Search Results (23)

To address the issues of insufficient capacity and difficult regeneration of adsorbents for phosphate removal from wastewater, in this study, FeOOH/Al₂O₃ adsorbents were successfully developed by in situ growing amorphous iron oxyhydroxide (FeOOH) within the pores of alumina (Al₂O₃) using a simple method. The physicochemical properties of FeOOH/Al₂O₃ adsorbents were characterized using X-ray Diffraction (XRD), N₂ adsorption/desorption analysis, and scanning electron microscopy (SEM). Additionally, their phosphate adsorption properties were comparatively investigated. The results revealed that FO-A-3, one of the FeOOH/Al₂O₃ samples prepared with Fe/Al molar ratio of 0.47, exhibited excellent adsorption capacity and a relatively fast adsorption rate, surpassing those of Al₂O₃ and amorphous FeOOH alone. The adsorption process of phosphate using FO-A-3 conformed to the pseudo-second-order kinetic model and the Langmuir isotherm model, with a maximum adsorption capacity of 131.00 mg/g. To tackle the problem of poor regeneration performance, this study innovatively proposed a repeatable and simple regeneration strategy. Experiments demonstrated that FO-A-3 maintained a relatively high adsorption capacity after four cycles of regeneration. Full article

This study aims to clarify the temperature-dependent degradation mechanisms of the steel–concrete interface in NaCl solution environments at the nanoscale, focusing on the key components of calcium silicate hydrate (C-S-H, the primary hydration product of cement) and iron oxyhydroxide (γ-FeOOH, a critical component of steel passive films in highly alkaline environments). Using Materials Studio software (2023) and molecular dynamics simulations, the evolution of the interface’s performance under temperatures ranging from 300 K to 390 K (corresponding to 27 °C to 117 °C) is systematically investigated. The results reveal that elevated temperatures degrade the performance of C-S-H/γ-FeOOH interfaces through three main mechanisms: (1) The stability of the hydration shell around aggressive ions is weakened, enabling these ions to occupy the coordination positions of calcium ions on the interface and form stable ion pairs with surface calcium ions, thereby weakening interfacial bonding. (2) The mobility of surface calcium ions is enhanced, reducing the strength of the interaction of ion pairs and diminishing the mediating role of calcium ions in connecting the C-S-H and γ-FeOOH phases. (3) Hydrogen bond stability at the interface decreases, as indicated by reduced hydrogen bond angles and numbers, coupled with increased hydrogen bond lengths. The above three reasons lead to a decrease in adsorption energy in the C-S-H/γ-FeOOH interface, which degrades the interface bond’s performance. Full article

The Mo:BiVO₄/FeOOH photoelectrode was synthesized through the deposition of FeOOH onto the surface of the Mo:BiVO₄ photoelectrode. The composite photoelectrode demonstrated a photocurrent of 1.8 mA·cm⁻², which is three times greater than that observed for pure BiVO₄. Furthermore, the glycerol conversion rate was recorded at 79 μmol·cm⁻²·h⁻¹, approximately double that of pure BiVO₄, while the selectivity for glyceraldehyde reached 49%, also about twice that of pure BiVO₄. The incorporation of Mo has been shown to enhance the stability of the BiVO₄. Additionally, Mo doping improves the efficiency of electron-hole transport and increases the carrier concentration within the BiVO₄. This enhancement leads to a greater number of holes participating in the formation of iron oxyhydroxide (FeOOH), thereby stabilizing the FeOOH co-catalyst within the glycerol conversion system. The FeOOH co-catalyst facilitates the adsorption and oxidation of the primary hydroxyl group of glycerol, resulting in the cleavage of the C−H bond to generate a carbon radical (C). The interaction between the carbon radical and the hydroxyl group produces an intermediate, which subsequently dehydrates to form glyceraldehyde (GLAD). 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

