Technology development for iron and cobalt Fischer-Tropsch catalysts
Author(s) -
B.H. Davis
Publication year - 1999
Publication title -
osti oai (u.s. department of energy office of scientific and technical information)
Language(s) - English
Resource type - Reports
DOI - 10.2172/775014
Subject(s) - fischer–tropsch process , catalysis , supercritical fluid , syngas , cobalt , chemistry , partial pressure , solvent , selectivity , inorganic chemistry , chemical engineering , organic chemistry , oxygen , engineering
The impact of deuterium on the Fischer-Tropsch (FT) synthesis was studied with a precipitated iron catalyst in the slurry phase. Deuterium has been used by several research groups to better understand the mechanism of CO hydrogenation. Inverse (k{sub H}/k{sub D} < 1), normal (k{sub H}/k{sub D} > 1) and no isotope effect (k{sub H}/k{sub D} = 1) have been reported. The conflicting results are thought to arise because rate of reaction is a combination of kinetic and equilibrium factors. In summary, the presence of boron produced only minor changes on the properties of the cobalt catalyst. In earlier studies, it was shown that the presence of boron made the catalyst less susceptible to poisoning by sulfur. Steady-state supercritical Fischer-Tropsch synthesis was studied in the work using a fixed-bed reactor and an unpromoted Co/SiO{sub 2} catalyst. This serves as the baseline for promoted catalyst studies. A pentane-hexane mixture was used as the supercritical solvent. Overall reactor pressure, syngas partial pressure and contact time were kept constant to obtain a valid comparison of the impact of solvent density in the catalytic activity and selectivity. Three different partial pressures of the mixture were chosen based on the density-pressure curve in order to investigate the pressure tuning effect to Fischer-Tropsch synthesis near critical region
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