Search Results (3,706)

Exploring materials for the uranium extraction from seawater holds great significance for the sustainable development of the nuclear industry. Though many adsorbents have been investigated to extract uranium, they still suffer from the issues of low adsorption performance and high production cost. In this work, biomass nanofiber adsorbents (PA-CS NFs) were prepared by the electrospinning of chitosan followed by functionalization with phytic acid. Based on the cost analysis, the preparation expense of PA-CS NFs was $16.4 kg⁻¹, lower than those of common synthetic polymer adsorbents. In addition, PA-CS NFs showed fast removal kinetics (equilibrium time = 60 min), high uptake capacity (457.8 mg g⁻¹), and good selectivity (the ratio of uranium/competing ion capacities > 3.8) from uranium spiked solution. PA-CS NFs also exhibited the ability to remove trace uranyl ions (distribution coefficient = 4.7 × 10⁵ mL g⁻¹) and satisfy recycling capacity. The experimental tests and theoretical calculations confirmed that the phosphate groups in the functionalized phytic acid displayed the main contribution to the uranyl ion adsorption, which had higher binding energy than the functional groups in chitosan. Benefiting from the good adsorption ability, low cost, and macroscopical membrane form, PA-CS NFs were applied to natural seawater for uranium extraction, and an extraction capacity of 4.52 mg g⁻¹ could be achieved after 35 days’ testing. On account of the obtained results, this study offers an efficient and low-cost nanofiber adsorbent for uranium extraction. Full article

The escalating issue of water pollution driven by rapid industrialization necessitates the development of advanced remediation technologies. In this study, a novel method for producing chromium (Cr(VI)) ion-imprinted biochar (Cr(VI)-IIP-PEI@NBC) from wheat residue was proposed. After acid-oxidative modifications, polyethyleneimine (PEI) and glutaraldehyde (GA) were employed as the functional monomer and crosslinker, respectively, to enhance the biochar’s selectivity and adsorption capacity. Under optimized conditions (pH 2.0, 55 °C), the adsorbent achieved a maximum Cr(VI) uptake of 212.63 mg/g, which was 2.3 times higher than that of the non-imprinted biochar. The material exhibited exceptional specificity (99.64%) for Cr(VI) and maintained >80% adsorption efficiency after five regeneration cycles, demonstrating excellent reusability. Comprehensive structural characterization via Fourier transform infrared spectroscopy (FT-IR), thermal gravimetric analysis (TGA), Brunner–Emmet–Teller measurements (BET), and Scanning Electron Microscopy (SEM) confirmed successful Cr(VI) imprinting in the biochar and its high thermal stability and mesoporous architecture, elucidating the mechanisms behind its superior performance. This study presents a sustainable and high-performance adsorbent for the efficient treatment of chromium-contaminated wastewater, with significant potential for industrial applications. Full article

Nanoparticle superlattices—periodic assemblies of uniformly spaced nanocrystals—bridge the nanoscale precision of individual particles with emergent collective properties akin to those of bulk materials. Recent advances demonstrate that multivalent ions and charged polymers can guide the co-assembly of nanoparticles, imparting electrostatic gating and enabling semiconductor-like behavior. However, the specific roles of anion geometry, valency, and charge density in mediating ion transport remain unclear. Here, we employ coarse-grained molecular dynamics simulations to investigate how applied electric fields (0–0.40 V/nm) modulate ionic conductivity and spatial distribution in trimethylammonium-functionalized gold nanoparticle superlattices assembled with four phosphate anions of distinct geometries and charges. Our results reveal that linear anions outperform ring-shaped analogues in conductivity due to higher charge densities and weaker interfacial binding. Notably, charge density exerts a greater influence on ion mobility than size alone. Under strong fields, anions accumulate at nanoparticle interfaces, where interfacial adsorption and steric constraints suppress transport. In contrast, local migration is governed by geometrical confinement and field strength. Analyses of transition probability and residence time further indicate that the rigidity and delocalized charge of cyclic anions act as mobility barriers. These findings provide mechanistic insights into the structure–function relationship governing ion transport in superlattices, offering guidance for designing next-generation ion conductors, electrochemical sensors, and energy storage materials through anion engineering. Full article

