钝化
溶解
腐蚀
硫酸盐
极化(电化学)
无机化学
Pourbaix图
水溶液
X射线光电子能谱
化学
硫酸钠
材料科学
被动性
电流密度
冶金
固溶体
钠
化学工程
作者
Mohammad Amin Razmjoo Khollari,Kashif Mairaj Deen,Edouard Asselin
标识
DOI:10.1038/s41529-025-00667-7
摘要
Understanding the dissolution and passivation of iron in aqueous environments is essential for enhancing its corrosion resistance and expanding its applications. We present Thermo-Kinetic (TK) diagrams for iron in deaerated solutions with no added sodium sulfate (Na 2 SO 4 ) and with 0.1 M Na 2 SO 4 over the pH range 1–14, constructed by integrating current density contours from potentiodynamic polarization with thermodynamic E-pH diagrams. TK diagrams indicate that in solutions with no added Na 2 SO 4 , iron passivates above pH 7, with a minimum passive current density (i p ) of 5 ×10 −6 mA·cm −2 at pH 8. The addition of 0.1 M Na 2 SO 4 delayed passivation until pH 12 and increased i p nearly tenfold. Galvanostatic (GS) polarization and EIS validated the TK diagram results. XPS after GS polarization revealed an FeOOH/Fe 2 O 3 film at pH 10, while Fe 3 O 4 /Fe 2 O 3 dominated at pH 12 and 14. These results clarify how sulfate compromises iron passivity and highlight TK diagrams as a powerful tool for mapping corrosion behavior.
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