Search Results (4,128)

Ethanolamine (EA) is a widely used yet toxic volatile organic compound (VOC). However, existing gas sensors for EA detection face persistent challenges in achieving exceptional sensitivity and low detection limits at room temperature (RT). In this study, a novel and high-performance EA sensor based on the MoO₃/BiOI composite was prefabricated using hydrothermal and cyclic impregnation methods. The response value toward 100 ppm EA reached 861.3, which was 3.5-times higher compared to that of pure MoO₃. In addition, the MoO₃/BiOI composite exhibited a low detection limit (0.13 ppm), excellent selectivity, short response/recovery times, exceptional repeatability and long-term stability. The outstanding gas sensing performance of the MoO₃/BiOI is attributed to the formation of a p-n heterojunction, synergistic effects between the two materials, abundant adsorbed oxygen species and superior charge transfer efficiency. The sensor developed in this work effectively addresses the long-standing challenges, demonstrating unprecedented practical application potential for EA gas detection. Simultaneously, this study provides a novel strategy, a new approach and a promising material for the subsequent development of advanced amine sensors. Full article

The Wufeng–Longmaxi (WF–LMX) shale gas reservoirs at depths > 3500 m in the Lu203–Yang101 well block, southern Sichuan Basin, possess great exploration potential, but their reservoir characteristics and high-production mechanisms remain unclear. In this study, we employed multi-scale analyses—including core geochemistry, X-ray diffraction (XRD), scanning electron microscopy (SEM), low-pressure N₂ adsorption, and nuclear magnetic resonance (NMR)—to characterize the macro- and micro-scale characteristics of these deep shales. By comparing with shallower shales in adjacent areas, we investigated differences in pore structure between deep and shallow shales and the main controlling factors for high gas-well productivity. The results show that the Long 11 sub-member shales are rich in organic matter, with total organic carbon (TOC) content decreasing upward. The mineral composition is dominated by quartz (averaging ~51%), which slightly decreases upward, while clay content increases upward. Porosity ranges from 1% to 7%; the Long11-1-3 sublayers average 4–6%, locally >6%. Gas content correlates closely with TOC and porosity, highest in the Long11-1 sublayer (6–10 m³/t) and decreasing upward, and the central part of the study area has higher gas content than adjacent areas. The micro-pore structure exhibits pronounced stratigraphic differences: the WF Formation top and Long11-1 and Long11-3 sublayers are dominated by connected round or bubble-like organic pores (50–100 nm), whereas the Long11-2 and Long11-4 sublayers contain mainly smaller isolated organic pores (5–50 nm). Compared to shallow shales nearby, the deep shales have a slightly lower proportion of organic pores, smaller pore sizes with more isolated pores, inorganic pores of mainly intraparticle types, and more developed microfractures, confirming that greater burial depth leads to a more complex pore structure. Type I high-quality reservoirs are primarily distributed from the top of the WF Formation to the Long11-3 sublayer, with a thickness of 15.6–38.5 m and a continuous thickness of 13–23 m. The Lu206–Yang101 area has the thickest high-quality reservoir, with a cumulative thickness of Type I + II exceeding 60 m. Shale gas-well high productivity is jointly controlled by multiple factors: an oxygen-depleted, stagnant deep-shelf environment, with deposited organic-rich, biogenic siliceous shales providing the material basis for high yields; abnormally high pore-fluid pressure with preserved abundant large organic pores and increased free gas content; and effective multi-stage massive fracturing connecting a greater reservoir volume, which is the key to achieving high gas-well production. This study provides a scientific basis for evaluating deep marine shale gas reservoirs in southern Sichuan and understanding the enrichment patterns for high productivity. Full article

The agricultural industry faces increasing environmental degradation due to the intensive use of conventional chemical fertilizers, leading to water pollution and alterations in soil composition. In addition, root-knot and cyst nematodes are major constraints to cucumber production, causing severe root damage and yield losses worldwide, underscoring the need for sustainable alternatives to conventional fertilization and pest management. Under greenhouse conditions, a four-month cultivation trial evaluated vegetable oil-, micronutrient-, and activated flavonoid-based biostimulants, applying Key Eco Oil^® (Miami, USA) via soil drench (every 15 days) combined with foliar sprays of CropBioLife^® (Victoria, Australia) and KeyPlex 120^® (Miami, USA) (every 7 days). Results showed reduced parasitic nematodes by 66% in soil and decreased gall formation by 41% in roots. Chlorophyll fluorescence and infrared gas analysis revealed higher oxygen-evolving complex efficiency (38%), increased PSII electron transport, improved the fluorescence decrease ratio, also known as the vitality index (Rfd), and higher CO₂ assimilation compared to conventional treatments. Processed cucumbers showed higher sugar and nearly double ascorbic acid content, with improved flesh consistency and color. Therefore, the application of these bioactive products significantly reduced nematode infestation while enhancing plant growth and physiological performance, underscoring their potential as sustainable tools for crop cultivation and protection. These results provide evidence that sustainable bioactive biostimulants improve plant resilience, productivity, and nutritional quality, offering also an environmentally sound approach to pest management. Full article

