Oxalate enhanced mechanism of hydroxyl-Fe-pillared bentonite during the degradation of Orange II by UV-Fenton process

J Hazard Mater. 2011 Jan 30;185(2-3):1477-81. doi: 10.1016/j.jhazmat.2010.10.071. Epub 2010 Oct 26.

Abstract

An enhanced method of hydroxyl-Fe-pillared bentonite (H-Fe-P-B) during the degradation of Orange II was studied to provide novel insight to interactions of degradation intermediates with heterogeneous catalyst in UV-Fenton system. Based on the degradation mechanism of Orange II, oxalate enhanced mechanism of H-Fe-P-B in heterogeneous UV-Fenton system was developed. The results showed that additional oxalate could increase the Fe leaching of H-Fe-P-B during heterogeneous UV-Fenton process, which led to higher mineralization efficiency of Orange II and lower energy consumption of treatment. When the concentrations of additional sodium oxalate increased up to 0.1 mmol L(-1), 0.2 mmol L(-1) and 0.4 mmol L(-1), the rate of Orange II degradation could increase 30%, 46% and 63%, respectively. The iron ions leached from catalyst could be adsorbed back to the catalyst again after the organic intermediates were mineralized completely. Then the catalyst of H-Fe-P-B could be reused and additional pollution caused by iron ions could be avoided.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azo Compounds / chemistry*
  • Bentonite / chemistry*
  • Benzenesulfonates / chemistry*
  • Hydrogen Peroxide / chemistry*
  • Iron / chemistry*
  • Oxalates / chemistry*
  • Spectrophotometry, Ultraviolet
  • Ultraviolet Rays*

Substances

  • Azo Compounds
  • Benzenesulfonates
  • Fenton's reagent
  • Oxalates
  • Bentonite
  • Hydrogen Peroxide
  • Iron
  • 2-naphthol orange