masterThesis
Síntese e caracterização de pós Ba(x)Sr(1-x)Co0,8Fe0,2O3- através do método de coprecipitação via oxalato
Fecha
2012-12-27Registro en:
PASSOS, Rafael Hernandez Damascena dos. Synthesis and Characterization of Powder Ba(x)Sr(1-x)Co0, 8Fe0,2O3- by Oxalate Co-precipitation Method. 2012. 67 f. Dissertação (Mestrado em Pesquisa e Desenvolvimento de Tecnologias Regionais) - Universidade Federal do Rio Grande do Norte, Natal, 2012.
Autor
Passos, Rafael Hernandez Damascena dos
Resumen
Ceramic powders based on oxides of perovskite-type structure is of fundamental interest
nowadays, since they have important ionic-electronic conductivity in the use of materials with
technological applications such as gas sensors, oxygen permeation membranes, catalysts and
electrolytes for solid oxide fuel cells (SOFC). The main objective of the project is to develop
nanostructured ceramic compounds quaternary-based oxide Barium (Br), Strontium (Sr), Cobalt
(Co) and Iron (Fe). In this project were synthesized compounds BaxSr(1-x)Co0, 8Fe0,2O3- (x
= 0.2, 0.5 and 0.8) through the oxalate co-precipitation method. The synthesized powders
were characterized by thermogravimetric analysis and differential thermal analysis (TGADTA),
X-ray diffraction (XRD) with the Rietveld refinement using the software MAUD and
scanning electron microscopy (SEM). The results showed that the synthesis technique used
was suitable for production of nanostructured ceramic solid solutions. The powders obtained
had a crystalline phase with perovskite-type structure. The TGA-DTA results showed that the
homogeneous phase of interest was obtained temperature above 1034°C. It was also observed
that the heating rate of the calcination process did not affect the elimination of impurities present
in the ceramic powder. The variation in the addition of barium dopant promoted changes
in the average crystallite size in the nanometer range, the composition being BSCF(5582)
obtained the lowest value (179.0nm). The results obtained by oxalate co-precipitation method
were compared with those synthesis methods in solid state and EDTA-citrate method