Search Results (513)

To enhance the anti-corrosion performance of storage tanks, Ni–SiC composites were successfully fabricated on the surface of Q345 steel substrate via the ultrasonic electrodeposition technique. The influence of ultrasonic power on the surface morphology, element content, phase structure, and anti-corrosion performance of Ni–SiC composites were explored utilizing a scanning electron microscope (SEM), X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), and an electrochemical workstation, respectively. SEM images showed that the Ni–SiC composites obtained at 120 W had a flat, dense surface morphology, with a uniform distribution of SiC nanoparticles (NPs) and a refined size of nickel grains. Meanwhile, the Si content (7.3 wt.%) of Ni–SiC composites prepared at 120 W was obviously higher than those obtained at 0 W (4.8 wt.%) and 60 W (6.1 wt.%). The thicknesses and adhesion force of Ni–SiC composites manufactured at 120 W were the largest of 103.5 μm and 51.2 N, respectively. XRD patterns presented that the diffraction peaks intensity and width of Ni–SiC composites manufactured at 120 W were lower and broader than that of Ni–SiC composites manufactured at 0 W and 60 W. A corrosion test illustrated that the Ni–SiC composites prepared at 120 W had the lowest corrosion current of 3.5 × 10⁻³ mA/cm², the lowest corrosive weight loss (4.2 mg) and corrosion rate (0.06 mg/h), while the corrosion potential was the highest of −0.41 V, which demonstrated the best anti-corrosion performance. In addition, the co-deposition mechanism of SiC NPs and Ni²⁺ ions was also analyzed. Full article

In organic solids, the heterogeneous distribution of organic molecules in the solid state gives rise to novel structure–property relationships. Here, we use transmission electron microscopy to investigate the aggregated structure of organic solid of a typical phosphorescent molecule Ir(ppy)₃ at the atomic scale. Through the identification of heavy Ir atoms in the molecular structure, we reveal the existence of organic crystals, clusters and single molecules in the solids. Through electron energy loss spectroscopy, we explore the vibration modes of molecules and lattices in the solids and possible perturbations by excitons induced by electron beam, which could affect the electroluminescent property of the molecules. Full article

Within the framework of an extensive conservation project involving multiple stained-glass windows of the Basilica of San Petronio in Bologna, Italy, this study reports the results of the diagnostic campaign on the rose window depicting Sant’Ambrogio between two angels holding the coats of arms of the Marsili family. The rose window is located in the homonymous chapel and, based on recent studies attributing the cartoon to the Bolognese painter Biagio Pupini, who was active in San Petronio from 1519, is dated to the early sixteenth century. No evidence was found regarding the workshop responsible for the production of the stained-glass window. The window showed no significant conservation issues, either in the glass elements or in the lead cames. However, the extensive degradation of the grisaille—likely caused by a low-quality mixture, improper firing, or aggressive cleaning—resulted in the loss of the original drawing. This study presents the results of non-invasive investigations on the glass tiles of the rose windows and the analyses of deposits present on their surfaces. Fiber Optic Spectroscopy (FOS) in transmittance, X Ray Fluorescence (XRF), and Hyper Spectral Imaging (HIS) in transmittance were used to investigate the glass composing the rose window. Fourier Transform Infrared Spectroscopy (FT-IR) was applied to study deposit samples collected from the external surface of the window. Additionally, only four glass samples, obtained from hidden areas or already detached fragments, were analyzed using Scanning Electron Microscope with Energy-Dispersive Spectroscopy (SEM-EDS). In addition, a photographic processing method is described, which enabled the recovery of the ghost image, the faint trace or imprint left by the grisaille on the glass during firing, allowing the conservators to faithfully reintegrate the original drawing. Full article

In high-sulfur environments, the failure risk of completion tubing increases due to the coupling effect of mechanical and electrochemical corrosion during the acidification production process. The corrosion behavior of P110SS tubing steel was investigated by an HTHP corrosion weight loss experiment and an electrochemical corrosion experiment. Scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS) were used to analyze the surface morphology of the corrosion products. In addition, a prediction model for the remaining service life of completion tubing under the synergistic effect of corrosion and stress was established during the acidification production process. The results show that acidification operations have a significant impact on the subsequent service life of tubing; the corrosion rate of P110SS tubing in the full acidification production process is much higher than that after the produced gas field solution corrosion treatment alone. Obvious pitting marks, micropores, and microchannels are observed in the corrosion product film of P110SS steel after acidification treatment, and the corrosion product film structure of P110SS steel is loose and honeycomb-like after acidification production treatment. The corrosion products are mainly FexSy and FeCO₃ after acidification production corrosion treatment. The corrosion during the acidification production stage is controlled by cathodic polarization. The remaining service life of tubing after production corrosion treatment can reach up to 29 years, while the remaining service life of tubing after acidification production corrosion treatment is significantly reduced, with a maximum of only 8 years. The research results have guiding significance for the selection, optimization, and design of high-sulfur-gas well tubing. Full article

