Photocatalytic degradation of tetracycline antibiotics using three-dimensional network structure perylene diimide supramolecular organic photocatalyst under visible-light irradiation

The occurrence of antibiotics in the ambient environment has raised serious concerns. In this work, the kinetics and mechanism of photocatalytic degradation tetracycline (TC) was investigated using three-dimensional network structure perylene diimide supramolecular organic photocatalyst (3D-PDI). Under visible-light irradiation, 3D-PDI exhibited excellent degradation performance and stability for several tetracycline-based antibiotics (e.g., tetracycline; chlortetracycline; oxytetracycline.). The adsorption and degradation rate of TC by 3D-PDI were 8.21 and 12.7 times higher than that of bulk-PDI. The enhanced adsorption and degradation performance of TC by 3D-PDI were mainly due to the larger specific surface area and Tr-electron conjugation of 3D network supramolecular system. Superoxide radical (O-center dot(2)-), hydrogen peroxide (H2O2) and hole (h(+)) the main reactive species (RSs) for TC degradation. Under the attack of photocatalytic RSs, TC undergoes hydroxylation, demethylation, aromatization, and ring-opening processes, and finally complete mineralization into CO2 and H2O. These results revealed that perylene diimide supramolecular photocatalyst may be efficiently applied for the remediation of tetracycline contaminated natural waters.