Step and steady shear responses of nearly monodisperse highly entangled 1,4-polybutadiene solutions |
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Authors: | Mohammad T. Islam Javier Sanchez-Reyes Lynden A. Archer |
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Affiliation: | 1.Department of Chemical Engineering, Texas A&M University, College Station TX 77843, USA,;2.School of Chemical and Biomolecular Engineering, Cornell University, Ithaca NY 14853, USA, |
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Abstract: | Nonlinear relaxation dynamics of highly entangled solutions of high molecular weight 1,4-polybutadiene (PB) in a PB oligomer are studied in steady shear and step shear flows. Polymer entanglement densities vary in the range 14hN/Ne(J)⣴, allowing systematic investigation of entanglement effects on nonlinear rheological response. In agreement with previous steady shear studies using well entangled polystyrene solutions, a flow regime is found where both the steady-state shear stress and first normal stress difference remain constant or increase quite slowly with shear rate, leading to a plateau in the steady-state orientation angle. The magnitude of the average orientation angle in the plateau range is in accordance with predictions of a recent theory by Islam and Archer (2001). In step shear, the nonlinear relaxation modulus G(t,%) is approximately factorable into time-dependent G(t) and strain-dependent h(%) functions only at long times, t>5k, where 5k,O(Fd0). This finding is consistent with earlier observations for entangled polystyrene solutions; however the complex crossing pattern in G(t,%)h-1(%) that precede factorability in the latter materials is not observed. For all but the most entangled sample, apparent shear damping functions h (%,t)=(G(t,%))/(G(t)) immediately following imposition of shear are in nearly quantitative accord with the damping function hDEIA predicted by Doi-Edwards theory. |
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