Photocatalytic degradation of X-3B dye by visible light using lanthanide ion modified titanium dioxide hydrosol system

被引:57
作者
Xie, YB [1 ]
Yuan, CW
Li, XZ
机构
[1] Southeast Univ, Key Lab Mol & Biomol Elect, Nanjing 210096, Peoples R China
[2] Hong Kong Polytech Univ, Dept Civil & Struct Engn, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; sol photocatalyst; visible light; photoactivity; lanthanide ion modification;
D O I
10.1016/j.colsurfa.2004.10.061
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The present work was focused on photocatalytic activity of sol photocatalysts. The lanthanide neodymium ion modified titania sol was prepared by chemical coprecipitation-peptization method and its photoactivity was studied by investigating the photodegradation efficiency of active brilliant red dye X-3B in hydrosol reaction system. It was noted that pure TiO2 and Nd3+-TiO2 sol particles had anatase crystalline structure, uniform nanoparticles distribution and spheral particle morphology, which were prepared at low temperature (70degreesC), ambient pressure and acidic condition (pH 1.5). This preparation method was much better than traditional high temperature calcination process to fabricate crystal TiO2. The average size was 10 nm for Nd3+-TiO2 and 25 nm for TiO2 sol particles. The sol photocatalysts in hydrosol system demonstrated better interfacial adsorption effect and photoactivity than commercial P25 TiO2 powder in suspension system, which was due to small particle size and well nanoparticles dispersion. Moreover, under visible light irradiation (vis, lambda > 400 nm), Nd3+-TiO2 sol showed higher photocatalytic activity than TiO2 Sol, which was ascribed to the electron trapping effect of modified Nd3+ ion on TiO2 Sol particles. Additionally, photosensitization-photocatalysis mechanism was discussed in the VIS/X-3B/Nd3+-TiO2 hydrosol reaction system. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 94
页数:8
相关论文
共 26 条
[11]   An investigation on photocatalytic activities of mixed TiO2-rare earth oxides for the oxidation of acetone in air [J].
Lin, J ;
Yu, JC .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1998, 116 (01) :63-67
[12]   Photocatalytic degradation of pesticide-acaricide formetanate in aqueous suspension of TiO2 [J].
Marinas, A ;
Guillard, C ;
Marinas, JM ;
Fernández-Alba, A ;
Aguëra, A ;
Herrmann, JM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2001, 34 (03) :241-252
[13]   Transparent anatase nanocomposite films by the sol-gel process at low temperatures [J].
Matsuda, A ;
Kotani, Y ;
Kogure, T ;
Tatsumisago, M ;
Minami, T .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2000, 83 (01) :229-231
[14]   Kinetic analysis of photoinduced reactions at the water semiconductor interface [J].
Minero, C .
CATALYSIS TODAY, 1999, 54 (2-3) :205-216
[15]   Decolorization of synthetic dyes by the Fenton reagent and the Cu/pyridine/H2O2 system [J].
Nerud, F ;
Baldrian, P ;
Gabriel, J ;
Ogbeifun, D .
CHEMOSPHERE, 2001, 44 (05) :957-961
[16]  
Poulios I, 1999, J CHEM TECHNOL BIOT, V74, P349, DOI 10.1002/(SICI)1097-4660(199904)74:4<349::AID-JCTB5>3.3.CO
[17]  
2-Z
[18]   Lanthanide oxide-doped titanium dioxide photocatalysts:: Novel photocatalysts for the enhanced degradation of p-chlorophenoxyacetic acid [J].
Ranjit, KT ;
Willner, I ;
Bossmann, SH ;
Braun, AM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (07) :1544-1549
[19]   Influence of metallic species on TiO2 for the photocatalytic degradation of dyes and dye intermediates [J].
Rao, KVS ;
Lavédrine, B ;
Boule, P .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2003, 154 (2-3) :189-193
[20]   Synthesis of zinc oxide nanoparticles with controlled morphology [J].
Wang, LN ;
Muhammed, M .
JOURNAL OF MATERIALS CHEMISTRY, 1999, 9 (11) :2871-2878