HfB2–SiC and HfB2–HfC–SiC dense composites have been prepared by self-propagating high-temperature synthesis (SHS) followed by spark plasma sintering (SPS) without the addition of any sintering aid. Starting from Hf, B4C, Si, and, when synthesizing the ternary system, also graphite powders, it was found that the SHS technique leads to the complete conversion of reactants to the desired products and the SPS allows for the full consolidation under the following optimal operating conditions: maximum dwell temperature (1800 ◦C), total processing time (30 min) and applied pressure (20MPa). The obtained ternary composite displayed relatively lowresistance to oxidation while the binary product exhibited low and thermally stable oxidation rate up to 1450 ◦C. In addition, the mechanical properties of both products are comparable to, and, in some cases better than, those related to analogous HfB2-based composites prepared with other processing routes. Moreover, the required consolidation conditions (processing time, temperature, and pressure) resulted to be milder in this investigation.
Consolidation via Spark Plasma Sintering of HfB2/SiC and HfB2/HfC/SiC Composite Powders obtained by Self-propagating High-temperature Synthesis
LICHERI, ROBERTA;ORRU', ROBERTO;MUSA, CLARA;LOCCI, ANTONIO MARIO;CAO, GIACOMO
2009-01-01
Abstract
HfB2–SiC and HfB2–HfC–SiC dense composites have been prepared by self-propagating high-temperature synthesis (SHS) followed by spark plasma sintering (SPS) without the addition of any sintering aid. Starting from Hf, B4C, Si, and, when synthesizing the ternary system, also graphite powders, it was found that the SHS technique leads to the complete conversion of reactants to the desired products and the SPS allows for the full consolidation under the following optimal operating conditions: maximum dwell temperature (1800 ◦C), total processing time (30 min) and applied pressure (20MPa). The obtained ternary composite displayed relatively lowresistance to oxidation while the binary product exhibited low and thermally stable oxidation rate up to 1450 ◦C. In addition, the mechanical properties of both products are comparable to, and, in some cases better than, those related to analogous HfB2-based composites prepared with other processing routes. Moreover, the required consolidation conditions (processing time, temperature, and pressure) resulted to be milder in this investigation.
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