Development and research of basalt plastic material for the flood protection structures

Due to the increasing number of catastrophic floods around the world, creation of an effective system to protect against natural disasters became particularly relevant. The paper investigates introduction of the basalt fiber to reinforce the composite sheet piles. Influence of the reinforcing fiber interlacing type on the nature of plastics destruction was established. Results of the work prove that basalt plastic (BP) exhibits higher climatic resistance than the fiberglass plastic (FGP). After post-curing, strength characteristics relative to the second year were decreasing by 15% with BP and by 22% with FGP in extension, and the strength limit in bending was decreasing by 12% with BP and by 47% with FGP. It was experimentally shown that under a long-term stationary thermal and humidity effect of 23°C/68RH, diffusion was observed on the basalt and fiberglass plastics consisting of two stages. The first stage had a satisfactory statistical error and was adequately approximated by the Fick’s diffusion model and the relaxation model. The second stage had an unsatisfactory statistical error for approximation and was of the spasmodic nature, while the jump in FGP was the largest indicating that the FGP was more susceptible to destruction exposed to the influence of long-term temperature and humidity regime of 23○С/68 RH, than the BP

Development and research of basalt plastic material for the flood protection structures

Due to the increasing number of catastrophic floods around the world, creation of an effective system to protect against natural disasters became particularly relevant. The paper investigates introduction of the basalt fiber to reinforce the composite sheet piles. Influence of the reinforcing fiber interlacing type on the nature of plastics destruction was established. Results of the work prove that basalt plastic (BP) exhibits higher climatic resistance than the fiberglass plastic (FGP). After post-curing, strength characteristics relative to the second year were decreasing by 15% with BP and by 22% with FGP in extension, and the strength limit in bending was decreasing by 12% with BP and by 47% with FGP. It was experimentally shown that under a long-term stationary thermal and humidity effect of 23°C/68RH, diffusion was observed on the basalt and fiberglass plastics consisting of two stages. The first stage had a satisfactory statistical error and was adequately approximated by the Fick’s diffusion model and the relaxation model. The second stage had an unsatisfactory statistical error for approximation and was of the spasmodic nature, while the jump in FGP was the largest indicating that the FGP was more susceptible to destruction exposed to the influence of long-term temperature and humidity regime of 23○С/68 RH, than the BP

Assessment of Extremely Cold Subarctic Climate Environment Destruction of the Basalt Fiber Reinforced Epoxy (BFRE) Rebar Using Its Moisture Uptake Kinetics

A quite simple method is proposed for the assessment of extremely cold subarctic climate environment destruction of the basalt fiber reinforced epoxy (BFRE) rebar. The method involves the comparison of experimentally obtained long-term moisture uptake kinetic curves of unexposed and exposed BFRP rebars. A moisture uptake test was carried out at the temperature of 60 °C and relative humidity of 98 ± 2% for 306 days. The plasticization can be neglected because of low-level moisture saturation (<0.41% wt.); the swelling and structural relaxation of the polymer network can be neglected due to the high fiber content of BFRP rebar; moisture diffusion into the basalt fibers can be neglected since it is a much lesser amount than in the epoxy binder. These assumptions made it possible to build a three-stage diffusion model. It is observed that an increase in the density of defects with an increase in the diameter of the BFRP rebar is the result of the technology of manufacturing a periodic profile. The diffusion coefficient of the BFRP rebar with a 6, 10, or 18 mm diameter increased at an average of 82.7%, 56.7%, and 30%, respectively, after exposure to the climate of Yakutsk during 28 months, whereas it was known that the strength indicators had been increased

Effect of Borpolymer on Mechanical and Structural Parameters of Ultra-High Molecular Weight Polyethylene

The paper presents the results of studying the effect of borpolymer (BP) on the mechanical properties, structure, and thermodynamic parameters of ultra-high molecular weight polyethylene (UHMWPE). Changes in the mechanical characteristics of polymer composites material (PCM) are confirmed and complemented by structural studies. X-ray crystallography (XRC), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and infrared spectroscopy (IR) were used to study the melting point, morphology and composition of the filler, which corresponds to the composition and data of the certificate of the synthesized BP. Tensile and compressive mechanical tests were carried out in accordance with generally accepted standards (ASTM). It is shown that BP is an effective modifier for UHMWPE, contributing to a significant increase in the deformation and strength characteristics of the composite: tensile strength of PCM by 56%, elongation at break by 28% and compressive strength at 10% strain by 65% compared to the initial UHMWPE, due to intensive changes in the supramolecular structure of the matrix. Structural studies revealed that BP does not chemically interact with UHMWPE, but due to its high adhesion to the polymer, it acts as a reinforcing filler. SEM was used to establish the formation of a spherulite supramolecular structure of polymer composites

Two-Layer Rubber-Based Composite Material and UHMWPE with High Wear Resistance

The aim of the study is the development of two-layer materials based on ultra-high-molecular-weight polyethylene (UHMWPE) and isoprene rubber (IR) depending on the vulcanization accelerators (2-mercaptobenzothiazole (MBT), diphenylguanidine (DPG), and tetramethylthiuram disulfide (TMTD)). The article presents the study of the influence of these accelerators on the properties and structure of UHMWPE. It is shown that the use of accelerators to modify UHMWPE leads to an increase in tensile strength of 28–53%, a relative elongation at fracture of 7–23%, and wear resistance of three times compared to the original UHMWPE. It has been determined that the introduction of selected vulcanization accelerators into UHMWPE leads to an increase in adhesion between the polymer and rubber. The study of the interfacial boundary of a two-layer material with scanning electron microscopy (SEM) and infrared spectroscopy (FTIR) showed that the structure is characterized by the presence of UHMWPE fibrils localized in the rubber material due to mechanical adhesion