The growing environmental concern over waste tire accumulation necessitates innovative recycling strategies in construction materials. Therefore, this study aims to develop and evaluate sustainable concrete by integrating waste tire rubber (WTR) aggregates of different sizes and recycled waste tire steel fibers (WTSFs), assessing their combined effects on the mechanical and microstructural performance of concrete through experimental and analytical approaches. WTR aggregates, consisting of fine (0–4 mm), small coarse (5–8 mm), and large coarse (11–22 mm) particles, were used at substitution rates of 0–20%; WTSF was used at volumetric dosages of 0–2%, resulting in a total of 40 mixtures. Mechanical performance was evaluated using density and pressure resistance tests, while microstructural properties were assessed using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). The findings indicate systematic decreases in density and compressive strength with increasing WTR ratio; the average strength losses were approximately 12%, 20%, and 31% at 5%, 10%, and 20% for WTR substitution, respectively. Among the WTR types, the most negative effect occurred in fine particles (FWTR), while the least negative effect occurred in coarse particles (LCWTR). The addition of WTSF compensated for losses at low/medium dosages (0.5–1.0%) and increased strength by 2–10%. However, high dosages (2.0%) reduced strength by 20–40% due to workability issues, fiber clumping, and void formation. The highest strength was achieved in the 5LCWTR–1WTSF mixture at 36.98 MPa (≈6% increase compared to the reference/control concrete), while the lowest strength was measured at 16.72 MPa in the 20FWTR–2WTSF mixture (≈52% decrease compared to the reference/control). A strong positive correlation was found between density and strength (r, Pearson correlation coefficient, ≈0.77). SEM and EDX analyses confirmed the weak matrix–rubber interface and the crack-bridging effect of steel fibers in mixtures containing fine WTR. Additionally, a hybrid prediction model combining physics-informed neural networks (PINNs) and CatBoost, supported by data augmentation strategies, accurately estimated compressive strength. Overall, the results highlight that optimized integration of WTR and WTSF enables sustainable concrete production with acceptable mechanical and microstructural performance. Full article

Tin slags generated during cassiterite smelting in Brazil contain significant amounts of technologically important metals such as niobium, tantalum, and zirconium. Improper disposal of these materials represents both an environmental concern and the loss of a valuable secondary source of critical elements. This study aimed to characterize a Brazilian tin slag sample to evaluate its composition, morphology, and potential for metal recovery. The material was homogenized and analyzed by laser diffraction (particle size), ICP-OES (chemical composition), X-ray diffraction (mineral phases), differential scanning calorimetry (metallic tin), and scanning electron microscopy with energy-dispersive spectroscopy (morphology). The slag exhibited a heterogeneous particle size distribution (D90 = 0.75 mm, D50 = 0.30 mm, D10 = 0.09 mm) and a complex multiphase structure composed mainly of silica, calcium silicate, and zirconia. The chemical analysis revealed 4.8 wt% Nb and 0.8 wt% Ta, along with high concentrations of Zr (11.1 wt%), confirming the material’s potential as a secondary resource. Thorium (2.7 wt%) and uranium (0.3 wt%) were also detected, indicating the presence of radioactive constituents. The detailed characterization of the slag provides essential insights into its chemical and mineralogical complexity, which directly influence the selection of suitable recovery routes. Understanding the distribution of Nb- and Ta-bearing phases within the refractory silicate–zirconia matrix is fundamental for defining pretreatment and leaching strategies. Therefore, this study establishes a necessary foundation for the design of efficient hydrometallurgical processes aimed at recovering critical metals from Brazilian tin slags. Full article

