Search Results (714)

This study explores the effect of cation adsorption on the shear strength and mineralogical characteristics of smectite-rich landslide clay collected from the Nishinotani landslide in Ehime Prefecture, Japan. Laboratory experiments were conducted using aqueous solutions of calcium, magnesium, and potassium chlorides at concentrations of 1000, 6000, and 12,000 mg/L. Ion chromatography, X-ray diffraction (XRD), and ring shear tests were conducted to evaluate the interaction between ion uptake and its influence on the change in shear strength. The results showed that calcium and potassium ion adsorption increased with both concentration and time, leading to enhanced residual shear strength and crystallinity, primarily due to stronger Coulombic interactions and favorable ionic size compatibility with smectite. Conversely, magnesium ions exhibited adverse effects, including reduced strength and mineral ordering, attributed to calcium leaching and weaker interparticle bonding. The findings indicate that selective cation exchange can be an effective, sustainable alternative to conventional landslide stabilization methods, especially in fine-grained, expansive clay systems. This work contributes to the development of geochemically engineered landslide mitigation strategies based on microstructural and mineralogical reinforcement. Full article

A zero-dimensional, non-isothermal analytical framework was developed to assess solid oxide fuel cell (SOFC) performance across a broad range of operating conditions. The model integrates the anode, electrolyte, interlayers, and cathode, while resolving the distinct physicochemical processes within each layer. Electrochemical impedance spectroscopy (EIS), followed by distribution of relaxation times (DRT) analysis, was implemented to probe relevant cell polarization resistances under open-circuit and load conditions. The modeling framework couples mass and charge transport, electrochemical reactions, and non-isothermal heat transfer, with multilayer discretization applied to capture localized material properties and operating conditions. It enables the estimation of electrolyte ionic conductivity and total ohmic resistance by accounting for microstructural and geometric parameters, while also quantifying activation energies, exchange current densities, and gas-diffusion-related polarization resistances. Simulations were conducted for an SOFC operating on pure hydrogen with varying oxygen concentrations at 700 °C, 660 °C, 620 °C, and 580 °C. The results were validated against experimental data. The analysis revealed that ohmic overpotential dominates total cell losses, even at high current densities, underscoring the importance of minimizing ionic resistance to improve overall SOFC performance. Full article

This work presents a detailed study of the coordination of Eu(III) with tartrate and oxalate ligands in aqueous solutions. The following techniques were employed: potentiometric titrations, 1D ¹H, ¹³C multinuclear NMR spectroscopy, 2D NMR experiments (COSY, HMQC, HMBC), and UV-Vis spectroscopy. Overall (cumulative) formation constants (logβ) were determined at ionic strengths of 0.1, 0.5, and 1.0, M KNO₃ over the temperature range 298–318 K. At 298 K, the oxalate complexes are significantly more stable (logβ = 7.63→15.70 as the ionic strength increases from 0.1 to 1.0 M) than the corresponding tartrate species (logβ = 5.11→8.87). Analysis of the temperature dependence of logβ shows that the Gibbs free energy change comprises both temperature-dependent terms and an approximately temperature-independent covalent contribution, the latter becoming strongly negative values in the tartrate system. The NMR data support a bidentate coordination mode involving deprotonated hydroxyl and carboxylate groups, whereas ¹⁷O NMR monitors the mechanism of water exchange within the Eu(III) hydration sphere. In the UV-Vis domain, a distinct blue shift in the absorption band is observed at 0.1 M KNO₃, while at 1.0 M KNO₃, the band shows a pronounced decrease in intensity, a hypochromic effect. This behavior can be attributed to increased structural distortion and a partial loss of coplanarity within the tartrate coordination environment. By contrast, the oxalate system behaves differently: the spectra, together with the thermodynamic data, support a more covalent Eu–O interaction, consistent with stabilization of Eu(III) by two dicarboxylate ligands adopting distinct coordination modes. Full article

