Development of an effervescence‐assisted dispersive liquid phase microextraction using a binary solvent as a simultaneous extraction and preconcentration approach specialized for the analysis of pesticides in grape juice without dilution

IF 1.3 Q4 CHEMISTRY, ANALYTICAL
M. Farajzadeh, Ali Hoboobi, S. Pezhhanfar, M. Mogaddam
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Abstract

In this study, a swift and economical extraction and preconcentration method called effervescence‐assisted dispersive liquid‐phase microextraction was developed to analyze the pesticide content of different grape juices. To propel the microextraction method, the sample was transferred to a conical bottom glass test tube, and ammonium chloride was added and vortexed to dissolve. Then, sodium bicarbonate and a mixture of 1,2‐dibromoethane and n‐hexane were added. The tube was located in a water bath and the produced carbon dioxide bubbles dispersed the extraction solvent into the sample. Finally, it was centrifuged and one microliter of the sedimented phase was injected into a gas chromatograph equipped with a flame ionization detector. Under the optimum conditions, the limits of detection and quantification ranged from 0.9 to 4.1 and 3.0 to 13.6 μg/L, respectively. Extraction recoveries and enrichment factors were achieved in the ranges of 36%–80% and 180%–404%, respectively. The inter‐ and intra‐day relative standard deviations were in the ranges of 3.4%–10.6% and 2.6%–9.7%, respectively. Also, the coefficients of determination in the calibration curves were ≥0.990. Short extraction time, no sorbent or costly apparatuses, using inexpensive chemicals, applying microliter levels of the extractant, and no dilution of the real samples are the highlights of the study.
开发一种使用二元溶剂的起泡辅助分散液相微萃取法,作为一种无需稀释即可同时进行萃取和预浓缩的分析葡萄汁中农药的专用方法
本研究建立了一种快速、经济的萃取预浓缩方法——气泡辅助分散液相微萃取法,用于分析不同葡萄汁中农药的含量。为了推进微萃取方法,将样品转移到锥形底玻璃试管中,加入氯化铵并旋转溶解。然后,加入碳酸氢钠和1,2 -二溴乙烷和正己烷的混合物。该管位于水浴中,产生的二氧化碳气泡将萃取溶剂分散到样品中。最后将沉淀相离心,取1微升注入装有火焰电离检测器的气相色谱仪中。在最佳条件下,检测限为0.9 ~ 4.1 μg/L,定量限为3.0 ~ 13.6 μg/L。提取回收率为36% ~ 80%,富集系数为180% ~ 404%。日间和日间的相对标准偏差分别在3.4%-10.6%和2.6%-9.7%之间。校正曲线的决定系数均≥0.990。提取时间短,不需要吸附剂或昂贵的仪器,使用廉价的化学品,使用微升级别的萃取剂,不稀释实际样品是该研究的亮点。
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来源期刊
SEPARATION SCIENCE PLUS
SEPARATION SCIENCE PLUS CHEMISTRY, ANALYTICAL-
CiteScore
1.90
自引率
9.10%
发文量
111
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