Search Results (1,771)

This study aimed to develop an industrially scalable coating route for enhancing the oxidation resistance of carbon fiber fabrics, a critical requirement for next-generation aerospace and high-temperature composite structures. To achieve this goal, synthesis of hexagonal boron nitride (h-BN) layers was achieved via a single wet step in which the fabric was impregnated with an ammonia–borane/THF solution and subsequently nitrided for 2 h at 1000–1500 °C in flowing nitrogen. Thermogravimetric analysis coupled with X-ray diffraction revealed that amorphous BN formed below ≈1200 °C and crystallized completely into (002)-textured h-BN (with lattice parameters a ≈ 2.50 Å and c ≈ 6.7 Å) once the dwell temperature reached ≥1300 °C. Complementary XPS, FTIR and Raman spectroscopy confirmed a near-stoichiometric B:N ≈ 1:1 composition and the elimination of O–H/N–H residues as crystallinity improved. Low-magnification SEM (100×) confirmed the uniform and large-area coverage of the BN layer on the carbon fiber tows, while high-magnification SEM revealed a progressive densification of the coating from discrete nanospheres to a continuous nanosheet barrier on the fibers. Oxidation tests in flowing air shifted the onset of mass loss from 685 °C for uncoated fibers to 828 °C for the coating produced at 1400 °C; concurrently, the peak oxidation rate moved ≈200 °C higher and declined by ~40%. Treatment at 1500 °C conferred no additional benefit, indicating that 1400 °C provides the optimal balance between full crystallinity and limited grain coarsening. The resulting dense h-BN film, aided by an in situ self-healing B₂O₃ glaze above ~800 °C, delayed carbon fiber oxidation by ≈140 °C. Overall, the process offers a cost-effective, large-area alternative to vapor-phase deposition techniques, positioning BN-coated carbon fiber fabrics for robust service in extreme oxidative environments. Full article

To evaluate the effect of nitrogen and hydrogen on the corrosion resistance of diamond-like carbon (DLC) coatings, potentiodynamic tests were carried out on DLC coatings deposited under various reactive atmosphere compositions on martensitically hardened 34CrAlNi steel. In order to replicate actual operating conditions of steel components, the tests were conducted both in a reference 3.5% NaCl solution and in natural mine waters, which are in direct contact with mining gearbox mechanisms. Although it is generally assumed that the addition of other elements tends to deteriorate the corrosion resistance of amorphous carbon coatings, such doping simultaneously improves adhesion to metallic substrates, and enhanced adhesion in turn contributes to improved corrosion resistance. Variation in the proportions of the doping elements altered the damage morphology on the sample surface, as well as the corrosion current density, corrosion potential, and polarization resistance. Improvements in corrosion resistance parameters correlated with the quality of the coating–substrate adhesion, evaluated in accordance with the VDI3918 standard. The most favorable properties were obtained for coatings deposited under a gas composition of N₂:CH₄:H₂ with a ratio of 3:4:2. Full article

Serpentinite rocks and their processing waste represent a valuable source of magnesium and silicon; however, their complex composition complicates the efficient recovery of individual components. This study investigates the combined acid–alkali processing of serpentinite waste from the Zhitikara deposit (Kazakhstan). In the acid leaching stage, sulfuric acid enables magnesium extraction, while subsequent treatment with sodium hydroxide (NaOH) facilitates the selective recovery of silica gel formed during acid attack. At the final neutralization step, amorphous silica is precipitated with a yield exceeding 60% of its initial content. The obtained silica was characterized using FTIR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), inductively coupled plasma mass spectrometry (ICP-MS, Thermo iCAP-Q), and nitrogen adsorption measurements via the BET method. It was established that the synthesized silica gel, according to the IUPAC classification, belongs to mesoporous materials, possesses a well-developed specific surface area (400 m²·g⁻¹), and is suitable for adsorption and catalytic applications. Full article

