Search Results (1,957)

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

Using multifunctional dual-cure smart bioactive resin luting agents (DRLs) offers benefits in adhesive dentistry, but their optical stability remains a concern. Their pre-cured form is a shear-thinning structure with thixotropic gel-like behavior. The effect of their hydrophilicity and different thicknesses of nanoceramic hybrid on the final shade of milled esthetic restorations needs further investigation. This study examined how the optical function deterioration of dual-cure smart bioactive resin luting agents used to bond a CAD/CAM nano-ceramic hybrid composite would influence the restoration’s final shade at three different thicknesses. A nanoceramic hybrid composite (GD) was cut into blocks and grouped by thickness (0.8, 1.0, 1.5 mm). Ten blocks from each group were assigned to subgroups based on the DRL type: Panavia SA Universal (PN), Predicta Bioactive (PR), and ACTIVA BioACTIVE (AC). Color and whiteness changes after a 24 h/day (24 days) coffee immersion were analyzed using statistical methods (ANOVA and Tukey’s HSD for ΔE₀₀; Welch’s ANOVA and Games-Howell for ΔWI_D and ΔL*). DRL type significantly affected ΔE₀₀, ΔWI_D, and ΔL* (p < 0.001). All materials showed the least color change and optical function deterioration at a restoration thickness of 1.5 mm, which was below the acceptability threshold (AT). Despite PR’s bioactive functionality, it maintained its primary optical function with the least color change at GD thicknesses of 1.0 and 1.5 mm (p < 0.001). AC exhibited the greatest ΔE₀₀ above AT, especially at a thickness of 0.8 mm (p < 0.001). ΔL*, ΔE₀₀, and ΔWI_D varied significantly based on DRL type, GD thickness, and the interaction between DRL and thickness (p < 0.05). This suggests that although dual-cure smart DRLs containing bioactive glasses are advantageous, their optical function shifts may become more noticeable in thin, translucent restorations. Increasing the restoration thickness can help mitigate this by altering the optical pathway. Full article

Canal wall down mastoidectomy (CWD) effectively eradicates cholesteatoma and chronic otitis media but frequently results in a problematic open mastoid cavity. Mastoid obliteration aims to reduce cavity-related morbidity. Bioceramic materials, including hydroxyapatite (HA), tricalcium phosphate (TCP), and bioactive glass (BAG), have been increasingly adopted because of their osteoconductive, biocompatible, and antimicrobial properties. This systematic review evaluates the clinical outcomes and complications of bioceramic mastoid obliteration following CWD. A systematic literature search of PubMed, Scopus, and Web of Science was conducted for studies published between 2005 and 2025, following PRISMA guidelines. Clinical studies reporting outcomes of bioceramic mastoid obliteration after CWD were included. Thirteen clinical studies were included. HA-, TCP-, and BAG-based materials demonstrated high obliteration success rates (>90% in most series). BAG S53P4 was consistently associated with low infection rates and favorable epithelialization, whereas earlier HA cement formulations were occasionally associated with revision-requiring complications. Bioceramic scaffolds represent safe and effective materials for mastoid obliteration after CWD. BAG offers additional antibacterial advantages, while HA provides predictable volume stability. Further prospective and comparative studies are required to establish material superiority and long-term outcomes. Full article

A series of biocomposites were elaborated by incorporating cellulose fibers, obtained from raw alfa plant, into a new polyurethane (PU) matrix synthesized from jojoba oil. The cellulose content was adjusted between 0% and 50%. To examine their properties, several characterization methods were employed. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) analyses confirmed that the extracted cellulose and the polyurethane matrix have high interfacial adhesion. Thermal stability was assessed using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). They indicate that the composites remained thermally stable in air up to 265 °C and exhibited glass transition temperatures (Tg) in the range of −38 to −7 °C, depending on the fiber percentage inside the polyurethane-based biocomposite. The corresponding mechanical properties increased with the addition of cellulose, reaching optimal improvement at 40% fiber content. Full article

This study aims to evaluate the potential of circular economy principles in earth-based construction using an experimental rammed earth building located in Pasłęk, Poland as a case study. The research focuses on end-of-life scenarios for earth materials, with particular emphasis on rammed earth, adobe, and compressed earth blocks stabilized with Portland cement. A scenario-based life-cycle assessment (LCA) was conducted to compare alternative demolition and reuse strategies, including manual and mechanical deconstruction, as well as on-site and off-site material reuse. Greenhouse gas emissions associated with demolition (Module C1) and transport (Module C2) were estimated for each scenario. The results indicate that manual deconstruction combined with local, on-site reuse leads to the lowest carbon footprint, whereas off-site reuse involving long-distance transport significantly increases greenhouse gas emissions. In addition, qualitative reuse pathways were identified for wood, glass, ceramics, and insulation materials. The study reveals a lack of standardized technical procedures for the recovery and reuse of stabilized earthen materials after demolition and highlights the importance of integrating end-of-life planning into the early design phase using digital tools such as material passports and BIM. The findings demonstrate that properly designed rammed earth systems can provide a viable low-tech solution for reducing construction waste and supporting circular material flows in the built environment. Full article

Transition metal (TM)-doped zinc oxide (ZnO) and zirconium dioxide (ZrO₂) nanocrystals exhibit complex correlations between crystal structure, defect chemistry, vibrational properties, and magnetic behavior that are strongly governed by synthesis route and dopant incorporation mechanisms. This review critically summarizes recent progress on Fe-, Mn-, and Co-doped ZnO and ZrO₂ nanocrystals synthesized by wet chemical, hydrothermal, and microwave-assisted hydrothermal methods, with emphasis on synthesis-driven phase evolution and apparent solubility limits. ZnO and ZrO₂ are treated as complementary host lattices: ZnO is a semiconducting, piezoelectric oxide with narrow solubility limits for most 3d dopants, while ZrO₂ is a dielectric, polymorphic oxide in which transition metal doping may stabilize tetragonal or cubic phases. Structural and microstructural studies using X-ray diffraction, electron microscopy, Raman spectroscopy, and Mössbauer spectroscopy demonstrate that at low dopant concentrations, TM ions may be partially incorporated into the host lattice, giving rise to diluted or defect-mediated magnetic behavior. When solubility limits are exceeded, nanoscopic secondary oxide phases emerge, leading to superparamagnetic, ferrimagnetic, or spin-glass-like responses. Magnetic measurements, including DC magnetization and AC susceptibility, reveal a continuous evolution from paramagnetism in lightly doped samples to dynamic magnetic states characteristic of nanoscale magnetic entities. Vibrational spectroscopy highlights phonon confinement, surface optical phonons, and disorder-activated modes that sensitively reflect nanocrystal size, lattice strain, and defect populations, and often correlate with magnetic dynamics. Rather than classifying these materials as diluted magnetic semiconductors, this review adopts a synthesis-driven and correlation-based framework that links dopant incorporation, local structural disorder, vibrational fingerprints, and magnetic response. By emphasizing multi-technique characterization strategies required to distinguish intrinsic from extrinsic magnetic contributions, this review provides practical guidelines for interpreting magnetism in TM-doped oxide nanocrystals and outlines implications for applications in photocatalysis, sensing, biomedicine, and electromagnetic interference (EMI) shielding. Full article

Designing the high-performance polyimides (PIs) for the biomimetic structures, which are used in extreme conditions, remains greatly challenging, due to the conflict between processability and thermal stability. Here, we report a series of silicon–alkyne-functionalized diamine-based polyimides that exhibit remarkable processability and thermal stability. The incorporation of bulky siloxy groups disrupts chain packing and increases free volume, enabling excellent solubility in polar solvents, while the rigid fluorene core enhances chain stiffness. DFT calculations confirm twisted molecular geometries (Si bond angle ≈ 103°, dihedral angle ≈ 89°) which weak π–π stacking, while heterogeneous electrostatic potentials enable favorable noncovalent interactions (e.g., C–F···H–C), promoting solvent diffusion. After thermal curing, the obtained product shows a high decomposition temperature (T_d5% = 560 °C), char yield of 72.0% at 800 °C, and glass transition temperature (T_g) of 354.6 °C. Meanwhile, locally planar fluorene units retain inherent thermal stabilization benefits through constrained rotational mobility. These results demonstrate a spatially decoupled siloxy–alkyne design that synergistically enhances molecular flexibility, disorder, and electronic stability, offering a molecular strategy for tailoring PI-based matrices to meet the demands of emerging biomimetic architectures and other high-performance composites operating under severe thermal loads. Full article

This study experimentally evaluates the mechanical and microstructural performance of single- and double-layer intraply hybrid composite (IRC) laminates produced using the hand lay-up method, focusing on Glass–Aramid (GA), Aramid–Carbon (AC), and Carbon–Glass (CG) configurations. Tensile, flexural, compressive, and density tests were conducted in accordance with relevant ASTM standards to assess the influence of hybrid type and layer number under field-representative manufacturing conditions. Microstructural investigations were performed using optical microscopy and scanning electron microscopy (SEM) to identify fabrication-induced imperfections and their relationship to mechanical behavior. The results demonstrate that increasing the laminate configuration from single to double layer significantly enhances mechanical performance across all hybrid types. Double-layer AC laminates exhibited the highest tensile strength (330.4 MPa) and Young’s modulus (11.93 GPa), corresponding to improvements of approximately 85% and 59%, respectively, compared to single-layer counterparts. In flexural loading, the highest strength was observed in double-layer CG laminates (97.14 MPa), while compressive strength was maximized in double-layer AC laminates (34.01 MPa), indicating improved stability and resistance to compression-driven failure. Statistical analysis confirmed that layer number is the dominant parameter governing mechanical response, exceeding the influence of hybrid configuration alone. Microstructural observations revealed fiber misorientation, incomplete resin impregnation, and localized voids inherent to manual fabrication. However, these imperfections were consistently distributed across all specimens and did not obscure comparative mechanical trends. Coefficients of variation generally remained below 10%, indicating acceptable repeatability despite non-ideal manufacturing conditions. Full article

