Naik Radhey M, Srivastava Abhishek, Prasad Surendra
Department of Chemistry, Lucknow University, Lucknow 226007, UP, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2008 Jan;69(1):193-7. doi: 10.1016/j.saa.2007.03.030. Epub 2007 Mar 24.
A new and highly sensitive catalytic kinetic method (CKM) for the determination of ruthenium(III) has been established based on its catalytic effect on the oxidation of l-phenylalanine (l-Pheala) by KMnO(4) in highly alkaline medium. The reaction has been followed spectrophotometrically by measuring the decrease in the absorbance at 526nm. The proposed CKM is based on the fixed time procedure under optimum reaction conditions. It relies on the linear relationship where the change in the absorbance (DeltaA(t)) versus added Ru(III) amounts in the range of 0.101-2.526ngml(-1) is plotted. Under the optimum conditions, the sensitivity of the proposed method, i.e. the limit of detection corresponding to 5min is 0.08ngml(-1), and decreases with increased time of analysis. The method is featured with good accuracy and reproducibility for ruthenium(III) determination. The ruthenium(III) has also been determined in presence of several interfering and non-interfering cations, anions and polyaminocarboxylates. No foreign ions interfered in the determination ruthenium(III) up to 20-fold higher concentration of foreign ions. In addition to standard solutions analysis, this method was successfully applied for the quantitative determination of ruthenium(III) in drinking water samples. The method is highly sensitive, selective and very stable. A review of recently published catalytic spectrophotometric methods for the determination of ruthenium(III) has also been presented for comparison.
基于钌(III)在高碱性介质中对高锰酸钾氧化L-苯丙氨酸(L-Pheala)的催化作用,建立了一种新的高灵敏度催化动力学方法(CKM)用于测定钌(III)。通过测量526nm处吸光度的降低,用分光光度法跟踪该反应。所提出的CKM基于最佳反应条件下的固定时间程序。它依赖于吸光度变化(ΔA(t))与0.101 - 2.526ng ml(-1)范围内添加的钌(III)量之间的线性关系。在最佳条件下,所提方法的灵敏度,即对应5分钟的检测限为0.08ng ml(-1),并随分析时间的增加而降低。该方法在测定钌(III)时具有良好的准确性和重现性。在存在几种干扰和非干扰阳离子、阴离子及聚氨基羧酸盐的情况下也对钌(III)进行了测定。高达20倍浓度的外来离子对钌(III)的测定均无干扰。除了分析标准溶液外,该方法还成功应用于饮用水样品中钌(III)的定量测定。该方法具有高灵敏度、高选择性且非常稳定。还对最近发表的用于测定钌(III)的催化分光光度法进行了综述以作比较。