Understanding of ammonium salts under-deposit corrosion: Electrochemical and AIMD investigations

被引:0
|
作者
Li, Ruidong [1 ,2 ]
Wang, Xiaodan [2 ]
Chen, Jukai [3 ]
Wang, Yueshe [2 ]
机构
[1] Northwest Univ, Sch Chem Engn, Xian 710069, Peoples R China
[2] Xi An Jiao Tong Univ, State Key Lab Multiphase Flow Power Engn, Xian 710049, Peoples R China
[3] China Univ Min & Technol, Sch Chem Engn & Technol, Xuzhou 221116, Peoples R China
基金
中国国家自然科学基金;
关键词
Interdigital electrode; Under-deposit corrosion; Interface; Dynamic deliquescence; INITIO MOLECULAR-DYNAMICS; MILD-STEEL; INHIBITORS; FILM; DFT; DERIVATIVES; NH4CL;
D O I
10.1016/j.corsci.2024.111887
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In -situ electrochemical experiments and ab initio molecular dynamics (AIMD) simulations are combined to investigate the under -deposit corrosion and hygroscopicity of ammonium salts on SAE 1020 steel interdigital electrodes. The findings indicate that the hygroscopicity of ammonium salts influences the evolution of the interface and the accumulation of the product film. The corresponding simulations reveal that the hydrolysis of NHa leads to the generation of a proton transfer chain, resulting in an elevation of H+ concentration. This hydrolysis behavior is effectively catalyzed on the Fe(1 0 0) surface, promoting the occurrence of anodic adsorption and cathodic hydrogen evolution reaction, thereby inducing corrosion.
引用
收藏
页数:14
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