Search Results (60)

Plasma-assisted nitrogen fixation is emerging as a promising alternative to the dominant industrial method of the Haber–Bosch (H–B) process, which is energy-intensive and environmentally detrimental. Nonthermal plasma technology represents a cutting-edge innovation with the potential to revolutionize nitrogen fertilizer (N-fertilizer) production, offering a more sustainable approach by operating under mild conditions, making it suitable for decentralized N-fertilizer production. Toward the goal, in this study, we demonstrate our development and test of a novel nonthermal plasma system for continuous on-site production of N-fertilizer. This technology results in a product of aqueous N-fertilizer on-site, from only air, water, and electricity without carbon emissions, directly applicable to plants, bypassing costly and hazardous multiple steps in the production and transportation of the industrial N-fertilizers. Full article

The object of this research is the process of water disinfection by means of high-frequency electrical discharge. The study addresses the problem of achieving high biological efficiency while reducing energy consumption and avoiding harmful by-products typical of traditional methods such as chlorination or UV irradiation. As a result, a comprehensive theoretical and experimental investigation was conducted, demonstrating that within 20 s of plasma exposure, E. coli, S. aureus, and P. aeruginosa bacteria were inactivated by 99.2–99.9%. The observed efficiency is explained by the synergistic action of reactive oxygen and nitrogen species (•OH, O₃, H₂O₂, NO₂⁻, NO₃⁻) formed in the plasma–water interface. The distinctive features of the obtained results include the establishment of optimal operating parameters-voltage U = 12–18 kV, frequency f ≈ 35 kHz, and gap distance d = 15 mm—under which the normalized specific energy input (SEI) was 6–9 kWh per cubic meter of water. This value represents the standard normalization used for plasma-based treatment systems, where the electrical energy delivered to the reactor is divided by the treated volume (1.0 L in our setup) and scaled to m³ for comparison with other studies, 30–40% lower than in previously reported plasma systems. The validated physicochemical model (Poisson, Navier–Stokes, and continuity equations) matched experimental data with R² ≥ 0.95, confirming its predictive capability for further scale-up. The practical significance of the results lies in the potential application of this method for decentralized and industrial water treatment systems. The reagent-free, energy-efficient, and environmentally safe nature of the proposed approach makes it suitable for sustainable water purification under real operating conditions. Full article

The Lower Cambrian Niutitang Formation was deposited precisely during the Cambrian Explosion period, a short-lived interval marked by drastic shifts in oceanic chemistry and climate. This stratigraphic sequence preserves a comprehensive record of early-ocean evolution and constitutes a world-class reservoir for rare and precious metals, widely termed the “poly-metallic enrichment layer”. Despite its metallogenic prominence, the genetic model for metal enrichment in the Niutitang Formation remains contentious. In this study, we employed inductively coupled plasma mass spectrometry (ICP-MS), carbon and sulfur analyzer, and X-ray fluorescence spectrometry (XRF) to quantify trace-metal abundances, redox-sensitive element distribution patterns, rare-earth element signatures, and total organic carbon contents. Results reveal that metal enrichment in the Niutitang Formation was governed by temporally distinct mechanisms. Member I records extreme enrichment in As, Ag, V, Re, Ba, Cr, Cs, Ga, Ge, Se and In. This anomaly was driven by the Great Oxidation Event and intensified upwelling that oxidized surface waters, elevated primary productivity and delivered abundant organic matter. Subsequent microbial sulfate reduction generated high H₂S concentrations, converting the water column to euxinic conditions. Basin restriction imposed persistent anoxia in bottom waters, establishing a pronounced redox stratification. Concurrent vigorous hydrothermal activity injected large metal fluxes, leading to efficient scavenging of the above metals at the sulfidic–anoxic interface. In Members II and III, basin restriction waned, permitting enhanced water-mass exchange and a concomitant shift from euxinic to anoxic–suboxic conditions. Hydrothermal metal fluxes declined, yet elevated organic-matter fluxes continued to sequester Ag, Mo, Ni, Sb, Re, Th, Ga, and Tl via carboxyl- and thiol-complexation. Thus, “organic ligand shuttling” superseded “sulfide precipitation” as the dominant enrichment mechanism. Collectively, the polymetallic enrichment in the Niutitang Formation reflects a hybrid model controlled by seawater redox gradients, episodic hydrothermal metal supply, and organic-complexation processes. Consequently, metal enrichment in Member I was primarily governed by the interplay between vigorous hydrothermal flux and a persistently sulfidic water column, whereas enrichment in Members II and III was dominated by organic-ligand complexation and fluctuations in the marine redox interface. This study clarifies the stage-dependent metal enrichment model of the Niutitang Formation and provides a theoretical basis for accurate prediction and efficient exploration of polymetallic resources in the region. Full article

