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RHEOLOGICAL BEHAVIOR OF POLYMER MELTS (II) MULTIPLE ENTANGLEMENT MODEL FOR PREDICTING THE DEPENDENCE OF VISCOELASTIC BEHAVIOR ON DEFORMATION STATE AND PRIMARY MOLECULAR WEIGHTS AND THEIR DISTRIBUTION

SONG Mingshi; WU Sizhu; YANG Jincai   

  1. Department of Polymer Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China
  • Received:1994-06-28 Revised:1995-03-10 Online:1996-09-28 Published:1996-09-28
  • Contact: SONG Mingshi

RHEOLOGICAL BEHAVIOR OF POLYMER MELTS (II) MULTIPLE ENTANGLEMENT MODEL FOR PREDICTING THE DEPENDENCE OF VISCOELASTIC BEHAVIOR ON DEFORMATION STATE AND PRIMARY MOLECULAR WEIGHTS AND THEIR DISTRIBUTION

宋名实; 吴丝竹; 杨金才   

  1. Department of Polymer Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China
  • 通讯作者: 宋名实

Abstract: In accordance with the memory function of Gaussian chain constraints in entangled polymermelts a set of material functions related to a certain"test flow"are formulated from the O-W-Ftype constitutive equation by the appropriate selection of the Cauchy-Green and Finger tensors.Thedependences of these material functions on the strain rate and the dependences of the linearviscoelastic functions on the primary molecular weight distribution and the entanglement sites sequencedistribution on polymer chain are derived from a multiple-entanglement model and a couple of mech-anisms of relaxation for the loop and terminal entanglement sites.When the primary polymer chainsare modelled with the Lansing-Kraemer molecular distribution function,a set of new relationshipsamong linear viscoelastic functions(η_0,ψ_(10)~0,η_(ext)~0 and τ_1)and the molecular weights and their distributionare formulated.These functions and relationships are verified with experimental data.

Key words: rheological behavior, constitutive equation, material function, molecular weight

摘要: In accordance with the memory function of Gaussian chain constraints in entangled polymermelts a set of material functions related to a certain"test flow"are formulated from the O-W-Ftype constitutive equation by the appropriate selection of the Cauchy-Green and Finger tensors.Thedependences of these material functions on the strain rate and the dependences of the linearviscoelastic functions on the primary molecular weight distribution and the entanglement sites sequencedistribution on polymer chain are derived from a multiple-entanglement model and a couple of mech-anisms of relaxation for the loop and terminal entanglement sites.When the primary polymer chainsare modelled with the Lansing-Kraemer molecular distribution function,a set of new relationshipsamong linear viscoelastic functions(η_0,ψ_(10)~0,η_(ext)~0 and τ_1)and the molecular weights and their distributionare formulated.These functions and relationships are verified with experimental data.

关键词: rheological behavior;constitutive equation;material function;molecular weight