The Kirkwood–Riseman Model of Polymer Solution Dynamics Is Qualitatively Correct

Author:

Phillies George David Joseph1ORCID

Affiliation:

1. Department of Physics, Worcester Polytechnic Institute, Worcester, MA 01609-2280, USA

Abstract

The Rouse model is the foundational basis of much of modern polymer physics. The period alternative, the Kirkwood–Riseman model, is rarely mentioned in modern monographs. The models are qualitatively different. The models do not agree as to how many internal modes a polymer molecule has. In the Kirkwood–Riseman model, polymers in a shear field perform whole-body rotation; in the Rouse model, polymers respond to shear with an affine deformation. We use Brownian dynamics to show that the Kirkwood–Riseman model for chain motion is qualitatively correct. Contrary to the Rouse model, in shear flow, polymer coils rotate. Rouse modes are cross-correlated. The amplitudes and relaxation rates of Rouse modes depend on the shear rate. Several alternatives to Rouse modes as collective coordinates are discussed.

Funder

computers and software out-of-pocket

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

Reference11 articles.

1. The Intrinsic Viscosities and Diffusion Coefficients of Flexible Molecules in Solution;Kirkwood;J. Chem. Phys.,1948

2. A Theory of the Linear Viscoelastic Properties of Dilute Solutions of Coiling Polymers;Rouse;J. Chem. Phys.,1953

3. Dynamics of Polymer Molecules in Dilute Solution: Viscoelasticity, Flow Birefringence, and Dielectric Loss;Zimm;J. Chem. Phys.,1956

4. Zur Theorie der orthogonalen Funktionensysteme;Haar;Math. Ann.,1910

5. Daubechies, I. (1992). CBMS-NSF Regional Conference Series in Applied Math, Society for Industrial and Applied Mathematics.

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