0 0
-v]2l En \/E21
0
0
0
0
0
0
1/G23
0
0
0
VE22 0 0
0 0 0 0
1/G12
0
0
0
0
-V23/E22 0
-vnl
Eu
-vJE22
(5)
0 1/G
where, the Young's moduli, shear moduli, and Poisson's ratios can be obtained from the fiber and matrix properties using the well known micro-mechanics expressions [2].
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3D Orthogonal Textile Reinforced Aluminum Matrix Composites
Additionally, compliance matrices of filler yarn Sf, and those of warp weaver yarn in x-direction (Swx) and in the z-direction (Swz) can be obtained. It should be noted proper coordinate transformation is required in the determination of these matrices. Depending upon the direction of the assumed load, either the iso-strain or the iso-stress condition can be assumed, and the selective volume averaging (SVA) process is required. Let us consider warp weavers, which consist of yarn segments in the x- and z-directions as shown in Fig. 3(b). If external load is applied in the x- or y-direction, uniform strain can be assumed in each segment. Thus, the stiffness matrix is utilized in the volume averaging, and the effective stiffness constants are expressed as follows. [C]
+ [C]( ^
[ C ] ( ) ux +luz
(6)
x
z
where, the subscript i means the in-plane property, and [Cm] and [Cwz] are inverse matrices of [Swx] and [Swz] as explained previously. It is noted that the volume is replaced with length of the yam due to the same cross-sectional area. When the load is applied in the z-direction, uniform stress can be assumed, and the similar equation can be written as Eqn. (6) except for utilizing compliance matrices. Thus, [ S
]
?
[ 5 ] (
ux + 2uz
(7)
x
z
where, the subscript o means the out-of-plane property hi the homogenization of sniffer and filler yarns elements, similar process can be applied, i.e., stiffness averaging under the in-plane load, and compliance averaging under the out-of-plane load. ^
^
^
^
(8)
Finally, the homogenization of the deformation property of block I and II (Fig. 3(a)) can be carried out by using SVA. x-direction: [CJ] = [ C " ] ( ^ ) + [C'](Vys + Vyf) y-direction: [sy] = [Swl](^-) + [Spi](Vys y
+ Vyf
)
(9) (10)
y
z-direction: [C Z ] = [C"°](^) + \C°\(ys
+Vyf
)
Volume Averaging of CTE hi order to determine the effective CTE of the warp weaver element, consider Fig. 3(b) again. Since the strain induced by the temperature change in a plane can be assumed constant (iso-strain), the effective CTE of the yam can be obtained by using Eqn. (4). The effective CTE in the thickness direction can also be found by assuming serial connection of the elements. (
ur+2u,
^
}
(12)
3D Orthogonal Textile Reinforced Aluminum Matrix Composites ^
^
1085 (13)
where, CTE matrices for each yarns are expressed upon the coordinate transformations. [awxf =[as]T ={a,,a2,a3,0,0,0} ; [am]T = {«2,a3,«1,0,0,0} [af]T ={a2,av a3,0,0,0}
(14)
where, a is the CTE of the unidirectional composites with subscripts 1 in the longitudinal direction, and subscripts 2 and 3 in the transverse direction. These CTE's can be obtained from the fiber and matrix properties based upon the micro-mechanics expressions [3]. The effective CTE for the block I in Fig. 3 can be determined by SVA depending upon stuffer and filler yarn arrangement under the assumed thermal condition. (15) V
V
ys + Vyf
yf
)+ l S ] [ c c ] ( ) +
V
V
yf
y
+
(16)
V
y{
Homogenization of the thermal deformation property of block I and II (Fig. 3) can be carried out by using SVA. x-direction: [a'] = [C'F{[C«][a«]fe)HC"l[a"lfc^)} y
y-direction: [ay] = [S>']-'{[Su"][awt](-^-) + [Spl][a>"]( " ~ *")} y
(18)
y
z-direction: [g-],[C1]-'{[C"][g'°](^) + F ] [ a 1 ( F ' " F f " ) ) y
(17)
y
(19)
y
Finally, CTE's of ORT textile composites can be selected from the corresponding components from Eqn. (17) to Eqn. (19) as follows: ax = a' ; ay = a{ ; az = a\
(20)
