Abstract
Magnetite nanoparticles (Fe3O4 NPs) are among the most effective Fenton-Like heterogeneous catalysts for degrading environmental contaminants. However, Fe3O4 NPs aggregate easily and have poor dispersion stability because of their magnetic properties, which seriously decrease their catalytic efficiency. In this study, a novel environmentally friendly method for synthesising Fe3O4@CA was proposed. Fe3O4 NPs were immobilized on the 3D cellulose aerogels (CAs) in order to augment the degradation efficiency of p-nitrophenol (PNP) treatment and make the separation of the catalyst accessible by vacuum filtration method. Besides, CAs were fabricated from a cellulose source extracted from water hyacinth by using different cross-linking agents, such as kymene (KM) and polyvinyl alcohol–glutaraldehyde system (PVA–GA), and other drying methods, including vacuum thermal drying and freeze drying, were evaluated in the synthesis process. As-synthesized samples were analysed by various methods, including Powder X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy dispersive X-ray analysis and Brunauer–Emmett–Teller. Then, using ultraviolet–visible spectroscopy, the difference in the degradability of PNP of the obtained material samples was also investigated to determine their potential applications. Results highlighted that the Fe3O4-3@CA-KF catalyst with an Fe3O4 loading of 0.40 g/gCA used KM as a cross-linker and the freeze-drying method demonstrated the highest PNP removal efficiency (92.5 %) in all Fe3O4@CA samples with a H2O2 content of 5 g/L. The degradation kinetics and well-fitted pseudo-first-order model were investigated. Notably, after five successive PNP degradation experiments, this catalyst retained ∼80 % of the ability to degrade PNP, indicating its outstanding reusability. In environmental remediation, this study provides valuable insights into the development of simply separated and high-efficiency catalysts for heterogeneous catalytic reactions.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have