Molecular Dynamics Simulations of Noble Gas Fractionation during Diffusion through Silica Nanopores

Abstract

Ne retention and slight enrichment of Kr-Xe relative to atmospheric levels have been found in biogenic chert samples. Previous studies suggested that the incorporation of noble gas atoms is dependent upon the structure rather than the environment. In this study, we perform molecular dynamics simulations of dissolved noble gas atomic diffusion through 1-4 nm diameter silica pores. Bulk-liquid-like water does not exist in the 1 nm diameter nanopores, which hinder noble gas diffusion into or out of the pores. In ≥2 nm diameter nanopores, noble gas atoms transport with bulk-liquid-like water into the center of the pores but size-controlled diffusive separation occurs at the layer of surface water and in the interior of the silica structure. The motion of large atoms (Kr and Xe) in surface water is governed by significant adsorption. Relatively small Ne atoms are able to cross the surface water layer and diffuse into the crystal interior. As a result of its moderate size and the negligible interaction with the interfacial surface, Ar lies beyond the adsorption and silica structure diffusion regimes. Therefore, our simulation results indicate that noble gas entrapment is expected to occur in nanoscale fluid circulation during sediment-to-chert lithification.