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机械化学辅助过硫酸盐活化用于从废旧锂离子电池中轻松回收金属。

Mechanochemically assisted persulfate activation for the facile recovery of metals from spent lithium ion batteries.

作者信息

Liang Zhilin, Peng Gangwei, Hu Jingping, Hou Huijie, Cai Chen, Yang Xiaorong, Chen Sijing, Liu Lu, Liang Sha, Xiao Keke, Yuan Shushan, Zhou Shoubin, Yang Jiakuan

机构信息

School of Environmental Science and Engineering, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan, Hubei, 430074, P.R.China; Hubei Provincial Engineering Laboratory of Solid Waste Treatment, Disposal and Recycling, 1037 Luoyu Road, Wuhan, Hubei, 430074, P.R.China.

School of Environmental Science and Engineering, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan, Hubei, 430074, P.R.China; Hubei Provincial Engineering Laboratory of Solid Waste Treatment, Disposal and Recycling, 1037 Luoyu Road, Wuhan, Hubei, 430074, P.R.China; State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan, Hubei, 430074, P.R.China.

出版信息

Waste Manag. 2022 Aug 1;150:290-300. doi: 10.1016/j.wasman.2022.07.014. Epub 2022 Jul 21.

Abstract

A novel mechanochemically assisted persulfate activation method was proposed in this study to enhance the leaching of valuable metals from lithium-ion batteries by combining ball-milling, advanced oxidation processes and sucrose reduction. By optimizing leaching parameters including temperature, pH, milling time and solid-to-liquid ratio, high leaching efficiencies of 97.1%, 94.0%, 87.6% and 93.8% can be achieved for Li, Ni, Co and Mn respectively. In the mechanochemical process, the breakage of covalent bonds in cathode material is facilitated by free radicals generated from zero valent iron activated ammonia persulfate as well as mechanochemical activation. To further explore the role of free radicals, the mechanism of ammonia persulfate activation by zero valent iron was elucidated, and SO was identified as the dominant reactive oxygen species in the mechanochemical process. Meanwhile, the synergistic effect of mechanochemically driven crystal dissolution and sulfate radical facilitated bond cleavage was revealed by ab initio molecular dynamics simulation. Moreover, the released metal was reduced by sucrose to a lower valent state of high solubility to promote transfer to the aqueous phase during the subsequent leaching process with dilute sulfuric acid. In this work, the insight on the mechanism of mechanochemical processes strengthened by free radicals may provide an inspiration for the recovery of valuable metals from LIBs.

摘要

本研究提出了一种新型机械化学辅助过硫酸盐活化方法,通过结合球磨、高级氧化过程和蔗糖还原,提高锂离子电池中贵金属的浸出率。通过优化浸出参数,包括温度、pH值、研磨时间和固液比,锂、镍、钴和锰的浸出效率分别可达到97.1%、94.0%、87.6%和93.8%。在机械化学过程中,零价铁活化过硫酸铵产生的自由基以及机械化学活化促进了正极材料中共价键的断裂。为了进一步探究自由基的作用,阐明了零价铁活化过硫酸铵的机理,并确定硫酸根自由基是机械化学过程中的主要活性氧物种。同时,通过从头算分子动力学模拟揭示了机械化学驱动的晶体溶解和硫酸根自由基促进的键断裂的协同效应。此外,在随后用稀硫酸浸出过程中,释放出的金属被蔗糖还原为高溶解度的低价态,以促进其转移到水相中。在这项工作中,对自由基强化机械化学过程机理的深入了解可能为从锂离子电池中回收贵金属提供启示。

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