Dynamics and rheology of a supercooled polymer melt in shear flow

Using molecular dynamics simulations, we study dynamics of a model polymer melt composed of short chains with bead number N = 10 in supercooled states. In quiescent conditions, the stress relaxation function G(t) is calculated, which exhibits a stretched exponential relaxation on the time scale of the α relaxation time τα and ultimately follows the Rouse dynamics characterized by the time τR ∼ N2τα. After application of shear , transient stress growth σxy(t)/ first obeys the linear growth ∫ 0tdt′G(t′) for strain less than 0.1 but saturates into a non-Newtonian viscosity for larger strain. In steady states, shear thinning and elongation of chains into ellipsoidal shapes take place for shear larger than τR−1. In such strong shear, we find that the chains undergo random tumbling motion taking stretched and compact shapes alternatively. We examine the validity of the stress–optical relation between the anisotropic parts of the stress tensor and the dielectric tensor, which are violated in transient states due to the presence of a large glassy component of the stress. We furthermore introduce time-correlation functions in shear to calculate the shear-dependent relaxation times, τα(T,) and τR(T,), which decrease nonlinearly as functions of in the shear-thinning regime. © 2002 American Institute of Physics.