Corrosion behavior of CoCrCu0.1FeMoNi high entropy alloy in 0.5 mol/L NaOH solution

被引:1
|
作者
Zhu, Hao-jie [1 ,2 ]
Han, Jian-yang [1 ]
Fang, Ke-wei [3 ]
Zheng, Zhi-bin [2 ]
Zhou, Hui-ling [1 ]
Yang, Lan-lan [1 ]
Qiao, Yan-xin [1 ]
Chen, Jian [4 ]
Cui, Jie [5 ]
Wang, Qiang [3 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Mat Sci & Engn, Zhenjiang 212003, Jiangsu, Peoples R China
[2] Guangdong Acad Sci, Inst New Mat, Guangdong Prov Key Lab Met Toughening & Applicat, Guangzhou 510650, Peoples R China
[3] Suzhou Nucl Power Res Inst, Measurement & Inspect Ctr, Suzhou 215004, Jiangsu, Peoples R China
[4] Univ Western Ontario, Dept Chem & Surface Sci Western, London, ON N6A 5B7, Canada
[5] Jiangsu Univ Sci & Technol, Sch Naval Architecture & Ocean Engn, Zhenjiang 212003, Jiangsu, Peoples R China
关键词
High entropy alloy; Micro-galvanic corrosion; Electrochemical corrosion; X-ray photoelectron spectroscopy; CAVITATION EROSION; STAINLESS-STEELS; GRAIN-SIZE; MICROSTRUCTURE; TEMPERATURE; RESISTANCE; NITROGEN; PASSIVATION; MOLYBDENUM; STABILITY;
D O I
10.1007/s42243-024-01407-y
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
The corrosion behavior of CoCrCu0.1FeMoNi high entropy alloy (HEA) in 0.5 mol/L NaOH solution was investigated using X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron microscopy, potentiodynamic polarization measurement, and electrochemical impedance spectroscopy. The results showed that the microstructure of this HEA displayed a dendritic morphology along with inter-dendritic regions. At the applied potential of -0.3, 0, and 0.1 V vs. saturated calomel electrode (SCE), no significant damage to the surface of the alloy was observed. At the applied potentials of 0.15 and 0.2 V vs. SCE, selective detachment and tearing of the microstructure on the alloy surface were observed, attributed to micro-galvanic corrosion. HEA demonstrates typical spontaneous passivation behavior and exhibits capacitance at all five applied potentials. The energy dispersive spectroscopy results indicate significant elemental segregation within HEA, with a decrease in the content of Cr2O3 in the passive film as the applied potential increases. Consequently, the protective efficacy of the passive film over the substrate in 0.5 mol/L NaOH solution was compromised.
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收藏
页数:13
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