Magnetic dispersive solid-phase extraction of triazole and triazine pesticides from vegetable samples using a hydrophilic-lipophilic sorbent based on maltodextrin- and β-cyclodextrin-functionalized graphene oxide

被引:16
|
作者
Majd, Mahshid [1 ]
Nojavan, Saeed [1 ]
机构
[1] Shahid Beheshti Univ, Dept Analyt Chem & Pollutants, Tehran 1983969411, Iran
关键词
beta-Cyclodextrin; Magnetic solid-phase extraction; Functionalized graphene oxide; Maltodextrin; Triazine herbicides; Triazole fungicides; Vegetable samples; EFFICIENT ADSORBENT; LIQUID-EXTRACTION; IONIC LIQUID; FUNGICIDES; NANOPARTICLES; MICROEXTRACTION; HERBICIDES;
D O I
10.1007/s00604-021-05039-x
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Maltodextrin- and beta-cyclodextrin-functionalized magnetic graphene oxide (mGO/beta-CD/MD), a novel hydrophilic-lipophilic composite, was successfully fabricated and used for the co-extraction of triazines and triazoles from vegetable samples before HPLC-UV analysis. mGO/beta-CD/MD was synthesized by chemical bonding of beta-CD and MD to the surface of mGO, using epichlorohydrin (ECH) as a linker. The successful synthesis of mGO/beta-CD/MD was confirmed by characterization tests, including attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), vibrating sample magnetometry (VSM), thermogravimetric analysis (TGA), energy-dispersive X-ray spectroscopy (EDX), Brunauer-Emmett-Teller (BET), and Barrett-Joyner-Halenda (BJH) analyses. The hydrophobic cavity of beta-CD and a large number of hydroxyl groups on the MD structure contributed to the co-extraction of mentioned pesticides with a wide range of polarity. Under the optimized condition (sorbent amount, 30 mg; desorption time, 10 min; desorption solvent volume, 300 mu L; desorption solvent, methanol/acetonitrile (1:1) containing 5% (v/v) acetic acid; extraction time, 20 min; and pH of sample solution, 7.0), good linearity within the range 1.0-1000 mu g L-1 (r(2) >= 0.992) was achieved. Extraction efficiencies were in the range 66.4-95.3%, and the limits of detection were 0.01-0.08 mu g L-1. Relative recoveries for spiked samples were obtained in the range 88.4-112.0%, indicating that the matrix effect was insignificant, and good precisions (intra- and inter-day) were also achieved (RSDs < 9.0%, n = 3). The results confirmed that the developed method was efficient for the determination of trace amounts of pesticides in potato, tomato, and corn samples.
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页数:12
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