Effect of water constituents on the degradation of sulfaclozine in the three systems: UV/TiO, UV/KSO, and UV/TiO/KSO.

Environ Sci Pollut Res Int

Université Lyon 1, CNRS, UMR 5256, Institut de recherches sur la catalyse et l'environnement de Lyon (IRCELYON), 2 avenue Albert Einstein, F-69626, Villeurbanne, France.

Published: January 2018

AI Article Synopsis

  • Bicarbonate (HCO) and phosphate (HPO) ions enhance the degradation of sulfaclozine (SCL) in certain advanced oxidation process (AOP) systems (UV/TiO and UV/TiO/KSO), while humic substances have a lesser impact.
  • The UV/KSO system is inhibited by humic substances and is unaffected by HCO and HPO, highlighting the different effects of these constituents on various AOPs.
  • The study also revealed that new reactive species formed in the presence of HCO and HPO, like carbonate (CO) and hydroxyl (·OH) radicals, contribute to the increased degradation rate of SCL.

Article Abstract

Bicarbonate, phosphate, chloride ions, and humic substances are among the constituents most widely present in natural waters. These non-target constituents can greatly affect the efficiency of advanced oxidation processes used for water decontamination due to their capacity to interfere with the adsorption of the target compounds on the surface of TiO, absorb photons, scavenge hydroxyl radicals (·OH), and generate photochemical reactive intermediates. In this work, the effect of these constituents on the degradation of sulfaclozine (SCL) was monitored in three different AOPs systems: UV/TiO, UV/KSO, and UV/TiO/KSO. It was shown that bicarbonate (HCO) and phosphate (HPO) ions enhanced the degradation of SCL in UV/TiO and UV/TiO/KSO systems whereas the addition of humic substances influenced these rates with a much smaller extent. On the other hand, the degradation rate of SCL in the UV/KSO system was not affected by the presence of HCO and HPO but was inhibited in the presence of humic substances. In addition, the different mechanisms that can take place in the presence of these constituents were discussed and the degradation rate enhancement in presence of HCO and HPO was attributed to the formation of new reactive species such as carbonate (CO) and hydroxyl (·OH) radicals activated by TiO holes (h). In the presence of chloride (Cl) and nitrate (NO) ions, an enhancement of SCL adsorption on the surface of TiO was observed. Finally, a comparative study of the degradation of SCL in river water and ultrapure water was reported.

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Source
http://dx.doi.org/10.1007/s11356-017-0629-3DOI Listing

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