A series of 3DOM cerium-based perovskite catalysts with
different
B-site elements were prepared by the colloidal crystal template method
and excess impregnation method with Cr, Ni, and Mn as the B-site elements.
The physical and chemical properties of the catalysts were investigated
by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET),
scanning electron microscopy (SEM), X-ray photoelectron spectroscopy
(XPS), hydrogen temperature-programmed reduction (H2-TPR),
and oxygen temperature-programmed desorption (O2-TPD) characterization
techniques. The results showed that the catalyst with Mn as the B-site
element had a high-quality macropore structure (pore size 200–250
nm), large specific surface area (45.26 m2/g), and abundant
surface adsorbed oxygen content (Oads/Olatt =
0.46). The addition of manganese enhanced the low-temperature reducibility,
and the main reduction peak was below 400 °C. The O2-TPD results showed that 3DOM CeMnO3 expressed the highest
adsorption oxygen content. The 3DOM CeMnO3 possessed the
best catalytic performance with T
50% =
102 °C and T
90% = 203 °C during
the catalytic oxidation of toluene. Intermediate product study hinted
that toluene was first converted into benzoic acid and benzaldehyde
and then further degraded into small molecules. The catalyst with
the best activity also exhibited good stability, and toluene degradation
rate remained above 85% at 200°C for more than 20 h of continuous
experiments.
To
achieve carbon peaking and carbon neutrality goals, the chemical
absorption method is the most widely used and mature carbon capture
technology. In this method, organic amine solution is a commonly used
absorbent for CO2 absorption. Biphasic solvents have been
designed due to their significant advantages in reducing energy consumption
for regeneration, and the development of new and efficient biphasic
solvents has become the current research focus. The CO2 absorption performance of absorbents with different ratios of triethylenetetramine
(TETA) and 1-diethylamino-2-propanol (1DMA2P) was investigated by
the bubbling absorption method, and it was found that the absorbent
of 2 mol/L TETA + 2 mol/L 1DMA2P biphasic solvent showed the best
performance. The volume of the rich phase after CO2 absorption
by the absorbent was 20% lower than that of the ethanolamine (MEA)
solution, and the CO2 absorption loading was as high as
0.656 mol CO2/mol of total amine. The absorption temperature
had little effect on absorption performance and the absorbent had
a lower rich-phase volume and better absorption performance when the
total amine concentration was 4 mol/L, and the optimum desorption
temperature was 393.15 K. Meanwhile, the material composition was
characterized by 13C NMR. It could be concluded that the
biphasic solvent generated carbamate and protonated amine after absorbing
CO2, and the reaction product was mainly concentrated in
the lower layer of the phase separation.
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