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Rational design of animal-derived biochar composite for peroxymonosulfate activation: Understanding the mechanism of singlet oxygen-mediated degradation of sulfamethoxazole

Authors :
Xu, Weicheng
Liang, Fawen
Liu, Zhang
Li, Shuai
Li, Jiesen
Jiang, Xueding
Pillai, Suresh C.
Wu, Xiaolian
Wang, Hailong
Xu, Weicheng
Liang, Fawen
Liu, Zhang
Li, Shuai
Li, Jiesen
Jiang, Xueding
Pillai, Suresh C.
Wu, Xiaolian
Wang, Hailong
Publication Year :
2024

Abstract

Animal-derived biochar are identified as a promising candidate for peroxymonosulfate (PMS) activation due to the abundant aromatics and oxygen-containing functional groups. The current investigation focuses on pig carcass-derived biochar (800-BA-PBC) by ball milling-assisted alkali activation. The results showed that 800-BA-PBC could effectively activate PMS and degraded 94.2% sulfamethoxazole (SMX, 10 mg/L) within 40 min. The reaction rate constant was found to be 47 times higher than that observed with PBC. The enhanced catalytic activity is mainly attributed to the increase in specific surface area, the increase content of oxygen-containing groups on the surface, and the formation of graphitic nitrogen. The quenching tests and electron paramagnetic resonance (EPR) analysis demonstrated that 1O2 is the main active species in the degradation of SMX. Moreover, the 800-BA-PBC + PMS system can maintain excellent degradation rate under different water quality, wide pH range, and the presence of different anions. The degradation pathways of SMX in the optimal system are also evaluated through intermediate identification and DFT calculation. These results indicate that the catalytic system has high anti-interference ability and practical application potential. This investigation provides new insight into the rational design of animal-derived biochar and develops a low-cost technology for the treatment of antibiotic containing wastewater. © 2023 Elsevier Ltd

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1415833011
Document Type :
Electronic Resource