Abstract
The extension of the homogeneity field of B12(B,C,Si)3 was established by sintering experiments in the B - rich corner of the B-C-Si system in the temperature range of 1000–2100°C. Below the ternary eutectic temperature of 1385°C the formation of B12(B,C,Si)3 is generated by a diffusion-controlled mono-molecular phase boundary reaction. Above this temperature, a ternary liquid phase exists which promotes dissolution-reprecipitation reactions. The maximum solid solubility of Si in the boron carbide lattice is 2.5 ± 0.3 at. -% at 2050° C. The increase of the aspect ratio co/ao of the unit cell with the Si-content indicates that Si occupies preferentially C-sites in the linear C-B-C chain and thereafter interstitial or icosahedral sites in prolongation of the chain.
As a result of the Si→C substitution, SiC-layers are precipitated around B12(B,C,Si)3 particles during liquid phase hot pressing which prevents an exaggerated grain growth and thus enhances strength and toughness. Pressureless sintering results in a high porosity because of unsuitable wetting conditions and evaporation-recordensation reactions.
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Telle, R. (1990). Structure and Properties of Si-Doped Boron Carbide. In: Freer, R. (eds) The Physics and Chemistry of Carbides, Nitrides and Borides. NATO ASI Series, vol 185. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-2101-6_16
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DOI: https://doi.org/10.1007/978-94-009-2101-6_16
Publisher Name: Springer, Dordrecht
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