Boosted elimination of florfenicol by BiOClxBr1-x solid solutions via photocatalytic ozonation under visible light

被引:5
|
作者
Tan, Lu [1 ]
Yuan, Zhenxi [1 ]
Chen, Weirui [2 ]
Lin, Ziyi [1 ]
Tang, Yiming [1 ,3 ,4 ,5 ]
Li, Laisheng [1 ,3 ,4 ,5 ]
Wang, Jing [1 ,3 ,4 ,5 ]
机构
[1] South China Normal Univ, Sch Environm, Guangzhou 510006, Peoples R China
[2] Guangdong Univ Technol, Sch Environm Sci & Engn, Guangzhou 510006, Peoples R China
[3] South China Normal Univ, Guangdong Prov Key Lab Chem Pollut & Environm Safe, Guangzhou 510006, Peoples R China
[4] South China Normal Univ, MOE Key Lab Theoret Chem Environm, Guangzhou 510006, Peoples R China
[5] Guangdong Prov Key Lab Funct Mat Environm Protect, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Solid solution; Photocatalysis; AOPs; Bismuth semiconductor; Florfenicol; BIOX X; ANILINE DEGRADATION; BR; CL; OXIDATION; ACID;
D O I
10.1016/j.jcis.2023.12.086
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, a series of BiOClxBr1-x (BCB) solid solutions are facilely designed for visible-light-driven photocatalytic ozonation (PCO) degradation of florfenicol (FF) in water environments, which could add to the library of efficient, cost-effective and robust nanocatalysts for water purification. BCB solid solutions in the structure of 2D nanosheets are achieved involving the etching of BiOBr "micro-flowers" with HCl at different concentrations, allowing a removal ratio of FF up to 97.3 % within 1 h, superior to bare BiOBr and bare BiOCl. A strengthened synergistic effect between photocatalysis and ozonation is substantiated, where the separation of photo-induced charge transfer is accelerated, the band gap is tuned and the utilization efficiency of ozone is enhanced. This facilitates the production of reactive oxygen species identified as center dot OH, center dot O2-, and 1O2 that will attack the FF molecule for degradation based on three pathways.
引用
收藏
页码:487 / 496
页数:10
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