Search Results (85)

This study focuses on the nameplate of Vila D. Bosco, a modern building in Macau from the time of Portuguese rule, and looks at the types of metal materials and surface coatings used, as well as how they corrode due to the tropical marine climate affecting the building’s metal parts. The study uses different techniques, such as X-ray fluorescence spectroscopy (XRF), scanning electron microscopy/energy dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), attenuated total internal reflectance Fourier transform infrared spectroscopy (ATR-FTIR), and cross-sectional microscopic analysis, to carefully look at the metal, corrosion products, and coating of the nameplate. The results show that (1) the nameplate matrix is a resulfurized steel with a high sulfur content (Fe up to 97.3% and S up to 1.98%), and the sulfur element is evenly distributed inside, which is one of the internal factors that induce corrosion. (2) Rust is composed of polycrystalline iron oxides such as goethite (α-FeOOH), hematite (α-Fe₂O₃), and magnetite (Fe₃O₄) and has typical characteristics of atmospheric oxidation. (3) The white and yellow-green coatings on the nameplate are oil-modified alkyd resin paints, and the color pigments are TiO₂, PbCrO₄, etc. The surface layer of the letters is protected by a polyvinyl alcohol layer. The paint application process leads to differences in the thickness of the paint in different regions, which directly affects the anti-rust performance. The study reveals the deterioration mechanism of resulfurized steel components in a subtropical polluted environment and puts forward repair suggestions that consider both material compatibility and reversibility, providing a reference for the protection practice of modern and contemporary architectural metal heritage in Macau and even in similar geographical environments. Full article

A facile low temperature hydrothermal-calcination approach was developed for the fabrication of β-FeOOH nanorods (NRs) and hollow-structure α-Fe₂O₃ magnetic nanorods (MNRs), and the products were characterized using SEM, TEM, XRD and VSM techniques. To achieve smaller-sized β-FeOOH NRs, the effects of Fe³⁺ concentration, the volume ratio of ethanol to water in solution, hydrothermal temperature, and hydrothermal time on the structure of the precursors were systematically investigated, and the nanorods with an average length 104 nm and diameter 36 nm were fabricated at hydrothermal temperature of 100 °C for 2 h using 0.15 M ferric chloride hexahydrate in 50% ethanol solution. Subsequently, the hollow-structure α-Fe₂O₃ MNRs with an average length of 67 nm, diameter of 20 nm, and thickness of 5 nm were successfully obtained via the calcination process at 400 °C for 2.5 h for versatile applications. Full article

A hydrothermal and combustion-reduction process with polyvinyl pyrrolidone (PVP) as a restricted growth agent and galactose as a reducing agent was developed for the fabrication of rod-like α-Fe₂O₃/Fe₃O₄ magnetic nanocomposites (MNCs). Firstly, β-FeOOH nanorods (NRs) were fabricated by the hydrothermal method, with PVP as a restricted growth agent. To obtain a smaller size for better applications in the biomedical field, the concentrations of FeCl₃ and PVP, the hydrothermal temperature, and the hydrothermal time were optimized as 0.171 M, 0.163 mM, 100 °C, and 8 h, and the fabricated β-FeOOH NRs were 193.1 nm in average length and 43.2 nm in average diameter. Then, with β-FeOOH NRs as precursors, α-Fe₂O₃/Fe₃O₄ MNCs were prepared via the combustion-reduction process with galactose as a reducing agent; the factors of the calcination temperature and time and the mass ratio of β-FeOOH and galactose were assessed as 300 °C, 0.5 h, and 1:2, respectively. The prepared α-Fe₂O₃/Fe₃O₄ MNCs under the optimized conditions were 81.6 nm in average length and 23.9 nm in average diameter, while their saturation magnetization reached 69.8 emu/g. Full article

It is difficult for traditional weathering steel (WS) to form a protective rust layer to withstand the chloride ions and high humidity. Hence, there is an urgent need to develop a new type of low-cost WS with excellent corrosion resistance in the containing NaCl environment. This study aims to determine the influence of Cu on the corrosion mechanism of 1%Ni WS in simulated containing NaCl atmospheric environments. By increasing the Cu content (0.15–0.55%), the corrosion resistance of WS is enhanced. The increasing Cu content promotes the formation of a stable and compact rust layer, significantly enriching the proportion of α-FeOOH to equip the rust layer with a physical barrier. The formation of CuO deposits in the holes and cracks make the rust layer more compact and uniform. The increased Cu content promotes the formation of CuFeO₂ and increases the content of NiFe₂O₄. The formation of CuFeO₂ and NiFe₂O₄ then equips the rust layer with a chemical barrier. Hence, the addition of Cu could enhance the resistance of 1%Ni WS to containing NaCl atmospheric environments. Full article

