新型氟化嵌段共聚物,用于超低能表面的构建和低凝聚能溶剂的分散稳定剂

M. Antonietti, S. Förster, M. A. Micha, S. Oestreich
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引用次数: 16

摘要

由聚苯乙烯和含有长氟化侧链的嵌段共聚物组成的嵌段共聚物是由市售聚苯乙烯-b-聚丁二烯嵌段共聚物通过两种非常有效的聚合物类似反应制成的。由于这些聚合物由具有疏水性和极疏水性的两个相互不混溶的嵌段组成,它们在各种介质中形成胶束,甚至在极疏水性溶剂中形成胶束,例如甲苯、四氢呋喃(THF)、全氟己烷、全氟(甲基环己烷)、六氟苯和1,1,2-三氯三氟乙烷(氟里昂113)。我们的聚合物在这种溶剂中作为有效的立体稳定剂是有用的第一个迹象是通过在溶剂中通过沉淀聚合制备的一些聚合物分散体的表征给出的。在固体状态下,通过定量小角x射线散射(SAXS)观察和表征了嵌段共聚物典型的中间相形成。这种薄膜的表面由氟化块控制,并表现出γSV = 15 mN/m数量级的超低表面能,低于聚四氟乙烯(PTFE)或聚二甲基硅氧烷(PDMS)的表面能。与聚四氟乙烯不同,所述聚合物的块状性质使热塑性加工和溶解在标准溶剂中,这是具有实际意义的。对涂有这些共聚物的膜的透气性测量显示出一些有趣的选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel fluorinated block copolymers for the construction of ultra-low energy surfaces and as dispersion stabilizers in solvents with low cohesion energy

Block copolymers consisting of polystyrene and a block containing long fluorinated side chains are made by two very effective polymer analogous reactions from commercially available polystyrene-b-polybutadiene block copolymers. Since these polymers consist of two mutually immiscible blocks with hydrophobic and very hydrophobic character they form micelles in a wide range of media down to very hydrophobic solvents, e. g. toluene, tetrahydrofurane (THF), perfluorohexane, perfluoro(methylcyclohexane), hexafluorobenzene and 1,1,2-trichlorotrifluoroethane (Freon 113). First indications that our polymers are useful as effective steric stabilizers in such solvents are given by characterization of some polymer dispersions made in the solvents via precipitation polymerization.

In the solid state, mesophase formation typical for block copolymers is observed and characterized by quantitative small angle X-ray scattering (SAXS). The surface of such films is controlled by the fluorinated block and exhibits an ultra-low surface energy of the order of γSV = 15 mN/m, below that of polytetrafluoroethylene (PTFE) or polydimethylsiloxanes (PDMS). Unlike PTFE, the blocky nature of the presented polymer enables thermoplastic processing and dissolution in standard solvents, which is of practical relevance. Gas-permeability measurements on membranes coated with these copolymers exhibit some interesting selectivities.

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