CuO/ZnO catalysts were examined by time-resolved X-ray absorption spectrosc
opy during oxidative reforming of methanol, tinder low oxygen conversion co
nditions, Cu2+ was the dominant copper species and combustion of methanol t
o carbon dioxide and water was the primary reaction. After complete oxygen
conversion, Cu2+ was reduced to Cu-0 while the principal activity of the ca
talyst shifted to steam reforming, where the dominant product was hydrogen.
Cu+ was observed as a transient species in the reduction of Cu2+ to Cu-0 a
nd no activity was attributed to it. Increasing the oxygen partial pressure
increased the rate of reduction of Cu2+ This observation was attributed to
a heating effect associated with an enhancement of the combustion rate. Ad
ditional experiments showed that the catalyst could recover its original ac
tivity after a reduction/oxidation cycle. (C) 2001 Academic Press.