Collection of Czechoslovak Chemical Communications - digital archive 

Abstract

Adsorption of butyl acetate on the mercury electrode in 1 M, 0.5 M or 0.1 M NaClO₄ is described. Differential capacity curves obtained in these solutions for various butyl acetate concentrations point to the strongest decrease in capacity in 0.1 M NaClO₄ for the smallest concentration of the ester tested. At the same time the heights of desorption peaks in the solutions tested decrease in the following order: 1 M > 0.5 M > 0.1 M NaClO₄. The obtained results show dynamic competitive adsorption in the ClO₄^--H₂O-ester system. In all the systems studied the zero charge potential values determined with a streaming electrode are shifted towards positive potential with increasing ester concentration. These results suggest that the polar molecule of the ester adsorbs on the mercury electrode with its hydrophobic end while hydrophilic ester group is directed towards the solution. The values of the relative surface excess obtained in the range of potentials where the strong adsorption occurs, virtually do not depend on the base electrolyte concentration. The values of the Gibbs energy of adsorption ∆G⁰ determined from the Frumkin isotherm have also similar values at base concentrations of the electrolyte tested. The values of interaction constant A are radically different: the adsorbed molecules undergo repulsive force in 1 M NaClO₄, whereas in 0.5 M and 0.1 M NaClO₄ they are under weak attraction. In the range of more negative potentials, the adsorption layer was investigated following the kinetics of the reduction of Zn⁺⁺ as a pilot ion. It was stated that the concentration of the base electrolyte fundamentally affects the process: the inhibition of butyl acetate decreases in the order 1 M > 0.5 M > 0.1 M NaClO₄.

Keywords: Electrochemistry; Adsorption; Butyl acetate; Mercury electrode; Zinc; Polarography.

References: 19 live references.