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Kinetic Analysis of Slow Monomer Addition in Synthesis of Hyperbranched Polymers

机译:超支化聚合物合成缓慢单体添加的动力学分析

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@@1.Introduction Owing to their unique structures and properties, hyperbranched polymers have extensive prospects of application and have drawn more and more attention. Kim et al.[1] first synthesized the hyperbranched polyphenylene by AB2 type monomers. So far, most hyperbranched polymers are prepared by Abg (g>1) type monomers[2] or the self-condensing vinyl polymerization (SCVP) of inimers[3]. However, both theory and experiment show that the molecular weight distribution of the hyperbranched polymers formed from one-pot synthesis is extremely broad at high conversion of monomers and it is difficult to control the molecular weight. The introduction of multifunctional core molecules in the hyperbranched polymerization process narrows polydispersities of the resulting hyperbranched polymerS[4]. Moreover, the polydispersity of polymers obtained can drastically decrease when monomers were slowly added to the reaction system[5]. In this work, we analysis the kinetic process and derive the expressions of distribution function and the various molecular parameters for the slow monomer addition polymerization process, with the conversion of monomers as variable.
机译:@@ 1.介绍了由于它们独特的结构和性质,超支化聚合物具有广泛的应用前景,并越来越受到关注。 Kim等人[1]首先通过AB2型单体合成超支化的聚苯。到目前为止,最多的超支化聚合物由ABG(G> 1)型单体[2]或内周的自凝乙烯基聚合(SCVP)制备[3]。然而,理论和实验既表明,由单盆合成形成的超支化聚合物的分子量分布在单体的高转化率下极宽,并且难以控制分子量。在超支化聚合过程中引入多官能核心分子使所得超支化聚合物的多分散性变窄[4]。此外,当将单体缓慢加入到反应体系中时,所获得的聚合物的多分散性可以急剧下降[5]。在这项工作中,我们分析了动力学过程并导出了分布函数的表达和用于缓慢单体加成聚合方法的分配功能和各种分子参数,随着单体的转化为可变。

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