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Characterization of nanoporous β-SiC fiber complex prepared by electrospinning and carbothermal reduction

机译:静电纺丝和碳热还原法制备纳米多孔β-SiC纤维复合物的表征

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摘要

The nanoporous /3-silicon carbide (SiC) nano-sized fiber complex were made from precursors of various ratios with (Si0_2) as silicon source and polyacylonitrile as carbon source by simple electrospinning method and economical carbothermal reduction. The prepared samples were characterized by SEM for surface shape, XRD for crystalline properties, TGA in air for oxygen resistance, and 3ET for porosity according to the precursor components (C/Si mol ratio). The samples with carbon ratio to silicon (C/Si) of five or more in the precursor showed he long fiber shape. Increasing the C/Si in the precursor solution tended to lead nigher -SiC crystalline and smaller crystallite size than low C/Si in the precursor solution because excess carbon could act as a dispersant and barrier to prevent neck srowth or adhesion of SiC. The prepared samples have superior oxidation resistance is a whole. The increment of the C/Si leads to the increment of porosity. Also, it seems that the gaseous pore development of carbon during carbothermal reduction eads to mainly small pores (micro- or mesopores).
机译:纳米多孔/ 3-碳化硅(SiC)纳米纤维复合物是通过简单的电纺丝方法和经济的碳热还原反应以多种比例的前驱体(以SiO 2_2为硅源,聚丙烯腈为碳源)制成的。根据前体组分(C / Si摩尔比),通过SEM表征表面形状,XRD表征晶体性能,空气中的TGA表征耐氧性,3ET表征孔隙率。前体中碳与硅的碳比(C / Si)为5或更高的样品显示出长纤维形状。与过量的碳可以充当分散剂和阻挡层,以防止颈长或SiC的粘附相比,增加前体溶液中的C / Si倾向于导致比前者溶液中低C / Si更高的-SiC晶体和较小的晶粒尺寸。所制备的样品整体具有优异的抗氧化性。 C / Si的增加导致孔隙率的增加。同样,在碳热还原过程中,碳的气孔发展似乎主要是小孔(微孔或中孔)。

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