Issue 38, 2022

Relying on the non-radical degradation of oxytetracycline by peroxymonosulfate activated with a magnetic Cu/Fe composite: performance and mechanism

Abstract

Oxytetracycline (OTC) is a typical antibiotic that poses a serious threat to the environment. However, traditional treatment methods suffer from low treatment efficiencies and potential secondary contamination. Therefore, there is a need to develop efficient, convenient, and environmentally friendly removal technology. In this paper, magnetic nano-Cu/Fe composites were successfully synthesized and used as the activator of peroxymonosulfate (PMS) to degrade OTC. The obtained catalysts with different ratios showed excellent degradation effects, especially the Cu/Fe-1 catalysts. The highest removal efficiency of OTC (93%) was achieved with 0.2 g L−1 PMS and 0.1 g L−1 catalyst in 60 min. The impacts of the catalyst and PMS dosages, initial temperature and pH, coexisting anions, microplastics, and real-life water samples were investigated. To explore the mechanism for OTC degradation, radical scavenging and electron spin resonance (EPR) experiments were carried out, and non-radical 1O2 was identified to be the main radical. TEM and XRD results show the presence of CuFe2O4 composites in Cu/Fe-1, which can promote the production of 1O2 and thus improve the OTC degradation efficiency. This work provides a new efficient, stable, low-cost, and environmentally friendly approach for the degradation of oxytetracycline.

Graphical abstract: Relying on the non-radical degradation of oxytetracycline by peroxymonosulfate activated with a magnetic Cu/Fe composite: performance and mechanism

Supplementary files

Article information

Article type
Paper
Submitted
24 Jun 2022
Accepted
02 Sep 2022
First published
05 Sep 2022

New J. Chem., 2022,46, 18251-18261

Relying on the non-radical degradation of oxytetracycline by peroxymonosulfate activated with a magnetic Cu/Fe composite: performance and mechanism

J. Sun, Q. Li, D. Zhang and D. Xia, New J. Chem., 2022, 46, 18251 DOI: 10.1039/D2NJ03125F

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