Fracture in glassy polymers: a molecular modeling perspective

Abstract

Over the past 25 years, molecular modeling and simulations have provided important insights into the physics of deformation and fracture of glassy polymers. This review presents an overview of key results discussed in the context of experimentally observed polymer behavior. Both atomistic and coarse-grained polymer models have been used in different deformation protocols to study elastic properties, shear yielding, creep, physical aging, strain hardening and crazing. Simulations reproduce most of the macroscopic features of plasticity in polymer glasses such as stress-strain relations and creep response, and reveal information about the underlying atomistic processes. Trends of the shear yield stress with loading conditions, temperature and strain rate, and the atomistic dynamics under load have been systematically explored. Most polymers undergo physical aging, which leads to a history-dependent mechanical response. Simulations of strain hardening and crazing demonstrate the nature of polymer entanglements in the glassy state and the role of local plasticity and provide insight into the origin of fracture toughness of amorphous polymers.