Abstract

High dispersion and high activity charcoal-supported molybdenum catalysts were prepared using incipient wetness and equilibrium adsorption methods. Activities and selectivities of these catalysts were tested after reducing the catalysts at 773 K in flowing hydrogen. It was found that all the catalysts, particularly those prepared by the equilibrium adsorption method, showed high activities in Fischer-Tropsch synthesis of C 1 to C 3 hydrocarbons. Potassium promotion increased the selectivity towards C 2 and C 3 hydrocarbons while reducing moderately the activity. Without potassium promotion, C 2+ selectivities of all the catalysts with metal loading of three weight percent or higher were about 50 ± 5% under differential reactor conditions. Promotion by potassium increased the C 2+ selectivity to as much as 70%. It was found that there was a critical potassium loading at which point the activity decrease levelled off. The method of potassium addition to the catalyst also plays a major role in determining the final activity.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call