Alkali resistance is a critical factor for the long-term performance of glass fibers in cementitious composites. While zirconium oxide doping has proven effective in enhancing the durability of basalt fibers, its high cost and limited solubility motivate the search for viable alternatives. This study presents the first systematic investigation of titanium dioxide (TiO₂) doping in basalt-based glasses across a wide compositional range (0–8 mol%). X-ray fluorescence and diffraction analyses confirm complete dissolution of TiO₂ within the amorphous silicate network, with no phase segregation. At low concentrations (≤3 mol%), Ti⁴⁺ acts as a network modifier in octahedral coordination ([TiO₆]), reducing melt viscosity and lowering processing temperatures. As TiO₂ content increases, titanium in-corporates into tetrahedral sites ([TiO₄]), competing with Fe³⁺ for network-forming positions and displacing it into octahedral coordination, as revealed by Mössbauer spectroscopy. This structural redistribution promotes phase separation and triggers the crystallization of pseudobrukite (Fe₂TiO₅) at elevated temperatures. The formation of a protective Ti(OH)₄ surface layer upon alkali exposure enhances chemical resistance, with optimal performance observed at 4.6 mol% TiO₂—reducing mass loss in NaOH and seawater by 13.3% and 25%, respectively, and improving residual tensile strength. However, higher TiO₂ concentrations (≥5 mol%) lead to pseudobrukite crystallization and a narrowed fiber-forming temperature window, rendering continuous fiber drawing unfeasible. The results demonstrate that TiO₂ is a promising, cost-effective dopant for basalt fibers, but its benefits are constrained by a critical solubility threshold and structural trade-offs between durability and processability. Full article

Magnesium alloy represents a typical category of biodegradable medical materials. However, the poor corrosion resistance and rapid degradation have significantly hindered the clinical adoption of magnesium alloy implants. This paper puts forward a method to improve the corrosion resistance of magnesium alloy by using an Fe-based composite coating. The microstructure and composition of the coating were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive spectroscopy (EDS). The corrosion resistance was evaluated through potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) measurements conducted in simulated body fluid, while the degradation behavior of the samples was evaluated by examining the hydrogen evolution volume and corrosion morphology during immersion tests. The results indicate that the composite coating exhibits a dual-layer structure, consisting of an amorphous carbon–fluorine transition layer and an iron-rich surface layer. After coating treatment, the corrosion current density of magnesium alloy decreased from 1.38 × 10⁻⁴ to 3.41 × 10⁻⁶ A/cm². Throughout a 28-day immersion period, the composite-coated sample demonstrated a remarkably low hydrogen evolution rate and maintained a smooth, intact surface. Furthermore, hemolysis and platelet adhesion tests confirmed the outstanding blood compatibility of the composite-coated magnesium alloy, showing an ultralow hemolysis rate of 0.1% and minimal platelet adhesion with well-preserved morphology. Full article

In situ high-temperature Raman spectroscopy (up to 550 °C) and infrared spectroscopy (up to 700 °C) were employed to analyze hydrous Fe-rich ringwoodite (Fo76 composition containing 0.69 wt% H₂O). The results demonstrate that the hydrous Fe-rich ringwoodite sample undergoes irreversible structural transformation above 300 °C at ambient pressure, converting to an amorphous phase. This indicates a lower thermal stability threshold compared to Fe-bearing ringwoodite (Fo90) with equivalent water content. Notably, identical infrared spectral evolution patterns were observed during heating (25–500 °C) for the studied Fo76 sample and previously reported Fo82/Fo90 specimens, suggesting minimal influence of iron content variation on hydroxyl group behavior. The material derived from Fe-rich ringwoodite through structural transformation at ~350 °C retains the capacity to preserve water within a defined temperature window (400–550 °C). In situ high-pressure Raman spectroscopy experiments conducted up to 20 GPa detected no notable structural modifications, suggesting that hydrous Fe-rich ringwoodite, hydrous Fe-bearing ringwoodite, and hydrous Mg-endmember ringwoodite exhibit comparable structural stability within this pressure range. 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

