An original method is proposed for preparing highly concentrated solutions of PAN copolymer in N-methylmorpholine-N-oxide (NMMO) and forming membranes for nanofiltration from these solutions. The high activity of the solvent with respect to the polymer provides short preparation time of spinning solutions in comparison with PAN solutions obtained in other solvents. The use of the rheological approach made it possible to find the optimal concentration for obtaining membranes. The formation of PAN membranes from the obtained solutions is proposed by the rolling method. The morphology of the formed membranes depends on the method of removing the precipitant from the sample. The features of the formed morphology of PAN membranes were studied by scanning electron microscopy. It was revealed that the use of water as a rigid precipitant leads to the formation of a homogeneous and symmetric morphology in the membrane. The average pore sizes in the membrane have been obtained by porosimetry. The study of the separating properties of PAN membranes revealed noteworthy values of the permeability and rejection for the anionic dyes Orange II and Remazol Brilliant Blue (74 and 97%, respectively). The mechanical properties of PAN membranes from solutions in NMMO are not inferior to analogs formed from commercially used direct solvents.

The research investigates the thermal behavior of mixed systems based on natural and artificial cellulose fibers used as precursors for carbon nonwoven materials. Flax and hemp fibers were employed as natural components; they were first chemically treated to remove impurities and enriched with alpha-cellulose. The structure, chemical composition, and mechanical properties of both natural and viscose fibers were studied. It was shown that fiber properties depend on the fiber production process history; natural fibers are characterized by a high content of impurities and exhibit high strength characteristics, whereas viscose fibers have greater deformation properties. The thermal behavior of blended compositions was investigated using TGA and DSC methods across a wide range of component ratios. Carbon yield values at 1000 °C were found to be lower for blended systems containing 10–40% by weight of bast fibers, with carbon yield increasing as the quantity of natural fibers increased. Thus, the composition of the cellulose composite affects carbon yield and thermal processes in the system. Using the Kissinger method, data were obtained on the value of the activation energy of thermal decomposition for various cellulose and composite systems. It was found that natural fiber systems have three-times higher activation energy than viscose fiber systems, indicating their greater thermal stability. Blends of natural and artificial fibers combine the benefits of both precursors, enabling the deliberate regulation of thermal behavior and carbon material yield. This approach opens up prospects for the creation of functional carbon materials used in various high-tech areas, including thermal insulation.

In this study, a new approach to stabilizing polypropylene (PP) melts using the bio-based antioxidant propyl gallate (PG) is considered. Since PG is extensively used in the food and cosmetics fields and its low doses do not cause reactions in humans, producing PP melts with PG is an interesting approach. Furthermore, PG is already actively used in the processing of natural polymers, for example, in the NMMO process. It is shown that introducing up to 0.2 wt.% PG into the system is sufficient to significantly reduce the decrease in melt viscosity during repeated PP processing. After five processing cycles, the viscosity of systems with PG decreases by less than an order of magnitude, while for melts without the antioxidant the viscosity drops by almost three orders of magnitude to 10 Pa s. For melts with antioxidant additives, the crossover point position in the frequency dependences remains virtually unchanged, indicating the preservation of the system’s elastic properties. Macrofibers were spun from the resulting melts, which can then be used for concrete reinforcement. For the spun fibers with PG, the strength decreased to 68.1 MPa after five passes, whereas for the PP fibers, the values did not exceed 31 MPa. The structure and properties of the fibers were studied using X-ray diffraction and IR spectroscopy, and contact angles were determined.