X-ray Diffraction Research Articles

Enhancing Adsorption Performance of Ce(III) by Amine-Thiourea and Aniline-Modified Magnetic Chitosan Nanocomposites.

To enhance the adsorption performance of chitosan for rare earth ions, two novel magnetic chitosan-based adsorbents were prepared by using chitosan-coated magnetic silica nanoparticles modified with amine-thiourea and aniline. The structure of copolymers was analyzed using characterization methods such as X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis, confirming the successful synthesis of modified magnetic chitosan nanocomposites. The investigation explored the influence of pH, contact time, dosage, initial concentration, and temperature on the adsorption performance. Comparative studies revealed a significantly enhanced adsorption performance after modification. The chitosan-coated magnetic silica nanoparticles modified with aniline (PAN-CS/Fe3O4@SiO2) reached adsorption saturation in about 120 min with a capacity of 136 mg/g, while the chitosan-coated magnetic silica nanoparticles modified with amine-thiourea (TSC-CS/Fe3O4@SiO2) exhibited a higher adsorption capacity of 156 mg/g for Ce(III). Both materials demonstrated strong agreement with the Langmuir isotherm model and pseudo-second-order kinetics. Thermodynamic analysis indicated that Ce(III) adsorption is both spontaneous and endothermic. Examination of the adsorption mechanisms suggested that the effective adsorption of Ce(III) is due to the strong synergistic effects of chelation and electrostatic interactions involving amino, carboxyl, and hydroxyl groups. This study demonstrates that chitosan modified with amine-thiourea and aniline is an effective approach to significantly enhance the rare earth ion adsorption by chitosan.

Preparation and characterization of a new Gd2O3-epoxy composite for neutron shielding applications

The current study aims to introduce a new polymeric composite consisting of epoxy resin as the matrix and gadolinium oxide (Gd2O3) as the neutron adsorption ingredient. The shielding performance of the composite was assessed by neutron attenuation experiments with an Am-Be source and polyethylene moderator. The results of these experiments showed an appreciable agreement with the Monte Carlo simulations. Other characteristics of the composite, including mechanical strength, thermal stability, microtexture, and its chemical compositions, were examined using standard tensile test, thermogravimetric analysis, X-ray diffraction, scanning electron microscopy, static light scattering analyses, and Fourier-transform infrared spectroscopy (FTIR). The results indicated that the new composites offer appreciable neutron absorption properties so that samples with 0.5%, 2%, 5%, and 10% Gd2O3 content could reduce the neutron beam intensity by 54%, 63%, 66%, and 70% at a thickness of 4 cm.

Nanostructured Coatings of 3d-Metals Produced by Green Chemistry Methods: Analysis of Inhomogeneities by Static and Dynamic Magnetic Methods

The study investigates carbon-containing coatings of 3d-metals (Ni, Co, Fe) produced by chemical deposition method using arabinogalactan. The coatings were analyzed using X-ray diffraction, FMR, and M(H) magnetometry. Measurement of M(H) in plane and perpendicular to the plane of the magnetic coatings allowed determining the distribution of demagnetizing factor in the studied coatings. The obtained distributions of the demagnetizing factor were used to analyze the angular dependences of the ferromagnetic resonance field. The values of magnetization and perpendicular anisotropy field were estimated. The paper illustrates the effect of texture on the magnetic parameters.

Utilizing Zn(Cu/Cr)Al-Layered Double Hydroxide-Based Photocatalysts for Effective Photodegradation of Environmental Pollutants

