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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/33579
Title: 
Characterization of the porosity developed in a new titania-alumina catalyst support prepared by the sol gel route
Author(s): 
Institution: 
  • Universidade Estadual Paulista (UNESP)
  • Universidade de São Paulo (USP)
  • Petrobras SA
ISSN: 
0021-8898
Abstract: 
Titanium oxide (TiO2) is a good candidate for support of hydrotreating catalysts but has the disadvantage of presenting a low surface area and a poor thermal stability when compared with Al2O3. A mixed TiO2-Al2O3 support was proposed as an alternative that is expected to be free from these drawbacks. The variation during firing of the nanoporous texture of supports composed of TiO2-Al2O3, TiO2 and Al2O3 was studied by small angle X-ray scattering (SAXS). The supports were prepared by the sol-gel route using Ti and Al isopropoxides. We have particularly analyzed the effects of acid and basic hydrolysis on the nanostructural features of catalyst supports fired at different temperatures. The nanopore radius distribution functions were determined from SAXS results assuming a simple model of spherical nanopores embedded in a homogeneous solid matrix. The modal pore radius in both pure TiO2 and pure Al2O3 supports grows from 1.3 to 2.2 nm as the firing temperature increases from 673 to 973 K. on the other hand, the modal pore radius in the mixed TiO2-Al2O3 support remains below 1.2 nm over the same range of firing temperatures. These results demonstrate the good thermal stability of the nanoporous texture of mixed TiO2-Al2O3 supports.
Issue Date: 
1-Jun-2003
Citation: 
Journal of Applied Crystallography. Copenhagen: Blackwell Munksgaard, v. 36, p. 469-472, 2003.
Time Duration: 
469-472
Publisher: 
Blackwell Munksgaard
Keywords: 
  • catalyst supports
  • sol-gel
  • nanoporous texture
Source: 
http://dx.doi.org/10.1107/S0021889803003819
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/33579
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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