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Preparation And Properties Of β-SiC/SiO2Fibers, SiO2and SiO2/ZnO Hollow Nanofibers By Electrospinning

Posted on:2013-10-29Degree:MasterType:Thesis
Country:ChinaCandidate:L N ZhangFull Text:PDF
GTID:2231330395980483Subject:Physical chemistry
Abstract/Summary:PDF Full Text Request
In this paper, β-SiC/SiO2micro/nano fibers, hydrophobic β-SiC/SiO2fibers, SiO2and SiO2/ZnO hollow nanofibers were obtained via electrospinning usingpolycarbosilane (PCS) and tetraethoxysilane (TEOS) as the raw materials, respectively.The influence of technological parameters on morphology of the fibers wassystematically studied, and the preparation processes were optimized. Themicrostructure, morphology and photoluminescence properties of the products werecharacterized by infrared spectrum (IR), X-ray diffraction (XRD), transmissionelectron microscopy (TEM), scanning electron microscopy (SEM) and fluorescencespectrophotometer. The main contents are as follows:1. The precursor was prepared by solution electrospinning using PCS as the rawmaterial, then, β-SiC/SiO2micro/nano fibers were obtained by curing treatment andsintering. The influence of PCS concentration, the sort and ratio of solution, additiveand curing treatment condition on morphology of the fibers and the photoluminescenceproperty were systematically studied. The results showed that the The optimizationprocess of the curing was that the precursor was cured in muffle furnace at190℃for8h, and the β-SiC/SiO2micro/nano fibers were prepared by calcining the precursor at1200℃for2h. The morphology of the product was mainly as same as that ofprecursor. Using xylene as solvent, controlling the concentration of PCS at60%70%,β-SiC/SiO2micro fibers with smooth surface and a diameter of10μm were obtained.The diameter of β-SiC/SiO2micro fibers reduced to12μm by adding10wt%TBAB/DMF in the spinning solution. Using xylene and DMF as solvent, controllingthe concentration of PCS at60%70%and the mass ratio of xylene and DMF at2:1, uniform β-SiC/SiO2nanofibers with an average diameter of500nm were obtained. Thephotoluminescence spectrum showed two emission peaks at367nm and466nm forβ-SiC/SiO2micro fibers.2. Hydrophobic β-SiC/SiO2fibers were prepared by surface modification ofβ-SiC/SiO2micro/nano fibers using AC-FAS as surface modifier. The influence offiber morphology on the hydrophobility and the photoluminescence properties ofmodified fibers were studied. The results showed that, the smaller the β-SiC/SiO2fiberdiameter, and the rougher the surface, the better hydrophobility. Water contact angle ofthe modified β-SiC/SiO2nanofibers was up to148°. The photoluminescence spectrashowed two emission peaks at338nm and410nm for hydrophobic β-SiC/SiO2microfibers and two emission peaks at336nm and416nm for hydrophobic β-SiC/SiO2nanofibers. It showed that the emission peak position of the photoluminescence wasslightly changed as the diameter of the fiber changed.3. Using TEOS or TEOS/ZnO as the raw materials, ethanol as solvent, PVP aspolymer template, the SiO2hollow nanofibers and SiO2/ZnO hollow nanofibers wereobtained by solution electrospinning. The ratio of the raw materials, the amount ofpolymer template, spinning voltage, injection rate and the amount of ZnOnanoparticles were optimized. Microstructure, morphology, specific surface area andphotoluminescence properties were investigated. The results showed that:(1) Optimum process for preparing the precursor of SiO2hollow nanofibers wasthat the volume ratio of TEOS and ethanol was1:3, the amount of PVP was50.062.5mg·mL-1, the injection rate was1.01.5mL·h-1, the applied voltage was2530kV, thetip-to-collector distance was15cm. SiO2hollow nanofibers with the diameter of300600nm, the wall thickness of about150nm and the inner diameter of about30nmwere obtained by curing treatment and sintering. The photoluminescence spectrumshowed two emission peaks at288nm and370nm for the SiO2hollow nanofibers.(2) Adding ZnO nanoparticles in TEOS/PVP/ethanol solution, SiO2/ZnO hollownanofibers were prepared according to the optimum process in (1). The influence ofthe amount of ZnO on the morphology of product was investigated principally. Theresults showed that ZnO was benefit for forming the hollow nanofibers, but it was notthe more the better. The optimized amount of ZnO was1020mg·mL-1. UniformSiO2/ZnO hollow nanofibers with the smooth surface, the diameter of300500nm, thewall thickness of about100nm and the inner diameter of about300nm were obtained atthe optimum process conditions. The photoluminescence spectrum showed two emission peaks at288nm and300500nm for the SiO2/ZnO hollow nanofibers.Compared with SiO2hollow nanofibers, SiO2/ZnO hollow nanofibers had strongerblue emission.
Keywords/Search Tags:β-SiC/SiO2fibers, SiO2/ZnO, hollow nanofibers, electrospinning, hydrophobility, photoluminescence
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