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Preparation of nano aluminum nitride powders by polymer network method
Ning Zhang,Tingting Fu,Feiyi Yang,Hongmin Kan,Xiaoyang Wang,Haibo Long,Liuyan Wang 한양대학교 세라믹연구소 2014 Journal of Ceramic Processing Research Vol.15 No.2
In this work, aluminum nitrate (Al(NO3)3), active carbon and C12H22O11 were used as raw materials. The nano aluminum nitride powders (AlN) were synthesis by polymer network method. Aluminum nitride (AlN) exhibits high thermal conductivity, low dielectric permittivity and good electric insulativity. It has a very high synthetic temperature, however, results in a high cost. The aim of this investigation is to develop a new method of fabricating ultra-fine AlN powders to lower the synthetic temperature of AlN. The influences of different carbon sources and the synthetic temperature on fabricating AlN powders via polymer network method were investigated, and the mechanism of AlN formation was also identified. The results indicated that as using sucrose (C12H22O11) as the carbon source, the optimum synthetic process condition for fabricating ultrafine AlN powders was at 1500 °C for 2 h. Comparing with the mechanical ball-milling method, the temperature of synthesizing AlN powders was lowered about 100 °C. Furthermore, the size of as-synthesized AlN was finer from 50 nm to 80 nm.
Zhang Ning,Liu Huan,Zhang Tianwen,Kan Hongmin,Wang Xiaoyang,Cui Xingyu 한양대학교 세라믹연구소 2016 Journal of Ceramic Processing Research Vol.17 No.3
The paper was prepared spherical hexagonal boron nitride with different microstructures under flowing ammoniaatmosphere. The effect of boron source component ratios (molar ratio of borax and boric acid) on the phase composition ofthe sample were studied: the work also explored the effect of boron source component ratio on the microstructure andadsorption performance of h-BN. Spherical hexagonal boron nitride had corresponding to shell structure, mesoporousstructure, and solid structure when the ratio of boron source components respectively was 1 : 0.5, 1 : 1, and 1 : 2. Between 1 : 1and 1:0.5, the former had an lower adsorptions at low relative pressures. On the contrary, the adsorption of former wouldincreased at higher relative pressures and reached up 276.02 cm3 g−1, and the maximum adsorption of the latter reached only228.20 cm3 g−1. Under any relative pressure, the adsorption capacity was the lowest when the boron source composition ratiowas 1 : 2.