Abstract

This paper addresses the effect of support pore sizes on the structure and performance of iron catalysts supported by mesoporous silicas in high-temperature Fischer–Tropsch synthesis. A combination of characterization techniques showed that the size of supported iron particles was controlled by catalyst pore sizes. The larger iron particles were localized in large-pore supports.Iron carbidization with carbon monoxide resulted in preferential formation of Hägg iron carbide (χ-Fe5C2). Larger iron oxide crystallites in large-pore supports were much easier to carbidize than smaller iron oxide counterparts in small-pore supports. The catalytic performance in Fischer–Tropsch synthesis was attributed to iron carbide. Higher Fischer–Tropsch reaction rates, higher olefin, and C5+ selectivity were observed over larger pore iron catalysts. High dispersion of iron oxide in small-pore silicas was not favorable for carbon monoxide hydrogenation because of poor iron carbidization.

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