ZrVTiNbAl高熵合金在酸性、中性和碱性水溶液中的极化研究

V. Dubey , P. Chakraborty , S. Roychowdhury , R. Tewari
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摘要

采用动电位极化实验和电化学阻抗谱(EIS)研究了轻质难熔高熵合金(ZrVTiNbAl)体系的电化学行为。在HNO3(1 M和0.1 M)、NaOH(1 M和0.1 M)和中性水溶液中进行了实验,并与SS304L在相同溶液中的实验结果进行了比较。ZrVTiNbAl有两种组成,一种是等原子的(命名为C1),另一种是非等原子的(35Nb25V25Ti10Al5Zr at%;名叫C2)。结果表明,高铝含量(~ 20 % Al)的等原子HEA (C1)在酸性和中性溶液中的耐蚀性优于C2(~ 10 % Al)和SS304L。通过无反被动行为、最低的无源电流密度和最低的腐蚀电流,证明了C1具有较高的耐腐蚀性。C2在1 M和0.1 M NaOH溶液中表现出很高的腐蚀电流密度和透溶,而SS304L在所有环境中都表现出透溶。在0.1 M HNO3和0.5 V条件下恒电位极化后的HEAs的辉光发射光谱和XPS分析(SCE)表明,在C1上形成的钝化膜含有所有合金元素的氧化物混合物,而C2上没有显示Al2O3的存在。Al₂O₃的存在促进了C1钝化膜的钝化行为,是C1钝化膜具有优异耐腐蚀性的关键因素。
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Polarisation studies of ZrVTiNbAl high entropy alloy in acidic, neutral and basic aqueous solution
The electrochemical behavior of a light weight refractory high entropy alloy (HEA) system (ZrVTiNbAl) was investigated by potentiodynamic polarization experiments and electrochemical impedance spectroscopy (EIS). Experiments were done in HNO3 (1 M and 0.1 M), NaOH (1 M and 0.1 M) and neutral aqueous solution and the results were compared with that of SS304L in the same solution. Two compositions of ZrVTiNbAl were used in this investigation, one equiatomic (named C1) and the other non-equiatomic (35Nb25V25Ti10Al5Zr at%; named C2). Results indicated that the corrosion resistance of the equiatomic HEA (C1) having higher aluminum content (∼20 at% Al) was better than that of both C2 (∼10 at% Al) and SS304L in acidic as well as neutral solution. The higher corrosion resistance of C1 was demonstrated through the absence of trans-passive behavior, lowest passive current density and the lowest corrosion current. C2 showed very high corrosion current density and transpassive dissolution in 1 M and 0.1 M NaOH solution while SS304L showed transpassive dissolution in all the environments. Glow discharge optical emission spectroscopy and XPS analysis of the HEAs after potentiostatic polarization in 0.1 M HNO3 at 0.5 V(SCE) indicated the passive film formed on C1 to contain a mixture of oxides of all the alloying elements while C2 did not show the presence of Al2O3 in the passive film. The presence of Al₂O₃ in the passive film of C1 was identified as the key factor contributing to its superior corrosion resistance, as it promoted passivation behavior.
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