Department of Environmental Science, Kongju National University, Kongju 314-701, Republic of Korea.
Anal Chim Acta. 2013 Mar 26;769:79-83. doi: 10.1016/j.aca.2013.01.036. Epub 2013 Jan 25.
A gas chromatography-mass spectrometric (GC-MS) method has been established for the determination of hydrazine in drinking water and surface water. This method is based on the derivatization of hydrazine with ortho-phthalaldehyde (OPA) in water. The following optimum reaction conditions were established: reagent dosage, 40 mg mL(-1) of OPA; pH 2; reaction for 20 min at 70 °C. The organic derivative was extracted with methylene chloride and then measured by GC-MS. Under the established condition, the detection and the quantification limits were 0.002 μg L(-1) and 0.007 μg L(-1) by using 5.0-mL of surface water or drinking water, respectively. The calibration curve showed good linearity with r(2)=0.9991 (for working range of 0.05-100 μg L(-1)) and the accuracy was in a range of 95-106%, and the precision of the assay was less than 13% in water. Hydrazine was detected in a concentration range of 0.05-0.14 μg L(-1) in 2 samples of 10 raw drinking water samples and in a concentration range of 0.09-0.55 μg L(-1) in 4 samples of 10 treated drinking water samples.
建立了测定饮用水和地表水中肼的气相色谱-质谱(GC-MS)方法。该方法基于水中原邻苯二醛(OPA)对肼的衍生化。建立了以下最佳反应条件:试剂用量,OPA 为 40mg mL(-1);pH 值为 2;70°C 下反应 20min。有机衍生物用二氯甲烷萃取,然后用 GC-MS 测定。在建立的条件下,以 5.0mL 地表水或饮用水为基体,检测限和定量限分别为 0.002μg L(-1)和 0.007μg L(-1)。校准曲线的线性良好,r(2)=0.9991(工作范围为 0.05-100μg L(-1)),准确度在 95-106%之间,水中测定的精密度小于 13%。在 10 个原水饮用水样品的 2 个样品中,肼的浓度范围为 0.05-0.14μg L(-1),在 10 个处理后饮用水样品的 4 个样品中,肼的浓度范围为 0.09-0.55μg L(-1)。