4.7 Article

Enhanced photocatalytic activation of peroxymonosulfate by CeO2 incorporated ZnCo-layered double hydroxide toward organic pollutants removal

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 263, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2021.118413

Keywords

ZnCo-LDH@CeO2; PMS; Visible light; Mechanism; Removal

Funding

  1. National Natural Science Foundation of China [21808243, U1662119, 21776314]
  2. National Key Research and Development Program of China [2017YFB0306600]
  3. Fundamental Research Funds for the Central Universities [17CX02061]

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In this study, ceria nanosheets incorporated zinc cobalt-layered double hydroxide composites were used as a heterogeneous photocatalyst in combination with peroxymonosulfate to degrade contaminants. The ZnCo-LDH@CeO2 /PMS system showed excellent photocatalytic removal performance, with 99.8% removal of phenol achieved in 30 minutes under optimal conditions. The efficient separation and transportation of photogenerated electrons and holes in ZnCo-LDH@CeO2 contributed to its enhanced performance.
In this study, ceria nanosheets incorporated zinc cobalt-layered double hydroxide composites (ZnCo-LDH@CeO2) were prepared and employed as a heterogeneous photocatalyst to degrade contaminants in combination with peroxymonosulfate (PMS). The morphologies and physicochemical properties of the as-prepared photocatalysts were characterized by various technologies. The ZnCo-LDH@CeO2 /PMS system exhibited the highest photocatalytic removal performance among a series of catalytic schemes with phenol (20 mg/L) as model compound and 99.8% removal was achieved after 30 min reaction under optimal conditions with 0.8 g/L PMS and 0.2 g/L catalyst at room temperature. The enhancement of more efficient separation and transportation of photogenerated electrons and holes for ZnCo-LDH@CeO2 than the two individual units was determined by transient photocurrent responses and electrochemical impedance spectroscopy instruments. The generated oxidizing species including SO4 center dot-, (OH)-O-center dot, O-center dot(2)-, and h(+) during the degradation process were analyzed by quenching experiments and electron paramagnetic resonance spectra, and the possible degradation mechanism was proposed. The satisfactory reusability and wide applications of ZnCo-LDH@CeO2 /PMS/vis system indicated a class of promising technology for various non-biodegradable organic pollutants remediation.

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