| Summary: | A combination of transient methods in a laboratory-scale trickle bed reactor and attenuated total reflection (ATR)-infrared spectroscopy was applied to gain insight into the reaction mechanism of the direct synthesis of hydrogen peroxide (DSHP) on a commercial 5 %Pd/C catalyst, with water and methanol used as solvents. During the transient studies, after the switch from water to methanol, an oscillatory pattern was observed in which methoxy and hydroxymethyl species were observed prior to the peroxide species. From the specific position and the maxima in the intensities of these species over time, an augmented reaction scheme for the DSHP in methanol was proposed, in which methanol can form hydroxymethyl species which act as co-catalysts to reduce absorbed oxygen species.
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