Abstract

It is known that thermodynamic properties of a system change upon confinement. To know how, is important for modelling of porous media. We propose to use Hill’s systematic thermodynamic analysis of confined systems to describe two-phase equilibrium in a nanopore. The integral pressure, as defined by the compression energy of a small volume, is then central. We show that the integral pressure is constant along a slit pore with a liquid and vapor in equilibrium, when Young and Young–Laplace’s laws apply. The integral pressure of a bulk fluid in a slit pore at mechanical equilibrium can be understood as the average tangential pressure inside the pore. The pressure at mechanical equilibrium, now named differential pressure, is the average of the trace of the mechanical pressure tensor divided by three as before. Using molecular dynamics simulations, we computed the integral and differential pressures, and p, respectively, analysing the data with a growing-core methodology. The value of the bulk pressure was confirmed by Gibbs ensemble Monte Carlo simulations. The pressure difference times the volume, V, is the subdivision potential of Hill, . The combined simulation results confirm that the integral pressure is constant along the pore, and that scales with the inverse pore width. This scaling law will be useful for prediction of thermodynamic properties of confined systems in more complicated geometries.

Highlights

  • It is well known that thermodynamic properties of fluids significantly change when the fluid phases become confined [1,2]

  • The literature offers, several definitions of the pressure inside a nano-porous material [15,16]. This situation calls for a robust definition of the representative elementary volume (REV) of the small system, to serve as a basis for a definition of pressure

  • In this work we have confirmed, using molecular dynamics simulations, that the integral pressure in a nano-confined single fluid in two phases is constant along a pore

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Summary

Introduction

It is well known that thermodynamic properties of fluids significantly change when the fluid phases become confined [1,2]. System properties were obtained by dividing the ensemble value by N In this way, he was able to deal with the impact of shape- and size-variation of the small system, within the normal structure of thermodynamics. The literature offers, several definitions of the pressure inside a nano-porous material [15,16] This situation calls for a robust definition of the representative elementary volume (REV) of the small system, to serve as a basis for a definition of pressure. Erdos et al [10] provided an expression for the ratio of the driving forces for adsorption into a pore, by means of the integral and differential pressures They expressed the ratio by the cross-correlation of the volume and the integral pressure

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