We investigated the application of an adsorbent fabricated from satsuma mandarin peel biomass using coating with poly(glycidyl methacrylate) followed by sequential treatment with hydroxylamine and hydrochloric acid for the remediation of hexavalent chromium-polluted water. The adsorbent was characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). Batch adsorption experiments were conducted wherein initial solution pH, initial chromium concentration, contact time, and temperature were varied. The adsorption equilibrium experimental data were well simulated by the Langmuir and Jovanovic models, pointing toward the formation of a monolayer of adsorbed chromium ions. The total chromium adsorption capacity of the functionalized satsuma mandarin peel adsorbent reached 219.28 mg g⁻¹ at initial pH 1.4 and 60 °C, markedly higher than 110.23 mg g⁻¹ at 30 °C. Where Cr(VI) was the sole chromium oxidation state in the initial solutions synthesized from potassium dichromate, the presence of Cr(III) ions in the final solutions confirmed Cr(VI) reduction. The results of this study show that the functionalized satsuma mandarin peel biomass is a potential candidate for use in the removal of hexavalent chromium from aqueous solution through reduction-coupled adsorption. Full article

The enrichment of cadmium (Cd) in farmland soil poses serious risks to agricultural safety and remains challenging to remediate. This study evaluated CaAl-layered double hydroxide (CaAl-LDH) as a highly efficient and stable passivator for Cd-contaminated soil. Laboratory adsorption tests demonstrated that Cd²⁺ adsorption on CaAl-LDH followed pseudo-second-order kinetics and the Langmuir model, indicating monolayer chemisorption, with a maximum capacity of 469.48 mg·g⁻¹ at pH 6. The adsorption mechanisms include surface complexation, interlayer anion exchange, dissolution–precipitation, and isomorphic substitution. A three-year field trial in Yongkang City, China showed that CaAl-LDH promoted the transformation of Cd in rhizosphere soil from the ion exchange state (F2) to the residual state (F7) and Fe–Mn oxidized state (F5), reducing the exchangeable Cd content by 26.71%. Consequently, Cd content in rice grains decreased by 68.42% in the first year and remained over 37% lower in the second year, consistently below the national food safety limit. Future research should focus on the optimization of material’s stability and application protocol. The results demonstrate that CaAl-LDH provides a cost-effective and sustainable strategy for the in situ passivation remediation of Cd-contaminated farmland, contributing to food safety and sustainable agriculture. Full article

Today, hydrogen is already widely regarded as up-and-coming source of energy. It is essential to meet energy needs while reducing environmental pollution, since it has a high energy capacity and does not emit carbon oxide when burned. However, for the widespread application of hydrogen energy, it is necessary to search new technical solutions for both its production and storage. A promising effective and cost-efficient method of hydrogen generation and storage can be the use of solid materials, including nanomaterials in which chemical or physical adsorption of hydrogen occurs. Focusing on the recommendations of the DOE, the search is underway for materials with high gravimetric capacity more than 6.5% wt% and in which sorption and release of hydrogen occurs at temperatures from −20 to +100 °C and normal pressure. This review aims to summarize research on hydrogen generation and storage using silicon nanostructures and silicon composites. Hydrogen generation has been observed in Si nanoparticles, porous Si, and Si nanowires. Regardless of their size and surface chemistry, the silicon nanocrystals interact with water/alcohol solutions, resulting in their complete oxidation, the hydrolysis of water, and the generation of hydrogen. In addition, porous Si nanostructures exhibit a large internal specific surface area covered by SiH_x bonds. A key advantage of porous Si nanostructures is their ability to release molecular hydrogen through the thermal decomposition of SiHx groups or in interaction with water/alkali. The review also covers simulations and theoretical modeling of H₂ generation and storage in silicon nanostructures. Using hydrogen with fuel cells could replace Li-ion batteries in drones and mobile gadgets as more efficient. Finally, some recent applications, including the potential use of Si-based agents as hydrogen sources to address issues associated with new approaches for antioxidative therapy. Hydrogen acts as a powerful antioxidant, specifically targeting harmful ROS such as hydroxyl radicals. Antioxidant therapy using hydrogen (often termed hydrogen medicine) has shown promise in alleviating the pathology of various diseases, including brain ischemia–reperfusion injury, Parkinson’s disease, and hepatitis. Full article

