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Updated: May 13, 2026

An Analog Macroscopic Technique for Studying Molecular Hydrodynamic Processes in Dense Gases and Liquids
Published on: December 4, 2017
Direct numerical simulations of anisotropic diffusion of spherical particles in sedimentation
Adnan Hamid1, Ryoichi Yamamoto
1Department of Chemical Engineering, Kyoto University, Kyoto 615-8510, Japan. hamid@cheme.kyoto-u.ac.jp
Abstract:
We investigated the scaling of the hydrodynamic velocity fluctuations and self-diffusion in the sedimentation of monodispersed spherical particles via direct numerical simulations using the smoothed profile method over a moderate range of volume fractions (0.01≤φ≤0.12). Hydrodynamic velocity fluctuations are visible at large Peclet numbers (Pe), and they scale as (φL/a)(1/2) at low volume fractions (φ≤0.04). Their characteristics become independent of volume fraction at moderate volume fractions (0.06≤φ≤0.12). Both vertical and horizontal self-diffusion coefficients scale as (L/a)(3/2)φ(1/2) at low volume fractions. At moderate volume fractions, the vertical diffusion scales as (L/a)(3/2)φ(-1/2); in contrast, the horizontal diffusion is saturated with respect to volume fraction. The diffusion anisotropy increases with increasing Pe and saturates at high Pe values. The saturated value remains unchanged at low volume fractions, whereas further increase in the volume fraction decreases this anisotropy. The reduction of this anisotropy is attributed to the φ(-1/2) scaling of the vertical relaxation time at moderate volume fractions; however, the horizontal relaxation time is independent of the volume fraction at this regime.

