4.6 Article

Polydopamine-reinforced magnetization of zeolitic imidazolate framework ZIF-7 for magnetic solid-phase extraction of polycyclic aromatic hydrocarbons from the air-water environment

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1452, Issue -, Pages 18-26

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2016.05.039

Keywords

Zeolitic imidazolate framework; Polycyclic aromatic hydrocarbons; PM2.5; Magnetic solid-phase microextraction

Funding

  1. National Natural Science Foundation of China [21305026, 41271249]
  2. Chinese Ministry of Science and Technology [2014BAC16B01]
  3. Zhejiang Provincial Natural Science Foundation of China [LQ13B050005]
  4. Scientific Research Foundation of Hangzhou Dianzi University [KYS205612034]

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Zeolitic imidazolate frameworks (ZIFs) consist of metal nodes connected to imidazolate linkers, having both the properties of metal-organic frameworks (MOFs) and inorganic zeolites, such as controllable pore sizes, high porosity and surface areas, as well as exceptional thermal and chemical stability, thereby making them a class of attractive materials for diverse analytical applications. In this study, we reported a facile magnetization process of ZIF-7 (zinc benzimidazolate) for simultaneous magnetic extraction of polycyclic aromatic hydrocarbons (PAHs) by simply mixing ZIF-7 and polydopamine (PDA)-coated Fe3O4 nanoparticles (PDA@Fe3O4) in solutions. Functional groups (-OH and -NH2), provided by PDA as a highly efficient molecular linker, could attract and anchor ZIF-7 through noncovalent adsorption and covalent cross-link interactions, thereby promoting the complete magnetization of ZIFs and enhancing their stability and reusability. The bridging ligand benzimidazolate, could be bonded with PAHs because of its high surface area, large pores, accessible coordinative unsaturated sites (pi-complexation), and,pi-pi stacking action. This ZIF-based magnetic solid-phase extraction (SPE), coupled with gas chromatography/tandem mass spectrometry (GC/MS), was further evaluated for analysis of PAHs from rainwater and air samples of particulate matter less than 2.5 mu m in diameter (PM2.5). The main effective parameters, including ionic strength, solution pH, extraction time, desorption solvent and desorption time, were investigated, respectively. Under optimized conditions, the developed method based on Fe3O4@PDA/ZIF-7 gave detection limits of 0.71-5.79 ng/L, and quantification limits of 2.50-19.2 ng/L for PAHs, respectively. The relathie standard deviations for intra-day and inter-day analyses were in the range of 3.1-9.1% and 6.1-12.7%, respectively. The PAHs founded in PM2.5 were in the range of 0.40-6.79 ng/m(3). Good recoveries (>82%) with low relative standard deviations (<9.2%) were achieved. This method was demonstrated to be an accurate, convenient and sensitive pretreatment procedure for trace analysis of environmental water and air samples. (C) 2016 Elsevier B.V. All rights reserved.

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