Search Results (3,057)

Nanoparticle superlattices—periodic assemblies of uniformly spaced nanocrystals—bridge the nanoscale precision of individual particles with emergent collective properties akin to those of bulk materials. Recent advances demonstrate that multivalent ions and charged polymers can guide the co-assembly of nanoparticles, imparting electrostatic gating and enabling semiconductor-like behavior. However, the specific roles of anion geometry, valency, and charge density in mediating ion transport remain unclear. Here, we employ coarse-grained molecular dynamics simulations to investigate how applied electric fields (0–0.40 V/nm) modulate ionic conductivity and spatial distribution in trimethylammonium-functionalized gold nanoparticle superlattices assembled with four phosphate anions of distinct geometries and charges. Our results reveal that linear anions outperform ring-shaped analogues in conductivity due to higher charge densities and weaker interfacial binding. Notably, charge density exerts a greater influence on ion mobility than size alone. Under strong fields, anions accumulate at nanoparticle interfaces, where interfacial adsorption and steric constraints suppress transport. In contrast, local migration is governed by geometrical confinement and field strength. Analyses of transition probability and residence time further indicate that the rigidity and delocalized charge of cyclic anions act as mobility barriers. These findings provide mechanistic insights into the structure–function relationship governing ion transport in superlattices, offering guidance for designing next-generation ion conductors, electrochemical sensors, and energy storage materials through anion engineering. Full article

Eight different types of tea bags were investigated in this work using dynamic light scattering, electrophoretic mobility and nanoparticle tracking analysis methods to determine the concentration and size of released particles from the bag materials at different temperatures and times. Infrared spectroscopy and calorimetric methods confirmed that the bag material consisted of synthetic (nylon or polypropylene) or natural polymers (cellulose). The size of the released particles lies in the range of 200 nm^–1 µm with an initial bimodal distribution and with an average diameter of about 600 nm. The concentration of released particles increases with increasing temperature and brewing time. The released particles of synthetic polymers remain quite stable and are not affected by natural enzymes, while cellulose particles are easily degraded by the proteolytic complex Morikrase. When analyzing the electrophoretic mobility, it was found that the released particles have a negative surface charge, which probably determines the absence of cytotoxicity established on the epithelial cell line Caco-2 even at the maximum values of the observed particle concentrations (14 × 10⁹ particle/L for synthetic polymers and 170 × 10⁹ particle/L for cellulose). Full article

The paper presents experimental results for a modified pulsed plasma thruster (PPT) with solid propellant, using a coaxial anode–cathode design. Graphite from pencil leads served as propellant, and a tungsten trigger electrode was tested to reduce carbonization effects. Experiments were performed in a vacuum chamber at 0.001 Pa, employing diagnostics such as discharge current/voltage recording, power measurement, ballistic pendulum, time-of-flight (TOF) method, and a Faraday cup. Current and voltage waveforms matched an oscillatory RLC circuit with variable plasma channel resistance. Key discharge parameters were measured, including current pulse duration/amplitude and plasma channel formation/decay dynamics. Impulse bit values, obtained with a ballistic pendulum, reached up to 8.5 μN·s. Increasing trigger capacitor capacitance reduced thrust due to unstable “pre-plasma” formation and partial pre-discharge energy loss. Using TOF and Faraday cup diagnostics, plasma front velocity, ion current amplitude, current density, and ion concentration were determined. Tungsten electrodes produced lower charged particle concentrations than graphite but offered better adhesion resistance, minimal carbonization, and stable long-term performance. The findings support optimizing trigger electrode materials and PPT operating modes to extend lifetime and stabilize thrust output. Full article

