Stimuli-Responsive Polymer Surfactants

S. Aoshima, S. Sugihara
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引用次数: 1

Abstract

Various amphiphilic block copolymers (polymer surfactants) possessing hydrophilic and hydrophobic segments were designed, prepared, and examined for stimuli-responsive selforganization in water. New polymer micelles or physical gels that would have this property were made by intermolecular hydrophobic interaction. Recent advances and related topics are initially summarized in this paper. Well-controlled block copoly (vinyl ether) s were synthesized in this study by living cationic polymerization of vinyl ethers with various functional groups. Not only hydrophilic polyalcohols and hydrophobic poly (alkyl vinyl ether) s, but thermally-responsive polymers with oxyethylene units as well were used as segments of diblock copolymers. When aqueous polymer solution was heated, characteristic physical gelation occurred in a certain temperature range corresponding to the particular properties of the segments. As other stimuli, the addition of selected organic compounds and H+ to the solution containing diblock copolymers was also examined as a means for obtaining physical gels via a mechanism similar to that in thermally-responsive systems.
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刺激响应型聚合物表面活性剂
设计、制备了各种具有亲疏水段的两亲嵌段共聚物(聚合物表面活性剂),并对其在水中的刺激响应自组织进行了研究。新的聚合物胶束或具有这种性质的物理凝胶是通过分子间疏水相互作用制成的。本文对近年来研究进展及相关课题进行了初步综述。本文采用活性阳离子聚合的方法,对含不同官能团的乙烯醚进行活性聚合,合成了控制良好的嵌段共聚物(乙烯醚)。不仅用亲水性聚醇和疏水性聚烷基乙烯醚,而且用氧乙烯基热响应聚合物作为二嵌段共聚物的节段。当聚合物水溶液被加热时,在特定的温度范围内发生了特征的物理凝胶化,这与聚合物段的特定性质相对应。作为其他刺激物,将选定的有机化合物和H+添加到含有二嵌段共聚物的溶液中,也可以通过类似于热响应系统的机制获得物理凝胶。
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