首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Dark cure studies of cationic photopolymerizations of epoxides: Characterization of kinetic rate constants at high conversions
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Dark cure studies of cationic photopolymerizations of epoxides: Characterization of kinetic rate constants at high conversions

机译:环氧阳离子光聚合的暗固化研究:高转化率下动力学速率常数的表征

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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.
机译:有效的传播速率常数(k(p);在所有传播的活性中心平均)针对苯缩水甘油醚在整个转化范围内的无溶剂阳离子光聚合反应进行了表征,包括其中传质限制变得重要的高转化率机制。发现k(p)作为转化率的函数的曲线在低转化率至中间转化率下显示出恒定的平稳值,随后在转化率阈值以上单调增加。为了解释这种趋势,提出在高转化率下光引发剂抗衡离子的扩散迁移率降低,而阳离子活性中心的迁移率由于反应性扩散而保持较高。因此,随着转化率的增加,活性中心和抗衡离子之间的平均距离可能增加,从而导致传播速率常数增加。根据温度,光引发剂阴离子和光引发剂浓度对k(p)值的分布进行了研究。随着光引发剂浓度的增加,有效传播速率常数的平稳值减小,而阈值转化率增加。所有的实验趋势都与高转化率下离子分离的拟议增加相符。 (C)2004年Wiley Periodicals,Inc.

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