Titanium dioxide is attractive for energy storage due to its abundance, stability, non-toxicity, low cost, and favorable electronic/optical properties. Colossal permittivity (CP) in co-doped TiO₂ is mainly linked to defect structures rather than intrinsic bulk behavior. This work studies the dielectric properties of TiO₂ co-doped with niobium and magnesium, synthesized by solid-state reaction. Grain size effects were examined by varying ball milling parameters of (½Mg½Nb)_0.05Ti_0.95O₂ and then were correlated with structure, morphology, and dielectric response. X-ray diffraction (XRD), infrared spectroscopy (FTIR), scanning electron microscopy and energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray photoelectron spectroscopy (XPS), and impedance spectroscopy (IS) (40 Hz–10⁶ Hz, 150–370 K) were employed for structural, morphological, and electrical characterization. XRD confirmed the rutile phase. For co-doped samples, larger grains yielded higher dielectric constants, reaching high permittivity (ε′ = 429, T = 300 K, f = 10 kHz at 500 rpm for 2 h). Lower loss tangent (tan δ = 0.11, T = 300 K, f = 10 kHz at 200 rpm for 2 h) is linked to Mg segregation at grain boundaries. The most conductive sample showed the highest dielectric constant, suggesting an IBLC polarization mechanism driven by grain boundary effects. XPS confirmed Nb and Mg incorporation, with Ti⁴⁺ dominant and minor Ti³⁺ from oxygen vacancies and surface hydroxylation/defects. Full article

This study focuses on the susceptibility and surface degradation of low-alloy carbon steel 42CrMo4 to corrosion and cavitation erosion, as this steel is widely used in marine environments with aggressive chemical species and harsh conditions. Due to its high strength and fatigue resistance, 42CrMo4 steel is often employed in offshore mechanical components such as shafts and fasteners as well as crane parts in ports and harbors. Various experimental methods, including corrosion and cavitation tests, were used to assess the steel’s surface integrity under extreme conditions. Surface changes were monitored using modern analytical tools for precise assessments, including image and morphological analyses, to quantify degradation levels and specific parameters of defects induced by corrosion and cavitation. Non-destructive techniques such as optical microscopy (OM), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and image analysis software were employed for the quantitative assessment of morphological parameters and elemental analysis. EDS analysis revealed changes in elemental composition, indicating corrosion products that caused significant mass loss and defect formation, with degradation increasing over time. The average corrosion rate of 42CrMo4 steel in a 3.5% NaCl solution reached a peak value of 0.846 mm/year after 120 days of exposure. Cavitation erosion behavior was measured based on mass loss, indicating the occurrence of different cavitation periods, with the steady-state period achieved after 60 min. The number of formed pits increased until 120 min, after which it decreased slightly. This indicates that a time frame of 120 min was identified as significant for changes in the mechanism of pit formation. Specifically, up to 120 min, pit formation was the dominant mechanism of cavitation erosion, while after that, as the number of pits slightly declined, the growth and merging of formed pits became the dominant mechanism. The cavitation erosion tests showed mass loss and mechanical damage, characterized by the formation of pits and cavities. The findings indicate that the levels of surface degradation were higher for corrosion than for cavitation. The presented approach also provides an assessment of the degradation mechanisms of 42CrMo4 steel exposed to corrosive and cavitation conditions. Full article

Magnetron sputtering offers a scalable route to magnetic topological insulators (MTIs) based on Cr-doped Sb₂Te₃. We combine a range of X-ray diffraction (XRD), reciprocal-space mapping (RSM), scanning transmission electron microscopy (STEM), scanning TEM-energy-dispersive X-ray spectroscopy (STEM-EDS), and X-ray absorption spectroscopy, and X-ray magnetic circular dichroism (XAS/XMCD) techniques to study the structure and magnetism of Cr-doped Sb₂Te₃ films. Symmetric $\theta$-2$\theta$ XRD and RSM establish a solubility window. Layered tetradymite order persists up to ∼10 at.-% Cr, while higher doping yields CrTe/Cr₂Te₃ secondary phases. STEM reveals nanocrystalline layered stacking at low Cr and loss of long-range layering at higher Cr concentrations, consistent with XRD/RSM. Magnetometry on a 6% film shows soft ferromagnetism at 5 K. XAS and XMCD at the Cr $L_{2,3}$ edges exhibits a depth dependence: total electron yield (TE; surface sensitive) shows both nominal Cr²⁺ and Cr³⁺, whereas fluorescence yield (FY; bulk sensitive) shows a much higher Cr²⁺ weight. Sum rules applied to TEY give $m_L=(0.20\pm 0.04)$${\mu }_{\mathrm{B}}$/Cr, and $m_S=(1.6\pm 0.2)$${\mu }_{\mathrm{B}}$/Cr, whereby we note that the applied maximum field (3 T) likely underestimates $m_S$. These results define a practical growth window and outline key parameters for MTI films. Full article

