High purity silicon carbide （SIC） powder was synthesized in-situ by chemical reaction between silicon and carbon powder. In order to ensure that the impurity concentration of the resulting SiC powder is suitable for...High purity silicon carbide （SIC） powder was synthesized in-situ by chemical reaction between silicon and carbon powder. In order to ensure that the impurity concentration of the resulting SiC powder is suitable for high-resistivity SiC single crystal growth, the preparation technology of SiC powder is different from that of SiC ceramic. The influence of the shape and size of carbon particles on the morphology and phase composition of the obtained SiC powder were discussed. The phase composition and morphology of the products were investigated by X-ray diffraction, Raman microspectroscopy and scanning electron microscopy. The results show that the composition of resulting SiC by in-situ synthesis from Si/C mixture strongly depends on the nature of the carbon source, which corresponds to the particle size and shape, as well as the preparation temperature. In the experimental conditions, flake graphite is more suitable for the synthesis of SiC powder than activated carbon because of its relatively smaller particle size and flake shape, which make the conversion more complete. The major phase composition of the full conversion products is β-SiC, with traces of α-SiC. Glow discharge mass spectroscopy measurements indicated that SiC powder synthesized with this chemical reaction method can meet the purity demand for the growth of high-resistivity SiC single crystals.展开更多
FeSiAl alloys ribbons synthesized by melt-quench were annealed in vacuum at 873 K for 60 rain. The flaky powders were prepared by milling the annealed ribbons for 70 h. After milling, the powders were heat treated at ...FeSiAl alloys ribbons synthesized by melt-quench were annealed in vacuum at 873 K for 60 rain. The flaky powders were prepared by milling the annealed ribbons for 70 h. After milling, the powders were heat treated at 573 K for 90 rain. The ordering degree of the powders lattice structure was analyzed by X-ray diffraction （XRD）. The measurement of specific saturation magnetization was carried out by vibrating samples magnetometer （VSM）. Complex permittivity and complex permeability in the frequency band of 0.5-18 GHz were measured with the vector network analyzer. The ordering degree of the superlattice structure increased from 0.2＇7 to 0.49. Complex permittivity and complex permeability decreased with increasing Si content. After ordering, the specific saturation magnetization decreased from 134.2 to 85.0 A.m2.kg-1. For use in anti-EMI material, the total contents of Si and Al in FeSiAl alloys should be controlled at a low level.展开更多
文摘High purity silicon carbide （SIC） powder was synthesized in-situ by chemical reaction between silicon and carbon powder. In order to ensure that the impurity concentration of the resulting SiC powder is suitable for high-resistivity SiC single crystal growth, the preparation technology of SiC powder is different from that of SiC ceramic. The influence of the shape and size of carbon particles on the morphology and phase composition of the obtained SiC powder were discussed. The phase composition and morphology of the products were investigated by X-ray diffraction, Raman microspectroscopy and scanning electron microscopy. The results show that the composition of resulting SiC by in-situ synthesis from Si/C mixture strongly depends on the nature of the carbon source, which corresponds to the particle size and shape, as well as the preparation temperature. In the experimental conditions, flake graphite is more suitable for the synthesis of SiC powder than activated carbon because of its relatively smaller particle size and flake shape, which make the conversion more complete. The major phase composition of the full conversion products is β-SiC, with traces of α-SiC. Glow discharge mass spectroscopy measurements indicated that SiC powder synthesized with this chemical reaction method can meet the purity demand for the growth of high-resistivity SiC single crystals.
文摘FeSiAl alloys ribbons synthesized by melt-quench were annealed in vacuum at 873 K for 60 rain. The flaky powders were prepared by milling the annealed ribbons for 70 h. After milling, the powders were heat treated at 573 K for 90 rain. The ordering degree of the powders lattice structure was analyzed by X-ray diffraction （XRD）. The measurement of specific saturation magnetization was carried out by vibrating samples magnetometer （VSM）. Complex permittivity and complex permeability in the frequency band of 0.5-18 GHz were measured with the vector network analyzer. The ordering degree of the superlattice structure increased from 0.2＇7 to 0.49. Complex permittivity and complex permeability decreased with increasing Si content. After ordering, the specific saturation magnetization decreased from 134.2 to 85.0 A.m2.kg-1. For use in anti-EMI material, the total contents of Si and Al in FeSiAl alloys should be controlled at a low level.
