The synthesis of barium zirconate was initiated by urea induced homogeneous precipitation followed by a ''low temperature'' thermal treatment. The kinetic of the reaction and the optimum urea/cation ratio have been determined by means of X-ray diffraction and Inductive Coupled Plasma analyses. It has been demonstrated that an amorphous zirconium hydrated oxide starts to precipitate followed by the precipitation of barium carbonate. A calcination at 1200 C during 2 h gives rise to the formation of a pure barium zirconate phase. Microstructural characterisations have been performed in order to evaluate the sintering behaviour. Dilatometric measurements, coupled with scanning electron microscopy analyses clearly indicate that barium carbonate decomposition process leads to the formation of internal porosity which severely limits the density of the material, even if a sintering was performed at 1500 C. A careful control of the heating profile seems to be necessary in order to produce dense materials. #

Barium zirconate is an interesting material for refractory applications as well as a good substrate for the manufacturing of high temperature superconductors. However, its solid state synthesis requires high temperature and provides inhomogeneous powder with a broad particle size distribution. In order to avoid these disadvantages, soft solution routes are of growing importance in the ceramic powder synthesis. Precipitation, decomposition of precursors, combustion techniques offer alternative ways to the solid state method. Advantages of these are a lower calcination temperature, production of homogeneous and fine monodisperse powders. The obtained powders have been characterised by XRD, IR, SEM and DTA / TG analysis. The influence of the synthesis conditions on the properties of BaZrO has been studied.

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