In this study, an N-ZnO/g-C3N4 (g-N-Z) Z-scheme photocatalyst was constructed using hydrothermal and high-temperature calcination. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and other tests were employed to characterise the catalytic material. The results showed that after N-ZnO modification, the separation efficiency of the photoinduced charge pairs and the utilisation of sunlight in the composites were improved. The kinetics experiments indicated that the degradation of atrazine (ATZ) in the g-N-Z/PDS/solar system was significantly better than that in the PDS/solar system. Under the action of the g-N-Z/PDS/solar system, the degradation rate of ATZ reached 83.88%, whereas in the PDS/solar system, it was only 31.76%. In addition, it was found that increasing the PDS concentration, g-N-Z dosage, and solution acidity effectively accelerated the removal of ATZ. The presence of HCO3-/CO32-, Cl-, and natural organic matter (NOM) inhibited the oxidation efficiency of the g-N-Z/PDS/solar system. Moreover, the presence of multiple reactive oxygen species (ROS) was confirmed using radical scavenging experiments to determine the contribution of each active component. Twelve oxidation intermediates of ATZ were obtained via liquid chromatography-tandem mass spectrometry (LC-MS/MS), and the mechanism of enhanced ATZ degradation in the g-N-Z/PDS/solar system was proposed. Actual water and cyclic photocatalytic experiments further suggest that g-N-Z has good application value in water treatment.
Keywords: Kinetics; Oxidation mechanism; PDS; Solar; g-N-Z.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.