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首页> 外文期刊>Analytical Letters >Simultaneous Determination of Gallium(III) and Indium(III) in Urine and Water Samples with Cloud Point Extraction and by Inductively Coupled Plasma Optical Emission Spectrometry
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Simultaneous Determination of Gallium(III) and Indium(III) in Urine and Water Samples with Cloud Point Extraction and by Inductively Coupled Plasma Optical Emission Spectrometry

机译:浊点萃取-电感耦合等离子体发射光谱法同时测定尿液和水样中的镓(Ⅲ)和铟(Ⅲ)

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摘要

A simple, sensitive, and selective method for the determination of gallium and indium in different samples at trace levels is presented. This method was based on complexation of analyzes with 2-(5-bromo-2- pyridylazo)-5-diethylaminophenol (5-Br-PADAP) in the presence of t-octylphenoxy-polyethoxyethanol (Triton X-100). After phase separation, the analyzed concentrations were determined by inductively coupled plasma optical emission spectrometry. Quantitative extraction of gallium and indium was performed at pH 7.0, 1.7 mmol L ~(-1), 5-Br-PADAP, 1.3% (w/v) Triton X-100 and at 75°C. The relative standard deviations (RSD) of this method were between 0.3% and 1.6% (C = 20 ng mL ~(-1), n = 9). The calibration curve is linear over the concentration range 6-200 ng mL ~(-1) for gallium and 2-200 ng mL ~(-1) for indium, respectively. The limits of detection (LOD) for gallium and indium were 0.72 and 0.28 ng mL ~(-1), respectively. The results showed the developed method was not susceptible to matrix effects, providing recoveries between 98% and 102%. The accuracy of the developed method was evaluated by the analysis of spiked certified reference materials. The developed method was successfully applied to gallium and indium determination in urine and lake water with satisfactory results.
机译:提出了一种简单,灵敏,选择性的测定痕量水平不同样品中镓和铟的方法。该方法基于在叔辛基苯氧基聚乙氧基乙醇(Triton X-100)存在下与2-(5-溴-2-吡啶基偶氮)-5-二乙基氨基苯酚(5-Br-PADAP)进行的络合分析。相分离后,通过电感耦合等离子体发射光谱法测定分析浓度。在pH 7.0、1.7 mmol L〜(-1),5-Br-PADAP,1.3%(w / v)Triton X-100和75°C下进行镓和铟的定量萃取。该方法的相对标准偏差(RSD)在0.3%和1.6%之间(C = 20 ng mL〜(-1),n = 9)。校准曲线分别在镓的6-200 ng mL〜(-1)和铟的2-200 ng mL〜(-1)的浓度范围内是线性的。镓和铟的检出限(LOD)分别为0.72和0.28 ng mL〜(-1)。结果表明,所开发的方法不易受基质影响,回收率在98%至102%之间。通过对加标的认证参考材料进行分析,评估了所开发方法的准确性。该方法成功应用于尿液和湖水中镓和铟的测定,结果令人满意。

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