Abstract

Extensive experiments with a flow reactor were performed to reliably detect the steady-state catalytic formation of ethylene oxide from ethylene and oxygen on an Ag(111) single crystal. For single crystals with their small surfaces, this had been a major experimental problem because of the low reaction probability of ethylene and cross-sensitivities in the mass spectra. Using 16O2 ethylene oxide could be detected on mass fragment m/z=43, using 18O2 on m/z=31 and m/z=45, but strong time-dependent background signals had to be subtracted. This was achieved by periodic temperature changes of the reactor. After proper inclusion of all effects, a mole fraction of ethylene oxide of only 3×10−5 with respect to the reaction gas mixture, which was unequivocally produced by catalysis on the Ag sample, could be determined with a signal-to-noise ratio of more than one order of magnitude above the detection limit.

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