In line with sustainable construction goals, this study investigates the synergistic use of amine-based grinding aids (GAs), triethanolamine (TEA), and triisopropanolamine (TIPA) to enhance grinding performance and cement properties. GAs were physically blended at varying TEA/TIPA ratios, and their effects on grinding efficiency, CO₂ emissions, and environmental footprint were assessed based on energy consumption per target Blaine fineness. The interaction of blended GAs with Ca²⁺ ions was modeled to understand adsorption behavior. Cement particle size distribution (PSD), Hausner ratio, Carr index, and angle of repose were analyzed to evaluate powder flowability. Scanning electron microscopy (SEM) was employed to examine microstructural changes. Finally, the Taguchi method statistically analyzed the effective parameters influencing system performance. Results demonstrated that the optimized blend containing 25% TEA and 75% TIPA improved grinding performance, enhanced polymer–ion interactions, refined PSD, and significantly increased powder flowability. Overall, the study underscores the potential of amine-based polymeric GAs in producing environmentally friendly, high-performance cement composites. Using a Taguchi design with the larger-is-better S/N criterion, the optimal formulation was determined to be 25% TEA and 75% TIPA at a dosage of 0.10%. ANOVA results indicated that the TEA content was the most significant factor, while the dosage had no statistically significant effect. Full article

Chromium (Cr), a toxic heavy metal, poses significant environmental and health risks when industrial effluents containing Cr are discharged untreated. Addressing this challenge, this study developed a selective chromium removal strategy using IRA-900 resin in a sulfuric acid system with sodium phosphite (NaH₂PO₃) as a complexing agent. In the NaH₂PO₃-H₂SO₄ system, IRA-900 resin exhibited exceptional selectivity for Cr³⁺ with minimal co-adsorption of competing ions. The adsorption process followed the Langmuir isotherm model (R² > 0.99), indicating monolayer chemisorption dominated by homogeneous active sites, and achieved a maximum capacity of 103.56 mg·g⁻¹. Characterization via XPS, FT-IR, and SEM-EDS revealed a two-step mechanism: Cr³⁺ reacts with H₂PO₃⁻ to form an anionic complex, and then the complex undergoes electrostatic interaction and ion exchange with chloride ions (Cl⁻) on the quaternary ammonium groups of the resin. The chromium-loaded resin demonstrated remarkable structural stability, resisting Cr³⁺ desorption under conventional elution conditions. This property provides a novel pathway for chromium solidification in industrial wastewater, effectively minimizing secondary pollution risks. This work advances the design of ligand-assisted ion-exchange systems for targeted heavy metal removal, offering both high selectivity and environmental compatibility in wastewater treatment. Full article

Lead (Pb) in soil poses serious environmental and health risks, and its removal requires complex and costly treatment methods to meet strict regulatory standards. To effectively address this challenge, innovative and efficient techniques are essential. Sepiolite-supported MnFe₂O₄ (MnFe₂O₄/SEP) composites were synthesized via a chemical co-precipitation method. The effects of MnFe₂O₄/SEP on soil pH, cation exchange capacity (CEC), available Pb content, Pb²⁺ uptake, and the activities of antioxidant enzymes in Brassica chinensis (Pak Choi) were examined. MnFe₂O₄/SEP showed superior Pb²⁺ adsorption compared to SEP alone, fitting Langmuir models, Dubinin-Radushkevich (D-R) models, Temkin models and pseudo-second-order kinetics. The maximum adsorption capacities at 298, 308, and 318 K were 459, 500 and 549 mg·g⁻¹, respectively. XPS analysis indicated that chemisorption achieved through ion exchange between Pb²⁺ and H⁺ was the main mechanism. MnFe₂O₄/SEP increased the soil pH by 0.2–1.5 units and CEC by 18–47%, while reducing available Pb by 12–83%. After treatment with MnFe₂O₄/SEP, acid-extractable and reducible Pb in the soil decreased by 14% and 39%, while oxidizable and residual Pb increased by 26% and 21%, respectively. In Brassica chinensis, MnFe₂O₄/SEP reduced Pb²⁺ uptake by 76%, increased chlorophyll content by 36%, and decreased malondialdehyde (MDA) levels by 36%. The activities of antioxidant enzymes—superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT)—were decreased by 29%, 38% and 17%, respectively. These findings demonstrate that MnFe₂O₄/SEP is an efficient Pb²⁺ adsorbent that immobilizes Pb in soil mainly through ion exchange, thereby providing a highly effective strategy for remediating Pb-contaminated soils and improving plant health. Full article

