Search Results (2,271)

Polyethylene waxes (PEWs) are considered promising mid-temperature phase change materials (PCMs). However, their low thermal conductivity limits both applicability and efficiency. One of the more interesting inorganic additives for PCMs is boron nitride (BN), which exhibits high thermal conductivity while remaining electrically insulating, excellent chemical and thermal stability, and good oxidation resistance. In this study, PEW was modified with hexagonal boron nitride (h-BN) in the range of 0.025 to 0.5 wt.%. Differential scanning calorimetry (DSC) results revealed that the addition of h-BN significantly alters the phase-transition behavior of polyethylene wax, broadens the melting and solidification temperature ranges, and reduces supercooling from 11 °C to 9 °C. Thermogravimetric analysis (TGA) showed that the incorporation of h-BN improves the thermal stability of the material. The temperature corresponding to 5% mass loss increased by about 50 °C after incorporation of more than 0.025% h-BN. The temperature of maximum mass-loss rate (T_DTGmax) was shifted about 8 °C toward higher temperatures. FTIR results indicate that h-BN does not change the chemical structure of polyethylene waxes, but does affect their morphology and physical properties by increasing the thermal conductivity from 0.30 to 0.40 mW/K. These effects enable the design of composites with tunable properties for energy-storage applications. Full article

Shape-stabilized phase change materials (SSPCMs) have been a promising thermal energy storage (TES) solution to combine the high energy density of solid-to-liquid (SL) PCMs and the structural stability of solid–solid PCMs. Although polymeric matrices have been used for their reduced cost and ease of processability, few have evaluated the use of crosslinked natural rubber (NR). In this study, we evaluate by differential scanning calorimetry (DSC) the preparation of room-temperature tailorable SSCPMs by the design of NR matrices with different crosslink density vulcanized by dicumyl peroxide (DCP) or sulphur, with special focus on the quantification of the content of PCM. The results indicate that the amount of PCM stable in the NR matrix is low, with PCM contents between 16 and 24% and enthalpies between 16 and 20 J·g⁻¹. Likewise, it is well-known that thermophysical properties of the PCMs vary upon confinement in a small-scale porous matrix. The confinement of the PCM in the rubber network results in a measured enthalpy below the expected value, and a melting point depression of up to 23.6 °C, dependent on crosslink density. These results highlight the structural complexity of NR-PCM composites and the need for further investigation. Full article

Powder bed fusion (PBF) is a widely adopted additive manufacturing (AM) process category that enables high-resolution fabrication across metals, polymers, ceramics, and composites. However, its inherent process complexity demands robust modeling to ensure quality, reliability, and scalability. This review provides a critical synthesis of advances in physics-based simulations, machine learning, and digital twin frameworks for PBF. We analyze progress across scales—from micro-scale melt pool dynamics and mesoscale track stability to part-scale residual stress predictions—while highlighting the growing role of hybrid physics–data-driven approaches in capturing process–structure–property (PSP) relationships. Special emphasis is given to the integration of real-time sensing, multi-scale modeling, and AI-enhanced optimization, which together form the foundation of emerging PBF digital twins. Key challenges—including computational cost, data scarcity, and model interoperability—are critically examined, alongside opportunities for scalable, interpretable, and industry-ready digital twin platforms. By outlining both the current state-of-the-art and future research priorities, this review positions digital twins as a transformative paradigm for advancing PBF toward reliable, high-quality, and industrially scalable manufacturing. Full article

The present study analyses the changes in antioxidative behavior of biodegradable Poly(lactic acid) (PLA)-based composite films with bioactive additives derived from pomegranate peel, an abundant agricultural by-product rich in antioxidants and antimicrobials. PLA-based composites were prepared by incorporating industrial-grade pomegranate peel powder (PoP) via melt extrusion at concentrations of 1–5 percent by weight (wt.%). For mechanical characterization, the resulting films were subjected to tensile testing. Their thermal properties were further characterized using thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), dynamic oxidation induction temperature measurements (OIT), complemented by Fourier-transform infrared spectroscopy (FT-IR), color analysis, rheology, scanning electron microscopy (SEM), and UV-Vis spectroscopy. Results show that the incorporation of PoP had no significant impact on the characteristic transition temperatures (Tg, Tm, and Tc) of PLA, indicating that the thermal behavior of the polymer matrix was largely preserved. However, while the thermo-oxidative stability of PLA was improved in the presence of PoP, with a maximum at 3 wt.% of PoP, increasing the OIT by 30 °C, the mechanical performance of the composite films was adversely affected, as evidenced by decreased tensile strength and elongation at break indication embrittlement, especially for ≥3 wt.% of PoP. Significant changes were observed in the films’ surface properties, as well as in their color parameters and UV transmittance values. Consequently, while PoP offers potential bioactive functionality for use as a sustainable additive, its content must be carefully optimized to maintain an acceptable balance between functionality and mechanical integrity. Full article