Periodontal disease represents a major global concern characterized by chronic biofilm-driven inflammation, excessive oxidative stress, progressive tissue destruction, and impaired regenerative capacity. Beyond conventional antimicrobial approaches, recent progress has shifted toward host-directed and regenerative therapeutic strategies aimed at restoring both oral function and tissue homeostasis. This review consolidates current developments in nanobiotechnology-based materials that modulate immune responses, scavenge reactive oxygen species, and promote angiogenesis and osteogenesis, thereby facilitating the effective regeneration of dental and periodontal tissues. Emphasis is placed on bioresponsive hydrogels, bioactive scaffolds, and gas-releasing platforms that integrate therapeutic regulation with tissue repair. The discussion further highlights key advances in polymeric and inorganic biomaterials designed to balance antibacterial action with cellular compatibility and regenerative potential. By linking pathophysiological mechanisms with material-guided healing processes, this review provides a comprehensive perspective on emerging nanobiotechnological solutions that bridge patho-therapeutics with regenerative and clinical dentistry. Full article

We report a defect-selective luminescence response in calcium-deficient hydroxyapatite (HAp) induced by electron and ion irradiation. Compacted HAp pellets prepared from hydrothermally grown nanofibers were investigated to analyze defect-related luminescence using photoluminescence (PL) and cathodoluminescence (CL) techniques, both before and after compaction. Low-energy electron beam irradiation (15 keV) produced a two-stage luminescent response, an initial enhancement arising from field-assisted activation of OH-channel vacancies (V_OH and V_OH + H_i), followed by an exponential decay attributed to defect annealing. Monochromatic transient CL measurements show that this rise–decay behavior is selective to the OH-related bands at 2.57 and 2.95 eV, whereas the 3.32 and 3.67 eV emissions exhibit only a monotonic exponential decay. The corresponding decay constants further indicate that the activated OH-channel vacancies anneal more rapidly than the other centers, consistent with their higher electron-capture probability and lower structural stability. In contrast, ${\mathrm{Ga}}^{+}$ ion irradiation (30 keV, 1.4 × 10⁻¹³ A/µm²) induced progressive monotonic luminescence quenching, primarily driven by selective annealing of oxygen vacancies in $\mathrm{P}{\mathrm{O}}_4^{3-}$ groups. These complementary pathways, electron-induced activation and ion-driven suppression, demonstrate that irradiation serves as a versatile tool for defect engineering in hydroxyapatite. Beyond providing fundamental insights into vacancy stability, these results open new routes for tailoring the optical, sensing, and bioimaging functionalities of HAp through controlled irradiation. Full article

Listeria monocytogenes (LM) contamination constitutes a paramount global threat to food safety, necessitating the urgent development of advanced, rapid, and non-destructive detection methodologies to ensure food security. This study successfully synthesized Bi₂WO₆ nanoflowers through optimized feed ratios of raw materials and further functionalized them with noble metal Au to construct a high-performance Au-Bi₂WO₆ composite nanomaterial. The composite exhibited high sensing performance toward acetoin, including high sensitivity (R_a/R_g = 36.9@50 ppm), rapid response–recovery kinetics (13/12 s), and excellent selectivity. Through UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS) and X-ray photoelectron spectroscopy (XPS) characterizations, efficient electron exchange between Au and Bi₂WO₆ was confirmed. This electron exchange increased the initial resistance of the material, effectively enhancing the response value toward the target gas. Furthermore, the chemical sensitization effect of Au significantly increased the surface-active oxygen content, promoted gas–solid interfacial reactions, and improved the adsorption capacity for target gases. Compared to conventional turbidimetry, the Au-Bi₂WO₆ nanoflower-based gas sensor demonstrates superior practical potential, offering a novel technological approach for non-destructive and rapid detection of foodborne pathogens. Full article

