Search Results (79)

The emulsification of a molten fusible metal alloy in a liquid epoxy matrix with its subsequent curing is a novel way to create a highly concentrated phase-change material. However, numerous challenges have arisen. The high interfacial tension between the molten metal and epoxy resin and the difference in their viscosities hinder the stretching and breaking of metal droplets during stirring. Further, the high density of metal droplets and lack of suitable surfactants lead to their rapid coalescence and sedimentation in the non-cross-linked resin. Finally, the high differences in the thermal expansion coefficients of the metal alloy and cross-linked epoxy polymer may cause cracking of the resulting phase-change material. This work overcomes the above problems by using nanosilica-induced physical gelation to thicken the epoxy medium containing Wood’s metal, stabilize their interfacial boundary, and immobilize the molten metal droplets through the creation of a gel-like network with a yield stress. In turn, the yield stress and the subsequent low-temperature curing with diethylenetriamine prevent delamination and cracking, while the transformation of the epoxy resin as a physical gel into a cross-linked polymer gel ensures form stability. The stabilization mechanism is shown to combine Pickering-like interfacial anchoring of hydrophilic silica at the metal/epoxy boundary with bulk gelation of the epoxy phase, enabling high metal loadings. As a result, epoxy shape-stable phase-change materials containing up to 80 wt% of Wood’s metal were produced. Wood’s metal forms fine dispersed droplets in epoxy medium with an average size of 2–5 µm, which can store thermal energy with an efficiency of up to 120.8 J/cm³. Wood’s metal plasticizes the epoxy matrix and decreases its glass transition temperature because of interactions with the epoxy resin and its hardener. However, the reinforcing effect of the metal particles compensates for this adverse effect, increasing Young’s modulus of the cured phase-change system up to 825 MPa. These form-stable, high-energy-density composites are promising for thermal energy storage in building envelopes, radiation-protective shielding, or industrial heat management systems where leakage-free operation and mechanical integrity are critical. Full article

Balancing high fluidity and stability is a critical challenge in deep-shaft cemented paste backfill (CPB) with high-concentration tailings. This study investigates the synergistic regulation mechanism of a combined admixture system comprising hydroxypropyl methylcellulose (HPMC) thickener and polycarboxylate (PCE) or Melamine-Formaldehyde Resin (MFR) superplasticizers on CPB rheology, mechanical strength, and microstructure. Results indicate that HPMC significantly enhanced anti-segregation performance via intermolecular bridging, substantially increasing yield stress and plastic viscosity. Upon PCE introduction, the steric hindrance provided by its side chains effectively disrupted HPMC-induced flocs and released entrapped water. Consequently, yield stress and plastic viscosity were reduced by up to 22.1% and 64.3%, respectively, with PCE exhibiting markedly superior viscosity-reducing efficiency compared to MFR. Mechanical testing revealed that PCE co-addition did not compromise early-age strength but enhanced 3, 7, and 28-day unconfined compressive strength (UCS) by refining pore structures and promoting the uniform distribution of hydration products. Microstructural analysis unveiled a competitive adsorption mechanism: preferential PCE adsorption dispersed particle agglomerates, while non-adsorbed HPMC formed a viscoelastic network within the pore solution, constructing a stable “dispersion-suspension” microstructure. This work provides a theoretical basis for optimizing high-performance backfill formulations. Full article

An epoxy resin can be crosslinked with an imidazole-based ionic liquid (IL), whose excess, provided its high melting temperature, can potentially form a dispersed phase to store thermal energy and produce a phase-change material (PCM). This work investigates the crosslinking of diglycidyl ether of bisphenol A (DGEBA) using 1-ethyl-3-methylimidazolium chloride ([EMIM]Cl) at its mass fractions of 5, 10, 20, 40, and 60%. The effect of [EMIM]Cl on the viscosity, curing rate, and curing degree was studied, and the thermophysical properties and morphology of the resulting crosslinked epoxy polymer were investigated. During the curing, [EMIM]Cl changes its role from a crosslinking agent (an initiator of homopolymerization) and a diluent of the epoxy resin to a plasticizer of the cured epoxy polymer and a dispersed phase-change agent. An increase in the [EMIM]Cl content accelerates the curing firstly because of the growth in the number of reaction centers, and then the curing slows down because of the action of the IL as a diluent, which reduces the concentration of reacting substances. In addition, a rise in the proportion of [EMIM]Cl led to the predominance of the initiation over the chain growth, causing the formation of short non-crosslinked molecules. The IL content of 5% allowed for curing the epoxy resin and elevating the stiffness of the crosslinked product by almost 7 times compared to tetraethylenetriamine as a usual aliphatic amine hardener (6.95 GPa versus 1.1 GPa). The [EMIM]Cl content of 20–40% resulted in a thermoplastic epoxy polymer capable of flowing and molding at elevated temperatures. The formation of IL emulsion in the epoxy matrix occurred at 60% [EMIM]Cl, but its hygroscopicity and absorption of water from surrounding air reduced the crystallinity of dispersed [EMIM]Cl, not allowing for an effective phase-change material to be obtained. Full article

