Recovery of light and heavy rare earth elements from apatite ore using sulphuric acid leaching, solvent extraction and precipitation

被引:94
作者
Battsengel, Ariuntuya [1 ]
Batnasan, Altansukh [2 ]
Narankhuu, Ariunbolor [1 ]
Haga, Kazutoshi [2 ]
Watanabe, Yasushi [2 ]
Shibayama, Atsushi [2 ]
机构
[1] Akita Univ, Grad Sch Engn & Resource Sci, 1-1 Tegata Gakuen Machi, Akita 0108502, Japan
[2] Akita Univ, Grad Sch Int Resource Sci, 1-1 Tegata Gakuen Machi, Akita 0108502, Japan
基金
日本学术振兴会;
关键词
Rare earth elements; Fluorapatite; Leaching; Solvent extraction; Precipitation; AQUEOUS-SOLUTIONS; LANTHANIDES; KINETICS; GYPSUM; SOLUBILITIES; SEPARATION; RESOURCES; YTTRIUM; CALCIUM; CERIUM;
D O I
10.1016/j.hydromet.2018.05.024
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
Apatite is one of the important host minerals of the rare earth elements (REEs). Separation of REEs from apatite has not been studied extensively compared with other main minerals such as monazite, bastnasite and xenotime. Therefore, it is essential to develop an effective method for recovery of REEs from apatite-based ores. This paper presents the results of laboratory studies for the recovery of rare earth elements from an apatite ore sample by using sulphuric acid leaching, solvent extraction, and precipitation processes. Results showed that the most effective dissolutions of light REEs (> 85%) and heavy REEs (>89%) from the apatite ore sample were achieved with a dilute sulphuric acid solution (1 M H2SO4) at a temperature of 20 degrees C in an hour. The heavy REEs present in the pregnant leach solution were almost entirely extracted using 1.2 M di-(2-ethylhexyl) phosphoric acid (D2EHPA) as a cation exchanger, while the most light REEs remained in the raffinate. The heavy REEs loaded into the organic phase were stripped completely by 3 M H2SO4 solution. REEs remained in raffinate and stripped into the aqueous solution were precipitated as RE oxalates by the addition of 0.08 M oxalic acid.
引用
收藏
页码:100 / 109
页数:10
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