Thermoelectric (TE) materials represent a critical frontier in sustainable energy conversion technologies, providing direct thermal-to-electrical energy conversion with solid-state reliability. The optimizations of TE performance demand a nuanced comprehension of structure–property relationships across diverse length scales. This review summarizes established and emerging spectroscopic and microscopic techniques used to characterize inorganic and polymer TE materials, specifically poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS). For inorganic TE, ultraviolet–visible (UV–Vis) spectroscopy, energy-dispersive X-ray (EDX) spectroscopy, and X-ray photoelectron spectroscopy (XPS) are widely applied for electronic structure characterization. For phase analysis of inorganic TE materials, Raman spectroscopy (RS), electron energy loss spectroscopy (EELS), and nuclear magnetic resonance (NMR) spectroscopy are utilized. For analyzing the surface morphology and crystalline structure, chemical scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD) are commonly used. For polymer TE materials, ultraviolet−visible–near-infrared (UV−Vis−NIR) spectroscopy and ultraviolet photoelectron spectroscopy (UPS) are generally employed for determining electronic structure. For functional group analysis of polymer TE, attenuated total reflectance–Fourier-transform infrared (ATR−FTIR) spectroscopy and RS are broadly utilized. XPS is used for elemental composition analysis of polymer TE. For the surface morphology of polymer TE, atomic force microscopic (AFM) and SEM are applied. Grazing incidence wide-angle X-ray scattering (GIWAXS) and XRD are employed for analyzing the crystalline structures of polymer TE materials. These techniques elucidate electronic, structural, morphological, and chemical properties, aiding in optimizing TE properties like conductivity, thermal stability, and mechanical strength. This review also suggests future research directions, including in situ methods and machine learning-assisted multi-dimensional spectroscopy to enhance TE performance for applications in electronic devices, energy storage, and solar cells. Full article

Microbiologically Influenced Corrosion (MIC) significantly endangers steel infrastructure, particularly in marine and buried environments, causing considerable economic and environmental damage. Sulphate-reducing bacteria (SRB) are primary supporters of MIC, accelerating iron corrosion through hydrogen sulfide production. Conventional mitigation strategies, including protective coatings and cathodic protection, often face challenges such as limited effectiveness against SRB and the aggressiveness of saltwater corrosion. This study explores a novel approach by directly introducing zinc oxide (ZnO) nanoparticles into the microbial medium to inhibit SRB activity and reduce MIC. Iron metal coupons were immersed in seawater under three conditions: control (seawater only), seawater with SRB, and SRB with ZnO nanoparticles. These coupons were used as electrodes in microbial fuel cells to obtain real-time voltage readings. At the same time, corrosion was evaluated using cyclic voltammetry (CV), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), mass loss, and pH measurements. Results demonstrate that ZnO nanoparticles significantly inhibited SRB growth, as confirmed by the antibiotic susceptibility test (ABST). It was revealed that the corrosion rate increased by 21.3% in the presence of SRB compared to the control, whereas the ZnO-added electrode showed a 21.7% reduction in corrosion rate relative to the control. SEM showed prominent corrosive products on SRB-exposed coupons. ZnO-added coupons exhibited a protective layer with grass-like whisker structures, and EDX results confirmed reduced sulfur and iron sulfide deposits, indicating suppressed SRB metabolic activity. ABST confirmed ZnO’s antimicrobial properties by producing clear inhibition zones. ZnO nanoparticles offer the dual benefits of antimicrobial activity and corrosion resistance by forming protective self-coatings and inhibiting microbial growth, making them a scalable and eco-friendly alternative to traditional corrosion inhibitors. This application can significantly extend the lifespan of iron structures, particularly in environments prone to microbial corrosion, demonstrating the potential of nanomaterials in combating microbiologically influenced corrosion (MIC). Full article

The paradigm shift from FinFET to gate-all-around nanosheet (GAA-NS) transistor architectures necessitates fundamental innovations in channel material engineering. This work addresses the critical challenge of pFET performance degradation in GAA-NS technologies through the development of an advanced selective etching process for strain-engineered SiGe channel formation. We present a systematic investigation of Si selective etching using CF₄/O₂/N₂ gas mixture in a remote plasma source reactor. It is demonstrated that the addition of N₂ to CF₄/O₂ plasmas significantly improves the selectivity of Si to SiGe (up to 58), by promoting NO* radical-induced passivation layer disruption on Si surfaces. Furthermore, an increase in the F:O ratio has been shown to mitigate stress-induced lateral micro-trenching (“Si-tip”), achieving near-zero tip length at high CF₄ flow (500 sccm) while retaining selectivity (>40). Transmission electron microscopy and energy-dispersive X-ray spectroscopy confirm the complete removal of the Si sacrificial layer with minimal SiGe channel loss, validating the process for high-performance SiGe GAA-NS FET integration. These findings provide critical insights into strain-engineered SiGe channel fabrication, enabling balanced NFET/PFET performance in next-generation semiconductor technologies. Full article

