Pt–Mg/Al2O3 soot oxidation
catalysts
were prepared by impregnating either magnesium acetate or magnesium
nitrate on alumina-supported platinum catalyst. The influence of Mg
addition on the structure and catalytic behaviors of Pt/Al2O3 catalysts were investigated by X-ray diffraction (XRD),
Brunauer–Emmett–Teller (BET) analysis, transmission
electron microscopy (TEM), H2 chemisorption, thermogravimetric
(TG) analysis, Fourier transform infrared spectroscopy (FTIR), NO
x
temperature-programmed desorption (NO
x
-TPD), NO temperature-programmed oxidation
(NO-TPO), and soot temperature-programmed oxidation (soot-TPO). In
spite of the coverage of surface Pt by magnesium species and the weakened
oxidation resistance of Pt, the Pt–Mg/Al2O3 catalyst derived from magnesium acetate exhibits a higher soot oxidation
activity than that prepared with magnesium nitrate, which is mainly
determined by the larger Pt particle size on this catalyst. Additionally,
the synergistic effect between Pt and Mg enhances the NO oxidation
activity and NO
x
storage capacity of Pt–Mg/Al2O3 catalyst. More NO2 is produced in
the temperature range of soot oxidation on this catalyst than on the
Mg-free Pt/Al2O3 catalyst with a similar Pt
particle size, which efficiently promotes the ignition of soot.