Correlations between dynamic fragility and dynamic mechanical properties of several amorphous polymers

被引:42
|
作者
Wu, Jinrong [1 ]
Huang, Guangsu [1 ]
Qu, Liangliang [1 ]
Zheng, Jing [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
Glass transition; Mechanical; Stress relaxation; Polymers and organics; Fragility; GLASS-FORMING LIQUIDS; THERMORHEOLOGICAL COMPLEXITY; TEMPERATURE-DEPENDENCE; TRANSITION TEMPERATURE; ENERGY LANDSCAPE; FORMERS; METHACRYLATE); MISCIBILITY; RELAXATION; VISCOSITY;
D O I
10.1016/j.jnoncrysol.2009.06.013
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In the present paper, dynamic mechanical properties were measured for several amorphous polymers ranging from strong to fragile. The results indicate that the storage modulus changes steadily, and the loss modulus peak and the tan delta peak are broader for strong glass-forming polymers. Three variables, the steepness index (S), the transition wideness (W) of storage modulus and the integration area (A) of tan delta, were defined to illustrate the potential correlation between the dynamic fragility index (m) and the dynamic mechanical properties. It is found that W and A can be correlated with m by power law equations, while an exponential relationship between S and m is observed. Moreover, as m decreases, the tan delta peak is more and more apart from the loss modulus peak and the point where the storage modulus begins to drop. These phenomena are interpreted in terms of chain packing efficiency. (C) 2009 Elsevier B.V. All rights reserved.
引用
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页码:1755 / 1759
页数:5
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