Search Results (3,068)

This study investigates the use of mussel shells (MSs), a biogenic by-product of the food industry, as a partial replacement for ground granulated blast furnace slag (GBFS) in alkali-activated mortars. Given their high CaCO₃ content, MSs represent a sustainable secondary raw material that reduces both waste disposal burden and reliance on natural resources, while offering a low-carbon alternative to conventional cement-based binders. Alkali-activated mussel shell/slag mortars (AAMSs) were produced with MS replacement ratios of 0%, 5%, 10%, 15%, and 20% by mass of GBFS. Sodium hydroxide (NaOH) and sodium silicate (Na₂SiO₃) were used as alkaline activators. Fresh specimens were cured at 60 °C for 48 h. The experimental program included workability, compressive and flexural strength, water absorption, porosity, density, capillarity, ultrasonic pulse velocity (UPV), and freeze–thaw (F-T) resistance tests. Increasing MS content slightly reduced flowability and mechanical strength, while increasing water absorption, porosity, and capillarity. The M0 series achieved the highest 28-day compressive strength (54.06 MPa), while M15 exhibited the highest flexural strength (5.23 MPa). Following F-T cycling, the 5% and 10% MS series demonstrated the best compressive strength (30 MPa). The 10% MS exhibits a relatively balanced overall performance, providing the best balance between mechanical performance, F-T resistance, and microstructural stability, as confirmed by scanning electron microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDS) analyses showing elevated Ca/Si ratios and the formation of Ca-rich crystalline phases. Full article

Al-Cu-Fe quasicrystalline coatings were deposited on AISI 321 stainless steel substrates by high-velocity oxy-fuel (HVOF) spraying at oxygen pressures of 3.0, 3.5, and 4.0 bar. The influence of oxygen pressure on the phase composition, microstructure, porosity, corrosion behavior, thermal stability, and microhardness of the coatings was investigated using X-ray diffraction (XRD), scanning electron microscopy coupled with energy-dispersive spectroscopy (SEM/EDS), ImageJ porosity analysis, electrochemical corrosion testing in 3.5 wt.% NaCl solution, simultaneous thermal analysis (TGA/DSC), and microhardness measurements. XRD analysis revealed the formation of quasicrystalline-related intermetallic phases together with Al, Fe₃Al₁₃, FeAl, Fe₃O₄, CuFe₂O₄, Cu₂O, and CuO phases. The coating deposited at 3.5 bar exhibited the lowest porosity (5.37%), the most homogeneous microstructure, and the largest residual coating thickness after corrosion testing. SEM and EDS analyses indicated that corrosion preferentially initiated at pores, splat boundaries, and phase interfaces, while the coating produced at 3.5 bar demonstrated the most stable surface condition after exposure to a 3.5 wt.% NaCl solution. Thermal analysis showed that all coatings remained stable up to 900 °C. Sample (a) exhibited the lowest mass loss and the highest thermal stability, whereas sample (b) demonstrated the most favorable combination of structural integrity, phase ordering, coating density, corrosion-related performance, and thermal stability. Microhardness values of the coatings ranged from 754 to 778 HV, significantly exceeding that of the AISI 321 substrate. The results demonstrate that oxygen pressure is a critical parameter controlling the microstructure and functional properties of HVOF-sprayed Al-Cu-Fe coatings, with 3.5 bar providing the most balanced set of properties. Full article

