摘要
The removal of bromide ions (Br − ) from water is critical, as these ions can generate bromate and brominated disinfection by-products that are toxic, carcinogenic, and corrosive. Previous research has not focused on the removal of Br − from water with a heavy presence of chloride ions (Cl − ). To address this research gap, we proposed a defective Zr-based metal–organic framework (MOF) to selectively remove trace Br − in environments with high concentrations of Cl − . We demonstrated that the open acidic sites on the secondary building units in a defective Zr-based MOF-808 (MOF-808-Cl) selectively removed the trace Br − in the presence of high concentration of Cl − using varying degrees of electrostatic interactions induced by their own polarizability. The Br − removal was performed with the mixed mechanism of ion-exchange and −adsorption, with contributions of approximately 70% and 30%, respectively. The Br − was successfully removed when the concentration of Cl − was 100 times higher than that of Br − . Our findings demonstrate the potential of MOF-808-Cl for industrial applications requiring trace ion removal and can provide insights for future research on selective ion removal in a competitive environment.
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