Polymer Glasses


Book Description

"the present book will be of great value for both newcomers to the field and mature active researchers by serving as a coherent and timely introduction to some of the modern approaches, ideas, results, emerging understanding, and many open questions in this fascinating field of polymer glasses, supercooled liquids, and thin films" –Kenneth S. Schweizer, Morris Professor of Materials Science & Engineering, University of Illinois at Urbana-Champaign (from the Foreword) This book provides a timely and comprehensive overview of molecular level insights into polymer glasses in confined geometries and under deformation. Polymer glasses have become ubiquitous to our daily life, from the polycarbonate eyeglass lenses on the end of our nose to large acrylic glass panes holding water in aquarium tanks, with advantages over glass in that they are lightweight and easy to manufacture, while remaining transparent and rigid. The contents include an introduction to the field, as well as state of the art investigations. Chapters delve into studies of commonalities across different types of glass formers (polymers, small molecules, colloids, and granular materials), which have enabled microscopic and molecular level frameworks to be developed. The authors show how glass formers are modeled across different systems, thereby leading to treatments for polymer glasses with first-principle based approaches and molecular level detail. Readers across disciplines will benefit from this topical overview summarizing the key areas of polymer glasses, alongside an introduction to the main principles and approaches.




The Physics of Glassy Polymers


Book Description

Since the publication of the first edition of The Physics of Glassy Polymers there have been substantial developments in both the theory and application of polymer physics, and many new materials have been introduced. Furthermore, in this large and growing field of knowledge, glassy polymers are of particular interest because of their homogeneous structure, which is fundamentally simpler than that of crystalline or reinforced materials. This new edition covers all these developments, including the emergence of the polymer molecule with its multiplicity of structure and conformations as the major factor controlling the properties of glassy polymers, using the combined knowledge of a distinguished team of contributors. With an introductory chapter covering the established science in the subject are and summarising concepts assumed in the later chapters, this fully revised and updated second edition is an essential work of reference for those involved in the field.




Understand the Mechanical Behaviors of Polymer Glasses Under Extension and Compression


Book Description

"It is of great fundamental important and practical interest to understand what controls the mechanical properties of polymeric glasses, such as shear yielding, necking, crazing, strain hardening and the brittle-ductile transition. Despite the tremendous efforts in the past decades to explorer the mechanical instabilities of polymer glasses, many topics about the nature of glass transition, nature of stress remain vague and under extensive debates. In this dissertation, we carried out a series of mechanical tests to study the mechanical response of polymeric glasses in both uniaxial extension and compression. Based on our recent phenomenological molecular model, this work investigates the origin of mechanical stress based on stress relaxation and brittle-ductile transition experiments of polymer glasses. Different from previous models emphasizing the inter-segmental contribution in stress, our stress relaxation experimental results revealed the important role of chain network by intra-chain connectivity and chain uncrossability. In Capture III, in room temperature stress relaxation experiments, we studied the stress relaxation behaviors of four different commercial polymer glasses under both extension and compression large ductile deformation over a wide range of rate. It was found that the initial stress relaxation rate after holding post-yield deformation is linearly proportional to the rate of prior deformation. While the pre-yield stress relaxation is logarithmically slow. This rate rescaling behaviors indicates the surviving segmental mobility in absence of ongoing deformation was due to the yield induced activation process. In Capture IV, to elucidate the nature of stress during deformation and stress relaxation, temperature for stress relaxation was increased to near Tg. All the pre-yield stress would vanish within fast segmental relaxation time independent of rate, while the initial post-yield stress relaxation can be either faster or far slower than the segmental dynamics dependents on prior deformation rate. Residual stress after large post-yield relaxation was observed to retain significant levels on the time scale much longer than the time scale for all the rate range investigated near Tg. Supporting results by MD simulation shown the chain network is essential in the mechanical response of uniaxial compression of glassy polymers through the chain network's lateral resistance to the lateral expansion and contribute to compressive stress. In Capture V and VI, to understand the role of chain network under uniaxial compression, we systematically studied how the structural change of chain network dictates whether the uniaxial compression of polymer glasses is ductile or suffers brittle fracture. Those structural characteristics of the perceived chain network can be changed by variation of molecular weight, molecular composition, and anisotropic reconstruction through melt stretching"--Website of ETD."




