Photocatalytic degradation of tetracycline antibiotics using delafossite silver ferrite-based Z-scheme photocatalyst: Pathways and mechanism insight

光催化 降级(电信) 化学 四环素类抗生素 四环素 催化作用 废水 化学工程 核化学 废物管理 有机化学 抗生素 计算机科学 生物化学 电信 工程类
作者
Jiayin Guo,Longbo Jiang,Jie Liang,Weihua Xu,Hanbo Yu,Jin Zhang,Shujing Ye,Wenle Xing,Xingzhong Yuan
出处
期刊:Chemosphere [Elsevier BV]
卷期号:270: 128651-128651 被引量:149
标识
DOI:10.1016/j.chemosphere.2020.128651
摘要

Tetracycline (TC), a widely used antibiotic, is easy to enter the aquatic ecosystem through soil erosion, livestock manure and wastewater discharge, resulting in a series of risks. The application of Z-scheme photocatalysts with efficient interface charge separation and transfer has been regard as an effective strategy for antibiotic degradation. Herein, a novel ternary Z-scheme Bi12O17Cl2/Ag/AgFeO2 was successfully synthesized by ultrasound-assisted ethanol reduction of Ag+ on the interface of Bi12O17Cl2 and AgFeO2. The Bi12O17Cl2/Ag/AgFeO2 Z-scheme system exhibited an enhanced photocatalytic degradation capability for TC, which was over 6.5 times and 2.4 times higher than those of AgFeO2 and Bi12O17Cl2/AgFeO2 system, respectively. The photocatalytic process of TC was explored, and the results indicated that an optimum catalyst concentration of 0.5 g L−1 and a primeval pH (without adjustment) favored the degradation process, while the introduction of exogenous anions (CO32−, SO42− and NO3−) and organic matter (HA) supressed the degradation of TC. Simultaneously, the possible pathway for the degradation process of TC was presented based on the liquid chromatography-mass spectrometry (LC-MS) analysis. Active species trapping experiments and ESR spectra revealed the significant contribution of O2− in the TC degradation, and verified the Z-scheme mechanism of the Bi12O17Cl2/Ag/AgFeO2 system.
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