1997
DOI: 10.1016/s0926-3373(96)00089-6
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FT-IR and EPR spectroscopic analysis of La1−xCexCoO3 perovskite-like catalysts for NO reduction by CO

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Cited by 47 publications
(23 citation statements)
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“…NO dissociatively adsorbs on a surface oxygen vacancy (□) (Equation (11)). The recombination of two adsorbed nitrogen species leads to the formation of N 2 (Equation (12)) while parallel pathways produce undesired N 2 O (Equation (13)) and isocyanate species (Equation (14)) [57]. The oxygen vacancy is restored by the reducing species in the gas phase (e.g., CO (Equation (15))).…”
Section: Reaction Mechanismsmentioning
confidence: 99%
“…NO dissociatively adsorbs on a surface oxygen vacancy (□) (Equation (11)). The recombination of two adsorbed nitrogen species leads to the formation of N 2 (Equation (12)) while parallel pathways produce undesired N 2 O (Equation (13)) and isocyanate species (Equation (14)) [57]. The oxygen vacancy is restored by the reducing species in the gas phase (e.g., CO (Equation (15))).…”
Section: Reaction Mechanismsmentioning
confidence: 99%
“…Many studies on perovskite catalysts have been reported [8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23].…”
Section: History Of Perovskite Catalystmentioning
confidence: 99%
“…In this manner, one can eliminate the costly steps of purchasing, transporting and storing the reductant. The vast majority of the catalysts reported for the NO + CO reaction are supported platinum group metals (Pt, Pd, Rh, Ir) [3][4][5], perovskite type oxides [6,7], and supported copper oxide [8]. Most of the reported catalysts require a high working temperature (773-873 K) to get reasonably high NO conversions.…”
Section: Introductionmentioning
confidence: 99%