Synthesis of new polymeric hindered amine light stabilizers: Performance evaluation in styrenic polymers
Polymeric hindered amine light stabilizers (HALSs), in which the HALS functionality was attached to the terminal isocyanate chain end of poly(styryl‐co‐styryl isocyanate), were synthesized by a two‐step process. First, cinnamoyl azide was prepared and copolymerized with styrene by a free‐radical cop...
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Published in: | Journal of applied polymer science Vol. 90; no. 4; pp. 1126 - 1138 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
24-10-2003
Wiley |
Subjects: | |
Online Access: | Get full text |
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Summary: | Polymeric hindered amine light stabilizers (HALSs), in which the HALS functionality was attached to the terminal isocyanate chain end of poly(styryl‐co‐styryl isocyanate), were synthesized by a two‐step process. First, cinnamoyl azide was prepared and copolymerized with styrene by a free‐radical copolymerization method. Polymeric low‐molecular‐weight and high‐molecular‐weight 2,2,6,6‐tetramethyl‐4‐pipridinol‐graft‐poly(styryl‐co‐styryl isocyanate) and 4‐amino‐2,2,6,6‐tetramethyl piperidine‐graft‐poly(styryl‐co‐styryl isocyanate) were synthesized by a grafting method. The photodegradation and stabilization of different grades of high‐impact polystyrene (HIPS) were studied at 55°C in air at different time intervals, and the photostabilizing efficiency of polymeric HALSs was compared with conventional light stabilizers, such as 2,2,6,6‐tetramethyl‐4‐pipridinol and bis(2,2,6,6‐tetramethyl‐4‐piperidinyl)sebacate. Polymeric HALSs showed significant improvements in the photostabilization of HIPS. The solubility and diffusion coefficient of polymeric HALSs were studied. The morphological changes in HIPS caused by photooxidation were also studied. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1126–1138, 2003 |
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Bibliography: | Council of Scientific and Industrial Research ark:/67375/WNG-XVT6R9HN-H istex:BF51AC3FE6D9D34D0CC94F48D1C961E04D6DDC6E ArticleID:APP12672 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.12672 |