Search Results (346)

Melamine formaldehyde particle boards (MFPBs), commonly utilized as a wooden decorative material in traditional architecture, demonstrate considerable performance deterioration with extended age, with reductions in essential flame retardancy and structural integrity presenting substantial risks to fire safety in structures. This research examines the impact of thermo-oxidative aging on the flame retardancy of MFPBs. The morphological evolution, surface composition, and flame-retardant characteristics of aged MFPBs were examined via scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TG), limiting oxygen index (LOI), and cone calorimeter (CCT). The results indicate that thermo-oxidative aging (60 °C, 1440 h) markedly reduces the activation energy (E, by 17.05%), pre-exponential factor (A, by 68.52%), LOI value (by 4%, from 27.5 to 26.4), and time to ignition (TTI, by 17.1%, from 41 s to 34 s) while augmenting the peak mass loss rate (MHRR, by 4.7%) and peak heat release rate (pHRR, by 20.1%). Subsequent investigation indicates that aging impairs the char layer structure on MFPB surfaces, hastens the migration and degradation of melamine formaldehyde resin (MFR), and alters the dynamic equilibrium between “MFR surface enrichment” and “thermal decomposition”. The identified degradation thresholds and failure mechanisms provide essential parameters for developing aging-resistant fireproof composites, meeting the pressing demands of building safety requirements and sustainable material design. Full article

With the continuous consumption of fossil energy and the related environmental problems, clean energy, especially the hydrogen energy-derived water electrolysis, has attracted wide attention. However, as a result of the high energy consumption of water electrolysis and the limitations of single-function catalysts, there is an urgent need for cheap and simple-to-make bifunctional catalysts. In this work, based on the NiFe-LDH that is usually used for OER (Oxygen Evolution Reaction), doping of heteroatoms was carried out and a bifunctional catalyst could be then prepared using biomass as the carbon source. The preparation of catalyst precursors and in situ reduction were performed through the coupling process of hydrothermal and pyrolysis to enhance the electrolytic activity of the catalyst. Results showed that the overpotentials required to reach a current density of 10 mA·cm⁻² for the HER and OER processes were 305.2 mV and 310.4 mV, respectively, which are superior to the commercial catalysts. In the subsequent characterization, the structural characteristics of the catalyst support and their structure–activity correlation with active metals were systematically investigated by TEM, XRD, and XPS analysis, providing mechanistic insights into the catalytic behavior. The basic catalytic mechanisms of HER and OER were also obtained: the HER process was due to the formation of a Ni₃Fe alloy structure during catalyst preparation, which changed the electronic structure of the catalyst, while the OER process was induced by the formation of a NiOOH intermediate. The research results are expected to provide new ideas and data support for the preparation of bifunctional catalysts. Full article

Significant uranium exploration breakthroughs have been achieved in the eolian deposits of the uranium reservoirs in the southwestern part of the Ordos Basin. The redox environment remains a crucial factor in controlling the migration and precipitation of uranium. This study, through rock mineralogical observations and hydrocarbon gas composition analysis, combined with the regional source rock and basin tectonic evolution history, reveals the characteristics of the reducing medium and the mineralization mechanisms involved in uranium ore formation. The Lower Cretaceous Luohe Formation uranium reservoirs in the study area exhibit a notable lack of common reducing media, such as carbonaceous debris and pyrite. However, the total hydrocarbon gases in the Luohe Formation range from 2967 to 20,602 μmol/kg, with an average of 8411 μmol/kg—significantly higher than those found in uranium reservoirs elsewhere in China, exceeding them by 10 to 100 times. Due to the absence of other macroscopically visible organic matter, hydrocarbon gases are identified as the most crucial reducing agent for uranium mineralization. These gases consist predominantly of methane and originate from the Triassic Yanchang Formation source rock. Faults formed during the Indosinian, Yanshanian, and Himalayan tectonic periods effectively connect the Cretaceous uranium reservoirs with the oil and gas reservoirs of the Triassic and Jurassic, providing pathways for the migration of deep hydrocarbon fluids into the Cretaceous uranium reservoirs. The multiphase tectonic evolution of the Ordos Basin since the Cenozoic has facilitated the development of faults, ensuring a sufficient supply of reducing media for uranium reservoirs in an arid sedimentary context. Additionally, the “Replenishment-Runoff-Drainage System” created by tectonic activity promotes a continuous supply of uranium- and oxygen-bearing fluids to the uranium reservoirs, resulting in a multi-energy coupling mineralization effect. Full article

