分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2014年
8期
1110-1116
,共7页
阮华%荣维广%宋宁慧%吉文亮%刘华良%马永建
阮華%榮維廣%宋寧慧%吉文亮%劉華良%馬永建
원화%영유엄%송저혜%길문량%류화량%마영건
QuEChERS%凝胶色谱-气相色谱-质谱%植物油%农药残留%快速筛查
QuEChERS%凝膠色譜-氣相色譜-質譜%植物油%農藥殘留%快速篩查
QuEChERS%응효색보-기상색보-질보%식물유%농약잔류%쾌속사사
QuEChERS%Gel permeation chromatography-gas chromatography-mass spectrometry%Vegetable oil%Pesticide residues%Fast screening
建立了葵花油、大豆油和玉米油中34种中高毒农药的快速筛查方法。样品采用改进的QuEChERS方法进行提取净化,提取液采用在线GPC-GC-MS检测。结果表明,34种农药在0.01~0.2 mg/L范围内具有良好的线性关系,相关系数为0.9913~0.9997。除p,p′-DDE, p,p′-DDD, p,p′-DDT外的31种农药在葵花油、大豆油和玉米油中的检出限分别为0.0692~2.28μg/kg,0.0559~2.01μg/kg,0.0584~2.14μg/kg;在0.05和0.1μg/g添加水平的平均回收率分别为70.3%~115.4%,69.5%~112.6%,70.2%~116.1%;相对标准偏差(RSD, n=6)分别为2.9%~13.3%,3.9%~13.5%,4.2%~12.1%。本方法具有操作便捷、快速等特点,适用于葵花油、大豆油和玉米油中34种农药残留的快速筛查与检测。
建立瞭葵花油、大豆油和玉米油中34種中高毒農藥的快速篩查方法。樣品採用改進的QuEChERS方法進行提取淨化,提取液採用在線GPC-GC-MS檢測。結果錶明,34種農藥在0.01~0.2 mg/L範圍內具有良好的線性關繫,相關繫數為0.9913~0.9997。除p,p′-DDE, p,p′-DDD, p,p′-DDT外的31種農藥在葵花油、大豆油和玉米油中的檢齣限分彆為0.0692~2.28μg/kg,0.0559~2.01μg/kg,0.0584~2.14μg/kg;在0.05和0.1μg/g添加水平的平均迴收率分彆為70.3%~115.4%,69.5%~112.6%,70.2%~116.1%;相對標準偏差(RSD, n=6)分彆為2.9%~13.3%,3.9%~13.5%,4.2%~12.1%。本方法具有操作便捷、快速等特點,適用于葵花油、大豆油和玉米油中34種農藥殘留的快速篩查與檢測。
건립료규화유、대두유화옥미유중34충중고독농약적쾌속사사방법。양품채용개진적QuEChERS방법진행제취정화,제취액채용재선GPC-GC-MS검측。결과표명,34충농약재0.01~0.2 mg/L범위내구유량호적선성관계,상관계수위0.9913~0.9997。제p,p′-DDE, p,p′-DDD, p,p′-DDT외적31충농약재규화유、대두유화옥미유중적검출한분별위0.0692~2.28μg/kg,0.0559~2.01μg/kg,0.0584~2.14μg/kg;재0.05화0.1μg/g첨가수평적평균회수솔분별위70.3%~115.4%,69.5%~112.6%,70.2%~116.1%;상대표준편차(RSD, n=6)분별위2.9%~13.3%,3.9%~13.5%,4.2%~12.1%。본방법구유조작편첩、쾌속등특점,괄용우규화유、대두유화옥미유중34충농약잔류적쾌속사사여검측。
A method for the simultaneous determination of 34 pesticides in sunflower oil, soybean oil and corn oil was developed. The samples were extracted and purified by a modified QuEChERS method, and then the supernatant was analyzed by on-line gel permeation chromatography-gas chromatography-mass spectrometry ( GPC-GC-MS ) . The linear range was from 0 . 01 to 0 . 2 mg/L with a good correlation coefficients ( r≥0. 9913). The average recoveries of 31 pesticides (except p,p′-DDE, p,p′-DDD, p,p′-DDT. For detail, please reference to section 3 . 6 ) ranged from 70 . 3% to 115 . 4%, 69 . 5% to 112 . 6% and 70 . 2% to 116 . 1%spiked at 0. 05 μg/g and 0. 1 μg/g with the relative standard deviations (RSDs, n=6) less than 13. 3%, 13. 5% and 12. 1% in sunflower oil, soybean oil and corn oil samples, respectively. The LODs of this method ranged from 0. 0692 to 2. 28, 0. 0559 to 2. 01 and 0. 0584 to 2. 14μg/kg (S/N=3) in sunflower oil, soybean oil and corn oil samples respectively. The convenient operation and versatility of this method are suitable for the fast screening and detection of 34 pesticide residues in sunflower oil, soybean oil and corn oil.