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Spectrophotometric Determination of Trace Amounts of Iron by Its Catalytic Effect on the Chlorpromazine-Hydrogen Peroxide Reaction

机译:氯丙嗪-过氧化氢催化光度法光度法测定痕量铁

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A catalytic photometric method for the determination of trace amounts of iron is proposed. In the presence of iron (FeII and FeIII), chlorpromazine is oxidized by hydrogen peroxide in a hydrochloric acid solution to form a red intermediate, which is further oxidized to a colorless compound. The reaction is followed by measuring an increase in the absorbance at 525nm; the absorbance/time curve increased with the increase in the reaction time, and reaches a maximum value. Since the slope of the linear range of absorbance/time curves increases with the increase in the iron concentration, tan α[=_??_(abs.)/_??_(sec.)] is used as a parameter for the iron determination. Under the optimum experimental conditions (0.011 M chlorpromazine, 0.43M hydrochloric acid, 0.12M hydrogen peroxide, 30°C), iron can be determined in the range 5-200μg l-1. The relative standard deviations are 0.8, 2.3 and 6.6% for 80, 40 and 10μg l-1, respectively. Under the reaction conditions, WVI, S2O32-, IO3-, I-, NO2- and BrO3- showed interference at concentrations of 1mg l-1. These ions showed no interference at concentrations one order lower. The procedure has been applied to the determination of iron in tap and natural fresh water samples.
机译:提出了一种催化光度法测定痕量铁的方法。在铁(FeII和FeIII)存在下,氯丙嗪在盐酸溶液中被过氧化氢氧化,形成红色中间体,该中间体进一步被氧化成无色化合物。反应后,测量525nm处吸光度的增加。吸光度/时间曲线随反应时间的增加而增加,并达到最大值。由于吸光度/时间曲线的线性范围的斜率随铁浓度的增加而增加,因此将tanα[= _Δε_(绝对)/ _Δε_(sec。)]用作参数。铁的决心。在最佳实验条件下(0.011 M氯丙嗪,0.43M盐酸,0.12M过氧化氢,30°C),铁的测定范围为5-200μgl-1。 80、40和10μgl-1的相对标准偏差分别为0.8、2.3和6.6%。在反应条件下,WVI,S2O32-,IO3-,I-,NO2-和BrO3-在浓度为1mg l-1时表现出干扰。这些离子在低一级浓度时没有显示出干扰。该程序已用于自来水和天然淡水样品中铁的测定。

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