Electrostatic Forces Research Articles

Analysis of nonlinear bending behavior of nano-switches considering surface effects

Nano-switch structures are important control elements in nanoelectromechanical systems and have potential applications in future nanodevices. This paper analyzes the effects of surface effects, geometric nonlinearity, electrostatic forces, and intermolecular forces on the nonlinear bending behavior and adhesion stability of nano-switches. Based on the Von Karman geometric nonlinearity theory, four types of boundary conditions for the nano-switch structure were specifically calculated. The results show that surface effects have a significant impact on the nonlinear bending and adhesion stability of nano-switches. Surface effects increase the adhesion voltage of the nano-switch and decrease its adhesion displacement, and as the size of the nano-switch structure increases, the impact of surface effects decreases. A comparative analysis of the linear theory and the nonlinear theory results shows that the adhesion voltage predicted by the linear theory is smaller than that predicted by the nonlinear theory. The effect of geometric nonlinearity increases as the size of the nano-switch structure increases, as the distance between the electrodes increases, and as the aspect ratio of the nano-switch structure increases. These findings provide theoretical support and reference for the design and use of future nanodevices and nanoelectromechanical systems.

Prey can detect predators via electroreception in air

Predators and prey benefit from detecting sensory cues of each other's presence. As they move through their environment, terrestrial animals accumulate electrostatic charge. Because electric charges exert forces at a distance, a prey animal could conceivably sense electrical forces to detect an approaching predator. Here, we report such a case of a terrestrial animal detecting its predators by electroreception. We show that predatory wasps are charged, thus emit electric fields, and that caterpillars respond to such fields with defensive behaviors. Furthermore, the mechanosensory setae of caterpillars are deflected by these electrostatic forces and are tuned to the wingbeat frequency of their insect predators. This ability unveils a dimension of the sensory interactions between prey and predators and is likely widespread among terrestrial animals.

Electrical detachment of triboelectrically charged bumpy particles from rough surfaces

The detachment of bumpy particles from smooth and rough surfaces through electrostatic fields was studied. The Johnson–Kendall–Roberts (JKR) adhesion model for elastic interface deformations was used to account for the individual bump adhesion, including the electrostatic forces. It was assumed that the elastic deformation of asperities determines the real contact area, and the effect of topographic properties of substrates was included in the analysis. For a fixed charge per unit mass, the Coulomb, the image, the dielectrophoretic, and the polarization forces acting on the particle in the presence of an imposed electric field were evaluated. The electrostatic detachment of bumpy toner particles for various applied electrostatic fields was studied. The triboelectric charges were concentrated on the hemispherical bumps, and the critical electric field strength needed to detach charged particles from surfaces with varying roughness levels was evaluated. It was shown that the particle charge, surface roughness, and the number of bumps significantly affect the removal of particles from surfaces. For higher charges (∼5 × 10−15 C ), decreasing the number of bumps from 22 to 14 and the roughness parameter from 0.83 to 0.77 approximately doubled the detachment field needed to remove 8.3 μ m polystyrene (PSL) particles from the aluminum oxide substrate. The model predictions are compared with the available experimental data, and good agreement was observed. The study’s findings predicting the electric field needed for charged particle removal could lead to more efficient copiers and electrostatic cleaning devices.

Stochastic model for migration and breakage of detrital and authigenic fines

Mobilisation of attached particles during flow in rocks occurs in geo-energy processes. Particle mobilisation, their migration through rocks and pore plugging yield significant decline in permeability and well injectivity and productivity. While much is currently known about the underlying mechanisms governing the detachment of detrital particles against attracting electrostatic forces, a critical gap exists in the theoretical understanding of detachment by breakage of widely spread authigenic particles, which naturally grow on rock grains during geological times. Previous works derived micro-scale mechanical equilibrium equations for both detrital and authigenic particles, and the upscaling procedure from particle to pore and core scales for detrital fines. In this paper, for the first time we derive a stochastic model for migration and breakage of authigenic fines and authigenic–detrital mixtures. This allows for core-scale transport modelling based on the particle-scale torque balance. We introduce a novel framework for predictive stochastic detachment modelling by particle–rock bond breakage that integrates the beam theory of elastic particle deformation, strength failure criteria and viscous flow around the attached particle. The analytical expressions for stress maxima and stress diagrams for a single particle allow determining the critical failure stresses, breakage points of the beam and breakage flow velocity. The mathematical model describing lab coreflood includes the maximum retention function for both authigenic and detrital fines. The matching laboratory coreflood data under increasing velocity at micro- and core-scales achieved high matching of the experimental data by the model. High matching validates the upscaling and downscaling procedures derived.

