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Separation of trace amount of silver using dispersive liquid-liquid based on solidification of floating organic drop microextraction

机译:基于悬浮有机液滴微萃取凝固的分散液-液分离痕量银

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摘要

In the present work, dispersive liquid-liquid microextraction based on solidification of floating organic drop was developed as a simple and rapid technique for separation of silver ions from aqueous samples. In this technique, 700 μX 0.02% of 5-(4'-dimethylamino benzyliden)-rhodanine (chelating agent) was added into the 10mL analyte sample in a test tube and 30.0 μX 1-undecanol (extraction solvent) was injected shortly thereafter. The test tubes were sonicated, centrifuged and then some effective parameters on extraction and complex formation, such as type and volume of extraction and disperser solvent, pH, the amount of chelating agent and extraction time were optimized. The effect of the interfering ions on the analytes recovery was also investigated. The calibration graph was linear in the range of 0.10-10.0ngm L~(-1) with detection limit of 0.056ngmL~(-1) (n = 8). The relative standard deviation (RSD) was±4.3% (n = 8, C=5.0 ng mL~(-1)) and the enrichment factor was 250.0. The proposed method was applied for extraction and determination of silver in different water samples.
机译:在当前的工作中,开发了一种基于漂浮有机液滴固化的分散液-液微萃取技术,该技术是一种从水样中分离银离子的简单快速的技术。在该技术中,将700μX0.02%的5-(4'-二甲基氨基苄基)-若丹宁(螯合剂)添加到试管中的10mL分析物样品中,然后不久注入30.0μX1-十一烷醇(萃取溶剂)。对试管进行超声处理,离心分离,然后优化了萃取和配合物形成的一些有效参数,例如萃取和分散剂的类型和体积,pH,螯合剂的量和萃取时间。还研究了干扰离子对分析物回收率的影响。校正曲线在0.10-10.0ngm L〜(-1)范围内呈线性,检出限为0.056ngmL〜(-1)(n = 8)。相对标准偏差(RSD)为±4.3%(n = 8,C = 5.0 ng mL〜(-1)),富集系数为250.0。该方法可用于不同水样中银的提取和测定。

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