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Microgelation in Free-Radical Crosslinking Polymerization and Copolymerization of Multivinyl Compounds

机译:自由基交联聚合中的微凝胶化合物和多聚乙烯基化合物的共聚合

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Earlier, Staudinger et al. [1] have reported styrene (St)-divinylbenzene (DVB) microgel. Thereafter, numerous reports on the microgel formation have been published in the homopolymerizations of multivinyl compounds and their copolymerizations with monovinyl monomers [2-6]. However, no microgelation was observed in the bulk polymerization of diallyl phthalate giving a quite low primary chain length [7] and also, in the monovinyl-divinyl copolymerizations with only a small amount of divinyl monomer [8]. Thus a detailed study on the microgelation, especially up to the gel point conversion, is required because the microgelation leads not only to the delayed gelation, but also to the microheterogeneity of network structures of three-dimensional polymers as closely related to their properties.
机译:早些时候,斯兰廷格等人。 [1]报道了苯乙烯(ST) - 二氨基苯(DVB)微凝胶。此后,已经在多聚乙烯化合物的均聚物和与单乙烯基单体的均聚物中公布了关于微凝胶形成的许多报道[2-6]。然而,在二烯丙基邻苯二甲酸酯的本体聚合中没有观察到微凝胶化,得到相当低的初级链长度[7],并且在单乙烯基 - 二乙烯基共聚中仅具有少量二乙烯基单体[8]。因此,需要对微胶质的详细研究,特别是凝胶点转化,因为微胶质不仅导致延迟凝胶化,而且还导致三维聚合物的网络结构的微孔,与其性质密切相关。

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