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Transalkylation of 1,4-diisopropylbenzene with naphthalene over dealuminated mordenites Научная публикация

Конференция 14th International Zeolite Conference
25-30 апр. 2004 , Cape Town
Журнал Studies in Surface Science and Catalysis
ISSN: 0167-2991
Вых. Данные Год: 2004, Том: 154, Номер: C, Страницы: 2163-2168 Страниц : 6 DOI: 10.1016/s0167-2991(04)80473-7
Авторы Nesterenko N.S. 1 , Timoshin S.E. 1 , Kuznetsov A.S. 1 , Montouillout V. 2 , Thibault-Starzyck F. 2 , Fernande C. 2 , Gilson J.P. 2 , Fajula F. 3 , Ivanova I.I. 1
Организации
1 Lomonosov Moscow State University
2 Universite de Caen
3 Institut Charles Gerhardt – UMR (CNRS)
Реферат: The transalkylation of diisopropylbenzene with naphthalene has been studied over two series of mordenite catalysts dealuminated by acid treatments and by combined calcination at 750°C and acid attack treatments, respectively. The nature and accessibility of the acid sites were studied by IR spectroscopy of adsorbed pyridine, 2,4,6-trimethylpyridine and 2,4,6-triethylpyridine. The highest yields of 2,6- and 2,7- diisopropylnaphtalenes and the highest stability of catalytic activity were observed over mordenites dealuminated by combined calcination and acid attack treatments. This dealumination procedure leads to the creation of a secondary mesopore network interconnecting structural micropores, which improves the acid sites accessibility, facilitates the transport of bulky reactants and products and prevents deactivation by pore blocking.
Библиографическая ссылка: Nesterenko N.S. , Timoshin S.E. , Kuznetsov A.S. , Montouillout V. , Thibault-Starzyck F. , Fernande C. , Gilson J.P. , Fajula F. , Ivanova I.I.
Transalkylation of 1,4-diisopropylbenzene with naphthalene over dealuminated mordenites
Studies in Surface Science and Catalysis. 2004. V.154. NC. P.2163-2168. DOI: 10.1016/s0167-2991(04)80473-7 Scopus OpenAlex
Идентификаторы БД:
Scopus: 2-s2.0-11844255397
OpenAlex: W83137537
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БД Цитирований
OpenAlex 5
Scopus 7
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