Search Results (854)

The ionic conductivity of EuCl₂ was investigated at high temperatures, including the melting point. Measurements were performed on polycrystalline specimens obtained by the solidification of the corresponding melt. The behavior of the conductivity and the apparent Arrhenius activation energy was characterized. It is suggested that the conductivity behavior results from anion sublattice disordering within the crystals up to the melting point. The variation in transport properties correlates well with the crystal structure of EuCl₂. The phase diagram of the LiCl–EuCl₂ binary system was constructed based on DSC measurements. This system was found to be a simple eutectic type featuring the incongruently melting compound LiEu₃Cl₇. The CALPHAD method was employed for thermodynamic modeling, incorporating both experimental and literature data for the LiCl–EuCl₂ system. Full article

This study explores an innovative approach based on deep eutectic solvent (DES)-synergistic ultrasonic-assisted extraction (UAE) of anthocyanins from blueberry pomace (BP). Choline chloride–lactic acid (ChCl-LA, 1:2) was identified as the most efficient DES and provided the highest anthocyanin recovery. The optimal conditions for ChCl-LA-synergistic UAE (ChCl-LA-UAE) were obtained as follows: ultrasonic power of 270 W, extraction time of 30 min, liquid-to-solid ratio of 35:1, and water content in ChCl-LA of 40%, achieving a total anthocyanin content (TAC) of 3.5168 mg/g, with R² = 0.9860. This value was significantly higher than those obtained with 70% ethanol (3.1962 mg/g) and pure water (1.9137 mg/g). SEM images revealed that ChCl-LA-UAE disrupted the surface structure of the samples, thereby promoting anthocyanin release. COSMO-RS simulations confirmed that ChCl-LA significantly enhanced the interaction between the solvent and the representative anthocyanin (cyanidin-3-O-glucoside, C3G), resulting in higher extraction efficiency. In vitro antioxidant assays further demonstrated that the synergistic system exhibited stronger antioxidant activity. Overall, ultrasonic-synergistic DES extraction could be an eco-friendly method for recovering high-value compounds from blueberry and its byproducts. Full article

The transition toward renewable and environmentally responsible materials has intensified interest in cellulose-based systems for use in sustainable packaging applications. Although cellulose offers biocompatibility, structural versatility, and tuneable physicochemical properties, conventional modification routes rely on harsh chemicals and generate environmentally burdensome effluents. In this study, an efficient and a potentially green strategy for cellulose modification was developed using acid-based deep eutectic solvents (DES) composed of choline chloride and lactic, acetic, or citric acid at different molar ratios. Under mild conditions (110 °C, 4 h), DES pretreatment reduced glucan content in sulphite pulp from 99% to 79–93%, depending on the hydrogen bond donor (HBD), while suggesting an apparent increase in relative crystallinity, from approximately 82% to 90%, as estimated by the Segal method. FTIR, XRD, and morphological analyses revealed the disruption of the hydrogen bonding network, enhanced fibrillation, and residual DES-derived functional groups detectable by FTIR. Although DES pretreatment increased structural order, it also reduced enzymatic digestibility due to the higher proportion of crystalline domains. Overall, the results demonstrate that acidic DES constitutes a sustainable and recyclable medium capable of modulating cellulose structure and generating materials with enhanced physicochemical properties. These findings suggest that DES-modified cellulose could serve as a potential reinforcement platform for future biodegradable packaging and bioplastic formulations, enabling the development of high-performance, renewable, and environmentally compliant packaging materials. Full article

Hot cracking in welding is a very complex phenomenon. It can happen in the weld metal zone during solidification but also in the heat-affected zone (HAZ). Hot cracking defects are material decohesion that occur at high temperatures along grain boundaries when the strain and strain rate exceed a certain level. The cracks can be internal or open to the surface in the weld bead. During a welding operation, different types of hot cracks can appear, such as hot cracking due to solidification, hot cracking due to liquation, hot cracking due to loss of ductility. The main factors favoring hot solidification cracking include the presence of residual elements and impurities, leading to the formation of a low-melting eutectic; the solidification mode; and mechanical restraints. This review paper gives an introduction to solidification cracking in stainless-steel welds, the weldability of the austenite grades, and the causes of solidification cracking occurrence. The main methods with which to detect and inspect cracks are investigated. Particular focus is placed on TIG (tungsten inert gas), also known as Gas Tungsten Arc Welding (GTAW). A review of the literature reveals that considerable progress has been made in terms of the improvement in the properties of the weld joint through the application of mitigation means and strategies. The effort made by researchers in understanding solidification cracking phenomena has been key to enhancing cracking resistance and ensuring the integrity of structures. Full article

