Search Results (43)

This study investigates the application of carbon nanotube (CNT)-enhanced epoxy adhesives for localised Joule heating-based curing in composite bonding. The electrical, thermal, and mechanical properties of epoxy with 0.25–1 wt% CNT loadings were evaluated. A simple CNT alignment method using DC voltage showed improved electrical conductivity, greatly reducing the percolation threshold. Transient thermal analysis using finite element modelling of representative volume elements revealed that aligned CNTs led to increased localised temperatures near the CNT clusters. The model was validated with infrared thermal imaging analysis, which also showed similar non-linear heat distribution and more uniform heating under higher CNT loading. Additionally, power distribution mapping was evaluated through inverse modelling techniques, suggesting different conductivity zones and cluster distribution within the single-lap joint. The numerical and experimental results demonstrated that CNT alignment significantly enhanced localised conductivity, thereby improving curing efficiency at lower voltages. The lap shear test results showed a peak shear strength of 10.16 MPa at 0.5 wt% CNT loading, 9% higher than pure epoxy. Scanning electron microscopy analysis confirmed the formation of aligned CNT clusters, and how CNT loading affected the failure modes, transitioning from cohesive to void-rich fracture patterns at a higher wt%. These findings establish CNT-enhanced Joule heating as a viable and scalable alternative for efficient composite bonding in aerospace and structural applications. Full article

Elastomers are made of chain-like molecules to form networks that can sustain large deformation. Rubbers are thermosetting elastomers that are obtained from irreversible curing reactions. Curing reactions create permanent bonds between the molecular chains. On the other hand, thermoplastic elastomers do not need curing reactions. Incorporation of appropriated filler particles, as has been practiced for decades, can significantly enhance mechanical properties of elastomers. However, there are fundamental questions about polymer matrix composites (PMCs) that still elude complete understanding. This is because the macroscopic properties of PMCs depend not only on the overall volume fraction ($\varphi$) of the filler particles, but also on their spatial distribution (i.e., primary, secondary, and tertiary structure). This work aims at reviewing how the mechanical properties of PMCs are related to the microstructure of filler particles and to the interaction between filler particles and polymer matrices. Overall, soft rubbery matrices dictate the elasticity/hyperelasticity of the PMCs while the reinforcement involves polymer–particle interactions that can significantly influence the mechanical properties of the polymer matrix interface. For $\varphi$ values higher than a threshold, percolation of the filler particles can lead to significant reinforcement. While viscoelastic behavior may be attributed to the soft rubbery component, inelastic behaviors like the Mullins and Payne effects are highly correlated to the microstructures of the polymer matrix and the filler particles, as well as that of the polymer–particle interface. Additionally, the incorporation of specific filler particles within intelligently designed polymer systems has been shown to yield a variety of functional and responsive materials, commonly termed smart materials. We review three types of smart PMCs, i.e., magnetoelastic (M-), shape-memory (SM-), and self-healing (SH-) PMCs, and discuss the constitutive models for these smart materials. Full article

This study presents the functionalization of silk fabric with SWCNT ink. The first step was the formation of a polydopamine (PDA) thin coating on the silk fabric to allow for effective bonding of SWCNTs. PDA formation was carried out directly on the fabric by means of polymerization of dopamine in alkali conditions. The Silk/PDA fabric was functionalized with SWCNT ink of different SWCNT concentrations by using the dip-coating method. IR and Raman analyses show that the dominant β-sheet structure of silk fibroin after the functionalization process remains unchanged. The heat resistance is even slightly improved. The hydrophobic silk fabric becomes hydrophilic after functionalization due to the influence of PDA and the surfactant in SWCNT ink. The ink significantly changes the electrical properties of the silk fabric, from insulating to conductive. The volume resistance changes by nine orders of magnitude, from 2.4 × 10¹² Ω to 2.3 × 10³ Ω for 0.12 wt.% of SWCNTs. The surface resistance changes by seven orders of magnitude, from 2.1 × 10¹² Ω to 2.4 × 10⁵ Ω for 0.17 wt.% of SWCNTs. The volume and surface resistance thresholds are determined to be about 0.05 wt.% and 0.06 wt.%, respectively. The low value of the percolation threshold indicates efficient functionalization, with high-quality ink facilitating the formation of percolation paths through SWCNTs and the influence of the PDA linker. Full article

