Search Results (252)

Common bean (Phaseolus vulgaris L.) is a critical protein-rich legume supporting food and nutritional security globally. However, Fusarium wilt, caused by Fusarium solani, remains a major constraint to production, with yield losses reaching up to 84%. While biocontrol strategies have been explored, most microbial agents are sourced from mesophilic environments and show limited effectiveness under abiotic stress. Here, we report the isolation and characterization of extremophilic Bacillus spp. from the hypersaline Lake Bogoria, Kenya, and their biocontrol potential against F. solani. From 30 isolates obtained via serial dilution, 9 exhibited antagonistic activity in vitro, with mycelial inhibition ranging from 1.07–1.93 cm 16S rRNA sequencing revealed taxonomic diversity within the Bacillus genus, including unique extremotolerant strains. Molecular screening identified genes associated with the biosynthesis of antifungal metabolites such as 2,4-diacetylphloroglucinol, pyrrolnitrin, and hydrogen cyanide. Enzyme assays confirmed substantial production of chitinase (1.33–3160 U/mL) and chitosanase (10.62–28.33 mm), supporting a cell wall-targeted antagonism mechanism. In planta assays with the lead isolate (B7) significantly reduced disease incidence (8–35%) and wilt severity (1–5 affected plants), while enhancing root colonization under pathogen pressure. These findings demonstrate that extremophile-derived Bacillus spp. possess robust antifungal traits and highlight their potential as climate-resilient biocontrol agents for sustainable bean production in arid and semi-arid agroecosystems. Full article

Hydrogen is a potential key component of a carbon-neutral energy carrier and an input to marine industrial processes. This study examines the consequences of coupled hydrogen release and marine environmental factors during floating photovoltaic hydrogen production (FPHP) system failures. A validated three-dimensional numerical model of FPHP comprehensively characterizes hydrogen leakage dynamics under varied rupture diameters (25, 50, 100 mm), transient release duration, dispersion patterns, and wind intensity effects (0–20 m/s sea-level velocities) on hydrogen–air vapor clouds. FLACS-generated data establish the concentration–dispersion distance relationship, with numerical validation confirming predictive accuracy for hydrogen storage tank failures. The results indicate that the wind velocity and rupture size significantly influence the explosion risk; 100 mm ruptures elevate the explosion risk, producing vapor clouds that are 40–65% larger than 25 mm and 50 mm cases. Meanwhile, increased wind velocities (>10 m/s) accelerate hydrogen dilution, reducing the high-concentration cloud volume by 70–84%. Hydrogen jet orientation governs the spatial overpressure distribution in unconfined spaces, leading to considerable shockwave consequence variability. Photovoltaic modules and inverters of FPHP demonstrate maximum vulnerability to overpressure effects; these key findings can be used in the design of offshore platform safety. This study reveals fundamental accident characteristics for FPHP reliability assessment and provides critical insights for safety reinforcement strategies in maritime hydrogen applications. Full article

The conventional spent lithium-ion batteries (LIBs) recycling method suffers from complex processes and excessive chemical consumption. Hence, this study proposes an electrochemical strategy for achieving reductant-free leaching of high-valence transition metals and efficient separation of valuable components from spent cathode sheets (CSs). An innovatively designed sandwich-structured electrochemical reactor achieved efficient reductive dissolution of cathode materials (CMs) while maintaining the structural integrity of aluminum (Al) foils in a dilute sulfuric acid system. Optimized current enabled leaching efficiencies exceeding 93% for lithium (Li), cobalt (Co), manganese (Mn), and nickel (Ni), with 88% metallic Al foil recovery via cathodic protection. Multi-scale characterization systematically elucidated metal valence evolution and interfacial reaction mechanisms, validating the technology’s tripartite innovation: simultaneous high metal extraction efficiency, high value-added Al foil recovery, and organic removal through single-step electrochemical treatment. The process synergized the dissolution of CM particles and hydrogen bubble-induced physical liberation to achieve clean separation of polyvinylidene difluoride (PVDF) and carbon black (CB) layers from Al foil substrates. This method eliminates crushing pretreatment, high-temperature reduction, and any other reductant consumption, establishing an environmentally friendly and efficient method of comprehensive recycling of battery materials. Full article

