The Nature of Active Sites in Pt–ReOX/TiO2 Catalysts for Selective Hydrogenation of Carboxylic Acids to Alcohols Научная публикация
Журнал |
Journal of Energy Chemistry
ISSN: 2095-4956 |
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Вых. Данные | Год: 2015, Том: 24, Номер: 5, Страницы: 646-654 Страниц : 9 DOI: 10.1016/j.jechem.2015.09.003 | ||||
Ключевые слова | Hexanoic acid, Hexanol, Nanoparticles, Platinum, Rhenium, Selective hydrogenation | ||||
Авторы |
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Организации |
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Реферат:
The highly dispersed Pt-ReOX (x 1) sites ca. 0.5 nm in size were formed via a successive and strong interaction of the
Re precursor with titania and then of the Pt complex with deposited low-valent rhenium oxide clusters. The size, charge and chemical composition were characterized by means of HRTEM/STEM with EDX mapping, XPS, and FTIRS. These sites with Re/Pt = 2 were shown to be highly active and selective in the hydrogenation of carboxylic acid to alcohol under very mild conditions (T = 130 °C, P = 50 bar). The reaction rate constant for the hydrogenation of hexanoic acid increased linearly with the Pt content. As for the homogeneous pincer-type Ru-organic complexes, the active Pt-ReO sites can dissociate heterolytically the molecular hydrogen with the formation of hydroxyl groups and Pt hydride for hydrogenation of the carboxylic group. Indeed, TOF of 20 h-1 and selectivity of 98%-99% are approaching the values typical of homogeneous catalysts. The first order kinetics described well the experimental data obtained in a wide range of reaction conditions. © 2015 Science Press and Dalian Institute of Chemical Physics.
Библиографическая ссылка:
Suknev A.
, Zaikovskii V.
, Kaichev V.
, Paukshtis E.
, Sadovskaya E.
, Balʹzhinimaev B.
The Nature of Active Sites in Pt–ReOX/TiO2 Catalysts for Selective Hydrogenation of Carboxylic Acids to Alcohols
Journal of Energy Chemistry. 2015. V.24. N5. P.646-654. DOI: 10.1016/j.jechem.2015.09.003 WOS Scopus РИНЦ OpenAlex
The Nature of Active Sites in Pt–ReOX/TiO2 Catalysts for Selective Hydrogenation of Carboxylic Acids to Alcohols
Journal of Energy Chemistry. 2015. V.24. N5. P.646-654. DOI: 10.1016/j.jechem.2015.09.003 WOS Scopus РИНЦ OpenAlex
Даты:
Поступила в редакцию: | 24 июн. 2015 г. |
Принята к публикации: | 12 авг. 2015 г. |
Опубликована в печати: | 1 сент. 2015 г. |
Опубликована online: | 14 сент. 2015 г. |
Идентификаторы БД:
Web of science: | WOS:000364260100015 |
Scopus: | 2-s2.0-84944720587 |
РИНЦ: | 24962843 |
OpenAlex: | W2394718958 |