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NO reduction with CO in the presence and absence of H2O over Pd/γ-Al2O3 and Pd-VOx/γ-Al2O3 catalysts: The formation of HNCO, NH3 and stable surface species

Paper ID Volume ID Publish Year Pages File Format Full-Text
42510 45928 2009 12 PDF Available
Title
NO reduction with CO in the presence and absence of H2O over Pd/γ-Al2O3 and Pd-VOx/γ-Al2O3 catalysts: The formation of HNCO, NH3 and stable surface species
Abstract

The reduction of NO by CO over Pd/γ-Al2O3 and Pd-VOx/γ-Al2O3 catalysts has been studied by combining activity and selectivity measurements with FTIR spectroscopy of gas phase products and adsorbed species under reaction conditions at 300 °C. Characterization of fresh, reduced samples, by H2 chemisorption, TEM and FTIR spectroscopy of adsorbed of CO and NO, indicated that the promoter is not covering the metal surface. Under dry conditions the rate of N2 formation is lowered on the vanadia-modified alumina but the production of N2O was not altered. As a result the selectivity to N2 decreased markedly on Pd-VOx/γ-Al2O3. FTIR and XPS characterization of used catalysts demonstrated that the negative effect of VOx on N2 formation is due to an oxidized state of Pd that develops under reaction conditions. FTIR analysis of the gas phase products showed that both catalysts produce small amounts of gas phase HNCO and NH3 with the participation of surface –OH groups. FTIR spectra of the catalysts surface under reaction conditions demonstrate the presence of isocyanate (–NCO) and hydrogen containing compounds derived from HNCO. These stable species are not responsible for the production of N2O, but contribute to deactivation of the catalyst. They are rapidly eliminated upon water injection with a brief high production of NH3. Under steady state conditions water increases the CO conversion and the selectivity to N2 and NH3 on Pd/γ-Al2O3. The most notable effect is a marked reduction in N2O production. On Pd-VOx/γ-Al2O3 water increases the conversion of both NO and CO, as well as the NH3 formation. The selectivity to N2 is not altered and it is lower than the ones of NH3 and N2O. On both catalysts the NH3 formation increases due to the rapid hydrolysis of –NCO and HNCO. The H2 participation in the process of NH3 formation is excluded due to the very low activity of Pd/γ-Al2O3 and Pd-VOx/γ-Al2O3 for the water–gas shift reaction.

Graphical abstractThe reduction of NO by CO over Pd/γ-Al2O3 and Pd-VOx/γ-Al2O3 catalysts has been studied by combining activity and selectivity measurements with FTIR spectroscopy. The rate of N2 formation decreases on Pd-VOx/γ-Al2O3. FTIR analysis of the gas phase products showed that all catalysts produce small amounts of HNCO (g) and NH3 (g) under dry conditions. Isocyanate species and other stable compounds derived from HNCO accumulate on the catalyst surface and lead to catalysts deactivation. In the presence of water the surface deposits are eliminated and the production of NH3 increases. On Pd/γ-Al2O the main effect of water is a lower production of N2O.Figure optionsDownload full-size imageDownload as PowerPoint slide

Keywords
NO + CO; NO + CO + H2O; Pd (palladium); V (vanadium); Isocyanate; Isocyanic acid; HNCO; Ammonia formation
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NO reduction with CO in the presence and absence of H2O over Pd/γ-Al2O3 and Pd-VOx/γ-Al2O3 catalysts: The formation of HNCO, NH3 and stable surface species
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis A: General - Volume 368, Issues 1–2, 31 October 2009, Pages 146–157
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis