A thermodynamically consistent constitutive equation describing polymer disentanglement under flow

Author:

Dolata Benjamin E.1ORCID,Olmsted Peter D.1ORCID

Affiliation:

1. Department of Physics and Institute for Soft Matter Synthesis and Metrology, Georgetown University, Washington DC, 20057

Abstract

We derive a thermodynamically consistent framework for incorporating entanglement dynamics into constitutive equations for flowing polymer melts. We use this to combine the convected constraint release (CCR) dynamics of Ianniruberto–Marriccui into a finitely extensible version of the Rolie–Poly model, and also include an anisotropic mobility as in the Giesekus model. The reversible dynamics are obtained from a free energy that describes both a finitely extensible conformation tensor and an ideal gas of entanglements along the chain. The dissipative dynamics give rise to coupled kinetic equations for the conformation tensor and entanglements, whose coupling terms describe shear-induced disentanglement. The relaxation dynamics of the conformation tensor follow the GLaMM and Rolie–Poly models, and account for reptation, retraction, and CCR. We propose that the relaxation time [Formula: see text] for entanglement recovery is proportional to the Rouse time [Formula: see text] which governs polymer stretch within the tube. This matches recent molecular dynamics simulations and corresponds to relaxing the entanglement number before the entire polymer anisotropy has relaxed on the longer reptation time [Formula: see text]. Our model suggests that claimed signatures of slow re-entanglement on the reptation time in step-strain experiments may be interpreted as arising from anisotropies in reptation dynamics.

Funder

National Science Foundation

Publisher

Society of Rheology

Subject

Mechanical Engineering,Mechanics of Materials,Condensed Matter Physics,General Materials Science

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