Microfluidics is considered a revolutionary interdisciplinary technology with substantial interest in various biomedical applications. Many non-Newtonian fluids often used in microfluidics systems are notably influenced by the external active fields, such as acoustic, electric, and magnetic fields, leading to changes in rheological behavior. In this study, a numerical investigation is carried out to explore the rheological behavior of non-Newtonian fluids in a T-shaped microfluidics channel integrated with complex micropillar structures under the influence of acoustic, electric, and magnetic fields. For this purpose, COMSOL Multiphysics with laminar flow, pressure acoustic, electric current, and magnetic field physics is used to examine rheological characteristics of non-Newtonian fluids. Three polymer solutions, such as 2000 ppm xanthan gum (XG), 1000 ppm polyethylene oxide (PEO), and 1500 ppm polyacrylamide (PAM), are used as a non-Newtonian fluids with the Carreau–Yasuda fluid model to characterize the shear-thinning behavior. Moreover, numerical simulations are carried out with different input parameters, such as Reynolds numbers (0.1, 1, 10, and 50), acoustic pressure (5 Mpa, 6.5 Mpa, and 8 Mpa), electric voltage (200 V, 250 V, and 300 V), and magnetic flux (0.5 T, 0.7 T, and 0.9 T). The findings reveal that the incorporation of active fields and micropillar structures noticeably impacts fluid rheology. The acoustic field induces higher shear-thinning behavior, decreasing dynamic viscosity from 0.51 Pa·s to 0.34 Pa·s. Similarly, the electric field induces higher shear rates, reducing dynamic viscosities from 0.63 Pa·s to 0.42 Pa·s, while the magnetic field drops the dynamic viscosity from 0.44 Pa·s to 0.29 Pa·s. Additionally, as the Reynolds number increases, the shear rate also rises in the case of electric and magnetic fields, leading to more chaotic flow, while the acoustic field advances more smooth flow patterns and uniform fluid motion within the microchannel. Moreover, a proposed experimental framework is designed to study non-Newtonian fluid mixing in a T-shaped microfluidics channel under external active fields. Initially, the microchannel was fabricated using a high-resolution SLA printer with clear photopolymer resin material. Post-processing involved analyzing particle distribution, mixing quality, fluid rheology, and particle aggregation. Overall, the findings emphasize the significance of considering the fluid rheology in designing and optimizing microfluidics systems under active fields, especially when dealing with complex fluids with non-Newtonian characteristics. Full article

Graphene oxide (GO) has been successfully used as a filler to modify various properties of polymers and fiber-reinforced composites. The resulting properties depend on the filler content and on the distribution of GO in the polymer matrix. In this work, for the first time, we introduced GO into the highly viscous DEN-438 epoxy novolac resin and investigated rheological properties of the resulting compositions. In particular, we studied the functions of complex viscosity, storage and loss moduli, and mechanical loss tangent on temperature and GO content. The unusual behavior of the newly prepared formulations compared to typical GO/epoxy mixtures was discovered. At low GO content, introduction of GO led not to an increase, but to a decrease in the resin viscosity, with the minimum registered at 0.29 wt.% GO. After this threshold value, viscosity increased with GO content, which we explained by formation of the liquid crystalline structure. At higher GO concentrations, the formulations changed their state from solid-like at rest to liquid-like under load, with the properties being highly desired for film binders. The discovered properties of the GO/novolac epoxy resin formulations suggest their potential use as the new generation of film binders for Resin Film Infusion technology. Full article

