Search Results (303)

To develop high-performance electrode materials for supercapacitors, in this paper, a heterostructured composite material of cerium sulfide and zinc sulfide quantum dots (CeS₂/ZnS QD) was successfully prepared by hydrothermal method. Characterization through scanning electron microscopy (SEM), X-ray diffraction (XRD), and transmission electron microscopy (TEM) showed that ZnS QD nanoparticles were uniformly composited with CeS₂, effectively increasing the active sites surface area and shortening the ion diffusion path. Electrochemical tests show that the specific capacitance of this composite material reaches 2054 F/g at a current density of 1 A/g (specific capacity of about 256 mAh/g), significantly outperforming the specific capacitance of pure CeS₂ 787 F/g at 1 A/g (specific capacity 98 mAh/g). The asymmetric supercapacitor (ASC) assembled with CeS₂/ZnS QD and activated carbon (AC) retained 84% capacitance after 10,000 charge–discharge cycles. Benefited from the synergistic effect between CeS₂ and ZnS QDs, the significantly improved electrochemical performance of the composite material suggests a promising strategy for designing rare-earth and QD-based advanced energy storage materials. Full article

In this study, a methacrylic derivative of xylan (XYLMA) was synthesized through transesterification reactions, with the aim of evaluating its physicochemical behavior and its interaction with kaolinite particles. Structural characterization by FT-IR and NMR spectroscopy confirmed the incorporation of methacrylic groups into the xylan (XYL) structure, with a degree of substitution of 0.67. Thermal analyses (TGA and DSC) showed a decrease in melting temperature and enthalpy in XYLMA compared to XYL, attributed to a loss of structural rigidity. Thermal analyses (TGA and DSC) revealed a decrease in the melting temperature and enthalpy of XYLMA compared to XYL, which is attributed to a loss of structural rigidity and a reduction in the crystalline order of the biopolymer. Aggregation tests in solution revealed that XYLMA exhibits amphiphilic behavior, forming micellar structures at a critical aggregation concentration (CAC) of 62 mg L⁻¹. In adsorption studies on kaolinite, XYL showed greater affinity than XYLMA, especially at acidic pH, due to reduced electrostatic forces and a greater number of hydroxyl groups capable of forming hydrogen bonds with the mineral surface. In contrast, modification with methacrylic groups in XYLMA reduced its adsorption capacity, probably due to the formation of supramolecular aggregates. These results suggest that interactions between xylan and kaolinite clay are key to understanding the role that hemicelluloses play in increasing copper recovery when added to flotation cells during the processing of copper sulfide ores with high clay content. Full article

The growing demand for high-energy, safe, and sustainable lithium-ion batteries has increased interest in nickel-rich cathode materials and solid-state electrolytes. This study presents a scalable wet-processing method for fabricating composite cathodes for all-solid-state batteries. The cathodes studied herein are high-nickel LiNi_0.90Mn_0.05Co_0.05O₂, NMC955, the sulfide-based electrolyte Li₆PS₅Cl, and alternative binders—polyvinyl alcohol (PVA) and polyisobutylene (PIB)—dispersed in toluene, a non-polar solvent compatible with the electrolyte. After fabrication, the cathodes were characterized using SEM/EDX, sheet resistance, and Hall effect measurements. Electrochemical tests were additionally performed in all-solid-state battery half-cells comprising the synthesized cathodes, lithium metal anodes, and Li₆PS₅Cl as the separator and electrolyte. The results show that both PIB and PVA formulations yielded conductive cathodes with stable microstructures and uniform particle distribution. Electrochemical characterization exposed that the PVA-based cathode outperformed the PIB-based counterpart, achieving the theoretical capacity of 192 mAh·g⁻¹ even at 1C, whereas the PIB cathode reached a maximum capacity of 145 mAh.g⁻¹ at C/40. Post-mortem analysis confirmed the structural integrity of the cathodes. These findings demonstrate the viability of NMC955 as a high-capacity cathode material compatible with solid-state systems. Full article

The aim of this work was to obtain biochar materials from plant biomass and to determine the changes occurring under the conditions of the pyrolysis process and physical activation, as well as to characterize the physicochemical characteristics of the produced products in terms of their practical use. The pyrolysis process was carried out at a temperature of 700 °C, under the flow of a protective gas, i.e., carbon dioxide, at a rate of 5.0 L/min. The pyrolysis processes were carried out in the absence and presence of an activating agent. For ecological safety, physical activation using water vapor was chosen. In the next stage of the work, biochars were produced and subjected to detailed physicochemical analysis. A scanning electron microscope with energy-dispersive SEM/EDS was used to determine the microstructure and changes in the chemical composition of the biochars. FTIR spectrophotometry was used to identify the functional groups present in the structures of biochars and to indicate changes occurring in the biomass during pyrolysis. Meanwhile, Raman spectroscopy was used to assess the ordering of the biochar structures based on the identification of spectral signals. The description of the specific surface areas of the biochars was made possible by studies conducted using a physical and chemical adsorption analyzer. Based on the obtained research results, the elementary structure, surface development, presence of functional groups on the surfaces of biochars and changes in the structure before and after activation with water vapor were determined. It was found that the biochars had functional groups, a well-developed specific surface area that increased after activation with water vapor, micropores and mesopores, as well as changes in structure under the influence of physical activation. It has been shown that the presence of functional groups influences the hydrogen sulfide sorption capacity. Full article

Silicon-based anodes have emerged as promising candidates for advanced lithium-ion batteries (LIBs) owing to their outstanding lithium storage capacity; however, the commercial implementation of silicon-based anodes is hindered primarily by their significant volumetric changes and the resulting solid electrolyte interphase (SEI) instability during the lithiation/delithiation process. To overcome these issues, electrolyte optimization, particularly through the use of functional additives and solid-state electrolytes, has attracted significant research attention. In this paper, we review the recent developments in electrolyte additives, such as vinylene carbonate, fluoroethylene carbonate, and silane-based additives, and new additives, such as dimethylacetamide, that improve the SEI stability and overall electrochemical performance of silicon-based anodes. We also discuss the role of solid electrolytes, including oxides, sulfides, and polymer-based systems, in mitigating the volume changes in Si and improving safety. Such approaches can effectively enhance both the longevity and capacity retention of silicon-based anodes. Despite significant progress, further studies are essential to optimize electrolyte formulation and solve interfacial problems. Integrating these advances with improved electrode designs and anode materials is critical for realizing the full potential of silicon-based anodes in high-performance LIBs, particularly in electric vehicles and portable electronics. Full article

The management of municipal solid waste remains a critical environmental and energy challenge across the European Union (EU), where a significant portion of waste still ends up in landfills, generating landfill gas (LFG) rich in methane and harmful impurities. In Latvia, despite national strategies to enhance circularity, untreated LFG is underutilized due to inadequate purification infrastructure, particularly in meeting biomethane standards. This study addressed this gap by proposing and evaluating an innovative, multistep LFG purification system tailored to Latvian conditions, with the aim of enabling the broader use of LFG for energy cogeneration and potentially biomethane injection. The research objective was to design, describe, and preliminarily assess a pilot-scale LFG purification prototype suitable for deployment at Latvia’s largest landfill facility—Landfill A. The methodological approach combined chemical composition analysis of LFG, technical site assessments, and engineering modelling of a five-step purification system, including desulfurization, cooling and moisture removal, siloxane filtration, pumping stabilization, and activated carbon treatment. The system was designed for a nominal gas flow rate of 1500 m³/h and developed with modular scalability in mind. The results showed that raw LFG from Landfill A contains high concentrations of hydrogen sulfide, siloxanes, and volatile organic compounds (VOCs), far exceeding permissible thresholds for biomethane applications. The designed prototype demonstrated the technical feasibility of reducing hydrogen sulfide (H₂S) concentrations to <7 mg/m³ and siloxanes to ≤0.3 mg/m³, thus aligning the purified gas with EU biomethane quality requirements. Infrastructure assessments confirmed that existing electricity, water, and sewage capacities at Landfill A are sufficient to support the system’s operation. The implications of this research suggest that properly engineered LFG purification systems can transform landfills from passive waste sinks into active energy resources, aligning with the EU Green Deal goals and enhancing local energy resilience. It is recommended that further validation be carried out through long-term pilot operation, economic analysis of gas recovery profitability, and adaptation of the system for integration with national gas grids. The prototype provides a transferable model for other Baltic and Eastern European contexts, where LFG remains an underexploited asset for sustainable energy transitions. Full article

Thermodynamic simulations of the H₂S removal from blast furnace gas by metal oxides were conducted to select a suitable metal desulfurizer. Notably, the Mn oxides demonstrated themselves as the optimal H₂S removal agents. They are characterized by the absence of radioactive pollution, high cost-effectiveness, high sulfur fixation potential, and non-reactivity with CO₂, CO, and CH₄. Through a comprehensive comparison of Mn oxides, the sulfur fixation potential and sulfur capacity were elucidated as follows: Mn₃O₄ > Mn₂O₃ > MnO₂ > MnO. The higher-valence manganese oxides were shown to have stronger oxidation ability, larger sulfur capacity, and the advantage of producing elemental sulfur with high utilization value during the reaction. After selecting Mn oxides as the optimal H₂S removal agents, an equilibrium component analysis of the regeneration process of the sulfided MnS was carried out. The results indicate that an oxygen amount that is 1.5 times that of MnS is the optimal dosage, and such an amount can oxidize all of the MnS at a relatively low temperature. Conversely, a diluted oxygen concentration can further reduce the temperature of the regeneration process, preventing the sintering of the regenerated desulfurizer and thus maintaining its reusability. This research provides a sufficient theoretical basis for the use of Mn oxides as active components of desulfurizers to remove H₂S from blast furnace gas and for the regeneration of MnS after desulfurization. Full article

Metal sulfides are promising anode candidates for sodium–ion batteries (SIBs) due to their high theoretical capacities. However, their practical application is limited by significant volume extension and sluggish Na⁺ diffusion during cycling, which lead to rapid capacity degradation and poor long-term stability. In this work, we report the rational design of a hollow triple-shelled high-entropy sulfide (NaFeZnCoNiMn)₉S₈, synthesized through sequential templating method under hydrothermal conditions. Transmission electron microscopy confirms its well-defined three-shelled architecture. The inter-shell voids effectively buffer Na⁺ insertion/desertion-induced volume extension, while the tailored high-entropy matrix enhances electronic conductivity and accelerates Na⁺ transport. This synergistic design yields outstanding performance, including a high initial Coulombic efficiency (ICE) of 94.1% at 0.1 A g⁻¹, low charge-transfer resistance (0.32~2.54 Ω), fast Na⁺ diffusion efficiency (10^−8.5–10^−10.5 cm² s⁻¹), and reversible capacity of 582.6 mAh g⁻¹ after 1600 cycles at 1 A g⁻¹ with 91.2% capacity retention. These results demonstrate the potential of high-entropy, multi-shelled architectures as a robust platform for next-generation durable SIB anodes. Full article

This study demonstrated the effectiveness of using autoclaved aerated concrete AAC waste as a low-cost filtering material for removing hydrogen sulfide (H₂S) from gas streams. A long-term experiment (89 days) was conducted in a packed bed reactor to purify synthetic biogas composed of N₂, CO₂, H₂S, and O₂. Optimal H₂S removal efficiencies, reaching up to 100%, were achieved under highly acidic conditions (pH ≈ 1–3) and low oxygen concentrations (<1%). In the presence of oxygen, calcium oxides in the AAC waste react with H₂S to form gypsum (CaSO₄ 2H₂O). The simultaneous removal of both oxygen and H₂S by AAC waste, following an approximate 2:1 molar ratio, may be particularly beneficial for biogas streams containing unwanted traces of oxygen. The transformation and lifespan of AAC waste were monitored through sulfur accumulation in the material and pressure drop measurements, which indicated structural changes in the AAC waste. At the end of its lifespan, the AAC waste exhibited an H₂S removal capacity of 185 g_H2S kg_AAC⁻¹. This innovative and sustainable process not only provides a cost-effective and environmentally sound solution for the simultaneous removal of H₂S and O₂ from biogas, but also promotes waste valorization and aligns with circular economy principles. Full article

The “shuttle effect” caused by the shuttling of soluble long-chain polysulfides between the anode and cathode electrodes has persistently hindered lithium–sulfur batteries (LSBs) from achieving stable and high-capacity performance. Numerous materials have been explored to mitigate the adverse effects of this phenomenon, among which metal oxides and metal sulfides are regarded as promising solutions due to their strong adsorption capability toward lithium polysulfides (LiPSs). However, the poor electrical conductivity of the metal oxides and sulfides, coupled with their inherent morphological limitations, makes it challenging to sustainably suppress LiPS shuttling. In this study, we designed a heterostructured catalyst composed of a metal oxide–metal sulfide heterostructure integrated with carbon nanotubes (CNTs). This design addresses the low conductivity issue of metal oxides/sulfides while optimizing the material’s morphology, enabling persistent LiPSs adsorption. Furthermore, the composite successfully facilitates three-dimensional (3D) Li₂S deposition. The assembled battery exhibits stable and high-capacity performance, delivering an initial discharge capacity of 622.45 mAh g⁻¹ at 2C and retaining 569.5 mAh g⁻¹ after 350 cycles, demonstrating exceptional cycling stability. Full article

In Chile, copper concentrate production through mineral flotation is increasing while production through hydrometallurgical processes is decreasing due to the depletion of oxidized ores. Using the idle capacity of hydrometallurgy plants for acid pretreatment of sulfate ores before the leaching stage is an attractive alternative; however, a deeper understanding of the process and the products of such treatment is required. In this study, the mineral species formed during acid pretreatment are characterized to identify new mineralogical species. Pretreatment was conducted at 50 °C with 210 kg/t H₂SO₄ over 15 days on a copper concentrate mainly composed of enargite (35.93%). The characterization techniques used were X-ray diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), and X-ray Photoelectron Spectroscopy (XPS). XRD identified copper sulfate (CuSO₄) formation and the disappearance of chalcocite/digenite (Cu₂S) and bornite (Cu₅FeS₄), indicating their transformation into sulfates. FESEM showed that enargite particles were oxidized, suggesting they did not form copper sulfates. The XPS results confirmed the presence of copper in species such as sulfides and sulfates. The results indicate that chalcocite and bornite transformed into copper sulfates, while chalcopyrite and enargite were only superficially oxidized. The combination of techniques allowed for a detailed identification of mineral transformations during pretreatment. Full article

Soil heavy metal contamination poses critical challenges to ecological sustainability in mining regions, particularly in acidic soils from copper sulfide mines. This study developed a sustainable remediation strategy using a carbonyl iron powder–biochar composite (CIP@BC) derived from agricultural waste (rice husk) and industrial byproducts. The composite was synthesized through an energy-efficient mechanical grinding method at a 10:1 mass ratio of biochar to carbonyl iron powder, aligning with circular economy principles. Material characterization revealed CIP particles uniformly embedded within biochar’s porous structure, synergistically enhancing surface functionality and redox activity. CIP@BC demonstrated exceptional Cu²⁺ immobilization capacity (910.5 mg·g⁻¹), achieved through chemisorption and monolayer adsorption mechanisms. Notably, the remediation process concurrently improved key soil health parameters. Soil incubation trials demonstrated that 6% CIP@BC application elevated soil pH from 4.27 to 6.19, reduced total Cu content by 29.43%, and decreased DTPA-extractable Cu by 67.26%. This treatment effectively transformed Cu speciation from bioavailable to residual fractions. Concurrent improvements in electrical conductivity (EC), cation exchange capacity (CEC), soil organic matter (OM), and soil water content (SWC) collectively highlighted the composite’s multifunctional remediation potential. This study bridges environmental remediation with sustainable land management through an innovative waste-to-resource approach that remediates acidic mine soils. The dual functionality of CIP@BC in contaminant immobilization and soil quality restoration provides a scalable solution. Full article

Cold stress, as an environmental factor that seriously restricts the growth, production and survival of plants, has received extensive attention in recent years. Nitric oxide (NO), as an important bioactive molecule, has emerged as a research focus in the domain of alleviating plant cold damage. In this review, the role of NO in enhancing plant cold tolerance and its underlying mechanisms, including interactions with signaling molecules, are discussed more extensively, and novel research directions and prospects are proposed according to existing research gaps. Interestingly, exogenous NO mitigates cold stress by strengthening antioxidant defense mechanisms, raising proline levels, enhancing photosynthetic capacity, and regulating glucose metabolism. More importantly, NO also interacts with cytoplasmic calcium ions (Ca²⁺), reactive oxygen species (ROS), glutathione (GSH), melatonin (MT), abscisic acid (ABA), ethylene (ETH) and hydrogen sulfide (H₂S). At the same time, in the process of NO alleviating cold stress, it regulates the expression of NO synthesis genes, cold response genes and antioxidant related genes, thereby improving the cold tolerance of plants, which may involve epigenetic reprogramming. This paper also points out the problems existing in the current research and the potential of NO in agricultural practice, and provides relevant theoretical references for future research in this field. Full article

¹³⁷Cs is a persistent β/γ-emitter (t_1/2 = 30.1 years) generated from ²³⁵U and ²³⁹Pu fission. It is a critical challenge to efficiently capture ¹³⁷Cs⁺ for nuclear waste management due to its high solubility, environmental mobility, and propensity for biological accumulation. Herein, we prepare a two-dimensional (2D) thiotitanate Rb_0.32TiS₂·0.75H₂O (denoted Rb-TiS₂) using a special molten salt synthesis method, “Mg + RbCl”. Rb-TiS₂ can selectively capture Cs⁺ from aqueous solutions. Its structure features a flexible anionic thiotitanate layer with Rb⁺ as counter ions located at the interlayer spaces. As an ion exchanger, it possesses high adsorption capacity (q_m^Cs = 232.70 mg·g⁻¹), rapid kinetics (the removal rate R > 72% within 10 min), and a wide pH tolerance range (pH = 4–12) for Cs⁺ adsorption. Through a single-crystal X-ray structural analysis, we elucidated the mechanism of Cs⁺ capture, revealing the ion exchange pathways between Cs⁺ and Rb⁺ in Rb-TiS₂. This work not only provides an important reference for the synthesis of transition metal sulfides with alkali metal cations but also proves the application prospect of transition metal sulfides in radionuclide remediation. Full article

Polyaniline (PANI) is currently one of the most extensively studied conductive polymers in the field of flexible gas sensors. However, sensors based on pure PANI generally suffer from problems such as low sensitivity and poor stability. To address these issues, in this work, a room-temperature hydrogen sulfide gas sensor of polyaniline/tungsten oxide/copper oxide (PANI/WO₃/CuO) was synthesized using in situ polymerization technology. This gas sensor displays a response value of 31.3% to 1 ppm hydrogen sulfide at room temperature, with a response/recovery time of 353/4958 s and a detection limit of 100 ppb. Such an excellent performance is attributed to the high surface area and large adsorption capacity of the ternary composite, as well as the multi-phase interface synergistic effect. Full article