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Determination of Trace Amounts of Lead Using the Flotation-spectrophotometric method

机译:浮选-分光光度法测定痕量铅。

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摘要

The present study describes a simple and highly selective method for separation, preconcentration and spectrophotometric determination of extremely low concentrations of lead. It is based on flotation of a complex of Pb2+ ions and Alizarin yellow between aqueous and n-hexane interface at pH = 6. The proposed procedure is also applied for determination of lead in both tap water and prepared sea water samples. Beer’s Law was obeyed over the concentration range of 3.86 × 10–8 To 8.20 × 10–7 molL−1 (8–170 ngmL−1) with an apparent molar absorptivity of 1.33 × 106 molL−1 cm−1 for a 100 mL aliquot of the water sample. The detection limit (n = 10) was 8.7 × 10–9 molL−1 (1.0 ngmL−1) and the Relative standard deviation (R.S.D), (n = 10) for 7.2 × 10–7 molL−1 (150 ngmL−1) of Pb (II) was 4.36%. A notable advantage of the method is that the determination of Pb (II) is free from the interference of almost all cations and ions found in the environment and waste water samples. The determination of Pb (II) in tap and synthetic seawater samples was also carried out by the present method. The results were satisfactorily comparable so that the applicability of the proposed method was confirmed to the real samples.
机译:本研究描述了一种用于分离,预浓缩和分光光度法测定极低浓度铅的简单且高度选择性的方法。它基于在pH = 6时水和正己烷界面之间的Pb2 +离子和茜素黄络合物的浮选。拟议的方法还适用于测定自来水和制备的海水样品中的铅。浓度在3.86×10–8至8.20×10–7 molL-1(8–170 ngmL-1)时符合比尔定律,对于100 mL,表观摩尔吸收率为1.33×106 molL-1 cm-1等分的水样。检出限(n = 10)为8.7×10–9 molL-1(1.0 ngmL-1),相对标准偏差(RSD)(n = 10)为7.2×10–7 molL-1(150 ngmL– 1)的Pb(II)为4.36%。该方法的显着优势在于,Pb(II)的测定不受环境和废水样品中发现的几乎所有阳离子和离子的干扰。用本方法还可以测定自来水和合成海水样品中的Pb(II)。结果令人满意地具有可比性,从而证实了所提出方法对实际样品的适用性。

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