Layered double hydroxides (LDHs) and their derived mixed oxides are emerging as a promising class of biocompatible inorganic lamellar nanomaterials. The detailed structure and textural characteristics of the synthesized LDH-based materials were examined using X-ray diffraction, Fourier transform infrared spectroscopy, and N2 adsorption/desorption isotherm. This study explored the removal efficiency of pharmaceutical tolperisone hydrochloride (TLP), as well as the herbicides quinmerac (QUI) and clomazone (CLO) from water, using dried and calcined LDH-based photocatalysts under simulated solar irradiation and UV irradiation. A higher removal efficiency was observed using UV irradiation, for all substrates. The most effective removal was achieved using ZnAl photocatalysts thermally treated at 100 °C (ZnAl 100) and 500 °C (ZnAl 500). The highest removal rates were observed in the TLP/ZnAl 100 and QUI/ZnAl 100 systems, achieving ~79% and ~86% removal after 75 min of treatment under UV. In contrast, the CLO/ZnAl 100 and CLO/ZnAl 500 systems achieved ~47% removal of CLO. Furthermore, this study investigated the role of reactive species to elucidate the mechanisms of photodegradation under UV. It was found that in the degradation of TLP and QUI in the presence of ZnAl 100 and ZnAl 500, the superoxide anion radical played the most important role.

Synthesis and Characterization of TiO2 Nanotubes for High-Performance Gas Sensor Applications

In this study, we investigated the fabrication, properties, and sensing applications of TiO2 nanotubes. A pure titanium metal sheet was used to demonstrate how titanium dioxide nanotubes can be used for gas-sensing applications through the electrochemical anodization method. Subsequently, X-ray diffraction indicated the crystallization of the titanium dioxide layer. Scanning electron microscopy and transmission electron microscopy then revealed the average diameter of the TiO2 nanotubes to be approximately 100 nm, with tube lengths ranging between 3 and 9 µm and the thickness of the nanotube walls being about 25 nm. This type of TiO2 nanotube was found to be suitable for NO2 gas sensor applications. With an oxidation time of 15 min, its detection of NO2 gas showed a good result at 250 °C, especially when exposed to a NO2 gas flow of 100 ppm, where a maximum NO2 gas response of 96% was obtained. The NO2 sensors based on the TiO2 nanotube arrays all exhibited a high level of stability, good reproducibility, and high sensitivity.

Strength and Microstructural Characteristics of Activated Fly Ash–Cement Paste

Incorporating high volumes of fly ash (FA) in filling materials reduces costs and carbon emissions, but low early strength limits its use. This study investigates the effects of sodium sulfate decahydrate (Na2SO4·10H2O) and calcium hydroxide (Ca(OH)2) as activators at concentrations of 0.5%, 1.0%, 1.5%, and 2.0% on the mechanical properties and microstructure of tailings–cement–fly ash composites. Compressive strength testing, X-ray diffraction (XRD), and scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS) were used to evaluate performance at different curing stages. Results indicate that all activators enhance early strength, with 2.0% Ca(OH)2 yielding the greatest improvement. Microstructural analysis showed that activators boost quartz reactivity and create denser structures. Na2SO4 promotes ettringite and gypsum formation, while Ca(OH)2 increases alkalinity, enhancing gel formation from FA. These findings clarify how activators improve the performance of activated fly ash–cement paste (AFCP).

Study the Antifungal Effects of Green Synthesized Silver Nanoparticles on the Aspergillus niger, Microsporum canis, and Candida albicans

: The increasing prevalence of drug-resistant fungal pathogens and the limitations of current antifungal therapies underscore the need for novel alternative treatments. This study aimed to evaluate the antifungal effects of green-synthesized silver nanoparticles (Ag NPs) on three clinically significant fungi: Aspergillus niger, Microsporum canis, and Candida albicans. Silver nanoparticles were synthesized using plant-based extracts to ensure eco-friendly production methods. The synthesized Ag NPs were characterized using UV spectrophotometry, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), dynamic light scattering (DLS), zeta potential measurements, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Characterization assays revealed spherical particles with colloidal stability, an average size of approximately 80 nm, a Polydispersity Index of 0.4, and a surface charge of 62.3 mV. Minimum inhibitory concentration (MIC) values demonstrated effective suppression of fungal growth at low nanoparticle concentrations. In conclusion, our study highlights the potential of green-synthesized Ag NPs as a promising alternative to conventional antifungal agents, emphasizing their significant advantages in biocompatibility and eco-friendliness. These findings could pave the way for a new era in treating fungal infections, particularly those caused by drug-resistant strains.

