光催化
降级(电信)
动力学
吸附
四环素类抗生素
四环素
矿化(土壤科学)
材料科学
催化作用
化学工程
分解
化学
光化学
物理化学
计算机科学
物理
有机化学
抗生素
工程类
电信
氮气
量子力学
生物化学
作者
Shushu Huang,Guodong Wang,Jiaqi Liu,Chunfang Du,Yiguo Su
出处
期刊:Chemcatchem
[Wiley]
日期:2020-05-28
卷期号:12 (17): 4431-4445
被引量:50
标识
DOI:10.1002/cctc.202000634
摘要
Abstract A novel direct Z‐scheme CuBi 2 O 4 /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 CuBi 2 O 4 /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 CuBi 2 O 4 /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.
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