Catalytic dehydration of glycerol over Cu-Fe-Al-based oxides: understanding changes in active sites throughout the reaction.

The glycerol conversion into acetol using Fe, Al and Cu-based oxides was investigated. XRD results indicate the formation of nanosized particles with high phase dispersion, however, Raman, Mössbauer, 27Al NMR and XPS spectroscopies suggest the presence of iron(iii) oxide, Al2O3 and CuO phases. The FTIR with pyridine adsorption revealed high Lewis acidity. The TPR profile showed the reduction temperature range for the Fe3+ and Cu2+ sites, indicating the suitable condition for pretreatment. The N2 adsorption-desorption isotherms indicated the presence of micro-mesopores with interesting textural properties and specific area varying between 71 and 220 m2 g-1, while the porous morphology was observed by SEM and TEM images. The optimized catalytic tests showed glycerol conversion of 60% and acetol selectivity of 92% with 17% of coke according to TG profile. The recycling tests confirmed the efficiency of the solid, reaching 28% conversion and 91% acetol selectivity after four reuses and, after reactivation in an oxidizing atmosphere, the catalytic performance obtained results close to the second reuse. The interaction between the different Lewis acid sites involved in the mechanisms for the acetol and coke formation on the catalyst surface is discussed. The charge distribution represented by colors which indicates the acid-base surface was evaluated by a simple theoretical-computational study based on the DFT approach. The synergy between the active sites indicates that the presence of Cu0/Cu+ drastically increases the acetol selectivity which is a more important characteristic than the high Lewis acidity of Fen+ and Al3+.

Photocatalytic degradation of ibuprofen using titanium oxide: insights into the mechanism and preferential attack of radicals.

The present work studied ibuprofen degradation using titanium dioxide as a photocatalyst. Mechanistic aspects were presented and the preferred attack sites by the OH˙ radical on the ibuprofen molecule were detailed, based on experimental and simple theoretical-computational results. Although some previous studies show mechanistic proposals, some aspects still need to be investigated, such as the participation of 4-isobutylacetophenone in the ibuprofen degradation and the preferred regions of attack by OH˙ radicals. The photodegradation was satisfactory using 0.03 g of TiO2 and pH = 5.0, reaching 100% decontamination in 5 min. The zeta potential curve showed the regions of attraction and repulsion between TiO2 and ibuprofen, depending on the pH range and charge of the species, influencing the amount of by-products formed. Different by-products have been identified by GC-MS, such as 4-isobutylacetophenone. Ibuprofen conversion to 4-isobutylacetophenone takes place through decarboxylation reaction followed by oxidation. The proposed mechanism indicates that the degradation of ibuprofen undergoes a series of elementary reactions in solution and on the surface. Three different radicals (OH˙, O2 -˙ and OOH˙) are produced in the reaction sequence and contribute strongly to the oxidation and mineralization of ibuprofen and by-products, but the hydroxyl radical has a greater oxidation capacity. The simple study using the DFT approach demonstrated that the OH˙ radical attacks preferentially in the region of the ibuprofen molecule with high electronic density, which is located close to the aromatic ring (C[double bond, length as m-dash]C bond). The presence of the OH˙ radical was confirmed through a model reaction using salicylic acid as a probe molecule.

Synthesis of Fe2SiO4-Fe7Co3 Nanocomposite Dispersed in the Mesoporous SBA-15: Application as Magnetically Separable Adsorbent.

The mixture containing alloy and oxide with iron-based phases has shown interesting properties compared to the isolated species and the synergy between the phases has shown positive effect on dye adsorption. This paper describes the synthesis of Fe2SiO4-Fe7Co3-based nanocomposite dispersed in Santa Barbara Amorphous (SBA)-15 and its application in dye adsorption followed by magnetic separation. Thus, it was studied the variation of reduction temperature and amount of hydrogen used in synthesis and the effect of these parameters on the physicochemical properties of the iron and cobalt based oxide/alloy mixture, as well as the methylene blue adsorption capacity. The XRD and Mössbauer results, along with the temperature-programmed reduction (TPR) profiles, confirmed the formation of Fe2SiO4-Fe7Co3-based nanocomposites. Low-angle XRD, N2 isotherms, and TEM images show the formation of the SBA-15 based mesoporous support with a high surface area (640 m2/g). Adsorption tests confirmed that the material reduced at 700 °C using 2% of H2 presented the highest adsorption capacity (49 mg/g). The nanocomposites can be easily separated from the dispersion by applying an external magnetic field. The interaction between the dye and the nanocomposite occurs mainly by π-π interactions and the mixture of the Fe2SiO4 and Fe7Co3 leads to a synergistic effect, which favor the adsorption.