Optimization of Crystal Structures in Polylithionite Concentrate: A Molecular Dynamics Approach to Lithium Extraction Efficiency

Molecular dynamics (MD) techniques offer significant potential for optimizing mineral extraction processes by simulating economically or physically restrictive conditions at the laboratory level. Lithium, a crucial metal in the electromobility era, exemplifies the need for ongoing re-evaluation of extraction techniques. This research aims to simulate the crystal structures of mineral species present in a polylithionite mineral concentrate [KLi2Al(Si4O10)(F,OH)2] using crystallographic data obtained from X-ray diffraction analysis. This study focuses on optimizing these structures, validating them through density comparisons, and determining the interaction parameter between the identified phases and lithium oxide (Li2O). The X-ray diffraction analysis revealed five predominant mineral phases: quartz (SiO2), calcite [Ca(CO3)], pyrite (FeS2), cassiterite (SiO2), and a compound Pb6O2(BO3)2SO4. Structural data, including lattice parameters, space groups, and atomic coordinates, were used to construct the crystal structures with Materials Studio 8.0, employing the Crystal Builder module. Optimization was performed using the Forcite module with the Smart optimization algorithm and the Universal force field. The interaction parameter (χ) indicated an affinity between lithium oxide and pyrite, as well as between calcite and quartz.

Imaging in-operando LiCoO2 nanocrystallites with Bragg coherent X-ray diffraction

Although the LiCoO2 (LCO) cathode material has been widely used in commercial lithium ion batteries (LIB) and shows high stability, LIB’s improvements have several challenges that still need to be overcome. In this paper, we have studied the in-operando structural properties of LCO within battery cells using Bragg Coherent X-ray Diffraction Imaging to identify ways to optimise the LCO batteries’ cycling. We have successfully reconstructed the X-ray scattering phase variation (a fingerprint of atomic displacement) within a ≈ (1.6 × 1.4 × 1.3) μm3 LCO nanocrystal across a charge/discharge cycle. Reconstructions indicate strained domains forming, expanding, and fragmenting near the surface of the nanocrystal during charging, with a determined maximum relative lattice displacements of 0.467 Å. While discharging, all domains replicate in reverse the effects observed from the charging states, but with a lower maximum relative lattice displacements of 0.226 Å. These findings show the inefficiency-increasing domain dynamics within LCO lattices during cycling.

Synthesis and Evaluation of Starch-Grafted-Poly[(Acrylic Acid)-Co-Acrylamide] Based Nanoclay Polymer Composite Fertilizers for Slow Release of Nitrogen in Soil

