Solid-Phase Extraction and Spectrophotometric Determination of Mercury with 6-Mercaptopurine in Environmental Samples

Mohammad Saber-Tehrani, Hamid Hashemi-Moghaddam, S. Waqif Husain, Karim Zare
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引用次数: 3

Abstract

A highly selective, sensitive and rapid method for the determination of trace amounts of inorganic mercury based on the reaction of Hg (II) with 6-mercaptopurine and the solid phase extraction of the complex on C18 membrane disks was developed. The 6-mercaptopurine selectively reacts with Hg (II) to form a complex in the pH range of 5-8. This complex was preconcentrated by solid phase extraction with C18 disks. An enrichment factor of 100 was achieved. The molar absorptivity of the complex is 0.26 ×10-6 L. mol-1. cm-1 measured at 315 nm. The Beer's law is obeyed in the concentration range of 0.002 – 0.048 μg mL-1. The relative standard deviation for eleven-replicated measurement of 0.04 μg mL-1 is 1.5 %. The detection limit is 0.001 μg mL-1 in the water samples. The advantage of the method is that the determination of Hg (II) is free from interference of almost all the cations and anions found in environment and wastewater samples. The determination of Hg (II) in water samples of different origins and marine sediment were carried out by the present method and cold vapor atomic absorption spectrometry (CVAAS). Also the method's accuracy was investigated by using SRM 2709. The obtained results by the present procedure were in good agreement with those of the CVAAS and certified value, so that the applicability of the proposed method was confirmed for the real samples.

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6-巯基嘌呤固相萃取光度法测定环境样品中的汞
基于Hg (II)与6-巯基嘌呤的反应和C18膜盘上络合物的固相萃取,建立了一种高选择性、高灵敏度和高快速测定痕量无机汞的方法。6-巯基嘌呤在5-8的pH范围内选择性地与Hg (II)反应形成络合物。用C18圆盘固相萃取法对该配合物进行预浓缩。富集系数达到100。配合物的摩尔吸收率为0.26 ×10-6 L. mol-1。Cm-1在315 nm处测量。在0.002 ~ 0.048 μg mL-1的浓度范围内符合比尔定律。0.04 μg mL-1 11次重复测定的相对标准偏差为1.5%。水样的检出限为0.001 μg mL-1。该方法的优点是汞(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。采用本方法和冷蒸汽原子吸收光谱法(CVAAS)测定了不同来源的水样和海洋沉积物中的汞(II)。并用srm2709对该方法的精度进行了研究。所得结果与CVAAS值和认证值吻合较好,从而证实了本文方法对实际样品的适用性。
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