Search Results (202)

The most important bauxite deposits in Türkiye are located in the Seydişehir (Konya) and Akseki (Antalya) regions, situated along the western Taurus Mountain, with a total reserve of approximately 44 million tons. Some of the bauxite deposits have been exploited for alumina since the 1970s. In this study, bauxite samples, collected from six different deposits were examined to determine their mineralogical and chemical composition, as well as their REE content, with the aim of identifying which bauxite types are enriched in REEs and assessing their economic potential. The samples included massive, oolitic, and brecciated bauxite types, which were analyzed using optical microscopy, X-ray diffraction (XRD), X-ray fluorescence (XRF) and inductive coupled plasma-mass spectrometry (ICP-MS), field emission scanning electron microscopy (FESEM-EDX), and electron probe micro-analysis (EPMA). Massive bauxites were found to be more homogeneous in both mineralogical and chemical composition, predominantly composed of diaspore, boehmite, and rare gibbsite. Hematite is the most abundant iron oxide mineral in all bauxites, while goethite, rutile, and anatase occur in smaller quantities. Quartz, feldspar, kaolinite, dolomite, and pyrite were specifically determined in brecciated bauxites. Average oxide contents were determined as 52.94% Al₂O₃, 18.21% Fe₂O₃, 7.04% TiO₂, and 2.69% SiO₂. Na₂O, K₂O, and MgO values are typically below 0.5%, while CaO averages 3.54%. The total REE content of the bauxites ranged from 161 to 4072 ppm, with an average of 723 ppm. Oolitic-massive bauxites exhibit the highest REE enrichment. Cerium (Ce) was the most abundant REE, ranging from 87 to 453 ppm (avg. 218 ppm), followed by lanthanum (La), which reached up to 2561 ppm in some of the massive bauxite samples. LREEs such as La, Ce, Pr, and Nd were notably enriched compared to HREEs. The lack of a positive correlation between REEs and major element oxides, as well as with their occurrences in distinct association with Al- and Fe-oxides-hydroxides based on FESEM-EDS and EPMA analyses, suggests that the REEs are present as discrete mineral phases. Furthermore, these findings indicate that the REEs are not incorporated into the crystal structures of other minerals through isomorphic substitution or adsorption. Full article

The Sierra Minera de Cartagena-La Unión, located in southeast of the Iberian Peninsula, has been significantly impacted by historical mining activities, which resulted in environmental degradation, including acid mine drainage (AMD) and heavy metal contamination. This study evaluates the potential of PRISMA hyperspectral imagery for multi-temporal mapping of AMD-related minerals in two mining-affected drainage basins: Beal and Gorguel. Key minerals indicative of AMD—iron oxides and hydroxides (hematite, jarosite, goethite), gypsum, and aluminium-bearing clays—were identified and mapped using band ratios applied to PRISMA data acquired over five dates between 2020 and 2024. Additionally, Sentinel-2 data were incorporated in the analysis due to their higher temporal resolution to complement iron oxide and hydroxide evolution from PRISMA. Results reveal distinct temporal and spatial patterns in mineral distribution, influenced by seasonal precipitation and climatic factors. Jarosite was predominant after torrential precipitation events, reflecting recent AMD deposition, while gypsum exhibited seasonal variability linked to evaporation cycles. Goethite and hematite increased in drier conditions, indicating transitions in oxidation states. Validation using X-ray diffraction (XRD), laboratory spectral curves, and a larger time-series of Sentinel-2 imagery demonstrated strong correlations, confirming PRISMA’s effectiveness for iron oxides and hydroxides and gypsum identification and monitoring. However, challenges such as noise, striping effects, and limited image availability affected the accuracy of aluminium-bearing clay mapping and limited long-term trend analysis. Full article

