Tetracycline degradation in the Fe3O4@HKUST-1/persulfate system: properties, activation mechanism, and degradation pathways

被引:3
|
作者
Wu, Tongtong [1 ]
Gao, Weili [1 ]
Zhang, Jiehe [1 ]
Hao, Mingxu [1 ]
Zhang, Shiyu [1 ]
Tao, Haisheng [1 ,2 ]
机构
[1] Anhui Normal Univ, Collaborat Innovat Ctr Recovery & Reconstruct Degr, Sch Ecol & Environm, Anhui Prov Engn Lab Water & Soil Pollut Control &, Wuhu 241000, Peoples R China
[2] Anhui Normal Univ, Coll Chem & Mat Sci, Anhui Lab Mol Based Mat, Wuhu 241000, Peoples R China
关键词
PHOTOCATALYTIC DEGRADATION; CATALYTIC DEGRADATION; PERSULFATE ACTIVATION; ADSORPTION; OXIDATION; REMOVAL; COPPER; WATER; PHOTODEGRADATION; ANTIBIOTICS;
D O I
10.1039/d3re00555k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As a typical antibiotic, tetracycline is ecotoxic and prone to bacterial resistance, producing superbugs and causing a public ecological crisis, thus raising the need to eliminate tetracycline from the aqueous environment. In this work, magnetic catalyst Fe3O4@HKUST-1 was prepared for catalyzing the degradation of tetracycline by persulfate. X-ray diffraction, scanning electron microscopy, and vibrating sample magnetometry were used to characterize the catalyst, and the results show that the catalyst had good crystallinity and magnetic properties. Tetracycline removal in the Fe3O4@HKUST-1/persulfate system reached84.80%, and the catalyst was easily recovered from the solution due to its good magnetic properties. Mechanism analysis revealed that the non-radical pathway was the main degradation channel in the Fe-3-O-4@HKUST-1/persulfate system, and(1)O(2)was the main reactive oxygen species generated from O-v on the surface of the Fe3O4@HKUST-1 catalyst. Tetracycline degradation was achieved by hydroxylation, demethylation, decarbonylation, dehydroxylation and the cleavage of C-N bonds. This finding holds significant value in further comprehension of the catalytic activation mechanism of metal-organic frameworks derivatives on persulfate and provides novel ideas for efficient water treatment technology development.
引用
收藏
页码:728 / 739
页数:12
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