Search Results (111)

This study investigates the design and performance of lime mortars incorporating multi-phase change material (multi-PCM) systems as thermally responsive rendering materials for building-envelope applications under variable conditions. Moving beyond conventional single-PCM lime mortar approaches, this work proposes a controlled multi-PCM design framework in which a fixed total PCM dosage is distributed across selected phase-transition windows. Mortars combining PCMs with different transition temperatures (5–25 °C and 18–25 °C) were produced using two PCM types: silica-supported form-stable systems and polymeric-shell microencapsulated systems supplied as powders or aqueous slurries. All formulations contained 20% PCM and were optimized with polymeric additives, including a polycarboxylate ether-based superplasticiser and a starch-derived adhesion enhancer, to ensure suitable workability and applicability as rendering materials. Microstructural analyses showed that form-stable PCMs generated more heterogeneous pore structures, whereas polymeric-shell microencapsulated systems maintained pore structures similar to PCM-free mortars. Mortars containing metakaolin exhibited enhanced mechanical performance and durability, in some cases outperforming reference mortars, highlighting the importance of matrix refinement in the successful incorporation of multi-PCM systems. Thermal characterization revealed that form-stable systems produced broader phase transitions due to component interactions, while polymeric-shell microencapsulation preserved distinct transitions and enabled a wider, more controllable activation range. Under dynamic thermal conditions (−10 to 50 °C), all multi-PCM mortars demonstrated effective temperature buffering, achieving reductions of up to 1.5 °C during heating and 1.1 °C during cooling. Environmental and economic analyses highlighted that the benefits of PCM incorporation depend on matching PCM transition temperatures to specific climatic and application requirements. These findings position multi-PCM lime mortars as a promising route towards climate-adapted, thermally responsive renders with distributed and tailorable activation profiles. Full article

The rapid development of cold chain logistics has generated a strong demand for high-performance phase change materials (PCMs). In this study, a composite PCM (CPCM) applicable to 5 °C cold chain logistics, integrated with PVA/CMC-Na hydrogel to maintain form stability, is developed. N-Tetradecane and water are employed as the primary cold storage media in the composite. Span 80, Tween 80 and borax are introduced into the composite as homogenizing agents and supercooling depressant, respectively. The main preparation steps of the CPCM include aqueous phase preparation, emulsifier compounding, oil-phase preparation, blending, homogenization, and molding, in sequence. Experimental results demonstrate that the CPCM exhibits a phase transition temperature of 0–5 °C, a latent heat of 236.2 J/g, a supercooling degree of no more than 0.5 °C, and a volume expansion ratio of 3%. Therefore, the CPCM is able to satisfy the cold storage demand for cold chain transportation with a target temperature of approximately 5 °C, and can serve as a superior-performance alternative to the PCMs currently used for similar applications in the market. Full article

The particle size of aggregate is a key factor affecting the mechanical properties and deformation capacity of cemented gangue filling body. In this study, coal gangue with a particle size range of (0.05, 20) mm was sieved into six groups of aggregate particles. Based on the Talbot gradation theory, cubic specimens with gradation indices n = 0.3, 0.4, 0.5, 0.6, and 0.7 were prepared for acoustic emission (AE) monitoring tests. The microstructure of the filling body was analyzed, and the failure characteristics and damage evolution laws of the cemented gangue filling body with different gradation indices were explored. The results show that the compressive strength reaches its maximum when n = 0.5. As the gradation index increases, the compressive strength of the specimens first increases and then decreases, and the specimens shift from primarily experiencing cleavage failure to shear failure. The curve of cumulative AE ringing count shows a bimodal distribution pattern, with both surge points and fracture points coexisting. The surge points can be regarded as precursor signals of backfill failure. The spatiotemporal evolution of AE events exhibits complex phased changes. An excessively small gradation index tends to form micropores and striped microcracks, reducing the compactness of the microstructure. An excessively large gradation index can lead to the formation of penetrative weak channels. A reasonable gradation index enables the mutual interlocking of aggregate particles, constructing a stable three-dimensional spatial skeleton structure. The dynamic trend of damage in the filling body can be captured based on AE analysis, and reverse guidance can be provided for parameter optimization of Talbot gradation, achieving a dynamic closed loop of “gradation design-AE monitoring-damage assessment-parameter optimization”. This not only enriches the application scenarios of acoustic emission analysis in graded materials, but also provides a new research approach and technical method for gradation design and safety assessment in scenarios where particle sizes are missing in practical engineering. Full article