The formation of acidic goaf water in abandoned coal mines poses significant environmental threats, especially in karst regions where the risk of groundwater contamination is heightened. This study investigates the geochemical processes responsible for the generation of acidic water through batch and column leaching experiments using coal mine surrounding rocks (CMSR) from Yangquan, China. The coal-bearing strata, primarily composed of sandstone, mudstone, shale, and limestone, contain high concentrations of pyrite (up to 12.26 wt%), which oxidizes to produce sulfuric acid, leading to a drastic reduction in pH (approximately 2.5) and the mobilization of toxic elements. The CMSR samples exhibit elevated levels of arsenic (11.0 mg/kg to 18.1 mg/kg), lead (69.5 mg/kg to 113.5 mg/kg), and cadmium (0.6 mg/kg to 2.6 mg/kg), all of which exceed natural crustal averages and present significant contamination risks. The fluorine content varies widely (106.1 mg/kg to 1885 mg/kg), with the highest concentrations found in sandstone. Sequential extraction analyses indicate that over 80% of fluorine is bound in residual phases, which limits its immediate release but poses long-term leaching hazards. The leaching experiments reveal a three-stage release mechanism: first, the initial oxidation of sulfides rapidly lowers the pH (to between 2.35 and 2.80), dissolving heavy metals and fluorides; second, slower weathering of aluminosilicates and adsorption by iron and aluminum hydroxides reduce the concentrations of dissolved elements; and third, concentrations stabilize as adsorption and slow silicate weathering regulate the long-term release of contaminants. The resulting acidic goaf water contains extremely high levels of metals (with aluminum at 191.4 mg/L and iron at 412.0 mg/L), which severely threaten groundwater, particularly in karst areas where rapid cross-layer contamination can occur. These findings provide crucial insights into the processes that drive the acidity of goaf water and the release of contaminants, which can aid in the development of effective mitigation strategies for abandoned mines. Targeted management is essential to safeguard water resources and ecological health in regions affected by mining activities. Full article

To investigate the corrosion resistance of 60Si2MnA spring steel coated with Zn-Al in a domestic atmospheric environment containing harmful salts, the corrosion environmental factors (temperature, humidity, deposited salts, and pH) were obtained through field research. The deliquescence and weathering behavior of harmful salts were studied using impedance methods to establish their characteristic curves. Additionally, a self-designed salt deposition test apparatus was employed to conduct accelerated atmospheric corrosion tests under constant salt deposition (10 g/m²) and controlled temperature and humidity conditions (20 °C/75% RH and 40 °C/75% RH) over different corrosion periods. The results show that noticeable red rust appeared on the samples after one month of corrosion. As the temperature increased, the consumption of the coating accelerated. XRD and Raman analyses reveal that the main corrosion products of the coating materials were ZnO, Zn(OH)₂, and Zn₅(CO₃)₂(OH)₆, while the red rust primarily consisted of iron oxides and hydroxides. In the early stages of corrosion, the self-corrosion current density was relatively low due to the protective effects of the coating and the corrosion product layer, indicating good corrosion resistance. However, in the later stages, the integrity of the coating and the corrosion product layer deteriorated, leading to a significant increase in the self-corrosion current density and a decline in corrosion resistance. This study provides a data foundation for understanding the corrosion behavior of Zn-Al-coated spring steel in atmospheric environments and offers theoretical insights for developing more corrosion-resistant coatings and optimizing anti-corrosion measures. Full article

The bioavailability of heavy metals is profoundly influenced by their interactions with active soil components (microorganisms, organic matter, and iron minerals). However, the effects of urease-producing bacteria combined with organo-Fe hydroxide coprecipitates (OFCs) on Cd accumulation in wheat, as well as the mechanisms underlying these effects, remain unclear. In this study, pot experiments integrated with high-throughput sequencing were employed to investigate the impacts of the urease-producing bacterial strain TJ6, ferrihydrite (Fh), and OFCs on Cd enrichment in wheat grains, alongside the underlying soil–microbial mechanisms. The results demonstrate that the strain TJ6-Fh/OFC consortium significantly (p < 0.05) reduced (50.1–66.7%) the bioavailable Cd content in rhizosphere soil while increasing residual Cd fractions, thereby decreasing (77.4%) Cd accumulation in grains. The combined amendments elevated rhizosphere pH (7.35), iron oxide content, and electrical conductivity while reducing (14.5–21.1%) dissolved organic carbon levels. These changes enhanced soil-colloid-mediated Cd immobilization and reduced Cd mobility. Notably, the NH₄⁺ content and NH₄⁺/NO₃⁻ ratio were significantly (p < 0.05) increased, attributed to the ureolytic activity of TJ6, which concurrently alkalinized the soil and inhibited Cd uptake via competitive ion channel interactions. Furthermore, the relative abundance of functional bacterial taxa (Proteobacteria, Gemmatimonadota, Enterobacter, Rhodanobacter, Massilia, Nocardioides, and Arthrobacter) was markedly increased in the rhizosphere soil. These microbes exhibited enhanced abilities to produce extracellular polymeric substances, induce phosphate precipitation, facilitate biosorption, and promote nutrient (C/N) cycling, synergizing with the amendments to immobilize Cd. This study for the first time analyzed the effect and soil science mechanism of urease-producing bacteria combined with OFCs in blocking wheat’s absorption of Cd. Moreover, this study provides foundational insights and a practical framework for the remediation of Cd-contaminated wheat fields through microbial–organic–mineral collaborative strategies. Full article

