Water-induced surface structure of poly(dimethylsiloxane)-containing block copolymers

被引:2
|
作者
Jo, Nam-Ju [1 ]
Chun, Jae Hwan [1 ]
Lim, Kwon Taek [2 ]
Jang, Ei-Sup [3 ]
Lee, Won-Ki [3 ]
机构
[1] Pusan Natl Univ, Dept Polymer Sci & Engn, Pusan 609735, South Korea
[2] Pukyong Natl Univ, Dept Imaging Syst Engn, Pusan 608739, South Korea
[3] Pukyong Natl Univ, Dept Polymer Engn, Pusan 608739, South Korea
基金
新加坡国家研究基金会;
关键词
triblock copolymers; poly(dimethylsiloxane) (PDMS); surface energy; water; chain mobility; ELECTRON-SPECTROSCOPY; TRIBLOCK COPOLYMERS; POLYURETHANE;
D O I
10.1007/s13233-013-1092-8
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two triblock copolymers, polyester-b-poly(dimethylsiloxane) (PDMS)-b-polyester, were synthesized by the ring-opening polymerization with both hydrophobic and water-repellent hydroxyl-terminated PDMS and hydrolytically degradable ester monomers. The T (g) s of the polyester blocks were controlled by E >-caprolactone/lactide mixture or lactide only. The surface composition of the triblock copolymers was measured by angle-dependent electron: X-ray photoelectron spectroscopy. The results showed that the PDMS block with a low surface energy in the copolymers was quite segregated in the surface region; the copolymer films showed significantly higher mole fractions of PDMS (0.78-0.86) at a low takeoff angle compared with their bulk mole fractions (0.015-0.02). When the films were exposed to water at 20 A degrees C for 70 min, the mole fractions of surface PDMS were decreased to 0.3-0.5 because of the water-repellent hydrophobicity and the chain mobility of both blocks.
引用
收藏
页码:821 / 825
页数:5
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