Nanostructures and Surface Hydrophobicity of Self-Assembled Thermosets Involving Epoxy Resin and Poly(2,2,2-trifluoroethyl acrylate)-block-Poly(ethylene oxide) Amphiphilic Diblock Copolymer

被引:45
作者
Yi, Fangping [1 ,2 ]
Zheng, Sixun [1 ,2 ]
Liu, Tianxi [3 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Polymer Sci & Engn, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[3] Fudan Univ, Dept Macromol Sci, Shanghai 200433, Peoples R China
关键词
BLOCK-COPOLYMERS; MECHANICAL-PROPERTIES; TRIBLOCK COPOLYMERS; DIAMINE BLENDS; POLYSTYRENE; MORPHOLOGIES; SEGREGATION; POLYMERS; BEHAVIOR; SYSTEMS;
D O I
10.1021/jp8082198
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Poly(2,2,2-trifluoroethyl acrylate)-block-poly(ethylene oxide) (PTFEA-b-PEO) amphiphilic diblock copolymer was synthesized via the reversible addition-fragmentation transfer polymerization of 2,2,2-triffluroethyl acrylate with dithiobenzoyl-terminated poly(ethylene oxide) as a chain-transfer agent. The amphiphilic diblock copolymer was incorporated into epoxy resin to prepare the nanostructured epoxy thermosets. The nanostructures were investigated by means of atomic force microscopy, small-angle X-ray scattering, and dynamic mechanical analysis. In terms of the miscibility of the subchains of the block copolymer with epoxy after and before curing reaction, it: is judged that the formation of the nanostructures follows the mechanism of self-assembly. The static contact angle measurements indicate that the nanostructured thermosets containing PTFEA-b-PEO diblock copolymer displayed a significant enhancement in surface hydrophobicity as well as a reduction in surface free energy. The improvement in surface properties was ascribed to the enrichment of the fluorine-containing subchain (i.e., PTFEA block) of the amphiphilic diblock copolymer on the surface of the nanostructured thermosets, which was evidenced by surface atomic force microscopy and energy-dispersive X-ray spectroscopy.
引用
收藏
页码:1857 / 1868
页数:12
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