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Mesoporous Bimetallic S-Doped Nanoparticles Prepared Via Hydrothermal Method for Enhanced Photodegradation of 4-Chlorophenol Publisher Pubmed



Taheri E1, 2 ; Fatehizadeh A1, 2 ; Hadi S1, 3 ; Amin MM1, 2 ; Khiadani M4 ; Ghasemian M1, 2 ; Rafiei N1, 3 ; Rezakazemi M5 ; Aminabhavi TM6
Authors
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Authors Affiliations
  1. 1. Department of Environmental Health Engineering, School of Health, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Environment Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Student Research Committee, School of Health, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. School of Engineering, Edith Cowan University, 270 Joondalup Drive, Joondalup, 6027, WA, Australia
  5. 5. Faculty of Chemical and Materials Engineering, Shahrood University of Technology, Shahrood, Iran
  6. 6. Center for Energy and Environment, School of Advanced Sciences, KLE Technological University, Hubballi, 580031, India

Source: Journal of Environmental Management Published:2024


Abstract

Magnesium oxides (MgO) have gained shown significant promise for a variety of applications, which can be modified by ions doping. In this study, bimetallic Ag-doped S–MgO nanoparticles were prepared by hydrothermal method and used for photocatalytic degradation of 4-chlorophenl (4-CP). EDX suggested the presence of no impurities, which mainly contained Mg, Ag, and S elements, suggesting that S and Ag were incorporated into the lattice of MgO as a result of successful doping. Estimated bandgap of Ag-doped S–MgO nanoparticles was 3.7 eV, lower than MgO (7.8 eV), but useful to improve optical characteristics and photocatalytic efficiency to degrade 4-CP up to a maximum of 99.60 ± 0.50%. The synergetic parameter during photocatalysis of 4-CP was 6.91, confirming the degradation of 4-CP. Quenching experiments proved the presence of hydroxyl radicals (•OH) and singlet dioxygen (1O2) that were critical in 4-CP degradation. The kinetics rate constant was increased by 24.8% from 0.086 ± 0.004 to 0.108 ± 0.005 min−1 by the addition of sulfate in the reaction medium. The work proposes a new synthetic method for preparing catalysts that are capable of producing in-situ •OH radicals and 1O2 to decompose the organic contaminants. © 2023 Elsevier Ltd
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