Iron cation impurities reportedly enhance the oxygen evolution reaction (OER) activity of Ni-based catalysts, and the enhancement of OER activity by Fe cations has been extensively studied. Meanwhile, Fe salts, such as iron hydroxide and iron oxyhydroxide, in the electrolyte improve the OER performance, but the distinct roles of Fe cations and Fe salts have not been fully clarified or differentiated. In this study, NiO electrodes were synthesized, and their OER performance was evaluated in KOH electrolytes containing goethite (α-FeOOH). Unlike Fe cations, which enhance the performance via incorporation into the NiO structure, α-FeOOH boosts OER activity by adsorbing onto the electrode surface. Surface analysis revealed trace amounts of α-FeOOH on the NiO surface, indicating that physical contact alone enables α-FeOOH to adsorb onto NiO. Moreover, interactions between α-FeOOH and NiO were observed, suggesting their potential role in OER activity enhancement. These findings suggest that Fe salts in the electrolyte influence OER performance and should be considered in the development of OER electrodes. Full article

The microbial reduction of Fe(III) is a major component of Fe cycling in terrestrial and aquatic environments and is affected by the Fe(III) mineralogy of the system. The majority of the research examining the bioreduction of Fe(III) oxides by Fe(III)-reducing bacteria (IRB) has focused on the reduction of poorly crystalline Fe(III) phases, primarily ferrihydrite; however, crystalline Fe(III) oxides like goethite (α-FeOOH) and hematite (α-Fe₂O₃) comprise the majority of Fe(III) oxides in soils. This study examined the bioreduction of goethite and hematite of geogenic and synthetic origin by Shewanella putrefaciens CN2, a well-studied model IRB, in laboratory incubations. Overall, the rate and extent of Fe(II) production were greater for goethite than for hematite, and for geogenic Fe(III) oxides relative to their synthetic analogs. Although there was substantial production of Fe(II) (i.e., >5 mM Fe(II)) in many of the systems, X-ray diffraction analysis of the solids at the end of the incubation did not indicate the formation of any Fe(II)-bearing secondary minerals (e.g., magnetite, siderite, green rust, etc.). The results of this study demonstrate the variability in the extent of bioreduction of geogenic goethite and hematite, and furthermore, that synthetic goethite and hematite may not be good analogs for the biogeochemical behavior of Fe(III) oxides in aquatic and terrestrial environments. Full article

The synthesis and characterization of iron oxide nanostructures, specifically snowflake architecture, are investigated for their potential applications in electrochemical sensing systems. A Raman spectroscopy analysis reveals phase diversity in the synthesized powders. The pH of the synthesis affects the formation of the hematite (α-Fe₂O₃) and goethite (α-FeOOH). Scanning electron microscopy (SEM) images confirm the distinct morphologies of the particles, which are selectively obtained through recrystallization during the elongated reaction time. An electrochemical analysis demonstrates the differing behaviors of the particles, with synthesis pH affecting the electrochemical activity and surface area differently for each shape. Cyclic voltammetry measurements reveal reversible dopamine detection processes, with snowflake iron oxide showing lower detection limits than a mixture of snowflakes and cube-like particles. This research contributes to understanding the relationship between iron oxide nanomaterials’ structural, morphological, and electrochemical properties. It offers practical insights into their potential applications in sensor technology, particularly dopamine detection, with implications for biomedical and environmental monitoring. Full article

The marine atmospheric corrosion behavior of 700L high-strength automotive beam steel exposed for 36 months was investigated by scanning electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and electrochemical technology. The corrosion kinetics of 700L steel followed the exponential function: D = 4.85t^1.23. The rust layers were mainly composited of γ-FeOOH, α-FeOOH, γ-Fe₂O₃, and Fe₃O₄, regardless of the exposure duration. With an extended exposure time, the porosity, cracking, and spalling of the rust layers increased, and the densification and thickness uniformity decreased. Electrochemical measurements displayed that the corrosion resistance of the rusted 700L steel gradually decreased with increasing exposure time. A good correlation was found between rust layer composition, microstructure, and corrosion resistance. Full article

