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机构地区:[1]上海工程技术大学材料工程学院,上海201600 [2]华东理工大学资源与环境工程学院,上海200237
出 处:《中国有色金属学报》2006年第6期1070-1075,共6页The Chinese Journal of Nonferrous Metals
基 金:国家自然科学基金资助项目(50204006)
摘 要:采用循环伏安法研究了700℃时46.5LiF-11.5NaF-42KF(摩尔分数,%)熔盐中Ti(Ⅳ)(c(K2TiF6)=0.2 mol/L)和B(Ⅲ)(c(KBF4)=0.4 mol/L)在铂电极上的电化学还原机理,计算了各还原步骤传递的电子数。研究了LiF-NaF-KF-K2TiF6-KBF4(c(K2TiF4)=0.3 mol/L,c(KBF4)=0.3,0.6,0.9 mol/L)熔盐中电化学合成TiB2的阴极过程机理。结果表明:Ti(Ⅳ)的电化学还原为三步电荷传递反应,且阴极过程近似可逆;B(Ⅲ)在铂电极上的电化学反应机理为简单的三电子一步反应,阴极过程近似可逆;Ti(Ⅳ)和B(Ⅲ)可在同一电位下发生共沉积并反应生成TiB2。The mechanism of the electrochemical reduction of Ti (Ⅳ) (c (K2 TiF6 )= 0. 2 mol/L) and B (Ⅲ) (c(KBF4) =0.4 mol/L) on the platinum electrode in 46.5LiF-11.5NaF-42KF (mole fraction, %) molten salt at 700 ℃ were investigated by means of the cyclic voltammetry technique. The cathode process of titanium diboride (TiB2) formation was also studied on the platinum electrode in the 46.5LiF-11.5NaF-42KF-Kz TiF6-KBF4 (c(K2TiF4 )= 0. 3 mol/L, c(KBF4)=0.3, 0.6, 0.9 mol/L)molten salt at 700 ℃. It is found that the electrochemical reduction of Ti (Ⅳ) proceeds in three-step charge transfer, the cathodic process is quasi-reversible. The electrochemical reduction of B( Ⅲ ) occurs in one-step charge transfer, the cathodic process is quasi-reversible. The electrolytic codeposition of Ti( Ⅳ ) and B( Ⅲ ) with the formation of TiB2 can he achieved.
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