Hydrogeological characterization of low permeability medium for conceptualization of a mine site in Eastern Turkey

The mining site in Eastern Anatolia of Turkey were encounter a significant risk of slope instability within the operational area. One of the processes that govern slope stability is the pore water pressure distribution. The conceptualization and characterization of porous media serve as fundamental prerequisites for the implementation of numerical methods aimed at predicting pore water distribution. This study aims to characterize the hydrogeological properties of water bearing rocks in the active mining site in Eastern Anatolia of Turkey. A total of 21 wells and drill holes were drilled in the study area to conduct in-situ tests, monitoring, and sampling. The large diameter wells drilled in surrounding the carbonate rocks were to determine the groundwater flow and boundary conditions and also wells tapped metasediments and diorite unit for hydraulic testing. The lugeon tests and installation of vibrating wire piezometers were carried out at small diameter drill holes to obtain localized hydraulic conductivity of metasediments and diorite at different depths and monitoring pore water pressure distribution along some critical cross-sections. The results obtained from these tests are used for developing hydrogeological conceptual model for groundwater flow. The results of in-situ tests show that the metasediment and diorite units act as a single hydrostratigraphic unit. The metasediments and diorite have high total porosity and low specific yield indicating that the pore water is retained by electrostatic forces in the medium and it resists flow due to low hydraulic conductivity. The vertical variation in hydraulic conductivity values indicates that the medium is highly heterogeneous.

Boosting Zn2+ intercalation in manganese oxides for aqueous zinc ion batteries via delocalizing the d-electrons spin states of Mn site

Rechargeable aqueous zinc-ion batteries (AZIBs) have received increasing attention on account of their eco-friendliness and low cost. However, the limited capacity and poor rate properties of cathodes remain a major challenge due to the low electrochemical reactivity of cathode materials and sluggish Zn2+ transport kinetics. Herein, we design a 1,5-naphthalenediamine (NAPD) pre-intercalate potassium manganese dioxide (KMO-NAPD) with high capacity and rate capability for AZIBs. The introduction of NAPD can delocalize the d-electrons spin states of the Mn site and activate the reactivity of KMO-NAPD for Zn2+ intercalation. Moreover, the interaction between intercalated Zn2+ and KMO-NAPD is weakened due to the decreased electrostatic interaction force, which promotes the diffusion of Zn2+. Consequently, the KMO-NAPD cathode exhibits high specific capacity (237 mAh g−1 at 1 A g−1) satisfying rate capability (129 mAh g−1 at 4 A g−1), and excellent cycling stability (85 % capacity retention after 1000 cycles). Furthermore, the fabricated AZIBs based on the KMO-NAPD exhibit a high energy density of 294.3 Wh kg−1 and a peak power density of 8.6 kW kg−1. This study opens up a new path for the development of high-energy organic-inorganic hybrid cathode materials with modulated electronic structures for advanced AZIBs.

Wave‐to‐Wire Model and Output Performance Analysis of a Point Absorption Wave Energy Converter Based on Triboelectric Nanogenerator

Herein, a point absorption wave energy converter (WEC) model combined with a contact–separation mode triboelectric nanogenerator (PAW TENG) is proposed. The model considers the interaction between the hydrodynamic forces captured by a point absorption conversion device of wave energy and the electrostatic force of the TENG. According to the established harmonic oscillation model of the buoy, the buoy's hydrodynamic properties and power generation characteristics are studied using finite element simulation and numerical simulation calculations. The best matching resistor circuit for PAW TENG in regular waves is investigated and analyzed. The electrical characteristics of the PAW TENG in the irregular wave spectrum are also solved. This work will provide design ideas for the experimental design of a novel point absorption WEC.

