Issue 3, 2024

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

Abstract

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 reached 84.80%, 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 Fe3O4@HKUST-1/persulfate system, and 1O2 was the main reactive oxygen species generated from Ov 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.

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

Supplementary files

Article information

Article type
Paper
Submitted
23 Oct 2023
Accepted
12 Dec 2023
First published
03 Jan 2024

React. Chem. Eng., 2024,9, 728-739

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

T. Wu, W. Gao, J. Zhang, M. Hao, S. Zhang and H. Tao, React. Chem. Eng., 2024, 9, 728 DOI: 10.1039/D3RE00555K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements