Abstract

Polymer material properties are strongly affected by entanglement effects. For long polymer chains and composite materials, they are expected to be at the origin of many technically important phenomena, such as shear thinning or the Mullins effect, which microscopically can be related to topological constraints between chains. Starting from fully equilibrated highly entangled polymer melts, we investigate the effect of isochoric elongation on the entanglement structure and force distribution of such systems. Theoretically, the related viscoelastic response usually is discussed in terms of the tube model. We relate stress relaxation in the linear and nonlinear viscoelastic regimes to a primitive path analysis (PPA) and show that tension forces both along the original paths and along primitive paths, that is, the backbone of the tube, in the stretching direction correspond to each other. Unlike homogeneous relaxation along the chain contour, the PPA reveals a so far not observed long-lived clustering of topological constraints along the chains in the deformed state.

Highlights

  • Polymer material properties are strongly affected by entanglement effects

  • The interplay of rather different time scales, which typically can be located between the Rouse time of an entanglement length τe and that of the whole chain τR,N makes a microscopic explanation of the Payne or the Mullins effects,[1−4] to name just two, rather difficult

  • Others employed primitive path network models to account for viscosity changes in entangled polymers upon elongational and shear flow.[21−24] They can rationalize viscosity changes for strain rates below the inverse Rouse time of the chains, they seem to fail for faster sample deformation

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Summary

Introduction

Polymer material properties are strongly affected by entanglement effects. For long polymer chains and composite materials, they are expected to be at the origin of many technically important phenomena, such as shear thinning or the Mullins effect, which microscopically can be related to topological constraints between chains. Others employed primitive path network models to account for viscosity changes in entangled polymers upon elongational and shear flow.[21−24] They can rationalize viscosity changes for strain rates below the inverse Rouse time of the chains, they seem to fail for faster sample deformation.

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