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无配体分散液液微萃取生物和食品样品中的铁及其电热原子吸收光谱法测定

Ligandless dispersive liquid--liquid microextraction of iron in biological and foodstuff samples and its determination by Electrothermal atomic absorption spectrometry.

作者信息

Madadizadeh Mohadeseh, Taher Mohammad Ali, Ashkenani Hamid

出版信息

J AOAC Int. 2013 Nov-Dec;96(6):1466-72. doi: 10.5740/jaoacint.12-459.

DOI:10.5740/jaoacint.12-459
PMID:24645530
Abstract

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 microg/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(IIl) ion at 0.1 microg/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.

摘要

报道了一种新的、简单且高效的方法,该方法包括无配体分散液液微萃取结合电热原子吸收光谱法,用于超痕量铁(III)的预富集和测定。分别使用四氯化碳和丙酮作为萃取溶剂和分散剂溶剂。对微萃取的一些有效参数进行了优化,如萃取溶剂和分散剂溶剂的选择、它们的体积、萃取时间和温度、盐和表面活性剂的影响以及pH值。在最佳条件下,铁(III)的校准曲线在0.02至0.46μg/L范围内呈线性,检测限和定量限分别为5.2和17.4 ng/L。在0.1μg/L浓度水平下对铁(III)离子进行七次重复测定的相对标准偏差为5.2%。操作简单、快速、成本低、重复性好以及萃取溶剂消耗低是该方法的主要优点。该方法成功应用于生物、食品和标准参考样品中铁的测定。

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