Thermal ablation behaviour of ultra-high temperature ceramic matrix composites made by RF enhanced chemical vapour infiltration

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Quantitative analysis of the residual stress and dislocation density distributions around indentations in alumina and zirconia toughened alumina (ZTA) ceramics

This is an Open Access Article. It is published by Elsevier under the Creative Commons Attribution 3.0 Unported Licence (CC BY). Full details of this licence are available at: http://creativecommons.org/licenses/by/3.0/Alumina, 10% and 20% ZTA with 1.5mol% yttria stabiliser were subjected to Vickers indentation testing with loads from 1 to 20kg. Cr fluorescence and Raman spectroscopy were applied to the indent centre and around the indentation in order to investigate the origin of the signal, the effect of indentation loads and zirconia phase transformation on the residual stress and plastic deformation in the plastic zone. The results suggested that with very strong laser scattering, the depth resolution of ZTA materials was very poor, which lead to a very significant amount of the signal being collected from the subsurface regions below the plastic zone. It was also found that zirconia phase transformation reduced the compressive residual stress in the alumina matrix within the plastic zone, except at the indentation centre, due to the tensile residual microstress generated by the zirconia phase transformation. In addition, the dislocation density on the indent surface of the ZTA samples was significantly reduced due to the restriction of crack propagation and energy absorption during the phase transformation process. At the indent centre, the zirconia phase transformation was suppressed by the high compressive stress, therefore, no significant difference between alumina and ZTA in terms of their residual stress and dislocation density were observed. Using TEM observation, it was found that the plastic zone microstructure of pure alumina is different from that of ZTA, which is consistent with the Cr fluorescence results

Solvothermal nanoYAG synthesis: Mechanism and particle growth kinetics

This paper was accepted for publication in the journal Journal of Supercritical Fluids and the definitive published version is available at http://dx.doi.org/10.1016/j.supflu.2015.09.031NanoYAG particles with spherical morphology have been synthesised using a solvothermal method; a structure sensitive reaction, where the chemical reaction and the particle growth kinetics are interdependent. It has been observed that the primary YAG particles agglomerated into ∼30 nm clusters via a self-assembled Ostwald ripening process along (2 1 1) planes, separated by a distance of ∼0.49 nm, at 270 °C and 2.0 MPa for 2 h. These nanoclusters coalesced into single nanoparticles of ∼30 nm in size and exhibited a smaller inter planar distance of ∼0.26 nm, corresponding to the (4 2 0) planes, when synthesized at 300 °C and 8.5 MPa for 2 h. in addition, the solvent 1,4-butanediol transformed into 1,4-diacetoxybutane, this will have undergone esterification by reacting with the terminal acetate groups cleaved from the precursor, yttrium acetate. The proposed mechanism based on the analytical evidence suggests that a complete dissolution of precursors facilitated the structural re-arrangement of atoms within the planes and lead to a significantly higher degree of crystallinity. Moreover, once the particles with (4 2 0) planes had formed, they were no longer involved in facile coalescence along their preferential planes due to their lower interfacial energy compared to the (2 1 1) planes. This led to control of the particle morphology and with little agglomeration occurring in the final nanopowder