A hybrid material composed of graphitic carbon nitride and magnetite (Fe3O4) for magnetic solid-phase extraction of trace levels of hydroxylated polycyclic aromatic hydrocarbons

被引:26
作者
Nian, Qixun [1 ]
Wang, Xuesheng [1 ]
Wang, Manman [1 ]
Zuo, Guifu [2 ]
机构
[1] North China Univ Sci & Technol, Sch Publ Hlth, 21 Bohai Rd, Tangshan 063210, Hebei, Peoples R China
[2] North China Univ Sci & Technol, Coll Mat Sci & Engn, 21 Bohai Rd, Tangshan 063210, Hebei, Peoples R China
关键词
Carbon-based materials; Magnetic composites; Adsorbent; Solvothermal method; Sample pretreatment; Urinary metabolites; Biological sample analysis; Urine; High performance liquid chromatography; Fluorescence detection; METABOLITES; NANOPARTICLES; EXPOSURE; FACILE; PAHS; MICROEXTRACTION; QUANTIFICATION; ADSORPTION; RISK;
D O I
10.1007/s00604-019-3607-2
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Magnetic carbon nitride composites were synthesized via a solvothermal reaction and developed as an effective adsorbent for magnetic solid-phase extraction of trace hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) from urine samples prior to their determination by HPLC. The sorbent was characterized by Fourier transform infrared spectrometry, X-ray diffractometry, scanning electron microscopy, vibrating sample magnetometry and solvent stability experiments. The adsorption of hydroxy-PAHs is better by a factor or 20 to 49 compared to bare Fe3O4 and comparable that of a commercial C-18 sorbent. The adsorbent amount, adsorption time and eluting solvent and volume were optimized. The complete extraction for the OH-PAHs at a level of 40ngmL(-1) and by using 4mg sorbent is completed within 3min. With an enzymatic hydrolyzed urine sample loading volume of 2mL, enhancement factors in the range of 9-10, and a limit of detection (at S/N=3) of 0.08ng.mL(-1) were achieved. The method showed a linear response in the 0.25-250ng.mL(-1) hydroxy-PAH concentration range, and intra-day and inter-day precisions are 1.5-7.7% and 2.2-8.7%, respectively. The recovery from spiked urine samples ranged from 90.1% to 102%. The sorbent was stable over 10 successive cycles of extraction/desorption of urine sample without significant loss of extraction efficiency. The method was successfully applied for the determination of OH-PAHs in urine samples of smoking volunteers.
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页数:9
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