Adsorption and reaction of CO and hydrogen on iron-based Fischer–Tropsch synthesis catalysts

Abstract

H 2, CO chemisorptions and the carbon hydrogenation on promoted iron Fischer–Tropsch synthesis (FTS) catalysts (Fe/SiO 2 and FeK/SiO 2) were investigated using temperature programmed surface reaction with X-ray photoelectron spectroscopy and laser Raman spectroscopy. It is found that potassium, used as promoter, does not lead to a distinct variation in the carbon species but changes the surface H/C ratio of carburized catalysts. Besides bulk iron carbide, several carbon species with different cluster sizes exist in the carburized catalysts, which have different reactivities towards hydrogen. The surface atomic carbon, the oligomerized carbon species and the bulk iron carbide are more reactive to hydrogen, whereas the large-size amorphous carbons are relatively inert to hydrogen. There is a good correlation between the chemisorption of H 2 or CO and the corresponding feed gas conversion activity in FTS reaction. Meanwhile, the methane selectivity is correlated with the hydrogenation capability of catalysts, indicating that the surface H concentration has an important effect on the selectivity of hydrocarbons.