In this study, we report the results of the structural characterization and electrochemical evaluation of novel cobalt-free layered Ruddlesden–Popper (RP) oxides, La₂SrFe₂O_7−δ and La₂SrFe_1.8Ga_0.2O_7−δ, as electrode materials for intermediate-temperature solid oxide cells. X-ray diffraction confirmed the formation of RP phases and phase stability after reducing treatment. The materials showed compatible thermal expansion behavior, with slightly lower thermal expansion coefficients for the Ga-doped composition. Oxygen pressure relaxation measurements demonstrated that the oxygen surface exchange coefficient increases with temperature and pO₂, while Ga substitution slightly reduces the O₂/oxide exchange rate, which may be associated with a lower concentration of oxygen vacancies. The electrical conductivity in air was higher for La₂SrFe₂O_7−δ than for the Ga-doped sample, while both compositions showed much lower conductivity under reducing conditions. Symmetrical cell impedance spectroscopy showed high polarization resistance for the electrodes, which was substantially reduced by applying a Ag current collector (0.43 Ω cm² for La₂SrFe₂O_7−δ and 0.73 Ω cm² for La₂SrFe_1.8Ga_0.2O_7−δ at 800 °C), consistent with the limited electronic conductivity of the oxide layers. Overall, both oxides exhibit structural stability, acceptable thermomechanical compatibility, and measurable oxygen exchange activity, making them promising candidates for further development as cobalt-free electrodes in solid oxide cells. Full article

Quaternary β-Ti-xTa-xZr-xNb (TTZN) alloys (x = 10, 20, and 30 wt%) were surface-modified by plasma electrolytic oxidation (PEO) to improve their surface properties. This treatment promotes the incorporation of bioactive ions, such as Ca and P, and favors the formation of a porous anodic surface resulting from the oxidation of the precursor metals. This study investigated how the addition of alloying elements (Zr, Ta, and Nb) influences oxide formation, PEO-induced pore morphology, wettability, and coating hardness. The surfaces were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS), Vickers microhardness testing, and wettability analysis. XRD analysis revealed that the TTZN10 alloy exhibited crystalline TiO₂ phases in the form of anatase and rutile. In contrast, the TTZN20 and TTZN30 alloys exhibited only cubic ZrO₂ diffraction peaks, while no TiO₂ peaks were detected within the detection limits of the XRD technique. Micrographs showed micrometric pores on all alloy surfaces. The TTZN20 alloy exhibited the highest porosity (31.8%), which correlated with lower hydrophilicity (θ = 79°) and high surface free energy (67 mJ/m²). After PEO treatment, all surfaces exhibited high hardness values ranging from 491 to 561 HV. The highest hardness was observed for TTZN10, attributed to the mixed anatase/rutile TiO₂ phase composition. Full article

Magnesium ammonium phosphate cement (MAPC) exhibits rapid setting, high early strength, and potential resistance to elevated temperatures, making it a promising material for rapid repair and fire-resistant applications. Gold tailings (GT), which contain thermally stable Si- and Al-rich components, show potential for improving the high-temperature performance of MAPC. However, the mechanisms by which GT affects the residual performance and phase evolution of MAPC after exposure to elevated temperatures remain insufficiently understood. In this study, GT was used to replace the total binder in MAPC mortar at mass replacement levels of 0%, 10%, 20%, and 30%, while the MgO/NH₄H₂PO₄ mass ratio in the remaining binder was kept constant. The effects of GT content on the workability of MAPC mortar, as well as its visual appearance, mechanical properties, mass loss rate, phase evolution, and microstructure after exposure to elevated temperatures, were investigated. The results showed that GT incorporation shortened the setting time and reduced the fluidity and room-temperature strength. After exposure to elevated temperatures, the GT-containing specimens exhibited higher strength retention and lower mass loss rates. After exposure to 1000 °C, the compressive strength of the specimen containing 30% GT reached 15.37 MPa, which was approximately 44.0% higher than that of the specimen without GT. Its flexural strength retention and mass loss rate were 47.42% and 9.84%, respectively. XRD and SEM results indicated that the formation of high-temperature residual phases, including Mg₃(PO₄)₂, Mg₂SiO₄, and aluminosilicates, may contribute to the improvement of the residual matrix structure after exposure to elevated temperatures. Overall, GT incorporation improved the residual mechanical properties of MAPC after exposure to elevated temperatures, and the specimen containing 30% GT showed comparatively superior performance within the experimental scope of this study. These findings provide a reference for the resource utilization of GT in MAPC-based heat-resistant repair materials. Full article

In this study, hexagonal titanium dioxide nanotubes (hTNTs) fabricated by sonoelectrochemical anodization were thermally modified in air to investigate the influence of annealing temperature and heating/cooling rate on phase evolution, structural stability and electrochemical behavior. The samples were annealed at 450 °C, 550 °C, and 650 °C for 2 h using heating/cooling rates of 6 °C/min, 10 °C/min, and 20 °C/min. The hexagonal nanotubular morphology remained preserved after thermal treatment. However, increasing annealing temperature and heating/cooling rate promoted crack formation due to the thermally induced stress relaxation and phase transformation. The anatase content increased with increasing heating/cooling rate, indicating kinetically limited anatase-to-rutile transformation, whereas annealing at 650 °C promoted partial rutile formation. Electrochemical studies demonstrated that annealing temperature and heating/cooling rate affected the electrochemical behavior of hTNTs through different mechanisms. Increasing annealing temperature promoted structural ordering and partial anatase-to-rutile transformation, leading to reduced current response and enhanced electrochemical stability. In contrast, heating/cooling rate significantly affected impedance behavior and diffusion-related processes, indicating changes in charge transfer kinetics and ion transport within the nanotubular oxide layer. The results demonstrate that thermal treatment kinetics play an important role in controlling the phase composition and electrochemical behavior of hTNTs, providing insight into the thermal optimization of hexagonal TiO₂ nanotubes for advanced functional applications. Full article

Lead-free [(Ba_0.85Ca_0.15)_1−1.5xNd_x][(Zr_0.1Ti_0.9)_0.995Mn_0.005]O₃ (x mol% Nd/Mn BCZT, x = 0.05, 0.1, 0.5, 1 mol%) ceramics were prepared by the traditional solid-state reaction method, in which the synergistic effects of sintering temperature and Nd/Mn co-doping on the phase structure, microstructural evolution, and electrical properties were systematically investigated. All ceramics exhibit a pure perovskite structure, with the tetragonal (P4mm) phase dominating at room temperature as confirmed by the X-ray diffraction Rietveld refinement. The sintering temperature (1475–1520 °C) is found to be the primary factor governing densification and grain growth, with the relative density peaking at 91.7% for the x = 0.5 mol% sample sintered at 1505 °C. Within this optimized processing window, increasing the Nd content induces a gradual migration of the Curie temperature (T_C) toward lower temperatures, accompanied by enhanced relaxor behavior. A highlight of this work is the strategic balance between piezoelectric activity and mechanical quality factor through a “donor–acceptor” co-doping mechanism. Specifically, for the x = 0.5 mol% ceramics, an exceptionally high mechanical quality factor (Q_m = 424.5) is achieved for samples sintered at 1490 °C, which is proposed to be associated with the temperature-modulated formation of ${Mn}_{Ti}^{″}-V_O^{••}$ defect dipoles, while a peak inverse piezoelectric coefficient $d_{33}^{*}$ of 685.1 pm/V is maintained at a sintering temperature of 1520 °C. Full article

TiO₂-based heterostructures have attracted considerable attention in photocatalytic pollutant degradation owing to their enhanced photoresponse and improved charge separation. The phase structure of TiO₂ strongly affects its band structure and interfacial charge-transfer behavior, making phase structure control critical for optimizing photocatalytic performance. However, due to the small difference in free energy among TiO₂ phase structure and the strong dependence of TiO₂ nucleation and growth on the local reaction environment, it remains challenging to precisely control the phase structure of TiO₂ in the TiO₂-based heterostructure nanomaterials. Herein, we achieved the phase engineering of TiO₂/MXene heterostructure nanomaterials through a solvent-regulation strategy. Specifically, by regulating the acetonitrile/water ratio in the hydrothermal solvent, TiO₂ with distinct phase structures was in situ grown on hydrothermally treated MXene nanosheets, resulting in two representative TiO₂/MXene heterostructure nanosheets: anatase TiO₂/MXene and rutile TiO₂/MXene. Acetonitrile likely acted as a surface-adsorbing agent during TiO₂ formation, stabilizing the anatase phase and promoting the preferential formation of anatase TiO₂. Benefiting from the optimized heterostructure, TiO₂/MXene heterostructure nanosheets promoted the generation of singlet oxygen (¹O₂), leading to enhanced photocatalytic degradation. Full article

