4.7 Article

A novel core-shell Fe@Co nanoparticles uniformly modified graphite felt cathode (Fe@Co/GF) for efficient bio-electro-Fenton degradation of phenolic compounds

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 760, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.143415

关键词

Fe@Co/graphite felt; Core-shell structure; Phenolic compounds; Degradation; Bio-electro-Fenton

资金

  1. Jiangsu Synergetic Innovation Center for Advanced Bio-Manufacture
  2. CAS Key Laboratory of Environmental and Applied Microbiology & Environmental Microbiology Key Laboratory of Sichuan Province
  3. Chengdu Institute of Biology, Chinese Academy of Sciences [KLCAS-2019-3]
  4. Key Research and Development Technology of Ningxia Hui Autonomous Region (special project for foreign science and technology cooperation) [2019BFH02008]
  5. National Key Research and Development Project [2019YFC1906602]
  6. National Natural Science Foundation of China [21777069]
  7. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

向作者/读者索取更多资源

In this study, a core-shell Fe@Co nanoparticles modified graphite felt was fabricated as the cathode by one-pot self-assembly strategy for the degradation of organic acids in the Bio-Electro-Fenton system, showing excellent electrochemical performance and catalytic reactivity.
In this study, a core-shell Fe@Co nanoparticles uniformly modified graphite felt (Fe@Co/GF) was fabricated as the cathode by one-pot self-assembly strategy for the degradation of vanillic acid (VA), syringic acid (SA), and 4-hydroxybenzoic acid (HBA) in the Bio-Electro-Fenton (BEF) system. The Fe@Co/GF cathode showed dual advantages with excellent electrochemical performance and catalytic reactivity not only due to the high electron transfer efficiency but also the synergistic redox cycles between Fe and Co species, both of which significantly enhanced the in situ generation of H2O2 and hydroxyl radicals (center dot OH) to 152.40 mu mol/L and 138.48 mu mol/L, respectively. In this case, the degradation rates of VA, SA, and HBA reached 100, 94.32, and 100%, respectively, within 22 h. Representatively, VA was degraded and ultimately mineralized via demethylation, decarboxylation and ring-opening reactions. This work provided a promising approach for eliminating typical recalcitrant organic pollutants generated by the pre-treatment of lignocellulose resources. (C) 2020 Elsevier B.V. All rights reserved.

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