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      Individual Molecular Dynamics of an Entangled Polyethylene Melt Undergoing Steady Shear Flow: Steady-State and Transient Dynamics

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          Abstract

          The startup and steady shear flow properties of an entangled, monodisperse polyethylene liquid (C 1000H 2002) were investigated via virtual experimentation using nonequilibrium molecular dynamics. The simulations revealed a multifaceted dynamical response of the liquid to the imposed flow field in which entanglement loss leading to individual molecular rotation plays a dominant role in dictating the bulk rheological response at intermediate and high shear rates. Under steady shear conditions, four regimes of flow behavior were evident. In the linear viscoelastic regime ( γ ˙ < τ d 1 ), orientation of the reptation tube network dictates the rheological response. Within the second regime ( τ d 1 < γ ˙ < τ R 1 ), the tube segments begin to stretch mildly and the molecular entanglement network begins to relax as flow strength increases; however, the dominant relaxation mechanism in this region remains the orientation of the tube segments. In the third regime ( τ R 1 < γ ˙ < τ e 1 ), molecular disentangling accelerates and tube stretching dominates the response. Additionally, the rotation of molecules become a significant source of the overall dynamic response. In the fourth regime ( γ ˙ > τ e 1 ), the entanglement network deteriorates such that some molecules become almost completely unraveled, and molecular tumbling becomes the dominant relaxation mechanism. The comparison of transient shear viscosity, η + , with the dynamic responses of key variables of the tube model, including the tube segmental orientation, S , and tube stretch, λ , revealed that the stress overshoot and undershoot in steady shear flow of entangled liquids are essentially originated and dynamically controlled by the S x y component of the tube orientation tensor, rather than the tube stretch, over a wide range of flow strengths.

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          Most cited references37

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          Shortest multiple disconnected path for the analysis of entanglements in two- and three-dimensional polymeric systems

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            Simulating the critical behaviour of complex fluids

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              Packing Length Influence in Linear Polymer Melts on the Entanglement, Critical, and Reptation Molecular Weights

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                Author and article information

                Journal
                Polymers (Basel)
                Polymers (Basel)
                polymers
                Polymers
                MDPI
                2073-4360
                12 March 2019
                March 2019
                : 11
                : 3
                : 476
                Affiliations
                Materials Research and Innovation Laboratory (MRAIL), Department of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, TN 37996, USA; mnafarse@ 123456vols.utk.edu
                Author notes
                [* ]Correspondence: bje@ 123456utk.edu (B.J.E.); bkhomami@ 123456utk.edu (B.K.)
                Author information
                https://orcid.org/0000-0003-2346-6797
                https://orcid.org/0000-0002-2378-5627
                Article
                polymers-11-00476
                10.3390/polym11030476
                6473836
                30960460
                09e7abe1-48ae-488f-a516-bf0f2862e922
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 29 January 2019
                : 07 March 2019
                Categories
                Article

                entangled polymer melts,linear polymers,nonequilibrium molecular dynamics simulations,steady and startup shear flows

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