Leaching mining of ion-adsorption rare earths degrades soil organic matter and hampers vegetation recovery. High-resolution UAV remote sensing enables large-scale monitoring of reclamation, yet vegetation detection accuracy is constrained by key challenges. Conventional three-channel detection struggles with terrain complexity, illumination variation, and shadow effects. Fixed UAV altitude and missing topographic data further cause resolution inconsistencies, posing major challenges for accurate vegetation detection in reclaimed land. To enhance multi-spectral vegetation detection, the model input is expanded from the traditional three channels to six channels, enabling full utilization of multi-spectral information. Furthermore, the Channel Attention and Global Pooling SPPF (CAGP-SPPF) module is introduced for multi-scale feature extraction, integrating global pooling and channel attention to capture multi-channel semantic information. In addition, the C2f_DynamicConv module replaces conventional convolutions in the neck network to strengthen high-dimensional feature transmission and reduce information loss, thereby improving detection accuracy. On the self-constructed reclaimed vegetation dataset, MRV-YOLO outperformed YOLOv8, with mAP@0.5 and mAP@0.5:0.95 increasing by 4.6% and 10.8%, respectively. Compared with RT-DETR, YOLOv3, YOLOv5, YOLOv6, YOLOv7, yolov7-tiny, YOLOv8-AS, YOLOv10, and YOLOv11, mAP@0.5 improved by 6.8%, 9.7%, 5.3%, 6.5%, 6.4%, 8.9%, 4.6%, 2.1%, and 5.4%, respectively. The results demonstrate that multichannel inputs incorporating near-infrared and dual red-edge bands significantly enhance detection accuracy for reclaimed vegetation in rare earth mining areas, providing technical support for ecological restoration monitoring. Full article

The removal of nickel from industrial wastewater necessitates efficient sorbent materials. This study investigates nanostructured potassium- and sodium-substituted aluminosilicate-based nanocomposites for this application. Materials were synthesized and characterized using SEM-EDS, XPS, XRD, FTIR, low temperature N₂ adsorption–desorption and Ni²⁺ adsorption experiments. SEM and XRD confirmed an X-ray amorphous structure attributable to fine crystallite size. The sodium-substituted material Na₂Al₂Si₂O₈ exhibited the lowest specific surface area (48.3 m²/g) among the tested composites. However, it demonstrated the highest Ni(II) sorption capacity (64.6 mg/g, 1.1 mmol/g) and the most favorable sorption kinetics, as indicated by a Morris-Weber coefficient of 0.067 ± 0.008 mmol/(g·min¹/²). Potassium-substituted analogs with higher Si/Al ratios showed increased surface area but reduced capacity. Analysis by XPS and SEM-EDS established that Ni(II) uptake occurs through a complex mechanism, involving ion exchange, surface complexation, and chemisorption resulting in the formation of new nickel-containing composite surface phases. The results indicate that optimal sorption performance for Ni(II) is achieved with sodium-based aluminosilicates at a low Si/Al ratio (Si/Al = 1). The functional characteristics of Na₂Al₂Si₂O₈ compare favorably with other silicate-based sorbents, suggesting its potential utility for wastewater treatment. Further investigation is needed to elucidate the precise local coordination environment of the adsorbed nickel. Full article

This study uses industrial wastewater from an aluminum factory to evaluate the phycoremediation efficiency of two green microalgal strains, Dictyosphaerium sp. and Tetradesmus obliquus. The industrial wastewater contained high levels of pollutants, including COD, ammonium, nitrate, phosphate, and heavy metal ions (Al³⁺, Cu²⁺, Cr³⁺, Zn²⁺, Mn²⁺, Cd²⁺). Four biomass conditions were tested: free-living cells (active living cells), immobilized cells (entrapped within alginate), dried biomass (non-living dried cells), and acid-treated dried biomass (chemically modified for enhanced adsorption). Both strains demonstrated significant pollutant removal, with living biomass (free and immobilized) achieving the highest nutrient and organic pollutant removal, and non-living biomass (dried and acid-treated) being more efficient for rapid heavy metal removal. Tetradesmus obliquus showed superior performance across most parameters, while Dictyosphaerium sp. exhibited the highest aluminum removal (99.4%, reducing Al from 481.2 mg/L to 10.2 mg/L). These findings highlight the potential of microalgae-based approaches and support species-specific strategies for cost-effective and sustainable phycoremediation of industrial wastewater. Full article

