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聚(甲基丙烯酸甲酯-共-2-全氟辛基乙基甲基丙烯酸酯)膜成膜过程中氟化部分的表面偏析:熵或焓的影响。

Surface segregation of fluorinated moieties on poly(methyl methacrylate-ran-2-perfluorooctylethyl methacrylate) films during film formation: Entropic or enthalpic influences.

机构信息

Department of Chemistry, Key Laboratory of Advanced Textile Materials and Manufacturing Technology of the Education Ministry, Zhejiang Sci-Tech University, Hangzhou 310018, China.

出版信息

J Colloid Interface Sci. 2010 Sep 1;349(1):205-14. doi: 10.1016/j.jcis.2010.05.042. Epub 2010 May 19.

Abstract

The effects of solvents, fluorinated monomer content and film-formation methods on the surface structures of random copolymers composed of methyl methacrylate (MMA) and 2-perfluorooctylethyl methacrylate (FMA) were investigated by contact angle goniometry, X-ray photoelectron spectroscopy, sum frequency generation (SFG) vibrational spectroscopy and surface tension measurement. It is found that, with cyclohexanone as the solvent, there is a critical FMA content of 9mol%, below which the copolymer films by spin coating have a more surface segregation extent of fluorinated moieties than those by solution casting; above which the copolymer films by solution casting have a more surface segregation extent of fluorinated moieties than those by spin coating. However, with toluene as solvent, the critical FMA content lowers down to 3mol%. We believe that the solvent nature and the content of fluorinated moieties in the random copolymer have the great effect because the combined effect of these two factors can determine the random copolymer chain conformations and their thermodynamic dominating factors in the solution and at the solution-air interface. A thermodynamic analysis combining the entropic and enthalpic effects is suggested to explain the observed phenomenon. This research is believed to obtain an enhanced understanding of the surface formation mechanism of the polymer films and thus demonstrate how to promote the segregation of fluorinated moieties at the polymer film surfaces.

摘要

采用接触角测量、X 射线光电子能谱、和频振动光谱以及表面张力测量等手段,研究了溶剂、含氟单体含量和成膜方法对甲基丙烯酸甲酯(MMA)和 2-全氟辛基乙基甲基丙烯酸酯(FMA)无规共聚物表面结构的影响。结果发现,以环己酮为溶剂时,存在一个临界 FMA 含量为 9mol%,低于此值时,旋涂共聚物膜的氟化物部分表面选择性程度高于溶液浇铸膜;高于此值时,溶液浇铸共聚物膜的氟化物部分表面选择性程度高于旋涂膜。然而,以甲苯为溶剂时,临界 FMA 含量降低至 3mol%。我们认为溶剂性质和无规共聚物中氟化物含量的影响很大,因为这两个因素的综合作用可以决定无规共聚物链在溶液中和溶液-空气界面的构象及其热力学主导因素。提出了一种结合熵和焓效应的热力学分析来解释所观察到的现象。该研究有助于深入了解聚合物膜的表面形成机制,并展示如何促进氟化物部分在聚合物膜表面的选择性富集。

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