Environmental issues related to phosphate and resource depletion have recently emerged as serious problems. This study focuses on solving the problems of phosphate removal and recovery using synthesized granular akaganeite (GAK). This study identified that akaganeite, which possesses an FeOOH structure in iron oxyhydroxide, can be synthesized and used as a reusable material. Immobilization with the core–shell method using polyethersulfone was applied as a strategy to recover phosphate anions from a trace of phosphate solution. GAK was successfully analyzed using SEM/TGA/BET to understand its physical properties. XRD and SAD pattern analyses suggested that the GAK powder form was amorphous in nature. The powdered akaganeite had a surface area of 231 mg²/g and a maximum adsorption capacity of 21.27 mg/g. To prevent the dispersion of powder during granulation, polyethersulfone was used as a scaffold since akaganeite particles can be effectively immobilized onto PES polymer scaffolds, as substantiated by the SEM/EDS results. Moreover, a lack of changes in the pore sizes suggested that physical properties remained unchanged. Furthermore, compared to the granular akaganeite, the surface area of powdered akaganeite decreased 4–5-fold. The adsorption kinetic of granular akaganeite fit the pseudo-second-order model. The powdered form displayed high removal efficiency, intimate with phosphate anions, when n > 1.0, instead of lower K_F. On the other hand, granular akaganeite showed lower affinity when n < 1.0, but appeared positive for an adsorbate with higher KF. This implies that the granulation of akaganeite with the PES polymer did not change its adsorption property, with the maximum adsorption capacity for granular akaganeite being 3.65 mg/g. Full article

Recovering iron from the bauxite residue (BR) is one of the long-standing challenges in the mining industry. However, there is a substantial lack of information in the literature regarding sample properties and iron extraction by reducing hydrogen. The present study aims at reducing a Greek BR using hydrogen, its characterization, and separating iron by magnetic separation processes. To this end, the reduced sample was characterized using X-ray diffractometry analysis (XRD), X-ray fluorescence spectrometer analysis (XRF), thermomagnetic analysis (TMA), automated mineralogy (AM), and scanning electron microscopy (SEM) coupled with energy dispersive spectroscopy (EDS). The effect of particle size (−200 + 100 µm, −100 + 75 µm, and <75 µm) was investigated through a medium-intensity magnetic separation (MIMS, Davis Tube) at 1000–2500 Gauss and a Slon^® magnetic separator (1000 G). The effects of solid content (3% and 10% w/w) in a wet low-intensity magnetic separation (WLIMS, 350 G) and a two-stage MIMS followed by WLIMS were investigated. It was revealed that through reduction at 500 °C and 2 h with 20 wt% NaOH under 5 vol.% H₂ + 95 vol.% N₂, iron oxides and ferric oxyhydroxide (Fe₂O₃ and FeOOH) were converted into magnetite (Fe₃O₄), whereas aluminum (oxy)hydroxides (Al(OOH), Al(OH)₃) were reacted with Na⁺ towards sodium aluminates (NaAlO₂). The AM observations indicated that only 3% of iron was in the phase of liberated magnetite, and the remaining was associated with Na, Al, and Ti phases with different intensities. The dissemination of iron throughout the matrix of the sample was recognized as the principal challenge in the physical separation processes. It was found that increasing magnetic intensity from 1000 G to 2500 G resulted in improved recovery for all studied particle size fractions in Davis Tube tests. The particle range of −106 + 74 µm was chosen as the most appropriate size to achieve the maximum Fe content of 41%. The results of WLIMS (350 G) showed the maximum Fe grade but revealed less recovery of 52% and 27% at 10% and 3% solid contents, respectively, compared to the Davis Tube trials. Full article

