Thermodynamic study of the adsorption of acridinium derivatives on the clay surface

Abstract

In this study, the adsorption behavior of mono-cationic acridinium derivatives on a synthetic clay mineral (Sumecton SA) was investigated. The acridinium derivatives were adsorbed on the clay surface without aggregation, as found from the changes in the absorption spectra of the acridinium derivatives with SSA and without SSA represented by two-component equilibrium systems of adsorbed and non-adsorbed components. Following the Langmuir isotherm analysis, the adsorption equilibrium constants and maximum adsorption amounts were determined for acridinium derivatives, and the Gibbs free energy change (ΔG) was calculated to be in the range of −33.8 to 40.0 kJ mol⁻¹ from the adsorption equilibrium constants. These results indicated that the adsorption of acridinium derivatives on the clay surface was an exergonic reaction. Moreover, thermodynamic parameters such as enthalpy change (ΔH) and entropy change (ΔS) were obtained from the temperature effect experiments. For all acridinium derivatives, ΔH (from −7.82 to −26.0 kJ mol⁻¹) and ΔS (0.047–0.088 kJ mol⁻¹ K⁻¹) were found to be negative and positive, respectively. It was suggested that not only electrostatic interactions, but also van der Waals forces and hydrophobic interactions played an important role in the adsorption of cationic aromatic molecules on the clay surface. Because these thermodynamic parameters showed a strong correlation with the molecular cross-sectional area of acridinium derivatives, it was suggested that the contribution of hydrophobic interactions became smaller as the molecular cross-sectional area became larger.