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Catalytic Epoxidation of Propylene with CO/O2 over Au/TiO2 Научная публикация

Журнал Applied Catalysis A: General
ISSN: 0926-860X , E-ISSN: 1873-3875
Вых. Данные Год: 2014, Том: 476, Страницы: 197-203 Страниц : 7 DOI: 10.1016/j.apcata.2014.02.036
Ключевые слова Gold catalysts, Propylene epoxidation, Propylene oxide
Авторы Sobolev Vladimir I. 1,2 , Koltunov Konstantin Yu. 1,3
Организации
1 Boreskov Institute of Catalysis, Russian Academy of Science, Pr. Akademika Lavrentieva 5, Novosibirsk 630090, Russia
2 Tomsk State University, 36 Lenina Ave., Tomsk 634050, Russia
3 Novosibirsk State University, Pirogova 2, Novosibirsk 630090, Russia

Реферат: Gold nanoparticles supported on TiO2 are known to catalyze vapor-phase epoxidation of propylene with molecular oxygen in the presence of H2 as the necessary reducing co reagent. Here, we report that carbon monoxide can be employed instead of hydrogen to accomplish similar reaction. The reaction of propylene, CO and O2 can be carried out in a flow reactor over Au/TiO2 at a temperature of 40–90 °C. The propylene oxide selectivity attains 80–97% at propylene conversion of 1.7–3.7%. The propylene oxide yield goes through the maximum as a function of reaction time, the maximal value being twice higher compared to yield of propylene oxide achieved by “traditional” reaction with H2/O2 mixture. Utilization efficiency of CO reaches 25%, which is comparable to that of H2 in the analogous reaction of propylene, H2 and O2. Proposed mechanism for the reaction involves the formation of specific oxygen species arising from O2 on catalytic sites reduced with CO. This is in line with generation of highly reactive oxygen species (detectable by oxygen isotopic exchange) on Au/TiO2 surface treated preliminarily with CO.
Библиографическая ссылка: Sobolev V.I. , Koltunov K.Y.
Catalytic Epoxidation of Propylene with CO/O2 over Au/TiO2
Applied Catalysis A: General. 2014. V.476. P.197-203. DOI: 10.1016/j.apcata.2014.02.036 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 2 сент. 2013 г.
Принята к публикации: 27 февр. 2014 г.
Опубликована online: 6 мар. 2014 г.
Опубликована в печати: 22 апр. 2014 г.
Идентификаторы БД:
Web of science: WOS:000336005600024
Scopus: 2-s2.0-84896471905
РИНЦ: 21867597
Chemical Abstracts: 2014:602116
Chemical Abstracts (print): 160:559441
OpenAlex: W2036425927
Цитирование в БД:
БД Цитирований
Web of science 18
Scopus 19
РИНЦ 18
OpenAlex 20
Альметрики: