聚合
化学
电子顺磁共振
激进的
自由基聚合
丙烯酸酯
链式转移
高分子化学
单体
光化学
动链长度
动力学
本体聚合
溶液聚合
聚合物
有机化学
核磁共振
量子力学
物理
作者
Hendrik Kattner,Michael Buback
出处
期刊:Macromolecules
[American Chemical Society]
日期:2017-05-15
卷期号:50 (11): 4160-4168
被引量:14
标识
DOI:10.1021/acs.macromol.7b00328
摘要
The SP–PLP–EPR (single pulse–pulsed laser polymerization–electron paramagnetic resonance) method has been used to measure the rate coefficients of termination, intramolecular transfer, and propagation for the radical polymerization of 20 wt % trimethylaminoethyl acrylate chloride (TMAEA) in the temperature range 0–90 °C. The high complexity of this acrylate system is due to water being the solvent, to the monomer being a strong electrolyte, and to both secondary chain-end radicals and tertiary midchain radicals being simultaneously present. The termination kinetics, which was analyzed by a chain-length-dependent scheme, largely differs from the situation met with nonionized radicals. The reliability of the rate coefficients obtained from the SP–PLP–EPR experiments has been demonstrated by the almost perfect agreement of TMAEA conversion vs time data from simulation, on the basis of these coefficients, and from the chemically initiated TMAEA polymerization experiment at 70 °C.
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