Uluozlu Ozgur Dogan, Tuzen Mustafa, Soylak Mustafa
Department of Chemistry, Faculty of Science and Arts, Gaziosmanpasa University, 60250 Tokat, Turkey.
Food Chem Toxicol. 2009 Oct;47(10):2601-5. doi: 10.1016/j.fct.2009.07.020. Epub 2009 Jul 24.
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).
本研究建立了一种用于水和食品样品中铬(III)和铬(VI)的形态分析方法。该方法基于使用镍(2+)/2-亚硝基-1-萘酚-4-磺酸共沉淀法对Cr(III)进行定量回收,回收率>95%。通过用浓硫酸和乙醇还原Cr(VI)后测定总铬含量。Cr(VI)通过总铬含量与Cr(III)含量之差计算得出。研究了分析变量,如pH值、沉淀量、用于Cr(III)最佳回收率的样品体积。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。预富集因子为50。铬(III)试剂空白的检测限(3σ)为1.33μg L-1。测定的相对标准偏差<7%,相对误差计算<6%。该方法通过茶叶(GBW 07605)和树枝叶(GBW 0703)标准物质进行了验证。该方法成功应用于天然水和食品样品(鱼、白奶酪、牛肉、红茶、煮小麦)中铬的形态分析。