Search results for "surface charge"

showing 10 items of 86 documents

The Role of Right Interpretation of Space Charge Distribution for Optimized Design of HVDC Cables

2019

In the field of high-voltage transmission systems, different degradation phenomena affect the reliability of the employed components. In particular, under dc stress, the space charge accumulation phenomenon is believed to be the most responsible of the dielectrics lifetime reduction. To measure the accumulated space charges in flat specimens, the pulsed electro-acoustic (PEA) method is one of the most used techniques. The working principle of the PEA cell is based on the acoustic waves propagation and detection. As is well known, the acoustic waves propagating in different means are partially transmitted and partially reflected. Therefore, the piezoelectric sensor of the PEA cell is subject…

010302 applied physicsPhysicsField (physics)Piezoelectric sensorPEA method020208 electrical & electronic engineeringhigh-voltage direct-current (HVdc)Charge (physics)modeling02 engineering and technologyMechanicsAcoustic wave01 natural sciencesSpace chargeSignalFinite-difference time-domain (FDTD) methodIndustrial and Manufacturing EngineeringSettore ING-IND/31 - ElettrotecnicaControl and Systems Engineering0103 physical sciences0202 electrical engineering electronic engineering information engineeringReflection (physics)space chargeSurface chargeElectrical and Electronic Engineering
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Onset of cohesion in cement paste

2004

It is generally agreed that the cohesion of cement paste occurs through the formation of a network of nanoparticles of a calcium-silicate-hydrate ("C-S-H"). However, the mechanism by which these particles develop this cohesion has not been established. Here we propose a dielectric continuum model which includes all ionic interactions within a dispersion of C-S-H particles. It takes into account all co-ions and counterions explicitly (with pure Coulomb interactions between ions and between ions and the surfaces) and makes no further assumptions concerning their hydration or their interactions with the surface sites. At high surface charge densities, the model shows that the surface charge of…

0211 other engineering and technologiesCementNanoparticleIonic bonding02 engineering and technologyDielectricCSHIonchemistry.chemical_compound021105 building & constructionElectrochemistryGeneral Materials ScienceSurface chargecalcium silicate hydrateCalcium silicate hydrateionic correlationsSpectroscopyMonte Carlo simulation[CHIM.MATE] Chemical Sciences/Material chemistryIonic radiusatomic force microscopySurfaces and Interfaces[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsC-S-HcohesionchemistryChemical physics[ CHIM.MATE ] Chemical Sciences/Material chemistryCohesion (chemistry)nanoparticlesAFM0210 nano-technology
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Matching the Directions of Electric Fields from Triboelectric and Ferroelectric Charges in Nanogenerator Devices for Boosted Performance

2020

Summary Embedding additional ferroelectric dipoles in contacting polymer layers is known to enhance the performance of triboelectricnanogenerator (TENG) devices. However, the influence of dipoles formed between the triboelectric surface charges on two contacting ferroelectric films has been ignored in all relevant studies. We demonstrate that proper attention to the alignment of the distinct dipoles present between two contacting surfaces and in composite polymer/BaTiO3 ferroelectric films can lead to up to four times higher energy and power density output compared with cases when dipole arrangement is mismatched. For example, TENG device based on PVAc/BaTiO3 shows energy density increase f…

0301 basic medicineMaterials sciencePolymers02 engineering and technologyArticle03 medical and health sciencesElectric field:NATURAL SCIENCES:Physics [Research Subject Categories]DevicesNanotechnologySurface chargelcsh:ScienceTriboelectric effectPower densityMultidisciplinarybusiness.industryNanogeneratorElectrostatic induction021001 nanoscience & nanotechnologyFerroelectricityDipole030104 developmental biologyElectromagnetic Field13. Climate actionOptoelectronicsNanoparticleslcsh:Q0210 nano-technologybusinessiScience
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Angular Trapping of Anisometric Nano-Objects in a Fluid

2012

We demonstrate the ability to trap, levitate, and orient single anisometric nanoscale objects with high angular precision in a fluid. An electrostatic fluidic trap confines a spherical object at a spatial location defined by the minimum of the electrostatic system free energy. For an anisometric object and a potential well lacking angular symmetry, the system free energy can further strongly depend on the object's orientation in the trap. Engineering the morphology of the trap thus enables precise spatial and angular confinement of a single levitating nano-object, and the process can be massively parallelized. Since the physics of the trap depends strongly on the surface charge of the objec…

