Search Results (107)

Shagamite, KFe₁₁O₁₇ (IMA 2020-091) was discovered in the ferrite zone of gehlenite hornfels from the Hatrurim Complex exposed near Mt. Ye’elim, Hatrurim Basin, Israel. The mineral occurs in outer zones of gehlenite rock blocks that were heterogeneously altered by high-temperature (>1200 °C) ferritization. Ferritization was induced by K-bearing fluids or melts, generated as a by-product of late combustion processes. Shagamite crystallized from a thin melt that formed on the rock surface during cooling to approximately 800–900 °C. It is mainly associated with minerals of the magnetoplumbite group like barioferrite, Sr-analog of barioferrite, and gorerite but also with magnetite, maghemite, harmunite, devilliersite and K(Sr,Ca)Fe₂₃O₃₆ hexaferrite. Shagamite is a modular compound with a β-alumina-type structure (P6₃/mmc, a = 5.9327 (5), c = 23.782 (3) Å, γ = 120°, V = 724.91 (13) ų, Z = 2), and it is isostructural with diaoyudaoite, NaAl₁₁O₁₇, and kahlenbergite, KAl₁₁O₁₇. Its structure is also closely related, though non-isotypic, to those of the magnetoplumbite-group minerals. Shagamite is dark brown with a semi-metallic luster and forms platy crystals flattened on (001). Its mean empirical formula is: (K_1.00Ca_0.15Mn²⁺_0.05Na_0.04Rb_0.01)_Σ1.25(Fe_10.36Mn²⁺_0.15Al_0.14Mg_0.12Zn_0.10Ni_0.07Cu_0.03Cr³⁺_0.02Ti⁴⁺_0.01)_Σ11.00O₁₇. The Vickers microhardness VHN₂₅ = 507 kg/mm² corresponds to a Mohs hardness of ~5. The calculated density, based on the empirical formula and unit-cell parameters, is 4.12 g·cm⁻³. The main bands in the Raman spectrum of shagamite occur at 685 and 715 cm⁻¹ and are assigned to ν₁(FeO₄)⁵⁻ tetrahedral vibrations. Full article

Layered compounds containing the T₂O plane (T = transition metal), which is the anti-type of the CuO₂ plane in cuprate superconductors, have been explored widely because of their diverse physical properties. Among them, KV₂Se₂O has attracted much attention due to its interesting physical properties, especially the magnetic order. In this work, we report a new isostructural chromium oxyselenide, RbCr₂Se₂O. It was synthesized using a solid-state method using Rb₂CO₃ as the source of Rb and O for the title compound, with the assistance of Ba. The compound crystallizes in the space group P4/mmm with lattice parameters a = 4.01123(8) Å and c = 7.49357(18) Å. Magnetic susceptibility measurements indicate an antiferromagnetic transition at 345 K for RbCr₂Se₂O and also above room temperature, as the Néel temperature is T_N ≈ 400 K for KV₂Se₂O. The analysis of variable temperature XRD data reveals the anisotropic thermal expansion of the RbCr₂Se₂O lattice. The almost unchanged lattice parameter a near the transition temperature and the broad peak with an onset temperature of ~360 K in the differential scanning calorimetry data may have a relationship with the magnetic ordering. The measurement of electrical resistivity demonstrates the semiconducting behavior of RbCr₂Se₂O. The thermal activation model and variable-range hopping model are proposed to describe the conduction mechanism in the high- and low-temperature ranges, respectively. Full article

Heavy metal enrichment in agricultural soils can affect crop safety, ecosystem functioning, and long-term land productivity, yet farm-scale screening is often constrained by limited routine monitoring data. This study develops a GIS-based framework that combines field-scale spatial analysis with explainable machine learning to characterize and predict heavy metal enrichment on an intensively managed cereal farm in eastern Kazakhstan. Topsoil samples (0 to 20 cm) were collected from 34 fields across eight campaigns between 2020 and 2023, yielding 241 composite field–campaign observations for eight metals (Pb, Cu, Zn, Ni, Cr, Mo, Fe, and Mn) and routine soil properties (humus, pH in H₂O, and pH in KCl). Concentrations were generally low but spatially heterogeneous, with wide observed ranges for several elements (for example, Pb 0.06 to 2.20 mg kg⁻¹, Zn 0.38 to 7.00 mg kg⁻¹, and Mn 0.20 to 38.0 mg kg⁻¹). We synthesized multi-metal structure using an HMI defined as the unweighted mean of z-standardized metal concentrations, which supported field-level screening of persistent enrichment and emerging hot spots. We then trained Extreme Gradient Boosting models using only humus and pH predictors and evaluated performance with field-based spatial block cross-validation. Predictive skill was modest but nonzero for several targets, including HMI (mean R² = 0.20), indicating partial spatial transferability under conservative validation. SHAP analysis identified humus content and soil acidity as dominant contributors to HMI prediction. Overall, the workflow provides a transparent approach for field-scale screening of heavy metal enrichment and establishes a foundation for future integration with satellite-derived covariates for broader monitoring applications. Full article

In this work, two novel nanoscale zero-valent iron (nZVI) composites (nanoscale zero-valent iron and copper-intercalated montmorillonite (MMT-nFe⁰/Cu⁰) and carbon microsphere-supported sulfurized nanoscale zero-valent iron (CMS@S-nFe⁰)) were used to treat soil contaminated with both Cr(VI) and p-nitrophenol (PNP), and added persulfate (PMS). Experiments found that the pollutant removal effect has a great relationship with the ratio of water to soil, the amount of catalyst, the amount of PMS, and the pH value. When the conditions are adjusted to the best (water–soil = 2:1, catalyst 30 g/kg, PMS 15 g/kg, pH 7–9), both materials fix Cr(VI) well and decompose PNP. The removal rates of Cr(VI) and PNP by the MMT-nFe⁰/Cu⁰ system are 90.4% and 72.6%, respectively, while the CMS@ S-nFe⁰ system is even more severe, reaching 94.8% and 81.3%. Soil column leaching experiments also proved that the fixation effect of Cr can last for a long time and PNP can be effectively decomposed. Through detection methods such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS), we found that Cr(VI) was effectively reduced to Cr(III) by Fe⁰ and Fe²⁺ ions and subsequently transformed into stable FeCr₂O₄ spinel oxides, and the groups produced after the decomposition of PNP could also help fix the metal. This work provides a way to simultaneously treat Cr(VI) and PNP pollution, and also allows the use of multifunctional nZVI composites in complex soil environments. Full article

Soils heavily contaminated with potentially toxic elements (PTEs) pose substantial risks to the environment and human health. However, conventional remediation methods are often plagued by high energy consumption and the potential for secondary pollution. To address this challenge, this study developed a synergistic system combining acidophilic bacteria with a Fe-modified anode, aiming to enhance the remediation of PTEs in such contaminated soils. This system integrates the following three core components: the catalytic function of Fe₃O₄–graphene-oxide (Fe₃O₄–GO) nanocomposites, the acclimation of microbial communities, and the optimization of process parameters—specifically, applied electric current, pH, and oxidation–reduction potential (ORP). Experimental treatments were designed to assess the individual and combined effects of three key factors: bacterial inoculation, the Fe-modified anode, and the addition of Fe₃O₄–GO. The results revealed that the integrated synergistic system effectively reduced the soil pH from 2.9 to 2.0 and maintained the ORP at approximately 600 mV. For PTE removal, the system achieved efficiencies of 89% for Zn, 85.89% for Cu, 66.3% for Pb, 77.89% for Cd, and 40.63% for Cr, respectively. In contrast, control groups lacking bacteria, applied current, or Fe₃O₄–GO exhibited significantly lower metal removal efficiencies. Notably, the bacteria-free treatment led to a more than 50% reduction in Cr removal. Additionally, the group with an unmodified anode only achieved 1/3 to 1/2 of the removal efficiencies observed in the full synergistic system; this discrepancy is likely attributed to reduced electron transfer efficiency and compromised microbial adhesion on the anode surface. These findings demonstrate that the coupling of electrochemical enhancement, acidophilic microbial activity, and Fe₃O₄–GO catalysis constitutes an effective and energy-efficient approach for remediating soils contaminated with high concentrations of PTEs while simultaneously minimizing the risk of secondary pollution. Full article