The deterioration of high-penetration asphalt pavements due to oxidative aging presents a significant challenge in highway maintenance. This study investigates the rejuvenation effect of three bio-oils, namely palm oil, soybean oil, and sunflower oil, on aged PEN 90 asphalt through an integrated approach combining experimental characterization and molecular dynamics (MD) simulations. Laboratory evaluations, including penetration, softening point, dynamic shear rheology (DSR), and Fourier Transform Infrared (FTIR) spectroscopy, were conducted to quantify the recovery of the physical, rheological, and chemical properties of aged high-penetration asphalt. MD simulations were conducted to provide insights into diffusion behavior and intermolecular interactions between bio-oil molecules and aged asphalt components. Experimental results show that bio-oils effectively restore the lost viscoelastic performance after long-term aging. An 8% dosage was determined as optimal, with rejuvenation efficiency decreasing in the order of SSO, SO, and PO. MD simulations clarify mechanisms by showing that soybean and palm oils have higher diffusion efficiency than sunflower oil, thus promoting the dispersion of asphaltene and resin. RDF shows that bio-oils enhance asphalt molecules’ short-range order via hydrogen bonds and van der Waals forces, which improves compatibility. Full article

Background: Digital light processing (DLP) 3D printing has emerged as a rapid alternative to labour-intensive micro-moulding for producing microneedle (MN) arrays, yet its use in biodegradable, dissolving MNs has been limited by proprietary, non-degradable resins. Methods: The current study proposed an innovative, biocompatible PEGDA–vinyl-pyrrolidone photo-resin with lithium phenyl(2,4,6-trimethylbenzoyl) phosphinate initiator, which systematically optimises its rheology and photo-reactivity for DLP printing. Resin formulations were evaluated through viscosity profiling, cure kinetics, FTIR, and ¹H NMR, and MN arrays were printed using a desktop DLP platform and characterised by optical microscopy, mechanical testing, thermal analysis, and dissolution studies. Results: A 40% PEGDA up-to 100% VP blend with 0.4% initiator was identified as providing rapid photopolymerisation, low shrinkage and complete vinyl conversion. Using a desktop DLP platform, 6 × 6 MN patches were printed in a single step without moulds and analysed by optical and scanning electron microscopy. The printed MNs reproduced CAD dimensions with <3% deviation, achieving a height of 1.40 ± 0.02 mm and a base thickness of 1.00 ± 0.01 mm, and showed a tip radius consistent with sharp penetration. Compression testing measured an array force of 32 N, corresponding to ~0.9 N per needle, exceeding the 0.2 N threshold for skin insertion. FTIR and ¹H NMR confirmed near-quantitative crosslinking, thermogravimetric and differential scanning calorimetry indicated stability at ambient conditions, and dissolution studies showed complete needle dissolution. Conclusions: An optimised PEGDA/VP resin yields geometrically precise, mechanically robust dissolving MNs in a single step, addressing the limitations of micro-moulding and paving the way for customisable, on-demand transdermal delivery of active molecules and biologics. Full article

This study provides a comprehensive quantitative comparison of three structurally distinct epoxy prepolymers—cycloaliphatic, novolac, and bis-aromatic (BADGE)—cured with a single hardener, methyl nadic anhydride (MNA), and catalyzed by 1-methylimidazole under strictly identical stoichiometric and thermal conditions. Each formulation was optimized in terms of epoxy/anhydride ratio and catalyst concentration to ensure meaningful cross-comparison under representative cure conditions. A multi-technique approach combining differential scanning calorimetry (DSC), dynamic rheometry, and thermogravimetric analysis (TGA) was employed to jointly assess cure kinetics, network build-up, and long-term thermal stability. DSC analyses provided reaction enthalpies and glass transition temperatures (Tg) ranging from 145 °C (BADGE-MNA) to 253 °C (cycloaliphatic ECy-MNA) after stabilization of the curing reaction under the chosen thermal protocol, enabling experimental fine-tuning of stoichiometry beyond the theoretical 1:1 ratio. Isothermal rheology revealed gel times of approximately 14 s for novolac, 16 s for BADGE, and 20 s for the cycloaliphatic system at 200 °C, defining a clear hierarchy of reactivity (Novolac > BADGE > ECy). Post-cure thermomechanical performance and thermal aging resistance (100 h at 250 °C) were assessed via rheometry and TGA under both dynamic and isothermal conditions. They demonstrated that the novolac-based resin retained approximately 93.7% of its initial mass, confirming its outstanding thermo-oxidative stability. The three systems exhibited distinct trade-offs between reactivity and thermal resistance: the novolac resin showed superior thermal endurance but, owing to its highly aromatic and rigid structure, limited flowability, while the cycloaliphatic resin exhibited greater molecular mobility and longer pot life but reduced stability. Overall, this work provides a comprehensive and quantitatively consistent benchmark, consolidating stoichiometric control, DSC and rheological reactivity, Tg evolution, thermomechanical stability, and degradation behavior within a single unified experimental framework. The results offer reliable reference data for modeling, formulation, and possible use of epoxy–anhydride thermosets at temperatures above 200 °C. Full article

