Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs

Recently, Fe-based metal-organic frameworks (MOFs) have attracted increasing attention and been widely used. To date, however, it is unknown whether they can be employed to degrade tetracycline, one of the most widely used antibiotics. This work therefore aims to provide such support by comparing th...

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Main Authors: Wang, Dongbo, Jia, Feiyue, Wang, Hou, Chen, Fei, Fang, Ying, Dong, Wenbo, Zeng, Guangming, Li, Xiaoming, Yang, Qi, Yuan, Xingzhong
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/139521
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1395212020-05-20T03:39:03Z Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs Wang, Dongbo Jia, Feiyue Wang, Hou Chen, Fei Fang, Ying Dong, Wenbo Zeng, Guangming Li, Xiaoming Yang, Qi Yuan, Xingzhong School of Chemical and Biomedical Engineering Engineering::Chemical engineering Metal-organic Frameworks (MOFs) Adsorption Recently, Fe-based metal-organic frameworks (MOFs) have attracted increasing attention and been widely used. To date, however, it is unknown whether they can be employed to degrade tetracycline, one of the most widely used antibiotics. This work therefore aims to provide such support by comparing the performance of three Fe-based MOFs (namely, Fe-MIL-101, Fe-MIL-100, and Fe-MIL-53) in removing tetracycline. Experimental results showed that Fe-MIL-101 exhibited the best performance in tetracycline removal, with 96.6% of tetracycline being removed (initial tetracycline concentration at 50 mg/L) while Fe-MIL-100 and Fe-MIL-53 removed 57.4% and 40.6% under the same conditions. Additionally, the effects of adding dosage, adsorption time, and initial concentration of tetracycline on degradation efficiency were examined. It was found that the adsorption and photocatalytic degradation effect was better with the increase of time, the optimum dosage of Fe-MIL-101 was 0.5 g/L and the removal efficiency decreased with the increasing of initial tetracycline concentrations. Moreover, the trapping experiments and ESR tests indicated that O2-, OH and h+ were the main active species in photocatalytic degradation process of tetracycline. Due to its high removal efficiency and simple synthesis, it could be used as a potential catalyst for degradation of tetracycline and other antibiotics. 2020-05-20T03:39:03Z 2020-05-20T03:39:03Z 2018 Journal Article Wang, D., Jia, F., Wang, H., Chen, F., Fang, Y., Dong, W., . . . Yuan, X. (2018). Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs. Journal of Colloid and Interface Science, 519, 273-284. doi:10.1016/j.jcis.2018.02.067 2190-8508 https://hdl.handle.net/10356/139521 10.1016/j.jcis.2018.02.067 29505989 2-s2.0-85042692297 519 273 284 en Journal of Colloid and Interface Science © 2018 Elsevier Inc. All rights reserved.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Engineering::Chemical engineering
Metal-organic Frameworks (MOFs)
Adsorption
spellingShingle Engineering::Chemical engineering
Metal-organic Frameworks (MOFs)
Adsorption
Wang, Dongbo
Jia, Feiyue
Wang, Hou
Chen, Fei
Fang, Ying
Dong, Wenbo
Zeng, Guangming
Li, Xiaoming
Yang, Qi
Yuan, Xingzhong
Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs
description Recently, Fe-based metal-organic frameworks (MOFs) have attracted increasing attention and been widely used. To date, however, it is unknown whether they can be employed to degrade tetracycline, one of the most widely used antibiotics. This work therefore aims to provide such support by comparing the performance of three Fe-based MOFs (namely, Fe-MIL-101, Fe-MIL-100, and Fe-MIL-53) in removing tetracycline. Experimental results showed that Fe-MIL-101 exhibited the best performance in tetracycline removal, with 96.6% of tetracycline being removed (initial tetracycline concentration at 50 mg/L) while Fe-MIL-100 and Fe-MIL-53 removed 57.4% and 40.6% under the same conditions. Additionally, the effects of adding dosage, adsorption time, and initial concentration of tetracycline on degradation efficiency were examined. It was found that the adsorption and photocatalytic degradation effect was better with the increase of time, the optimum dosage of Fe-MIL-101 was 0.5 g/L and the removal efficiency decreased with the increasing of initial tetracycline concentrations. Moreover, the trapping experiments and ESR tests indicated that O2-, OH and h+ were the main active species in photocatalytic degradation process of tetracycline. Due to its high removal efficiency and simple synthesis, it could be used as a potential catalyst for degradation of tetracycline and other antibiotics.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Wang, Dongbo
Jia, Feiyue
Wang, Hou
Chen, Fei
Fang, Ying
Dong, Wenbo
Zeng, Guangming
Li, Xiaoming
Yang, Qi
Yuan, Xingzhong
format Article
author Wang, Dongbo
Jia, Feiyue
Wang, Hou
Chen, Fei
Fang, Ying
Dong, Wenbo
Zeng, Guangming
Li, Xiaoming
Yang, Qi
Yuan, Xingzhong
author_sort Wang, Dongbo
title Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs
title_short Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs
title_full Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs
title_fullStr Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs
title_full_unstemmed Simultaneously efficient adsorption and photocatalytic degradation of tetracycline by Fe-based MOFs
title_sort simultaneously efficient adsorption and photocatalytic degradation of tetracycline by fe-based mofs
publishDate 2020
url https://hdl.handle.net/10356/139521
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