4.7 Article

Degradation of trimethoprim by sulfate radical-based advanced oxidation processes: kinetics, mechanisms, and effects of natural water matrices

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 44, Pages 62572-62582

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-15146-0

Keywords

Sulfate radical; Trimethoprim; UV; persulfate; Kinetics model

Funding

  1. National Nature Science Foundation of China [52000183]
  2. China Postdoctoral Science Foundation [2020M683665XB]
  3. Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle Open Fund [ES202080088]
  4. Key Project of Scientific Research Project of Hunan Provincial Department of Education [20A523]
  5. Central South University of Forestry and Technology Introduced Talent Research Startup Fund [2020YJ010]
  6. Postdoctoral Oriented Training Program of Yunnan Province
  7. Hunan Provincial Innovation Foundation For Postgraduate [CX20200731]

Ask authors/readers for more resources

The study found that free radical reactions in UV-activated persulfate systems significantly promoted the degradation of trimethoprim (TMP). Factors such as persulfate concentration, natural organic matter, and chloride ions all influence the degradation rate of TMP. Transition metal ions in industrial wastewater have a synergistic effect on TMP degradation in UV/PS systems.
In this study, we investigated the removal efficiency of a broad-spectrum antimicrobial agent trimethoprim (TMP) in a UV-activated persulfate system(UV/PS). The pseudo-first-order reaction kineticmodel based on the steady-state hypothesis was used to explain TMP degradation behavior in UV-activated persulfate system. Due to the low quantum yield and molar absorptivity of TMP at 254 nm, the direct photolysis of TMP was slower. Since the free radicals generated by adding H2O2 or PS to the system can react with TMP, the degradation rate was significantly accelerated, and SO4 center dot- played a dominant role in the UV/PS system. k(HO center dot,TMP) and k(SO4 center dot-,TMP) were determined by the pseudo-first-order reaction kinetic model to be 6.02x10(9) and 3.88x10(9) M(-1)s(-1), respectively. The values were consistent with competitive kinetic measurements. The pseudo-first-order reaction kinetics model can predict and explain the effect of PS concentration, natural organicmatter, and chloride ion on the TMPdegradation in the UV/ PS system. The observed pseudo first-order rate constants for TMP degradation (k(obs)) increased with the persulfate concentration, but it significantly decreased in the presence of NOMand chloride. SO42- has no effect on the degradation of TMP, while HCO3- promotes the degradation and NO3- inhibits the degradation. The common transition metal ion (such as Cu2+, Zn2+, and Co2+) in industrial wastewater has a synergistic effect on theTMP degradation in theUV/PS system, but excessivemetal ions will lead to a decrease of the degradation rate.

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