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Connection between thermodynamics and dynamics of simple fluids in highly attractive pores

Published

Author(s)

William P. Krekelberg, Vincent K. Shen, Daniel W. Siderius, Thomas M. Truskett, Jeffrey R. Errington

Abstract

We investigate the structural and diffusive dynamics properties of a model fluid in highly-absorptive cylindrical pores. At subcritical temperatures, self diffusion displays three distinct regimes as a function of average pore density ρ: 1) a decrease in self-diffusivity with increasing ρ at low ρ, 2) constant self-diffusivity with respect to varying ρ at moderate density, and 3) a decrease in self-diffusivity with increasing ρ at high density. These regimes are closely linked to the thermodynamic properties of the fluid in the pore, specifically, the adsorption isotherm, isosteric heat of adsorption, and the density profile. We show that, the three diffusivity regimes qualitatively correpsond to three distinct adsorption regimes: monolayer formation, multilayer adsorption, and pore filling.
Citation
Langmuir
Volume
29

Keywords

Self-diffusivity, gas adsorption, molecular dynamics, confined fluids, physical properties

Citation

Krekelberg, W. , Shen, V. , Siderius, D. , Truskett, T. and Errington, J. (2013), Connection between thermodynamics and dynamics of simple fluids in highly attractive pores, Langmuir, [online], https://doi.org/10.1021/la4037327 (Accessed July 24, 2024)

Issues

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Created October 25, 2013, Updated November 10, 2018