Creating stable hydrophobic surfaces by poly(butyl methacrylate) end- capped with 2-perfluorooctylethyl methacrylate units

被引:19
作者
Yang, Juping [1 ]
Ni, Huagang [1 ]
Wang, Xiaofang [1 ]
Zhang, Wei [1 ]
Wang, Xinping [1 ]
机构
[1] Zhejiang Sci Tech Univ, Key Lab Adv Textile Mat & Mfg Technol, Educ Minist, Dept Chem, Hangzhou 310018, Peoples R China
关键词
surface free energy; perfluoroalkyl side chain; surface structure; self-assembly; hydrophobic surface; surface reconstruction;
D O I
10.1007/s00289-007-0743-3
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
It is a challenge to fabricate fluorine-containing polymer surface with low-energy properties and superior long-lasting barrier properties as well as lower fluorine content. In this paper, poly( butyl methacrylate) end-capped with 2-perfluorooctylethyl methacrylate units ( PBMA-ec-FMA), having the so-called push-me/pull-you structures, have been synthesized by ATRP and their surface properties were investigated. This structure was in favorable of the longer -(CF2)(7)CF3 moieties self-assembling on the polymer surface during film formation, which resulted in better chain alignment and packing of the longer -( CF2) 7CF3 moieties. Therefore, the contact angles of water and paraffin oil on the surface of the end-capped PBMA were 118 degrees and 84 degrees, respectively, approaching that of poly(2-perfluorooctylethyl methacrylate) homopolymer, even though the content of FMA was 0.34 mol% ( the average polymerization degree of PFMA units is 1). However, more than 9 mol% was necessary for the relative random copolymer (PBMA-r-PFMA) to reach these values of the contact angle. Regardless of the wetting properties, the end-capped PBMA by fluorinated methacrylate has better resistance to surface reconstruction than PBMA-rPFMA random copolymer even though FMA content in PBMA-ec-FMA is much lower than that in random copolymer. Therefore, it may be a facile method to create stable hydrophobic surfaces with lower price.
引用
收藏
页码:105 / 115
页数:11
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