Efficient Removal of Antibiotic Resistance Genes through 4f-2p-3d Gradient Orbital Coupling Mediated Fenton-Like Redox Processes.

Angew Chem Int Ed Engl

Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Department of Chemistry, School of Science, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, 300072, Tianjin, P. R. China.

Published: November 2023

AI Article Synopsis

  • Peroxymonosulfate (PMS) effectively eliminates antibiotic resistance genes (ARGs) through both radical and nonradical processes, but improving its activation remains challenging.
  • A new Co-doped CeVO catalyst (Co-CVO) was developed to enhance electron cycling and optimize the activation of PMS, achieving a rapid removal of eARGs at a high degradation rate.
  • This catalyst promotes efficient mineralization of ARGs (83.4%) and demonstrates notable performance in a continuous flow reactor over extended periods, reducing ecological risks associated with ARGs in wastewater.

Article Abstract

Peroxymonosulfate (PMS) mediated radical and nonradical active substances can synergistically achieve the efficient elimination of antibiotic resistance genes (ARGs). However, enhancing interface electron cycling and optimizing the coupling of the oxygen-containing intermediates to improve PMS activation kinetics remains a major challenge. Here, Co doped CeVO catalyst (Co-CVO) with asymmetric sites was constructed based on Ce 4f-O 2p-Co 3d gradient orbital coupling. The catalyst achieved approximately 2.51×10 copies/mL of extracellular ARGs (eARGs) removal within 15 minutes, exhibited ultrahigh degradation rate (k=1.24 min ). The effective gradient 4f-2p-3d orbital coupling precisely regulates the electron distribution of Ce-O-Co active center microenvironment, while optimizing the electronic structure of Co 3d states (especially the occupancy of e ), promoting the adsorption of oxygen-containing intermediates. The generated radical and nonradical generated by interfacial electron cycling enhanced by the reduction reaction of PMS at the Ce site and the oxidation reaction at the Co site achieved a significant mineralization rate of ARGs (83.4 %). The efficient removal of ARGs by a continuous flow reactor for 10 hours significantly reduces the ecological risk of ARGs in actual wastewater treatment.

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http://dx.doi.org/10.1002/anie.202313298DOI Listing

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