1989
DOI: 10.1016/s0166-9834(00)83386-2
|View full text |Cite
|
Sign up to set email alerts
|

Structure and selectivity changes in vanadia-titania catalysts used to promote the reduction of nitric oxide with ammonia

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
5
0

Year Published

1991
1991
2002
2002

Publication Types

Select...
7
1
1

Relationship

0
9

Authors

Journals

citations
Cited by 12 publications
(5 citation statements)
references
References 12 publications
0
5
0
Order By: Relevance
“…The anatase is a low-temperature modification of titania, and the phase transition to rutile generally occurs above 973 K. The vanadia supported on anatase TiO 2 is a classical example of support enhancement of active phase, especially if the vanadium oxide is applied to titania as a monomolecular layer. The optimal catalytic activity and selectivity is achieved when one monolayer of vanadia is dispersed on anatase phase of TiO 2 . , The structure of highly dispersed VO x species present on the TiO 2 surface in V 2 O 5 /TiO 2 catalysts has been studied extensively in the recent past by various spectroscopic techniques including laser Raman spectra, 51 V NMR, , ESR, , EXAFS, and ESCA. The V 2 O 5 /TiO 2 catalyst system has been employed in selective oxidation and ammoxidation of aromatic hydrocarbons and alcohols. In environmental catalytic applications V 2 O 5 /TiO 2 catalysts in combination with WO 3 have been successfully employed for selective catalytic reduction of NO x reactions. …”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…The anatase is a low-temperature modification of titania, and the phase transition to rutile generally occurs above 973 K. The vanadia supported on anatase TiO 2 is a classical example of support enhancement of active phase, especially if the vanadium oxide is applied to titania as a monomolecular layer. The optimal catalytic activity and selectivity is achieved when one monolayer of vanadia is dispersed on anatase phase of TiO 2 . , The structure of highly dispersed VO x species present on the TiO 2 surface in V 2 O 5 /TiO 2 catalysts has been studied extensively in the recent past by various spectroscopic techniques including laser Raman spectra, 51 V NMR, , ESR, , EXAFS, and ESCA. The V 2 O 5 /TiO 2 catalyst system has been employed in selective oxidation and ammoxidation of aromatic hydrocarbons and alcohols. In environmental catalytic applications V 2 O 5 /TiO 2 catalysts in combination with WO 3 have been successfully employed for selective catalytic reduction of NO x reactions. …”
Section: Introductionmentioning
confidence: 99%
“…[19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36] In environmental catalytic applications V 2 O 5 /TiO 2 catalysts in combination with WO 3 have been successfully employed for selective catalytic reduction of NO x reactions. [37][38][39][40][41][42][43][44] In the present investigation we report the characterization of vanadium oxide catalysts supported on various modifications of TiO 2 (anatase, rutile, and titania containing anatase and rutile) by XRD, ESR, and oxygen chemisorption methods. We also report the differences in catalytic properties exhibited by these catalysts during vapor-phase ammoxidation of 3-picoline to nicotinonitrile.…”
Section: Introductionmentioning
confidence: 99%
“…Supported vanadium oxide catalysts have been widely investigated as they represent an important group of catalysts for a number of selective oxidation reactions as well as the reduction of NO with NH 3 . The bulk oxides cannot generally be employed in industrial applications because of their lack of thermal/mechanical strength. In addition, the surface structure of vanadia dispersed on supported oxides is very different from that of bulk phase and consequently exhibits a unique role in catalytic activity and selectivity.…”
Section: Introductionmentioning
confidence: 99%
“…Vanadia-based catalysts are being used commercially to reduce NO* levels as prescribed by Clean Air Act Amendments (CAAA) of 1990. Due to their high NO* removal efficiencies and SO2 resistant properties these catalysts have received a great deal of attention in the past few years (Bosch et al, 1986; Bauerle et al, 1975; Bauerle et al, 1978;Morikawa et al, 1981;Nam et al, 1986; Haber et al, 1986;Inomata et al, 1982;Janssen, 1988;Hotter et al, 1989). While our understanding of the catalytic phenomena involved in the SCR reaction network has significantly increased through some of the recent studies (Haber et al, 1986;Janssen, 1988; Odriozola et al, 1989; Ramis et al, 1990;Topsoe, 1991; Went et al, 1992a,b,c), there still remain questions in the literature regarding the nature of active sites, the elementary steps that take place on the catalyst surfaces, the adsorption/desorption behavior of nitric oxide and ammonia, and the role of the support material.…”
Section: Introductionmentioning
confidence: 99%