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作 者:兰腾芳[1,2] 郑尊涛[3] 李薇[1] 李莉[1]
机构地区:[1]中国科学院动物研究所,农业虫害鼠害综合治理研究国家重点实验室,北京100101 [2]长江大学农学院,湖北荆州434025 [3]农业部农药检定所,北京100125
出 处:《农药学学报》2013年第1期113-116,共4页Chinese Journal of Pesticide Science
摘 要:建立了同时测定生姜中8种酰胺类除草剂(炔苯酰草胺、敌稗、乙草胺、异丙甲草胺、甲草胺、丁草胺、丙草胺、苯噻草胺)残留的气相色谱(GC-ECD)分析方法。样品经乙酸乙酯超声提取(加入少量氢氧化钠溶液调节pH值至7),乙二胺-N-丙基硅烷(PSA)净化,气相色谱检测。结果表明:在0.01~1 mg/L范围内,8种除草剂的线性相关系数均大于0.995,检出限(LOD)为4~10μg/kg,定量限(LOQ)为0.05 mg/kg;在0.05、0.1和1 mg/kg 3个添加水平下的平均回收率在79.0%~111.2%之间,相对标准偏差(RSD)为0.9%~11.5%。An analytical method for the simultaneous determination of residues of 8 amide herbicides ( propyzamide, propanil, acetochlor, metolachlor, alachlor, butachlor, pretilachlor, mefenacet ) in fresh ginger using gas chromatography with electron capture detector (GC-ECD) was developed. The samples were extracted with ethyl acetate by ultrasonic, pH was adjusted to 7 with NaOH solution for reducing interference and further clean-up was carried out by primary secondary amine. It showed that good linearity was obtained between 0.01 and 1 mg/L with correlation coefficients above 0. 995. The limits of detection were 4 - 10 μg/kg and the limits of quantification were 0.05 mg/kg. Fortified recoveries at 0.05,0. 1 and 1 mg/kg were between 79.0% and 111.2% with the relative standard deviations (RSD) from 0.9 % to 11.5 %, respectively.
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