Search Results (638)

In recent years, flow batteries have emerged as a crucial technological solution for large-scale energy storage, leveraging their unique power-capacity decoupling characteristics and long cycle life to demonstrate significant potential in applications such as renewable energy integration and grid frequency regulation. Based on differences in electrolyte systems, mainstream flow battery technologies are primarily categorized into three types: all-vanadium redox flow batteries (VRFBs), iron-chromium redox flow batteries (ICFBs), and zinc-based redox flow batteries (ZRFBs). However, each of these technologies faces critical challenges in practical commercialization: VRFBs are constrained by cost pressures due to fluctuations in vanadium resource prices and relatively low energy efficiency; ICFBs require urgent solutions to issues such as hydrogen evolution side reactions at the negative electrode and the sluggish kinetic responses of the Cr³⁺/Cr²⁺ redox couple; while ZRFBs grapple with safety concerns such as zinc dendrite growth and morphology instability. To overcome these technical bottlenecks, extensive innovative research has been conducted in key materials (electrodes, ion-exchange membranes, electrolytes). Against this backdrop, this paper systematically reviews recent advances in the modification and optimization of flow battery technologies and conducts an extended discussion on the emerging organic redox flow batteries in recent years. Full article

Heavy metal pollution is characterized by long-term accumulation and recalcitrance to degradation, which poses a serious threat to soil ecosystems and groundwater environments. To improve the remediation efficiency of biochar for cadmium (Cd)-contaminated soil, this study took unmodified biochar (BC) as the control and systematically explored the remediation potential of NaOH–KMnO₄–FeCl₃ composite-modified biochar (GBC). Combined with a Brassica napus L. pot experiment, the effects of modified biochar on soil Cd passivation, soil physicochemical properties, and B. napus biomass were analyzed. After composite modification, GBC had its surface ash removed and exhibited a more regular pore structure, with successful loading of iron–manganese oxides. Although partial changes in the microporous structure caused a decrease in CO₂ adsorption, the number of surface-active sites increased. Both biochars significantly increased soil carbon content, nitrogen and phosphorus nutrient levels, and electrical conductivity, while promoting B. napus biomass accumulation and reducing its Cd enrichment. Among them, the GBC-1.5 treatment group exhibited the most significant increase in B. napus biomass, which was 33.66% higher than that of the control group (CK). However, soil pH increased with the increase in BC but decreased with the increase in GBC application rate. In terms of Cd passivation effect, both biochars showed excellent remediation performance. When the application rate was 3%, the Cd passivation rate of the GBC-3 treatment group reached 35.87%, which was 5.29% higher than that of the BC-3 treatment group. The loading of iron–manganese oxides further enhanced the effectiveness and stability of chemical adsorption. This study provides an important reference for achieving sustainable utilization of soil heavy metal remediation. Full article

This study focuses on the surface materials of rammed-earth walls of Fujian Tulou in Xiaoshu Village, exploring the microscopic characteristics of rammed earth in different orientations and the microclimate adaptation mechanism and degradation law of the walls. Specimens were collected from the inner and outer surface soil layers of the four directional walls of a representative Tulou. SEM, XRD, and XRF analyses were performed to characterize the materials’ microstructure, mineral composition, and elemental distribution, with the test results correlated to the microclimatic conditions of each wall orientation. The conclusion is as follows: (1) The microscopic particle size of rammed earth exhibits significant directional differences at dual scales of 300 nm and 2 μm. Solar radiation duration and wind speed are positively correlated with the coefficient of variation in particle size. (2) The southeast and north walls were the most severely damaged (soil loss, quartz enrichment: 79.9%), the west wall had minor cracks, the north wall showed slight salt crystallization (Halite = 0.3%), and the east wall exhibited moisture-related moss growth. (3) Traditional organic additives (bamboo strips, rice husks) mitigate deterioration and enhance structural integrity. (4) The diversity of soil color (related to hematite and iron oxide) can serve as a simple indicator of deterioration. This study has proposed differentiated protection schemes for the “microclimate-compounds” on walls facing different directions on the rammed-earth surface of the Tulou. The findings provide a theoretical basis for orientation-specific conservation of Tulou heritage and offer scientific references for the modification of modern rammed-earth materials. Full article

Anthropogenic CO₂ emissions have accelerated climate change, prompting the need for effective capture technologies. Adsorption using clay-based sorbents offers an eco-friendly alternative, although performance often requires enhancement. This study explored mechanochemical modification of two halloysite-rich kaolin clay samples—iron-poor (Hal) and iron-rich (HalFe)—using locust bean gum and quillaja saponin and compared their CO₂ uptake with the calcined counterparts (CHal, CHalFe). All samples were characterized using standard techniques, and their CO₂ uptake was measured volumetrically across 0.1–20 bar and 15–35 °C. Modified sorbents showed enhanced mesoporosity and binding sites, increasing CO₂ uptake by up to 26% at 20 bar (11.85 mg/g) and 125% at 1 bar (2.25 mg/g). Calcination, however, reduced surface area and sorption capacity. Isosteric heat values remained within the physisorption range, as supported by FTIR, XRF, and XPS, which showed no bulk carbonate formation. These sorbents show lower CO₂ uptakes than conventional ones. Yet their low costs, abundance, biocompatibility, and solvent-free synthesis indicate strong potential for large-scale applications, especially for low-pressure implementations such as landfills. Further detailed studies on kinetics, thermodynamics, and sorbent regeneration are needed. Spent sorbents can potentially be repurposed for subsequent use in other applications, e.g., water treatment, construction materials, thereby minimizing waste production and supporting circular economy principles. Full article

Cemented tailings backfill (CTB) is widely used in mining operations due to its operational simplicity, reliable performance, and environmental benefits. However, the poor consolidation of fine tailings with ordinary Portland cement (OPC) remains a critical challenge, leading to excessive backfill costs. This study addresses the utilization of modified manganese slag (MMS) as a supplementary cementitious material (SCM) for fine tailings from an iron mine in Anhui, China. Sodium silicate (Na₂SiO₃) modification coupled with melt-water quenching was implemented to activate the pozzolanic reactivity of manganese slag (MS) through glassy structure alteration. The MMS underwent comprehensive characterization via physicochemical analysis, X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR) to elucidate its physicochemical attributes, mineralogical composition, and glassy phase architecture. The unconfined compressive strength (UCS) of the CTB samples prepared with MMS, OPC, tailings, and water (T-MMS) was systematically evaluated at curing ages of 7, 28, and 60 days. The results demonstrate that MMS predominantly consists of SiO₂, Al₂O₃, CaO, and MnO, exhibiting a high specific surface area and extensive vitrification. Na₂SiO₃ modification induced depolymerization of the highly polymerized Q⁴ network into less-polymerized Q² chain structures, thereby enhancing the pozzolanic reactivity of MMS. This structural depolymerization facilitated formation of stable gel products with low calcium–silicon ratios, conferring upon the T-MMS10 sample a 60-day strength of 3.85 MPa, representing a 94.4% enhancement over the T-OPC. Scanning electron microscopy–energy dispersive spectroscopy (SEM-EDS) analysis revealed that Na₂SiO₃ modification precipitated extensive calcium silicate hydrate (C-S-H) gel formation and pore refinement, forming a dense networked framework that superseded the porous microstructure of the control sample. Additionally, the elevated zeta potential for T-MMS10 engendered electrostatic repulsion, while the aluminosilicate gel provided imparted lubrication, collectively improving the flowability of the composite slurry exhibiting a 26.40 cm slump, which satisfies the requirements for pipeline transportation in backfill operations. Full article

Copper (Cu) and zinc (Zn) are critical for global high-tech industries and national economic security. With high-grade mineral depletion, recycling valuable metals from iron ore tailings has become a sustainable solution. A Peruvian mining company’s iron ore tailing reprocessing faces a severe challenge: surging lead (Pb) content due to increased excavation depth has rendered the original Cu-Zn bulk flotation flowsheet ineffective, causing excessive impurities in concentrates. This study first characterized the occurrence states of Cu, Pb, and Zn via multi-analytical techniques. A novel Cu-Pb-Zn iso-flotation process with step-by-step depression, coupled with optimized reagents, was proposed. It abandons initial CuSO₄ activation to reduce separation difficulty and uses targeted depressants for efficient impurity removal. Closed-circuit tests yielded a Cu concentrate (26.57% grade, 56.08% recovery) with Pb/Zn contents reduced to 2.97%/9.80%, and a Zn concentrate (44.95% grade, 75.56% recovery) with Cu/Pb controlled at 1.15%/8.31%. Experimental results demonstrate that this new flowsheet effectively mitigates the impact of high Pb content, restoring production efficiencies and offering a valuable precedent for industrial process modification. Full article

Water polluted by dye colorants has been on the rise in the last decade. This is due to the over reliance on the textile industry, and it is holding a high economic value in most countries. This industry is the highest consumer of fresh water whilst also discharging several natural and synthetic pollutants to the environment. Several methods have been used for the removal of these pollutants and one of the most efficient technologies to be developed includes the photocatalysis method, via advanced oxidation processes. This review highlights the developments of green iron oxide nanoparticles as photocatalysts in the last decade. It was noted that tuning and controlling the phytochemical concentration and synthesis conditions, can assist with forming uniform and non-agglomerated materials, as this has limited the vast usage of these materials in major applications. Also, upon controlling the synthesis conditions, improved surface area and charge separation efficiency was noted. Their limitations and need for modification through forming composites are highlighted. Moreover, future perspectives are given on the use of green IONPs as photocatalysts. Full article

Recent advancements in nanotechnology and materials science have enabled the development of magnetic photocatalysts with improved efficiency, stability, and reusability, offering a promising approach for wastewater treatment. The integration of magnetic nanoparticles (MNPs) into photocatalytic processes has gained significant attention as a sustainable method for addressing emerging pollutants—such as antibiotics and pharmaceutical compounds—which pose environmental and public health risks, including the proliferation of antibiotic resistance. Surface modification techniques, specifically applied to MNPs, are employed to enhance their photocatalytic performance by improving surface reactivity, reducing nanoparticle agglomeration, and increasing photocatalytic activity under both visible and ultraviolet (UV) light irradiation. These modifications also facilitate the selective adsorption and degradation of target contaminants. Importantly, the modified nanoparticles retain their magnetic properties, allowing for facile separation and reuse in multiple treatment cycles via external magnetic fields. This review provides a comprehensive overview of recent developments in surface-modified MNPs for wastewater treatment, with a focus on their physicochemical properties, surface modification strategies, and effectiveness in the removal of antibiotics from aqueous environments. Furthermore, the review discusses advantages over conventional treatment methods, current limitations, and future research directions, emphasizing the potential of this technology for sustainable and efficient water purification. Full article

Nanoparticles based on gallium ferrite are explored as potential agents for magnetic fluid hyperthermia due to their magnetic performance and biocompatibility. In this study, Ga_xFe_3−xO₄ systems (0 ≤ x ≤ 1) were synthesized by co-precipitation of iron chlorides, with part of the series modified by a chitosan shell. Structural analysis confirmed single-phase formation across the studied range, while microscopy revealed irregular morphology, broad size distribution, and aggregation into mass-fractal-like assemblies. Chitosan was observed to coat groups of particles rather than single crystallites. Under an alternating magnetic field, all samples exhibited efficient heating, with specific absorption rate values generally increasing with gallium content. The composition Ga_0.73Fe_2.27O₄ showed the highest SAR—83.4 ± 2.2 W/g at 2.8 mg/mL, 532 kHz, 15.3 kA/m, and SAR values rose with decreasing concentration. Cytotoxicity assays without magnetic activation indicated no harmful effect, while chitosan-coated nanoparticles enhanced fibroblast viability and lowered metabolic activity of HeLa cells. Higher Ga content (x = 0.66) combined with chitosan modification was identified as optimal for hyperthermia. The results demonstrate the biomedical potential of these nanoparticles, while emphasizing the need to reduce shape heterogeneity, aggregation, and sedimentation for improved performance. Full article

Remediating cadmium (Cd) contamination in aquatic and terrestrial environments has become an urgent environmental priority. Biochar has been widely employed for heavy metal removal due to its wide availability, strong adsorption capacity, and potential for recycling agricultural waste. In this study, samples of alkali–Fe-modified biochar (Fe@NaOH-SBC, Fe@NaOH-HBC, and Fe@NaOH-MBC) were prepared from agricultural wastes (ginger straw, Sichuan pepper branches, and kiwi leaves) through NaOH and FeCl₃·6H₂O modification. A comprehensive characterization confirmed that the alkali–Fe-modified biochar exhibits a higher specific surface area, richer functional groups, and successful incorporation of the iron oxides Fe₃O₄ and α-FeOOH. The fitting parameter qmax from the Langmuir model indicates that the alkali–Fe modification of carbon significantly enhanced its maximum capacity for Cd²⁺ adsorption. Furthermore, a synergistic effect was observed between iron oxide loading and alkali modification, outperforming alkali modification alone. Furthermore, a 30-day soil incubation experiment revealed that the application of alkali–Fe-modified biochar significantly increased soil pH, SOM, and CEC while reducing the available cadmium content by 13.34–33.94%. The treatment also facilitated the transformation of highly bioavailable cadmium species into more stable, less bioavailable forms, thereby mitigating their potential entry into the food chain and the associated human health risks. Moreover, short-term spinach seed germination experiments confirmed that treatments with varying additions of alkali–Fe-modified biochar mitigated the inhibition of seed physiological processes by high concentrations of available cadmium to varying degrees. Overall, this study provides a sustainable and effective strategy for utilizing agricultural waste in the remediation of cadmium-contaminated water and soil systems. Full article

Diabetic retinopathy (DR), a leading cause of vision loss in diabetic patients, involves complex pathological mechanisms including neurodegeneration, microvascular damage, inflammation, and oxidative stress. Recent studies have identified ferroptosis—a ferrodependent cell death mechanism—as playing a pivotal role in DR development. Existing evidence indicates that oxidative stress and mitochondrial dysfunction induced by hyperglycemia may contribute to retinal damage through the ferroptosis pathway in DR. Ferroptosis inhibitors such as Ferostatin-1 have demonstrated protective effects against DR in animal models. The core mechanisms of ferroptosis involve iron homeostasis imbalance and lipid peroxidation, with key regulatory pathways including GPX4-dependent and non-dependent mechanisms (such as FSP1-CoQ10). Within the signaling network, Nrf2 inhibits ferroptosis, p53 promotes it, while Hippo/YAP functions are environment-dependent. Non-coding RNAs and epigenetic modifications (e.g., DNA methylation and histone modifications) also participate in regulation. In DR, iron overload, GPX4 dysfunction, and p53 upregulation collectively induce ferroptosis in various types of retinal cells, making these pathways potential therapeutic targets. This review not only elaborates the role of iron metabolism imbalance and ferroptosis pathway in the occurrence and development of DR but also summarizes the new therapeutic approaches of DR targeting ferroptosis pathway. Investigating the relationship between ferroptosis and DR not only helps unravel its core pathophysiological mechanisms but also provides theoretical foundations for developing novel therapeutic approaches. Full article

Amorphous nano zero-valent iron (A-nZVI) was synthesized via liquid-phase reduction and ethylenediamine (EDA) modification to enhance trichloroethylene (TCE) dechlorination. A-nZVI showed a cauliflower-like morphology, where 20–50 nm primary particles formed 500–1000 nm secondary agglomerates with a high surface area. Compared with crystalline nZVI (C-nZVI), A-nZVI exhibited higher electron transfer efficiency and stronger reducing capability (potentiodynamic polarization analysis). TCE removal followed a two-stage model: a rapid adsorption–reduction phase (pseudo-second-order; q_e = 9.48 mg/g, R² = 0.998) and a slower degradation phase (pseudo-first-order; k = 0.0125 h⁻¹, R² = 0.994). No toxic intermediates (e.g., dichloroethylene or vinyl chloride) were detected; products were mainly acetylene, ethylene, and ethane. The electron utilization efficiency increased from 8.47% (C-nZVI) to 15.32% (A-nZVI), while hydrogen evolution decreased by 32%. EDA formed Fe–N coordination bonds that facilitated electron transfer and stabilized the amorphous structure. A-nZVI retained 40% of its activity after four cycles under neutral to alkaline conditions. Full article

