Enhanced oxytetracycline removal coupling with increased power generation using a self-sustained photo-bioelectrochemical fuel cell

被引:29
|
作者
Sun, Jian [1 ]
Xu, Wenjing [1 ]
Yang, Ping [1 ]
Li, Nan [1 ]
Yuan, Yong [1 ]
Zhang, Hongguo [2 ]
Wang, Yujie [1 ]
Ning, Xunan [1 ]
Zhang, Yaping [1 ]
Chang, Kenlin [3 ]
Peng, Yenping [4 ]
Chen, Kufan [5 ]
机构
[1] Guangdong Univ Technol, Inst Environm Hlth & Pollut Control, Guangdong Key Lab Environm Catalysis & Hlth Risk, Sch Environm Sci & Engn,Guangzhou Key Lab Environ, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangzhou Univ, Guangzhou Univ Linkoping Univ Res Ctr Urban Susta, Guangzhou 510006, Guangdong, Peoples R China
[3] Natl Sun Yat Sen Univ, Inst Environm Engn, Gaoxiong 80424, Taiwan
[4] Tunghai Univ, Dept Environm Sci & Engn, Taichung 40704, Taiwan
[5] Natl Chi Nan Univ, Dept Civil Engn, Nanto 54561, Taiwan
基金
中国国家自然科学基金;
关键词
Photo-bioelectrochemical fuel cell; Bioanode; Electron transfer; Oxytetracycline removal; Power generation; Enhancement; ANTIBIOTIC-RESISTANCE GENES; POLYCHLORINATED BIPHENYL; BIODEGRADATION; OXIDATION; TETRACYCLINE; REDUCTION; COMMUNITY; CHLORAMPHENICOL; FERMENTATION; CONTAMINANTS;
D O I
10.1016/j.chemosphere.2018.12.152
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Photo-bioelectrochemical fuel cell (PBFC) represents a promising technology for enhancing removal of antibiotic pollutants while simultaneously sustainable transformation of organic wastes and solar energy into electricity. In this study, simultaneous antibiotic removal and bioelectricity generation were investigated in a PBFC with daily light dark cycle using oxytetracycline (OTC) as a model compound of antibiotic. The specific OTC removal rate increased by 61% at an external resistance of 50 Omega compared to that in the open-circuit control, which was attributed to bioelectrochemically enhanced co-metabolic degradation in the presence of the bioanode. The OTC removal was obviously accelerated during illumination of cathode in contrast with a dark cathode due to the higher driving force for anodic bioelectrochemical reaction by using photosynthetic oxygen as cathodic electron acceptor during illumination than that using nitrate in dark. The bioelectrocatalytic activity of anodic biofilm was continuously enhanced even at an initial OTC concentration of up to 50 mg L-1. The degradation products of OTC can function as mediators to facilitate the electron transfer from bacteria to the anode, resulting in 1.2, 1.76 and 1.8 fold increase in maximum power output when 10, 30 and 50 mg L-1 OTC was fed to the bioanode, compared to the OTC-free bioanode, respectively. The OTC feeding selective enriched OTC-tolerant bacterial community capable of degrading complex organic compounds and producing electricity. The occurrence of ARGs during bioelectrochemical degradation of OTC was affected more greatly by the succession of the anodic bacterial community than the initial OTC concentration. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:21 / 29
页数:9
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