Mixtures of powders essentially differing in their particle morphology and size were applied to prepare polycrystals in a Y₂O₃-ZrO₂ system. An yttria–zirconia solid solution nanometric powder with a Y₂O₃ concentration of 3.5% was prepared by subjecting co-precipitated gels to hydrothermal treatment at 240 °C. The crystallization occurred in distilled water. The pure zirconia powders composed of elongated and sub-micrometer size particles were also manufactured through the hydrothermal treatment of pure zirconia gel, although in this case, the process took place in the NaOH solution. Mixtures of the two kinds of powder were prepared so as to produce a mean composition corresponding to an yttria concentration of 3 mol%. Compacts of this powder mixture were sintered, and changes in phase composition vs. temperature were studied using X-ray diffraction. The dilatometry measurements revealed the behavior of the powder compact during sintering. The polished surfaces revealed the microstructure of the resulting polycrystal. Additionally, the electron back scattering diffraction technique (EBSD) allowed us to identify symmetry between the observed grains. Hardness, fracture toughness, and mechanical strength measurements were also performed.

Crystallization under hydrothermal conditions allowed us to prepare nanometric powders in the MgO–ZrO₂ system of different magnesia concentrations. Sintering runs of these powder compacts studied using dilatometry measurements during heating and cooling revealed essential differences in their behavior. The microstructure of the resulting polycrystal is strongly related to the magnesia content in the starting powder, which strongly influences the phase composition of the resulting material and its mechanical properties. It should be emphasized that the novel processing method of such materials differs from the usual applied technology and leads to magnesia–zirconia materials of a different microstructure than that of “classical” materials of this kind.

Yttria stabilized tetragonal zirconia polycrystals were prepared using mixtures of two different powders. One is composed of nanometric particles of 3.5mol% Y2O3 solid solution in ZrO2 and the other one of pure zirconia particles. The latter shows elongated particles of about 200 nm length and monoclinic symmetry and the former consists of isometric tetragonal particles of about 7 nm size. Both powders were synthesized under hydrothermal conditions at 240?C in water (the 3.5mol% Y2O3-ZrO2 solid solution) or in 4M NaOH solution (the pure ZrO2 powder). Two homogenous mixtures of these powders were prepared; the one with 5wt.% and the other one with 10 wt.% of the elongated zirconia particles. Compacts of 10mm diameter were isostatically pressed (250MPa) and sintered in a dilatometer furnace at 1400?C with no soaking time. A set of samples heated up to the selected temperatures allowed us to follow phase changes of the materials vs. temperature by X-ray diffraction. It was confirmed that all materials show tetragonal symmetry at the final temperature (1400?C). Density and mean grain size decrease with the elongated zirconia particle additives. The dense samples were polished and their hardness and fracture toughness were determined by Vickers indentation. No hardness changes, due to the elongated zirconia particles additives, were observed, but essential increase of fracture toughness occurred. The observations of the crack runs suggest crack deflection as a potential mechanism of the fracture toughness increase.

An alumina-toughened zirconia (ATZ) material, fabricated using a procedure consisting of the common sintering of two different zirconia powders, was tested using the ball-on-disc method in a temperature range between room temperature and 500 °C. Corundum balls were used as a counterpart. The ATZ composite behaviour during tests was compared with that of commonly used α-alumina and tetragonal zirconia sintered samples. At temperatures over 350 °C, a drastic decrease in the wear rate of the material was detected. SEM analyses proved that, in such conditions, nearly the whole surface of the sliding material was covered with a layer of deformed submicrometric grains, which limited contact with the part of material that was not deformed. The mentioned layer was relatively strongly connected with the material, increased its resistance, and decreased its coefficient of friction. As a reference, commonly used materials, namely commercial alumina and tetragonal zirconia, were tested. The wear parameters of the composite were significantly better than those registered for the materials prepared of commercial powders.