A predictive parameter for the shape memory behavior of thermoplastic polymers

被引:33
|
作者
Xiao, Rui [1 ,2 ]
Yakacki, Christopher M. [3 ]
Guo, Jingkai [2 ]
Frick, Carl P. [4 ]
Nguyen, Thao D. [2 ]
机构
[1] Hohai Univ, Coll Mech & Mat, Dept Engn Mech, Inst Soft Matter Mech, Nanjing 210098, Jiangsu, Peoples R China
[2] Johns Hopkins Univ, Dept Mech Engn, Baltimore, MD 21218 USA
[3] Univ Colorado, Dept Mech Engn, Denver, CO 80217 USA
[4] Univ Wyoming, Dept Mech Engn, Laramie, WY 82071 USA
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
modeling; shape-memory polymers; stimuli-sensitive polymers; thermoplastics; unrecoverable strain; viscoelastic properties; TEMPERATURE MEMORY; THERMOMECHANICAL BEHAVIOR; FINITE STRAIN; NETWORKS; POLYURETHANES; MODEL;
D O I
10.1002/polb.23981
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We present an experimental and modeling study of the effect of programming conditions on the shape-memory behaviors of amorphous thermoplastic polymers. Experimentally we measure the influence of deformation temperature, strain rate and relaxation time on the thermomechanical properties and shape-memory response of poly(para-phenylene), which is a stiff and strong aromatic thermoplastic. To understand the underlying mechanism, we develop a viscoelastic model, which contains multiple discrete relaxation processes with broad distribution of relaxation time. The model parameters of the relaxation spectrum are obtained from the master curve of small strain-stress relaxation tests using time-temperature superposition. The model predictions show good agreement with experimental observations, including the stress response and shape-memory response under various conditions. We applied the model to study the effect of the programming conditions on the shape recovery performance. The results show that the relaxation modulus at the end of the programming process was a predictor of the recovery speed and recoverable strain ratio. This provides a design metric to optimize the shape programming process for shape recovery. (c) 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 1405-1414
引用
收藏
页码:1405 / 1414
页数:10
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