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在 CsCl 基熔盐中电化学回收稀土离子的研究。

An investigation into the electrochemical recovery of rare earth ions in a CsCl-based molten salt.

机构信息

School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing, 100083, PR China.

出版信息

J Hazard Mater. 2011 May 30;189(3):821-6. doi: 10.1016/j.jhazmat.2011.03.027. Epub 2011 Mar 16.

Abstract

A CsCl-based melt, was used as a supporting electrolyte for a fuel cycle in pyrochemical separation, as it has a high solubility for lanthanide oxide. Cyclic voltammetry and square wave voltammetry were carried out to investigate the cathodic reduction of those rare earth ions. The results prove that the cathodic process of La(III) ions dissolved in a CsCl-based melt, with a one-step reduction La(3+)+3e(-)=La, and is similar to those of other reports which have utilised LiCl-KCl or CaCl(2)-KCl molten salt systems. However, for the Ce(III) ions that dissolved in a CsCl-based melt, there is a significant difference when compared with published literature as there are two reduction steps instead of the reported single step Ce(3+)+e(-)=Ce(2+) and Ce(2+)+2e(-)=Ce. In order to explain the novel result, a detailed investigation was focused on the cathodic process of Ce(III) in a CsCl-based melt. The identification of the M-O (M=La, Ce) compounds that are stable in the electrolyte, as well as the determination of their solubility products, were carried out by potentiometric titration using an oxide ion sensor. Furthermore, the E-pO(2-) (potential-oxide ion) diagram for the M-O stable compound was constructed by combining both theoretical and experimental data.

摘要

采用氯化铯基熔盐作为高温冶金分离燃料循环的支持电解质,因为它对氧化镧有很高的溶解度。采用循环伏安法和方波伏安法研究了这些稀土离子的阴极还原。结果表明,溶解在氯化铯基熔盐中的镧(III)离子的阴极过程为 La(3+)+3e(-)=La,与利用 LiCl-KCl 或 CaCl(2)-KCl 熔盐体系的其他报道相似。然而,对于溶解在氯化铯基熔盐中的铈(III)离子,与已发表的文献相比存在显著差异,因为有两个还原步骤,而不是报道的单一步骤 Ce(3+)+e(-)=Ce(2+) 和 Ce(2+)+2e(-)=Ce。为了解释这一新的结果,我们对氯化铯基熔盐中铈(III)的阴极过程进行了详细研究。通过使用氧化物离子传感器进行电位滴定,确定了电解质中稳定存在的 M-O(M=La、Ce)化合物及其溶解度积。此外,通过结合理论和实验数据,构建了 M-O 稳定化合物的 E-pO(2-)(电位-氧离子)图。

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