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Gas chromatographic method for the determination of hexaconazole residues in black tea*

机译:气相色谱法测定红茶中的六康唑残留量*

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摘要

A highly reliable, quantitative and sensitive analytical method for determining the residues of the fungicide, hexaconazole in black tea is described. The proposed method is based on liquid-liquid extraction followed by gas chromatographic determination, using nitrogen phosphorus detector (GC-NPD) for the identification and quantitation of hexaconazole. The most appropriate solvent mixture for extracting hexaconazole residues from black tea was n-hexane:acetone at 1:1 (v/v). The extract was cleaned up by adsorption column chromatography using activated florisil. Performance of the method was assessed by evaluating quality parameters such as recovery value, repeatability, reproducibility, linearity and limits of detection and quantitation. When the method was assessed for repeatability, the percentage of recovery ranged between 86% and 96% while the relative standard deviation was between 0.30% and 2.35%. In studies on reproducibility the recovery ranged from 81% to 85% and relative standard deviation from 1.68% to 5.13%, implying that the method was reliable. A field trial was conducted to verify the application of this method with real samples. Results prove that the validated method was suitable for extracting hexaconazole residues.
机译:描述了一种用于测定红茶中杀菌剂六康唑的残留量的高度可靠,定量和灵敏的分析方法。所提出的方法基于液-液萃取,然后进行气相色谱测定,使用氮磷检测器(GC-NPD)进行六康唑的鉴定和定量。从红茶中提取六康唑残留物的最合适的溶剂混合物是正己烷:丙酮(1:1(v / v))。通过使用活化的弗洛里西尔的吸附柱色谱法纯化提取物。该方法的性能通过评估质量参数(如回收率,重复性,再现性,线性度以及检测和定量限)进行评估。当评估该方法的可重复性时,回收率在86%至96%之间,而相对标准偏差在0.30%至2.35%之间。在可重复性研究中,回收率从81%到85%不等,相对标准偏差从1.68%到5.13%不等,这表明该方法是可靠的。进行了现场试验,以验证该方法在实际样品中的应用。结果证明该方法适用于提取六康唑残留物。

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