In situ recycling of Al foil and cathode materials from spent lithium-ion batteries through exogenous advanced oxidation

被引:4
|
作者
Yan, Shuxuan [1 ]
Ou, Yudie [1 ]
Li, Xueping [2 ]
Yuan, Lu [3 ,4 ]
Chen, Xiangping [3 ,4 ]
Zhou, Tao [1 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Hunan Prov Key Lab Chem Power Sources, Changsha 410083, Peoples R China
[2] Guangxi Minzu Univ, Coll Chem & Chem Engn, Key Lab Chem & Engn Forest Prod, State Ethn Affairs Commiss, Nanning 530006, Peoples R China
[3] Hunan Normal Univ, Coll Chem & Chem Engn, Changsha 410081, Peoples R China
[4] Hunan Normal Univ, Natl & Local Joint Engn Lab New Petro Chem Mat & F, Changsha 410081, Peoples R China
关键词
Spent lithium-ion batteries; PVDF degradation; Exfoliation mechanism; In-situ recycling; Exogenous advanced oxidation process; DEGRADATION; FACILE; METALS; SYSTEM; WASTE;
D O I
10.1016/j.seppur.2023.124788
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The efficient and sustainable recycling of spent lithium-ion batteries (LIBs), especially valuable metal enriched cathodes, is critical to achieve the goals of carbon peaking and carbon neutrality of new energy industry. However, current energy-intensive separation technologies to liberate cathode materials from current collector can hardly balance urgent requirements to sustainability and efficiency. Herein, an improved advanced oxidation technology based on ultrasonic assisted S2O82--Fe2+-H+ system (USFH) was innovatively proposed to exfoliate the cathode materials from Al foil through the selective degradation of polyvinylidene difluoride binders (PVDF), with the emphasis on degradation mechanism. Experimental results illustrate that nearly all of coating materials were effectively separated from Al foil under the optimized conditions. Then, the density function theory (DFT) calculations and possible chemical reactions were conducted to reveal the detailed degradation mechanism for PVDF. It can be discovered that the functional groups in PVDF will be attacked by free radicals generated in USFH, leading to defluoridation with the formation of oxyorganics containing oxygen groups (e.g. C=O, O-H) and fracture of C-C skeleton to olefins, carboxylic acids, ketones and alkanes with shorter carbon chains, along with exfoliation of organic intermediates into solution. It may promise a green and efficient alternative by novel improved advanced oxidation technology with sound fundamental theory for in-situ recycling of spent LIBs.
引用
收藏
页数:10
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