{"title":"Investigation of the electrochemical behaviour of praseodymium ions in a LiF-PrF3-Pr6O11 molten salt system","authors":"Shumei Chen, Peng Xukun, Mingyang Tan, Qiang Li, Chunfa Liao, Xu Wang, Xinyu Wu","doi":"10.1016/j.jelechem.2024.118724","DOIUrl":null,"url":null,"abstract":"<div><div>Understanding the electrochemical of paseodymium ions in molten salt is essential to improve electrolytic efficiency. To elucidate the electroreduction mechanism of praseodymium ions and overcome the limitations associated with regulating the yield of praseodymium metal in the industrial praseodymium electrolysis process, the electrochemical behaviour of praseodymium on the W working electrode surface in the LiF-PrF<sub>3</sub>-Pr<sub>6</sub>O<sub>11</sub> molten salt system was determined by square–wave voltammetry, chronoamperometry, cyclic voltammetry and potentiometry analyses. The results indicated that the reduction of Pr<sup>3+</sup> on the W cathode is a one-step quasireversible Pr<sup>3+</sup>/Pr reduction process controlled by diffusion of the LiF-PrF<sub>3</sub> and (LiF-PrF<sub>3</sub>)<sub>eut</sub>-Pr<sub>6</sub>O<sub>11</sub> electrolytes at 1223 K Pr<sup>3+</sup> in the LiF-PrF<sub>3</sub>-Pr<sub>6</sub>O<sub>11</sub> molten salt has a diffusion coefficient of <em>D<sub>Pr3+/Pr</sub></em> = 0.20 × 10<sup>−8</sup>–4.11 × 10<sup>−8</sup> cm<sup>2</sup>·s<sup>−1</sup>. The incorporation of Pr<sub>6</sub>O<sub>11</sub> increased the electrochemical activity of Pr<sup>3+</sup> in the LiF-PrF<sub>3</sub> system. Pr crystallization on the W electrode was achieved by three-dimensional progressive nucleation.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"974 ","pages":"Article 118724"},"PeriodicalIF":4.1000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665724007021","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Understanding the electrochemical of paseodymium ions in molten salt is essential to improve electrolytic efficiency. To elucidate the electroreduction mechanism of praseodymium ions and overcome the limitations associated with regulating the yield of praseodymium metal in the industrial praseodymium electrolysis process, the electrochemical behaviour of praseodymium on the W working electrode surface in the LiF-PrF3-Pr6O11 molten salt system was determined by square–wave voltammetry, chronoamperometry, cyclic voltammetry and potentiometry analyses. The results indicated that the reduction of Pr3+ on the W cathode is a one-step quasireversible Pr3+/Pr reduction process controlled by diffusion of the LiF-PrF3 and (LiF-PrF3)eut-Pr6O11 electrolytes at 1223 K Pr3+ in the LiF-PrF3-Pr6O11 molten salt has a diffusion coefficient of DPr3+/Pr = 0.20 × 10−8–4.11 × 10−8 cm2·s−1. The incorporation of Pr6O11 increased the electrochemical activity of Pr3+ in the LiF-PrF3 system. Pr crystallization on the W electrode was achieved by three-dimensional progressive nucleation.
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
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