Flash Joule Heating Upgraded Li Leaching of Residues from Spent LiFePO4 Cathodes for Superior Catalytic Degradation of Pollutants

浸出(土壤学) 催化作用 阴极 材料科学 化学工程 热解 降级(电信) 化学 环境科学 有机化学 计算机科学 电信 工程类 物理化学 土壤科学 土壤水分
作者
Hua Shang,Wenting Yang,Zhelin He,Jiewen Luo,Fengbo Yu,Chao Jia,Xiangdong Zhu
出处
期刊:ACS ES&T engineering [American Chemical Society]
卷期号:5 (3): 724-731 被引量:1
标识
DOI:10.1021/acsestengg.4c00645
摘要

The rapid development of new energy sources has produced large quantities of battery-derived spent LiFePO4 cathodes (SLICs), whose recycling has attracted growing attention in recent years. Previous SLICs recycling approaches have focused on the recovery of Li resources, neglecting the Fe-enriched residues obtained after Li recovery. Generally, Fe-enriched residues cannot be effectively converted to active Fe species using traditional methods, thereby limiting their upgrading. This study uses the emerging flash Joule heating (FJH) technology to upgrade Fe-enriched residues, and its performance was independent of Li leaching pathways. Common Li leaching protocols were initially applied to extract Li and produce residues enriched with FeC2O4, FeO(OH), FePO4, and Fe3O4. Subsequently, ultrahigh temperature and electrical stripping were performed by FJH treatment, promoting Fe–O bond breakage within the various Fe phases and generating low-coordinated Fe0 nanoparticles, as confirmed by extended X-ray absorption fine structure analysis. The unique low-coordinated Fe0 nanoparticles present in the FJH-derived composites promoted the enhanced catalytic degradation of chloramphenicol following peroxydisulfate activation, in relation to that achieved through traditional pyrolysis-derived composites. Furthermore, the developed continuous FJH process demonstrated the potential for the large-scale recycling of Fe-enriched residues and promoted the conversion of Fe-enriched residues after Li recovery.
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