The Xth European Colloid and Interface Society (ECIS) Conference was conducted jointly with its Finnish counterpart (PKS-YKS) in Abo (Turku), Finland, in September 1996.
The focus was placed on the following topics:
- Properties of microemulsion systems; - Structure and interactions in thin films; - Biocolloids and vesicles; - Structure and interactions in dispersions; - Polymers at solid interfaces; - Polymers in solutions.
This volume presents a balanced and representative selection of the papers presented at the conference.

"Imagination and shrewd guesswork are powerful instruments for acquiring scientific knowledge . . . " 1. H. van't Hoff The last decades have witnessed a rapid growth of quantum chemistry and a tremendous increase in the number of very accurate ab initio calculations of the electronic structure of molecules yielding results of admirable accuracy. This dramatic progress has opened a new stage in the quantum mechanical description of matter at the molecular level. In the first place, highly accurate results provide severe tests of the quantum mecha nics. Secondly, modern quantitative computational ab initio methods can be synergetically combined with various experimen tal techniques thus enabling precise numerical characterization of molecular properties better than ever anticipated earlier. However, the role of theory is not exhausted in disclosing the fundamental laws of Nature and production of ever increasing sets of data of high accuracy. It has to provide additionally a means of systematization, recognition of regularities, and ratio nalization of the myriads of established facts avoiding in this way complete chaos. Additional problems are represented by molecular wavefunctions provided by the modern high-level computational quantum chemistry methods. They involve, in principle, all the information on molecular system, but they are so immensely complex that can not be immediately understood in simple and physically meaningful terms. Both of these aspects, categorization and interpretation, call for conceptual models which should be preferably pictorial, transparent, intuitively appealing and well-founded, being sometimes useful for semi quantitative purposes."

Dedicated to Professor Manfred Gordon on the Occasion of His 70th Birthday

The word Polyethylene was probably first pronounced in a lecture which M. P. E. Berthelot delivered on April ,27, 1863 to the Chemical Society in Paris, reporting on the "polymerization" of various simple organic compounds (1). Much later this work appeared twice in the literature before the classical ICI breakthrough in the 1930's which is so colorfully described in Ballard's lecture. Once it came up at the end of the last century when H. von Pechmann obtained "a white flocculant material" from the decomposition of diazomethane which, one year later, was termed to be "polymethylene" - (CH ) - from E. Bamberger 2 and F. Tschiemer (1). At that time the investigators were disappointed about this product because it was not what they had expected to find in their experiments. As a result any further work was discontinued. The second time that the word polyethylene appeared in the literature to describe a "white solid powder" was in 1930 when C. S. Marvel and M. E. P. Friedericks (2) attempted to prepare alkylated As compounds in which all five valencies were covalently bonded to five monovalent-aTkyl groups. They reacted Tetra-ethyl-arsenium bromide with butyllithium and expected to get tetra ethyl butyl arsenium. Instead they obtained LiBr + AsEt3 + gaseous products. Delicate and somewhat time-consuming analysis gave a surprising result: ethane and C 's were there in the 4 expected quantities but ethylene was missing - or almost missing - in the gas mixture.

Epoxy resins are regarded as thermosetting resins and have found various c- mercial applications after crosslinking with adequate curing agents [1-3]. H- ever, some epoxy resins have been used as thermoplastic resins without curing agents. Figure 1 shows the applications of epoxy resins that are classi?ed to three categories: thermosets in combination with curing agents, thermoplastics wi- out curing agents, and raw materials for modi?cation. The use in thermoplastics is not popular compared with the two other applications. Typical thermoplastic applications are found in stabilizers for vinyl resins, toners for copying - chines, ?re retardants for engineering plastics, and sizing material for glass or carbon ?bers. The epoxy resin most frequently used is the oligomer of the diglycidyl ether of bisphenol-A (DGEBA) whose chemical structure is shown below [1-3]. The DGEBA is composed of linear molecules with different molecular weights according to the variation of the repeated number (n) in the structural formula.

Molecular manipulation of nano- and microstructures paves the way to produce organic polymer materials by design. Such architectures comprise both the synthesis and the kinetics and thermodynamics of macromolecular organization and is the theme of this volume. The book consists of four articles reviewing living polymerization to produce precisely defined linear polyesters, comparing them to other living polymerization techniques. The articles also deal with the synthesis of polymeric dendrimers, either by the convergent or divergent approach; block copolymers synthesis, to define micromorphology in high performance polymers; and thereby tailoring their thermal, chemical, mechanical and dielectrical properties, and finally kinetics and thermodynamics for microstructural organization in macroporous thermosets.

Organometallic chemistry is a well established research area at the interface of organic and inorganic chemistry. In recent years this field has undergone a ren aissance as our understanding of organometallic structure, properties and mechanism has opened the way for the design of organometallic compounds and reactions tailored to the needs of such diverse areas as medicine, biology, materials and polymer sciences and organic synthesis. For example, in the de velopment of new catalytic processes, organometallic chemistry is helping meet the challenge to society that the economic and environmental necessities of the future pose. As this field becomes increasingly interdisciplinary, we recognize the need for critical overviews of new developments that are of broad significance. This is our goal in starting this new series Topics in Organometallic Chemistry. The scope of coverage includes a broad range of topics of pure and applied or ganometallic chemistry, where new breakthroughs are being achieved that are of significance to a larger scientific audience. Topics in Organometallic Chemistry differs from existing review series in that each volume is thematic, giving an overview of an area that has reached a stage of maturity such that coverage in a single review article is no longer possible. Furthermore, the treatment addresses a broad audience of researchers, who are not specialists in the field, starting at the graduate student level. Discussion of possible future research directions in the areas covered by the individual volumes is welcome."