With increasingly stringent requirements for wear resistance and reliability of functional coatings for heavily loaded friction units, a relevant challenge in materials science is to establish the relationships between the parameters of reactive pulsed magnetron sputtering and the tribo-mechanical properties of TiN/CrN multilayer systems. In this study, TiN/CrN multilayer coatings were deposited by reactive pulsed magnetron sputtering using separate titanium and chromium targets. The effect of the nitrogen flow rate (0.20–0.36 L/h) during chromium sputtering on the structure, phase composition, and mechanical and tribological properties of the coatings was investigated at a fixed nitrogen flow rate of 0.08 L/h for titanium. SEM, EDS, and XRD showed that increasing the nitrogen flow rate leads to a non-monotonic change in coating thickness (2.0–2.6 µm), caused by the transition of the chromium target from the metallic to the poisoned sputtering mode. At low N₂ flow rates, a subnitride Cr₂N phase forms in the structure, whereas at the optimal flow rate of 0.32 L/h the coating consists of stable TiN, CrN, and (Cr_0.5Ti_0.5)N phases. The coating nanohardness was 20–23 GPa and the Young’s modulus was 250–300 GPa. The best tribological performance was achieved at a nitrogen flow rate of 0.32 L/h, coefficient of friction μ ≈ 0.5 and a minimum wear rate of 1 × 10⁻⁵ mm³/(m·N), which correlates with the highest H³/E² value. It is shown that independent control of the CrN layer stoichiometry using separate targets can affect the tribo-mechanical properties of the TiN/CrN multilayer system. Full article

The intermittent and variable nature of solar energy poses challenges for maintaining stable thermal performance in solar heating systems. One effective approach to mitigate this limitation is to store surplus thermal energy during periods of high solar irradiance and release it when solar input is insufficient. Phase change materials (PCMs) are particularly suitable for this purpose due to their ability to absorb and release large amounts of latent heat during phase transition. The aim of this work is to develop a mathematical model of a flow-through tank containing a phase change material in the form of a spherical packed bed. Including longitudinal dispersion in the model equations allows for a more accurate description of the heat transfer process in a tank containing PCM elements. Simulation calculations based on the model were carried out to demonstrate its potential applicability to practical problems. The influence of the following parameters on the process was investigated: tank volume, water flow rate, phase change temperature, process duration, dispersion coefficient during water flow, radius of the packed-bed elements, and cyclic variations of the inlet water temperature. A significant influence of the axial dispersion coefficient in the tank containing PCM on the outlet water temperature profile was demonstrated. It was found that the internal heat transfer coefficient within the packing elements containing PCM falls within the range of 58–145 W/(m²K). Full article

Phase change materials (PCMs) have emerged as a key enabler of high-performance, low-carbon buildings through latent heat-based thermal energy storage. This paper presents a systematic and critical synthesis of advances in PCM technologies for building applications published between 2022 and 2025, analyzing over 300 peer-reviewed studies to evaluate thermal performance, economic viability, environmental impact, and climate adaptability across three integration approaches: passive, active, and hybrid systems. The studies analyzed show that passive envelope integration employing macroencapsulated or form-stable PCMs in walls, roofs, and glazing is reported to deliver 15–45% energy savings with payback periods of 8–15 years, primarily through enhanced thermal inertia and indoor temperature stabilization. Active systems, which couple PCMs with HVAC, heat pumps, or air handling units, are found to achieve 20–40% energy reductions and shorter payback periods (3–8 years) by enabling load shifting, peak shaving, and improved coefficient of performance (COP). Hybrid configurations integrating passive and active strategies with AI-driven control demonstrate, in the literature, the highest potential, with reported energy savings of up to 50%, though they entail greater complexity and capital cost. The review further highlights material-level innovations, including ternary composite PCMs, bio-based alternatives, and nano-enhanced formulations that address intrinsic limitations such as low thermal conductivity (0.1–0.3 W/m·K for organics) and cycling instability. Despite significant progress, critical gaps persist in standardized testing protocols, long-term field validation, comprehensive lifecycle assessments, and real-world scalability, particularly in tropical and cold climates. By bridging material science, building physics, and energy system engineering, this work provides a forward-looking roadmap to accelerate the deployment of PCM-based solutions in the global decarbonization of the built environment. Full article

