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首页> 外文期刊>European Polymer Journal >Study of amphiphilic poly(1-dodecene-co-para-methylstyrene)-graft-poly (ethylene glycol): Part I. Preparation of poly(1-dodecene-co-para-methylstyrene) copolymer and its molecular weight regulation
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Study of amphiphilic poly(1-dodecene-co-para-methylstyrene)-graft-poly (ethylene glycol): Part I. Preparation of poly(1-dodecene-co-para-methylstyrene) copolymer and its molecular weight regulation

机译:两亲性聚(1-十二烯-对-对甲基苯乙烯)-接枝聚乙二醇的研究:第一部分。聚(1-十二烯-对-对甲基苯乙烯)共聚物的制备及其分子量调节

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Poly(1-dodecene-co-para-methylstyrene) copolymers with a broad composition range were prepared by an MgCl2 supported TiCl4 catalyst. The effects of temperature and hydrogen on catalyst activity were investigated. It was found that catalyst activity reached a maximum at around 60 C, and then decreased with the rising temperature. Hydrogen showed an activation effect on the Ziegler-Natta catalyst. H-1 NMR and C-13 NMR spectra showed that para-methylstyrene (pMS) could be effectively and randomly incorporated into the copolymer chains. The single glass transition indicated there was no block sequence in the copolymer. The copolymerization reaction was examined by the reactivity ratios of comonomers and the relatively low reactivity ratios of 1-dodecene and pMS indicated that both of them had little tendency of consecutive insertion and should be homogeneously distributed in the copolymer chains. Furthermore, the molecular weights of copolymers were regulated by chain transfer agents (diethyl zinc and hydrogen) and temperature. The molecular weights reduced greatly with the addition of diethyl zinc and hydrogen and with the increasing temperature. (c) 2008 Elsevier Ltd. All rights reserved.
机译:用MgCl2负载的TiCl4催化剂制备了具有宽组成范围的聚(1-十二烯-对-对甲基苯乙烯)共聚物。研究了温度和氢气对催化剂活性的影响。发现催化剂活性在约60℃达到最大值,然后随温度升高而降低。氢对齐格勒-纳塔催化剂显示出活化作用。 H-1 NMR和C-13 NMR光谱表明对甲基苯乙烯(pMS)可以有效且无规地掺入共聚物链中。单玻璃化转变表明在共聚物中没有嵌段序列。通过共聚单体的反应率检查共聚反应,并且1-十二碳烯和pMS的相对低的反应率表明它们两者几乎没有连续插入的趋势并且应该均匀地分布在共聚物链中。此外,共聚物的分子量由链转移剂(二乙基锌和氢)和温度调节。随着二乙基锌和氢的添加以及温度的升高,分子量大大降低。 (c)2008 Elsevier Ltd.保留所有权利。

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