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通过干式氯化从锂辉石中提取锂的新途径。

Novel extraction route of lithium from α-spodumene by dry chlorination.

作者信息

Fosu Allen Yushark, Kanari Ndue, Bartier Danièle, Vaughan James, Chagnes Alexandre

机构信息

Université de Lorraine, CNRS, GeoRessources F-54000 Nancy France

School of Chemical Engineering, The University of Queensland Brisbane QLD 4072 Australia.

出版信息

RSC Adv. 2022 Aug 2;12(33):21468-21481. doi: 10.1039/d2ra03233c. eCollection 2022 Jul 21.

Abstract

Processing spodumene for lithium is challenging as it requires a high temperature transformation of the natural α-monoclinic form to β-tetragonal form, usually followed by acid baking and digestion. This three-step extraction process requires significant heat energy, acid, process complexity and residence time, leading to both operating and capital costs. An approach which helps to eliminate this challenge will therefore be a milestone in processing spodumene. This study, thus, investigates a direct chlorination of α-spodumene using calcium chloride followed by water leaching of the residue to recover lithium, which reduces the energy requirement and number of unit operations. HSC Chemistry software was used to simulate the process using both phases (α and β) of the mineral up to 1100 °C prior to experimental investigation. The α-form was the only polymorph identified in residues after leaching, suggesting that the extraction is directly from the α-phase. However, an initial formation of a metastable β-form followed by a fast synthesis of lithium chloride from it is also suspected. Under optimal conditions of calcium chloride/spodumene molar ratio of 2.0, and 1000 °C treatment for 60 minutes, almost 90 percent lithium chloride was extracted and 85 percent was recovered to the leach solution with the remainder exiting with the off-gas. An apparent activation energy of about 122 ± 6 kJ mol was obtained at temperatures ranging from 800 to 950 °C during the process.

摘要

锂辉石锂加工具有挑战性,因为它需要将天然α单斜晶型高温转化为β四方晶型,通常随后进行酸焙烧和消解。这种三步提取过程需要大量热能、酸、工艺复杂性和停留时间,导致运营成本和资本成本都很高。因此,一种有助于消除这一挑战的方法将是锂辉石加工的一个里程碑。因此,本研究考察了使用氯化钙对α-锂辉石进行直接氯化,然后对残渣进行水浸提以回收锂,这降低了能源需求和单元操作数量。在进行实验研究之前,使用HSC Chemistry软件在高达1100°C的温度下对矿物的两个相(α相和β相)进行了过程模拟。浸出后残渣中唯一鉴定出的多晶型物是α型,这表明提取直接来自α相。然而,也怀疑最初形成了亚稳β型,随后从中快速合成了氯化锂。在氯化钙/锂辉石摩尔比为2.0、1000°C处理60分钟的最佳条件下,几乎90%的氯化锂被提取出来,85%被回收至浸出液中,其余部分随废气排出。在此过程中,在800至950°C的温度范围内获得了约122±6 kJ/mol的表观活化能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b01/9345300/51e8ca1b3b79/d2ra03233c-f1.jpg

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