Abstract

Catalytic partial oxidation (CPO) of methane has been investigated over Co/Al 2 O 3 catalysts with different metal (0.1 wt.% of Ni, Pt, Rh, Ru or Pd) and oxide (<4 wt.% Fe 3 O 4 /Cr 2 O 3 , La 2 O 3 , SnO 2 or K 2 O) promoters. A comparison with Ni- and Fe-based catalysts was performed. Methane conversions and selectivities were determined in the temperature range 200–750 °C at atmospheric pressure in a continuous fixed-bed quartz reactor. Catalytic partial oxidation (CPO) of methane has been investigated over Co/Al 2 O 3 catalysts with different metal (0.1 wt.% of Ni, Pt, Rh, Ru or Pd) and oxide (<4 wt.% Fe 3 O 4 /Cr 2 O 3 , La 2 O 3 , SnO 2 or K 2 O) promoters. A comparison with Ni- and Fe-based catalysts was performed. Methane conversions and selectivities were determined in the temperature range 200–750 °C at atmospheric pressure in a continuous fixed-bed quartz reactor. The scope was to identify factors for control of product selectivity and investigate the potential of low temperature operation. The unpromoted 10 wt.% Co/Al 2 O 3 catalyst showed stable steady-state performance at 650 °C in the gas hourly space velocity range 15–180 N l CH 4 /g cat h. Equilibrium behaviour was observed during ramping (−1 °C/min) until a sudden extinction occurred around 450 °C, seemingly coinciding with O 2 breakthrough. Addition of 0.1 wt.% metal promoter, particularly Pt and Rh, caused the activity to be maintained to lower temperatures. While Rh maintained H 2 formation, Pt promoted combustion at low temperatures. Addition of 0.1 wt.% Ni by co-impregnation promoted carbon formation and deactivation. Addition of surface oxides typically promoted instability, deactivation and combustion. While the performance of Ni catalysts was superior to Co catalysts at low temperatures, Fe-based catalysts showed combustion activity in the whole temperature range. A hydrogen yield according to equilibrium predictions seems to be the best possible achievement.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.