EXPERIMENT AND RESULTS In the fabrication of 3D orthogonal woven fabric preforms, 12K carbon fibers were used for the stuffer and filler yarn and the 3K carbon fibers were used for the warp weaver. The composite was fabricated by the pressure infiltration casting (PIC) process using a permanent metallic mold [4]. Strain gages (WK-06-062AP-350, Micro-Measurement) were utilized for the measurement of CTE. Temperature of the test specimen was increased from 20 °C to 180 °C by the increment of 20 °C. The input data of the sample geometry and thermo-mechanical properties of fiber and matrix are summarized in Table 1. The geometric data were obtained from the microstructures of the sample section. The thermo-mechanical data of the constituent materials were taken from a data brochure and metal handbook. These data were utilized in the calculation of the thermo-mechanical properties of the unidirectional composites from the micro-mechanics expressions. Table 2 summarizes the comparison between the model prediction and the test
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3D Orthogonal Textile Reinforced Aluminum Matrix Composites
results. Although fairly good correlation can be observed for ay, a large discrepancy (22%) exists in the case of ax. The main reason for this discrepancy may be due to the warpage of preforms during pressure infiltration casting process. Another possibility is that the thermo-mechanical properties were obtained from literature. To validate the accuracy of the model, it is recommended to measure the properties for the unidirectional composites. TABLE I Input data of sample geometry and thermo-mechanical property of constituent materials
Geometric data 3D textile composites (unit: mm) w»,= 0.57; ^ = 033 ws = 3.6 ; ts = 0.42 wf= 2.27 ; //= 0.133 K-=0.65
Vf=57,.l%
Thermo-mechanical data
T300 carbon fiber E,f
y =24GPa
Aluminum En = 57 GPa v = 0 33 c^ = 23.5 (i/°C
; G23f= 14.3 GPa
f=0,26
= -0.5u/°C ; op = 7.0 u/°C
(Note) f/ is the measured fiber volume fraction of composites. TABLE II Comparison of test results and model predictions in 3D ORT textile composites
Coefficient of thermal . . ,„„. expansion (unit: |^/C) a, a2
«..-.. Prediction
„» Measurement
8.05 5.73
6.6 5.8
CONCLUSION (1) The geometric characteristics and the effective coefficient of thermal expansion of three-dimensional orthogonal textile composites were predicted from the analytical model. Homogenization was based upon the volume averaging of stiffness and compliance coupled with CTE of warp weaver, stuffer and filler yarns. (2) In order to confirm the analytic model, samples were fabricated by vacuum assisted pressure infiltration method. Strain gages were utilized in the measurement of CTE of the sample. Fairly good agreement has been observed between the model prediction and the test results for ay. However, a large discrepancy exists in the case of ax. Acknowledgement This research was supported by a grant from the Information Display R&D Center of the 21st Century Frontier R&D Program and National Research Laboratory funded by the Ministry of Science and Technology, Republic of Korea. REFERENCES 1 2 3 4
Byun JH, Chou TW. Mechanics of Textile Composites. In: Kelly A, Zweben C, editors. Comprehensive Composite Materials. Amsterdam: Elsevier; 2000; chapter 22. Chou TW. Microstructural design of fiber composites, Cambridge University Press, New York, 1992. Tsai SW, Hahn HT Introduction to Composite Materials, Technomic Publishing Co., Westport, Connecticut, USA, 1980. Lee SK, Byun JH, Hong SH. Effect of fiber geometry on the elastic constants of the plain woven fabric reinforced aluminum matrix composites; Materials Science and Engineering 2003;A347: 346-358.
Permeability of Sisal Textile Reinforced Composites by Resin Transfer Molding Yan Li Department of Engineering Mechanics and Technology Tongji University, Shanghai, 200092, P. R. China Yiu-Wing Mai and Lin Ye Centre for Advanced Materials Technology (CAMT) Department of Mechanical & Mechatronic Engineering, J07 The University of Sydney, Sydney, NSW 2006, Australia
ABSTRACT In this paper, linear flow model based on Darcy's law was used in the experiment to measure permeability of sisal textile. Kozeny-carman equation was used to predict the permeability of sisal textile and Kozeny constant was calculated through experimental results. Both experimental and predicted permeability values of sisal textiles were compared. Effects of fibre surface treatments on the permeability of sisal textile were also studied in this paper.