The corrosion behavior of open-cell AlSn6Cu-based composites, one reinforced with SiC particles and the other with Al₂O₃ particles, was investigated. The composites were fabricated via liquid-state processing, employing both squeeze casting and the replication method, and they produced in two distinct pore size ranges (800–1000 µm and 1000–1200 µm). Corrosion performance was systematically evaluated through gravimetric (weight loss) measurements and electrochemical techniques, including open-circuit potential monitoring and potentiodynamic polarization tests. Comprehensive microstructural and phase analyses were conducted using X-ray diffraction, energy-dispersive X-ray spectroscopy, and scanning electron microscopy. The results revealed that both reinforcement type and pore architecture have a significant impact on corrosion resistance. Al₂O₃-reinforced composites consistently outperformed their SiC-containing counterparts, and pore enlargement generally improved performance for the unreinforced alloy and the Al₂O₃ composite but not for the SiC composite. Overall, the optimal corrosion resistance is achieved by pairing a coarser-pore architecture (1000–1200 µm) with Al₂O₃ reinforcement, which minimizes both instantaneous (electrochemical) and cumulative (gravimetric) corrosion metrics. This study addresses a gap in current research by providing the first detailed assessment of corrosion in open-cell AlSn6Cu-based composites with controlled pore architectures and different ceramic reinforcements, offering valuable insights for the development of advanced lightweight materials for harsh environments. Full article

The advent of graphene has catalyzed extensive exploration into two-dimensional (2D) materials, among which gallium selenide (GaSe)—a layered semiconductor—stands out for its promise in optoelectronic and nanoscale device applications. To elucidate the intricate correlation between structure and electronic properties, and to enable performance optimization at the atomic scale, we employ advanced characterization methodologies. In this work, atomic-resolution Scanning Transmission Electron Microscopy (STEM) and Electron Energy Loss Spectroscopy (EELS) are utilized to investigate the structural and electronic characteristics of GaSe. STEM imaging confirms the atomic-level uniformity and verifies the β-GaSe phase, while EELS measurements reveal a thickness-dependent, tunable bandgap that decreases from 3.8 eV to 2.4 eV as the crystal thickness increases from approximately 1 nm to 30 nm—a trend attributable to quantum confinement effects. Full article

Background and Objectives: Chairside bleaching can alter enamel morphology and mineral content. This in vitro study compared surface changes and elemental shifts after three in-office protocols using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). Materials and Methods: Forty-two human premolars/molars were sectioned; matched halves served as control or received Opalescence Quick 45% carbamide peroxide (CP), Opalescence Boost 40% hydrogen peroxide (HP), or BlancOne Ultra+ 35% HP with light activation. Gels were applied per manufacturers’ instructions. SEM assessed topography (×500–×1100); EDS quantified atomic percent of O, Ca, P, C and trace elements. One-way ANOVA compared Ca and P between bleached groups (α = 0.05). Results: Controls showed compact surfaces with preserved Ca and P. After Quick, SEM revealed roughness, fissures and microcracks; Ca fell from 11.5 to 12.5 to 9.53–11.73 at% and P from 7.5 to 8.9 to 7.41–8.59 at%. Boost produced mild superficial restructuring and granular deposits with variable Ca 13.80–27.94 at% and P 7.32–14.65 at%. BlancOne Ultra+ caused diffuse erosion and loss of prismatic clarity with marked demineralization (Ca 1.42–7.85 at%, P 1.22–6.71 at%); C rose locally to 46.61 at%. Across bleached groups, Ca and P differed significantly (both p < 0.001). Oxygen remained dominant (~39–50 at%) in all spectra; occasional Al/Si/Cl/K likely reflected residues or preparation artifacts. Conclusions: All protocols produced surface and compositional alterations, with a severity gradient: BlancOne Ultra+ > Boost > Quick. High-concentration, light-activated HP yielded the largest Ca/P losses. Clinically, neutral-pH, non-activated or chemically activated regimens and immediate post-bleach remineralization should ideally be used when feasible, particularly before adhesive procedures. Full article