The α-SiC in 0.5μm size powders were coated with Al_2O_3 and Y_2O_3 by a coprecipitation coating (CPC) method forfabrication of SiC/YAG composites. The same powder preparation was carried out by conventional mechanical mixing(MM) method for comparison. Two kinds of SiC/YAG composites were manufactured by pressureless sintering usingthe different powders, named CPC composite and MM composite thereafter respectively. It is shown that the CPCcomposite has the advantages of homogeneous distribution of YAG phase and of being sintered to high density ata low temperature, 100℃ lower than that of MM composite. The strength (573 MPa) and hardness (23.3 GPa) ofthe CPC composite are significantly higher than those (323 MPa and 13.5 GPa) of the MM composite, respectively.
Low cost silicon carbon nanometer powder was synthesized by carbothermal reduction method with nanometer SiO2 and carbon as raw material. Its synthesis thermodynamics were discussed. The influence of La on TG-DSC curve was also analyzed. It indicated that the synthesis process of SiC powder had two steps. In the first step two medial productions of SiOg and COg formed, and in the second step, β-SiC was finally synthesized. After 0.3% La added, at the first step, the initiatory forming temperature of producing SiO(g) and CO(g) declined from 1351.4 to 1250.9 ℃, and the thermal activation energy decreased from 223.6 to 34.7 J·g-1; at the second step the initiatory forming temperature of synthesizing β-SiC powder declined from 1526.5 to 1357.8 ℃, and the thermal activation energy decreased from 693.7 to 295.7 J·g-1. Without La added, the best synthesis technology for β-SiC powder was 1550 ℃ for 120 min, average powder diameter was bigger about 150 nm. With La added, the best synthesis technology was 1500 ℃ for 120 min, average powder diameter was about 100 nm.
