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The Catalytic Performance of CO Oxidation over MnOx-ZrO2 Catalysts: The Role of Synthetic Routes Full article

Journal Catalysts
ISSN: 2073-4344
Output data Year: 2023, Volume: 13, Number: 1, Article number : 57, Pages count : 15 DOI: 10.3390/catal13010057
Tags catalyst; CO oxidation; manganese oxide; fluorite; solid solution; zirconia
Authors Bulavchenko Olga A. 1,2 , Konovalova Valeriya P. 1,2 , Saraev Andrey A. 1,2 , Kremneva Anna M. 1 , Rogov Vladimir A. 1,2 , Gerasimov Evgeny Yu. 1,2 , Afonasenko Tatyana N. 3
Affiliations
1 Boreskov Institute of Catalysis SB RAS, Lavrentiev Ave., 5, Novosibirsk 630090, Russia
2 Department of Physics, Novosibirsk State University, Pirogova, 2, Novosibirsk 630090, Russia
3 Center of New Chemical Technologies, Boreskov Institute of Catalysis, Neftezavodskaya 54, Omsk 644040, Russia

Funding (1)

1 Ministry of Science and Higher Education of the Russian Federation 075-15-2022-263

Abstract: MnOx-ZrO2 catalysts prepared by co-precipitation and vacuum impregnation were calcined at 400–800 °C and characterized by powder X-ray diffraction, textural studies, high-resolution transmission electron microscopy, temperature-programmed reduction, X-ray absorption near edge structure, and X-ray photoelectron spectroscopy. The catalytic activity was tested in the CO oxidation reaction. The activity of the co-precipitated samples exceeds that of the catalysts prepared by vacuum impregnation. The characterization studies showed that the nature of the active component for the catalysts obtained by co-precipitation differs from that of the catalysts obtained by impregnation. In the impregnation series, the most active catalyst was obtained at a temperature of 400 °C; its increased activity is due to the formation of MnO2 oxide nanoparticles containing Mn4+ and low-temperature reducibility. An increase in the synthesis temperature leads to the formation of less active Mn2O3, catalyst sintering, and, accordingly, deterioration of the catalytic properties. In the case of co-precipitation, the most active CO oxidation catalysts are formed by calcination at 650–700 °C in air. In this temperature interval, on the one hand, a MnyZr1−yO2−x solid solution is formed, and on the other hand, a partial separation of mixed oxide begins with the formation of highly dispersed and active MnOx. A further increase in temperature to 800 °C leads to complete decomposition of the solid solution, the release of manganese cations into Mn3O4, and a drop in catalytic activity.
Cite: Bulavchenko O.A. , Konovalova V.P. , Saraev A.A. , Kremneva A.M. , Rogov V.A. , Gerasimov E.Y. , Afonasenko T.N.
The Catalytic Performance of CO Oxidation over MnOx-ZrO2 Catalysts: The Role of Synthetic Routes
Catalysts. 2023. V.13. N1. 57 :1-15. DOI: 10.3390/catal13010057 WOS Scopus РИНЦ AN OpenAlex publication_identifier_short.sciact_ihcp_identifier_type
Dates:
Submitted: Nov 14, 2022
Accepted: Dec 23, 2022
Published online: Dec 27, 2022
Published print: Jan 1, 2023
Identifiers:
Web of science: WOS:000914727400001
Scopus: 2-s2.0-85146705500
Elibrary: 53957566
Chemical Abstracts: 2023:199932
OpenAlex: W4312224699
publication_identifier.sciact_ihcp_identifier_type: 3907
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Scopus 7
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