Enrichment and sensitive determination of phthalate esters in environmental water samples: A novel approach of MSPE-HPLC based on PAMAM dendrimers-functionalized magnetic-nanoparticles

被引:61
作者
Wu, Yalin [1 ]
Zhou, Qingxiang [1 ]
Yuan, Yongyong [1 ]
Wang, Hongyuan [1 ]
Tong, Yayan [1 ]
Zhan, Yali [1 ]
Sheng, Xueying [1 ]
Sun, Yi [1 ]
Zhou, Xianqi [1 ]
机构
[1] China Univ Petr, State Key Lab Petr Pollut Control, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
基金
中国国家自然科学基金;
关键词
Phthalate esters; Magnetic solid-phase extraction; PAMAM dendrimers; High performance liquid chromatography; Environmental water samples; SOLID-PHASE EXTRACTION; PERFORMANCE LIQUID-CHROMATOGRAPHY; ACID-ESTERS; MICROEXTRACTION; REMOVAL; GRAPHENE; CARBON; ADSORPTION; ADSORBENTS; METALS;
D O I
10.1016/j.talanta.2019.120213
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Phthalate esters (PAEs) are an important kind of environmental endocrine disrupting chemicals, and have attracted great attention in environmental field. Present study described a new method for rapid and sensitive determination of PAEs including dibenzyl phthalate (DPhP), dibutyl phthalate (DnPP), and dicyclohexyl phthalate (DCHP) from aqueous matrices based on magnetic solid-phase extraction. Polyamidoamine (PAMAM) dendrimers-grafted magnetic-nanoparticles were synthesized and characterized, and the expected integration of more multifunctional sites of PAMAM dendrimers and rapid separation property was utilized for method development. To achieve the best extraction efficiency, several important parameters were optimized including the dosage of the adsorbent, sample pH, kind and volume of eluent, extraction time, desorption time, ionic strength. Under the optimal conditions, three phthalate esters were well enriched and simultaneously determined by high performance liquid chromatography with variable wavelength detector (VWD). Excellent linearities were observed in the range of 0.1-600 mu g L-1 for DPhP and DnPP and 0.5-600 mu g L-1 for DCHP, and all correlation coefficients (R-2) were larger than 0.997. The limits of detection (LODs, S/N = 3) were ranged from 0.025 to 0.16 mu g L-1. The spiked recoveries of PAEs in real water samples were in the range of 93.5-101.8% with satisfied relative standard deviations (RSDs) ranging from 0.9 to 4.1%. The prepared magnetic materials have shown good adsorption capability for PAEs and the developed method earned merits such as high sensitivity, simplicity, rapidness and environmental friendliness, which can be used as a robust alternative tool for monitoring PAEs in water samples.
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页数:10
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