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Influence of [H]-donating activity of hydrocarbons on transformations of thiophene compounds under catalytic cracking conditions Научная публикация

Журнал Petroleum Chemistry
ISSN: 0965-5441 , E-ISSN: 1531-8532
Вых. Данные Год: 2012, Том: 52, Номер: 1, Страницы: 55-59 Страниц : 5 DOI: 10.1134/S0965544112010082
Авторы Potapenko O.V. 1 , Doronin V.P. 1 , Sorokina T.P. 1
Организации
1 Institute of Hydrocarbon Processing Problems, Siberian Branch, Russian Academy of Sciences

Реферат: Transformations of 2-methylthiophene and benzothiophene together with n-undecane, declaim, or cumene under conditions of catalytic cracking have been studied. It has been found that enhancement of the [H]-donating activity in the order cumene < n-undecane < decalin leads to an increase in the degree of conversion of organic sulfur compounds, predominantly yielding hydrogen sulfide. An increase in the amount of 2-methylthiophene and benzothiophene alkylation and condensation products in the liquid products of cracking is observed in this case. Schemes of conversion of these compounds under catalytic cracking conditions have been proposed. The dependence of the degree of conversion of thiophene compounds into hydrogen sulfide on the ability of the catalyst to mediate hydrogen transfer reactions has been revealed. © Pleiades Publishing, Ltd., 2012.
Библиографическая ссылка: Potapenko O.V. , Doronin V.P. , Sorokina T.P.
Influence of [H]-donating activity of hydrocarbons on transformations of thiophene compounds under catalytic cracking conditions
Petroleum Chemistry. 2012. V.52. N1. P.55-59. DOI: 10.1134/S0965544112010082 WOS Scopus РИНЦ OpenAlex
Оригинальная: Потапенко О.В. , Доронин В.П. , Сорокина Т.П.
Влияние [H]-донорной активности углеводородов на превращения тиофеновых соединений в условиях каталитического крекинга
Нефтехимия. 2012. Т.52. №1. С.60-65. РИНЦ
Даты:
Поступила в редакцию: 29 мар. 2011 г.
Опубликована в печати: 1 янв. 2012 г.
Опубликована online: 26 янв. 2012 г.
Идентификаторы БД:
Web of science: WOS:000300729700009
Scopus: 2-s2.0-84856512097
РИНЦ: 17975212
OpenAlex: W1984121016
Цитирование в БД:
БД Цитирований
Scopus 14
Web of science 13
OpenAlex 19
Альметрики: