Synthetic Polymer-Polymer Composites

819 Pages·2012·48.068 MB·English

by  Debes Bhattacharyya, Stoyko Fakirov

Debes Bhattacharyya
Stoyko Fakirov
Synthetic
Polymer-Polymer
Composites
Bhattacharyya, Fakirov
Synthetic Polymer-Polymer Composites

Debes Bhattacharyya
Stoyko Fakirov
Synthetic
Polymer-Polymer
Composites
Hanser Publishers, Munich Hanser Publications, Cincinnati
The Editors:
Prof. Dr. Debes Bhattacharyya,
The University of Auckland, Department of Mechanical Engineering,
Centre for Advanced Composite Materials (CACM), Private Bag 92019, Auckland 1142, New Zealand
Prof. Dr., DSc Stoyko Fakirov,
The University of Auckland, Centre for Advanced Composite Materials, Private Bag 92019, Auckland 1142,
New Zealand
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Library of Congress Cataloging-in-Publication Data
Synthetic Polymer-Polymer Composite / Debes Bhattacharyya, Stoyko Fakirov.
p. cm.
Includes bibliographical references and indexes.
ISBN 978-1-56990-510-4 (hardcover) -- ISBN 1-56990-510-X (hardcover) -- ISBN 978-3-446-42277-3
(hardcover) 1. Polymeric composites. I. Bhattacharyya, D. II. Fakirov, Stoyko.
TA418.9.C6S96 2012
547’.7--dc23
2012001955
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Preface
The awareness about adverse environmental impacts of synthetic, petroleum-based poly-
mers is steadily increasing and has already caused some worldwide concern. What is more,
this concern is ascending because of the use of synthetic polymers is increasing rather
than decreasing. A good example in this respect is the usage of poly(ethylene terephthalate)
(PET) whose production has an annual growth of 10%, mostly due to its excellent prop-
erties as packaging material for various products that include pressurized beverages, food
articles and medicines. The expected future growth is strongly supported by the fact that
a large percentage of food products is often wasted because of bad or lack of packaging.
In their efforts to change the situation, many countries, such as China and India, are
likely to increase the usage of plastics packaging containers. However, in many countries
legislations are introduced to control the amount of plastics used. For example, in the
European Union, it will be not allowed after 2015 to use in the cars manufacturing plastics
having more than 5 wt% incineration quota*.
A decade or so ago, researchers believed that the commonly used polymer composites,
comprising about 30% glass fibers, would be replaced by nanocomposites having only 2
to 5 wt% nano-sized materials as reinforcement. Unfortunately, this expectation has turned
out to be somewhat elusive and researchers have started to look for alternative ways of
replacing the traditional glass fibers with natural, biodegradable materials, mostly with
fibrous structure. The potential of this approach has been demonstrated in our book
entitled Engineering Biopolymers: Homopolymers, Blends and Composites (Hanser Publica-
tion, 2007).
In this book we show another approach for replacing glass and other inorganic fibers
as reinforcements for polymer composites. This replacement could be again synthetic,
petroleum-based polymer but prepared as fibers, micro- or nanofibrils. Of course, this
approach is not as advantageous as using natural fibers that are biodegradable and eco-
friendly. At the same time, the synthetic polymer-polymer composites seem to be much
more acceptable from the environmental point of view because they, being organic in
* A. Bismarck et al., Plant fibres as reinforcement for green composites, in Natural Fibres, Biopolymers, and
Biocomposites (Eds. A. Mohanty, M. Misra and L. T. Drzal) CRC/Taylor & Francis, 2005, pp. 37–108.
nature, are prone to incineration process. In addition to their environmental advantages,
compared to the polymer composites with mineral reinforcements with high weight/volume
fractions, they are likely to possess much better specific mechanical properties. This positive
attribute allows them to be used to manufacture lightweight products and structures, a
fact that has particular importance in the transportation and packaging industries.
This book is an attempt to collate information from a group internationally known
researchers and demonstrate the state-of-the-art applications of synthetic, but organic in
nature, materials as carbon fibers, carbon nanotubes, synthetic polymers in the forms of
fibers, and micro-/nanofibrils as replacements of mineral reinforcements. We would like
to thank all the contributors for their willingness to participate in this exercise and being
patient during the compilation work. The editors also wish to thank the Centre for
Advanced Composite Materials, University of Auckland for providing a range of facilities
and the Ministry of Science and Innovation, New Zealand for financially supporting
Dr. Fakirov.
D. Bhattacharyya
S. Fakirov
Auckland, November 2011
Contents
PART I INTRODUCTION
Chapter 1 Manufacturing and Processing
of Polymer Composites
J. Schuster, M. Duhovic, D. Bhattacharyya
1.1. Introduction........................................................................................................... 3
1.2. Autoclave-processing.............................................................................................. 5
1.2.1. Introduction.................................................................................................... 5
1.2.2. Equipment...................................................................................................... 5
1.2.3. Laminate assembly......................................................................................... 5
1.2.4. Process description......................................................................................... 6
1.2.5. Further developments..................................................................................... 7
1.3. Pultrusion.............................................................................................................. 7
1.3.1. Introduction.................................................................................................... 7
1.3.2. Equipment...................................................................................................... 7
1.3.3. Process description......................................................................................... 8
1.4. Filament winding and placement techniques........................................................10
1.4.1. Filament winding...........................................................................................10
1.4.2. Tape-laying....................................................................................................15
1.5. Liquid composite molding.....................................................................................18
1.5.1. Introduction...................................................................................................18
1.5.2. LCM processes with single sided tools..........................................................19
1.5.3. Double sided tool LCM processes..................................................................23
1.6. Thermoforming of semifinished thermoplastic composite sheets..........................26
1.6.1. Double belt press forming .............................................................................26
