Search Results (678)

This study investigates the mechanical and thermal properties of polypropylene (PP) composites incorporating pumice, a naturally occurring porous volcanic rock with high SiO₂ content, sourced from three regions in Türkiye (Nevşehir, Alaçatı, and Kütahya). Pumice was processed to particle sizes below 10 microns to maximize nucleating effectiveness, and composites were fabricated by melt compounding. The distinct mineralogical composition, porosity, and surface chemistry of the pumice samples enabled systematic evaluation of how regional variations influence crystallization and mechanical performance. A multi-analytical characterization approach, including thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray diffraction (XRD), and standardized mechanical tests (tensile, flexural, and impact), was applied. Results revealed that Alaçatı pumice at 0.1 wt% increased the impact strength of PP by about 11%, while maintaining stiffness. This demonstrates that pumice, unlike conventional fillers, can simultaneously enhance toughness and rigidity. Thermal analysis confirmed improved stability, with higher degradation onset and maximum decomposition temperatures observed in pumice-filled PP. DSC results indicated that certain pumice loadings promoted nucleation and increased crystallinity, while excessive amounts disrupted chain packing. SEM examinations confirmed uniform dispersion at low loadings, with agglomeration at higher levels reducing impact resistance. This work provides the first systematic demonstration of pumice powders as effective nucleating agents in PP, combining regional mineralogical diversity with measurable performance benefits. These findings indicate that pumice can serve as a sustainable, low-cost alternative to conventional nucleating agents, with potential applications in polymer components requiring improved toughness and thermal stability. Full article

This study investigates iron acetylacetonate (Fe(acac)₃) as a catalyst for enhancing high-temperature oxidation (HTO) during in situ combustion (ISC) of heavy oil. Thermal analysis revealed that Fe(acac)₃ decomposes at 360 °C to form crystalline magnetite (Fe₃O₄). This transformation precedes the HTO regime. Differential scanning calorimetry demonstrated significantly intensified HTO reactions in catalytic systems, as peak temperatures were lower than those in non-catalytic reactions. Kinetic analysis showed that the catalyst reduces HTO activation energy by 15.6%, substantially increasing reaction rates across the HTO temperature range. X-ray powder diffraction confirmed that the mixed-valence Fe²⁺/Fe³⁺ configuration in the magnetite structure facilitates electron transfer during oxidation, enabling more complete combustion at lower temperatures. These findings represent a novel approach to catalyst design, from general activity to temperature-specific activation for a more stable and efficient in situ combustion process. Full article

This study investigates TNM-type titanium aluminide alloys, representing the third generation of β-stabilized γ-TiAl heat-resistant materials. The aim of this work is to study the combustion characteristics and to produce compact materials via the free SHS compaction method from initial powder reagents taken in the following ratio (wt%): 51.85Ti–43Al–4Nb–1Mo–0.15B, as well as to determine the effect of high-temperature isothermal annealing at 1000 °C on the structure and properties of the obtained materials. Using free SHS compression (self-propagating high-temperature synthesis), we synthesized compact materials from a 51.85Ti–43Al–4Nb–1Mo–0.15B (wt%) powder blend. Key combustion parameters were optimized to maximize the synthesis temperature, employing a chemical ignition system. The as-fabricated materials exhibit a layered macrostructure with wavy interfaces, aligned parallel to material flow during compression. Post-synthesis isothermal annealing at 1000 °C for 3 h promoted further phase transformations, enhancing mechanical properties including microhardness (up to 7.4 GPa), Young’s modulus (up to 200 GPa) and elastic recovery (up to 31.8%). X-ray powder diffraction, SEM, and EDS analyses confirmed solid-state diffusion as the primary mechanism for element interaction during synthesis and annealing. The developed materials show promise as PVD targets for depositing heat-resistant coatings. Full article

