In this work, the results of investigation of the effect of polymer composite melts electrical conductance increase with time are presented. The conductance time dependencies were obtained for composites based on polypropylene filled with carbon nanoparticles of different types. The dependencies were analyzed to demonstrate the possibility of correlation of the conductance kinetics with different composite parameters, such as the filler geometry. Additional studies were carried out, such as electron microscopy study, conductance measurements after consecutive surface layer removal, and composite melt conductance measurements using a three-electrode scheme. The results showed that the increased electrical conductance of the composite materials can be attributed to the formation of an enriched with the filler particles surface layer, which happens during the stay of the composite in a melt state. Analysis of the experimental data, along with the results of numerical modeling, allowed to suggest a possible filler distribution transformation scheme. The physical premises behind the investigated effect are discussed.

In this work, the results of a complex investigation of structure and properties of nanodiamond soot (NDS) of detonation synthesis are presented. Size distribution of NDS particles, dispersed in different liquid media, was investigated using dynamic light scattering and laser diffraction analysis methods. The results of the investigation, as well as the results of zeta-potential measurements, allowed us to characterize the agglomeration process of the NDS particles as independent of the medium, making NDS a good model filler for research of composite-modified nanosized particles. Additional data obtained using scanning electron microscopy, scanning tunneling microscopy, atomic force microscopy, X-ray diffraction, and Raman spectroscopy, demonstrated that in NDS the spherical nanodiamond (ND) particles with diameter ~5 nm are densely packed into strong-coupled aggregates with diameter ~300 nm, surrounded by graphite nanoribbons. X-ray diffraction analysis estimated the volume fraction of NDs in NDS as ~45 vol.%, simultaneously showing that the graphite is not defective, which was confirmed with the electron diffraction method. It was demonstrated that this structure of NDS allows to efficiently use NDS as a filler for polymer composites to increase polymer characteristics such as electrical conductivity or tribological characteristics, similarly to conventionally applied fillers such as carbon black.

A number of thioether-containing zirconium siloxanes, differing in their composition and metal atom shielding degree with a siloxy substituent, were synthesized and characterized. Synthesis of such compounds made it possible to evaluate the effect of sulfur atoms’ presence in the cured compositions on their dielectric properties, as well as to evaluate their curing ability and influence on mechanical characteristics compared to the sulfur-free analogs obtained earlier. Studying a wide range of compositions differing in their content and ratio of metallosiloxane and silica components revealed that such systems are still typical dielectrics. At the same time, the introduction of thioether groups can provide increased dielectric constant and conductivity in comparison with previously obtained sulfur-free similar compositions in the <10² Hz frequency range (dielectric constant up to ~10–30 at frequency range 1–10 Hz). As before, the dielectric parameters increase is directly determined by the silica component proportion in the cured material. It is also shown that varying sulfur-containing zirconium siloxanes structure and functionality and its combination with previously obtained sulfur–free analogs, along with varying the functionality and rubber chain length, can be an effective tool for changing the dielectric and mechanical material parameters in a wide range (tensile strength 0.5–7 Mpa, elastic deformation 2–300%), which determine the prospects for the use of such cured systems as dielectric elastomers for various purposes.

The article presents the results of research on electrically conductive hard-to-burn composite materials based on polyethylene, graphite, and some flame retardants. It is shown that optimal electrical conducting properties and the flammability rating (V₀) in accordance with UL 94 test are achieved by modifying the graphite-containing composite material based on low-pressure polyethylene with ammonium polyphosphate and (or) aluminum hydroxide. It is shown that the percolation threshold of a composite material based on high-pressure polyethylene and graphite is observed at significantly higher values of the mass fraction of graphite. It is concluded that the reduction of the percolation threshold of polyethylene when filled with graphite is facilitated by an increase in the degree of crystallinity of the binder, and the formation of structured continuous conducting clusters in the composite material is observed at lower values of the mass fraction of the filler. As a result, the thermal conductivity and heat resistance of the composite material are increased owing to more efficient delocalization of the supplied heat. A number of electrically conductive hard-to-burn materials were obtained and characterized. These data allow us to directly adjust the values of the specific volume electrical resistance, physical and mechanical properties, heat resistance, and, to a certain extent, flame resistance.

Chitosan is one of the promising compounds for use in various fields of medicine. However, for successful application, materials based on it must be insoluble in water and have specified physical and mechanical properties. In this work, we studied the interaction of N-methylolacrylamide (NMA) and chitosan upon concentration of the solutions, both under the action of UV radiation and without it, which results in curing of the polymer matrix. The main products, proposed mechanisms of the crosslinking reaction, and the influence of external conditions on these processes have been revealed using NMR, IR, and UV spectroscopy. It was found that the reaction proceeds along three pathways. The main reactions proceed with the amino groups of chitosan, and the hydroxymethyl and vinyl groups of NMA. Studies have shown that for the formation of insoluble materials based on chitosan, the best content in the initial cast solution is 2 wt% of chitosan at 0.25 wt% concentration of NMA. Films formed from such solutions possessed high strength and deformation characteristics, namely an elastic modulus of about 1500 GPa, a strength of about 30 MPa, and an elongation at break of about 100%.

A representative series of functional branched metallosiloxane oligomers was used to obtain polydimethylsiloxane-based composites highly filled with a metallosiloxane component. Physical and mechanical characteristics of compositions obtained strongly depends on metallosiloxane structure and composition. It is shown that it is possible to regulate the strength and elastic properties of the systems under consideration within wide limits, as well as to influence the morphology of the material. The resulting materials are rather thermo-oxidatively stable and can also maintain high mobility of polydimethylsiloxane chains.