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Preparation of Titanium Dioxide Nanoparticles Immobilized on Polyacrylonitrile Nanofibres for the Photodegradation of Methyl Orange

机译:加固聚丙烯腈纳米纤维的二氧化钛纳米粒子的制备,以光降解甲基橙

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摘要

Herein, we describe the synthesis of titanium dioxide (TiO2) nanoparticles by the hydrolysis and condensation of titanium tetrachloride. The resulting nanoparticles were immobilized on polyacrylonitrile (PAN) based nanofibres by an electrospinning technique in order to allow simple isolation and reuse of titania semiconductor photocatalyst. The composite nanofibres were heat treated to convert the polymer nanofibres to carbon nanofibres and to convert amorphous TiO2 to crystalline TiO2. X-ray diffraction (XRD) analysis showed that the rutile phase was themajor phase and the equatorial peaks of PAN disappeared after heat treatment at 600 degrees C. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) analysis confirmed that some TiO2 nanoparticles were encapsulated whereas some were surface residing on the electrospun nanofibres. The TiO2 nanoparticles were found to lower the cyclization temperature of PAN as indicated by differential scanning colorimetry (DSC) and differential thermal analysis (DTA). Photocatalytic studies on the degradation of methyl orange dye under UV light irradiation showed that composite nanofibres were capable of degrading organic contaminants in water. The carbon nanofibres with surface residing titanium dioxide nanoparticles (TiO2/CNF-SR) showed the highest photocatalytic activity (59.35% after 210 minutes) due to direct contact between the TiO2 photocatalyst and methyl orange.
机译:在此,我们通过四氯化钛的水解和缩合来描述二氧化钛(TiO 2)纳米颗粒的合成。通过静电纺丝技术将所得纳米颗粒固定在基于聚丙烯腈(锅)的纳米纤维上,以便简单地分离和重用二氧化钛半导体光催化剂。将复合纳米纤维进行热处理以将聚合物纳米纤维转化为碳纳米纤维,并将无定形TiO 2转化为结晶TiO 2。 X射线衍射(XRD)分析表明,金红石相是OjOR相位,并且在600摄氏度下热处理后PAN的赤道峰消失。透射电子显微镜(TEM)和扫描电子显微镜(SEM)分析证实了一些TiO2纳米颗粒封装,而有些是驻留在电纺纳米纤维上的表面。发现TiO2纳米颗粒,以降低平底锅的环化温度,如差分扫描比色法(DSC)和差分热分析(DTA)所示。紫外光照射下甲基橙染料降解的光催化研究表明,复合纳米纤维能够降解水中有机污染物。由于TiO 2光催化剂和甲基橙之间直接接触,具有表面驻留二氧化钛纳米颗粒(TiO2 / CNF-SR)的碳纳米纤维(TiO 2 / CNF-SR)显示出最高的光催化活性(210分钟后59.35%)。

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