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Synthesis of ultra-fine porous tin oxide fibres and its process characterization

机译:超细多孔氧化锡纤维的合成及其工艺表征

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摘要

Porous rutile-structured SnO_2 fibres, with their length of several millimetres, diameter from 100 nm to 40 mu m and potentials for sensor applications, were synthesized from a precursor solution of poly(ethylene oxide) (PEO), chloroform (CHCl_3) and dimethyldineodecanoate tin (C_(22)H_(44)O_4Sn) using electrospinning and metal-organic decomposition techniques. Fourier-transform infrared spectroscopy, thermogravimetric and differential thermal analysis and x-ray diffraction were used to characterize the synthesized fibres so as to reveal the series of physical and chemical changes occurring from the starting chemicals to the final product of ultra-fine SnO_2 fibres: the solvent CHCl_3 evaporates during the electrospinning; the organic groups in PEO and C_(22)H_(44)O_4Sn decompose, with Sn-C bond in C_(22)H_(44)O_4Sn replaced by Sn-O between 220 and 300 deg C, and the atomic arrangement transforms into the genesis of a rutile-type lattice between 300 and 380 deg C; the incipient lattice finally develops into the rutile structure during heat treatment at higher temperatures up to 600 deg C.
机译:由聚环氧乙烷(PEO),氯仿(CHCl_3)和二甲基二癸二酸酯的前体溶液合成了金红石结构的多孔SnO_2纤维,其长度为几毫米,直径为100 nm至40μm,具有用于传感器的潜力。锡(C_(22)H_(44)O_4Sn)使用静电纺丝和金属有机分解技术。使用傅里叶变换红外光谱,热重和差热分析以及X射线衍射对合成纤维进行表征,以揭示从超细SnO_2纤维的起始化学物质到最终产物的一系列物理和化学变化:电纺丝过程中溶剂CHCl_3蒸发; PEO和C_(22)H_(44)O_4Sn中的有机基团分解,C_(22)H_(44)O_4Sn中的Sn-C键在220至300摄氏度之间被Sn-O取代,原子排列转变为在300至380摄氏度之间的金红石型晶格的形成;最初的晶格在高达600摄氏度的高温热处理过程中最终发展成金红石结构。

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