4.6 Article

Magnetic covalent triazine framework for rapid extraction of phthalate esters in plastic packaging materials followed by gas chromatography-flame ionization detection

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1525, Issue -, Pages 32-41

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2017.10.025

Keywords

Magnetic covalent triazine framework composite; Magnetic solid phase extraction; Phthalate esters; Gas chromatography-flame ionization detection; Plastic packaging materials

Funding

  1. National Nature Science Foundation of China [21575107, 21575108, 21675118]
  2. Science Fund for Creative Research Groups of NSFC [20921062]
  3. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences [KF2010-04]
  4. Large-scale Instrument and Equipment Sharing Foundation of Wuhan University [LF20170799]

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Covalent triazine frameworks (CTFs), featuring with high surface area, good thermal, chemical and mechanical stability, are good adsorbents in sample pretreatment. Herein, magnetic CTFs/Ni composite was prepared by in situ reduction of nickel ions on CTFs matrix with a solvothermal method. The prepared CTFs/Ni composite exhibited good preparation reproducibility, high chemical stability, and high extraction efficiency for targeted phthalate esters (PAEs) due to pi-pi interaction and hydrophobic effect. The porous structure of CTFs/Ni composite benefited the fast transfer of target PAEs from aqueous solution to the adsorbents, and the integrated magnetism contributed to the rapid separation of adsorbents from sample and elution solution. Based on it, a novel method of magnetic solid phase extraction (MSPE) combined with gas chromatography-flame ionization detector (GC-FID) was developed for the analysis of PAEs including dimethyl phthalate (DMP), diethyl phthalate (DEP), di-n-butyl phthalate (DBP), benzyl butyl phthalate (BBP), di-2-ethylhexl phthalate (DEHP), and di-n-octyl phthalate (DNOP) in plastic packaging materials. Under the optimal experimental conditions, the limits of detection (LODs, S/N = 3) for six PAEs were found to be in the range of 0.024-0.085 mg/kg. The linear range was 0.32-16 mg/kg for DMP, DEP, 0.08-80 mg/kg for DBP, 0.16-32 mg/kg for BBP, DEHP, and 0.32-32 mg/kg for DNOP, respectively. The enrichment factors ranged from 59 to 88-fold (theoretical enrichment factor was 133-fold). The proposed method was successfully applied to the analysis of PAE5 in various plastic packaging materials with recoveries in the range of 70.6-119% for the spiked samples. This method is characterized with short operation time, high sensitivity, low consumption of harmful organic solvents and can be extended to the analysis of other trace aromatic compounds. (C) 2017 Elsevier B.V. All rights reserved.

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