Conversion of Dimethyl Disulfide in the Presence of Zeolites Научная публикация
Журнал |
Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210 |
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Вых. Данные | Год: 2008, Том: 49, Номер: 2, Страницы: 253-260 Страниц : 8 DOI: 10.1134/S0023158408020134 | ||
Ключевые слова | Zeolite; DMDS; Strong Acid Site;Dimethyl Sulfide; Dimethyl Disulfide | ||
Авторы |
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Организации |
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Реферат:
Dimethyl disulfide conversion in the presence of zeolites was studied at atmospheric pressure and T = 190–350°C. For all catalysts, the products of the reaction at T = 190°C—methanethiol, dimethyl sulfide, and hydrogen sulfide—result directly from dimethyl disulfide. The relative reaction rate and the dimethyl sulfide selectivity decreases in the order HZSM-5 ≥ CoHZSM-5 > HNaY > NaX, NaY. The methanethiol formation selectivity changes in the reverse order. The highest methanethiol selectivity at T = 190°C is shown by the sodium zeolites; the highest dimethyl sulfide selectivity, by the high-silicz zeolite HZSM-5. Raising the reaction temperature increases the reaction rate and changes the process route: at high temperatures, dimethyl disulfide decomposes to methanethiol, which then condenses to yield dimethyl sulfide and hydrogen sulfide. The observed regularities are explained in terms of the different acidic properties of the zeolite surfaces.
Библиографическая ссылка:
Mashkina A.V.
, Paukshtis E.A.
, Krivoruchko O.P.
, Khairulina L.N.
Conversion of Dimethyl Disulfide in the Presence of Zeolites
Kinetics and Catalysis. 2008. V.49. N2. P.253-260. DOI: 10.1134/S0023158408020134 WOS Scopus РИНЦ
Conversion of Dimethyl Disulfide in the Presence of Zeolites
Kinetics and Catalysis. 2008. V.49. N2. P.253-260. DOI: 10.1134/S0023158408020134 WOS Scopus РИНЦ
Оригинальная:
Машкина А.В.
, Паукштис Е.А.
, Криворучко О.П.
, Хайрулина Л.Н.
Превращение диметилдисульфида в присутствии цеолитов
Кинетика и катализ. 2008. Т.49. №2. С.266-273. РИНЦ
Превращение диметилдисульфида в присутствии цеолитов
Кинетика и катализ. 2008. Т.49. №2. С.266-273. РИНЦ
Даты:
Поступила в редакцию: | 27 нояб. 2006 г. |
Опубликована в печати: | 1 мар. 2008 г. |
Опубликована online: | 20 янв. 2011 г. |
Идентификаторы БД:
Web of science | WOS:000254964400013 |
Scopus | 2-s2.0-42149176014 |
РИНЦ | 13587002 |
Chemical Abstracts | 2008:466794 |
Chemical Abstracts (print) | 150:285171 |
OpenAlex | W2070068495 |