Nitrogen (N) losses from conventional N fertilizers contribute to environmental degradation and low N use efficiency. Highlighting the need for slow-release fertilizers (SRFs) to mitigate these problems, this study aims to develop slow-release N fertilizers using starch-grafted-poly[(acrylic acid)-co-acrylamide] based nanoclay polymer composites (NCPCs) and investigate their efficacy for slow N delivery in soil. Three types of NCPCs, NCPC(A) (poly [(acrylic acid)-co-acrylamide]), NCPC(W) (wheat starch-grafted-poly[(acrylic acid)-co-acrylamide), and NCPC(M) (maize starch-grafted-poly[(acrylic acid)-co-acrylamide) were prepared and characterized using FTIR spectroscopy and X-ray diffraction techniques. N-release behaviour of the products was assessed under two distinct soils, i.e., Assam (Typic Hapludults, pH 4.2) and Delhi (Typic Haplustepts, pH 7.9) soils. Additionally, the effects of varying soil moisture and temperature levels on N release were studied in the Assam soil. The N-release kinetics of the synthesized fertilizers were assessed using zero-order, first-order, Higuchi, and Korsmeyer−Peppas models. Degradability of the NCPCs was evaluated by measuring evolved CO2–C under various soil conditions as an indicator of microbial degradation. The results indicated that NCPC fertilizers significantly slowed down the release of N compared to urea. According to the R2 values obtained, it was evident that the first-order kinetic model most accurately describes the N release from both urea and NCPC-based N fertilizers in the studied soils. Among the formulations, NCPC(A) exhibited the lowest N release (42.94–53.76%), followed by NCPC(M) (51.05–61.70%), NCPC(W) (54.86–67.75%), and urea (74.33–84.27%) after 21 days of incubation. The rate of N release was lower in the Assam soil compared to the Delhi soil, with higher soil moisture and temperature levels accelerating the release. Starch addition improved the biodegradability of the NCPCs, with NCPC(W) showing the highest cumulative CO2-C evolution (18.18–22.62 mg g−1), followed by NCPC(M) (15.54–20.97 mg g−1) and NCPC(A) (10.89–19.53 mg g−1). In conclusion, NCPC-based slow-release fertilizers demonstrated a more gradual N release compared to conventional urea and the inclusion of starch enhanced their degradability in the soil, which confirms their potential for sustainable agricultural applications. However, soil properties and environmental factors influenced the N release and degradation rates of NCPCs.

Chain-like Pentanuclear Complexes: Syntheses, Crystal Structures and Long-range Electronic Interactions of Cyanido-Bridged M2Ru3 (M = Fe, Ru).

In this work, we report the design and synthesis of two chain-like pentanuclear cyanido-bridged complexes trans-[Ru(bpy)2(μ-CN)2][cis-Ru(bpy)2(μ-NC)M(dppe)Cp*]2[PF6]4(M = Fe, 14+; M = Ru, 24+) and the electronic communication properties of their oxidized products 1m+ (m = 6, 7, 8) and 2n+ (n = 5, 6, 7, 8). The single-crystal X-ray diffraction analysisof 1m+ (m = 4, 6, 7) and 24+ show that 14+ and 24+ possess a Z-type array structure, 17+ is a U-type one, and 16+ exhibits both the types. The investigations indicate that both 1 and 2 show an extraordinarily strong electronic interaction between the two side Ru across the central NC-Ru-CN, leading to the formation of a fully delocalized cyanidometal Ru-Ru-Ru bridge for both three-electron oxidized states 17+ and 27+. Moreover, it should be noted that in 1 there exists no electronic interaction between the two terminal Fe ions. Upon substitution of Fe by Ru, however, 2 exhibits an electronic interaction between the two terminal metal ions across the trinuclear cyanidometal CN-Ru-NC-Ru-CN-Ru-NC bridge which is up to 20 Å.

The role of BaTiO3 nanoparticles as photocatalysts in the synthesis and characterization of novel fruit dyes is investigated.