10120 Department of ChemistryOptics and Photonics3104 Condensed Matter PhysicsSilverMaterials scienceMacromolecular SubstancesSurface PropertiesStatic Electricity2210 Mechanical EngineeringMetal Nanoparticles1600 General ChemistryBioengineeringTrap (computing)OpticsOrientation (geometry)540 ChemistryNano-ElectrochemistryNanotechnologyScattering RadiationGeneral Materials ScienceFluidicsSurface chargeParticle Size1502 Bioengineeringbusiness.industryPhysicsMechanical EngineeringElectrostatic unitsDNAGeneral ChemistryCondensed Matter Physics2500 General Materials ScienceSymmetry (physics)KineticsHydrodynamicsLevitationAnisotropybusinessNano Letters
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Surface charges at the CaF2/water interface allow very fast intermolecular vibrational-energy transfer

2020

Abstract We investigate the dynamics of water in contact with solid calcium fluoride, where at low pH, localized charges can develop upon fluorite dissolution. We use 2D surface‐specific vibrational spectroscopy to quantify the heterogeneity of the interfacial water (D2O) molecules and provide information about the sub‐picosecond vibrational‐energy‐relaxation dynamics at the buried solid/liquid interface. We find that strongly H‐bonded OD groups, with a vibrational frequency below 2500 cm−1, display very rapid spectral diffusion and vibrational relaxation; for weakly H‐bonded OD groups, above 2500 cm−1, the dynamics slows down substantially. Atomistic simulations based on electronic‐structu…

540 Chemistry and allied sciencesMaterials science530 Physics2D sum-frequency generation010402 general chemistry01 natural sciencesCatalysisVibrational energy relaxationSurface chargeDiffusion (business)DissolutionResearch Articlesenergy transfer010405 organic chemistryIntermolecular forceGeneral ChemistryInterfacial Chemistryab-initio molecular dynamics530 Physik0104 chemical sciencesDipoleSolvation shellChemical physicsMolecular vibration540 Chemiesolid/liquid interfacesResearch Article
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Buildup of Ultrathin Multilayer Films by a Self-Assembly Process: II. Consecutive Adsorption of Anionic and Cationic Bipolar Amphiphiles and Polyelec…

1991

We have recently reported on the consecutive physisorption of anionic and cationic bipolar amphiphiles onto charged surfaces, adsorbed out of aqueous solutions [1]. Here, we extend our previous concept to multipolar compounds such as polyelectrolytes. In contrast to the bipolar amphiphile system, it is not necessary to separate single charges by a rigid unit, when the polyelectrolyte is adsorbed from sufficiently concentrated solutions. In this case the physisorbed layer does not bind with all ionic groups to the surface and exposes free ionic groups at the new film/solution interface. Therefore a polyelectrolyte layer can replace a layer of bipolar amphiphiles in the consecutive buildup of…

AdsorptionAqueous solutionMaterials scienceChemical engineeringGeneral Chemical EngineeringMonolayerAmphiphileIonic bondingNanotechnologySurface chargeSelf-assemblyPolyelectrolyteBerichte der Bunsengesellschaft für physikalische Chemie
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Microscopic Insights into the Fluorite/Water Interfaces from Vibrational Sum Frequency Generation Spectroscopy

2016

Water/mineral interfaces are central to a wide range of environmental and technological processes. In this report we provide a quantitative, molecular-level understanding of the CaF2/water interface using Density Functional Theory-based molecular dynamics simulations. In particular through the comparison of calculated Vibrational Sum Frequency Generation spectra to the experimental ones, we give a structural characterisation of the interface at different pH. At low pH, the surface is positively charged, causing a substantial degree of water ordering. Our results suggest that the surface charge originates from the dissolution of fluoride ions of the topmost layer, rather than from proton ads…

