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Magnetic deep eutectic solvent-based ultrasoundassisted liquid-liquid microextraction for determination of hexanal and heptanal in edible oils followed by gas chromatography-flame ionization detection

机译:基于磁性深度共晶溶剂的超声波液体微萃取,用于测定食用油中己醛和庚醇的测定,然后是气相色谱 - 火焰电离检测

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摘要

Use of a novel magnetic deep eutectic solvent (MDES), consisting of the inexpensive and simple components [choline chloride/para-cresol] [FeCl4] was examined using ultrasound-assisted liquid-liquid microextraction and back-extraction methods to determine hexanal and heptanal in edible oils. The MDES was specified using vibrating sample magnetometry (VSM), proton nuclear magnetic resonance (H-1-NMR), CHN elemental analysis, as well as Raman and Fourier-transform-infrared (FT-IR) spectroscopy. Effective factors, including the volume of back-extraction solvent (L), MDES (L) volume, as well as extraction and back-extraction times (min) were optimized through a Box-Behnken design. Under optimal conditions, the calibration graphs of both analytes were linear at 0.05-100 mg L-1, with correlation coefficients 0.999. The limit of detection and limit of quantification was 19-25 g L-1 and 63-83 g L-1, respectively. This method was used to determine target analytes in spiked samples of edible oils; the relative mean recovery ranged from 94% to 102%.
机译:使用具有廉价和简单的组分[胆碱氯化物/对甲酚] [FECL4]的新型磁深共晶溶剂(MDES),采用超声辅助液 - 液 - 液体微萃取和后萃取方法检查己醛和庚烷在食用油中。使用振动样品磁体(VSM),质子核磁共振(H-1-NMR),CHN元素分析以及拉曼和傅立叶变换红外(FT-IR)光谱指定MDES。通过Box-Behnken设计优化了有效因素,包括背提取溶剂(L),MDES(L),MDES(L)的体积以及提取和后提取时间(min)。在最佳条件下,两种分析物的校准图是线性的,0.05-100mg L-1,相关系数& 0.999。定量的检测极限分别为19-25g L-1和63-83g L-1。该方法用于确定可食用油样品中的靶分析物;相对平均恢复范围为94%至102%。

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