This study employs a mono-caprylate waterborne polyurethane microencapsulation technique to construct a core–shell phase-change microcapsule system with a structured composite core material. By integrating a silica network with phase change materials (ethyl palmitate/paraffin), a stable core material is formed. The silica not only acts as a physical framework to prevent leakage but also regulates the phase change temperature and latent heat through molecular interactions at its surface active sites. The shell layer polyurethane, derived from a fatty acid monoglyceride prepolymer, exhibits a structure highly similar to that of the core material, ensuring efficient and complete encapsulation, while the aqueous system aligns with green manufacturing requirements. The system successfully achieves two types of performance-tunable microcapsules: the silica–ethyl palmitate type exhibits a broad phase change temperature range near room temperature, while the silica–paraffin type demonstrates high latent heat of phase change in the medium-temperature range. This diversity in performance broadens the material’s application scenarios. Its broad temperature range characteristic is particularly suitable for building energy efficiency and electronic thermal management fields, effectively mitigating temperature fluctuations and reducing energy consumption, demonstrating significant application value and innovative potential. Full article

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

Background: Using Huanglian Jiedu decoction (HJD) as a model, this study systematically compares the traditionally prepared combined decoction with mixtures of separately decocted components, focusing on differences in chemical composition, material properties, and transcriptomic responses. Methods: To maintain consistency, both the combined HJD decoction and the single-herb mixture were prepared using a standardized method, and their chemical profiles were analyzed by HPLC and UPLC-MS/MS to identify constituent differences. Physical properties were examined through key parameter measurements and phase behavior analysis, and the integration of chemical and physical data identified the components driving the observed material changes. Transcriptome sequencing compared the two decoction types, highlighting differentially expressed genes and the major regulatory pathways involved. Results: HPLC analysis showed a clear redistribution of components between the two decoction methods, with the combined decoction containing higher levels of alkaloids such as coptisine chloride, epiberberine, palmatine chloride, jatrorrhizine hydrochloride, and phellodendrine chloride, while the single decoction mixture had higher levels of berberine hydrochloride and baicalin. In the combined decoction, the berberine hydrochloride content was 37.04 mg/g, and the baicalin content was 15.57 mg/g; in the single decoction, the berberine hydrochloride content was 41.15 mg/g; in the combined decoction, the baicalin content was 40.07 mg/g. UPLC-MS/MS analysis confirmed clear differences between the two decoctions, mainly in flavonoid and alkaloid compositions. The combined decoction contains 110 flavonoid compounds and 67 alkaloid compounds, while the single decoction contains 100 flavonoid compounds and 80 alkaloid compounds. Physical measurements showed that the combined decoction had higher total dissolved solids, conductivity, and salinity, while the single decoction had higher resistivity. The combined decoction had a TDS of 2480 mg/L, σ of 4.95 ms/cm, S of 0.26%, and ρ of 202 Ω·cm; the single decoction had a TDS of 1190 mg/L, σ of 2.37 ms/cm, S of 0.12%, and ρ of 419 Ω·cm. Phase separation analysis indicated that the combined decoction formed a stable nanoscale phase structure, whereas the single decoction remained unstable. Transcriptome sequencing at various concentrations revealed marked differences in gene expression between the two preparations, reflecting their distinct biological activities. Conclusions: Analysis showed clear differences in chemical composition, physical properties, and gene expression in the combined decoction. Taking Huanglian Jiedu decoction as a representative example, we systematically compared the specific differences between combined and single decoction methods, providing a reference basis for subsequent pharmacodynamic evaluation and clinical application. Full article

