Viscoelasticity of the polydomain-monodomain transition in main-chain liquid crystal elastomers

被引:59
|
作者
Azoug, A. [1 ]
Vasconcellos, V. [1 ]
Dooling, J. [1 ]
Saed, M. [2 ]
Yakacki, C. M. [2 ]
Nguyen, T. D. [1 ]
机构
[1] Johns Hopkins Univ, Dept Mech Engn, Baltimore, MD 21218 USA
[2] Univ Colorado, Dept Mech Engn, Denver, CO 80202 USA
基金
美国国家科学基金会;
关键词
Liquid crystal elastomers; Soft elasticity; Polydomain; Monodomain; Viscoelasticity; NEMATIC ELASTOMERS; STRESS-RELAXATION; PHASE-BEHAVIOR; ELASTICITY; NETWORK;
D O I
10.1016/j.polymer.2016.06.022
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 goal of this study was to explore the rate-dependent behavior of the stretch-induced polydomain-monodomain (PM) transition of a liquid crystal elastomer (LCE). The main-chain LCE was synthesized and then cross-linked in the nematic polydomain state. The PM transition caused a soft-elastic behavior, which was measured using uniaxial tensile tests at multiple strain rates and temperatures. The main finding was that we were able to apply the temperature-dependent shift factor determined for the small strain behavior and in the frequency domain to create master curves for the large-strain response in the strain rate domain. The soft elasticity phenomenon was absent from the stress-strain curve at equilibrium. The results also suggest that the relaxation mechanisms of the network, and not of the mesogen orientation, dominate the rate-dependent behavior. Finally, we observed a relatively slow recovery behavior, suggesting the presence of an additional slow relaxation mechanism. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:165 / 171
页数:7
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