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超临界二氧化碳中的分散聚合。

Dispersion polymerizations in supercritical carbon dioxide.

出版信息

Science. 1994 Jul 15;265(5170):356-9. doi: 10.1126/science.265.5170.356.

Abstract

Conventional heterogeneous dispersion polymerizations of unsaturated monomers are performed in either aqueous or organic dispersing media with the addition of interfacially active agents to stabilize the colloidal dispersion that forms. Successful stabilization of the polymer colloid during polymerization results in the formation of high molar mass polymers with high rates of polymerization. An environmentally responsible alternative to aqueous and organic dispersing media for heterogeneous dispersion polymerizations is described in which supercritical carbon dioxide (CO(2)) is used in conjunction with molecularly engineered free radical initiators and amphipathic molecules that are specifically designed to be interfacially active in CO(2). Conventional lipophilic monomers, exemplified by methyl methacrylate, can be quantitatively (>90 percent) polymerized heterogeneously to very high degrees of polymerization (>3000) in supercritical CO(2) in the presence of an added stabilizer to form kinetically stable dispersions that result in micrometer-sized particles with a narrow size distribution.

摘要

常规的不饱和单体的多相分散聚合反应在添加界面活性剂的水相或有机分散介质中进行,以稳定形成的胶体分散体。聚合过程中聚合物胶体的成功稳定化导致高摩尔质量聚合物的形成,具有高聚合速率。本文描述了一种替代水相和有机分散介质的环境友好方法,即在多相分散聚合中使用超临界二氧化碳(CO(2)),同时使用分子设计的自由基引发剂和两亲分子,这些分子专门设计在 CO(2)中具有界面活性。传统的亲脂性单体,如甲基丙烯酸甲酯,可以在超临界 CO(2)中定量(>90%)异相聚合到非常高的聚合度(>3000),在添加稳定剂的情况下形成动力学稳定的分散体,得到具有窄粒径分布的微米级颗粒。

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