The thermal stabilities of palladium
(Pd) catalysts supported on
MCM-41-modified Pd/Al2O3 calcination at 1000
°C were investigated for the adsorption and catalytic combustion
of ethanol. MCM-41 (0, 30, 50, 70, and 100 wt %)-modified Al2O3 materials were prepared by the in situ coprecipitation
method. The catalysts were characterized by N2 adsorption–desorption,
X-ray diffraction, and scanning electron microscopy–energy
dispersive spectrometry. It was found that MCM-41 less than 50 wt
% was conductive to the increase in specific surface area and pore
volume of the catalysts even after 1000 °C calcination which
had a positive relationship with the adsorption performance of ethanol.
Pd/Al2O3, prepared in this study, presented
a sheet-like morphology which could attach on the surface of MCM-41.
Meanwhile, the introduction of MCM-41 into Al2O3 could hinder the phase transition of γ-Al2O3 to δ-Al2O3 and prevent the collapse
of the pore structure in MCM-41, thus avoiding the aggregation of
Pd particles effectively at 1000 °C. Cat-50% (50 wt % MCM-41
into Pd/Al2O3) showed the best ethanol adsorption
performance with the longest breakthrough time and highest adsorption
capacity at 40, 60, and 80 °C because of its good textual properties,
while Cat-70% presented the highest activity with higher CO2 yield at 200 °C, reaching 90% ethanol conversion at 220 °C,
owing to its good dispersion of Pd particles. In addition, the introduction
of MCM-41 could inhibit the production of acetaldehyde to some extent.
The long-term stability test demonstrated that MCM-41-modified Pd/Al2O3 had good stability for catalytic oxidation of
ethanol for the stable conversion for 500 h at 300 °C and gas
hourly space velocity of 10,000 h–1.