首页> 外文期刊>International Research Journal of Pure and Applied Chemistry >Selective Extraction and Determination ofArsenic (III) and Arsenic (V) in Some FoodSamples by Cloud-Point Extraction Coupledwith Hydride Generation Atomic AbsorptionSpectrometry
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Selective Extraction and Determination ofArsenic (III) and Arsenic (V) in Some FoodSamples by Cloud-Point Extraction Coupledwith Hydride Generation Atomic AbsorptionSpectrometry

机译:浊点萃取-氢化物发生原子吸收光谱法选择性萃取和测定某些食品中的砷(Ⅲ)和砷(Ⅴ)

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Aims: To develop a new selective approach for the extraction and determination of trace amounts of As(III) and As(V) in some food samples by cloud point extraction (CPE) using two new synthesized ligands coupled with hydride-generation atomic absorption spectrometry (HG-AAS).Study Design: All significant variables for both As (III) and As (V) species that impact the separation and determination steps were studied by one factor-at-a-time (OFAT) optimization. Place and Duration of Study: Department of Chemistry, College of Science for Women, University of Baghdad, Baghdad, Iraq between October 2012 and May 2013. Methodology: The method involved the selective complexation of As (III) with 7-(6-BrBTA8HQ) or As (V) with 7-(6-MBTA8HQ) at certain pH values. Then the two complexes were individually extracted into a non-ionic surfactant (Triton X-114) and separated by centrifugation from which the two species were individually determined by means of HG-AAS. The established method was applied to the determination of the two As species in the fish and honey samples with satisfactory results where the detection limits of the method in the sample were of 0.0033 and 0.0065 μg g-1 for As (III); 0.0063 and 0.0125 μg g-1 or As(V) in fish and honey samples respectively.Results: Under the optimum established conditions, the enrichment factors of 80 and 73.7 fold were obtained for As (III) and As (V) respectively leading to detection limits of 1.3 ng mL-1 of As(III) and 2.5 ng mL-1 for As(V) in aqueous solution. The Beer’s law was obeyed in concentration range of 1.5-100 ng mL-1 for As (III) and 4-150 ng mL-1 for As (V). The accuracy of the method was checked by the standard additions procedure. The percent recoveries of As (III) and As (V) were found to be in the range of 98.3-99.3% and 98-101.6% respectively. Conclusion: The establish method avoids the steps of oxidation/reduction of As species giving good analytical figures of merit and being most suitable for the determination of two As species individually in the selected samples and other food matrices.
机译:目的:建立一种新的选择性方法,该方法使用两种新的合成配体结合氢化物发生原子吸收光谱法通过浊点萃取(CPE)萃取和测定某些食品样品中的痕量砷(III)和砷(V) (HG-AAS)研究设计:通过一次一次性因素(OFAT)优化研究了影响分离和测定步骤的As(III)和As(V)物种的所有重要变量。研究地点和持续时间:2012年10月至2013年5月,伊拉克巴格达,巴格达大学,女子学院,化学系,化学方法。方法:该方法涉及将As(III)与7-(6-BrBTA8HQ进行选择性络合)或在特定pH值下具有7-(6-MBTA8HQ)的As(V)。然后将两种复合物分别萃取到非离子型表面活性剂(Triton X-114)中,并通过离心分离,通过HG-AAS从中分别确定两种物质。所建立的方法用于鱼和蜂蜜样品中两种砷的测定,结果令人满意,样品中砷(III)的检出限为0.0033和0.0065μgg-1。结果:在最佳建立条件下,As(III)和As(V)的富集因子分别为0.0063和0.0125μgg-1或As(V)。水溶液中As(III)的检出限为1.3 ng mL-1,As(V)的检出限为2.5 ng mL-1。遵守比尔定律,砷(III)的浓度范围为1.5-100 ng mL-1,砷(V)的浓度范围为4-150 ng mL-1。通过标准添加程序检查方法的准确性。发现As(III)和As(V)的回收率分别在98.3-99.3%和98-101.6%之间。结论:建立的方法避免了砷种类的氧化/还原步骤,具有良好的分析价值,最适合于选定样品和其他食品基质中两种砷种类的单独测定。

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