Well cementing is an important step in oil and gas development. It uses cement to seal the formation and the casing, preventing fluid leakage. However, when conducting offshore oil well cementing operations, deep-water formations are usually weakly consolidated soils, and it is difficult to form a good cementation between the cement and formation. Therefore, enhancing the strength of the formation is one of the effective measures. This study uses the microbial-induced carbonate precipitation technology to cement sandy formations containing clay minerals. The triaxial tests were conducted to evaluate the consolidation effectiveness in the presence of three clay minerals: montmorillonite, illite, and kaolinite. X-ray computed tomography was utilized to characterize microscopic pore parameters, while thermogravimetric analysis, X-ray diffraction, and surface potential measurements were applied to analyze the mechanisms of clay minerals affecting microbial consolidation. The results showed that microbial mineralization mainly affects the cohesion of the samples. The cohesion of the montmorillonite sample increased from 20 kPa to 65.4 kPa, an increase of up to 3.27 times. The other two samples (illite and kaolinite) had increases of only 0.33 times and 1.82 times. Although the strength of the montmorillonite sample increased the most, unexpected large pores appeared with a diameter of over 120 µm, accounting for 7.1%. This is mainly attributed to the mineral expansion property. The expansion of the minerals will trap more microorganisms in the sample, thereby generating more calcium carbonate. And it also reduced the gaps between sand particles, creating favorable conditions for the connection of calcium carbonate. Although the surface charge of the minerals also affects the attachment of microorganisms, all three minerals have negative charges and a difference of no more than 0.84 mV (pH = 9). Therefore, the expansion property of the minerals is the dominant factor affecting the mechanical and microstructure of the sample. Full article

Background/Objectives: Understanding the interactions between nanoparticles and mucosal tissues is crucial for the development of advanced drug delivery systems, as the diffusion behavior of nanoparticles through mucus is strongly influenced by their size and surface properties, and the viscoelastic nature of the hydrogel matrix. In this study, we investigated the impact of nanoparticle size, surface charge, and hydrogel crosslinking density on nanoparticle diffusion in a mucus model in vitro. Method: Citrate-stabilized and PEGylated 30 and 100 nm gold nanoparticles were used as a model of nanoparticle and their diffusion through mucus-mimicking mucin-based hydrogels of two different crosslinking densities was assessed. Results: Citrate-stabilized 30 nm nanoparticles demonstrated greater diffusion in hydrogels mimicking native mucus compared to more densely crosslinked ones, reaching approximately 50.3 ± 0.2% diffusion within the first 5 min of the assay. This size-dependent effect was not observed for the 100 nm citrate-stabilized nanoparticles, which showed limited diffusion in both hydrogel types. To confer different surface charge, gold nanoparticles were functionalized by the conjugation of poly(ethylene glycol) (PEG) derivatives of identical molecular weight with different terminal moieties (neutral, and positively and negatively charged) to modulate the surface charge and assess their interaction with the negatively charged mucin matrix. PEGylated particles exhibited significantly greater mobility than their citrate-stabilized counterparts, regardless of size or hydrogel density owing to the muco-penetration effect of PEG. Among PEGylated particles, the neutral and negatively charged 30 nm variants demonstrated higher diffusion than the positively charged ones due to weaker interactions with the negatively charged mucin hydrogel. For the 100 nm particles, the neutral PEGylated nanoparticles exhibited greater diffusion than their positively charged counterparts. Conclusions: Overall findings could provide valuable insights into the more rational design of nanoparticle-based drug delivery systems targeting mucosal tissues. Full article

The direct deposition of highly concentrated polyelectrolyte complexes based on poly(ethyleneimine) (PEI) and poly(sodium methacrylate) (PMANa) onto inorganic sand microparticles (F100 and F200) resulted in the formation of versatile core-shell composites with fast removal properties in dynamic conditions toward anionic charged pollutants. Herein, in situ-generated nonstoichiometric PEI/PMANa polyelectrolyte complexes were directly precipitated as a soft organic shell onto solid sand microparticles at a 5% mass ratio (organic/inorganic part = 5%, w/w%). The sorption of an anionic model pollutant (Indigo Carmine (IC)) onto the composite particles in dynamic conditions depended on the inorganic core size, the flow rate, the bed type (fixed or fluidized) and the initial dye concentration. The maximum sorption capacity, after 10 cycles of sorption/desorption of IC onto F100@P5% and F200@P5%, was between 16 and 18 mg IC/mL composite. The newly synthesized core-shell composites could immobilize IC at a high flow rate (8 mL/min), either from concentrated (C_IC = 60 mg/L) or very diluted (C_IC = 0.2 mg/L) IC aqueous solution, demonstrating that this type of material could be promising in water treatment or efficient in solid-phase extraction (concentration factor of 2000). Full article

