A Thermodynamic-Consistent Model For The Thermo-Chemo-Mechanical Couplings In Amorphous Shape-Memory Polymers

Chemically-responsive amorphous shape-memory polymers (SMPs) can transit from the temporary shape to the permanent shape in responsive to solvents. This effect has been reported in various polymer-solvent systems. However, limited attention has been paid to the constitutive modeling of this behavior. In this work, we develop a fully thermo-chemomechanical coupled thermodynamic framework for the chemically-responsive amorphous SMPs. The framework shows that the entropy, the chemical potential and the stress can be directly obtained if the Helmholtz free energy density is defined. Based on the entropy inequality, the evolution equation for the viscous strain, the temperature and the number of solvent molecules are also derived. We also provide an explicit form of Helmholtz free energy density as an example. In addition, based on the free volume concept, the dependence of viscosity and diffusivity on the temperature and solvent concentration is defined. The theoretical framework can potentially advance the fundamental understanding of chemically-responsive shape-memory effect. Meanwhile, it can also be used to describe other important physical processes such as the diffusion of solvents in glassy polymers.