Analysis of the Volmer–Krishtalic mechanism for the chlorine electrode reaction

The dependencies of the current density and surface coverage of the adsorbed intermediates on overpotential were established without kinetic approximations for the chlorine electrode reaction under the Volmer–Krishtalic mechanism. Tafelian regions were obtained which slope values cannot be derived from the use of the rate determining step criteria, such as 2.3026(2RT/3F) and 2.3026(RT/F), as well as two or three Tafel regions with different slopes in the same anodic or cathodic curve. The existence of limiting kinetic current densities was also demonstrated. Finally, the results obtained were analysed and discussed, comparing them with those obtained by the usual methods. Keywords: Chlorine evolution, Volmer–Krishtalic mechanism, Tafel slope

Hydrogen oxidation reaction: Evidences of different electrocatalytic activity between α and β Pd–H

The hydrogen oxidation reaction (hor) was studied in steady state conditions on a palladium thin film electrode supported on a gold rotating disc. The electrode surface was characterized by cyclic voltammetry and SEM observation. The hydrogen absorption process was analysed by open circuit potential decay in an acid solution saturated with hydrogen and the kinetic measurements were carried out potentiostatically in the same solution. The results obtained show a marked change on the dependence of the current density on overpotential due to the transition between the α and β phases of the Pd–H system. These results were correlated with appropriate kinetic expressions and the corresponding electrocatalytic activity of both phases was estimated. Keywords: Palladium thin film, Hydrogen oxidation reaction, Electrocatalytic activit

Vapor Pressure of Saturated Aqueous Solutions of Potassium Sulfate from 310 K to 345 K

The experimental evaluation of the vapor pressure of saturated aqueous solutions of potassium sulfate was carried out in the range of temperatures 310 K≤T≤345 K. The experimental data were used to determine the corresponding values of the water activity in such solutions. The analytical expressions as a function of temperature of both, vapor pressure and water activity, were obtained from the correlation of the experimental results. The vapor pressure expression was also extrapolated to a different temperature range in order to make a comparison with the results obtained by other authors