Vat photopolymerization 3D printing, including stereolithography (SLA), digital light processing (DLP), and masked SLA (mSLA), has transformed dental device fabrication by enabling precise and customizable components. However, the rheological behavior of photopolymer resins is a critical factor that governs the printability, accuracy, and performance of printed parts. This review surveys the role of viscosity, shear-thinning, and thixotropy in defining the “printability window” of dental resins and explores the relationship between these properties and the formulation and final material performance. Rheological characterization using rotational rheometry provides key insights, with shear rate sweeps and thixotropy tests quantifying whether a resin behaves as Newtonian or pseudoplastic. The literature shows that optimal printability typically requires resins with low to moderate viscosity at shear, moderate thixotropy for stability, and formulations balanced between high-strength oligomers and low-viscosity diluents. The addition of fillers modifies the viscosity and dispersion, which can improve reinforcement but may reduce print resolution if not optimized. Thermal and optical considerations are also coupled with rheology, affecting the curing depth and accuracy. In conclusion, controlling resin rheology is essential for bridging material formulation with reliable clinical outcomes, guiding both resin design and printer process optimization in modern dental applications. Full article

In the field of enhanced oil recovery (EOR), particularly for water control in high-temperature reservoirs, there is a critical need for effective in-depth water shutoff and conformance control technologies. Polymer-based in situ-cross-linked gels are extensively employed for enhanced oil recovery (EOR), yet their short gelation time under high-temperature reservoir conditions (e.g., >120 °C) limits effective in-depth water shutoff and conformance control. To address this, we developed a hydrogel system via the in situ cross-linking of polyacrylamide (PAM) with phenolic resin (PR), reinforced by silica sol (SS) nanoparticles. We employed a variety of research methods, including bottle tests, viscosity and rheology measurements, scanning electron microscopy (SEM) scanning, density functional theory (DFT) calculations, differential scanning calorimetry (DSC) measurements, quartz crystal microbalance with dissipation (QCM-D) measurement, contact angle (CA) measurement, injectivity and temporary plugging performance evaluations, etc. The composite gel exhibits an exceptional gelation period of 72 h at 130 °C, surpassing conventional systems by more than 4.5 times in terms of duration. The gelation rate remains almost unchanged with the introduction of SS, due to the highly pre-dispersed silica nanoparticles that provide exceptional colloidal stability and the system’s pH changing slightly throughout the gelation process. DFT and SEM results reveal that synergistic interactions between organic (PAM-PR networks) and inorganic (SS) components create a stacked hybrid network, enhancing both mechanical strength and thermal stability. A core flooding experiment demonstrates that the gel system achieves 92.4% plugging efficiency. The tailored nanocomposite allows for the precise management of gelation kinetics and microstructure formation, effectively addressing water control and enhancing the plugging effect in high-temperature reservoirs. These findings advance the mechanistic understanding of organic–inorganic hybrid gel systems and provide a framework for developing next-generation EOR technologies under extreme reservoir conditions. Full article

This study investigates the use of carbonized hemp fiber (CHF) as a reinforcement for phenol resorcinol formaldehyde (PRF)-based fiber composites. The hemp fiber was carbonized slowly up to 1000 °C under N₂ with a yield of 18%. Compression-molded composites were prepared with CHF and then compared to hemp (HF) and wood fiber (WF) at 0 to 50% loading with PRF resin. The flow characteristics of the uncured composites were determined by dynamic rheology and showed pseudoplastic behavior; the composites show promise as extrudable materials. The flexural strength of the HF composites (69 MPa for 40% HF) was higher than the CHF composites. The thermal stability of the composites was determined by thermogravimetric analysis (TGA), and the CHF composites were more stable than the HF and WF composites. Carbonization was shown to enhance both the thermal stability and the hydrophobicity of the composites, which is expected to lead to less susceptibility to weathering and biological attack. Formulations of 50% WF, 50% CHF, and 30% HF fiber loadings with PRF were able to be extruded into rods. Extruded CHF composites showed better mechanical properties than the HF and WF composites. Full article

