K.P.P.R. Mohan Reddy, P. Govind Chowdary, V. Krishna Reddy, P. Raveendra Reddy
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引用次数: 6
摘要
提出了一种高灵敏度、高选择性的动力学分光光度法测定纳克银的方法。该方法是基于银(I)的催化活性来促进亚铁氰化钾与2,4,6-三吡啶-1,3,5-三嗪(TPTZ)之间的绿色形成,否则在pH 2.0下是一个非常缓慢的反应。在银的存在下,绿色溶液的吸收光谱显示出两个强度几乎相等的峰,一个在405 nm处,另一个在600 nm处。在5 ~ 410 ng mL-1和10 ~ 610 ng mL-1波长范围内,实验溶液的吸光度随银(I)含量的增加而成比例增加。优化了pH、试剂浓度、亚铁氰化物浓度、时间对最大反应速率的影响等实验条件。测定其摩尔吸光度为1.57 × 106 L mol-1 cm-1,桑德尔灵敏度为0.065 ng cm-2,检出限为1.6 ng mL-1,检出限为4.8 ng mL-1,相对标准偏差(n = 8)为0.81%。研究了不同离子对银测定的影响。该方法适用于合金、生物样品、废水、纯水和阿育吠陀药品中银的测定。
Catalytic-Kinetic Determination of Silver(I) Using Hexacyanoferrate(II) and 2,4,6-Tripyridyl-1,3,5-Triazine(TPTZ)
A highly sensitive and selective kinetic spectrophotometric method is proposed for the determination of silver in nanogram quantities. The method is based on catalytic activity of silver(I) in enhancing the green colour formation between potassium ferrocyanide and 2,4,6-tripyridyl-1,3,5-triazine (TPTZ) which is otherwise a very slow reaction at pH 2.0. The absorbance spectrum of the green coloured solution in presence of silver showed two peaks of almost equal intensity one at 405 nm and another at 600 nm. At both the wavelengths the absorbance of the experimental solution increased proportionally with the amount of silver(I) in the range 5 – 410 ng mL-1 and 10 – 610 ng mL-1 respectively. Other experimental conditions like pH, reagent concentration, ferrocyanide concentration and effect of time for obtaining maximum reaction rate were optimized. The molar absorptivity, Sandell's sensitivity, detection limit, determination limit and relative standard deviation (n = 8) were determined as 1.57 × 106 L mol-1 cm-1, 0.065 ng cm-2, 1.6 ng mL-1, 4.8 ng mL-1 and 0.81 % respectively. The effect of various diverse ions on the determination of silver was studied. The method was applied for the determination of silver in alloys, biological samples, effluents, real water and in ayurvedic medicines.