Pilot-scale evaluation of micropollutant abatements by conventional ozonation, UV/O3, and an electro-peroxone process

Water Res. 2018 Jul 1:138:106-117. doi: 10.1016/j.watres.2018.03.044. Epub 2018 Mar 16.

Abstract

The electro-peroxone (E-peroxone) process is an emerging ozone-based advanced oxidation process (AOP) that has shown large potential for micropollutant abatement in water treatment. To evaluate its performance under more realistic conditions of water treatment, a continuous-flow pilot E-peroxone system was developed and compared with conventional ozonation and a UV/O3 process for micropollutant abatements in various water matrices (groundwater, surface water, and secondary wastewater effluent) in this study. With a specific ozone dose of 1.5 mg O3/mg DOC, micropollutants that have high and moderate reactivity with ozone (O3) (diclofenac, naproxen, gemfibrozil, and bezafibrate) could be sufficiently abated (>90% abatement) in the various waters by all three processes. However, ozone-resistant micropollutants (ibuprofen, clofibric acid, and chloramphenicol) were abated only by ∼32-68%, 68-91%, and 73-90% during conventional ozonation of the selected groundwater, surface water, and secondary wastewater effluent, respectively. By electro-generating H2O2 or applying UV irradiation to enhance O3 transformation to •OH during ozonation, the E-peroxone and UV/O3 processes similarly enhanced the abatement efficiencies of ozone-resistant micropollutants by ∼15-43%, ∼5-15%, and ∼5-10% in the groundwater, surface water, and secondary wastewater effluent, respectively. In addition, the E-peroxone and UV/O3 processes significantly reduced bromate formation during the treatment of the three waters compared to conventional ozonation. Due to its higher efficiency, the E-peroxone process reduced ∼10-53% of the energy consumption required to abate the concentration of chloramphenicol (the most ozone-resistant micropollutant spiked in the waters) by 1 order of magnitude in the three waters compared to conventional ozonation. In contrast, the UV/O3 process consumed approximately 4-10 times higher energy than conventional ozonation. This pilot-scale study demonstrates that the E-peroxone process can provide a feasible, effective, and energy-efficient alternative for micropollutant abatement and bromate control in water and wastewater treatment.

Keywords: Advanced oxidation; Bromate; Emerging contaminant; Energy efficiency; Pharmaceutical; Water and wastewater treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bromates / chemistry
  • Hydrogen Peroxide / chemistry*
  • Oxidation-Reduction
  • Ozone / chemistry*
  • Pharmaceutical Preparations / chemistry
  • Pharmaceutical Preparations / radiation effects
  • Ultraviolet Rays*
  • Waste Disposal, Fluid / methods*
  • Wastewater / analysis
  • Water Pollutants, Chemical / chemistry*
  • Water Pollutants, Chemical / radiation effects*

Substances

  • Bromates
  • Pharmaceutical Preparations
  • Waste Water
  • Water Pollutants, Chemical
  • Ozone
  • Hydrogen Peroxide