Titanium-containing nanoparticles have emerged as materials of significant technological importance due to their multifunctional properties and excellent performance. With their expanding applications, the amount of TiO₂ nanoparticles (TNPs) being released into the soil environment has increased significantly. This review addresses the gap in current research, which has predominantly focused on the environmental behavior of TNPs in aquatic systems while lacking systematic integration of the synergetic mechanism of adsorption–transformation–ecological effects in soil systems and its guiding value for practical applications. It deeply reveals the interaction mechanisms between TNPs and environmental pollutants. TNPs exhibit outstanding adsorption performance towards environmental pollutants such as heavy metals and organic compounds. Specifically, the maximum adsorption capacities of titanate nanowhiskers for the heavy metal ions Cu(II), Pb(II), and Cr(III) are 143.9 mg·g⁻¹, 384.6 mg·g⁻¹, and 190.8 mg·g⁻¹, respectively. Additionally, 1-hydroxydinaphthoic acid surface-modified nano-TiO₂ exhibits an adsorption rate of up to 98.6% for p-nitrophenol, with an enrichment factor of 50-fold. The transformation process of TNPs after pollutant adsorption profoundly affects their environmental fate, among which pH is a critical controlling factor: when the environmental pH is close to the point of zero charge (pHpzc = 5.88), TNPs exhibit significant aggregation behavior and macroscopic sedimentation. Meanwhile, factors such as soil solution chemistry, dissolved organic matter, and microbial activities collectively regulate the aggregation, aging, and chemical/biological transformation of TNPs. In the soil ecosystem, TNPs can exert both beneficial and detrimental impacts on various soil organisms, including bacteria, plants, nematodes, and earthworms. The beneficial effects include alleviating heavy metal stress, serving as a nano-fertilizer to supply titanium elements, and acting as a nano-pesticide to enhance plants’ antiviral capabilities. However, excessively high concentrations of TiO₂ can stimulate plants, induce oxidative stress damage, and impair plant growth. This review also highlights promising research directions for future studies, including the development of safer-by-design TNPs, strategic surface modifications to enhance functionality and reduce risks, and a deeper understanding of TNP–soil microbiome interactions. These avenues are crucial for guiding the sustainable application of TNPs in soil environments. Full article

Addressing the challenges of energy production and environmental sustainability necessitates the development of advanced materials capable of facilitating both photocatalytic reduction and oxidation processes. Here, we report a Z-scheme Ag₃PO₄/CuBi₂O₄ heterojunction photocatalyst, which was fabricated via the in situ anisotropic growth of Ag₃PO₄ nanoparticles on the ends of CuBi₂O₄ microrods. The prepared heterojunction exhibits a low lattice mismatch (~3%) and features a covalently bonded interface, anchored by oxygen atoms, with the formation of P-O-Cu bonds. This interface synergizes with the built-in electric field to drive an efficient Z-scheme charge transfer mechanism, significantly enhancing the separation and migration of carriers. Furthermore, the interfacial chemical bonds induce electron redistribution that effectively weakens the Ag-O bond, thereby activating surface lattice oxygen. As a result, the photocatalyst shows remarkably improved performance for photocatalytic oxygen evolution synchronized with Cr(VI) reduction by enabling both the conventional adsorbate evolution mechanism and the lattice oxygen mechanism. This work provides critical insights into the design of efficient photocatalysts. Full article

