Dark cure studies of cationic photopolymerizations of epoxides: Characterization of kinetic rate constants at high conversions

被引:27
|
作者
Sipani, V [1 ]
Kirsch, A [1 ]
Scranton, AB [1 ]
机构
[1] Univ Iowa, Dept Chem & Biochem Engn, Seamans Ctr 4133, Iowa City, IA 52242 USA
关键词
cationic photopolymerization; kinetics; propagation; conversion; photoinitiator concentration; photopolymerization; kinetics (polym.);
D O I
10.1002/pola.20209
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The effective propagation rate constant (k(p); averaged over all the propagating active centers) was characterized for solvent-free cationic photopolymerizations of phenyl glycidyl ether over the entire range of conversions, including the high conversion regime in which mass transfer limitations become important. The profile for the k(p) as a function of conversion was found to exhibit a constant plateau value at low to intermediate conversions, followed by a monotonic increase above a threshold value of conversion. To explain this trend, it is proposed that at high conversion the diffusional mobility of the photoinitiator counterion is reduced whereas the mobility of the cationic active center remains high because of reactive diffusion. Therefore, with increasing conversion, the average distance between the active centers and counterions may increase, resulting in an increase in the propagation rate constant. The profiles for the k(p) values were investigated as a function of the temperature, photoinitiator anion, and photoinitiator concentration. As the photoinitiator concentration was increased, the plateau value of the effective propagation rate constant decreased whereas the threshold conversion increased. All of the experimental trends are consistent with the proposed increase in ion separation at high conversions. (C) 2004 Wiley Periodicals, Inc.
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页码:4409 / 4416
页数:8
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