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首页> 外文期刊>Analytical Sciences >Potentiometric Determination of Bromate Using an Fe(III)-Fe(II) Potential Buffer by Circulatory Flow-Injection Analysis
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Potentiometric Determination of Bromate Using an Fe(III)-Fe(II) Potential Buffer by Circulatory Flow-Injection Analysis

机译:Fe(III)-Fe(II)电位缓冲剂通过循环流动注射分析电位法测定溴酸盐

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A method for the potentiometric determination of bromate by circulatory flow injection analysis (CFIA) is described. The procedure involves the use of an Fe(III)-Fe(II) potential buffer solution, which is recycled via a reservoir. The analytical method is based on a linear relationship between the concentration of bromate and a very transient potential change in the electrode potential due to the generation of intermediate bromine during the reaction of bromate with the Fe(III)-Fe(II) potential buffer solution, which also contains NaBr, (NH4)6Mo7O24 and H2SO4. An aliquot (5 µl) of a bromate sample solution was injected into the stream of the potential buffer solution, 100 ml of which was circulated at a flow rate of 1 ml/min; the potential buffer solution stream was then returned to the reservoir after passing through a flow-through redox electrode detector. A potential change due to the reaction of the injected sample with the potential buffer in a reaction coil was measured with the detector in the form of a peak signal. The effects of the bromide, sulfuric acid and Fe(III)-Fe(II) concentrations in the potential buffer, and length of the reaction coil on the peak heights were examined in order to optimize the proposed CFIA method. The analytical sensitivities to bromate were 5.6 mV/µM for 1 × 10-2 M and 30.9 mV/µM for 1 × 10-3 M in the concentration of Fe(III)-Fe(II) in a potential buffer solution containing 0.35 M NaBr, 0.2% (NH4)6Mo7O24 and 1 M H2SO4. The detection limit of bromate obtained by a 1 × 10-3 M Fe(III)-Fe(II) potential buffer solution was 0.02 µM (2.5 ppb). The numbers of repetitive determinations in which the relative sensitivities within 5% were regarded as being tolerated were ca. 4000 and 2000 for the use of only 100 ml of 1 × 10-2 M and 1 × 10-3 M Fe(III)-Fe(II) potential buffer solution, respectively.
机译:描述了一种通过循环流动注射分析(CFIA)电位测定溴酸盐的方法。该程序涉及使用Fe(III)-Fe(II)潜在的缓冲溶液,该溶液可通过储罐循环使用。该分析方法基于溴酸盐浓度与电极电位中非常短暂的电位变化之间的线性关系,该电位变化是由于在溴酸盐与Fe(III)-Fe(II)电位缓冲溶液反应过程中生成了中间溴,其中还包含NaBr,(NH4)6Mo7O24和H2SO4。将等分试样(5 µl)的溴酸盐样品溶液注入潜在的缓冲溶液流中,将其100 ml以1 ml / min的流速循环;潜在的缓冲溶液流在通过流通式氧化还原电极检测器后返回到储存器。用检测器以峰值信号的形式测量由于注入的样品与电抗线圈中的电势缓冲液的反应引起的电势变化。为了优化所提出的CFIA方法,研究了溴化物,硫酸和Fe(III)-Fe(II)浓度在电势缓冲液中的浓度以及反应线圈长度对峰高的影响。在潜在的含0.35 M缓冲溶液中的Fe(III)-Fe(II)浓度下,对溴酸盐的分析灵敏度对于1×10-2 M为5.6 mV / µM,对于1×10-3 M为30.9 mV / µM。 NaBr,0.2%(NH4)6Mo7O24和1 M H2SO4。通过1×10-3 M Fe(III)-Fe(II)电位缓冲溶液获得的溴酸盐的检出限为0.02 µM(2.5 ppb)。相对耐受性在5%以内的容许重复性测定的数量为。 4000和2000仅分别使用100 ml 1×10-2 M和1×10-3 M Fe(III)-Fe(II)潜在缓冲溶液。

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