Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
220571 | Journal of Electroanalytical Chemistry | 2009 | 5 Pages |
The electro-oxidation mechanism of trace amounts of sodium hypochlorite (<4.0 mg Cl dm−3) in an aqueous medium has been studied by employing the potential sweep method and double-potential step chronocoulometry. These methods confirmed the occurrence of the competition reaction of the Faradaic-based hypochlorite and the non-Faradaic-based formation of platinum oxide. In the hypochlorite-free solution, the amount of platinum oxide formed during the non-Faradaic reaction was approximately 1.3 pmol cm−2; however, with an increase in the amount of sodium hypochlorite, the amount of platinum oxide gradually decreased to approximately 0.2 pmol cm−2. The results of this study suggest that the electro-oxidation of trace amounts of hypochlorite, particularly amounts less than 1.0 mg Cl dm−3, is strongly inhibited by the initial formation of platinum oxide in a non-Faradaic reaction.