Fe(III) oxides were prepared as free nanoparticles and on DNA templates via the precipitation of Fe(III) salts with NaOH in the presence/absence of DNA. Through control of the pH and temperature, FeOOH and Fe₂O₃ were synthesised. The formation of templated materials FeOOH/DNA and Fe₂O₃/DNA was confirmed using UV-Vis absorption and FTIR spectra. The direct optical gap of Fe₂O₃/DNA was estimated as 3.2 eV; the absorption by FeOOH/DNA and Fe₂O₃/DNA at longer wavelengths is weaker, but consistent with indirect gaps near 2 eV. X-ray photoelectron spectra confirmed the presence of Fe(III) and DNA in the templated samples. Analysis of the X-ray diffraction patterns of both templated and non-templated FeOOH and Fe₂O₃ demonstrated that the materials were the α-FeOOH and α-Fe₂O₃ polymorphs with crystallite diameters of the DNA-templated materials estimated as 7.6 nm and 6.8 nm. Transmission electron microscopy showed needle-like crystals of both FeOOH and Fe₂O₃, but the Fe₂O₃ contains some globular structures. In contrast, the morphology of FeOOH/DNA and Fe₂O₃/DNA consists of needle-like crystallites of the respective oxides organised into complex dendritic structures with a length on the 10 μm scale formed by the DNA molecules. Finally, scanned conductance microscopy provided evidence for the conductivity of the FeOOH/DNA after alignment via molecular combing on an Si/SiO₂ substrate. Fe₂O₃/DNA did not exhibit any detectable conductivity. Full article

Sediment microbial fuel cells (SMFC) are bioelectrochemical systems that can use different wastes for energy production. This work studied the implementation of nanoparticles (NPs) of α-FeOOH (goethite, which is well-known as a photoactive catalyst) in the electrodes of an SMFC for its potential use for dye removal. The results obtained demonstrate the feasibility of the NPs activation with the electrical potential generated in the electrodes in the SMFC instead of the activation with light. The NPs of α-FeOOH were synthesized using a hydrothermal process, and the feasibility of a conductive bio-composite (biofilm and NPs) formation was proven by X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), and electrochemical techniques. The improvement of the power density in the cell was more than twelve times higher with the application of the bio-composite, and it is attributed mostly to the presence of NPs. The results also demonstrate the NPs effect on the increase of the electron transfer, which resulted in 99% of the COD removal. The total electrical energy produced in 30 days in the SMFC was 1.2 kWh based on 1 m² of the geometric area of the anode. The results confirm that NPs of α-FeOOH can be used to improve organic matter removal. Moreover, the energy produced due to its activation through the potential generated between the electrodes suggests the feasibility of its implementation for dye removal. Full article

The corrosion behaviors of two bridge steels (Q345q and Q500q) under simulated ultraviolet irradiation and a wet–dry alternating (UVWD) environment were studied. Weight loss measurement, stereomicroscope observation, SEM, XRD, and electrochemical impedance spectroscopy (EIS) were performed to investigate the influence of the coupled environment. The results revealed that the corrosion rates of Q345q and Q500q were significantly accelerated by the synergistic effect of UV light exposure and alternating wet–dry conditions. Numerous voids and cracks could be observed throughout the thickened rust layers, enabling the corrosive substances to easily penetrate through the rust layer. Q500q exhibited better corrosion resistance than Q345q due to the addition of Mo, Cr, and Ni as corrosion-resistant elements, which tended to transform the rust layer into α-FeOOH rather than γ-FeOOH during later stages of corrosion. Full article

