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基于磁性离子液体的搅拌棒分散液液微萃取法测定天然水中痕量挥发性多环芳烃

Trace determination of volatile polycyclic aromatic hydrocarbons in natural waters by magnetic ionic liquid-based stir bar dispersive liquid microextraction.

作者信息

Benedé Juan L, Anderson Jared L, Chisvert Alberto

机构信息

Department of Analytical Chemistry, University of Valencia, 46100 Burjassot, Valencia, Spain.

Department of Chemistry, Iowa State University, Ames, IA 50011, USA.

出版信息

Talanta. 2018 Jan 1;176:253-261. doi: 10.1016/j.talanta.2017.07.091. Epub 2017 Aug 1.

Abstract

In this work, a novel hybrid approach called stir bar dispersive liquid microextraction (SBDLME) that combines the advantages of stir bar sorptive extraction (SBSE) and dispersive liquid-liquid microextraction (DLLME) has been employed for the accurate and sensitive determination of ten polycyclic aromatic hydrocarbons (PAHs) in natural water samples. The extraction is carried out using a neodymium stir bar magnetically coated with a magnetic ionic liquid (MIL) as extraction device, in such a way that the MIL is dispersed into the solution at high stirring rates. Once the stirring is ceased, the MIL is magnetically retrieved onto the stir bar, and subsequently subjected to thermal desorption (TD) coupled to a gas chromatography-mass spectrometry (GC-MS) system. The main parameters involved in TD, as well as in the extraction step affecting the extraction efficiency (i.e., MIL amount, extraction time and ionic strength) were evaluated. Under the optimized conditions, the method was successfully validated showing good linearity, limits of detection and quantification in the low ng L level, good intra- and inter-day repeatability (RSD < 13%) and good enrichment factors (18 - 717). This sensitive analytical method was applied to the determination of trace amounts of PAHs in three natural water samples (river, tap and rainwater) with satisfactory relative recovery values (84-115%), highlighting that the matrices under consideration do not affect the extraction process.

摘要

在本研究中,一种名为搅拌棒分散液液微萃取(SBDLME)的新型混合方法被用于准确、灵敏地测定天然水样中的十种多环芳烃(PAHs)。该方法结合了搅拌棒吸附萃取(SBSE)和分散液液微萃取(DLLME)的优点。萃取过程使用涂覆有磁性离子液体(MIL)的钕搅拌棒作为萃取装置,通过高速搅拌使MIL分散于溶液中。搅拌停止后,MIL通过磁力吸附到搅拌棒上,随后进行热脱附(TD)并与气相色谱-质谱联用仪(GC-MS)系统相连。评估了热脱附以及影响萃取效率的萃取步骤中的主要参数(即MIL用量、萃取时间和离子强度)。在优化条件下,该方法成功得到验证,呈现出良好的线性关系、低纳克每升水平的检测限和定量限、良好的日内和日间重复性(相对标准偏差<13%)以及良好的富集因子(18 - 717)。该灵敏的分析方法被应用于测定三种天然水样(河水、自来水和雨水)中的痕量PAHs,获得了令人满意的相对回收率(84 - 115%),突出表明所考虑的基质不影响萃取过程。

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