Stabilizing thermoplastic polymers against thermal degradation is an important aspect that must be addressed during material development and becomes critical in the case of bio-polymers, which often reveal reduced thermal stability and a narrow processing temperature window. Herein, we propose a new methodology to analyze and compare the thermal stability of thermoplastic materials, exampled by several types of bio-polyesters, such as aliphatic PBS and PBSA, aliphatic-aromatic PBAT and PBST, and amorphous PHBV, and evaluate the impact of thermal stabilizer on their processability and thermal stability. The proposed method relies on multi-step torque rheometry experiments that involve controlled cycling of the tested material under varied thermal conditions, shear forces, and processing times to acquire and evaluate the changes in flow behavior of the sample after its processing. By monitoring polymer melt behavior and comparing the changes before and after repetitive processing steps, we can gain valuable insights into the material performance and stabilizing efficiency of additives. The thermal stability of polymers and the efficiency of thermal stabilizers can be assessed by means of the relative change in temperature-normalized torque, $∆\tau \left(\%\right)$, measured after different processing steps. Significantly, we demonstrate that the obtained $∆\tau \left(\%\right)$ values correlate with changes in the molar mass of neat polymers as a result of their processing. The proposed approach enables a semi-quantitative evaluation of the thermal stability of various polymers and the study of the efficiency of thermal stabilizers and their performance, providing a robust strategy for optimizing compound formulations, particularly regarding the optimal fractions required. Full article

Medium-entropy alloys (MEAs) represent a promising class of materials for solid-state hydrogen storage due to their high hydrogen affinity, structural stability, and tunable properties. In this work, a compositional series of (TiZrNbTa)_{100−x}Al_x (x = 0–10 at. %) MEAs were prepared and systematically investigated to clarify the influence of aluminum addition on microstructure, mechanical response, and hydrogen sorption behavior. The alloys were synthesized by arc melting, homogenized by annealing, and characterized using microscopy, X-ray diffraction, density measurements, microhardness testing, nanoindentation, and hydrogen absorption/desorption experiments. Hydrogen sorption was evaluated by isobaric absorption measurements at 2 MPa H₂ over two consecutive cycles, complemented by thermogravimetric desorption analysis of hydrogenated samples. The results show that aluminum addition significantly affects activation behavior, hydrogen uptake, and residual hydrogen retention, while simultaneously increasing hardness and elastic modulus in a non-linear manner. The alloy containing 5 at. % Al exhibits the most balanced performance, combining reduced activation temperature in the second absorption cycle, relatively high hydrogen capacity, and moderate mechanical stiffness. These findings demonstrate that controlled aluminum alloying is an effective strategy for tailoring hydrogen–metal interactions and optimizing the performance of TiZrNbTa-based MEAs for solid-state hydrogen storage applications. Full article

Organic phase change materials show potential for thermal energy storage, but their scalable implementation is limited by fixed phase change temperatures, molten leakage, and low thermal conductivity. To address the temperature constraint, a binary eutectic system of 1-tetradecanol and 1,10-decanediol is prepared, expanding the operational temperature range for building thermal management. Compositing the eutectic with expanded graphite yields a composite material that exhibits a low leakage and a markedly improved thermal conductivity of 4.642 W/(m·K), which is approximately 12 times that of the pure eutectic. The composite maintains distinct phase transition properties, with melting and solidification temperatures of 37.77 °C and 29.38 °C and corresponding latent heats of 218.80 J/g and 216.66 J/g. It also demonstrates a good cycling stability, retaining over 87% of the original latent heat after 2000 thermal cycles. While these findings remain valid under controlled conditions, further studies are required to evaluate their practical feasibility and long-term durability in real-world scenarios. This work establishes a systematic approach for fabricating composite phase change materials and provides a promising candidate for building thermal management applications. Full article