Electrochemical carbon dioxide reduction reaction (CO₂RR) offers a promising route to mitigate climate change while simultaneously enabling renewable energy storage and the sustainable production of value-added chemicals. A wide variety of CO₂RR reactor designs have been developed, including both liquid-phase cells and gas-phase configurations. Among these, gas-phase systems, particularly flow-cell and membrane electrode assembly (MEA) designs, have become the primary focus of recent research due to their ability to overcome mass transport limitations and operate at high currents. While catalyst development has received considerable attention in advancing CO₂RR performance, the role of membranes in these gas-phase electrolyzers has been less systematically reviewed. This article addresses that gap by critically examining the functions, advantages, and limitations of the major membrane classes used in CO₂ electrolysis: anion exchange membranes, cation exchange membranes, bipolar membranes, and non-ion-exchange porous membranes within flow-cell and MEA configurations. We highlight how membrane properties influence local pH regulation, water management, crossover behavior, and overall reactor performance, while emphasizing that product identity is primarily catalyst-determined. By analyzing recent progress and remaining challenges, this review provides design insights for membrane selection and development toward efficient, stable, and scalable CO₂ electrolysis systems. Full article

The trade-off between the ionic conductivity and the stability of the proton exchange membrane (PEM) is a major concern in the development of PEM water electrolysis (PEMWE). This review focuses on the design and fabrication of homogeneous and composite PEMs for water electrolysis and establishes the structure–performance relationships between the membrane chemical/physical structures and their efficiency metrics—specifically, proton conductivity, hydrogen permeability, and chemical and mechanical stability. A special focus is placed on the fundamental connection between the microstructure and performance of membrane materials. At the molecular level, we systematically illustrate the design principles for main chains, side chains, and sulfonate groups, covering both fluorinated PEMs (encompassing perfluorinated and partially fluorinated membranes) and non-fluorinated PEMs (including aromatic polymers with heteroatom backbones and all-carbon backbones). At the macroscopic level, the review provides an in-depth exploration of two primary modification strategies: creating composites with organic polymers and with inorganic nanofillers. In summary, this review elucidates how these composite approaches leverage material synergies to improve the membrane’s mechanical integrity, proton conduction efficiency, and chemical resistance and offers a theoretical framework for the rational design of next-generation, high-performance PEMs to advance the commercialization of PEMWE technology. Full article

Phenomena associated with an ion-exchange membrane (IEM) in contact with an ionic solution, such as its selectivity and ionic transport, commonly occur when an ion approaches the membrane surface. Because of this, if a change occurs in the IEM/Solution interfacial region, then it is expected that these processes will be affected. For example, if the IEM surface is modified with an electronic conducting polymer (ECP), then its selectivity and the phenomena associated with ionic transport will change. These changes can be quantified by parameters such as the permselectivity, the contact angle, and others, and are associated with the hydrophilic/hydrophobic balance of its surface. This work reports the characterization of commercial anion-exchange membrane samples modified voltammetrically with polyaniline (PAni) obtained at different temperatures (10, 15, and 20 °C). Among the main results obtained, it was found that with an increase in synthesis temperature of the PAni, the membrane’s permselectivity will increase from 0.757 to 0.782 to 0.808. While contrary behavior is observed in the case of the contact angle, since an increase in the synthesis temperature will cause a greater hydrophilic character when going from 67° to 53° to 50°. According to this work, these trends in the properties of the modified membranes are related to the morphological characteristics of PAni deposits conferred by the variation in the synthesis temperature. Full article

Waste electrical and electronic equipment (WEEE) is a rapidly growing waste stream rich in precious metals, with gold in particular being concentrated in printed circuit boards and other high-value components. Historically, industrial recycling has relied on pyrometallurgy and non-selective hydrometallurgical leaching. These recovery routes have major drawbacks, including high energy demand, corrosion, the use of toxic reagents, and the complexity of pregnant leach solutions, which complicate downstream gold recovery. This review aims to synthesize recent advances in selective gold recovery from WEEE using a speciation-driven approach. Mechanical pretreatment and physical beneficiation methods are critically assessed as processes for concentrating gold and reducing the amount of material sent to downstream hydrometallurgical leaching. Different lixiviants, from conventional cyanide to halide-based, as well as greener chemistries such as thiosulfate and thiourea, are assessed for gold dissolution from the WEEE stream. Assessment of different extraction methods, including sorbents, ion exchange resins, solvent/ionic liquid, direct reduction/precipitation, and electrochemical recovery, is conducted. The review concludes with guidelines for potential process integration and highlights the need for scalable, reusable lixiviants and sorbent materials validated under realistic multi-metal conditions in real WEEE leachate. Full article

