4.6 Article

Magnetic micro-solid-phase-extraction of polycyclic aromatic hydrocarbons in water

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1440, 期 -, 页码 23-30

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2016.02.046

关键词

Magnetic chitosan; Graphene oxide; Micro-solid-phase-extraction; Gas chromatography-mass spectrometry

资金

  1. National University of Singapore Environmental Research Institute [R-706-000-100-414]
  2. Singapore National Research Foundation
  3. Singapore Economic Development Board (SPORE) [COY-15-EWI-RCFSA/N197-1]

向作者/读者索取更多资源

A novel sorbent, magnetic chitosan functionalized graphene oxide (MCFG) was synthesized and used in the micro-solid-phase-extraction (mu-SPE) and gas chromatography-mass spectrometric (GC-MS) analysis of polycyclic aromatic hydrocarbons (PAHs) from water. Through the use of the magnetic sorbent, the mu-SPE device also functioned as a stir bar during extraction. Three types of MCFG were prepared using glutaraldehyde cross-linked chitosan and graphene oxide with different amounts of magnetic nanoparticles (Fe3O4) (0.05 g, 0.07 g and 0.1 g). The material was characterized using Fourier transform infrared spectroscopy and field emission scanning electron microscopy. Parameters affecting the extraction such as the type of sorbent, extraction and desorption times, volume of sample solution and type of desorption solvent were optimized. Under the most favourable conditions, the highest extraction was obtained by using the composite prepared with 0.1 g of Fe3O4. For the latter material as sorbent, the linearity of the analytes was in the range of 0.01 and 100 mu g L-1 for naphthalene, fluoranthene and pyrene while acenaphthylene and phenanthrene exhibited linearity in the range of 0.05 and 100 mu g L-1. For fluorene and anthracene, the linearity range was from 0.01 to 50 mu g L-1. The coefficients of determination (r(2)) associated with the above linear ranges were higher than 0.987. The limits of detection from GC-MS analysis of the seven PAHs were in the range 0.2-1.8 ng L-1; limits of quantification were between 0.8 and 5.9 ng L-1 while the relative standard deviations (RSDs) varied from 2.1 to 8.2%. The recoveries of the method for the compounds at spiking levels of 1 and 5 mu g L-1 were in the range 67.5-106.9% with RSDs below 15%. The enrichment factors were found to be in between 67 and 302. The developed method afforded an interesting and innovative approach using MCFG as an efficient and promising sorbent. (C) 2016 Elsevier B.V. All rights reserved.

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