RESUMEN
The novel bimetallic MOF, ZnCu-MOF-74, has been evaluated for the remediation of tetracycline-contaminated water. ZnCu-MOF-74 was obtained at room temperature, avoiding high pressure and temperature. ZnCu-MOF-74 exhibited chemical stability in the 4-8 pH range. The adsorption result analysis was described using the Elovich kinetic model and the Langmuir adsorption isotherm, suggesting a physicochemical process. The maximum adsorption capacity was estimated at 775.66 mg g-1. The pH of the solution and the presence of ions such as NO3-, SO42-, Na+, Mg2+, Cl-, and Ca2+ had no influence on the removal of tetracycline. In addition, π-interactions and metal complexation were proposed as possible adsorption mechanisms through FT-IR and XPS. ZnCu-MOF-74 showed outstanding cyclability performance, preserving its adsorption capacity after 4 adsorption-desorption cycles, besides exhibiting chemical stability, proving the benefits of applying ZnCu-MOF-74 in the water treatment process.
RESUMEN
The development of adsorbents for air pollutant remediation and effective monitoring is of interest. Then, the effect of the APTES functionalization ratio on the impact of the adsorption and detection of SO2 molecules was evaluated. The higher APTES functionalization material (SBA-15_6.1APTES) shows a high uptake of 1.15 mmol g-1 at 0.001 bar and 298 K. Fluorescence, time-resolved photoluminescence, and quantum yield experiments revealed a turn-on effect specifically for SO2 molecules, indicating high selectivity, suggesting host-to-guest energy transfer. Attractively, XPS measurement provided an understanding of the mechanism, suggesting hydrogen bonding and dipole-dipole interactions as the main interactions between SO2 molecules and SBA-15_6.1APTES. DFT calculations were performed to confirm these interactions. Furthermore, this study highlights the application of SBA-15 materials with different amino modifications for SO2 treatment and provides insight into the interaction mechanism using experimental techniques.
RESUMEN
A lipoma is a tumor of adipose tissue cells that can develop anywhere in the body, usually at the subcutaneous level without invading adjacent structures. Its most common location is on the back and extremities. According to the literature, it is considered common in both sexes; however, it is mentioned that it occurs more frequently in females. Clinically, it presents as a slow-growing, painless mass. Although the diagnosis is clinical, an imaging study is usually performed for confirmation and to obtain information about its location, relationship with adjacent structures, and surgical planning. The definitive treatment involves surgical resection with histopathological analysis, providing a definitive diagnosis to rule out malignancy. In the present case report, we will present a 45-year-old female patient, with no significant medical history, who comes for evaluation due to a tumor in her right shoulder approximately 5 cm in size with gradual growth to 20 cm over 12 years, seeking evaluation due to clinical manifestations. A surgical protocol was initiated, with magnetic resonance imaging (MRI) considered the imaging study of choice according to the literature, where a superficial location was observed. A surgical plan was made that included complete resection and histopathological analysis, with post-surgical evaluations at two, four, and six months post-surgery showing no signs of recurrence, remission of symptoms of nerve compression, and appropriate wound healing.
RESUMEN
The Al(III)-based MOF CYCU-3 exhibits a relevant SO2 adsorption performance with a total uptake of 11.03 mmol g-1 at 1 bar and 298 K. CYCU-3 displays high chemical stability towards dry and wet SO2 exposure. DRIFTS experiments and computational calculations demonstrated that hydrogen bonding between SO2 molecules and bridging Al(III)-OH groups are the preferential adsorption sites. In addition, photoluminescence experiments demonstrated the relevance of CYCU-3 for application in SO2 detection with good selectivity for SO2 over CO2 and H2O. The change in fluorescence performance demonstrates a clear turn-on effect after SO2 interaction. Finally, the suppression of ligand-metal energy transfer along with the enhancement of ligand-centered π* â π electronic transition was proposed as a plausible fluorescence mechanism.