A Novel CuBi2O4/BiOBr Direct Z-scheme Photocatalyst For Efficient Antibiotics Removal: Synergy of Adsorption and Photocatalysis on Degradation Kinetics and Mechanism Insight

被引:55
作者
Huang, Shushu [1 ]
Wang, Guodong [1 ]
Liu, Jiaqi [1 ]
Du, Chunfang [1 ]
Su, Yiguo [1 ]
机构
[1] Inner Monglia Univ, Coll Chem & Chem Engn, Hohhot 010021, Peoples R China
基金
中国国家自然科学基金;
关键词
Adsorption; photocatalysis; Z-scheme; antibiotics removal; photocatalytic mechanism; CHARGE SEPARATION EFFICIENCY; ENHANCED DRIVING-FORCE; TETRACYCLINE HYDROCHLORIDE; AQUEOUS-SOLUTIONS; ACTIVATED CARBON; HETEROJUNCTION; WATER; FABRICATION; BIOBR; COMPOSITE;
D O I
10.1002/cctc.202000634
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
A novel direct Z-scheme CuBi2O4/BiOBr heterostructural photocatalyst was developed aiming to modulate the adsorption ability and photocatalytic degradation performance toward antibiotics. Tetracycline as the model antibiotics was found to show pH value and temperature dependent adsorption capacity over CuBi2O4/BiOBr. The adsorption process was fitted to Pseudo-second-order and Elovich kinetic models and adsorption isotherm was followed Freundich isotherm model. Junction of CuBi(2)O(4)and BiOBr can modulate the surface feature and interfacial interactions, leading to direct Z-scheme charge kinetics for improved photocatalytic activity. The adsorptive capability and photocatalytic performance of CuBi2O4/BiOBr heterojunction showed great improvement in comparison with pristine CuBi(2)O(4)and BiOBr. The mineralization process and intermediates for tetracycline degradation were identified by total organic carbon analysis and liquid chromatograph-tandem mass spectrometry. Plausible transformation pathway and photocatalytic mechanism were proposed. Radical trapping experiments indicated that photogenerated holes and O(2)(-)active species played crucial roles in photocatalytic tetracycline decomposition.
引用
收藏
页码:4431 / 4445
页数:15
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