Ti–6Al–4V is the primary titanium alloy for aerospace, biomedical, and additive manufacturing applications; however, the high cost of powders produced by atomization limits their widespread adoption. This study aims to develop a cost-effective method for producing chemically homogeneous pre-alloyed Ti–6Al–4V powders from titanium sponge. A combined process is proposed, involving the hydrogenation of titanium sponge, mechanical alloying of the hydride phase with Al and V powders, and subsequent vacuum dehydrogenation. The formation of the brittle δ-TiH₂ phase facilitated intensive material comminution and effective distribution of the alloying elements. According to laser diffraction data, the median particle size decreased from 450 to 30–35 µm. X-ray diffraction (XRD) analysis confirmed the sequential α-Ti → δ-TiH₂ transition and the formation of a stable α + β two-phase structure characteristic of Ti–6Al–4V following dehydrogenation. SEM observations demonstrated that the final powders predominantly consist of individual fractured particles with limited hard agglomeration, favorable for powder flowability and compaction behavior. EDS analysis indicated a relatively homogeneous microscale distribution of Al and V without observable large-scale segregation. The synthesized powders exhibited low impurity levels, with O < 0.07 wt.% and H < 0.02 wt.%. The developed approach represents a promising and economical alternative to expensive atomization techniques for powder metallurgy and additive manufacturing. Full article

Copper and its alloys are widely used in electrical, automotive, aerospace, and energy applications because of their excellent thermal and electrical conductivity. However, the low hardness and poor wear resistance of pure Cu limit its use under tribologically demanding sliding conditions. In this study, Cu matrix composites reinforced with 1 wt.% boron carbide (B₄C), boron (B), chromium (Cr), cobalt (Co), alumina (Al₂O₃), and graphite (Gr) were fabricated by powder metallurgy and comparatively evaluated under identical processing and testing conditions. Phase constitution and microstructural characteristics were analyzed by XRD, SEM, and EDS, while mechanical and tribological behavior was assessed by Vickers hardness and dry sliding wear tests. All reinforcements improved the hardness of the Cu matrix compared with unreinforced Cu. The hardness increase followed the order Cu–B₄C (68.91%) > Cu–B (66.43%) > Cu–Gr (63.97%) > Cu–Al₂O₃ (61.79%) > Cu–Cr (42.69%) > Cu–Co (36.04%). Dry sliding wear tests, performed under a 10 N normal load, 0.05 m s⁻¹ sliding speed, and 1000 m sliding distance against a 316L stainless-steel ball, showed that all reinforced composites exhibited lower mass loss and more stable sliding behavior than pure Cu. Among all samples, Cu–B₄C displayed the best wear performance, with a 154.8% improvement in wear resistance relative to pure Cu. SEM analysis of the worn surfaces revealed that reinforcement addition reduced severe plastic deformation, groove formation, and delamination, leading to a more stable wear regime. Graphite- and boron-containing composites benefited from interfacial lubrication and contact stabilization, whereas B₄C and Al₂O₃ improved wear resistance through rigid-particle strengthening and enhanced load-bearing capacity. By comparing ceramic, metalloid, metallic, oxide, and solid-lubricating reinforcements at the same low addition level and under identical processing and testing conditions, this study provides a reinforcement-selection framework for Cu-based composites requiring improved hardness and dry-sliding durability. Full article