Indium is a strategically important metal, essential for the production of transparent conductive oxides, flat panel displays, thin-film photovoltaics, and advanced optoelectronic devices. Due to its limited natural abundance and its occurrence in trace amounts alongside other metals in both primary and secondary sources, the recovery of indium through efficient separation techniques has gained increasing attention. This review discusses three major separation strategies for indium recovery: solvent extraction, ion-exchange, and membrane processes, applied to both synthetic solutions and real leachates. D2EHPA has demonstrated its applicability as an effective agent for indium separation, not only in solvent extraction but also as an impregnating agent in polymer resins and membranes. While solvent extraction achieves high recovery rates, ion-exchange resins and membrane-based methods offer significant advantages in terms of reusability, reduced chemical consumption, and minimal environmental impact. The selective separation of indium from impurities such as Fe³⁺ and Sn²⁺ remains a key consideration, which can be addressed by optimizing feed solution conditions or adjusting the selective stripping stages. A comparative overview of these methods is provided, focusing on separation efficiency, operational conditions, and potential integration into close-loop systems. The article highlights recent innovations and outlines the challenges involved in achieving sustainable indium recovery, in line with circular economy principles. Full article

Polyphenols are a structurally diverse group of plant secondary metabolites widely recognized for their antioxidant, anti-inflammatory, antimicrobial, and chemoprotective properties, which have stimulated their extensive use in food, pharmaceutical, nutraceutical, and cosmetic products. However, their chemical heterogeneity, wide polarity range, and strong interactions with plant matrices pose major challenges for efficient extraction, separation, and reliable analytical characterization. This review provides a critical overview of contemporary strategies for the extraction, separation, and identification of polyphenols from plant-derived matrices. Conventional extraction methods, including maceration, Soxhlet extraction, and percolation, are discussed alongside modern green technologies such as ultrasound-assisted extraction, microwave-assisted extraction, pressurized liquid extraction, and supercritical fluid extraction. Particular emphasis is placed on environmentally friendly solvents, including ethanol, natural deep eutectic solvents, and ionic liquids, as sustainable alternatives that improve extraction efficiency while reducing environmental impact. The review further highlights chromatographic separation approaches—partition, adsorption, ion-exchange, size-exclusion, and affinity chromatography—and underlines the importance of hyphenated analytical platforms (LC–MS, LC–MS/MS, and LC–NMR) for comprehensive polyphenol profiling. Key analytical challenges, including matrix effects, compound instability, and limited availability of reference standards, are addressed, together with perspectives on industrial implementation, quality control, and standardization. Full article

Achieving sustainable land restoration in southern Chinese ionic rare earth mining areas remains a significant challenge due to the extended duration and low efficiency of conventional remediation approaches. Although the hyperaccumulator Dicranopteris pedata possesses a remarkable capacity for rare earth element (REE) enrichment, a significant knowledge gap exists regarding how to effectively combine exogenous organic acids with agronomic practices like clipping to enhance its remediation efficiency in an environmentally sustainable manner. Crucially, the potential environmental risks associated with such synergistic strategies have not been systematically evaluated, hindering their practical application. To address this, our study focused on Dicranopteris pedata and employed integrated pot and soil column leaching experiments to systematically analyze the effects of different concentrations of citric acid and tartaric acid on REE migration and transformation within the soil–plant system. The results demonstrated that exogenous organic acids significantly reduced soil pH and promoted the conversion of REEs from the residual to the exchangeable fraction. Specifically, the 20 mmol·kg⁻¹ citric acid treatment increased the proportion of exchangeable REEs by 43.46%. Furthermore, organic acid treatments significantly altered the REE uptake patterns in Dicranopteris pedata, inhibiting the translocation and accumulation of REEs in the aboveground tissues. Soil column leaching experiments revealed that citric acid drove the migration of REEs to deeper soil layers, with the concentration peaking at 288.33 mg·kg⁻¹ at a depth of 6–8 cm; concomitantly, the REE content in the leachate reached its maximum on the 5th day. This study demonstrates that the combined application of 20 mmol·kg⁻¹ citric acid and 100% clipping management increased the annual REE accumulation in Dicranopteris pedata to 4.85 g·m⁻², thereby significantly shortening the theoretical remediation period from 25.0 years in the control to 12.1 years. Soil column leaching experiments indicated no significant secondary pollution risk associated with this strategy. These findings provide a feasible, low-risk, and sustainable technical strategy for the synergistically enhanced remediation of REE-contaminated soils, offering a promising path for ecological restoration and sustainable land management in degraded mining ecosystems. Full article

