Solvent extraction kinetics of Sm(III), Eu(III) and Gd(III) with 2-ethylhexyl phosphoric acid-2-ethylhexyl ester

被引:10
|
作者
Chen, Zhuo [1 ]
Wang, Yundong [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, State Key Lab Chem Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Rare earth elements (REEs); Extraction; Kinetics; Model; CONSTANT INTERFACIAL CELL; LAMINAR-FLOW; CHLORIDE MEDIUM; IONIC LIQUIDS; D2EHPA; ACID; SEPARATION; ELEMENTS; SYSTEMS; LA(III);
D O I
10.1016/j.cjche.2017.06.022
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Solvent extraction kinetics of Sm (III), Eu (III) and Gd (III) from hydrochloric acid have been focused on using 2-ethylhexyl phosphoric acid-2-ethylhexyl ester (P507) with Anordning for Kontinuerlig Undersokning av Fordelningsfaktore vid Vatske Extraction (AKUFVE). Compared with the conventional set-up, some advantages emerge obviously, for example, fast phase separation, easy operation and convenience of kinetic data acquisition. First of all, the extraction mechanism was discussed based on the dimeric model of P507. Secondly, the effects of stirring speed were investigated and 420 r . min(-1) was determined of the following experiments. The effects of pH, concentration of rare earth elements (REEs) and P507 on the extraction rate were analyzed. The results indicated that the extraction mechanism changed with the increasing concentration of P507. Then, the experiments with different temperature were carried out. It turned out that the values of apparent activation energy (E-a) for Sm(III), Eu(III) and Gd(III) extracted by P507 were 26.80 kJ.mol(-1), 13.40 kJ.mol(-1) and 11.10 kJ . mol(-1) respectively, the resistance of the entire process was limited by diffusion or both of diffusion and reaction. Finally, the correlation equations were obtained, and the theoretical results fit with the experimental data well, most relative error was within +/- 30%. (C) 2017 The Chemical Industry and Engineering Society of China, and Chemical Industry Press. All rights reserved.
引用
收藏
页码:317 / 321
页数:5
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