Electrochemical deprotonation of phosphate on stainless steel

Voltammetric experiments performed in phosphate buffer at constant pH 8.0 on platinum and stainless steel revealed clear reduction currents, which were correlated to the concentrations of phosphate. On the basis of the reactions proposed previously, a model was elaborated, assuming that both H2PO4 and HPO4 2 underwent cathodic deprotonation, and including the acid–base equilibriums. A kinetic model was derived by analogy with the equations generally used for hydrogen evolution. Numerical fitting of the experimental data confirmed that the phosphate species may act as an efficient catalyst of hydrogen evolution via electrochemical deprotonation. This reaction may introduce an unexpected reversible pathway of hydrogen formation in the mechanisms of anaerobic corrosion. The possible new insights offered by the electrochemical deprotonation of phosphate in microbially influenced corrosion was finally discussed

SURFACE EFFECTS IN THE HYDROGEN EVOLUTION REACTION ON NI-ZN ALLOY ELECTRODES IN ALKALINE-SOLUTIONS

Hydrogen evolution reaction was studied on Ni-Zn (25% of Ni before leaching) in 1 M NaOH at 25 degrees C. These electrodes were characterized by very low Tafel slopes of 67 mV dec(-1). Other techniques used included potential and current pulse, potential relaxation in an open circuit, and ac impedance spectroscopy. Analysis of the experimental results led to the conclusion that hydrogen adsorption in the surface layers was responsible for the observed behavior. Influence of the oxidation of the electrode surface and the addition of poisons, thiourea and cyanides, were also studied. These processes inhibit the hydrogen absorption and restore ''normal'' Tafel slopes. Kinetic parameters of the hydrogen evolution reaction were determined