Perfluorosulfonic acid (PFSA) membranes suffer from severe conductivity decay caused by dehydration at elevated temperatures, hindering their application in medium- to high-temperature proton exchange membrane fuel cells (MHT-PEMFCs). To address this, Nafion/SiO₂ composite membranes with systematically varied filler contents were fabricated via a sol–gel-assisted casting strategy to enhance hydration stability and proton transport. Spectroscopic and microscopic analyses reveal a homogeneous nanoscale dispersion of SiO₂ within the Nafion matrix, along with strong interfacial hydrogen bonding between SiO₂ and sulfonic acid groups. These interactions effectively suppress polymer crystallinity and stabilize hydrated ionic domains. Thermogravimetric analysis confirms markedly improved water retention in the composite membranes at intermediate temperatures. Proton conductivity measurements at 50% relative humidity (RH) identify the Nafion/SiO₂-3 membrane as exhibiting optimal transport behavior, delivering the highest conductivity of 61.9 mS·cm⁻¹ at 120 °C and significantly improved conductivity retention compared to Nafion 117. Furthermore, single-cell tests under MHT-PEMFC conditions (120 °C, 50% RH) demonstrate the practical efficacy of these membrane-level enhancements, with the Nafion/SiO₂-3 membrane exhibiting an open-circuit voltage and peak power density 11.2% and 8.9% higher, respectively, than those of pristine Nafion under identical MEA fabrication and operating conditions. This study elucidates a clear structure–property–transport relationship in SiO₂-reinforced PFSA membranes, demonstrating that controlled inorganic incorporation is a robust strategy for extending the operational temperature window of PFSA-based proton exchange membranes toward device-level applications. Full article

Cadmium (Cd) contamination in agricultural systems poses significant ecotoxicological risks through bioaccumulation in food chains. While lime-based amendments are widely applied for Cd immobilization, mechanistic understanding of bioavailability control pathways remains limited. This study employed a meta-analysis methodology based on 260 datasets from 55 publications to systematically investigate the mechanisms and differences in the effectiveness of calcium hydroxide, calcium carbonate, and calcium oxide in regulating Cd migration in acidic soil–plant systems. The study revealed that lime-based materials synergistically regulated Cd migration through two processes: chemical fixation and ionic competition. Results showed lime application reduced soil available Cd by 33.0%, decreased grain Cd by 44.8%, increased soil pH by 15.6%, and enhanced exchangeable Ca by 35.2%. Chemical fixation was evidenced by Cd transformation from labile to stable forms (residual Cd: +29.5%, acid-soluble Cd: −17.5%). Ionic competition was quantitatively confirmed through strong negative correlation between exchangeable Ca and grain Cd (R² = 0.704). Among the materials, Ca(OH)₂ exhibits the highest efficiency in rapid pedogenic passivation (58.7% reduction in available Cd), whereas CaCO₃ demonstrates superior long-term grain Cd attenuation (65.7% inhibition) via sustained Ca²⁺ release and rhizosphere-regulated dissolution. This study advances mechanistic understanding of Cd bioavailability control and establishes quantitative frameworks for predicting ecotoxicological outcomes, providing scientific basis for optimizing remediation strategies to minimize Cd transfer through agricultural food chains. Full article

Soil salinity is recognized as a critical abiotic stress that limits plant growth on marginal lands. The cup plant (Silphium perfoliatum L.), a perennial bioenergy species with high biomass potential, has been proposed for cultivation on saline-degraded soils; however, its physiological responses to different types of salinity stress, particularly alkaline and neutral salt stress, remain insufficiently characterized. In the present study, the physiological responses of the cup plant to neutral (NaCl) and alkaline (NaHCO₃) salt stress at concentrations of 100, 200, and 300 mM were evaluated in a pot experiment conducted under controlled conditions. The assessed indicators included relative chlorophyll content (CCI), chlorophyll fluorescence parameters (F_v/F_m, F_v/F₀, PI), and gas exchange characteristics, namely net photosynthetic rate (P_N), stomatal conductance (g_s), transpiration rate (E), and intercellular CO₂ concentration (C_i). Salinity reduced most physiological parameters, although some, such as maximum photochemical efficiency of PSII (F_v/F_m) and transpiration rate (E), did not show a clear dose-dependent response. Alkaline salt stress induced more pronounced reductions in the physiological parameters than neutral salt stress. At the first measurement, at the highest salt concentration, the chlorophyll content decreased by 49.0% and the P_N parameter by 77.8% under NaHCO₃ treatment, whereas under NaCl conditions the decreases were 29.0% and 51.3%, respectively, compared to the control. At 300 mM NaHCO₃, the chlorophyll content and photosynthetic rate were substantially reduced compared with those recorded under the corresponding NaCl treatment. Even at the moderate salinity level of 100 mM NaHCO₃, reductions in photosynthetic performance were detected relative to the control. Overall, photosynthetic efficiency and gas exchange in the cup plant were markedly impaired by salinity, particularly under conditions of high bicarbonate concentration. The results offer a deeper understanding of the physiological limitations of S. perfoliatum under acute salt stress and demonstrate that alkaline salinity, associated with elevated pH due to HCO₃⁻, exacerbates stress effects beyond the osmotic and ionic impacts of neutral salinity. These results highlight the potential of S. perfoliatum for sustainable biomass production on salt-affected soils, supporting renewable energy generation and environmentally responsible land use. Full article

The discovery of cathode materials that simultaneously exhibit high oxygen-reduction activity, robust stability, and low cost is pivotal to moving solid oxide fuel cells (SOFCs) from the laboratory into commercial deployment. To address this challenge, we compile the largest perovskite dataset to date parameterized by the oxygen tracer surface exchange coefficient (k^*). Using only readily obtainable elemental and structural descriptors, we develop machine-learning models that surpass existing approaches in both accuracy and computational efficiency. Specifically, by integrating Mahalanobis-distance-based applicability-domain analysis with random forest-enhanced property descriptors and support vector regression, we high-throughput-screen 1.3 million ABO3 compositions and curate a candidate list that balances thermodynamic stability, cost, and oxygen-reduction activity. Beyond prediction accuracy, SHAP interpretation reveals strong physical correlations between the enhanced descriptors and k^*, highlighting the coefficient of thermal expansion, O p-band center, and A-site ionic radius as the dominant factors governing oxygen exchange kinetics. Finally, we identify 209 promising perovskite cathodes predicted to outperform LSC in the low-temperature regime, offering promising directions for experimental realization of practical low-temperature SOFCs. Full article

Northwestern Jiangxi Province is rich in metasilicic acid (as H₂SiO₃) mineral water resources. Investigating their hydrogeochemical characteristics and formation mechanism is crucial for the rational utilization of water resources and the sustainable development of the local mineral water industry. Taking the Taoping water source area in northwestern Jiangxi as a case study, 11 sets of groundwater and surface water samples were systematically collected. By comprehensively applying mathematical statistics, ionic ratios, and isotopic analyses, the hydrogeochemical characteristics and formation processes of metasilicic acid-type mineral water were examined. The results indicate that: (1) The mineral waters in the area are weakly alkaline and belong to the metasilicic acid type, with concentrations ranging from 22.0 to 67.0 mg/L, of which 75% exceed 30 mg/L. (2) The primary hydrochemical types are HCO₃⁻–Ca·Na, HCO₃⁻–Ca·Mg, and HCO₃⁻–Ca. Analysis of stable isotopes (δ¹⁸O and δ²H) and tritium (³H) indicates that metasilicic acid mineral water is primarily recharged by atmospheric precipitation, with an apparent groundwater age of approximately 60 years. (3) The enrichment of metasilicic acid primarily results from the weathering and leaching of silicate minerals, coupled with cation exchange. K⁺ and Na⁺ are mainly derived from silicate minerals such as feldspars and halite, whereas Ca²⁺ and Mg²⁺ originate primarily from carbonate minerals like calcite and dolomite. During recharge, atmospheric precipitation infiltrates the aquifer, dissolving aluminosilicate and siliceous minerals in the surrounding rocks, thereby releasing metasilicic acid into the groundwater and ultimately forming the metasilicic acid-type mineral water. Full article