The mechanism of propagation in free-radical copolymerization

被引:0
作者
Davis, TP [1 ]
机构
[1] Univ New S Wales, Ctr Adv Macromol Design, Sch Chem Engn & Ind Chem, Sydney, NSW 2052, Australia
关键词
copolymerization; radical; mechanism; terminal; penultimate;
D O I
10.1002/1099-0518(20010301)39:5<597::AID-POLA1030>3.0.CO;2-Q
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A brief overview of free-radical copolymerization kinetics is presented. Recent developments have highlighted the shortcomings of the terminal (or Mayo-Lewis) model. However. for many practical reasons, approximate models are useful for assisting our understanding of any given copolymerization reaction and allowing comparisons with the vast database on copolymerization reactions. Terminal model reactivity ratios have limited meaning, so it may be imprudent to use these values as a quantitative measurement of radical reactivity. Presently, experimental limitations restrict the amount of information that can be obtained by models being fitted to composition or propagation rate data; therefore, the direct measurement of radical reactivity is required together with high-level quantum calculations. (C) 2001 John Wiley & Sons. Inc.
引用
收藏
页码:597 / 603
页数:7
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