摘要
研究了pH值在1.0～1.5磷酸介质中,柠檬酸存在下,痕量钒对溴酸钾氧化对乙酰基偶氮胂的褪色反应及其动力学条件,建立了测定痕量钒的新方法。本法表观摩尔吸光系数ε_(max)=2.64×10~6 L·mol^(-1)·cm^(-1),线性范围为0～10ng·ml^(-1),检出限为1.41×10^(-11)g·L^(-1)。方法用于测定自来水、湖水、芹菜样中痕量钒(V),取得了令人满意的结果。
A new method was developed for the determination of trace vanadium in which vanadium (V) catalyzes the decoloring reaction of p-acetylarsenazo with potassium bromate in phosphoric acid medium in the presence of citric acid. The apparent molar absorptivity of the method is epsilon = 2.64 x 10(6) L(.)mol(-1 .) cm(-1) at 532 nm. The linear range of the determination of vanadium is 0similar to10 ng(.)ml(-1). The detection limit of the method for vanadium is 1.41 x 10(-11) g(.)L(-1). The method has been used in the determination of trace vanadium in tap water, lake water and celery samples with satisfactory results. The possible kinetic mechanism of the reaction was proposed.
出处
《稀有金属材料与工程》
SCIE
EI
CAS
CSCD
北大核心
2004年第2期222-224,共3页
Rare Metal Materials and Engineering
基金
长春理工大学留学归国人员科研专项基金(40103/129159)
关键词
痕量钒(V)
对乙酰基偶氮胂
溴酸钾
催化动力学光度法
trace amount of vanadium(V)
p-acetylarsenazo
potassium bromate
catalytic kinetic spectrophotometry
