Search Results (89)

One of the most effective methods of improving the properties of aluminium alloys is grain refining using Al-Ti-B master alloys. In contrast, zirconium is a key alloying element, used mainly in 2xxx and 7xxx series aluminium alloys, where it contributes to dispersion enhancement and reduces the rate of dynamic recrystallisation. However, even trace amounts of zirconium—just a few hundredths of ppm—significantly reduce the performance of Al-Ti-B grain refiners, a phenomenon known as ‘Zr poisoning’. This study investigates the impact of holding time and the level of Al-5Ti-1B addition on the microstructure and properties of an AlMgSi(Cu) alloy containing 0.15 wt.% Zr, cast as 7-inch DC billets. The structure and phase distribution were characterised using optical microscopy (OM), scanning electron microscopy (SEM) with energy-dispersive spectroscopy (EDS), and transmission electron microscopy (TEM). Grain size and morphology were evaluated through macrostructure analysis (etched cross-sections and polarised light microscopy), while chemical and elemental distributions were analysed via SEM-EDS and STEM-EDS mapping. Additionally, Brinell hardness measurements were conducted across the billet diameter to assess the correlation between grain size and mechanical properties. The results show that reducing holding time and increasing the Al-5Ti-1B addition improves grain refinement efficiency despite the presence of Zr. The finest grain structure (150–170 μm) and most homogeneous hardness distribution were achieved when the grain refiner was continuously fed during casting at 80 ppm B. These findings are supported by the literature and contribute to a deeper understanding of the Zr poisoning effect and its mitigation through optimized casting practice. Full article

Designing supramolecular gelators with targeted properties is very difficult and mainly relies on structural modifications of known gelator molecules. However, very often, even minor modifications can result in the complete loss of gelation capabilities. In the present work, we have studied the influence and role of the silver nanoparticles (AgNPs) and trisodium citrate (TSC) additives on the self-assembly process of alanine derivative gelator (C₁₂Ala) and intermolecular interactions resulting in hydrogel systems of enhanced stability and sustainability. The effect of phase separation and diversity of supramolecular microstructures of gelator internal matrix on the composition of the investigated tricomponent system was studied thoroughly with thermal analysis methods (TGA/DSC), high-resolution nuclear magnetic resonance spectroscopy (HR-MAS NMR), and polarising optical microscopy (POM). The molecular mechanism of gelation and the interactions responsible for enhanced properties of nanosilver hydrogels was determined and described, indicating the synergistic role of TSC and AgNPs in the self-assembly process. Full article

Titanium (Ti) alloys are widely used in biomedical applications but face challenges like poor biological activity and corrosion at modular interfaces. Strontium (Sr)-doped micro-arc oxidation (MAO) surfaces are proposed to improve biocompatibility and tribocorrosion resistance. This study examines the electrochemical behaviour of Ti surfaces treated with 0.0013 M and 0.13 M Sr-doped MAO via open circuit potential, potentiodynamic polarisation, and electrochemical impedance spectroscopy in a basic physiological solution at 37 °C. The results indicate that higher Sr concentrations led to lower passivation current densities (more than two times lower than at the lowest Sr concentration) and reduced barrier layer capacitance (more than one and a half times lower than at the lowest Sr concentration), suggesting improved corrosion resistance for Sr-enriched MAO treatments on Ti implants. Full article

Paint loss is one of the main forms of deterioration in historical wall paintings, generally restored by the application of chromatic reintegration. In the specific case of outdoor exposed paintings, it is essential to find a binder that will withstand diverse weather conditions. Since chromatic reintegrations have to be compatible with the original painting, fresco paint mock-ups were manufactured and compared to chromatic reintegrations made with an aqueous colloidal dispersion of silica nanoparticles as binder. The physical compatibility was studied by colour spectrophotometry and measurements of static contact angle, gloss, and roughness values, together with a peeling test, stereomicroscopy, and polarised light microscopy. They were also characterised from a mineralogical, chemical, and molecular point of view using X-ray diffraction, X-ray fluorescence and Fourier-transform infrared spectroscopy. The microtexture was studied by scanning electron microscopy with energy-dispersive X-ray spectroscopy. Chromatic reintegrations showed similar roughness and lower gloss values than frescoes, and the nano-silica binder ensured the natural breathability of the wall. Overall, the chemical nature of pigments was highly influential. The reintegrations with silicate-based pigments were more homogenous, with hardly any fissures, while those carried out with sulphide- or oxide-based pigments were severely cracked. The use of verdigris is discouraged due to the lack of affinity between the binder and the pigment. Full article

