Gas phase chemistry in catalytic combustion of methane/air mixtures over platinum at pressures of 1 to 16 bar

The gas-phase combustion of fuel-lean methane/air premixtures over platinum was investigated experimentally and numerically in a laminar channel-flow catalytic reactor at pressures 1 bar ⩽ p ⩽ 16 bar . In situ, spatially resolved one-dimensional Raman and planar laser induced fluorescence (LIF) measurements over the catalyst boundary layer were used to assess the concentrations of major species and of the OH radical, respectively. Comparisons between measured and predicted homogeneous (gaseous) ignition distances have led to the assessment of the validity of various elementary gas-phase reaction mechanisms. At low temperatures ( 900 K ⩽ T ⩽ 1400 K ) and fuel-to-air equivalence ratios ( 0.05 ⩽ φ ⩽ 0.50 ) typical to catalytic combustion systems, there were substantial differences in the performance of the gaseous reaction mechanisms originating from the relative contribution of the low- and the high-temperature oxidation routes of methane. Sensitivity analysis has identified the significance of the chain-branching reaction CHO + M = CO + H + M on homogeneous ignition, particularly at lower pressures. It was additionally shown that C2 chemistry could not be neglected even at the very fuel-lean conditions pertinent to catalytic combustion systems. A gas-phase reaction mechanism validated at 6 bar ⩽ p ⩽ 16 bar has been extended to 1 bar ⩽ p ⩽ 16 bar , thus encompassing all catalytic combustion applications. A reduced gas-phase mechanism was further derived, which when used in conjunction with a reduced heterogeneous (catalytic) scheme reproduced the key catalytic and gaseous combustion characteristics of the full hetero/homogeneous reaction schemes.