Volume 120, Issue 1 pp. 466-473

Degradation and initiation polymerization mechanism of α-methylstyrene-containing macroinitiators

Shan Jiang

Shan Jiang

Department of Materials Science and Engineering, Jiangsu Polytechnic University, Changzhou 213016, People's Republic of China

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Jianping Deng

Jianping Deng

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China

Department of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China

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Qiang Yu

Qiang Yu

Department of Materials Science and Engineering, Jiangsu Polytechnic University, Changzhou 213016, People's Republic of China

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Wantai Yang

Corresponding Author

Wantai Yang

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China

Department of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China===Search for more papers by this author
First published: 14 October 2010
Citations: 10

Abstract

Copolymers obtained from radical copolymerization of α-methylstyrene (AMS) and glycidyl methacrylate (GMA) behave as macroinitiators, when heated in the presence of a second monomer, giving rise to block copolymers. The relevant degradation and initiation polymerization mechanism of the macroinitiators were studied. Thermal depropagation of the macroinitiators generated monomers, identified by 1H-NMR, photoionization mass spectroscopy and FT-IR. According to the results of structure analysis by GPC, ESR and NMR spectroscopy, the AMS-GMA (head-head) and AMS-AMS (head-head) bonds in the macroinitiators are easily scissored providing free radicals when the temperature is above 80°C. The radicals lead to subsequent polymerization of the second monomer, and thereby block copolymers are formed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011

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