Search Results (110)

In order to address vibration and noise challenges in modern industry while satisfying the lightweighting requirements for aerospace and transportation applications, the development of polymer elastomers integrating both lightweight and high-damping properties holds substantial significance. This study developed polyurethane (PU) with optimized damping and mechanical properties at room temperature through monomer composition optimization. Hollow glass microspheres (HGMs) were introduced into the PU matrix to increase stiffness and reduce density, though this resulted in decreased tensile strength (Rm) and loss factor (tanδ). To further improve mechanical and damping properties, we applied a carbon coating to the surface of the HGMs to optimize the interface between the HGMs and the PU matrix, and systematically investigated the energy dissipation and load-bearing behavior of PU composites. The effect of enhanced interface damping of HGM@C/PU resulted in broadening of the effective damping temperature range (tanδ ≥ 0.3) and higher maximum loss factor (tanδ_max) compared to HGM/PU at equivalent filler loading. The tensile and dynamic properties significantly improved due to optimized interfacial adhesion. In PU composites reinforced with 10 wt% HGM and HGM@C, a 46.8% improvement in Rm and 11.0% improvement in tanδ_max occurred after carbon coating. According to acoustic testing, average transmission loss of HGM/PU and HGM@C/PU with the same filler content showed a difference of 0.3–0.5 dB in 500–6300 Hz, confirming that the hollow structure of the HGMs was preserved during carbon coating. Full article

During the operation of structures, the components and materials from which they are made are exposed to various environmental, technological, and operational impacts. In this context, the use of a modified water-dispersion composition containing finely dispersed fillers with enhanced protective and performance characteristics proves to be effective. This article examines the development of a paint-and-coating composition using hollow glass microspheres and modified diatomite as finely dispersed fillers. The influence of technological factors on the properties of coating materials based on a synthesized acrylic dispersion and fillers—such as modified diatomite and hollow glass microspheres ranging from 20 to 100 μm in size with a bulk density of 0.107–0.252 g/cm³—is analyzed. The optimal formulation of the coating materials was determined to ensure the required coating quality. Experimental results demonstrate the improved strength and hardness of the coating due to the use of acrylic dispersion obtained through an emulsifier-free method and modifiers in the form of finely dispersed fillers. It has been established that the resulting samples also exhibit high adhesion to mineral and metallic substrates, along with excellent corrosion resistance. Moreover, the incorporation of acrylic dispersion contributes to increased elasticity of the coating, resulting in improved resistance to washing and abrasion. The developed protective material can be applied to a variety of surfaces, including walls, ceilings, and roofs of buildings and structures, pipelines, and many other applications. Thus, modified water-dispersion compositions based on synthesized acrylic dispersion showed the following results: resistance to sticking—5, which is the best; chemical resistance and gloss level with standard single-phase acrylic dispersion—no destruction or change in gloss. The adhesion of coatings cured under natural conditions and under the influence of UV radiation was 1 point. The developed formulations for obtaining water-dispersion paint and varnish compositions based on synthesized polymer dispersions, activated diatomite, and hollow glass microspheres, meet all the regulatory requirements for paint and varnish materials in terms of performance, and in terms of economic indicators, the cost of 1 kg of paint is 30% lower than the standard. Full article

This research investigates a novel hybrid E-glass fiber coated with a thin amorphous carbon (coke) layer, referred to as GF@C, designed to enhance the affinity of fiber with a polymer matrix. Acrylonitrile butadiene styrene (ABS), an engineering thermoplastic, was selected as the matrix to form the composite. The carbon coating was produced by pyrolyzing a lubricant oil (Lo) layer applied to the glass fiber strands. To promote the formation of graphite crystallites during carbonization, a small amount (x wt.% of Lo) of coronene (Cor) was added to Lo as a dopant. The resulting doped fibers, denoted GF@C_Lo-Cor(x%), were embedded in ABS at 70 wt.%, leading to significant improvements in mechanical properties. At the optimal doping level (x = 5), the composite achieved a Young’s modulus of 1.02 GPa and a tensile strength of 6.96 MPa, substantially higher than the 0.4 GPa and 3.81 MPa observed for the composite with the pristine GF. This enhancement is attributed to a distribution of graphite crystallites and their graphitization extent in the carbon coating, which improves interfacial bonding and increases chain entanglement. Additionally, GF@C_Lo-Cor(x%)–ABS composites (x = 0 and 5) exhibit significantly higher dielectric constant–temperature profiles than GF–ABS, attributed to the formation of diverse chain adsorption states on the C-coating. Full article