An oat protein isolate is an ideal raw material for producing a wide range of plant-based products. However, oat protein exhibits weak functional properties, particularly in emulsification. Casein-based ingredients are commonly employed to enhance emulsifying properties as a general practice in the food industry. pH-shifting processing is a straightforward method to partially unfold protein structures. This study modified a mixture of an oat protein isolate (OPI) and casein by combining a pH adjustment (adjusting the pH of two solutions to 12, mixing them at a 3:7 ratio, and maintaining the pH at 12 for 2 h) with an atmospheric cold plasma (ACP) treatment to improve the emulsifying properties. The results demonstrated that the ACP treatment significantly enhanced the solubility of the OPI/casein mixtures, with a maximum solubility of 82.63 ± 0.33%, while the ζ-potential values were approximately −40 mV, indicating that all the samples were fairly stable. The plasma-induced increase in surface hydrophobicity supported greater protein adsorption and redistribution at the oil/water interface. After 3 min of treatment, the interfacial pressure peaked at 8.32 mN/m. Emulsions stabilized with the modified OPI/casein mixtures also exhibited a significant droplet size reduction upon extending the ACP treatment to 3 min, decreasing from 5.364 ± 0.034 μm to 3.075 ± 0.016 μm. The resulting enhanced uniformity in droplet size distribution signified the formation of a robust interfacial film. Moreover, the ACP treatment effectively enhanced the emulsifying activity of the OPI/casein mixtures, reaching (179.65 ± 1.96 m²/g). These findings highlight the potential application value of OPI/casein mixtures in liquid dairy products. In addition, dairy products based on oat protein are more conducive to sustainable development than traditional dairy products. Full article

With the rapid progression of global industrialization and urbanization, emerging contaminants (ECs) have become pervasive in environmental media, posing considerable risks to ecosystems and human health. While multidisciplinary evidence continues to accumulate regarding their environmental persistence and bioaccumulative hazards, critical knowledge gaps persist in understanding their spatiotemporal distribution, cross-media migration mechanisms, and cascading ecotoxicological consequences. This review systematically investigates the global distribution patterns of ECs in aquatic environments over the past five years and evaluates their potential ecological risks. Furthermore, it examines the performance of various treatment technologies, focusing on economic cost, efficiency, and environmental sustainability. Methodologically aligned with PRISMA 2020 guidelines, this study implements dual independent screening protocols, stringent inclusion–exclusion criteria (n = 327 studies). Key findings reveal the following: (1) Occurrences of ECs show geographical clustering in highly industrialized river basins, particularly in Asia (37.05%), Europe (24.31%), and North America (14.01%), where agricultural pharmaceuticals and fluorinated compounds contribute disproportionately to environmental loading. (2) Complex transboundary pollutant transport through atmospheric deposition and oceanic currents, coupled with compound-specific partitioning behaviors across water–sediment–air interfaces. (3) Emerging hybrid treatment systems (e.g., catalytic membrane bioreactors, plasma-assisted advanced oxidation) achieve > 90% removal for recalcitrant ECs, though requiring 15–40% cost reductions for scalable implementation. This work provides actionable insights for developing adaptive regulatory frameworks and advancing green chemistry principles in environmental engineering practice. Full article