Hydrogen energy offers high energy density and carbon-free combustion, making it a promising fuel for next-generation propulsion and power generation systems. Hydrogen offers approximately three times more energy per unit mass than natural gas, and its combustion yields only water as a byproduct, making it an exceptionally clean and efficient energy source. Materials used in hydrogen-fueled combustion engines must exhibit high thermal stability as well as resistance to corrosion caused by high-temperature water vapor. This study introduces a novel ceramic matrix composite (CMC) designed for such harsh environments. The composite is made of yttria-stabilized zirconia (YSZ) fiber-reinforced silicoboron carbonitride [Si(B)CN]. CMCs were fabricated via the polymer infiltration and pyrolysis (PIP) method. Multiple PIP cycles, which help to reduce the porosity of the composite and enhance its properties, were utilized for CMC fabrication. The Si(B)CN precursor formed an amorphous ceramic matrix, where the presence of boron effectively suppressed crystallization and enhanced oxidation resistance, offering superior performance than their counter part. Thermogravimetric analysis (TGA) confirmed negligible mass loss (≤3%) after 30 min at 1350 °C. The real-time ablation performance of the CMC sample was assessed using a hydrogen torch test. The material withstood a constant heat flux of 185 W/cm² for 10 min, resulting in a front-surface temperature of ~1400 °C and a rear-surface temperature near 700 °C. No delamination, burn-through, or erosion was observed. A temperature gradient of more than 700 °C between the front and back surfaces confirmed the material’s effective thermal insulation performance during the hydrogen torch test. Post-hydrogen torch test X-ray diffraction indicated enhanced crystallinity, suggesting a synergistic effect of the oxidation-resistant amorphous Si(B)CN matrix and the thermally stable crystalline YSZ fibers. These results highlight the potential of YSZ/Si(B)CN composites as high-performance materials for hydrogen combustion environments and aerospace thermal protection systems. Full article

Harnessing solar energy is crucial for applications such as water desalination through solar collectors, where efficient conversion of solar radiation into thermal energy is required. In this study, electroless nickel–phosphorus (Ni-P) coatings and their carbon black (CB) nanoparticle composites were successfully deposited and evaluated as selective solar absorbers. The coatings exhibited compact, crack-free, and amorphous structures composed mainly of Ni(OH)₂ and NiOOH, as confirmed by SEM-EDS, XRD, FTIR, and Raman analyses. Increasing the pH enhanced the deposition rate and coating thickness while reducing the phosphorus content. Incorporation of CB nanoparticles was confirmed, though it slightly decreased coating thickness. Optical characterization revealed high absorptance and low emissivity across all samples, with the Ni-P coating produced at higher pH (C1) achieving the best performance (brightness L* = 29.0; figure of merit α − ε = 0.84). Aging tests further demonstrated the resilience of this sample, maintaining a figure of merit of 0.81. These findings establish Ni-P coatings, particularly at higher pH, as promising and safer alternatives to conventional chromium-based solar selective coatings. Full article

The removal of nickel from industrial wastewater necessitates efficient sorbent materials. This study investigates nanostructured potassium- and sodium-substituted aluminosilicate-based nanocomposites for this application. Materials were synthesized and characterized using SEM-EDS, XPS, XRD, FTIR, low temperature N₂ adsorption–desorption and Ni²⁺ adsorption experiments. SEM and XRD confirmed an X-ray amorphous structure attributable to fine crystallite size. The sodium-substituted material Na₂Al₂Si₂O₈ exhibited the lowest specific surface area (48.3 m²/g) among the tested composites. However, it demonstrated the highest Ni(II) sorption capacity (64.6 mg/g, 1.1 mmol/g) and the most favorable sorption kinetics, as indicated by a Morris-Weber coefficient of 0.067 ± 0.008 mmol/(g·min¹/²). Potassium-substituted analogs with higher Si/Al ratios showed increased surface area but reduced capacity. Analysis by XPS and SEM-EDS established that Ni(II) uptake occurs through a complex mechanism, involving ion exchange, surface complexation, and chemisorption resulting in the formation of new nickel-containing composite surface phases. The results indicate that optimal sorption performance for Ni(II) is achieved with sodium-based aluminosilicates at a low Si/Al ratio (Si/Al = 1). The functional characteristics of Na₂Al₂Si₂O₈ compare favorably with other silicate-based sorbents, suggesting its potential utility for wastewater treatment. Further investigation is needed to elucidate the precise local coordination environment of the adsorbed nickel. Full article

