A new Fe3O4-MWCNTs-reinforced hollow fiber solid/liquid phase microextraction-based natural deep eutectic solvent for determination of trace phthalate esters in aqueous samples using HPLC–DAD

IF 2.2 4区 化学 Q2 Engineering
Nabil N. AL-Hashimi, Qusi K. Alomoush, Amjad H. El-Sheikh, Nada A. Alsakhen, Thaer Barri, Jafar I. Abdelghani, Abdelrahim M. Alqudah
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Abstract

Herein, we present a new eco-friendly microextraction method based on the magnetite/multi-walled carbon nanotubes reinforced and natural deep eutectic-filled hollow fiber solid/liquid phase microextraction, abbreviated as HF-SLPME, combined with HPLC–DAD analysis. This method has been developed to determine trace levels of phthalate esters, including diethyl phthalate, benzyl butyl phthalate, and di-iso-butyl phthalate in urine, blood plasma, tap water, and groundwater samples. The natural deep eutectic solvents were prepared using terpenoid-derived natural compounds containing menthol and camphor in various ratios. The HF-SLPME device was constructed by reinforcing and immobilizing the synthesized Fe3O4-MWCNTs within the pores of a 2.5 cm segment of hollow fiber microtube through ultrasonication, followed by filling the lumen with the natural deep eutectic solvent with both ends heat sealing. The extraction process was conducted in direct immersion mode. Values of crucial variables for HF-SLPME were optimized through a multivariate methodology based on a central composite design, with 30 extraction tests performed to determine the best conditions. The method exhibited good linearity (correlation coefficients R2 > 0.996) over a dynamic range lower than 0.927–103 µg L−1. The results show that the limits of detection/quantification for the chosen PEs ranged from 0.19 to 0.27/ 0.65 to 0.92 µg L−1 with enrichment factor˃ 37.24. As evidenced by intra- and inter-day precisions, satisfactory reproducibility was achieved with relative standard deviations (RSDs) below 3.7% and 5.1%, respectively. The recoveries of the selected phthalate esters from spiked real samples ranged from 88.4 to 111.1%, with relative standard deviations between 2.3 and 6.5%. This HF-SLPME-HPLC–DAD method offered a new, cost-effective, sensitive microextraction approach for determining and quantifying phthalate esters in aqueous samples with complex matrices.

Abstract Image

基于天然深共晶溶剂的新型 Fe3O4-MWCNT 增强中空纤维固/液相微萃取技术,用于 HPLC-DAD 法测定水样中的痕量邻苯二甲酸酯类化合物
本文介绍了一种基于磁铁矿/多壁碳纳米管增强天然深共晶填充中空纤维固/液相微萃取(简称HF-SLPME)并结合HPLC-DAD分析的新型环保微萃取方法。该方法可用于检测尿液、血浆、自来水和地下水样品中邻苯二甲酸酯类化合物(包括邻苯二甲酸二乙酯、邻苯二甲酸丁苄酯和邻苯二甲酸二异丁酯)的痕量水平。天然深共晶溶剂是用含薄荷醇和樟脑的萜类天然化合物按不同比例制备的。高频-SLPME 装置的构建方法是:通过超声波将合成的 Fe3O4-MWCNT 加固并固定在 2.5 厘米长的中空纤维微管孔隙中,然后在管腔中注入天然深共晶溶剂,并将两端热封。萃取过程以直接浸泡模式进行。通过基于中心复合设计的多元方法对高频-SLPME 的关键变量值进行了优化,共进行了 30 次萃取试验,以确定最佳条件。在低于 0.927-103 µg L-1 的动态范围内,该方法表现出良好的线性关系(相关系数 R2 > 0.996)。结果表明,所选 PE 的检出/定量限为 0.19 至 0.27/ 0.65 至 0.92 µg L-1,富集因子˃ 37.24。从日内和日间的精确度来看,重现性令人满意,相对标准偏差(RSD)分别低于 3.7% 和 5.1%。在实际样品中添加所选邻苯二甲酸酯的回收率为 88.4% 至 111.1%,相对标准偏差为 2.3% 至 6.5%。这种高频-SLPME-HPLC-DAD方法为测定和定量复杂基质水样中的邻苯二甲酸酯类化合物提供了一种新的、经济有效的灵敏微萃取方法。
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来源期刊
Chemical Papers
Chemical Papers Chemical Engineering-General Chemical Engineering
CiteScore
3.30
自引率
4.50%
发文量
590
期刊介绍: Chemical Papers is a peer-reviewed, international journal devoted to basic and applied chemical research. It has a broad scope covering the chemical sciences, but favors interdisciplinary research and studies that bring chemistry together with other disciplines.
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