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Activation of Peroxymonosulfate Using Spent Li-Ion Batteries for the Efficient Degradation of Chloroquine Phosphate

Authors :
Zhenzhong Hu
Jia Luo
Sheng Xu
Peng Yuan
Shengqi Guo
Xuejing Tang
Boxiong Shen
Source :
Catalysts, Vol 13, Iss 4, p 661 (2023)
Publication Year :
2023
Publisher :
MDPI AG, 2023.

Abstract

Recycling and reusing spent lithium-ion batteries (LIBs) have gained a lot of attention in recent years, both ecologically and commercially. The carbon nanotube-loaded CoFe2O4 (CoFe2O4@CNTs) composite was made using a solvothermal technique utilizing wasted LIBs as the starting material and carbon nanotubes as support, and it was used as an efficient peroxymonosulfate (PMS, HSO5−) activator to degrade chloroquine phosphate (CQP). Scanning electron microscopy (SEM), transmission electron microscopy (TEM), an energy dispersive spectrometer (EDS), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), and X-ray photoelectron spectroscopy (XPS) were utilized to characterize the physical and chemical properties of the catalyst generated. The impacts of CoFe2O4@CNTs dosage, PMS concentration, reaction temperature, initial pH value, starting CQP concentration, and co-existing ions have undergone extensive experimental testing. In comparison to bare CoFe2O4, the CoFe2O4@CNTs demonstrated increased catalytic activity, which might be attributed to their super electron transport capacity and large surface area. In ideal conditions, the mineralization efficiency and removal efficiency of 10 mg/L CQP approached 33 and 98.7%, respectively. By employing external magnets, the CoFe2O4@CNTs catalyst may be simply recycled and reused several times. The potential reaction mechanism in the CoFe2O4@CNTs/PMS system was also investigated. In summary, this study indicates that CoFe2O4@CNTs generated from spent lithium-ion batteries have a high potential in PMS activation for CQP and other pollutant degradation.

Details

Language :
English
ISSN :
20734344
Volume :
13
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Catalysts
Publication Type :
Academic Journal
Accession number :
edsdoj.b66658aa64614488aae96ca92a80a23a
Document Type :
article
Full Text :
https://doi.org/10.3390/catal13040661