Defect engineering has recently emerged as a cutting-edge discipline for precise modulation of electronic structures in nanomaterials, shifting the paradigm in nanoscience from passive ‘inherent defect tolerance’ to proactive ‘defect-controlled design’. The deliberate introduction of defect—including vacancies, dopants, and interfaces—breaks the rigid symmetry of crystalline lattices, enabling new pathways for optimizing catalysis performance. This review systematically summarizes the mechanisms underlying defect-mediated electronic structure at active sites regulation, including (1) reconstruction of the electronic density of states, (2) tuning of coordination microenvironments, (3) charge transfer and localization effects, (4) spin-state and magnetic coupling modulation, and (5) dynamic defect and interface engineering. These mechanisms elucidate how defect-induced electronic restructuring governs catalytic activity and selectivity. We further assess advanced characterization techniques and computational methodologies for probing defects-induced electronic states, offering deeper mechanistic insights at atomic scales. Finally, we highlight recent breakthroughs in defect-engineered nanomaterials for catalytic applications, including hydrogen evolution reaction (HER), oxygen evolution reaction (OER) and beyond, while discussing existing challenges in scalability, defect stability, and structure–property causality. This review aims to provide actionable principles for the rational design of defects to tailor electronic structures toward next-generation energy technologies. Full article

Myelodysplastic syndromes are a group of clonal hematopoietic stem cell disorders characterized by ineffective hematopoiesis, peripheral cytopenia, and dysplasia in one or more myeloid lineages, with a variable risk of progression to acute myeloid leukemia. In addition to well-characterized genetic and epigenetic abnormalities, oxidative stress has emerged as a critical contributor to the pathophysiology of myelodysplastic syndrome. Reactive oxygen species and reactive nitrogen species can induce cumulative DNA damage, mitochondrial dysfunction, and altered redox homeostasis, promoting genomic instability and clonal evolution. Elevated oxidative stress in patients with myelodysplastic syndromes has been linked to increased apoptosis of hematopoietic stem and progenitor cells, disruption of the bone marrow microenvironment, and progression toward leukemic transformation. Moreover, ROS-related pathways, such as TP53 mutations and epigenetic dysregulation, interact with the key molecular drivers of myelodysplastic syndrome. Given these findings, oxidative stress is now recognized not only as a hallmark of disease biology but also as a potential therapeutic target. Antioxidant-based strategies and agents that modulate redox signaling are being investigated for their ability to restore hematopoietic function and enhance treatment efficacy. This review provides an overview of the current biology of myelodysplastic syndrome, highlights the connections between oxidative stress and disease mechanisms, and explores emerging redox-targeted therapeutic approaches. Full article

This work provides a comprehensive investigation into the synergistic effects of zirconium and oxygen on the microstructural evolution, high-temperature oxidation resistance, and mechanical properties of γ-phase Ti52AlxZr alloys (x = 0, 0.5, 1, and 2 at.%) under systematically controlled oxygen concentrations. Unlike prior studies that have examined these alloying elements in isolation, this study uniquely decouples the contributions of interstitial (oxygen) and substitutional (zirconium) solutes by employing low (LOx) and high (HOx) oxygen levels. Alloys were synthesized via vacuum arc melting and subsequently subjected to homogenization annealing at 1250 °C for 100 h to ensure phase and microstructural stability. Characterization techniques including scanning electron microscopy (SEM), X-ray diffraction (XRD), and electron backscatter diffraction (EBSD) were employed to elucidate phase constitution and grain morphology. Zirconium addition was found to stabilize the γ-TiAl matrix, suppress α₂-phase formation, and promote grain coarsening in LOx specimens. Conversely, elevated oxygen concentrations led to α₂-phase precipitation along grain boundaries. Mechanical testing, comprising Vickers hardness and uniaxial compression at ambient and elevated temperatures (800 °C), revealed that both zirconium and oxygen significantly enhanced strength and hardness, with Ti52Al2Zr delivering optimal mechanical performance. Moreover, zirconium substantially improved oxidation resistance by promoting the formation of a thinner, adherent Al₂O₃ scale while simultaneously inhibiting TiO₂ growth. Collectively, the findings demonstrate the critical role of zirconium in engineering advanced γ-TiAl-based intermetallics with superior high-temperature structural integrity and oxidation resistance. Full article