The present study investigates the effect of different concentrations of Na₂WO₄ and graphene oxide dispersed composite additives on the structure and corrosion resistance of 6063 aluminum alloy micro-arc oxidation (MAO) coatings in a silicate electrolyte. The characterisation of the microstructure, cross-sectional morphology, elemental distribution, and phase composition of the films was conducted utilising scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and X-ray diffraction (XRD). The corrosion resistance of the films was tested by prolonged immersion for 24 h, 72 h, 168 h, and 240 h, with measurement of kinetic potential polarisation curves and impedance modulus in a 3.5 wt.% NaCl solution. The densification of the films was enhanced with increasing mass concentration of Na₂WO₄ and dispersed graphene oxide in the electrolyte, and the thickness initially increased and then decreased. The film containing 6 g of Na₂WO₄ and 10 mL of graphene oxide dispersion (G10-6) exhibited optimal densification and thickness, with an I_corr value of 3.01 × 10⁻⁶ A·cm⁻² and a low-frequency impedance film value of 10⁸ Ω·cm², thereby demonstrating the most advanced corrosion resistance among the films. The densification and corrosion resistance of the films were enhanced by the incorporation of Na₂WO₄ and graphene oxide dispersion into the alkaline electrolyte. Full article

The nanosecond pulsed fibre laser (NsPFL) treatment is extensively employed to distinguish hospital surgical instruments (micro-surgical forceps, surgical blades, orthopaedic drills, and high-precision laparoscopic tools), which are generally composed of stainless steel. Nevertheless, if the laser parameters are not properly optimised, this process may unintentionally provoke corrosion. Maintaining the structural integrity of these materials is essential for ensuring patient safety and minimising long-term costs. This work aims to optimise the laser scanning parameters for marking 316L stainless steel (316L SS), seeking to improve its corrosion resistance. The corrosion behaviour was assessed by using open circuit potential (OCP), potentiodynamic polarisation curves (PPc), and electrochemical impedance spectroscopy (EIS) techniques, conducted in 0.9% wt NaCl solution at a controlled temperature of 25 ± 1 °C. A comprehensive study employing optical profilometry has significantly enhanced our understanding of the corrosion micromechanisms of 316L SS, comparing specimens both with and without NsPFL treatment. Considering applications involving environments rich in chloride ions, the results indicated that the NsPFL-316L SS samples demonstrated markedly enhanced performance compared to the untreated base material after 48 h of immersion in 0.9% wt NaCl solution. This improvement is particularly noteworthy given the widespread utilisation of 316L SS in the manufacturing of surgical instruments, where corrosion resistance is of paramount importance. Full article

The microstructure evolution of Al_0.3FeCoNiCr_x (x = 0, 0.3, 0.5, 1, 1.5) high-entropy alloys (HEAs) were studied using X-Ray diffraction technique and scanning electron microscope equipped with energy dispersive spectrometer. The short-term and long-term corrosion behaviours of these alloys in 3.5 wt.% NaCl solution were studied by electrochemical impedance spectroscopy, potentiodynamic polarisation measurement, immersion test and corrosion morphology analysis. The results show that all the designed HEAs present single-phase FCC structure, and the increase in Cr content changes the microstructural morphology from cellular to a typical dendritic–interdendritic state. Without the influence of phase transformation, the corrosion resistance of Al_0.3FeCoNiCr_x HEAs gradually increases with the increase in Cr content. Our designed alloys exhibit excellent corrosion resistance compared to the existing HEAs in the AlFeCoNiCr composition system. Full article

Commercially available 316L (1.4404) stainless steel is commonly used for industrial filtration due to its combination of good material properties, particularly its corrosion resistance, which is a critical factor for filters in corrosive (e.g., saltwater) environments. Recently, laser powder bed fusion (LPBF) has enabled new more complex and efficient filtration pieces to be manufactured from this material. However, it is critical to know how the corrosion resistance is affected by this manufacturing strategy. Here, the corrosion resistance of LPBF manufactured 316L stainless steel is compared with wrought 316L sheet. The corrosion of the samples in saltwater was assessed with asymmetric electrochemical noise, potentiodynamic polarisation curve, and electrochemical impedance spectroscopy. The samples before and after corrosion were examined with scanning electron microscopy and energy-dispersive spectroscopy. The LPBF samples had higher corrosion resistance than the sheet samples and were more noble. The corrosion resistance of the LPBF sample increased with time, while the wrought sample corrosion resistance reduced over time. The corrosion mechanism of both samples was stable with time, formed of a passive film process and a bared material process. This paper presents the first study about the temporal evolution of the LPBF 316L stainless steel corrosion mechanism. Full article