This research is to assess the potential use of phosphate sludge from the Gafsa (Tunisia) phosphate laundries as an alternative raw material for the manufacture of ecological refractory bricks. Feasibility was evaluated through comprehensive physico-chemical and mineralogical characterizations of the raw materials using X-ray diffraction (XRD), X-ray fluorescence (XRF), Fourier-transform infrared spectroscopy (FTIR), and thermal analysis (TGA-DTA). Bricks were formulated by substituting phosphate sludge with clay and diatomite, then activated with potassium silicate solution to produce geopolymeric materials. Specific formulations exhibited mechanical performance ranging from 7 MPa to 26 MPa, highlighting the importance of composition and minimal water absorption values of approximately 17.8% and 7.7%. The thermal conductivity of the bricks was found to be dependent on the proportions of diatomite and clay, reflecting their insulating potential. XRD analysis indicated the formation of an amorphous aluminosilicate matrix, while FTIR spectra confirmed the development of new chemical bonds characteristic of geopolymerization. Thermal analysis revealed good stability of the materials, with mass losses mainly related to dehydration and dehydroxylation processes. Environmental assessments showed that most samples are inert or non-hazardous, though attention is required for those with elevated chromium content. Overall, these findings highlight the viability of incorporating phosphate sludge into fired brick production, offering a sustainable solution for waste valorization in accordance with the circular economy. Full article

In this study, high-conductivity W-doped Ga₂O₃ thin films were successfully fabricated by directly depositing a composition of Ga₂O₃ with 10.7 at% WO₃ (W:Ga = 12:100) using electron beam evaporation. The resulting thin films were found to be amorphous. Due to the ohmic contact behavior observed between the W-doped Ga₂O₃ film and platinum (Pt), Pt was used as the contact electrode. Current-voltage (J-V) measurements of the W-doped Ga₂O₃ thin films demonstrated that the samples exhibited significant current density even without any post-deposition annealing treatment. To further validate the excellent charge transport characteristics, Hall effect measurements were conducted. Compared to undoped Ga₂O₃ thin films, which showed non-conductive characteristics, the W-doped thin films showed an increased carrier concentration and enhanced electron mobility, along with a substantial decrease in resistivity. The measured Hall coefficient of the W-doped Ga₂O₃ thin films was negative, indicating that these thin films were n-type semiconductors. Energy-Dispersive X-ray Spectroscopy was employed to verify the elemental ratios of Ga, O, and W in the W-doped Ga₂O₃ thin films, while X-ray photoelectron spectroscopy analysis further confirmed these ratios and demonstrated their variation with the depth of the deposited thin films. Furthermore, the W-doped Ga₂O₃ thin films were deposited onto both p-type and heavily doped p⁺-type silicon (Si) substrates to fabricate heterojunction diodes. All resulting devices exhibited good rectifying behavior, highlighting the promising potential of W-doped Ga₂O₃ thin films for use in rectifying electronic components. Full article

