Abstract
The dependence of the melt flow of polymers on temperature is of both theoretical and commercial importance. A useful representation of the temperature dependence of the shear‐dependent viscosity, based on superposition of flow curves at various temperatures, has previously been presented by the author for several olefin polymers. This method is extended in the current work to styrene and styrene‐acrylonitrile based polymers. The melt viscosity‐temperature dependence of a broad range of styrenic polymers and copolymers, ranging from polystyrene to 82 percent AN styrene‐acrylonitrile copolymer, with and without rubber inclusions, was investigated. Flow curves at the various temperatures were found to be superimposable, as had earlier been found to be the case for olefin polymers, and a unique quantitative relationship between the superposition shift factors and temperature was found applicable to the entire family of polymers. The resultant energy of activation for viscous flow is in excellent agreement with previously published results for polystyrene Newtonian viscosities, and the magnitude of the shift factors is consistent with a limited set reported for ABS polymers. Independent tests of the derived relationships provided excellent prediction of measured viscosities. Thus, it is considered that a general viscosity‐temperature relationship has been defined for this family of polymers, independent of molecular structural detail.