Oxynitride catalysis reductant in oxygen-enriched condition and preparation method thereof
A technology of oxynitride and reducing agent, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc.
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Embodiment 1
[0042] Zirconium source, cerium source, lanthanum source, and yttrium source are all nitrates of corresponding metals, and the surfactant is polyoxyethylene polyoxypropylene copolymer F127. According to formula ratio (weight ratio):
[0043] 8Zr(NO 3 ) 4 :10Ce(NO 3 ) 3 :2La(NO 3 ) 3 :Y(NO 3 ) 3 :9F127:250H 2 O; hydrothermal crystallization treatment at 110-150°C for 24 hours; synthesize a precursor sample of yttrium / lanthanum doped cerium-zirconium oxide composite with high specific surface area and high dispersion, and disperse in aqueous solution after centrifugation and drying At the same time, a certain proportion of γ-alumina sol was added, mixed and stirred for 5 hours, and then dried by centrifugation. After drying at 100°C for 3 hours, it was calcined in a muffle furnace to remove the organic surfactant to obtain the prepared yttrium / lanthanum-doped aluminum cerium zirconium oxide composite nanomaterial, calcining temperature: 500°C; calcining time 4 Hour. I...
Embodiment 2
[0051] The proportion of the formula in Example 1 is constant, and the calcining temperature is 1000° C.-2 hours, and its XRD diffraction pattern is as follows: figure 2 b; transmission electron microscope photo as Figure 5 . It can be seen that the catalytic promoter of this composite system has good thermal stability, and it still maintains a stable cubic crystal phase after heat treatment at 1000°C. The broadened diffraction peaks indicate that it is still in the nanocrystalline grain size range at this time, and there are no abnormal grains. Growth phenomenon; It can be seen intuitively from the transmission electron microscope that the mesoporous structure is still intact.
Embodiment 3
[0053] The formula ratio of the yttrium / lanthanum doped cerium-zirconium composite oxide in Embodiment 1 is kept unchanged, and it is directly dried after hydrothermal treatment, filtration and washing, and then calcined at 500° C. for 4 hours without adding alumina components. The N of its sample 2 -Adsorption analysis profile such as image 3 As shown in b, it can be seen that the specific surface area of the sample without adding alumina components is significantly lower than that of the sample in Embodiment 1 after being calcined at 500 degrees, and the pore size distribution range becomes wider, indicating that the mesoporous structure becomes relatively It is loose, which also shows that the addition of alumina components plays an important role in stabilizing the mesoporous structure and increasing the specific surface area.
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