This study utilized capric acid (CA), lauric acid (LA), myristic acid (MA), palmitic acid (PA), and stearic acid (SA) as alternative feedstocks to conduct theoretical analyses on ten fatty acid-based ternary eutectic systems. By leveraging the Schrader equation, phase diagrams for each system were constructed, and their theoretical eutectic points were calculated. The CA-LA-MA (capric acid–lauric acid–myristic acid) ternary system was selected as a representative for experimental fabrication: differential scanning calorimetry (DSC) was employed to characterize its thermal properties, while Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA) were used to assess its functional group composition and thermal stability, respectively. Theoretical calculations indicate that the ten ternary eutectic systems exhibit melting temperatures ranging from 17.11 °C to 37.61 °C, with phase change latent heats spanning 167.8 J·g⁻¹ to 189.6 J·g⁻¹. For the CA-LA-MA system, experimental DSC results confirm that its eutectic melting temperature is 16.0 °C (accompanied by a phase change latent heat of 177.0 J·g⁻¹, with minor deviations from theoretical predictions attributed to reagent impurities and operational errors). TGA characterization further reveals that the CA-LA-MA mixture has an initial weight loss temperature (corresponding to ~1% mass loss) of 115.6 °C and an extrapolated onset weight loss temperature of 164.8 °C, confirming reliable thermal stability below 100 °C—consistent with its low-temperature application design. These results validate the consistency between theoretical predictions and experimental data, and demonstrate that fatty acid-based ternary eutectic mixtures are promising candidates for low-temperature thermal energy storage applications. Full article

Friction Stir Processing (FSP) has emerged as an advanced solid-state surface engineering technique for tailoring high-performance surface architectures in metal matrix composites (MMCs). By combining localized thermo-mechanical deformation with controlled material flow, FSP enables grain refinement, homogeneous dispersion of reinforcement, and strong interfacial bonding without melting or altering bulk properties. This review critically examines the role of FSP in enhancing the mechanical, tribological, and corrosion performance of composites, with emphasis on process–structure–property relationships. Key strengthening mechanisms, including grain boundary strengthening, load transfer, particle pinning, and defect elimination, are systematically discussed, along with their implications for wear resistance, fatigue life, and durability. Special attention is given to corrosion and tribo-corrosion behavior, highlighting electrochemical mechanisms such as micro-galvanic interactions, passive film stability, and interfacial chemistry. Furthermore, the eco-efficiency, industrial viability, and sustainability advantages of FSP are evaluated in comparison with conventional surface modification techniques. The review concludes by identifying critical challenges and outlining future research directions for the scalable, multifunctional, and sustainable design of composite surfaces. Full article

This study investigates the activation mechanism of boron-doped carbon (BMC) catalysts for the degradation of the antibiotic sulfamethoxazole (SMX) via persulfate (PMS) activation. The catalysts were synthesized using a sequential double-melting calcination method, resulting in mesoporous carbon nanosheets characterized by hierarchical macro-mesopores and atomically dispersed dual active sites. Comprehensive characterization was performed using BET, SEM, TEM, FT-IR, XPS, XRD, and Raman techniques. The optimized BMC catalyst demonstrated excellent performance, achieving complete removal of sulfamethoxazole (100%) and a high mineralization rate (~90%) within 45 min. Mechanistic analysis, including electron paramagnetic resonance (EPR), revealed that the degradation predominantly follows a singlet oxygen (1O2)-dominated pathway. The system exhibited broad applicability to various pollutants, along with notable operational stability and robust resistance to common environmental interferents. Persulfate activation was primarily attributed to boron-active sites, while the hierarchical mesoporous structure facilitated both pollutant enrichment and catalytic efficiency. Full article

Per- and polyfluoroalkyl substances (PFASs), as a class of “permanent chemicals” with high environmental persistence and bioaccumulation, have attracted much attention. In this study, we focused on the molecular mechanism of the interaction between perfluoroalkyl acids (PFAAs) and peroxisome proliferator-activated receptor δ (PPARδ). Using molecular docking, binding free energy calculation, and structural analysis, we systematically investigated the binding modes, key amino acid residues, and binding energies of 20 structurally diverse PFAAs with PPARδ. The results showed that the binding energies of PFAAs with PPARδ were significantly affected by the molecular weight, the number of hydrogen bond donors, and the melting point of PFAAs. PFAAs with smaller molecular weights and fewer hydrogen bond donors showed stronger binding affinity. The binding sites were concentrated in high-frequency amino acid residues such as TRP-256, ASN-269, and GLY-270, and the interaction forces were dominated by hydrogen and halogen bonds. PFAAs with branched structure of larger molecular weight (e.g., 3m-PFOA, binding energy of −2.92 kcal·mol⁻¹; 3,3m₂-PFOA, binding energy of −2.45 kcal·mol⁻¹) had weaker binding energies than their straight-chain counterparts due to spatial site-blocking effect. In addition, validation group experiments further confirmed the regulation law of binding strength by physicochemical properties. In order to verify the binding stability of the key complexes predicted by molecular docking, and to investigate the dynamic behavior under the conditions of solvation and protein flexibility, molecular dynamics simulations were conducted on PFBA, PFOA, 3,3m₂-PFOA, and PFHxA. The results confirmed the dynamic stability of the binding of the high-affinity ligands selected through docking to PPARδ. Moreover, the influence of molecular weight and branched structure on the binding strength was quantitatively verified from the perspectives of energy and RMSD trajectories. The present study revealed the molecular mechanism of PFAAs interfering with metabolic homeostasis through the PPARδ pathway, providing a theoretical basis for assessing its ecological and health risks. Full article

