Publications by authors named "Haijuan Tao"

Covalent organic frameworks (COFs), when utilized as solid-phase microextraction (SPME) coating materials, exhibit remarkable abilities to concentrate phenols by thousands-fold owing to their vast surface area and exceptional stability. However, the prevalent micropores inherent in COFs can impede rapid mass transfer of target molecules, prolonging SPME extraction times. To addresses this limitation, this work introduces a novel approach by integrating hierarchical porous structures into COFs, leveraging polystyrene microspheres as hard templates during the in situ growth process of the SPME coating.

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The recovery of precious metals (PMs) from secondary resources has garnered significant attention due to environmental and economic considerations. Covalent organic frameworks (COFs) have emerged as promising adsorbents for this purpose, owing to their tunable pore size, facile functionalization, exceptional chemical stability, and large specific surface area. This review provides an overview of the latest research progress in utilizing COFs to recover PMs.

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The extraction performance of materials is highly related to their physical structure. However, the precise impact of ordered pore structure in covalent organic frameworks (COFs) on extraction performance are still puzzling. To look insight into this, a series of COFs with varying degrees of ordered pore structures were prepared at room temperature by adjusting reaction time and their extraction efficiencies toward phenolic compounds were investigated.

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Solid-phase microextraction (SPME) is a green, environmentally friendly, and efficient technique for sample pre-treatment. Covalent organic frameworks (COFs), a class of porous materials formed by covalent bonds, have gained prominence owing to their remarkable attributes, including large specific surface area, tunable pore size, and robust thermal/chemical stability. These characteristics have made COFs highly appealing as potential coatings for SPME fiber over the past decades.

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