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Photocatalytic degradation of neonicotinoid insecticides using sulfate-doped Ag3PO4 with enhanced visible light activityoa mark
  • Lee, Youn Jun ;
  • Kang, Jin Kyu ;
  • Park, Seong Jik ;
  • Lee, Chang Gu ;
  • Moon, Joon Kwan ;
  • Alvarez, Pedro J.J.
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Publication Year
2020-12-15
Publisher
Elsevier B.V.
Citation
Chemical Engineering Journal, Vol.402
Keyword
Neonicotinoid insecticidesPhotocatalytic degradationPhotoinduced holeSulfate doped Ag3PO4Visible light photocatalyst
Mesh Keyword
Charge transfer resistanceFirst-order rate constantsNeonicotinoid insecticidesPhoto catalytic degradationPhotocatalytic efficiencySpectrophotometer measurementsVisible light activated photocatalystsVisible light photocatalytic activity
All Science Classification Codes (ASJC)
Chemistry (all)Environmental ChemistryChemical Engineering (all)Industrial and Manufacturing Engineering
Abstract
Visible light-activated photocatalysts offer a promising approach to remove recalcitrant organic contaminants from water without adding chemicals, using free solar energy. In this study, sulfate-doped silver phosphate (SO4-Ag3PO4) was prepared using a simple precipitation method, and its visible light photocatalytic activity against seven neonicotinoid insecticides currently available on the market was evaluated. The characteristics of the photocatalysts were analyzed using diffuse reflectance-UV/visible spectrophotometer measurements and electrochemical impedance spectroscopy analysis. Photocatalytic degradation of all tested insecticides under visible light irradiation was significantly enhanced by SO4 doping, which decreased band gap energy and charge transfer resistance. The apparent first-order rate constant (kapp) with SO4-Ag3PO4 varied depending on the insecticides (0.003–0.432/min), and was at least 5.4-fold faster than that with pristine Ag3PO4, in the order of thiacloprid (TCP) > nitenpyram (NTP) > imidacloprid (ICP) > clothianidin (CTD) > acetamiprid (ATP) > thiamethoxam (TMX) > dinotefuran (DTF). Even after four reuse cycles, SO4-Ag3PO4 maintained over 75% of its initial photocatalytic efficiency. Reactive species trapping experiments indicated that photoinduced electron holes (h+) were the most important oxidant for ICP degradation.
ISSN
1385-8947
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/31405
DOI
https://doi.org/10.1016/j.cej.2020.126183
Fulltext

Type
Article
Funding
This work was supported by the National Research Foundation (NRF) of Korea [Grant no. NRF-2018R1C1B5044937]. Partial funding for PJA was provided by the United States National Science Foundation (NSF) Engineering Research Center (ERC) for Nanotechnology-Enabled Water Treatment ( EEC-1449500 ).This work was supported by the National Research Foundation (NRF) of Korea [Grant no. NRF-2018R1C1B5044937]. Partial funding for PJA was provided by the United States National Science Foundation (NSF) Engineering Research Center (ERC) for Nanotechnology-Enabled Water Treatment (EEC-1449500).
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Lee, Chang-Gu  Image
Lee, Chang-Gu 이창구
Department of Environmental and Safety Engineering
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