首页> 外文期刊>Journal of Hazardous Materials >Chromium-zinc ferrite nanocomposites for the catalytic abatement of toxic environmental pollutants under ambient conditions
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Chromium-zinc ferrite nanocomposites for the catalytic abatement of toxic environmental pollutants under ambient conditions

机译:铬锌铁氧体纳米复合材料在环境条件下催化消除有毒环境污染物

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HighlightsOxidizing power of zinc ferrite nanocomposites increases with chromium substitution.Direct correlation between surface acidity and catalytic activity of composites.Rate of reaction is strongly dependent on catalyst amount and its composition.Composite is reusable with negligible leaching, indicating heterogeneous mechanism.AbstractCatalytic abatement of 4-chlorophenol, 2,4-dichlorophenol and 2,4-dichlorophenoxy acetic acid in water was investigated by peroxide oxidation over chromium substituted zinc ferrite nanocomposites at ambient conditions. The structural and chemical properties of composites synthesized by sol-gel auto combustion method was studied by X-ray diffraction, Fourier Transform Infra-Red spectroscopy, Transmission Electron Microscopy, surface area, X-ray Fluorescence spectroscopy, Temperature Programmed Reduction and Desorption techniques. Complete removal of 4-CP, DCP and 2,4-D was achieved within 60, 75 and 90min with 96.7/90.5%, 93.88/77.23% and 88.55/62.1% of COD/TOC removal respectively at 298K and 343K. Influence of reaction variables including reaction temperature, oxidant concentration, substrate concentration, catalyst dosage and its composition on the removal efficiency was studied. Kinetic study revealed that wet peroxide oxidation followed a first order kinetic model with rate constant and activation energy of 3.5×10−2min−1/10.7kJ/mole, 9.5×10−3min−1/12.9kJ/mole and 2.29×10−2min−1/17.7kJ/mole respectively for 4-CP, DCP and 2,4-D. The results of five consecutive catalytic runs from X-ray diffraction, Brunauer Emmet Teller surface area and leaching studies from Atomic Absorption Spectrophotometry (AAS) revealed the excellent stability of the catalyst. Scavenging effect ofn-butanol on hydroxyl radical indicated a heterogeneous free radical mechanism.
机译: 突出显示 铁铬酸锌纳米复合材料的氧化能力随铬的取代而增加。 复合材料的表面酸度和催化活性之间直接相关。 反应速度强烈依赖 使用NE可以复合使用明显的浸出,表明机制不同。 < ce:abstract xmlns:ce =“ http://www.elsevier.com/xml/common/dtd” xmlns =“ http://www.elsevier.com/xml/ja/dtd” id =“ abs0010” view = “ all” class =“ author”> 摘要 在环境条件下,通过过氧化物氧化铬取代的铁酸锌纳米复合材料,研究了水中4-氯苯酚,2,4-二氯苯酚和2,4-二氯苯氧基乙酸的催化减量作用。 。通过X射线衍射,傅立叶变换红外光谱,透射电子显微镜,表面积,X射线荧光光谱,程序升温还原和解吸技术研究了溶胶-凝胶自燃法合成的复合材料的结构和化学性质。在60、75和90分钟内,分别在298K和343K处分别完成了96.7 / 90.5%,93.88 / 77.23%和88.55 / 62.1%的COD / TOC去除,可以完全去除4-CP,DCP和2,4-D。研究了反应温度,氧化剂浓度,底物浓度,催化剂用量及其组成等反应变量对去除效率的影响。动力学研究表明,湿式过氧化物氧化遵循一阶动力学模型,速率常数和活化能为3.5×10 − 2 min −1 /10.7kJ/mol,9.5×10 -3 min − 1 /12.9kJ/mole和2.29×10 − 2 min − 1 sup> /17.7kJ/mol。 X射线衍射,Brunauer Emmet Teller表面积连续五次催化运行的结果以及原子吸收分光光度法(AAS)的浸出研究表明,该催化剂具有出色的稳定性。 n -丁醇对羟基自由基的清除作用表明了自由基的异构机制。

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