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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Preconcentration of trace uranium from seawater with solid phase extraction followed by differential pulse polarographic determination in chloroform eluate
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Preconcentration of trace uranium from seawater with solid phase extraction followed by differential pulse polarographic determination in chloroform eluate

机译:固相萃取对海水中痕量铀进行预浓缩,然后在氯仿洗脱液中进行差分脉冲极谱法测定

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摘要

In the present study, an effective method is presented for the separation and preconcentration of uranium (VI) by solid phase extraction (SPE). For this purpose, U(VI) oxinate is formed by the reaction of U(VI) with 8-hydroxy-quinoline and adsorbed onto the octylsilane (C-8) SPE cartridge. The analyte is completely eluted with chloroform and determined by differential pulse polarography. The SPE conditions were optimized by evaluating the effective factors such as pH, oxine concentration, type and concentration of buffer and masking agent. By the proposed method a preconcentration factor more than 100 was achieved. The average recovery of uranium (VI) oxinate (0.1 mg l~(-1) was 99.8%. The relative standard deviation was 1.6% for seven replicate determinations of uranyl ion in the solution with a concentration 20 μg l~(-1). Some concomitant ions such as Ca~(+2), Mg~(+2) and Fe~(+3) which interfere in extraction or determination process of uranium were masked with EDTA in aqueous phase during the extraction process. The proposed method was successfully used for the determination of uranium in Caspian Sea and Persian Gulf water samples.
机译:在本研究中,提出了一种通过固相萃取(SPE)分离和预浓缩铀(VI)的有效方法。为此,U(VI)含氧酸酯是通过U(VI)与8-羟基喹啉的反应形成的,并被吸附到辛基硅烷(C-8)SPE柱上。分析物完全用氯仿洗脱,并通过差动脉冲极谱法测定。通过评估有效因素,例如pH,oxine浓度,缓冲液和掩蔽剂的类型和浓度,优化了SPE条件。通过提出的方法,实现了超过100的预浓缩系数。铀(VI)含氧铀(0.1 mg l〜(-1)的平均回收率为99.8%。七次重复测定浓度为20μgl〜(-1)的铀酰离子时的相对标准偏差为1.6%。 。在萃取过程中,水相中的EDTA掩盖了干扰铀萃取或测定过程的一些伴生离子,如Ca〜(+2),Mg〜(+2)和Fe〜(+3)。被成功用于里海和波斯湾水样中铀的测定。

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