丙烯腈
共聚物
键裂
高分子化学
苯乙烯
β-断裂
化学
材料科学
聚合物
有机化学
催化作用
激进的
自由基取代
出处
期刊:Journal of polymer science
[Wiley]
日期:1970-09-01
卷期号:8 (9): 2679-2688
被引量:13
标识
DOI:10.1002/pol.1970.150080932
摘要
Abstract The chain‐scission reaction which occurs in copolymers of styrene and acrylonitrile has been studied at temperatures of 262, 252, and 240°C. Under these conditions volatilization is negligible, and chain scission can be studied in virtual isolation. At 262°C three kinds of chain scission are discernible, namely, at weak links which are associated with styrene units, “normal” scission in styrene segments of the chain and scission associated with the acrylonitrile units. The rate constants for normal scission and scission associated with acrylonitrile units are in the ratio of approximately 1 to 30. The molecular weight of the copolymer has no effect on the rates of scission. At 252°C the same general behavior is observed for the copolymers containing up to 24.9% acrylonitrile. The 33.4% acrylonitrile copolymer is anomalous, however. At 240°C the trends observed at 262°C appear to break down completely although individual experiments are quite reproducible. This behavior at the lower temperatures is believed to be associated with the fact that the melting points of the various copolymers are in this temperature range. Thus the viscosity of the medium, which should be expected to have a strong influence on the chain scission reaction, will be changing rapidly with temperature, copolymer composition, and molecular weight in this temperature range.
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