The current investigation is focused on the development of composite membranes based on polymeric ionic liquids (PILs) containing imidazolium and pyridinium polycations with various counterions, including hexafluorophosphate, tetrafluoroborate, and bis(trifluoromethylsulfonyl)imide. A combination of spectroscopic methods was used to identify the synthesized PILs and characterize their interaction with carbon dioxide. The density and surface free energy of polymers were performed by wettability measurements, and the results are in good agreement with the permeability and selectivity obtained within the gas transport tests. It was shown that the membranes with a selective layer based on PILs exhibit relatively high permeability with CO₂ and high ideal selectivity CO₂/CH₄ and CO₂/N₂. Additionally, it was found that the type of an anion significantly affects the performance of the obtained membranes, with the most pronounced effect from bis-triflimide-based polymers, showing the highest permeability coefficient. These results provide valuable insights into the design and optimization of PIL-based membranes for natural and flue gas treatment.

This work explored the zinc nanoparticles obtained by the one-stage induction flow levitation method. A 10 kW tube generator with an operating frequency of 440 kHz was used. The process used 8 mm diameter zinc granules (2 g weight) with a purity of 99.9%. Zinc wire was fed to replace the evaporated metal from the granule surface. This method productivity was 30 g/h of nanoparticles. In addition, various methods were used to characterize the resulting nanoparticles: scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-Ray fluorescence analysis (XRF), dynamic light scattering (DLS), porosimetry and inductively coupled plasma atomic emission spectroscopy (ICP-MS). The resulting nanoparticle size, determined by SEM and porosimetry, was 350 nm, while the size of the primary crystallites was 21 nm. The amount of impurities in the resulting nanoparticles did not exceed 1000 ppm.

The present research provides data on the density (ρ), viscosity (η) and ability to absorb carbon dioxide of systems containing amine, molecular solvent (MS) and choline chloride (ChCl), with the investigation of the physical properties of both neat amine/MS/ChCl mixtures and their samples after complete CO₂ saturation. The effect of the mixture composition was studied by varying amine from primary (monoethanolamine, MEA) to secondary (diethanolamine, DEA) and tertiary (triethanolamine, TEA) amine, and the degree of its substitution from a mono- (MEA, DEA and TEA) to a doubly-substituted (ethylenediamine, EDA) compound. The role of an MS was investigated via the exchange of ethylene glycol (EG) with water and dimethylsulfoxide (DMSO). In addition, the influence of the CO₂ absorption promoters present in the ternary MEA/EG/ChCl mixture at an amount of 5 wt. % was also investigated. We show that an increase in ρ and η in the amine/EG/ChCl mixture affects the properties of neat amines. This suggests that in the studied ternary mixtures, the nature of the interspecies interactions is very similar to those in the previously studied MEA/EG/ChCl system. When EG was exchanged for H₂O or DMSO, a decrease in ρ and an increase in η were observed. A comparison of the data with the corresponding properties of the systems composed of each pair of the mixture components indicates that the intensity and/or number of interspecies interactions in the present ternary mixtures were stronger than those in pure H₂O, DMSO and MEA. While in the presence of promoters no significant changes in the studied properties were found, for the corresponding CO₂-saturated samples, the ρ and η increased proportionally to the amount of absorbed gas. This was also the case for all the systems studied in the present research. The overall CO₂ absorption of the EG-based mixtures decreased when going from primary to secondary and tertiary amines; it was 21% higher for the MEA/H₂O/ChCl system compared to the mixtures containing EG and DMSO, which, in turn, showed similar absorption capacities. When the promoters were added to the MEA/EG/ChCl mixture, the highest capacity was found for the piperazine-containing system.

TiC nanoparticles less than 16 nm in size have been prepared in a single step from bulk titanium carbide by the induction flow levitation (IFL) method. The method has a number of advantages: high production rate (up to 100 g/h), the ability to vary the nanoparticle size in a wide range (0.5–500 nm), and contactless heating (up to 2500°C). Moreover, it meets green chemistry principles. In this gas phase method, a levitating metal is heated by a high-frequency electromagnetic field. The synthesized titanium carbide nanoparticles have been characterized by a variety of physicochemical techniques: transmission electron microscopy, scanning electron microscopy, X-ray diffraction, low-temperature nitrogen adsorption measurements, and dynamic light scattering. The results demonstrate that IFL is one of the most promising methods for the preparation of nanoparticles and ensures high purity and a small particle size of single-step synthesis products.