Preparation, characterization, and catalytic properties for the SCR of NO by NH3 of V2O5/TiO2 catalysts prepared by equilibrium deposition filtration

被引:60
作者
Georgiadou, I
Papadopoulou, C
Matralis, HK
Voyiatzis, GA
Lycourghiotis, A
Kordulis, C
机构
[1] Univ Patras, Dept Chem, GR-26500 Patras, Greece
[2] FORTH, Inst Chem Engn & High Temp Chem Proc, GR-26500 Patras, Greece
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1998年 / 102卷 / 43期
关键词
D O I
10.1021/jp973187y
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
V2O5/TiO2 catalysts of varying vanadium content were prepared at various pH's and concentrations of the impregnation solution using the equilibrium deposition filtration (EDF) method. Moreover, corresponding catalysts were prepared using the conventional wet impregnation (WI) method. The above catalysts were exhaustively characterized using BET, AEM, FT-IR, DRS, LRM, XPS, TPR, and TPD of NH3 and tested for the SCR of NO by NH3 in the temperature range 250-450 degrees C. It was found that the application of EDF results in V2O5/TiO2 catalysts with relatively high dispersity of the vanadia supported phase, homogeneous distribution of this phase on the support particles, and quite strong interactions between the supported vanadia phase and the surface of titania, and inhibits the formation of supported V2O5 crystallites. The catalysts prepared by EDF exhibited better activity and selectivity than those prepared by conventional WI. Decrease of the impregnation pH in the EDF preparations from 8 to 4.5 caused an increase in the vanadium content from 2.6 to 3.6 wt % V2O5 which, in turn, provoked very important differences in the physicochemical properties of the EDF catalysts (increase of the surface coverage of the titania by the vanadia phase and decrease of the mean value of the vanadia phase-support interactions). The above explained the increase, with the vanadium content, of the activity and selectivity of the V2O5/TiO2 EDF catalysts.
引用
收藏
页码:8459 / 8468
页数:10
相关论文
共 58 条
[1]  
ANDERSSON SLT, 1990, CATAL LETT, V7, P351
[2]  
ANDESSON A, 1982, J CATAL, V144, P144
[3]  
ARCO MD, 1986, J CATAL, V99, P19
[4]   STRUCTURE AND REACTIVITY OF TITANIA-SUPPORTED OXIDES .2. CHARACTERIZATION OF VARIOUS VANADIUM-OXIDE ON TITANIA CATALYSTS BY X-RAY PHOTOELECTRON-SPECTROSCOPY [J].
BOND, GC ;
ZURITA, JP ;
FLAMERZ, S .
APPLIED CATALYSIS, 1986, 27 (02) :353-362
[5]   STRUCTURE AND REACTIVITY OF TITANIA-SUPPORTED OXIDES .1. VANADIUM-OXIDE ON TITANIA IN THE SUBMONOLAYER AND SUPER-MONOLAYER REGIONS [J].
BOND, GC ;
ZURITA, JP ;
FLAMERZ, S ;
GELLINGS, PJ ;
BOSCH, H ;
VANOMMEN, JG ;
KIP, BJ .
APPLIED CATALYSIS, 1986, 22 (02) :361-378
[6]   Advances in the mechanism of deposition of the CrO42-, HCrO4-, and Cr2O72- species on the surface of titania consisting of anatase and rutile [J].
Bourikas, K ;
Spanos, N ;
Lycourghiotis, A .
LANGMUIR, 1997, 13 (03) :435-444
[7]   Advances in the mechanism of deposition of MoO42- and Mo7O246- species on the surface of titania consisted of anatase and rutile [J].
Bourikas, K ;
Spanos, N ;
Lycourghiotis, A .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1996, 184 (01) :301-318
[8]   Mechanism of deposition of vanadium-oxo, species on the ''anatase/electrolytic solution'' interface [J].
Bourikas, K ;
Georgiadou, I ;
Kordulis, C ;
Lycourghiotis, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (42) :8499-8506
[9]   SURFACE-STRUCTURE AND REACTIVITY OF VANADIUM-OXIDE SUPPORTED ON TITANIUM-DIOXIDE - V2O5/TIO2 (RUTILE) CATALYSTS PREPARED BY HYDROLYSIS [J].
CAVANI, F ;
CENTI, G ;
FORESTI, E ;
TRIFIRO, F ;
BUSCA, G .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1988, 84 :237-254
[10]  
CAVANI F, 1987, PREPARATION CATALYST, V5, P227