Difference in temperature effect on the polymerizations between triallyl isocyanurate and its isomer triallyl cyanurate
Autor: | Tsuneo Nakanishi, Tsuyoshi Kubo, Yoshihiro Takayama, Hiroyuki Aota, Akira Matsumoto, Akinori Kameyama, Katsuyuki Watanabe |
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Rok vydání: | 2000 |
Předmět: |
Steric effects
chemistry.chemical_classification Degree of unsaturation Reaction mechanism Polymers and Plastics Bulk polymerization Organic Chemistry Radical polymerization Kinetics technology industry and agriculture General Physics and Astronomy macromolecular substances Polymer stomatognathic diseases chemistry Polymerization Polymer chemistry Materials Chemistry |
Zdroj: | European Polymer Journal. 36:673-677 |
ISSN: | 0014-3057 |
DOI: | 10.1016/s0014-3057(99)00129-9 |
Popis: | The temperature effect on the polymerization of triallyl isocyanurate (TAIC) was explored in detail as compared with its isomer triallyl cyanurate (TAC), since TAIC and TAC are commercially important as crosslinking agents with comonomers, and for aftercuring preformed polymers at elevated temperatures. Thus, the relative rate Rp(TAIC)/Rp(TAC) decreased with temperature, accompanied by the reversed rate feature, as the higher rate for TAIC polymerization has been reported previously at 60°C [3] . No inversion was observed for the gel point and primary chain length, although the difference between TAIC and TAC polymerizations became smaller. The initial residual unsaturation decreased obviously with raised temperature for TAC polymerization, whereas only a slight decrease was observed for TAIC. These results are discussed mechanistically in terms of allyl polymerization and the steric effect caused by the bulky side-chain groups. |
Databáze: | OpenAIRE |
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