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首页> 外文期刊>Hydrometallurgy >Purification of synthetic laterite leach solution by solvent extraction using D2EHPA
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Purification of synthetic laterite leach solution by solvent extraction using D2EHPA

机译:使用D2EHPA进行溶剂萃取纯化合成红土浸出液

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摘要

The world mineral industry is experiencing an unprecedented interest in nickel-cobalt extraction from laterite ores through acid pressure leach and SX-EW processes. The recovery of cobalt and nickel from the leach solution through direct solvent extraction is of great interest as this would result in significant capital and operating cost savings. In the direct solvent extraction approach, the separation of zinc, calcium, copper and, in particular, manganese from cobalt and nickel is highly important. A series of shakeout tests was undertaken to investigate the fundamentals of the separation of the above impurities from cobalt and nickel using di-2-ethylhexyl phosphoric acid (D2EHPA) in kerosene.D2EHPA p11-extraction isotherms from solutions each containing a single element showed that the extraction order for the seven elements of interest as a function of pH_(50) was Zn(2+)> Ca(2+)> Mn(2+)> Cu(2+)> Co(2+)> Ni(2+)> Mg(2+). This confirmed that manganese would be extracted from sulfate solution ahead of cobalt and nickel. Extraction isotherms from solutions containing Zn, Ca, Mn, Cu, Co, Ni and Mg showed that the separation of zinc and calcium from the other elements was not difficult and the separation of copper and manganese from cobalt and nickel was possible.The separation of manganese from cobalt and nickel by D2EHPA in kerosene was affected by temperature and pH. At pH 3.0, better separation of manganese from cobalt and nickel was achieved at room temperature (23deg C). At pH 3.5, better separation of manganese from cobalt was achieved at room temperature (23deg C). However, better separation of manganese from nickel could be obtained at elevated temperatures (40-60deg C). The McCabe-Thiele diagram for the system showed that at pH 3.5 and 40deg C, two theoretical extraction stages at A/O ratio 1:1 were needed to extract 99.9percent manganese from the aqueous solution and to reduce the manganese concentration from 2.0 g/L to 3 ppm.Multiple stage extraction with fresh aqueous solution showed that cobalt and nickel were crowded out by zinc and manganese. Multiple stage extraction with fresh organic solution showed that manganese and copper in the aqueous solution were eliminated. Multiple stage scrubbing of the loaded organic solution with manganese solution indicated that after one stage of contact, only about 3 ppm cobalt and nickel were present in the organic solution.
机译:世界矿产行业对通过酸压浸提和SX-EW工艺从红土矿石中提取镍钴的兴趣空前高涨。通过直接溶剂萃取从浸出溶液中回收钴和镍引起了极大的兴趣,因为这将节省大量的资金和运营成本。在直接溶剂萃取方法中,从钴和镍中分离锌,钙,铜,尤其是锰非常重要。进行了一系列摇晃试验,以研究在煤油中使用二-2-乙基己基磷酸(D2EHPA)从钴和镍中分离上述杂质的基本原理.D2EHPA p11等温线从均含单个元素的溶液中萃取的等温线表明:七个目标元素的提取顺序与pH_(50)的关系为Zn(2 +)> Ca(2 +)> Mn(2 +)> Cu(2 +)> Co(2 +)> Ni( 2 +)> Mg(2+)。这证实了将从钴和镍之前的硫酸盐溶液中提取锰。从含锌,钙,锰,铜,钴,镍和镁的溶液中提取等温线表明,从其他元素中分离锌和钙并不困难,并且可以从钴和镍中分离铜和锰。 D2EHPA在煤油中通过钴和镍制得的锰受温度和pH值的影响。在pH 3.0下,室温(23℃)下锰与钴和镍的分离效果更好。在pH 3.5下,室温(23℃)下锰与钴的分离效果更好。但是,在高温(40-60摄氏度)下,锰与镍的分离效果更好。该系统的McCabe-Thiele图显示,在pH 3.5和40°C下,需要两个理论萃取阶段(A / O比例为1:1)才能从水溶液中萃取99.9%的锰并将锰浓度从2.0 g / L至3 ppm。用新鲜水溶液进行多步萃取表明,钴和镍被锌和锰挤出。用新鲜有机溶液进行多步萃取表明,消除了水溶液中的锰和铜。用锰溶液对负载的有机溶液进行多级洗涤表明,在接触的一级之后,有机溶液中仅存在约3 ppm的钴和镍。

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