Catalytic activation of O2 by Al0-CNTs-Cu2O composite for Fenton-like degradation of sulfamerazine antibiotic at wide pH range

[Display omitted] •A novel Al0-CNTs-Cu2O composite was prepared and characterized.•Al0-CNTs-Cu2O was capable of activating O2 to H2O2, OH and O2- at wide pH range.•The removal efficiency of SMR and TOC was 73.91 % and 56.80 %, respectively.•Al0-CNTs-Cu2O had a good reusability for the activation of...

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Veröffentlicht in:Journal of hazardous materials 2020-09, Vol.396, p.122751-122751, Article 122751
Hauptverfasser: Liu, Yong, Tan, Ni, Guo, Jinrui, Wang, Jianlong
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Sprache:eng
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Zusammenfassung:[Display omitted] •A novel Al0-CNTs-Cu2O composite was prepared and characterized.•Al0-CNTs-Cu2O was capable of activating O2 to H2O2, OH and O2- at wide pH range.•The removal efficiency of SMR and TOC was 73.91 % and 56.80 %, respectively.•Al0-CNTs-Cu2O had a good reusability for the activation of O2. In this study, a novel Al°-CNTs-Cu2O composite, capable of activating O2 to generate H2O2 and further to reactive oxygen species (ROSs) at a wide pH range, was synthetized, characterized and applied for the degradation of sulfamerazine. In the activation of O2 by Al°-CNTs-Cu2O composite, H2O2 was generated from the reaction of O2 with Al°-CNTs, which could be catalytically decomposed into O2− and OH by Cu2O, the formed Cu(II) could be rapidly reduced to Cu2O by Al°-CNTs in composite, which made Al°-CNTs-Cu2O composite reusable and decreased the leaching of copper ions into solution. The removal efficiency of SMR and TOC was 73.91 % and 56.80 %, respectively at initial pH = 5.8, T = 20 °C, O2 flow rate = 100 mL/min, Al°-CNTs-Cu2O dosage = 2 g/L, SMR = 50 mg/L, and reaction time = 60 min. The removal efficiency of SMR kept almost unchanged and the concentration of copper ions in solution was below 0.5 mg/L. The Al°-CNTs-Cu2O/O2 process could be used as a novel catalyst for the degradation of refractory organic contaminants in water and wastewater by Fenton-like process at a wide pH range through the in situ generation of H2O2.
ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2020.122751