开发概念性直接溶剂萃取(DSX)路线和流程图,以生产红土硫酸浸出液中的纯化浓缩钴和镍溶液

IF 4.8 2区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Hydrometallurgy Pub Date : 2024-04-23 DOI:10.1016/j.hydromet.2024.106321
Alexandre Silva Guimarães , Georgio Patrício de Souza Resende , Iranildes Daniel dos Santos , Marcelo Borges Mansur
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引用次数: 0

摘要

直接溶剂萃取(DSX)被用于从含有 Ca、Cu、Mg、Mn 和 Zn 等杂质的合成硫液中生产纯化的浓镍和浓钴溶液,该溶液模拟了硫化-焙烧-浸出过程中铁、铝和铬沉淀后得到的溶液。商用萃取剂 Versatic 10、Cyanex 272、D2EHPA 和 TBP 被用于 3 个溶剂萃取回路。在第一回路中,温度为 40 °C,在 O/A = 2:1 和 pH 值为 6.5 的条件下,Versatic 10(0.5 M)在 3 个阶段中完全萃取了铜、锌、镍和钴,剩余的锰(萃取了 54%)以及大部分的钙和镁留在了尾渣中。在 O/A = 5:1 和 pH 值为 6.5 的条件下,共萃取的 Ca 和 Mg 分 2 个阶段从负载的 Versatic 10 中完全洗脱。在 O/A = 9:1 的条件下,使用合成镍废电解液(60 g/L 镍,2 M H2SO4)分两个阶段从 Versatic 10 萃取液中剥离出其他金属。在 50 °C的条件下,使用Cyanex 272(0.64 M)对带液进行第二次循环。需要三个阶段才能完全萃取出钴、铜、锰和锌(O/A = 2:1,pH 值为 4),而含有 82 克/升镍的废液被认为适合电积。在 O/A = 5:1 和 pH 值为 4 的条件下,只需一个阶段就能将共萃取的 Ni(II) 从负载的 Cyanex 272 中完全洗脱出来。在 O/A = 10:1 的条件下,使用合成的 Co 废电解质(45 g/L Co,1 M H2SO4),分两个阶段从洗脱负载的 Cyanex 272 中剥离出所有的 Co、Cu、Mn 和 Zn。含有 58.4 g/L Co 的废液被送入第三回路,使用 D2EHPA(0.6 M)+ TBP(0.73 M)协同系统,在 50 °C 下运行。在 pH 值为 2 和 O/A = 1:3 的条件下,D2EHPA + TBP 系统分两个阶段完全萃取了锌(II),而在 pH 值为 3.5 和 O/A = 2:1 的条件下,分两个阶段完全萃取了贫锌废液中的锰(II)和铜(II)。含 58.3 g/L Co 的废液被认为适合电积。在 O/A = 2.5:1 的条件下,使用 1 M H2SO4 分 3 个阶段从负载的 D2EHPA + TBP 中剥离出铜(II)、锰(II)和锌(II)。对所有回路中萃取剂的实际摩尔数和表观平衡常数进行了估算。报告还提供了纯化概念路线的流程图。
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Development of a conceptual direct solvent extraction (DSX) route and a flowsheet to produce purified concentrated cobalt and nickel solutions representing sulfuric acid leach liquor of laterite

Direct solvent extraction (DSX) was applied to produce purified concentrated Ni and Co solutions from a synthetic sulfuric liquor containing Ca, Cu, Mg, Mn, and Zn as impurities, which simulates the solution obtained by the sulfation-roasting-leaching process after precipitation of Fe, Al, and Cr. The commercial extractants Versatic 10, Cyanex 272, D2EHPA, TBP were used in 3 solvent extraction circuits. In the first circuit, operated at 40 °C, Versatic 10 (0.5 M) fully extracted Cu, Zn, Ni, and Co in 3 stages at O/A = 2:1, and pH 6.5, leaving remaining Mn (54% was extracted) and most of the Ca and Mg in the raffinate. The co-extracted Ca and Mg were fully scrubbed off the loaded Versatic 10 in 2 stages at O/A = 5:1, and pH 6.5. The other metals were stripped out of the Versatic 10 extract using a synthetic Ni spent electrolyte (60 g/L Ni, 2 M H2SO4) in 2 stages at O/A = 9:1. This loaded strip liquor was subjected to a second circuit with Cyanex 272 (0.64 M) operated at 50 °C. Three stages were required to fully extract Co, Cu, Mn, and Zn (O/A = 2:1, pH 4), whereas the raffinate containing 82 g/L Ni was deemed suitable for electrowinning. The co-extracted Ni(II) was fully scrubbed off the loaded Cyanex 272 in only 1 stage at O/A = 5:1, and pH 4. All Co, Cu, Mn, and Zn were stripped out from the scrubbed loaded Cyanex 272 in 2 stages at O/A = 10:1 using a synthetic Co spent electrolyte (45 g/L Co, 1 M H2SO4). The raffinate containing 58.4 g/L Co was submitted to a third circuit using a D2EHPA (0.6 M) + TBP (0.73 M) synergistic system operated at 50 °C. Zinc(II) was fully extracted by the D2EHPA + TBP system in 2 stages at pH 2 and O/A = 1:3, while Mn(II) and Cu(II) were fully extracted from the Zn-depleted raffinate in 2 stages at pH 3.5 and O/A = 2:1. The raffinate containing 58.3 g/L Co was deemed suitable for electrowinning. Copper(II), Mn(II), and Zn(II) were stripped out from the loaded D2EHPA + TBP in 3 stages at O/A = 2.5:1 using 1 M H2SO4. The real number of moles of extractants involved in the extractions and apparent equilibrium constants were estimated for all circuits. A flowsheet of the purification conceptual route is presented.

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来源期刊
Hydrometallurgy
Hydrometallurgy 工程技术-冶金工程
CiteScore
9.50
自引率
6.40%
发文量
144
审稿时长
3.4 months
期刊介绍: Hydrometallurgy aims to compile studies on novel processes, process design, chemistry, modelling, control, economics and interfaces between unit operations, and to provide a forum for discussions on case histories and operational difficulties. Topics covered include: leaching of metal values by chemical reagents or bacterial action at ambient or elevated pressures and temperatures; separation of solids from leach liquors; removal of impurities and recovery of metal values by precipitation, ion exchange, solvent extraction, gaseous reduction, cementation, electro-winning and electro-refining; pre-treatment of ores by roasting or chemical treatments such as halogenation or reduction; recycling of reagents and treatment of effluents.
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