Min Hee Woo

Enhanced Catalytic Performance by Zirconium Phosphate‐Modified SiO2‐Supported RuCo Catalyst for Fischer–Tropsch Synthesis

Our zirconium phosphate (ZrP)‐promoted Ru/Co/ZrP/SiO2 catalyst reveals a high catalytic activity and stability during Fischer–Tropsch synthesis. Surface modification with ZrP on SiO2 support with an appropriate amount of phosphorous component prevents cobalt particle aggregation and enhances its stability. These positive effects of ZrP are mainly induced by the spatial confinement of cobalt particles in a thermally stable ZrP matrix, and the catalytic performance was greatly improved when the P/(Zr+P) molar ratio was 0.134 on the CoZrP(0.5) catalyst.

Thermally Stabilized Cobalt-Based Fischer–Tropsch Catalysts by Phosphorous Modification of Al2O3: Effect of Calcination Temperatures on Catalyst Stability

A phosphorous‐modified Al2O3 support was prepared by the impregnation method and applied for the preparation of cobalt‐based Fischer–Tropsch synthesis (FTS) catalysts (Co/P–Al2O3), which were calcined at different temperatures. The Co/P–Al2O3 showed a significant increase of thermal stability with a higher catalytic performance without severe deactivation even above a calcination temperature of 600 °C compared with the unmodified Co/Al2O3. These findings are explained by the suppressed cobalt aluminate formation and less pronounced aggregation of cobalt particles. The suppressed aggregation of cobalt particles is attributed to the localized presence of aluminum phosphate by forming a thermally stable metal–phosphorous oxo‐species on Al2O3 surfaces thus suppressing the migration of cobalt particles to the outer pore mouths of the support. These effects significantly enhance the catalytic activity with a higher thermal stability of the catalysts.