Enhanced performance of ZIF-8 nanocrystals hybrid monolithic composites via an in-situ growth strategy for efficient capillary microextraction of perfluoroalkyl phosphonic acids

Abstract

Enrichment of perfluoroalkyl phosphonic acids (PFPAs) is of great significance and challenging for environmental monitoring, due to their toxic and persistent nature, highly fluorinated character as well as low concentration. Herein, novel metal-organic frameworks (MOFs) hybrid monolithic composites were prepared via metal oxide-mediated in situ growth strategy and utilized for capillary microextraction (CME) of PFPAs. A porous pristine monolith was initially obtained by copolymerization of the zinc oxide nanoparticles (ZnO-NPs)-dispersed methacrylic acid (MAA) with ethylenedimethacrylate (EDMA) and dodecafluoroheptyl acrylate (DFA). Afterwards, nanoscale-facilitated transformation of ZnO nanocrystals into the zeolitic imidazolate framework-8 (ZIF-8) nanocrystals was successfully realized via the dissolution-precipitation of the embedded ZnO-NPs in the precursor monolith in the presence of 2-methylimidazole. Experimental and spectroscopic results (SEM, N2 adsorption-desorption, FT-IR, XPS) revealed that the coating of ZIF-8 nanocrystals significantly increased the surface area of the obtained ZIF-8 hybrid monolith and endowed the material abundant surface-localized unsaturated zinc sites. The proposed adsorbent showed highly enhanced extraction performance for PFPAs in CME, which was mainly ascribed to the strong fluorine affinity, Lewis acid/base complexing, anion-exchange, and weakly π-CF interaction. The coupling of CME with LC-MS enables effective and sensitive analysis of ultra-trace PFPAs in environment water and human serum. The coupling method demonstrated low detection limits (2.16–4.12 ng L−1) with satisfactory recoveries (82.0–108.0%) and precision (RSDs ≤6.2%). This work offered a versatile route to design and fabricate selective materials for emerging contaminant enrichment in complicated matrices.