This paper reports a novel catalytic process for the destruction of ch
lorinated hydrocarbons. Based on CH4-steam reforming reactions, the ap
proach gives high levels of conversion (5-nines possible) at high spac
e velocities (2-3 x 10(5) h(-1)) and temperatures (650-750 degrees C).
Products comprise CO, CO2, H-2 and HCl and no others were identified.
Rapid deactivation by parallel thermal pyrolysis reactions occurs if
high conversion is not maintained. The presence of Cl species poisons
CH4-steam reforming and water gas shift activities, but the effect is
only temporary and disappears when the Cl compounds are removed from t
he feed. Kinetic studies on methyl chloride have been carried out and
show a Langmuir-Hinshelwood type behavior, from which a proposed mecha
nism involving dual-site surface dissociation is suggested. Comparison
s with other common chlorocarbons show similarities, with the exceptio
n that 1,1,1-trichloroethane is very sensitive to thermal pyrolysis an
d gives faster deactivation.