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Electrochemical Behavior of Pb-Co Anodes in Sulfuric Acid Electrolyte Containing Cl- Ions
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1.School of Materials Science and Engineering, Hebei University of Engineering, Handan 056038, China;2.Zhuzhou Smelting Group Co., Ltd, Zhuzhou 412000, China;3.School of Metallurgy and Environment, Central South University, Changsha 410083, China

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Fund Project:

National Natural Science Foundation of China (51904085, 51904086, U20A20272); Supported by Zhuzhou Smelting Group Co., Ltd (ZYKJ20220408003); Natural Science Foundation of Hebei Province (E2021402056); Science and Technology Research and Development Program of Handan City (21422101235)

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    Abstract:

    Pb-Co anodes with different Co contents (0.5wt%, 1wt%, and 2wt%) were prepared by powder metallurgy, and the traditional Pb-Ca-Sn anode was used as the reference for comparison. The electrochemical behavior of the anodes in the electrolyte containing 160 g/L H2SO4 and 500 mg/L Cl- ions was evaluated by electrochemical measurements. The phase composition, surface morphologies, and element distribution of the anodic oxide layers after galvanostatic polarization for 72 h were investigated. With increasing the Co content, the anodic potential, charge transfer resistance, and oxygen evolution overpotential of the Pb-Co anodes are decreased gradually. After galvanostatic polarization for 72 h, the oxygen evolution overpotential of Pb-2wt% Co anode is lower than that of Pb-Ca-Sn anode by 101 mV. In addition, due to the presence of Cl- ions, the charge transfer is improved, the oxygen evolution reaction is inhibited, and the oxide layer is deteriorated.

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[Wang Shuai, Liu Ying, Xu Dong, Lin Wenjun, Wang Yong, Zhao Shuo, Yang Juan, Zhou Xiangyang. Electrochemical Behavior of Pb-Co Anodes in Sulfuric Acid Electrolyte Containing Cl- Ions[J]. Rare Metal Materials and Engineering,2023,52(5):1565~1572.]
DOI:10.12442/j. issn.1002-185X.20220805

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History
  • Received:October 14,2022
  • Revised:January 06,2023
  • Adopted:February 14,2023
  • Online: May 31,2023
  • Published: May 29,2023