Modeling of nonlinear viscoelastic-viscoplastic behavior of glassy polymers based on intramolecular rotation of molecular chains

被引:0
作者
Aoyagi, Yoshiteru [1 ]
Camboulives, Louis Narita [1 ]
机构
[1] Tohoku Univ, Dept Finemech, Sendai, Japan
关键词
Glassy polymers; Nonlinear viscoelastic-viscoplastic model; Sub-glass transition temperature condition; Finite element simulation; Intramolecular rotation of molecular chains; MECHANICALLY COUPLED THEORY; CONSTITUTIVE MODEL; DENSITY-FLUCTUATIONS; HYDROSTATIC-PRESSURE; AMORPHOUS POLYMERS; LARGE DEFORMATIONS; YIELD; POLYCARBONATE; TEMPERATURE; RELAXATION;
D O I
10.1016/j.ijplas.2025.104328
中图分类号
TH [机械、仪表工业];
学科分类号
0802 ;
摘要
In recent years, there has been progress in the development of constitutive models for reproducing the mechanical properties of glassy polymers, but there are limitations to conventional models, such as increased complexity and the number of material parameters. In this study, a new model was proposed to describe the nonlinear viscoelastic-viscoplastic behavior under loading, unloading, and cyclic loading conditions at temperatures below the glass transition temperature. The anelastic strain was considered in addition to elastic strain and plastic strain, which is based on three states: a stable state, a metastable state in tension, and a metastable state in compression. The numerical results obtained with the present model were compared with those obtained with the latest existing model and with the experimental results to investigate the ability to model both viscoelasticity and viscoplasticity. The proposed model stands out for its capacity to predict nonlinear viscoelasticity and viscoplasticity for various loading conditions with only simple thermal activation processes. The 22 material parameters required are fewer than those of recent models used for comparison. This is because the proposed model expresses the viscoelastic phenomena during loading and unloading in a unified manner.
引用
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页数:25
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