静电纺丝法合成以腐植酸和聚丙烯腈为基材的纳米碳纤维

B. Yermagambet, M. Kazankapova, A. Nauryzbayeva, Z. Kassenova
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引用次数: 0

摘要

本文介绍了在实验室条件下,用电纺丝法从麦库本盆地氧化煤和聚丙烯腈(PAN)中制备基于腐殖酸的碳纳米纤维(CNFs)的方法。电极间电压值为20-25kV。测定了所研究样品的元素组成,研究了样品的表面形貌,揭示了碳纤维的改性类型。能量色散X射线光谱和扫描电子显微镜(SEM)的结果表明,初始CNF的化学成分(C-48.73%)和碳纤维的直径范围为148.6nm至1.36μm。并对所得样品进行了氧化和碳化处理。碳经氧化和碳化后的元素组成分别为87.75%和89.16%,纤维直径为117.5nm-1.03微米。碳化CNF的拉曼散射结果表明,其石墨化程度为-23.97%,I(D)/I(G)=0.7,I(G)/I)=1.4。这种材料的电阻为27欧姆。基于腐殖酸和PAN的CNFs的SEM图谱,发现样品在氧化和碳化后的结构保持了原始的纤维结构。研究还发现,纳米纤维的直径从1μm减小到117.5 nm,这可能与原始产品中挥发性和非均相成分的释放以及结构更薄的多孔细丝的形成有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SYNTHESIS OF CARBON NANOFIBERS BASED ON HUMIC ACID AND POLYACRYONITRILE BY ELECTROSPINNING METHOD
The article describes a method for obtaining carbon nanofibers (CNFs) based on humic acid from oxidized coal of the Maikuben basin and polycarlonitrile (PAN) by electrospinning in laboratory conditions. The value of the interelectrode voltage was 20-25 kV. The elemental composition was determined and the surface morphology of the studied sample was studied, the type of modification of the carbon fiber was revealed. As a result of energy dispersive X-ray spectroscopy and scanning electron microscopy (SEM), the chemical composition of the initial CNF (C-48.73%) and the diameter of carbon fibers, which ranged from 148.6 nm to 1.36 μm, were found. The processes of oxidation and carbonization of the obtained samples were also carried out. The elemental composition of carbon after oxidation and carbonization was 87.75 and 89.16%, respectively, the diameter of the fibers was 117.5 nm -1.03 microns. The results of Raman scattering of light (RS) of carbonized CNF showed the degree of graphitization - 23.97%, the ratio I (D) / I (G) = 0.7, I (G) / I (D) = 1.4. The resistance of this material was 27 ohms. On the basis of SEM patterns of CNFs based on humic acid and PAN, it was found that the structure of the sample after oxidation and carbonization retains the original fibrous structure. It was also found that the diameter of nanofibers decreases from 1 μm to 117.5 nm, which may be associated with the release of volatile and heterogeneous components of the original product and the formation of a more structural thin porous filament.
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