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Bengt Kronberg

Swedish Institute

Publishes on Surfactants and Colloidal Systems, Advanced Polymer Synthesis and Characterization, Analytical Chemistry and Chromatography. 134 papers and 6.3k citations.

134Publications
6.3kTotal Citations

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Top publicationsby citations

Surfactants and Polymers in Aqueous Solution
Cited by 3k

Many industrial formulations such as detergents, paints, foodstuff and cosmetics contain both surfactants and polymers and their interaction govern many of the properties. This book is unique in that it discusses the solution chemistry of both surfactants and polymers and also the interactions between the two. The book, which is based on successful courses given by the authors since 1992, is a revised and extended version of the first edition that became a market success with six reprints since 1998. Surfactants and Polymers in Aqueous Solution is broad in scope, providing both theoretical insights and practical help for those active in the area. This book contains a thorough discussion of surfactant types and gives information of main routes of preparation. A chapter on novel surfactants has been included in the new edition. Physicochemical phenomena such as self-assembly in solution, adsorption, gel formation and foaming are discussed in detail. Particular attention is paid to the solution behaviour of surfactants and polymers containing polyoxyethylene chains. Surface active polymers are presented and their interaction with surfactants is a core topic of the book. Protein-surfactant interaction is also important and a new chapter deals with this issue. Microemulsions are treated in depth and several important application such as detergency and their use as media for chemical reactions are presented. Emulsions and the choice of emulsifier is discussed in some detail. The new edition also contains chapters on rheology and wetting. Surfactants and Polymers in Aqueous Solution is aimed at those dealing with surface chemistry research at universities and with surfactant formulation in industry.

Surface Chemistry of Surfactants and Polymers
Cited by 378

© 2014 John Wiley & Sons, Ltd. All rights reserved. This book gives the reader an introduction to the field of surfactants in solution as well as polymers in solution. Starting with an introduction to surfactants the book then discusses their environmental and health aspects. Chapter 3 looks at fundamental forces in surface and colloid chemistry. Chapter 4 covers self-assembly and 5 phase diagrams. Chapter 6 reviews advanced self-assembly while chapter 7 looks at complex behaviour. Chapters 8 to 10 cover polymer adsorption at solid surfaces, polymers in solution and surface active polymers, respectively. Chapters 11 and 12 discuss adsorption and surface and interfacial tension, while Chapters 13- 16 deal with mixed surfactant systems. Chapter 17, 18 and 19 address microemulsions, colloidal stability and the rheology of polymer and surfactant solutions. Wetting and wetting agents, hydrophobization and hydrophobizing agents, solid dispersions, surfactant assemblies, foaming, emulsions and emulsifiers and microemulsions for soil and oil removal complete the coverage in chapters 20-25.

Morphology development of polymeric microparticles in aqueous dispersions. I. Thermodynamic considerations
Donald C. Sundberg, Anthony P. Casassa, John Pantazopoulos et al.|Journal of Applied Polymer Science|1990
Cited by 265

Abstract A thermodynamic analysis of polymer particle morphology highlights the role of interfacial tensions in controlling particle structure. The influence of the surfactant and the nature of the incompatible polymers is seen through their individual and collective effects upon these interfacial tensions. It has been found that by simply changing the type of surfactant used in the emulsion the particle morphology can change from core‐shell to hemispherical, in agreement with thermodynamic predictions. Several apparently different morphologies (hemispherical, sandwich, multiple lobes) have been found to coexist at the same time within a single emulsion, suggesting that they may be simply different states of phase separation and not thermodynamically stable, unique morphologies. The thermodynamic analyses are independent of particle size and method of emulsion processing. Experimental evidence shows that the morphology of particles formed via in situ polymerization (as in a synthetic latex) is controlled by interfacial tensions in the same manner as those particles formed via solvent evaporation from a solution of an incompatible polymer pair (as in an artificial latex or microencapsulation).