LiF-CaF2-BaF2-ZrO2熔盐中Zr4+在钨电极上的电化学还原机理

Electrochemical reduction mechanism of Zr4+ on tungsten electrode in LiF-CaF2-BaF2-ZrO2 molten salt

  • 摘要: 以LiF-CaF2-BaF2为熔盐体系, ZrO2为原料, 1 373 K条件温度下利用循环伏安法, 计时电位法, 计时电流法, 研究锆离子在钨电极上的电化学过程,对不同ZrO2含量0.5 %,0.7 %,0.9 %的熔盐体系进行电化学分析,研究结果表明:Zr4+在钨电极上还原是通过两步得电子反应, 即Zr4++2e→Zr2+,Zr2++2e→Zr,相对参比电极铂还原峰分别为0.9 V和1.2 V,析出过程是受扩散控制的准可逆反应. 1 373 K时Zr4+在LiF-CaF2-BaF2-ZrO2熔盐中的扩散系数D为6.7×10-6 cm2/s.

     

    Abstract: The electrochemical process of Zr4+ on the tungsten electrode at the temperature of 1 373 K was studied through the methods of cyclic voltammetry, chronopotentiometry and chronoamperometry when LiF-CaF2-BaF2was taken as the molten salt system, and ZrO2 as the raw material.This paper has carried out an electrochemical analysis for molten salt with different ZrO2 contents of 0.5 %, 0.7 %, 0.9 %. The results show that the electrochemical reduction of Zr4+on the tungsten electrode is caused by two electrode reactions, namely Zr4++2e→Zr2+ and Zr2++2e→Zr. As a result, platinum reduction peak of the relative reference electrode is 0.9 V and 1.2 V respectively, which proves that this process is a quasi-reversible reaction controlled by diffusion. The diffusion coefficient of Zr4+ in the molten salt is 6.7×10-6 cm2/s at 1 373 K.

     

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