Particle accelerators are powerful tools in fundamental research, medicine, and industry that provide high-energy beams that can be used to study matter and to enable advanced applications. The state-of-the-art particle accelerators are fundamentally constructed from superconducting radio-frequency (SRF) cavities, which act as resonant structures for the acceleration of charged particles. The performance of such cavities is governed by inherent superconducting material properties such as the transition temperature, critical fields, penetration depth, and other related parameters and material quality. For the last few decades, bulk niobium has been the preferred material for SRF cavities, enabling accelerating gradients on the order of ~50 MV/m; however, its intrinsic limitations, high cost, and complicated manufacturing have motivated the search for alternative strategies. Among these, sputter-deposited superconducting thin films offer a promising route to address these challenges by reducing costs, improving thermal stability, and providing access to numerous high-T_c superconductors. This review focuses on progress in sputtered superconducting materials for SRF applications, in particular Nb, NbN, NbTiN, Nb₃Sn, Nb₃Al, V₃Si, Mo–Re, and MgB₂. We review how deposition process parameters such as deposition pressure, substrate temperature, substrate bias, duty cycle, and reactive gas flow influence film microstructure, stoichiometry, and superconducting properties, and link these to RF performance. High-energy deposition techniques, such as HiPIMS, have enabled the deposition of dense Nb and nitride films with high transition temperatures and low surface resistance. In contrast, sputtering of Nb₃Sn offers tunable stoichiometry when compared to vapour diffusion. Relatively new material systems, such as Nb₃Al, V₃Si, Mo-Re, and MgB₂, are just a few of the possibilities offered, but challenges with impurity control, interface engineering, and cavity-scale uniformity will remain. We believe that future progress will depend upon energetic sputtering, multilayer architectures, and systematic demonstrations at the cavity scale. Full article

Microplastics (MPs), as an emerging persistent contaminant, pose a potential threat to ecosystems and human health. The adsorptive removal of MPs from aqueous environments using magnetic nanoparticles has become a particularly promising remediation technology. Nevertheless, there remain significant knowledge gaps regarding its adsorption mechanism, especially how the key physical properties of magnetic nanoparticles regulate their adsorption behavior towards MPs. This study first investigated the relationship between the particle size of Fe₃O₄ nanoparticles and their adsorption efficacy for MPs. The results demonstrated a non-monotonic, size-dependent adsorption of MPs by Fe₃O₄ nanoparticles, with the adsorption efficiency and capacity following the order: 300 nm > 15 nm > 100 nm. This non-linear relationship suggested that factors other than specific surface area (which would favor smaller particles) are significantly influencing the adsorption process. Isotherm analysis indicated that the adsorption is not an ideal monolayer coverage process. Kinetic studies showed that the adsorption process could be better described by the pseudo-second-order model, while intra-particle diffusion played a critical role throughout the adsorption process. Furthermore, the effect of pH on adsorption efficiency was examined, revealing that the optimal performance occurs under neutral to weak acidic conditions, which is consistent with measurements of surface charges of nanoparticles. These findings suggest that the adsorption is not determined by specific surface area but is dominated by electrostatic interactions. The size-dependent adsorption of MPs by Fe₃O₄ nanoparticles provides new insights for the modification of magnetic adsorbents and offers a novel perspective for the sustainable and efficient remediation of environmental MPs pollution. Full article

In this study, four types of Fe₃O₄-based magnetic nanospheres were functionalized with distinct surface groups to examine how surface chemistry influences their co-transport with tetracycline (TC) in porous media. The functional groups investigated are carboxyl (−COOH), epoxy (−EPOXY), silanol (−SiOH), and amino (−NH₂). Particles bearing −COOH, −EPOXY, or −SiOH are negatively charged, facilitating their transport through porous media, whereas −NH₂-modified particles acquire a positive charge, leading to strong electrostatic attraction to the negatively charged TC and quartz sand, and consequently substantial retention with reduced mobility. Adsorption of TC onto Fe₃O₄-MNPs is predominantly chemisorptive, driven by ligand exchange and the formation of coordination complexes between the ionizable carboxyl and amino groups of TC and the surface hydroxyls of Fe₃O₄-MNPs. Additional contributions arise from electrostatic interactions, hydrogen bonding, hydrophobic effects, and cation–π interactions. Moreover, the carboxylate moiety of TC can coordinate to surface Fe centers via its oxygen atoms. Molecular dynamics simulations reveal a hierarchy of adsorption energies for TC on the differently modified surfaces: Fe₃O₄-NH₂ > Fe₃O₄-EPOXY > Fe₃O₄-COOH > Fe₃O₄-SiOH, consistent with experimental findings. The results underscore that tailoring the surface properties of engineered nanoparticles substantially modulates their environmental fate and interactions, offering insights into the potential ecological risks associated with these nanomaterials. Full article

