Time–Concentration Superposition for Linear Viscoelasticity of Polymer Solutions

Author:

Li Can-Qi1ORCID,Winter Horst Henning2,Fan Yuan-Qi1,Xu Geng-Xin1,Yuan Xue-Feng1ORCID

Affiliation:

1. Institute for Systems Rheology, Guangzhou University, No. 230 West Outer Ring Road, Higher Education Mega-Center, Panyu District, Guangzhou 510006, China

2. Chemical Engineering and Polymer Science & Engineering, University of Massachusetts Amherst, Silvio O. Conte National Center for Polymer Research, 120 Governors Drive, Amherst, MA 01003-3110, USA

Abstract

The concentration dependence of linear viscoelastic properties of polymer solutions is a well-studied topic in polymer physics. Dynamic scaling theories allow qualitative predictions of polymer solution rheology, but quantitative predictions are still limited to model polymers. Meanwhile, the scaling properties of non-model polymer solutions must be determined experimentally. In present paper, the time–concentration superposition (TCS) of experimental data is shown to be a robust procedure for studying the concentration scaling properties of binary and ternary polymer solutions. TCS can not only identify whether power law scaling may exist or not, and over which concentration range, but also unambiguously estimate the concentration scaling exponents of linear viscoelastic properties for a range of non-model polymer solutions.

Funder

Ministry of Science and Technology of the People’s Republic of China

U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Bioenergy Technologies Office

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

Reference15 articles.

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2. De Gennes, P.G. (1979). Scaling Concepts in Polymer Physics, Cornell University Press.

3. Doi, M., and Edwards, S.F. (1986). The Theory of Polymer Dynamics, Oxford University Press.

4. Effect of concentration and thermodynamic interaction on the viscoelastic properties of polymer solutions;Colby;Macromolecules,1991

5. Ferry, J.D. (1980). Viscoelastic Properties of Polymer, John Wiley & Son Inc.

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