The potential of electrically conductive graphene nanoplatelets (GNPs)/epoxy, multi-walled carbon nanotubes (MWNCTs)/epoxy and hybrid GNPs-MWCNTs/epoxy nanocomposites as adhesives for out-of-autoclave (OoA) and in-the-field CFRP repair via Joule heat curing was investigated. Scanning electron microscopy revealed a good dispersion of the nanoparticles in the matrix in all the nanocomposite adhesives above their percolation thresholds, which led to a homogeneous distribution of the heat generated during Joule CFRP repair. The joints bonded with neat epoxy and the nanocomposites showed similar lap shear strengths, with the addition of nanoparticles enhancing the fatigue performance of the adhesively bonded joints relative to when neat epoxy was used as an adhesive and oven-cured. The interfacial and cohesive failure mechanisms were found to coexist in all the cases, with an increasing dominance of the cohesive when nanofillers were embedded into the adhesive. No effect of the specific type of nanofiller incorporated into the epoxy as the conductive component was observed on the mechanical performance of the bonded joints, with the adhesives containing MWCNTs showing similar results to those filled with GNPs at considerably lower loadings due to their lower percolation thresholds. The independence of the properties regardless of the curing method highlights the promise of these Joule-cured adhesives for industrial applications. Full article

The manufacturing of Diels–Alder (D-A) crosslinked epoxy nanocomposites is an emerging field with several challenges to overcome: the synthesis is complex due to side reactions, the mechanical properties are hindered by the brittleness of these bonds, and the content of carbon nanotubes (CNT) added to achieve electroactivity is much higher than the percolation thresholds of other conventional resins. In this work, we develop nanocomposites with different D-A crosslinking ratios (0, 0.6, and 1.0) and CNT contents (0.1, 0.3, 0.5, 0.7, and 0.9 wt.%), achieving a simplified route and avoiding the use of solvents and side reactions by selecting a two-step curing method (100 °C-6 h + 60 °C-12 h) that generates the thermo-reversible resins. These reversible nanocomposites show ohmic behavior and effective Joule heating, reaching the dissociation temperatures of the D-A bonds. The fully reversible nanocomposites (ratio 1.0) present more homogeneous CNT dispersion compared to the partially reversible nanocomposites (ratio 0.6), showing higher electrical conductivity, as well as higher brittleness. For this study, the nanocomposite with a partially reversible matrix (ratio 0.6) doped with 0.7 CNT wt.% was selected to allow us to study its new smart functionalities and performance due to its reversible network by analyzing self-healing and thermoforming. Full article

In recent years, the use of biomaterials has been required from the viewpoint of biocompatibility of electronic devices. In this study, the proton conductivity of Glycyl-L-serine (Gly-Ser) was investigated to clarify the relationship between hydration and proton conduction in peptides. From the crystal and conductivity data, it was inferred that the proton conductivity in hydrated Gly-Ser crystals is caused by the cleavage and rearrangement of hydrogen bonds between hydration shells formed by hydrogen bonds between amino acids and water molecules. Moreover, a staircase-like change in proton conduction with hydration was observed at n = 0.3 and 0.5. These results indicate that proton transport in Gly-Ser is realized by hydration water. In addition, we also found that hydration of GSGS and GS50 can achieve proton conduction of Gly-Ser tetrameric GSGS and GS50 containing repeating sequences. The proton conductivity at n = 0.3 is due to percolation by the formation of proton-conducting pathways. In addition to these results, we found that proton conductivity at GS50 is realized by the diffusion constant of 3.21 × 10⁻⁸ cm²/s at GS50. Full article

Many endothermic liquid–liquid transitions, occurring at a temperature T_n+ above the melting temperature T_m, are related to previous exothermic transitions, occurring at a temperature T_x after glass formation below T_g, with or without attached crystallization and predicted by the nonclassical homogenous nucleation equation. A new thermodynamic phase composed of broken bonds (configurons), driven by percolation thresholds, varying from ~0.145 to Δε, is formed at T_x, with a constant enthalpy up to T_n+. The liquid fraction Δε is a liquid glass up to T_n+. The solid phase contains glass and crystals. Molecular dynamics simulations are used to induce, in NiTi₂, a reversible first-order transition by varying the temperature between 300 and 1000 K under a pressure of 1000 GPa. Cooling to 300 K, without applied pressure, shows the liquid glass presence with Δε = 0.22335 as memory effect and T_n+ = 2120 K for T_m = 1257 K. Full article