This paper presents the physical, hydrogeological, and geochemical characterizations of two types of tailings: one from the nickel–cobalt (Ni–Co) and the other from the lead–zinc (Pb–Zn) industries. The study is restricted only to Ni and Zn ions behavior. The mineralogical composition of the studied tailings is primarily composed of oxides and hydroxides of iron, aluminum, and silica. Based on their grain size, these wastes are geotechnically classified as low plasticity silts, with permeability ranging from 10⁻⁸ m/s to less than 10⁻⁹ m/s. Batch and column flow tests, along with metal transport tests using heavy metal-contaminated wastewater, reveal that these tailings have an adsorption capacity for metals such as nickel (Ni) and zinc (Zn) ranging from 2000 to 6000 mg/kg of solid. This high adsorption capacity surpasses that of many clayey soils used for sealing municipal, industrial, mining, and metallurgical waste deposits. Additionally, these wastes can neutralize the acidity of wastewater. The results indicate that the mineralogical composition and pH of these tailings are key factors determining their adsorption characteristics and mechanisms. Due to their characteristics, these tailings could be evaluated for use as low-permeability reactive geochemical barriers (LPRGB) in the conditioning of repositories for the storage of industrial, urban, mining and metallurgical waste. This would allow large volumes of tailings to be repurposed effectively. Full article

Transition metal oxides (TMOs) are considered to be highly promising materials for supercapacitor electrodes due to their low cost, multiple convertible valence states, and excellent electrochemical properties. However, inherent limitations, including restricted specific surface area and low electrical conductivity, have largely restricted their application in supercapacitors. In this paper, core–shell heterostructures of nickel–iron layered double hydroxide (NiFe-LDH) nanosheets uniformly grown on CuCo₂O₄ nanoneedles were synthesized by hydrothermal and calcination methods. It is found that the novel core–shell structure of CuCo₂O₄@NiFe-LDH improves the electrical conductivity of the electrode materials and optimizes the charge transport path. Under the synergistic effect of the two components and the core–shell heterostructure, the CuCo₂O₄@NiFe-LDH electrode achieves an ultra-high specific capacity of 323.4 mAh g⁻¹ at 1 A g⁻¹. And the capacity retention after 10,000 cycles at 10 A g⁻¹ is 90.66%. In addition, the assembled CuCo₂O₄@NiFe-LDH//RGO asymmetric supercapacitor device achieved a considerable energy density (68.7 Wh kg⁻¹ at 856.3 W kg⁻¹). It also has 89.36% capacity retention after 10,000 cycles at 10 A g⁻¹. These properties indicate the great potential application of CuCo₂O₄@NiFe-LDH in the field of high-performance supercapacitors. Full article

This study analyzes the effects of varying H₂S and CO₂ concentrations and temperature on the pH of geothermal fluids flowing through superduplex S32750 stainless-steel pipelines, classified as corrosion-resistant alloys (CRAs). Corrosive decay is evaluated by comparing OLI Studio software simulations with experimental data from the literature. The results indicate that an increase in the partial pressure of either gas lowers pH levels, with temperature exerting a more pronounced exponential effect on corrosion than gas partial pressure. When both gases are present, the dominant gas dictates the corrosion behavior. In cases where CO₂ and H₂S are in equal proportions, FeS₂ forms as the primary corrosive product due to the higher potential corrosivity of H₂S. The H₂S/CO₂ ratio influences the formation of passive films containing chromium oxides or hydroxides (Cr₂O₃, Cr(OH)₃), iron oxides (Fe₂O₃, Fe₃O₄), or iron sulfides (FeS). Full article

The quality of strong-flavor baijiu largely depends on the physicochemical properties and prokaryotic microbial activities of pit mud. However, the impact of the iron-bearing minerals in pit mud on its prokaryotic microbial communities remains unknown. This study examined the differences in the prokaryotic communities between 2-year, 40-year, and 100-year pit mud and yellow soil (the raw material for pit mud), as well as the impacts of environmental factors, particularly iron-bearing minerals, on the structure and diversity of these prokaryotic communities. The results indicated that there were significant differences in the composition of prokaryotic microorganisms between yellow soil and pit mud. As the fermentation pit aged, the relative abundance of dominant fermentation bacteria (including Petrimonas, Syntrophomonas, Clostridium, etc.) and hydrogenotrophic methanogens in the pit mud increased. The relative abundance of Lactobacillus in the 2-year pit mud was low (0.33%). Under laboratory conditions, goethite (a typical crystalline iron mineral, denoted as Fe_c) reduced the physiological and metabolic activity of Lacticaseibacillus paracasei JN01 in a concentration-dependent manner. The results of the physicochemical analysis showed that the contents of total iron (TFe) and Fe_c significantly decreased, while the contents of Fe(II) and amorphous iron (hydr)oxides (Fe_o) significantly increased with an increasing fermentation pit age. TFe and Fe_c were significantly negatively correlated with both the Chao1 and Shannon indexes and functional microorganisms such as Clostridium_sensu_stricto_12, Sedimentibacter, and hydrogenotrophic methanogens. The current results contribute to our understanding of the aging process of pit mud from the perspective of the interaction between iron-bearing minerals and prokaryotic microorganisms. Full article

