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A silica-silver nanocomposite obtained by sol-gel method in the presence of silver nanoparticles

机译:银纳米粒子存在下通过溶胶-凝胶法获得的二氧化硅-银纳米复合材料

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摘要

Silver nanopar ticles (AgNPs) were obtained by a redox reaction, using a glucose-containing cyclosiloxane as a reduction agent and stabilizer. Then the AgNPs aqueous solution was used as the reaction medium for the sol-gel process, star ting from tetraethylor thosilicate (TEOS) as silica precursor. The nanocomposite material resulted (SilAg) after solvent removal, aging and calcination and was investigated by infrared spectroscopy (FT-IR), atomic force microscopy (AFM), scanning electron microscopy coupled with energy dispersive X-ray system (SEM/EDX), transmission electron microscopy (TEM), energy-dispersive X-ray fuorescence spectroscopy (EDXRF), X-ray diffraction (XRD) and dynamic vapor sorption (DVS). The results were compared to model silicas obtained without silver. A higher condensation degree in SilAg was obtained due to the basic medium used in the frst step and was confrmed by a sorption capacity lower than for the model silicas. The solid surface area calculated with GAB analysis using DVS data for the water vapors is 210 m2 g~(-1). The nanocomposite showed good catalytic activity for hydrogen peroxide decomposition.
机译:使用含葡萄糖的环硅氧烷作为还原剂和稳定剂,通过氧化还原反应获得了银纳米颗粒(AgNP)。然后,将AgNPs水溶液用作溶胶-凝胶工艺的反应介质,由四乙基或原硅酸盐(TEOS)作为二氧化硅前体进行调制。去除溶剂,老化和煅烧后得到的纳米复合材料(SilAg),并通过红外光谱(FT-IR),原子力显微镜(AFM),扫描电子显微镜和能量色散X射线系统(SEM / EDX)进行了研究,透射电子显微镜(TEM),能量色散X射线荧光光谱(EDXRF),X射线衍射(XRD)和动态蒸气吸附(DVS)。将结果与没有银获得的模型二氧化硅进行比较。由于在第一步中使用了碱性介质,因此在SilAg中获得了更高的缩合度,并且其吸附能力低于模型二氧化硅。使用DVS数据通过GAB分析计算得出的水蒸气的固体表面积为210 m2 g〜(-1)。该纳米复合材料对过氧化氢显示出良好的催化活性。

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