职业与健康 ›› 2025, Vol. 41 ›› Issue (12): 1625-1629.

• 论著 • 上一篇    下一篇

离子色谱法同时测定饮用水中8种除草剂和植物生长调节剂

马晓曼1, 石红梅2, 李韵冰1, 张来颖1, 高丽红3, 王玉江1   

  1. 1.北京市丰台区疾病预防控制中心理化检验科,北京 100070;
    2.河北医科大学公共卫生学院,河北 石家庄 050017;
    3.赛默飞世尔科技(中国)有限公司,北京 100013
  • 收稿日期:2025-03-25 修回日期:2025-04-02 出版日期:2025-06-15 发布日期:2025-12-11
  • 通信作者: 王玉江,主任技师,E-mail:yujiangwang@126.com
  • 作者简介:马晓曼,女,主管技师,主要从事理化检验工作。
  • 基金资助:
    国家自然科学基金(82373626)

Simultaneous determination of eight herbicides and plant growth regulators in drinking water by ion chromatography

MA Xiaoman1, SHI Hongmei2, LI Yunbing1, ZHANG Laiying1, GAO Lihong3, WANG Yujiang1   

  1. 1. Department of Physical and Chemical Testing, Fengtai Center for Diseases Control and Prevention, Beijing 100070, China;
    2. School of Public Health, Hebei Medical University, Shjiazhuang, Hebei 050017, China;
    3. Thermo Fisher Scientific Inc, Beijing 100013, China
  • Received:2025-03-25 Revised:2025-04-02 Online:2025-06-15 Published:2025-12-11
  • Contact: WANG Yujiang,Chief technician,E-mail:yujiangwang@126.com

摘要: 目的 采用离子色谱法,建立前处理简单、仅需普通试剂,就可以达到同时测定饮用水中2,4-滴、调节膦、氨甲基膦酸、草铵膦、乙烯利、草甘膦、增甘膦和灭草松等8种除草剂和植物生长调节剂的检测方法。方法 水样依次经0.2 μm微孔滤膜和Ba/Ag/H柱过滤后上机,利用2~60 mmol/L氢氧化钾梯度淋洗程序,在IonPac AS19色谱柱得到有效分离,经抑制器降低背景值后用电导检测器检测。结果 8种待测物在0.002~0.200 mg/L(0.005~0.200 mg/L)浓度范围内线性关系良好,相关系数(r)均 >0.999;方法检出限为0.000 2~0.003 6 mg/L,定量限为0.000 6~0.011 1 mg/L;在低、中、高3个浓度添加水平的回收率为94.3%~108.6%,相对标准偏差(relative standard deviations,RSD)为0.592%~4.425%(n=7)。与国标法对比的检测结果差异无统计学意义(P>0.05)。结论 所建立的方法操作简单、分离效果好,准确性、精密度和灵敏度均较好,适用于饮用水日常监测任务。

关键词: 离子色谱, 饮用水, 除草剂, 植物生长调节剂, 同时测定

Abstract: Objective To develop a detection method for simultaneous determination of eight herbicides(including 2,4-D,fosamine,aminomethylphosphonic acid,glufosinate,ethephon,glyphosate,glyphosine,and bentazone) and plant growth regulators in drinking water by ion chromatography,which has a simple pretreatment process and only requires common reagents. Methods The water sample is sequentially filtered through a 0.2 μm microporous membrane and a Ba/Ag/H cartridge before being introduced into the system. The effective separation is achieved on an IonPac AS19 chromatographic column using a 2-60 mmol/L potassium hydroxide gradient elution program. After the background signal is reduced by a suppressor,the analytes are detected by a conductivity detector. Results The eight analytes exhibit excellent linearity within the concentration range of 0.002-0.200 mg/L(0.005-0.200mg/L),with correlation coefficients(r) all >0.999. The method demonstrates detection limits ranging 0.000 2-0.003 6 mg/L and quantification limits ranging 0.000 6-0.011 1 mg/L. At low,medium,and high spiked concentration levels,the recovery rates range from 94.3% to 108.6%,with relative standard deviations(RSD) between 0.592% and 4.425%(n=7). Compared with the national standard method,the detection results showed no statistically significant difference(P>0.05). Conclusion This method is characterized by its simplicity of operation,effective separation,and satisfactory accuracy,precision and sensitivity,making it suitable for routine monitoring of drinking water.

Key words: Ion chromatography, Drinking water, Herbicide, Plant growth regulators, Simultaneous determination

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