INTRODUCTION Sisal fibre is a kind of natural fibre which has high specific strength and modulus, no health risk during processing, easy availability in some countries and renewability [1, 2]. But the most attractive aspect for the utilization of this kind of fibre is its low cost [3]. Nowadays, the advantages of sisal fibres have raised great interest among materials scientists and engineers. Many researches have been done on the investigations of mechanical and physical properties of sisal fibre reinforced composites including improving the interfacial properties between sisal fibres and polymer resins [4-7]. Finding a low cost and effective manufacturing method for this economic material, however, is an important aspect for the application of sisal fibres. Resin transfer molding (RTM) is an effective and economic processing method for the manufacturing of advanced composite materials [8-10]. The infiltration of matrix into reinforcement and its consolidation are accomplished at the same time. This can improve the working efficiency quite a lot, thus lower the manufacturing cost. The key for RTM technology is to let the resin impregnate preform as soon as possible, before resin cures so that undesirable flaws, such as incomplete filling, non-uniform wetting and void can be avoided. Permeability is a parameter used to describe the easiness o'f liquid resin impregnating preforms. It is a complex function of woven pattern, tow structure, packing characteristics and intra-tow properties [11]. Most of the works which have been done before are focused on working out computational models to predict the permeability of the preforms. The permeability value of "Correspondence Author, Department of Engineering Mechanics and Technology, Tongji University, Shanghai 200092, PR. China, Fax: 86-21-65982383, E-mail: [email protected]
1088
Permeability of Sisal Textile Reinforced Composites
reinforcement is usually predicted based on the theoretical models developed for liquid resin flowing through porous media [12]. hi this study, linear flow of the liquid resin injected from a side inlet based on Darcy's law was adopted to measure the permeability values of sisal textile. Predicted values based on Kozeny-Carman equation were compared with the experimental results. The effects of fibre surface treatments on the permeability of sisal textile were also investigated in this paper. MATERIALS AND EXPERIMENT Materials Sisal textiles were obtained from Guangxi province, China. They were plain woven and have same properties in the orthogonal directions. The average diameter of sisal fibre is around 300 urn. Vinyl ester resin used in the present study was provided by Ashland Chemical. It was cured at room temperature and post cured at 120°C for 2 hours. Sisal textiles were heated at 120°C before used and before fibre surface treatments to get rid of the absorbent moisture. Two chemicals were selected to treat sisal textile which are gamma-methacryloxpropyl silane and permanganate. Experiment When resin flows through the preform during RTM process, the flow behavior of the polymer can be regarded as following Darcy's law [13]. When the flow of the matrix in the reinforcement is one-dimensional, Darcy's law can be simplified as: x2=^-P-t V
(1)
where, P is the pressure difference between two points along flow direction, x is the flow distance between those two points, r| is the viscosity of the fluid and K is the permeability. This equation provides theoretical basis for experimental measurement of permeability. Based on equation (1), an experimental method to measure permeability of reinforcement was set up. The design of this experiment is based on the vacuum aided RTM (VARTM). Usually, the thicknesses of the products made by RTM are much smaller than the other two dimensions. So the flow of the resin through the thickness can be neglected and regarded as in-plain two-dimensional flow. In order to get onedimensional flow of the matrix through the preform, a linear side injection gate was adopted. So, the flow of the resin through the fabric can be assumed as in one direction, i.e. the flow direction. Measure and record the positions of flow front of the matrix, x, and their correspondent time, t, during the impregnating process. When x2 is plotted against t, a straight line is produced. The the permeability of the preforms can be calculated.
Permeability of Sisal Textile Reinforced Composites
1089
RESULTS AND DISCUSSION Theoretical Prediction If the liquid flows along the fibre direction, the Kozeny-Carman equation can be simplified as:
4k.
(2)
Where Kx is the permeability in the fibre direction, rf is the fibre radius, kx is the Kozeny constant in the fibre direction and Vf is the fibre volume fraction. It can be seen that permeability of preform is proportional to (1-Vf)3/ Vf2. 1 layer, 2 layers and 3 layers of permanganate treated sisal textile were used to make the composites with different fibre volume fractions. Figure 1 shows permeability of sisal textile versus fibre volume fraction expression (1-Vf)3/ Vf2. A linear line curve fitting is also shown in the Figure. Kozeny constant can be calculated from the slope of the line. Table I compares the permeability values predicted by Kozeny-Carman equation with experimental results. They show good agreement with each other. All the predicted values and experimental results are in the same order of magnitude. So the Kozeny constant predicted by the present work can be used to predict the permeability of sisal textile in its future applications by Kozeny-Carman equation provided the fibre volume fraction was known. This provides a theoretical basis for the prediction of processing parameters for the production of sisal fibre reinforced composites. Effect of Fibre Surface Treatments on the Permeability of Sisal Textile From the experimental results it was observed that the square of flow distance of vinyl ester inside untreated sisal textile, silane treated sisal textile and permanganate treated sisal textile versus the correspondent time during RTM process showed very good linear relationships, which is consistent with Darcy's law. From the slopes of these curves, the permeability values of these textiles can be calculated by equation (1) and shown in Table II. Comparisons of sisal textile with synthetic preforms which
FIGURE 1 Relationship of permeability versus fibre volume fraction. (The scatters are experimental results and the line is the linear curve fitting according to Kozeny-Carman equation)
1090
Permeability of Sisal Textile Reinforced Composites
have similar fibre volume fractions are also made. It is clearly shown that fibre surface treatments have great effect on the permeability of sisal textile, especially silane treatment. The permeability value has been increased more than 2 times. High permeability is beneficial to improve the quality of composite product and working efficiency made by RTM method. Table 1 also clearly indicates that sisal fibre has better processing properties than synthetic fibres and sisal fibre is probably the most suitable reinforcement for RTM technology to make fibre reinforced composites.