Halloysite nanotubes immobilized by copper itaconic acid complexes as smoke suppressant for soft polyvinyl chloride

AbstractCurrently, there are few reports of core–shell‐structured smoke suppressants that can provide a growth substrate and stabilize the char layer. In response to this problem, core–shell nanoparticles of halloysite nanotubes (HNTs) coated with copper itaconate complex were prepared by layer‐by‐layer assembly method. The electrostatic forces between HNTs and copper ions and the coordination between the itaconic acid and copper ions contributed this synthesis. The micromorphology, chemical composition, and structure of HNT@CuC5H4O4 were characterized, and its effects on the flame‐retardant and smoke‐inhibition properties, mechanical properties, and thermal stability of the soft polyvinyl chloride (PVC) were investigated. The results showed that the core–shell structure of HNT@CuC5H4O4 contributed to its homogeneous dispersion in PVC and the formation of interlocking mesh structure. Thus, the incorporation of HNT@CuC5H4O4 enhanced the strength and stiffness of soft PVC without sacrificing its ductility. Besides, copper ions on HNT@CuC5H4O4 could promote the cross‐linking carbonization of the PVC at high temperature. The formed char layer catalyzed by CuC5H4O4, together with its attached three‐dimensional network structure of HNT constituted a compact and continuous char layer with high thermal stability, which effectively prevented the release of combustible volatiles and toxic gases as well as heat transfer.

Improved comprehensive adhesion performance of aggregate- recycled asphalt interface via incorporating steel slag

Steel slag, a typical industrial waste, reveals high alkalinity and abundant texture, endowing its excellent adhesion performance with asphalt and facilitating its implementation in recycled asphalt mixture. While few studies focused on the interaction mechanism and comprehensive adhesion performance of steel slag- recycled asphalt interface. Hence, this topic merits further exploration. In this study, the interface models of steel slag-asphalt were established and their interface parameters also were surveyed. And the comprehensive evaluation index of adhesion performance was explored by the improved radar chart. The experimental results elaborate that steel slag exhibits the larger surface energy of 46.69 mJ/m2 and higher percentage of dispersion component of 76.6 %. Recycled asphalt-steel slag demonstrates the greater adhesion work, the smaller exfoliated work and the larger adhesive destructive force than recycled asphalt-basalt, indicating its superior adhesion ability. Steel slag-asphalt molecule behaves the lower radial distribution function and larger interfacial bonding energy due to the dual provision of van der Waals force and electrostatic adsorption force. The exfoliated work in experiment and adhesion work in simulation presents a Pearson correlation coefficient of −0.683, resulting in their strong negative correlation. Steel slag-recycled asphalt interface with the higher comprehensive evaluation index of 0.9155 reveals the superior comprehensive adhesion performance than basalt- recycled asphalt.

THE DEPENDENCE OF ACID-BASE EQUILBRIA AND ACIDITY CONSTANTS OF CONGO RED IN BUFFER SOLUTIONS ON THE IONIC STRENGTH

In this study, the spectrophotometric studies of aqueous ethanol solution of Congo red in various buffers solutions at room temperature 25oC and at different ionic strength of 0.05, 0.1, 0.3, and 0.5 KCl mol L-1 were investigated. The acidity constants of Congo red were estimated by three different methods. The two protonation stages were observed in pH range 2 - 4 and 4 - 6 as result as protonation of amino group and azo groups. The dependence of absorption spectra of Congo red on the ionic strength of solutions which exhibited blue shift with increases ionic strength in addition the shape and intensity were varied. Therefore, the acid-base equilibria shifted toward the higher pHs with the rise in ionic strength. Also, the acidity constants were affected by the ionic strength which the acidity constants decrease with increasing ionic strength of solution because the electrostatic interaction force increased.

Selective flotation separation of gypsum and quartz using dodecyl amine hydrochloride as collector: Mechanism and application

The selective flotation separation of gypsum and quartz in phosphogypsum (PG) is an urgent problem that is very important for the high‐value utilization of PG. In the work, dodecyl amine hydrochloride (DH) was introduced as a collector for the selective flotation separation of gypsum and quartz. The flotation property and selective mechanism of DH on the surface of gypsum and quartz were researched by single mineral flotation experiments, Fourier transform attenuated total reflection infrared spectroscopy analyzer, zeta potential analyzer, X‐ray photoelectron spectrum, molecular dynamic (MD) simulation, etc. Additionally, H+ was introduced into the mineral‐water system simulated by MD to take into account the effect of acidic conditions on the adsorption of DH. The pre‐adsorption of H+ on the quartz surface under strongly acidic conditions hindered the electrostatic force adsorption of DH on the quartz surface. Furthermore, DH was adopted as a collector in the direct flotation recovery of gypsum from PG, and the gypsum concentrates with productivity of 69.85%, CaSO4·2H2O content of 96.33%, and whiteness of 55.00% were obtained. The SiO2 content in the gypsum concentrate decreased from 9.08% to 0.616%. It suggested that DH could serve as a promising collector in the selective separation of gypsum and quartz in PG via flotation.

