Boreskov Institute of Catalysis SB RAS, Novosibirsk, Russia
Boreskov Institute of Catalysis SB RAS, Novosibirsk, Russia
Boreskov Institute of Catalysis SB RAS, Novosibirsk, Russia
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PP-44EFFECT OF REDUCTION CONDITIONS OF 20%Co/(Hβ +50%Al)CATALYST ON THE CATALYST PROPERTIES IN HYDROCARBONSYNTHESIS FROM CO AND H 2Potapova S.N., Mikhailova Ya.V., Svidersky S.A., Loginova A.N.United research and development centre, <strong>Russia</strong>, Moscow, Leninsky pr. 55/1, b.2.research-centre@yrd.ruSearch for new ways to use associated and natural gas is <strong>of</strong> great importance infuel sources utilization. One <strong>of</strong> promising methods for large-scale processes isproduction <strong>of</strong> synthetic liquid hydrocarbons via Fischer-Tropsch synthesis over cobaltcatalysts. In the presence <strong>of</strong> these catalytic systems, normal paraffins are mainlyformed with yield and composition depending not only on composition <strong>of</strong> a catalystbut also on the conditions <strong>of</strong> its activation before the synthesis. Formation <strong>of</strong> activesurface <strong>of</strong> cobalt catalyst is known to occur during its reduction with hydrogen.Reduction conditions have an impact on the ratio between metallic and oxide phaseswhich, in its turn, determines catalytic properties <strong>of</strong> a system, particularly selectivityto C 5+ hydrocarbons and methane. Large amount <strong>of</strong> hydrogen is required to reduce(activate) commercial Fischer-Tropsch catalysts. Consumption <strong>of</strong> hydrogen can belowered by its dilution with inert gases (helium, nitrogen, argon) to provide H 2 contentfrom 5 to 100 vol.%. However, there is a limited number <strong>of</strong> studies considering themethod.The aim <strong>of</strong> our study was to investigate the influence <strong>of</strong> 20%Со/(Нβ+50%Al)catalyst reduction conditions, particularly hydrogen dilution with nitrogen and helium,on its properties in hydrocarbon synthesis from CO and H 2 .20%Со/(Нβ+50%Al) catalyst has been prepared by the technique described inpatent [1]. Hydrocarbon synthesis from CO and H 2 was performed in a flow unit withfixed-bed catalyst at P=2.0 MPa and syngas space velocity <strong>of</strong> 1000 hr –1 . Thecatalysts were activated either with pure hydrogen or with reducing mixtures(10%Н 2 +N 2 ) or (10%Н 2 +Нe) at 400°C. In all the cases the total amount <strong>of</strong> purehydrogen passed was 7.5 l.All the catalysts were active in hydrocarbon synthesis from CO and H 2 .Over the whole temperature range <strong>of</strong> the synthesis the largest CO conversionand liquid hydrocarbon yield were achieved over the sample reduced with pure133