Polymeric Liquids and Networks: Structure and Properties is the first book of two by William W. Graessley that presents a unified view of flexible-chain polymer liquids and networks. The topics of both volumes range from equilibrium properties to dynamic response, finite deformation behavior and non-Newtonian flow. The second book will be titled Polymeric Liquids and Networks: Dynamics and Rheology. These various aspects of the field were developed over the past 70 years by researchers from many academic disciplines. The infusion of fresh viewpoints continually invigorated and enriched the field, making polymeric liquids and networks a truly interdisciplinary subject. The lack of a common terminology and perspective, however, has led to compartmentalization, making it difficult for a newcomer, even one technically trained, to gain a broad appreciation of the field and to see the relationships among its various parts. The aim of these two books, without diluting the substance, is to achieve a desired unity.Polymeric Liquids and Networks emphasizes fundamental principles and a molecular viewpoint. The conceptual basis of theories underlying each topical area is explained with derivations sometimes outlined briefly and sometimes given in detail. Technical terminology is kept to a minimum necessary for coherent presentation. The goal of the text is to provide an informed understanding rather than detailed technical proficiency. Theory, experiment, and simulation are woven together as appropriate for achieving a balanced view. The books are designed to serve academic and industrial needs, consolidating the understanding of topics with both practical and fundamental significance, and written from a technical but non-specialized perspective.The books deal mainly with non-polar and weakly polar species and largely with results derived from experiments on structurally well-defined systems. The objective is not to ignore

This second part of a two-volume treatise covers continuum background along with experimental observations. The work offers readers a solid grounding in the principles that underlie the dynamics and rheological behavior of flexible chain polymer liquids and networks.

This revision of an introductory text examines Newtonian liquids and polymer fluid mechanics. It begins with a review of the main ideas of fluid dynamics as well as key points of Newtonian fluids.

Liquid crystal displays were discovered in the 1960s, and today we continue to enjoy the benefits of that fundamental discovery and its translation into a wide variety of products. Like liquid crystals, polymers are unusual materials, and have similarly enjoyed a great deal of research attention because of their vast applications and uses and compl

Polymer science is a technology-driven science. More often than not, technological breakthroughs opened the gates to rapid fundamental and theoretical advances, dramatically broadening the understanding of experimental observations, and expanding the science itself. Some of the breakthroughs involved the creation of new materials. Among these one may enumerate the vulcanization of natural rubber, the derivatization of cellulose, the giant advances right before and during World War II in the preparation and characterization of synthetic elastomers and semi crystalline polymers such as polyesters and polyamides, the subsequent creation of aromatic high-temperature resistant amorphous and semi-crystal line polymers, and the more recent development of liquid-crystalline polymers mostly with n~in-chain mesogenicity. other breakthroughs involve the development of powerful characterization techniques. Among the recent ones, the photon correlation spectroscopy owes its success to the advent of laser technology, small angle neutron scattering evolved from n~clear reactors technology, and modern solid-state nuclear magnetic resonance spectroscopy exists because of advances in superconductivity. The growing need for high modulus, high-temperature resistant polymers is opening at present a new technology, that of more or less rigid networks. The use of such networks is rapidly growing in applications where they are used as such or where they serve as matrices for fibers or other load bearing elements. The rigid networks are largely aromatic. Many of them are prepared from multifunctional wholly or almost-wholly aromatic kernels, while others contain large amount of stiff difunctional residus leading to the presence of many main-chain "liquid-crystalline" segments in the "infinite" network.

Hypercrosslinked network polymers present a new class of polymeric materials with very wide application possibilities, including adsorption technology, ion exchange, HPLC, analytical chemistry, nanotechnology (nanocomposites), medical polymers - First book describing the theory, practice of preparation and use of polymeric adsorbing materials with the emphasis on new hypercrosslinked polystyrene-type polymers - Written by the originators of the concept of hypercrosslinked polymers - Complex phenomena are explained by appealing to common sense, analogies and well-known effects, rather than complex mathematical treatment and computer modelling - Reviews many Russian, German and even Czech language publications - Contains numerous experimental data in the form of Figures and Tables

This book contains the plenary lectures from international experts, which were presented during the International Conference Polymer Networks, held in Moscow, April 1991. The book covers different areas of physics and chemistry of polymer networks, generated by the formation of chemical bonds. New theoretical and experimental results concerning the synthesis, structure and properties of such networks as recently obtained in scientific centres world-wide are extensively presented.