With increasing energy demands, fuel cells are a popular avenue for portability and low waste emissions. Hydrogen fuel cells are popular due to their potential output power and clean waste. However, due to storage and transport concerns, hydrogen peroxide fuel cells are a promising alternative. Although they have a lower output potential compared to hydrogen fuel cells, peroxide can act as both the oxidizing and reducing agent, simplifying the structure of the cell. In addition to reducing the complexity, hydrogen peroxide is stable in liquid form and can be stored in less demanding methods. This paper investigates chelated metals as electrode material for hydrogen peroxide fuel cells. Chelated metal complexes are ring-like structures that form from binding organic or inorganic compounds with metal ions. They are used in medical imaging, water treatment, and as catalysts for reactions. Copper(II) phthalocyanine, phthalocyanine green, poly(copper phthalocyanine), bis(ethylenediamine)copper(II) hydroxide, iron(III) ferrocyanine, graphene oxide decorated with Fe₃O₄, zinc phthalocyanine, magnesium phthalocyanine, manganese(II) phthalocyanine, cobalt(II) phthalocyanine are investigated as electrode materials for peroxide fuel cells. In this study, the performance of these materials is evaluated using cyclic voltammetry. The voltammograms are compared, as well as observations are made during the materials’ use to measure their effectiveness as electrode material. There has been limited research comparing the use of these chelated metals in the context of hydrogen peroxide fuel cells. Through this research, the goal is to further the viability of hydrogen peroxide fuel cells. Poly(copper phthalocyanine) and graphene oxide doped with iron oxides had strong redox catalytic activity for use in acidic peroxide single-compartment fuel cells, where the poly(copper phthalocyanine) electrode compound generated the highest peak power density of 7.92 mW/cm² and cell output potential of 0.634 V. Full article

The reliance on acidic working environments presents a significant bottleneck in the development and widespread application of peroxymonosulfate (PMS)-activated high-valent iron-oxo systems and iron-based catalysts. In this study, we present a system of non-homogeneous activation of peroxymonosulfate that is capable of overcoming the acidic environment in heterogeneous to generate continuous non-radicals for the selective degradation of organic pollutants such as sulfamethoxazole. The system takes advantage of amphiprotic hydroxides to create a homogeneous neutral pH microenvironment at the heterogeneous interface of the catalyst. The generation of the neutral pH microenvironment is capable of inducing the formation of high-valent iron-oxo species and a more stable cycling of iron ions in the iron-based material., promoting sustained catalytic activity A series of design quenching experiments, electron paramagnetic resonance (EPR) experiments, and three-dimensional excitation-emission matrix fluorescence spectroscopy (3D-EEM) which were conducted to assess the selectivity of FeCo-LDH/PMS under high salt or natural organic conditions, as well as its effectiveness in treating real wastewater. These findings offer a novel approach to overcoming pH limitations and enhancing the selectivity of target pollutants in advanced oxidation processes (AOPs). Full article

The influence of static pressure during focused ultrasonic rolling extrusion on the corrosion resistance of GCr15 bearing steel was investigated. Quenched GCr15 bearing steel served as the subject of this study, wherein ultrasonic rolling extrusion was performed using a CNC lathe. Static pressure levels of 200 N, 400 N, and 500 N were applied during the experiments. Following the preparation of samples, which included grinding and cleaning, electrochemical assessments were conducted utilizing an electrochemical workstation. These assessments encompassed measurements of open-circuit potential, Tafel polarization, and electrochemical impedance spectroscopy, employing a three-electrode configuration. Additionally, the microstructural characteristics of the samples were examined using scanning electron microscopy, optical microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The findings indicate that an increase in static pressure results in a forward shift of the open-circuit potential and a reduction in corrosion susceptibility. Tafel analysis revealed an increase in linear polarization resistance, a decrease in corrosion current, and a positive shift in corrosion potential. The impedance spectroscopy results demonstrated that both the modulus of low-frequency impedance and charge transfer resistance increased with elevated static pressure. Microstructural analysis indicated that higher static pressure contributes to a smoother and more compact surface, with a reduction in defects. The primary corrosion products identified were iron oxides and hydroxides. In conclusion, the corrosion resistance of GCr15 bearing steel subjected to ultrasonic rolling extrusion is enhanced as static pressure increases. Full article