This study focuses on epoxy hybrid systems prepared by incorporating multi-wall carbon nanotubes (MWCNTs) and graphene nanosheets (GNs) at two fixed filler amounts: below (0.1 wt%) and above (0.5 wt%), with varying MWCNT:GN mix ratios. The hybrid epoxy systems exhibited remarkable electrical performance, attributed to the π–π bond interactions between the multi-wall carbon nanotubes and the graphene layers dispersed in the epoxy resin matrix. The material’s properties were characterized through dynamic mechanical and thermal analyses over a wide range of temperatures. In addition to excellent electrical properties, the formulated hybrid systems demonstrated high mechanical performance and thermal stability. Notably, the glass transition temperature of the samples reached 255 °C, and high storage modulus values at elevated temperatures were observed. The hybrid systems also displayed thermal stability up to 360 °C in air. By comparing the mechanical and electrical performance, the formulation can be optimized in terms of the electrical percolation threshold (EPT), electrical conductivity, thermostability, and mechanical parameters. This research provides valuable insights for designing advanced epoxy-based materials with multifunctional properties. Full article

Recent discovery and investigation of the flow of glasses under the electron beams of transmission electron microscopes raised the question of eventual occurrence of such type effects in the vitrified highly radioactive nuclear waste (HLW). In connection to this, we analyse here the flow of glasses and glass–liquid transition in conditions of continuous electron irradiation such as under the e-beam of transmission electron microscopes (TEM) utilising the configuron (broken chemical bond) concept and configuron percolation theory (CPT) methods. It is shown that in such conditions, the fluidity of glasses always increases with a substantial decrease in activation energy of flow at low temperatures and that the main parameter that controls this behaviour is the dose rate of absorbed radiation in the glass. It is revealed that at high dose rates, the temperature of glass–liquid transition sharply drops, and the glass is fully fluidised. Numerical estimations show that the dose rates of TEM e-beams where the silicate glasses were fluidised are many orders of magnitude higher compared to the dose rates characteristic for currently vitrified HLW. Full article

Microbially induced calcite precipitation (MICP) is a green bio-inspired soil solidification technique that depends on the ability of urease-producing bacteria to form calcium carbonate that bonds soil grains and, consequently, improves soil mechanical properties. Meanwhile, different treatment methods have been adopted to tackle the key challenges in achieving effective MICP treatment. This paper proposes the combined method as a new MICP treatment approach, aiming to develop the efficiency of MICP treatment methods and simulate naturally cemented soil. This method combines the premixing, percolation, and submerging MICP methods. The strength outcomes of Portland-cemented and MICP-cemented sand using the percolation and combined methods were compared. For Portland-cemented sand, the UCS values varied from 0.6 MPa to 17.2 MPa, corresponding to cementation levels ranging from 5% to 30%. For MICP-cemented sand, the percolation method yielded UCS values ranging from 0.5 to 0.9 MPa, while the combined method achieved 3.7 MPa. The strength obtained by the combined method is around 3.7 times higher than that of the percolation method. The stiffness of bio-cemented samples varied between 20 and 470 MPa, while for Portland-cemented sand, it ranged from 130 to 1200 MPa. In terms of calcium carbonate distribution, the percolation method exhibited higher concentration at the top of the sample, while the combined method exhibited more precipitation at the top and perimeter, with less concentration in the central bottom region, equivalent to 10% of a half section’s area. Full article

Contact network models are recent alternatives to equation-based models in epidemiology. In this paper, the spread of disease is modeled on contact networks using bond percolation. The weight of the edges in the contact graphs is determined as a function of several variables in which case the weight is the product of the probabilities of independent events involving each of the variables. In the first experiment, the weight of the edges is computed from a single variable involving the number of passengers on flights between two cities within the United States, and in the second experiment, the weight of the edges is computed as a function of several variables using data from 2012 Kenyan household contact networks. In addition, the paper explored the dynamics and adaptive nature of contact networks. The results from the contact network model outperform the equation-based model in estimating the spread of the 1918 Influenza virus. Full article

