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New Ammonia Synthesis Catalysts Based on Supported Potassium Carbonyl Ruthenates as Precursors of Catalytically Active Ruthenium Particles and Potassium Promoter Научная публикация

Журнал Journal of Molecular Catalysis A: Chemical
ISSN: 1381-1169
Вых. Данные Год: 2004, Том: 219, Номер: 1, Страницы: 149-153 Страниц : 5 DOI: 10.1016/j.molcata.2004.04.031
Ключевые слова Ammonia synthesis, Metallic potassium, Potassium carbonyl metallates, Ruthenium, Supported catalysts
Авторы Yunusov S.M. 1 , Kalyuzhnaya E.S. 1 , Moroz B.L. 2 , Ivanova A.S. 2 , Reshetenko T.V. 2 , Avdeeva L.B. 2 , Likholobov V.A. 2 , Shur V.B. 1
Организации
1 A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilov Street 28, Moscow 119991, Russia
2 K.G. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Ac. Lavrent’ev Avenue 5, Novosibirsk 630090, Russia

Информация о финансировании (1)

1 Российский фонд фундаментальных исследований 02-03-32681

Реферат: New supported “single-component” ruthenium catalysts for ammonia synthesis are reported. For preparation of the catalysts, various potassium carbonyl ruthenates such as K2[Ru6(CO)18] (K:Ru=1:3), K4[Ru4(CO)12] (K:Ru=1:1), K6[Ru6(CO)16] (K:Ru=1:1), K6[Ru4(CO)11] (K:Ru=1.5:1) and K2[Ru(CO)4] (K:Ru=2:1) were used as precursors of both catalytically active ruthenium particles and potassium promoter while graphite-like carbon “Sibunit” was utilized as a support. The studied catalysts have been compared in their activity with the previously described K2[Ru4(CO)13]-based catalyst (K:Ru=1:2) on “Sibunit”. It has been established that the rate of the ammonia synthesis at 300 °C over these catalysts increases with the increase in the K:Ru ratio in the starting carbonyl metallate, reaching a maximum in the case of the K6[Ru4(CO)11]-based sample. On further enhancement in the K:Ru ratio, i.e. when the K2[Ru(CO)4] catalyst is used, the rate of the ammonia formation noticeably diminishes. The activity of the K2[Ru(CO)4]-based catalyst in the ammonia synthesis can be considerably augmented on the replacement of “Sibunit” by catalytic filamentous carbon CFC-III or MgO. The use of γ-Al2O3 or carbon-coated γ-Al2O3 as supports decreases the reaction rate. An introduction of metallic potassium into the K2[Ru(CO)4] catalysts on “Sibunit” and CFC-III accelerates strongly the process of the ammonia synthesis. The highest activity is exhibited by the K2[Ru(CO)4]+K system on “Sibunit” at the metallic potassium to carbon molar ratio of 0.08. On using this catalyst (3.55 g), the steady ammonia concentration in the gas flow at 300 °C and 1 atm amounts to 71.1% of the equilibrium value while at 350 and 400 °C the process of the ammonia synthesis fully reaches the equilibrium. In its efficiency in the ammonia production at 250–300 °C, the K2[Ru(CO)4]+K catalyst on “Sibunit” carbon significantly exceeds the previously developed K2[Ru4(CO)13]+K catalyst on the same support.
Библиографическая ссылка: Yunusov S.M. , Kalyuzhnaya E.S. , Moroz B.L. , Ivanova A.S. , Reshetenko T.V. , Avdeeva L.B. , Likholobov V.A. , Shur V.B.
New Ammonia Synthesis Catalysts Based on Supported Potassium Carbonyl Ruthenates as Precursors of Catalytically Active Ruthenium Particles and Potassium Promoter
Journal of Molecular Catalysis A: Chemical. 2004. V.219. N1. P.149-153. DOI: 10.1016/j.molcata.2004.04.031 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 21 янв. 2004 г.
Принята к публикации: 30 апр. 2004 г.
Опубликована online: 7 июн. 2004 г.
Опубликована в печати: 1 сент. 2004 г.
Идентификаторы БД:
Web of science: WOS:000222878700018
Scopus: 2-s2.0-3042793151
РИНЦ: 13455835
Chemical Abstracts: 2004:561886
Chemical Abstracts (print): 142:267420
OpenAlex: W2047001997
Цитирование в БД:
БД Цитирований
Web of science 12
Scopus 14
РИНЦ 12
OpenAlex 14
Альметрики: