R. F. T. Stepto

Glossary of basic terms in polymer science (IUPAC Recommendations 1996)

Titular Members: G. Allegra (Italy, to 1989); R. E. Bareiss (Germany, to 1993); N. M. Bikales (USA, Secretary to 1987); K. Hatada (Japan, Associate Member from 1987, Titular Member from 1989); A. D. Jenkins (UK, Chairman to 1985, Associate Member to 1987); J. Kahovec (Czech Republic, Associate Member from 1987, Titular Member from 1991); P. Kratochvíl (Czech Republic, Chairman to 1991); E. Maréchal (France, Associate Member from 1991, Titular Member from 1993); W. V. Metanomski (USA, Associate Member from 1987, Titular Member from 1991); I. Mita (Japan, Titular Member to 1989, Associate Member to 1991); C. Noël (France, to 1993); I. M. Papisov (Russia, to 1987, Associate Member to 1991); V. P. Shibaev (Russia, from 1987); R. F. T. Stepto (UK, Associate Member from 1987, Titular Member from 1989, Chairman from 1991); U. W. Suter (Switzerland, to 1991, Associate Member to 1993); W. J. Work (USA, Associate Member from 1985, Secretary from 1987).

Definitions of terms relating to the structure and processing of sols, gels, networks, and inorganic-organic hybrid materials (IUPAC Recommendations 2007)

This document defines terms related to the structure and processing of inorganic, polymeric, and inorganic-organic hybrid materials from precursors, through gels to solid products. It is divided into four sections - precursors, gels, solids, and processes - and the terms have been restricted to those most commonly encountered. For the sake of completeness and where they are already satisfactorily defined for the scope of this document, terms from other IUPAC publications have been used. Otherwise, the terms and their definitions have been assembled in consultation with experts in the relevant fields. The definitions are intended to assist the reader who is unfamiliar with sol-gel processing, ceramization, and related technologies and materials, and to serve as a guide to the use of standard terminology by those researching in these areas.

Terminology of polymers and polymerization processes in dispersed systems (IUPAC Recommendations 2011)

A large group of industrially important polymerization processes is carried out in dispersed systems. These processes differ with respect to their physical nature, mechanism of particle formation, particle morphology, size, charge, types of interparticle interactions, and many other aspects. Polymer dispersions, and polymers derived from polymerization in dispersed systems, are used in diverse areas such as paints, adhesives, microelectronics, medicine, cosmetics, biotechnology, and others. Frequently, the same names are used for different processes and products or different names are used for the same processes and products. The document contains a list of recommended terms and definitions necessary for the unambiguous description of processes, products, parameters, and characteristic features relevant to polymers in dispersed systems.

Definition of terms related to polymer blends, composites, and multiphase polymeric materials (IUPAC Recommendations 2004)

The document defines the terms most commonly encountered in the field of polymer blends and composites. The scope has been limited to mixtures in which the components differ in chemical composition or molar mass and in which the continuous phase is polymeric. Incidental thermodynamic descriptions are mainly limited to binary mixtures although, in principle, they could be generalized to multicomponent mixtures. The document is organized into three sections. The first defines terms basic to the description of polymer mixtures. The second defines terms commonly encountered in descriptions of phase domain behavior of polymer mixtures. The third defines terms commonly encountered in the descriptions of the morphologies of phase-separated polymer mixtures.

DEFINITIONS OF TERMS RELATING TO REACTIONS OF POLYMERS AND TO FUNCTIONAL POLYMERIC MATERIALS (IUPAC Recommendations 2003)

The document defines the terms most commonly encountered in the field of polymer reactions and functional polymers. The scope has been limited to terms that are specific to polymer systems. The document is organized into three sections. The first defines the terms relating to reactions of polymers. Names of individual chemical reactions are omitted from the document, even in cases where the reactions are important in the field of polymer reactions. The second section defines the terms relating to polymer reactants and reactive polymeric materials. The third section defines the terms describing functional polymeric materials.

Definitions of terms relating to the structure and processing of sols, gels, networks, and inorganic-organic hybrid materials

This document defines terms related to the structure and processing of inorganic, polymeric, and inorganic-organic hybrid materials from precursors, through gels to solid products. It is divided into four sections-precursors, gels, solids, and processes- and the terms have been restricted to those most commonly encountered. For the sake of completeness and where they are already satisfactorily defined for the scope of this document, terms from other IUPAC publications have been used. Otherwise, the terms and their definitions have been assembled in consultation with experts in the relevant fields. The definitions are intended to assist the reader who is unfamiliar with sol-gel processing, ceramization, and related technologies and materials, and to serve as a guide to the use of standard terminology by those researching in these areas.

9: Definitions of Terms Related to Polymer Blends, Composites, and Multiphase Polymeric Materials (2004)

The document defines the terms most commonly encountered in the field of polymer blends and composites. The scope has been limited to mixtures in which the components differ in chemical composition or molar mass and in which the continuous phase is polymeric. Incidental thermodynamic descriptions are mainly limited to binary mixtures although, in principle, they could be generalized to multicomponent mixtures. The document is organized into three sections. The first defines terms basic to the description of polymer mixtures. The second defines terms commonly encountered in descriptions of phase domain behavior of polymer mixtures. The third defines terms commonly encountered in the descriptions of the morphologies of phase-separated polymer mixtures. Reproduced from: Pure Appl. Chem., Vol. 76, No. 11, pp. 1985–2007, 2004.

Terminology of polymers containing ionizable or ionic groups and of polymers containing ions (IUPAC Recommendations 2006)

This document defines the terms most commonly encountered in the field of polymers containing ionizable or ionic groups and polymers containing ions. The scope of the document has been limited to organic polymers. Inorganic materials, such as certain phosphates, silicates, etc., which also may be considered ionic polymers, are excluded from the present document. The terms selected are those that are widely used in the field of polymers containing ionizable or ionic groups and polymers containing ions. Only those terms that could be defined without ambiguity are considered. The terms are listed in alphabetical order, and cross-references to definitions given in other documents are provided.

Studies of cyclic and linear poly(dimethyl siloxanes): 10. Calculations of radii of gyration

A Monte Carlo method has been devised for calculating the conformation-dependent properties of cyclic poly(dimethyl siloxanes) (PDMS), using Flory, Crescenzi and Marks rotational isomeric state model. Calculated values of the mean-square radii of gyration 〈s2r〉 of ring molecules unperturbed by excluded volume effects and containing 8–100 skeletal atoms are compared with the 〈s2l〉 values for the corresponding unperturbed chain molecules. Exact enumeration methods were also employed for rings [(CH3)2SiO]w2 with w ⩽ 24 and the results found to be in close agreement with those obtained by the Monte Carlo method. The ratio 〈s2l〉〈s2r〉 was found to attain limiting values close to 2.0 for w > 30, in agreement with theoretical predictions.

Rate theory of irreversible linear random polymerisation. Part 2.—Application to intramolecular reaction in A—A + B—B type polymerisations

The theory described in the preceding paper is extended to include intramolecular reactions in A—A + B—B type polymerisations. The extension is described in a general way and a limiting form is applied to previously published data giving total ring fractions during the formation of linear polyurethanes. The interpretations afforded by the present approach and by previous analyses of the data are discussed and compared.