Gallium (Ga)-based liquid metal (LM) composites, particularly those based on eutectic gallium–indium (EGaIn) and related alloys, have emerged as a promising materials platform for soft and deformable energy storage owing to their unique combination of metallic conductivity, fluidic deformability, and adaptive interfaces. Despite rapid advances in LM-enabled devices, binders remain insufficiently understood and are still commonly regarded as passive structural components. Here, we present a comprehensive binder-centered perspective for LM composites, establishing the binder as a key regulator of electro-chemo-mechanical coupling, interfacial stability, transport behavior, and processability in soft energy systems. We show that tailored binder chemistries in Ga-based LM systems—including stretchable batteries, printable conductors, and soft electrochemical devices—govern LM droplet dispersion, suppress coalescence and leakage, and preserve conductive percolation under large deformation, while enabling room-temperature fabrication and printability through rheological regulation and interfacial wetting. Beyond mechanical confinement, emerging binder functionalities—including dynamic bonding, supramolecular interactions, ionically conductive networks, and reversible polymer architectures—enable self-healing interfaces, adaptive transport pathways, and robust adhesion in deformable devices. By integrating recent advances in stretchable batteries, flexible supercapacitors, printable electronics, and multifunctional soft energy systems, we establish a unified multiscale framework linking binder molecular design to device-level electrochemical and mechanical performance. We further discuss sustainability and manufacturing considerations, including recyclable polymer networks, low-temperature fabrication, and scalable processing strategies. Finally, we outline current challenges and future opportunities toward programmable binder systems with tunable viscoelasticity, interfacial reactivity, and adaptive functionality. This Review establishes binder-centered engineering as a key pathway for transforming LM composites from proof-of-concept materials into resilient, manufacturable, and multifunctional soft energy technologies for wearable, stretchable, and biointegrated electronics. Full article

Under lead–bismuth eutectic (LBE) corrosion conditions, the multilayer oxide layer that forms on T91 steel adversely affects on its thermal conductivity. This study systematically conducted corrosion experiments under varying temperatures, durations, oxygen concentrations, and bismuth (Bi) content. By combining microstructural characterization with laser flash measurements of thermal conductivity, the evolution of T91 thermal conductivity under different corrosion conditions was revealed. Based on these findings, molecular dynamics simulations based on the neuroevolution potential (NEP) framework were employed to construct a T91/Fe-Cr spinel/Fe₃O₄ multilayer heterojunction model, enabling precise determination of the intrinsic thermal resistances at the two interfaces. By coupling the interfacial thermal resistances with experimental data, the macroscopic effective thermal conductivities of Fe-Cr spinel and Fe₃O₄ in real corrosion environments were calculated to be 1.68 W/(m·K) and 2.19 W/(m·K), respectively. These values are significantly lower than those reported for pure phases, thus revealing the inhibitory effect of defects and pores in actual oxide layers on heat transport. This research establishes a multiscale analytical method spanning from atomic-scale interfacial thermal resistance to macroscopic heat transfer properties of oxide layers, thereby providing a theoretical basis and data support for the thermal performance evaluation and service life prediction of LFR structural materials. Full article

The work is a continuation of studies , focused on the development of fundamental principles of aluminum activation by low-melting metals forming eutectic alloys with fine-grained structure and limited solid solubility. The aim of this work is to investigate the mechanism and kinetics of the interaction of aluminum-based eutectic alloys with water and aqueous electrolytes. Analysis of phase diagrams of binary systems (Al–Ga, Al–In, In–Ga, Al–Sn, Sn–Ga, Al–Zn, Zn–Ga) shows that alloy composition governs surface heterogeneity and reactivity. Ternary and quaternary systems (Al–In–Ga, Al–Sn–Ga, Al–In–Sn–Ga) exhibit enhanced interaction with water due to increased heterogeneity, leading to the formation of numerous microgalvanic couples and accelerated aluminum dissolution. The process is characterized by the stationary potential of aluminum and involves coupled chemical, electrochemical, and topochemical stages described by the Avrami–Erofeev equation, with n ≈ 1.27–2.07. An increase in the In–Ga or In–Sn–Ga fraction reduces the activation energy: 9.1 kcal/mol (82% Al–9% Ga–9% Sn), 11.4 kcal/mol (92% Al–4% Ga–4% In), and 15.5 kcal/mol (91% Al–3% Ga–3% In–3% Sn). Full article

