Search Results (493)

Corrosion in maritime ballast tanks is a major driver of maintenance costs and operational risks for maritime assets. Inspections are hampered by complex geometries, hazardous conditions, and the limitations of conventional methods, particularly visual assessment, which struggles with subjectivity, accessibility, and early detection, especially under coatings. This paper critically examines these challenges and explores the potential of Light Detection and Ranging (LiDAR) and Hyperspectral Imaging (HSI) to form the basis of improved inspection approaches. We discuss LiDAR’s utility for accurate 3D mapping and providing a spatial framework and HSI’s potential for objective material identification and surface characterization based on spectral signatures along a wavelength range of 400-1000nm (visible and near infrared). Preliminary findings from laboratory tests are presented, demonstrating the basic feasibility of HSI for differentiating surface conditions (corrosion, coatings, bare metal) and relative coating thickness, alongside LiDAR’s capability for detailed geometric capture. Although these results do not represent a deployable system, they highlight how LiDAR and HSI could address key limitations of current practices and suggest promising directions for future research into integrated sensor-based corrosion assessment strategies. Full article

Superhydrophobic coatings possess distinct wettability characteristics and hold significant potential in metal corrosion protection and underwater drag reduction. However, their practical application is often hindered by poor durability arising from the fragility of their micro/nanostructured surface roughness. In this study, a durable superhydrophobic coating featuring a hierarchical, hydrangea-like micro/nanostructure was successfully fabricated on an aluminum alloy substrate via a simple one-step cold-spraying technique. The coating consisted of hydrangea-shaped SiO₂ nanoparticles modified with 1H,1H,2H,2H-perfluorodecyltrimethoxysilane (PFDT) to produce multiscale roughness, while epoxy resin (EP) served as the binding matrix to enhance mechanical integrity. The hydrangea-like SiO₂ nanostructures were characterized by solid cores and wrinkled, petal-like outgrowths. This unique morphology not only increased the surface roughness but also provided more active sites for air entrapment, thereby enhancing the coating’s overall performance. The h-SiO₂@PFDT-EP composite coating exhibited excellent superhydrophobicity, with a WCA of 170.1° ± 0.8° and a SA of 2.7° ± 0.5°. Durability was evaluated through sandpaper abrasion, tape peeling, acid and alkali immersion, artificial weathering, and salt spray tests. The results demonstrated that the coating retained stable superhydrophobic performance under various environmental stresses. Compared with bare 6061 aluminum and EP coatings, its corrosion current density was reduced by four and three orders of magnitude, respectively. Furthermore, the coating achieved a maximum drag-reduction rate of 31.01% within a velocity range of 1.31–7.86 m/s. The coating also displayed excellent self-cleaning properties. Owing to its outstanding durability, corrosion resistance, and drag-reducing capability, this one-step fabricated superhydrophobic coating showed great promise for applications in marine engineering and defense. Full article

We studied the adsorption thermodynamics and mechanism behind the binding of nitric oxide (NO) in the interior surfaces and structural fragments of the high metal center density microporous Metal-Organic Framework (MOF) CPO-27-Cu, by gas sorption, at a series of temperatures. For the purpose of comparison, we also measured the corresponding CO₂ adsorption isotherms, and as a result, the isosteric heats of adsorption for the two studied adsorptives were derived, being in the range of 12–15 kJ/mol for NO at loadings up to 0.5 NO molecules per formula unit (f.u.) of the bare compound (C₄O₃HCu), and 23–25 kJ/mol CO₂ in the range 0–1 CO₂ per f.u. Microscopically, the mode of NO binding near the square pyramid Cu(II) centers was directly accessed with the use of in situ NO gas adsorption X-ray Absorption Spectroscopy (XAS). Additionally, during the vacuum/temperature activation of the material and consequent NO adsorption, the electronic state of the Cu-species was monitored by observing the corresponding X-ray Near Edge Spectra (XANES). Contrary to the previously anticipated chemisorption mechanism for NO binding at Cu(II) species, we found that at slightly elevated temperatures, under ambient, but also cryogenic conditions, only relatively weak physisorption takes place, with no evidence for a particular adsorption preference to the coordinatively unsaturated Cu-centers of the material. Full article

