4.8 Article

UV/Sodium percarbonate for bisphenol A treatment in water: Impact of water quality parameters on the formation of reactive radicals

期刊

WATER RESEARCH
卷 219, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2022.118457

关键词

AOPs; Carbonate radical anion; Hydroxyl radical; Steady state concentrations; Transformation pathways

资金

  1. International Collaborative Research Project of National Natural Science Foundation of China [51720105001]
  2. China Scholarship Council (CSC) scholarship [201406780006]
  3. GSG Research Fellowship by Graduate Student Government at University of Cincinnati
  4. Herman Schneider Professorship in the College of Engineering and Applied Sciences, University of Cincinnati
  5. Fulbright Commission in Brazil

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This study investigates the impact of water quality parameters on the formation of radical anions and BPA degradation in UV/SPC and UV/H2O2 systems. The rise in pH decreases the steady state concentration of HO•, resulting in a decrease in BPA degradation rate.
Reported herein is an investigation of the impact of water quality parameters on the formation of carbonate radical anion (CO & BULL;?3) and hydroxyl radical (HO & BULL;) in UV/sodium percarbonate (UV/SPC) system versus in UV/ hydrogen peroxide (UV/H2O2) system for bisphenol A (BPA) degradation in water. Pathways of CO & BULL;? 3 oxidation of BPA were proposed in this study based on the evolution of direct transformation products of BPA. Observed in this study, the degradation of BPA in the UV/SPC system was slower than that in the UV/H2O2 system in the secondary effluents collected from a local wastewater treatment plant due to the significant impact of coexisting constituents in the matrices on the former system. Single water quality parameter (e.g., solution pH, common anion, or natural organic matter) affected radical formations and BPA degradation in the UV/SPC system in a way similar to that in the UV/H2O2 system. Namely, the rise of solution pH decreased the steady state concentration of HO & BULL; resulting in a decrease in the observed pseudo first-order rate constant of BPA (kobs). Chloride anion and sulfate anion played a negligible role over the examined concentrations; nitrate anion slightly suppressed the reaction at the concentration of 20 mM; bicarbonate anion decreased the steady state concentrations of both CO & BULL;?3 and HO & BULL; exerting significant inhibition on BPA degradation. Different extents of HO & BULL; scavenging were observed for different types of natural organic matter in the order of fulvic acid > mixed NOM > humic acid. However, the impact was generally less pronounced on BPA degradation in the UV/SPC system than that in the UV/H2O2 system due to the existence of CO & BULL;?3. The results of this study provide new insights into the mechanism of CO & BULL;? 3 based oxidation and new scientific information regarding the impact of water quality parameters on BPA degradation in the sytems of UV/SPC and UV/H2O2 from the aspect of reactive radical formation, which have reference value for UV/SPC application in wastewater treatment.

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