Recycling metals from lithium ion battery by mechanical separation and vacuum metallurgy

[Display omitted] •No any chemical additives are added in whole recycling process.•High value-added Li2CO3 and Mn3O4 are in situ recovered without any additive.•Mechanical treatment is used in the recovery process to improve the handling capacity. The large-batch application of lithium ion batteries...

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Veröffentlicht in:Journal of hazardous materials 2017-09, Vol.338, p.124-131
Hauptverfasser: Xiao, Jiefeng, Li, Jia, Xu, Zhengming
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] •No any chemical additives are added in whole recycling process.•High value-added Li2CO3 and Mn3O4 are in situ recovered without any additive.•Mechanical treatment is used in the recovery process to improve the handling capacity. The large-batch application of lithium ion batteries leads to the mass production of spent batteries. So the enhancement of disposal ability of spent lithium ion batteries is becoming very urgent. This study proposes an integrated process to handle bulk spent lithium manganese (LiMn2O4) batteries to in situ recycle high value-added products without any additives. By mechanical separation, the mixed electrode materials mainly including binder, graphite and LiMn2O4 are firstly obtained from spent batteries. Then, the reaction characteristics for the oxygen-free roasting of mixed electrode materials are analyzed. And the results show that mixed electrode materials can be in situ converted into manganese oxide (MnO) and lithium carbonate (Li2CO3) at 1073K for 45min. In this process, the binder is evaporated and decomposed into gaseous products which can be collected to avoid disposal cost. Finally, 91.30% of Li resource as Li2CO3 is leached from roasted powders by water and then high value-added Li2CO3 crystals are further gained by evaporating the filter liquid. The filter residues are burned in air to remove the graphite and the final residues as manganous-manganic oxide (Mn3O4) is obtained.
ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2017.05.024