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    磁固相萃取-高效液相色谱-串联质谱法测定环境水样中的苯脲类除草剂残留

    Determination of Phenylurea Herbicide Residues in Environmental Water by High Performance Liquid Chromatography-Tandem Mass Spectrometry Coupled with Magnetic Solid Phase Extraction

    • 摘要: 通过水热合成法制备磁性类沸石咪唑酯材料(Fe3O4@ZIF-8),采用扫描电子显微镜、透射电子显微镜和傅里叶变换红外光谱仪对该材料进行表征。将50 mg Fe3O4@ZIF-8加入100 mL水样中,于40℃振荡吸附10 min后,将Fe3O4@ZIF-8进行磁分离,弃去水样,加入0.5 mL乙腈,涡旋解吸1 min,将洗脱液转移,重复解吸3次,合并洗脱液,用氮气吹至近干后用甲醇-0.1%(体积分数)甲酸溶液(6+4)混合溶液溶解并定容至500 μL,经0.22 μm有机滤膜过滤,滤液在Agilent Zorbax Eclipse XDB-C18反相色谱柱(50 mm×3 mm,1.8 μm)上分离,以甲醇-0.1%(体积分数)甲酸溶液为流动相进行梯度洗脱,质谱分析中采用电喷雾离子源和多反应监测模式。4种苯脲类除草剂质量浓度均在0.01~20.0 μg·L-1内与峰面积呈线性关系,检出限(3S/N)为1.03~3.00 ng·L-1。对空白水样进行加标回收试验,回收率在78.8%~106%之间,相对标准偏差(n=6)小于7.0%。

       

      Abstract: The magnetic zeolitic imidazole ester material (Fe3O4@ZIF-8) was prepared by hydrothermal synthesis method, and was characterized by scanning electron microscope, transmission electron microscope and Fourier transform infrared spectrometer. 50 mg of Fe3O4@ZIF-8 was added to 100 mL of water sample, and the mixture was shaken at 40℃ for 10 min of adsorption. After Fe3O4@ZIF-8 was magnetically separated and the water sample was discarded, 0.5 mL of acetonitrile was added and the mixture was vortexed for 1 min for desportion, the eluate was transferred, and desorption was repeated three times. The combined eluate was dried by nitrogen blowing, the residue was dissolved with a mixed solution of methanol and 0.1% (φ) formic acid solution (6+4), and the volume of the solution was made up to 500 μL. After the solution was filtered through a 0.22 μm organic filter, the filtrate was seperated on an Agilent Zorbax Eclipse XDB-C18 chromatographic column (50 mm×3 mm, 1.8 μm), with a mixture of methanol and 0.1% (φ) formic acid solution as the mobile phase for gradient elution. Electrospray ion source and multi-reaction monitoring mode were selected in mass spectrometry analysis. Linear relationships were found between peak areas of 4 phenylurea herbicides and the corresponding mass concentrations in the same range of 0.01-20.0 μg·L-1, and the detection limits (3S/N) were in the range of 1.03-3.00 ng·L-1. Test for recovery was made by standard addition method to blank sample, giving results in the range of 78.8%-106%, with RSDs (n=6) less than 7.0%.

       

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