This study employed the water-thermal coupled high-temperature
CO2 gasification method using Zhundong coal as the raw
material to prepare porous carbon materials. A dual-function catalyst
for NO
x
adsorption and reduction was prepared
by loading Cu, Mn, and Ce components onto the carbon material through
hydrothermal impregnation. The influence of metal loading content
on the pore structure, surface functional groups, and synergistic
effects between metals in the carbon-based catalyst was investigated
during the preparation process. In the process of NO
x
removal using carbon-based catalysts, the primary components
comprise two distinct phases: NO
x
adsorption
and CO-SCR experiments. The experimental sequence involves the initial
execution of NO
x
adsorption tests, succeeded
by subsequent reduction treatments. These processes are undertaken
systematically to comprehensively investigate the attributes of the
catalyst. The physical and chemical parameters of the samples were
characterized using XRD, Raman, H2-TPR, NO
x
-TPD, and other techniques. Finally, the NO
x
adsorption and reduction mechanism of representative
samples were deeply analyzed using in situ DRIFTS. The results showed
that when the loading amounts of Cu, Mn, and Ce were 0.006, 0.012,
and 0.003 g, respectively, the pore structure of the catalyst was
excellent, with a NO
x
adsorption performance
(q
e) of 16.23 mg/g, and the NO conversion
rate reached 66% at 200 °C. This is mainly attributed to the
enhanced interaction between metal species on the catalyst surface
by optimizing the metal content on the carbon support, which promotes
the dissociation of NO in the NO + CO reaction. In situ DRIFTS results
confirmed that NO and CO adsorb on the catalyst surface, and CO* reacts
with NO* to produce N2 and CO2, following the
Langmuir–Hinshelwood mechanism.