The use of natural organic extracts in nanoparticle synthesis can reduce environmental impacts and reagent costs. With that purpose in mind, a novel biosynthesis procedure for the formation of magnetic iron-oxide nanoparticles (IONPs) using Eucalyptus globulus extract in an aqueous medium has been systematically carried out. First, the biosynthesis was optimized for various extract concentrations, prepared by decoction and infusion methods, and yielded IONPs with sizes from 4 to 9 nm. The optimum concentration was found at 5% w/v, where the biosynthesis reaction time and ammonium hydroxide amount were the lowest of all samples. This extract concentration was tested, including in replicated samples, for a scale-up process, yielded a total mass of 70 g. It was found by Rietveld and electron microscopy analyses that the structural and morphological properties, such as crystalline and particle sizes (9 nm), are equivalent when scaling the synthesis process. ⁵⁷Fe Mössbauer spectroscopy results indicated that Fe ions are atomically ordered and in a trivalent state in all samples, corroborating with structural results found by X-ray diffraction. Magnetic analysis showed that the scale-up sample exhibited ferrimagnetic-like behavior suitable for magnetic remediation performance (55 emu g⁻¹). The eucalyptus functionalization was demonstrated by thermogravimetric measurements, whereas the colloidal analysis supported the stability of the magnetic suspensions at pH = 7 (zeta potential > −20 mV). The kinetic adsorption performance indicated a fast kinetic adsorption time of 40 min and remarkable removal efficiency of 96% for lubricant removal from water (emulsion systems). The infrared analysis confirmed the presence of the eucalyptus chemical groups even after the removal experiments. These results suggest that the scale-up sample can be recovered for future and sustainable magnetic remediation processes. Full article

Iron oxides and hydroxides (Fe-OH) extracted from natural sources have garnered significant attention for their diverse catalytic applications. This article provides a comprehensive overview of the catalytic potential of naturally occurring Fe-OH, focusing on the influence of natural sources and preparation methods on their morphological characteristics and application in heterogeneous catalysis. The unique physicochemical properties of these catalysts, including their high surface area, redox activity, and tunable surface chemistry, make them promising candidates for various catalytic processes. The review discusses key catalytic reactions facilitated by natural Fe-OH, such as advanced oxidation processes (AOPs), electrochemical applications, catalytic cracking, and biodiesel production. Furthermore, it highlights recent advancements and challenges in utilizing these materials as heterogeneous catalysts. By presenting an analysis of the catalytic potential of natural iron oxides, this review aims to stimulate further research about the use of these materials, which are widely distributed in the Earth’s crust. Full article

The Falakra geosite is located at the northern shoreline of the island of Limnos, Greece, and exhibits an array of unusual geomorphological features developed in late Cenozoic sandstones. Deposition of the primary clastic sediments was overprinted by later, low-temperature hydrothermal fluid flow and interstitial secondary calcite formation associated with nearby volcanic activity. Associated sandstone cannonballs take center stage in a landscape built by joints, Liesengang rings and iron (hydr)oxide precipitates, constituting an intriguing site of high aesthetic value. The Falakra geosite is situated in an area with dynamic erosion processes occurring under humid weather conditions. These have evidently sculpted and shaped the sandstone landscape through a complex interaction of wave- and wind-induced erosional processes aided by salt spray wetting. This type of geosite captivates scientists and nature enthusiasts due to its unique geological and landscape features, making its sustainable conservation a significant concern and topic of debate. Here, we provide detailed geological and remote sensing mapping of the area to improve the understanding of geological processes and their overall impact. Given the significance of the Falakra geosite as a unique tourist destination, we emphasize the importance of developing it under sustainable management. We propose the segmentation of the geosite into four sectors based on the corresponding geological features observed on site. Sector A, located to the west, is occupied by a lander-like landscape; to the southeast, sector B contains clusters of cannonballs and concretions; sector C is characterized by intense jointing and complex iron (hydr)oxide precipitation patterns, dominated by Liesengang rings, while sector D displays cannonball or concretion casts. Finally, we propose a network of routes and platforms to highlight the geological heritage of the site while reducing the impact of direct human interaction with the outcrops. For constructing the routes and platforms, we propose the use of serrated steel grating. Full article