固相微萃取
色谱法
新烟碱
杀虫剂
化学
相(物质)
气相色谱-质谱法
益达胺
有机化学
农学
生物
质谱法
作者
Musiiwa V. Sengane,Masixole Sihlahla,Philiswa N. Nomngongo,Nomvano Mketo
标识
DOI:10.1016/j.sampre.2025.100152
摘要
A greener sample preparation method based on magnetic solid phase microextraction (MSPμE) was developed for the preconcentration of neonicotinoid pesticides (acetamiprid, imidacloprid, thiacloprid and thiamethoxam) in vegetable oil samples followed by separation and quantification using high performance liquid chromatography with diode array detector (HPLC-DAD). Different characterisation techniques such as Fourier Transform Infrared Spectroscopy (FTIR), Powder X-ray diffraction analysis (PXRD), Thermogravimetric Analysis (TGA), Transmission electron microscopy (TEM), and scanning electron microscope and energy-dispersive X-ray spectroscopy (SEM-EDS) confirmed the synthesised magnetic nano adsorbents (Fe 3 O 4 , Fe 3 O 4 @Al 2 O 3 and Fe 3 O 4 @Al 2 O 3 /AC). The most influential parameters affecting MSPμE of NEOs by Fe 3 O 4 @Al 2 O 3 /AC were examined using a multivariate optimisation approach and 8 min extraction time, 13 pH, 9 mg adsorbent mass, and 0.5 mL eluent volume were optimal parameters. The proposed Fe3O4@Al2O3/AC method showed high accuracy (80–119.21%) and precision (≤10 %) for all the investigated NEOs. Additionally, the obtained limit of detection (LOD) ranged from 0.5–1.76 ng µL -1 , the limit of quantification (LOQ) ranged from 1.87–6.62 ng µL -1 and satisfactory high preconcentration factors (73.02- 407.0) were comparable with literature reported studies. The Analytical GREEness calculator AGREE, BAGI and NEMI analysis confirmed greenness of MSPμE. After that, the validated MSPμE method was applied to real vegetable oil samples (avocado, canola, olive and sunflower), and fortunately, all the investigated NEOs were below LODs of the proposed MSPμE /HPLC-DAD methods.
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