The state of Zirconia Suported Platinum Catalysts for CO2/CH4 Reforming

Abstract

In Pt/ZrO2 catalysts used for CO2/CH4 reforming to syngas, not all accessible Pt contributes equally to the activity of the catalyst. The cataalytic activity is determined by the accessibility of Pt on the Pt-ZrO2 perimeter. Thes is explained in terms of the CO2 activation via carbonate species on the support which must be in the proximity of the Pt particles to react with the methane activated on the metal. The significance of the support is also emphasized by the low activity of Pt black and Pt/SiO2, which were incapable of forming carbonates on the support. The perimeter concentration of Pt/ZrO2 can be changed by changing the Pt concentration in the catalyst or by increasing the calcination temperature which causes sintering of the Pt particles. In contrast to the calcination temperature, the reduction temperature did not influence the activity although the hydrogen chemisorption capacity was merkedly decreased by increasing the reduction temperature. As sintering was excluded on basis of particle size determination from EXAFS results a SMSI state on Pt/ZrO2 during high temperature reduction is concluded to exist. This state does not persist under reaction conditions due tot the presence of absorbed oxygen from CO2 dissociation.