A Thermo-Mechanically Coupled Large-Deformation Theory for Amorphous Polymers Across the Glass Transition Temperature

Amorphous thermoplastic polymers are important engineering materials; however, their nonlinear, strongly temperature- and rate-dependent elastic-viscoplastic behavior is still not very well understood, and is modeled by existing constitutive theories with varying degrees of success. There is no generally agreed upon theory to model the large-deformation, thermo-mechanically-coupled, elastic-viscoplastic response of these materials in a temperature range which spans their glass transition temperature. Such a theory is crucial for the development of a numerical capability for the simulation and design of important polymer processing operations, and also for predicting the relationship between processing methods and the subsequent mechanical properties of polymeric products. In this manuscript we briefly summarize a few results from our own recent research [1–4] which is intended to fill this need.