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Nanostructured thermoset epoxy resin templated by an amphiphilic poly(ethylene oxide)-block-poly(dimethylsiloxane) diblock copolymer
被引:38
|作者:
Guo, Qipeng
[1
]
Chen, Fei
Wang, Ke
Chen, Ling
机构:
[1] Deakin Univ, Ctr Mat & Fibre Innovat, Geelong, Vic 3217, Australia
[2] Monash Univ, Dept Mat Engn, Clayton, Vic 3800, Australia
[3] Inst Mat Res & Engn, Singapore 117602, Singapore
关键词:
blends;
block copolymers;
crystallization;
phase behavior;
thermosets;
D O I:
10.1002/polb.20947
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
An amphiphilic poly(ethylene oxide)-block-poly(dimethylsiloxane) (PEO-PDMS) diblock copolymer was used to template a bisphenol A type epoxy resin (ER); nanostructured thermoset blends of ER and PEO-PDMS were prepared with 4,4'-methylenedianiline (MDA) as the curing agent. The phase behavior, crystallization, hydrogen-bonding interactions, and nanoscale structures were investigated with differential scanning calorimetry, Fourier transform infrared spectroscopy, transmission electron microscopy, and small-angle X-ray scattering. The uncured ER was miscible with the poly(ethylene oxide) block of PEO-PDMS, and the uncured blends were not macroscopically phase-separated. Macroscopic phase separation took place in the MDA-cured ER/PEO-PDMS blends containing 60-80 wt % PEO-PDMS diblock copolymer. However, the composition-dependent nanostructures were formed in the cured blends with 10-50 wt % PEO-PDMS, which did not show macroscopic phase separation. The poly(dimethylsiloxane) microdomains with sizes of 10-20 nm were dispersed in a continuous ER-rich phase; the average distance between the neighboring microdomains was in the range of 20-50 nm. The miscibility between the cured ER and the polyethylene oxide) block of PEO-PDMS was ascribed to the favorable hydrogen-bonding interaction. (c) 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3042-3052, 2006.
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页码:3042 / 3052
页数:11
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