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Physics of Polymer Networks presents the proceedings of the 29th Europhysics Conference on Macromolecular Physics held in Merseburg, Germany. The main topics of this volume are: - Theory of networks; - Formation of networks; - Sol-gel transition; - Experimental investigations on structure and properties of polymer networks.
Polymer Physics provides and introduction to the field for upper level undergraduates and first year graduate students. Any student with a working knowledge of calculus, physics and chemistry should be able to read this book. The essential tools of the polymer physical chemist or engineer are derived in this book without skipping any steps.
Modern polymer materials are designed by applying principles of correlation between chemical structure, physical macrostructure and technological properties. Fundamentals of polymer physics are explained in this book without excessive use of calculations. Four main sections treat relaxation of polymers, melting and crystallization, the mechanism of deformation in thermoplastics, elastomers and multiphase systems, and thermodynamics of mixing and swelling of polymers and polymer networks. The book presents the theoretical models of polymer physics in a comprehensive style and relates their applicability to real polymer systems in terms of the available experimental observations.
Rubber elasticity is an important sub-field of polymer science. This book is in many ways a sequel to the authors' previous, more introductory book, Rubberlike Elasticity: A Molecular Primer (Wiley-Interscience, 1988), and will in some respects replace the now classic book by L.R.G. Treloar, The Physics of Rubber Elasticity (Oxford, 1975). The present book has much in common with its predecessor, in particular its strong emphasis on molecular concepts and theories. Similarly, only equilibrium properties are covered in any detail. Though this book treats much of the same subject matter, it is a more comprehensive, more up-to-date, and somewhat more sophisticated treatment.
The workshop on the "Molecular Basis of Polymer Networks", held October 5- 7, 1988 in 1iilich, FRG, continued a series of workshops jointly organized by the Institute Laue Langevin (ILL) in Grenoble, and the Institute of Solid State Physics of the KFA, 1iilich. The aim of this workshop was to provide a platform for discussions between theoreticians and experimentalists interested in the physics of polymer networks, in the hope that the two types of discussion would be synergistic. As revealed by the title of this workshop, the main focus of the lectures was on molecular aspects of the problem. The individual parts of these proceedings cover various approaches. Following quite general comments from a physicist examining the situation from "outside", various new theoretical concepts are developed. During the last decade the advent of Small Angle Neutron Scattering (SANS) has allowed the molecular structure of polymer networks to be studied and thus the reliability of the theories to be tested directly at the molecular level. Recent advances in this field are presented. The use of new techniques such as 2H NMR or QELS and the refinements of more classical, mechanical experimental measure ments have provided new information about the relation between the macroscopic behavior and the microscopic structure of polymer networks. Some recent results in this area are discussed for both chemically cross-linked networks and gels built by specific interchain interactions.
This volume of the series gives an overview on Rigid Polymer Networks written by two reputed experts in the field. A broad range of densely-branched, highly-crosslinked aromatic networks and gels of increasing rigidity are discussed, with special emphasis on aromatic rigid liquid-crystal polymer networks. The synthetic procedures to create the networks are briefly described and extensively referenced. Features of one-step and two-step rigid networks in their pre-gel and post-gel states are discussed. Some first steps are then taken in the theoretical treatment of LCP networks with long aromatic segments of decreasing stiffness. The current state of theory dealing with the broader class of highly-crosslinked rigid aromatic networks and gels is finally mentioned.
The series Advances in Polymer Science presents critical reviews of the present and future trends in polymer and biopolymer science. It covers all areas of research in polymer and biopolymer science including chemistry, physical chemistry, physics, material science. The thematic volumes are addressed to scientists, whether at universities or in industry, who wish to keep abreast of the important advances in the covered topics. Advances in Polymer Science enjoys a longstanding tradition and good reputation in its community. Each volume is dedicated to a current topic and each review critically surveys one aspect of that topic, to place it within the context of the volume. The volumes typically summarize the significant developments of the last 5 to 10 years and discuss them critically, presenting selected examples, explaining and illustrating the important principles and bringing together many important references of primary literature. On that basis, future research directions in the area can be discussed. Advances in Polymer Science volumes thus are important references for every polymer scientist, as well as for other scientists interested in polymer science - as an introduction to a neighboring field, or as a compilation of detailed information for the specialist. Review articles for the individual volumes are invited by the volume editors. Single contributions can be specially commissioned. Readership: Polymer scientists, or scientists in related fields interested in polymer and biopolymer science, at universities or in industry, graduate students.
For several decades, polymer science has sought to rationalize the mechanical and thermodynamic properties of polymer networks largely within the framework of statistical thermodynamics. Much of this effort has been directed toward the rubbery rather than the glassy state. It is generally assumed that networks possess an av erage composition to which average properties may be assigned; from such a continuum view, a powerful analysis of such properties as modulus, swelling, birefringence and thermoelasticity has emerged. In the years following the rise of polymer characterization (the late 40's and early 50's), many scientists began to study ap parent relations between the properties of linear polymer molecules and the networks obtainable therefrom. This search was also stimu lated by the wide range of applications of polymer networks in com mercial elastomers, thermosets and coatings. Frequently, these data were confidently matched with curves obtained from statisti cally describable models of networks of ghost chains, uniformly distributed in space. More recently, it has become apparent that polymer chains in networks are not as ideal as assumed in the formulation of statis tical models, and there has been a shift in emphasis towards the less than ideal, perturbed and possibly inhomogeneous networks which are more frequently encountered in practice. The continuum approach, however, had to be developed before inhomogeneous systems could be described; the present volume, therefore, contains both views.
Biological and Synthetic Polymer Networks contains 36 papers selected from the papers presented at NETWORKS 86, the 8th Polymer Networks Group Meeting. NETWORKS 86 was held in Elsinore, Denmark, on 31 August 5 September 1986. A total of nine invited main lectures and 68 contributed papers were presented at the meeting. A wide range of important biological and synthetic materials consist of three-dimensional polymer networks. The properties range from very stiff structural materials to extremely flexible rubbery materials and gels. Most polymer networks are permanent networks held together by covalent bonds. Such networks are insoluble but they may swell considerably in good solvents. Polymer networks held together by ionic bonds, hydrogen bonds or so-called entanglements are of a more temporary nature. At long times they exhibit a tendency to flow, and they are soluble in good solvents. The paper by Professor Walther Burchard and his co-workers, 'Covalent, Thermoreversible and Entangled Networks: An Attempt at Comparison', serves as a general introduction to polymer networks. The book contains both theoretical and experimental papers on the formation, characterisation and properties of polymer networks. Two topics were given special sessions at the meeting, namely Biological Networks and Swelling of Polymer Networks.