Rare-earth cuprates for ceramic colouring application: An investigation

Autores: Kar, J.K.|Kar, J.K.|Stevens, R.|Bowen, C.R.
Fuente: Journal of alloys and compounds
455 (1-2), 121-129
2008

The possible use of rare-earth cuprates R2BaCuO5 and R2Cu2O5 (R= rare earth) type compounds for high temperature (above 1000º C ceramic pigment application is presented in this paper. The traditional ceramic powder mixing method was adopted for the manufacture of various samples (pigment powders) used in this study. Yellow-green coloured powders with a variation in the intensity were obtained with R2BaCuO5 (R = Sm) at different calcination temperatures (950-1050º C) and soaking time up to 12 h. These powders were then optimized in terms of colour by altering the calcinations temperature. The products with the most attractive colour were obtained with the sample calcined at 1050º C. The same yellow-green colour powders were observed when Sm was replaced by other rare earth oxides such as Ho, Yb, Er and calcined at the same temperature, except for Y. In the case of the Y addition, a dark green coloured powder was observed. The X-ray diffraction pattern o f the samples indicated R2BaCuO5 (R = rare earth) to be the major phase present in each case, although traces of CuO and the respective rare earth oxides were still present. For R2Cu2O5 (R = Dy), a bluish-green coloured pigment powders with a variation in their intensity were observed when calcined between (950 and 1050º C with a 2 h soaking time. The best result (as far as intense colour is concerned) was noticed with the sample calcined at 950º C. The same bluish-green colour powders were observed when Dy was replaced by other rare earths such as Yb, Ho, Er and Y. SEM micrographs of both types of compounds (R2BaCuO5 and R2Cu2O5) obtained at various calcination temperatures revealed the presence of agglomerates in the samples, with an average grain size in the range 1-3 mu m. All the pigment powders of the type R2BaCuO5 with the exception of the Sm-doped materials were unstable at 1070º C and produced a bubble rich surface (yttrium being the worst) when introduced into an unleaded commercial transparent glaze. In the case of Sm the yellow-green coloured powder turned to a light green. Similarly all the bluish-green coloured powders were unstable in the glaze except R = Dy and Y. In the case of Dy, a raindrop effect was observed 0on the surface of the ceramic tiles.

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