D Ayushi, Sengupta Arijit, Kumar Sangita D, Kumbhar A G, Venkateswaran G
Analytical Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085, India.
Int J Anal Chem. 2011;2011:813061. doi: 10.1155/2011/813061. Epub 2011 Jul 12.
A simple, rapid and accurate method for the determination of monoethanolamine (MEA) in PHWR steam-water circuits has been developed. MEA is added in the feed water to provide protection against corrosion while hydrazine is added to scavenge dissolved oxygen. The quantitative determination of MEA in presence of hydrazine was accomplished using derivatization ion chromatography with conductometric detection in nonsuppressed mode. A Metrosep cation 1-2 analytical column and a Metrosep cartridge were used for cation separation. A mixture of 4 mM tartaric acid, 20% acetone and 0.05 mM HNO(3) was used as eluent. Acetone in the mobile phase leads to the formation of different derivatives with MEA and hydrazine. The interferences due Na(+) and NH(4) (+) were eliminated by adopting a simple pretreatment procedure employing OnGuard-H cartridge. The limit of detection limit of MEA was 0.1 μg mL(-1) and the relative standard deviation was 2% for the overall method. The recovery of MEA added was in the range 95%-102%. The method was applied to the determination of MEA in steam generator water samples.
已开发出一种用于测定压水堆蒸汽 - 水回路中单乙醇胺(MEA)的简单、快速且准确的方法。在给水中添加MEA以提供防腐蚀保护,同时添加肼以清除溶解氧。在肼存在的情况下,采用衍生化离子色谱法并在非抑制模式下进行电导检测来完成MEA的定量测定。使用Metrosep阳离子1 - 2分析柱和Metrosep柱进行阳离子分离。以4 mM酒石酸、20%丙酮和0.05 mM HNO₃的混合物作为洗脱液。流动相中的丙酮会导致MEA和肼形成不同的衍生物。通过采用使用OnGuard - H柱的简单预处理程序消除了Na⁺和NH₄⁺的干扰。MEA的检测限为0.1 μg mL⁻¹,整个方法的相对标准偏差为2%。添加的MEA回收率在95% - 102%范围内。该方法应用于蒸汽发生器水样中MEA的测定。