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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1 October 1975
Research Article|
October 01 1975
Potentiodynamic Studies of Antimony in Acidic and Alkaline Solutions
Ken Nobe
Ken Nobe
*School of Engineering and Applied Science, University of California, Los Angeles.
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Online ISSN: 1938-159X
Print ISSN: 0010-9312
© 1975 National Association of Corrosion Engineers
1975
CORROSION (1975) 31 (10): 364–369.
Citation
L. L. Wikstrom, Ken Nobe; Potentiodynamic Studies of Antimony in Acidic and Alkaline Solutions. CORROSION 1 October 1975; 31 (10): 364–369. https://doi.org/10.5006/0010-9312-31.10.364
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