Highly heat-resistant and low-dielectric materials are crucial for achieving high-frequency communication, high-density integration, and high-temperature stability in modern electronics. In this work, surface modification of hollow silica microspheres (HGMs) using a silane coupling agent ((3-aminopropyl)triethoxysilane, KH550) yielded KHGM particles with a coating content of approximately 9.3 wt%, which were subsequently incorporated into high-performance polyarylene ether nitrile (PEN) polymers to fabricate composite films. The modified nanoparticles demonstrated significantly enhanced compatibility with the polymer matrix, while their hollow structure effectively reduced the dielectric constant of the composite film. When loaded with 50 wt% KHGM particles, the PEN-based composite film exhibited an elevated glass transition temperature of 198 °C and achieved a dielectric constant as low as 2.32 at 1 MHz frequency, coupled with dielectric loss below 0.016; compared with pure PEN, the dielectric constant of PEN/KHGM-50% decreased by 26.47%. Additionally, the composite demonstrated excellent water repellency. These advancements provide high-performance material support for applications in electronic communications, aerospace, and related fields. Full article

Polyester-glass laminates are widely used to reinforce underground steel fuel tanks due to their excellent corrosion resistance and mechanical performance. However, the management of these composites at the end of their service life poses significant challenges, particularly in terms of material recovery and environmental impact. This study investigates both the structural benefits and recyclability of polyester-glass laminates. Numerical simulations confirmed that reinforcing corroded steel tank shells with a 5 mm GFRP (Glass Fiber Reinforced Polymer) coating reduced the maximum equivalent stress by nearly 50%, significantly improving mechanical integrity. In parallel, thermogravimetric and microscopic analyses were conducted on waste GFRP samples subjected to pyrolysis, gasification, and combustion. Among the methods tested, pyrolysis proved to be the most favorable, allowing substantial organic degradation while preserving the structural integrity of the glass fiber fraction. However, microscopy revealed that the fibers were embedded in a dense char matrix, requiring additional separation processes. Although combustion leaves the fibers physically loose, pyrolysis is favored due to better preservation of fiber mechanical properties. Combustion resulted in loose and morphologically intact fibers but exposed them to high temperatures, which, according to the literature, may reduce their mechanical strength. Gasification showed intermediate performance in terms of energy recovery and fiber preservation. The findings suggest that pyrolysis offers the best trade-off between environmental performance and fiber recovery potential, provided that appropriate post-treatment is applied. This work supports the use of pyrolysis as a technically and environmentally viable strategy for recycling polyester-glass laminates and encourages further development of closed-loop composite waste management. Full article

To enhance the high-temperature resistance of silicone rubber and meet the application requirements of flexible conductive silicone rubber under elevated temperature conditions, this study adopts a chemical modification strategy by introducing phenyl groups into the molecular chains of silicone rubber to improve its thermal resistance. High-phenyl-content hydroxyl-terminated silicone oil (MPPS) was used as the polymer backbone, and vinylmethyldimethoxysilane (VDMS) served as the chain extender. Through a silanol condensation reaction, vinylmethylphenyl polysiloxane (VMPPS) with a crosslinkable structure was synthesized, providing reactive sites for subsequent vulcanization and molding. Subsequently, needle-like silver-coated glass fiber (AGF) conductive fillers were prepared via a green and environmentally friendly electroless silver plating method. These fillers were incorporated into the phenyl polysiloxane matrix to impart electrical conductivity to the phenyl silicone rubber while synergistically enhancing its thermal resistance. Finally, thermally resistant conductive silicone rubber was fabricated through high-temperature vulcanization, and the key properties of the material were systematically characterized. The synthesized phenyl polysiloxane exhibited a number-averaged molecular weight of up to 181,136, with a PDI of 2.43. When the loading of AGF reached 25 phr, the phenyl silicone rubber composite achieved the electrical percolation threshold, exhibiting a conductivity of 7.12 S/cm. With a further increase in AGF content to 35 phr, the composite demonstrated excellent thermal stability, with a 5% weight loss temperature of 478 °C and a residual mass of 37.36% at 800 °C. Moreover, after thermal aging at 100 °C for 72 h, the conductivity degradation of the phenyl silicone rubber was significantly lower than that of commercial silicone rubber, indicating outstanding electrical stability. This study provides an effective approach for the application of flexible electronic materials under extreme thermal environments. Full article

