Fracture strengths and microstructures of Si3N4/SiC nanocomposites fabricated by in-situ process
Introduction
Various processes have been followed to produce Si3N4/SiC nanocomposites. It was reported that the Si-C-N powder production as a precursor of nanocomposites via the pyrolysis of a polymethylsilazane precursor, (1) laser irradiation of gas mixtures, (2) and laser interaction with droplets of a liquid hexamethyldisilazane precursor.(3) Also, powder mixing method was used for fabrication of Si3N4/SiC nanocomposites. 4, 5 More recently, we developed a new route to in-situ fabricate Si3N4/SiC nanocomposites, assuming that Si3N4 and/or silicon oxide reacts with free carbon formed by decomposition of a polymer during heat treatments.(6) This reaction yielded a homogeneously dispersed Si3N4/SiC nanocomposite, thereby eliminating the use of SiC powder with more efficient processing.
In this study, the 3-point bending test was used for measuring fracture strength of the fabricated Si3N4/SiC nanocomposite and the phases of samples were analyzed by X-ray diffraction (XRD) method. The microstructure of Si3N4/SiC nanocomposite were analyzed by transmission electron microscopy (TEM). From the results of these investigations, we tried to explain the relationship between microstructure/grain boundary phases and fracture strength of the in situ processed Si3N4/SiC nanocomposite.
Section snippets
Experimental procedure
Si3N4/SiC nanocomposite was prepared by in situ process using α-Si3N4 powder and commercial polymers. In situ process means that a polymer will be converted to the carbon and it transformed to SiC particles by several heat treatments. The used α-Si3N4 powder (SN-E10, Ube Industries, Tokyo, Japan) had a mean particle size of 200 nm and contained oxygen (<1.26 vol.%) as a main impurity.
The phenolic resin ([-CH2(C6H5)OH-]n, Phenolite 739, Kangnam Chemicals, Incheon, Korea; 3511g/mol) was used for
Results and discussion
Fig. 1 shows that the results of fracture strength of SNP4-4Y and SNP4-8Y at room temperature and 1400°C. They show the average value of 1100MPa at room temperature and 800MPa at 1400 °C. The reason of retain of high temperature strength at 1400°C might be the hinder of grain boundary sliding by SiC nanoparticles.
From the observation of microstructure of SNP4-8Y (Fig. 2), the SiC nanoparticles are well distributed in grain or grain boundaries. The agglomerates (CNx phases) are not observed.
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