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Alumina-Supported Palladium–Silver Bimetallic Catalysts with Single-Atom Pd1 Sites in the Liquid-Phase Hydrogenation of Substituted Alkynes Научная публикация

Журнал Kinetics and Catalysis
ISSN: 1608-3210 , E-ISSN: 0023-1584
Вых. Данные Год: 2020, Том: 61, Номер: 6, Страницы: 869-878 Страниц : 10 DOI: 10.1134/s0023158420060129
Авторы Rassolov A.V. 1 , Bragina G.O. 1 , Baeva G.N. 1 , Mashkovsky I.S. 1 , Stakheev A.Yu. 1
Организации
1 Zelinsky Institute of Organic Chemistry Russian Academy of Sciences Moscow Russia

Реферат: The catalytic characteristics of Pd–Ag/Al2O3 bimetallic catalysts with an Ag/Pd atomic ratio of 0.03–3.0 have been studied in the selective liquid-phase hydrogenation of diphenylacetylene and 1-phenyl-1-propyne. It has been found that an increase in the Ag/Pd ratio leads to a significant increase in selectivity, which, however, is accompanied by a decrease in the catalyst activity. Comparison with data of an earlier structural study suggests that an increase in selectivity observed with an increase in the Ag/Pd ratio to 0.5–1.0 is attributed to the following two factors: (1) the suppression of the formation of palladium hydride and (2) an increase in the fraction of “single-atom” Pd1 sites isolated from each other by Ag atoms on the surface of the Pd–Ag nanoparticles. An increase in the Ag/Pd value to 2.0–3.0 leads to a further increase in the selectivity, which exceeds the selectivity of a commercial Lindlar catalyst (Pd–Pb/CaCO3). In this case, the most probable cause of the high selectivity is the formation of the single-atom Pd1 sites on the surface of the Pd–Ag alloy and an increase in the stability of the structure.
Библиографическая ссылка: Rassolov A.V. , Bragina G.O. , Baeva G.N. , Mashkovsky I.S. , Stakheev A.Y.
Alumina-Supported Palladium–Silver Bimetallic Catalysts with Single-Atom Pd1 Sites in the Liquid-Phase Hydrogenation of Substituted Alkynes
Kinetics and Catalysis. 2020. V.61. N6. P.869-878. DOI: 10.1134/s0023158420060129 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000603310400006
Scopus: 2-s2.0-85098260025
OpenAlex: W3114327758
Цитирование в БД:
БД Цитирований
OpenAlex 24
Scopus 17
Web of science 16
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