Gold nanoclusters supported on different materials as catalysts for the selective alkyne semihydrogenation

[EN] Catalysts based on gold nanoclusters supported by different materials have been used for the selective semi hydrogenation of phenylacetylene to styrene. The most active species were formed by catalyst thermal activation in a reductive atmosphere. It is shown that the activity and selectivity of...

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Detalles Bibliográficos
Autores: López-Hernández, I., Truttmann, V., Barrabés, N., Rupprechter, G., Rey Garcia, Fernando|||0000-0003-3227-5669, Mengual Cuquerella, Jesús|||0000-0002-8507-509X, Palomares Gimeno, Antonio Eduardo|||0000-0002-6480-6607
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/194523
Acceso en línea:https://riunet.upv.es/handle/10251/194523
Access Level:acceso abierto
Palabra clave:Alkynes
Gold nanoclusters
Selective hydrogenation
Support
Hydrotalcite
TECNOLOGIA DEL MEDIO AMBIENTE
INGENIERIA QUIMICA
Descripción
Sumario:[EN] Catalysts based on gold nanoclusters supported by different materials have been used for the selective semi hydrogenation of phenylacetylene to styrene. The most active species were formed by catalyst thermal activation in a reductive atmosphere. It is shown that the activity and selectivity of these catalysts is mainly controlled by the interaction of the gold nanoclusters with the support, as demonstrated by using materials with high surface area and different acidity/basicity, i.e. MgO, Al2O3 and Mg/Al hydrotalcite. There is an important influence of the acid/base properties of the support on the selectivity. Higher activity is obtained for gold supported on basic materials (MgO and hydrotalcite) and the best results are obtained with the Au catalyst supported on the MgAl hydrotalcite exhibiting high activity and the best selectivity to the alkene. This was explained by the intermediate basicity of the support that favors the heterolytic cleavage of H2 while avoiding the overreduction of the alkynes to alkanes.