Coarse-grained molecular dynamics simulations that incorporate explicit water-mediated hydrophilic/hydrophobic interactions are employed to track spatiotemporal evolution of diblock copolymer aggregation in initially homogeneous solutions. A phase portrait of the observed morphologies and their quantitative geometric features such as aggregation numbers, packing parameters, and radial distribution functions of solvent/monomers are presented. Energetic and entropic measures relevant to self-assembly such as specific solvent accessible surface area (SASA) and probability distribution functions (pdfs) of segmental stretch of copolymer chains are analyzed. The simulations qualitatively capture experimentally observed morphological diversity in diblock copolymer solutions. Topologically simpler structures predicted include spherical micelles, vesicles (polymersomes), lamellae (bilayers), linear wormlike micelles, and tori. More complex morphologies observed for larger chain lengths and nearly symmetric copolymer compositions include branched wormlike micelles with Y-shaped junctions and cylindrical micelle networks. For larger concentrations, vesicle strands, held together by hydrogen bonds, and “giant” composite aggregates that consist of lamellar, mixed hydrophobic/hydrophilic regions and percolating water cores are predicted. All structures are dynamic and exhibit diffuse domain boundaries. Morphology transitions across topologically simpler structures can be rationalized based on specific SASA measurements. PDFs of segmental stretch within vesicular assemblies appear to follow a log-normal distribution conducive for maximizing configuration entropy. Full article

Zinc oxide nanostructures have real potential in different scientific fields. In the case of these nanostructures, it was found that the morphology of ZnO plays an essential role in developing further applications, but it is necessary a rigorous control of the main factors which influence the size, shape, agglomeration tendency, uniformity, and orientation of the nanostructures. In the present paper, our efforts are oriented to synthesize different types of ZnO nanostructures by chemical method, and optimization was achieved with varying parameters, such as the concentration of precursors, types of solvents, pH, time, or temperature, as well as the parameters required for thermal treatment. To obtain the characteristic structural and morphological information, ZnO nanostructures were investigated using Fourier transform infrared spectrometry (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD). SEM analysis confirms that the morphology and size of the ZnO nanostructures depend on the process parameters. The XRD results reveal that the synthesized samples have a wurtzite crystalline structure, and FTIR spectra show the presence of Zn-O bonding. The wetting capacity of continuous ZnO surfaces with different morphologies was studied by measuring the contact angle, indicating that the wetting and percolation capacity, depend on the orientation of the synthesized nanostructures. Full article

Porous polymer monolith materials of 2-mm thickness were obtained by visible light-induced radical polymerization of oligocarbonate dimethacrylate (OCM-2) in the presence of 1-butanol (10 to 70 wt %) as a porogenic additive. The pore characteristics and morphology of polymers were studied by mercury intrusion porosimetry and scanning electron microscopy. Monolithic polymers with both open and closed pores up to 100 nm in size are formed when the alcohol content in the initial composition is up to 20 wt %. The pore structure in such materials is a system of holes in the bulk of the polymer (hole-type pores). Open interconnected pores with a specific volume up to 2.22 cm³/g and modal pore size up to 10 microns are formed in the volume of the polymer with 1-butanol content of more than 30 wt %. Such porous monoliths are a structure of covalently bonded polymer globules (interparticle-type pores). The free space between the globules represents a system of open interconnected pores. In the transition region of 1-butanol concentrations (from 20 to 30 wt %), areas with both structures and intermediate frameworks, as well as honeycomb structures of polymer globules connected by bridges, are fixed on the polymer surface. It was found that the transition from one type of pore system to another is accompanied by a sharp change in the strength characteristics of the polymer. Approximation of experimental data using the sigmoid function made it possible to determine the concentration of the porogenic agent in the vicinity of which the percolation threshold is observed. Full article

The production of flexible electronic systems includes stretchable electrical interconnections and flexible electronic components, promoting the research and development of flexible conductors and stretchable conductive materials with large bending deformation or torsion resistance. Silver nanowires have the advantages of high conductivity, good transparency and flexibility in the development of flexible electronic products. In order to further prepare system-level flexible systems (such as autonomous full-software robots, etc.), it is necessary to focus on the conductivity of the system’s composite conductor and the robustness of the system at the physical level. In terms of conductor preparation processes and substrate adhesion strategies, the more commonly used solutions are selected. Four kinds of elastic preparation processes (pretensioned/geometrically topological matrix, conductive fiber, aerogel composite, mixed percolation dopant) and five kinds of processes (coating, embedding, changing surface energy, chemical bond and force, adjusting tension and diffusion) to enhance the adhesion of composite conductors using silver nanowires as current-carrying channel substrates were reviewed. It is recommended to use the preparation process of mixed percolation doping and the adhesion mode of embedding/chemical bonding under non-special conditions. Developments in 3D printing and soft robots are also discussed. Full article