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液相色谱法测定饮用水中的九种氨基甲酸甲酯

Liquid chromatographic determination of nine N-methylcarbamates in drinking water.

作者信息

Morrica Patrizia, Fidente Paola, Seccia Serenella

机构信息

Department of Pharmaceutical and Toxicological Chemistry, University of Napoli 'Federico II', Via D. Montesano 49, 80131 Napoli, Italy.

出版信息

Biomed Chromatogr. 2005 Jan;19(1):107-10. doi: 10.1002/bmc.426.

Abstract

A multi-residue method for the simultaneous extraction from drinking water using solid-phase extraction on LiChrolut EN [poly(styrene-divinylbenzene), PSDVB] and determination of nine N-methylcarbamate pesticides (NMCs) (aldicarb, its metabolites i.e. aldicarb sulfone and aldicarb sulfoxide and carbaryl, carbofuran, dioxacarb, ethiofencarb, methomyl and propoxur) using reversed-phase liquid chromatography was studied. A 1000-fold pre-concentration was achieved and the method was used for determination of the nine pesticides in water, with limits of detection in the range 3-15 ng L(-1). For all compounds the recoveries determined at the 0.1 and 1 microg L(-1) level generally ranged from 85 to 104% with relative standard deviations (RSD) of 1.4-8.8%.

摘要

研究了一种多残留方法,该方法采用LiChrolut EN[聚(苯乙烯-二乙烯基苯),PSDVB]固相萃取从饮用水中同时萃取,并使用反相液相色谱法测定九种N-甲基氨基甲酸酯类农药(NMCs)(涕灭威及其代谢物涕灭威砜、涕灭威亚砜、西维因、克百威、恶虫威、乙硫苯威、灭多威和残杀威)。实现了1000倍预浓缩,该方法用于测定水中的九种农药,检测限在3-15 ng L(-1)范围内。对于所有化合物,在0.1和1 μg L(-1)水平测定的回收率一般在85%至104%之间,相对标准偏差(RSD)为1.4%-8.8%。

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