In this study, the effects of exposure to seawater on the material properties of glass fiber-reinforced polymer (GFRP) and carbon fiber-reinforced polymer (CFRP) samples were investigated. The samples were stored in seawater with a salinity of 3.3–3.7% and a temperature of 23.5 °C taken from the Aegean Sea in September for different periods (1, 2, 3, 6 and 15 months). The samples prepared in accordance with the ASTM D5868-01 standard were subjected to axial impact testing. In the first stage of this study, moisture retention percentages were determined, and, then, axial impact tests were performed. In the tests, a total of 36 samples bonded with single-lap adhesive were subjected to 30 Joule impact energy, and their mechanical strength was evaluated. In line with the experimental results, moisture absorption and axial impact energy values were compared in order to determine the most durable composite material connection, and the most durable connection was selected by evaluating the mechanical properties. Damage analysis on the samples was performed at the DEU Science and Technology Application and Research Center with ZEISS GEMINI SEM 560. (Oberkochen, Germany). The fracture surfaces of the CFRP and GFRP samples after gold coating were examined in detail with a scanning electron microscope, and their interface properties and internal structures were observed. The fracture toughness of GFRP specimens increased from 4.6% in a dry environment to 27.96% after 15 months in seawater. CFRP specimens increased from 4.2% in a dry environment to 11.96% after 15 months in seawater, but the increase was less pronounced compared to GFRP. According to the experimental results, CFRP samples exhibited superior mechanical performance compared to GFRP samples. Full article

Dopamine (DA) is a neurotransmitter that works in the brain. It plays several important roles in executive functions, including motor control, memory, mood, motivation, and reward. DA imbalances are associated with diseases in the nervous system such as Parkinson’s disease, schizophrenia, Alzheimer’s disease, and attention deficit hyperactivity disorder (ADHD). Therefore, the development of a biosensor for the detection of precise amounts of DA is of great interest. In this research, polypyrrole-3-carboxylic acid/polypyrrole/gold nanoparticle (PP3C/PPy/AuNPs) composites were developed for the electrochemical detection of DA. Firstly, a PP3C/PPy/AuNPs composite thin film was synthesized by electropolymerization on a fluorine-doped tin oxide (FTO)-coated glass substrate. Subsequently, cyclic voltammetry (CV), scanning electron microscopy (SEM), and differential pulse voltammetry (DPV) were used for the characterization and study of the efficiency of the obtained conducting polymer–gold nanoparticle composite thin film for the detection of DA. The proposed electrochemical sensor showed good sensitivity and selectivity for the detection of DA with a wide detection linear range from 5 to 180 μM (R² = 0.9913). The limit of detection (LOD) and limit of quantitation (LOQ) values were 9.72 nM and 0.032 μM, respectively. Therefore, it can be concluded that the electrochemically fabricated PP3C/PPy/AuNPs composite thin film can be applied as an electrochemical biosensor for the detection of dopamine for the early diagnosis of various neurological disorders in the future. Full article

