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首页> 外文期刊>Journal of AOAC International >Ligandless dispersive liquid-liquid microextraction of iron in biological and foodstuff samples and its determination by electrothermal atomic absorption spectrometry.
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Ligandless dispersive liquid-liquid microextraction of iron in biological and foodstuff samples and its determination by electrothermal atomic absorption spectrometry.

机译:生物和食品样品中铁的无配体液-液微萃取及其电热原子吸收光谱法测定。

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摘要

A new, simple, and efficient method comprising ligandless dispersive liquid-liquid microextraction combined with electrothermal atomic absorption spectrometry is reported for the preconcentration and determination of ultratrace amounts of Fe(III). Carbon tetrachloride and acetone were used as the extraction and disperser solvents, respectively. Some effective parameters of the microextraction such as choice of extraction and disperser solvents, their volume, extraction time and temperature, salt and surfactant effect, and pH were optimized. Under the optimum conditions, the calibration curve was linear in the range of 0.02 to 0.46 micro g/L of Fe(III), with LOD and LOQ of 5.2 and 17.4 ng/L, respectively. The RSD for seven replicated determinations of Fe(III) ion at 0.1 micro g/L concentration level was 5.2%. Operational simplicity, rapidity, low cost, good repeatability, and low consumption of extraction solvent are the main advantages of the proposed method. The method was successfully applied to the determination of iron in biological, food, and certified reference samples.
机译:报道了一种新的,简单而有效的方法,该方法包括无配体分散液-液微萃取与电热原子吸收光谱法相结合,用于超痕量Fe(III)的富集和测定。四氯化碳和丙酮分别用作萃取溶剂和分散剂。优化了微萃取的一些有效参数,如萃取和分散剂溶剂的选择,其体积,萃取时间和温度,盐和表面活性剂的作用以及pH值。在最佳条件下,Fe(III)的校正曲线在0.02至0.46 micro g / L的范围内呈线性,LOD和LOQ分别为5.2和17.4 ng / L。在0.1 micro g / L浓度水平下重复测定Fe(III)离子的7次重复测定的RSD为5.2%。该方法的主要优点是操作简单,快速,成本低,重复性好,萃取溶剂消耗少。该方法已成功应用于生物,食品和认证参考样品中铁的测定。

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