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In situ time-resolved FTIR spectroscopy was used to study the reaction mechanism of partial oxidation of methane (POM) to synthesis gas and the reaction of CH4/O2/He (2/1/45, molar ratio) gas mixture with adsorbed CO species over Rh/SiO2, Ru/γ-Al2O3 and Ru/SiO2 catalysts at 500-600℃. It was found that CO is the primary product of POM reaction over reduced and working state Rh/SiO2 catalysts. Direct oxidation of CH4 is the main pathway of synthesis gas formation over Rh/SiO2 catalyst. CO2 is the primary product of POM over Ru/γ-Al2O3 and Ru/SiO2 catalysts. The dominant reaction pathway for synthesis gas formation over Ru/γ-Al2O3 catalyst is via the reforming reactions of CH4 with CO2 and H2O. For the POM reaction over Rh/SiO2 and Ru/γ-Al2O3 catalysts, consecutive oxidation of surface CO species is an important pathway of CO2 formation.
In situ time-resolved FTIR spectroscopy was used to study the reaction mechanism of partial oxidation of methane (POM) to synthesis gas and the reaction of CH4 / O2 / He (2/1/45, molar ratio) gas mixture with adsorbed CO species Over Rh / SiO2, Ru / γ-Al2O3 and Ru / SiO2 catalysts at 500-600 ° C. It was found that CO is the primary product of POM reaction over reduced and working state Rh / SiO2 catalysts. Direct oxidation of CH4 is the main pathway of synthesis gas formation over Rh / SiO2 catalyst. CO2 is the primary product of POM over Ru / γ-Al2O3 and Ru / SiO2 catalysts. The dominant reaction pathway for synthesis gas formation over Ru / γ-Al2O3 catalyst is via the reforming reactions of CH4 with CO2 and H2O. For the POM reaction over Rh / SiO2 and Ru / γ-Al2O3 catalysts, consecutive oxidation of surface CO species is an important pathway of CO2 formation.