Abstract

A molecular network theory incorporating the concept of entanglement disruption and regeneration was previously developed to describe not only steady‐state but also transient rheological properties of monodisperse polymer melts and concentrated solutions. The viscoelastic responses of these systems are dominated by a rapid segmental motion at short times and a more sluggish, structure‐dependent network relaxation process at long times. In a binary blend of monodisperse fractions, the entangled network is composed of chains of two different lengths. The chain dynamics, and thus the characteristic response time, of each component in such a system is influenced by the presence of the coexistent component. This interaction is accommodated by a simple mixing assumption, which leads to accurate predictions of composition‐dependent linear viscoelastic properties, such as zero‐shear viscosity. In addition, the model gives an excellent description of the shear‐rate‐dependent viscosity curves of binary blends of va...

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