Hydrogen is a promising alternative to fossil fuels, but its efficient storage presents significant challenges. Polymer composite vessels, especially those made from carbon fiber-reinforced plastic (CFRP), are gaining attention, due to their high strength-to-weight ratio for storing compressed or cryogenic hydrogen. The latest Type V tanks, which lack internal liners, rely solely on fiber composites for both structural integrity and gas containment, enhancing the storage volume-to-weight ratio and supporting recycling. However, this linerless design faces the challenge of preventing gas permeation. Epoxy resins, widely used in aerospace carbon fiber-reinforced composites (CFRCs), offer excellent processability and load-bearing capabilities. The addition of high-aspect-ratio nanofillers can enhance the gas barrier properties, which are essential for preventing hydrogen leakage, while also improving the mechanical, electrical, and thermal properties of the nanocomposites. This study focuses on epoxy-based composites with expanded graphite, aiming to optimize their physical properties and processing for Type V tanks, using a rheological framework to evaluate their processability and multifunctionality in transport applications. Full article

The effect of the addition of polyvinylpyrrolidone (PVP) to polyamide resins was studied using polyamide 6 (PA6) and an amide copolymer with a low melting point (PA-L). For the PA6/PVP blends, the crosslinking reaction occurred during rheology measurements in the molten state. The blends did not show a phase-separated structure. Furthermore, the crystallization of PA6 was greatly inhibited by PVP addition. These results suggest that the PVP chains were dissolved in PA6 in the molten state, although the effect of the crosslinking reaction on the structure development is unknown. In the case of the PA-L/PVP blends, melt-mixing and the rheology measurements were performed at low temperature to avoid the crosslinking reaction. It was found that PVP was miscible with PA-L in the molten state when the PVP content was 10 and 15 wt%. The intermolecular interaction between the polyamide resins and PVP was detected from the peak shift of the infrared absorbance. PVP addition enhanced the moisture content in both polyamide resins and decreased the contact angle with water droplets. These results suggested that the surface properties and mechanical properties of polyamide resins, which are affected by the moisture content, are modified by PVP addition. Full article

Epoxy resins are extensively employed as adhesives and matrices in fibre-reinforced composites. As polymers, they possess a viscoelastic nature and are prone to creep and stress relaxation even at room temperature. This phenomenon is also responsible for time-dependent failure or creep fracture due to cumulative strain. Several constitutive equations have been used to describe the mechanical time-dependent response of polymers. These models have been proposed over the past six decades, with minimal direct and practical confrontation. Each model is associated with a specific application or research group. This work assesses the predictive performance of four distinct time-dependent constitutive models based on experimental data. The models were deemed sufficiently straightforward to be readily integrated into practical engineering analyses. A range of loading cases, encompassing constant strain rate, creep, and relaxation tests, were conducted on a commercial epoxy resin. Model parameter calibration was conducted with a minimum data set. The extrapolative predictive capacity of the models was evaluated for creep loading by extending the tests to five decades. The selected rheological models comprise two viscoelastic models based on Volterra-type integrals, as originally proposed by Schapery and Rabotnov; one viscoplastic model, as originally proposed by Norton and Bailey; and the Burger model, in which two springs and two dashpots are combined in a serial and parallel configuration. The number of model parameters does not correlate positively to superior performance, even if it is high. Overall, the models exhibited satisfactory predictive performance, displaying similar outcomes with some relevant differences during the unloading phases. Full article

Polybenzoxazine (PBz) resins exhibit excellent mechanical, thermal, and adhesive properties, making them interesting candidates for coating applications. Moreover, thanks to the incorporation of exchangeable ester bonds within the PBz network, the coating presents healable properties that are catalyzed by the intrinsic presence of tertiary amine within the PBz backbone. Unfortunately, these tertiary amine functions are also responsible for the limited resistance of such systems to acid environments by protonation. To address this limitation, the protection of tertiary amines inherent to the PBz network was investigated in this study by incorporating an aromatic group close to the amine function to minimize its protonation via hindrance/mesomeric effects. More precisely, benzoxazine precursors based on monoethanolamine (mea) and aminophenylethyl alcohol (Apa) were synthesized and tested as protective coatings of aluminium alloy substrates (AA1050). The resins were characterized by NMR, FTIR, rheology, TGA, DSC, and DMA. PBz synthesized from Apa exhibits enhanced thermal stability, reduced swelling rates in both water and acid, and shortened relaxation times. After application via solvent casting on AA1050 substrates, the acid resistance of the coatings was evaluated. Electrochemical impedance spectroscopy results demonstrated better resistance of the Apa-based resins in 0.1 M sulfuric acid after one month of immersion. Full article