Dual activation of peroxymonosulfate with FeS 2 @Co 3 O 4-C catalyst and visible light for the efficient degradation of tetracycline

Wang X., Lu Y., Imanova G., Komarneni S., Ma J.

JOURNAL OF ALLOYS AND COMPOUNDS, vol.1002, 2024 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 1002
  • Publication Date: 2024
  • Doi Number: 10.1016/j.jallcom.2024.175474
  • Journal Name: JOURNAL OF ALLOYS AND COMPOUNDS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, PASCAL, Aerospace Database, Chemical Abstracts Core, Chimica, Communication Abstracts, Compendex, INSPEC, Metadex, Public Affairs Index, Civil Engineering Abstracts
  • Azerbaijan State University of Economics (UNEC) Affiliated: No

Abstract

Antibiotics have garnered global attention as a pressing concern due to their wide spread discharge to the environment and resulting significant threats to both human health and the environment. The Sulfate Radicalbased Advanced Oxidation Processes (SR-AOPs) technique has already been verified as an effective process for pollutant degradation. Herein, FeS 2 @Co 3 O 4-C composites, utilizing ZIF-67-derived Co 3 O 4-C as the substrate material, were fabricated using a single-step solvothermal technique for the degradation of tetracycline (TC) by activated peroxymonosulfate (PMS) in combination with visible light irradiation. In the FeS 2 @Co 3 O 4-C/PMS/Vis system, the FeS 2 @Co 3 O 4-C showed better activation performance than the single chemical activation system or photocatalytic system, with 97.2 % TC removed in 20 min. The FeS 2 @Co 3 O 4-C composite material was thoroughly investigated employing X-ray diffraction (XRD) for analyzing its crystal structure, transmission electron microscopy (TEM) for detailed structural insights, scanning electron microscopy (SEM) for morphological examination, and X-ray photoelectron spectroscopy (XPS) for the elemental valence states. The quenching experiments, along with EPR test, revealed that the primary active oxygen species consisted of 1 O 2 , O 2 & sdot;- , and h + . The results presented here suggest the impressive stability and recyclability of FeS 2 @Co 3 O 4-C making it a potential candidate as an efficient catalyst for initiating the activation of PMS in degrading persistent organic pollutants present in water.