Effects of styrene oligomers and polymers on the suspension polymerization behavior and properties of expandable polystyrene
Styrene oligomers are formed by a free‐radical mechanism during the thermal polymerization of styrene in storage. The effects of these compounds on the preparation of expandable polystyrene (EPS) were investigated with respect to suspension polymerization behavior and the properties of the impregnat...
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Published in | Journal of applied polymer science Vol. 110; no. 1; pp. 453 - 458 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
05.10.2008
Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | Styrene oligomers are formed by a free‐radical mechanism during the thermal polymerization of styrene in storage. The effects of these compounds on the preparation of expandable polystyrene (EPS) were investigated with respect to suspension polymerization behavior and the properties of the impregnated polystyrene beads produced. Styrene dimers and trimers up to concentrations of 0.2 wt % did not affect the stability of the suspension during the polymerization and impregnation stages. Besides differentiated effects on the particle size distributions of the polymers and on the polymerization rate, no chain‐transfer activity of the oligomers was observed, and this confirmed the assignment of chain transfer to the Diels–Alder dimer in the literature. The investigation of the foaming behavior of the pentane‐impregnated EPS beads indicated a significant reduction of the prefoaming density caused by styrene dimers and trimers. This behavior resulted from a decrease in the glass‐transition temperatures of these polymers. The effects of high‐molecular‐weight polystyrene, formed in addition to oligomers during storage by the thermal polymerization of styrene, on the polymerization behavior and polymer properties of EPS were also investigated. The results showed a significant impact on the suspension stability that was dependent on the concentration of the high‐molecular‐weight polystyrene. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 |
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Bibliography: | ArticleID:APP28531 ark:/67375/WNG-NVFHPXVJ-N istex:C23325F89A97AE0C6EBBFB53E5437F0BEF63DAA5 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.28531 |