This study investigated an efficient approach for extracting saponins from Panax japonicus using deep eutectic solvents (DES) coupled with ultrasound-assisted (UA) extraction, and compared its performance with the methanol extraction method. Twenty-six DES were screened, and choline chloride–urea was selected as the optimal solvent. The total extraction yield was evaluated based on the sum of the yields of chikusetsusaponin IVa (CS-IVa) and ginsenoside Ro (G-Ro). The extraction process was optimized using single-factor experiments combined with an orthogonal array design. Molecular dynamics (MD) simulation was applied to reveal the extraction mechanism at the molecular level. The results showed that the optimal conditions were as follows: a choline chloride-to-urea molar ratio of 1:3, a solid-to-liquid ratio of 1:50, a water content of 60%, an ultrasonic temperature of 40 °C, and an ultrasonic time of 60 min. Under these conditions, the total extraction yield of Panax japonicus saponins reached 7.4%, which was 13% higher than that obtained with the pharmacopeia methanol extraction method. MD simulation demonstrated that DES weakens intermolecular interactions among saponins through hydrogen bonds and van der Waals forces, promoting the dispersion of saponin aggregates and enabling efficient dissolution. Compared with CS-IVa, G-Ro displayed a more pronounced solvation effect, which was likely attributed to the difference in the number of polar sites in their molecular structures. The UA-DES extraction method established herein is green and efficient. It provides a practical reference for the industrial extraction of Panax japonicus saponins and a theoretical foundation for mechanistic studies on natural product extraction using DES. Full article

316L stainless steel and T91 heat-resistant steel are key structural materials for lead-cooled fast reactors (LFRs). Lead–bismuth eutectic (LBE) corrosion induces oxide layer formation and remarkably degrades thermal conductivity, endangering reactor safety and efficiency. Systematic experimental studies on and predictive tools for the thermal conductivity of stainless steels after LBE corrosion are currently scarce. To address the lack of experimental data and predictive capabilities regarding changes in thermal conductivity following LBE corrosion, this study experimentally obtained thermal conductivity data from stainless steels after lead–bismuth corrosion and developed machine learning models to predict thermal conductivity under multi-parameter coupled LBE corrosion conditions. Three machine learning models were established using material composition and corrosion parameters as inputs. Overall, the hyperparameter-optimized Gradient Boosting Regression model showed competitive predictive performance with low overall prediction error. The model therefore provides a preliminary data-driven tool for estimating the thermal conductivity of corroded 316L stainless steel and T91 heat-resistant steel, thereby providing technical support for material selection, thermal design, and safety assessment of LFRs, with further specimen-level validation required for broader engineering application. Full article

Thermal regulation of lithium-ion (Li-ion) battery modules is a critical constraint for electric vehicle (EV) safety and durability, particularly during high-C-rate operation. Phase change materials (PCMs) have emerged as promising passive solutions due to their latent heat storage capability; however, current literature is heavily biased toward organic paraffin-based systems and lacks structured benchmarking across PCM categories and integration architectures. This review provides a systematic comparative assessment of PCM-based battery thermal management systems (BTMSs) comprising organic, inorganic, and eutectic materials under EV-relevant discharge conditions. The review is structured according to the conventional classification of PCMs; however, the available literature is predominantly focused on organic materials, particularly paraffin-based PCMs, leading to greater depth of analysis for this category. Thermophysical properties are analyzed in conjunction with discharge rate, module configuration, and hybrid cooling strategies. The results indicate that peak temperature mitigation is weakly correlated with latent heat magnitude when thermal conductivity remains below critical values. Conductivity-enhanced composites incorporating expanded graphite or metal foams significantly improve heat diffusion, reducing hotspot intensity and inter-cell temperature gradients under medium-to-high C-rates. Pure passive PCM systems exhibit thermodynamic limitations during sustained high-power operation due to saturation effects, underscoring the need for hybrid architectures for continuous heat rejection. This work establishes a structured benchmarking framework and demonstrates that effective thermal conductivity, integration strategy, and discharge-dependent design dominate BTMS performance over latent heat alone. The findings also reveal that inorganic and eutectic PCM-based BTMSs remain comparatively less explored in the literature, particularly at the battery module level and under realistic electric vehicle operating conditions, highlighting opportunities for future research. Full article