The structural application of Fiber-Reinforced Polymers (FRP) is significantly hindered by their inherent thermal sensitivity. This paper presents a comprehensive review of the fire performance of FRP materials and FRP-concrete systems, spanning from material-scale degradation to structural-scale response. Distinct from previous studies, this review explicitly distinguishes between the fire behavior of internally reinforced FRP-reinforced concrete members and externally applied systems, including Externally Bonded Reinforcement (EBR) and Near-Surface Mounted (NSM) techniques. The thermal and mechanical degradation mechanisms of FRP constituents—specifically reinforcing fibers and polymer matrices—are first analyzed, with a focused discussion on the critical role of the glass transition temperature T_g. A detailed comparative analysis of the pros and cons of organic (epoxy-based) and inorganic (cementitious) binders is provided, elaborating on their respective bonding mechanisms and thermal stability under fire conditions. Furthermore, the effectiveness of various fire-protection strategies, such as external insulation systems, is evaluated. Synthesis of existing research indicates that while insulation thickness remains the dominant factor governing the fire survival time of EBR/NSM systems, the irreversible thermal degradation of polymer matrices poses a primary challenge for the post-fire recovery of FRP-reinforced structures. This review identifies critical research gaps and provides practical insights for the fire-safe design of FRP-concrete composite structures. Full article

Toughening modification of epoxy resin (EP) matrices is important for advancing high-performance fiber-reinforced composites. A promising strategy involves the use of multi-component additive systems. However, synergistic effects in such additive systems are difficult to achieve for multidimensional performance optimization due to insufficient interfacial interactions and competing toughening mechanisms. Herein, a “hard–soft” biphasic synergistic toughening system was engineered for epoxy resin, composed of furan-ring-grafted polyhedral oligomeric silsesquioxane (FPOSS) and liquid polysulfide rubber. The hybrid toughening agent significantly enhanced the integrated performance of the epoxy system: Young’s modulus, tensile strength, and elongation at break increased by 13%, 56%, and 101%, respectively. These improvements are attributed to the formation of enriched molecular chain entanglement sites and optimized dispersion, facilitated by nucleophilic addition reactions between flexible rubber segments and rigid FPOSS units with the epoxy matrix. The marked enhancement in toughness primarily stems from the synergistic toughening mechanism involving “crazing pinning” and “crazing-shear band”. Concurrently, FPOSS incorporation effectively modulated the curing reaction kinetics, rendering the process more gradual while substantially elevating the glass transition temperature (T_g) of the cured system by 16.82 °C and endowing it with superior thermal degradation stability. This work provides a simple and unique strategy to leverage multi-scale mechanisms for the construction of epoxy-based composites with good toughness and strength, and enhanced heat resistance. Full article

This study investigates a metakaolin-based geopolymer matrix in which two types of non-recyclable mirror glass waste (MGW) were used as alternative aggregates. The composition, properties and contents of MGW materials as well as their impact on the structure and performance of the geopolymer composites (MGW-Gs) have been characterized using X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TG), and Fourier transform infrared spectroscopy (FTIR). Mechanical properties, porosity and thermal conductivity have been evaluated, and compared with silica sand reference composites. The results show that MGW-based composites achieved flexural strengths of 3.9–5.7 MPa and compressive strengths of 60–70 MPa, which are lower than those of sand-based materials (8–11 MPa and up to 93.5 MPa, respectively) but remain adequate performance for applications with moderate load. FTIR analysis has indicated that the incorporation of MGW does not adversely affect the geopolymer network. All composites display similar porosity (approximately 18–22%) and water absorption (12–14%), while MGW incorporation has improved their thermal stability and significantly reduced their thermal conductivity to values below 0.53 W·m⁻¹·K⁻¹, compared with up to 1.09 W·m⁻¹·K⁻¹ for sand-based composites, emphasizing their insulation potential and sustainability benefits. The findings indicate that MGW aggregates can influence the microstructure, mechanical performance, and thermal properties of geopolymer composites, suggesting their potential use in specific construction applications. Full article

