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Investigation on electrochemical removal of CaCl2 from LiCl-KCl melts ( EI收录)
文献类型:期刊文献
英文题名:Investigation on electrochemical removal of CaCl2 from LiCl-KCl melts
作者:Shen, Miao[1]; Li, Bing[1]; Yu, Jianguo[1]
机构:[1] National Reaction Engineering Key Laboratories, National Engineering Research Center for Integrated Utilization of Salt Lake Resource, East China University of Science and Technology, Shanghai 200237, China
年份:2012
卷号:62
起止页码:153
外文期刊名:Electrochimica Acta
收录:EI(收录号:20120514724816)
语种:英文
外文关键词:Calcium - Lithium compounds - Removal - Deposition rates - Ions - Reduction - Chlorine compounds - Electrolysis - Electrodes - Potassium compounds
摘要:In order to investigate the possibility of electroseparation of CaCl 2 from CaCl2-LiCl-KCl melts prior to Li+ reduction, Ca2+ and Li+ ions reduction potentials in the melts were investigated by cyclic voltammetry (CV) and chronopotentiometry (CP) on both a tungsten and a tin electrodes. The potential difference between the two ions in CaCl2 (0.5 wt%)-LiCl-KCl melts was 0.2 V at 953 K analyzed by CV. About 0.4 V reduction potential difference between Ca 2+ and Li+ ions was observed on chronopotentiograms recorded on a tungsten electrode in CaCl2 (2.0 wt%)-LiCl-KCl melts either at 723 K or 953 K, which can meet the requirements of total electroseparation. Tin electrode can shift the reduction potentials of Ca 2+ and Li+ to more positive ones and also can improve Ca deposition rate and removal efficiency. After 3.0 h electrolysis on solid tungsten at -3.4 V vs. Cl2/Cl- and liquid tin cathode at -3.0 V vs. Cl2/Cl-, the Ca/Li (weight ratio) in the melts changed from 3/25 before electrolysis to 2.6/25 and 0.76/25 respectively, analyzed by ICP. Under stirring, even higher removal rates of 83.65 wt% and 94.66 wt%, corresponding to 0.54/25 and 0.16/25 of Ca/Li have been obtained for 3.0 h and 6.0 h electrolysis at -3.0 V vs. Cl2/Cl- on a tin electrode. Clearly, stirring availably increases the Ca2+ ions diffusion rate and its electrochemical reaction rate. ? 2011 Elsevier Ltd.
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