@article {1568,
	title = {Tracer diffusion in hard sphere fluids from molecular to hydrodynamic regimes},
	journal = {Journal of Chemical Physics},
	volume = {125},
	number = {20},
	year = {2006},
	note = {ISI Document Delivery No.: 110UZTimes Cited: 6Cited Reference Count: 43Sokolovskii, R. O. Thachuk, M. Patey, G. N.},
	month = {Nov},
	pages = {10},
	type = {Article},
	abstract = {Molecular dynamics is employed to investigate tracer diffusion in hard sphere fluids. Reduced densities (rho(*)=rho sigma(3), sigma is the diameter of bath fluid particles) ranging from 0.02 to 0.52 and tracers ranging in diameter from 0.125 sigma to 16 sigma are considered. Finite-size effects are found to pose a significant problem and can lead to seriously underestimated tracer diffusion constants even in systems that are very large by simulation standards. It is shown that this can be overcome by applying a simple extrapolation formula that is linear in the reciprocal cell length L-1, allowing us to obtain infinite-volume estimates of the diffusion constant for all tracer sizes. For higher densities, the range of tracer diameters considered spans diffusion behavior from molecular to hydrodynamic regimes. In the hydrodynamic limit our extrapolated results are clearly consistent with the theoretically expected slip boundary conditions, whereas the underestimated values obtained without extrapolation could easily be interpreted as approaching the stick limit. It is shown that simply adding the Enskog and hydrodynamic contributions gives a reasonable qualitative description of the diffusion behavior but tends to overestimate the diffusion constant. We propose another expression that fits the simulation results for all densities and tracer diameters. (c) 2006 American Institute of Physics.},
	keywords = {BOUNDARY-CONDITIONS, BROWNIAN PARTICLE, COEFFICIENT, DYNAMICS SIMULATION, friction, KINETIC-THEORY, RIGID PARTICLES, SINGLE-PARTICLE MOTION, SIZE DEPENDENCE, TRANSPORT-COEFFICIENTS, VELOCITY-AUTOCORRELATION FUNCTION},
	isbn = {0021-9606},
	url = {<Go to ISI>://000242408100031},
	author = {Sokolovskii, R. O. and Thachuk, M. and Patey, G. N.}
}
@article {4364,
	title = {Improved initial density dependence of the viscosity and a corresponding states function for high pressures},
	journal = {Physica a-Statistical Mechanics and Its Applications},
	volume = {260},
	number = {1-2},
	year = {1998},
	note = {ISI Document Delivery No.: 135WLTimes Cited: 24Cited Reference Count: 50},
	month = {Nov},
	pages = {31-48},
	type = {Article},
	abstract = {The initial density correction to gaseous viscosity using accurate realistic potentials of the noble gases is evaluated using the Rainwater-Friend theory. It is shown that this theory works satisfactorily for densities up to about 2 mol dm(-3). Due to the superimposability of the noble gas potential functions, a universal function of the reduced second viscosity virial coefficient is obtained over the entire reduced temperature range. At densities beyond the range of the theory, a variant of the excess viscosity is developed, by which the viscosity of the different gases can be easily calculated above the critical temperature for pressures up to 900 MPa. The accuracy of this method is within the experimental uncertainties. (C) 1998 Elsevier Science B.V. All rights reserved.},
	keywords = {11 POLYATOMIC GASES, ARGON, COEFFICIENT, COEFFICIENTS, EQUILIBRIUM, high-pressure excess viscosity, NOBLE-GASES, ORGANIC VAPORS, PHYSICAL-PROPERTIES, Rainwater-Friend theory, second viscosity virial, TEMPERATURE, THERMAL-CONDUCTIVITY, TRANSPORT-PROPERTIES, VISCOSITY},
	isbn = {0378-4371},
	url = {<Go to ISI>://000076825600004},
	author = {Najafi, B. and Ghayeb, Y. and Rainwater, J. C. and Alavi, S. and Snider, R. F.}
}