Blended Nephelium lappaceum and Durio zibethinus wastes for activated carbon production via microwave-ZnCl2 activation: optimization for methylene blue dye removal

Herein, this work targets to employ the blended fruit wastes including rambutan (Nephelium lappaceum) peel and durian (Durio zibethinus) seed as a promising precursor to produce activated carbon (RPDSAC). The generation of RPDSAC was accomplished through a rapid and practical procedure (microwave-ZnCl2 activation). To evaluate the adsorptive capabilities of RPDSAC, its efficacy in eliminating methylene blue (MB), a simulated cationic dye, was measured. The Box–Behnken design (BBD) was utilized to optimize the crucial adsorption parameters, namely A: RPDSAC dose (0.02–01 g/100 mL), B: pH (4–10), and C: time (2–6 min). The BBD design determined that the highest level of MB removal (79.4%) was achieved with the condition dosage of RPDSAC at 0.1 g/100 mL, contact time (6 min), and pH (10). The adsorption isotherm data is consistent with the Freundlich concept, and the pseudo-second-order versions adequately describe the kinetic data. The monolayer adsorption capacity (qmax ) of RPDSAC reached 120.4 mg/g at 25 °C. Various adsorption mechanisms are involved in the adsorption of MB dye onto the surface of RPDSAC, including π–π stacking, H-bonding, pore filling, and electrostatic forces. This study exhibits the potential of the RPDSAC as an adsorbent for removal of toxic cationic dye (MB) from contaminated wastewater.

Low-Cytotoxic Core-Sheath ZnO NWs@TiO2-xNy Triggered Piezo-photocatalytic Antibacterial Activity.

Sonophotodynamic antimicrobial therapy (SPDAT) is recognized as a highly efficient biomedical treatment option, known for its versatility and remarkable healing outcomes. Nevertheless, there is a scarcity of sonophotosensitizers that demonstrate both low cytotoxicity and exceptional antibacterial effectiveness in clinical applications. In this paper, a novel ZnO nanowires (NWs)@TiO2-xNy core-sheath composite was developed, which integrates the piezoelectric effect and heterojunction to build dual built-in electric fields. Remarkably, it showed superb antibacterial effectiveness (achieving 95% within 60 min against S. aureus and ∼100% within 40 min against E. coli, respectively) when exposed to visible light and ultrasound. Due to the continuous interference caused by light and ultrasound, the material's electrostatic equilibrium gets disrupted. The modification in electrical properties facilitates the composite's ability to attract bacterial cells through electrostatic forces. Moreover, Zn-O-Ti and Zn-N-Ti bonds formed at the interface of ZnO NWs@TiO2-xNy, further enhancing the dual internal electric fields to accelerate the excited carrier separation to generate more reactive oxygen species (ROS), and thereby boosting the antimicrobial performance. In addition, the TiO2 layer limited Zn2+ dissolution into solution, leading to good biocompatibility and low cytotoxicity. Lastly, we suggest a mechanistic model to offer practical direction for the future development of antibacterial agents that are both low in toxicity and high in efficacy. In comparison to the traditional photodynamic therapy systems, ZnO NWs@TiO2-xNy composites exhibit super piezo-photocatalytic antibacterial activity with low toxicity, which shows great potential for clinical application as an antibacterial nanomaterial.