Titanium alloys are of significant value in aerospace, biomedical, and marine engineering applications due to their excellent specific strength and favorable biocompatibility. As a crucial interstitial solute, oxygen significantly influences the mechanical properties of titanium alloys. However, excessive oxygen content can lead to severe embrittlement and a significant reduction in ductility. This paper systematically reviews the mechanisms of microstructural evolution induced by oxygen in conventionally manufactured titanium alloys and their impact on mechanical properties, highlighting that conventional processes require complex post-treatments (PT) to achieve a balance between strength and plasticity. This assessment further explores the regulatory mechanisms of oxygen on the microstructure and mechanical properties of laser additive manufactured (LAM) titanium alloys, elucidating the fundamental phenomena regarding the oxygen–microstructure–property relationship. Finally, based on the current research progress, this paper provides an outlook on the future development directions and key research priorities in this field. This review offers valuable insights into the role of oxygen in titanium alloys and the development of high-performance titanium alloys. Full article

To address mass transport limitations in carbon nanofiber membrane electrodes for overall water splitting, a self-supporting nitrogen-doped hollow carbon nanofiber membrane embedded with Co/Co₂P heterojunctions (Co/Co₂P-NCNFs-H) was fabricated via continuous coaxial electrospinning. The architecture features uniform hollow channels (200–250 nm diameter, 30–50 nm wall thickness) and a high specific surface area (254 m² g⁻¹), as confirmed by SEM, TEM, and BET analysis. The Co/Co₂P heterojunction was uniformly dispersed on nitrogen-doped hollow carbon nanofibers through electrospinning, leverages interfacial electronic synergy to accelerate charge transfer and optimize the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). Electrochemical tests demonstrated exceptional catalytic activity, achieving current densities of 100 mA cm⁻² at ultralow overpotentials of 405.6 mV (OER) and 247.9 mV (HER) in 1.0 M KOH—surpassing most reported transition metal catalysts for both half-reactions. Moreover, the electrode exhibited robust long-term stability, maintaining performance for nearly 20 h at 0.6 V (vs. Ag/AgCl) (OER) and over 250 h at −1.5 V (vs. Ag/AgCl) (HER), attributed to the mechanical integrity of the hollow architecture and strong metal–carbon interactions. This work demonstrates that integrating hollow nanostructures (enhanced mass transport) and heterojunction engineering (optimized electronic configurations) creates a scalable strategy for designing efficient bifunctional catalysts, offering significant promise for sustainable hydrogen production via water electrolysis. Full article

Over the last decade, polymeric carbon nitrides (PCNs) have received exponentially growing attention as metal-free photocatalytic platforms for green energy generation and environmental remediation. Although PCNs can be easily synthesized from abundant precursors in a powdered form, progress in the field of photoelectrochemical applications requires effective methods for the fabrication of PCN films endowed with suitable mechanical stability and modular chemico-physical properties. In this context, as a proof-of-concept, we report herein on a simple and versatile chemical vapor infiltration (CVI) strategy for one-step PCN growth on porous Ni foam substrates, starting from melamine as a precursor compound. Interestingly, tailoring the reaction temperature enabled to control the condensation degree of PCN films from melem/melon hybrids to melon-like materials, whereas the use of different precursor amounts directly affected the mass and morphology of the obtained deposits. Altogether, such features had a remarkable influence on PCN electrochemical performances towards the oxygen evolution reaction (OER), yielding, for the best performing systems, Tafel slopes as low as ≈65 mV/dec and photocurrent density values of ≈1 mA/cm² at 1.6 V vs. the reversible hydrogen electrode (RHE). Full article

