Glucose oxidase-based biocatalytic acid-leaching process for recovering valuable metals from spent lithium-ion batteries

被引:43
作者
Fan, Ersha [1 ]
Shi, Pingchuan [1 ]
Zhang, Xiaoxiao [1 ]
Lin, Jiao [1 ]
Wu, Feng [1 ,2 ]
Li, Li [1 ,2 ]
Chen, Renjie [1 ,2 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing Key Lab Environm Sci & Engn, Beijing 100081, Peoples R China
[2] Collaborat Innovat Ctr Elect Vehicles, Beijing, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Gluconic acid; Glucose oxidase; Biocatalysis; Spent LIBs; Leaching; HYDROMETALLURGICAL PROCESS; SELECTIVE RECOVERY; CATHODE MATERIALS; COBALT; KINETICS; LI; OPTIMIZATION;
D O I
10.1016/j.wasman.2020.06.047
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
An environmentally benign leaching process for recovering valuable metals from the cathodes of spent lithium-ion batteries was developed. Glucose oxidase produced by Aspergillus niger can oxidize glucose to give the leaching agent gluconic acid. The presence of gluconic acid was proven by mass spectrometry. The cathode material morphology was characterized by X-ray diffractometry and scanning electron microscopy, and the efficiencies with which valuable metals were leached from the Li(NixCoyMnz)O-2 material were determined by inductively coupled plasma optical emission spectroscopy. More than 95% of the Co, Li, Mn, and Ni were leached from spent lithium-ion batteries using a solid/liquid ratio of 30 g/L, 1 M gluconic acid leaching solution, a 1 vol% H2O2 reductant solution, a temperature of 70 degrees C, and a reaction time of 80 min. The leaching kinetics were perfectly described by the Avrami equation. The apparent activation energies for leaching of Li, Ni, Co, and Mn were determined as 41.76, 42.84, 43.59, and 45.35 kJ/mol, respectively, indicating that the surface chemical reaction is the rate-controlling step during this leaching process. This mild biocatalysis-aided acid leaching process is a promising method for effectively recovering valuable metals from spent lithium-ion batteries. (C) 2020 Published by Elsevier Ltd.
引用
收藏
页码:166 / 173
页数:8
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