In this work, a rotating disk electrode was used to measure the cathodic kinetics on stainless steel as a function of diffusion layer thickness (6 to 60 mu m) and chloride concentration (0.6 to 5.3 M NaCl). It was found that, while the cathodic kinetics followed the Levich equation for large diffusion layer thicknesses, the Levich equation overpredicts the mass-transfer limited current density for diffusion layer thicknesses less than 20 mu m. Also, an unusual transitory response between the activation and mass-transfer controlled regions was observed for small diffusion layer thicknesses that was more apparent in lower concentration solutions. The presence and reduction of an oxide film and a transition in the oxygen reduction mechanism were identified as possible reasons for this response. The implications of these results on atmospheric corrosion kinetics under thin electrolyte layers is discussed. (C) The Author(s) 2018. Published by ECS.
CITATION STYLE
Alexander, C. L., Liu, C., Alshanoon, A., Katona, R. M., Kelly, R. G., Carpenter, J., … Schindelholz, E. (2018). Oxygen Reduction on Stainless Steel in Concentrated Chloride Media. Journal of The Electrochemical Society, 165(13), C869–C877. https://doi.org/10.1149/2.0181813jes
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