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Mo (IV) adsorption from nitric acid media by Di-(2-ethylhexyl) phosphoric acid (D2EHPA) coated silanized magnetite nanoparticles

机译:二(2-乙基己基)磷酸(D2EHPA)包覆的硅烷化磁铁矿纳米粒子从硝酸介质中吸附钼(IV)

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Di-(2-ethylhexyl) phosphoric acid coated silanized magnetite nanoparticles were applied for the rapid removal and fast adsorption of molybdenum ions from simulated nitric acid solutions. The characterization of the developed adsorbent was carried out using various analytical techniques such as Transmission electron microscopy (TEM), X-ray diffraction pattern (XRD) and Fourier transform infrared spectroscopy (FT-IR). The Transmission electron microscopy photographs showed that the silanized magnetite nanoparticles were roughly spherical in shape and the average size of these particles is very close to the average size of bare magnetite particles. The binding of silane polymer and Di-(2-ethylhexyl) phosphoric acid on the magnetite nanoparticles was confirmed through Fourier transform infrared spectroscopy. From the optimized influential parameters, it was found that as the acid (HNO3) concentration increases, the effect of this element vanishes and at concentrations above 1 M, this element has practically no influence on molybdenum adsorption. Regarding the effect of these elements on the process, the maximum K-d is obtained in a 0.75 M nitric acid solution which is 2780 mL/g. While on the other hand the increase in initial NH3 concentration decreases the desorption K-d values. The studies on the adsorption of Mo (IV) ions revealed that maximum adsorption efficiency was achieved with 0.5 M nitric acid. Also the adsorption of Mo (IV) from a solution containing Al, Ce, Cu, Fe, Ca and Si revealed that maximum adsorption efficiency was achieved in 0.75 M nitric add. Finally the Mo (IV) ion loaded particles were desorbed with NH3 as desorption agent. (c) 2016 Elsevier B.V. All rights reserved.
机译:将二(2-乙基己基)磷酸包覆的硅烷化磁铁矿纳米颗粒用于从模拟硝酸溶液中快速去除和快速吸附钼离子。使用各种分析技术,如透射电子显微镜(TEM),X射线衍射图(XRD)和傅里叶变换红外光谱(FT-IR),对开发的吸附剂进行表征。透射电子显微镜照片显示,硅烷化的磁铁矿纳米颗粒的形状大致为球形,并且这些颗粒的平均尺寸非常接近裸露的磁铁矿颗粒的平均尺寸。通过傅立叶变换红外光谱法证实了硅烷聚合物和二-(2-乙基己基)磷酸在磁铁矿纳米颗粒上的结合。从最优化的影响参数中发现,随着酸(HNO3)浓度的增加,该元素的作用消失,而在1 M以上的浓度下,该元素对钼的吸附几乎没有影响。关于这些元素对工艺的影响,在0.75 M硝酸溶液中以2780 mL / g获得最大K-d。另一方面,初始NH3浓度的增加会降低解吸K-d值。 Mo(IV)离子的吸附研究表明,使用0.5 M的硝酸可获得最大的吸附效率。同样,从含有Al,Ce,Cu,Fe,Ca和Si的溶液中吸附Mo(IV)也表明,在添加0.75 M硝酸时可获得最大的吸附效率。最后,用NH 3作为脱附剂使Mo(IV)离子负载的粒子脱附。 (c)2016 Elsevier B.V.保留所有权利。

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