This paper proposes a mathematical description of nitriding atmospheres obtained from a one-component ammonia ingoing atmosphere and a two-component ammonia inlet nitrogen-diluted atmosphere. The Fe-N phase equilibrium diagrams of the nitriding atmosphere in the hydrogen content-temperature (Q-T) system for selected NH₃/N₂ atmosphere compositions are presented. The nitriding atmosphere obtained with different degrees of nitrogen dilution of the ingoing atmosphere was characterized. It has been shown that in processes carried out in nitriding atmospheres obtained from a two-component atmosphere with nitrogen, there is no direct relationship between the value of the nitrogen potential and the degree of dilution of the ingoing atmosphere with nitrogen. It has been shown analytically and confirmed experimentally that with changes in the degree of dilution of ammonia with nitrogen, the hydrogen content of the nitriding atmosphere and, consequently, the nitrogen availability of the nitriding atmosphere change. Using the example of nitriding AISI 52100 steel, it has been experimentally demonstrated that the change in nitrogen availability, caused by a change in the degree of dilution of the ingoing atmosphere with nitrogen, is not accompanied by a change in the value of the nitrogen potential. It has also been shown that the change in the nitrogen availability of the nitriding atmosphere, induced by the change in the composition of the aNH₃/bN₂ ingoing atmosphere, affects the kinetics of nitrogen mass gain in the nitrided layer and the distribution of nitrogen mass between the iron nitride layer and the solution zone. It has also been shown that with the change in nitrogen availability, what changes in addition to the thickness of the iron nitride layer is also the phase composition of the layer. Using gravimetric tests, the mass of nitrogen in the iron nitride layer and the solution zone has been determined. To describe the equilibrium between the NH₃/H₂ atmosphere and nitrogen in the different iron phases, a modified Lehrer diagram in the coordinate system of temperature and hydrogen content in the nitriding atmospheres (T-Q) has been proposed. Full article

Arginine plays a critical role in biomolecular interactions due to its guanidinium side chain, which enables multivalent electrostatic and hydrogen bonding contacts. In this study, atomistic molecular dynamics simulations were conducted across a broad concentration range (26–605 mM) to investigate the thermodynamic and structural features of arginine self-assembly in aqueous solution. Key observables—including hydrogen bond count, radius of gyration, contact number, and isobaric heat capacity—were analyzed to characterize emergent behavior. A three-regime aggregation pattern (dilute, cooperative, and saturated) was identified and quantitatively modeled using the Hill equation, revealing a non-linear transition in clustering behavior. Spatial analyses were supplemented with trajectory-based clustering and radial distribution functions. The heat capacity peak observed near 360 mM was interpreted as a thermodynamic signature of hydration rearrangement. Trajectory analyses utilized both GROMACS tools and the MDAnalysis library. While force field limitations and single-replica sampling are acknowledged, the results offer mechanistic insight into how arginine concentration modulates molecular organization—informing the understanding of biomolecular condensates, protein–nucleic acid complexes, and the design of functional supramolecular systems. The findings are in strong agreement with experimental observations from small-angle X-ray scattering and differential scanning calorimetry. Overall, this work establishes a cohesive framework for understanding amino acid condensation and reveals arginine’s concentration-dependent behavior as a model for weak, reversible molecular association. Full article

Natural deep eutectic solvents (NaDESs) are emerging solvents for their yield when used for extraction of different molecules, including polyphenols. NaDESs are a cutting-edge technology that offers numerous advantages, including cheap cost, safety, effectiveness and environmental friendliness. However, due to NaDES’ high boiling point, the recovery and separation of compounds after the extraction is the bottleneck of the process. In this work, two affordable methods were tested for the recovery of phenolic compounds from three binary NaDESs (composed of choline chloride mixed separately with lactic acid, tartaric acid or glycerol as hydrogen bond donors): the antisolvent and the liquid–liquid extraction methods. The former was assessed by diluting the extracts with different aliquots of water, employed as antisolvent, which was ineffective. For the liquid–liquid extraction method, ethyl acetate (EtOAc), acetonitrile (ACN), 2-chlorobutane (2-CB) and 2-methyltetrahydrofuran (2-MeTHF) were compared. Except for ACN, all solvents were perfectly immiscible with the three NaDESs, forming biphasic systems that were analyzed by colorimetric assays and HPLC/MS. 2-MeTHF applied on a 10-fold water dilution of the NaDES extract reached recovery percentages higher than 90% for most of the non-anthocyanin phenols and good recovery (up to 80%) for some anthocyanins. 2-MeTHF appears to be the first known solvent capable of extracting anthocyanins from NaDESs. Finally, a two-step liquid–liquid extraction performed firstly with EtOAc and subsequently with 2-MeTHF is proposed for the separation of different phenolic fractions. Full article

