5 research outputs found

    Cation segregation in an oxide ceramic with low solubility: Yttrium doped α-alumina

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    The segregation behaviour of a cation (yttrium) with a low solubility in the polycrystalline oxide host (α-Al2O3) has been investigated at temperatures between 1450 and 1650°C using analytical scanning transmission electron microscopy. Three distinct segregation regimes were identified. In the first, the yttrium adsorbs to all grain boundaries with a high partitioning coefficient, and this can be modelled using a simple McLean-Langmuir type absorption isotherm. In the second, a noticeable deviation from this isotherm is observed and the grain boundary excess reaches a maximum of 9 Y-cat/nm2 and precipitates of a second phase (yttrium aluminate garnet, YAG) start to form. In the third regime, the grain boundary excess of the cation settles down to a value of 6–7 Y-cat/nm2 that is in equilibrium with the YAG precipitates. In a material (accidentally) co-doped with Zr, the Zr seems to behave in a similar way to the Y and the Y + Zr grain boundary excess behaves in the same way as the Y grain boundary excess in the pure Y-doped system. In this latter system, Y-stabilised cubic zirconia is precipitated in addition to YAG at higher Y + Zr concentrations

    The effect of yttrium on densification and grain growth in alpha-alumina

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    The grain growth and densification have been investigated in very high-purity α-alumina doped with varying amounts of yttrium (0 to 3000 wt ppm of yttria) and sintered in air at 1450, 1550 and 1650 °C. Yttrium doping inhibited densification and coarsening at 1450 °C, but had very little effect at 1550 °C and no effect at 1650 °C. The change in densification behaviour is suggested to be related to the transition with increasing temperature from grain boundary diffusion to lattice diffusion controlled densification. The coarsening rate increases faster with temperature than the densification rate. This was correlated with a higher measured activation energy for grain growth than for the diffusion processes, which control the densification
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