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The Catalytic Performance of CO Oxidation over MnOx-ZrO2 Catalysts: The Role of Synthetic Routes Научная публикация

Журнал Catalysts
ISSN: 2073-4344
Вых. Данные Год: 2023, Том: 13, Номер: 1, Номер статьи : 57, Страниц : 15 DOI: 10.3390/catal13010057
Ключевые слова catalyst; CO oxidation; manganese oxide; fluorite; solid solution; zirconia
Авторы 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
Организации
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

Информация о финансировании (1)

1 Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) 075-15-2022-263

Реферат: 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.
Библиографическая ссылка: 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 CAPlus OpenAlex ЦНХТ ID
Даты:
Поступила в редакцию: 14 нояб. 2022 г.
Принята к публикации: 23 дек. 2022 г.
Опубликована online: 27 дек. 2022 г.
Опубликована в печати: 1 янв. 2023 г.
Идентификаторы БД:
Web of science: WOS:000914727400001
Scopus: 2-s2.0-85146705500
РИНЦ: 53957566
Chemical Abstracts: 2023:199932
OpenAlex: W4312224699
ЦНХТ ID: 3907
Цитирование в БД:
БД Цитирований
Web of science 6
Scopus 7
РИНЦ 5
OpenAlex 7
Альметрики: