4.8 Article

Catalytic degradation of ciprofloxacin by a visible-light-assisted peroxymonosulfate activation system: Performance and mechanism

期刊

WATER RESEARCH
卷 173, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2020.115559

关键词

Peroxymonosulfate; Visible light; BiVO4; Catalytic degradation; Water treatment; Mechanism

资金

  1. National Key R&D Program of China [2018YFC0406303]
  2. National Natural Science Foundation of China [21590812, 51908528, 51538011, 51821006]
  3. Postdoctoral Innovation Talent Support Program of China [BX20180290]
  4. China Postdoctoral Science Foundation [2018M640595]
  5. Fundamental Research Funds for the Central Universities [WK2060120001]

向作者/读者索取更多资源

Peroxymonosulfate (PMS) is extensively used as an oxidant to develop the sulfate radical-based advanced oxidation processes in the decontamination of organic pollutants and various PMS activation methods have been explored. Visible-light-assisted PMS activation to construct a Fenton-like process has shown a great potential for pollution control. In our work, BiVO4 nanosheets were prepared using a hydrothermal process and used to activate PMS under visible light. A rapid degradation of ciprofloxacin (CIP) was achieved by dosing PMS (0.96 g/L), BiVO4 (0.32 g/L) under visible light with a reaction rate constant of 77.72-fold higher than that in the BiVaavisible light process. The electron spin resonance and free radical quenching experiments indicate that reactive species of center dot O-2(-).H+ and SO4 center dot- all worked, where h(+), center dot OH and SO4 center dot- were found as the dominant contributors to the CIP degradation. The spectroscopic analyses further demonstrate that the photoinduced electrons were directly involved in the PMS acti- vation process. The generated was partially utilized to activate PMS and more center dot OH was produced because of the chain reactions between SO4 center dot- and H2O/OH-. In this process, PMS acted as an electron acceptor to transfer the photo-induced charges from the conduction band of BiVO4 and PMS was successfully activated to yield the high-powered oxidative species. From the degradation intermediates of CIP detected by a liquid-chromatography-mass spectrometer, the possible degradation pathways were proposed. The substantially decreased toxicity of CIP after the reaction was also observed. This work might provide new insights into the visible-light-assisted PMS activation mechanisms and is useful to construct environmentally-friendly catalytic processes for the efficient degradation of organic pollutants. (C) 2020 Elsevier Ltd. All rights reserved.

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