Additive manufacturing (AM) has emerged as a pivotal technology in component fabrication, renowned for its capabilities in freeform fabrication, material efficiency, and integrated design-to-manufacturing processes. As a critical branch of AM, metal additive manufacturing (MAM) has garnered significant attention for producing metal parts. However, process anomalies during MAM can pose safety risks, while internal defects in as-built parts detrimentally affect their service performance. These concerns underscore the necessity for robust in-process monitoring of both the MAM process and the quality of the resulting components. This review first delineates common MAM techniques and popular in-process monitoring methods. It then elaborates on the fundamental principles of acoustic emission (AE), including the configuration of AE systems and methods for extracting characteristic AE parameters. The core of the review synthesizes applications of AE technology in MAM, categorizing them into three key aspects: (1) hardware setup, which involves a comparative analysis of sensor selection, mounting strategies, and noise suppression techniques; (2) parametric characterization, which establishes correlations between AE features and process dynamics (e.g., process parameter deviations, spattering, melting/pool stability) as well as defect formation (e.g., porosity and cracking); and (3) intelligent monitoring, which focuses on the development of classification models and the integration of feedback control systems. By providing a systematic overview, this review aims to highlight the potential of AE as a powerful tool for real-time quality assurance in MAM. Full article

With the growing demand for eco-friendly food packaging, poly(butylene adipate-co-terephthalate) (PBAT)/polylactic acid (PLA) composite films have emerged as promising biodegradable alternatives, but their inherent limitations (e.g., poor antioxidant capacity, weak UV stability, and insufficient antimicrobial activity) hinder practical applications. This study aimed to address these drawbacks by incorporating Rosmarinus officinalis L. extract (RM) as a natural multifunctional additive. PBAT/PLA/RM blend films with RM concentrations of 0.1%, 0.3%, 0.5%, and 1% were fabricated via melt extrusion and blown film processing. Key characterizations were conducted to evaluate thermal stability, mechanical properties, morphology, antioxidant activity, UV-shielding performance, antimicrobial efficacy, and biodegradability. The results showed that RM significantly enhanced the antioxidant capacity of the films, with the highest DPPH radical scavenging activity achieved at 0.3% RM. UV-blocking performance improved incrementally with increasing RM concentration, and films containing ≥0.5% RM filtered over 90% of UVA and UVB radiation. All composite films met biodegradability standards, with over 90% degradation observed after 240 days of composting, though RM prolonged the initial degradation stage by inhibiting early microbial activity. However, the antimicrobial effect of RM was limited, and concentrations exceeding 1% caused film stickiness, impeding processing. This work demonstrates that RM is a viable natural additive for functionalizing PBAT/PLA films, offering enhanced antioxidant and UV-shielding properties while maintaining biodegradability, thus providing a promising solution for sustainable food packaging. Full article

Additive manufacturing (AM) has emerged as a key enabling technology in contemporary dental manufacturing, driven by its capacity for customization, geometric complexity, and seamless integration with digital design workflows. This article presents a technology-oriented narrative review of additive manufacturing in dental implant production, focusing on dominant processing routes, material systems, and emerging research trends rather than a systematic or critical appraisal of the literature. An indicative descriptive analysis of publications indexed in the Web of Science and Scopus databases between 2014 and 2024 was used to contextualize the technological development of the field and identify major research directions. Emphasis was placed on metal powder bed fusion technologies, specifically Selective Laser Melting (SLM) and Direct Metal Laser Sintering (DMLS), which enable the fabrication of titanium implants with controlled porosity and enhanced osseointegration. Ceramic AM approaches, including SLA, DLP, and PBF, are discussed in relation to their potential for aesthetic dental restorations and customized prosthetic components. The publication trend overview indicates a growing interest in ceramic AM after 2020, an increasing focus on hybrid and functionally graded materials, and persistent challenges related to standardization and the availability of long-term clinical evidence. Key technological limitations—including manufacturing accuracy, material stability, validated metrology, and process reproducibility—are highlighted alongside emerging directions such as artificial intelligence-assisted workflows, nanostructured surface modifications, and concepts enabling accelerated or immediate clinical use of additively manufactured dental restorations. 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