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Volume 5 Issue 3
Sep.  1998
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K Ogura, W Lou, M Nakayama,  and T Fukum, Potential Oscillations of a Stainless Steel Electrode during Galvanostatic Polarization in a Mixed Solution of Sulfuric and Chromic Acids, J. Univ. Sci. Technol. Beijing, 5(1998), No. 3, pp. 134-139.
Cite this article as:
K Ogura, W Lou, M Nakayama,  and T Fukum, Potential Oscillations of a Stainless Steel Electrode during Galvanostatic Polarization in a Mixed Solution of Sulfuric and Chromic Acids, J. Univ. Sci. Technol. Beijing, 5(1998), No. 3, pp. 134-139.
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Materials

Potential Oscillations of a Stainless Steel Electrode during Galvanostatic Polarization in a Mixed Solution of Sulfuric and Chromic Acids

  • Potential oscillations of a stainless steel electrode galvanostatically anodized have been observed in a mixture of chromic and sulfuric acids. The potential regularly oscillated between 1.6 V vs. SCE (lower) and 2.1V (upper) with a certain frequency. The potential values are affected neither by the composition of chromic and sulfuric acids nor by the magnitude of applied current density although the potential frequency is very sensitive to these parameters. This phenomenon is interpreted in terms of the repeated formation and disappearance of the saturated layer of dichromate ions on the electrode surface. Such scheme is consistent with the in situ FTIR spectroscopic result that the concentration of Cr2O72- ions on the electrode surface increased with time during the polarization at the lower potential but the change in concenetion of Cr2O72- ions was negligible at the higher potential.
  • Materials

    Potential Oscillations of a Stainless Steel Electrode during Galvanostatic Polarization in a Mixed Solution of Sulfuric and Chromic Acids

    + Author Affiliations
    • Potential oscillations of a stainless steel electrode galvanostatically anodized have been observed in a mixture of chromic and sulfuric acids. The potential regularly oscillated between 1.6 V vs. SCE (lower) and 2.1V (upper) with a certain frequency. The potential values are affected neither by the composition of chromic and sulfuric acids nor by the magnitude of applied current density although the potential frequency is very sensitive to these parameters. This phenomenon is interpreted in terms of the repeated formation and disappearance of the saturated layer of dichromate ions on the electrode surface. Such scheme is consistent with the in situ FTIR spectroscopic result that the concentration of Cr2O72- ions on the electrode surface increased with time during the polarization at the lower potential but the change in concenetion of Cr2O72- ions was negligible at the higher potential.
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