Supercapacitors (SCs) offer a potential replacement for traditional lithium-based batteries in energy-storage devices thanks to the increased power density and stable charge–discharge cycles, as well as negligible environmental impact. Given this, a vast array of materials has been explored for SCs devices. Among the materials, iron oxyhydroxide (FeOOH) has gained significant attention in SC devices, owing to its superior specific capacitance, stability, eco-friendliness, abundance, and affordability. However, FeOOH has certain limitations that impact its energy storage capabilities and thus implicate the need for optimizing its structural, crystal, electrical, and chemical properties. This review delves into the latest advancements in FeOOH-based materials for SCs, exploring factors that impact their electrochemical performance. To address the limitations of FeOOH’s materials, several strategies have been developed, which enhance the surface area and facilitate rapid electron transfer and ion diffusion. In this review, composite materials are also examined for their synergistic effects on supercapacitive performance. It investigates binary, ternary, and quaternary Fe-based hydroxides, as well as layered double hydroxides (LDHs). Promising results have been achieved with binder-free Fe-based binary LDH composites featuring unique architectures. Furthermore, the analysis of the asymmetric cell performance of FeOOH-based materials is discussed, demonstrating their potential exploitation for high energy-density SCs that could potentially provide an effective pathway in fabricating efficient, cost-effective, and practical energy storage systems for future exploitations in devices. This review provides up-to-date progress studies of novel FeOOH’s based electrodes for SCs applications. Full article

The work investigates the effect of sulfuric acid baking on rare earth element (REE) extraction from two waste rock samples from a phosphate mine. The role of different mineralogical assemblages and the degree of alteration (i.e., weathering), and the behavior of the main impurities–iron, phosphorus, and calcium–on REE extraction are emphasized. For both samples, the sulfuric acid baking at 25 °C, during 15 min, H₂SO₄:sample (w/w) mass ratio of 0.45:1 is the best condition for achieving the selective leaching of REE. For the iron rich-sample, the increase in temperature reduces REE extraction and increases iron dissolution. The corresponding sulfuric acid consumed by goethite (α-FeOOH) from 25 °C to 160 °C acid baking is ten times higher than that required for the monazite (REEPO₄) reaction. Conversely, higher REE and lower iron extraction are observed by increasing (sulfuric acid/sample) mass ratio (0.95:1). Due to the high sulfuric concentration during dissolution, a local saturation zone close to the dissolution front caused the precipitation of iron oxyhydroxides. The calcium-rich sample shows lower REE extraction by leaching (63% maximum) mainly due to the entrapment of REE-bearing minerals by a gypsum layer, and lanthanide’s uptake by calcium sulfate compounds formed during leaching. The results were discussed with the help of a detailed characterization of the residues. Full article

One-dimensional anisotropic nanoparticles are of great research interest across a wide range of biomedical applications due to their specific physicochemical and magnetic properties in comparison with isotropic magnetic nanoparticles. In this work, the formation of iron oxides and oxyhydroxide anisotropic nanoparticles (ANPs) obtained by the co-precipitation method in the presence of urea was studied. Reaction pathways of iron oxide and oxyhydroxide ANPs formation are described based on of X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and pulse magnetometry studies. It is shown that a nonmonotonic change in the Fe₃O₄ content occurs during synthesis. The maximum content of the Fe₃O₄ phase of 47.4% was obtained at 12 h of the synthesis. At the same time, the reaction products contain ANPs of α-FeOOH and submicron isotropic particles of Fe₃O₄, the latter formation can occur due to the oxidation of Fe²⁺ ions by air-oxygen and Ostwald ripening processes. A subsequent increase in the synthesis time leads to the predominant formation of an α-FeOOH phase due to the oxidation of Fe₃O₄. As a result of the work, a methodological scheme for the analysis of iron oxide and oxyhydroxide ANPs was developed. Full article

