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Polar, functionalized diene-based materials. 1. Bulk, solution, and emulsion free radical polymerization of 2-cyanomethyl-1,3-butadiene

机译:极性,功能化的二烯基材料。 1. 2-氰基甲基-1,3-丁二烯的本体,溶液和乳液自由基聚合

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The bulk, solution, and emulsion free radical polymerizations of 2-cyanomethyl-1,3-butadiene were studied. Traditional bulk free radical polymerization kinetics were observed, giving polymers with [M-n] values of 20 x 10(3)-60 x 10(3) g/mol and polydispersities near 1.5. In solution polymerization, the highest molecular weight (82 x 10(3) g/mol at 53% conversion) was obtained in tetrahydrofuran, with a broader polydispersity attributed to chain transfer to the solvent. In these two types of polymerizations, the Diels-Alder side product yield was affected by initiator concentration, solvent concentration, and polymerization time. Emulsion polymerization gave the highest molecular weight of poly(2-cyanomethyl-1,3-butadiene) to date of 128 x 10(3) g/mol in significantly shorter reaction time than bulk or solution reactions. Finally, the polymer microstructure of approximately 95% 1,4 and 5% 4,3 structure was determined, with the percent cis-1,4 (36-45%) varying with the polymerization temperatures. The glass transition temperature of poly(2-cyanomethyl-1,3-butadiene) is near -18 degrees C, based on the molecular weight and the microstructure. [References: 22]
机译:研究了2-氰基甲基-1,3-丁二烯的本体,溶液和乳液自由基聚合。观察到传统的本体自由基聚合动力学,得到[M-n]值为20 x 10(3)-60 x 10(3)g / mol且多分散度接近1.5的聚合物。在溶液聚合中,在四氢呋喃中获得了最高的分子量(在53%的转化率下为82 x 10(3)g / mol),更宽的多分散性归因于链转移到溶剂中。在这两种类型的聚合反应中,Diels-Alder副产物的收率受引发剂浓度,溶剂浓度和聚合时间的影响。到目前为止,乳液聚合的最高分子量为128 x 10(3)g / mol的聚(2-氰基甲基-1,3-丁二烯),比本体或溶液反应的反应时间短得多。最后,确定了约95%的1,4和5%的4,3结构的聚合物微结构,其中顺式1.4,%(36-45%)的百分比随聚合温度而变化。基于分子量和微观结构,聚(2-氰基甲基-1,3-丁二烯)的玻璃化转变温度接近-18℃。 [参考:22]

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