With the rapid advances of the electronics industry, a large amount of acidic etching waste solutions (AEWS) for etching Printed Circuit Board (PCB) are generated, which require complete remediation and sustainable recycling to avoid environmental pollution and wasting of resources. Herein, the novel purification technology for the acidic copper-containing etching waste solution was exploited via integrated alkali gradient pH control (3.0, 3.2, and 3.5). At pH 3.0, the system demonstrated selective metal removal with 94.02% efficiency for Fe and 82.60% for Mn. Elevating the pH to 3.2 enabled effective elimination of Zn (59.32%), Cr (59.46%), and Al (33.24%), while maintaining minimal copper loss (8.16%). Further pH adjustment to 3.5 achieved enhanced removal efficiencies of 97.86% (Fe), 91.30% (Mn), 59.38% (Zn), 62.10% (Cr), 21.66% (Ca), 34.05% (Al), and 26.66% (Co), with copper retention remaining high at 70.83% (29.17% loss). Furthermore, using the purified AEWS (pH 3.2) as precursor, high-purity nano-CuO was successfully synthesized through a Cu₂(OH)₃Cl conversion-calcination process, exhibiting 99.20% CuO purity with 0.0012% chlorine content and <0.1% metallic impurities. The development and application of the purification technology for AEWS containing copper, along with the production methodology for high-purity CuO, were significant to the fields of electronic information industry, environmental engineering, green industry and sustainable development of the ecological environment. Full article

Rouaite (Cu₂(OH)₃NO₃) long hexagonal multilayered nanoplates with high purity and high crystallinity were prepared from acidic reaction solution (pH = 4.4–4.8) with the assistance of ZnO. The ZnO-assisted strategy is remarkably different from the conventional synthetic protocol that was regularly carried out in alkaline solution (pH > 11). The rouaite multilayer nanoplates displayed exceptionally high catalytic activity in the catalytic wet peroxide oxidation (CWPO) of Congo red (CR). The catalytic efficiency for CR decolorization achieved an impressive 96.3% in 50 min under near-neutral (pH = 6.76) and ambient conditions (T = 20 °C, p = 1 atm), without increasing the temperature and/or decreasing the pH value to acidic region (pH = 2–3) as is commonly employed in CWPO process for improved degradation efficiency. Full article

Five requeijão samples, classified as Brazilian cream cheeses, were developed: one control (without guabiroba pulp (Campomanesia xanthocarpa O. Berg) and four with 5, 10, 15, and 20% (m/m) guabiroba pulp. They were evaluated for pH, water activity (aw), color, texture, multi-mineral composition, carotenoid content, and microstructure. The addition of guabiroba pulp reduced pH and maintained Aw. The samples with 5%, 10%, 15%, and 20% guabiroba pulp presented a yellow–reddish coloration. The formulation with 5% had the lowest values of firmness, resilience, texture, and spreadability. From 10% onwards, an increase in cohesiveness and a reduction in creaminess were observed. The sample with 15% presented better spreadability, while the 20% sample had adhesiveness similar to the control. No traces of Al, As, Cd, Co, Cr, Cu, Fe, Mn, Pb, or Se were detected. The detected elements, in descending order, were Na, Ca, P, S, K, Mg, Sr, and Zn. β-carotene was predominant, with guabiroba pulp enhancing α-carotene, β-carotene, β-cryptoxanthin, and λ-carotene levels, especially at 20% pulp. Microstructure analysis by scanning electron microscopy (SEM) showed no significant differences. These findings highlight the potential of guabiroba pulp as a functional ingredient in requeijão, enhancing its carotenoid profile while maintaining desirable textural and physicochemical properties. Full article

