Nanostructured aluminium oxide powders obtained by aspartic acid-nitrate gel-combustion routes

In this work, two new gel-combustion routes for the synthesis of Al2O3 nanopowders with aspartic acid as fuel are presented. The first route is a conventional stoichiometric process, while the second one is a non-stoichiometric, pH-controlled process. These routes were compared with similar synthesi...

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Detalhes bibliográficos
Autores: Gardey Merino, María Celeste, Lascalea, Gustavo Enrique, Sánchez, Laura M., Vazquez, Patricia Graciela, Cabanillas, Edgardo Domingo, Lamas, Diego Germán
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2010
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/77473
Acesso em linha:http://hdl.handle.net/11336/77473
Access Level:acceso abierto
Palavra-chave:Nanostructured Materials
Oxide Materials
X-Ray Diffraction
https://purl.org/becyt/ford/2.10
https://purl.org/becyt/ford/2
Descrição
Resumo:In this work, two new gel-combustion routes for the synthesis of Al2O3 nanopowders with aspartic acid as fuel are presented. The first route is a conventional stoichiometric process, while the second one is a non-stoichiometric, pH-controlled process. These routes were compared with similar synthesis procedures using glycine as fuel, which are well-known in the literature. The samples were calcined in air at different temperatures, in a range of 600-1200 °C. They were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and BET specific surface area. Different phases were obtained depending on the calcination temperature: amorphous, γ (metastable) or α (stable). The amorphous-to-γ transition was found for calcination temperatures in the range of 700-900 °C, while the γ-to-α one was observed for calcination temperatures of 1100-1200 °C. The retention of the metastable γ phase is probably due to a crystallite size effect. It transforms to the α phase after the crystallite size increases over a critical size during the calcination process at 1200 °C. The highest BET specific surface areas were obtained for both nitrate-aspartic acid routes proposed in this work, reaching values of about 50 m2/g. © 2009 Elsevier B.V. All rights reserved.