首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Speciation and separation of Cr(VI) and Cr(III) using coprecipitation with Ni2+/2-Nitroso-1-naphthol-4-sulfonic acid and determination by FAAS in water and food samples.
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Speciation and separation of Cr(VI) and Cr(III) using coprecipitation with Ni2+/2-Nitroso-1-naphthol-4-sulfonic acid and determination by FAAS in water and food samples.

机译:与Ni2 + / 2-亚硝基-1-萘酚-4-磺酸共沉淀并通过FAAS测定水和食品样品中的Cr(VI)和Cr(III)的形态和分离。

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摘要

A speciation procedure for chromium(III) and chromium(VI) in the water and food samples has been established in the presented work. The procedure presented based on quantitative recoveries of Cr(III)>95% using coprecipitation of Ni(2+)/2-Nitroso-1-naphthol-4-sulfonic acid. The total chromium was measured after reduction of Cr(VI) by concentrated H(2)SO(4) and ethanol. The Cr(VI) was calculated as the difference between the total Cr content and the Cr(III) contents. The analytical variables, pH, amounts of precipitate, sample volume for optimum recoveries of Cr(III) were investigated. The influences of the some alkaline and earth alkaline ions and some transition metals on the recoveries of analyte ions were also investigated. The preconcentration factor was 50. The detection limit (3 sigma) of the reagent blank for chromium(III) was 1.33 microg L(-1). The relative standard deviations for determinations were found to be <7%, and % of relative error was calculated <6%. The method was validated by certified reference materials of tea (GBW 07605) and bush branches and leaves (GBW 0703). The procedure was successfully applied to the speciation of chromium in natural water and food samples (fish, white cheese, cow's meat, black tea, boiled wheat).
机译:在目前的工作中,已经建立了水和食品样品中铬(III)和铬(VI)的形成方法。提出的程序基于使用Ni(2 +)/ 2-亚硝基-1-萘酚-4-磺酸的共沉淀对Cr(III)> 95%的定量回收率。在用浓H(2)SO(4)和乙醇还原Cr(VI)之后测量总铬。 Cr(VI)计算为总Cr含量和Cr(III)含量之差。研究了Cr(III)最佳回收率的分析变量,pH,沉淀量,样品量。还研究了一些碱金属和碱土金属离子以及一些过渡金属对分析物离子回收率的影响。预浓缩系数为50。铬(III)试剂空白的检测极限(3 sigma)为1.33 microg L(-1)。发现用于测定的相对标准偏差为<7%,并且计算的相对误差%<6%。该方法已通过茶叶(GBW 07605)和灌木枝叶的认证参考材料(GBW 0703)的验证。该方法已成功应用于天然水和食物样品(鱼,白奶酪,牛肉,红茶,煮熟的小麦)中铬的形态分析。

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