Influence of Anodizing Parameters on Tribological Properties and Wettability of Al2O3 Layers Produced on the EN AW-5251 Aluminum Alloy

The article presents the effect of anodizing parameters of the EN AW-5251 aluminum alloy on the thickness and roughness of Al₂O₃ layers as well as their wettability and tribological properties in a sliding combination with the T7W material. The input variables were the current density of 1, 2, 3 A/dm² and the electrolyte temperature of 283, 293, 303 K. The tribological tests were performed on the T-17 tester in reciprocating motion, in conditions of technically dry friction. The tests were carried out on a 15 km road with a constant average slip speed of 0.2 m/s and a constant unit pressure of 1 MPa. The measurement of the wettability of the layers was performed using the sitting drop method, determining the contact angles on the basis of which the surface free energy was calculated. The profilographometric measurements were made. The analysis of the test results showed that the anodizing parameters significantly affect the thickness of the Al₂O₃ layers. The performed correlation analysis also showed a significant relationship between the roughness parameters and the wettability of the surface of the layers, which affects the ability to create and maintain a sliding film, which in turn translates into sliding resistance and wear of the T7W material. The analysis of friction and wear tests showed that the layer with hydrophobic properties produced at a current density of 1 A/dm² in an electrolyte at a temperature of 283 K is the most favorable for sliding associations with T7W material.     

Processing of Al2O3-AlN Ceramics and Their Structural,Mechanical, and Tribological Characterization

The aim of this study is to present a novel, lower sintering temperature preparation, processing, structural, mechanical, and tribological testing of the AlN-Al₂O₃ ceramics. The precursor powder of AlN was subjected to oxidation in ambient environment at 900 °C for 3, 10, and 20 h, respectively. These oxidized powders were characterized by SEM and XRD to reveal their morphology, phase, and crystal structure. The SEM results showed coarse powder particles and the presence of aluminum oxide (Al₂O₃) phase at the surface of aluminum nitride (AlN). The XRD analysis has shown increasing aluminum-oxy-nitride conversion of aluminum nitride as the holding time of oxidation increased. The highest percentage of conversion of AlN powder to AlN-Al₂O₃ was observed after 10 h. Simultaneously the powders were compacted and sintered using the hot isostatic pressing (HIP) under inert environment (N₂ gas) at 1700 °C, 20 MPa for 5 h. This led to the compaction and increase in density of the final samples. Mechanical tests, such as bending test and tribology tests, were carried out on the samples. The mechanical properties of the samples were observed to improve in the oxidized samples compared to the precursor AlN. Moreover, applying longer oxidation time, the mechanical properties of the sintered samples enhanced significantly. Optimum qualitative (microstructure, oxide percentage) and quantitative (tribology, hardness, and bending tests) properties were observed in samples with 10-h oxidation time.     

Thermodynamic Properties,Viscosity, and Structure of CaO–SiO2–MgO–Al2O3–TiO2–Based Slag

The effect of TiO₂ and the MgO/Al₂O₃ ratio on the viscosity, heat capacity, and enthalpy change of CaO–SiO₂–Al₂O₃–MgO–TiO₂ slag at constant heat input was studied. The variation of slag structure was analyzed by the calculation of activation energy and FTIR spectrum measurements. The results showed that the heat capacity and enthalpy change of the slag decreased with the increase of TiO₂ content. Under constant heat supply, the fluctuations in slag temperature were relatively apparent, and the temperature of slag increased as the TiO₂ content increased. The viscosity of slag decreased due to the increase in slag temperature. Increasing the MgO/Al₂O₃ ratio could decrease the temperature and viscosity of slag. The effect of increasing the MgO/Al₂O₃ ratio on the viscosity was more pronounced than the decreasing temperature caused by increasing the MgO/Al₂O₃ ratio. The apparent activation energy decreased with increasing TiO₂ content and MgO/Al₂O₃ ratio. The Ti–O bonds formed with TiO₂ addition, and the Ti–O bonds were weaker than Si–O bonds, which resulted in the decrease in heat capacity and viscosity of slag.     

Fabrication of r-GO/GO/α-Fe2O3/Fe2TiO5 Nanocomposite Using Natural Ilmenite and Graphite for Efficient Photocatalysis in Visible Light

Hematite (α-Fe₂O₃) and pseudobrookite (Fe₂TiO₅) suffer from poor charge transport and a high recombination effect under visible light irradiation. This study investigates the design and production of a 2D graphene-like r-GO/GO coupled α-Fe₂O₃/Fe₂TiO₅ heterojunction composite with better charge separation. It uses a simple sonochemical and hydrothermal approach followed by L-ascorbic acid chemical reduction pathway. The advantageous band offset of the α-Fe₂O₃/Fe₂TiO₅ (TF) nanocomposite between α-Fe₂O₃ and Fe₂TiO₅ forms a Type-II heterojunction at the Fe₂O₃/Fe₂TiO₅ interface, which efficiently promotes electron-hole separation. Importantly, very corrosive acid leachate resulting from the hydrochloric acid leaching of ilmenite sand, was successfully exploited to fabricate α-Fe₂O₃/Fe₂TiO₅ heterojunction. In this paper, a straightforward synthesis strategy was employed to create 2D graphene-like reduced graphene oxide (r-GO) from Ceylon graphite. The two-step process comprises oxidation of graphite to graphene oxide (GO) using the improved Hummer’s method, followed by controlled reduction of GO to r-GO using L-ascorbic acid. Before the reduction of GO to the r-GO, the surface of TF heterojunction was coupled with GO and was allowed for the controlled L-ascorbic acid reduction to yield r-GO/GO/α-Fe₂O₃/Fe₂TiO₅ nanocomposite. Under visible light illumination, the photocatalytic performance of the 30% GO/TF loaded composite material greatly improved (1240 Wcm⁻²). Field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM) examined the morphological characteristics of fabricated composites. X-ray photoelectron spectroscopy (XPS), Raman, X-ray diffraction (XRD), X-ray fluorescence (XRF), and diffuse reflectance spectroscopy (DRS) served to analyze the structural features of the produced composites.     

