Influence of the thermal treatment conditions and composition of bimetallic catalysts Fe—Pd/SiO2 on the catalytic properties in phenylacetylene hydrogenation
- Авторлар: Shesterkina A.A.1, Kozlova L.M.1, Kirichenko O.A.1, Kapustin G.I.1, Mishin I.V.1, Kustov L.M.1,2
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Мекемелер:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Department of Chemistry, M. V. Lomonosov Moscow State University
- Шығарылым: Том 65, № 2 (2016)
- Беттер: 432-439
- Бөлім: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/237125
- DOI: https://doi.org/10.1007/s11172-016-1317-z
- ID: 237125
Дәйексөз келтіру
Аннотация
The supported bimetallic Fe—Pd/SiO2 catalysts with the different Fe (0.025—8 mass.%) and Pd (0.05—3.2 mass.%) loadings were synthesized by the incipient wetness impregnation of support. The samples were heat-treated under different conditions (calcination in air at 240—350 °C or reduction in an H2 flow at 400 °C). The X-ray phase analysis revealed the formation of Pd0, α-Fe2O3 and Fe3O4 phases after calcination of the samples at 240—260 °C. The reduction of the calcined Fe—Pd samples in an H2 flow at 400 °C enables the formation of Fe0 nanoparticles of size 17—20 nm. The synthesized catalytic systems were studied in the selective hydrogenation of phenylacetylene at room temperature and atmospheric pressure in a solvent (ethanol, propanol). The catalytic properties of the Fe—Pd catalysts depend on the nature of solvent, catalyst composition, and thermal treatment conditions. The application of the Fe—Pd bimetallic catalysts with a low Pd loading of 0.05—0.1 mass.% made it possible to reach the high activity and selectivity to styrene (91%) at the complete conversion of phenylacetylene.
Авторлар туралы
A. Shesterkina
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: anastasiia.strelkova@mail.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
L. Kozlova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: anastasiia.strelkova@mail.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
O. Kirichenko
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: anastasiia.strelkova@mail.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
G. Kapustin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: anastasiia.strelkova@mail.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
I. Mishin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: anastasiia.strelkova@mail.ru
Ресей, 47 Leninsky prosp., Moscow, 119991
L. Kustov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences; Department of Chemistry, M. V. Lomonosov Moscow State University
Email: anastasiia.strelkova@mail.ru
Ресей, 47 Leninsky prosp., Moscow, 119991; Building 3, 1 Leninskie Gory, Moscow, 119992
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