Negatively charged hydrochar from Aesculus indica waste: A sustainable material for enhanced Li-S batteries performance

This study presents a negatively charged hydrochar from Aesculus indica waste, employing a microwave-assisted hydrothermal carbonization (HTC) method at very low temperatures (120∼200 °C). The research shows the utilization of these negatively-charged-oxygen-containing hydrochars in lithium-sulfur (Li-S) batteries effectively mitigates polysulfide shuttling through electrostatic repulsive forces and simultaneously facilitate uniform lithium-ion transportation, leading to substantial improvement in battery performance. Through detailed investigations into the HTC reaction mechanism, the concentration of the negatively charged oxygen functional groups is tunable by controlling the carbonization process, which could further improve the enhancement effects. Furthermore, negatively-charged-oxygen-containing hydrochars were utilized as modified separator in Li-S batteries to enhance the electrochemical performance. The batteries assembled with hydrochar modified separator, has an initial discharge capacity of 1216 mAh g−1 at 0.1 C, and after 200 cycles at 1 C, its reversible discharge capacity was still 800 mAh g−1 with more than 80 % capacity retention. This research not only provides an efficient method for the utilization of waste biomass, but also offers a new approach for the preparation of negatively charged carbon for lithium-sulfur batteries.

Exploring high hydrostatic pressure effects on anthocyanin binding to serum albumin and food-derived transferrins

This study investigated the effects of high hydrostatic pressure (HHP) on the binding interactions of cyanindin-3-O-glucoside (C3G) to bovine serum albumin, human serum albumin (HSA), bovine lactoferrin, and ovotransferrin. Fluorescence quenching revealed that HHP reduced C3G-binding affinity to HSA, while having a largely unaffected role for the other proteins. Notably, pretreating HSA at 500 MPa significantly increased its dissociation constant with C3G from 24.7 to 34.3 μM. Spectroscopic techniques suggested that HSA underwent relatively pronounced tertiary structural alterations after HHP treatments. The C3G-HSA binding mechanisms under pressure were further analyzed through molecular dynamics simulation. The localized structural changes in HSA under pressure might weaken its interaction with C3G, particularly polar interactions such as hydrogen bonds and electrostatic forces, consequently leading to a decreased binding affinity. Overall, the importance of pressure-induced structural alterations in proteins influencing their binding with anthocyanins was highlighted, contributing to optimizing HHP processing for anthocyanin-based products.

Impact of silt chemical composition on deflocculation and coagulation of clay-rich paste

This paper investigates the impact of the chemical composition of two silts, quartz and limestone, on the deflocculation/coagulation process for poured earth application. The driving mechanisms behind the evolution of the rheological behavior after the addition of sodium hexametaphosphate are highlighted through zeta potential measurementand the chemical changes with ICP-OES and 31P MAS NMR spectroscopy. The first results show that adding sodium hexametaphosphate into the quartz silt modifies its inter-particle forces through electrostatic repulsion forces induced by the adsorption of phosphate anions onto the quartz structure. For limestone paste, the deflocculation mechanism is affected by the dissolution of the calcite. This dissolution leads to a release of Ca2+ cations and an increase in the paste's pH, reducing the paste deflocculation rate. These dissolved Ca2+ cations in the solution conduct to a partial coagulation making the delayed flocculation targeted initially with the addition of magnesium oxide less effective.

A novel Pt2+ complex containing 1,4-benzodioxan-6-amine: Stability, DNA binding, and antitumor effects against human breast cancer cells

In this work, a new platinum(II) complex was prepared by the reaction of K2PtCl4 with 1,4-benzodioxan-6-amine (bda) at room temperature in the molar ratio 2:1 (L:M). The complex was characterized by physicochemical (elemental analysis, TGA/DTA, and conductivity measurements) and spectroscopic methods (UV–Vis, FTIR, 1H, 13C and 195Pt NMR). According to the spectroscopic data, two bda ligands coordinate to the platinum ion in a monodentate manner through the nitrogen atom to give the complex cis-[PtCl2(bda)2]. Stability studies were carried out under different conditions and showed that the complex is stable in pure DMF, although it undergoes slow solvolysis in DMSO. The interaction of this complex with calf thymus DNA (CT-DNA) was studied using circular dichroism (CD), electronic absorption and fluorescence spectroscopy. The complex binds to CT-DNA with a Kb value of 1.06 ​× ​103 ​M−1 and according to data from CD and fluorescence spectroscopy, appears to interact with DNA by electrostatic forces and or other no intercalative binding mode. Compared to cisplatin, the complex exhibited good cytotoxic activity and selectivity against the MCF-7 tumor cell line, displaying an IC50 value of 17.33 ​± ​1.1 ​μM, as well as inhibited MCF-7 ​cells migration.

