4.7 Article

Novel strategy towards in-situ recycling of valuable metals from spent lithium-ion batteries through endogenous advanced oxidation process

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 457, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jhazmat.2023.131818

关键词

Spent lithium-ion batteries; Valuable metals; Pretreatment; Endogenous advanced oxidation process; Exfoliation mechanism

向作者/读者索取更多资源

In this study, a self-activated and ultrasonic-induced endogenous advanced oxidation process (EAOP) was developed for the selective removal of PVDF and in-situ extraction of Li from waste LiFePO4 (LFP) to improve the recycling efficiency of valuable metals from spent LIBs. The optimized conditions allowed for the detachment of over 99 wt% of cathode materials from Al foils, with high purity Al foils and Li2CO3 (>99.9% purity) recovered. The ultrasonic induction of S2O82- by LFP generated an increased amount of SO4•− radicals, which attacked PVDF binders for degradation, and further oxidation of these radicals achieved complete ionization of Li from LFP powders. This work presents a novel strategy for efficient and in-situ recycling of valuable metals from spent LIBs with minimal environmental impact.
Efficient and sustainable recycling of metal resources from spent lithium-ion batteries (LIBs) is critical for the metal resources security and environment protection. However, the intact exfoliation of cathode materials (CMs) from current collectors (Al foils) and selective extraction of Li towards the in-situ and sustainable recycling of cathodes from spent LIBs are still pending issues. A self-activated and ultrasonic-induced endogenous advanced oxidation process (EAOP) was proposed in this study for selective removal of PVDF and in-situ extraction of Li from CMs of waste LiFePO4 (LFP) to address the above issues. Over 99 wt% CMs can be detached from Al foils after EAOP treatment under the optimized operation conditions. High purity of Al foil can be directly recycled as metallic forms and nearly 100 % of Li can be in-situ extracted from the detached CMs and then recovered as Li2CO3 (>99.9 % in purity). With induction and reinforcement of ultrasonic, S2O82-was self-activated by LFP to generate an increased amount of SO4 & BULL; radicals that will attack the PVDF binders to ensure their degradation. The degradation pathway of PVDF and density functional theory (DFT) calculation can also support the analytical and experimental results. Then, the complete and in-situ ionization of Li can be achieved by the further oxidization of SO4 & BULL;� radicals from LFP powders. This work provides a novel strategy towards efficient and in-situ recycling of valuable metals from spent LIBs with minimized environmental footprint.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据