This article deals with the influence of electron-beam radiation on the micro-mechanical, thermo-mechanical, and structural properties of selected polymers. In the search for the desired improvement of polymers, it is possible to use, inter alia, one particular possible modification—Namely, crosslinking—Which is a process during which macromolecular chains start to connect to each other and, thus, create the spatial network in the structure. In the course of the treatment of the ionizing radiation, two actions can occur: crosslinking and scission of macromolecules, or degradation. Both these processes run in parallel. Using the crosslinking technology, standard and technical polymers can acquire the more “expensive” high-tech polymeric material properties and, thus, replace these materials in many applications. The polymers that were tested were selected from across the whole spectra of thermoplastics, ranging from commodity polymers, technical polymers, as well as high-performance polymers. These polymers were irradiated by different doses of beta radiation (33, 66, 99, 132, 165, and 198 kGy). The micro-mechanical and thermo-mechanical properties of these polymers were measured. When considering the results, it is obvious that irradiation acts on each polymer differently but, always when the optimal dose was found, the mechanical properties increased by up to 36%. The changes of micro-mechanical and thermo-mechanical properties were confirmed by structural measurement when the change of the micro-hardness and modulus corresponded to the crystalline phase change as determined by X-ray and gel content.

This article aimed to compare various mechanical properties of epoxy/graphene and epoxy/halloysite nanocomposites. Graphene nanoplatelets (GnPs) and halloysite nanotubes (HNTs) were used as fillers at different concentrations. The studied fillers were dispersed in the epoxy resin matrices. Elastic–plastic mechanical behavior modulation was observed utilizing the fillers’ nanoparticles and carboxyl-terminated butadiene–acrylonitrile copolymer rubber-modified epoxy resin. The hypothesis of the possible preceding inter-particle gliding of the individual GnPs in the complex resin nanocomposite matrix during mechanical testings was also confirmed. Increased ductility (elongation at break increased from 0.33 mm [neat matrix] to 0.46 mm [1 wt% GnPs] [39% increase]) and plasticity of the GnP nanocomposite samples were observed. In contrast, the decreasing mechanical stiffness as reflected in the decreased Young’s modulus of elasticity (from 3.4 to 2.7 GPa [20% decrease]) was found for the epoxy/HNT nanocomposites. The obtained dynamic stiffness of the investigated nanocomposites confirmed the complexity of the mechanical response of the studied material systems as a combination of the ductile and brittle phenomena.

Two different nanosized mineral fillers (nano calcium carbonate and nanoclay) were used in the high density poly(ethylene) (HDPE) composites pilot plant production. Structural and mechanical properties of the prepared composites were examined in this study. The homogenous filler distribution was confirmed in the tested samples by scanning electron microscopy, transmission electron microscopy, and energy dispersive spectroscopy analyses. The fillers’ fortifying effect on polymer composites’ mechanical performance was confirmed as indicated by the increased elastic modulus and indentation modulus. Additionally, the possible modulation of the plastic-elastic mechanical behavior was confirmed by the type of the filler as well as its concentration used in the final composites testing articles.

In industrial applications, the potential of basalt fibre-reinforced polymer (BFRP) composite pipes as a compelling alternative to glass and carbon fibre-reinforced composite pipes is recognized. Their high recyclability makes them a viable option for aerospace, marine, and automotive applications. In this study, a comparison is made between the mechanical properties of virgin basalt–epoxy composite pipes and graphene-modified counterparts. To conduct the experiments, pipe section specimens were prepared using a flex grinding machine. Graphene nanoplatelets (GnPs), serving as an exceptional reinforcing material, were uniformly incorporated into the basalt–epoxy composites at a specific concentration. The inclusion of these nanoplatelets resulted in significant changes in mechanical stiffness compared to the virgin basalt–epoxy composite pipes. A series of tests, including uniaxial tensile, Charpy impact, microhardness, Shore D hardness, uniaxial 3-point bending, and dynamic displacement transmissibility tests, were carried out to assess the mechanical properties of both graphene-reinforced and virgin basalt–epoxy pipes. The findings indicated that the pure basalt–epoxy composite exhibited lower ductility compared to the graphene basalt–epoxy composites after undergoing uniaxial mechanical loading. Non-destructive dynamic mechanical vibration testing was used to investigate the complex mechanical response of the materials under examination. The observed complex frequency-dependent responses reflected the mutual ductile/brittle mechanical performance of the developed composites.

This paper was focused on application of the perlite mineral as the filler for polymer nanocomposites in technical applications. A strong effect of the perlite nano-filler on high-density poly(ethylene) (HDPE) composites’ mechanical and thermal properties was found. Also found was an increase of the Young’s modulus of elasticity with the increasing filler concentration. Increased stiffness from the mechanical tensile testing was confirmed by the nondestructive vibrator testing as well. This was based on displacement transmissibility measurements by means of forced oscillation single-degree-of freedom method. Fracture toughness showed a decreasing trend with increasing perlite concentration, suggesting occurrence of the brittle fracture. Furthermore, ductile fracture processes were observed as well at higher filler concentrations by means of SEM analysis. There was also found relatively strong bonding between polymer chains and the filler particles by SEM imagining.