A fiber Bragg grating (FBG)-based ocean temperature and depth sensor structure is proposed. The pressure sensing section employs a secondary sensitization design comprising a piston and the polycarbonate buffer, while the temperature sensing section utilizes an FBG encapsulated within a metal silver tube, accompanied by a temperature compensation structure. Simulation analyses verify the enhanced sensitivity of the proposed configuration. By selecting suitable materials for the piston, metal tube, and polymer, and optimizing the dimensions of key components, the sensitivity of the bare FBG sensor is significantly improved through the combined effects of the piston, polymer, and metal tube. After optimization, the sensor exhibits a pressure sensitivity of 1.33 nm/MPa and a temperature sensitivity of 102.77 pm/°C, meeting the high-precision detection requirements for ocean temperature and depth sensing. The experimental results show that the temperature sensitivity is 109.9 pm/°C within the temperature range of −5~35 °C, and that the pressure sensitivity is 1.63 nm/MPa within the pressure range of 1~10 MPa. These results confirm that the sensor is well-suited for high-precision ocean temperature and depth measurements. Full article

Hypochlorous acid solutions are used as effective disinfectants in many settings, including operating rooms and other hospital environments. During and after the COVID-19 pandemic, their use increased significantly, and this work stems from that development. In fact, despite their undoubtedly excellent properties, these solutions can constitute a very aggressive system for a variety of different materials that are very common in those environments. Materials that can be subject to corrosion include steels, copper-based alloys, and components in electronic devices. This work aims to investigate the responses of these materials to long but intermittent exposures to HClO disinfectant solutions. It consists of a compatibility test, performed on several reference materials with HClO used as a surface disinfectant, connected with NaCl’s eventual presence/deposition over them. To perform the investigations in a manner consistent with the duration of compatible laboratory analyses, the samples were immersed in electrolytically prepared HClO solutions for 750 h, which is a duration considered equivalent to normal exposure to disinfectant aerosols over 3 years. Analyzing the large amount of experimental data gathered yielded interesting results. Where the exposure of non-metallic materials or steel did not lead to compatibility issues, bare metals showed degradation due to salt deposition. This article summarizes the morphological studies, i.e., a huge experimental work conducted at the ENEA IMPACT lab in Bologna and part of the PhD work of the corresponding author. Full article

Herein, we report on the synthesis of Ni and Zn clusters on the surface of TiO₂ as well as their bimetallic NiZn analogs. The materials were prepared by incipient wet impregnation of colloidal TiO₂ followed by microwave (MW) irradiation to graft the clusters to TiO₂ surface. The materials were further immobilized onto glass slides and exhibited high surface area, high mechanical stability, and porosity with accessible pores. The main species responsible for visible light degradation of microcystin LR via the interface charge transfer (IFCT) of excited e⁻ to surface metal clusters were found to be O₂^•− and h⁺. The optimal nominal grafting concentration was 0.5 wt.% for Ni and 1.0 wt.% for Zn, while for the bimetal modification (NiZn), the optimal nominal concentration was 0.5 wt.%. Compared to monometallic, bimetallic grafting showed a lower kinetic constant, albeit still improved compared to bare TiO₂. Bimetal-modified titania showed a lower photocurrent compared to single metal-grafted TiO₂ and poorer interfacial charge transport, namely, more recombination sites—possibly at the interface between the Ni and Zn domains. This work highlights the efficiency of using MW irradiation for grafting sub-nano-sized metallic species to TiO₂ in a homogeneous way. However, further strategies using MW irradiation for the structural design of bimetallic cocatalysts can be implemented in the future. Full article

