High Efficiency Removal Performance of Tetracycline by Magnetic CoFe2O4/NaBiO3 Photocatalytic Synergistic Persulfate Technology

Author:

Zhang Juanxiang1,Zhang Shengnan1,Bian Xiuqi12,Yin Yaoshan1,Huang Weixiong3ORCID,Liu Chong4ORCID,Liang Xinqiang5,Li Fayong1

Affiliation:

1. College of Water Resources and Architectural Engineering, Tarim University, Alaer 843300, China

2. College of Architecture Engineering, Shandong Vocational and Technical University of Engineering, Jinan 250200, China

3. School of Environmental Studies, China University of Geosciences, Wuhan 430074, China

4. Department of Chemical & Materials Engineering, University of Auckland, Auckland 0926, New Zealand

5. Key Laboratory of Environment Remediation and Ecological Health, Ministry of Education, College of Environmental and Resources Sciences, Zhejiang University, Hangzhou 310058, China

Abstract

The widespread environmental contamination resulting from the misuse of tetracycline antibiotics (TCs) has garnered significant attention and study by scholars. Photocatalytic technology is one of the environmentally friendly advanced oxidation processes (AOPs) that can effectively solve the problem of residue of TCs in the water environment. This study involved the synthesis of the heterogeneous magnetic photocatalytic material of CoFe2O4/NaBiO3 via the solvothermal method, and it was characterized using different characterization techniques. Then, the photocatalytic system under visible light (Vis) was coupled with peroxymonosulfate (PMS) to explore the performance and mechanism of degradation of tetracycline hydrochloride (TCH) in the wastewater. The characterization results revealed that CoFe2O4/NaBiO3 effectively alleviated the agglomeration phenomenon of CoFe2O4 particles, increased the specific surface area, effectively narrowed the band gap, expanded the visible light absorption spectrum, and inhibited recombination of photogenerated electron–hole pairs. In the Vis+CoFe2O4/NaBiO3+PMS system, CoFe2O4/NaBiO3 effectively activated PMS to produce hydroxyl radicals (·OH) and sulfate radicals (SO4−). Under the conditions of a TCH concentration of 10 mg/L−1, a catalyst concentration of 1 g/L−1 and a PMS concentration of 100 mg/L−1, the degradation efficiency of TCH reached 94% after 100 min illumination. The degradation of TCH was enhanced with the increase in the CoFe2O4/NaBiO3 and PMS dosage. The solution pH and organic matter had a significant impact on TCH degradation. Notably, the TCH degradation efficiency decreased inversely with increasing values of these parameters. The quenching experiments indicated that the free radicals contributing to the Vis+CoFe2O4/NaBiO3+PMS system were ·OH followed by SO4−, hole (h+), and the superoxide radical (O2−). The main mechanism of PMS was based on the cycle of Co3+ and Co2+, as well as Fe3+ and Fe2+. The cyclic tests and characterization by XRD and FT-IR revealed that CoFe2O4/NaBiO3 had good degradation stability. The experimental findings can serve as a reference for the complete removal of antibiotics from wastewater.

Funder

Bingtuan Science and Technology Program

President’s foundation of Tarim University

the earmarked fund for XJARS

Publisher

MDPI AG

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