4.7 Article

Fabrication of hollow covalent-organic framework microspheres via emulsion-interfacial strategy to enhance laccase immobilization for tetracycline degradation

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 421, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.129743

Keywords

H-COF-OMe; Laccase; Interfacial defects; Emulsion interfacial polymerization; High activity and stability; Fast degradation kinetics of tetracycline

Funding

  1. National Natural Science Foundation of China [21968003, 21666004, 21676059]
  2. National Natural Science Foundation of Guangxi Province [2020GXNSFGA297001, 2017GXNSFFA198009]
  3. Innovation and Entrepreneurship Training Program of Guangxi Zhuang Autonomous Region [201910593044]
  4. Opening Project of Guangxi Key Laboratory of AgroEnvironment [2020KF04]

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H-COF-OMe was fabricated using emulsion interfacial polymerization, exhibiting a hollow spherical microstructure and unique defects-rich interface, with high loading capacity and activity recovery for laccase. It efficiently stabilized the active conformation of laccase, leading to significantly enhanced tetracycline degradation performance. This work suggested a novel COF synthesis strategy as laccase immobilization supporters for high TC degradation, showing promising potential for degradation of organic pollutants.
Hollow covalent organic framework microsphere (H-COF-OMe) using TAPB and DMTP with enriched interfacial defects was fabricated via emulsion interfacial polymerization and in turn applied as a novel host for high laccase loading and tetracycline (TC) degradation. Benefited from the space-confined growth in the multiphase solvent interface, H-COF-OMe exhibited hollow spherical microstructure, high surface area and unique defects-rich interface. Attributed to these intriguing aspects, H-COF-OMe achieved maximum loading capacity of 567 mg/ g and activity recovery of 85% for laccase. H-COF-OMe efficiently stabilized the active conformation of laccase from structural distortion via multiple binding sites, which endowed Lac@H-COF-OMe significantly higher pH, thermal, and storage stabilities, and reusability than free laccase and Lac@COF-OMe. Interestingly, the hollow morphology and defective interface of Lac@H-COF-OMe accelerated the diffusion of TC and shortened the reaction pathway, which endowed it with markedly enhanced TC degradation and recycling performance than many state-of-the-art catalysts. Significantly, Lac@H-COF-OMe (20 mg) could achieve 99% degradation of 50 mg/L tetracycline (50 mL) within 100 min. Monitoring of the intermediate products indicated that Lac@H-COFOMe showed outstanding detoxification performance of the degradation products. This work suggested a novel COF synthesis strategy as laccase immobilization supporters for high TC degradation, which makes it as a promising candidate for degradation of organic pollutants.

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