Magnesium as a biodegradable metal implant has garnered attention. Nevertheless, its rapid degradation rate and insufficient osseointegration restrict its clinical applications. In order to enhance the corrosion resistance and bioactivity of magnesium alloys, superhydrophobic hydroxyapatite (HA) layers were synthesized on micro-arc oxidized (MAO)-treated AZ31B magnesium alloy through liquid-phase deposition. This study examined the surface morphology, phase composition, bonding strength, wettability, electrochemical properties, and in vitro mineralization of the synthesized coatings. The study results demonstrated that the improved corrosion resistance of composite coatings in Hank’s solution is due to the formation of a protective HA layer. The inclusion of the MAO coating significantly enhances the bonding strength between the hydroxyapatite (HA) layer and the bare magnesium alloy. The concentration of NaH₂PO₄ affects both the microstructure and wettability. The composite coating exhibited excellent osseointegration capabilities, with new HA layers observed after immersing the samples in simulated body fluid (SBF) solution for three days. These findings suggest that the combination of MAO and solution treatment presents a promising method for enhancing biocompatibility and reducing magnesium degradation, thus making it a viable option for biodegradable implant applications. Full article

The development of bioactive coatings for metallic implants is essential to enhance osseointegration and improve implant longevity. In this study, composite thin films based on bioactive glass and melittin were synthesized using the matrix-assisted pulsed laser evaporation technique and deposited onto titanium substrates. The coatings were characterized using physicochemical analysis methods, including scanning electron microscopy, atomic force microscopy, contact angle measurements, Fourier transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, and electrochemical impedance spectroscopy. Simulated body fluid immersion tests were also conducted to assess bioactivity over time. Scanning electron microscopy and atomic force microscopy revealed dense, irregular surface textures with nanoscale features and an average roughness of ~120 nm, favorable for cell adhesion. Contact angle measurements showed a significant shift from hydrophobic (~95° for bare titanium) to moderately hydrophilic (~62° for the bioglass and melittin coating) surfaces, indicating improved biocompatibility. Electrochemical impedance spectroscopy demonstrated enhanced corrosion resistance in simulated body fluid, with the coating exhibiting a ~45% decrease in impedance magnitude after 12 h of immersion, compared to only 4% for bare titanium. Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy analyses confirmed the progressive formation of a carbonated apatite layer after 7 days of simulated body fluid exposure, suggesting high bioactivity and osteoconductive potential. The combined effects of bioactive glass and melittin in the thin film structure offer promising applications in orthopedic and dental implants, enhancing both biological performance and structural integrity. Full article

Multifunctional reinforced polymer composites provide an ideal platform for next-generation smart materials applications, enhancing matrix properties like electrical and thermal conductivity. Reinforcements are usually based on functional metal alloys, inorganic compounds, polymers, and carbon nanomaterials. The latter have drawn significant interest in developing high-performance smart composites due to their exceptional mechanical, electrical, and thermal properties. The increasing demand for highly complex functional structures has led additive manufacturing to become a reference technology for the production of smart material components. In this study, laser sintering technology was adopted to manufacture nano-graphite/nylon-12 composites with a carbon-based particle reinforcement content of up to 10% in weight. The results showed that the addition of the filler led to the fabrication of samples that reached an electrical conductivity of around 4·10⁻⁴ S/cm, in contrast to the insulating behavior of a bare polymeric matrix (i.e., lower than 10⁻¹⁰ S/cm), while maintaining a low production cost, though at the expense of mechanical performance under both tensile and bending loads. Full article

