Synthesis and characterization of La2O3/TiO2-xFx and the visible light photocatalytic oxidation of 4-chlorophenol

被引:38
作者
Cao, Guangxiu [2 ,3 ]
Li, Yaogang [2 ]
Zhang, Qinghong [1 ]
Wang, Hongzhi [2 ]
机构
[1] Donghua Univ, Engn Res Ctr Adv Glasses Mfg Technol, MOE, Shanghai 201620, Peoples R China
[2] Donghua Univ, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[3] Shangqiu Normal Univ, Dept Chem, Shangqiu 476000, Peoples R China
关键词
Visible light; Photocatalytic oxidation; TiO2; 4-Chlorophenol; DOPED TITANIUM-DIOXIDE; TIO2; PHOTOCATALYSTS; SPRAY-PYROLYSIS; NITROGEN; DEGRADATION; CARBON; NANOPARTICLES; EFFICIENT; LANTHANUM; BORON;
D O I
10.1016/j.jhazmat.2010.01.101
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this work, we investigated the synergetic effect of La and F on the visible light photocatalytic activity of TiO2 catalysts. La2O3/TiO2-xFx photocatalysts were prepared by a simple sol-gel process using tetrabutyl titanate (TBT). La(NO3)(3) and NH4F as precursors. XPS results revealed that La2O3 accumulated on the surface of TiO2, which enhanced the surface area of TiO2 and inhibited the recombination of electron-hole pairs. It also showed that two kinds of fluorine species were formed and these increased the acid active sites and enhanced the oxidation potential of the photogenerated holes in the valance band. UV-vis diffuse reflection spectra of La2O3/TiO2-xFx showed that intraband gap states were present and these are probably responsible for its absorption of visible light while the intrinsic absorption band was shifted slightly to a longer wavelength. At molar ratios of La and F to Ti of 1.5:100 and 5:100 and after calcination at 500 degrees C. the degradation rate of 4-chlorophenol (4-CP) over the sample was about 1.2-3.0 times higher than that of the other doped samples and undoped TiO2. The total organic carbon (TOC) removal rates of 4-CP showed that 4-CP was mineralized efficiently in the presence of the sample under visible light illumination. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:440 / 449
页数:10
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