The partial oxidation of methane to synthesis gas has been studied in
a continuous flow reactor using a Rh/alpha-Al2O3 catalyst under condit
ions as close as possible to those industrially relevant: pressures up
to 800 kPa and temperatures higher than 1274 K in order to avoid the
formation of carbon and to obtain high equilibrium selectivities to CO
and H-2. Intrinsic kinetic data were obtained when the feed was dilut
ed with helium. Gas-phase reactions were found to occur at 500 kPa whe
n the feed was not diluted. A reaction network has been derived from e
xperimental results in which oxygen conversions range from 0 to 1. CO2
, C2H6 and H2O are the primary products. C2H4 is formed by oxidative d
ehydrogenation of C2H6 CO and H-2 are formed by reforming of CH4 by CO
2 and H2O; an additional direct route to CO and H-2 at low oxygen conv
ersions cannot be excluded. The catalyst appears to be present in two
states, the transition being at an oxygen conversion of 0.4 under the
conditions used. The support probably enhances oxidation reactions by
reverse spillover of oxygen or hydroxyl species onto rhodium. The supp
ort as such behaves similarly to the catalyst at low oxygen conversion
s, but shows no reforming activity.