Ozone (O3), as an environmentally friendly oxidant, is widely used to remove emerging pollutants and ensure the safety of the water supply, whereas the restricted accessibility of O3 and limited collision frequency between pollutants and O3 will inevitably reduce the ozonation efficiency. To promote the chemical reactions between O3 and target pollutants, here we developed a novel gas-solid-liquid reaction interface dominated triphase ozonation system using a functional hydrophobic membrane with an adsorption layer as the O3 distributor and place where chemical reactions occurred. In the triphase system, the functional hydrophobic membrane simultaneously improved the interface adsorption performance of emerging pollutants and the access pathway of O3, leading to a marked enhancement of interfacial pollutant concentration and O3 levels. These synergistic qualities result in high ciprofloxacin (CIP) removal efficiency (94.39%) and fast apparent reaction rate constant (kapp, 2.75 × 10-2 min-1) versus a traditional O3 process (41.82% and 0.48 × 10-2 min-1, respectively). In addition, this triphase system was an advanced oxidation process involving radical participation and showed excellent degradation performance of multiple emerging pollutants. Our findings highlight the importance of gas-solid-liquid triphase reaction interface design and provide new insight into the efficient removal of emerging pollutants by the ozonation process.
Keywords: Bubble-less mass transfer; Cross-linked cyclodextrin; Emerging pollutants; Ozonation; Triphase reaction interface.