In the present work, the photocatalytic activity against the natural dye extracted from the novel fruits has been studied by the BaTiO3 nanoparticles (NPs) under a ultra-violet (UV) light source. The large concentrations of an essential phenolic agent present in this phytochemical extract superimposed with cloths fibers make strong stain and degrade into another form of toxic, which is excluded from the many textiles industries as the colorful waste waters without recycling and removal of that dye pigments have been investigated using both photodegradation and photoluminescence techniques. The entitled nanoparticles (NPs) were prepared using the soft chemical root-modified solvothermal synthesis combo method and exposure to heat treatment such that the annealing process has been done for different temperatures ranging from 100°C to 250°C. As for as concern the characterization, as a start, structural and morphology studies have been reported here that highly crystalline oriented peaks data using powder x-ray diffraction techniques (PXRD) as well as the surface morphology including the size, shape, and mass distribution using the field emission scanning electron microscopy (FESEM) techniques, which purely belong to rutile tetragonal structure of the crystal system and circular and noncircular flakes like rough surface morphology materials respectively. The lattice dissociation constant 'ε' value of the BaTiO3 NPs has determined to be ~2.71 × 10-3 using the Williamson-Hall (W-H plot) analysis of crystallographic data. In the UV visible spectroscopy findings, since the extreme quantum confinement of BaTiO3 nanoflakes/nanodisc, the optical energy bandgap has been estimated to be a range of 1.98 to 2.67 eV (~2.48 eV) found from the Tauc plot analysis, which contributes to the significantly owing to the enhanced photocatalytic efficiency with excellent performance along exciton formation, superoxide ions, and hydroxyl free radicals generations under UV-vis light irradiation resulting in efficient degradation of typical novel fruit organic dye. Photoluminescence spectra observed at room temperature and low temperature have been observed for the BaTiO3 nanoflakes, which exhibit the blue emission due to the crystalline defects such as the appearance of Ba vacancies leads to the conceivable beginning of p-type conductivity and the origination of free exciton emission reveals the direct bandgap transition nature of nanoflakes. RESEARCH HIGHLIGHTS: According to our findings, 89.71% of the natural syzygium cumin is degraded by photocatalysis reaction. As a plausible mechanism for the destruction of natural dyes under solar light, photocatalytic destruction has been proposed. The reaction between these reactive free radical species leads to high efficiency photodegradation with a short decay time. In addition to water treatment and environmental cleaning applications, the excellent performance of this photocatalyst makes it a promising candidate for other applications. Hence, the synthesized BaTiO3 nanoflakes showcase a highly significant advancement towards the development of a textiles dye recycling method.

Magnetocaloric and Magnetostrictive Properties of the Tb(Co,In)<sub>2</sub> Laves Phases

Multicomponent polycrystalline TbInxCo2–x (with х = 0–0.2) solid solutions are prepared for the first time, and their crystal structure and magnetic, magnetocaloric, and magnetostrictive properties are studied. X-ray diffraction patterns taken at room temperature demonstrate mainly the presence of the cubic C15 Laves phase in all samples. As the indium content increases to x = 0.1, the lattice parameter is found to increase; the further increase in the indium content to х = 0.2 leads to a decrease in the lattice parameter. In this case, the Curie temperature TC monotonically increases to 245 K. The isotheral magnetic entropy change ΔSmag is calculated in accordance with magnetic measurements using the thermodynamic Maxwell’s relation. At a magnetic field change from 0 to 1.8 T, the maximum entropy change monotonically decreases and, for composition with x = 0.2, is 1.8 J/(kg∙К). As the indium content increases to x = 0.05, the volume magnetostriction increases. The further increase in the indium concentration leads to the decrease in the peak values and their shift to high temperatures.

Hydrothermal synthesis of rGO and MnCoS composite for enhanced supercapacitor application

Nanostructured materials incorporating transition metal sulfides have demonstrated considerable potential across various applications, particularly in the realms of energy production and storage. Sulfide-based material preparation is a challenging and costly procedure that requires a high temperature and reducing atmosphere. This work reports that manganese cobalt sulfide (MCS) and reduced graphene oxide composite manganese cobalt sulfide (rMCS) were successfully prepared through a hydrothermal method. Various characterization techniques were employed to analyze the prepared materials, including X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller analysis, and X-ray photoelectron spectroscopy. In a three-electrode system, MCS and rMCS electrodes exhibit an excellent specific capacitance of 1695 and 1925 F g−1 at 1 A g−1 current density respectively. MCS delivers the capacitance retention of 99% and rMCS exhibits the capacitance retention of 100% capacitance retention over 5000 consecutive cycles. The constructed asymmetric supercapacitor electrode (rMCS//rGO) exhibits the energy and power density of 64 Wh kg−1 at 799 W kg−1, respectively with outstanding cyclic stability of 97.4% even after 10,000 cycles. The exceptional electrochemical properties of MCS with rGO composite electrode indicate that they would make an outstanding electrode material for cutting-edge energy storage devices.

