Yu Lin, Zhao Siying, Guo Jianping, Si Mengying, Liao Qi, Wang Yunyan, Li Qingzhu, Yang Zhihui, Yang Weichun
School of Metallurgy and Environment, Central South University, Changsha 410083, China.
School of Metallurgy and Environment, Central South University, Changsha 410083, China; Chinese National Engineering Research Centre for Control & Treatment of Heavy Metal Pollution, Changsha 410083, China.
Waste Manag. 2025 Aug 1;204:114965. doi: 10.1016/j.wasman.2025.114965. Epub 2025 Jun 19.
Lithium smelting slag (LSS), a hazardous by-product from lithium carbonate production, present potential environmental risks due to its geochemically association with, thallium (Tl)-a highly toxic element activated during lithium extraction process. This study developed a novel NHOH·HCl-oxalic acid-citric acid reductive leaching system for efficient Tl detoxification from LSS. 91.7 % Tl leaching rate was achieved under optimized conditions: oxalic acid/citric acid molar ratio 1:1, the molar ratio of NHOH·HCl/oxalic acid-citric acid molar ratio 3:1, compound leaching agent concentration 0.48 mol L (NHOH·HCl/oxalic acid-citric acid concentration 0.36 mol L/0.06 mol L-0.06 mol L), liquid-solid ratio 5.5:1, temperature 50 °C, and a NHOH·HCl concentration of 0.1 mol L during the enhanced leaching step. The toxic leaching concentration of Tl in the leached residue was less than the general industrial solid waste Class I standard threshold (5 μg L). It is revealed that Tl in LSS mainly existed in a reducible fraction (bound to Fe-Mn oxides), and encapsulated within gypsum phase. The synergistic leaching mechanism of Tl from LSS by NHOH·HCl-oxalic acid-citric acid reductive leaching system involved gypsum phase dissolution by citric acid and oxalic acid synergistically, and reductive release of Tl bound to iron-manganese oxides mainly by NHOH·HCl. Leaching kinetics and thermodynamics studies confirmed that the reductive leaching process follows the shrinking core model under diffusion control, and the low activation energy for Tl leaching (18.934 kJ/mol) further confirms that Tl leaching kinetics are governed by reagent transport through boundary layers rather than chemical bond breaking. This work established a green, efficient, and economical approach for the Tl detoxification in LSS.
锂冶炼渣(LSS)是碳酸锂生产过程中产生的一种有害副产品,由于其在地球化学上与铊(Tl)相关联,而铊是锂提取过程中被活化的剧毒元素,因此存在潜在的环境风险。本研究开发了一种新型的NHOH·HCl - 草酸 - 柠檬酸还原浸出体系,用于从锂冶炼渣中高效去除铊。在优化条件下,铊的浸出率达到了91.7%:草酸/柠檬酸摩尔比为1:1,NHOH·HCl/草酸 - 柠檬酸摩尔比为3:1,复合浸出剂浓度为0.48 mol/L(NHOH·HCl/草酸 - 柠檬酸浓度为0.36 mol/L/0.06 mol/L - 0.06 mol/L),液固比为5.5:1,温度为50℃,强化浸出步骤中NHOH·HCl浓度为0.1 mol/L。浸出渣中铊的有毒浸出浓度低于一般工业固体废物一类标准阈值(5 μg/L)。研究表明,锂冶炼渣中的铊主要以可还原态(与铁 - 锰氧化物结合)存在,并包裹在石膏相中。NHOH·HCl - 草酸 - 柠檬酸还原浸出体系对锂冶炼渣中铊的协同浸出机制包括柠檬酸和草酸协同溶解石膏相,以及主要由NHOH·HCl使与铁 - 锰氧化物结合的铊发生还原释放。浸出动力学和热力学研究证实,还原浸出过程遵循扩散控制下的收缩核模型,铊浸出的低活化能(18.934 kJ/mol)进一步证实铊浸出动力学受试剂通过边界层的传输控制,而非化学键断裂。本工作建立了一种绿色、高效且经济的锂冶炼渣中铊解毒方法。