This work was focused on the rust conversion of proanthocyanidins (PC) for goethite (α-FeOOH), akaganeite (β-FeOOH) and lepidocrocite (γ-FeOOH), trying to show the potential of PC as an eco-friendly corrosion inhibitor and rust converter for archaeological steel conservation. The experiment used a rusted steel screw from Lingzhao Xuan of the Forbidden City in the Qing Dynasty and three kinds of pure iron oxyhydroxides as research samples. By means of micro-Raman, FTIR, XRD, XPS, SEM and EIS, PC had the ability to chemically react with iron oxyhydroxides in the rust, forming amorphous PC-FeOOH with a marked signal about 1384 cm⁻¹ as phenolic-Fe in infrared properties. The original relatively stable iron oxides were not induced to phase transformation and still remained. The converted rust layer could be more stable in the corrosive medium and increased the corrosion potential more effectively. Both the rust layer resistance and the charge transfer resistance of the archaeological samples were improved by at least 3 times with 5.0 g/L of PC, which could reasonably stabilize the archaeological rust and hindered external corrosive penetration into the core. It was a mild protection material that showed satisfactory performance for archaeological steel cultural heritage and has a good application prospect. Full article

Arsenic is a potentially toxic element (PTE) that is widely present in groundwater, with concentrations often exceeding the WHO drinking water guideline value (10.0 μg/L), entailing a prominent risk to human health due to long-term exposure. We investigated its origin in groundwater in a study area located north of Rome (Italy) in a volcanic-sedimentary aquifer. Some possible mineralogical sources and main mechanisms governing As mobilization from a representative volcanic tuff have been investigated via laboratory experiments, such as selective sequential extraction and dissolution tests mimicking different release conditions. Arsenic in groundwater ranges from 0.2 to 50.6 μg/L. It does not exhibit a defined spatial distribution, and it shows positive correlations with other PTEs typical of a volcanic environment, such as F, U, and V. Various potential As-bearing phases, such as zeolites, iron oxyhydroxides, calcite, and pyrite are present in the tuff samples. Arsenic in the rocks shows concentrations in the range of 17–41 mg/kg and is mostly associated with a minor fraction of the rock constituted by FeOOH, in particular, low crystalline, containing up to 70% of total As. Secondary fractions include specifically adsorbed As, As-coprecipitated or bound to calcite and linked to sulfides. Results show that As in groundwater mainly originates from water-rock interaction processes. The release of As into groundwater most likely occurs through desorption phenomena in the presence of specific exchangers and, although locally, via the reductive dissolution of Fe oxy-hydroxides. Full article

Iron oxyhydroxides (FeOOHs) appear to be the optimal group of materials among inorganic adsorbents for the removal of phosphates from water, providing significant adsorption capacities. This research work presents a thermodynamic study of phosphate adsorption by examining five different FeOOHs sorbent nanomaterials. The otablebtained results indicated that the adsorption process in these cases was spontaneous. When the experiments were performed using distilled water, akageneite (GEH), schwertmannite, and tetravalent manganese feroxyhyte (AquAsZero), displaying ΔH° values of 31.2, 34.7, and 7.3 kJ/mole, respectively, presented an endothermic adsorption process, whereas for goethite (Bayoxide) and lepidocrocite, with ΔH° values of −11.4 and −7.7 kJ/mole, respectively, the adsorption process proved to be exothermic. However, when an artificial (according to NSF) water matrix was used, GEH, schwertmannite, lepidocrocite, and AquAsZero presented ΔH° values of 13.2, 3.3, 7.7, and 3.3 kJ/mole, respectively, indicative of an endothermic process, while only for Bayoxide, with ΔH° of −17 kJ/mole, the adsorption remained exothermic. The adsorption enthalpy values generally decreased with the NSF water matrix, probably due to the competition for the same adsorption sites by other co-existing anions as well to the possible formation of soluble phosphate complexes with calcium; however, an overall positive effect on the uptake of phosphates was observed. Full article

