停止流动注射化学发光法测定天然水中过氧化氢

S. H. Fan, B. T. Hart, I. D. McKelvie
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引用次数: 9

摘要

介绍了一种快速、灵敏的流动注射化学发光法测定天然水中微量过氧化氢的方法。该方法是在碱性介质中以钴(II)催化发光氨与过氧化氢反应。采用十二烷基硫酸钠(SDS)作为增感剂,SDS的存在大大加快了反应速度,增强了CL强度。在CL反应中引入FI停流技术以提高灵敏度。考察了化学发光反应的最佳条件。采样频率为50 hr−1,进样量为100µL。过氧化氢在高纯水中的检出限为0.5 nM,定义为空白标准偏差的3倍,工作线性范围为1 ~ 105 nM。15 nM和52 nM过氧化氢测定的相对标准偏差分别为2.8和2.3% (n = 11)。该方法已应用于天然水样中过氧化氢的测定。©2000 John Wiley &儿子,Inc。实验室机器人与自动化[j], 2000
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of hydrogen peroxide in natural waters by stopped-flow injection analysis with chemiluminescence detection

A rapid, sensitive flow injection (FI) method with chemiluminescence (CL) detection for the determination of trace amounts of hydrogen peroxide in natural water is described. This method is based on the reaction of luminol with hydrogen peroxide catalysed by cobalt(II) in an alkaline medium. Sodium dodecyl sulphate (SDS) was used as sensitizer agent, and its presence greatly accelerated the reaction and enhanced the CL intensity. An FI stopped-flow technique was introduced to the CL reaction to increase sensitivity. Optimal conditions for the chemiluminescence reaction were examined. The sampling frequency was 50 hr−1 for injection volumes of 100 µL. The detection limit of hydrogen peroxide, defined as 3 times the standard deviation of the blank, was 0.5 nM in high purity water, and the working linear range was 1 to 105 nM. For the determination of 15 nM and 52 nM hydrogen peroxide, the relative standard deviations were 2.8 and 2.3% respectively (n = 11). The method has been applied to the determination of hydrogen peroxide in natural water samples. © 2000 John Wiley & Sons, Inc. Lab Robotics and Automation 12:149–156, 2000

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