ChemInform Abstract: Polarization Behavior of a Cobalt Rotating Disc Electrode in Sulfuric Acid Solutions in the Absence and Presence of Chloride Ions.

ChemInform ◽  
2010 ◽  
Vol 22 (31) ◽  
pp. no-no
Author(s):  
D. SAZOU ◽  
M. PAGITSAS
1979 ◽  
Vol 57 (19) ◽  
pp. 2560-2563 ◽  
Author(s):  
Hélio C. Chagas

Electrosorption at the platinum rotating disc electrode in sulfuric acid solutions of selenite, selenate, selenide, and tellurite gives rise to isopotential points in the potential range where oxidation of platinum occurs. The data are analyzed with the framework of the model put forward by Untereker and Bruckenstein. Since similar behavior is observed for the selenite, selenate, and selenide systems, it is tentatively inferred that a common electrosorbed species, possibly selenium itself, may be involved in these systems.


2003 ◽  
Vol 68 (1-3) ◽  
pp. 141-150 ◽  
Author(s):  
A. Mayboroda ◽  
I.D. Troshkina ◽  
A.M. Chekmarev ◽  
H. Lang

CORROSION ◽  
1972 ◽  
Vol 28 (3) ◽  
pp. 77-82 ◽  
Author(s):  
WESLEY B. CROW ◽  
JAMES R. MYERS ◽  
J. V. JEFFREYS

CORROSION ◽  
1965 ◽  
Vol 21 (9) ◽  
pp. 277-287 ◽  
Author(s):  
J. R. MYERS ◽  
F. H. BECK ◽  
M.G. FONTANA

Abstract Anodic polarization behavior of annealed high-purity Ni, Cr and selected Ni-Cr alloys in hydrogen-saturated, 1, 5, 10 and 20N sulfuric acid solutions was investigated at 25 ± 1 C (77 F) using a potentiostatic technique. All specimens except pure Ni in 20N acid had an active-to-passive transition. Decreasing acid concentration increased passive potential range of pure Ni while acid concentration did not appreciably affect the passive region of pure Cr or the Ni-Cr alloys. Increasing acid concentration and decreasing chromium content increased the secondary passivation tendency in the transpassive region. No oxygen evolved in the transpassive region except for pure Ni and the higher nickel alloys. Tafel slopes for anodic dissolution, early transpassive region and oxygen evolution were determined. Corrosion potentials for pure Ni and Ni-Cr alloys containing up to 90 w/o Cr behaved as a reversible hydrogen electrode over the pH range 1.63 to −0.44. This linear relationship did not exist for the higher acid concentrations. Slope dependence for pure Cr and the 99Cr-1Ni alloy was −0.110. A minimum in critical current density versus percent Cr curves was established at 90 to 95 w/o Cr. Passivation potentials were determined. Passive current density decreased with increasing chromium content over the composition range 0 to 33 w/o Cr. It was established that increased specimen purity decreases the magnitude of critical current density and shifts corrosion and passivation potentials in the noble potential direction.


1978 ◽  
Vol 56 (15) ◽  
pp. 2042-2048 ◽  
Author(s):  
Hélio C. Chagas

The Cr6+/Cr3+ reduction in aqueous solution is studied in the presence of sulfate and chloride ions by the rotating disc electrode method. In the low chromic acid concentration region, the results exhibit some differences in relation to those obtained using more concentrated solutions. However, it is demonstrated that in the presence of sulfate and chloride ions there is a chemical reaction preceding the electrochemical process, confirming a previous suggestion. Results for Cr6+/Cr3+ reduction process in perchloric acid medium at various temperatures are presented and a reduction mechanism is suggested.


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