Determination of trace amounts of selenium in natural spring waters and tea samples by catalytic kinetic spectrophotometry

R. Gürkan, Nevalnur Zeynep Gürkan
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引用次数: 1

Abstract

In this work, a new kinetic method is described for the determination of trace Se(IV) in natural spring waters and commercial tea samples. The method is based on the activation of Se(IV) onto the indicator reaction in acidic medium. The reaction was monitored using a fixed time approach of 20 min at 680 nm. The variables affecting the reaction rate were evaluated and optimized. The method allows the determination of Se(IV) in the range of 0.0125-1.0 mg L-1 with a detection limit of 3.6 µg L-1. The precision was in range of 0.63-3.15% (as RSD %) with a higher recovery than 98.6%. The method has been found to be selective against matrix effect. The method was applied to the speciation analysis of inorganic Se species present in the selected samples. The method was statistically validated by analysis of two certified samples and comparing the obtained results to those of HG-AAS analysis. Also, the total Se levels of the samples were determined by using both methods after conversion of Se(VI) into Se(IV) in ultrasonic bath in acidic medium for 30 min at 85-90 °C. The results were in good agreement with those of HG-AAS. The Se(VI) level of the samples was calculated from the difference between amounts of total Se and Se(IV).
催化动力学分光光度法测定天然泉水和茶叶样品中痕量硒
本文建立了一种新的测定天然泉水和商品茶叶样品中痕量硒(IV)的动力学方法。该方法是基于Se(IV)在酸性介质中对指示剂反应的活化。采用固定时间方法监测反应,时间为20 min,波长为680 nm。对影响反应速率的因素进行了评价和优化。本方法对硒(IV)的测定范围为0.0125 ~ 1.0 mg L-1,检出限为3.6µg L-1。精密度为0.63 ~ 3.15% (RSD %),回收率高于98.6%。该方法对基体效应具有选择性。将该方法应用于所选样品中无机硒的形态分析。通过对两个认证样品的分析,并将所得结果与HG-AAS分析结果进行比较,对该方法进行了统计验证。将Se(VI)转化为Se(IV),在85 ~ 90℃的酸性介质中超声浴30 min后,用两种方法测定样品的总Se水平。结果与HG-AAS相吻合。根据样品中总硒量与硒(IV)量之差计算样品中的硒(VI)水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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