Electrocatalytic nitrate reduction reaction (NO₃⁻RR) to ammonia (NH₃) presents an alternative, sustainable approach to ammonia production. However, the existing catalysts suffer from poor NH₃ yield under lower concentrations of NO₃⁻, and the kinetic understanding of bimetal catalysis is lacking. In this study, a Co₃O₄–modified Cu₂₊₁O nanowire (CoCuNWs) catalyst with a high specific surface area was synthesized to effectively produce NH₃ from a 10 mM KNO₃ basic solution. CoCuNWs demonstrated a high NH₃ yield rate of 0.30 mmol h⁻¹ cm⁻² with an NH₃ Faradaic efficiency (FE) of 96.7% at −0.2 V vs. RHE, which is 1.5 times higher than the bare Cu₂₊₁O NWs. The synergistic effect between Co₃O₄ and Cu₂₊₁O significantly enhanced both the nitrate conversion and ammonia yield. Importantly, it is revealed that the surface of CoCuNWs is kinetically more easily saturated with NO₃⁻ (NO₂⁻) ions than that of Cu₂₊₁O NWs, as evidenced by both the higher current density and the plateau occurring at higher NO_x⁻ concentrations. In addition, CoCuNWs exhibit a higher diffusion coefficient of NO₃⁻, being 1.6 times higher than that of Cu₂₊₁O NWs, which also indicates that the presence of Co₃O₄ could promote the diffusion and adsorption of NO₃⁻ on CoCuNWs. Moreover, the ATR–SEIRAS analysis was applied to illustrate the reduction pathway of NO₃⁻ to NH₃ on CoCuNWs, which follows the formation of the key intermediate from *NO₂⁻, *NO, *NH₂OH to *NH₃. This work presents a strategy for constructing dual–metal catalysts for NO₃⁻RR and provides an insight to understand the catalysis from the perspective of the kinetics. Full article

This study presents a comparative analysis of gold nanoparticles electrodeposited on different two-dimensional materials used as electrode substrates, graphene (Gr) and MoS₂, or co-deposited with the metallic material MoS₂. The morphological and electrochemical data demonstrate the efficiency of the electrodeposition process and the preferability of gold nanoparticles for certain attachment sites depending on the nature of the material used as a substrate and the deposition method used. The electrocatalytic activity of the gold nanoparticles obtained in these configurations was evaluated via the oxidation of nitrite ions (NO₂⁻), using both qualitative and quantitative approaches, by cyclic voltammetry and amperometry techniques. The electrocatalytic activity of gold nanoparticles co-deposited with MoS₂ is superior compared to that of gold nanoparticles deposited either on bare gold electrodes or on 2D materials (graphene and MoS₂), showing good performance with a specific sensitivity of 1.043 μA µM⁻¹ cm⁻² on the linear range of 0.5–600 µM nitrite, with a limit of detection of 0.16 µM and good anti-interference ability. Full article

Background/Objectives: We sought to confirm the performance and safety of the Pantera Lux paclitaxel-coated balloon (pDCB) when used as per the instructions for use at a single high-volume center. Methods: In this retrospective analysis, 386 consecutive patients were categorized into three groups: the treatment of drug-eluting stent in-stent restenosis (DES-ISR) lesions (n = 191), bare-metal stent in-stent restenosis (BMS-ISR) lesions (n = 127), and de novo lesions (n = 68). The primary endpoint at 12 months was target-lesion revascularization (TLR). Secondary endpoints were device success, target-vessel myocardial infarction (TV-MI), and cardiac death. Results: The baseline characteristics were balanced between the groups, with a median age of 71.3 years, 25% being female, 32% being diabetic. The majority presented with chronic coronary syndrome (82.9%). Type C lesions were more often observed in the DES-IRS group as compared with the BMS-IRS and de novo groups (15.6% vs. 7.9% vs. 7.4%, p < 0.001). Cutting balloons were more often used in the DES-IRS group (41.0% vs. 19.7% vs. 1.5%, p < 0.001). The residual stenosis rate was 7.6% vs. 3.3% vs. 7.3% (p = 0.002). The TLR at 12 months was 8.9% vs. 2.4% vs. 1.5% (p = 0.013). Device success was achieved in 98.8% vs. 98.5% vs. 100% of cases (p = 0.8). TV-MI occurred in 3.2% vs. 0.8% vs. 1.5% (p = 0.5) and cardiac death in 2.6% vs. 0.0% vs. 2.9% (p = 0.13) in DES-IRS vs. BMS-IRS vs. de novo lesions. Conclusions: In this single-center observation, we confirmed the safety and efficacy of the Pantera Lux paclitaxel-coated balloon for the treatment of DES-IRS, BMS-IRS, and de novo lesions with low TLR rates at 12 months. Full article

