摘要
建立了人参中18种有机氯农药及其异构体残留量的气相色谱分析方法。样品以30mL石油醚-丙酮(1∶1,体积比)为提取剂,冰浴超声提取15 min,重复2次,提取液用浓硫酸净化,采用HP-5与DB1701毛细管色谱柱双柱定性分离,气相色谱-电子捕获检测器(GC-ECD)测定。结果表明:该方法在10、50、100μg/kg 3个水平下的添加回收率除艾氏剂与苯氟磺胺在62%左右外,其余分别在75.1%~107.7%、72.1%~98.6%和71.5%~105.4%,相对标准偏差(RSD)分别为2.5%~11.3%、2.6%~12.5%和1.1%~11.2%;方法的检出限为3.14μg/kg,定量限为10μg/kg。
A gas chromatographic method for determination of 18 organochlorine pesticides in Ginsene was established.Clean up by sulfonation treatment was optimized.The procedure involves ultrasonic extraction [acetone/petroleum ether(1∶ 1)as the extract solvent],concentrated sulphuric acid as clean-up method and determination by GC-ECD.Result showed that the percentage recoveries were 75.1%-107.7%,72.1%-98.6%,71.5%-105.4%(except aldrin and dichlofluanid were 62%),and the relative standard deviation(RSD) were 2.5%-11.3%,2.6%-12.5%,1.1%-11.2%.The limit of detection(LOD) of the method was 3.14 μg/kg,the limit of quantification(LOQ) was 10 μg/kg.
出处
《农药学学报》
CAS
CSCD
北大核心
2011年第3期299-303,共5页
Chinese Journal of Pesticide Science
基金
国家重大创新药专项(2009ZX09502-027
2009ZX09308-006
2009ZX09308-001-1-5)
关键词
人参
气相色谱
有机氯农药
多残留
Ginsene
gas chromatograohy
organochlorine pesticides
multiresidue