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Oxy-apatite reaction sintering of colloidal and classic ceramic processed powders
Oxy-apatites are promising electrolyte materials for intermediate-temperature solid oxide fuel cells, IT–SOFC. However the requirements of electrolytes make necessary the preparation of dense films with the appropriated composition to show good electrical properties; in this way, colloidal processin...
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Published in: | Ceramics international 2012-04, Vol.38 (3), p.1851-1858 |
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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: | Oxy-apatites are promising electrolyte materials for intermediate-temperature solid oxide fuel cells, IT–SOFC. However the requirements of electrolytes make necessary the preparation of dense films with the appropriated composition to show good electrical properties; in this way, colloidal processing is a key issue.
This work involves the application of colloidal processing for four oxygen-excess oxy-apatites, La9.67(Si6O24)O2.5, La10(Si6O24)O3, La10(Si5.5Al0.5O24)O2.75 and La10(Si5Al1O24)O2.5 and their characterization (phases, microstructure and electrical properties). The results have been compared with those obtained by classical ceramic method to assure the same composition without loosing properties. Samples with the desired compositions were obtained by reaction sintering of La2O3, SiO2 and Al2O3. La10(Si5.5Al0.5O24)O2.75 prepared by colloidal processing and heated at 1923K showed the highest conductivity value, 3.0×10−2Scm−1 at 973K. Furthermore, its residual porosity was very low. On the other hand, La10(Si6O24)O3 stoichiometry was tried by colloidal and ceramic methods under several experimental conditions. Unfortunately, the obtained oxy-apatite seems to have slightly lower lanthanum content. In spite of previous reports claiming the preparation of stoichiometric La10(Si6O24)O3, this study cannot support these findings. |
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ISSN: | 0272-8842 1873-3956 |
DOI: | 10.1016/j.ceramint.2011.10.010 |