ABSTRACT
The global presence of pharmaceutical pollutants in water sources represents a burgeoning public health concern. Recent studies underscore the urgency of addressing this class of emerging contaminants. In this context, our work focuses on synthesizing a composite material, FexOy/MAF-32, through a streamlined one-pot reaction process, as an adsorbent for diclofenac, an emerging environmental contaminant frequently found in freshwater environments and linked to potential toxicity towards several organisms such as fish and mussels. A thorough characterization was performed to elucidate the structural composition of the composite. The material presents magnetic properties attributed to its superparamagnetic behavior, which facilitates the recovery efficiency of the composite post-diclofenac adsorption. Our study further involves a comparative analysis between the FexOy/MAF-32 and a non-magnetic counterpart, comprised solely of 2-ethylimidazolate zinc polymer. This comparison aims to discern the relative advantages and disadvantages of incorporating magnetic iron oxide nanoparticles in the contaminant removal process facilitated by a coordination polymer. Our findings reveal that even a minimal incorporation of iron oxide nanoparticles substantially enhanced the composite's overall performance in pollutant adsorption.
ABSTRACT
In this research, changes in several characteristics of partially reduced titania were studied. The reduction process used made it possible to gradually observe changes in the material depending on the amount of reducing agent used. We used NaBH4 to impregnate commercial TiO2 with isopropyl alcohol. Impregnated TiO2 nanoparticles were dried and thermally treated in a nitrogen flow to obtain blue titania samples. Thorough spectroscopic characterization showed that oxygen atoms from hydroxyl groups, as well as from the surface, and the lattice of TiO2 was consumed. This caused changes in the surface and even in the bulk of TiO2 when the amount of reducing agent used was increased. Structural, optical, superficial, and textural characteristics were studied using XRD, Raman, DRS UV-Vis-NIR, Mid-DRIFT, XPS, and nitrogen adsorption/desorption isotherms. A photocatalytic test of the degradation of methylene blue dye was performed. Among different effects on the mentioned characteristics, we found evidence of changes in the surface properties of the blue titania samples and their probable effect on the photocatalytic properties. The reduction process implied a preponderant decrease in the surface hydrophilicity of the reduced samples, an effect shown for the first time in this type of material.
ABSTRACT
Zeolites are not often used directly as photocatalysts. Their framework and nanocavities have served as support or hosts for photoactive materials or traces of transition metals functioning as photoactive sites for catalysing decomposition and oxidation reactions in the gas phase. Research in this area has been limited to a few synthetic zeolites and in this context, efforts are directed to the preparation of new zeolite-based photocatalysts, when in nature there is an abundance of materials with properties yet to be discovered. We report the application of a natural clinoptilolite-mordenite zeolite as an efficient self-photocatalytic material for the decomposition of caffeine in aqueous solution. Adsorption experiments, combined with textural, crystallographic, and spectroscopic characterization were performed comparatively for the natural zeolite, a synthetic homologue, and the iron-exchanged zeolite. The neat zeolite containing 1.2 wt% of endogenous iron exhibited 99% decomposition of caffeine after 4 h irradiation and a faster reaction rate, followed by the synthetic sample. In contrast, the iron-loaded sample was the less effective zeolite because of pore blocking. Caffeine adsorption occurred on the outer zeolite surface and the photoproducts were hydroxylated pyrimidine rings and linear amide derivatives.
ABSTRACT
Carbon-TiO2 sulfated composites were obtained from TiOSO4 · xH2O and glycerol as the TiO2 and carbon sources, respectively. The precursor xerogels were prepared in a one-step ultrasonic-assisted sol-gel reaction, followed by thermal treatment at 400°C under a nitrogen atmosphere to produce carbon-TiO2 sulfated composites. XRD, micro-Raman, SEM, and TEM studies showed that the composites consisted of nanocrystalline clusters of TiO2 and carbon. Ultrasonication in glycerol promoted the crystallinity of the xerogel precursors prior to thermal treatment. X-ray powder diffraction and Raman spectroscopy studies confirmed that glycerol also facilitated the formation of small crystallites. The band gaps of carbon-TiO2 composites with two different carbon loadings were found to be 3.06 eV and 2.69 eV. By contrast, the band gap of TiO2 prepared by our method was 3.53 eV. Calcination of the precursors led to an unusual increase in the specific surface and porosity of the composites compared to TiO2. The photocatalytic activities of the prepared composites were tested in a decomposition assay of Acid Orange 7. The reaction was monitored by UV-vis spectrophotometry and by LC-ESI-(Qq)-TOF-MS-DAD. Some intermediate species were identified by LC-ESI-QTOF-MS.
