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Cobalt Stabilization through Mesopore Confinement on TiO(2) Support for Fischer–Tropsch Reaction

[Image: see text] Cobalt supported on mesostructured TiO(2) catalysts has been prepared by a wet-impregnation method. The Co/TiO(2) catalytic system showed better catalytic performance after support calcination at 380 °C. Co nanoparticles appeared well distributed along the mesopore channels of TiO(...

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Detalles Bibliográficos
Autores principales: Platero, F., Todorova, S., Aoudjera, L., Michelin, L., Lebeau, B., Blin, J. L., Holgado, J. P., Caballero, A., Colón, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523356/
https://www.ncbi.nlm.nih.gov/pubmed/37771503
http://dx.doi.org/10.1021/acsaem.3c01432
Descripción
Sumario:[Image: see text] Cobalt supported on mesostructured TiO(2) catalysts has been prepared by a wet-impregnation method. The Co/TiO(2) catalytic system showed better catalytic performance after support calcination at 380 °C. Co nanoparticles appeared well distributed along the mesopore channels of TiO(2). After reduction pretreatment and reaction, a drastic structural change leads to mesopore structure collapse and the dispersion of the Co nanoparticles on the external surface. Along this complex process, Co species first form discrete nanoparticles inside the pore and then diffuse out as the pore collapses. Through this confinement, a strong metal–support interaction effect is hindered, and highly stable metal active sites lead to better performance for Fischer–Tropsch synthesis reaction toward C(5+) products.