TY - JOUR
T1 - Exploration of sequential mechanochemical activation and complexation leaching for enhanced recovery of valuable metals from spent lithium-ion batteries
AU - Gao, Guilan
AU - Luo, Xingmin
AU - Liu, Nuo
AU - Yang, Tianyi
AU - Zhang, Xiaojiao
AU - Guan, Jie
AU - Chen, Shuai
AU - Zhang, Rui-Qin
AU - Guo, Yaoguang
PY - 2023/9
Y1 - 2023/9
N2 - An efficient sequential mechanochemical activation and complexation leaching for enhanced recovery of valuable metals from spent lithium-ion batteries was explored. The cathode material of lithium cobalt oxide (LiCoO2) was firstly ground in a planetary ball mill, and then diluted into an ethylene diamine tetraacetic acid (EDTA) and hydrogen peroxide (H2O2) leaching solution. One hundred percent of cobalt (Co) and 98.2% of lithium (Li) could be leached from the activated LiCoO2 materials compared with the non-activated (the leaching efficiencies of 7.9% for Co and 4.1% for Li), indicating that the mechanochemical activation process could significantly improve the EDTA/H2O2 mixed liquor complexation leaching of valuable metals from spent LIBs. The involved kinetics and mechanism were explored by carrying out characterization and theoretical calculations. Results demonstrated that an exponential kinetic model could well describe the mechanochemical process, and the Avrami equation leaching model provided a satisfactory fitting relevant for the subsequent improved leaching process. The breakage of the layer structure, the Co–O-Co unit, and the LiCoO2 surface, along with a decrease in activation energy, resulted in the enhancement of the leaching efficiency following mechanochemical activation. Enhanced leaching of Co was owing to the reduction of Co(III) to Co(II) instantaneously forming Co(II)-EDTA chelates. The acidity of EDTA and H2O2 promoted upgrade dissolution of lithium after mechanochemical activation for LiCoO2. This efficient and benign recovery process is of great significance for recycling spent LIBs. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
AB - An efficient sequential mechanochemical activation and complexation leaching for enhanced recovery of valuable metals from spent lithium-ion batteries was explored. The cathode material of lithium cobalt oxide (LiCoO2) was firstly ground in a planetary ball mill, and then diluted into an ethylene diamine tetraacetic acid (EDTA) and hydrogen peroxide (H2O2) leaching solution. One hundred percent of cobalt (Co) and 98.2% of lithium (Li) could be leached from the activated LiCoO2 materials compared with the non-activated (the leaching efficiencies of 7.9% for Co and 4.1% for Li), indicating that the mechanochemical activation process could significantly improve the EDTA/H2O2 mixed liquor complexation leaching of valuable metals from spent LIBs. The involved kinetics and mechanism were explored by carrying out characterization and theoretical calculations. Results demonstrated that an exponential kinetic model could well describe the mechanochemical process, and the Avrami equation leaching model provided a satisfactory fitting relevant for the subsequent improved leaching process. The breakage of the layer structure, the Co–O-Co unit, and the LiCoO2 surface, along with a decrease in activation energy, resulted in the enhancement of the leaching efficiency following mechanochemical activation. Enhanced leaching of Co was owing to the reduction of Co(III) to Co(II) instantaneously forming Co(II)-EDTA chelates. The acidity of EDTA and H2O2 promoted upgrade dissolution of lithium after mechanochemical activation for LiCoO2. This efficient and benign recovery process is of great significance for recycling spent LIBs. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
KW - Complexation
KW - Mechanochemical activation
KW - Metal extraction
KW - Theoretical calculation
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UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85164147249&origin=recordpage
U2 - 10.1007/s11581-023-05098-5
DO - 10.1007/s11581-023-05098-5
M3 - RGC 21 - Publication in refereed journal
SN - 0947-7047
VL - 29
SP - 3585
EP - 3596
JO - Ionics
JF - Ionics
IS - 9
ER -