This paper summarises the research carried out so far on barniz de Pasto objects from the Victoria and Albert Museum (V&A) and outlines future areas of development for our collection of Indigenous lacquer from Latin America. The V&A was the first UK public institution to identify objects decorated with barniz de Pasto within its collection. Two of these were acquired in 2015 and 2018; others had entered the collection between 1855 and 1902 but were recognised as barniz de Pasto only after 2018. The acquisition in 2015 of a cabinet marked the start of a research campaign to understand the materiality and context of all the museum’s barniz de Pasto objects. The analytical techniques used included X-radiography, polarised light microscopy and digital microscopy, Raman microscopy, X-ray fluorescence (point and scanning), chromatography (py-GC–MS and LC–DAD–MS), Fourier transform infrared spectroscopy, X-ray diffraction, and X-ray micro-computed tomography. Unexpected discoveries were made along the way, including the characterisation and documentation of mercury white (mercury(I) chloride, or calomel) used as a white pigment, a world first. Gel-based cleaning methods were used to remove a non-original, discoloured, natural varnish covering nearly the entire surface of one of the objects, and the recent overpaint on its lid, revealing original surfaces which had been repaired and drastically repainted in the second half of the twentieth century. Full article

With the increasing focus on decarbonisation of the transport sector, it is imperative to consider routes to electrify vehicles beyond those achievable using lithium-ion battery technology. These include heavy goods vehicles and aerospace applications that require propulsion systems that can provide gravimetric energy densities, which are more likely to be delivered by fuel cell systems. While the discussion of light-duty vehicles is abundant in the literature, heavy goods vehicles are under-represented. This paper presents an overview of the electrochemical degradation of a proton exchange membrane fuel cell integrated into a simulated Class 8 heavy goods range-extender fuel cell hybrid electric vehicle operating in urban driving conditions. Electrochemical degradation data such as polarisation curves, cyclic voltammetry values, linear sweep voltammetry values, and electrochemical impedance spectroscopy values were collected and analysed to understand the expected degradation modes in this application. In this application, the proton exchange membrane fuel cell stack power was designed to remain constant to fulfil the mission requirements, with dynamic and peak power demands managed by lithium-ion batteries, which were incorporated into the hybridised powertrain. A single fuel cell or battery cell can either be operated at maximum or nominal power demand, allowing four operational scenarios: maximum fuel cell maximum battery, maximum fuel cell nominal battery, nominal fuel cell maximum battery, and nominal fuel cell nominal battery. Operating scenarios with maximum fuel cell operating power experienced more severe degradation after endurance testing than nominal operating power. A comparison of electrochemical degradation between these operating scenarios was analysed and discussed. By exploring the degradation effects in proton exchange membrane fuel cells, this paper offers insights that will be useful in improving the long-term performance and durability of proton exchange membrane fuel cells in heavy-duty vehicle applications and the design of hybridised powertrains. Full article

This paper investigates the oil on canvas painting Boat scene (1974) by Liu Kang (1911–2004), belonging to the National Gallery Singapore (NGS). The focus is on disfiguring paint protrusions in a specific area and colour in the composition. Moreover, in search of the possible factors responsible for the creation of the protrusions, the structure and composition of the paint layers were determined. Three possible reasons were put forward to explain this phenomenon: deliberate textural effects, the expansion of metal soaps and unintentional paint contamination during the artistic process. Investigative techniques such as technical photography, digital microscopy, optical microscopy (OM), polarised light microscopy (PLM), field emission scanning electron microscope (FE-SEM-EDS) and attenuated total reflectance micro-Fourier transform infrared spectroscopy (ATR μ-FTIR) were employed to analyse paint layers, including protrusion samples. The analyses revealed that the protrusions resulted from an unintentional contamination of the oil paint during the artistic process by dry fragments of different pigment mixtures bound in drying oil. Zinc soaps were found in significant concentrations within the protrusions and other parts of the painted scene. Nevertheless, the metal soaps do not pose a direct risk to the integrity of the paint layers at the time of this research. The analyses highlight the potential challenges caused by the protrusions that conservators may face while caring for the painting. The research contributes to our ongoing comprehension of the artist’s working process. Full article

Background: This study aims to evaluate the percutaneous permeation profiles of caffeic acid (CA) from the cubic and hexagonal liquid crystalline phases of Pluronic P123/water mixtures. Method: The resulting drug-loaded mesophases were subjected to characterisation through deuterium nuclear magnetic resonance spectroscopy and polarised optical microscopy observations. These analyses aimed to evaluate the structural changes that occurred in the mesophases loading with CA. Additionally, steady and dynamic rheology studies were conducted to further explore their mechanical properties and correlate them to the supramolecular structure. Finally, CA release experiments were carried out at two different temperatures to examine the behaviour of the structured systems in a physiological or hyperthermic state. Results: As the concentration of the polymer increases, an increase in the viscosity of the gel is noted; however, the addition of caffeic acid increases microstructure fluidity. It is observed that the temperature effect conforms to expectations. The increase in temperature causes a decrease in viscosity and, consequently, an increase in the rate of permeation of caffeic acid. Conclusions: The CA permeation profile from the prepared formulations is mostly dependent on the structural organisation and temperature. Cubic mesophase LLC 30/CA showed greater skin permeation with good accumulation in the skin at both tested temperatures. Full article

