Properties and catalytic activity of NOx reduction of alumina-titania catalysts prepared by sol-gel method

被引:18
作者
Kawabata, K
Yoshimatsu, H
Fujiwara, K
Yabuki, T
Osaka, A
Miura, Y
机构
[1] Okayama Ceram Res Fdn, Bizen 7050021, Japan
[2] Ind Technol Ctr Okayama Prefecture, Okayama 7011296, Japan
[3] Okayama Univ, Fac Engn, Dept Biosci & Technol, Okayama 7008530, Japan
[4] Okayama Univ, Fac Environm Sci & Technol, Dept Environm Chem & Mat, Okayama 7008530, Japan
关键词
D O I
10.1023/A:1004632211927
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The alumina-titania catalysts were prepared from various alumina and titania sources by sol-gel method, which were metal alkoxide and metal alkoxide modified with organic groups. Specific surface area, pore size distribution, solid acidity and catalytic activity of NO reduction for the alumina-titania catalysts depended on the alumina and titania sources. The alumina-titania catalyst prepared from metal alkoxide for alumina source and metal alkoxide modified with organic groups for titania source exhibited higher activity of NO reduction than the other alumina-titania catalysts. Catalytic activity of NO reduction for the alumina-titania catalysts depended on specific surface area and solid acidity. It was suggested that solid acidity of the alumina-titania catalysts depended on the coordination structure of Al atoms and the homogeneity of alumina and titania components. (C) 1999 Kluwer Academic Publishers.
引用
收藏
页码:2529 / 2534
页数:6
相关论文
共 27 条
[1]   OUTSTANDING PROBLEMS IN THE KAOLINITE-MULLITE REACTION SEQUENCE INVESTIGATED BY SI-29 AND AL-27 SOLID-STATE NUCLEAR MAGNETIC-RESONANCE .2. HIGH-TEMPERATURE TRANSFORMATIONS OF METAKAOLINITE [J].
BROWN, IWM ;
MACKENZIE, KJD ;
BOWDEN, ME ;
MEINHOLD, RH .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1985, 68 (06) :298-301
[2]  
*CHEM SOC JAP, 1991, EXP COURS CHEM 5 NMR, P235
[3]  
*COMM REF CAT JAP, 1991, SHOKUBAI, V33, P249
[4]   SELECTIVE REDUCTION OF NO BY HYDROCARBONS AND OXYGENATED HYDROCARBONS OVER METAL-OXIDE CATALYSTS [J].
HAMADA, H .
CATALYSIS TODAY, 1994, 22 (01) :21-40
[5]  
HAMADA H, 1991, SHOKUBAI, V33, P320
[6]  
HAMADA H, 1993, SEKIYU GAKKAISHI, V36, P149
[7]  
HAMADA H, 1997, NEW CERAMICS, V7, P41
[8]  
HATTORI A, 1988, NEW CHEM CATALYST, P143
[9]  
HATTORI H, 1988, NEW CHEM CATALYST, P175
[10]  
HAYASHI S, 1993, SOLID NMR MAT, P52