K- and Ca-promoted ferrosilicates for the gas-phase epoxidation of propylene with O2
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Título: | K- and Ca-promoted ferrosilicates for the gas-phase epoxidation of propylene with O2 |
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Autor/es: | García Aguilar, Jaime | Cazorla-Amorós, Diego | Berenguer-Murcia, Ángel |
Grupo/s de investigación o GITE: | Materiales Carbonosos y Medio Ambiente |
Centro, Departamento o Servicio: | Universidad de Alicante. Departamento de Química Inorgánica | Universidad de Alicante. Instituto Universitario de Materiales |
Palabras clave: | Sol-gel | Propylene epoxidation | Alkali promotion | Ferrosilicate | Dyoxygen |
Área/s de conocimiento: | Química Inorgánica |
Fecha de publicación: | 25-may-2017 |
Editor: | Elsevier |
Cita bibliográfica: | Applied Catalysis A: General. 2017, 538: 139-147. doi:10.1016/j.apcata.2017.03.031 |
Resumen: | In the propylene epoxidation reaction with Fe-SiO2 catalysts the presence of iron oxide particles has a detrimental effect due to the total combustion of propylene on these iron species. Thus, the complete elimination of the iron oxide particles is presented as a preliminary strategy in order to increase the selectivity towards propylene oxide in iron-based catalysts. In this sense, a simple post-treatment of the catalysts with alkali or alkaline-earth elements (such as K or Ca, respectively) has proven effective in the total elimination of these iron oxide particles. Furthermore, the addition of K and Ca has modified the physico-chemical properties of the catalysts, decreasing their superficial acidity and (for higher K or Ca loadings) masking/blocking the active sites responsible for the catalytic reaction. With all this, it is shown that K has a higher efficiency removing the iron oxide particles compared with Ca (for the same molar ratios) and that a higher amount of K (compared to Fe) is required for the complete elimination of the iron oxide particles. A considerable propylene oxide selectivity enhancement (up to 65%) has been obtained for the K-promoted Fe0.005SiO2 and Fe0.01SiO2 catalysts using O2 as sole oxidant. |
Patrocinador/es: | We thank the Spanish Ministry of Economy and Competitiveness (MINECO), Generalitat Valenciana and FEDER (CTQ2015-66080-R MINECO/FEDER and PROMETEOII/2014/010) for financial support. J.G.A. thanks the Spanish Ministry of Economy and Competitiveness (MINECO) for his fellowship (BES-2013-063678). |
URI: | http://hdl.handle.net/10045/67793 |
ISSN: | 0926-860X (Print) | 1873-3875 (Online) |
DOI: | 10.1016/j.apcata.2017.03.031 |
Idioma: | eng |
Tipo: | info:eu-repo/semantics/article |
Derechos: | © 2017 Elsevier B.V. |
Revisión científica: | si |
Versión del editor: | http://dx.doi.org/10.1016/j.apcata.2017.03.031 |
Aparece en las colecciones: | INV - MCMA - Artículos de Revistas |
Archivos en este ítem:
Archivo | Descripción | Tamaño | Formato | |
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2017_Garcia-Aguilar_etal_ApplCatA_final.pdf | Versión final (acceso restringido) | 1,07 MB | Adobe PDF | Abrir Solicitar una copia |
2017_Garcia-Aguilar_etal_ApplCatA_revised.pdf | Versión revisada (acceso abierto) | 3 MB | Adobe PDF | Abrir Vista previa |
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