Viscoelasticity of randomly branched polymers in the critical percolation class

Charles P. Lusignan, Thomas H. Mourey, John C. Wilson, and Ralph H. Colby
Phys. Rev. E 52, 6271 – Published 1 December 1995
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Abstract

We report viscosity, recoverable compliance, and molecular weight distribution of a series of randomly branched polyester samples below their gel point. From the static characterization we determine τ=2.17±0.08 (95%) for the exponent controlling the mass distribution, indicating that this system belongs to the critical percolation universality class. We find that viscosity diverges at the gel point with an exponent s=1.36±0.09 (95%), in agreement with a simple bead-spring (Rouse) model without hydrodynamic or topological interactions. Similarly, the recoverable compliance diverges at the threshold with an exponent t=2.71±0.30 (95%), consistent with the idea that kBT of elastic energy is stored per correlation volume. The complex shear modulus obeys a power law in frequency with exponent u=0.659±0.015 (95%), thereby confirming the dynamical scaling law u=t/(s+t). (c) 1995 The American Physical Society

  • Received 15 May 1995

DOI:https://doi.org/10.1103/PhysRevE.52.6271

©1995 American Physical Society

Authors & Affiliations

Charles P. Lusignan

  • Department of Physics and Astronomy, University of Rochester, Rochester, New York 14627

Thomas H. Mourey

  • Analytical Technology Division, Eastman Kodak Company, Rochester, New York 14650-2136

John C. Wilson

  • Office Imaging, Eastman Kodak Company, Rochester, New York, 14650-2129

Ralph H. Colby

  • Imaging Research and Advanced Development, Eastman Kodak Company, Rochester, New York, 14650-2109

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Vol. 52, Iss. 6 — December 1995

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