The Competitive Adsorption of Water and Methanol on a Hybrid Silica Stationary Phase in Supercritical Fluid Chromatography

Abstract

This study investigates the adsorption of methanol, water, and their mixture in a hybrid silica stationary phase with supercritical carbon dioxide as a mobile phase in supercritical fluid chromatography (SFC). The adsorption isotherms of methanol and water were determined by two dynamic methods: the elution by characteristic point (ECP) method and the inverse method (IM). Both the single-component and competitive bi-Langmuir models were pre-selected for the inverse method. The initial parameters of the single-component isotherm for both methanol and water were estimated with the ECP method by fitting the experimental data to the bi-Langmuir isotherm model. Then, using the inverse method, we refined the single-component isotherm parameter values, which were then further used for determining the competitive isotherm of the methanol–water mixture. The elution profile of the (methanol–water) mixture sample was calculated by the equilibrium-dispersive (ED) model. The results indicated that there is a good agreement between the experimental band profile and the calculated band profile, which was obtained from the parameters of the competitive bi-Langmuir isotherm model, revealing a competition between methanol and water to reach the adsorption sites. Furthermore, the saturation capacity of the adsorption sites in the stationary phase decreased in the case of the mixture sample compared to those for the single-component sample.