Ni-W Catalysts Supported on Mesoporous SBA-15: Trace W Steering CO2 Methanation
A series of Ni-W catalysts supported on mesoporous SBA-15 with different Ni:W ratios(Ni x W/SBA-15, Ni-5%, x =1, 10, 50) was prepared and fully characterized by powder X-ray diffraction(PXRD), Brunner-Emmet-Teller(BET), transmission electronic microscopy(TEM), H 2 -temperature programmed reduction(H...
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Veröffentlicht in: | Chemical research in Chinese universities 2022-12, Vol.38 (6), p.1504-1511 |
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Sprache: | eng |
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Zusammenfassung: | A series of Ni-W catalysts supported on mesoporous SBA-15 with different Ni:W ratios(Ni
x
W/SBA-15, Ni-5%,
x
=1, 10, 50) was prepared and fully characterized by powder X-ray diffraction(PXRD), Brunner-Emmet-Teller(BET), transmission electronic microscopy(TEM), H
2
-temperature programmed reduction(H
2
-TPR), and X-ray photoelectron spectroscopy(XPS). High-resolution TEM images, XPS measurements, H
2
-TPR experiments coupled with PXRD results determined the evolution of Ni and W species. It is found that a trace amount of W from H
2
WO
4
can significantly improve Ni dispersion on SBA-15 (Ni
50
W/SBA-15) with Ni
0
and non-stoichiometric WO
x
species as small as
ca
. 3.6 nm. The prepared Ni
x
W/SBA-15 was utilized for CO
2
hydrogenation, which showed that a higher W content restrained the CO
2
hydrogenation while a lower W ratio promoted both conversion rate and selectivity for methane compared with Ni/SBA-15. The Ni
50
W/SBA-15 catalyst showed the best performance with a 93.3% CO
2
conversion rate and 99.7% selectivity for methane at 400
o
C under 0.1 MPa and maintained
ca
. 97% initial performance for 24 h. Tracking product evolution experiments by
in-situ
Fourier transform infrared spectrascopy(FTIR) indicated that a small amount of W can modify the surface of Ni particles by geometric coverage and electronic modification, which facilitates the adsorption of the CO intermedia and results in the formation of CH
4
. This work provides a new clue to fabricating efficient CO
2
conversion bimetallic materials. |
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ISSN: | 1005-9040 2210-3171 |
DOI: | 10.1007/s40242-022-2096-8 |