The aim of this study was to synthesize, characterize, and investigate the biomedical effects of nanoscale cerium phosphate obtained via different synthesis techniques, as well as to evaluate the influence of various CePO₄ concentrations on cells involved in skin structure regeneration (human mesenchymal stem cells, keratinocytes, and fibroblasts) and establish their antioxidant properties. Methods and Results: Cerium(III) orthophosphate was obtained by precipitation with ammonium dihydrogen phosphate from a nitrate solution. By changing the initial concentrations of the solutions and the drying and annealing temperatures, the best conditions for obtaining nanosized phosphate powders were established. The structure of rhabdophane was obtained by X-ray diffraction analysis, and the particle sizes were measured by transmission electron microscopy. The particle sizes ranged from 2 to 10 nm in the transverse direction and 20 to 50 nm in the longitudinal direction. Studies on cell lines have shown a high level of safety, as well as the regenerative potential of CePO₄ nanoparticles, which have a stimulating effect on the proliferation of MSCs at concentrations of 10⁻² to 10⁻³ M for 48 h after application and stimulate the metabolism of human keratinocytes and fibroblasts at a wide range of concentrations (10⁻³ to 10⁻⁵ M). A dose-dependent antioxidant effect of small CePO₄ nanoparticles at a concentration of 10⁻² to 10⁻⁵ has been established, which is stronger than ascorbic acid. Conclusions: A method for obtaining cerium phosphate nanoparticles with beneficial biomedical effects was developed. The non-cytotoxicity and regenerative potential of CePO₄ were established at a wide range of concentrations on different cell lines that are involved in the healing of skin wounds, as were their antioxidant properties. Full article

Aluminum nitride (AlN) powder, a cornerstone material for advanced ceramics. This study examines the low-temperature formation of AlN crystals as well as their phase transformation by employing amorphous aluminum oxalate (AAO) as a novel precursor for carbothermal reduction, contrasting it with conventional aluminum hydroxide (Al(OH)₃). Through characterization using X-ray diffraction (XRD), scanning electron microscopy (SEM), High-Resolution Transmission Electron Microscope (HRTEM), ²⁷Al Magic-Angle Spinning Nuclear Magnetic Resonance (²⁷Al-MAS-NMR) energy-dispersive spectroscopy (EDS), and Fourier-transform infrared spectroscopy (FTIR), we unraveled the phase evolution pathways and the formation of AlN. Key findings reveal striking differences between the two precursors. When Al(OH)₃ was used, no AlN phase was detected at 1350 °C, and even at 1500 °C, the AlN obtained with significant residual alumina impurities. In contrast, the AAO precursor demonstrated exceptional efficiency: nano-sized α-Al₂O₃ formed at 1050 °C, followed by the emergence of AlN phases at 1200 °C, ultimately gaining the pure AlN at 1500 °C. The phase transformation sequence—Al(OH)₃ → γ-Al₂O₃ (950 °C) → (α-Al₂O₃ + δ-Al₂O₃) (1050 °C) → (AlN + α-Al₂O₃) (1200 °C~ 1350 °C) → AlN (≥1500 °C)—highlights the pivotal role of nano-sized α-Al₂O₃ in enabling low-temperature nano AlN synthesis. By leveraging the unique properties of AAO, we offer a transformative strategy for synthesizing nano-sized AlN powders, with profound implications for the ceramics industry. Full article

p-toluenesulfonic acid (pTSA) was used for the synthesis of porous silica xerogels while applying different synthesis conditions. Key parameters included acid concentration, drying temperature and the method of acid removal. The resulting organic–inorganic composites were investigated by nitrogen physisorption, X-ray powder diffraction (XRD), solid-state NMR and thermal analysis. The results demonstrated that both the drying temperature and quantity of the pTSA significantly influenced the pore structure of the xerogels. The utilization of such strong acids like pTSA yielded high surface area and pore volume, as well as narrow pore size distribution. Environmentally friendly template removal by solvent extraction produced materials with superior textural properties compared to traditional calcination, enabling the recovery and reuse of pTSA with over 95% efficiency. A selected mesoporous silica xerogel was modified by a simple two-step post-synthesis procedure with 1-(2-Hydroxyethyl) piperazine (HEP). High CO₂ adsorption capacity was determined for the HEP-modified material in dynamic conditions. The isosteric heat of adsorption revealed the stronger interaction between functional groups and CO₂ molecules. Total CO₂ desorption could be achieved at 60 °C. Leaching of the silica functional groups could not be detected even after four consecutive adsorption cycles. These findings provide valuable insights into the sustainable synthesis of tunable piperazine-modified mesoporous silica xerogels with potential applications in CO₂ capture. Full article

