Abstract
The electrochemical behavior of iron in neutral solutions of perchlorate and low borate concentrations was investigated using cyclic voltammetry and the rotating ring-disc electrode techniques. In solutions containing just perchlorate, iron passivation was observed at potentials higher than the potential of an anodic peak corresponding to the active range at which the dissolution of Fe2+ and Fe3+ species was detected. When borate is added to the solution, this anodic peak decreased as well as the amount of the active soluble species. The increase of pH, keeping the borate and perchlorate concentrations constant, was found to be less effective at promoting iron passivation than the increase of borate concentration. The results demonstrated that the interaction between borate ion and the electrode surface occurs by chemical adsorption according to the Langmuir isotherm.
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