This comprehensive review systematically explores the molecular design and functional applications of nano-smooth hydrophilic ionic polymer surfaces. Beginning with advanced fabrication strategies—including plasma treatment, surface grafting, and layer-by-layer assembly—we critically evaluate their efficacy in eliminating surface irregularities and tailoring wettability. Central to this discussion are the types of ionic groups, molecular configurations, and counterion hydration effects, which collectively govern macroscopic hydrophilicity through electrostatic interactions, hydrogen bonding, and molecular reorganization. By bridging molecular-level insights with application-driven design, we highlight breakthroughs in oil–water separation, anti-fogging, anti-icing, and anti-waxing technologies, where precise control over ionic group density, the hydration layer’s stability, and the degree of perfection enable exceptional performance. Case studies demonstrate how zwitterionic architectures, pH-responsive coatings, and biomimetic interfaces address real-world challenges in industrial and biomedical settings. In conclusion, we synthesize the molecular mechanisms governing hydrophilic ionic surfaces and identify key research directions to address future material challenges. This review bridges critical gaps in the current understanding of molecular-level determinants of wettability while providing actionable design principles for engineered hydrophilic surfaces. Full article

Considering the poor conductivity of Fe₂O₃ and the weak oxygen evolution reaction associated with it, surface hole accumulation leads to electron hole pair recombination, which inhibits the photoelectrochemical (PEC) performance of the Fe₂O₃ photoanode. Therefore, the key to improving the PEC water oxidation performance of the Fe₂O₃ photoanode is to take measures to improve the conductivity of Fe₂O₃ and accelerate the reaction kinetics of surface oxidation. In this work, the PEC performances of Fe₂O₃ photoanodes are synergistically improved by combining loaded an FeOOH cocatalyst and oxygen vacancy doping. Firstly, amorphous FeOOH layers are successfully prepared on Fe₂O₃ nanostructures through simple photoassisted electrodepositon. Then oxygen vacancies are introduced into FeOOH-Fe₂O₃ through plasma vacuum treatment, which reduces the content of Fe-O (O_L) and Fe-OH (-OH), jointly promoting the generation of oxygen vacancies. Oxygen vacancy can increase the concentration of most carriers in Fe₂O₃ and form photo-induced charge traps, promoting the separation of electron holes and enhancing the conductivity of Fe₂O₃. The other parts of -OH act as oxygen evolution catalysts to reduce the reaction obstacle of water oxidation and promote the transfer of holes to the electrode/electrolyte interface. The performance of FeOOH-Fe₂O₃ after plasma vacuum treatment has been greatly improved, and the photocurrent density is about 1.9 times higher than that of the Fe₂O₃ photoanode. The improvement in the water oxidation performance of PEC is considered to be the synergistic effect of the cocatalyst and oxygen vacancy. All outstanding PEC response characteristics show that the modification of the cocatalyst and oxygen vacancy doping represent a favorable strategy for synergistically improving Fe₂O₃ photoanode performance. Full article

Catalyzing hydrogen evolution reaction (HER) is a key process in high-efficiency proton exchange membrane water electrolysis (PEMWE) devices. To replace the use of Pt-based HER catalyst, tungsten carbide (W₂C) is one of the most promising non-noble-metal-based catalysts with low cost, replicable catalytic performance, and durability. However, the preparation access to scalable production of W₂C catalysts is inevitable. Herein, we introduced a facile protocol to achieve the tungsten carbide species by plasma treatment under a CH₄ atmosphere from the WO₃ precursor. Moreover, the heterogeneous structure of the tungsten carbide/tungsten oxide nanosheets further enhances the catalytic activity for HER with the enlarged specific surface area and the synergism on the interfaces. The prepared tungsten carbide/tungsten oxide heterostructure nanosheets (WO_3-x-850-P) exhibit exceptional HER catalytic activity and stable longevity in acid electrolytes. This work provides a facile and effective method to construct high-performance and non-precious-metal-based electrocatalysts for industrial-scale water electrolysis. Full article

