4.7 Article

Effervescence-assisted dual microextraction of PAHs in edible oils using lighter-than-water phosphonium-based ionic liquids and switchable hydrophilic/hydrophobic fatty acids

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 413, 期 7, 页码 1983-1997

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03167-0

关键词

Effervescent microextraction; Low-density phosphonium-based ionic liquid; Fatty acid; Polycyclic aromatic hydrocarbons; Edible oil

资金

  1. Natural Science Foundation of China [21876125, 22076134]
  2. Zhejiang Provincial Natural Science Foundation [LY19B070010]
  3. Wenzhou Science and Technology Project [S20180025]
  4. National Innovation and Entrepreneurship Training Program for College Students [201910343059S]
  5. Research and Development Fund of Wenzhou Medical University [QTJ19018]

向作者/读者索取更多资源

A novel effervescence-assisted dual microextraction method, combining phosphonium-based ionic liquids and switchable hydrophilic/hydrophobic fatty acids, was developed for quick extraction of polycyclic aromatic hydrocarbons in edible oils. The optimized method showed high accuracy and precision in detecting six PAHs in edible oils, indicating great potential for practical application.
Herein, we developed a novel effervescence-assisted dual microextraction method, abbreviated as EM-LPSH, using lighter-than-water phosphonium-based ionic liquids (LPILs) and switchable hydrophilic/hydrophobic fatty acids (SHFAs). The EM-LPSH method was utilized for quick enrichment/extraction of polycyclic aromatic hydrocarbons (PAHs) in edible oils. Owing to lower density than water, LPILs used as the first extractant were floated on the upper layer of the aqueous phase, leading to a convenient separation/collection compared with traditional heavier-than-water imidazolium-based ionic liquids. Interestingly, SHFAs play triple functions: a dispersive solvent in the microextraction process, an acidic source in effervescent reaction, and the second extractant in dual microextraction, due to switchability from hydrophilicity to hydrophobicity. Consequently, the integration of LPILs with SHFAs greatly enhanced the extraction efficiency for PAHs owing to the quick dual microextraction process. Some important variables were rigorously optimized using a one-factor-at-a-time approach. Under optimized conditions, the EM-LPSH/HPLC-FLD method provided a wide linear range (0.07 similar to 0.63-200 mu g kg(-1)), satisfactory recovery (80.12-103.27%), and low limit of detection (0.02-0.19 mu g kg(-1)), as well as high intra-day and inter-day precision (0.03-6.55) for six PAHs in edible oils. By using certified reference material in olive oil samples (GBW10162), the recoveries ranged from 97.40 to 98.39%, demonstrating high accuracy and precision. According to the detected levels of PAHs in six unheated and heated oils, their edible safety was evaluated in detail. In short, the newly developed method is simple, convenient, and highly efficient, thereby showing great prospects for application in conventional monitoring of trace-level PAHs in edible oils.

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