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出 处:《石油化工》2007年第6期575-578,共4页Petrochemical Technology
基 金:国家自然科学基金项目(2047404220574049)
摘 要:以偶氮二异丁腈为引发剂,在醋酸乙烯酯(VAc)的普通自由基聚合反应体系中加入少量碘,原位生成了碘化物α-碘代异丁腈,该碘化物在聚合过程中起可逆的链转移剂的作用,合成了含碘端基的聚醋酸乙烯酯(PVAc-I);考察了反应温度、原料配比对聚合反应的影响。实验结果表明,反应温度为75℃较适宜VAc的聚合;在该温度下,VAc通过衰减链转移自由基聚合法可合成相对分子质量可控、相对分子质量分布较窄(Mw/Mn≤1.41)的PVAc-I,并用核磁共振仪对PVAc-I的结构进行了表征。PVAc-I与甲基丙烯酸甲酯的嵌段共聚实验结果表明,PVAc-I末端的碘具有活性,合成的嵌段共聚物聚醋酸乙烯酯-b-甲基丙烯酸甲酯的相对分子质量分布窄(Mw/Mn=1.43)。Iodic - end - group poly ( vinyl acetate) ( PVAc - I) was synthesized from vinyl acetate (VAc) by degenerative chain transfer radical polymerization in presence of iodine with 2.2' - azobisisobutyronitrile (AIBN) as initiator. In the polymerization, radicals initiated from AIBN firstly reacted in situ with iodine to produce α -iodoisobutyronitrile (CH3)2(CN)CI, which then acted as chain transfer agent in the polymerization. Effects of reaction temperature and n(VAc) : n(AIBN) : n( 12 ) on the polymerization were investigated. PVAc -I with adjustable relative molecular mass and narrow relative molecular mass distribution(Mw/Mn≤1. 41 ) can be synthesized at 75 ℃. The PVAc -I was characterized by means of ^1H NMR. Iodine at the end of PVAc - I molecule is active, which is proved by block copolymerization of PVAc - I and methyl methacrylate. The block copolymer poly ( vinyl acetate) - b - methyl methacrylate with narrow relative molecular mass distribution ( Mw/Mn = 1.43 ) is obtained.
关 键 词:醋酸乙烯酯 聚醋酸乙烯酯 碘端基的聚醋酸乙烯酯 碘 衰减链转移自由基聚合 链转移剂
分 类 号:TQ325.5[化学工程—合成树脂塑料工业]
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