Against the backdrop of escalating global carbon emissions, the steel industry urgently requires a transition toward green and low-carbon practices. As a conditionally carbon-neutral renewable energy source, biochar holds potential for replacing traditional fossil-based reducing agents. This study aims to investigate the mechanism and performance differences between biochar (wood char, bamboo char) and conventional reducing agents (semi-coke, coke powder, anthracite) in the direct reduction process of carbon-bearing briquettes. Through reduction experiments simulating rotary kiln conditions, combined with analysis of reducing agent gasification characteristics, carbon-to-oxygen (C/O) molar ratio control, X-ray diffraction (XRD), and microstructural examination, the high-temperature behavior of different reducing agents was systematically evaluated. Results indicate that biochar exhibits superior gasification reactivity due to its high specific surface area and developed pore structure: wood char and bamboo char show significantly enhanced reaction rates above 1073 K, approaching complete conversion at 1173 K. In contrast, anthracite and coke powder, characterized by dense structures and low specific surface areas, failed to achieve complete gasification even at 1273 K. Pellets containing bamboo char achieved the highest metallization rate (90.16%) after calcination at 1373 K. The compressive strength of the pellets first decreased and then increased with rising temperature, consistent with the trend in metallization rate. The mechanism analysis indicates that the high reactivity and porous structure of biochar promote rapid CO diffusion and synergistic gas–solid reactions, significantly accelerating the reduction of iron oxides and the formation of metallic iron. Full article

This study addresses the development of advanced anode materials for lithium-ion batteries by investigating the high-entropy perovskite La(Co_0.2Mn_0.2Fe_0.2Ni_0.2Cu_0.2)O₃. The material was synthesized via spray drying of aqueous metal nitrate solutions, followed by calcination at various temperatures (800 °C/1 h, 1000 °C/1 h, 1000 °C/2 h, 1100 °C/1 h) to optimize structural properties. Structural analysis using X-ray diffraction confirmed the formation of a single-phase perovskite in the sample calcined at 1100 °C for 1 h, while SEM/EDS revealed homogeneous elemental distribution. Electrochemical testing of the powders as anode materials in coin-type lithium-ion cells revealed a trend of slightly increasing capacity over 150 cycles, with capacity ultimately reaching 617 mAh g⁻¹, indicating progressive electrochemical activation. Although the samples share the same composition, variations in calcination conditions resulted in differences in capacity and cycling behavior. These results demonstrate that synthesis parameters critically influence the electrochemical performance of high-entropy perovskites. The findings suggest that such materials have potential as stable anodes for next-generation lithium-ion batteries, contributing to improved durability and efficiency in energy-storage technologies. Full article

Boriding is widely used in various industries due to the unique combination of high mechanical, corrosion, and tribological properties of boride layers formed on the surface of steel components. In this work, the powder boriding of 40 Kh steel was investigated in a closed capsule using a specially prepared powder mixture containing boric acid as the boron source. Boriding was carried out in a furnace at 850, 900, and 950 °C for 10 h. The resulting boride layers were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD), which confirmed that all three coatings consist exclusively of the Fe₂B phase. It was found that with increasing temperature, the thickness of the boride layer increased from 68 μm to 160 μm. The tribological properties were evaluated using the pin-on-disk method, followed by analysis of the wear surfaces using optical profilometry and SEM. The most significant reduction in wear rate was observed at 850 °C, where the wear decreased by a factor of 4.2—from 8.471 × 10⁻⁵ to 1.999 × 10⁻⁵ mm³·N⁻¹·m⁻¹. In addition, the hardness increased fivefold compared to the untreated material. These results demonstrate the high potential of diffusion boriding for enhancing the operational performance of parts subjected to severe wear conditions. Full article

