Potentiodynamic polarization of antimony in acidic and alkaline solutions has been investigated. In acidic solutions, two transition potentials were observed at about the equilibrium potentials of the Sb/Sb2O3 and the Sb2O3/Sb2O5 reactions. Both anodic and cathodic Tafel behavior was observed for these reactions. The anodic and cathodic Tafel slopes are 100 and 150 mV/decade, respectively, for the Sb2O3/Sb2O5 reaction. For the latter, the cathodic reaction is first order and the anodic reaction is zero order with respect to the hydrogen ion concentration. A mechanism for the Sb2O3/Sb2O5 reaction is proposed which is consistent with the experimental kinetic data. In alkaline solutions, only the Sb/Sb2O3 reaction was observed. In both acidic and alkaline solutions the differential capacitance of active antimony is substantially larger than the differential capacitance of passive antimony.

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