On a thermodynamic foundation of Eyring rate theory for plastic deformation of polymer solids

Abstract

The plastic deformation of almost all solid polymers can be represented by a thermally activated rate process involving the motion of cooperative mobile elements over potential barriers, based on the Eyring activated rate theory. The present study shows that the governing equations for the Eyring rate theory can be completely derived based on the principle of microscopic reversibility in the framework of non-equilibrium dynamics.