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Kinetic Spectrophotometric Determination of Trace Amounts of Iodide in Food Samples

机译:动力学分光光度法测定食品样品中痕量的碘化物

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摘要

A simple, selective and sensitive kinetic method has been developed for the determination of trace amounts of iodide. This method is based on a catalytic effect of iodide on the reaction between Janus Green and bromate in acidic media. Trace amounts of iodide increase the rate of a reaction that is monitored spectrophotometrically at 618 nm by a fixed-time method at 30 s. Effective parameters on the reaction rate, such as the concentration of reactants, temperature and reaction time, were investigated and the optimum conditions were obtained (6.0 × 10−2 mol L−1 of sulfuric acid, 2.50 × 10−5 mol L−1 of Janus Green, 1.75 × 10−2 mol L−1 of bromate, 30°C and 180 s). The calibration curve was linear between 0.5 – 190.0 μg L−1 of iodide, and the relative standard deviations (n = 5) for 10.0 and 100.0 μg L−1 of iodide were 1.2 and 1.8%, respectively. The limit of detection was 0.12 μg L−1 of iodide concentration. The effects of various substances upon the reaction rate were determined for assigning the selectivity of the method. The proposed method was successfully applied to the determination of iodide in food samples. The new developed method was found to have fairly good selectivity, sensitivity, simplicity and rapidity.
机译:已经开发了一种简单,选择性和敏感的动力学方法,用于测定痕量的碘化物。该方法基于碘化物对酸性介质中Janus绿色和溴酸盐之间的反应的催化作用。痕量的碘化物增加了通过30秒的定时方法在618nm下在618nm下监测分光光度素的反应速率。研究了反应速率的有效参数,例如反应物,温度和反应时间的浓度,得到最佳条件(6.0×10-2摩尔L-1,硫酸,2.50×10-5摩尔L-1 Janus Green,1.75×10-2 mol L-1溴酸盐,30°C和180s)。校准曲线在0.5-190.0μgL-1之间的碘化物之间是线性的,并且分别为10.0和100.0μgL-1的相对标准偏差(n = 5)分别为1.2和1.8%。检测极限为碘化物浓度为0.12μg。确定各种物质对反应速率的影响,用于分配方法的选择性。所提出的方法成功地应用于食品样品中碘化物的测定。发现新的开发方法具有相当良好的选择性,敏感性,简单性和快速。

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