Issue 12, 2023

Robust degradation of tetracycline antibiotic through recyclable Fe3S4/Ti3C2MXene composites

Abstract

The efficient and sustainable removal of tetracycline (TC) from wastewater is a matter of great significance. In this study, we present a novel technique that effectively degrades TC by harnessing the synergistic effects of Fe3S4/Ti3C2MXene. The Fe3S4/Ti3C2MXene composite, specifically designed for this purpose, exhibits exceptional magnetic properties derived from Fe3S4. Our research demonstrates that this composite significantly enhances TC degradation through Fenton activity, achieving an impressive degradation rate of over 90%. Notably, when TC is subjected to the Fe3S4/Ti3C2MXene + H2O2 system, it generates a substantial amount of reactive oxygen species, including ˙OH and ˙O2. Among these species, ˙OH, primarily produced on the surface of Fe3S4/Ti3C2MXene, plays a dominant role in TC degradation. In contrast, pristine Fe3S4 or Ti3C2MXene alone does not exhibit comparable degradation capabilities under similar conditions. Moreover, the Fe3S4/Ti3C2MXene composite demonstrates excellent reusability and high stability over four consecutive cycles. Gas/liquid chromatography–mass spectrometry (GC/LC–MS) analysis was utilized to identify the intermediates of TC degradation, and a possible degradation pathway was proposed. These findings highlight the potential of Fe3S4/Ti3C2MXene composites in enhancing the Fenton degradation process and unveil an encouraging tactic for the successful elimination of TC from wastewater.

Graphical abstract: Robust degradation of tetracycline antibiotic through recyclable Fe3S4/Ti3C2MXene composites

Supplementary files

Article information

Article type
Paper
Submitted
21 Aug. 2023
Accepted
25 Okt. 2023
First published
25 Okt. 2023

Environ. Sci.: Nano, 2023,10, 3401-3413

Robust degradation of tetracycline antibiotic through recyclable Fe3S4/Ti3C2MXene composites

P. Sanga, J. Chen, J. Xiao, B. Liu, H. Saad Al-mashriqi and H. Qiu, Environ. Sci.: Nano, 2023, 10, 3401 DOI: 10.1039/D3EN00560G

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