TABLE I Comparisons of permeability obtained from experiment and Kozeny-Carman equation
Fibre volume fraction [%1 15.11 16.67 16.98 16.77 25.13 26.34 33.12 35.48 34.38 33.33 31.34 30.68 32.31
Experimental permeability [1010m2] 107.81 99.48 86.56 87.23 35.46 38.96 7.43 4.53 6.69 7.68 7.36 8.97 7.26
Predicted permeability [1010m2] 119.05 92.51 88.18 91.09 29.53 25.59 12.12 9.48 10.62 11.85 . 14.64 15.72 13.20
TABLE II Permeability of sisal and synthetic textile
Fibre Untreated sisal Permanganate treated sisal Silane treated sisal Woven glass fabric Woven carbon fabric
Fibre volume fraction [%] 32 32 30 30 36
Permeability [10-10m2] 6.38 7.26 15.4 5.66 5.12
Usually, the flow of resin through the preform includes inter-bundle flow and intrabundle flow [14]. The higher permeability of sisal textile compared with glass and carbon textile was caused by the larger fibre diameters of sisal textile. From the stacking theory, it is known that the larger the fibre diameters are, the larger the cavities between fibres exist. Larger fibre diameters will facilitate the inter-bundle flow which is the predominant flow during the infiltration process because interbundle flow is faster than intra-bundle flow and more matrix flow through interbundles. As discussed before, permanganate, as an oxidant, can etch sisal fibre surface. Scanning electronic micrograph of a permanganate treated sisal fibre shows that a fibre bundle was broken down into many small fibres, hence increasing the flow
Permeability of Sisal Textile Reinforced Composites
1091
channels for vinyl ester (Figure 2). This enables the flow easier and faster, and leads to a higher permeability. But the increased flow channels belong to intra-bundle flow which would not affect the whole filling process very much. So, the permeability of sisal textile was improved after permanganate treatment compared with untreated ones, but not too much. Silane treatment method has different mechanism with permanganate treatment in improving interfacial properties between sisal fibres and vinyl ester resin. Silane treatment is a kind of chemical method which introduces functional groups onto sisal fibre surface. It is known that sisal fibre is mainly made up of cellulose which has large amount of hydroxyl groups. No reactive functional groups attached on the fibre surface and this makes the surface non-polarity. However, with the existence of moisture, silane can react with cellulose of sisal fibre. The resultant chemicals attached on sisal fibres after chemical reactions is: CH2CH3CCOO(CH2)3Si(OH)2OG. These chemical molecules lead to strong polarity to sisal fibre and increase the surface tension as well [15]. So the induced polarity facilitates the filtration of vinyl ester through sisal textile greatly. This explains why silane treatment can improve the permeability of sisal textile from 6.38xlO"10 m2 to 15.4xlO'10 m2.
(a)
(b)
FIGURE 2 Fibre surface structures (a) permanganate treated sisal fibre; (b) untreated sisal fibre
CONCLUSIONS Experimental measurement of linear flow of the matrix injected from a side gate based on Darcy's law is an effective method to evaluate the permeability of sisal textile. Predicted permeability values calculated from Kozeny constant show good agreement with experimental results. Kozeny-Carman equation can be used to predict the permeability of sisal textile as long as the fibre volume fraction is given. Fibre surface treatments show great effect on the permeability of sisal textile. By introducing strong polarity functional groups onto sisal fibre surface, silane treatment can increase the permeability of sisal textile by almost two times. This is beneficial for the processing of sisal textile reinforced composites by RTM. Permanganate can break down sisal bundles into small fibres, thus increase the flow channels inside the preform and hence the permeability.
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Permeability of Sisal Textile Reinforced Composites
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Murherjee, P. S. and Satyanarayana, K. G. 1984. Structure and Properties of Some Vegetable Fibres, Part 1 Sisal Fibre. Journal of Materials Science, 19: 3925-3934 Chand, N., Sood, S., Rohatgi, P. K. and Sayanarayana, K. G. 1984. Resources, Structure, Properties and Uses of Natural Fibres of Madhya Pradesh. Journal of Scientific and Industrial Research, 43: 489-499 Bisanda, E. T. N. and Ansell, M. P. 1992. Properties of Sisal - CNSL Composites. Journal of Materials Science, 27: 1690-1700 Varghese, S., Kuriakose, B. Thomas, S. and Koshy, A. T. 1994. Mechanical and Viscoelastic Properties of Short Fibre Reinforced Natural Rubber Composites: Effects of Interfacial Ddhesion, Fibre Loading, and Orientation. Journal of Adhesion Science & Technology, 8: 235-248 Bisanda, E. T. N. and Ansell, M. P. 1991. The Effect of Silane Treatment on the Mechanical and Physical Properties of Sisal - Epoxy Composites. Composites Science and Technology, 41: 165178 Pavithran, C , Mukherjee, P. S., Brahmakumar, M. and Damodaran, A. D. 1988. Impact Performance of Sisal - Polyester Composites. Journal of Materials Science Letters, 7: 825-826 Rong, M. Z., Li, R. K. Y., Ng, C. N., Tjong, S. C , Mai, Y. W. and Zeng, H. M. 1998. Effect of Ffibre Pretreatment on the Impact Fracture Toughness of Sisal Fibre Reinforced Polymer Composites, in Pro. First Asian-Australian Conference on Composite Materials (ACCM — 1), pp433-l to 433-4 Lee, L. J. 1997. Liquid Composite Molding, Advanced Composites Manufacturing. Timothy G. Gutowski, John Willey & Sons, Inc., pp393. Tari, M. J., Bals, A., Park, J., Lin, M. Y. and Hahn, H. T. 1998. Rapid Prototyping of Composite Parts Using Resin Transfer Molding and Laminated Object Manufacturing, Composites Part A: Applied Science and Manufacturing, 29: 651-661 Lehmann, U. and Michaeli, W. 1998. Cores Lead to an Automated Production of Hollow Composite Parts in Resin Transfer Moulding, Composites Part A: Applied Science and Manufacturing, 29: 803-810 Velten, K., Lutz, A. and Friedrich, K. 1999. Quantitative Characteriszation of Porous Materials in Polymer Processing, Composites Science and Technology, 59: 495-504 Choi, M. A., Lee, M. H., Chang, J. and Lee, S. J. 1998. Permeability Modeling of Fibrous Media in Composite Processing, Journal of Non-Newtonian Fluid Mechanics, 79: 585-598 Darcy, H. 1956. Les fontainespublique de la ville de Dijon. Paris: Dalmont. Lekakou, C , Johari, M. A. K., Norman, D. and Bader, M. G. 1996. Measurement Techniques and Effects on In-plane Permeability of Woven Cloths in Resin Transfer Moulding, Composites: Part A 27A: 401-408 Li, Y. 2002. PhD dissertation, School of Aerospace, Mechanical and Mechatronic Engineering, The University of Sydney, Sydney, NSW, Australia.