The surging demand for lithium-ion batteries (LIBs) has intensified the need for sustainable recovery of critical metals such as lithium, manganese, cobalt, and nickel from spent cathodes. While conventional hydrometallurgical and pyrometallurgical methods are widely used, they involve high energy consumption, hazardous waste generation, and complex processing steps, underscoring the urgency of developing eco-friendly alternatives. This study presents a novel, water-enhanced deep eutectic solvent (DES) system composed of choline chloride and D-glucose for the efficient leaching of valuable metals from spent LiMn-based battery cathodes. The DES was synthesized under mild conditions and applied to dissolve cathode powder, with leaching performance optimized by varying temperature and duration. Under optimal conditions (100 °C, 24 h), exceptional recovery efficiencies were achieved: 98.9% for lithium, 98.4% for manganese, and 71.7% for nickel. Material characterization using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and inductively coupled plasma mass spectrometer (ICP-MS) confirm effective phase dissolution and metal release. Although this DES system requires relatively higher temperature and longer reaction time compared to traditional acid leaching, it offers clear advantages in terms of non-toxicity, biodegradability, and elimination of strong oxidizing agents. These results demonstrate the potential of water-enhanced choline chloride–glucose DES as a green alternative for future development in sustainable battery recycling, supporting circular economy objectives. Full article

This work reports a low-cost, microwave-assisted wet chemistry synthesis of zinc antimonate (ZnSb₂O₆) powders with a trirutile structure, yielding highly homogeneous, nanometric particles. X-ray diffraction (XRD) confirmed the formation of the trirutile phase with lattice parameters of a = 4.664 Å and c = 9.263 Å, and an estimated crystallite size of 42 nm. UV–vis spectroscopy revealed a bandgap of 3.35 eV. Scanning electron microscopy (SEM) showed that ethylenediamine, as a chelating agent, formed porous microstructures of microrods and cuboids, ideal for enhanced gas adsorption. Brunauer–Emmett–Teller (BET) analysis revealed a specific surface area of 6 m²/g and a total pore volume of 0.0831 cm³/g, indicating a predominantly mesoporous structure. The gas sensing properties of ZnSb₂O₆ pellets were evaluated in CO and C₃H₈ atmospheres at 100, 200, and 300 °C. The material exhibited high sensitivity at 300 °C, where the maximum responses were 5.86 for CO at 300 ppm and 1.04 for C₃H₈ at 500 ppm. The enhanced sensitivity at elevated temperatures was corroborated by a corresponding decrease in electrical resistivity. Furthermore, the material demonstrated effective photocatalytic activity, achieving up to 60% degradation of methylene blue and 50% of malachite green after 300 min of UV irradiation, with the process following first-order reaction kinetics. These results highlight that ZnSb₂O₆ synthesized by this method is a promising bifunctional material for gas sensing and photocatalytic applications. Full article

The present study investigates post-emplacement zeolitization processes in two widespread pyroclastic units from Central Italy: the Cimina Ignimbrite and the Sorano Ignimbrite. A total of seventy-five samples from ten outcrops were analyzed using optical and environmental scanning electron microscopy, electron probe microanalysis, X-ray powder diffraction, and inductively coupled plasma optical emission spectrometry. Analytical results allow the mineral distribution, zeolite composition, textural relationships, and geochemical features of the zeolite-bearing rocks to be defined. In the Cimina Ignimbrite, zeolitization affects the glassy portion of the groundmass, where the glass transforms into a medium- to high-temperature mineral assemblage dominated by clinoptilolite-Ca and cristobalite. This transformation is restricted to the innermost parts of the deposit. In contrast, zeolitization in the Sorano Ignimbrite involves the entire glassy fraction of pumice clasts, with extensive alteration of the glass into medium- to low-temperature zeolites such as chabazite-K and phillipsite-K. The results reveal a significant correlation between the chemical composition of the juvenile material and that of the newly formed zeolites in both types of ignimbrites, particularly in the Sorano Ignimbrite. Zeolitization in Central Italy ignimbrites likely occurs in a natural autoclave-like setting, where hot fluids remain trapped in the deposit for a long time. Full article

