首页> 外文期刊>Journal of Chemistry >The Development of a New Kinetic Spectrophotometric Method for the Determination of Vanadium(V) Based on its Catalytic Effect on the Oxidation of Malachite Green Oxalate by Bromate in Acidic and Micellar Medium
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The Development of a New Kinetic Spectrophotometric Method for the Determination of Vanadium(V) Based on its Catalytic Effect on the Oxidation of Malachite Green Oxalate by Bromate in Acidic and Micellar Medium

机译:基于酸性胶束介质溴酸盐催化作用的新动力学分光光度法的开发基于其催化作用对酸性和胶束培养基溴酸盐的催化作用

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A new, simple, sensitive and selective kinetic spectrophotometric method was developed for the determination of ultra trace amounts of vanadium(V). The method is based on the catalytic effect of vanadium(V) on the oxidation of malachite green oxalate (MG) by bromate in acidic and micellar medium. The reaction was monitored spectrophotometrically by measuring the decrease in the absorbance of malachite green oxalate (MG) at 625 nm with a fixed-time method. The decrease in the absorbance of MG is proportional to the concentration of vanadium(V) in the range of 1-100 ng/mL with a fixed time of 0.5-2 min from the initiation of the reaction. The limit of detection is 0.71 ng/mL of vanadium(V). The relative standard deviation for the determination of 5, 30, 50 ng/mL of vanadium(V) was2.5% 2.6%, 2.4% and respectively. The method was applied to the determination of vanadium(V) in water samples.
机译:开发了一种新的,简单,灵敏和选择性的动力学分光光度法,用于测定超痕量钒(V)。该方法基于钒(V)在酸性和胶束介质中溴酸盐对孔雀石绿色草酸盐(Mg)氧化的催化作用。通过测量625nm以固定时间方法测量625nm的孔雀石绿色草酸盐(Mg)的吸光度降低来监测分光光度法的反应。 Mg的吸光度降低与1-100ng / ml的钒(v)的浓度成比例,其从反应开始的0.5-2分钟的固定时间为0.5-2分钟。检测限为0.71ng / ml钒(V)。用于测定5,30,50ng / ml钒(V)的相对标准偏差为2.5%2.6%,2.4%。该方法应用于水样中钒(V)的测定。

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