Photocatalytic degradation and removal mechanism of ibuprofen via monoclinic BiVO4 under simulated solar light

被引:78
作者
Li, Fuhua [1 ]
Kang, Yapu [1 ]
Chen, Min [1 ]
Liu, Guoguang [1 ]
Lv, Wenying [1 ]
Yao, Kun [1 ]
Chen, Ping [1 ]
Huang, Haoping [1 ]
机构
[1] Guangdong Univ Technol, Sch Environm Sci & Engn, Guangzhou Higher Educ Mega Ctr, 100 Waihuan Xi Rd, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
BiVO4; Photocatalytic degradation; Ibuprofen; Kinetics; Mechanism; VISIBLE-LIGHT; HYDROTHERMAL SYNTHESIS; BISMUTH VANADATE; TITANIUM-DIOXIDE; IRRADIATION; WATER; PHENOL; OXIDATION; PHOTODEGRADATION; BEHAVIOR;
D O I
10.1016/j.chemosphere.2016.02.045
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Characterized as by X-ray diffraction, scanning electron microscopy and UV-vis diffuse reflectance spectra techniques, BiVO4 photocatalyst was hydrothermally synthesized. The photocatalytic degradation mechanisms of ibuprofen (IBP) were evaluated in aqueous media via BiVO4. Results demonstrated that the prepared photocatalyst corresponded to phase-pure monoclinic scheelite BiVO4. The synthesized BiVO4 showed superior photocatalytic properties under the irradiation of visible-light. The photocatalytic degradation rate of IBP decreased with an increase in the initial IBP concentration. The degradation process followed first-order kinetics model. At an IBP concentration of 10 mg L-1, while a BiVO4 concentration of 5.0 g L-1 with pH value of 4.5, the rate of IBP degradation was obtained as 90% after 25 min. The photocatalytic degradation of IBP was primarily accomplished via the generation of superoxide radical (O-2(center dot-)) and hydroxyl radicals ((OH)-O-center dot). During the process of degradation, part of the (OH)-O-center dot was converted from the O-2(center dot-). The direct oxidation of holes (h+) made a minimal contribution to the degradation of IBP. 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:139 / 144
页数:6
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