With the rapid advancement of energy storage technologies, there is a growing demand for affordable, efficient, and environmentally benign battery systems. Sodium-ion batteries (SIBs) present a promising alternative to lithium-ion systems due to sodium’s high abundance and similar electrochemical properties. Particular attention is given to developing NASICON -sodium (Na) super ionic conductor, type cathode materials, especially Na3V2(PO4)3, which exhibits high thermal and structural stability. This study focuses on the sol–gel synthesis of Na₃V₂(PO₄)₃ using citric acid and ethylene glycol, as well as investigating the effect of annealing temperature (400–1000 °C) on its structural and electrochemical properties. Phase composition, morphology, textural characteristics, and electrochemical performance were systematically analyzed. Above 700 °C, a highly crystalline NASICON phase free of secondary impurities was formed, as confirmed by X-ray diffraction (XRD). Microstructural evolution revealed a transition from a loose amorphous structure to a dense granular morphology, accompanied by changes in specific surface area and porosity. The highest surface area (67.40 m²/g) was achieved at 700 °C, while increasing the temperature to 1000 °C caused pore collapse due to sintering. X-ray photoelectron spectroscopy (XPS) confirmed the predominant presence of V³⁺ ions and the formation of V⁴⁺ at the highest temperature. The optimal balance of high crystallinity, uniform elemental distribution, and stable texture was achieved at 900 °C. Electrochemical testing in a Na/NVP half-cell configuration delivered an initial capacity of 70 mAh/g, which decayed to 55 mAh/g by the 100th cycle, attributed to solid-electrolyte interphase (SEI) formation and irreversible Na⁺ trapping. These results demonstrate that the proposed approach yields high-quality Na₃V₂(PO₄)₃ cathode materials with promising potential for sodium-ion battery applications. Full article

In recent years, apatite-based materials have garnered significant interest, particularly for applications in tissue engineering. Apatite is most commonly employed as a coating for metallic implants, as a component in composite materials, and as scaffolds for bone and dental tissue regeneration. Among its various forms, hydroxyapatite (HAP) is the most widely used, owing to its natural occurrence in human and animal hard tissues. An emerging area of research involves the use of fluoride-substituted apatite, particularly fluorapatite (FAP), which can serve as a direct fluoride source at the implant site, potentially offering several biological and therapeutic advantages. However, substituting HAP with FAP may lead to unforeseen changes in material behavior due to the differing physicochemical properties of these two calcium phosphate phases. This study investigates the effects of replacing hydroxyapatite with fluorapatite in ceramic–polymer composite materials incorporating β-1,3-glucan as a bioactive polymeric binder. The β-1,3-glucan polysaccharide was selected for its proven biocompatibility, biodegradability, and ability to form stable hydrogels that promote cellular interactions. Nitrogen adsorption analysis revealed that FAP/glucan composites had a significantly lower specific surface area (0.5 m²/g) and total pore volume (0.002 cm³/g) compared to HAP/glucan composites (14.15 m²/g and 0.03 cm³/g, respectively), indicating enhanced ceramic–polymer interactions in fluoride-containing systems. Optical profilometry measurements showed statistically significant differences in profile parameters (e.g., Rp: 134 μm for HAP/glucan vs. 352 μm for FAP/glucan), although average roughness (Ra) remained similar (34.1 vs. 27.6 μm, respectively). Microscopic evaluation showed that FAP/glucan composites had smaller particle sizes (1 μm) than their HAP counterparts (2 μm), despite larger primary crystal sizes in FAP, as confirmed by TEM. XRD analysis indicated structural differences between the apatites, with FAP exhibiting a reduced unit cell volume (524.6 ų) compared to HAP (528.2 ų), due to substitution of hydroxyl groups with fluoride ions. Spectroscopic analyses (FTIR, Raman, ³¹P NMR) confirmed chemical shifts associated with fluorine incorporation and revealed distinct ceramic–polymer interfacial behaviors, including an upfield shift of PO₄³⁻ bands (964 cm⁻¹ in FAP vs. 961 cm⁻¹ in HAP) and OH vibration shifts (3537 cm⁻¹ in FAP vs. 3573 cm⁻¹ in HAP). The glucan polymer showed different hydrogen bonding patterns when combined with FAP versus HAP, as evidenced by shifts in polymer-specific bands at 888 cm⁻¹ and 1157 cm⁻¹, demonstrating that fluoride substitution significantly influences ceramic–polymer interactions in these bioactive composite systems. Full article

