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Effect of Light on Reactions over Sulfated Zirconia Научная публикация

Журнал Journal of Catalysis
ISSN: 0021-9517 , E-ISSN: 1090-2694
Вых. Данные Год: 1998, Том: 176, Номер: 2, Страницы: 294-304 Страниц : 11 DOI: 10.1006/jcat.1998.2027
Ключевые слова BENZENE CATION-RADICALS; ZSM-5 ZEOLITES; ACID SITES; BUTANE ISOMERIZATION; CRYSTAL PHASE; METAL-OXIDES; CATALYSTS; ION; MECHANISM; HYDROCARBONS
Авторы Bedilo Alexander F. 1 , Kim Vladimir I. 1 , Volodin Alexander M. 1
Организации
1 Boreskov Institute of Catalysis, Novosibirsk 630090, Russia

Информация о финансировании (2)

1 Российский фонд фундаментальных исследований 97-03-32566
2 Российский фонд фундаментальных исследований 94-03-08690

Реферат: The effect of illumination with visual and near-UV light on the isomerization and cracking of n-pentane and formation of radical cations from benzene and its derivatives over sulfated zirconia has been studied. Sulfated zirconia proved to have very strong acceptor sites capable of ionizing benzene and methylbenzenes to corresponding radical cations. The ionization of aromatic molecules could be initiated with visual light. The presence of oxygen in the gas phase appeared to strengthen the acceptor sites and shift the photoreaction red edge to longer wavelengths. Electron donor–acceptor complexes are shown to be key intermediates in the ionization of aromatic molecules on sulfated zirconia. A qualitative correlation between the presence of the strongest acceptor sites and the isomerization activity was observed. Illumination with visual light significantly increased the pentane cracking selectivity with little effect on the isomerization activity. Pentane cracking is proposed to proceed via dimerization initiated by the charge transfer with the formation of unstable radical cations.
Библиографическая ссылка: Bedilo A.F. , Kim V.I. , Volodin A.M.
Effect of Light on Reactions over Sulfated Zirconia
Journal of Catalysis. 1998. V.176. N2. P.294-304. DOI: 10.1006/jcat.1998.2027 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 18 июл. 1997 г.
Принята к публикации: 29 янв. 1998 г.
Опубликована в печати: 10 июн. 1998 г.
Опубликована online: 25 мая 2002 г.
Идентификаторы БД:
Web of science: WOS:000074276900003
Scopus: 2-s2.0-0001051209
РИНЦ: 13302422
Chemical Abstracts: 1998:393025
Chemical Abstracts (print): 129:122373
OpenAlex: W2004128713
Цитирование в БД:
БД Цитирований
Web of science 25
Scopus 26
РИНЦ 24
OpenAlex 24
Альметрики: