4.7 Article

Defect- and nitrogen-rich porous carbon embedded with Co NPs derived from self-assembled Co-ZIF-8 @ anionic polyacrylamide network as PMS activator for highly efficient removal of tetracycline hydrochloride from water

期刊

CHEMICAL ENGINEERING JOURNAL
卷 443, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.136439

关键词

Co-ZIF-8; Anionic polyacrylamide; Zn defect sites; Peroxymonosulfate; Tetracycline hydrochloride

资金

  1. China?s Na-tional Natural Science Foundation [51978491]

向作者/读者索取更多资源

The design of N-doped carbon-based nanomaterials for efficient heterogeneous activation of peroxymonosulfate (PMS) for environmental remediation has drawn the attention of researchers. In this study, N-doped porous carbon-encapsulated Co nanoparticles were successfully prepared by pyrolyzing the zeolite imidazolium framework (Co-ZIF-8) @ anionic polyacrylamide (APAM) network composite. The obtained nanomaterials showed excellent efficiency and stability in breaking down tetracycline hydrochloride (TC center dot HCl) using activated PMS. The CZA-1000/PMS system achieved a separation efficiency of 99.8% within 30 minutes.
The design of N-doped carbon-based nanomaterials for efficient heterogeneous activation of peroxymonosulfate (PMS) for environmental remediation has piqued the attention of many researchers. In this study, precise temperature control vaporized Zn to form defects, and N-doped porous carbon-encapsulated Co nanoparticles were successfully generated by pyrolyzing the zeolite imidazolium framework (Co-ZIF-8(CZ)) @ anionic polyacrylamide (APAM) network composite (Co-ZIF-8@APAM (CZA)). Benefiting from the defect structure and enhanced N content doped Co particles, the obtained nanomaterials exhibited excellent effect and stability on tetracycline hydrochloride (TC center dot HCl) breakdown by activated PMS. The separation efficiency of TC center dot HCl in the CZA-1000/PMS system was 99.8% within 30 min and was 2.43 times more than pure Co-ZIF-8/PMS. In addition, the study investigated potential factors including pH, the coexistence of anions/cations/halide ions, TC center dot HCl, Ciprofloxacin Hydrochloride (CPFX center dot HCl), and TC center dot HCl removal from natural water. CZA-1000/PMS system kept excellent performance. Through EPR, Raman spectroscopy, and XPS, the mechanism exploration revealed that the N-doped carbon modified with Co nanoparticles generated the oxygen defects and promoted the catalytic activity and stability. The radical and nonradical oxidation co-acted on TC center dot HCl degradation.

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