The membrane dipole potential that arises from the interfacial water and constitutive dipolar groups of lipid molecules modulates the interaction of amphiphiles and proteins with membranes. Consequently, its determination for lipid mixtures resembling the existing diversity in biological membranes is very relevant. In this work, the dipole potentials of monolayers, formed at the air–water interface, from pure or mixed lipids (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (POPE), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidyserine (POPS), sphingomyelin (SpM) and cholesterol) were measured and correlated with the mean area per lipid. The results showed that, as previously observed, cholesterol increases the dipole potential in correspondence with the decrease in the average area per lipid. At the small mole fractions encountered in biomembranes, the presence of the negatively charged lipid POPS increases the dipole potentials of monolayers despite inducing an increase in the average area per lipid. Additionally, the inclusion of POPE in POPC:cholesterol monolayers disrupts the area condensation induced by cholesterol while increasing the membrane dipole moment, leading to a small reduction in the dipole potential. This trend is reinforced for the quaternary POPC:cholesterol:POPE:POPS 4:3:2:1 system, which mimics the inner leaflets of eukaryotic plasma membranes. In agreement with previous works, the replacement of phosphocholine lipids with sphingomyelin leads to a decrease in the dipole potential. Together, this results in a lower dipole potential for the SpM-enriched outer leaflet, generating a non-zero transbilayer dipole potential in the asymmetric plasma membranes of eukaryotic cells. Full article

A cold atmospheric-pressure He-plasma jet (CAPPJ) interacts with air and water, producing reactive oxygen and nitrogen species (RONS), including biologically active ions, radicals, and molecules such as NO_x, H₂O₂, HNO₃, HNO₂, and O₃. These compounds can activate interfacial redox processes in biological tissues. The CAPPJ can oxidize N₂ to HNO₃ and water to H₂O₂ at the interface between plasma and water. It can also induce the oxidation of water-soluble redox compounds in various organisms and in vitro. This includes salicylic acid, hydroquinone, and mixtures of antioxidants such as L (+)-ascorbic acid sodium salt with NADPH. It can react with redox indicators, such as ferroin, in a three-phase system consisting of air, CAPPJ, and water. Without reducing agents in the water, the CAPPJ will oxidize the water and decrease the pH of the solution. When antioxidants such as ascorbate, 1,4-hydroquinone, or NADPH are present in the aqueous phase, the CAPPJ oxidizes these substances first and then oxidizes water to H₂O₂. The multielectron mechanisms of the redox reactions in the plasma-air/water interfacial area are discussed and analyzed. Full article

The article investigates the potential for producing hydrogen by combining the methods of water splitting under cavitation and the chemical activation of aluminum in a high-speed cavitation–jet flow generated by a specialized hydrodynamic reactor. The process of cavitation and water spraying causes the liquid heating itself until it reaches saturated vapor pressure, resulting in the creation of vapor–gaseous products from the splitting of water molecules. The producing of vapor–gaseous products can be explained through the theory of non-equilibrium low-temperature plasma formation within a high-speed cavitation–jet flow of fluid. Special focus is also given to the interactions occurring at the interface boundary phase of aluminum and liquid under cavitation condition. The primary solid products formed on aluminum surfaces are bayerite, copper oxides (I and II), iron carbide, and a compound of magnesium oxides and aluminum hydroxide. A high hydrogen yield of 60% was achieved when using a 0.1% sodium hydroxide solution as a working liquid compared to demineralized water. Moreover, hydrogen methane was also detected in the volume of the vapor–gas mixture, which could be utilized to address the challenges of decarbonization and the recycling of aluminum-containing solid industrial and domestic waste. This work provides a contribution to the study of the mechanism of hydrogen generation by cavitation–jet processing of water and aqueous alkali solutions, in which conditions are created for double cavitation in the cavitation–jet chamber of the hydrodynamic reactor. Full article

Plasma from electric discharges can be used in the abatement of volatile organic compounds (VOCs). The application of gas-phase pulsed corona discharge (PCD) in air–water mixtures provides favorable conditions for the oxidation of VOCs at unsurpassed energy efficiency. This research investigates the impact of water sprinkling on PCD performance in the oxidation of m-xylene as a model compound. Experimental research into the plasma treatment of continuous air flow was undertaken using the PCD reactor in dry and water-sprinkled modes. Water sprinkling more than doubled the m-xylene oxidation rate, which can be attributed to abundant OH-radicals produced at the plasma–water interface. Water sprinkling substantially reduced the formation of nitrous oxide, which is considered to be a secondary pollutant in the outlet air. Ozone is considered a by-product helping the subsequent photocatalytic oxidation of potential residues and photocatalyst maintenance. The use of water-sprinkled PCD is a promising approach to energy-efficient abatement of VOCs. Full article

This study presents the synthesis and characterization of polyimide (PI-2) films incorporated with spirulina powder for potential biomedical applications. The synthesis of PI-2 was achieved through a two-step polycondensation reaction using N-methyl-2-pyrrolidone (NMP) as the solvent. The incorporation of spirulina was systematically varied to investigate its effects on the structural and surface properties of the hybrid materials. Scanning electron microscopy revealed a tightly bound interface between spirulina and the PI-2 matrix, indicating effective dispersion and strong interfacial adhesion. Profilometry and Raman spectroscopy confirmed the homogeneous integration of spirulina within the polymer matrix, with resulting variations in surface roughness and chemistry. Contact angle measurements demonstrated altered wettability characteristics, with increased hydrophilicity observed with spirulina incorporation. Furthermore, blood component interaction studies indicated the variations in adhesion behavior observed for red blood cells, platelets, and plasma proteins. Water uptake studies revealed enhanced absorption capacity in PI-2 films loaded with spirulina, highlighting their potential suitability for applications requiring controlled hydration. Overall, this comprehensive characterization elucidates the potential of PI-2/spirulina hybrid materials for diverse biomedical applications, offering tunable properties that can be tailored to specific requirements. Full article

This paper studies the dynamics of the development of laser breakdown plasma in aqueous colloids of dysprosium nanoparticles by analyzing the time patterns of plasma images obtained using a high-speed streak camera. In addition, the distribution of plasma flashes in space and their luminosity were studied, and the amplitude of acoustic signals and the rate of generation of new chemical products were studied depending on the concentration of dysprosium nanoparticles in the colloid. Laser breakdown was initiated by pulsed radiation from a nanosecond Nd:YAG laser. It is shown that the size of the plasma flash, the speed of motion of the plasma–liquid interface, and the lifetime of the plasma flash decrease with an increasing concentration of nanoparticles in the colloid. In this case, the time delay between the beginning of the laser pulse and the moment the plasma flash reaches its maximum intensity increases with increasing concentrations of nanoparticles. Varying the laser fluence in the range from 67 J/cm² to 134 J/cm² does not lead to noticeable changes in these parameters, due to the transition of the breakdown plasma to the critical regime. For dysprosium nanoparticles during laser breakdown of colloids, a decrease in the yield of hydrogen peroxide and an increase in the rate of formation of hydroxyl radicals per water molecule, characteristic of nanoparticles of rare earth metals, are observed, which may be due to the participation of nanoparticles and hydrogen peroxide in reactions similar to the Fenton and Haber–Weiss reactions. Full article

Human society annually produces nearly 100 billion gallons of wastewater, containing approximately 3600 GWh of energy. This study introduces a proof of concept utilizing graphene materials to extract and instantly store this energy. A hybrid device, mimicking a microbial fuel cell, acts as both a battery and supercapacitor. Wastewater serves as the electrolyte, with indigenous microorganisms on the graphene electrode acting as biocatalysts. The device features a capacitive electrode using a 3D nickel foam modified with a plasma-exfoliated graphene mixture. Compared to controls, the Gr/Ni configuration shows a 150-fold increase in power output (2.58 W/m²) and a 48-fold increase in current density (12 A/m²). The Gr/Ni/biofilm interface demonstrates outstanding charge storage capability (19,400 F/m²) as confirmed by electrochemical impedance spectroscopy. Microscopy, spectroscopy, and electrochemical tests were employed to elucidate the superior performance of Gr/Ni electrodes. Ultimately, the capacitive energy extracted from wastewater can power small electrical equipment in water infrastructure, addressing energy needs in remote regions without access to a typical power grid. Full article