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Dehydrogenation of n-Butane to Butadiene-1,3 on an Alumina-Chromium Catalyst. Part 1: Kinetics of Dehydrogenation and Reactions of Coke Formation Научная публикация

Журнал Catalysis in Industry
ISSN: 2070-0504 , E-ISSN: 2070-0555
Вых. Данные Год: 2024, Том: 16, Номер: 4, Страницы: 413–423 Страниц : 11 DOI: 10.1134/S2070050424700259
Ключевые слова kinetic model, n-butane, butadiene-1,3, dehydrogenation, hydrocracking, coke formation
Авторы Ovchinnikova E.V. 1 , Petrov R.V. 1 , Chumachenko V.A. 1 , Noskov A.S. 1
Организации
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia

Информация о финансировании (1)

1 Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) FWUR-2024-0037

Реферат: The kinetics of n-butane dehydrogenation to butadiene is studied with temperature (T) variation of 550–625°C, duration of dehydrogenation stage (t) of 5–30 min, and space velocity (V) of 4400–35200 h−1 on industrial catalyst K-CrOx/γ-Al2O3 at a fraction of 56–94 μm. The catalyst is stabilized before studies. The granulated catalyst in a reduction–dehydrogenation–regeneration cycle at 593°C, and then as a fraction of 56–94 μm in dehydrogenation–regeneration cycle at 650°C. The maximum selectivity toward butadiene of ~25 mol % is achieved with n-butane conversion of 26–30% (V = 35200 h−1), T = 600 °C, and t = 5 min, while the maximum yield of butadiene ~10 mol % is obtained with an increase in conversion up to ~50% (V = 8800 h–1) under the same conditions. Raising T to 625°C and t to 30 min and lowering V to ~4400 h–1 increases the selectivity toward byproducts to ~50 mol %. It is found that the energy of activation for the rates of product formation falls in the order by-products > butylene > butadiene. A kinetic model is proposed that describes the formation of butadiene via butylene, the formation of ethane/ethylene and methane/propylene by-products during butylene hydrocracking, and secondary conversions of by-products, plus the formation of coke and its effect on catalyst activity. In the model, the inhibition of dehydrogenation reactions by components of reaction mixture is described by a mechanism in which the limiting stage is a surface reaction on two active centers. The adequacy of the kinetic model is confirmed by good agreement between the calculated and experimental results
Библиографическая ссылка: Ovchinnikova E.V. , Petrov R.V. , Chumachenko V.A. , Noskov A.S.
Dehydrogenation of n-Butane to Butadiene-1,3 on an Alumina-Chromium Catalyst. Part 1: Kinetics of Dehydrogenation and Reactions of Coke Formation
Catalysis in Industry. 2024. V.16. N4. P.413–423. DOI: 10.1134/S2070050424700259 WOS Scopus РИНЦ OpenAlex
Оригинальная: Овчинникова Е.В. , Петров Р.В. , Чумаченко В.А. , Носков А.С.
Дегидрирование н-бутана в бутадиеН-1,3 на алюмохромовом катализаторе: 1. Кинетика реакций дегидрирования и коксообразования
Катализ в промышленности. 2024. Т.24. №3. С.16-28. DOI: 10.18412/1816-0387-2024-3-16-28 РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 5 окт. 2023 г.
Принята к публикации: 13 дек. 2023 г.
Опубликована в печати: 1 дек. 2024 г.
Опубликована online: 27 янв. 2025 г.
Идентификаторы БД:
Web of science: WOS:001408605200011
Scopus: 2-s2.0-85217661731
РИНЦ: 80240199
OpenAlex: W4406869204
Цитирование в БД: Пока нет цитирований
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