A polyamidoamine-based hydrogel (H-M-GLY) and its montmorillonite-based composite (H-M-GLY/MMT) were studied as selective cleaning materials for cultural heritage conservation. H-M-GLY was synthesized from a glycine-based polyamidoamine oligomer with acrylamide terminals (M-GLY) through radical polymerization at pH 7.3 and had a basic character. The M-GLY oligomer was in turn synthesized from N,N′-methylenebisacrylamide and glycine in a 1:0.85 molar ratio. H-M-GLY/MMT was obtained by cross-linking a 1:0.1—weight ratio—M-GLY/MMT mixture at pH 4.0, to promote polyamidoamine-MMT interaction. The composite hydrogel absorbed less water than the plain hydrogel and proved tougher, due to montmorillonite’s electrostatic interactions with the positively charged M-GLY units. Scanning electron microscopic analysis showed that MMT was uniformly dispersed throughout the hydrogel. Both hydrogels were subjected to ink bleeding tests on papers written with either iron gall or India ink. Microscopic observation revealed neither bleeding nor release of hydrogel fragments. Being basic, H-M-GLY successfully deacidified the surface of aged paper. H-M-GLY/MMT, swollen in a 1:9 ethanol/water solution, was found to be effective in removing wax, known to trap carbonaceous particles and form dark stains on artistic artifacts. This study demonstrates the great potential of polyamidoamine-based hydrogels as versatile selective cleaning systems for cellulosic and other cultural heritage materials. Full article

(1) Background: gold nanoparticles (AuNPs) are of particular interest in biomedical research because they possess unique optical properties. In particular, its localized surface plasmon resonance is widely used for photothermal therapy and for detecting molecular interactions at nanoparticle surfaces. To enhance circulation time and biocompatibility, nanoparticles are often coated to shield their hydrophobic character. (2) Methods: we explored the seed-growth method to coat AuNPs with phospholipids to improve colloidal stability. (3) Results: various charged phospholipids were tested, and particle size and zeta potential were characterized. The monodispersity of the coated nanoparticles strongly depends on the narrow size distribution of both gold nanoparticles seeds and lipid vesicles. Achieving stable coated AuNPs with zwitterionic lipids such as phosphatidylcholine was challenging, whereas coatings containing phosphatidylglycerol did not compromise nanoparticle stability. (4) Conclusions: coating AuNPs with phospholipids via the seed-growth method has potential but requires further optimization to improve reproducibility and achieve stable nanoparticles with near-neutral surface charge. Full article

Seawater has been widely used in copper–molybdenum flotation plants due to the shortage of fresh water and the high cost of seawater desalination, especially in arid regions. There have been many studies concerning the molybdenite flotation in seawater. Due to the complication of seawater flotation, it is difficult to identify the key factors affecting molybdenite recoveries. It is known that the unique structure of molybdenite plays an important role in molybdenite flotation. The anisotropic property of molybdenite leads to the different surface properties of basal and edge plane surfaces. Electrochemical properties of sulfides have a significant effect on the surface properties which affect the flotation performance. Therefore, it is important to understand the surface electrochemical properties such as surface chemistry, redox processes, and reaction kinetics of molybdenite’s two different surfaces in seawater, and to determine what affects the molybdenite flotation behaviors in seawater. In this study, the surface properties of molybdenite basal and edge plane surfaces in both fresh water and seawater were investigated through various electrochemical techniques. Open circuit potential (OCP) measurement indicated that edge plane surfaces were easier to be oxidized than basal plane surfaces. Cyclic voltammetry (CV) studies showed that the basal plane surfaces were stable with a low electrochemical reactivity, while the edge plane surfaces had relatively high electrochemical reactivity. In addition, the redox property of the molybdenite surface was enhanced in seawater, which is a key to the improvement of fine molybdenite flotation in seawater. Electrochemical impedance spectroscopy (EIS) measurements further confirmed the stability of basal plane surfaces and indicated a greater charge transfer ability of edge plane surfaces in seawater. Different molybdenite particle sizes with different basal and edge ratios were applied in the flotation in both fresh water and seawater; the results illustrated that molybdenite flotation was enhanced in seawater especially to fine particles. The flotation and electrochemical studies reveal that the electrochemical reactivity of edge plane surface plays an important role in molybdenite seawater flotation. Full article

