关键词: 共价有机骨架, 点击反应, 全氟化合物

Abstract:

Perfluorinated compounds (PFCs) are widely used in textiles, fire protection, metal electroplating, and semiconductor production owing to their hydrophobic and oil-repellent characteristics. However, they are also persistent organic pollutants. The uncontrolled discharge of PFCs into the environment has led to serious global pollution. PFCs pose severe reproductive, neural, immune, and other threats to human health by accumulating through the food chain. Thus, the development and application of high-performance extraction materials has become a research hotspot in efforts to achieve the accurate detection of trace PFCs in environmental waters. Most traditional PFC adsorbents present a number of disadvantages, such as low adsorption selectivity, slow diffusion, and poor reusability. Covalent organic frameworks (COFs) are crystalline polymers with ordered porous structures, large specific surface areas, and high chemical and thermal stability. These frameworks can easily be functionalized for the desired purpose. In this paper, spherical amino-functionalized COFs (denoted COF-NH₂) were fabricated via a two-step method to effectively enrich/remove PFCs from water. First, vinyl covalent organic framework (Vinyl COF) was synthesized at room temperature using 1,4-diradical-2,5-divinylbenzene (Dva) and 1,3,5-tris(4-aminophenyl)benzene (Tab) as building blocks. Then, thioether-bridged aromatic amine-functionalized spherical COF-NH₂ was synthesized through a thiol-alkenyl click reaction using 4-aminothiophenol as the functional monomer. COF-NH₂ showed good dispersion in water owing to its abundant amino groups, forming multiple hydrogen bonds with the F atoms of PFCs. The synergistic hydrophobic interactions between the organic skeleton of the COF and alkyl carbon chains of the PFCs led to enhanced adsorption efficiency. The produced Vinyl COF and COF-NH₂ were characterized by Fourier transform infrared spectroscopy (FT-IR), field-emission scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), and Brunner-Emmet-Teller (BET) measurements. The results confirmed that spherical COF-NH₂ materials with a homogeneous size distribution were successfully fabricated. The obtained COF-NH₂ microspheres had a diameter of approximately 500 nm and exhibited high thermal stability as well as a large specific surface area and pore volume. The adsorption kinetics, isotherm adsorption models, pH effects, and regeneration properties of COF-NH₂ were also investigated, and the results indicated that the adsorption of PFCs by COF-NH₂ conformed to the pseudo-second-order kinetic and Langmuir isotherm adsorption models. The obtained COF-NH₂ microspheres can be applied over a wide pH range, and the best adsorption effect was achieved in neutral and alkaline environments. After five cycles of regeneration and reuse, the COF-NH₂ microspheres retained their good adsorption efficiency for PFCs. The adsorption mechanism was mainly attributed to the synergistic effect of hydrogen bonding and hydrophobic interactions between COF-NH₂ and the PFCs. The extraction efficiencies of the microspheres toward five PFCs (perfluorobutyric acid, perfluorovaleric acid, perfluorohexanoic acid, perfluorooctanoic acid, and perfluorononanoic acid) in tap and Pearl River water samples were between 91.76% and 98.59%, with relative standard deviations (RSDs) (n=3) varying from 0.82% to 3.8%; these findings indicate that the obtained COF-NH₂ is promising for the extraction of PFCs from complex water samples. Given their uniform size distribution, high thermal stability, good adsorption performance, and reusability, the novel spherical COF-NH₂ materials developed in this study may be used as solid-phase extraction materials or filled into liquid chromatographic columns for the enrichment, separation, and detection of PFCs in complex samples.

Key words: covalent organic frameworks (COFs), click reactions, perfluorinated compounds (PFCs)