Hydrogel-based adsorbents have gained increasing recognition in recent years due to their promising potential for pollutant removal. However, conventional hydrogels often suffer from low mechanical strength over prolonged use. Therefore, this study explores the incorporation of silica extracted from bamboo culm (Dendrocalamus asper) to enhance the mechanical stability of hydrogel beads composed from carboxymethyl cellulose (CMC), chitosan (CS), and magnetite ferrofluid (Fe₃O₄), through cross-linking. We hypothesize that silica enhances the mechanical properties of magnetite hydrogel beads without compromising their adsorption capacity. The extracted silica was confirmed with FTIR and EDS analysis. The synthesized CMC-CS-Fe₃O₄-Si hydrogel beads were characterized using FTIR and SEM. Its stability was assessed through dry weight loss measurements, while its adsorption efficiency was evaluated using batch adsorption experiments. The silica-incorporated hydrogel exhibited enhanced mechanical and thermal stability under various pH and temperature conditions, without negatively affecting its adsorption performance, achieving maximum adsorption capacities of 53.00 mg/g for Cr (VI) and 85.06 mg/g for Cu (II). Desorption and regeneration studies confirmed the reusability of the hydrogel for more than four cycles. Overall, the interaction between the hydrogel and silica resulted in excellent adsorption performance, improved mechanical properties, and long-term reusability, making this a promising hydrogel adsorbent for wastewater remediation. Full article

Copper oxide nanoparticles (CuO-NPs) induce neurological diseases, including neurobehavioral defects and neurodegenerative diseases. Direct evidence indicates that CuO-NPs induce inflammation in the central nervous system and cause severe neurotoxicity. However, the mechanism of CuO-NP-induced damage to the nervous system has rarely been studied, and the toxicity of different CuO-NP particle sizes and their copper ion (Cu²⁺) precipitation in microglia (BV2 cells) is worth exploring. Therefore, this study investigated CuO-NPs with different particle sizes (small particle size: S-CuO-NPs; large particle size: L-CuO-NPs), Cu²⁺ with equal molar mass (replaced by CuCl₂ [Equ group]), and Cu²⁺ precipitated in a cell culture solution with CuO-NPs (replaced by CuCl₂ [Pre group]), and examined the mechanism of action of each on BV2 microglia after co-culture for 12 h and 24 h. The activity of BV2 cells decreased, the morphology was damaged, and the apoptosis rate increased in all the exposed groups. Toxicity increased time- and dose-dependently, and was highest in the Equ group, followed by the S-CuO-NPs, L-CuO-NPs, and Pre groups, respectively. Subsequently, we investigated the mechanism of S-CuO-NP-induced cell injury, and revealed that S-CuO-NPs induced oxidative stress and inflammatory response and increased the membrane permeability of BV2 cells. Moreover, S-CuO-NPs reduced the ratio of p-CSF-1R/CSF-1R, p-PLCγ2/PLCγ2, p-extracellular signal-regulated kinase (ERK)/ERK, p-Nrf2/Nrf2, and Bcl-2/Bax protein expression in microglia, and elevated cleaved caspase-3 expression. The CSF-1R/PLCγ2/ERK/Nrf2 apoptotic pathway was activated. The downregulation of CX3CR1, CSF-1R, brain-derived neurotrophic factor (BDNF), and IGF-1 protein expression indicates impairment of the repair and protection functions of microglia in the nervous system. In summary, our results reveal that CuO-NPs promote an increase in inflammatory molecules in BV2 microglia through oxidative stress, activate the CSF-1R/PLCγ2/ERK/Nrf2 pathway, cause apoptosis, and ultimately result in neurofunctional damage to microglia. Full article

The circular economy practice of using waste to fertilize plants should be more widespread. It is a means to manage natural resources sustainably in agriculture. This approach is in line with organic and sustainable farming strategies, reducing the cultivation costs. Organic waste dumped into a landfill decomposes and emits greenhouse gases. This can be reduced through its application to energy crops, which not only has a positive impact on the environment but also improves the soil quality and increases yields. However, organic waste with increased content of heavy metals, when applied to the soil, can also pose a threat. Using Miscanthus × giganteus M 19 as a test plant, an experiment with a randomized block design was established in four replications in Central–Eastern Poland in 2018. Various combinations of organic waste (municipal sewage sludge and spent mushroom substrate) were applied, with each dose containing 170 kg N ha⁻¹. After three years (in 2020), the soil content of total nitrogen (N_t) and carbon (C_t) was determined by elemental analysis, with the total content of P, K, Ca, Mg, S, Na, Fe, Mn, Mo, Zn, Ni, Pb, Cr, Cd, and Cu determined by optical emission spectrometry, after wet mineralization with aqua regia. For the available forms of P and K, the Egner–Riehm method was used, and the Schachtschabel method was used for the available forms of Mg. The total content of bacteria, actinomycetes, and fungi was also measured. The application of municipal sewage sludge (SS) alone and together with spent mushroom substrate (SMS) improved the microbiological composition of the soil and increased the content of N_t and C_t and the available forms of P₂O₅ and Mg more than the application of SMS alone. SMS did not contaminate the soil with heavy metals. In the third year, their content was higher after SS than after SMS application, namely for Cd by 12.2%, Pb by 18.7%, Cr by 25.3%, Zn by 16.9%, and Ni by 14.7%. Full article

