Solubility of Metal Oxides under Control of Basicity by Electrolysis in Fused Na2SO4
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The dissolution behavior of NiO, Co<SUB>3</SUB>O<SUB>4</SUB>, Fe<SUB>2</SUB>O<SUB>3</SUB>, Fe<SUB>3</SUB>O<SUB>4</SUB>, SiO<SUB>2</SUB>, Al<SUB>2</SUB>O<SUB>3</SUB> and Cr<SUB>2</SUB>O<SUB>3</SUB> powders under the control of the O<SUP>2−</SUP> activity of fused Na<SUB>2</SUB>SO<SUB>4</SUB> by electrochemical polarization was investigated. As a result, the increase in the quantity of electricity for the anodic reaction with increasing polarization potential for the platinum electrode caused an increase in the basicity(−log a<SUB>Na2O</SUB>) of the fused Na<SUB>2</SUB>SO<SUB>4</SUB>, while the increase in the quantity of electricity for cathodic reaction with decreasing polarization potential caused a decrease in basicity of the fused Na<SUB>2</SUB>SO<SUB>4</SUB>. The solubility of NiO and Co<SUB>3</SUB>O<SUB>4</SUB> in fused Na<SUB>2</SUB>SO<SUB>4</SUB> increased in the anodic potential region. However, their solubility did not increase in the cathodic potential region. The solubility of Fe<SUB>2</SUB>O<SUB>3</SUB> and Fe<SUB>3</SUB>O<SUB>4</SUB> slightly increased in the anodic potential region. The solubility of SiO<SUB>2</SUB> did not increase in the anodic potential region, whereas the solubility of SiO<SUB>2</SUB> increased with a decrease in the polarization potential in the cathodic potential region. The solubility of Al<SUB>2</SUB>O<SUB>3</SUB> and Cr<SUB>2</SUB>O<SUB>3</SUB> increased in the cathodic and anodic potential regions. The solubility of Al<SUB>2</SUB>O<SUB>3</SUB> was larger than that of Cr<SUB>2</SUB>O<SUB>3</SUB>. We found that the resistance of acid and basic dissolution for oxides could be estimated by the electrochemical polarization method.
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