Publications

Abstract : A molecular level understanding of the structure of water-methane interface is important due to its role in methane hydrate nucleation and atmospheric chemistry. Using classical molecular dynamics simulations, we investigated the structure of water-methane interface and the adsorption of methane molecules on the water surface. The molecular level roughness of the surface and its effect on adsorption of methane are examined. An increase in the pressure is found to increase the amplitude of humps and wells on the rough water surface. The layer of methane molecules that are in direct contact with the surface and the adsorbed methane molecules above the first layer are identified. It is revealed that a greater fraction of methane molecules that are in direct contact with the surface are present at the humps than at the wells. In contrast, the density of adsorbed methane molecules above the first molecular layer of methane is found to be more above the wells. The non-uniform distribution of methane adsorbed on the water surface is explained in terms of the interaction between methane and water. The distribution of adsorbed methane molecules above the water surface indicates a clear preference for the gas molecule to enter the liquid phase through the humps of the surface. The results suggest that the roughness of water surface has a crucial role in the process of methane dissolution.