Viscoelastic polyurethane foams were prepared using four different bio-based polyols derived from coconut oil (CO), palm oil (PO), duck fat (DF), and pork fat (PF), employing up to 20 wt.% of the polyol component in a conventional formulation. The introduction of bio-polyols into the polyurethane formulation gave rise to an early minor decomposition of modified foams at low temperatures; however, the overall thermal stability improved slightly by the elimination of some intermediate decomposition stages. The glass transition temperature of foams was only moderately influenced and remained in the typical temperature range (around 10 °C). The effect of biopolyol type and content (5–20 wt.%) on the mechanical properties of the foams was investigated over the temperature range −20 to 40 °C. At 20 and 40 °C, all foams exhibited comfortable viscoelastic properties suitable for furniture applications. Hysteresis and the damping behavior of foams were also influenced by biopolyol type and concentration, with CO and DF providing enhanced energy absorption. Overall, these bio-based foams demonstrate potential for eco-friendly, high-performance applications, although their use at temperatures below 10 °C may be limited by increased stiffness. Full article

The bioinspired superhydrophobic surfaces have demonstrated many fascinating performances in fields such as self-cleaning, anti-corrosion, anti-icing, energy-harvesting devices, and antibacterial coatings. However, developing a low-cost, feasible, and scalable production approach to fabricate robust superhydrophobic surfaces has remained one of the main challenges in the past decades. In this paper, we propose an uncommon method for the fabrication of a durable superhydrophobic coating on the surface of the glass slide (GS). By utilizing the screen printing method and high-temperature curing, the epoxy resin grid (ERG) coating was uniformly and densely loaded on the surface of GS (ERG@GS). Subsequently, the hydrophobic silica (H-SiO₂) was deposited on the surface of ERG@GS by the impregnation method, thereby obtaining a superhydrophobic surface (H-SiO₂@ERG@GS). It is demonstrated that the micro-grooves in ERG can provide a large specific surface area for the deposition of low surface energy materials, while the micro-columns can offer excellent protection for the superhydrophobic coating when it is subjected to mechanical wear. It is important to note that micro-columns, micro-grooves, and nano H-SiO₂ jointly form the micro–nano structure, providing a uniform and robust rough structure for the superhydrophobic surface. Therefore, the combination of a micro–nano rough structure, low surface energy material, and air cushion effect endow the material with excellent durability and superhydrophobic property. The results show that H-SiO₂@ERG@GS possesses excellent self-cleaning property, mechanical durability, and chemical stability, indicating that this preparation method of the robust superhydrophobic coating has significant practical application value. Full article

This work investigated the comparative performance of two fluidized bed agglomeration systems for producing instant coconut milk powder: a commercially manufactured unit and a hybrid dryer previously modified into a fluidized bed agglomerator. Three binder solutions, distilled water, xanthan gum, and xyloglucan polysaccharide, were employed to examine how equipment configuration and binder type influence key powder properties. The aim was to evaluate the effects of fluidized bed agglomerator design and binder selection on coconut milk powder characteristics, including moisture content, bulk density, solubility, and glass transition temperature. All samples, including the non-agglomerated control, exhibited moisture contents ranging from 2.1% and 2.6% (w.b.), meeting the criterion for safe long-term storage. Powders produced with hydrocolloid binders (xanthan gum and xyloglucan) possessed lower bulk densities than those agglomerated with water, reflecting the formation of more open particle structures. When identical binders were applied, the two agglomerators produced comparable solubility outcomes, although water-based agglomerates consistently dissolved the fastest. Differential scanning calorimetry indicated a substantial increase in glass transition temperature after agglomeration, confirming improved structural stability. Overall, the results demonstrate that both agglomeration systems effectively enhanced the physicochemical and functional characteristics of coconut milk powder, with only minor variations that were attributable to equipment design. Full article

Copolymers of polyphenylene sulfone and polyarylene ether nitrile were synthesized using nucleophilic polycondensation. 2,6-difluorobenzonitrile (DFBN), 4,4′-dihydroxybiphenyl, and 4,4′-dichlorodiphenyl sulfone were used as monomers. The structure of the obtained copolymers was confirmed by means of IR spectroscopy, and their solubility in various solvents was studied. Thermal properties were studied using differential scanning calorimetry (DSC) and thermogravimetric analysis, as well as a set of basic mechanical properties. It was found that both thermal stability and glass transition temperature are virtually independent of the copolymer composition, while samples with a DFBN monomer content of more than 75% exhibit a melting peak in the region of 357 °C on the DSC curves, indicating an increase in the degree of crystallinity, accompanied by a deterioration in the solubility of these polymers. With increasing DFBN content, a uniform increase in elastic modulus is observed, and both bending and tensile strength increase significantly. However, the introduction of DFBN segments into the polyphenylene sulfone structure leads to a decrease in impact strength. Full article