Neutrophils, accounting for 50–70% of circulating leukocytes, exhibit remarkable plasticity in tumor biology. Depending on tumor type and microenvironmental cues, they can exert either anti-tumor or pro-tumor effects. During tumor initiation, neutrophils exposed to chronic inflammation secrete cytokines and oncogenic microRNAs that promote genomic instability and malignant transformation. In tumor progression, neutrophils adopt context-dependent phenotypes and execute diverse functions, including polarization into anti-tumor (N1) or pro-tumor (N2) subsets; secretion of inflammatory and angiogenic mediators; formation of neutrophil extracellular traps (NETs); production of reactive oxygen and nitrogen species (e.g., H₂O₂ and nitric oxide); and modulation of immune cell infiltration and function within the tumor microenvironment. During metastasis, neutrophils facilitate cancer dissemination through three principal mechanisms: (1) promoting epithelial–mesenchymal transition (EMT) via inflammatory signaling, adhesion molecule interactions, and lipid metabolic support; (2) establishing pre-metastatic niches by remodeling distant organ stroma through NETs and matrix metalloproteinases; and (3) reactivating dormant tumor cells in response to chronic inflammation, viral infection, or stress hormones. Collectively, neutrophils function as central regulators across all stages of tumor evolution, influencing cancer growth, immune evasion, and metastatic progression. This review aims to provide a comprehensive synthesis of neutrophil-mediated mechanisms in the tumor microenvironment and highlight emerging strategies for neutrophil-targeted cancer therapy. Full article

Objects with the B[e] phenomenon, whose defining features are the presence of forbidden emission lines and infrared excess coming from circumstellar dust, represent a broad range of evolutionary stages from pre-main-sequence to planetary nebulae. They are important for understanding mechanisms of the circumstellar matter formation and evolution. However, it is not easy to discover them, especially among faint stars, as forbidden emission lines are usually weak and hardly noticeable in low-resolution spectra. We developed photometric criteria to search for candidate objects with this phenomenon based on a combination of optical and near-infrared color indices and found nearly 40 objects that satisfy these criteria. Spectroscopy of the candidates allows us to make more confident conclusions on their classification. We present the results of our photometric and spectroscopic observations of six objects, which are part of a large list of ∼40 objects that satisfy our photometric selection criteria for candidate objects with the B[e] phenomenon. Forbidden lines of neutral oxygen were clearly detected in the optical spectrum of one object (VES 683) and suspected in three others. One object, AS 415, is most likely a binary system with components that exhibit partial eclipses but without the B[e] phenomenon, while IRAS 20402 + 4638 may be a luminous member of the FS CMa objects group. Full article

Lithium–air batteries (LABs) possess the highest energy density among all energy storage systems, and have drawn widespread interest in academia and industry. However, many arduous challenges are still to be conquered, one of them is Li₂CO₃, which is a ubiquitous product in LABs. It is inevitably produced but difficult to decompose; therefore, Li₂CO₃ is perceived as the “Achilles’ heel of LABs”. Among various approaches to addressing the Li₂CO₃ issue, developing Li₂CO₃-decomposing redox mediators (RMs) is one of the most convenient and versatile, because they can be electrochemically oxidized at the gas cathode surface, then they diffuse to the solid-state products and chemically oxidize them, recovering the RMs to a pristine state and avoiding solid-state catalysts’ contact instability with Li₂CO₃. Furthermore, because of their function mechanism, they can double as catalysts for Li₂O₂/LiOH decomposition, which are needed in LABs/LOBs anyway regardless of Li₂CO₃ incorporation due to the sluggish kinetics of oxygen reduction/evolution reactions. This review summarizes the progress in Li₂CO₃-decomposing RMs, including halides, metal–chelate complexes, and metal-free organic compounds. The insights into and discrepancies in the mechanisms of Li₂CO₃ decomposition and corresponding catalysis processes are also discussed. Full article

