高效液相色谱法检测生活饮用水中微量甲醛

    Determination of trace formaldehyde in drinking water by HPLC

    • 摘要:
      目的 建立高效液相色谱法检测生活饮用水中甲醛。
      方法 甲醛在酸性条件下, 55℃水浴中与2, 4-二硝基苯肼反应40min, 生成的甲醛-2, 4-二硝基苯腙产物用正己烷提取。经高效液相色谱C18(250 mm×4.6mm, 5μm) 色谱柱分离, 以乙腈-水(v: v, 70:30)洗脱, 在最大吸收波长355 nm下测定。
      结果 水中甲醛在0.006~2.00μg/mL范围内, 相关系数(r)优于0.999 2, 线性关系良好, 检出限为0.002μg/mL。该方法加标回收率为90.0%~106.0%, 相对标准偏差(RSD)为1.20%~3.79%, 乙醛在4.00μg/mL下不干扰实验。
      结论 该方法操作简单, 灵敏度高, 重现性好, 结果准确, 满足生活饮用水中微量甲醛的测定。

       

      Abstract:
      Objective To establish a high-performance liquid chromatography (HPLC) method for determination of formaldehyde in drinking water.
      Methods Formaldehyde reacted with 2, 4-dinitrophenylhydrazine in an acidic medium in a water bath at 55℃ for 40 minutes to form the formaldehyde-2, 4-dinitrophenylhydrazone product, which was extracted with n-hexane. The product was separated by the C18 (250 mm×4.6 mm, 5 μm) column of high-performance liquid chromatograph, and eluted with acetonitrile-water (v: v, 70:30). The detection was carried out at the maximum absorption wavelength of 355 nm.
      Results The content of formaldehyde in drinking water ranged from 0.006 μg/mL to 2.00 μg/mL, and the correlation coefficient (r) was greater than 0.9992, indicating a good linear relationship. The detection limit was 0.002 μg/mL. The spike recovery rate of the method was 90.0%-106.0%, with the relative standard deviation of 1.20%-3.79%. Acetaldehyde had no interference with the experimentation at 4.00 μg/mL.
      Conclusion The established method is simple to operate, has high sensitivity and good repeatability, and allows the generation of accurate results, meeting the requirements for measurement of trace formaldehyde in drinking water.

       

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