<p>The combined impact of alternating current (AC) density and ammonium ion content on the anti-corrosion property of CoCrFeMnNi HEA in a 3.5 wt.% NaCl solution was researched via electrochemical test, atomic force microscope (AFM), and scanning electron microscopy (SEM). Elevated corrosion rate and metastable pitting density confirm that the corrosion resistance of the HEA is gradually declined with rising NH<sub>4</sub><sup>+</sup> concentration. Increasing AC density induces a transition of the alloy surface status from passivated to active, signifying that a violent anodic dissolution reaction occurs. When AC interference is exerted, the passivation film on the HEA becomes noticeably non-compact, inhomogeneous, and thin, accompanied by a rise in flaw amount. Moreover, the synergistic impact between i<sub>AC</sub> and ammonium ion leads to the production of larger and denser corrosion pits on the matrix. The augmented adsorption of aggressive ions and increased H<sup>+</sup> observably reduce the barrier capability of the protective passivation film, thereby intensifying the corrosion of the alloy, as testified by the rapid rise of corrosion current density.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Analysis of Corrosion Characteristics for CoCrFeMnNi HEA Induced by Alternating Current Interference in NaCl Solution Contaminated with Ammonium Ion

  • Y. Q. Lu,
  • M. Zhu,
  • W. Lan,
  • Y. F. Yuan

摘要

The combined impact of alternating current (AC) density and ammonium ion content on the anti-corrosion property of CoCrFeMnNi HEA in a 3.5 wt.% NaCl solution was researched via electrochemical test, atomic force microscope (AFM), and scanning electron microscopy (SEM). Elevated corrosion rate and metastable pitting density confirm that the corrosion resistance of the HEA is gradually declined with rising NH4+ concentration. Increasing AC density induces a transition of the alloy surface status from passivated to active, signifying that a violent anodic dissolution reaction occurs. When AC interference is exerted, the passivation film on the HEA becomes noticeably non-compact, inhomogeneous, and thin, accompanied by a rise in flaw amount. Moreover, the synergistic impact between iAC and ammonium ion leads to the production of larger and denser corrosion pits on the matrix. The augmented adsorption of aggressive ions and increased H+ observably reduce the barrier capability of the protective passivation film, thereby intensifying the corrosion of the alloy, as testified by the rapid rise of corrosion current density.