Reactive powder concrete (RPC) is widely used in large-scale bridges, and its durability in coastal areas has become a significant concern. Straw fibers have been evidenced to improve the mechanical properties of concrete, while research on their influence on the chloride corrosion resistance of RPC is deficient. Therefore, it is essential to establish the relationships between the quantities and parameters of straw fibers and the properties of the resulting concrete. In this study, the mass loss rates (MLRs), the relative dynamic modulus of elasticity (RDME), the electrical resistance (R), the AC impedance spectrum (ACIS), and the corrosion rates of steel-bar-reinforced RPC mixed with 0%–4% straw fibers by volume of RPC were investigated. A scanning electron microscope (SEM) and X-ray diffraction (XRD) were used to analyze the corrosion of steel bars. The reinforced RPC specimens were exposed to a 3% NaCl dry-wet alternations (D-As) and 3% NaCl freeze-thaw cycles (F-Cs) environment. The results show that, after adding 1%–4% straw fibers, the setting time and slump flow of fresh RPC were reduced by up to 16.92% and 12.89%. The MLRs were −0.44%–0.43% and −0.38%–0.42%, respectively, during the D-As and F-Cs. The relationship between the RDME and the fiber volume ratio was the quadratic function, and it was improved by 9.34%–13.94% and 3.01%–5.26% after 10 D-As and 100 F-Cs, respectively. Incorporating 4% straw fibers reduced the R values of the reinforced RPC specimens by up to 22.90% and decreased the corrosion rates after 10 D-As and 100 F-Cs by 26.08% and 82.29%, respectively. The impedance value was also increased. Moreover, a dense, ultra-fine iron layer and α-FeO(OH) were observed in the rust of rebars by SEM and XRD, as the corrosion resistance of rebars was enhanced. The results indicate that straw fibers improved the corrosion resistance of RPC, which can serve as a protective material to inhibit concrete cracking and thereby prevent rebar oxidation. This study provides theoretical support for the investigation of surface phenomena in reinforced RPC with straw fibers. Full article

The skeletons of marine sponges are ancient biocomposite structures in which mineral phases are formed on 3D organic matrices. In addition to calcium- and silicate-containing biominerals, iron ions play an active role in skeleton formation in some species of bath sponges in the marine environment, which is a result of the biocorrosion of the metal structures on which these sponges settle. The interaction between iron ions and biopolymer spongin has motivated the development of selected extreme biomimetics approaches with the aim of creating new functional composites to use in environmental remediation and as adsorbents for heavy metals. In this study, for the first time, microporous 3D spongin scaffolds isolated from the cultivated marine bath sponge Hippospongia communis were used for electro-assisted deposition of iron oxides such as goethite [α-FeO(OH)] and lepidocrocite [γ-FeO(OH)]. The obtained iron oxide phases were characterized with the use of scanning electron microscopy, FTIR, and X-ray diffraction. In addition, mechanisms of electro-assisted deposition of iron oxides on the surface of spongin, as a sustainable biomaterial, are proposed and discussed. Full article

This article aims to investigate the atmospheric corrosion of carbon steel in a marine environment abundant in hydrogen sulfide (H₂S) resulting from the decomposition of Sargassum seaweed. To accomplish this, four sites with varying degrees of impact were chosen along the coast of Martinique. The corrosion rates of steel were evaluated through mass loss measurements. After one year of exposure, the corrosion rates were notably high, particularly in atmospheres rich in Cl⁻ ions and H₂S, ranging from 107 µm to 983 µm. Complementing these findings, surface and product morphologies were characterized using scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). These analyses revealed a significant degradation of the corrosion surface in the most affected atmospheres compared to those unaffected by Sargassum seaweed strandings. Lepidocrocite (γFeOOH) was identified as the predominant product regardless of the exposure atmosphere. However, goethite (αFeOOH) was found to be present in atmospheres most impacted by H₂S. Full article

Throughout the nuclear power production process, the disposal of radioactive waste has consistently raised concerns about environmental safety. When the metal tanks used for waste disposal are corroded, radionuclides seep into the groundwater environment and eventually into the biosphere, causing significant damage to the environment. Hence, investigating the adsorption behavior of radionuclides on the corrosion products of metal tanks used for waste disposal is an essential component of safety and evaluation protocols at disposal sites. In order to understand the adsorption behavior of important radionuclides ⁶⁰Co, ⁵⁹Ni, ⁹⁰Sr, ¹³⁵Cs and ¹²⁹I on α-FeOOH, the influences of different pH values, contact time, temperature and ion concentration on the adsorption rate were studied. The adsorption mechanism was also discussed. It was revealed that the adsorption of key nuclides onto α-FeOOH is significantly influenced by both pH and temperature. This change in surface charge corresponds to alterations in the morphology of nuclide ions within the system, subsequently impacting the adsorption efficiency. Sodium ions (Na⁺) and chlorate ions (ClO₃⁻) compete for coordination with nuclide ions, thereby exerting an additional influence on the adsorption process. The XPS analysis results demonstrate the formation of an internal coordination bond (Ni–O bond) between Ni²⁺ and iron oxide, which is adsorbed onto α-FeOOH. Full article