Modeling shape-memory effects in amorphous polymers

被引:6
|
作者
Xiao, Rui [1 ]
机构
[1] Hohai Univ, Coll Mech & Mat, Dept Engn Mech, Nanjing 210098, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
shape-memory polymers; constitutive modeling; glass transition; temperature-memory effects;
D O I
10.1016/j.matpr.2019.05.324
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The time-dependent behavior of glass transition can be used to achieve shape-memory behaviors in amorphous polymers. Thus, modeling the shape-memory effect in amorphous polymers requires considering the viscoelastic/viscoplastic behaviour across the glass transition region. Here, we discuss our past efforts to develop constitutive models for the glass transition behavior of amorphous polymers to predict the shape-memory behavior under a variety of conditions. We first demonstrate that a viscoelastic model with multiple relaxation processes can describe the temperature memory effect and multiple shape-memory effect in amorphous thermosets and thermoplastics. The viscoelastic model is further extended to a viscoplastic model. Comparison with experimental results shows that the viscoplastic model can accurately predict the partially constrained shape recovery of polymers programmed below the glass transition temperature. Finally, we present a constitutive model to describe the effect of solvent absorption on the thermomechanical properties and shape-memory behavior of amorphous polymers. We derive an explicit function to describe the influence of solvent concentration on viscosity and implement the model for finite element analysis. The thermo-chemo-mechanical coupled model is able to describe the isothermal recovery of programmed SMPs in water. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1462 / 1468
页数:7
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