Surface morphology and dewettability of self-organized thermosets involving epoxy and POSS-capped poly(ethylene oxide) telechelics

被引:20
作者
Wang, Lei
Zheng, Sixun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Polymer Sci & Engn, Shanghai 200240, Peoples R China
关键词
Polymers; Inorganic compounds; Composite materials; Nanostructures; Surfaces; OLIGOMERIC SILSESQUIOXANES POSS; POLYHEDRAL OLIGOSILSESQUIOXANE; AMPHIPHILIC TELECHELICS; MECHANICAL RELAXATION; POLYSTYRENE; NETWORKS; RESIN; MICROSTRUCTURE; NANOSTRUCTURES; POLYMERIZATION;
D O I
10.1016/j.matchemphys.2012.07.051
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A heptaphenyl polyhedral oligomeric silsesquioxane-capped poly(ethylene oxide) (POSS-capped PEO) telechelics was synthesized via the Huisgen 1,3-dipolar cycloaddition between 3-azidopropylheptaphenyl POSS and alpha,omega-dialkynyl-terminated poly(ethylene oxide). The organic inorganic amphiphile was incorporated into epoxy to obtain the organic inorganic nanocomposites. The morphology of the nanocomposites was investigated by means of atomic force microscopy (AFM) and dynamic mechanical thermal analysis (DMTA). It was found that the epoxy thermosets containing POSS-capped PEO telechelics were microphase-separated. The formation of the nanophases in the thermosets followed a self-assembly mechanism. The static contact angle measurements show that the nanocomposites displayed a significant enhancement in surface hydrophobicity as well as reduction in surface free energy. The improvement in surface dewettability was ascribed to the enrichment of POSS cages at the surface of the nanocomposites and the formation of the specific surface morphology as evidenced by X-ray photoelectron spectroscopy (XPS) and surface atomic force microscopy (AFM). (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:744 / 754
页数:11
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