Influence of molecular weight on dynamic crossover temperature in linear polymers

被引:26
|
作者
Pawlus, S. [1 ]
Kunal, K. [1 ]
Hong, L. [1 ]
Sokolov, A. P. [1 ]
机构
[1] Univ Akron, Dept Polymer Sci, Akron, OH 44325 USA
基金
美国国家科学基金会;
关键词
polymers; glass transition; dynamic crossover;
D O I
10.1016/j.polymer.2008.04.040
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Dielectric and light scattering spectra of two linear polymers, polyisoprene (PIP) and polystyrene (PS), were analyzed in broad temperature and frequency range above the glass transition temperature, T-g. The crossover temperature, T-C, was estimated using two approaches: (i) derivative analysis of relaxation times proposed by Stickel and (ii) Mode-Coupling Theory approach. Both estimates provide consistent values. T-C varies with molecular weight (MW) in both polymers, while the ratio T-C/T-g changes significantly with MW in PS only. It appears that the segmental relaxation time at T-C has value tau(T-C) similar to 10(-7) S for both polymers independent of MW and similar to the value reported for many non-polymeric glass-forming systems. No sign of the dynamic crossover has been observed in the chain relaxation around T-C of the segmental dynamics. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2918 / 2923
页数:6
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