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A finite deformation constitutive model for thermally activated amorphous shape memory polymers
被引:14
作者:
Gu, Jianping
[1
,2
]
Sun, Huiyu
[1
]
Fang, Changqing
[1
]
机构:
[1] Nanjing Univ Aeronaut & Astronaut, State Key Lab Mech & Control Mech Struct, Nanjing 210016, Peoples R China
[2] Nanjing Inst Technol, Dept Mat Engn, Nanjing, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Shape memory polymers;
finite deformation;
constitutive model;
glass transition;
structural relaxation;
THERMOMECHANICAL BEHAVIOR;
MECHANISMS;
RECOVERY;
RUBBER;
D O I:
10.1177/1045389X14544147
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
A thermoviscoelastic-thermoviscoplastic finite deformation constitutive model incorporating structural and stress relaxation is developed for thermally activated amorphous shape memory polymers. In this study, the nonlinear Adam-Gibbs model is used to describe the structural relaxation. Furthermore, a modified Argon scalar equation is proposed for the viscous flow as the temperature crosses T-g. In addition, as the Arruda-Boyce eight-chain model captures the hyperelastic behavior of the material up to large stretches, it is used here to represent the partial material behavior of shape memory polymers. To further feature the macroscopic post-yield strain softening behavior, the phenomenological evolution rule is also implemented. Comparisons of numerical simulations and the thermomechanical experiments conducted on an ether-based polyurethane shape memory polymer show acceptable agreement.
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页码:1530 / 1538
页数:9
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