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An electrospun magnetic nanocomposite for a facile micro-scaled analysis approach

机译:一种用于静电微尺度分析方法的电纺磁性纳米复合材料

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摘要

A magnetic polyurethane (PU] nanocomposite was synthesized by an electrospinning technique and applied for isolation and preconcentration of fluoxetine from aquatic and biological samples. The nanocomposite was electrospun using a PU polymer solution containing the dispersed magnetic nanoparticles. The magnetic properties of iron nanoparticles, along with the use of an electrospinning technique, led to the formation of a suitable sorbent toward isolation of fluoxetine. The magnetic PU nanofibers could be subsequently removed from the sample solution by applying a permanent magnet. The scanning electron microscopy (SEM) image of the magnetic PU nanofibers confirms that their diameters are in the range of 68-113 nm. The major parameters influencing the morphology of the magnetic PU nanofibers, comprising the weight ratio of iron and PU components, the applied voltage and the coating time, were optimized. Moreover, parameters including the eluting solvent amount of sorbent, extraction time, pH and salinity of aqueous samples were considered for optimization. The detection limit of the developed method under optimized conditions and using fluorescence spectrometry was 1 μg L~(-1). The relative standard deviation (n = 5) at a concentration level of 150 μg L~(-1) was 2%. The method was linear in the range of 50-5000 μg L~(-1) with a correlation coefficient of 0.9997. The whole procedure proved to be conveniently rapid, efficient and economical to extract fluoxetine from environmental and biological samples. Eventually, the developed method was applied to the analysis of water, urine, milk and plasma samples and relative recoveries of 76 to 99% were achieved.
机译:通过静电纺丝技术合成了磁性聚氨酯(PU)纳米复合材料,并将其用于水生生物样品中氟西汀的分离和预浓缩,然后使用包含分散的磁性纳米颗粒的PU聚合物溶液对纳米复合材料进行电纺丝。通过使用静电纺丝技术,形成了适合于氟西汀分离的吸附剂,随后可以通过应用永磁体从样品溶液中去除磁性PU纳米纤维。证实PU纳米纤维的直径在68-113 nm范围内,并优化了影响磁性PU纳米纤维形态的主要参数,包括铁和PU成分的重量比,施加电压和涂覆时间。 ,参数包括吸附剂的洗脱溶剂量,萃取时间e,考虑优化水性样品的pH和盐度。该方法在优化条件下,采用荧光光谱法的检出限为1μgL〜(-1)。浓度水平为150μgL〜(-1)时的相对标准偏差(n = 5)为2%。该方法在50-5000μgL〜(-1)范围内呈线性,相关系数为0.9997。事实证明,从环境和生物样品中提取氟西汀的整个过程方便,快速,高效且经济。最终,将开发的方法应用于水,尿液,牛奶和血浆样品的分析,相对回收率达到76%至99%。

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