The effects of activated carbon supports on the structure and properties of TiO2 nanoparticles prepared by a sol-gel method

被引:101
作者
Li, Youji [1 ]
Zhang, Shiying
Yu, Qumin
Yin, Wenbin
机构
[1] Jishou Univ, Coll Chem & Chem Engn, Hunan 416000, Peoples R China
[2] Hunan Univ, Coll Mat Sci & Engn, Hunan 410082, Peoples R China
[3] Changsha Coll, Dept Chem & Environm Engn, Hunan 410003, Peoples R China
关键词
crystallites; sol-gel method; nanomaterials; titanium composites; activated carbon;
D O I
10.1016/j.apsusc.2007.05.057
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
TiO2-coated activated carbon (TiO2/AC) composites and pure TiO2 powders were prepared by a sol-gel method using tetrabutylorthotitanate as a precursor. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), differential thermal analysis (DTA), X-ray photoelectron spectrum (XPS) and nitrogen absorption. The photoactivity of samples was evaluated by methylene blue (MB) degradation. The analysis results show that compared with pure TiO2 powders, the spherical-shaped TiO2 particles are well-dispersed in the AC matrix and the size of the resulting TiO2 crystallites decreases to below 40 mu with increasing phase transformation temperature. The AC matrix creates anti-calcination effects and shows interfacial energy effects that control the growth of the TiO2 particles, baffle the anatase to rutile phase transition, and cumber the TiO2 particles to agglomerate. Compared with the surface areas of TiO2 powders, the combination of TiO2 and AC forms composites with high surface areas which are slightly affected by calcination temperature. By AC support, the photoactivity of TiO2 is increased in MB photocatalytic course, possible because active carbon increases photocatalytic activity of TiO2 particles by producing high concentration of organic compound near TiO2, and small-size TiO2 particles are well-dispersed on the surface of AC. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:9254 / 9258
页数:5
相关论文
共 18 条
[1]  
BEATA T, 2004, J PHOTOCH PHOTOBIO A, V167, P127
[2]   A STRUCTURAL INVESTIGATION OF TITANIUM-DIOXIDE PHOTOCATALYSTS [J].
BICKLEY, RI ;
GONZALEZCARRENO, T ;
LEES, JS ;
PALMISANO, L ;
TILLEY, RJD .
JOURNAL OF SOLID STATE CHEMISTRY, 1991, 92 (01) :178-190
[3]   The surface science of titanium dioxide [J].
Diebold, U .
SURFACE SCIENCE REPORTS, 2003, 48 (5-8) :53-229
[4]   Deposition of anatase on the surface of activated carbon [J].
El-Sheikh, AH ;
Newman, AP ;
Al-Daffaee, H ;
Phull, S ;
Cresswell, N ;
York, S .
SURFACE & COATINGS TECHNOLOGY, 2004, 187 (2-3) :284-292
[5]   PHOTOCATALYTIC ACTIVITY OF ULTRA-FINE RUTILE IN METHANOL WATER SOLUTION AND DEPENDENCE OF ACTIVITY ON PARTICLE-SIZE [J].
HARADA, H ;
UEDA, T .
CHEMICAL PHYSICS LETTERS, 1984, 106 (03) :229-231
[6]   INFLUENCE OF THE DENSITY OF SURFACE HYDROXYL-GROUPS ON TIO2 PHOTOCATALYTIC ACTIVITIES [J].
KOBAYAKAWA, K ;
NAKAZAWA, Y ;
IKEDA, M ;
SATO, Y ;
FUJISHIMA, A .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1990, 94 (12) :1439-1443
[7]   Photocatalytic degradation of methyl orange in a sparged tube reactor with TiO2-coated activated carbon composites [J].
Li, YJ ;
Li, XD ;
Li, JW ;
Yin, J .
CATALYSIS COMMUNICATIONS, 2005, 6 (10) :650-655
[8]   Photocatalytic reduction of CO2 using surface-modified CdS photocatalysts in organic solvents [J].
Liu, BJ ;
Torimoto, T ;
Yoneyama, H .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1998, 113 (01) :93-97
[9]   Degradation of bisphenol A in water by TiO2 photocatalyst [J].
Ohko, Y ;
Ando, I ;
Niwa, C ;
Tatsuma, T ;
Yamamura, T ;
Nakashima, T ;
Kubota, Y ;
Fujishima, A .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (11) :2365-2368
[10]   Chemistry of NO2 on oxide surfaces:: Formation of NO3 on TiO2(110) and NO2⇆O vacancy interactions [J].
Rodriguez, JA ;
Jirsak, T ;
Liu, G ;
Hrbek, J ;
Dvorak, J ;
Maiti, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (39) :9597-9605