With increasing demand for Li-ion batteries, studies are focusing on enhancing battery performance and safety. However, studies on battery cases remain scarce. Herein, we propose the use of super duplex stainless steel SAF2507, which is a two-phase (austenite + ferrite) steel, for battery casings. Unlike conventional AISI304, SAF2507 maintains its corrosion resistance and strength at high temperatures and precipitates a secondary phase at approximately 975 °C. However, the effects of Ni plating on this secondary phase are not well documented. Therefore, the electroless Ni plating of SAF2507 after secondary-phase precipitation was studied. Briefly, heat treatment at 1000 °C was used to induce precipitation, and the electroless Ni plating behaviour over varying plating periods was analysed using open-circuit potential, potentiodynamic polarisation, and electrochemical impedance spectroscopy measurements. The plating state and corrosion behaviour were examined using scanning electron microscopy. Heat-treated SAF2507 steel with a secondary phase exhibited excellent electroless Ni plating behaviour, which enhances the safety and durability of Li-ion batteries. Furthermore, uniform plating and electrochemical behaviour were achieved after 180 s, suggesting that SAF2507 is superior to AISI304. These findings contribute to the development of safer and more efficient batteries and address the growing demand for Li-ion battery case materials. Full article

Carbon steel is subjected to several pretreatments to enable its use in highly corrosive environments, such as marine structures. However, its surface treatment is problematic owing to various processes, and these problems can be solved by replacing it with super duplex stainless steel (SDSS), which exhibits remarkable strength and corrosion resistance owing to its austenite and ferrite phases. EN 1.4410 and EN 1.4501 are the most extensively used SDSS grades in marine structures, as they exhibit exceptional strength and corrosion resistance in seawater. This study subjected EN 1.4410 and EN 1.4501 samples to specific heat treatment after casting and observed their structural alterations through field emission scanning electron microscopy. Their passivation states, with or without the Cu and W layers, were determined by examining their corrosion properties through open-circuit potential measurements, electrostatic polarisation tests, electrochemical impedance spectroscopy (EIS), and critical pitting temperature (CPT) analysis. The inclusion of Cu significantly improved the uniform corrosion resistance within the passivation layers, whereas the addition of W enhanced the pitting resistance (E_pit, CPT). Additionally, the EIS analysis confirmed a double-layer structure in the passivation layer of EN 1.4501. Moreover, Cu did not act as a strengthening element of the passivation layer, whereas W significantly reinforced it. Full article

Ancient Ardaxšīr Khwarrah, today known as Shahr-e Gur, situated near the modern town of Firuzabad in Fars, Iran, holds historical significance as the inaugural capital city of the Sasanian Empire. During archaeological excavations conducted in 2005 by an Iranian–German team directed by Mas‘oud Azarnoush and Dietrich Huff, a mud-brick complex was uncovered, revealing a remarkably well-preserved stretch of wall painting and a polychrome painted floor. The discovery prompted the hypothesis of a potential funerary context dating back to the Sasanian period. Both the wall painting and painted floor have suffered extensive deterioration attributed to the environmental conditions of the archaeological site, which was inscribed on the UNESCO World Heritage List in 2020. To address the urgent need for preservation and further understanding of the site’s artistic and structural elements, an emergency diagnostic project was initiated. Non-invasive investigations were carried out on the wall and floor by optical digital microscopy and portable energy-dispersive X-ray fluorescence. Additionally, representative minute samples underwent analysis through various techniques, including micro-X-ray fluorescence, polarised light microscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy, micro-Raman spectroscopy, micro-Fourier Transform Infrared Spectroscopy, gas chromatography-mass spectrometry and pyrolysis coupled with gas chromatography-mass spectrometry. The palette of the floor and mural paintings were identified to contain red and yellow ochres, lead-based pigments, carbon black and bone white. The unexpected presence of Egyptian blue mixed with green earth was recognised in the green hues of the wall painting. The detection of protein material in both the wall painting and polychrome floor indicates the use of “a secco” technique, thereby shedding light on the artistic practices employed in Ardaxšīr Khwarrah. Full article