Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism Insights
Batch experiments were performed to investigate the effect of several environmental factors on atenolol (ATL) degradation efficiency, including catalyst crystal phase (anatase TiO<sub>2</sub>, rutile TiO<sub>2</sub>, and mixed phase), catalyst dosage, UV-LED wavelength and in...
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doaj-b7ce2f2b459c48149d5d8374e994a5aa2020-11-25T00:56:43ZengMDPI AGCatalysts2073-43442019-10-0191187610.3390/catal9110876catal9110876Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism InsightsZhilin Ran0Liping Wang1Yuanhang Fang2Cong Ma3Shaofeng Li4Institute of Innovational Education Research, School of Transportation and Environment, Shenzhen Institute of Information Technology, Shenzhen 518172, ChinaSchool of Environmental Science and Engineering, Chang’an University, Xi’an 710064, ChinaShenzhen Water Affairs (Group) Co. Ltd., Shenzhen 518033, ChinaState Key Laboratory of Separation Membranes and Membrane Processes, School of Environmental Science and engineering, Tiangong University, Tianjin 300387, ChinaDepartment of Building and Environmental Engineering, Shenzhen Polytechnic, Shenzhen 518055, ChinaBatch experiments were performed to investigate the effect of several environmental factors on atenolol (ATL) degradation efficiency, including catalyst crystal phase (anatase TiO<sub>2</sub>, rutile TiO<sub>2</sub>, and mixed phase), catalyst dosage, UV-LED wavelength and intensity, co-existing anions, cations, and pH. The mixed phase (2 g/L) exhibited the best photocatalytic activity at 365 nm, with ATL (18.77 µM) completely oxidized within 1 h. These results suggest that: (i) The mixed phase exhibits the highest activity due to its large specific surface area and excellent charge separation efficiency. (ii) ATL can be effectively degraded using mixed phase TiO<sub>2</sub> combined with UV-LED technology and the ATL degradation efficiency could reach 100% for 60 min; (iii) ATL photodegradation was more effective under 365 nm UV-LED than 254 nm, which was caused by the effect of light-induced charge separation; (iv) the ATL Degradation efficiency(De) decreased with an increase in initial ATL concentrations; and (v) co-existing anions and cations had different effects on the ATL De, mainly by changing the concentration of hydroxyl radicals. Considering that UV-LED is more energy-saving and environmentally friendly, and commercial TiO<sub>2</sub> is cheap and easy to obtain, our research provides feasibility for practical application.https://www.mdpi.com/2073-4344/9/11/876ultraviolet light emitting diodeadvanced oxidation processnano titanium dioxidephotocatalysishydroxyl radicalatenolol |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhilin Ran Liping Wang Yuanhang Fang Cong Ma Shaofeng Li |
spellingShingle |
Zhilin Ran Liping Wang Yuanhang Fang Cong Ma Shaofeng Li Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism Insights Catalysts ultraviolet light emitting diode advanced oxidation process nano titanium dioxide photocatalysis hydroxyl radical atenolol |
author_facet |
Zhilin Ran Liping Wang Yuanhang Fang Cong Ma Shaofeng Li |
author_sort |
Zhilin Ran |
title |
Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism Insights |
title_short |
Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism Insights |
title_full |
Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism Insights |
title_fullStr |
Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism Insights |
title_full_unstemmed |
Photocatalytic Degradation of Atenolol by TiO<sub>2</sub> Irradiated with an Ultraviolet Light Emitting Diode: Performance, Kinetics, and Mechanism Insights |
title_sort |
photocatalytic degradation of atenolol by tio<sub>2</sub> irradiated with an ultraviolet light emitting diode: performance, kinetics, and mechanism insights |
publisher |
MDPI AG |
series |
Catalysts |
issn |
2073-4344 |
publishDate |
2019-10-01 |
description |
Batch experiments were performed to investigate the effect of several environmental factors on atenolol (ATL) degradation efficiency, including catalyst crystal phase (anatase TiO<sub>2</sub>, rutile TiO<sub>2</sub>, and mixed phase), catalyst dosage, UV-LED wavelength and intensity, co-existing anions, cations, and pH. The mixed phase (2 g/L) exhibited the best photocatalytic activity at 365 nm, with ATL (18.77 µM) completely oxidized within 1 h. These results suggest that: (i) The mixed phase exhibits the highest activity due to its large specific surface area and excellent charge separation efficiency. (ii) ATL can be effectively degraded using mixed phase TiO<sub>2</sub> combined with UV-LED technology and the ATL degradation efficiency could reach 100% for 60 min; (iii) ATL photodegradation was more effective under 365 nm UV-LED than 254 nm, which was caused by the effect of light-induced charge separation; (iv) the ATL Degradation efficiency(De) decreased with an increase in initial ATL concentrations; and (v) co-existing anions and cations had different effects on the ATL De, mainly by changing the concentration of hydroxyl radicals. Considering that UV-LED is more energy-saving and environmentally friendly, and commercial TiO<sub>2</sub> is cheap and easy to obtain, our research provides feasibility for practical application. |
topic |
ultraviolet light emitting diode advanced oxidation process nano titanium dioxide photocatalysis hydroxyl radical atenolol |
url |
https://www.mdpi.com/2073-4344/9/11/876 |
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