Sulfonated Chitosan Gel Membrane with Confined Amine Carriers for Stable and Efficient Carbon Dioxide Capture.

Capturing carbon dioxide (CO2) from flue gases is a crucial step towards reducing CO2 emissions. Among the various carbon capture methods, facilitated transport membranes (FTMs) have emerged as a promising technology for CO2 capture owing to their high efficiency and low energy consumption in separating CO2. However, FTMs still face the challenge of losing mobile carriers due to weak interaction between the carriers and membrane matrix. Herein, we report a sulfonated chitosan (SCS) gel membrane with confined amine carriers for effective CO2 capture. In this structure, diethylenetriamine (DETA) as a CO2-mobile carrier is confined within the SCS gel membrane via electrostatic forces, which can react reversibly with CO2 and thus greatly facilitate its transport. The SCS ion gel membrane allows for the fast diffusion of amine carriers within it while blocking the diffusion of nonreactive gases, like N2. Thus, the prepared membrane exhibits exceptional CO2 separation capabilities when tested under simulated flue gas conditions with CO2 permeance of 1155 GPU and an ultra-high CO2/N2 selectivity of above 550. Moreover, the membrane retains a stable separation performance during the 170 h continuous test. The excellent CO2 separation performance demonstrates the high potential of gel membranes for CO2 capture from flue gas.

Dielectric Elastomer Actuators with Enhanced Durability by Introducing a Reservoir Layer.

A Dielectric Elastomer Actuator (DEA) consists of electrodes with a dielectric layer between them. By controlling the design of the electrodes, voltage, and frequency, the operating range and speed of the DEA can be adjusted. These DEAs find applications in biomimetic robots, artificial muscles, and similar fields. When voltage is applied to the DEA, the dielectric layer undergoes compression and expansion due to electrostatic forces, which can lead to electrical breakdown. This phenomenon is closely related to the performance and lifespan of the DEA. To enhance stability and improve dielectric properties, a DEA Reservoir layer is introduced. Here, stability refers to the ability of the DEA to perform its functions even as the applied voltage increases. The Reservoir layer delays electrical breakdown and enhances stability due to its enhanced thickness. The proposed DEA in this paper is composed of a Reservoir layer and electrode layer. The Reservoir layer is placed between the electrode layers and is independently configured, not subjected to applied voltage like the electrode layers. The performance of the DEA was evaluated by varying the number of polymer layers in the Reservoir and electrode designs. Introducing the Reservoir layer improved the dielectric properties of the DEA and delayed electrical breakdown. Increasing the dielectric constant through the DEA Reservoir can enhance output characteristics in response to electrical signals. This approach can be utilized in various applications in wearable devices, artificial muscles, and other fields.

The synergistic effect of typical chiral organic acids and solution chemistry conditions on the transport of 2-arylpropionic acid chiral derivatives in porous media

The hazards of man-made chiral compounds are of great public concern, with reports of worrying stereoselective compounds and an urgent need to assess their transport. This study evaluated the transport of 2-arylpropionic acid derivatives enantiomers (2-APA) in porous media under a variety of solution chemistry conditions via column packing assays. The results revealed the introduction of Malic acid (MA) enantiomers enhanced the mobility of 2-APA enantiomers, but the enhancement effect was different for different 2-APA enantiomers. Batch sorption experiments confirmed that the MA enantiomers occupied the sorption site of the quartz sand, thus reducing the deposition of the 2-APA enantiomer. Homo- or heterochirality between 2-APA and MA dominates the transport of 2-APA enantiomers, with homochirality between them triggering stronger retention and vice versa. Further evaluating the effect of solution chemistry conditions on the transport of 2-APA enantiomers, increased ionic strength attenuated the mobility of 2-APA enantiomers, whereas introduced coexisting cations enhanced the retention of 2-APA enantiomers in the column. The redundancy analyses corroborated these solution chemistry conditions were negatively correlated with the transport of 2-APA enantiomers. The coupling of pH and these conditions reveals electrostatic forces dominate the transport behavior and stereoselective interactions of 2-APA enantiomers. Distinguishing the transport of enantiomeric pair helps to understand the difference in stereoselectivity of enantiomers and promises to remove the more hazardous one.