Catalytic Performance of Co3O4 on Different Activated Carbon Supports in the Benzyl Alcohol Oxidation

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Título: Catalytic Performance of Co3O4 on Different Activated Carbon Supports in the Benzyl Alcohol Oxidation
Autor/es: Cordoba, Misael | Miranda, Cristian | Lederhos, Cecilia R. | Coloma, Fernando | Ardila, Alba | Fuentes, Gustavo A. | Pouilloux, Yannick | Ramírez, Alfonso
Grupo/s de investigación o GITE: Materiales Avanzados
Centro, Departamento o Servicio: Universidad de Alicante. Servicios Técnicos de Investigación
Palabras clave: Benzyl alcohol | Oxidation | Activated carbon | Cobalt oxide | Heterogeneous catalysts
Área/s de conocimiento: Química Inorgánica
Fecha de publicación: 12-dic-2017
Editor: MDPI
Cita bibliográfica: Cordoba M, Miranda C, Lederhos C, Coloma-Pascual F, Ardila A, Fuentes GA, Pouilloux Y, Ramírez A. Catalytic Performance of Co3O4 on Different Activated Carbon Supports in the Benzyl Alcohol Oxidation. Catalysts. 2017; 7(12):384. doi:10.3390/catal7120384
Resumen: Co3O4 particles were supported on a series of activated carbons (G60, CNR, RX3, and RB3). Incipient wetness method was used to prepare these catalysts. The effect of the structural and surface properties of the carbonaceous supports during oxidation of benzyl alcohol was evaluated. The synthetized catalysts were characterized via IR, TEM, TGA/MS, XRD, TPR, AAS, XPS, and N2 adsorption/desorption isotherm techniques. Co3O4/G60 and Co3O4/RX3 catalysts have high activity and selectivity on the oxidation reaction reaching conversions above 90% after 6 h, without the presence of promoters. Catalytic performances show that differences in chemistry of support surface play an important role in activity and suggest that the presence of different ratios of species of cobalt and oxygenated groups on surface in Co3O4/G60 and Co3O4/RX3 catalysts, offered a larger effect synergic between both active phase and support increasing their catalytic activity when compared to the other tested catalysts.
Patrocinador/es: The author acknowledges the financial support from University of Cauca (project ID VRI 3573). M. Cordoba thanks COLCIENCIAS (Young Researchers Program 2012-Call 566), the Research Institute of Catalysis and Petrochemistry—INCAPE (Argentina), Design of Advanced Catalytic Materials Group, Department of Process Engineering, Universidad Autónoma Metropolitana—Iztapalapa, UAM-I (Mexico), and the group of Zeolites and Solids from Université de Poitiers (France).
URI: http://hdl.handle.net/10045/73468
ISSN: 2073-4344
DOI: 10.3390/catal7120384
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Revisión científica: si
Versión del editor: http://dx.doi.org/10.3390/catal7120384
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