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author:

Huang, Y.-L. (Huang, Y.-L..) [1] | Li, D.-Z. (Li, D.-Z..) [2] | Fu, X.-Z. (Fu, X.-Z..) [3] | Wang, X.-X. (Wang, X.-X..) [4]

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Scopus PKU CSCD

Abstract:

The La3+-doped TiO2 photocatalyst was prepared by the improved sol-gel and impregnation method. XRD, N2 adsorption, UV-Vis diffuse reflection spectroscopy and surface photovoltage spectroscopy (SPS) were applied to study the effect of La3+ doping. At the same time, the photocatalytic process of TiO2 and La3+-doped TiO 2 catalysts for degradation of ethylene, acetone, benzene were further studied by means of in situ FTIR. The result indicated that La 3+ doping could enhance the photocatalytic activities of ethylene, acetone, benzene to some extend as compared with pure TiO2. The increase in photoactivity is probably due to higher content of anatase, smaller particle size, higher specific surface area and lager band gap. In addition, the higher photocatalytic activity of La3+-doped TiO2 may be attributed to the stronger photovoltage signal and the effective separation of photo-generated electron-hole pairs. The result also showed that ethylene could be photocatalytically oxidized to CO2. The acetone and benzene may be photocatalytically oxidized to propionic acid and phenol, quinone, respectively.

Keyword:

in situ FTIR; La3+ doping; Organic contaminants; Photocatalytic oxidation; TiO2

Community:

  • [ 1 ] [Huang, Y.-L.]Chemistry and Chemical Engineering Department, Minjiang University, Fuzhou 350108, China
  • [ 2 ] [Li, D.-Z.]Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 3 ] [Fu, X.-Z.]Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 4 ] [Wang, X.-X.]Research Institute of Photocatalysis, Fuzhou University, Fuzhou 350002, China

Reprint 's Address:

  • [Huang, Y.-L.]Chemistry and Chemical Engineering Department, Minjiang University, Fuzhou 350108, China

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Source :

Chinese Journal of Inorganic Chemistry

ISSN: 1001-4861

Year: 2006

Issue: 7

Volume: 22

Page: 1275-1281

0 . 5 8 3

JCR@2006

0 . 8 0 0

JCR@2023

JCR Journal Grade:4

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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