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With the aim of providing a deeper insight into possible mechanisms of biological self-organization, this thesis presents new approaches to describe the process of self-assembly and the impact of spatial organization on the function of membrane proteins, from a statistical physics point of view. It focuses on three important scenarios: the assembly of membrane proteins, the collective response of mechanosensitive channels and the function of the twin arginine translocation (Tat) system. Using methods from equilibrium and non-equilibrium statistical mechanics, general conclusions were drawn that demonstrate the importance of the protein-protein interactions. Namely, in the first part a general aggregation dynamics model is formulated, and used to show that fragmentation crucially affects the efficiency of the self-assembly process of proteins. In the second part, by mapping the membrane-mediated forces into a simplified many-body system, the dynamic and equilibrium behaviour of interacting mechanosensitive channels is derived, showing that protein agglomeration strongly impacts its desired function. The final part develops a model that incorporates both the agglomeration and transport function of the Tat system, thereby providing a comprehensive description of this self-organizing process.

Block Copolymer Surfactant Mixtures in Aqueous Solution: Can we Achieve Size and Shape Control by Co-Micellization?, by Thomas Hellweg; Non-ionic Thermoresponsive Polymers in Water, by Vladimir Aseyev, Heikki Tenhu and Francoise Winnik; From Coordination Polymers to Hierarchical Self-Assembled Structures, by Yun Yan, Arie de Keizer, Martien A. Cohen Stuart and Nicolaas A. M. Besseling; Processes of Ordered Structure Formation in Polypeptide Thin Film Solutions, by Ioan Botiz, Helmut Schlaad and Gunter Reiter; Amphiphilic Polymers at Interfaces, by Katarzyna Kita-Tokarczyk, Mathias Junginger, Serena Belegrinou and Andreas Taubert;"

The second edition of this textbook is identical with its fourth German edi tion and it thus has the same goals: precise definition of basic phenomena, a broad survey of the whole field, integrated representation of chemistry, physics, and technology, and a balanced treatment of facts and comprehen sion. The book thus intends to bridge the gap between the often oversimpli fied introductory textbooks and the highly specialized texts and monographs that cover only parts of macromolecular science. The text intends to survey the whole field of macromolecular science. Its organization results from the following considerations. The chemical structure of macromolecular compounds should be inde pendent of the method of synthesis, at least in the ideal case. Part I is thus concerned with the chemical and physical structure of polymers. Properties depend on structure. Solution properties are thus discussed in Part II, solid state properties in Part III. There are other reasons for dis cussing properties before synthesis: For example, it is difficult to understand equilibrium polymerization without knowledge of solution thermodynamics, the gel effect without knowledge of the glass transition temperature, etc. Part IV treats the principles of macromolecular syntheses and reactions.

The liquid crystalline state may be identified as a distinct and unique state of matter which is characterised by properties which resemble those of both solids and liquids. It was first recognised in the middle of the last century through the study of nerve myelin and derivatives of cholesterol. The research in the area really gathered momentum, however, when as a result of the pioneering work of Gray in the early 1970's organic compounds exhibiting liquid crystalline properties were shown to be suitable to form the basis of display devices in the electronic products. The study of liquid crystals is truly multidisciplinary and has attached the attention of physicists, biologists, chemists, mathematicians and electronics engineers. It is therefore impossible to cover all these aspects fully in two small volumes and therefore it was decided in view of the overall title of the series to concentrate on the structural and bonding aspects of the subject. The Chapters presented in these two volumes have been organised to cover the following fundamental aspects of the subiect. The calculation of the structures of liquid crystals, an account of their dynamical properties and a discussion of computer simulations of liquid crystalline phases formed by Gay Berne mesogens. The relationships between molecular conformation and packing are analysed in some detail. The crystal structures of liquid crystal mesogens and the importance of their X ray scattering properties for characterisational purposes are discussed.

The 13th Conference of the European Colloid and Interface Society (ECIS 99) was held in September 1999 in Dublin, Ireland. It brought together scientists from academic research and industry within the field of physics and chemistry of colloids and interfaces. The Conference focused on the following topics: - Surfactant colloids;
- Polymer colloids and solid particles;
- Food colloids;
- Soft matter interfaces;
- Biosystems;
- Rheology;
- Experimental methods in colloid and interface science.

Das Buch enthalt Kapitel uber: N. Kinjo, M. Ogata, Ibaraki-ken; K. Nishi, Tokyo; A. Kaneda, Yokohama, Japan: Epoxyd-Formmassen als Einschlussmaterialien fur mikroelektronische Gerate Yu.S. Lipatov, T.E. Lipatova, L.F. Kosyanchuk, Kiev, UdSSR: Synthese und Struktur struktureller Makromolekule K. Horie, I. Mita, Tokyo, Japan: Reaktionen und Photodynamik in polymeren Festkorpern Yu.K. Godovsky, V.S. Papkov, Moskau, UdSSR: Thermotrope Mesophasen elementorganischer Polymere

This monograph gives a detailed introductory exposition of research results for various models, mostly two-dimensional, of directed walks, interfaces, wetting, surface adsorption (of polymers), stacks, compact clusters (lattice animals), etc. The unifying feature of these models is that in most cases they can be solved analytically. The methods used include transfer matrices, generating functions, recurrence relations, and difference equations, and in some cases involve utilization of less familiar mathematical techniques such as continued fractions and q-series. The authors emphasize an overall view of what can be learned generally of the statistical mechanics of anisotropic systems, including phenomena near surfaces, by studying the solvable models. Thus, the concept of scaling and, where known, finite-size scaling properties are elucidated. Scaling and statistical mechanics of anisoptropic systems in general are active research topics. The volume provides a comprehensive survey of exact model results in this field.