Synchronous removal of oxytetracycline and Cr(Ⅵ) in Fenton-like photocatalysis process driven by MnFe2O4/g-C3N4: Performance and mechanisms

被引:7
|
作者
Li Y. [1 ]
Wang S. [4 ]
Guo H. [2 ]
Zhou J. [3 ]
Liu Y. [3 ]
Wang T. [3 ]
Yin X. [3 ]
机构
[1] Ningxia Academy of Environmental Sciences (Co., LTD.), Yinchuan
[2] College of Biology and the Environment, Nanjing Forestry University, Nanjing
[3] College of Natural Resources and Environment, Northwest A&F University, Shaanxi Province, Yangling
[4] College of Environmental Science and Engineering, Yangzhou University, Jiangsu, Yangzhou
基金
中国国家自然科学基金;
关键词
Cr(Ⅵ); g-C[!sub]3[!/sub]N[!sub]4[!/sub; MnFe[!sub]2[!/sub]O[!sub]4[!/sub; Oxytetracycline; Photocatalysis;
D O I
10.1016/j.chemosphere.2024.141371
中图分类号
学科分类号
摘要
Complex wastewater has more complicated toxicity and potential harm to organisms, and synchronous REDOX of complex pollutants in wastewater has always been a bottleneck in the development of advanced oxidation technology. Herein, a Fenton-like photocatalytic system (MnFe2O4/g-C3N4 heterojunction composites) was established to simultaneously remove oxytetracycline (OTC) and Cr(Ⅵ) in this study. The MnFe2O4/g-C3N4 heterojunction composites exhibited outstanding catalytic performances for OTC and Cr(Ⅵ) removal, and more than 90% of OTC and nearly 100% of Cr(Ⅵ) were simultaneously removed within 1 min photocatalysis. The photo-generared electrons and holes played significant roles in Cr(Ⅵ) reduction and OTC degradation, respectively. Moreover, the heterojunction formed between g-C3N4 and MnFe2O4 effectively accelerated the separation and migration of photogenerated carriers. The OTC degradation was mainly initiated by cracking of benzene rings, degradation of substituents, and removal of groups such as –OH, –NH2, –CH3, and –CONH2, resulting in generation of small molecular substances; Cr(Ⅲ) was the main reduction product of Cr(Ⅵ). Meanwhile, the MnFe2O4/g-C3N4 heterojunction composites also exhibited excellent stability and reusability in removal of OTC and Cr(Ⅵ). © 2024 Elsevier Ltd
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