Selective reduction of NO with NH3 on a new iron-vanadyl phosphate catalyst

被引:22
作者
Bagnasco, G
Busca, G
Galli, P
Massucci, MA
Melanová, K
Patrono, P
Ramis, G
Turco, M
机构
[1] Univ Naples Federico II, Dipartimento Ingn Chim, I-80125 Naples, Italy
[2] Univ Genoa, Fac Ingn, Ist Chim, I-16129 Genoa, Italy
[3] Univ Roma La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
[4] Univ Pardubice, Pardubice 53009, Czech Republic
[5] Acad Sci Czech Republ, Joint Lab Solid State Chem, Prague, Czech Republic
[6] CNR, IMAI, I-00016 Monterotondo, Rome, Italy
关键词
iron-vanadyl phosphate; NOx removal; ammonia adsorption; water vapour;
D O I
10.1016/S0926-3373(00)00169-7
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
The compound [Fe(H2O)](0.20)(VO)(0.80)PO4 was studied for NH3-adsorption properties and catalytic activity towards NO reduction by NH3, Adsorption properties were studied by means of temperature programmed desorption (TPD) and FT-IR techniques. FT-IR investigation gave evidence of the presence of strong Lewis acid sites and less strong Bronsted acid sites, The NH3 uptake increased in the presence of water vapour due to an increase in the concentration of surface acid sites and due to some NH3 intercalation. Catalytic activity measurements, performed under diluted feed conditions at T = 250-450 degreesC and a contact time of 9 x 10(-3) s, gave NO conversion up to 60%, with small N2O production. Addition of water vapour to the feed caused not only a slight decrease in NO and NH3 conversion but also a marked decrease in N2O formation, thus enhancing the reaction selectivity. This behaviour was ascribed to an inhibiting effect of water on NH3 oxidation. (C) 2000 Elsevier Science B.V, All rights reserved.
引用
收藏
页码:135 / 142
页数:8
相关论文
共 41 条
[1]   DETERMINATION OF THE SURFACE-ACIDITY OF LAYERED METAL PHOSPHATES BY NH3 TEMPERATURE-PROGRAMMED DESORPTION [J].
BAGNASCO, G ;
CIAMBELLI, P ;
LAGINESTRA, A ;
TURCO, M .
THERMOCHIMICA ACTA, 1990, 162 (01) :91-97
[2]   TG/DTA, XRD and NH3-TPD characterization of layered VOPO4•2H2O and its Fe3+-substituted compound [J].
Bagnasco, G ;
Benes, L ;
Galli, P ;
Massucci, MA ;
Patrono, P ;
Turco, M ;
Zima, V .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 1998, 52 (02) :615-630
[3]  
Bagnasco G, 1997, STUD SURF SCI CATAL, V110, P643
[4]  
Bagnasco G, 1998, STUD SURF SCI CATAL, V119, P653
[5]  
BAGNASCO G, 2000, IN PRESS J THERM ANA, V61
[6]   Thermal, structural and acidic characterization of some vanadyl phosphate materials modified with trivalent metal cations [J].
Benes, L ;
Galli, P ;
Massucci, MA ;
Melanova, K ;
Zima, V .
JOURNAL OF THERMAL ANALYSIS, 1997, 50 (03) :355-364
[7]  
BENES L, 1986, INORG CHIM ACTA, V114, P47
[8]   INTERCALATION OF ALIPHATIC-AMINES INTO LAYERED STRUCTURE OF VANADYL PHOSPHATE [J].
BENES, L ;
HYKLOVA, R ;
KALOUSOVA, J ;
VOTINSKY, J .
INORGANICA CHIMICA ACTA, 1990, 177 (01) :71-74
[9]  
Bosch H., 1986, CATAL TODAY, V2, P369, DOI DOI 10.1016/0920-5861(88)80002-6
[10]  
BRONWYN LD, 1995, J CATAL, V154, P107