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Effects of cerium incorporation on the catalytic oxidation of benzene over flame-made perovskite La1-xCexMnO3 catalysts
Perovskite-type La1-xCexMnO3 (x= 0-10%) catalysts were prepared by flame spray pyrolysis and their activities during the catalytic oxidation of benzene were examined over the temperature range of 100-450 ℃. The structural properties and reducibility of these materials were also characterized by X-ra...
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Published in: | Particuology 2015-04, Vol.19 (2), p.60-68 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Perovskite-type La1-xCexMnO3 (x= 0-10%) catalysts were prepared by flame spray pyrolysis and their activities during the catalytic oxidation of benzene were examined over the temperature range of 100-450 ℃. The structural properties and reducibility of these materials were also characterized by X-ray diffraction (XRD), N2 adsorption/desorption, H2 temperature-programmed reduction (H2-TPR) and X-ray photoelectron spectroscopy (XPS). The incorporation of Ce was found to improve the benzene oxidation activity, and the perovskite in which x was 0.1 exhibited the highest activity. Phase composition and surface elemental analyses indicated that non-stoichiometric compounds were present. The incorporation of Ce had a negligible effect on the specific surface area of the perovskites and hence this factor has little impact on the catalytic activity. Introduction of Ce^4+ resulted in modification of the chemical states of both B-site ions and oxygen species and facilitated the reducibility of the perovskite. The surface Mn^4+/Mn^3+ ratio was increased as a result of Ce^4+ substitution, while a decrease in the surface-adsorbed O/lattice O (Oads/Olatt) ratio was observed. The relationship between the surface elemental ratios and catalytic activity was established to allow a better understanding of the process by which benzene is oxidized over perovskites. |
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ISSN: | 1674-2001 2210-4291 |
DOI: | 10.1016/j.partic.2014.07.001 |