<p>A series of measurements including electrochemical measurements, atomic force microscope and immersion test were employed to investigate the impact of SO<sub>4</sub><sup>2−</sup> concentration over a range of 0 to 20&#xa0;g/L on the anti-corrosion performance of FeCoNi MEA in a simulated ocean environment. With the increase in the concentration of&#xa0;SO<sub>4</sub><sup>2−</sup>, the corrosion resistance of the MEA is severely damaged, which is demonstrated by the significant increase of i<sub>p</sub> value, metastable pitting number and corrosion rate, as well as the occurrence of fused corrosion pit. The negative influence of&#xa0;SO<sub>4</sub><sup>2−</sup>&#xa0;on the anti-corrosion property results from its cyclic acidification reaction, which generates unstable iron compound that is unfavorable for protecting the substrate. The addition of SO<sub>4</sub><sup>2−</sup> increases the flaw amount of surface passivation film, which provides the increased pathways for the infiltration of corrosive&#xa0;Cl<sup>−</sup> and H<sup>+</sup>, weakening the protective capability. Metal elements in the substrate are comprehensively dissolved, resulting in the production of pit.</p>

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Revealing the Influence of Sulfate Ion on Corrosion Characteristics of FeCoNi Medium-Entropy Alloy in Simulated Seawater Environment

  • Z. X. Ye,
  • M. Zhu,
  • Y. F. Yuan,
  • J. L. Yang

摘要

A series of measurements including electrochemical measurements, atomic force microscope and immersion test were employed to investigate the impact of SO42− concentration over a range of 0 to 20 g/L on the anti-corrosion performance of FeCoNi MEA in a simulated ocean environment. With the increase in the concentration of SO42−, the corrosion resistance of the MEA is severely damaged, which is demonstrated by the significant increase of ip value, metastable pitting number and corrosion rate, as well as the occurrence of fused corrosion pit. The negative influence of SO42− on the anti-corrosion property results from its cyclic acidification reaction, which generates unstable iron compound that is unfavorable for protecting the substrate. The addition of SO42− increases the flaw amount of surface passivation film, which provides the increased pathways for the infiltration of corrosive Cl and H+, weakening the protective capability. Metal elements in the substrate are comprehensively dissolved, resulting in the production of pit.