Hosseini Mohammad Saeid, Hashemi-Moghaddam Hamid
Department of Chemistry, Faculty of Science, Birjand University, P.O. Box 79, Birjand, Iran.
Talanta. 2005 Sep 15;67(3):555-9. doi: 10.1016/j.talanta.2005.01.010. Epub 2005 Jul 1.
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 HgI(4)(2-) and ferroin between aqueous and n-heptane interface at pH 5. The ion-associate was then separated and treated with ammonia and dithizone solutions to extract only the mercury chelate with CH(2)Cl(2). The measurement is feasible when the volume of the water sample containing Hg(II) was varied over 50-800ml. Beer's law was obeyed over the concentration range of 8x10(-9) to 1.6x10(-7)moll(-1) with an apparent molar absorptivity of 6.53x10(6)lmol(-1)cm(-1) for a 500ml aliquot of the water sample. The detection limit (n=7) was 5.0x10(-10)moll(-1) and the R.S.D. (n=5) for 8.0x10(-7)moll(-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(II) 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.
本文描述了一种用于分离、预富集和分光光度法测定极低浓度汞的简单且高选择性方法。该方法基于在pH 5条件下,HgI(4)(2-)与邻二氮菲亚铁离子的离子缔合物在水相和正庚烷界面间的浮选。然后将该离子缔合物分离,并用氨和双硫腙溶液处理,仅用CH(2)Cl(2)萃取汞螯合物。当含Hg(II)的水样体积在50 - 800ml范围内变化时,测量是可行的。对于500ml水样等分试样,在8×10(-9)至1.6×10(-7)moll(-1)的浓度范围内符合比尔定律,表观摩尔吸光系数为6.53×10(6)lmol(-1)cm(-1)。检测限(n = 7)为5.0×10(-10)moll(-1),8.0×10(-7)moll(-1)的Hg(II)的相对标准偏差(n = 5)为3.7%。该方法的一个显著优点是Hg(II)的测定不受环境和废水样品中几乎所有阳离子和阴离子的干扰。采用本方法和冷蒸气原子吸收光谱法(CV - AAS)对自来水、合成海水和人发样品中的Hg(II)进行了测定。结果令人满意地可比,从而证实了所提出方法对实际样品的适用性。