Phase Formation,Mechanical Strength,and Bioactive Properties of Lithium Disilicate Glass–Ceramics with Different Al2O3 Contents

Owing to its excellent mechanical properties and aesthetic tooth-like appearance, lithium disilicate glass–ceramic is more attractive as a crown for dental restorations. In this study, lithium disilicate glass–ceramics were prepared from SiO₂–Li₂O–K₂O–P₂O₅–CeO₂ glass systems with various Al₂O₃ contents. The mixed glass was then heat-treated at 600 °C and 800 °C for 2 h to form glass–ceramic samples. Phase formation, microstructure, mechanical properties and bioactivity were investigated. The phase formation analysis confirmed the presence of Li₂Si₂O₅ in all the samples. The glass–ceramic sample with an Al₂O₃ content of 1 wt% showed rod-like Li₂Si₂O₅ crystals that could contribute to the delay in crack propagation and demonstrated the highest mechanical properties. Surface treatment with hydrofluoric acid followed by a silane-coupling agent provided the highest micro-shear bond strength for all ceramic conditions, with no significant difference between ceramic samples. The biocompatibility tests of the material showed that Al₂O₃-added lithium disilicate glass–ceramic sample was bioactive, thus activating protein production and stimulating the alkaline phosphatase (ALP) activity of osteoblast-like cells.     

Reinforced 3D Composite Structures of γ-, α-Al2O3 with Carbon Nanotubes and Reduced GO Ribbons Printed from Boehmite Gels

The ability of boehmite to form printable inks has sparked interest in the manufacturing of 3D alumina (Al₂O₃) and composite structures by enabling direct ink writing methods while avoiding the use of printing additives. These materials may exhibit high porosity due to the printing and sintering procedures, depending on the intended application. The 3D-printed porous composite structures of γ-Al₂O₃ and α-Al₂O₃ containing 2 wt.% of carbon nanotubes or reduced graphene oxide ribbons were fabricated from boehmite gels, followed by different heat treatments. The reinforcing effect of these carbon nanostructures was evidenced by compression tests carried out on the different alumina structures. A maximum relative increase of 50% in compressive strength was achieved for the γ-Al₂O₃ composite structure reinforced with reduced graphene oxide ribbons, which was also accompanied by an increase in the specific surface area.     

Highly Active Co3O4-Based Catalysts for Total Oxidation of Light C1–C3 Alkanes Prepared by a Simple Soft Chemistry Method: Effect of the Heat-Treatment Temperature and Mixture of Alkanes

In the present work, a simple soft chemistry method was employed to prepare cobalt mixed oxide (Co₃O₄) materials, which have shown remarkably high activity in the heterogeneously catalyzed total oxidation of low reactive VOCs such as the light alkanes propane, ethane, and methane. The optimal heat-treatment temperature of the catalysts was shown to depend on the reactivity of the alkane studied. The catalytic activity of the Co₃O₄ catalysts was found to be as high as that of the most effective catalysts based on noble metals. The physicochemical properties, from either the bulk (using XRD, TPR, TPD-O₂, and TEM) or the surface (using XPS), of the catalysts were investigated to correlate the properties with the catalytic performance in the total oxidation of VOCs. The presence of S1 low-coordinated oxygen species at the near surface of the Co₃O₄-based catalysts appeared to be linked with the higher reducibility of the catalysts and, consequently, with the higher catalytic activity, not only per mass of catalyst but also per surface area (enhanced areal rate). The co-presence of propane and methane in the feed at low reaction temperatures did not negatively affect the propane reactivity. However, the co-presence of propane and methane in the feed at higher reaction temperatures negatively affected the methane reactivity.     

Core-Shell Fe2O3@La1−xSrxFeO3−δ Material for Catalytic Oxidations: Coverage of Iron Oxide Core,Oxygen Storage Capacity and Reactivity of Surface Oxygens

A series of Fe₂O₃@LSF (La_0.8Sr_0.2FeO_3−δ perovskite) core-shell materials (CSM) was prepared by infiltration of LSF precursors gel containing various complexants and their mixtures to nanocrystalline aggregates of hematite followed by thermal treatment. The content of LSF phase and amount of carboxyl groups in complexant determine the percent coverage of iron oxide core with the LSF shell. The most conformal coating core-shell material was prepared with citric acid as the complexant, contained 60 wt% LSF with 98% core coverage. The morphology of the CSM was studied by HRTEM-EELS combined with SEM-FIB for particles cross-sections. The reactivity of surface oxygen species and their amounts were determined by H₂-TPR, TGA-DTG, the oxidation state of surface oxygen ions by XPS. It was found that at complete core coverage with perovskite shell, the distribution of surface oxygen species according to redox reactivity in CSM resemble pure LSF, but its lattice oxygen storage capacity is 2–2.5 times higher. At partial coverage, the distribution of surface oxygen species according to redox reactivity resembles that in iron oxide.