Effect of the Calcination Temperature and Composition of the MnOx–ZrO2 System on Its Structure and Catalytic Properties in a Reaction of Carbon Monoxide Oxidation
The effect of the calcination temperature and composition of the MnO x –ZrO 2 system on its structural characteristics and catalytic properties in the reaction of CO oxidation was studied. According to X-ray diffraction analysis and H 2 thermo-programmed reduction data, an increase in the calcinatio...
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Veröffentlicht in: | Kinetics and catalysis 2018, Vol.59 (1), p.104-111 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The effect of the calcination temperature and composition of the MnO
x
–ZrO
2
system on its structural characteristics and catalytic properties in the reaction of CO oxidation was studied. According to X-ray diffraction analysis and H
2
thermo-programmed reduction data, an increase in the calcination temperature of Mn
0.12
Zr
0.88
O
2
from 450 to 900°C caused a structural transformation of the system accompanied by the disintegration of solid solution with the release of manganese ions from the structure of ZrO
2
and the formation of, initially, highly dispersed MnO
x
particles and then a crystallized phase of Mn
3
O
4
. The dependence of the catalytic activity of MnO
x
–ZrO
2
in the reaction of CO oxidation on the calcination temperature takes an extreme form. A maximum activity was observed after heat treatment at 650–700°C, i.e., at limiting temperatures for the occurrence of a solid solution of manganese ions in the cubic modification of ZrO
2
. If the manganese content was higher than that in the sample of Mn
0.4
Zr
0.6
O
2
, the phase composition of the system changed: the solid solution phase was supplemented with Mn
2
O
3
and β-Mn
3
O
4
phases. The samples of Mn
0.4
Zr
0.6
O
2
–Mn
0.6
Zr
0.4
O
2
exhibited a maximum catalytic activity; this was likely due to the presence of the highly dispersed MnO
x
particles, which were not the solid solution constituents, on their surface in addition to an increase in the dispersity of the solid solution. |
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ISSN: | 0023-1584 1608-3210 |
DOI: | 10.1134/S0023158418010019 |