With the increasing global demand for sustainable building materials, coal gangue, as a potential supplementary cementitious material (SCM), has attracted widespread attention. Coal gangue is primarily composed of clay minerals, among which the kaolinite content can significantly enhance its cementitious properties after activation. However, there are various grades of coal gangues, which restrain their application, especially for the low kaolinite content coal gangue. This paper investigates the feasibility of using iron-rich coal gangue with low kaolinite content as a cement substitute through high-temperature activation treatment. In the current study, activated coal gangue replaced cement clinker at proportions of 10%, 15%, and 20%, which was further mixed with limestone powder to form a new cementitious material system. The mechanical attributes of the systems were assessed using compressive strength and microhardness tests. The influence of hydration products and microstructural changes on system performance was further explored through electrochemical impedance spectroscopy (EIS) and quantitative X-ray diffraction (XRD) analysis. The findings suggest that a well-balanced addition of coal gangue can effectively substitute for cement clinker, thereby enhancing both the mechanical properties and microstructure of the systems. These results demonstrate that through appropriate activation treatments, coal gangue can be utilized as an effective SCM. While traditional SCMs like fly ash (FA) and ground granulated blast-furnace slag (GGBFS) have near-zero allocated carbon footprints, their global supply is diminishing and increasingly unreliable. In contrast, our approach valorizes a vast industrial waste stream, aligning with circular economy principles and offering a scalable, sustainable, and low-carbon alternative for the construction industry. Full article

Boron oxide is introduced into slag as a flux, significantly lowering the liquidus temperature; however, this advantage is accompanied by several undesirable consequences. This study aims to evaluate the impact of boron oxide addition on the wetting reactivity of the CaO-SiO₂-MgO-Al₂O₃-B₂O₃ slag system, particularly on platinum and graphite substrates, which are commonly utilized for wettability investigations of such systems. The slag system was modified to incorporate varying concentrations of B₂O₃, reaching up to 30 wt%, with the addition of this oxide at the expense of CaO and SiO₂ in a constant ratio, while the contents of Al₂O₃ and MgO remained unchanged. High-temperature wettability tests were conducted at temperatures up to 1550 °C under a flow of high-purity argon atmosphere (99.9999%). For the platinum substrate, the results indicated non-reactive wetting, characterized by a decrease in wetting angles with increasing temperature and boron oxide content. Conversely, for the graphite substrate, the nature of wetting varied, resulting in either reactive or non-reactive behavior depending on the B₂O₃ content. Following the high-temperature experiments, additional analyses were performed using scanning electron microscopy (SEM) and energy-dispersive spectrometry (EDS). Furthermore, the powdered oxide systems underwent characterization through Fourier transform infrared spectroscopy (FTIR) and X-ray powder diffraction (XRPD). Full article

Porous CaCO₃ vaterite particles have been widely used as drug carriers for biomedical applications due to their high biocompatibility and low production costs. However, controlling the particle size and porosity of CaCO₃ nanoparticles with the desired crystalline phase is still challenging. In this study, we have systematically investigated the preparation of CaCO₃ nanoparticles under various conditions including precursor types/ratios/concentrations, additive concentrations (ethylene glycol), and temperatures. The materials were fully characterized by optical microscopy, scanning and transmission electron microscopy, infrared spectroscopy, powder X-ray diffraction, dynamic laser scattering, thermogravimetric analysis, and gas sorption. The impacts of the reaction parameters were rationalized and the mechanism for the formation of porous vaterite particles was suggested. It was possible to produce porous vaterite nanoparticles (200 nm) under the optimized conditions, which were further used as drug carrier to upload a model drug curcumin. The potential of using these vaterite particles for controlled drug release was demonstrated. Full article