In this work, the removal of Cu(II) ions from an aqueous effluent was studied using an Mg/Fe layered double hydroxide (LDH) as the adsorbent. The material was synthesized and characterized before and after the adsorption process to identify structural and morphological changes induced by copper uptake. Techniques such as X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), ultraviolet-visible spectroscopy (UV-Vis), Raman spectroscopy, and nitrogen physisorption (BET) were employed to confirm the interaction between the metal ions and the LDH surface. The LDH-Mg/Fe exhibited a high maximum adsorption capacity of 526 mg/g, and the adsorption kinetics followed a pseudo-second-order model, achieving over 90% removal of Cu(II) within 2.5 h. The Cu(II)-loaded material was subsequently evaluated as a sustainable catalyst in two applications: (i) an organic synthesis via “click” chemistry, reaching yields of up to 85%, and (ii) the decoloration of Congo Red via a Fenton-like process, achieving a decoloration efficiency of at least 84%. These dual uses demonstrate the potential of Cu(II)-loaded LDH as a cost-effective and environmentally friendly approach to simultaneous pollutant removal and catalytic valorization. Full article

This study investigates the corrosion inhibition efficiency of [2-(thiophen-2-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole] and its Zn and Cu complexes for mild steel in 1.0 M HCl. The ligand was selected for its non-toxic profile and high electron density, favoring strong adsorption onto the metal surface. Electrochemical methods, including EIS, PDP, LPR, and CASP, were employed to evaluate the inhibitors’ performance. The results showed a significant decrease in corrosion current density and increased polarization resistance, with the Zn complex achieving the highest inhibition efficiency (93.8%). EIS fitting confirmed the formation of a protective film with high charge transfer and film resistance. Surface analyses by SEM and EDS revealed smoother steel morphology and inhibitor adsorption. XPS confirmed the presence of Fe³⁺, Zn²⁺and Cu²⁺ oxides, as well as all active inhibitor elements on the surface, supporting a mixed inhibition mechanism. The enhanced performance of the metal complexes is attributed to synergistic effects between the metal ions and the heterocyclic ligand, offering a promising strategy for the design of effective and environmentally friendly corrosion inhibitors. Full article

In recent years, apatite-based materials have garnered significant interest, particularly for applications in tissue engineering. Apatite is most commonly employed as a coating for metallic implants, as a component in composite materials, and as scaffolds for bone and dental tissue regeneration. Among its various forms, hydroxyapatite (HAP) is the most widely used, owing to its natural occurrence in human and animal hard tissues. An emerging area of research involves the use of fluoride-substituted apatite, particularly fluorapatite (FAP), which can serve as a direct fluoride source at the implant site, potentially offering several biological and therapeutic advantages. However, substituting HAP with FAP may lead to unforeseen changes in material behavior due to the differing physicochemical properties of these two calcium phosphate phases. This study investigates the effects of replacing hydroxyapatite with fluorapatite in ceramic–polymer composite materials incorporating β-1,3-glucan as a bioactive polymeric binder. The β-1,3-glucan polysaccharide was selected for its proven biocompatibility, biodegradability, and ability to form stable hydrogels that promote cellular interactions. Nitrogen adsorption analysis revealed that FAP/glucan composites had a significantly lower specific surface area (0.5 m²/g) and total pore volume (0.002 cm³/g) compared to HAP/glucan composites (14.15 m²/g and 0.03 cm³/g, respectively), indicating enhanced ceramic–polymer interactions in fluoride-containing systems. Optical profilometry measurements showed statistically significant differences in profile parameters (e.g., Rp: 134 μm for HAP/glucan vs. 352 μm for FAP/glucan), although average roughness (Ra) remained similar (34.1 vs. 27.6 μm, respectively). Microscopic evaluation showed that FAP/glucan composites had smaller particle sizes (1 μm) than their HAP counterparts (2 μm), despite larger primary crystal sizes in FAP, as confirmed by TEM. XRD analysis indicated structural differences between the apatites, with FAP exhibiting a reduced unit cell volume (524.6 ų) compared to HAP (528.2 ų), due to substitution of hydroxyl groups with fluoride ions. Spectroscopic analyses (FTIR, Raman, ³¹P NMR) confirmed chemical shifts associated with fluorine incorporation and revealed distinct ceramic–polymer interfacial behaviors, including an upfield shift of PO₄³⁻ bands (964 cm⁻¹ in FAP vs. 961 cm⁻¹ in HAP) and OH vibration shifts (3537 cm⁻¹ in FAP vs. 3573 cm⁻¹ in HAP). The glucan polymer showed different hydrogen bonding patterns when combined with FAP versus HAP, as evidenced by shifts in polymer-specific bands at 888 cm⁻¹ and 1157 cm⁻¹, demonstrating that fluoride substitution significantly influences ceramic–polymer interactions in these bioactive composite systems. Full article