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Impact of water matrices on oxidation effects and mechanisms of pharmaceuticals by ultraviolet-based advanced oxidation technologies: A review

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 844, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.157162

Keywords

Ultraviolet; Water matrices; Degradation kinetics; Transformation products; Electrical energy per order

Funding

  1. National Key Research and Development Project of China [2019YFD1100204]
  2. Fundamental Research Funds for the Central Universities [FRF-MP-20-33]

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The binding between water components and pharmaceuticals influences the migration and transformation of pollutants. Different water matrices have either enhancing or inhibiting effects on drug degradation. The electrical energy demands for different oxidation processes can vary. It is important to assess the cost-benefit and formation of toxic by-products, as well as compare degradation pathways and products in the presence of different water matrices.
The binding between water components (dissolved organic matters, anions and cations) and pharmaceuticals influences the migration and transformation of pollutants. Herein, the impact of water matrices on drug degradation, as well as the electrical energy demands during UV, UV/catalysts, UV/O3, UV/H2O2-based, UV/persulfate and UV/ chlorine processes were systemically evaluated. The enhancement effects of water constituents are due to the powerful reactive species formation, the recombination reduction of electrons and holes of catalyst and the catalyst regenera-tion; the inhibition results from the light attenuation, quenching effects of the excited states of target pollutants and reactive species, the stable complexations generation and the catalyst deactivation. The transformation pathways of the same pollutant in various AOPs have high similarities. At the same time, each oxidant also can act as a special nu-cleophile or electrophile, depending on the functional groups of the target compound. The electrical energy per order (EEO) of drugs degradation may follow the order of EEOUV > EEOUV/catalyst > EEOUV/H2O2 > EEOUV/PS > EEOUV/chlorine or EEOUV/O3. Meanwhile, it is crucial to balance the cost-benefit assessment and toxic by-products formation, and the comparison of the contaminant degradation pathways and productions in the presence of different water matrices is still lacking.

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