首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of the limits of identification and quantitation of selected organochlorine and organophosphorous pesticide residues in surface water by full-scan gas chromatography/mass spectrometry
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Determination of the limits of identification and quantitation of selected organochlorine and organophosphorous pesticide residues in surface water by full-scan gas chromatography/mass spectrometry

机译:全扫描气相色谱/质谱法测定地表水中选定的有机氯和有机磷农药残留的鉴定和定量限

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In this work, we report a reliable method for quantitation and determination of the limits of identification of 14 organochlorine and organophosphorous pesticide (OPP) residues in surface water. The method features the simultaneous identification and quantitation of targeted pesticides and the possibility of identification of any other eluting compounds. The method is based on liquid-liquid extraction (LLE) with a mixture of petroleum ether and dichloromethane (70:30, v/v) followed by gas chromatographic separation and a full-scan mass spectrometric detection (GC-MS). The method presents a new validation parameter, limit of identification (LOI) which is defined for our purpose as the lowest analyte concentration that yields a library searchable mass spectrum. The method is linear over the range 0.048-1.20 mu g L (1) for nine pesticides and 0.024-0.60 mu g L-1 for the other five pesticides. Correlation coefficients vary between 0.988 and 0.998. Limits of detection (LODs) vary between 0.005 and 0.05 mu g L-1 for 4,4'-DDT and LOIs vary between 0.012 and 0.048 mu g L-1 (c) 2005 Elsevier B.V. All rights reserved.
机译:在这项工作中,我们报告了一种可靠的定量和确定地表水中14种有机氯和有机磷农药(OPP)残留限量的方法。该方法具有目标农药的同时鉴定和定量以及鉴定其他洗脱化合物的可能性。该方法基于用石油醚和二氯甲烷(70:30,v / v)的混合物进行液-液萃取(LLE),然后进行气相色谱分离和全扫描质谱检测(GC-MS)。该方法提供了一个新的验证参数,即鉴定极限(LOI),出于我们的目的,该极限被定义为产生库可检索质谱的最低分析物浓度。该方法在9种农药的0.048-1.20μg L(1)和其他5种农药的0.024-0.60μg L-1范围内是线性的。相关系数在0.988和0.998之间变化。 4,4'-DDT的检出限(LOD)在0.005至0.05μg L-1之间,LOI在0.012至0.048μgL-1之间变化(c)2005 Elsevier B.V.保留所有权利。

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