固相萃取-高效液相色谱法检测水中多种拟除虫菊酯类农药

沈登辉, 单晓梅, 陆蓓蓓, 谢继安

沈登辉, 单晓梅, 陆蓓蓓, 谢继安. 固相萃取-高效液相色谱法检测水中多种拟除虫菊酯类农药[J]. 环境与职业医学, 2013, 30(1): 49-52.
引用本文: 沈登辉, 单晓梅, 陆蓓蓓, 谢继安. 固相萃取-高效液相色谱法检测水中多种拟除虫菊酯类农药[J]. 环境与职业医学, 2013, 30(1): 49-52.
SHEN Deng-hui , SHAN Xiao-mei , LU Bei-bei , XIE Ji-an . Determination of Five Pyrethroids in Water Using Solid Phase Extraction High Performance Liquid Chromatography[J]. Journal of Environmental and Occupational Medicine, 2013, 30(1): 49-52.
Citation: SHEN Deng-hui , SHAN Xiao-mei , LU Bei-bei , XIE Ji-an . Determination of Five Pyrethroids in Water Using Solid Phase Extraction High Performance Liquid Chromatography[J]. Journal of Environmental and Occupational Medicine, 2013, 30(1): 49-52.

固相萃取-高效液相色谱法检测水中多种拟除虫菊酯类农药

基金项目: 安徽省自然科学基金资助项目(编号:11040606M216)
详细信息
    作者简介:

    沈登辉(1989-),男,硕士生;研究方向:环境卫生学,E-mail:anyixiaoshen@163.com

    通讯作者:

    单晓梅,Email:xiaomeishan@126.com

Determination of Five Pyrethroids in Water Using Solid Phase Extraction High Performance Liquid Chromatography

More Information
    Corresponding author:

    SHAN Xiao-mei ,Email:xiaomeishan@126.com

  • 摘要:
    [目的] 研究同时测定水中甲氰菊酯、氯氟氰菊酯、溴氰菊酯、氰戊菊酯、氯菊酯5种拟除虫菊酯类农药污染物的固相萃取-高效液相色谱方法。

    [方法] 水样经C18小柱富集,以异丙醇洗脱,采用光电二极管阵列检测器检测,利用C18色谱柱分离,以乙腈溶液和纯水为流动相等梯度洗脱,流速1.0 mL/min,在波长205 nm进行测定,外标法定量。

    [结果] 5种拟除虫菊酯类农药在0.0~5.0 mg/L浓度范围内具有良好的线性关系,方法最低检测质量浓度为0.025~0.050 μg/L,回收率范围为88.0%~102.2%,相对标准偏差为1.0%~3.8%。

    [结论] 该固相萃取-高效液相色谱法灵敏、准确,适用于水源水及生活饮用水中痕量拟除虫菊酯类农药残留的检测。

     

    Abstract:
    [Objective] To establish a method for the simultaneous determination of 5 pyrethroids in source water or drinking water, i.e. fenpropathrin, cyhalothrin, deltamethrin, fenvalerate, and permethrin, using solid phase extraction combined with high performance liquid chromatography.

    [Methods] The water samples were extracted and condensed with solid-phase extraction using C18 cartridges and eluted by isopropanol. Separation was carried out on a Waters Sunfire C18 column, using acetonitrile and water as mobile phase gradient model at a flow rate of 1.0 mL/min, with detective wavelength at 205 nm. Quantification was calculated by an external standard method.

    [Results] The linear range of proposed determination methodology was 0.0-5.0 mg/L. The minimum detectable concentration was 0.025-0.050 μg/L. The recoveries were between 88.0% and 102.2% with a relative standard deviation in the range of 1.0%-3.8%.

    [Conclusion] The method is sensitive, accurate, and applicable to detect the trace pyrethroid residues in source water and drinking water.

     

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出版历程
  • 收稿日期:  2012-02-01
  • 刊出日期:  2017-06-23

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