The moldic pore-vuggy reservoirs of the Ma5₄-Ma5₁ sub-member in the Majiagou Formation, central Ordos Basin, are key targets for deep natural gas exploration, yet the alteration mechanisms and controlling factors of burial-stage pressure-released water karstification remain unclear. Herein, an integrated methodology encompassing core observation, thin-section analysis, and geochemical testing was adopted to systematically clarify the development characteristics and multi-factor coupling control mechanisms of this karst process. Results show that burial-stage pressure-released water karst is dominated by overprinting on pre-existing syndepositional and supergene pore networks, forming complex reservoir spaces via synergistic selective dissolution. The development of preferential dissolution zones is jointly controlled by differential compaction of the weathering crust, permeability heterogeneity of the overlying strata and weathered crust, and diagenetic fluid properties. After the supergene diagenetic stage, differential tectonic deformation and burial compaction induced overpressure in pore fluids, which drove acidic pressure-released water to migrate along high-permeability pathways such as the “sandstone windows” overlying the Ordovician weathering crust. These fluids preferentially dissolved high-permeability moldic pore-vuggy dolomites in paleo-karst platforms and steep slope zones, whereas tight micritic dolomites served as effective barriers. The acidic environment sustained by organic acids and H₂S in pressure-released water promoted carbonate dissolution, and carbon-oxygen isotopes as well as pyrite δ³⁴S values verify that the fluids were derived from mudstone compaction. This study reveals that the distribution of high-quality reservoirs is jointly determined by the synergistic preservation of moldic pore-vuggy systems in paleo-karst platforms and steep slopes and directional alteration of pressure-released water along preferential pathways, providing crucial geological guidance for the evaluation of deep carbonate reservoirs. Full article

The presence of aberrant double-stranded DNA (dsDNA) in the cytoplasm of cells is sensed by unique pattern recognition receptors (PRRs) to trigger innate immune response. The cyclic GMP–AMP synthase (cGAS)–stimulator of interferon genes (STING) signaling pathway is activated by the presence of non-self or mislocalized self-dsDNA from nucleus or mitochondria released in response to DNA damage or cellular stress in the cytoplasm. Activation of cGAS leads to the synthesis of the second messenger cyclic GMP–AMP (cGAMP), which binds and activates STING, triggering downstream signaling cascades that result in the production of type I interferons (IFNs) and proinflammatory cytokines. Here, we show that diverse immunostimulatory dsDNA ligands and chemotherapy agents like Doxorubicin and Taxol trigger the integrated stress response (ISR) by activating endoplasmic reticulum (ER) stress kinase, protein kinase RNA-like ER kinase (PERK), in addition to the canonical IFN pathways. PERK-mediated phosphorylation and inactivation of the alpha subunit of eukaryotic translation initiation factor-2 (eIF2α) result in the formation of stress granules (SGs). SG formation by dsDNA was significantly reduced in PERK knockout cells or by inhibiting PERK activity. Transcriptional induction of IFNβ and cytokines, ISR signaling, and SG formation by dsDNA was dampened in cells lacking PERK activity, STING, or key stress-granule nucleating protein, Ras-GAP SH3 domain-binding protein 1 (G3BP1), demonstrating an important role of the signal transduction pathway mediated by STING and SG assembly. Lastly, STING regulates reactive oxygen species (ROS) production in response to DNA damage, highlighting the crosstalk between DNA sensing and oxidative stress pathways. Together, our data identify STING–PERK–G3BP1 signaling axis that couples cytosolic DNA sensing to stress response pathways in maintaining cellular homeostasis. Full article

In this study, pectin packaging films were enhanced with selected phenolic acids, including caffeic, coumaric, ferulic, gallic, protocatechuic, and sinapic acids. Edible films were created from apple pectin aqueous solutions that were plasticised with glycerol. The evaluation covered various properties, including optical, barrier, mechanical, thermal, structural, and antioxidant activity. The findings showed that phenolic acids are beneficial and compatible components for pectin films. A higher barrier against UV-VIS light and mechanical strength, as well as a more resilient structure, was observed. All the films exhibited a compact and uniform structure, along with transparency and a light colour. The addition of phenolic acids caused greater permeability to oxygen and carbon. Except for caffeic and protocatechuic acids, which resulted in lower values of permeability for both gases, the other acids improved gas transmission. Fourier transform infrared spectroscopy (FT-IR) analysis confirmed several functional groups, including hydroxyl (−OH) and carbonyl (C=O) groups. All films containing phenolic acids demonstrated increased antioxidant activity, with variations depending on the specific compound. Full article

