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Mechanism of the Transpassive Dissolution and Secondary Passivation of Chromium in Sulphuric Acid Solutions

机译:铬溶液中铬的钝化溶解和二次钝化机理

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The transpassive dissolution and secondary passivation of Cr in 1... 10 M H_2SO_4 solutions were studied by a combination of different electrochemical methods. The steady-state polarization curves for transpassive dissolution exhibited a Tafel behaviour with a slope being independent on the acid concentration. Lower dissolution rates were measured for higher acid concentrations. Ring-disk measurements showed a release of both soluble Cr(VI) and Cr(III) during transpassivity. Impedance spectra were qualitatively similar in all acid concentrations, comprising one capacitive and two inductive semicircles. A kinetic model comprising two parallel transpassive dissolution paths was consistent with the experimental results. Typical passivation diagrams were observed for Cr in 10 M H_2SO_4, and a secondary passive state was established at higher potentials. The formation of the secondary passive film was confirmed by contact electric resistance (CER) measurements. A renewed version of the surface charge approach was consistent with the experimental results in the region of the secondary passivation.
机译:结合不同的电化学方法,研究了Cr在1 ... 10 M H_2SO_4溶液中的过钝溶解和二次钝化。被动渗透的稳态极化曲线表现出Tafel行为,其斜率与酸浓度无关。对于较高的酸浓度,测得的溶解度较低。环盘测量表明,在钝化过程中,可溶性Cr(VI)和Cr(III)均释放。在所有酸浓度下,阻抗谱在质量上都相似,包括一个电容性和两个电感性半圆。包含两个平行的超被动溶解路径的动力学模型与实验结果一致。在10 M H_2SO_4中观察到Cr的典型钝化图,并在较高电势下建立了次级钝态。通过接触电阻(CER)测量确认了第二无源膜的形成。表面电荷方法的更新版本与二次钝化区域中的实验结果一致。

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