Sol-gel preparation of TiO2-ZrO2 thin films supported on glass rings:: Influence of phase composition on photocatalytic activity

被引:74
作者
Hernández-Alonso, MD
Tejedor-Tejedor, I
Coronado, JM
Soria, J
Anderson, MA
机构
[1] CSIC, Inst Catalisis & Petroleoquim, Madrid 28049, Spain
[2] Univ Wisconsin, Environm Chem & Technol Program, Madison, WI 53706 USA
关键词
photocatalysis; TiO2; ZrO2; anatase; solid solutions; nanoparticles; TG-DTA; Raman spectroscopy; band gap;
D O I
10.1016/j.tsf.2005.07.256
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In order to optimize the characteristics of TiO2-ZrO2 thin films supported on glass for the photocatalytic removal of VOCs, acidic sols of different composition (ZrO2, TiO2 and Ti-Zr mixed oxides) have been prepared using metal alkoxides as starting materials. The photoactive oxides were deposited on "Raschig rings" of borosilicate glass using a dip-coating technique. The phase composition of the thin films was controlled during the sol preparation stage to produce either (1) Ti0.90Zr0.10O2 solid solutions, or (2) ZrO2/TiO2 binary metal oxides (10% and 20% molar content of Zr). The particle size of the different sols was measured by photon correlation spectroscopy, and the xerogels were characterized by XRD, N-2 adsorption isotherms, and TG-DTA, so as to monitor the modifications induced by the thermal treatments. Raman spectroscopy was used to determine the crystalline structure of the supported TiO2-ZrO2 oxides, which in all cases corresponded to the anatase phase. The band gap of the thin films was estimated from the UV-vis spectra, and none of them differed significantly from that of unmodified TiO2. The photoactivity of the coated glass "Raschig rings" was measured for the oxidation of acetone and methylcyclohexane vapors using, respectively, total recycle and single pass plug flow photoreactors. The results obtained indicate that, for the same Zr content, the photoactivity of the films containing binary metal oxides is slightly higher than that of the solid solution. In contrast, specific surface area seems to have little influence on the performance of the thin films. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 131
页数:7
相关论文
共 24 条
[1]   The design and development of highly reactive titanium oxide photocatalysts operating under visible light irradiation [J].
Anpo, M ;
Takeuchi, M .
JOURNAL OF CATALYSIS, 2003, 216 (1-2) :505-516
[2]   Electrostatic sol-spray deposition (ESSD) and characterisation of nanostructured TiO2 thin films [J].
Chen, CH ;
Kelder, EM ;
Schoonman, J .
THIN SOLID FILMS, 1999, 342 (1-2) :35-41
[3]   Photocatalytic oxidation of ketones in the gas phase over TiO2 thin films:: a kinetic study on the influence of water vapor [J].
Coronado, JM ;
Zorn, ME ;
Tejedor-Tejedor, I ;
Anderson, MA .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 43 (04) :329-344
[4]   THE GAS-PHASE PHOTOCATALYTIC MINERALIZATION OF BENZENE ON POROUS TITANIA-BASED CATALYSTS [J].
FU, XZ ;
ZELTNER, WA ;
ANDERSON, MA .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1995, 6 (03) :209-224
[5]   Enhanced photocatalytic performance of titania-based binary metal oxides: TiO2/SiO2 and TiO2/ZrO2 [J].
Fu, XZ ;
Clark, LA ;
Yang, Q ;
Anderson, MA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (02) :647-653
[6]   Visible light-activated nanosized doped-TiO2 photocatalysts [J].
Fuerte, A ;
Hernández-Alonso, MD ;
Maira, AJ ;
Martínez-Arias, A ;
Fernández-García, M ;
Conesa, JC ;
Soria, J .
CHEMICAL COMMUNICATIONS, 2001, (24) :2718-2719
[7]   ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[8]  
Kawahara T, 2002, ANGEW CHEM INT EDIT, V41, P2811, DOI 10.1002/1521-3773(20020802)41:15<2811::AID-ANIE2811>3.0.CO
[9]  
2-#
[10]   Patterned TiO2/SnO2 bilayer type photocatalyst.: 2.: Efficient dehydrogenation of methanol [J].
Kawahara, T ;
Konishi, Y ;
Tada, H ;
Tohge, N ;
Ito, S .
LANGMUIR, 2001, 17 (23) :7442-7445