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Abstract: Tantalum carbide with a TaC0.9 composition was sintered to 96% relative density by spark plasma sintering at 1400°C for 5min, using commercial micrometric Ta and TaC powders as the starting materials. This achievement was dependent on the delicate rearrangement of the heating process which limits evaporation–condensation and promotes the mass transportation in association with 0.9TaC+Ta=TaC0.9 reaction. The dense TaC0.9 ceramic had a uniform microstructure composed of equiaxed grains, and showed flexure strength up to ∼498MPa. [Copyright &y& Elsevier]

Abstract: Nano-sized Si–B–C–N powders nearly amorphous with different mole ratio of Si/C were prepared by mechanical alloying (MA) technique using cubic silicon (c-Si), hexagonal boron nitride (h-BN) and graphite powder (Cp) as starting materials, then consolidated at 1800°C under a pressure of 40MPa for 3min by spark plasma sintering (SPS). Sub-micrometer sized β-SiC and nano-sized BCN phase were formed as the final components in the ceramics. The grain size of the β-SiC tend to be a little coarser with the increase of the Si/C ratio as well as their total content, but no changes are observed for the fine sub-micrometer structure characteristics of β-SiC and BCN grains. Mechanical properties of the Si–B–C–N ceramics were found remarkably increased with the increase of the mole ratio of Si/C and their total relative content. Thermal physical properties, including thermal diffusivity, heat capacity, thermal conductivity, as well as thermal expansion coefficient were also studied. [Copyright &y& Elsevier]

Abstract: Y-α-SiAlON (Y1/3Si10Al2ON15) ceramics with 5wt.%BaAl2Si2O8 (BAS) as an additive were synthesized by spark plasma sintering (SPS). The kinetic of densification, phase transformation sequences and grain growth during sintering process were investigated. Full densification could be achieved by 1600°C without holding and using a heating rate of 100°Cmin−1, but the transformation from α-Si3N4 to α-SiAlON is not completed simultaneously with the densification process. The equilibrium phase assemblage could be reached after SPS at 1800°C for 5min and the resultant material possesses self-reinforced microstructure with high hardness of 19.2GPa and fracture toughness of 6.8MPam1/2. The complete crystallization of BAS is beneficial to the high temperature mechanical properties. The obtained could maintain the room strength up to 1300°C. [Copyright &y& Elsevier]

A series of TiB 2 –TiC composites were successfully fabricated through one-step and two-step pressureless sintering using powders obtained by high-energy ball-milling. Effects of ball-milling time on crystal size and morphology of powders as well as microstructural evolution and mechanical properties of TiB 2 –TiC composites were investigated. The crystal size of TiB 2 –TiC powders decreases to 14.7 nm after ball milling for 30 h. Two-step pressureless sintering is beneficial to the densification process without obvious grain coarsening. The core-rim structure of carbides in TiB 2 –TiC composites is formed by nonuniform diffusion of W atoms from the outside to the interior of TiC grains. The phenomenon of selective solution of WC into TiC grains was carried out through experiments and verification of first-principles DFT calculations. An in-situ TiB 2 plate toughened microstructure is developed for TiB 2 -40 wt %TiC composites two-step sintered at 1500 °C for 4 h and 2000 °C for 1 h with excellent comprehensive performances. [ABSTRACT FROM AUTHOR]