以水为唯一溶剂从 NMC 电池中回收材料。

IF 8 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Journal of Environmental Management Pub Date : 2024-07-09 DOI:10.1016/j.jenvman.2024.121710
Anirudha Karati , Prashant P. Gargh , Sabyasachi Paul , Sourav Das , Pranav Shrotriya , Ikenna C. Nlebedim
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引用次数: 0

摘要

我们报告了一种无害环境的大容量镍锰钴(NMC)电池回收方法,即通过电化学方法将锂浓缩在阳极上,然后仅用水进行回收。镍锰钴袋式电池的循环表明,在 5C 充电速率下,锂回收的潜力最大。将从放电和拆卸电池中提取的阳极浸没在去离子水中,可使锂溶解并从铜箔中回收石墨。在 4C 充电速率下循环使用的 NMC 袋装电池中,每 100 毫克阳极、铜集流体和隔膜最多可提取 13 毫克锂盐。通过 X 射线光电子能谱测定,从低 C 速率循环电池中提取的锂盐富含碳酸锂,而从高 C 速率循环电池中提取的锂盐富含锂氧化物和过氧化物。本方法可成功用于回收所有袋装电池组件:锂、石墨、铜和铝集流体、隔膜以及正极活性材料。
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Materials recovery from NMC batteries with water as the sole solvent

We report an environmentally benign recycling approach for large-capacity nickel manganese cobalt (NMC) batteries through the electrochemical concentration of lithium on the anode and subsequent recovery with only water. Cycling of the NMC pouch cells indicated the potential for maximum lithium recovery at a 5C charging rate. The anodes extracted from discharged and disassembled cells were submerged in deionized water, resulting in lithium dissolution and graphite recovery from the copper foils. A maximum of 13 mg of lithium salts per 100 mg of the anode, copper current collector, and separator was obtained from NMC pouch cell cycled at a 4C charging rate. The lithium salts extracted from batteries cycled at low C-rates were richer in lithium carbonate, while the salts from batteries cycled at high C-rates were richer in lithium oxides and peroxides, as determined by X-Ray photoelectron spectroscopy. The present method can be successfully used to recover all the pouch cell components: lithium, graphite, copper, and aluminum current collectors, separator, and the cathode active material.

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来源期刊
Journal of Environmental Management
Journal of Environmental Management 环境科学-环境科学
CiteScore
13.70
自引率
5.70%
发文量
2477
审稿时长
84 days
期刊介绍: The Journal of Environmental Management is a journal for the publication of peer reviewed, original research for all aspects of management and the managed use of the environment, both natural and man-made.Critical review articles are also welcome; submission of these is strongly encouraged.
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