4.7 Article

Enhanced activation of persulfate by nitric acid/annealing modified multi-walled carbon nanotubes via non-radical process

Journal

CHEMOSPHERE
Volume 220, Issue -, Pages 514-522

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2018.12.136

Keywords

Nitric acid/annealing modification; Carbon nanotubes; Singlet oxygen; Persulfate activation; Phenol

Funding

  1. National Natural Science Foundation of China [51634010, 51474246]
  2. Major Science and Technology projects in Gansu province [1602FXDC007]

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This study aim to explore art effective approach of persulfate (PS) activation based on multi-walled carbon nanotubes (CNTs) for the phenol degradation. The nitric acid/annealing modified CNTs were obtained by oxidation with concentrated nitric acid followed by annealing at various high temperatures (400-1000 degrees C). The modified CNTs catalysts were characterized and their catalytic degradation performances of phenol with PS were investigated. The results reveal that the modified CNTs can obviously enhance the phenol removal. The catalytic activity is improved by nitric acid modification and obviously influenced by the annealing temperature. PS concentration and solution pH could also affect the catalytic degradation of phenol. The mechanism of enhanced PS activation by the nitric acid/annealing modified CNTs was proposed that the nitric acid modification resulted in more defective edges and oxygen containing groups, and subsequent annealing at high temperate facilitated the conversion of sp(3) to sp(2) carbon, then the catalytic activity for PS activation was enhanced by the active sites of C=O group and sp(2)-hybridized carbon at the defective edges. In addition, a non-radical process of phenol degradation was demonstrated in terms of the radical quenching tests and electron paramagnetic resonance (EPR) spectra analyses. It is suggested that O-1(2) is likely the main reactive specie generated in PS activation by the modified CNTs for the phenol removal. (C) 2018 Published by Elsevier Ltd.

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