A novel procedure for anodic reaction quantitative restructuration and its application in pure magnesium

IF 10.7
Corrosion Communications Pub Date : 2026-03-01 Epub Date: 2025-07-08 DOI:10.1016/j.corcom.2024.10.003
Junli Sun , Qixin Yan , Jianlei Song , Donghu Li , Qian Wang , Kunkun Deng , Yinghui Wei , Lifeng Hou
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引用次数: 0

Abstract

The anodic dissolution behavior of pure magnesium in sodium chloride solution was characterized using a synchronous online monitoring system. Concurrently, the film-forming magnesium was quantitatively characterized using a Thermal Gravimetric Analyzer (TGA). By combining these two analyses, the anodic reaction during the process of anodic polarization of magnesium was comprehensively described for the first time. This novel procedure allows for detailed examination of the quantitative relationship between film-forming magnesium and dissolved magnesium. To elucidate the anomalous hydrogen evolution, a plausible local active site mechanism was proposed. This mechanism suggests that uneven current distribution causes the local active dissolution, creating a potential difference that leads to the formation of micro-galvanic couples and subsequently anomalous hydrogen evolution.
一种新的阳极反应定量重组方法及其在纯镁中的应用
采用同步在线监测系统对纯镁在氯化钠溶液中的阳极溶解行为进行了表征。同时,用热重分析仪(TGA)对成膜镁进行了定量表征。结合这两种分析方法,首次对镁阳极极化过程中的阳极反应进行了较为全面的描述。这种新颖的程序允许详细检查成膜镁和溶解镁之间的定量关系。为了解释氢的异常演化,提出了一个合理的局部活性位点机制。该机制表明,不均匀的电流分布导致局部活性溶解,产生电位差,导致微电偶的形成和随后的异常析氢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.30
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0.00%
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