Monolayer transition metal supported on titania catalysts for the selective catalytic reduction of NO by NH3

被引:53
作者
Bourikas, K
Fountzoula, C
Kordulis, C [1 ]
机构
[1] Univ Patras, Dept Chem, GR-26500 Patras, Greece
[2] FORTH ICE HT, Inst Chem Engn & High Temp Chem Proc, GR-26500 Patras, Greece
关键词
V2O5TiO2; Cr2O3/TiO2; MoO3/TiO2; WO3/TiO2 monolayer catalysts; transition metal supported titania catalysts; equilibrium deposition filtration (EDF); selective catalytic reduction (SCR); nitric oxide; ammonia; active phase-support interactions; DRS; XPS;
D O I
10.1016/j.apcatb.2004.04.001
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
Monolayer catalysts were prepared by supporting transition metal ionic (t.m.i.)-oxo species (VOx, CrOx, MoOx and WOx) on the TiO2 (anatase) surface using the equilibrium-deposition-filtration (EDF) technique. The prepared samples were characterized by N-2 adsorption, UV/Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS) and tested for the selective catalytic reduction of NO by NH3 (NH3-SCR) in the temperature range 250-450 degreesC. Using the EDF method the transition metal ion (V, Cr, Mo or W) loading of the supported Titania catalysts achieved at monolayer coverage follows the order V > Mo > W > Cr. It is mainly determined by the deposition of polymeric t.m.i.-oxo species on the surface of titania in the impregnation step. The activity of the corresponding monolayers follows the order V > Cr > Mo > W. It was also demonstrated that the activity of the above catalysts correlates well with the intensity of a DRS absorption band appearing at ca. 400 nm. The intensity of this absorption band, which is considered as a measure of the extent of interactions exerted between the active phase and the support surface, depends on the kind and the amount of the transition metal. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:145 / 153
页数:9
相关论文
共 66 条
[41]   SODIUM-DOPED V2O5/TIO2 SYSTEMS - AN XRD, DTA, TG/DTG, IR, V-UV, TPR, AND XANES STUDY [J].
MALET, P ;
MUNOZPAEZ, A ;
MARTIN, C ;
RIVES, V .
JOURNAL OF CATALYSIS, 1992, 134 (01) :47-57
[42]   COMPARISON AND ANALYSIS OF INTRINSIC KINETICS AND EFFECTIVENESS FACTORS FOR THE CATALYTIC REDUCTION OF NO WITH AMMONIA IN THE PRESENCE OF OXYGEN [J].
MARANGOZIS, J .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1992, 31 (04) :987-994
[43]   SELECTIVE OXIDATION OF TOLUENE OVER V2O5/TIO2 CATALYSTS - EFFECT OF VANADIUM LOADING AND OF MOLYBDENUM ADDITION ON THE CATALYTIC PROPERTIES [J].
MATRALIS, HK ;
PAPADOPOULOU, C ;
KORDULIS, C ;
ELGUEZABAL, AA ;
CORBERAN, VC .
APPLIED CATALYSIS A-GENERAL, 1995, 126 (02) :365-380
[44]  
MATRALIS HK, 1997, POLISH J APPL CHEM, V41, P275
[45]   Characterization and reactivity of TiO2-supported MoO3 De-Nox SCR catalysts [J].
Nova, I ;
Lietti, L ;
Casagrande, L ;
Dall'Acqua, L ;
Giamello, E ;
Forzatti, P .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 17 (03) :245-258
[46]   On the relationship between the preparation method and the physicochemical and catalytic properties of the CoMo/γ-Al2O3 hydrodesulfurization catalysts [J].
Papadopoulou, C ;
Vakros, J ;
Matralis, HK ;
Kordulis, C ;
Lycourghiotis, A .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 261 (01) :146-153
[47]  
Papadopoulou C, 1996, B SOC CHIM BELG, V105, P247
[48]   TiO2-supported metal oxide catalysts for low-temperature selective catalytic reduction of NO with NH3I.: Evaluation and characterization of first row transition metals [J].
Peña, DA ;
Uphade, BS ;
Smirniotis, PG .
JOURNAL OF CATALYSIS, 2004, 221 (02) :421-431
[49]  
Pope M. T., 1994, ENCY INORGANIC CHEM, V6
[50]   CHARACTERIZATION OF TUNGSTA TITANIA CATALYSTS [J].
RAMIS, G ;
BUSCA, G ;
CRISTIANI, C ;
LIETTI, L ;
FORZATTI, P ;
BREGANI, F .
LANGMUIR, 1992, 8 (07) :1744-1749