論文

査読有り
2015年5月

Decomposition of methyl orange using C-60 fullerene adsorbed on silica gel as a photocatalyst via visible-light induced electron transfer

APPLIED CATALYSIS B-ENVIRONMENTAL
  • Ryo Wakimoto
  • ,
  • Tamako Kitamura
  • ,
  • Fuyu Ito
  • ,
  • Hisanao Usami
  • ,
  • Hiroshi Moriwaki

166
開始ページ
544
終了ページ
550
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.apcatb.2014.12.010
出版者・発行元
ELSEVIER SCIENCE BV

Visible-light induced electron transfer reactions of C-60 fullerene adsorbed on silica gel (C-60/SiO2 powder) to methyl orange in water have been studied. The C-60/SiO2 powder was simply prepared by mixing a toluene solution of the C-60 fullerene with silica gel followed by evaporating the toluene. Irradiation by visible light (>420 nm) of the methyl orange aqueous solution (25 mu M) in the presence of the C-60/SiO2 powder and ascorbic acid resulted in the decomposition of the methyl orange. These results showed that the degradation conversion reached 96% after a 25-min visible light irradiation. The reaction also occurred by the irradiation of sunlight. The reductive products of methyl orange, N,N-dimethyl-p-phenylenediamine and sulfanilic acid, were ascertained and monitored by liquid chromatography/mass spectrometry (LC/MS). The reaction did not occur in the dark and in the absence of C-60/SiO2 or ascorbic acid. The possible mechanism of the reaction is discussed. Furthermore, the C-60/SiO2 powder was applied to a continuous flow system for the photodecomposition of methyl orange. C-60/SiO2 powder was packed in a glass tube. The methyl orange solution was pumped into the glass tube, and the tube was irradiated by visible light or sunlight. The continuous decomposition of methyl orange was achieved by this method. (C) 2014 Elsevier B.V. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.apcatb.2014.12.010
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000348753400060&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.apcatb.2014.12.010
  • ISSN : 0926-3373
  • eISSN : 1873-3883
  • Web of Science ID : WOS:000348753400060

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