The influence of chromium substitution on an iron–titanium catalyst used in the selective catalytic reduction of NO

The selective catalytic reduction (SCR) of NO by NH3 over chromium-substituted Fe titanate catalysts with different amounts of chromium has been studied. The experiments revealed that the amount of chromium in the catalyst is a crucial factor for high activity. Fe0.5Cr0.5TiOx showed the highest acti...

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Published inJournal of catalysis Vol. 292; pp. 32 - 43
Main Authors Karami, Asghar, Salehi, Vajiheh
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.08.2012
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Abstract The selective catalytic reduction (SCR) of NO by NH3 over chromium-substituted Fe titanate catalysts with different amounts of chromium has been studied. The experiments revealed that the amount of chromium in the catalyst is a crucial factor for high activity. Fe0.5Cr0.5TiOx showed the highest activity. A series of Cr-substituted Fe–Ti compounds were prepared by the co-precipitation method and were systematically investigated as catalysts for the selective catalytic reduction (SCR) of NO by NH3. A variety of analytical techniques revealed that the Cr substitution amount affects the N2 selectivity, SCR activity, redox behavior of NH3/NOx, adsorption ability, and structure of catalysts in terms of surface properties, porosity, mobility of lattice oxygen, oxidative ability of Cr species, ratio of Brønsted acid sites and Lewis acid sites, NOx adsorption capacity, and structural disorder and distortion. In a series of FeaCr1−aTiOx (a=1, 0.75, 0.5, 0.2, 0) catalysts, Fe0.5Cr0.5TiOx showed the highest activity because of the optimized interactions of Fe, Cr, and Ti species in this catalyst.
AbstractList The selective catalytic reduction (SCR) of NO by NH3 over chromium-substituted Fe titanate catalysts with different amounts of chromium has been studied. The experiments revealed that the amount of chromium in the catalyst is a crucial factor for high activity. Fe0.5Cr0.5TiOx showed the highest activity. A series of Cr-substituted Fe–Ti compounds were prepared by the co-precipitation method and were systematically investigated as catalysts for the selective catalytic reduction (SCR) of NO by NH3. A variety of analytical techniques revealed that the Cr substitution amount affects the N2 selectivity, SCR activity, redox behavior of NH3/NOx, adsorption ability, and structure of catalysts in terms of surface properties, porosity, mobility of lattice oxygen, oxidative ability of Cr species, ratio of Brønsted acid sites and Lewis acid sites, NOx adsorption capacity, and structural disorder and distortion. In a series of FeaCr1−aTiOx (a=1, 0.75, 0.5, 0.2, 0) catalysts, Fe0.5Cr0.5TiOx showed the highest activity because of the optimized interactions of Fe, Cr, and Ti species in this catalyst.
A series of Cr-substituted Fe–Ti compounds were prepared by the co-precipitation method and were systematically investigated as catalysts for the selective catalytic reduction (SCR) of NO by NH₃. A variety of analytical techniques revealed that the Cr substitution amount affects the N₂ selectivity, SCR activity, redox behavior of NH₃/NOₓ, adsorption ability, and structure of catalysts in terms of surface properties, porosity, mobility of lattice oxygen, oxidative ability of Cr species, ratio of Brønsted acid sites and Lewis acid sites, NOₓ adsorption capacity, and structural disorder and distortion. In a series of FeₐCr₁₋ ₐTiOₓ (a=1, 0.75, 0.5, 0.2, 0) catalysts, Fe₀.₅Cr₀.₅TiOₓ showed the highest activity because of the optimized interactions of Fe, Cr, and Ti species in this catalyst.
The selective catalytic reduction (SCR) of NO by NH3 over chromium-substituted Fe titanate catalysts with different amounts of chromium has been studied. The experiments revealed that the amount of chromium in the catalyst is a crucial factor for high activity. Fe0.5 Cr0.5 TiO x showed the highest activity. A series of Cr-substituted Fe-Ti compounds were prepared by the co-precipitation method and were systematically investigated as catalysts for the selective catalytic reduction (SCR) of NO by NH3 . A variety of analytical techniques revealed that the Cr substitution amount affects the N2 selectivity, SCR activity, redox behavior of NH3 /NO x , adsorption ability, and structure of catalysts in terms of surface properties, porosity, mobility of lattice oxygen, oxidative ability of Cr species, ratio of Brønsted acid sites and Lewis acid sites, NO x adsorption capacity, and structural disorder and distortion. In a series of Fe a Cr1- a TiO x (a =1, 0.75, 0.5, 0.2, 0) catalysts, Fe0.5 Cr0.5 TiO x showed the highest activity because of the optimized interactions of Fe, Cr, and Ti species in this catalyst. [PUBLICATION ABSTRACT]
Author Karami, Asghar
Salehi, Vajiheh
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  surname: Salehi
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Keywords Cr substitution
Redox behavior
NOx adsorption
Selective catalytic reduction
NO
Acidic site
Adsorption capacity
Mobility
Distortion
Iron
Selectivity
Chemical reduction
Precipitation
Brönsted acid
Substitution
Surface properties
Adsorption structure
Titanium
Oxidation
Lewis acid
Nitrogen oxide
Oxygen
Catalytic reaction
Lewis site
Transition metal
Bronsted site
Ammonia
Heterogeneous catalysis
Adsorption
Chromium
Porosity
Catalyst
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Snippet The selective catalytic reduction (SCR) of NO by NH3 over chromium-substituted Fe titanate catalysts with different amounts of chromium has been studied. The...
A series of Cr-substituted Fe–Ti compounds were prepared by the co-precipitation method and were systematically investigated as catalysts for the selective...
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SubjectTerms adsorption
ammonia
analytical methods
Catalysis
Catalysts
Chemistry
Chromium
Colloidal state and disperse state
coprecipitation
Cr substitution
Exact sciences and technology
General and physical chemistry
Iron
Lewis acids
nitric oxide
nitrogen
NOx adsorption
oxygen
porosity
Porous materials
Redox behavior
Selective catalytic reduction
Surface physical chemistry
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
Titanium
Title The influence of chromium substitution on an iron–titanium catalyst used in the selective catalytic reduction of NO
URI https://dx.doi.org/10.1016/j.jcat.2012.04.007
https://www.proquest.com/docview/1024668803
Volume 292
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