Index of Authors Abadi, M. T. 195-200 Abbasi, F. 811-816 Abdul Khalil, H. P. S. 15-20, 149-153 Ageetha, S. 903-907 Ahmad, F. 545-550,651-657 Ai, X. 772-777 Al-Assafi, S. 509-514 Ambika, R. 903-907 Atadero, B. 1012-1017 Atherton, K. 957-962 Babu, P. E. J. 629-634 Bae, S.-I. 500-505 Bai, R. X. 337-342 Bao, N. Z. 823-827 Bechtold, G. 828-833 Ben, G. 908-913 Bhattacharyya, D. 154-162, 796-802 Bochenek, B. 257-263 Boey, F. 106-111 Boorboor, D. 357-362 Bruijn, P. 124-130 Burchill, P. J. 515-520,969-974 Byun, J.-H. 488-493,1081-1086 Cantwell, W. 852-857 Cardew-Hall, M. 852-857 Chang, H. R. 748-752 Chang, P. 615-620 Chen, D. H. 46-51 Chen, H. B. 409-415,416-421 Chen, H. R. 337-342 Chen, H.-S. 62-67 Chen, L. 713-718 Chen,X. H. 187-192 Chen, Z. P. 124-130 Chen, Z.-R. 858-863,1032-1037 Cheng, L. J. 288-293 Chiang, C.-L. 742-747,748-752,784-789 Chiu, W. K. 1025-1031 Cho, M. 249-254 Cho, S.-S. 846-851 Cho, Y. J. 100-105 Choi, Y.-G. 1032-1037 Choupani, N. 403-408 Chow, W. S. 790-795 Chu,W. 169-174 Chuang,W.-P. 731-735 Chung, D. S. 658-662 Compston, P. 852-857 Cox, B.N. 615-620 Cui, Y. H. 695-700 Daghyani, H. R. 195-200,313-318 Dai, Y. 588-593,594-599 Darbari, A. M. 325-330 Darling, A. 1052-1057 Das, B. B.903-907
Davuluri, S. P. 719-724 Diao, X. X. 349-354 Dias, M. L. 163-168 Ding, X. 52-56 Dong, Z.-X. 665-670 Du, S. Y. 926-930,1064-1069 Duan, K. 433-438 Dunlop, L. A. 131-136 Easteal, A. J. 796-802,894-899 Enoki, M. 658-662 Ertiin, T. 21-26 Fainleib, A. 175-180,181-186 Fang, D.-N. 665-670 Fang, Z. 1052-1057 Fariborz, S. 195-200 Fasce, L. 163-168 Feih, S. 445-451 Feng, X. 46-51,823-827 Ferreira, A. J. M. 229-234 Foliente, G. 1005-1011 Friedrich, K. 571-576,671-676,754-759 Frontini, P. 163-168 Fu, S. Y. 68-71,472-476,707-712 Fukui, E. 1058-1063 Fukui, T. 397-402,1047-1051 Fukunaga, H. 677-682 Funabashi, M. 57-61 Funami, K. 370-375 Galea, T. 27-32 Gao, X.-L. 363-369 Gardiner, C. P. 131-136,969-974 Ghaffarian, S. R. 357-362,577-582 Gokdag.E. 187-192 Gonno, H. 9-14 Gou, J. H. 683-668 Grigoryeva, O. 175-180,181-186 Gupta, M. 635-638 Haddadi-asl, V. 72-77 Halliwell, R. 27-32 Ham, K.-C. 500-505 Hamada, H. 218-222,397-402,466-471,621626,1041-1046,1047-1051 1058-1063 Han, K. S. 276-281,870-875 Han, M.-S. 500-505 Han, S. Y. 270-275 Harper, L. T. 521-526 Hasan, MD. A. 846-851 Hatakeyama, H. 57-61 Hatta, S. 9-14,527-532 Hayashi, Y. 1070-1075 He, C. B. 713-718 He, M. 823-827 Heo, S. I. 870-875 Hirose, S. 57-61
1094
Index of Authors
Hodzic, A. 41-45,565-570 Hoffman, M. 94-99,331-336 Hong, C.-H. 264-269,963-968 Hong, S. H. 658-662,1081-1086 Hosokawa, K. 207-211 Hosseini-Toudeshky, H. 313-318 Hou, M. 805-810 Houshyar, S. 41-45,565-570 Hsu, C.-W. 742-747, 784-789 Hu, C. G. 689-694 Hu, N. 679-684 Hu, X. 106-111, Hu, X. Z. 433-438 Hu, Y. Q. 639-644 Hu, Z. Q. 639-644 Huang, C.J. 707-712 Huang, H. T. 943-948 Huang, H.-C. 212-217 Huang, J. C. 701-706 Huang, N. 999-1004 Huang, X. P. 772-777 Hwang, B.-S. 488-493 Hwang, I. H. 477-481 Hwang, W. 294-298
Kim, G.-I. 249-254 Kim, H. Y. 658-662 Kim, H.-C. 766-771 Kim, J.-K. 689-694 Kim, J.-S. 249-254 Kim, S. J. 477-481 Kim, S. S. 282-287 Kim, S.-H. 981-986 Kim, W.-S. 981-986 Kim, Y. J. 137-142 Kimpara, I. 370-375,376-381 Kimura, T. 9-14,527-532 Kitipomchai, S. 975-980 Kobayashi, H. 1018-1024 Komiya, I. 1058-1063 Kong, C. D. 83-87 Kong, H. 888-893 Kramer, L. 683-688 Kruckenberg, T. 858-863 Kuan, H.-C. 731-735,736-741,742-747,748752,778-783 Kung, H.-K. 62-67 Kurashiki, T. 1070-1075,1076-1080 Kuwahara, J. 987-992