The molecular structure and mechanical resilience of the binder are crucial for mitigating volume expansion, maintaining electrode structural integrity, and enhancing the cycling stability of silicon-based anode materials in lithium-ion batteries. In this study, from the perspective of binder molecular structural design, commercial carboxymethyl cellulose (CMC) was modified with silk protein (SF), which has good mechanical properties and abundant surface functional groups, to address issues such as high brittleness, poor compliance and easy cracking of the electrode structure during charge and discharge cycles, and to enhance the mechanical properties of the CMC-based binder and its interaction with silicon particles, so as to improve the cycle stability of silicon-based materials. The mechanical properties of the CMC binder were significantly improved and the interaction between the binder and the surface of the silicon particles was enhanced by the addition of SF. When the SF content was optimized at 6 wt%, the electrode exhibited the best electrochemical performance, delivering a specific capacity of 1182 mAh/g at a high current density of 5000 mA/g, and retaining a capacity of 1138 mAh/g after 50 cycles at 1000 mA/g, demonstrating excellent electrochemical durability. Full article

Soil contamination with heavy metals (HM) poses a risk to human health and can impact different soil functions. This study aimed to determine the influence of heavy metal pollution on the physical and physicochemical characteristics of the two profiles of alluvial–deluvial soil under grassland located at different distances from the Aurubis-Pirdop Copper smelter in Bulgaria. Data for soil particle-size distribution, soil bulk and particle densities, mineralogical composition, soil organic carbon contents, cation exchange properties, surface charge, soil water retention curves, pore size distribution—obtained by mercury intrusion porosimetry (MIP)—and thermal properties were obtained. The contents of Pb, Cu, As, Zn, and Cd were above the maximum permissible level in the humic horizon and decreased with depth and distance from the Copper smelter. Depending on HM speciation, the correlations are established with SOC and most physicochemical parameters. It can be concluded that the HMs impact the clay content, specific surface area, distribution of pores, and the water stability of soil aggregate fraction 1–3 mm to varying degrees. Full article

With the rapid development of renewable energy and the continuous pursuit of efficient energy utilization, distributed photovoltaic power generation has been widely used in village-level microgrids. As a key platform connecting distributed photovoltaics with users, energy storage systems play an important role in alleviating the imbalance between supply and demand in VMG. However, current energy storage systems rely heavily on lithium batteries, and their frequent charging and discharging processes lead to rapid lifespan decay. To solve this problem, this study proposes a hybrid energy storage system combining supercapacitors and lithium batteries for VMG, and designs a hybrid energy storage scheduling strategy to coordinate the “source–load–storage” resources in the microgrid, effectively cope with power supply fluctuations and slow down the life degradation of lithium batteries. In order to give full play to the active support ability of supercapacitors in suppressing grid voltage and frequency fluctuations, the scheduling optimization goal is set to maximize the sum of the virtual inertia time constants of the supercapacitor. In addition, in order to efficiently solve the high-complexity model, the reason for choosing the snow goose algorithm is that compared with the traditional mathematical programming methods, which are difficult to deal with large-scale uncertain systems, particle swarm optimization, and other meta-heuristic algorithms have insufficient convergence stability in complex nonlinear problems, SGA can balance global exploration and local development capabilities by simulating the migration behavior of snow geese. By improving the convergence effect of SGA and constructing a multi-objective SGA, the effectiveness of the new algorithm, strategy and model is finally verified through three cases, and the loss is reduced by 58.09%, VMG carbon emissions are reduced by 45.56%, and the loss of lithium battery is reduced by 40.49% after active support optimization, and the virtual energy inertia obtained by VMG from supercapacitors during the scheduling cycle reaches a total of 0.1931 s. Full article