Activity of Selective Catalytic Reduction of NO over V2O5/TiO2 Catalysts Preferentially Exposed Anatase {001} and {101} Facets
Three V 2 O 5 /TiO 2 catalysts with V 2 O 5 loading of 3 wt% were fabricated by wet impregnation, in which the TiO 2 supports had different crystal types, including the octahedral TiO 2 (preferentially exposed anatase {101} facets, labeled as TiO 2 -O), the sheet TiO 2 (preferentially exposed anatas...
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Veröffentlicht in: | Catalysis letters 2017-04, Vol.147 (4), p.934-945 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Three V
2
O
5
/TiO
2
catalysts with V
2
O
5
loading of 3 wt% were fabricated by wet impregnation, in which the TiO
2
supports had different crystal types, including the octahedral TiO
2
(preferentially exposed anatase {101} facets, labeled as TiO
2
-O), the sheet TiO
2
(preferentially exposed anatase {001} facets, labeled as TiO
2
-S), and the commercial TiO
2
(TiO
2
-P25), giving the three corresponding catalysts, respectively. The activities and the effects of H
2
O and SO
2
over the V
2
O
5
/TiO
2
catalysts for the selective catalytic reduction (SCR) of NO by NH
3
were investigated. It was found that the crystal facets of TiO
2
nanoparticles played an essential role in the catalytic activity. The V
2
O
5
/TiO
2
-S catalyst exhibited the better catalytic activity than the V
2
O
5
/TiO
2
-O and V
2
O
5
/TiO
2
-P25 catalysts for the NH
3
-SCR reaction. The N
2
sorption isotherm measurement (BET), X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), temperature-programmed reduction (H
2
-TPR), temperature-programmed desorption (NH
3
-TPD), X-ray photoelectron spectra (XPS) and
in-situ
diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS) characterizations showed that the good dispersion and reducibility of vanadium species, and the high concentration of chemisorbed oxygen of the V
2
O
5
/TiO
2
-S catalyst could be responsible for the enhancement in the activity of NH
3
-SCR reaction over the catalyst.
Graphical Abstract |
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ISSN: | 1011-372X 1572-879X |
DOI: | 10.1007/s10562-017-1989-5 |