This study deals with the reconstruction of the paleoenvironment and the paleoclimate situation of the middle–upper Eocene sediments in the northwest Fayum area. The reconstruction is based on comprehensive stratigraphical and geochemical analyses of major oxides and trace elements for selected sediment samples from the Gehannam Formation (Bartonian–Priabonian), the Birket Qarun and the Qasr El Sagha formations (Priabonian). The sedimentological features coupled with paleo-redox trace elemental ratios (Ni/Co, V/Cr, U/Th, V/(V + Ni), and Cu/Zn), paleosalinity (Sr/Ba, Mg/Al ×100, Ca/Al), and paleowater depth (Fe/Mn) proxies, indicate that deposition took place in a shallow marine agitated environment with high oxygen levels. Paleoclimate indicators (Sr/Cu, Rb/Sr, K₂O₃/Al₂O₃, Ga/Rb, C-value, CIA, and CIW) suggest warm and prevailing arid climatic conditions, with minor humid periods at some intervals. The observed low values of the total organic carbon (TOC) are attributed to significant high sediment influx, predominant oxygenated conditions, and poor primary productivity, which is further confirmed by low values of paleoprimary productivity proxies (P, Ni/Al, Cu/Al, P/Al and P/Ti, and Ba_bio ratios). These findings enhance our understanding of the Eocene environments and provide insights into sedimentation processes during this period. Full article

The multielement pyrochlore of the composition Bi_1.57Mn_1/3Cr_1/3Cu_1/3Nb₂O_9−Δ (sp. gr. Fd-3m:2, 10.4724 Å) containing transition element atoms—chromium, manganese and copper in equimolar amounts—was synthesized for the first time using the solid-phase reaction method. The microstructure of the ceramics is grainless and has low porosity. The sample is characterized by reflection in the red (705 nm) color region. The band gap for the direct allowed transition in the sample is 1.68 eV. The parameters of the Bi5d, Nb3d, Сr2p, Mn2p, and Cu2p X-ray photoelectron spectroscopy (XPS) spectra for the mixed pyrochlore are compared with the parameters of transition element oxides. For the complex pyrochlore, a characteristic shift in the Bi4f and Nb3d spectra to the region of lower energies by 0.15 and 0.60 eV, respectively, is observed. According to the XPS Cu2p and Mn2p spectra of pyrochlore, copper, and manganese cations are in a mixed charge state; they mainly have an effective charge of +2/+3, and the Cr2p spectrum is a superposition of the spectra of chromium ions in the charge state of +3, +4, +6. At 24 °С, the permittivity of the sample in the frequency range (10⁴–10⁶ Hz) weakly depends on the frequency and is equal to ~100, the dielectric loss tangent is 0.017. The activation energy of conductivity is equal to 0.41 eV. The specific electrical conductivity of Bi_1.57Cr_1/3Cu_1/3Mn_1/3Nb₂O_9−Δ increases with the temperature increasing from 1.8 × 10⁻⁵ Ohm⁻¹·m⁻¹ (24 °С) to 0.1 Ohm⁻¹·m⁻¹ (330 °С). Nyquist curves for the sample are modeled by equivalent electrical circuits. Full article