Ionic-liquid-modified magnetic nanoparticles as a solid-phase extraction adsorbent coupled with high-performance liquid chromatography for the determination of linear alkylbenzene sulfonates in water samples

萃取(化学) 色谱法 化学 固相萃取 洗脱 磁性纳米粒子 吸附 离子强度 离子液体 傅里叶变换红外光谱 检出限 十二烷基苯磺酸钠 样品制备 纳米颗粒 分析化学(期刊) 材料科学 肺表面活性物质 水溶液 化学工程 有机化学 工程类 纳米技术 催化作用 生物化学
作者
Junyu Lu,Fanggui Ye,Xiuxiang Huang,Lianqiang Wei,Dongmei Yao,Shengying Li,Miao Ou-Yang,Hongfang Lai
出处
期刊:Journal of Separation Science [Wiley]
卷期号:40 (5): 1133-1141 被引量:13
标识
DOI:10.1002/jssc.201601144
摘要

Novel ionic-liquid-functionalized Fe3O4 magnetic nanoparticles were synthesized by the thiol-ene click reaction. The prepared functionalized Fe3O4 nanoparticles possessed multiple interactions, such as electrostatic, hydrophobic, and π–π interactions. The functionalized Fe3O4 nanoparticles were characterized by using Fourier transform infrared spectroscopy, X-ray diffraction, vibrating sample magnetometry, and transmission electron microscopy. Four kinds of linear alkylbenzene sulfonates, namely, sodium decylbenzenesulfonate, sodium undecylbenzene sulfonate, sodium dodecylbenzenesulfonate, and sodium tridecylbenzenesulfonate, were selected as model compounds to evaluate the applicability of adsorbents for extraction and subjected to high-performance liquid chromatography analysis. In addition, the effects of various parameters, such as sorbent amount, pH value, ionic strength, sample volume, extraction time, and elution conditions on extraction efficiency were studied in detail. Under the optimum conditions, good linearities were attained, with correlation coefficients between 0.9912 and 0.9968. The proposed method exhibited limits of detection ranging from 0.061 to 0.099 μg/L for all the target analytes. The spiked recoveries of the target analytes in real water samples ranged from 86.3 to 107.5%, with relative standard deviations lower than 7.96%. The enrichment factors of the analytes ranged from 364 to 391, indicating that the obtained functionalized Fe3O4 nanoparticles can effectively extract trace target analytes from environmental water samples.

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