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One-step synthesis of cumene from benzene and acetone over a bifunctional catalyst Научная публикация

Журнал Catalysis in Industry
ISSN: 2070-0504 , E-ISSN: 2070-0555
Вых. Данные Год: 2015, Том: 7, Номер: 4, Страницы: 282-286 Страниц : 5 DOI: 10.1134/s2070050415040133
Авторы Shutkina O.V. 1 , Ponomareva O.A. 1,2 , Ivanova I.I. 1,2
Организации
1 Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, 119991 Russia
2 Lomonosov Moscow State University, Moscow, 119991 Russia
Реферат: The hydroalkylation of benzene with acetone on a bifunctional solid catalyst containing silicasupported copper and beta zeolite is studied. The effects of temperature (100–230°C), pressure (0.1–3 MPa), and composition of the reaction mixture (benzene: acetone) on the process are revealed. It is shown that optimal conditions for the reaction are the following: temperature of 150–170°C, pressure of 1–3 MPa, and (4–9): 1 molar ratio of benzene to acetone. At 170°C, 1 MPa, and a 9-fold dilution of acetone with benzene, the conversion of acetone is as high as 98% and the yield of the desired products (cumene and diisopropylbenzenes) is 94%, which is comparable to the parameters of the industrial process of benzene alkylation with propylene. Using acetone as an alkylating agent instead of propylene makes the proposed hydroalkylation method more attractive, due to the excess of cheap acetone.
Библиографическая ссылка: Shutkina O.V. , Ponomareva O.A. , Ivanova I.I.
One-step synthesis of cumene from benzene and acetone over a bifunctional catalyst
Catalysis in Industry. 2015. V.7. N4. P.282-286. DOI: 10.1134/s2070050415040133 WOS Scopus РИНЦ OpenAlex
Оригинальная версия: Шуткина О.В. , Пономарева О.А. , Иванова И.И.
Одностадийный синтез кумола из бензола и ацетона на бифункциональном катализаторе
Катализ в промышленности. 2015. №4. С.37-41. DOI: 10.18412/1816-0387-2015-4-37-41 РИНЦ CAPlusCAРЖ ВИНИТИ
Даты:
Поступила в редакцию: 25 мар. 2015 г.
Опубликована в печати: 1 окт. 2015 г.
Опубликована online: 29 дек. 2015 г.
Идентификаторы БД:
Web of science: WOS:000372437900006
Scopus: 2-s2.0-84952034528
РИНЦ: 26928104
OpenAlex: W2297318895
Цитирование в БД:
БД Цитирований
OpenAlex 8
Web of science 7
Scopus 7
Альметрики: