The behavior of different species during the temperature-programmed surface
reaction (TPSR) of methane over various catalysts is traced by an on-line
mass spectrometer. It is demonstrated that the transformation of MoO3 to mo
lybdenum carbide hinders the activation of methane as well as the succeedin
g aromatization in the TPSR. If this transformation process is done before
the reaction, the temperature needed for methane activation and benzene for
mation will be greatly lowered (760 K and 847 K, respectively). It is stron
gly suggested that molybdenum carbide is one of the active center of this c
atalytic process.