Polydimethylsiloxane (PDMS) is known for its exceptional mechanical properties, chemical stability, and flexibility. Recent advancements have focused on developing functional PDMS composites by integrating various functional fillers, including polymers, ceramics, and metals, for advanced applications such as electronics, medical devices, and aerospace. Consequently, there is a growing need to investigate PDMS composites to achieve higher filler loadings offering enhanced mechanical performance. This study addresses this need by utilizing the high molecular weight (MW) PDMS resin we have developed, offering its high elongation capacity of up to >6500%. We incorporated boron (B), hollow glass microballoons (HGMs), and tungsten-coated hollow glass microballoons (WHGMs) into the developed high MW PDMS. The resulting composites demonstrated excellent elastic properties and significant compression resilience (35–80%) and elastic modulus (1.28–10.15 MPa) at high filler loadings (~60 vol.%). Specifically, B/PDMS composites achieved up to 67.6 vol.% of B, HGM/PDMS composites held up to 68.6 vol.% of HGM, and WHGM/PDMS composites incorporated up to 54.0 vol.% of WHGM. These findings highlight the potential of high MW PDMS for developing high-performance PDMS composites suitable for advanced applications such as aerospace, automotive, and medical devices. Full article

The protective effect of polyurea (PU) coatings on polymer matrix composite (PMC) panels subjected to high-velocity ballistic impacts, particularly as a potential replacement material for large power transformer (LPT) tanks, has not been extensively reported in the literature. This study addresses the gap by presenting a numerical investigation into the ballistic performance of PMC panels with PU coatings. Due to the complex nature and high cost of experimental testing, this research relies on finite element modeling to predict the panels’ responses under impact. Glass fiber/epoxy and carbon fiber/epoxy composite panels were tested individually and in hybrid configurations while being subjected to simulated 400 m/s steel projectile impacts. This study first investigates the impact damage evolution in uncoated panels, analyzing the arrest depth as a function of the panel thickness. It then evaluates the effect of PU coatings on the ballistic response. The results demonstrate that PU coatings are three times more effective in protecting both glass and carbon fiber panels from penetration compared to simply increasing the panel thickness. Additionally, the utilization of PU coatings led to a reduction in cost, mass, and thickness while still preventing penetration of the projectile in the models. Full article

Fiber coatings protect the glass surface of fiber from extrinsic environmental factors. The coating of shape memory alloy over fiber is useful in sensor fabrication where the state of deformation is affected by the phase transformation of the coated material. In addition, coated plastic fibers can be used in elevated temperature environments. To this end, the present research aims to investigate the effect of the Ni-Ti-Sn composite coating over the fiber. Homogeneous particle distribution, agglomeration, porosity and the ability to obtain uniform coating thickness have been general concerns in fiber coatings. Hence, the present study comprehensively investigated the mechanical and thermal behavior as well as morphological properties of Ni-Ti-Sn nanopowders deposited on polymer fiber optics. Five sets of polyamide-coated samples with different Ni-Ti-Sn proportions were fabricated and characterized. Morphological studies confirmed that an even coating thickness enhanced the mechanical integrity and optical performance. The optimum composition demonstrated superior tensile strength of 29.5 MPa and a 25% increase in elongation compared to the uncoated sample. The Ni-Ti-Sn alloy composition investigated in the present study is promising for industrial applications where thermal stability and mechanical performance are warranted. Full article

Environmental issues and the reduction of fossil fuel resources will lead to the partial or total substitution of petroleum-based materials with natural, raw, renewable ones. One expanding domain is the obtaining of engineering materials from vegetable oils for sustainable, eco-friendly polymers for different applications. Herein, the authors propose a simplified and green synthesis pathway for a thermally curable, acrylated and epoxidized soybean oil matrix formulation containing only epoxidized soybean oil, acrylic acid, a reactive diluent (5%) and just 0.15 mL of catalyst. The small amount of reactive diluent significantly reduced the initial system viscosity while eliminating the need for adding solvent, hardener, activator, etc. Both the thermally cured composite with a 2% TiO₂ microparticle filler and its pristine matrix were comparably characterized in terms of structural, thermal, morphological, dielectric and wettability by Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetry, scanning electron microscopy, broadband dielectric spectrometry and contact angle measurements. The 2% filler in the composite generated superior thermal stability via lower mass loss (48.89% vs. 57.14%) and higher degradation temperatures (395 °C vs. 387 °C), increased the glass transition temperature from −20 °C to −10 °C, rendered the microcomposite hydrophobic by increasing the contact angle from 88° to 96° and enhanced dielectric properties compared to the pristine matrix. All investigations recommend the microcomposite for protective coatings, capacitors, sensors and electronic circuits. This study brings new contributions to green chemistry and sustainable materials. Full article

