Photocatalytic degradation of ibuprofen on S-doped BiOBr

被引:71
|
作者
Liu, Yang [1 ]
Hu, Zhuofeng [2 ]
Yu, Jimmy C. [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China
[2] Sun Yat Sen Univ, Sch Environm Sci & Engn, Guangdong Prov Key Lab Environm Pollut Control &, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalytic degradation; Ibuprofen; BiOBr; Doping; Oxygen vacancies; PERSONAL CARE PRODUCTS; VISIBLE-LIGHT; OXYGEN VACANCIES; BACTERIAL INACTIVATION; DRINKING-WATER; NANOSHEETS; BIOCL; PHARMACEUTICALS; PHOSPHORUS; PPCPS;
D O I
10.1016/j.chemosphere.2021.130376
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Doping heterogeneous atoms into BiOX is recognized as an effective method to improve its photo-catalytic activity. Here, S-doped BiOBr (S-BiOBr) was synthesized via a solvothermal method in the absence of water, which is supposed to substitute O as S2- in the lattice. This material is firstly used for the visible-light-driven degradation of ibuprofen, a model anti-inflammatory drug. The degradation efficiency of S-BiOBr is much higher than that of pure BiOBr. The degradation kinetic constant for S-BiOBr (2.48 x 10(-2) min(-1)) is about 3 times as high as that of pure BiOBr (0.83 x 10(-2) min(-1)). It is found that S-doping tunes the band structure of BiOBr, leading to a narrower band gap and thus higher utilization efficiency of visible light. The degradation of ibuprofen on S-BiOBr can be attributed to the generation of H2O2 and OH radicals. OH radical plays a synergistic role along with holes in the photo-catalytic degradation process, which is supposed to be better than the reported single hole- or superoxide-dominant reaction. This work reveals a previously unrecognized and more efficient method for the degradation of organic contaminants on BiOBr. (C) 2021 Elsevier Ltd. All rights reserved.
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页数:8
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