Catalytic behaviors of Co-Mn/TiO2catalysts for Fischer-Tropsch synthesis

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The 15%(Co-Mn)/TiO2,(Co/Mn=1/6) catalyst was prepared using fusion procedure and studied for the conversion of synthesis gas to C2 ~ 4 olefins.The effects of calcination conditions and operation conditions such as the H 2 / CO molar feed ratio at different temperatures,gas hourly space velocity(GHSV) and total reaction pressure on the catalytic performance of catalyst were investigated.The stability of the catalyst during 150 h at optimal operation conditions(t = 250℃ H2 /CO= 2/1,GHSV=1 500 h-1 and p =0.3 MPa) has been investigated.It is found that this catalyst is high stable for production C2 ~ 4 olefins.Characterizations of both precursors and calcined catalysts by powder X-ray diffraction,scanning electron microscopy(SEM),Brunauer-Emmett-Teller(BET) specific surface area measurement and thermal analysis methods such as thermal gravimetric analysis(TGA) and differential scanning calorimetry(DSC) show that the different preparation method influences the catalyst precursor structure and morphology. The 15% (Co-Mn) / TiO2, (Co / Mn = 1/6) catalyst was prepared using fusion procedure and studied for the conversion of synthesis gas to C2 ~ 4 olefins. These effects of calcination conditions and operation conditions such as as the H 2 / CO molar feed ratio at different temperatures, gas hourly space velocity (GHSV) and total reaction pressure on the catalytic performance of catalyst were investigated. The stability of the catalyst during 150 h at optimal operation conditions (t = 250 ° C H2 / CO = 2/1, GHSV = 1500 h-1 and p = 0.3 MPa) has been investigated. It is found that this catalyst is high stable for C2 ~ 4 olefins. Characterizations of both precursors and calcined catalysts by powder X -ray diffraction, scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) specific surface area measurement and thermal analysis methods such as thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) show that the different preparation method influences the catalyst precursor struc ture and morphology.
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