AdsorptionProtonChemistryHydrogen bondChemical physicsAnalytical chemistryDensity functional theorySurface chargeDissolutionIonSum frequency generation spectroscopy
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N-Propyl-N′-2-pyridylurea-modified silica as mixed-mode stationary phase with moderate weak anion exchange capacity and pH-dependent surface charge r…

2018

Herein, we present a novel silica-based stationary phase modified with N-propyl-N'-2-pyridylurea selector. Due to the weakly basic properties of the pyridine selector and the presence of residual silanols after selector immobilization, a zwitterionic surface with a pI observed at approximately pH 5.5 was measured by electrophoretic light scattering in pH-dependent ζ-potential determinations. The capability of the new N-propyl-N'-2-pyridylurea-modified silica to serve as mixed-mode stationary phase was investigated. For this purpose, it was characterized under RP and HILIC conditions using test mixtures. Subsequent classification of this stationary phase in comparison to in-house and commerc…

AnionsPyridinesSurface PropertiesSilicon dioxideAnalytical chemistryUridine Triphosphate02 engineering and technology01 natural sciencesBiochemistryUridine DiphosphateAnalytical Chemistrychemistry.chemical_compoundUreaSurface chargeAnion Exchange ResinsChromatographyIon exchangeChemistryElutionHydrophilic interaction chromatography010401 analytical chemistryOrganic ChemistryGeneral MedicineHydrogen-Ion ConcentrationChromatography Ion ExchangeSilicon Dioxide021001 nanoscience & nanotechnology0104 chemical sciencesMixed-mode chromatographyElectrophoretic light scatteringUridine Monophosphate0210 nano-technologySelectivityHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
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Surface-anchored counterions on weak chiral anion-exchangers accelerate separations and improve their compatibility for mass-spectrometry-hyphenation

2017

In the present work we propose new variants of chiral stationary phases (CSP) with tert-butylcarbamoylquinine (tBuCQN) as chiral selector molecule. Four tBuCQN-CSPs with distinct bonding chemistries are compared in terms of their pH-dependent surface charge by ζ-potential determinations, by achiral and chiral liquid chromatographic tests and LC-ESI-MS hyphenation. In one embodiment tBuCQN was immobilized on 3-mercaptopropylmethylsilyl-modified silica by thiol-ene click reaction (brush type CSP with selector coverage of 0.38mmol/g). In another embodiment, poly-(3-mercaptopropyl)-methylsiloxane was coated onto vinylized silica particles in presence of tBuCQN and radical initiator. The tBuCQN …

AnionsSiloxanesSulfonic acid010402 general chemistry01 natural sciencesBiochemistryMass SpectrometryAnalytical ChemistryEndcappingMoleculeSulfhydryl CompoundsSurface chargeIonschemistry.chemical_classificationChromatographyQuinineElutionOsmolar Concentration010401 analytical chemistryOrganic ChemistryStereoisomerismGeneral MedicineSilicon Dioxide0104 chemical scienceschemistryIonic strengthCounterionEnantiomerChromatography LiquidJournal of Chromatography A
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Acid–Base Properties and Surface Charge Distribution of the Water-Soluble Au102(pMBA)44 Nanocluster

2016

The pKa of the p-mercaptobenzoic acid (pMBA) ligands in the Au102(pMBA)44 nanocluster was measured by using acid–base and IR titration. The observed macroscopic pKa = 6.18 ± 0.05 is significantly more basic than that of free pMBA (pKa = 4.16), and the protonation behavior is anticooperative according to the Hill coefficient n = 0.64 ± 0.04. The cluster is truly water-soluble when more than 22 and insoluble when fewer than 7 ligands are in the deprotonated state. In order to obtain more insight into the anticooperative character, the cluster was modeled at pH ∼6.2 using constant pH molecular dynamics simulations. The pKa values of the individual pMBAs are in the range of 5.18–7.58, depending…

Base (chemistry)acid–base propertiesInorganic chemistryProtonation02 engineering and technology010402 general chemistry01 natural sciencescharge distributionMolecular dynamicsDeprotonationCluster (physics)Surface chargePhysical and Theoretical Chemistryta116chemistry.chemical_classificationChemistryCharge density021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyPhysical chemistryTitration0210 nano-technologygold nanoclustersJournal of Physical Chemistry C
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