Tremella fuciformis polysaccharides (TFPS) exhibit anti-inflammatory and gut-microbiota-modulating activities, but conventional extraction methods often show limited efficiency and may affect polysaccharide structural integrity. This study optimized a deep eutectic solvent (DES)-based extraction method with potential environmental advantages for TFPS, characterized the major purified fraction, and evaluated its effects in a dextran sulfate sodium (DSS)-induced experimental colitis model. Extraction parameters for the choline chloride–lactic acid DES system were refined through single-factor testing combined with response surface methodology. The purified fraction TFPS-1 was characterized by chromatographic, spectroscopic, methylation, and NMR analyses, and its biological effects were assessed in DSS-treated mice. Under the optimized conditions, the TFPS yield reached 33.09 ± 1.52%, representing a 77.6% increase compared with hot-water extraction. TFPS-1 was identified as a low-molecular-weight glucan mainly containing α-(1→4)- and β-(1→6)-linked glucose residues. In experimental colitis mice, TFPS-1 alleviated body weight loss, colon shortening, and histopathological injury; increased mucus secretion and barrier-related gene expression; reduced pro-inflammatory cytokines; increased IL-10; and partially adjusted gut microbiota composition. These results indicate that DES-based extraction is an efficient strategy for preparing TFPS and provide evidence that TFPS-1 may be further explored as a food-derived polysaccharide ingredient for intestinal protection in experimental colitis-related contexts. Full article

Aqueous zinc–iodine batteries (AZIBs) are emerging as highly promising candidates for next-generation, grid-scale energy storage due to the intrinsic safety of water-based electrolytes, the high theoretical capacity of the zinc anode, and the rapid conversion kinetics of the iodine cathode. However, the practical commercialization of AZIBs is severely impeded by formidable interfacial instabilities, including the uncontrollable growth of zinc dendrites, parasitic hydrogen evolution reactions (HER), and the notorious polyiodide (I₃⁻, I₅⁻) shuttle effect. These macroscopic degradation modes are fundamentally rooted in the robust [Zn(H₂O)₆]²⁺ primary solvation sheath and the immense thermodynamic driving force for polyiodide dissolution in highly polar aqueous media. To address these interconnected challenges, electrolyte engineering has evolved into the most potent, holistic strategy. This comprehensive review systematically evaluates the latest advancements in electrolyte engineering for AZIBs. We first deeply decipher the fundamental thermodynamic mechanisms governing Zn²⁺ desolvation and iodine multiphase conversion. Subsequently, we critically analyze cutting-edge regulation paradigms, including water-in-salt (WIS) and localized high-concentration electrolytes (LHCE), cosolvent networks, functional molecular additives, deep eutectic solvents (DES), and quasi-solid-state hydrogels. By integrating in situ/operando spectroscopic characterizations with multiscale theoretical computations (such as MD and DFT), we elucidate the structure–activity relationships at the atomic level. Finally, we provide strategic perspectives on the future trajectories of the field, emphasizing the stabilization of multi-electron (I⁻/I⁰/I⁺) halogen chemistry, AI-driven high-throughput screening, and the rigorous standardization of Ah-level pouch cell engineering for extreme-environment applications. Full article

