Fabrication of MoS2@Fe3O4 Magnetic Catalysts with Photo-Fenton Reaction for Enhancing Tetracycline Degradation
Zhusheng Liu, Jia-Hong Sun, Bing Liu, Yanan Chen, Wei Feng
Abstract
Tetracycline (TCs) is widely used in the treatment of human and animal infectious disease. TCs gives rise to a growing threat to the human health and environment protection due to its overuse. Therefore, it is important to remove TCs contaminants from waste effluents. In this work, MoS2@Fe3O4 catalytic material was fabricated by the simple hydrothermal method, which was applied in the photo-Fenton system to degrade TCs. The crystal structure, surface morphology, elemental composition, chemical state, electrochemical properties, and separability of MoS2@Fe3O4 catalytic materials were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM), conventional and high-resolution transmission electron microscopy (TEM/HRTEM), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), and vibrating sample magnetometry (VSM). Furthermore, MoS2@Fe3O4 could degrade 98.6% of TCs within 60 min under the optimum reaction conditions (the catalyst dosage of 3 g/L, H2O2 concentration of 5 mmol/L, the initial TCs concentration of 50 mg/L, and the initial pH of 5), which was a significant increase compared with pure Fe3O4. MoS2 can accelerate the Fe3+/Fe2+ cycle through electron transfer from Mo4+ to Fe3+, resulting in the improvement in the degradation efficiency of TCs. The quenching and electron paramagnetic resonance (EPR) results showed that OH• and photogenic hole h+ was the main active species in the photo-Fenton system. What is more, MoS2@Fe3O4 catalytic materials had remarkable stability and reusability, and can be handily regained via magnetic separation technology in a real scenario.