Understanding the Environmental Sensitivity of Copper‐Metal Oxides Interactions in Cu/ZnO and Cu/Al2O3 Catalysts

AbstractTernary Cu/ZnO/Al2O3 catalysts are one of the most important industrial catalysts and show excellent activity in methanol reforming reaction. However, it is challenging to elucidate the metal support interactions, which critically influence the catalyst structure and performance, due to their environmentally sensitive nature. This study examines the interactions between Cu and Al2O3 and ZnO, after reductive treatments of the Cu/Al2O3 and Cu/ZnO model catalysts with varying temperatures and hydrogen concentration. A combination of Brunner‐Emmet‐Teller (BET) measurements, X‐ray diffraction (XRD), N2O titration, diffuse reflectance infrared Fourier transformations spectroscopy (DRIFTS) and high‐resolution transmission electron microscopy (HRTEM) provided comprehensive insights into the structural evolution of the catalysts.

Isolation and characterization of a resistance Bacillus subtilis for soil stabilization and dust alleviation purposes

Dust poses environmental, geological, health, and economic concerns, and microorganisms can help mitigate these adverse consequences by improving soil properties. Microbial calcium carbonate precipitation (MICP) has been found to be an efficient strategy for increasing soil strength, reducing soil porosity, and preventing erosion; however, severe environmental conditions such as pH and high temperatures may impede this process. To identify the best strain for MICP, 60 bacteria strains were obtained from arid soils using the enrichment culture technique. They were tested for the capacity of calcium carbonate deposition and biocement synthesis in stress environments. Phenotypic characterization indicated that the majority of the bacterial isolates were gram-positive and rod-shaped, with strong catalase and oxidase enzyme activity. Furthermore, MALDI-TOF MS identification revealed that the isolates were from the Bacillus and Pseudomonas genera. Scanning Electron Microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD) were used to analyze the microstructures and composition of bacterial cement. The results represented that B. subtilis isolate S56 has a higher production yield and forms distinctive calcite crystals as a result of fast urease synthesis. B. subtilis isolate S56 can be applied in situ to reduce soil erosion and dust pollution. This study reveals the potential of the B. subtilis S56 strain for soil consolidation and dust prevention in harsh environments and has the prospect of promoting its application in desertification control and ecological restoration.

Enhancing Vanadium Redox Flow Battery Performance with ZIF-67-Derived Cobalt-Based Electrode Materials

Vanadium redox flow batteries (VRFBs) have emerged as a promising energy storage solution for stabilizing power grids integrated with renewable energy sources. In this study, we synthesized and evaluated a series of zeolitic imidazolate framework-67 (ZIF-67) derivatives as electrode materials for VRFBs, aiming to enhance electrochemical performance. Four materials—Co/NC-700, Co/NC-800, Co3O4-350, and Co3O4-450—were prepared through thermal decomposition under different conditions and coated onto graphite felt (GF) electrodes. X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) analyses confirmed the structural integrity and distribution of the active materials. Electrochemical evaluations revealed that electrodes with ZIF-67-derived coatings exhibited significantly lower charge transfer resistance (Rct) and higher energy efficiency (EE) compared to uncoated GF electrodes. Co/NC-800//GF delivered the highest energy efficiency and discharge capacity among the tested configurations, maintaining stable performance over 100 charge–discharge cycles. These results indicate that Co/NC-800 holds great potential for use in VRFBs due to its superior electrochemical activity, stability, and scalability.

Enhancing Sustainable Production of Biodiesel from Xanthoceras sorbifolia Bunge Oil Using Bio-Based Heterogeneous Catalyst

