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首页> 外文期刊>Macromolecular reaction engineering >Estimation of Reactivity Ratios in the RAFT Copolymerization of Styrene and Glycidyl Methacrylate
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Estimation of Reactivity Ratios in the RAFT Copolymerization of Styrene and Glycidyl Methacrylate

机译:苯乙烯和甲基丙烯酸缩水甘油酯的RAFT共聚中的反应率估算

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The bulk reversible addition-fragmentation chain transfer (RAFT) copolymerization of glycidyl methacrylate (GMA) and styrene (S) at several GMA molar feed fractions in the presence of 2-cyano isopropyl dodecyl trithiocarbonate as RAFT agent and 1,10-azobis(cyclohexane carbonitrile) as initiator is reported. The reaction conditions are similar to those used in the industrial production of crystal and high-impact polystyrene by free radical polymerization with the purpose of synthesizing well-defined copolymers in current industrial processes with only minor changes. Reactivity ratios calculated with linear Kelen-Tudos, extended Kelen-Tudos, and nonlinear regression (error in all variables) methods are reported. The results obtained suggest that the RAFT process modifies copolymer composition development. Increased preference for the monomer with the higher reactivity ratio is observed.
机译:在2-氰基异丙基十二烷基三硫代碳酸酯作为RAFT剂和1,10-偶氮双(环己烷)存在下,甲基丙烯酸缩水甘油酯(GMA)和苯乙烯(S)在几个GMA摩尔进料分数下的本体可逆加成-断裂链转移(RAFT)共聚据报道,以乙腈为引发剂。反应条件类似于通过自由基聚合在晶体和高抗冲聚苯乙烯的工业生产中使用的那些条件,其目的是在当前的工业过程中仅需很小的变化即可合成定义明确的共聚物。报告了使用线性Kelen-Tudos,扩展的Kelen-Tudos和非线性回归(所有变量均存在误差)方法计算的反应率。获得的结果表明,RAFT方法改变了共聚物组成的发展。观察到对具有较高反应性比率的单体的偏好增加。

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