魏红. 气相色谱—电子捕获检测法测定水中5种农药残留[J]. 环境卫生学杂志, 2021, 11(1): 98-103. DOI: 10.13421/j.cnki.hjwsxzz.2021.01.020
    引用本文: 魏红. 气相色谱—电子捕获检测法测定水中5种农药残留[J]. 环境卫生学杂志, 2021, 11(1): 98-103. DOI: 10.13421/j.cnki.hjwsxzz.2021.01.020
    WEI Hong. Determination of Five Pesticide Residues in Water by Gas Chromatography-Electron Capture Detection[J]. Journal of Environmental Hygiene, 2021, 11(1): 98-103. DOI: 10.13421/j.cnki.hjwsxzz.2021.01.020
    Citation: WEI Hong. Determination of Five Pesticide Residues in Water by Gas Chromatography-Electron Capture Detection[J]. Journal of Environmental Hygiene, 2021, 11(1): 98-103. DOI: 10.13421/j.cnki.hjwsxzz.2021.01.020

    气相色谱—电子捕获检测法测定水中5种农药残留

    Determination of Five Pesticide Residues in Water by Gas Chromatography-Electron Capture Detection

    • 摘要:
      目的 利用气相色谱—电子捕获检测法同时测定水中莠去津、林丹、百菌清、毒死蜱和溴氰菊酯5种农药残留。
      方法 水样经液液萃取,无水硫酸钠脱水后直接进样测定;针对影响回收率的因素进行了试验,优化了溶剂的选择及用量、氯化钠用量;采用外标法定量,进行低、中、高三个添加水平的加标回收率测定,每个水平测定6次。
      结果 该方法在测定的含量范围内标准曲线线性关系良好,相关系数均>0.999 6,方法检出限为(0.01~0.30)μg/L,3种浓度的水样加标回收率为90.5%~110.0%,相对标准偏差(RSD)为0.4%~3.2%。
      结论 该方法样品无需浓缩,操作简便、干扰少、分析速度快、灵敏度高、线性良好、精密度和准确度均较好,适用于水样中5种农药残留的测定。

       

      Abstract:
      Objective To determine atrazine, lindane, chlorothalonil, chlorpyrifos, and deltamethrin simultaneously in water samples by gas chromatography- electron capture detection.
      Methods Pretreated by liquid-liquid extraction and dehydrated with anhydrous sodium sulfate, water samples were, directly injected into the gas chromatograph for determination. The tests were done to optimize the sorts and amount of solvent, and the amount of sodium chloride used in this method which were the factors affecting the recovery rates. The spiked recovery rates at three concentration levels (low, medium, and high) were determined by adding the external standard samples. Each concentration level was determined for six times.
      Results The standard curves obtained by this method showed good linear correlation within the determined range of concentration, and the coefficients were all over 0.999 6. The detection limits were at the range from 0.01 μg/L to 0.30 μg/L, the average recovery rates were 90.5%-110.0%, with the relative standard deviation ranged from 0.4% to 3.2%.
      Conclusion This method was suitable for determination of five pesticide residues simultaneousiy in water samples, which was simple to operate without being concentrated, less interference, rapid analysis, good sensitivity and linearity, high precision and accuracy.

       

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