Biomass fluidized bed gasification technology has attracted significant attention due to its high efficiency and clean energy conversion capabilities. However, its industrial application has been limited by insufficient technological maturity. This paper systematically reviews the research progress on biomass fluidized bed gasification characteristics; compares the applicability of bubbling fluidized beds (BFBs), circulating fluidized beds (CFBs), and dual fluidized beds (DFBs); and highlights the comprehensive advantages of CFBs in large-scale production and tar control. The gas–solid flow characteristics within CFB reactors are highly complex, with factors such as fluidization velocity, gas–solid mixing homogeneity, gas residence time, and particle size distribution directly affecting syngas composition. However, experimental studies have predominantly focused on small-scale setups, failing to characterize the impact of flow dynamics on gasification reactions. Therefore, numerical simulation has become essential for in-depth exploration. Additionally, this study analyzes the influence of different gasification agents (air, oxygen-enriched, oxygen–steam, etc.) on syngas quality. The results demonstrate that oxygen–steam gasification eliminates nitrogen dilution, optimizes reaction kinetics, and significantly enhances syngas quality and hydrogen yield, providing favorable conditions for downstream processes such as green methanol synthesis. Based on the current research landscape, this paper employs numerical simulation to investigate oxygen–steam CFB gasification at a pilot scale (500 kg/h biomass throughput). The results reveal that under conditions of O₂/H₂O = 0.25 and 800 °C, the syngas H₂ volume fraction reaches 43.7%, with a carbon conversion rate exceeding 90%. These findings provide theoretical support for the industrial application of oxygen–steam CFB gasification technology. Full article

Olive mill wastewater (OMW) represents a toxic waste generated during olive oil production (30 million m³/year). Its phytotoxicity and resistance to biodegradation are mainly due to the presence of polyphenols. Methodologies able to remove these organic compounds from this waste to allow the safe dispose of OMW have been developed, and among them, the most effective are oxidation procedures. In this context, we propose an alternative chemical treatment based on the oxidation of OMW using diluted hydrogen peroxide and seleno-organic compounds (diphenyl diselenide and diseleno-bis-benzoic acid) selected as eco-friendly bioinspired catalysts. The effectiveness of the protocol was monitored by Folin–Ciocalteu (F-C) quantification and NMR quantification. The results demonstrated that the greatest reduction in the total phenols content—up to 96%—was achieved using the highest concentrations of catalyst (0.6% _w/w) and oxidant (10% _v/v). Moreover, a toxicological evaluation was carried out using the marine bacteria Aliivibrio fischeri, revealing a significant decrease in toxicity. The EC₅₀ value increased from 0.089 mg/L in the untreated OMW to 18.740 mg/L in the treated sample after removal of the residual catalyst and peroxides. Full article

