首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >A new portable switchable hydrophilicity microextraction method for determination of vanadium in microsampling micropipette tip syringe system couple with ETAAS
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A new portable switchable hydrophilicity microextraction method for determination of vanadium in microsampling micropipette tip syringe system couple with ETAAS

机译:一种新的便携式可切换亲水性微萃取方法,用于测定叶片微内采样微纤维尖端注射器系统叶片的钒

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摘要

First time we launch an innovative and simple portable in a closed micropipette tip switchable hydrophilicity microextraction syringe system (mu S-SHS) couple with electrothermal atomic absorption spectroscopy (ETAAS) was developed for preconcentration and determination of vanadium using 2-(5-Bromo-2-pyridylazo)-5-diethylaminophenol (5-Br-PADAP), as complexing. In the proposed method decanoic acid was used as a switchable hydrophilicity extraction solvent and their polarity was switched on and off (water miscible/immiscible) by simply changing their pH. The phase separation was induced by simply adding sulfuric acid that switch off hydrophilicity (nondispersed/immiscible) of decanoic acid. The metal complex enriched phase (V-(5-Br-PADAP-SHS) was separated by simply removing the aqueous phase through manually dispensed syringe system. Then finally acidic ethanol drawn into the syringe contains metal complex enriched SHS phase to reduce viscosity and directly injected into the ETAAS by using an enclosed micropipette tip syringe system. The multivariate strategy was applied to screen out and optimized the variables. Limit of detection (LOD), enhancement factor (EF) and relative standard deviation (RSD) were found 0.0075 mu g L-1, 120 and 2.91%, respectively. Certified reference material of riverine water (SLRS-4), Apple leaves (NIST SRM 1515) and a standard addition method was used to validate the present method. Developed method was applied to water and food samples. We successfully applied the proposed method to analyze vanadium in different real food and water samples.
机译:我们第一次启动一个创新和简易携带在一个封闭的微量移液器尖端转换的亲水性微注射器系统(MU S-SHS)夫妇与电热原子吸收光谱(ETAAS)的开发,使用2-(5-溴 - 富集和钒的测定2-吡啶基偶氮)-5-二乙氨基(5-溴-PADAP),作为配位。在所提出的方法癸酸被用作转换的亲水性提取溶剂和它们的极性,通过简单地改变它们的pH和关闭(水混溶性/不混溶的)切换。相分离诱导癸酸仅仅是添加硫酸该开关关断的亲水性(非色散的/不混溶的)。的金属配合物富集相(N-(5-BR-PADAP-SHS)通过简单地通过手动分配的注射器体系中除去水相分离,然后抽入注射器最后酸性乙醇中含有金属络合物富集SHS相以降低粘度,并直接通过使用封闭的微量移液器尖端注射器系统注入ETAAS。多元策略用于筛选出和优化的变量。检测限(LOD),增强因子(EF)和相对标准偏差(RSD)被发现0.0075亩克L-1,分别120和2.91%。河流水的认证标准物质(SLRS-4),苹果叶(NIST SRM 1515)和标准添加法来验证本发明的方法。建立的方法适用于水和食品样品。我们成功地应用所提出的方法来分析不同钒真正的食物和水样中。

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