کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
62726 | 47652 | 2008 | 9 صفحه PDF | دانلود رایگان |

It is widely accepted in the catalysis literature that the bulk MO bond of bulk mixed metal oxides controls catalytic activity. In the present study, for the first time, the bulk MO bond lengths (strengths) and the surface catalytic activity of bulk metal vanadates and molybdates were quantitatively compared to allow examination of this long-standing hypothesis. The bulk MO bond lengths were obtained from crystallographic studies and also determined by Raman spectroscopy. The surface catalytic activity was determined by CH3OH-temperature programmed surface reaction (TPSR) spectroscopy and steady-state methanol oxidation. The CH3OH-TPSR experiments provided the first-order rate constants for breaking of the CH bond for the decomposition of the surface CH3O* intermediate to H2CO and the number of catalytic active sites (NsNs). The corresponding steady-state methanol oxidation studies provided the equilibrium adsorption constant (KadsKads) for breaking the methanol OH bond and the specific reaction rate (TOF). The findings clearly demonstrate the lack of correlations among krdskrds, KadsKads, TOF, and the bulk MO bond length (strength). This finding is not so surprising when one considers that the adsorption step involves breaking the methanol OH bond and the rate-determining step involves breaking the surface methoxy CH bond on surface MOx sites, not bulk MO bond-breaking.
Journal: Journal of Catalysis - Volume 256, Issue 1, 15 May 2008, Pages 145–153