Volume 42, Issue 4 pp. 960-974
Article

Controlled, radical reversible addition–fragmentation chain-transfer polymerization in high-surfactant-concentration ionic miniemulsions

J. B. McLeary

J. B. McLeary

Division of Polymer Science, Department of Chemistry, University of Stellenbosch, Private Bag X1, Matieland 7602, South Africa

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M. P. Tonge

M. P. Tonge

Division of Polymer Science, Department of Chemistry, University of Stellenbosch, Private Bag X1, Matieland 7602, South Africa

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D. de Wet Roos

D. de Wet Roos

Sastech R&D, Sasol Technology (Pty) Limited, P.O. Box 1, Sasolburg 1947, South Africa

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R. D. Sanderson

R. D. Sanderson

Division of Polymer Science, Department of Chemistry, University of Stellenbosch, Private Bag X1, Matieland 7602, South Africa

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B. Klumperman

Corresponding Author

B. Klumperman

Division of Polymer Science, Department of Chemistry, University of Stellenbosch, Private Bag X1, Matieland 7602, South Africa

Technische Universiteit Eindhoven, Faculteit Scheikundige Technologie, Den Dolech 2, 5612 AZ Eindhoven, The Netherlands

Eindhoven University of Technology, Laboratory of Polymer Chemistry, P.O. Box 513, NL-5600 MB Eindhoven, The NetherlandsSearch for more papers by this author
First published: 06 January 2004
Citations: 64

Abstract

Living free-radical polymerization of methacrylate and styrenic monomers with ionic surfactants was carried out with reversible addition–fragmentation chain transfer in miniemulsion with different surfactant types and concentrations. The previously reported problem of phase separation was found to be insignificant at higher surfactant concentrations, and control of the molar mass and polydispersity index was superior to that of published miniemulsion systems. Cationic and anionic surfactants were used to examine the validity of the argument that ionic surfactants interfere with transfer agents. Ionic surfactants were suitable for miniemulsion polymerization under certain conditions. The colloidal stability of the miniemulsions was consistent with the predictions of a specific model. The living character of the polymer that comprised the latex material was shown by its transformation into block copolymers. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 960–974, 2004

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