Thaysensosa3286

Today, nanoparticles are effectively used in different areas. Initially, physical and chemical methods were used in the synthesis of nanoparticles. Biosynthesis (green synthesis) has emerged as an alternative to overcome the toxic effects of chemically synthesized nanoparticles. In this study, green synthesis of silver nanoparticles (AgNPs) with the leaf extract of Anthurium andraeanum was performed. UV-Vis spectrophotometry, scanning transmission electron microscopy, and XRD were applied to characterize the biosynthesized nanoparticles. As a result of the characterization, the spectra showed that a spectrum at a wavelength of about 419 nm and a spherical size of 38 nm nanoparticles was formed. Antibacterial and biofilm inhibition activities of AgNPs against gram-positive and gram-negative bacteria were determined. AgNPs at a concentration of 1 mg/mL showed antibacterial activity against all of the bacterial strains. In the antibiofilm activity study, the highest inhibition percentage was obtained against the P. fluorescens strain at 87.1%, at a concentration of 0.5 mg/mL.In this study, microwave-assisted ammonia decomposition reaction was investigated over molybdenum incorporated catalysts. Due to the selective, volumetric, and noncontact heating properties of the microwave system, higher conversion values could be achieved at relatively lower reaction temperatures, which is important for on-site COx-free hydrogen production. Multiwall carbon nanotube-supported molybdenum catalysts were prepared following the impregnation procedure with different metal loading (3.5%-12.5% wt%), and inductively coupled plasma, nitrogen physisorption, X-ray diffraction, and transmission electron microscopic techniques were employed to characterize the fresh and used samples. Reaction experiments were performed under the flow of pure ammonia with a gas hourly space velocity of 36,000 mL/gcat.h for both the microwave and conventionally heated reaction systems. It was found that ammonia conversion was obtained even at 400 °C, reaching 40%, and total conversion was observed even at 450 °C, while the activities of these catalysts were negligible at a reaction temperature lower than 550 °C, in the conventional heated system, which included an electrically heated furnace. Crystals of α-Mo2C as well as MoO2 were observed in the structures of the synthesized catalysts and the formation of nitride species was more easily observable under microwave heating, possibly due to the nitridation of molybdenum carbide species during the reaction.Silsesquioxane-based transition-metal complexes have come to the forefront due to the ability of silsesquioxane to control nanostructures and properties. However, some difficulties in complete complexation and purification limit the widespread use of transition-metal-based supramolecular coordination complexes comprising silsesquioxane. Herein, 2 different approaches have been proposed for the synthesis of metallo-supramolecular materials on the basis of ruthenium(II)-terpyridine functional double-layer silsesquioxane (DDSQ) (Tpy/Ru-DDSQ) (Routes 1 and 2). In Route 1, complexation was followed by functionalization of DDSQ with the ligand, whereas in Route 2, complexation was performed before the ligand was inserted into the DDSQ. Tpy/Ru-DDSQ obtained from both approaches was characterized by 1H NMR, X-ray photoelectron spectrometer, and FTIR and found in the same structure. Both methods were fully discussed and their merits were explored. The complexation yield of the routes was similar. However, the results based on NMR and UV-Vis spectroscopy demonstrated that the incorporation rate of DDSQ into the complex was quite high in Route 2. As far as is known, this is the first study based on the effects of complexing Tpy ligands before/after binding to the target compound, particularly to silsesquioxane-based materials.Activated carbon (AC), a porous material with high pore volume, attracts increasing attention owing to its potential applications in several fields. The development of a porous structure in AC marginally relies on both the treatment methods and the type of precursor. Thus far, both renewable and nonrenewable precursor sources have been used to synthesize AC with high surface area and pore volume. This study presents the synthesis of AC via physicochemical treatment of waste oil fly ash (OFA), a waste material produced from power plants. The aim was to produce AC by adding surface pores and surface functional groups to the basal plane of OFA. Toward this objective, OFA was first chemically leached/activated with various combinations of H2SO4 and H3PO4, and then physically activated with CO2 at 900 °C. The chemical activation step, synergistically combined with CO2 activation, resulted in an increase of 24 times the specific surface area of the OFA. The maximum increase in surface area was obtained for the sample physicochemically treated with 100% H2SO4 . IACS-010759 cost Moreover, the spectroscopic analysis confirmed the presence of acid functional groups after the chemical treatment step. To explore the surface heterogeneity, adsorptive potential distribution in terms of surface energy was also discussed as a function of the surface coverage. Following chemical activation, the OFA surface became heterogeneous. A major portion of the AC showed surface energy in the range of 40-50 erg/K, which was further increased as a result of physical activation at a higher temperature. Thus, the synergism created by physicochemical activation resulted in a material with high surface area and pore volume, and excellent adsorption characteristics. From the findings of this study, it was concluded that OFA is a cost-effective and environmentally benign precursor for the synthesis of AC.Cyclodextrins (CDs) are natural, nontoxic, and biodegradable macrocyclic oligosaccharides. As supramolecular hosts, CDs have numerous applications in many aspects. However, nonsubstituted CDs have the disadvantages of solubility, unspecific recognition sites, and weak interactions with guest molecules. Therefore, new CD-based derivatives are successfully designed, synthesized, and widely used in various fields. This contribution outlines the research progress in CD derivatives. In particular, this review emphasizes the synthesis and application of CDs modified through functionalization in definite positions, random substitution, and reconstruction of the skeleton. At the end of this review, a summary and future directions are presented.