4.7 Article

Peroxymonosulfate activation on carbon nano-onions modified graphitic carbon nitride via light-tuning radical and nonradical pathways

Journal

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2021.106592

Keywords

Carbon nano-onions; Graphitic carbon nitride; Norfloxacin; Active species; Degradation pathways

Funding

  1. Zhejiang Provincial Natural Science Foundation of China [LY21E090004]
  2. National Natural Science Foundation of China [52070103]
  3. Key Research and Development Program of Zhejiang Province [2020C03082]
  4. K. C. Wong Magna Fund in Ningbo University

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The carbon-based catalyst CN-CNO prepared in this study exhibited enhanced degradation of NOR under PMS activation compared to conventional C3N4. The combination of CNO with g-C3N4 improved the photogenerated-electron mobility, resulting in outstanding oxidative performance under visible light irradiation. This study provides novel insights into the fabrication and application of carbon-based catalysts for efficient antibiotic pollution elimination in aquatic environments.
Carbon-based catalyst has unique advantages as peroxymonosulfate (PMS) activator due to its unique structure and metal-free characteristics. Herein, the carbon nano-onions modified graphitic carbon nitride (CN-CNO) were prepared via the facile ultrasonic-assisted method in different proportions. With the aid of visible-light, the CN-CNO catalyst possessed a much better PMS activation capacity for norfloxacin (NOR) degradation than con-ventional C3N4. The incorporation of CNO with g-C3N4 provided an effective interface afforded by the 7C-7C stacking interaction, which significantly enhanced photogenerated-electron mobility as evidenced by electron microscopy and electrochemical studies. Radical quenching experiments and EPR illustrated that the outstanding oxidative performance of CN-CNO/PMS system originated from the h(+), O-2(center dot-), SO4 center dot-, center dot OH and O-1(2) under visible-light irradiation. In addition, in the absence of light, CN-CNO/PMS system exhibited nonradical degradation for NOR through the possible surface-bound complexes mediated electron transfer pathway, confirmed by radical scavenging, substrate specificity test and ATR-FTIR spectra. According to the NOR degradation path analysis, complete intermediates were detected under visible light. This study supplies new insight into the fabrication and application of carbon-based catalysts for efficient antibiotic pollution elimination in aquatic environments.

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