Modern tendencies in the kinetics of heterogeneous catalytic reactions asso
ciated with the consideration of the interaction of the catalyst with the r
eaction medium (including the conjugation of the catalytic reaction with th
e transformation of the catalyst) and of the participation of chemisorbed i
ntermediates in heterogeneous catalysis were examined. It was shown that th
ese effects are responsible for nonlinearity in the kinetic description of
catalytic processes even for simple reactions occurring at equivalent activ
e sites. These effects complicate the structure of the kinetic scheme and m
ake more difficult solving the reverse kinetic problem of establishing the
mechanism of a reaction from its kinetic characteristics. For the synthesis
of methanol, as an example, it was demonstrated that the kinetic model of
reactions involving firmly sorbed products is similar to the classical mode
l of two-center reactions. It was argued that the contribution from the non
uniformity of the surface is not as great as previously believed.