Effect of the rare earth in the perovskite-type mixed oxides AMnO{sub 3} (A=Y, La, Pr, Sm, Dy) as catalysts in methanol oxidation

Journal Article · Sat Nov 15 00:00:00 EST 2008 · Journal of Solid State Chemistry

DOI:https://doi.org/10.1016/j.jssc.2008.07.029· OSTI ID:21212089

Levasseur, B ^[1]

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1. Department of Chemical Engineering, Laval University, Sainte-Foy, Que., G1K 7P4 (Canada)

The effect of the rare earth in the perovskite-type mixed oxides AMnO{sub 3} (A=Y, La, Pr, Sm, Dy) on catalytic properties in methanol oxidation was investigated in this work. The perovskites were prepared by reactive grinding in order to enhance the specific surface area in comparison with other classical synthesis procedures. These catalysts were characterized by N{sub 2} adsorption, X-ray diffraction, H{sub 2} temperature-programmed reduction (TPR-H{sub 2}), O{sub 2}-, CH{sub 3}OH- and CO{sub 2}-temperature-programmed desorption (TPD). The activity of the five catalysts under study in the methanol oxidation reaction was evaluated. The behaviour of the {alpha}-O{sub 2} from the surface of the perovskite was strongly related to the nature of the A-site cation and particularly to its electronegativity but also to its density. Concerning the {beta}-O{sub 2} from the bulk, the rare earth only induces an indirect effect notably due to structural modifications. As suggested in a previous study, the activity in methanol oxidation was directly linked with the surface oxygen density. Under an excess of {alpha}-oxygen, the reaction intermediate was found to be a monodentate carbonate that decomposes into CO{sub 2}. The stability of monodentate carbonates was also found to be related to the electronegativity of the rare earth during both CH{sub 3}OH- and CO{sub 2}-temperature-programmed desorption. However, as soon as a lack of {alpha}-oxygen was observed in the structure, the dominant reaction intermediate was a bidentate carbonate that induces a consumption of anion vacancies in spite of the production of CO{sub 2}. Nevertheless, the accumulation of these carbonates leads to a decrease in the oxidation rate since their desorption requires high temperatures. - Graphical abstract: Perovskite-type mixed oxides AMnO{sub 3} (with A=Y, La, Pr, Sm, Dy) with high specific surface area were prepared by reactive grinding. The influence of the rare earth on the two kinds of oxygen in the perovskite structure ({alpha}-O{sub 2} and {beta}-O{sub 2}) was correlated with a variety of intrinsic properties of the A-site cation. Moreover, the catalytic performance of the samples for methanol oxidation was evaluated.

• OSTI ID: 21212089
• Journal Information: Journal of Solid State Chemistry, Vol. 181, Issue 11; Other Information: DOI: 10.1016/j.jssc.2008.07.029; PII: S0022-4596(08)00407-6; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0022-4596
• Country of Publication: United States
• Language: English

Related Subjects

37 INORGANIC
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
CARBON DIOXIDE
CARBONATES
CATALYSTS
DESORPTION
DYSPROSIUM COMPOUNDS
ELECTRONEGATIVITY
HYDROGEN
LANTHANUM COMPOUNDS
METHANOL
OXIDATION
PEROVSKITE
PRASEODYMIUM COMPOUNDS
SAMARIUM COMPOUNDS
SPECIFIC SURFACE AREA
VACANCIES
X-RAY DIFFRACTION
YTTRIUM COMPOUNDS