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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Zyl, W. E. Van
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Publications (4/4 displayed)
- 2004Friction behaviour of solid oxide lubricants as second phase in alpha-Al2O3 and stabilised ZrO2 compositescitations
- 2003Densification of zirconia-hematite nanopowderscitations
- 2002Hybrid Polyamide/Silica Nanocomposites
- 2002Synthesis and characterisation of dual-phase Y-TZP and RuO2 nanopowders: dense electrode precursors.citations
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article
Synthesis and characterisation of dual-phase Y-TZP and RuO2 nanopowders: dense electrode precursors.
Abstract
The synthesis and characterisation of nanopowders in the dual-phase system tetragonal-Y2O3-doped ZrO2 (Y-TZP) and RuO2 are described. Five powders were prepared from a co-precipitation (CP) method with stoichiometric variation in the RuO2 content (5–46 mol%) and two powders were prepared from solid-phase mechanical mixing of the above oxides prepared separately. In the CP method, an aqueous chlorometal solution containing appropriate precursor ions was co-precipitated in a concentrated aqueous ammonia (pH y14) solution. Following filtration, washing and drying (100 uC), the CP synthesis route yielded black coloured amorphous powders. Crystalline dual-phase powders were obtained after calcination in stagnant air at 600 uC for 2 h. The average Y-TZP and RuO2 crystallite sizes were, respectively, 10 and 20 nm, i.e. a nano/nano powder. The powders were characterised by X-ray diffraction (XRD), transmission electron microscopy (TEM), backscatter Raman spectroscopy (ZrO2 phase determination) and quantitative X-ray fluorescence (XRF). Time-dependent calcination experiments for samples of similar composition revealed that under the synthesis conditions employed, a composite was formed where a fraction of the crystalline RuO2 phase was initially dissolved in the ZrO2 phase and which gradually transforms to a more stable, distinctly dual-phase system upon prolonged (¢20 h) calcination at 600 uC.