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Highly Selective Catalytic Propylene Glycol Synthesis from Alkyl Lactate over Copper on Silica: Performance and Mechanism Научная публикация

Журнал Applied Catalysis B: Environmental
ISSN: 0926-3373 , E-ISSN: 1873-3883
Вых. Данные Год: 2012, Том: 119-120, Страницы: 340-347 Страниц : 8 DOI: 10.1016/j.apcatb.2012.03.003
Ключевые слова Alkyl lactate, Copper-silica, Hydrogenolysis, Propylene glycol
Авторы Simonov Mikhail N. 1 , Zaikin Pavel A. 2 , Simakova Irina L. 1
Организации
1 Boreskov Institute of Catalysis, Novosibirsk 630090, Russia
2 Novosibirsk Institute of Organic Chemistry, Novosibirsk 630090, Russia

Реферат: Catalytic alkyl lactate hydrogenolysis over silica-supported copper at atmospheric hydrogen pressure and temperature range 433-493 K provides an eco-friendly green alternative to the petroleum-based process for propylene glycol synthesis. It was shown that catalytic activity strongly depends on copper loading and the most active catalyst contains ca. 45 wt.% Cu. General peculiarities of methyl and butyl lactate hydrogenolysis were studied demonstrating that an overall reaction rate increases with reaction temperature increase but a selectivity to propylene glycol decreases due to enhanced concurrent dehydrogenation of propylene glycol to a by-product hydroxyacetone. It was found that the amount of propylene glycol formed during the reaction is determined by thermodynamic equilibrium between propylene glycol and hydroxyacetone that results in propylene glycol selectivity of 96% at full butyl lactate conversion at 453 K. Overall mechanism of alkyl lactate transformation involving formation of intermediate hemiacetal over bifunctional Cu/SiO2 catalyst was proposed
Библиографическая ссылка: Simonov M.N. , Zaikin P.A. , Simakova I.L.
Highly Selective Catalytic Propylene Glycol Synthesis from Alkyl Lactate over Copper on Silica: Performance and Mechanism
Applied Catalysis B: Environmental. 2012. V.119-120. P.340-347. DOI: 10.1016/j.apcatb.2012.03.003 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 13 нояб. 2011 г.
Принята к публикации: 6 мар. 2012 г.
Опубликована online: 6 мар. 2012 г.
Опубликована в печати: 1 мая 2012 г.
Идентификаторы БД:
Web of science: WOS:000304691700040
Scopus: 2-s2.0-84859485580
РИНЦ: 17982098
Chemical Abstracts: 2012:659414
Chemical Abstracts (print): 156:666823
OpenAlex: W2038698974
Цитирование в БД:
БД Цитирований
Web of science 22
Scopus 22
РИНЦ 19
OpenAlex 25
Альметрики: