Synthesis of carbon nanofibers supported cobalt catalysts for Fischer–Tropsch process

•Support crystallinity clearly influenced on the metal particle size.•Co/CNF-1 and Co/CNF-2 showed the highest activity and selectivity to CO2 and CH4.•Co/CNF-3 sample presented the highest selectivity to long-chained hydrocarbons.•Metal sintering was significant in catalysts with small metal partic...

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Veröffentlicht in:Fuel (Guildford) 2013-09, Vol.111, p.422-429
Hauptverfasser: Díaz, José Antonio, Martínez-Fernández, Miriam, Romero, Amaya, Valverde, José Luis
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creator Díaz, José Antonio
Martínez-Fernández, Miriam
Romero, Amaya
Valverde, José Luis
description •Support crystallinity clearly influenced on the metal particle size.•Co/CNF-1 and Co/CNF-2 showed the highest activity and selectivity to CO2 and CH4.•Co/CNF-3 sample presented the highest selectivity to long-chained hydrocarbons.•Metal sintering was significant in catalysts with small metal particles.•Catalyst fouling by long-chained hydrocarbons slow down the reaction. In this paper, CNFs prepared at three different temperatures (1023, 873 and 723K, called CNF-1, CNF-2 and CNF-3, respectively) were used as supports for cobalt-based catalysts in the Fischer–Tropsch Synthesis (FTS). The supports and cobalt catalysts were characterized by nitrogen adsorption–desorption, temperature-programmed reduction (TPR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) techniques; the metal content of the cobalt-based catalysts was analyzed by atomic absorption. The activity and selectivity of the CNFs supported catalysts were studied at 523K, 20bar and H2/CO=2. Co/CNF-1 and Co/CNF-2 were very active and showed high selectivity to CH4 and CO2, without further deactivation, whereas the less active catalyst Co/CNF-3 led to the highest selectivity to long-chained hydrocarbons (C5+) and under was a remarkable deactivation. Used catalysts were characterized by nitrogen adsorption–desorption, XRD and TGA. Results confirmed that all the catalysts underwent catalyst fouling as a consequence of C5+ hydrocarbons formation whereas catalyst Co/CNF-3 presented a notably metal sintering by coalescence.
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In this paper, CNFs prepared at three different temperatures (1023, 873 and 723K, called CNF-1, CNF-2 and CNF-3, respectively) were used as supports for cobalt-based catalysts in the Fischer–Tropsch Synthesis (FTS). The supports and cobalt catalysts were characterized by nitrogen adsorption–desorption, temperature-programmed reduction (TPR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) techniques; the metal content of the cobalt-based catalysts was analyzed by atomic absorption. The activity and selectivity of the CNFs supported catalysts were studied at 523K, 20bar and H2/CO=2. Co/CNF-1 and Co/CNF-2 were very active and showed high selectivity to CH4 and CO2, without further deactivation, whereas the less active catalyst Co/CNF-3 led to the highest selectivity to long-chained hydrocarbons (C5+) and under was a remarkable deactivation. Used catalysts were characterized by nitrogen adsorption–desorption, XRD and TGA. 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subjects Applied sciences
Carbon nanofibers
Catalysis
Catalyst deactivation
Catalysts
Cobalt
Deactivation
Energy
Energy. Thermal use of fuels
Exact sciences and technology
Fischer–Tropsch
Fouling
Fuels
Hydrocarbons
Selectivity
Synthesis
title Synthesis of carbon nanofibers supported cobalt catalysts for Fischer–Tropsch process
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