Ichimura,J. 319-324 Inoda, M. 1041-1046 Iscioglu, G. 21-26 Issam, A. M. 15-20, 149-153
Lam, H. F. 975-980 Lam, S. W. 461-465 Latif, M. Ridzuan. A. 545-550 Law, S. 343-348 Lee, C.-C. 931-936 Lee, D. G. 282-287 Lee, D. H. 864-869 Lee, H.-J. 846-851 Lee, H.-Y. 583-587 Lee, J. W. 83-87 Lee, J.-J. 766-771,981-986 Lee, J.-R. 583-587 Lee,L. S. 1012-1017 Lee, S. K. 270-275 Lee, S. M. 282-287 Lee, S.-E. 766-771 Lee, S.-K.1O81-1O86 Lee, T.-M. 784-789 Lee, W. II 864-869 Leong, K. H. 557-562 Lessard, L. B. 349-354 Lewinsohn, C. A. 603-608 Li, K. 363-369 Li.L.F. 68-71,707-712 Li, M. 68-71 Li, Q. F. 926-930 Li, Q. Y. 382-387 Li, R.-Y. 609-614 Li, S. L. 926-930 Li, Y. (P. 12) 68-71 Li, Y. (P.177)1087-1092 Liang, G.G.H. 894-899 Liang, J. 1064-1069 Liang, Z. Y. 683-688 Liang, Z.-Q. 494-499
Jayaraman, K. 27-32 Ji, X. 588-593,594-599 Jiang, T. H. 683-688 Jiang, X.H. 46-51 Joe, C.-R. 299-304 Johnstone, B. 834-839,840-845 Jones, F. 143-148 Jung, C.K. 276-281 Jung, K. 100-105 Kadokura, K. 9-14 Kalyanasundaram, S. 852-857 Kameyama, M. 677-682 Kang, D.-H. 264-269, 963-968 Kang, M. K. 864-869 Kang, T. J. 100-105 Karad, S. 143-148 Karbhari, V. M. 169-174, 288-293,1012-1017 Karger-Kocsis, J. 181-186,409-415,790-795 Karunaratne, B. S. B. 817-822 Katzos, A. 243-248 Kayis, B. 551-556 Kendall, K. N. 521-526 Khatibi, A. A. 422-427 Khondker, O. A. 397-402,1047-1051 Kim B.-S. 299-304 Kim, A. 846-851 Kim, C.-G. 264-269, 766-771 Kim, C.-U. 264-269,963-968 Kim, C.-W. 237-242,963-968
Index of Authors Lievana, E. 181-186 Lin, R. J. T. 154-162 Liu,C. 823-827 Liu, H.-X. 428-432 Liu, H.-Y. 307-312,428-432 Liu, J. 725-730 Liu, L. 118-123 Liu.S.L. 416-421 Liu, T.X. 713-718 Lopez, A. 482-487 Low, I. M . 112-117,482-487 Lu, L. 635-638 Lu, M. 834-839,840-845 Lu, S.-C. 748-752 Lu, X. 3-8 Lu, X. H. (p. 134) 823-827 Lu, X. H. (p.116) 713-718 Lii, Z. J. 772-777 Luo, Y. 571-576 Ma, C.-C. M. 731-735,736-741,742-747,748752, 778-783,784-789,876-881 Ma, S. 52-56 Mahajerin, E. 201-206 Mahmood, U. 112-117 Mai, Y.-W. 307-312,403-408,433-438,588593,594-599,645-650,834-839,840-845,10871092 Masoomi, M. 577-582 Mathys, Z. 969-974, Matsumoto, K. 207-211,1076-1080 McGuckin, D. 388-393 Mills, T. 27-32 Min, B.-G. 583-587 Miyano, Y. 319-324 Mizutani, T. 937-942 Mohafezatkar, F. 72-77 Mohamed, A. T. 452-458 Mohammadi, N. 577-582 Mohd Ishak, Z. A. 790-795 Moon, R. 94-99,331-336 Mosse, L. 852-857 Mouritz, A. P. 615-620,888-893 Murakawa, H. 603-608 Nakada, M. 319-324 Nakai, A. 218-222,397-402,466-471,621626,1041-1046,1047-1051,1058-1063 Nakai, Y. 439-444 Nakanishi, Y. 1076-1080 Narita, T. 1058-1063 Nazokdast, H. 72-77 Ngatimin, W. 88-93 Ni, J. H. 539-544 Nisar, H. 545-550 Nishi, T. 937-942 Nosier, A. 223-228 O'Brien, E. 957-962 Ochi, A. 621-626