Spontaneous coal combustion accounts for more than 90% of mine fires, and at the same time, the ‘dual carbon’ strategy requires fire prevention and extinguishing materials to have both low-carbon and environmentally friendly functions. To meet on-site application needs, a composite gel with fast injection, flame retardant, and CO₂ adsorption functions was developed. PVA-PEI-PAC materials were selected as the gel raw materials, and an orthogonal test with three factors and three levels was used to optimize the gelation time parameters to identify the optimal formulation. The microstructure of the gel, CO₂ adsorption performance, as well as its inhibition rate of CO, a marker gas of coal spontaneous combustion, and its effect on activation energy were systematically characterized through SEM, isothermal/temperature-programmed/cyclic adsorption experiments, and temperature-programmed gas chromatography. The results show that the optimal gel formulation is 14% PVA, 7% PEI, and 5.5% PAC. The gel microstructure is continuous, dense, and rich in pores, with a CO₂ adsorption capacity at 30 °C and atmospheric pressure of 0.86 cm³/g, maintaining over 76% efficiency after five cycles. Compared with raw coal, a 10% gel addition reduces CO release at 170 °C by 25.97%, and the temperature-programmed experiment shows an average CO inhibition rate of 25% throughout, with apparent activation energy increased by 14.96%. The gel prepared exhibited controllable gelation time, can deeply encapsulate coal, and can efficiently adsorb CO₂, significantly raising the coal–oxygen reaction energy barrier, providing an integrated technical solution for mine fire prevention and extinguishing with both safety and carbon reduction functions. Full article

Oxidation can lead to intrinsic degradation and loss in the load-bearing capacity of ceramic matrix composites (CMCs) in high-temperature service, thereby compromising structural integrity and operational safety. To elucidate the mechanism of its oxidation effects, this study predicted the oxygen diffusion coefficient within 2.5D woven C/SiC fibre bundles based on gas diffusion and oxidation kinetics theory, and subsequently constructed a meso-scale constitutive model incorporating oxidation damage and fibre defect distribution. Furthermore, a micro-scale framework for yarns was established by integrating interfacial slip behaviour, and an RVE model for 2.5D woven C/SiC was constructed based on X-ray computed tomography reconstruction of the actual microstructure. Building upon this foundation, an oxidation constitutive model applicable to loading–unloading cycles was proposed and validated through high-temperature oxidation tests at 700 °C, 900 °C, and 1100 °C. Results demonstrate that this model effectively characterizes the strength degradation and stiffness reduction caused by oxidation, enabling prediction of CMCs’ mechanical properties under oxidizing conditions and providing a physics-based foundation for the reliable design and life assessment of C/SiC components operating in oxidizing environments. Full article

Cracking occurred in the surface coating of a screw rotor during shale gas well operations. To determine whether the coating cracks could contribute to the failure of the 42CrMo substrate, the microstructure and morphology of surface cracks and local corrosion pits were examined and analyzed using a metallographic microscope, an SEM, and an EDS. To investigate the cross-sectional morphology and elemental distribution of corrosion pits, EDS mapping was performed. The composition of the corrosion products was characterized using Raman spectroscopy and XPS. In addition, four-point bend stress corrosion tests were conducted on screw rotor specimens under simulated service conditions. The results indicate that the P and S contents in the screw rotor substrate exceeded the specified limits, whereas its tensile and impact strengths satisfied the standard requirements. The microstructure consisted of tempered sorbite and ferrite, along with a small amount of sulfide inclusions. The corrosion products on the fracture surface were primarily identified as FeOOH, Fe₃O₄, and Cr(OH)₃. All specimens failed during the four-point bend tests. The chlorine (Cl) content in the corroded regions reached up to 8.05%. These findings demonstrate that the crack resistance of the 42CrMo screw rotor was markedly reduced under the simulated service conditions of 130 °C in a saturated, oxygenated 25% CaCl₂ solution. The study concludes that stress concentration induced by sulfide inclusions in the screw rotor, together with the combined effects of chloride ions, dissolved oxygen, and applied load, promotes the initiation and propagation of stress corrosion cracking. Therefore, it is recommended to strictly control the chemical composition and inclusion content of the screw rotor material and to reduce the oxygen content of the drilling fluid, thereby mitigating the risk of corrosion-induced cracking of the rotor. Full article