1.6.2. Continuous compression molding..................................................................26
1.6.3. Roll forming...................................................................................................27
1.7. Combined forming processes.................................................................................29
1.7.1. Thermoforming and injection/compression molding.....................................29
1.7.2. Pultrusion/impregnation and roll forming....................................................29
1.8. Post processing of composites...............................................................................30
1.8.1. Welding of thermoplastics.............................................................................31
1.9. Conclusions and outlook.......................................................................................32
References: ....................................................................................................................32
viii Contents
Chapter 2 Melting of Polymer-Polymer Composites
by Particulate Heating Promoters
and Electromagnetic Radiation
T. Bayerl, A. Benedito Borrás, J.-I. Andrés Gallego,
B. Galindo Galiana, P. Mitschang
2.1. Introduction..........................................................................................................39
2.2. State of the art .....................................................................................................40
2.2.1. Induction heating ..........................................................................................41
2.2.2. Microwave heating.........................................................................................43
2.3. Selective melting using particulate fillers .............................................................48
2.3.1. Selective melting by induction.......................................................................49
2.4. Selective melting by microwave radiation.............................................................57
2.4.1. Effect of different susceptor materials...........................................................57
2.4.2. Influence of dispersion quality.......................................................................60
2.5. Concepts for an industrial application..................................................................61
2.6. Conclusions and outlook.......................................................................................62
Acknowledgements ........................................................................................................63
References .....................................................................................................................63
Further Reading............................................................................................................64
Chapter 3 Inter-Particle Distance and Toughening Mechanisms
in Particulate Thermosetting Composites
H. S. Kim
3.1. Introduction..........................................................................................................65
3.2. Various conditions for fracture surface morphology.............................................66
3.3. Inter-particle/void distance and toughening mechanism......................................67
3.3.1. Theoretical inter-particle distance.................................................................68
3.3.2. Method for inter-particle distance measurement...........................................69
3.3.3. Statistical properties of inter-particle distance..............................................74
3.3.4. Experimental inter-void distance and toughness...........................................81
3.4. Toughening mechanisms in the presence of compressive stress
around particles/voids ..........................................................................................89
3.4.1. Necessary conditions for cavitation...............................................................89
3.4.2. Graphical understanding of compressive stress around particles..................90
3.4.3. Creating compressive stress around modifier particles
as a toughening method ................................................................................91
Contents ix
3.4.4. Production of mechanical testing specimens.................................................92
3.4.5. Mechanical properties of toughened epoxies .................................................93
3.4.6. Fracture surface morphology examination ....................................................93
3.4.7. Stress intensity factor influenced by compressive residual stress..................97
3.4.8. Mohr circle analysis for fracture surface morphology..................................100
3.4.9. Interaction of toughening mechanisms........................................................106
3.5. Conclusions.........................................................................................................111
References ...................................................................................................................112
PART II POLYMER-POLYMER COMPOSITES WITH
PREMADE FIBROUS REINFORCEMENT
Chapter 4 Fracture Behavior of Short Carbon Fiber Reinforced
Polymer Composites
S. P. Bao, G. D. Liang, S. C. Tjong
4.1. Introduction........................................................................................................119
4.2. Deformation of SCF-reinforced composites ........................................................120
4.2.1. Carbon fiber-polymer matrix interface........................................................120
4.2.2. Fiber length.................................................................................................124
4.2.3. Matrix microstructure.................................................................................126
4.2.4. Fiber orientation..........................................................................................128
4.3. Fiber hybridization.............................................................................................130
4.4. Fracture toughness of SCF-reinforced composites..............................................132
4.5. Fatigue failure.....................................................................................................138
4.6. Conclusions and outlook.....................................................................................141
References ...................................................................................................................141
Chapter 5 Polymer-Carbon Nanotube Composites:
Melt Processing, Properties and Applications
S. Pegel, T. Villmow. G. Kasaliwal, P. Pötschke
5.1. Introduction........................................................................................................145
5.2. Microscopy based characterization of dispersion, distribution,
and alignment of nanotubes in polymer matrices...............................................148
5.2.1. Light microscopy .........................................................................................148
5.2.2. Transmission electron microscopy ...............................................................149