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首页> 外文期刊>European Polymer Journal >Controlled/'living' atom transfer radical polymerization of methyl methacrylate in the synthesis of triblock copolymers from a poly(oxyethylene) macroinitiator
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Controlled/'living' atom transfer radical polymerization of methyl methacrylate in the synthesis of triblock copolymers from a poly(oxyethylene) macroinitiator

机译:从聚(氧乙烯)大分子引发剂合成三嵌段共聚物中甲基丙烯酸甲酯的受控/“活”原子转移自由基聚合

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摘要

Atom transfer radical polymerization of methyl methacrylate initiated by a poly(oxyethylene) macroinitiator by the esterification of PEG 1500 with 2-chloro propionyl chloride was synthesized. These polymerization proceeds both in bulk and solution with a quantitative initiation efficiency. leading to A-B-A triblock copolymers. The macroinitiators P, and their block copolymers were characterized by FT-IR, FT-NMR and GPC analyses. in bulk polymerization. the kinetic study showed that the relationship between vs time was linear showing that there is a constant concentration of active species throughout the polymerization and follow the first order kinetics with respect to monomer, Moreover, the experimental molecular weight of the block copolymers increased linearly with the monomer conversion and the polydispersity index remained between 1.3 and 1.5 throughout the polymerization. No formation of homo poly(methyl methacrylate) could also be detected, and all this confirms that the bulk polymerization proceeds in a controlled/"living" manner. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 27]
机译:合成了由聚(氧乙烯)大分子引发剂引发的甲基丙烯酸甲酯的原子转移自由基聚合反应,该反应是通过PEG 1500与2-氯丙酰氯的酯化反应而引发的。这些聚合以定量引发效率在本体和溶液中进行。导致A-B-A三嵌段共聚物。通过FT-IR,FT-NMR和GPC分析表征大分子引发剂P及其嵌段共聚物。在本体聚合中。动力学研究表明,时间与时间之间的关系呈线性关系,表明整个聚合过程中活性物质的浓度恒定,并且相对于单体遵循一级动力学。而且,嵌段共聚物的实验分子量随分子量的增加而线性增加。在整个聚合过程中,单体转化率和多分散指数保持在1.3和1.5之间。也没有检测到均聚聚(甲基丙烯酸甲酯)的形成,所有这些证实本体聚合以受控/“活性”方式进行。 (C)2002 Elsevier ScienceLtd。保留所有权利。 [参考:27]

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