Adsorption of butyl acetate on mercury electrode and its effect on electroreduction of Zn cations

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 soluti ons for various butyl acetate concentrations point to the strongest decreas e in capacity in 0.1 hi NaClO4 for the smallest concentration of the ester tested. At the same time the heights of desorption peaks in the solutions t ested decrease in the following order: 1 M > 0.5 M > 0.1 M NaClO4. The obta ined results show dynamic competitive adsorption in the ClO4--H2O-ester sys tem. In all the systems studied the zero charge potential values determined with a streaming electrode are shifted towards positive potential with inc reasing ester concentration. These results suggest that the polar molecule of the ester adsorbs on the mercury electrode with its hydrophobic end whil e hydrophilic ester group is directed towards the solution. The values of t he relative surface excess obtained in the range of potentials where the st rong adsorption occurs, virtually do not depend on the base electrolyte con centration. The values of the Gibbs energy of adsorption DeltaG(0) determin ed from the Frumkin isotherm have also similar values at base concentration s of the electrolyte tested. The values of interaction constant A are radic ally different: the adsorbed molecules undergo repulsive force in 1 M NaClO 4, 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 f ollowing the kinetics of the reduction of Zn++ as a pilot ion. It was state d 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.