Catalytic membranes, as a combination of heterogeneous advanced oxidation and membrane technology reaction systems, have important application prospects in the treatment of dyes and other organics. In practical applications, it is still challenging to construct catalytic membranes with excellent removal efficiency and fouling mitigation. Herein, molybdenum disulfide-iron oxyhydroxide (MoS₂-FeOOH) was fabricated using iron oxide and MoS₂ nanoflakes, which were synthesized by the hydrothermal method. Furthermore, by changing the concentration of MoS₂-FeOOH, the MoS₂-FeOOH/polyethersulfone (PES) composite ultrafiltration membrane was obtained with improved hydrophilicity, permeability, and antifouling capacity. The pure water flux of the composite membrane reached 385.3 L/(m²·h), which was 1.7 times that of the blank PES membrane. Compared with the blank membrane, with the increase of MoS₂-FeOOH content, the MoS₂-FeOOH/PES composite membranes had better adsorption capacity and catalytic performance, and the membrane with 3.0% MoS₂-FeOOH content (M4) could be achieved at a 60.2% methylene blue (MB) degradation rate. In addition, the membrane flux recovery ratio (FRR) of the composite membrane also increased from 25.6% of blank PES membrane (M0) to more than 70% after two cycles of bovine serum albumin (BSA) filtration and hydraulic cleaning. The membrane with 2.25% MoS₂-FeOOH content (M3) had the best antifouling performance, with the largest FRR and the smallest irreversible ratio (R_ir). Catalytic self-cleaning of the composite membrane M3 recovered 95% of the initial flux with 0.1 mol/L H₂O₂ cleaning. The MoS₂-FeOOH/PES composite membranes with the functions of excellent rejection and antifouling capacity have a good prospect in the treatment of printing and dyeing wastewater composed of soluble dyes. Full article

This study investigated the effect of Cr alloying element on the corrosion properties of automotive carbon steel (0.1C, 0.5Si, 2.5Mn, Fe Bal., composition given in wt.%) in aqueous and atmospheric conditions using electrochemical measurement and cyclic corrosion tests. Three steels with 0, 0.3, and 0.5 wt.% Cr were studied by electrochemical impedance spectroscopy. Polarization resistance (R_p) of 0.3 Cr and 0.5 Cr steels was higher than that of 0 Cr steel, and the R_p also increased as the Cr content increased. Therefore, Cr increases the corrosion resistance of automotive carbon steel immersed in a chloride ion (Cl⁻)-containing aqueous solution. In the cyclic corrosion test results, Cl⁻ was concentrated at the metal/rust interface in all of the steels regardless of Cr content. The Cl⁻ was uniformly concentrated and distributed on the 0 Cr steel, but locally and non-uniformly concentrated on the Cr-added steels. The inner rust layer consisted of β-FeOOH containing Cl⁻ and Cr-goethite, while the outer rust layer was composed of amorphous iron oxyhydroxide mixed with various types of rust. FeCl₂ and CrCl₃ are formed from the Cl⁻ nest developed in the early stage, and the pitting at CrCl₃-formed regions are locally accelerated because Cr is strongly hydrolyzed to a very low pH. Full article

Rare diseases affect a small part of the population, and the most affected are children. Because of the low availability of patients for testing, the pharmaceutical industry cannot develop drugs for the diagnosis of many of these orphan diseases. In this sense, the use of benzothiazole compounds that are highly selective and can act as spectroscopy probes, especially the compound 2-(4′-aminophenyl)benzothiazole (ABT), has been highlighted. This article reports the design of potential contrast agents based on ABT and iron to develop a new material with an efficient mechanism to raise the relaxation rate, facilitating diagnosis. The ABT/δ-FeOOH hybrid material was prepared by grafting (N-(4’-aminophenyl) benzothiazole-2-bromoacetamide) on the surface of the iron oxyhydroxide particles. FTIR spectra confirmed the material formations of the hybrid material ABT/δ-FeOOH. SEM analysis checked the covering of nanoflakes’ surfaces in relation to the morphology of the samples. The theoretical calculations test a better binding mode of compound with iron oxyhydroxide. Theoretical findings show the radical capture mechanism in the stabilization of this new material. In this context, Fe³⁺ ions are an electron acceptor from the organic phase. Full article