4.7 Article

Activation of persulfate by magnetic zirconium-doped manganese ferrite for efficient degradation of tetracycline

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 423, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.130283

Keywords

ZrO2; Radicals; Tetracycline; Application feasibility; Mechanism

Funding

  1. Natural Sciences Foundation of Jiangxi Province [20171BAB206047]
  2. Scientific Research Project of Jiangxi Provincial Department of Education [GJJ200617]
  3. Key Research Development Program of Jiangxi Province [20203BBGL73230]

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The study developed an innovative approach for efficient removal of tetracycline in water environment by activating persulfate with oxide-based materials (ZrO2/MnFe2O4). Various factors affecting tetracycline degradation efficiency were investigated, and optimal conditions were determined. The study revealed the contributions of three radicals to rapid tetracycline degradation in the ZrO2/MnFe2O4-10/PDS system.
Tetracycline (TC) is a typical antibiotic that is eco-toxic and easily causes bacterial resistance, and thus it is necessary to eliminate tetracycline from the water environment. In this study, an innovative TC removal approach was developed by activation of persulfate (PDS) using oxide-based materials fabricated via lowtemperature co-precipitation: Zr oxide/MnFe2O4 (ZrO2/MnFe2O4). The effects of Fe/Zr molar ratio, the dose of ZrO2/MnFe2O4 and PDS, initial pH, TC concentration, co-existing anions, natural organic matter on TC degradation were investigated. Under optimal conditions (Fe/Zr = 10, PDS = 6.0 mM, ZrO2/MnFe2O4-10 = 0.20 g/L, and pH = 7.1), the TC degradation efficiency of 85.2% could be achieved after 120 min. Besides, the TC degradation efficiency was different extents inhibited by inorganic anions (H2PO-4 >HCO3- > NO3- > Cl-) and organic substances (EDTA > HA). Furthermore, the results of quenching experiments, electron paramagnetic resonance (EPR) analysis, and X-ray photoelectron spectroscopy (XPS) spectra analysis demonstrated that three radicals (hydroxyl radicals (.OH), sulfate radicals (SO.-4 ), and superoxide radicals (O.-2 )) contribute to rapid TC degradation in ZrO2/MnFe2O4-10/PDS system. Particularly, the ZrO2/MnFe2O4-10 exhibited superparamagnetic property and excellent stability, which was conducive to the effective recovery and utilization of the catalyst through the external magnetic field. Based on the degradation products determined by ultra-performance liquid chromatography-mass spectrometry (UPLC-MS), the possible four degradation pathways of TC degradation were proposed in the ZrO2/MnFe2O4-10/PDS system. This study indicates the ZrO2/MnFe2O4 composite is an efficient and environmentally catalyst for PDS oxidation of organic pollutants.

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