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Selective Oxidation of Methanol to Form Dimethoxymethane and Methyl Formate over a Monolayer V2O5/TiO2 Catalyst Научная публикация

Журнал Journal of Catalysis
ISSN: 0021-9517 , E-ISSN: 1090-2694
Вых. Данные Год: 2014, Том: 311, Страницы: 59-70 Страниц : 12 DOI: 10.1016/j.jcat.2013.10.026
Ключевые слова Methanol oxidation, Monolayer catalyst, Near ambient pressure X-ray photoelectron spectroscopy, Vanadium pentoxide
Авторы Kaichev V.V. 1,2 , Popova G.Ya. 1 , Chesalov Yu.A. 1 , Saraev A.A. 1 , Zemlyanov D.Y. 3 , Beloshapkin S.A. 4 , Knop-Gericke A. 5 , Schlögl R. 5 , Andrushkevich T.V. 1 , Bukhtiyarov V.I. 1,2
Организации
1 Boreskov Institute of Catalysis of SB RAS, Lavrentieva Ave. 5, 630090 Novosibirsk, Russia
2 Novosibirsk State University, Pirogova St. 2, 630090 Novosibirsk, Russia
3 Birck Nanotechnology Center, Purdue University, 1205 West State Street, West Lafayette, IN 47907-2100, USA
4 Materials and Surface Science Institute, University of Limerick, Limerick, Ireland
5 Fritz-Haber-Institute of MPG, Faradayweg 4-6, D-14195 Berlin, Germany

Информация о финансировании (2)

1 Российский фонд фундаментальных исследований 13-03-00128
2 European Commission CT-2004-506008

Реферат: The oxidation of methanol over highly dispersed vanadia supported on TiO2 (anatase) has been investigated using in situ Fourier transform infrared spectroscopy (FTIR), near ambient pressure X-ray photoelectron spectroscopy (NAP XPS), X-ray absorption near-edge structure (XANES), and a temperature-programmed reaction technique. The data were complemented by kinetic measurements collected in a flow reactor. It was found that dimethoxymethane competes with methyl formate at low temperatures, while the production of formaldehyde is greatly inhibited. Under the reaction conditions, the FTIR spectra show the presence of non-dissociatively adsorbed molecules of methanol, in addition to adsorbed methoxy, dioxymethylene, and formate species. According to the NAP XPS and XANES data, the reaction involves a reversible reduction of V5+ cations, indicating that the vanadia lattice oxygen participates in the oxidation of methanol via the classical Mars–van Krevelen mechanism. A detailed mechanism for the oxidation of methanol on vanadia catalysts is discussed.
Библиографическая ссылка: Kaichev V.V. , Popova G.Y. , Chesalov Y.A. , Saraev A.A. , Zemlyanov D.Y. , Beloshapkin S.A. , Knop-Gericke A. , Schlögl R. , Andrushkevich T.V. , Bukhtiyarov V.I.
Selective Oxidation of Methanol to Form Dimethoxymethane and Methyl Formate over a Monolayer V2O5/TiO2 Catalyst
Journal of Catalysis. 2014. V.311. P.59-70. DOI: 10.1016/j.jcat.2013.10.026 WOS Scopus РИНЦ CAPlusCA OpenAlex
Файлы: Полный текст от издателя
Даты:
Поступила в редакцию: 16 июл. 2013 г.
Принята к публикации: 31 окт. 2013 г.
Опубликована online: 15 дек. 2013 г.
Опубликована в печати: 1 мар. 2014 г.
Идентификаторы БД:
Web of science: WOS:000333489500008
Scopus: 2-s2.0-84890534431
РИНЦ: 21861965
Chemical Abstracts: 2014:283689
Chemical Abstracts (print): 160:310361
OpenAlex: W2057044003
Цитирование в БД:
БД Цитирований
Web of science 127
Scopus 135
РИНЦ 137
OpenAlex 133
Альметрики: