Search Results (2,184)

In this study, a composite powder explosion suppressant (MVTS–NaHCO₃) was prepared via the wet coating method of the solution–crystallization (WCSC) process, using modified vanadium–titanium slag (VTS) as the carrier and NaHCO₃ as the active suppressive component. A 20 L spherical explosion apparatus and a transparent pipeline explosion propagation test system were employed to investigate the effects of the composite powder explosion suppressant with different mass fractions (0%, 10%, 20%, 30%, 40%, 50%) on the explosion pressure and micro-mechanism of polyacrylonitrile (PAN) dust. The experimental results indicated that the MVTS–NaHCO₃ composite powder exhibited a significant suppression effect on PAN dust explosions. In the confined 20 L vessel, complete suppression was achieved when the mass fraction of the composite powder explosion suppressant exceeded 30%, with a maximum explosion pressure reduction of 53.2%. In the semi-open pipeline, 40% composite powder explosion suppressant reduced the maximum explosion pressure to 0.08 MPa (a reduction rate of 82.6%), and complete suppression was achieved at a mass fraction of 50%. Microstructural analysis revealed that the suppression performance of the composite powder explosion suppressant is attributed to the synergetic effects of physical and chemical mechanisms. Physically, NaHCO₃ decomposes endothermically (100 kJ/mol), releasing CO₂ and H₂O and thereby diluting the oxygen concentration, while the porous structure of MVTS enhances dispersibility. Chemically, the hydroxyl groups on the surface of MVTS bond with NaHCO₃, delaying its decomposition, while metal hydroxides (e.g., Al(OH)₃) decompose thermally to form Al₂O₃, which adsorbs and quenches free radicals (e.g., ·OH, ·H), thereby inhibiting chain reactions. This study provides new insights for the resource utilization of VTS and the prevention and control of industrial dust explosions. The findings have important reference value for optimizing explosion suppressant formulations and improving the intrinsic safety. Full article

In this work, the impact of hydrogen plasma treatment on the electrical and electronic quality of multicrystalline silicon (mc-Si) was systematically investigated using plasma-enhanced chemical vapor deposition (PE-CVD). Hydrogen radicals generated in the plasma effectively passivate dangling bonds, reducing electrically active defects and enhancing material quality. Optimized PE-CVD conditions were applied to promote efficient hydrogen incorporation and surface modification. Optical characterization, including reflectivity measurements and FT-IR spectroscopy, confirms the formation of Si–H bonds and a significant reduction in surface reflectivity of up to 66% at 600 nm. Electrical and optoelectronic analyses reveal pronounced improvements in carrier lifetime and diffusion length, increased by 200% and 79%, respectively. In addition, dark current–voltage (I–V) measurements show a 32% decrease in series resistance and a 51% increase in shunt resistance, indicating enhanced charge transport and suppressed leakage currents. These macroscopic electrical improvements are supported by light beam-induced current (LBIC) measurements, which demonstrate a 14% increase in grain boundary current, confirming effective hydrogen passivation and reduced recombination. Overall, hydrogen plasma PE-CVD treatment is shown to significantly improve the electronic quality and photovoltaic performance of mc-Si solar cells. Full article

This study employed UPLC-MS/MS to determine the contents of major polyphenolic compounds and proanthocyanidins (PCs) in Kyoho grape seeds, optimized the extraction method and conditions for PCs using response surface methodology (RSM), and further evaluated the scavenging activities of PCs against 2,2-diphenyl-1-picrylhydrazyl (DPPH) and hydroxyl (•OH) radicals as well as their effects on growth, immunity, and oxidative stress in mice. Three hundred and sixty 3-week-old male mice (42.28 ± 0.31 g) were assigned to a single factor complete randomized trial design and fed with six different diets including 0 mg/kg vitamin E(VE) + 0 mg/kg PCs, 100 mg/kg VE, 25 mg/kg PCs + 75 mg/kg VE, 50 mg/kg PCs + 50 mg/kg VE, 75 mg/kg PCs + 25 mg/kg VE and 100 mg/kg PCs, respectively. The results demonstrated that PCs were identified as the predominant phenolic compounds, accounting for 29.6% of total phenolic substances in Kyoho grape seeds. Additionally, the ultrasound-assisted extraction method was superior to the shaker-assisted and low-temperature infiltration extraction methods, with optimal conditions of 60% ethanol concentration, material-to-liquid ratio of 1:20 g/mL, temperature of 30 °C, and extraction time of 50 min. Scanning electron microscopy (SEM) revealed that ultrasound treatment effectively disrupted the seed surface structure, facilitating PC release. In vitro, PCs exhibited significantly stronger DPPH and hydroxyl radical (•OH) scavenging activities than vitamin C (VC), Trolox, and gallic acid. Compared with the control group, mice fed diets containing PCs and VE showed higher superoxide dismutase (SOD) activity, glutathione peroxidase (GSH-PX) activity, and total antioxidant capacity (TAOC), Catalase (CAT), GPX and inflammation factor 10 (IL-10) genes levels in the serum and liver (p < 0.05), whereas the levels of immunoglobulin G (IgG), immunoglobulin A (IgA), immunoglobulin M (IgM), tumor necrosis factor α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6), as well as the mRNA expression of IL-1β and TNF-α, showed the opposite trend (p < 0.05). In conclusion, the antioxidant capacity of PCs was stronger than that of VC and VE. The addition of PCs improved the antioxidant activity and immune function of mice. Full article

The activation of molecular oxygen driven by solar energy presents a cost-effective and environmentally friendly approach in the area of environmental purification. Carbon quantum dots and semiconductor nanocomposite photocatalysts serve as an effective strategy for enhancing the separation and transport of photogenerated carriers, thereby boosting the activation of molecular oxygen. In this study, we prepared 0D tea biomass quantum dots (T-BCDs) coupled with 2D PbBiO₂Br nanosheets, which demonstrate enhanced molecular oxygen activation under visible light irradiation and were synthesized using a solvothermal method. Transmission electron microscopy (TEM) analysis reveals that T-BCDs, with diameters of approximately 5 nm, are uniformly distributed on the surface of PbBiO₂Br. Notably, experimental results indicate a strong covalent interaction between PbBiO₂Br and T-BCDs, which enhances the absorbance of visible light, facilitates the transfer and separation of interfacial photogenerated carriers, and promotes the conversion of molecular oxygen into superoxide radicals. The degradation rate constant of ciprofloxacin achieved with 5 mL T-BCDs/PbBiO₂Br is 3.3 times greater than that obtained with pure PbBiO₂Br. This research offers a promising strategy for the development of efficient 0D/2D photocatalysts aimed at sustainable environmental remediation. Full article

As global oil and gas exploration extends to deep and ultra-deep formations, high-temperature and high-salt environments have become major challenges for drilling fluid viscosifiers. In this study, a hydrophobic associative polymer viscosifier, HATA, was synthesized via free-radical copolymerization using acrylamide (AM), 2-acrylamido-2-methylpropanesulfonic acid (AMPS), sodium styrene sulfonate (SSS), and stearyl methacrylate (SMA) as monomers, and its structure was systematically characterized, while its performance and action mechanism in a 4 wt% bentonite base slurry were evaluated. The results show that the base slurry modified with 3 wt% HATA maintains an apparent viscosity retention ratio of 69.20% following 16 h of hot rolling at 180 °C, with an API filtration loss of only 7.2 mL, and its HTHP filtration loss is 73.72% lower than that of the blank bentonite slurry system; this viscosifier sustains effective viscosity and yield point of the drilling fluid system at 200 °C and in 36 wt% NaCl brine. HATA achieves viscosity enhancement and filtration control by regulating surface charges of bentonite particles, constructing stable three-dimensional networks, and stabilizing clay hydration layers, thus presenting a high-performance viscosifier formulation for high-temperature and high-salinity water-based drilling fluids with important theoretical and engineering application values. Full article

Photocatalytic H₂O₂ synthesis emerges as a promising green substitute for the energy-intensive anthraquinone process, yet its efficiency is limited by rapid charge recombination and limited surface active sites in bulk polymeric semiconductors. Herein, we report a topology-directed strategy to tailor the interlayer interactions of graphitic carbon nitride (g-C₃N₄), yielding ultrathin nanosheets with optimized electronic structures. The resulting catalyst exhibits an exceptional H₂O₂ production rate of 1.34 mmol g⁻¹ h⁻¹ under visible light, surpassing bulk g-C₃N₄ by a factor of 2.48. Water contact angle measurements confirm the superior hydrophilicity of the engineered nanosheets, facilitating interfacial mass transfer, while in situ FTIR and EPR spectroscopies unravel that the abundant exposed active sites optimize the adsorption configuration of the key *OOH intermediate and promote the generation of •O₂⁻ and •OH radicals. Regarding charge transfer dynamics, in situ EPR trapping experiments and Kelvin probe force microscopy (KPFM) reveal that the attenuated interlayer coupling induces a robust internal electric field, effectively suppressing carrier recombination and prolonging the exciton lifetime by a factor of 1.249. This work establishes a quantitative structure–activity relationship between interlayer engineering and exciton dynamics, offering a reliable protocol for the rational design of high-performance molecular photocatalysts. Full article

The exceptional stability of C-F bonds renders PFAS highly persistent in aqueous environments, posing significant challenges for conventional treatment technologies. While plasma-based technologies show promise, their efficiency is often limited by poor gas–liquid mass transfer in bulk liquid. Here, an in-house constructed ultrasonic atomization–dielectric barrier discharge (UEN-DBD) system was developed to promote PFAS degradation under non-thermal plasma conditions. Ultrasonic atomization generated microdroplets, which promoted PFAS enrichment at the surface of microdroplets and facilitate interactions with plasma-generated reactive species. Using perfluorooctanoic acid (PFOA) and perfluorooctanesulfonate (PFOS) as model compounds, degradation behavior was evaluated over an initial concentration range of 0.01–1.0 ppm. At 0.01 ppm, degradation efficiencies of 96.06% for PFOA and 94.86% for PFOS were achieved within 5 min. Electron paramagnetic resonance (EPR) spectroscopy confirmed the formation of oxidative radicals (·OH) and suggested a mixed redox environment involving reactive species, potentially including superoxide (O₂·⁻) or hydrated electrons (e_aq⁻), in the discharge-treated system. High-resolution mass spectrometry results are consistent with a stepwise chain-shortening pathway dominated by successive –CF₂– scission, while fluoride-release measurements provided supporting evidence for partial defluorination. These findings advance the understanding of plasma-assisted PFAS degradation at the gas–liquid interface and provide a basis for the further development of plasma-assisted PFAS treatment strategies. Full article

This study reports the synthesis and evaluation of diclofenac-derived organotin(IV) complexes as photostabilizing additives for poly(vinyl chloride) (PVC). Diclofenac was selected as a ligand due to its aromatic structure and heteroatom-rich framework, enabling the formation of stable tin-based complexes with potential UV-absorbing and radical-scavenging properties. The synthesized di- and tri-organotin complexes were incorporated into PVC films at 0.5 wt.% and exposed to UV irradiation (365 nm) for up to 300 h to assess their stabilizing efficiency. Photodegradation was monitored by tracking changes in carbonyl, polyene, and hydroxyl indices, as well as weight loss and surface deterioration. Compared with blank PVC and ligand-containing films, the organotin-modified samples exhibited significantly slower growth of degradation indices, reduced mass loss, and improved surface integrity after irradiation. Among the evaluated additives, the tributyltin complex demonstrated the highest photostabilizing performance, showing superior retention of chlorine content and lower surface roughness parameters. Overall, the results indicate that diclofenac-based organotin(IV) complexes are effective photostabilizers for PVC, with the tributyltin derivative emerging as the most promising candidate for enhancing the durability of PVC materials under UV exposure. Full article

The purpose of this study is the exploration of the catalytic performance of a ZSM-5 zeolite produced from iron-rich fly ash, without any additional iron loading, in removing paracetamol via a heterogenous Fenton reaction. The structural and textural characterization by powder X-ray diffraction and N₂ adsorption isotherms showed that a pure ZSM-5 phase was synthesized, but lower crystallinity and textural parameters were obtained when compared with commercial ZSM-5. The XPS analysis revealed significant amounts of iron and yttrium, which enhanced the electronic properties of the samples’ surface when compared with iron-impregnated commercial ZSM-5. The catalytic reaction was followed through UV-spectroscopy and kinetic models were applied to the data; the best fit was obtained for a pseudo-first-order model. All fly ash-based zeolites showed increased paracetamol removal when compared with commercial iron-loaded ZSM-5, which may be attributed to the more disordered structure, able to accommodate large paracetamol species (dimers). On the other hand, the effect of yttrium on the electronic properties of iron sites may increase the ^●OH radical formation, thus increasing the paracetamol removal rate, despite the progressive drop on paracetamol removal upon regeneration–reuse cycles due to Fe leaching. Full article

The secondary effluent from printing and dyeing wastewater contains recalcitrant organic pollutants, such as azo dye derivatives. Their persistence in aquatic environments not only creates ecological risks but also hampers the high-value reuse of reclaimed water. This study investigated the influence of typical binary anions on the degradation performance of low-concentration azo dye wastewater using a Ti/RuO₂-IrO₂ anode electrochemical oxidation system. The results demonstrated that maximum COD removal efficiency could reach 50.22%, and the controlling factors synergistically regulated the contribution and competition between Reactive Chlorine Species and free radicals. This led to a characteristic “rapid rise–decline–slow rebound” phenomenon in the COD removal rate, with the inflection points co-influenced by the current density, conductivity, and binary anion ratio of the electrochemical process. Furthermore, it alters the degradation pathway of the azo dye to “azo bond cleavage → demethylation/desulfonation → dehydroxylation/deamination oxidation → benzene ring opening”. Within a fixed duration of 60 min, the Response Surface Methodology model identified the optimal COD degradation conditions as follows: current density of 19.72 mA/cm², Cl⁻/SO₄²⁻ ratio of 5.40, and conductivity of 8.30 mS/cm. This research elucidates the differences between the electrochemical oxidation degradation pathway of low-concentration azo dye wastewater under the regulation of typical binary anions and the conventional pathway. It also reveals the regulatory effects of current density, conductivity, and binary anion ratio on the degradation patterns. Full article

This study evaluated the electrochemical and oxidative performance of titanium-supported RuO₂–SnO₂–Sb₂O₅ mixed metal oxide electrodes (hereafter denoted as RuO₂–SnO₂–Sb₂O₅/Ti) for degrading three aniline-based dyes and their mixture using electro-oxidation (EOx), electro-Fenton (EF), and photoelectron-Fenton (PEF) processes. Electrochemical characterization showed quasi-reversible redox behavior and fast electron-transfer kinetics, while SEM, AFM, and EDS analyses revealed a rough surface with fissures and agglomerates that increased the real electroactive area to 4.85 cm², supporting the high catalytic activity. Spectroscopic analyses confirmed the functional groups typical of azo dyes, and RNO assays verified sustained hydroxyl-radical production during electrolysis. Current density was the main operational factor: at 50 mA cm⁻², decolorization exceeded 90% due to enhanced ^•OH generation, whereas higher initial dye concentrations decreased reaction rates because of surface saturation and diffusion limitations. Among the oxidation processes, EF was most effective for Brown KK and Brown 5VR, EOx performed best for Brown NT, and PEF showed a slight advantage for the dye mixture owing to UV-assisted regeneration of reactive species. COD removal followed similar trends, with Brown KK mineralizing fastest and Brown 5VR showing the highest recalcitrance. Analysis of H₂O₂ and active chlorine indicated that EOx favors the accumulation of chlorine-derived oxidants, whereas PEF maximizes H₂O₂ conversion to ^•OH and reduces chlorinated by-products, positioning PEF as the most efficient and environmentally favorable option for treating chloride-containing wastewater. Full article

Streptococcus sanguinis (S. sanguinis) is an oral commensal and early colonizer of the tooth surface that contributes to dental biofilm homeostasis. Zinc oxide nanoparticles (ZnO NPs) are often incorporated into dental restorative materials to enhance mechanical performance and confer antibacterial properties; however, their effects on S. sanguinis have not been thoroughly studied. Here, we investigated the antimicrobial and antibiofilm efficacy of ZnO NPs against this bacterial species. ZnO NPs exhibited a minimal inhibitory concentration (MIC) of 100 µg/mL and caused rapid, dose-dependent suppression of intracellular ATP levels and overall metabolic activity within 2–4 h of exposure. ZnO NPs induced reactive oxygen species (ROS) production in a dose-dependent manner. The free radical scavenger α-tocopherol partly prevented the antibacterial effect of ZnO NPs, suggesting that lipid peroxidation contributes to ZnO NP-mediated toxicity, although it is not the sole mechanism involved. Short-term exposure (2 h) to ZnO NPs did not significantly affect membrane integrity or cellular morphology, whereas prolonged treatment (24 h) resulted in pronounced membrane permeabilization, membrane hyperpolarization, and cellular swelling. Computational morphometric analyses of high-resolution scanning electron microscopy (HR-SEM) images of planktonic growing bacteria after a 24 h treatment confirmed a significant, dose-dependent increase in cell surface area and surface roughness. Importantly, ZnO NPs also reduced the metabolic activity and compromised the structural integrity of mature, preformed biofilms. Collectively, these findings demonstrate that ZnO NPs exert antimicrobial and antibiofilm effects against S. sanguinis through early metabolic inhibition associated with oxidative stress followed by progressive membrane dysfunction. Full article

The valorization of agro-industrial by-products is a sustainable approach to recovering high-value bioactive compounds. In this study, Opuntia ficus-indica (L.) Mill. seed press residues were investigated as a source of phenolic and flavonoid compounds using microwave-assisted extraction (MAE). A multi-step optimization strategy was implemented, combining preliminary single-factor experiments (OVAT), response surface methodology based on a Box–Behnken design (BBD), and machine learning modeling using K-nearest neighbors coupled with the dragonfly algorithm (KNN_DA), followed by desirability-based validation. The effects of ethanol concentration (50–100%), microwave power (400–800 W), extraction time (2–4 min), and liquid-to-solid ratio (30–50 mL/g) were evaluated on Folin–Ciocalteu reducing capacity (FCRC), AlCl₃ complexation response, and antioxidant activity assessed by DPPH radical scavenging and reducing power assays. Optimal conditions were identified at 50% ethanol, 800 W microwave power, 4 min extraction time, and a liquid-to-solid ratio of 47.28 mL/g. Under these conditions, FCRC reached 376.85 ± 0.23 mg GAE/100 g DW and 49.16 ± 0.33 mg QE/100 g DW for AlCl₃ complexation response, with prediction errors of 2.80% and 0.82%, respectively. The optimized extracts exhibited enhanced antioxidant activity. These findings confirm MAE as a rapid and environmentally friendly technique and highlight the predictive performance of the KNN_DA model for process optimization. Full article

Selenium (Se) enrichment in yeast represents a promising strategy for producing organic Se with high bioavailability. However, a systematic understanding of how Se incorporation alters intact protein structure and function across diverse strains remains lacking. This study investigated four yeast species (Saccharomyces cerevisiae, Kluyveromyces marxianus, Kluyveromyces lactis, and Torulaspora delbrueckii) using multi-spectroscopic and radical scavenging assays. Despite moderate growth inhibition (10.4–27.7%), all strains accumulated substantial Se (1164–2858 µg/g). Structural analysis revealed that Se induced strain-dependent protein conformational perturbations. Specifically, in selenium-enriched Saccharomyces cerevisiae, where Se was predominantly incorporated as selenomethionine (SeMet, 85.80%), a significant structural relaxation occurred. This was characterized by decreased rigid β-sheet content, increased flexible random coils, and a substantial enhancement in surface hydrophobicity. Crucially, Pearson correlation analysis revealed that functional enhancements were synergistically governed by specific Se speciation and secondary structural remodeling. Enhanced DPPH^• scavenging activity was positively correlated with changes in β-sheet and random coil structures. Selenomethionine content was also significantly correlated with increased scavenging of ^•OH and ABTS^•+. Consequently, Saccharomyces cerevisiae uniquely achieved highly significant (p < 0.001) antioxidant improvements, whereas other strains showed moderate or non-significant responses despite high Se yields. Our findings demonstrate that the antioxidant efficacy of selenoproteins is not solely determined by total Se content but is fundamentally driven by the targeted bioconversion of SeMet and its associated structural relaxation. Full article

A synergistic and magnetically recoverable NiFe₂O₄–MWCNT–CA nanocomposite was developed for efficient UV-driven photodegradation of hazardous organic pollutants. Biogenic NiFe₂O₄ nanoparticles synthesized using Costus speciosus extract exhibited a crystallite size of 32.5 nm, which increased to 83.6 nm upon incorporation into the MWCNT–cellulose acetate matrix. XRD confirmed the preservation of the cubic spinel structure, while VSM analysis showed maintained ferrimagnetic behavior with a saturation magnetization of 9.64 emu/g, enabling rapid magnetic separation. Although BET analysis revealed a reduction in surface area from 112.46 to 30.99 m²/g due to hybridization, the conductive MWCNT network significantly enhanced charge separation and interfacial electron transport. The composite displayed a widened optical bandgap of 5.3 eV, necessitating UV excitation for photocatalytic activity. Under UV irradiation, it achieved rapid degradation of methylene blue (97%) and Congo red (91%) at 20 mg/L, with corresponding rate constants of 0.119 and 0.076 min⁻¹. Scavenger experiments confirmed hydroxyl radicals (•OH) as the dominant reactive species, followed by photogenerated holes (h⁺). These results demonstrate a robust and synergistically engineered photocatalyst with high efficiency in removing organic pollutants under UV illumination. Full article