The kinetics of CO2 reforming of methane has been studied at 976-1033K on a
commercial NiO/CaO/Al2O3 catalyst in a packed-bed continuous reactor. The
reaction was carried out at atmospheric pressure and CO2/CH4 ratio > 2. The
Hougen-Watson rate models were fitted to experimental data assuming the di
ssociative adsorption of methane as the rate-determining step. The reaction
rate showed an effective reaction order of about unity for CH4. The appare
nt activity energy was found to be 104kJ . mol(-1). Therefore the kinetic r
eaction parameters were determined and a possible reaction mechanism was pr
oposed.