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February 22, 2026Catalysts0 citationsOpen Access

ZnFe2O4-N-BC Bifunctional Catalyst in Visible Light−Peroxydisulfate Coupled System in Norfloxacin Degradation

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XHXiaoxian HuDZDi ZhangXLXinyu Li

Key Points

  • The aim is to explore the efficiency and mechanism of ZnFe2O4-N-BC as a catalyst in degrading norfloxacin under visible light and peroxydisulfate conditions.
  • Utilized ZnFe2O4-N-BC catalyst in a visible light-peroxydisulfate system.
  • Conducted optical absorption and charge transfer analyses.
  • Performed radical quenching experiment and EPR analysis to determine reactive species involved.
  • Used HPLC-MS for identifying degradation intermediates and pathways.
  • Achieved a degradation rate constant 22.7 times higher in the coupled system than the separate systems.
  • Demonstrated an apparent enhancement factor of 26.3% compared to internal controls.
  • Identified key reactive species contributing to degradation in the order: 1O2 > SO4− > O2−· > ·OH > h+.
  • Displayed a wider pH adaptability of the coupled system.

Abstract

Using norfloxacin (NOR) as the target pollutant, the synergism and degradation mechanism of ZnFe2O4-N-BC (MNBC), a nitrogen (N) and zinc ferrite (ZnFe2O4) co-doped biochar bifunctional catalyst (BC), in visible light (VIS)−peroxydisulfate (PDS) coupled system, were elucidated, and the synergistic mechanism was further supported by optical absorption and photo-induced charge transfer analyses. The results indicate that the degradation rate constant of the ZnFe2O4-N-BC/Vis-PDS system is 22.7 and 17.4 times higher than that of the ZnFe2O4-N-BC/Vis and ZnFe2O4-N-BC/PDS systems, respectively. More importantly, an apparent enhancement factor of 26.3% was obtained relative to the internal control systems. In addition, the coupled system showed a wider pH adaptation range. Furthermore, the radical quenching experiment and EPR analysis further revealed that multiple reactive species (including SO4−, O2−·, ·OH, h+, and 1O2) were involved in the degradation of NOR, and their relative contributions followed the order: 1O2 > SO4− > O2−·> ·OH > h+. Finally, HPLC-MS analysis was performed to identify the key degradation intermediates of NOR, and thus to propose its possible transformation pathways.

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Cite This Study

Hu et al. (2026) studied this question.

synapsesocial.com/papers/699a9d8e482488d673cd37f5https://doi.org/10.3390/catal16020196
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