In this work, a multifunctional surface engineering strategy was developed to impart both flame-retardant and hydrophobic properties to cotton fabrics. In the first stage, cellulose fibers were modified with poly(methylvinyl)siloxane containing trimethoxysilyl groups, 2,4,6,8-tetramethyl-divinyl-bis(trimethoxysilylpropyltioethyl)cyclotetrasiloxane, or tetrakis(vinyldimethylsiloxy)tetrakis(trimethoxysilylpropyltioethyl)octasilsesquioxane (POSS). All modifiers contained alkoxysilyl groups capable of forming covalent bonds with cellulose hydroxyl groups. The modification was performed using a dip-coating process followed by thermal curing. This procedure enabled the formation of Si-O-C linkages and the generation of a reactive organosilicon layer on the cotton surface. In the second step, O,O′-diethyl dithiophosphate was grafted directly onto the vinyl-functionalized fabrics via a thiol-ene click reaction. This process resulted in the formation of a phosphorus- and sulfur-containing protective layer anchored within the siloxane-based network. The obtained hybrid coatings were characterized using Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and SEM-EDS. These analyses confirmed the presence and uniform distribution of the modifiers on the fiber surface. Microscale combustion calorimetry demonstrated a substantial reduction in the heat release rate. Thermogravimetric analysis (TG/DTG) revealed increased char formation and altered thermal degradation pathways. The limiting oxygen index (LOI) increased for all modified fabrics, confirming enhanced flame resistance. Water contact angle measurements showed values above 130°, indicating effective hydrophobicity. As a result, multifunctional textile surfaces were obtained. In addition, the modified fabrics exhibited partial durability toward laundering and retained measurable flame-retardant and hydrophobic performance after repeated washing cycles.

The study aimed to determine the influence of shear stress during real-life industrial processes such as compression molding and injection molding to different cavities on the crystallization of the isotactic polypropylene nucleated with a novel silsesquioxane-based β-nucleating agent. Octakis(N²,N⁶-dicyclohexyl-4-(3-(dimethylsiloxy)propyl)naphthalene-2,6-dicarboxamido)octasilsesquioxane (SF-B01) is a highly effective nucleating agent (NA) based on the hybrid organic-inorganic silsesquioxane cage. The samples containing various amounts of the silsesquioxane-based and commercial iPP β-nucleants (0.01–0.5 wt%) were prepared by compression molding and injection molding, including forming in the cavities with different thicknesses. The study of the thermal properties, morphology, and mechanical properties of iPP samples allows for obtaining comprehensive information about the efficiency of silsesquioxane-based NA in shearing conditions during the forming. As a reference sample, iPP nucleated by commercial β-NA (namely N²,N⁶-dicyclohexylnaphthalene-2,6-dicarboxamide, NU-100) was used. The static tensile test assessed the mechanical properties of pure and nucleated iPP samples formed in different shearing conditions. Variations of the β-nucleation efficiency of the silsesquioxane-based and commercial nucleating agents caused by shear forces accompanying the crystallization process during forming were evaluated by differential scanning calorimetry (DSC) and wide-angle X-ray scattering (WAXS). The investigations of changes in the mechanism of interactions between silsesquioxane and commercial nucleating agents were supplemented by rheological analysis of crystallization. It was found that despite the differences in the chemical structure and solubility of the two nucleating agents, they influence the formation of the hexagonal iPP phase in a similar way, taking into consideration the shearing and cooling conditions.

Waterborne polyurethane cationomer coatings modified with 1,3-bis(3(3-(propoxy-2-ol-)-9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide)-3-propyloxy))tetramethyldisiloxane (TMDS–AGE–DOPA) containing phosphorus and silicon atoms were obtained. Their structures were confirmed by Fourier transform infrared (FTIR) spectroscopy. The effect of TMDS–AGE–DOPA on thermal properties, flame retardancy, and surface characteristics (gloss, contact angle, surface free energy), as well as performance properties (hardness, impact resistance), was investigated. A coupled TG-FTIR technique was employed for evolved gas analysis. Thermal stability decreased with the addition of the modifier, while the glass transition temperature increased from −19 to 25 °C. The modifier improved the flame retardancy of the material by shifting the peak temperature of the heat release rate (T_PHRR) to lower values. The gloss of the coatings was very high (>90 GU at all angles studied), although it decreased with increasing modifier content. The presence of phosphorus moieties from the modifier enhanced hydrophilicity, raising surface free energy (SFE) from 37.9 to 44.0 mJ/m². The coatings are soft materials with a Persoz hardness in the range of 0.05–0.32. The modifier increased hardness but reduced impact strength. The obtained cationomers can be applied as environmentally friendly coatings on hydrophilic surfaces such as textiles, glass, or wood.