RESUMEN
A novel tertiary magnetic ZnFe2O4/BiOBr/rGO visible light-driven photocatalytic system was successfully synthesized from graphite, bismuth nitrate pentahydrate, iron (III) nitrate, and zinc nitrate precursors. The produced materials were characterized regarding micro-structure, chemical composition and functional groups, surface charge properties, photocatalytic characteristics such as band gap energy (Eg), recombination rate of charge carriers, and magnetic properties. ZnFe2O4/BiOBr/rGO heterojunction photocatalyst exhibited a saturation magnetization of 7.5 emu/g, and a visible light response (Eg = 2.08 eV). Thus, under visible light, these materials could generate effective charge carriers responsible for forming free hydroxyl radicals (HOâ¢) for degrading organic pollutants. ZnFe2O4/BiOBr/rGO also exhibited the lowest charge carriers recombination rate compared to all individual components. The construction of ZnFe2O4/BiOBr/rGO system resulted in 1.35 to 2.55 times higher in photocatalytic degradation of DB 71 compared to individual components. At the optimal conditions (0.5 g/L catalyst load and pH 7.0), the ZnFe2O4/BiOBr/rGO system could completely degrade 30 mg/L DB 71 after 100 min. DB 71 degradation process was best described by the pseudo-first-order model, with the coefficient of determination within the range of 0.9043-0.9946 for all conditions. HO⢠radicals were mainly responsible for degrading the pollutant. The photocatalytic system could be effortlessly regenerated, very stable, which showed an efficiency of >80.0 % after 5 repetitive runs regarding the DB 71 photodegradation. The photocatalyst was easily recovered by a magnet. This research provides a novel approach for producing an effective and practical photocatalyst that can be applied in real organic pollutants-containing waste water treatment systems.
RESUMEN
Novel N,C,S-TiO2/WO3/rGO Z scheme photocatalyst was successfully synthesized from graphite, TIOT, and ammonium metatungstate precursors. Material characteristics such as crystal structure, surface morphology, functional groups, specific surface area, elemental composition, band gap energy, and electron-hole recombination were characterized by XRD, TEM, BET, SEM/EDX, FT-IR, UV-VIS, and PL methods. The as-synthesized novel N,C,S-TiO2/WO3/rGO Z-scheme heterojunction photocatalyst exhibited visible light-driven photocatalytic activity (the band gap energy = 2.24 eV), could generate both effective electrons and holes, and presented the lowest electron-hole recombination rate compared to all individual components. Different factors impacting the photocatalytic decomposition of Direct Blue 71 (DB 71) by the N,C,S-TiO2/WO3/rGO system were studied. The results showed that pH of the solution, catalyst load, DB 71 initial concentration, and reaction time affected the DB 71 photocatalytic degradation efficiency. The DB 71 degradation completed after 100 min with a typical efficiency of over 91%, which was much better than other photocatalytic systems. The DB 71 degradation process followed the pseudo-first-order kinetics model with coefficients of determination > 0.95 for all conditions. The photocatalyst was easily regenerated, and exhibited a very good stability, with a photocatalytic degradation efficiency of over 83.0% after 3 cycles.