J Mater Sci Technol ›› 2001, Vol. 17 ›› Issue (03): 375-382.

• Research Articles • Previous Articles     Next Articles

Rheological behavior for polymer melts and concentrated solutions Part VII: A quantitative verification for the molecular theory of non-linear viscoelasticity with entanglement constraints in polymer melts

Mingshi SONG, Chen ZHANG, Guixian HU   

  1. Research Institute of Polymeric Materials, Beijing University of Chemical Technology, Beijing 100029, China
  • Received:1999-12-08 Revised:2000-04-29 Online:2001-05-28 Published:2009-10-10
  • Contact: Mingshi SONG

Abstract: Based on the molecular theory of non-linear viscoelasticity with constrained entanglements in polymer melts, the material functions in simple shear flow were formulated, the theoretical relations between. eta((gamma) over dot), psi (10)((gamma) over dot) and shear rate ((gamma) over dot), and topologically constrained dimension number n ' and a were derived. Linear viscoelastic parameters (eta (0) and G(N)(0)) and topologically constrained dimension number (n ' a and <()over bar>) as a function of the primary molecular weight (M-n), molecular weight between entanglements (M-C) and the entanglement sites sequence distribution in polymer chain were determined. A new method for determination of viscoelastic parameters (eta (0), psi (10), G(N)(0) and J(e)(0)), topologically constrained dimension number (n ', a and v) and molecular weight (M-n, M-c and M-e) from the shear flow measurements was proposed. It was used to determine those parameters and structures of HDPE, making a good agreement between these values and those obtained by other methods. The agreement affords a quantitative verification for the molecular theory of nonlinear viscoelasticity with constrained entanglement in polymer melts.

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