Nanoplasmonic structures have emerged as a promising approach to address light trapping limitations in thin-film optoelectronic devices. This study investigates the integration of metallic nanoparticle arrays onto nanocrystalline silicon (nc-Si:H) thin films to enhance optical absorption through plasmonic effects. Using finite-difference time-domain (FDTD) simulations, we systematically optimize key design parameters, including nanoparticle geometry, spacing, metal type (Ag and Al), dielectric spacer material, and absorber layer thickness. The results show that localized surface plasmon resonances (LSPRs) significantly amplify near-field intensities, improve forward scattering, and facilitate coupling into waveguide modes within the active layer. These effects lead to a measurable increase in integrated quantum efficiency, with absorption improvements reaching up to 30% compared to bare nc-Si:H films. The findings establish a reliable design framework for engineering nanoplasmonic architectures that can be applied to enhance performance in photovoltaic devices, photodetectors, and other optoelectronic systems. Full article

Electrochemical reduction is a promising strategy for the dechlorination of halogenated organic compounds, offering advantages such as enhanced electron transfer efficiency and increased hydrogen atom concentration. It has garnered significant attention for application in mitigating halogenated disinfection by-products (DBPs) in drinking water, owing to its high efficiency and simple operation. In this study, trichloroacetic acid (TCAA), a representative DBP, was selected as the target contaminant. A novel composite cathode comprising a metal–organic framework MIL-53(Fe)@C supported on an Nd magnet (MIL-53(Fe)@C-MAG) and its dechlorination performance for TCAA were systematically investigated. The innovative aspect of this study is the magnetic attachment of the MOF catalyst to the carbonized cathode surface treated through carbonization, which fundamentally differs from conventional solvent-based adhesion methods. Compared to the bare electrode, the MIL-53(Fe)@C-MAG achieved a TCAA removal efficiency exceeding 96.03% within 8 h of contact time. The structural characterization revealed that the α-Fe⁰ crystalline phase serves as the primary active center within the MIL-53(Fe)@C catalyst, facilitating efficient electron transfer and TCAA degradation. The scavenger experiments revealed that TCAA reduction involves a dual pathway: direct electron transfer and atomic hydrogen generation. The modified MIL-53(Fe)@C-MAG electrode exhibited robust electrolytic performance over a broad pH range of 3–7, with TCAA removal efficiency showing a positive correlation with current density within the range of 10–50 mA/cm². Furthermore, the electrode maintained exceptional stability, retaining more than 90% removal efficiency after five consecutive operational cycles. The versatility of the system was further validated by the rapid and efficient dechlorination of various chlorinated DBPs, demonstrating the broad applicability of the electrode. The innovative magnetic composite electrode demonstrates a significant advancement in electrochemical dechlorination technology, offering a reliable and efficient solution for the purification of drinking water contaminated with diverse halogenated DBPs. These results provide valuable insights into the development of electrolysis for dechlorination in water treatment applications. Full article

In this study, we highlight the use of the alkaline earth metal barium (Ba) for the impregnation of Ag₃PO₄ (AgP). AgP was synthesized via co-precipitation and subsequently impregnated with a Ba²⁺-containing solution, followed by hydrothermal treatment to obtain Ba-AgP. The addition of barium significantly influenced both the crystallinity and crystallite size. Ba impregnation enhanced the crystallinity of AgP and promoted the growth of its crystallites. It was confirmed that Ba²⁺ was homogeneously distributed on the surface of AgP, with only a slight effect on particle shape. Ba-impregnated Ag₃PO₄ (Ba-AgP) exhibited improved photocatalytic activity for the degradation of methyl orange (MO) under visible light compared to bare AgP. The optimal impregnation concentration of Ba²⁺ was determined to be 6%. This enhancement is attributed to the role of Ba²⁺ in facilitating the separation of photogenerated electron–hole pairs, which also contributed to the improved stability of AgP. The active species h⁺, ·OH, and O₂·⁻ were all identified as essential for the MO degradation process, with h⁺ being the most significant contributor. Full article