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Fe3O4@SiO2@VAN Nanoadsorbent Followed by GC-MS for the Determination of Polycyclic Aromatic Hydrocarbons at Ultra-Trace Levels in Environmental Water Samples

Nanomaterials 2022 9 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Yu Tian, Zhigang Xu, Zhimin Liu, Xiaoxi Si, Fengmei Zhang, Wei Jiang

Summary

Researchers synthesized vancomycin-functionalized silica-coated magnetic nanoparticles (Fe3O4-SiO2-VAN) for magnetic solid-phase extraction of polycyclic aromatic hydrocarbons from environmental water samples, achieving detection limits of 0.03 to 0.16 micrograms per liter with extraction recoveries of 82 to 116% and relative standard deviations under 13% when coupled to GC-MS analysis.

Study Type Environmental

In the present study, silica-coated magnetic nanoparticles functionalized with vancomycin (Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>@VAN) were synthesized. The Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>@VAN nanocomposite was used as a sorbent for the magnetic solid-phase extraction (MSPE) of polycyclic aromatic hydrocarbons (PAHs) from environmental water, followed by GC-MS. The nanocomposite was characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, vibrating sample magnetometry, and nitrogen sorption. Various experimental parameters were optimized, including extraction condition and desorption condition. Results show that Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>@VAN combined the advantages of nanomaterials and magnetic separation technology, showing excellent dispersibility and high selectivity for PAHs in environmental water sample. Under the optimal extraction conditions, an analytical method was established with the sensitive limit of detection (LOD) of 0.03-0.16 μg L<sup>-1</sup>. The method was successfully applied for the analysis of environmental water samples. The relative standard deviations (%) were in the range of 0.50-12.82%, and the extraction recovery (%) was in the range of 82.48% and 116.32%. MSPE-coupled gas chromatography-mass spectrometry quantification of PAHs is an accurate and repeatable method for the monitoring of PAH accumulation in environmental water samples. It also provides an effective strategy for the tracing and quantification of other environmental pollutants in complex samples.

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