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首页> 外文期刊>Journal of separation science. >Extraction and preconcentration technique for triazole pesticides from cow milk using dispersive liquid-liquid microextraction followed by GC-FID and GC-MS determinations
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Extraction and preconcentration technique for triazole pesticides from cow milk using dispersive liquid-liquid microextraction followed by GC-FID and GC-MS determinations

机译:分散液-液微萃取-GC-FID和GC-MS测定牛奶中三唑类农药的提取和预浓缩技术

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摘要

A simple and rapid dispersive liquid-liquid microextraction (DLLME) technique coupled with gas chromatography-flame ionization detection (GC-FID) and gas chromatography-mass spectrometry (GC-MS) was developed for the extraction, preconcentration, and analysis of triazole pesticides (penconazole, hexaconazole, tebuconazole, triticonazole, and difenoconazole) in cow milk samples. Initially to 5 mL milk sample, NaCl and acetonitrile were added as salting-out agent and extraction solvent, respectively. After manual shaking, the mixture was centrifuged. In the presence of sodium chloride, a two-phase system was formed: upper phase, acetonitrile containing triazole pesticides and lower phase, aqueous phase containing soluble compounds and the precipitated proteins. After the extraction of pesticides from milk, a portion of supernatant phase (acetonitrile) was removed, mixed with chloroform at microliter level and rapidly injected by syringe into 5 mL distilled water. In this process, triazole pesticides were extracted into fine droplets of chloroform (as extraction solvent). After centrifugation, the fine droplets of chloroform were sedimented in bottom of the conical test tube. Finally, GC-FID and GC-MS were used for the separation and determination of analytes in the sedimented phase. Some important parameters like type of solvent for extraction of pesticides from milk, salt amount, the volume of extraction solvent, etc., which affect the extraction efficiency, were completely studied. Under the optimum conditions, enrichment factors were in the range of 156-380. The linear ranges of calibration curves were wide and limits of detection (LODs) and limits of quantification (LOQs) were between 4-58 and 13-180 μg/L, respectively. This method is very simple and rapid, requiring <15 min for sample preparation.
机译:结合气相色谱-火焰电离检测(GC-FID)和气相色谱-质谱(GC-MS),开发了一种简单快速的分散液-液微萃取(DLLME)技术,用于三唑类农药的提取,预浓缩和分析。 (牛奶中的苯康唑,六康唑,戊唑醇,曲康唑和苯甲酰氟康唑)。最初,向5 mL牛奶样品中分别添加NaCl和乙腈作为盐析剂和提取溶剂。手动摇动后,将混合物离心。在氯化钠的存在下,形成两相系统:上层相,含三唑农药的乙腈和下层相,含可溶性化合物和沉淀蛋白质的水相。从牛奶中提取农药后,除去一部分上清相(乙腈),以微升水平与氯仿混合,并通过注射器快速注入5 mL蒸馏水中。在此过程中,将三唑类农药提取为氯仿细小滴(作为提取溶剂)。离心后,氯仿的细小液滴沉淀在锥形试管的底部。最后,GC-FID和GC-MS用于分离和测定沉淀相中的分析物。全面研究了影响牛奶提取效率的重要参数,如牛奶中农药的提取溶剂类型,盐分,提取溶剂的体积等。在最佳条件下,富集因子在156-380之间。校准曲线的线性范围宽,检测限(LOD)和定量限(LOQ)分别在4-58和13-180μg/ L之间。该方法非常简单,快速,样品准备时间不到15分钟。

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