Structural health monitoring (SHM) of composite materials is of great significance in various practical applications. However, it is a challenge to accurately monitor the damage of composites without affecting their mechanical properties. In this paper, an embedded sensing layer based on carbon nanotube-coated glass fiber is designed, combined with electrical resistance tomography (ERT) for in situ damage monitoring. Multi-wall carbon nanotube-coated glass fiber (MWCNT-GF) is prepared and embedded into laminates as an in situ sensing layer. Low-velocity impact experiments demonstrate that the embedded sensing layer has high compatibility with the composite laminates and has no adverse effect on its impact response; although, the energy absorption behavior of glass fiber-reinforced polymer (GFRP) laminates containing MWCNT-GF occurs about 10% earlier than that of GFRP laminates overall. ERT technology is used to analyze the laminates after a low-velocity impact test. The results show that the in situ monitoring method with the embedded MWCNT-GF sensing layer can achieve high precision in imaging localization of impact damage, and the error of the detected damage area is only 4.5%. Full article

The primary characteristic of ablative materials is their fire resistance. This study explored the development of cost-effective ablative materials formed into application-specific shapes by using a polymer matrix reinforced with ceramic powder. A thermoplastic (polypropylene; PP) and a thermoset (polyester; UPE) matrix were used to manufacture ablative materials with 50 wt% silicon carbide (SiC) particles. The reference composites (50 wt% SiC) were compared to those with 1 and 3 wt% short glass fibers (0.5 mm length) and to composites using a 1 and 3 wt% glass fiber mesh. Fire resistance was tested using a butane flame (900 °C) and by measuring the transmitted heat with a thermocouple. Results showed that the type of polymer matrix (PP or UPE) did not influence fire resistance. Composites with short glass fibers had a fire-resistance time of 100 s, while those with glass fiber mesh tripled this resistance time. The novelty of this work lies in the exploration of a specific type of material with unique percentages of SiC not previously studied. The aim is to develop a low-cost coating for industrial warehouses that has improved fire-protective properties, maintains lower temperatures, and enhances the wear and impact resistance. Full article

Fiber-reinforced composites (FRCs) represent a promising class of engineering materials due to their mechanical performance. However, the vast majority of FRCs are currently manufactured using carbon and glass fibers, which raises concerns because of the difficulties in recycling and the reliance on finite fossil resources. On the other hand, the use of natural fibers is still hampered due to the problems such as, e.g., differences in polarity between the reinforcement and the polymer matrix components, leading to a significant decrease in composite durability. In this work, we present a natural fiber-reinforced composite (NFRC), incorporating plasma pre-treated flax fibers as the reinforcing element, thermoplastic polylactic acid (PLA) as a matrix, and a key point of the current study—a thermoset coating based on epoxidized linseed oil for adhesion improvement. Using atmospheric plasma-jet treatment allows for increasing the fiber’s surface energy from 20 to 40 mN/m. Furthermore, a thermoset coating layer based on epoxidized linseed oil, in conjunction with dodecyl succinic anhydride (DDSA) as a curing agent and 2,4,6-tris(dimethyl amino methyl) phenol (DMP-30) as a catalyst, has been developed. This coated layer exhibits a decomposition temperature of 350 °C, and there is a substantial increase in the dispersive surface-energy part of the coated flax fibers from 8 to 30 mN/m. The obtained natural fiber-reinforced composite (NFRC) was prepared by belt-pressing with a PLA film, and its mechanical properties were evaluated by tensile testing. The results showed an elastic modulus up to 18.3 GPa, which is relevant in terms of mechanical properties and opens up a new pathway to use natural-based fiber-reinforced bio-based materials as a convenient approach to greener FRCs. Full article