Application of transient-time correlation functions to nonequilibrium molecular-dynamics simulations of elongational flow

B. D. Todd
Phys. Rev. E 56, 6723 – Published 1 December 1997
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Abstract

The transient-time correlation function (TTCF) technique of Morriss and Evans [Mol. Phys. 54, 629 (1985); Phys. Rev. A 35, 792 (1987); Mol. Phys. 61, 1151 (1987); Phys. Rev. A 38, 4142 (1988); Statistical Mechanics of Nonequilibrium Liquids (Academic, London, 1990)] is applied to the case of an atomic fluid undergoing steady isothermal elongational flow. It is found that nonequilibrium molecular-dynamics TTCF calculations of the diagonal elements of the pressure tensor are extremely efficient for small applied strain rates, where the signal-to-noise ratio for the equivalent direct time-averaged pressures is far too low. At higher strain rates, TTCF is seen to faithfully reproduce the long-time steady-state values of the pressures, but is unable to account for observed transient oscillations. The technique thus provides an unambiguous means of calculating the long-time steady-state response of a fluid under steady elongational flow and opens the possibility of studying more complex molecular fluids under relatively weak flow, allowing for greater simulation time compared to the relaxation time of the fluid.

  • Received 21 May 1997

DOI:https://doi.org/10.1103/PhysRevE.56.6723

©1997 American Physical Society

Authors & Affiliations

B. D. Todd

  • Cooperative Research Centre for Polymers, CSIRO Division of Molecular Science, Private Bag 10, Clayton South MDC, Victoria 3169, Australia

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Vol. 56, Iss. 6 — December 1997

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