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首页> 外文期刊>Journal of Applied Polymer Science >The transient nature of maximum maleic anhydride grafting of polypropylene: A mechanistic approach based on a consecutive reaction model. II. A comparison of the batch solution and molten state processes
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The transient nature of maximum maleic anhydride grafting of polypropylene: A mechanistic approach based on a consecutive reaction model. II. A comparison of the batch solution and molten state processes

机译:聚丙烯最大马来酸酐接枝的暂态性质:基于连续反应模型的机械方法。二。分批溶液和熔融状态过程的比较

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摘要

This article compares the batch solution and molten state chemical modification of an atactic polypropylene to yield a grafted polypropylene. Short reaction times appear to be sufficient and indeed necessary for the highest graft yields to be obtained if degradative processes occurring in both reaction media are to be avoided. The consecutive reactions for the optimized grafting reaction pathway were proposed for the solution process in an earlier article. The present work attempts to correlate this pathway with that of the molten state process. Grafted succinic anhydride groups react with two resorcine molecules to yield grafted succinyl-fluorescein groups. This work considers the resorcine units as true molecular probes, to be able to stabilize and activate the complexes formed between the succinic anhydride groups and the propylene sequence. This work shows the unsteady and later dynamic character of the process. (c) 2007 Wiley Periodicals, Inc.
机译:本文比较了无规聚丙烯的间歇溶液和熔融态化学改性,以制得接枝聚丙烯。如果要避免在两种反应介质中发生降解过程,则短的反应时间似乎足够并且确实对于获得最高的接枝产率是必要的。在较早的文章中提出了用于溶液工艺的优化接枝反应途径的连续反应。当前的工作试图将该途径与熔融过程的途径联系起来。接枝的琥珀酸酐基团与两个间苯二酚分子反应生成接枝的琥珀酰荧光素基团。这项工作认为间苯二酚单元是真正的分子探针,能够稳定和激活在琥珀酸酐基团和丙烯序列之间形成的络合物。这项工作显示了该过程的不稳定和后来的动态特征。 (c)2007年Wiley Periodicals,Inc.

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