Sodium-ion batteries (SIBs) have arisen as a potential alternative to lithium-ion batteries (LIBs) as a result of the abundant availability of sodium resources at low production costs, making them in line with the United Nations Sustainable Development Goals (SDGs) for affordable and clean energy (Goal 7). The current review intends to comprehensively analyse the various modification techniques deployed to improve the performance of cathode materials for SIBs, including element doping, surface coating, and morphological control. These techniques have demonstrated prominent improvements in electrochemical properties, such as specific capacity, cycling stability, and overall efficiency. The findings indicate that element doping can optimise electronic and ionic conductivity, while surface coatings can enhance stability in addition to mitigating side reactions throughout cycling. Furthermore, morphological control is an intricate technique to facilitate efficient ion diffusion and boost the use of active materials. Statistically, the Cr-doped NaV_1−xCr_xPO₄F achieves a reversible capacity of 83.3 mAh/g with a charge–discharge performance of 90.3%. The sodium iron–nickel hexacyanoferrate presents a discharge capacity of 106 mAh/g and a Coulombic efficiency of 97%, with 96% capacity retention over 100 cycles. Furthermore, the zero-strain cathode Na₄Fe₇(PO₄)₆ maintains about 100% capacity retention after 1000 cycles, with only a 0.24% change in unit-cell volume throughout sodiation/desodiation. Notwithstanding these merits, this review ascertains the importance of ongoing research to resolve the associated challenges and unlock the full potential of SIB technology, paving the way for sustainable and efficient energy storage solutions that would aid the conversion into greener energy systems. Full article

This study presents the effects of using pyrite aggregate in field concretes on the mechanical, surface performance, and algal growth tendency of concrete. The substitution of pyrite influences the process of hydration, as the gradual release of its iron- and sulfur-bearing components shifts the reaction mechanism, leading to differences in phase formation and some modification in the pore structure of the cement matrix. Three different concrete mixes (PB0, PB2.5%, and PB7.5%) were designed by replacing 0%, 2.5%, and 7.5% of the total weight of sand and crushed sand with ground pyrite as a fine aggregate. Prismatic specimens of 80 × 100 × 200 mm were produced from these mixtures and mechanical properties such as flexural, splitting tensile, and abrasion were investigated after 28 days of curing. Then, to determine the effect of pyrite on concrete surface properties, pyrite was substituted on the surface of three concrete specimens produced in 50 × 240 × 500 mm dimensions at rates of 0, 1, and 3 kg/m². These specimens were divided into two groups: one group was exposed to clean water drops at a constant flow rate in a closed environment, and the other group was exposed to dirty water in an open environment, and observed for 2 months. At the end of the process, sections of 50 × 80 × 200 cm³ were taken from the specimens and friction, abrasion and flexural tests were carried out. The results of the study demonstrate that a 7.5% pyrite substitution improves both flexural and shear strength by 38%. At the same time, pyrite substitution prevented algal growth on the surface of field concrete under clean water and delayed its formation in those under contaminated water. Finally, it was observed that pyrite, when used in concrete mix and surface applications, optimizes mechanical performance and environmental durability. Full article

Prussian blue (PB) and its analogs (PBAs) are interesting materials for electrochemical applications due to their tunable redox chemistry and open framework structure. In this study, hexacyanoferrates (HCF) containing iron (FeHCF), cobalt (CoHCF), and nickel (NiHCF) were synthesized via potentiostatic electrodeposition. Cyclic voltammetry revealed distinct redox behaviors. Morphological characterization (SEM, EDX) demonstrated uniform, pyramidal film growth for FeHCF and CoHCF. Otherwise, NiHCF presented a cracked film with cubic clusters on top due to residual stress. Despite this, homogeneous element distribution was found for all samples. Structural characterization (TEM and XRD) confirmed a cubic lattice crystal structure for all films, with systematic lattice contraction from Fe to Co to Ni due to decreasing atomic radius. Raman and XPS data revealed a shift toward Fe²⁺ dominant oxidation states and modifications in C≡N bonding, with the influence of K⁺ and water occupancy in the PBAs framework. These findings illustrate how metal substitution and deposition parameters can tune the structural and electrochemical properties of PBA films, presenting a strategic route to design tailored electrodes. Full article