Sciact
  • EN
  • RU

Synthesis of Crystalline Metal Silicates Having Zeolite Structure and Study of Their Catalytic Properties Научная публикация

Журнал Journal of Molecular Catalysis
ISSN: 0304-5102
Вых. Данные Год: 1985, Том: 31, Номер: 3, Страницы: 355-370 Страниц : 16 DOI: 10.1016/0304-5102(85)85118-X
Авторы Ione K.G. 1 , Vostrikova L.A. 1 , Mastikhin V.M. 1
Организации
1 Institute of Catalysis
Реферат: The possibility of isomorphous heterocharged substitution (IHS) of Si4+ by Men+ cations of elements of Groups I – VIII (where n ≠ 4) in crystalline non-aluminium silicates with the ZSM structure has been examined. The silicates were synthesized in hydrothermal conditions in the presence of Men+ and tetrabutylammonium bromide. The catalytic activity of the silicates in methanol conversion into hydrocarbons has been determined. The state of Men+ in crystallization products was studied by EPR and NMR methods. As shown, the probability of Men+ fixation in tetrahedral oxygen surroundings in the silicate framework can be predicted on the basis of the Pauling criterion. Acid-base catalytic activity was found only for silicates with Men+ cations in IHS positions. Both the rate and selectivity of methanol conversion to hydrocarbons depend on the e/r of cations, because the number of Men+ which can be occluded in the IHS positions in the silicate framework depends on this parameter.
Библиографическая ссылка: Ione K.G. , Vostrikova L.A. , Mastikhin V.M.
Synthesis of Crystalline Metal Silicates Having Zeolite Structure and Study of Their Catalytic Properties
Journal of Molecular Catalysis. 1985. V.31. N3. P.355-370. DOI: 10.1016/0304-5102(85)85118-X WOS Scopus РИНЦ CAPlusCA OpenAlex Sciact
Даты:
Поступила в редакцию: 8 июн. 1984 г.
Принята к публикации: 11 февр. 1985 г.
Опубликована в печати: 1 авг. 1985 г.
Опубликована online: 2 окт. 2001 г.
Идентификаторы БД:
Web of science: WOS:A1985ANU2200009
Scopus: 2-s2.0-0022111225
РИНЦ: 30975944
Chemical Abstracts: 1985:493555
Chemical Abstracts (print): 103:93555
OpenAlex: W2056000105
Sciact: 12820
Цитирование в БД:
БД Цитирований
Scopus 77
OpenAlex 75
Альметрики: