Relaxations in polystyrene below the glass transition studied by viscosity measurement

Abstract The shear viscosity of organic glass polystyrene has been determined under pure shear deformation mode from room temperature up to the glass transition temperature. A mechanical model of series connection of anelasticity and viscosity was used to determine the viscosity of the material. Relaxation time for the viscous flow was determined as a function of temperature. The relaxation was composed of two thermal-activation type relaxation processes: the high temperature relaxation (HTR) and the low temperature relaxation (LTR). In both relaxations the relaxation time was represented as τ=τo exp(E/kBT), and the values of τ0 and E were different in specimens treated differently – aged, loaded, and annealed. The observed τ0 and E were not independent of each other but a compensation effect, a linear decrease of logτ0 with increased E, was seen. The results were explained using the idea of cooperative relaxations of relaxing elements. HTR and LTR were considered to correspond to the structural and the slow relaxations, respectively, and the relaxing elements could respectively be a single atom or molecule and a segment in molecular chains.