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The Efficacy of the Vuv/O3 Process Run in a Continuous-Flow Fluidized Bed Reactor for Simultaneous Elimination of Favipiravir and Bacteria in Aqueous Matrices Publisher Pubmed



Kiyanmehr K1 ; Moussavi G1 ; Mohammadi S1 ; Naddafi K2 ; Giannakis S3
Authors
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Authors Affiliations
  1. 1. Department of Environmental Health Engineering, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
  2. 2. Department of Environmental Health Engineering, Faculty of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Universidad Politecnica de Madrid, E.T.S. Ingenieros de Caminos, Canales y Puertos, Departamento de Ingenieria Civil: Hidraulica, Energia y Medio Ambiente, Unidad docente Ingenieria Sanitaria, c/ Profesor Aranguren, s/n, Madrid, ES-28040, Spain

Source: Chemosphere Published:2022


Abstract

The efficacy of the Vacuum UV/Ozonation (VUV/O3) process was evaluated for the degradation of favipiravir (FAV). It was found that coupling O3 and VUV resulted in a considerable synergistic catalytic effect on FAV removal. The VUV/O3 process performed better in moderately alkaline conditions than in acidic ones; complete FAV degradation and 99.4% TOC removal were achieved within 10 and 60 min, respectively. HO• played the dominant role in FAV degradation, with a second-order reaction rate constant with HO• at 1.05 × 1010 M−1 s−1. The VUV/O3 process could effectively treat tap water spiked with FAV. Efficient FAV and TOC removal, as well as total bacterial inactivation, was attained when treating municipal secondary effluent by the VUV/O3 process. Finally, the VUV/O3 process was operated in a continuous-flow mode in a fluidized-bed (FBR) reactor for treating FAV-spiked tap water. Complete degradation and 75.1% mineralization of 10 mg/L FAV were obtained at a hydraulic retention time of 1 and 8 min, respectively. The findings clearly suggest that the VUV/O3 process operated in a continuous-flow FBR is a promising, efficient technology for the removal of novel and emerging contaminants, such as the antiviral FAV. © 2022 Elsevier Ltd