摘要:本实验采用三级四级杆液质联用仪,建立并优化了马铃薯和土壤中烯草酮的残留分析的方法。经优化后的方法为:在锥形瓶中称取样品5.00 g,加入20.0 mL超纯水,2.0 mL乙酸铅,加入20.0 mL乙腈,在摇床上摇晃2 h后抽滤,盐析,静置分层。取上层清液1 mL,用30 mgC18分散固相萃取填料进行净化,净化后的溶液用0.22 μm微孔滤膜过滤,装入进样小瓶上机。流动相为乙腈-水-甲酸(体积比60∶40∶0.1),流速0.3 mL/min;柱温为35 ℃;进样量4 μL。离子对360.1/164.1为定量离子,对烯草酮残留进行定量分析。实验进行了三个添加水平测试,分别为0.05 mg•kg-1、0.1 mg•kg-1和0.2 mg•kg-1,得到的平均回收率为85.3%~86.8%,相对平均偏差(RSD)小于5%。烯草酮在马铃薯上的最大残留限量为0.1 mg•kg-1,该方法的检出限为0.010 mg•kg-1,定量限为0.020 mg•kg-1,该方法的准确性、精确性以及灵敏度符合农药残留分析测定的要求。8930
关键字:烯草酮,残留分析,液质联用,马铃薯
Distribution of Clethodim in potato and soil
Abstract:In this study,we use the three quadrupole LC-MS instrument,the analysis method of clethodim residues in potato and soil is established and optimized.The method after optimization is: weigh 5.00 g sample in the conical flask,add 20.0 mL ultrapure water,2.0 mL lead acetate,20.0 mL acetonitrile, shaking 2 h in a shaker,filtration, salting rested,stratification.Take the supernatant fluid 1 mL,With 30 mgC18 dispersive solid-phase extraction packing for purificatio,after purification, the solution with 0.22 um microporous membrane filter, load the sample vial and Ready to machine.Mobile phase is acetonitrile - water - formic acid (volume ratio 60:40:0.1), the flow rate of 0.3 mL/min; Column temperature of 35 ℃; Sample quantity 4 uL.Ion on 360.1/164.1 is quantitative ion,ion pair 360.1/164.1 as a quantitative ion,analysis residues of clethodim.Experiment was carried out three add level test,respectively are 0.05 mg•kg-1,0.1 mg•kg-1,0.2 mg•kg-1.The average recovery was 85.3% ~ 85.3%, average relative deviation (RSD) is less than 5%.The method detection limit is 0.010 mg•kg-1, quantitative limit is 0.020 mg•kg-1, accuracy, precision and sensitivity of this method meets the requirement of pesticide residue analysis determination.
Keywords: Clethodim, residue analysis, LC-MS, potato