腐蚀
吸附
催化作用
化学
阴极保护
材料科学
溶解度
无机化学
冶金
化学工程
电化学
有机化学
物理化学
电极
工程类
作者
Jihui Leng,Y. Frank Cheng,Kexi Liao,Yuanjie Huang,Feilong Zhou,Shuai Zhao,Xin Liu,Qing Zou
标识
DOI:10.1016/j.engfailanal.2022.106332
摘要
To enhance the understanding of the corrosion mechanism on rapid perforation failure, the corrosion behavior of L245N with the synergistic effect of O2-Cl− and different Cl− contents in CO2-O2-Cl− environment were studied by weight-loss test and characterization analysis. It showed that the O2 was the dominant factor inducing localized corrosion and the synergistic effect of O2-Cl− in CO2-O2-Cl− environment mainly accounted for the growth of the corrosion, because porous Fe oxides generated by O2 promoted the mass transfer and catalysis of Cl− and Cl− in turn promoted the expansion of localized corrosion pits. The increase of the Cl− under low content enhanced the synergistic effect with O2, while high content of Cl− (3000–5000 mg/L) could reduce the solubility of CO2/O2 and replace the adsorption of corrosive medium and ions on the substrate surface, inhibiting the cathodic process of corrosion reaction.
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