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Reduction of Double Manganese–Cobalt Oxides: in situ XRD and TPR Study Научная публикация

Журнал Dalton Transactions
ISSN: 1477-9226 , E-ISSN: 1477-9234
Вых. Данные Год: 2018, Том: 47, Номер: 47, Страницы: 17153-17159 Страниц : 7 DOI: 10.1039/c8dt04137g
Ключевые слова High resolution transmission electron microscopy; Hydrogen; Manganese oxide; Solid solutions; Transmission electron microscopy; X ray diffraction
Авторы Bulavchenko Olga A. 1,2 , Gerasimov Evgeny.Y. 1,2 , Afonasenko Tatyana N. 3
Организации
1 Boreskov Institute of Catalysis SB RAS, Lavrentieva Ave. 5, Novosibirsk, Russia
2 Novosibirsk State University, Pirogova Str. 2, Novosibirsk, Russia
3 Institute of Hydrocarbons Processing SB RAS, Neftezavodskaya Str. 54, Omsk, Russia

Информация о финансировании (1)

1 Российский фонд фундаментальных исследований 18-33-00542 (АААА-А18-118042890005-8)

Реферат: The work reported here was aimed at determining differences in redox properties of simple and double oxides. Comparison between the reduction of double oxides (Mn,Co)3O4 and simple oxides Co3O4 and Mn3O4 was performed using in situ X-ray diffraction (XRD), temperature-programmed reduction (TPR) and transmission electron microscopy (TEM). The double oxides with a ratio of cations Mn : Co = 1 : 1 were prepared by the coprecipitation method and contained a mixture of 50% MnCo2O4 and 50% CoMn2O4. It was shown that the mechanism of reduction of double oxides with hydrogen differs significantly from the processes occurring on simple oxides. For simple cobalt and manganese oxides, transformations Co3O4 → CoO → Co and Mn3O4 → MnO are observed under a hydrogen atmosphere. The reduction of mixed-metal oxides occurs in two steps. In the first step, at 300–450 °C, (Mn,Co)3O4 transforms to (Mn,Co)O solid solutions. In situ XRD under isothermal conditions illustrates that Co-rich Co2MnO4 oxide starts to be reduced to Co0.6Mn0.4O first, and then Mn-rich Mn2CoO4 passes into Mn0.6Co0.4O. In the second step, at 450–700 °C, the reduction of solid solutions (Mn,Co)O to metallic cobalt Co and MnO proceeds. Again, the reduction begins with transformation of Co-rich oxide with the Co0.6Mn0.4O structure. The temperature of appearance of the intermediate phase (Mn,Co)O shifts to the higher values as compared to those observed for CoO, and to lower temperatures as compared to MnO during simple oxide reduction.
Библиографическая ссылка: Bulavchenko O.A. , Gerasimov E.Y. , Afonasenko T.N.
Reduction of Double Manganese–Cobalt Oxides: in situ XRD and TPR Study
Dalton Transactions. 2018. V.47. N47. P.17153-17159. DOI: 10.1039/c8dt04137g WOS Scopus РИНЦ CAPlusCA PMID OpenAlex
Даты:
Поступила в редакцию: 16 окт. 2018 г.
Принята к публикации: 17 окт. 2018 г.
Опубликована online: 23 нояб. 2018 г.
Опубликована в печати: 21 дек. 2018 г.
Идентификаторы БД:
Web of science: WOS:000452112100036
Scopus: 2-s2.0-85058156283
РИНЦ: 38676371
Chemical Abstracts: 2018:2296550
Chemical Abstracts (print): 170:87975
PMID (PubMed): 30468212
OpenAlex: W2900790381
Цитирование в БД:
БД Цитирований
Web of science 46
Scopus 48
РИНЦ 45
OpenAlex 49
Альметрики: