Search Results (652)

Porous Ni, Ni–Ir, and Ni–Pt electrodes were prepared on Ni substrates by molten-salt Al co-deposition followed by dealloying. SEM/EDS and XRD confirmed a Raney-type porous network with Ir or Pt present across the layer. A urea oxidation reaction (UOR) was tested in 1 M NaOH + 0.33 M urea by cyclic voltammetry and chronoamperometry at +0.40 V vs. SCE (60 min). Smooth Ni showed near-zero current. Porous Ni resulted in ~11 mA cm⁻² initially and ~9 mA cm⁻² after 60 min. Porous Ni–Ir started at ~7 mA cm⁻² and fell to ~2 mA cm⁻² within 5 min, indicating fast deactivation, likely due to Ir-oxide formation that suppresses the Ni²⁺/Ni³⁺ redox couple. Porous Ni–Pt remained at ~11 mA cm⁻² over 60 min, consistent with a stable Ni–Pt effect in which Pt aids urea adsorption/activation while Ni provides the redox path for oxidation. Overall, Pt improves UOR performance, whereas Ir lowers it under these conditions. Full article

The biological effects of magnetic fields (MFs) have been studied and applied in medicine over the past four decades. However, the influence of high-intensity pulse magnetic fields (HI-PMFs), theorized to exert even stronger biological effects, is rarely reported. Herein, a study was conducted to investigate the biological effects of 2.5 T HI-PMF on the model organism Escherichia coli and its corresponding physiological alterations. After being treated by HI-PMF, a notable increase was observed in its intracellular NADH/NAD⁺ ratio, coupled with an improved cell survival rate. Transcriptome analysis revealed significant upregulation of genes related to glucose metabolism. Subsequent experiments confirmed that if the initial intracellular glucose level was relatively high and markedly decreased after being treated with HI-PMF, the cell density would significantly rise, owing to the alleviated inhibition of cell division. On the contrary, a lower initial intracellular glucose level led to cell death under HI-PMF. Furthermore, reactive oxygen species (ROS) production was proved to be the main cause attributed to the above phenomena. Therefore, our study suggests that HI-PMF treatment promotes ROS production, enhances cellular glucose metabolism, and consequently influences cell division and survival rate according to the initial level of intracellular glucose. Full article

The role of sedimentary heterogeneity in reactive transport processes is becoming increasingly important as closed open-pit lignite mines are converted into post-mining lakes or pumped hydropower storage reservoirs. Flooding of the open pits introduces constant oxygen-rich inflows that reactivate pyrite oxidation within internal mine dumps. A reactive transport model coupling groundwater flow, advection–diffusion–dispersion, and geochemical reactions was applied to a 2D cross-section of a water-saturated mine dump to determine the processes governing pyrite oxidation. Spatially correlated fields representing permeability and pyrite distributions were generated via exponential covariance models reflecting the end-dumping depositional architecture, supported by a suite of scenarios with systematically varied correlation lengths and variances. Simulation results covering a time span of 100 years quantify the impact of heterogeneous permeability fields that result in preferential flow paths, which advance tracer breakthrough by ~15 % and increase the cumulative solute outflux up to 139 % relative to the homogeneous baseline. Low initial pyrite concentrations (0.05 wt %) allow for deeper oxygen penetration, extending oxidation fronts over the complete length of the modeling domain. Here, high initial pyrite concentrations (0.5 wt %) confine reactions close to the inlet. Kinetic oxidation allows for more precise simulation of redox dynamics, while equilibrium assumptions substantially reduce the computational time (>10×), but may oversimplify the redox system. We conclude that reliable risk assessments for post-mining redevelopment should not simplify numerical models by assuming average homogeneous porosity and mineral distributions, but have to incorporate site-specific spatial heterogeneity, as it critically controls acid generation, sulfate mobilization, and the timing of contaminant release. Full article

Traditional Fe-based materials are limited for Cr(VI) remediation due to low reactivity, oxidation, and aggregation. Although chitosan coatings improve stability, they hinder efficient liquid-solid separation. To overcome this, a novel phosphorus-modified magnetic chitosan adsorbent (PCC/Fe₃O₄) was synthesized using Fe₃O₄ as the core and tetrakis hydroxymethyl phosphonium sulfate (THPS) as a cross-linking agent. The composite exhibited a high surface area (20.67 m²/g) and superparamagnetism, enabling easy magnetic recovery. PCC/Fe₃O₄ demonstrated superior Cr(VI) removal capabilities compared to unmodified chitosan and raw Fe₃O₄, achieving a saturated adsorption capacity of 23.6 mg/g under the selected conditions (pH 6, initial Cr(VI) concentration of 1 mg/L), which were chosen to balance adsorption efficiency, adsorbent stability, and environmental relevance. The main removal mechanism includes electrostatic attraction, redox reaction, and ligand exchange. PCC/Fe₃O₄ maintained 86% efficiency after 5 d aging and >90% efficiency after five cycles, demonstrating excellent stability and reusability and strong potential for practical environmental remediation. Full article

Biocatalysis is fundamental to biological processes and sustainable chemical productions. Over time, the biocatalysis strategy has been widely researched. Initially, biomanufacturing and catalysis of high-value chemicals were carried out through direct immobilization and application of biocatalysts, including natural enzymes and living cells. With the evolution of green chemistry and environmental concern, hybrid photoelectro-biocatalysis (HPEB) platforms are seen as a new approach to enhance biocatalysis. This strategy greatly expands the domain of natural biocatalysis, especially for bio-based components. The selective valorization of renewable furan derivatives, such as 5-hydroxymethylfurfural (HMF) and furfural, is central to advancing biomass-based chemical production. Biocatalysis offers high chemo-, regio-, and stereo-selectivity under mild conditions compared with traditional chemical catalysis, yet it is often constrained by the costly and inefficient regeneration of redox cofactors like NAD(P)H. Photoelectrocatalysis provides a sustainable means to supply reducing equivalents using solar or electrical energy. In recent years, hybrid systems that integrate biocatalysis with photoelectrocatalysis have emerged as a promising strategy to overcome this limitation. This review focuses on recent advances in such systems, where photoelectrochemical platforms enable in situ cofactor regeneration to drive enzymatic transformations of furan-based substrates. We critically analyze representative coupling strategies, materials and device configurations, and reaction engineering approaches. Finally, we outline future directions for developing efficient, robust, and industrially viable hybrid catalytic platforms for green biomass valorization. Full article

Two diphosphonates, etidronic acid (HEDP) and zoledronic acid (ZOL), were radiolabelled with ¹⁶¹Tb and evaluated as potential bone-targeting radiopharmaceuticals. Radiolabeling was performed at pH 7, achieving high radiolabeling yields (greater than 98%) and demonstrating excellent in vitro stability in saline and human serum. Both radiolabeled complexes exhibited hydrophilic behavior, a strong binding affinity to hydroxyapatite, and moderate to high plasma protein binding. Biodistribution studies in healthy Wistar rats demonstrated that ¹⁶¹Tb-HEDP and ¹⁶¹Tb-ZOL achieve high and stable skeletal uptake with rapid blood clearance and minimal soft tissue accumulation. ¹⁶¹Tb-HEDP favored higher initial bone localization, while ¹⁶¹Tb-ZOL showed lower renal and hepatic accumulation, indicating higher safety and selectivity. Compared to unchelated ¹⁶¹TbCl₃, both diphosphonate complexes exhibited significantly higher bone-to-kidney and bone-to-liver ratios, resulting in superior targeting. Complementary experiments with non-radioactive terbium were performed to investigate the redox behavior and confirm complex formation, providing valuable insight into the stability and binding modes of the ligands. Both terbium and the ligands displayed well-defined redox behavior within the potential range of −1 to 1.7 V, with complex formation evidenced by shifts in the oxidation peaks. Density functional theory (DFT) calculations further supported these findings, showing that both phosphonate groups of a ligand coordinate to Tb³⁺, while the hydroxyl groups in HEDP enable intermolecular hydrogen bonding, contributing to additional structural stabilization. Results encourage further investigations of ¹⁶¹Tb-labeled diphosphonates as promising candidates for radionuclide therapy of bone metastases and other skeletal diseases. Full article

Reactive oxygen species (ROS) are versatile determinants of cell fate, tipping the balance between survival and death. By exceeding critical thresholds or perturbing compartment-specific signaling, ROS can initiate, modulate, or suppress regulated cell death (RCD). Importantly, their influence extends across the full spectrum of currently characterized RCD modalities. 19 distinct forms of cell death—including both long-established and recently described entities—are shaped by ROS, either as triggers, modulators, or inhibitors. Beyond pathway-specific effects, ROS promote crosstalk between death programs, enabling switches from one mode to another and determining whether outcomes are inflammatory or non-inflammatory. By systematically integrating 19 RCD types, the unifying role of ROS emerges as both gatekeeper and connector of diverse death pathways. Such a comprehensive perspective underscores the centrality of redox imbalance in cell fate control and highlights its broader implications for inflammation and disease. Full article

Renewable energy sources, such as photovoltaic panels and wind turbines, are increasingly integrated into domestic systems to address energy scarcity, rising demand, and climate change. However, their intermittent nature requires efficient energy storage systems (ESS) for stability and reliability. This systematic review, conducted in accordance with PRISMA guidelines, aimed to evaluate the size and chemical composition of battery energy storage systems (BESS) in household renewable energy applications. A literature search was conducted in Scopus in August 2025 using predefined keywords, and studies published in English from 2015 onward were included. Exclusion criteria included book chapters, duplicate conference proceedings, geographically restricted case studies, systems without chemistry or size details, and those focusing solely on electric vehicle batteries. Of 308 initially retrieved records, 83 met the eligibility criteria and were included in the analysis. The majority (92%) employed simulation-based approaches, while 8% reported experimental setups. No formal risk-of-bias tool was applied, but a methodological quality check was conducted. Data were synthesized narratively and tabulated by chemistry, nominal voltage, capacity, and power. Lithium-ion batteries were the most prevalent (49%), followed by lead–acid (13%), vanadium redox flow (3.6%), and nickel–metal hydride (1.2%), with the remainder unspecified. Lithium-ion dominated due to high energy density, long cycle life, and efficiency. Limitations of the evidence include reliance on simulation studies, heterogeneity in reporting, and limited experimental validation. Overall, this review provides a framework for selecting and integrating appropriately sized and composed BESS into domestic renewable systems, offering implications for stability, efficiency, and household-level sustainability. The study was funded by the PNRR NEST project and Sapienza University of Rome Grant. Full article

The DNA Damage Response (DDR) network is an essential machinery for maintaining genomic integrity, with DDR defects being implicated in cancer initiation, progression, and treatment resistance. Moreover, oxidative stress, an imbalance between reactive oxygen species production and antioxidant defense, can significantly impact cell viability, leading to cell death or survival. Herein, we tested the hypothesis that DDR-related signals and redox status measured in multiple myeloma (MM) cell lines correlate with the sensitivity to genotoxic insults. At baseline and following irradiation with Ultraviolet C (UVC; 50 J/m²) or treatment with melphalan (100 μg/mL for 5 min) DDR-related parameters, redox status expressed as GSH/GSSG ratio and apurinic/apyrimidinic sites were evaluated in a panel of eleven human MM cell lines and one healthy B lymphoblastoid cell line. We found that MM cell lines with increased apoptosis rates displayed significantly higher levels of endogenous/baseline DNA damage, reduced GSH/GSSG ratio, augmented apurinic/apyrimidinic lesions, decreased nucleotide excision repair and interstrand crosslinks repair capacities, and highly condensed chromatin structure. Taken together, these findings demonstrate that DDR-related parameters and redox status correlate with the sensitivity of MM cells to DNA-damaging agents, specifically melphalan, and, if further validated, may be exploited as novel sensitive/effective biomarkers. Full article

The eco-toxicological impacts caused by organic pollutants in aquatic environments have emerged as a global concern in recent decades, resulting from the potential hazards they present to ecosystem integrity and human health. Decorating active components on mesoporous silica is considered a popular approach by which to obtain synergistic effects in persulfate activation for sustainable water decontamination. However, at present there has been no review focusing solely, specifically and comprehensively on this field. Therefore, this paper places an emphasis on the latest research progress on the synthesis and physicochemical properties of functionalized mesoporous silica materials as well as their catalytic performance. The preparation methods included co-condensation, impregnation, grinding–calcination, hydrothermal synthesis and chemical precipitation, and their synthesis parameters played a major role in the characterization of materials, thereby affecting pollutant elimination. Metal redox cycles, nonmetallic activation and confinement effects contributed to persulfate activation. Targeted pollutants were degraded via radical pathways, non-radical pathways, or a combination of the two. The effects and causes of operational conditions (catalyst and persulfate dosage, initial pollutant concentration, temperature, initial pH, co-existing anions, and natural organic matter) varied across the degradation systems, and they were categorized and summarized in detail. Furthermore, functionalized mesoporous silica presented excellent reusability, stability and applicability in practical application. Finally, current potential directions for further research and sustainable development in this field were also prospected. This critical analysis aims to fuel the evolution of functionalized mesoporous silica catalyst-driven persulfate system application in water treatment and to bridge prevailing knowledge gaps. Full article

Reactive oxygen species (ROS) are formed by the incomplete reduction of oxygen and play a crucial role in both physiological function and pathological process, being controlled by enzymatic and non-enzymatic antioxidant systems. However, excessive ROS production can exceed the body’s antioxidant capacity, resulting in oxidative stress and causing cell death and oxidation of important biomolecules. In this context, the inhibition and/or modulation of ROS has been shown to be effective in reducing pain, oxidative stress, and inflammation. Among ROS, superoxide anion (O₂^•−) is the first free radical to be formed through the mitochondrial electron transport chain (ETC) or by specific enzymes systems, such as the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX) complex. O₂^•− plays a significant role in the development and maintenance of pain associated with inflammatory conditions through direct or indirect activation of primary nociceptive neurons and, consequently, peripheral and central sensitization. Experimentally, potassium superoxide (KO₂, a O₂^●− donor) is used to initiate O₂^●− mediated inflammatory and nociceptive responses, making it important for studying the mechanisms associated with ROS-induced pain and evaluating potential therapeutic molecules. This review addresses the production and regulation of O₂^•−, highlighting its biosynthesis, redox control, and its physiological and pathological roles in the development of inflammatory pain, as well as the pharmacological therapies under development aimed at its generation and/or action. Full article

Supercapacitors (SCs) are widely acknowledged for their high-power density as energy storage devices; designing electrode materials with both high efficiency and exceptional energy density remains a significant challenge. In this study, a flower-like iron-doped molybdenum sulfide on graphene nanosheets (FMS/G) was synthesized through a simple, efficient, and scalable solvothermal approach. The FMS/G composite demonstrated exceptional performance when employed as both positive and negative electrodes, owing to the effective incorporation of iron into the MoS₂ crystal lattice. This doping induces defects and facilitates abundant redox reactions, ultimately boosting electrochemical performance. The FMS/G composite demonstrates an ultrahigh specific capacitance of 931 F g⁻¹ at 1 A g⁻¹, along with excellent rate capability, retaining 582 F g⁻¹ at 20 A g⁻¹. It also exhibits remarkable cycling stability, maintaining 90.5% of its initial capacitance after 10,000 cycles. Furthermore, the assembled FMS/G-3//FMS/G-3 supercapacitor device achieves a superior energy density of 64.7 Wh kg⁻¹ at a power density of 0.8 kW kg⁻¹ with outstanding cycling stability, retaining 92% of its capacitance after 10,000 cycles. The remarkable capabilities of the flower-like FMS/G composite underscore its noteworthy potential for promoting effective energy storage systems. Full article

This work examines the effect of gadolinium (Gd) promotion on nickel-based SBA-16 catalysts for the dry reforming of methane (DRM), with the goal of improving syngas production by optimizing catalyst composition and operating conditions. Catalysts with varying Gd loadings (0.5–3 wt.%) were synthesised using co-impregnation. XRD, N₂ physisorption, FTIR, XPS, and H₂-TPR–CO₂-TPD–H₂-TPR were used to examine the structural features, textural properties, surface composition, and redox behaviour of the catalysts. XPS indicated formation of enhanced metal–support interactions, while initial and post-treatment H₂–TPR analyses showed that moderate Gd loadings (1–2 wt.%) maintained a balanced distribution of reducible Ni species. The catalysts were tested for DRM performance at 800 °C and a gas hourly space velocity (GHSV) of 42,000 mL g⁻¹ h⁻¹. 1–2 wt.% Gd-promoted catalysts achieved the highest H₂ (~67%) and CO yield (~76%). Response surface methodology (RSM) was used to identify optimal reaction conditions for maximum H₂ yield. RSM predicted 848.9 °C temperature, 31,283 mL g⁻¹ h⁻¹ GHSV, and a CH₄/CO₂ ratio of 0.61 as optimal, predicting a H₂ yield of 96.64%, which closely matched the experimental value of H₂ yield (96.66%). The 5Ni–2Gd/SBA-16 catalyst exhibited minimal coke deposition, primarily of a graphitic character, as evidenced by TGA–DSC and Raman analyses. These results demonstrate the synergy between catalyst design and process optimization in maximizing DRM efficiency. Full article

Musculoskeletal disorders are a major cause of lameness in horses, often necessitating innovative regenerative strategies to restore joint function and improve quality of life. This study investigated the effects of platelet-rich plasma (PRP), ozonized PRP, hyaluronic acid, paracetamol, and polyacrylamide hydrogel (NOLTREX^®) on the behavior of mesenchymal stem cells (MSCs) derived from equine synovial fluid. Synovial fluid samples were collected under strict cytological criteria to ensure viability, followed by in vitro expansion and phenotypic characterization of MSCs. Cultures were supplemented with the tested preparations, and cellular proliferation and viability were evaluated at 24 h, 72 h, and 7 days. PRP significantly promoted MSC proliferation in a time- and dose-dependent manner, with maximal effect at 10%. Hyaluronic acid stimulated growth, most pronounced at 1 mg/mL, while paracetamol induced a concentration-dependent proliferative response, strongest at 100 μg/mL. NOLTREX displayed a biphasic effect, initially inhibitory at high concentrations but stimulatory at 7 days. Ozonized PRP showed concentration-dependent redox activity, with lower doses maintaining viability and higher doses producing an initial suppression followed by delayed stimulation. Collectively, these findings support the therapeutic potential of PRP and related biologic preparations as intra-articular regenerative therapies in equine medicine, while underscoring the importance of dose optimization and standardized protocols to facilitate clinical translation. Full article

For the first time, the kinetics of isothermal curing and thermal degradation of polyethylene glycol maleate (pEGM)–based systems and their composites with mineral fillers were investigated in the presence of a benzoyl peroxide/N,N-Dimethylaniline redox-initiating system. DSC analysis revealed that the curing process at 20 °C can be described by the modified Kamal autocatalytic model; the critical degree of conversion (α_c) decreases with increasing content of the unsaturated polyester pEGM and in the presence of fillers. In particular, for unfilled systems, α_c was 0.77 for pEGM45 and 0.60 for pEGM60. TGA results demonstrated that higher pEGM content and the incorporation of fillers lead to increased thermal stability and residual mass, along with a reduction in the maximum decomposition rate (dTGₘₐₓ). Calculations using the Kissinger–Akahira–Sunose and Friedman methods also confirmed an increase in the activation energy of thermal degradation (E_a): E_KAS was 419 kJ/mol for pEGM45 and 470 kJ/mol for pEGM60, with the highest values observed for pEGM60 systems with fillers (496 kJ/mol for SiO₂ and 514 kJ/mol for CaCO₃). Rheological studies employing three-interval thixotropy tests revealed the onset of thixotropic behavior upon filler addition and an increase in structure recovery after deformation of up to 56%. These findings underscore the potential of pEGM-based systems for low-temperature curing and for the design of composite materials with improved thermal resistance. Full article