Catalytic wet oxidation of 2,4-dichlorophenol solutions: activity of the manganese-cerium composite catalyst and biodegradability of the effluent stream

Water Environ Res. 2002 Jan-Feb;74(1):28-32. doi: 10.2175/106143002x139721.

Abstract

Aqueous solutions containing 100 to 1000 mg/L of 2,4-dichlorophenol (2,4-DCP) were oxidized in an upflowing fixed-bed reactor in this study of manganese-cerium composite catalysts, which were prepared by the coprecipitation of both manganese nitrate and ceric nitrate at various molar concentrations. Results showed that 2,4-DCP conversion by wet oxidation in the presence of the manganese-cerium composite catalysts was a function of the molar ratio of the manganese-cerium catalyst. The kinetic behavior of 2,4-DCP oxidation with catalysis could be explained by using a zero-order rate expression. Total organic carbon (TOC) removal by wet oxidation in the absence of any catalyst was nil, while approximately 68% TOC reduction was achieved during wet oxidation over a manganese-cerium (7:3 mol/mol) catalyst at 160 degrees C and an oxygen partial pressure of 1.0 MPa. Moreover, the 5-day biochemical oxygen demand/chemical oxygen demand ratios of all the effluent streams were determined to be greater than 0.45 as the wet catalytic processes were carried out at a liquid hourly space velocity less than 24 h (-1), indicating that they could be made more amenable to further biological treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Biodegradation, Environmental / drug effects
  • Carbon / metabolism
  • Catalysis / drug effects
  • Cerium / pharmacology
  • Chlorine / pharmacology
  • Chlorophenols / metabolism*
  • Equipment Design
  • Manganese / pharmacology
  • Models, Biological
  • Oxidation-Reduction
  • Oxygen / pharmacology*
  • Waste Disposal, Fluid / methods*
  • Water Purification / methods

Substances

  • Chlorophenols
  • Cerium
  • Manganese
  • Chlorine
  • Carbon
  • 2,4-dichlorophenol
  • Oxygen