Journal
JOURNAL OF HAZARDOUS MATERIALS
Volume 380, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jhazmat.2019.120888
Keywords
Adsorption; Catalytic ozonation; Micropollutant; Model
Categories
Funding
- NSFC [51878370]
- National Special Program of Water Pollution Control and Management [2017ZX07202]
- special fund of State Key Joint Laboratory of Environment Simulation and Pollution Control [18LO1ESPC]
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This study evaluated the prediction of emerging contaminant (EC) removal during heterogeneous catalytic ozonation by chemical kinetic models. Six ECs with differing ozone reactivity were spiked in a synthetic water and a groundwater, then treated by conventional ozonation and heterogeneous catalytic ozonation with alpha- or beta-MnO2 catalysts. Results show that catalysts did not considerably influence the removal of ECs with high and intermediate ozone reactivity (diclofenac, gemfibrozil, and bezafibrate), but enhanced the removal efficiencies of ECs with low ozone reactivity (2,4-dichlorophenoxyacetic acid, clofibric acid, and ibuprofen) to varied extent ((-)10-30%). The removal efficiencies of ECs could be reasonably predicted using chemical kinetic models based on the ozone (O-3) and hydroxyl radical ((OH)-O-center dot) rate constants of ECs, pseudo-first-order rate constants observed for EC adsorption on the MnO2 catalysts, and O-3 and (OH)-O-center dot exposures observed for catalytic ozonation. Furthermore, the model reveals that ECs are removed mainly by O-3 and/or center dot OH oxidation during heterogeneous catalytic ozonation, while adsorption of ECs on catalysts contributes negligibly. Therefore, the removal efficiencies of ECs could be satisfactorily predicted using a simplified model based only on the O-3 and (OH)-O-center dot rate constant and the O-3 and (OH)-O-center dot exposures.
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