This study utilizes a zero-dimensional, constant-pressure, perfectly stirred reactor (PSR) model within the Cantera framework to examine the combustion characteristics of hydrogen, methane, methanol, and propane, both singly and in hydrogen-enriched mixtures. The impact of the equivalence ratio (ϕ = 0.75, 1.0, 1.5), fuel composition, and residence duration on temperature increase, heat release, ignition delay, and emissions (NO_x and CO₂) is methodically assessed. The simulations are performed under steady-state settings to emulate the ignition and flame propagation processes within pre-chambers and primary combustion zones of internal combustion engines. The results demonstrate that hydrogen significantly improves combustion reactivity, decreasing ignition delay and increasing peak flame temperature, especially at short residence times. The incorporation of hydrogen into hydrocarbon fuels, such as methane and methanol, enhances ignition speed, improves thermal efficiency, and stabilizes lean combustion. Nevertheless, elevated hydrogen concentrations result in increased NO_x emissions, particularly at stoichiometric equivalence ratios, due to higher flame temperatures. The examination of fuel mixtures at varying hydrogen concentrations (10–50% by mole) indicates that thermal performance is optimal under stoichiometric settings and diminishes in both fuel-lean and fuel-rich environments. A thermodynamic model was created utilizing classical combustion theory to validate the heat release estimates based on Cantera. The model computes the heat release per unit volume (MJ/m³) by utilizing stoichiometric oxygen demand, nitrogen dilution, fuel mole fraction, and higher heating values (HHVs). The thermodynamic estimates—3.61 MJ/m³ for H₂–CH₃OH, 3.43 MJ/m³ for H₂–CH₄, and 3.35 MJ/m³ for H₂–C₃H₈—exhibit strong concordance with the Cantera results (2.82–3.02 MJ), thereby validating the physical consistency of the numerical methodology. This comparison substantiates the Cantera model for the precise simulation of hydrogen-blended combustion, endorsing its use in the design and development of advanced low-emission engines. Full article

This study investigates the potential of sugar beet pulp (SBP), a lignocellulosic by-product of sugar production, as a low-cost substrate for biohydrogen and biomass generation using Escherichia coli under dark fermentation conditions. Two strains—BW25113 wild-type and a genetically engineered septuple mutant—were employed. SBP was pretreated via thermochemical hydrolysis, and the effects of substrate concentration, dilution, and glycerol supplementation were evaluated. Hydrogen production was highly dependent on substrate dilution and nutrient balance. The septuple mutant achieved the highest H₂ yield in 30 g L⁻¹ SBP hydrolysate (0.75% sulfuric acid) at 5× dilution with glycerol, reaching 12.06 mmol H₂ (g sugar)⁻¹ and 0.28 mmol H₂ (g waste)⁻¹, while the wild type under the same conditions yielded 3.78 mmol H₂ (g sugar)⁻¹ and 0.25 mmol H₂ (g waste)⁻¹. In contrast, undiluted hydrolysates favored biomass accumulation over H₂ production, with the highest biomass yield (0.3 g CDW L⁻¹) obtained using the septuple mutant in 30 g L⁻¹ SBP hydrolysate without glycerol. These findings highlight the potential of genetically optimized E. coli and optimized hydrolysate conditions to enhance the valorization of agro-industrial waste, supporting future advances in sustainable hydrogen bioeconomy and integrated waste biorefineries. Full article

Rapid and cost-effective measurements of the autofluorescence of wine can provide valuable information on the brand, origin, age, and composition of wine and may be helpful for the authentication of wine and detection of forgery. The list of fluorescent components of wines includes flavonoids, phenolic acids, stilbenes, some vitamins, aromatic amino acids, NADH, and Maillard reaction products. Distinguishing between various fluorophores is not simple, and chemometrics are usually employed to analyze the fluorescence spectra of wines. Front-face fluorescence is especially useful in the analysis of wine, obviating the need for sample dilution. Front-face measurements are possible using most plate readers, so they are commonly available. Additionally, the use of fluorescent probes allows for the detection and quantification of specific wine components, such as resveratrol, oxygen, total iron, copper, hydrogen sulfite, and haze-forming proteins. Fluorescence measurements can thus be useful for at least a preliminary rapid evaluation of wine properties. Full article