Photochemical degradation is a major removal pathway for pharmaceutical pollutants in water, and dissolved organic matter (DOM) in water is an important factor affecting this process. This study investigates the differential effects of seasonally-varied dissolved organic matter (DOM) from Songhua River and Liao River on the photodegradation of pharmaceutical pollutants, using levofloxacin (LFX), sulfamethoxazole (SMZ), and ibuprofen (IBP) as target compounds. The results demonstrated that summer and autumn DOM inhibited the photodegradation of LFX and SMZ through light screening and dynamic quenching effects, with inhibition rates of 35.1% and 55.5%, respectively, whereas winter DOM enhanced degradation through photo-oxidation mechanisms. DOM from Songhua River and Liao River significantly promoted the photodegradation of IBP. Quenching experiments showed differences in the contributions of photochemically reactive intermediates (PPRIs) to the photodegradation of different target pollutants, with hydroxyl radicals (•OH) dominating LFX photodegradation (48.79% contribution), excited triplet states of DOM (³DOM*) dominating SMZ photodegradation (85.20% contribution), and singlet oxygen (¹O₂) dominating IBP photodegradation (79.89% contribution). The photodegradation pathways were elucidated by measuring the photodegradation by-products of the target pollutants: LFX mainly underwent piperazine ring cleavage and oxidative decarboxylation, SMZ underwent isoxazole ring opening and deamination during photodegradation, and IBP underwent photodecarboxylation and oxidation reactions. Under the influence of the DOM from the Songhua River and Liao River, the generation of multiple photodegradation by-products led to an increasing trend in the acute toxicity of target pollutants to luminescent bacteria. This investigation elucidates the dual regulatory mechanisms of natural aquatic DOM on both photo-induced degradation pathways and toxicity evolution dynamics of pharmaceutical contaminants, which is of great significance for understanding the photochemical transformation behavior and risk assessment of pharmaceutical pollutants in aquatic environments. Full article

Refractory metal-based Mo-Si-B alloys have long been considered the most promising candidates for replacing nickel-based superalloys in the aerospace and energy sector due to their outstanding mechanical properties and good oxidation of the Mo-silicide phases. In general, the addition of vanadium to Mo-Si-B alloys leads to a significant density reduction, while small amounts of titanium provide additional strengthening without changing the phase evolution within the Mo_ss-Mo₃Si-Mo₅SiB₂ phase field. In this work, high-energy ball milling studies on Mo-40V-9Si-8B, substituting both molybdenum and vanadium with 2 and 5 at. % Ti in all constituents, were performed to evaluate the potential milling parameters and investigate the effects of Ti doping on the milling characteristics and phase formation of these multicomponent alloys. After different milling durations, the powders were analysed with regard to their microstructure, particle size, oxygen concentration and microhardness. After heat treatment, the silicide phases (Mo,V)₃Si and (Mo,V)₅SiB₂ precipitated homogeneously within a (Mo,V) solid solution matrix phase. Thermodynamic phase calculations using the CALPHAD method showed good agreement with the experimental phase compositions after annealing, confirming the stability of the observed microstructure. Full article

Bifidobacterium animalis is a widely used probiotic with significant health benefits, but its application is limited by oxygen sensitivity. Our laboratory previously developed an oxygen-tolerant B. animalis AR668-R1 using adaptive laboratory evolution under aerobic culture, but the molecular mechanism remains unclear. In this work, compared to the wild-type parental strain B. animalis AR668, 212 upregulated and 390 downregulated proteins were identified in AR668-R1 under aerobic conditions through comparative proteomic analysis. Enrichment analysis of the differentially expressed proteins between AR668 and AR668-R1 identified the potential oxygen-tolerant related pathways, including the translation process, transmembrane transport system, and carbohydrate metabolism. Furthermore, five potential oxygen-tolerance proteins (DapE, Mth2, MutT, Eno, and MsrAB) were validated by RT-qPCR that may contribute to the aerobic growth of AR668-R1. Through gene overexpression validation, Mth2 (7,8-dihydro-8-oxoguanine triphosphatase) was found to enhance the growth of AR668-R1 by 19.8% compared to the empty plasmid control under aerobic conditions. Our finding provides valuable insights into the oxygen-tolerant mechanisms of B. animalis at the protein level. Full article