Kinetic behaviour of three samples of samarium oxide (cubic (Sm-1), mo
noclinic (Sm-3) and mixed cubic-monoclinic (Sm 2)) were studied in the
oxidative coupling of methane using a gradientless flow circulation s
ystem. The specific rate of C-2-product formation differed by a factor
of 6-8 for Sm-1 and Sm-3. The specific activity for CO formation did
not depend upon the crystal structure of samarium oxide while the rate
of formation of CO2 was different for the samples studied. It is prop
osed that formation of CO and CO2 occurs via different reaction routes
. The rate of CO2 formation at high CH4/O-2 ratio is limited by oxidan
t activation or surface CO2-complex decomposition.