Curcuminoids from Curcuma longa L. (curcumin, demethoxycurcumin, bisdemethoxycurcumin) are attractive bioactives yet constrained by low water solubility and chemical instability. Herein, we introduce a Supramolecular Deep Eutectic Solvent (SupraDES) as a “Janus” green platform, combining extraction and stabilization with a subsequent solvent-to-material strategy. Eight NaDES/SupraDES formulations based on choline chloride (ChCl) or betaine with glycerol (Gly) or citric acid (CitA), with/without β-cyclodextrin (βCD), were assessed. The extinction coefficients of the most promising solvents were extrapolated at 425 nm for the UV–vis quantification of curcuminoids, to determine extraction performance. The SupraDES ChCl:Gly:βCD gave the best performance during the first solvent screening, improving at the same time the bioactive stability (after 30-day, 47.5% loss vs. 62.8% of ChCl:Gly alone). Subsequent microwave-assisted extraction (MAE) optimization identified 80 °C as the optimal process temperature, with near-equilibrium reached within 15 min (3139.4 µgCurc/gEXT). Peleg modelling (R² = 0.997) indicated a fast extraction rate and limited benefit from longer residence times. Finally, the curcuminoid-loaded SupraDES was incorporated into polyvinyl alcohol (PVA) networks crosslinked with CitA and 2,5-bis(hydroxymethyl)furan (BHMF); thermal analysis confirmed the formation of a stable crosslinked structure. To the best of our knowledge, this is the first report of a βCD-based SupraDES acting as a Janus platform that couples supramolecular extraction of lipophilic bioactives with their direct incorporation into bio-based polymeric materials, exemplifying an integrated green chemistry approach aligned with circular bioeconomy principles. Full article

In this work, a non-standardized hypereutectic aluminum–silicon alloy AlSi21Cu5MgCr intended for the automotive industry is presented. The modification of the alloy is performed with the conventional modifier phosphorus in an amount of 0.04 wt%. The applied metallurgical treatment is the basis for the obtained modified structure. It has been established that after conducting the T6 heat treatment, the free silicon crystals are reduced to 26.9 µm, and the eutectic silicon crystals are spherical in shape and have dimensions not exceeding 8 µm. The macrohardness of the studied alloy is 168.5HV_10/10, a value significantly higher than that required for this type of alloy, which is in the range of 95 ÷ 137 HV (90 ÷ 130 HB). The microhardness of the α-phase in the composition of the eutectic is 154 µHV_50/10, which indicates that after quenching a saturated solid solution was fixed, and during the artificial aging process secondary strengthening phases were formed and separated. A CrAlN hard coating was deposited on the alloy surface. The mechanical properties of the coating were characterized by a hardness of 14 GPa, whereas the AlSi21Cu5MgCr substrate had a hardness of 2 GPa. The results showed considerable improvement of the hardness of the new alloy and well-tuned elastic–plastic properties. The obtained adhesive properties are compatible with this class of materials. The composition of the CrAlN hard coating is homogeneously distributed on the alloy surface and the morphology is improved. The investigations showed that CrAlN hard coatings could successfully be applied for the modification of the surface of AlSIMgCu alloys. Full article

To address the demand for lightweight, high-performance Al-Si-Mg alloys in aerospace and automotive industries, this work proposes a novel synergistic strengthening strategy by combining rare-earth Y microalloying and in situ synthesized ZrB₂ nanoparticles to construct a hybrid reinforcement architecture. The effects of Y-ZrB₂ additions on the microstructure, crystallographic orientation evolution, and mechanical properties of Al-Si-Mg alloys were systematically investigated via XRD, SEM, EBSD, and tensile/hardness tests. Results show that compared with the base alloy and single-modified alloys, the co-addition of Y and ZrB₂ simultaneously enhances mechanical properties and optimizes grain structure. The optimal comprehensive performance is achieved at 0.3 wt.% Y + 2 wt.% ZrB₂ after T6 heat treatment, with ultimate tensile strength of 332.87 MPa, yield strength of 271.35 MPa, elongation of 16.24%, and Vickers hardness of 153.9 HV. Phase analysis and SEM-EDS confirm a synergistic coupling relationship between Y-rich phases and ZrB₂ nanoparticles. EBSD characterization reveals that Y-ZrB₂ modification has negligible effect on the morphology and crystallographic orientation stability of primary α-Al grains, but effectively regulates the lattice rotation, texture redistribution, and growth behavior of eutectic Si. At the optimal composition, the fraction of high-angle grain boundaries (HAGBs) reaches a maximum of 34.3%. Furthermore, the synergistic effect significantly increases the geometrically necessary dislocation (GND) density and reduces the Schmid factor of the dominant {111}⟨110⟩ slip system, thus enhancing dislocation strengthening and plastic deformation resistance. This work clarifies the intrinsic strength-ductility synergy mechanism of Y-ZrB₂ co-modified Al-Si-Mg alloys, paving a new pathway for the development of advanced lightweight aluminum alloys. Full article