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Structure and properties of bifunctional catalysts based on zirconia modified by tungsten oxide obtained by polymeric precursor method
Bifunctional catalysts of Pt/WO x –ZrO 2 (PWZ) type with 1 wt% of Pt and 10, 15 and 20 wt% of tungsten were synthesized by polymeric precursor calcined at 600, 700 and 800 °C and characterized by several techniques. Such catalysts were active in the n-heptane isomerization with high selectivity to b...
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Published in: | Applied catalysis. A, General General, 2008-06, Vol.342 (1), p.56-62 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Bifunctional catalysts of Pt/WO
x
–ZrO
2 (PWZ) type with 1
wt% of Pt and 10, 15 and 20
wt% of tungsten were synthesized by polymeric precursor calcined at 600, 700 and 800
°C and characterized by several techniques. Such catalysts were active in the
n-heptane isomerization with high selectivity to branched product.
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Bifunctional catalysts of Pt/WO
x
–ZrO
2 (PWZ) type with 1
wt% of Pt and 10, 15 and 20
wt% of tungsten were synthesized by polymeric precursor method and after they were calcined at 600, 700 and 800
°C. The structural and textural properties of the catalysts were by X-ray diffraction (XRD), Fourier-transformed infrared spectroscopy (FTIR), N
2 adsorption measurement, temperature programmed reduction by derivative thermogravimetry (TPR–DTG) and transmission electron microscopy (TEM). X-ray diffractogram revealed the presence of tetragonal ZrO
2 and platinum (Pt) as the main phases. The infrared spectra of the catalysts showed bands due O–W–O and W
O bonds. The catalysts showed specific surface area values in the range of 30–160
m
2
g
−1. TPR profile showed reduction peaks at high temperatures that were related with the reduction of WO
x
species. Such catalysts were active in the
n-heptane isomerization with high selectivity to branched product. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2007.12.036 |