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FABRICATION OF SILICON-BASED CERAMIC SYNTHESIZED FROM MESOPOROUS CARBON-SILICA NANOCOMPOSITES

机译:从介孔碳 - 二氧化硅纳米复合材料中合成硅基陶瓷的制造

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Mesoporous carbon-silica (C-SiO_2) nanocomposites with different C/SiO_2 molar ratios were used as precursor for fabricating silicon-based ceramics. Different silicon carbide nanostructures were synthesized by carbothermal reduction of mesoporous C-SiO_2 nanocomposites via different heat treatments under argon. X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and nitrogen adsorption-desorption analysis were used to characterize C-SiO_2 nanocomposites and SiC products. The major morphologies formed from the mesoporous C-SiO_2 nanocomposites were nanoparticles and nanofibers. With higher quantity of P123, which is the surfactant for the mesopores, the BET surface area and pore volume increased, inducing a decrease of nanofibers. The mesoporous precursors were also heated at 1200 °C for 15 hours to make a nearly dense structure and then heatedto the final temperature. The products were almost nanoparticles which had a larger size than those heated directly to 1450 °C. Therefore carbothermal reduction of mesoporous C-SiO_2 precursors appears to be an effective means of accelerating the reaction and controlling SiC nanostructures.
机译:具有不同C / SiO_2摩尔比的介孔碳 - 二氧化硅(C-SiO_2)纳米复合材料用作制造硅基陶瓷的前体。通过氩气下的不同热处理通过介孔C-SiO_2纳米复合材料进行不同的碳化硅纳米结构。 X射线衍射,扫描电子显微镜,透射电子显微镜和氮吸附 - 解吸分析用于表征C-SiO_2纳米复合材料和SiC产物。由中孔C-SiO_2纳米复合材料形成的主要形态是纳米颗粒和纳米纤维。具有较高量的P123,其是中孔的表面活性剂,BET表面积和孔体积增加,诱导纳米纤维的降低。中孔前体也在1200℃下加热15小时,使得几乎致密的结构,然后加热至最终温度。产物几乎纳米颗粒的尺寸比直接加热至1450℃的纳米颗粒。因此,介孔C-SiO_2前体的碳热还原似乎是加速反应和控制SiC纳米结构的有效方法。

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