Polymerization of Diallyl Alkyl Isocyanurates

Autor: Tsukasa Matsumoto, Mikio Hirabayashi, Tsuneo Nakanishi, Akinori Kameyama, Katsuyuki Watanabe, Akira Matsumoto, Hiroyuki Aota
Rok vydání: 1998
Předmět:
Zdroj: Journal of Macromolecular Science, Part A. 35:1889-1893
ISSN: 1520-5738
1060-1325
DOI: 10.1080/10601329808000559
Popis: Polymerizations of several diallyl alkyl isocyanurates were investigated to explore in more detail the steric effect observed in the polymerization of triallyl isocyanurate [3, 5], as compared to its isomer triallyl cyanurate, by changing alkyl groups from methyl, propyl, hexyl, and octyl up to lauryl. The rate of polymerization, the gel point, the cyclization constant, and the primary chain length were evaluated. For example, the primary chain length increased with an increase in the bulkiness of the alkyl group as expected, although in the polymerization of diallyl lauryl isocyanurate it decreased as a reflection of reduced rate of propagation due to the enhanced steric effect arising from a very bulky lauryl group.
Databáze: OpenAIRE