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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Sensitized extraction spectrophotometric determination of Hg(II) with dithizone after its flotation as ion-associate using iodide and ferroin
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Sensitized extraction spectrophotometric determination of Hg(II) with dithizone after its flotation as ion-associate using iodide and ferroin

机译:双硫zone浮选为碘离子和铁蛋白后用双硫fer敏化萃取光度法测定汞(Ⅱ)

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This paper describes a simple and highly selective method for the separation, preconcentration and spectrophotometric determination of extremely low concentration of mercury. The method is based on the flotation of an ion-associate of HgI42- and ferroin between aqueous and n-heptane interface atpH 5. The ion-associate was then separated and treated with ammonia and dithizone solutions to extractonly the mercury chelate with CH2Cl2. The measurement is feasible when the volume of the water sample containing Hg(II) was varied over 50-800 ml. Beer ' s law was obeyed over the concentration range of 8 x 10(-9) to 1.6 x 10(-7) Mol 1(-1) with an apparent molar absorptivity of 6.53 x 10(6) l Mol(-1) cm(-1) for a 500 ml aliquot of the water sample. The detection limit (n = 7) was 5.0 x 10(-10) mol l(-1) and the R.S.D. (n = 5) for 8.0 x 10(-7) mol l(-1) of Hg(II) was 3.7%. A notable advantage of the method is that the determination of Hg(II) is free from the interference of almost all cations and anions found in the environmental and waste water samples. The determination of Hg(11) in tap, synthetic sea water and human hair samples was carried out by the present method and cold vapor atomic absorption spectrometry (CV-AAS). The results were satisfactorily comparable so that the applicability of the proposed method was confirmed to the real samples. (c) 2005 Elsevier B.V. All rights reserved.
机译:本文介绍了一种用于分离,预浓缩和分光光度法测定极低汞含量的简单且高度选择性的方法。该方法基于pH值为5的HgI42和铁蛋白在水和正庚烷界面之间的离子缔合剂的浮选。然后分离离子缔合剂,并用氨水和双硫zone溶液处理,仅用CH2Cl2萃取汞螯合物。当含Hg(II)的水样品的体积变化超过50-800 ml时,该测量是可行的。在8 x 10(-9)至1.6 x 10(-7)Mol 1(-1)的浓度范围内遵守比尔定律,表观摩尔吸收率为6.53 x 10(6)l Mol(-1) cm(-1)取500 ml等分的水样。检出限(n = 7)为5.0 x 10(-10)mol l(-1),R.S.D。对于8.0 x 10(-7)mol l(-1)的Hg(II)(n = 5)为3.7%。该方法的显着优势在于,测定Hg(II)不受环境样品和废水样品中几乎所有阳离子和阴离子的干扰。用本方法和冷蒸气原子吸收光谱法(CV-AAS)测定自来水,合成海水和人发样品中的Hg(11)。结果令人满意地具有可比性,从而证实了该方法在实际样品中的适用性。 (c)2005 Elsevier B.V.保留所有权利。

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