4.7 Article

Highly efficient microwave-assisted Fenton degradation of metacycline using pine-needle-like CuCo2O4 nanocatalyst

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 373, Issue -, Pages 1158-1167

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2019.05.097

Keywords

Fenton reaction; Microwave; CuCo2O4; Antibiotics

Funding

  1. National Natural Science Foundation of China [21674028]
  2. University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2016075]
  3. Excellent Youth Science Fundation of Heilongjiang University [JCL201703]
  4. Open Project of State Key Laboratory of Supramolecular Structure and Materials [Sklssm 2019029]

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The heterogeneous Fenton reaction was a powerful technique for degrading organics in wastewater. However, it usually took a long time to meet efficiency requirement. To solve this problem, herein, pine-needle-like CuCo2O4 was prepared and applied as a catalyst in a microwave-assisted Fenton reaction (MAFR) towards antibiotic metacycline (MTC). The optimized degradation condition was 500 mu L of H2O2, 10.0 mg of catalyst, 50 mg/L of MTC, and 90 degrees C of temperature, under which MTC was degraded within 4.0 min. Dynamics data revealed that the activation energy of MAFR was 17.3 kJ/mol, which was much lower than that of the corresponding heterogeneous Fenton reaction (52.2 kJ/mol). Owing to the synergistic effect of combining Cu(II)/Cu(I) and Co(III)/Co (II) sites, the reaction rate constant of CuCo2O4 nanoneedles (7.2x10(-1) min(-1)) was much higher than that of the CuO (1.3x10(-1) min(-1)), Co3O4 (2.2x10(-1) min-1), and mixed CuO+ Co3O4 (1.5x10(-1) min(-1)) references. CuCo2O4 nanoneedles could be easily separated from the reaction solution, and their degradation efficiency remained 86.4% after the 5th cycle. To study the catalytic mechanism, radical trapping experiments were performed, and the results revealed that center dot OH played a dominating role in the degradation process. A possible degradation pathway of MTC was investigated, and it was determined that hydroxylation, de-alkylation, dehydroxylation, and ring-opening reactions were involved for final inorganic molecules.

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