In this paper, the thermodynamic properties of terpene mixtures were investigated because they represent a promising group of compounds, usually extracted from biomass, with their most notable application as fuel performance enhancers. The densities, viscosities, refractive indices, and ultrasonic speeds of sound were measured for three binary mixtures, citral + chloroform, limonene + chloroform, and linalool + chloroform, across the full composition range at temperatures between 288.15 K and 323.15 K under atmospheric pressure. Using experimental data, excess molar volumes, viscosity deviations, refractive index deviations, and isentropic compressibility, deviations were calculated. Additionally, properties such as partial molar volumes, excess partial molar volumes, partial molar volumes at infinite dilution, and apparent molar volumes were derived. The excess and deviation properties were analyzed using the Redlich–Kister equation. A single mathematical model, the Heric–Brewer–Jouyban–Acree model, was used to represent densities, viscosities, refractive indices, and ultrasonic speeds of sound. The results obtained in this work suggest that dispersive interactions dominate in the limonene and linalool binary mixtures, while hydrogen bonding plays a significant role in the citral + chloroform system. In summary, dispersive interactions are dominant in nonpolar systems like limonene and linalool, while hydrogen bonding significantly affects the citral-chloroform mixture, where the polar groups in citral interact with chloroform molecules. These differences in intermolecular forces help explain the distinct behavior of each mixture. The modeling outcomes demonstrated that the Heric–Brewer–Jouyban–Acree model accurately correlated the experimental thermodynamic properties, with average percent deviations below 1% for all three systems. Full article

The venting process is one of the most important events during the thermal runaway (TR) of lithium-ion batteries (LIBs) in determining fire accidents, while different ambient pressures will exert an influence on the venting events as well as the TR. Ternary nickel–cobalt–manganese (NCM) batteries with a 75% state of charge (SOC) were employed to conduct TR tests under different ambient pressures in a sealed chamber with dilute oxygen. It was found that elevated ambient pressure results in milder ejections in terms of jet temperature and mass loss. Gas venting characteristics were also obtained. Additionally, the amount of carbon dioxide (CO₂), hydrogen (H₂), methane (CH₄), and ethylene (C₂H₄) released increase with ambient pressure, while carbon monoxide (CO) varies inversely with ambient pressure. The higher the ambient pressure is, the greater the flammability risk is. The molar amount of C, H, O, and total gases released shows a positive correlation with the maximum battery temperature and ambient pressure. This study will support the design of safety valves and help reveal the effects of venting events on the evolution of TR. Full article

Rapid and precise detection of hydrogen sulfide (H₂S) at trace levels is critical for industrial safety and environmental air quality monitoring, yet existing methods often struggle with cost, speed, or sensitivity. A cost-effective cavity ring-down spectroscopy (CRDS) analyzer is presented, incorporating a novel digital locking circuit for sequential laser-cavity mode matching. This system demonstrates rapid and precise hydrogen sulfide (H₂S) detection capability at parts-per-billion (ppb) concentration levels. Compared to traditional wavelength meters, our system delivers a 140-fold improvement in frequency interval precision (0.07 MHz, 0.027% relative uncertainty). Allan variance analysis under vacuum conditions demonstrates a sensitivity limit of 3 × 10⁻¹² cm⁻¹ at a 60-s averaging time. Validated through calibrated gas dilution tests, the analyzer detects a 4 ppb H₂S absorption signal with a signal-to-noise ratio (SNR) > 6, establishing a 2 ppb detection limit (3σ criterion). This innovative approach meets stringent industrial and environmental requirements, offering a significant advancement in trace gas-sensing technology. Full article

This study aims to develop a novel use of baker’s yeast in biosorption as a sustainable metal recovery process for cost-effective and practical applications in recovering copper and zinc from waste gravity-thickened sludge generated at livestock wastewater treatment facilities. The supernatant of the acid-extracted product was separated from the residues through centrifugation. To ensure cost efficiency, the supernatant was treated with 2N acetic acid for 24 h, with the addition of hydrogen peroxide, and used for the biosorption experiments. The filtrated supernatant was adjusted to various pH values (4.5, 5.0, and 5.5) to explore the effects of acidity on the subsequent biosorption of extracted zinc and copper by baker’s yeast. A diluted molasses solution was added to the filtrate as a carbon source to support yeast growth during the 4 h biosorption experiments. The results revealed that the removal efficiency of zinc from the filtrate by baker’s yeast was 97.3%, while the removal efficiency for copper was about 48.8% at pH 5.5 with a reaction time of 4 h. In summary, this combined approach is expected to reduce and recycle heavy metals in livestock sludge. Acetic acid with hydrogen peroxide can extract copper and zinc from the sludge, and baker’s yeast can absorb both metals from the filtrate at pH 5.5 in a 4 h reaction time. This technological innovation has the potential to transform waste management practices in the livestock industry, contributing to resource recovery and environmental sustainability. Full article