The swift exhaustion of natural oil reserves and worsening environmental issues have prompted the quest for an economical method to produce biofuels. The superiority of heterogeneous catalysis promotes the development of bio-based catalysts. Carbon materials prepared from agricultural and forestry biomass waste have good application prospects in catalysis. In the present study, Xanthoceras sorbifolia shell waste was used as the raw material, Xanthoceras sorbifolia Bunge Carbon (XC) was used as the catalyst carrier, and K2CO3 was used as the activator to prepare a heterogeneous catalyst (KXC). The heterogeneous catalyst was characterized by scanning electron microscopy-energy dispersion X-ray spectroscopy (SEM-EDS), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and Brunauer–Emmett–Teller (BET) and X-ray photoelectron spectroscopy (XPS) analysis techniques to evaluate its chemical composition, structure, and physical morphology. EDS and XPS revealed the presence of K metal, which provided an alkaline site for the transesterification reaction to produce biodiesel. The biodiesel yield was observed by gas chromatography−mass spectrometry (GCMS). Under the reaction conditions of a methanol-to-oil molar ratio of 12:1, a reaction time of 90 min, a temperature of 65 °C, and a catalyst loading of 4 wt.% using 25KXC-600-4, the yield of biodiesel can reach 95.13 ± 0.82%. After being repeated five times, the yield was still 58.11 ± 3.80%. The catalyst has no waste generation, and has the characteristics of simple preparation and environmental friendliness, which make it a green heterogeneous catalyst for biodiesel production.

Ce-Doped Iron Oxide Anticorrosive Coatings: Effect of c(Ce4+):c(Fe3+) Ratio on Structure, Morphology, and Coating Anticorrosion Performance

Utilizing hydrothermal methods, Ce-doped iron oxide nanoparticles were synthesized from precursor solutions under different c(Ce4:c(Fe3+) precursor solutions. The effects of the c(Ce4+):c(Fe3+) ratio in the precursor solutions on the nanoparticle morphology and nanoparticle structure of the Ce-doped iron oxide were investigated using X-Ray diffraction, transmission electron microscopy, and scanning electron microscopy. Fourier transform infrared spectroscopy (FTIR) was used to examine the bond energy strength of the Ce-doped iron oxide nanoparticles. The electrochemical properties of the Ce-doped iron oxide nanoparticles were tested using an electrochemical workstation and a saltwater immersion resistance test. The corrosion resistance of Ce-doped iron oxide coatings at different c(Ce4+):c(Fe3+) ratios was systematically analyzed, uncovering corrosion resistance mechanisms and self-healing capabilities. The results show that as the c(Ce4+):c(Fe3+) ratio decreases, the lattice constants of the samples increase along with the average grain size. Both smaller and larger c(Ce4+):c(Fe3+) ratios are detrimental to lattice distortion in α-Fe2O3. The reduced number of valence electrons provided by cerium ions in Ce-doped iron oxide hinders the generation of holes and exerts a minor influence on the crystal band structure, leading to weaker electrochemical stability. The Ce-doped iron oxide coating prepared at a c(Ce4+):c(Fe3+) ratio of 1:60 readily generates a higher number of reactive hydroxyl radicals during corrosion, thus exhibiting enhanced self-healing capabilities and corrosion resistance.

Surface modification of high-speed steel (HSS) drills by plasma nitriding and cathodic cage tin deposition

Cutting tools made of high-speed steel have significant economic and technological importance. To enhance their productivity, thermochemical treatments are sought to improve both surface mechanical and tribological properties. Plasma nitriding and thin film deposition are widely employed for this purpose. In this study, modifications were made to M2 high-speed steel drills through plasma nitriding at temperatures of 400°C and 450°C. Cathodic cage TiN plasma deposition was also performed, varying the dwell time at a fixed temperature of 450°C. Characterization techniques included optical microscopy, X-ray diffraction (XRD), Vickers microhardness testing, and scanning electron microscopy (SEM). Performance tests were carried out to evaluate the behavior of the drills in relation to wear when machining AISI 1020 steel. It was observed that longer deposition times promote more uniform and thicker layers, and higher nitriding temperatures result in thicker nitride layers. An increase in hardness was noticeable in all deposition and nitriding treatments, with the nitrided samples exhibiting the highest hardness. During performance tests, the cathodic cage plasma TiN deposition demonstrated greater potential for application in HSS drills, with a treatment lasting 4 h providing the best results.