1095 Ochi, S. 33-38 Ogi, K. 914-919 Oh, D.-J. 237-242 Oh, J. 249-254 Okabe, T. 993-998 Okabe, Y. 937-942,987-992 Okano, M. 218-222,466-471 Pacheco, E. B. A. V., 163-168 Paget, C. A. 957-962 Pai, B. C. 629-634 Park, D. C. 282-287 Park, J. Y. 270-275 Park, S.H. 276-281 Park, S.-J. 583-587 Park, S.-W. 963-968 Park, Y.-H. 864-869 Paton, R. 124-130,888-893 Phung, T. 124-130 Pillai, U. T. S. 629-634 Poon, C.-K. 949-954 Pyrz, R. 257-263 Qiu, G.-X. 494-499 Rezaeepazhand, J. 223-228,325-330,920-925 Rispler, A. 243-248,533-538 Rodriguez Pita, V. J. 163-168 Rong, M. Z. 3-8,571-576,671-676 Rosalie, S. C. 1025-1031 Ruan, W. H. 671-676 Rudd, C. D., 521-526 Rutgers, L. 94-99,331-336 Sabouri, H. 920-925 Sadeghi, G. 313-318 Sakata, K. 908-913 Savci, S. 551-556 Savithri, S. 629-634 Schubel, P. J. 521-526 Sekine, N. 319-324 Seltzer, R. 163-168 Serizawa, H. 603-608 Shanks, R. A. 41-45,565-570 Shen, Z. 472-476 Shi, Y. W. 645-650 Shimamoto, A. 931-936 Shimamura, Y. 1018-1024 Shin, S. J. 100-105 Shojaei, A. 357-362,811-816 Sikorsky, C. 1012-1017 Simpson, G.J. 515-520 Smith, C.834-839,840-845 Sobolev, K. 21-26, Soh, A. K. 665-670 Song, J.-I. 500-505 Song, S.-H. 237-242 Song, S.-W. 488-493 S0rensen, B.F. 445-451 Soutis, C. 83-87
1096 StJohn, N. A. 131-136 Starly, B. 1052-1057 Starostenko, O. 175-180,181-186 Su, H.-Y. 731-735,778-783 Su, Z. 999-1004,1005-1011,1032-1037 Sugimoto, K. 218-222,466-471,621-626,10411046 Sun, W. 1052-1057 Sun, X. N. 243-248 Suzuki, K. 370-375,376-381 Suzuki, T. 527-532
Index of Authors Wetzel, B. 571-576 Whitbourn, J. 88-93 Wo, D. Z. 695-700 Wong, S.-C. 106-111,713-718,719-724 Wood, M. D. K. 243-248 Wouterson, E. 106-111 Wu, H.-L. 876-881 Wu, J. S. 409-415,416-421,725-730 Wu, L. X. 169-174 Wu, Z. J. 118-123,926-930 Xiao, K. Q. 760-765
Tahani, M. 223-228 Tai, H., 742-747 Takagi, H. 33-38 Takao, Y. 914-919 Takeda, N. 937-942,987-992,993-998 Takura, R. 33-38 Tamaue, H. 987-992 Tanaka, H. 439-444 Tao, J. 695-700 Tao, X. M. 461-465 Tay, K. W. 635-639 Tilbrook, M. 94-99,331-336 Todoroki, A. 1018-1024 Tolstov.A. 175-180,181-186 Tong, L. Y. 243-248 Tsai, J.-L. 701-706 Tsuji, R. 937-942 Tiirker, P. 21-26 Turner, T. A. 521-526 Ueda, M. 1018-1024 Uhl.F.M. 719-724 Um, M.-K. 488-493 Vaihola, S. 482-487 Varley, R. 557562 Veidt, M. 975-980 Verpoest, I. 1070-1075 Vilaiphand, W. 482-487 Vimala, P. 903-907 Wan Rosli, W. D. 149-153 Wang, B. 683-688 Wang, C. P. 778-783 Wang, D. F. 118-123 Wang, K. J. 882-887 Wang, K. S. 1064 Wang, M. 337-342 Wang, S. S. 187-192 Wang,X. M. 1005-1011 Wang, Y. M. 52-56,78-82,539-544 Wang, Y. P. 78-82 Warrior, N. A. 521-526 Webster, D. C. 719-724
Yan, C. 343-348,639-644 Yan, Q. 68-71 Yan, W.I 54-162 Yan, W. Y. 307-312 Yang, C.-H 609-614 Yang, J.-C. 742-747 Yang, J.-L. 754-759 Yang, S. C. 472-476 Yang, Y. C. 870-875 Yang, Z. H. 823-827 Yashiro, S. 993-998 Ye, L. 88-93,343-348,388-393,403-408,472476,588-593,594-599,639-644,645-650,805810,834-839,840-845,858-863,999-1004,10051011,1032-1037,1087-1092 Ye, Z.-M. 428-432 Yeginobali, A. 21-26 Yeh, M.-K. 212-217 Yi, X.-S. 494-499,882-887 Yip, M.-C. 609-614 You, C.-S. 294-298 Yu, S. W. 382-387 Yu, T. X. 461-465 Yu, X. B. 388-393 Yuan, Q. 88-93 Yuan, X. W. 796-802 Yun, J. C. 870-875 Zako,M. 1070-1075,1076-1080 Zebarjad, S. M. 223-228 Zhang, A. D. 52-56 Zhang, B. M. 118-123, 926-930 Zhang, C. 683-688 Zhang, H. 539-544 Zhang, H. F. 639-644 Zhang, L. C. 760-765 Zhang, M. Q. 3-8,571-576,671-676 Zhang, X. P. 88-93,645-650 Zhang, Y.H. 68-71,707-712 Zhang, Z. 754-759, Zhao, J. 772-777 Zhou, L. M. 943-948,949-954 Zou, L. M. 539-544