M-type hexaferrites are widely used in magnetic applications, and tailoring their properties via aliovalent substitution requires a detailed understanding of charge compensation and cation distribution. In this work, Mg²⁺/M⁴⁺ (M = Zr, Hf) co-substituted BaFe₁₂O₁₉ was synthesized via Na₂CO₃ flux and comprehensively characterized by wavelength-dispersive X-ray spectroscopy, powder and single-crystal X-ray diffraction, Rietveld refinement, X-ray absorption near-edge structure, and magnetic measurements. Increasing substitution levels x, y in BaFe_12−x−yMg_xM_yO₁₉ result in increasing lattice parameters and decreasing the room-temperature magnetic parameters saturation magnetization, remanence, and coercivity, while remanence and coercivity increase at low temperatures. Secondary phases form for nominal substitution ≥ 1. Zr⁴⁺ and Hf⁴⁺ preferentially occupy the 4f₂ site, whereas Mg²⁺ is distributed over multiple sites, as indicated by polyhedral volume analysis. Wavelength-dispersive X-ray spectroscopy confirms homogeneous elemental distribution within individual crystals but reveals significant variation in substitution levels within batches. The maximum degree of substitution for the tetravalent metals was y ≈ 1.2–1.7, with lower Mg incorporation of x ≈ 0.9–1.1. Charge compensation was found to be partially achieved via vacancy formation, while minor Fe²⁺ contributions cannot be excluded. Full article

Titanium-bearing blast furnace slag is rich in high-melting-point titanium-containing minerals including perovskite, melilite and spinel, which result in the loss of titanium resources and hinder the comprehensive utilization of such slag. On this basis, combined with process mineralogy theories, this study adopted multiple characterization methods, including a polarized light microscope with transmitted and reflected light, XRD and EPMA. These simulations reveal that the bulk SiO₂ content dictates titanium distribution among the mineral phases, thereby laying a solid foundation for the subsequent experiments. Meanwhile, quantitative analyses were performed on the microstructure, mineral composition and perovskite grain size of the slag. The occurrence state and migration law of titanium in the slag were systematically investigated. The results show that the microstructure of titanium-bearing blast furnace slag presents a porphyritic structure at different SiO₂ levels. Its main mineral phases include perovskite, pyroxene, spinel and glass. Titanium is predominantly hosted in perovskite, with small amounts distributed in the pyroxene, spinel and glass phases. Reducing the SiO₂ content facilitates the formation and grain coarsening of perovskite and promotes the migration of titanium from pyroxene and glass into perovskite. When the SiO₂ content is 20%, the perovskite content reaches 44.3%. Among them, the proportion of grains larger than 40 μm is 59.94%, and the distribution ratio of titanium in perovskite is 86.78%. Under the experimental conditions of this study, 20% SiO₂ is the optimal level. These findings can provide a theoretical reference for the efficient separation and recovery of titanium from titanium-bearing blast furnace slag. Full article

Chromic materials exhibiting reversible changes in optical properties under external stimuli represent an important class of smart materials with applications in smart windows, sensors, and optoelectronic devices. Transition-metal oxides (TMOs) provide a versatile platform for chromic functionality due to their coupled structural, electronic, and optical properties. In this review, the chromic response of selected TMO thin films is analyzed using both microscopic and phenomenological approaches. The microscopic description is based on many-body theory, including Green’s function methods and correlation effects, while the macroscopic optical response is described using Drude–Lorentz and Tauc–Lorentz models within the effective medium approximation. Chromic behavior in TMOs is shown to originate from two principal mechanisms: (i) electronic and structural reconstruction driven by Peierls–Mott metal–insulator phase transitions, leading to thermochromism (notably in VO₂ and V₂O₃), and (ii) formation of localized states driven by small-polaron injection, giving rise to electrochromism, gasochromism, and photochromism. The models are applied to representative systems, including VO₂, WO₃, NiO, and TiO₂, demonstrating the chromic changes in the dielectric function spectra. These results highlight chromism in TMOs as a multiscale phenomenon linking microscopic interactions with macroscopic optical response. Full article