Novel multifunctional fibrous materials were prepared by simultaneous dual spinneret electrospinning of two separate solutions differing in composition. This technique allowed for the preparation of materials built of two types of fibers: fibers from poly(vinyl alcohol) (PVA), chitosan (Ch), and rosmarinic acid (RA), and poly(L-lactide) (PLA) fibers containing lidocaine hydrochloride (LHC). Confocal laser scanning microscopy (CLSM) analyses showed that both types of fibers are present on the surface and in the bulk of the new materials. The presence of all components and some interactions between them were proven by attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. RA and LHC were in an amorphous state in the fibers, and their presence affected the temperature characteristics and the crystallinity, as detected by differential scanning calorimetry (DSC) and X-ray diffraction analyses (XRD). The presence of PVA/Ch/RA fibers enabled the hydrophilization of the surface of the multifunctional fibrous materials (the water contact angle value was 0°). The newly developed materials demonstrated adequate mechanical properties, making them suitable for use in wound dressing applications. The RA-containing fibrous mats possessed high radical-scavenging activity (ca. 93%), and the combining with LHC led to an enhancement of this effect (ca. 98.5%). RA-containing fibrous mats killed all the pathogenic bacteria S. aureus and E. coli and decreased the titer of fungi C. albicans by ca. 0.4 log for a contact time of 24 h. Therefore, the new materials are prospective as antibacterial and atraumatic functional wound dressings, as systems for local drug delivery, and in medical skincare. Full article

The potential for creating composite cements by incorporating fly ash is demonstrated. Analysis revealed that the fly ash examined consists of 69.66 wt. % silicon oxide, 21.34 wt. % aluminum oxide, 1.57 wt. % calcium oxide and 2.78 wt. % iron oxide. Fly ash mainly consists of quartz (SiO₂), goethite (FeO(OH)) and mullite (3Al₂O₃·2SiO₂). The properties of the cement composition containing 5 to 25 wt. % fly ash were studied. Incorporating fly ash enhances system dispersion, promotes mixture uniformity, and stimulates the pozzolanic reaction. Compositions of composite cements consisting of 90% CEM I 42.5 and 10% fly ash were developed. The cement stone based on the obtained composite cement had a compacted structure with a density of 2.160 g/cm³, which is 9.4% higher than the control sample. It is shown that when composite cement containing 10% fly ash interacts with water, hydration reactions of cement minerals (C₃S, C₂S, C₃A and C₄AF) begin first. This is accompanied by the formation of hydrate neoplasms, such as calcium hydroxide (Ca(OH)₂) and calcium hydrosilicates (C-S-H). Fly ash particles containing amorphous silica progressively participate in a pozzolanic reaction with Ca(OH)₂, leading to the formation of additional calcium hydrosilicates phases. This process enhances structural densification and reduces the porosity of the cement matrix. After 28 days of curing, the compressive strength of the resulting composite cements ranged from 42.1 to 54.2 MPa, aligning with the strength classes 32.5 and 42.5 as specified by GOST 31108-2020. Full article

This study demonstrates the successful preparation of pristine and modified PVC polymer films with (0.7, 1.0, 2.0, and 3.0 wt%) Cr_1.4Ca_0.6O₄ by the solution casting method. These films were characterized using XRD, FTIR, XPS, SEM, TGA, and a UV–vis spectrophotometer. The XRD confirmed the amorphous nature of PVC films and a tetragonal zircon-type structure of Cr_1.4Ca_0.6O₄ as a dopant in the PVC polymer. The XPS survey spectra of pristine Cr_1.4Ca_0.6O₄ and its composites with PVC reveal essential insights into the materials’ surface composition and chemical states. The spectra clearly show peaks corresponding to O1s, Ca2p, and Cr2p, with the Cr2p signals being notably weaker than the other peaks. SEM images showed a uniform distribution of Cr_1.4Ca_0.6O₄ within the PVC polymer films despite the presence of some minor agglomerations. The TGA analysis revealed that incorporating Cr_1.4Ca_0.6O₄ enhanced the thermal stability of PVC films, particularly at a 0.7 wt% concentration of Cr_1.4Ca_0.6O₄. Moreover, incorporation of Cr_1.4Ca_0.6O₄ improved the optical parameters of PVC films, i.e., linear refractive index, nonlinear refractive index, and optical susceptibility. These findings proposed the modified PVC with Cr_1.4Ca_0.6O₄ for optoelectronic applications. Full article