首页> 外文期刊>Analytical and bioanalytical chemistry >Use of dicyclohexano-18-crown-6 to separate traces of silver(I) from potassium thiocyanate in hydrochloric acid media, and determination of the silver by atomic absorption spectrometry
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Use of dicyclohexano-18-crown-6 to separate traces of silver(I) from potassium thiocyanate in hydrochloric acid media, and determination of the silver by atomic absorption spectrometry

机译:在盐酸介质中使用二环己酮-18-冠-6分离痕量的银(I)和硫氰酸钾,并通过原子吸收光谱法测定银

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摘要

Solvent extraction with 0.05 mol L~(-1) dicyclohexano-18-crown-6 (DC18C6) in 1,2-dichloroethane, coupled with flame atomic absorption spectrometry (AAS), has been investigated as a new method for separation of trace amounts of silver(I) from 0.05 mol L~(-1) potassium thiocyanate in 1.0 mol L~(-1) hydrochloric acid media and quantification of the amount of silver present. The method is based on the formation of an extractable ion-association product, [DC18C6·K]~+[Ag(SCN)_2]~-, with a metal-to-crown ether ratio of 1:1 (as derived from slope analysis data). Stripping of the extracted silver(I) in the 1,2-dichloroethane phase was achieved within 5 min by use of 3.0 mol L~(-1) potassium thiocyanate. Reducing the concentration of acid in the sample solution to 0.1 mol L~(-1) improved the preconcentration factor severalfold. Excellent tolerance of the proposed method to the presence of foreign ions in solution with silver(I) was demonstrated. A detection limit of 13 ng mL~(-1) was derived from the mean value of the blank plus three times its standard deviation. The method was used to determine traces of silver(I) after separation from gold(III), platinum(IV), and palladium(II) matrices on the basis of extractability differences with 18-membered crown ethers under specified conditions. The efficiency of the adopted ion-association mechanism for silver(I) extraction was apparent from the average recovery of 96% for spiked standards by use of the back-washing technique. The proposed extraction procedure was applied to the determination of traces of silver(I) in a selection of chemical reagents.
机译:研究了在1,2-二氯乙烷中用0.05 mol L〜(-1)二环己基-18-冠-6(DC18C6)萃取溶剂,结合火焰原子吸收光谱法(AAS),作为痕量分离的新方法溶于1.0 mol L〜(-1)盐酸介质中的0.05 mol L〜(-1)硫氰酸钾中的银(I),并对存在的银量进行定量。该方法基于可萃取的离子缔合产物[DC18C6·K]〜+ [Ag(SCN)_2]〜-的形成,金属与冠醚之比为1:1(源自斜率)。分析数据)。通过使用3.0 mol L〜(-1)硫氰酸钾,在5分钟内实现了1,2-二氯乙烷相中萃取银(I)的汽提。将样品溶液中的酸浓度降低至0.1 mol L〜(-1)可以将预浓缩系数提高数倍。证明了所提出的方法对银(I)溶液中存在外来离子的极好的耐受性。从空白的平均值加上其标准偏差的三倍得出检测限为13 ng mL〜(-1)。该方法用于根据在指定条件下与18元冠醚的可萃取性差异来确定与金(III),铂(IV)和钯(II)基质分离后的痕量银(I)。通过使用反洗技术从加标标准品的平均回收率达到96%,可以明显看出采用的离子缔合机制萃取银(I)的效率。拟议的提取程序用于选择化学试剂中痕量银(I)的测定。

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