Textural Analysis of Sulphated ZrO–SiO Sol–Gel Catalytic Supports by N Sorption and X-Ray Diffraction
The textural properties of sulphated ZrO 2 –SiO 2 catalytic supports of different compositions were investigated through N 2 sorption and X-ray diffraction (conventional and SAXS) methods. The materials were synthesised by the sol–gel procedure from a mixture of zirconium(IV) tert-butoxide and tetra...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Hindawi - SAGE Publishing
2001-12-01
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Series: | Adsorption Science & Technology |
Online Access: | https://doi.org/10.1260/0263617011494628 |
Summary: | The textural properties of sulphated ZrO 2 –SiO 2 catalytic supports of different compositions were investigated through N 2 sorption and X-ray diffraction (conventional and SAXS) methods. The materials were synthesised by the sol–gel procedure from a mixture of zirconium(IV) tert-butoxide and tetraethyl orthosilicate. The final products were obtained after drying at 125°C followed by calcination at 400°C. The porous structures of the substrates were found to depend on their composition: at low zirconia contents these were formed by slit cavities while at high ZrO 2 concentrations the void structure became open; both cavities and necks were of similar size. In the first case, the pore size distribution function could be obtained from an analysis of the ascending boundary curve of the N 2 isotherm since adsorption occurred on a flat surface. In the second case, a unique pore-size distribution was obtained either from the ascending or descending boundary curves of the N 2 isotherm. A tubular geometry seemed appropriate for the description of the sorption characteristics of these substrates. Primary descending scanning curves traced within the hysteresis loops of samples having high ZrO 2 contents offered further textural information. X-Ray diffraction methods provided compound identification, evidence of phase segregation between ZrO 2 and SiO 2 , and particle and pore-size distributions. |
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ISSN: | 0263-6174 2048-4038 |