Studies of the complete oxidation of methane on a Pt electrode-catalys
t in the cell with a solid proton-conducting electrolyte (CH4 + O-2, P
t\SrCe0.92Dy0.08O3\Pt, H2O + N-2) were carried out. The non-Faradaic e
ffect of electrochemical hydrogen pumping on the rate of methane oxida
tion has been demonstrated. The induced change in the reaction rate at
anodic polarization of a Pt electrode-catalyst was over two orders of
magnitude higher than the rate of hydrogen pumping from the reaction
zone through the electrolyte.