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Evaluation of photocathode coupling-mediated hydroxychloroquine degradation in a single-chamber microbial fuel cell based on electron transfer mechanism and power generation
被引:7
|作者:
Wang, Chengzhi
[1
]
Xing, Yi
[1
]
Zhang, Kangning
[1
]
Zheng, Huizi
[1
]
Zhang, Ya-nan
[1
]
Zhu, Xiaolin
[1
]
Yuan, Xing
[1
]
Qu, Jiao
[1
]
机构:
[1] Northeast Normal Univ, Sch Environm, Changchun 130024, Jilin, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Microbial fuel cell;
Photocathode;
Electricity;
Hydroxychloroquine;
ELECTRICITY;
COMMUNITY;
ENERGY;
PERFORMANCE;
CHALLENGES;
REDUCTION;
REACTORS;
LIGHT;
FILMS;
MFC;
D O I:
10.1016/j.jpowsour.2022.232625
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
A photocathode-microbial electrochemical coupling system (PC-MFC) using black phosphorus-doped titanium dioxide nanobelt (BP/TB) as a photocatalyst is constructed for the degradation of hydroxychloroquine (HCQ, used to treat COVID-19). The degradation efficiency of HCQ (100 mg/L) in coupling system is 73.7% within 8 h, higher than that of photocatalysis (69.5%), MFC (25.6%), and adsorption (9.6%). The photocathode coupling facilitates subsequent bioelectric treatment, resulting in complete degradation of HCQ (100 mg/L) within 96 h in PC-MFC, much higher than in MFC (51.1%). Illumination of PC-MFC significantly increases the cathodic abundance of Pseudomonadales ord. (from 1.83% to 66.30%), accumulates biomass, improves the electrochemical behaviors of photocathode and bioanode, and finally increases the maximum power from 241 to 280 mW/m2. The electron transfer pathways depende on nicotinamide adenine dinucleotide dehydrogenase, succinate dehydrogenase and terminal oxidase. The coupled system enhances the dechlorination reduction of HCQ and reduces the biotoxicity of its degradation pathway. PC-MFC represents a new strategy for the treatment and energy recovery of refractory organic compounds in wastewater.
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页数:12
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