Fischer Tropsch synthesis from a simulated biosyngas feed over Co(x)/SiO 2 catalysts: Effect of Co-loading

Medina, C; García R; Reyes, P; Escalona, N.; Fierro, J.L.G.

Keywords: adsorption, catalysis, xps, spectroscopy, electron, crystal, hydrocarbons, size, spectra, reduction, transmission, synthesis, silicon, co, reactors, liquid, biomass, polymer, ratio, ray, microscopy, surface, catalysts, steel, tem, cobalt, bed, wet, photoelectron, blends, fraction, loading, reactor, gasification, impregnation, biosyngas, compounds, fischer-tropsch, chemical, of, Reaction, X, (chemical), Stainless, 2, effect, atomic, fixed, Large, coverages, Crystallite, Temperature-programmed, Martensitic, Syn-gas, Co/SiO

Abstract

A series of Co/SiO 2 catalysts containing 10-30 wt.% Co were prepared by wet impregnation and tested in the Fischer Tropsch reaction using a simulated syngas (CO/H 2) mixture similar to that obtained in biomass gasification. The catalysts characterization included N 2 adsorption, temperature programmed reduction (TPR), X-ray photoelectron spectra (XPS) and transmission electron microscopy (TEM) techniques. The reaction was carried out in a stainless steel fixed bed reactor at 300 °C and 1 MPa. In general, activity increased almost linearly with increasing Co-loading, reaching maximum at about 20 wt.% Co and then levelled off. These results correlate with that derived from XPS. The Co/Si surface atomic ratios increased almost linearly up to about 20 wt.% Co due to gradual surface coverage by Co species. At higher loadings, cobalt form large crystal aggregates. The selectivity to C 8-C 9 hydrocarbons increases whereas the C 14+ hydrocarbon follows an opposite trend upon increasing Co-loading. It was also observed that the selectivity to liquid fraction is a function of the Co crystallite size, that is longer hydrocarbons chains are formed on the smaller cobalt crystallites. © 2009 Elsevier B.V. All rights reserved.

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Título de la Revista: APPLIED CATALYSIS A-GENERAL
Volumen: 373
Número: 1-2
Editorial: Elsevier
Fecha de publicación: 2010
Página de inicio: 71
Página final: 75
URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-74049090182&partnerID=q2rCbXpz