Search Results (4)

In this study, a novel magnetic nanocatalyst based on tin ferrite (SnFe₂O₄) was synthesized via a chemical co-precipitation method and thoroughly characterized using XRD, SEM, TGA-DTG, BET, FTIR, and FTIR-pyridine techniques. The catalyst exhibited high crystallinity, a mesoporous structure with a specific surface area of 79.7 m²/g, and well-defined Lewis and Brønsted acid sites. Its catalytic performance was assessed in the esterification of glycerol with acetic acid to produce monoacetin (MAG), diacetin (DAG), and triacetin (TAG). A Box–Behnken experimental design was employed to evaluate the influence of temperature, catalyst loading, and the acetic-acid-to-glycerol molar ratio on product distribution and glycerol conversion. Statistical analysis and regression modeling revealed excellent predictive accuracy (R² > 0.99), confirming the robustness of the model. Optimal reaction conditions (110 °C, 2 wt.% catalyst, and AA/GLY ratio of 3.6) yielded a maximum glycerol conversion of 93.2% and a combined DAG and TAG yield of ~59.1%. These results demonstrate the high efficiency and selectivity of the synthesized SnFe₂O₄ catalyst, making it a promising candidate for sustainable glycerol valorization. Full article

This study intended to fabricate a novel Fenton-like catalyst by supporting the rod-like MIL-88A and the magnetic tin ferrite nanoparticles (SnFe₂O₄) on the MXene sheets (MIL-88A/SnFe₂O₄@MXene). The well fabrication and determination of the MIL-88A/SnFe₂O₄@MXene properties were investigated using SEM, XPS, VSM, Zeta potential, XRD, and FTIR tools. The Fenton-like degradation reaction of CR by MIL-88A/SnFe₂O₄@MXene was thoroughly studied to identify the optimal proportions of the catalyst components, the impact of CR and H₂O₂ concentrations, as well as the effect of raising the temperature and the pH medium of the catalytic system and the catalyst dosage. Kinetics studies were executed to analyze the decomposition of CR and H₂O₂ using First-order and Second-order models. Furthermore, the degradation mechanism was proposed based on the scavenging test that proceeded in the presence of chloroform and t-butanol, in addition to the XPS analysis that clarified the participation of the containing metal species: Fe, Sn, and Ti, and the formation of a continual redox cycle. The obtained intermediates during the CR degradation were defined by GC–MS. A recyclability test was performed on MIL-88A/SnFe₂O₄@MXene during five runs of the Fenton-like degradation of CR molecules. Finally, the novel MIL-88A/SnFe₂O₄@MXene Fenton-like catalyst could be recommended as a propitious heterogeneous catalyst with a continuous redox cycle and a recyclability merit. Full article

Electrodeposited bismuth ferrite (BiFeO₃) thin films on fluorine-doped tin oxide (FTO) substrate were employed as photoanodes in the photoelectrocatalytic degradation of methylene blue. The BiFeO₃ thin films electrodeposited for 300 s, 600 s, 1200 s, 1800 s and 3600 s were characterised with XRD, field emission scanning electron microscopy (FESEM) and UV–vis diffuse reflectance spectroscopy. SEM images displayed different morphology at different electrodeposition times which affects the photoelectrocatalytic (PEC) performances. The FESEM cross-sectional area was used to measure the thickness of the film. The optical properties showed that the band gaps of the photoanodes were increasing as the electrodeposition time increased. The photocurrent response obtained showed that all thin film photoanodes responded to visible light and lower charge transfer resistance (from electrochemical impedance spectroscopy studies) was observed with photoanodes electrodeposited at a shorter time compared to those at a longer time. The PEC application of the photoanode for the removal of methylene blue (MB) dye in water showed that the percentage degradation decreased with an increase in electrodeposition time with removal rates of 97.6% and 70% observed in 300 s and 3600 s electrodeposition time, respectively. The extent of mineralisation was measured by total organic carbon and reusability studies were carried out. Control experiments such as adsorption, photolysis, photocatalysis and electrocatalysis processes were also investigated in comparison with PEC. The electrodeposition approach with citric acid exhibited improved electrode stability while mitigating the problem of catalyst leaching or peeling off during the PEC process. Full article

The continuously growing need for clean water has increased research looking for new and efficient ways to treat wastewater. Due to its magnetic properties, Bismuth ferrite, a photo-catalyst, has introduced a novel field of photo-catalysis where the photo-catalytic material could easily be separated from the aqueous solution after wastewater treatment. Herein, a new type of photo-catalysts, composed of Gadolinium (Gd) and Tin (Sn), co-doped Bismuth Ferrite deposited over graphene nanoplatelet surface have been synthesized using a two-step method. In first step, Gd (fixed concentration 10%) and Sn (5%, 15%, 20% and 25%) were doped inside bismuth ferrite (BFO) host using sol-gel method (namely the BGFSO nanoparticles, abbreviated for Gd and Sn doped BFO). In the second step, BGFSO nanoparticles were introduced onto GNPs using co-precipitation method (namely the BGFSO/GNP nanohybrids). The x-ray photoelectron spectroscopy confirmed the chemical bonding between co-doped BFO and GNP sheets via oxy and hydroxyl groups. The photocatalytic activities of the nanohybrids under both, visible light and dark conditions have been increased, and the maximum degradation activity (74%) of organic dye Congo-red (CR) is obtained for 25% Sn-doped BGFSO/GNP nanohybrid. The photocatalytic activity may be attributed to enhanced adsorption capability, electron storage properties of graphene and the presence of oxygen-rich species inside nanohybrids. Based on the current overgrowing population and need for clean water, these materials present versatile potential as catalysts for wastewater treatment. Full article