Model supported palladium and palladium-molybdenum catalysts prepared
from organometallic precursors and previously characterized by a varie
ty of chemical and physical methods were examined by IR spectroscopy o
f NO chemisorption and tested for their activities as catalysts in the
competitive NO + CO + O-2 reaction. The IR results reveal distinctive
behavior of the catalyst made from a bimetallic precursor, and the ac
tivity results show that this catalyst is more selective for NO reduct
ion than the other catalysts, but its stability is vulnerable to the r
eaction conditions. The high selectivity is attributed to Pd-Mo intera
ctions, which are inferred to be stronger in the catalyst prepared fro
m a bimetallic precursor than in catalysts prepared from monometallic
precursors.