Next-generation wastewater treatment and recycling rely on membrane-based processes, but they face a trade-off among permeability, selectivity, and fouling resistance. In the present study, thin-film nanocomposite (TFN) membranes were fabricated by incorporating a ternary TiO₂-SiO₂-biochar nanofiller into a polysulfone (PSf) support using nonsolvent-induced phase separation, after which m-phenylenediamine and trimesoyl chloride were used via interfacial polymerization to produce a selective polyamide layer. The membrane compositions were M1 (22 wt.% PSf), M2 (22 wt.% PSf/0.5 wt.% TiO₂/0.5 wt.% SiO₂/0.5 wt.% biochar), and M3 (polyamide-coated M2). FTIR, XRD, SEM, contact-angle, porosity, and mechanical analyses supported successful membrane formation and changes in morphology, wettability, and structural strength after nanofiller incorporation and TFC coating. The addition of a nanofiller increased the hydrophilicity of the membranes by decreasing the water contact angle from 98.6 ± 0.8° for pristine PSf to 35.6 ± 1.5° for the nanocomposite membrane. Consequently, the pure-water permeability increased from 21 to 37 L m⁻² h⁻¹ bar⁻¹. After polyamide layer formation, the optimized TFN membrane maintained a contact angle of 55.4 ± 3.8° and achieved a high Congo red rejection of 98% with permeate flux of 7–9 L m⁻² h⁻¹ bar⁻¹. The membrane also showed good antifouling performance, with flux recovery ratios exceeding 90%. For heavy-metal-containing solutions, the optimized membrane showed apparent removal efficiencies of 78–98% for multivalent heavy metals (Pb²⁺, Hg²⁺, Cd²⁺, Mn²⁺, Zn²⁺, Cu²⁺, Ni²⁺, Fe³⁺, As³⁺, and Cr⁶⁺). Static adsorption tests showed the order M2 > M3 > M1, confirming that exposed TiO₂-SiO₂-biochar sites contribute to pollutant uptake, while the superior filtration performance of M3 is attributed to the combined effect of the polyamide selective layer and adsorption-assisted interactions. Overall, the TiO₂-SiO₂-biochar-based TFN membrane provides a promising platform for dye removal and preliminary heavy-metal attenuation from contaminated water. Full article

The development of lightweight aluminum matrix composites with improved mechanical performance and thermal stability using sustainable reinforcement materials remains a significant challenge in structural materials engineering. Although ceramic-reinforced aluminum composites exhibit enhanced strength and thermal resistance, the potential of bio-derived snail shell particles as environmentally sustainable reinforcements remains insufficiently explored. In this study, snail-shell-reinforced AA6061 aluminum matrix composites were fabricated by stir casting to investigate their microstructural characteristics, mechanical behavior, phase composition, and thermal stability. Snail shell particles, predominantly composed of CaCO₃, were processed to particle sizes of 50–75 µm before incorporation into the molten aluminum matrix. Characterization was performed using scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), X-ray diffraction (XRD), tensile and hardness testing, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The results revealed relatively uniform particle dispersion and satisfactory matrix–reinforcement interfacial compatibility. The tensile strength increased from 155 ± 5 MPa for the unreinforced alloy to 211 ± 4.8 MPa for the reinforced composite, corresponding to an improvement of approximately 36%, while elongation increased from 2.4 ± 0.2% to 4.6 ± 0.4% (92%). XRD analysis confirmed the presence of Al, CaCO₃, Mg₂Si, and minor CaO phases, indicating successful reinforcement incorporation and strengthening phase formation. Thermal analysis demonstrated enhanced thermal stability, increased residual mass retention, and improved resistance to thermal degradation. This work demonstrates that bio-derived snail shell particles are viable and environmentally sustainable reinforcements for lightweight aluminum matrix composites intended for structural engineering applications. Full article