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Spectrophotometric Kinetic Determination of Ultra Trace Amounts of Vanadium(V) Based on The Oxidation of Rhodamine B by Bromate in Sulfuric Acid Medium

机译:硫酸介质中溴酸盐氧化若丹明B的动力学光度法测定痕量钒(V)

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摘要

A new, simple, sensitive and selective catalytic spectrophotometric method was developed for the determination of trace amounts of V(V). The method is based on the catalytic effect of yanadium(V) on the oxidation of rhodamine B by bromate in acidic medium, The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of rhodamine B at 554 nm with a fixed-time method. The decrease in the absorbance of rhodamine B is proportional to the concentration of V(V) in concentration range 0.02-20 ng/mL, with a fixed time of 0.5-2.0 min from initiation of the reaction.The limit of detection ofV(V) is 0.011 ng/mL. The relative standard deviation of 2.0 and 10.0 ng/mL V(V) was 2.6 and 2.8 %, respectively. The method was applied to the determination of vanadium(V) in natural water.
机译:建立了一种新的,简单,灵敏和选择性的催化分光光度法,用于测定痕量的V(V)。该方法是基于钒(V)对酸性介质中溴酸盐对罗丹明B的催化催化作用,通过分光光度法通过固定时间法测量554 nm下罗丹明B的吸光度来监测反应。罗丹明B吸光度的降低与浓度范围0.02-20 ng / mL的V(V)成正比,从反应开始的固定时间为0.5-2.0分钟。 )为0.011 ng / mL。 2.0和10.0 ng / mL V(V)的相对标准偏差分别为2.6%和2.8%。该方法用于测定天然水中的钒(V)。

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