An Introduction to the Mechanical Properties of Solid Polymers


Book Description

Provides a comprehensive introduction to the mechanical behaviour of solid polymers. Extensively revised and updated throughout, the second edition now includes new material on mechanical relaxations and anisotropy, composites modelling, non-linear viscoelasticity, yield behaviour and fracture of tough polymers. The accessible approach of the book has been retained with each chapter designed to be self contained and the theory and applications of the subject carefully introduced where appropriate. The latest developments in the field are included alongside worked examples, mathematical appendices and an extensive reference. Fully revised and updated throughout to include all the latest developments in the field Worked examples at the end of the chapter An invaluable resource for students of materials science, chemistry, physics or engineering studying polymer science







Mechanical Properties and Testing of Polymers


Book Description

This volume represents a continuation of the Polymer Science and Technology series edited by Dr. D. M. Brewis and Professor D. Briggs. The theme of the series is the production of a number of stand alone volumes on various areas of polymer science and technology. Each volume contains short articles by a variety of expert contributors outlining a particular topic and these articles are extensively cross referenced. References to related topics included in the volume are indicated by bold text in the articles, the bold text being the title of the relevant article. At the end of each article there is a list of bibliographic references where interested readers can obtain further detailed information on the subject of the article. This volume was produced at the invitation of Derek Brewis who asked me to edit a text which concentrated on the mechanical properties of polymers. There are already many excellent books on the mechanical properties of polymers, and a somewhat lesser number of volumes dealing with methods of carrying out mechanical tests on polymers. Some of these books are listed in Appendix 1. In this volume I have attempted to cover basic mechanical properties and test methods as well as the theory of polymer mechanical deformation and hope that the reader will find the approach useful.




Mechanical Properties of Solid Polymers


Book Description

A concise, self-contained introduction to solid polymers, the mechanics of their behavior and molecular and structural interpretations. This updated edition provides extended coverage of recent developments in rubber elasticity, relaxation transitions, non-linear viscoelastic behavior, anisotropic mechanical behavior, yield behavior of polymers, breaking phenomena, and other fields.







Segmental Dynamics of Polymer Glasses During Deformation


Book Description

A probe reorientation technique is used to measure changes in the segmental dynamics of polymer glasses during and after deformation. In this thesis, experiments are performed on poly(lactic acid) (PLA) and lightly crosslinked poly(methyl methacrylate) (PMMA) glasses in which fluorescent probe molecules, N,N'-dipentyl-3,4,9,10-perylenedicarboximide (DPPC), are dispersed. Glasses are subject to constant strain rate deformation and cyclic loading/unloading using a custom-built deformation apparatus that allows for concurrent fluorescence detection. The work described in this thesis provides quantitative dynamics and mechanical data that can test existing models and theories that describe the nonlinear deformation of polymer glasses. This is expected to improve predictions of the mechanical properties of polymer glasses and expand the utility of these materials in engineering applications. The segmental dynamics of PLA glasses between Tg - 15 K and Tg - 25 K are monitored during uniaxial extension at constant strain rates from 6x10^(-6) to 3x10^(-5) s-1. Segmental relaxation times are decreased by up to a factor of 30 in the plastic flow regime relative to the undeformed state. In the plastic flow regime, the segmental relaxation time is related to the local strain rate via a power law. Additionally, is it observed that the segmental dynamics become more homogeneous during deformation. Comparisons to previous probe reorientation experiments on lightly crosslinked PMMA and various models of polymer glass deformation are discussed. The effects of cyclic loading/unloading on the segmental dynamics and mechanical properties of lightly crosslinked PMMA glasses between Tg - 10 K and Tg - 25 K are investigated. Sets of 5000 tensile loading/unloading cycles are performed, with cycle extension strains ranging from 0.003 to 0.007. After cycling, segmental dynamics either remained unchanged or were faster relative to an undeformed sample. Surprisingly, the mechanical properties were unchanged after cycling under all investigated conditions. No evidence of overaging was observed in the optical or mechanical measurements as a result of these cyclic loading/unloading experiments; comparison of the results to various simulations and experiments are discussed.