A growing number of fires and explosions in energy storage plants have been triggered by the thermal runaway of lithium-ion batteries. Owing to the complex physicochemical properties of these batteries, their fire safety issues remain unresolved and constitute a major obstacle to the large-scale deployment of energy storage systems. Compared with conventional extinguishing media, liquid nitrogen (LN₂) offers a dual suppression mechanism, i.e., rapid endothermic vaporization and oxygen displacement by inert nitrogen gas, making it highly suitable for lithium-ion battery fire control. However, the key operational parameters governing its suppression efficiency remain unclear, leading to excessive or insufficient LN₂ use in practice. This study established a dedicated experimental platform and designed 10 experimental conditions, each repeated three times, to investigate the propagation of thermal runaway between adjacent batteries and to quantify the suppression performance of LN₂ under varying nozzle diameters and injection strategies. Results demonstrate that under identical injection pressures, larger nozzle diameters significantly outperform smaller ones in cooling and suppression efficiency. The optimal nozzle diameter was found to be 14 mm, achieving a cooling efficiency of 40%. Furthermore, intermittent LN₂ injection of equal total mass outperformed continuous injection, with a 45 s intermittent duration achieving a cooling efficiency of 63%, 23% higher than continuous injection. These findings provide quantitative guidance for the design of LN₂-based suppression systems in large-scale lithium-ion battery energy storage modules. Full article

This study examines the high-temperature degradation of Hastelloy C276, a corrosion-resistant nickel-based alloy, during exposure to combustion products generated by methane and 99% cracked ammonia. Using a high-pressure optical combustor (HPOC) at 4 bar and exhaust temperatures of 815–860 °C, standard tensile specimens were exposed for five hours to fully developed post-flame exhaust gases, simulating real industrial turbine or burner conditions. The surfaces and subsurface regions of the samples were analysed using scanning electron microscopy (SEM; Zeiss Sigma HD FEG-SEM, Carl Zeiss, Oberkochen, Germany) and energy-dispersive X-ray spectroscopy (EDX; Oxford Instruments X-MaxN detectors, Oxford Instruments, Abingdon, United Kingdom), while mechanical properties were evaluated by tensile testing, and the gas-phase compositions were tracked in detail for each fuel blend. Results show that exposure to methane causes moderate oxidation and some grain boundary carburisation, with localised carbon enrichment detected by high-resolution EDX mapping. In contrast, 99% cracked ammonia resulted in much more aggressive selective oxidation, as evidenced by extensive surface roughening, significant chromium depletion, and higher oxygen incorporation, correlating with increased NO_x in the exhaust gas. Tensile testing reveals that methane exposure causes severe embrittlement (yield strength +41%, elongation −53%) through grain boundary carbide precipitation, while cracked ammonia exposure results in moderate degradation (yield strength +4%, elongation −24%) with fully preserved ultimate tensile strength (870 MPa), despite more aggressive surface oxidation. These counterintuitive findings demonstrate that grain boundary integrity is more critical than surface condition for mechanical reliability. These findings underscore the importance of evaluating material compatibility in low-carbon and hydrogen/ammonia-fuelled combustion systems and establish critical microstructural benchmarks for the anticipated mechanical testing in future work. Full article

Advanced ceramics are known for their lightweight, high-temperature resistance, corrosion resistance, and biocompatibility. They are crucial in energy conversion, environmental protection, and aerospace fields. This review highlights the recent advancements in ceramic matrix composites, high-entropy ceramics, and polymer-derived ceramics, alongside various fabrication techniques such as three-dimensional printing, advanced sintering, and electric-field-assisted joining. Beyond the fabrication process, we emphasize how different processing methods impact microstructure, transport properties, and performance metrics relevant to catalysis. Additive manufacturing routes, such as direct ink writing, digital light processing, and binder jetting, are discussed and normalized based on factors such as relative density, grain size, pore architecture, and shrinkage. Cold and flash sintering methods are also examined, focusing on grain-boundary chemistry, dopant compatibility, and scalability for catalyst supports. Additionally, polymer-derived ceramics (SiOC, SiCN, SiBCN) are reviewed in terms of their catalytic performance in hydrogen evolution reaction, oxygen evolution reaction, oxygen reduction reaction, and CO₂ reduction reaction. CeO₂-ZrO₂ composites are particularly highlighted for their use in environmental catalysis and high-temperature gas sensing. Furthermore, insights on the future industrialization, cross-disciplinary integration, and performance improvements in catalytic applications are provided. Full article