This article presents the surface morphology effect of silicon carbide (SiC) particles on the polyurethane binder’s structure formation in a dispersed-filled composite. The difference in the morphology and surface relief of filler particles was ensured by the implementation of plasma chemical modification. As a result of this modification, the filler consisted of core-shell particles characterized by a SiC core and a carbon shell (SiC@C), as well as a carbon shell decorated with silicon nanoparticles (SiC@C/SiNP) or nanos (SiC@C/SiNW). The study of the relaxation properties of polyurethane composites has shown that the strongest limiting effect on the molecular mobility of boundary layer’s chain segments is exerted by a highly developed surface with a complex relief of SiC@C/SiNP and SiC@C/SiNW particles. An empirical method was proposed to find the polymer fractions spent on the formation of the boundary, transition and bulk layers of the polymer matrix in the composite. It was shown that the morphology of the filler particles’ surface does not affect the dependence of the boundary layer thickness on the filler’s volume fraction. However, with an increase in the degree of surface development, the boundary layer thickness decreases.

The paper describes the effect of the addition of alumina nanofibers on the mechanical properties of the epoxy resin. Alumina nanofibers functionalized with epoxypropyl functional groups are used in this work. The dependence of the mechanical characteristics on the amount of the additive, as well as the features of its distribution in the material, is investigated. In the work, nanocomposites were obtained, which are epoxy resin with aluminum oxide nanofibers. The mechanical properties of the samples were studied by bending tests and differential mechanical analysis (DMA). It has been shown that the addition of alumina nanofibers leads to an increase in ultimate flexural strength. The maximum of this increase is near the percolation threshold of alumina nanofibers in epoxy resin. With the addition of 0.2% alumina nanofibers, the ultimate flexural strength increases from 41 to 71 MPa. It is shown that after exceeding the percolation threshold of nanofibers, the ultimate strength decreases. In this case, the elastic modulus increases from 0.643 to 0.862 GPa. DMA is shown that the glass transition temperature decreases with increasing amount of the additive. This indicates a decrease in the molecular weight of the polymer. By implication, this suggests that the hardener connects the epoxypropyl functional groups on the nanofibers and the epoxy groups in the resin, and as a result of this process, the nanofibers become natural polymer chain length limiters. The data obtained from mechanical testing and differential mechanical analysis can be used to strengthen epoxy resins in polymer composite materials and molding compositions.

A plasma-chemical method for the modification of silicon carbide particles is presented, which makes it possible to obtain particles with a controlled surface morphology. The variable parameter of particle processing was the ratio of the fraction of plasma-forming (Ar) and additional (H) gases. It was shown that at Ar/H = 100/0, the formation of a carbon shell is observed; at Ar/H ratios of 91/9 and 84/16, the particles are characterized by a carbon shell decorated with silicon nanoparticles or nanowires, respectively. The modified particles were analyzed using scanning electron microscopy and Raman spectroscopy.

The degradation pattern of bacterial poly-3-hydroxybutyrate (PHB) in dimethylformamide (DMF) and dioxane solutions at 100 °C assisted by ethylenediamine, 1,4-diaminobutane and monoaminoethanol was studied. When diamines were introduced into the PHB solution in DMF in the amount of 1 mol of the reagent to 5 or 10 mol of PHB monomers, a rapid decrease in the molecular weight of the polymer was observed. The initial value of the weight average molecular weight (M_w) 840 kDa had decreased by 20–30 times within the first 10–20 min of the experiment, followed by its gradual decrease to several thousand Da. When a similar molar quantity of aminoethanol was added, the molecular weight decreased slower. PHB had been degrading much slower in the dioxane solution than in DMF. By varying the number of reagents, it was possible to reach stabilization of the M_w at 1000–3000 Da when using diamines and 8000–20,000 Da using aminoethanol. ¹H NMR analysis of the oligomers revealed of amino and amido groups forming in their structure. From the opposite end of the polymer chain, residues of 3-hydroxybutyric, crotonic and isocrotonic acids were formed during degradation. Differential scanning calorimetry indicated that after oligomerization there was a decrease in the melting point from 178 °C to 140–170 °C depending on the decrease in the molecular weight. The method proposed can be used for obtaining aminated PHB oligomers.