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Protocol for Relative Hydrodynamic Assessment of Tri-leaflet Polymer Valves
Published on: October 17, 2013
Revisiting the Stokes-Einstein relation without a hydrodynamic diameter
Lorenzo Costigliola1, David M Heyes2, Thomas B Schrøder1
1"Glass and Time," IMFUFA, Department of Science and Environment, Roskilde University, P.O. Box 260, DK-4000 Roskilde, Denmark.
Abstract:
We present diffusion coefficient and shear viscosity data for the Lennard-Jones fluid along nine isochores above the critical density, each involving a temperature variation of roughly two orders of magnitude. The data are analyzed with respect to the Stokes-Einstein (SE) relation, which breaks down gradually at high temperatures. This is rationalized in terms of the fact that the reduced diffusion coefficient and the reduced viscosity are both constant along the system's lines of constant excess entropy (the isomorphs). As a consequence, is a function of T/T Ref(ρ) in which T is the temperature, ρ is the density, and T Ref(ρ) is the temperature as a function of the density along a reference isomorph. This allows one to successfully predict the viscosity from the diffusion coefficient in the studied region of the thermodynamic phase diagram.
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