To meet the massive increase in energy demand, extensive research has been conducted over the past few decades on developing clean and sustainable energy storage methods. Hydrogen is considered as one of the most promising future energy carriers due to its high energy density and renewability, but it requires storage. Storing hydrogen using metal hydride offers several advantages, including stability, safety compactness and reversibility of the hydrogen absorption/desorption process. Thermal management during hydrogen storage using metal hydride is critically important since the reaction between the metal and hydrogen is highly exothermic. We are aiming to develop thermal storage systems based on composite phase change materials (CPCMs) that absorb the heat generated during hydrogen absorption and release it during desorption, in an effort to improve energy storage efficiency. Lightweight, shape-stable CPCMs are prepared by loading the selected organic phase change materials into expanded graphite and hydrophobic monolithic silica aerogel. The chemical structure, microstructure, thermal properties and leakage of CPCMs are investigated. These samples were subjected to variable power electrical heating to simulate the heat generated during hydrogen reaction, forming lanthanum hydride, according to its published reaction kinetics. Full article

The significant energy consumption and contribution to greenhouse gas emissions by the construction sector need careful attention to explore innovative sustainable solutions for improving the energy efficiency and thermal comfort of building envelopes. The integration of phase-change materials (PCMs) into building commodities is a favorable technology for minimizing energy consumption and enhancing thermal performance. This review paper covers the impact of PCM incorporation into construction materials, such as walls, roofs, and glazing units. Additionally, it examines different embedding techniques like direct incorporation, immersion, macro and micro-encapsulation, and form and shape-stable PCM. Factors affecting the thermal performance of PCM-integrated buildings, including melting temperature, thickness, position, volumetric change, vapor pressure, density, optical properties, latent heat, thermal conductivity, chemical stability, and climate conditions, are elaborated. Furthermore, the latest experimental and numerical simulations, as well as modeling techniques, evident from case studies, are investigated. Ultimately, the advantages of PCM integration, including energy savings, peak load reduction, improvement in interior comfort, and reduced heating, ventilation, and air-conditioning dependence, are explained alongside the limitations. Finally, the recent progress and future potential of PCM-integrated construction materials are discussed, focusing on innovations in this field, addressing the status of policies in line with the United Nations Sustainable Development Goals, and outlining research potential for the future. Full article

The aim of this study is an interdisciplinary assessment of the potential of cement pastes to permanently bind carbon dioxide (CO₂) under anaerobic digestion conditions, considering technological, microstructural, environmental, and economic aspects. The research focused on three types of Portland cement: CEM I 52.5N, CEM I 42.5R-1, and CEM I 42.5R-2, differing in phase composition and reactivity, which were evaluated in terms of their carbonation potential and resistance to chemically aggressive environments. The cement pastes were prepared with a water-to-cement ratio of 0.5 and subjected to 90-day exposure in two environments: a reference environment (tap water) and a fermentation environment (aqueous suspension of poultry manure simulating biogas reactor conditions). XRD, TG/DTA, SEM/EDS, and mercury intrusion porosimetry were applied to analyze CO₂ mineralization, phase changes, and microstructural evolution. XRD results revealed a significant increase in calcite content (e.g., for CEM I 52.5N from 5.9% to 41.1%) and the presence of vaterite (19.3%), indicating intense carbonation under organic conditions. TG/DTA analysis confirmed a reduction in portlandite and C-S-H phases, suggesting their transformation into stable carbonate forms. SEM observations and EDS analysis revealed well-developed calcite crystals and the dominance of Ca, C, and O, confirming effective CO₂ binding. In control samples, hydration products predominated without signs of mineralization. The highest sequestration potential was observed for CEM I 52.5N, while cements with higher C₃A content (e.g., CEM I 42.5R-2) exhibited lower chemical resistance. The results confirm that carbonation under fermentation conditions may serve as an effective tool for CO₂ emission management, contributing to improved durability of construction materials and generating measurable economic benefits in the context of climate policy and the EU ETS. The article highlights the need to integrate CO₂ sequestration technologies with emission management systems and life cycle assessment (LCA) of biogas infrastructure, supporting the transition toward a low-carbon economy. Full article