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Pollutant Abatement of Nitrogen-Based Fuel Effluents over Mono- and Bimetallic Pt/Ru Catalysts

[Image: see text] Mono- and bimetallic alloy Pt and Ru catalysts supported on γ-Al(2)O(3) have been investigated for the reduction of pollutants (NO(x), NH(3), and CO) generated during the continuous combustion of an aqueous urea ammonium nitrate fuel. A Pt/Ru alloy with a Pt25/Ru75 atomic ratio has...

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Detalles Bibliográficos
Autores principales: Kutteri, Deepa Ayillath, Mosevitzky, Bar, Epstein, Michael, Shter, Gennady E., Grader, Gideon S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645125/
https://www.ncbi.nlm.nih.gov/pubmed/31457367
http://dx.doi.org/10.1021/acsomega.7b01344
Descripción
Sumario:[Image: see text] Mono- and bimetallic alloy Pt and Ru catalysts supported on γ-Al(2)O(3) have been investigated for the reduction of pollutants (NO(x), NH(3), and CO) generated during the continuous combustion of an aqueous urea ammonium nitrate fuel. A Pt/Ru alloy with a Pt25/Ru75 atomic ratio has been found to have higher activity and selectivity than those of a 50/50 alloy and monometallic catalysts. Among monometallic catalysts, Ru was more selective toward N(2) formation, whereas Pt showed a higher selectivity toward NH(3) formation. For Ru, it was observed that the oxidizing atmosphere of NO(x) pollutants caused the formation of RuO(2), whereas Ru in the Pt/Ru alloy was stable under these conditions. Temperature (250–500 °C) and pressure (1–8 MPa) studies over Ru and 25/75 Pt/Ru have concluded that the alloy catalyst at 400 °C and 5 MPa reduced the pollutants to a minimum level with high yields of N(2) (99.7%) and CO(2) (99.9%). It was also observed that the 25/75 Pt/Ru catalyst remained stable up to 100 h of thermal treatment at 400 °C. Minimal pollutants were obtained at a weight hourly space velocity = 11 822 h(–1). Characterization studies of the spent catalyst showed that metal particles were sintered over a period of time (8 h) and the γ-Al(2)O(3) support was transformed into θ- and α-phases under the hydrothermal reaction conditions.