The work is focused on the study of the influence of the cellulose type and processing parameters on the structure, morphology, and permeability of cellulose films. The free volume of the cellulose films was evaluated by the sorption of n-decane, which is a non-solvent for cellulose. The structural features of the membranes and their morphology were studied using X-ray diffraction, IR spectroscopy, SEM, and AFM methods. The characteristic features of the porous structure and properties of cellulose films regenerated from cellulose solutions in the N-methylmorpholine-N-oxide (NMMO) and cellophane films were compared. Generally, cellulose films obtained from solutions in NMMO have a higher permeability and a lower rejection (as measured using Orange II dye) as compared to cellophane films. It was also found that the cellulose films have a higher ultimate strength and modulus, whereas the cellophane films are characterized by higher elongation at break.
Composite fibers and films based on cellulose and betulin were spun for the first time from solutions in N-methylmorpholine-N-oxide using the dry–wet jet method. The rheological properties of the composite solutions did not reveal any fundamental difference from those of the cellulose solutions. Introduction of betulin into the cellulose matrix (up to 10%) led to a decrease in the mechanical properties of the obtained fibers. The structure of the composite fibers was analyzed using SEM and X-ray diffraction methods. It was shown that the introduction of an additive into the cellulose matrix led to a decrease in the structural ordering of the cellulose. Comparative studies of the antibacterial activity of the composite films on Escherichia coli (E. coli) were carried out. The antifungal activity of the composite films was estimated using the strain of the O-97 Trichoderma viride Pers ex Fr (Gause Institute of New Antibiotics, Moscow, Russia).
In the present study, one of the possible methods of the bacterial cellulose processing is proposed via its dissolution in N-methylmorpholine-N-oxide using the stage of mechano-chemical activation of the solid polymer–solvent system. Preliminary solid-phase activation is apparently a decisive factor affecting the dissolution rate of bacterial cellulose in N-methylmorpholine-N-oxide. The effects of bacterial cellulose concentration, solvent nature, degree of polymerization and temperature on dissolution time were studied. The rheological behavior of the solutions does not change at 120 °C for at least half an hour that allowed us to process such solutions for films preparation. The films from these solutions by means of dry-wet jet spinning in aqueous coagulant were formed. The structure of the nascent cellulose and formed films was tested by the X-ray diffraction method and SEM. The thermal behavior of the films revealed an increase in the carbon yield for the formed films compared to the nascent bacterial cellulose. The process of film pyrolysis is accompanied by exothermic effects, which are not typical for wood cellulose. Some reasons of such thermal behavior are considered.
This review examines scientific and engineering strategies for adapting bituminous and asphalt concrete materials to the highly diverse climates of Central Asia. The region’s sharp gradients—from arid lowlands to cold mountainous zones—expose pavements to thermal fatigue, photo-oxidative aging, freeze–thaw cycles, and wind abrasion. Existing climatic classifications and principles for designing thermally and radiatively resilient pavements are summarized. Special emphasis is placed on linking binder morphology, rheology, and climate-induced transformations in composite bituminous systems. Advanced characterization methods—including dynamic shear rheometry (DSR), multiple stress creep recovery (MSCR), bending beam rheometry (BBR), and linear amplitude sweep (LAS), supported by FTIR, SEM, and AFM—enable quantitative correlations between phase composition, oxidative chemistry, and mechanical performance. The influence of polymeric, nanostructured, and biopolymeric modifiers on stability and durability is critically assessed. The review promotes region-specific material design and the use of integrated accelerated aging protocols (RTFOT, PAV, UV, freeze–thaw) that replicate local climatic stresses. A climatic rheological profile is proposed as a unified framework combining climate mapping with microstructural and rheological data to guide the development of sustainable and durable pavements for Central Asia. Key rheological indicators—complex modulus (G*), non-recoverable creep compliance (Jnr), and the BBR m-value—are incorporated into this profile.
Polypropylene (PP) is a highly sought-after synthetic polymer. Due to its properties, it has wide applications in a number of industries. One-dimensional molded materials (fibers and strands) are widely used in the textile and construction sectors. Concrete reinforcing using PP fiber is an intriguing use in construction. Fiber can be provided in two forms: fine fibers (microfiber) and extrudates (macrofiber). The macrofiber has a length of up to 60 mm and a thickness of up to 300 microns. The aim of the work was to obtain PP-based macrofibers from recycled polymer using the natural antioxidant tocopherol. The initial polymer is used to produce the fiber, whereas, in this work, it is proposed to use a secondary PP. Vitamin E, a natural antioxidant, was added to the system to stabilize the melts. It has been demonstrated that adding up to 0.5% Vitamin E reduces the heat degradation of the polymer and yields melts with the appropriate viscoelastic characteristics. Rheological data was used to determine the fiber’s formability window. Macrofibers were derived from melts with varying histories. Their structure was investigated using X-ray structural analysis and IR spectroscopy, and their mechanical characteristics were assessed.
This study focuses on the development of environmentally sustainable polypropylene (PP)-based composites with the potential for biodegradability by incorporating cellulose and the oligomeric siloxane ES-40. Targeting industrial applications such as fused deposition modeling (FDM) 3D printing, ES-40 was employed as a precursor for the in situ formation of silica particles via hydrolytic polycondensation (HPC). Two HPC approaches were investigated: a preliminary reaction in a mixture of cellulose, ethanol, and water, and a direct reaction within the molten PP matrix. The composites were thoroughly characterized using rotational rheometry, optical microscopy, differential scanning calorimetry, and dynamic mechanical analysis. Both methods resulted in composites with markedly reduced crystallinity and shrinkage compared to neat PP, with the lowest shrinkage observed in blends prepared directly in the extruder. The inclusion of cellulose not only enhances the environmental profile of these composites but also paves the way for the development of PP materials with improved biodegradability, highlighting the potential of this technique for fabricating more amorphous composites from crystalline or semi-crystalline polymers for enhancing the quality and dimensional stability of FDM-printed materials.