Molecular relaxation in cross-linked poly(ethylene glycol) and poly(propylene glycol) diacrylate networks by dielectric spectroscopy

被引:24
|
作者
Kalakkunnath, Sumod
Kalika, Douglass S.
Lin, Haiqing
Raharjo, Roy D.
Freeman, Benny D.
机构
[1] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
[2] Univ Kentucky, Ctr Mfg, Lexington, KY 40506 USA
[3] Univ Texas, Ctr Energy & Environm Resources, Dept Chem Engn, Austin, TX 78758 USA
基金
美国国家科学基金会;
关键词
membranes; poly(ethylene oxide); dielectric spectroscopy;
D O I
10.1016/j.polymer.2006.11.046
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The molecular relaxation characteristics of rubbery amorphous crosslinked networks based on poly(ethylene glycol) diacrylate [PEGDA] and poly(propylene glycol) diacrylate [PPGDA] have been investigated using broadband dielectric spectroscopy. Dielectric spectra measured across the sub-glass transition region indicate the emergence of an intermediate "fast" relaxation in the highly crosslinked networks that appears to correspond to a subset of segmental motions that are more local and less cooperative as compared to those associated with the glass transition. This process, which is similar to a distinct sub-T-g relaxation detected in poly(ethylene oxide) [PEO], may be a general feature in systems with a sufficient level of chemical or physical constraint, as it is observed in the crosslinked networks, crystalline PEO, and PEO-based nanocomposites. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:579 / 589
页数:11
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