Search results for "FILM"

showing 10 items of 4577 documents

Electronic Perspective on the Electrochemistry of Prussian Blue Films

2009

The derivative of the voltabsommetric scans, together with previous nano-electrogravimetric and X-ray diffraction results, allow different electrochemical processes to be distinguished during the Prussian blue (PB) voltammetric scan. Potassium, proton, and hydrated proton counterions involved in PB electrochemistry are related here to the electrochemical reactions of specific Fe sites. Potassium counterions show two different sites for their insertion: one located in the crystalline framework and another in ferrocyanide vacancies. From the monitoring of electroactive Fe sites, the covalent-exchange model is suggested as one of the first approaches to explain the origin of the PB magnetic or…

chemistry.chemical_classificationPrussian blueProtonIon exchangeRenewable Energy Sustainability and the EnvironmentPotassiumInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsElectrochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryX-ray crystallographyMaterials ChemistryElectrochemistryCounterionFerrocyanideJournal of The Electrochemical Society
researchProduct

Usefulness of F(dm/dQ) Function for Elucidating the Ions Role in PB Films

2007

The conversion process of "insoluble" prussian blue (PB) films into the "soluble" structure has been followed by the simultaneous measurement of current and mass changes during voltammetric experiments and focusing on the possibilities of the use of the instantaneous mass/electrical charge ratio at each potential. A similar procedure was used for the analysis of the mechanism of reduction of PB films to the Everitt's salt form and to follow the partial dissolution of iron species during the oxidation to the prussian yellow form. The possibility of covering PB films by Nafion membranes, which make difficult the transport of anions through it, allows us to discern the role of anions in the so…

chemistry.chemical_classificationPrussian blueRenewable Energy Sustainability and the EnvironmentAnalytical chemistrySalt (chemistry)Nafion membraneCondensed Matter PhysicsElectric chargeSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonchemistry.chemical_compoundchemistrySolubilizationMaterials ChemistryElectrochemistryDissolutionJournal of The Electrochemical Society
researchProduct

Rheological behaviour, filmability and mechanical properties of biodegradable polymer films

2014

The rheological properties in shear flow and non isothermal elongational flow of two biodegradable polymers, belonging to two different classes of materials, have been measured and compared with those of a film blowing grade high density polyethylene in order to assess the filmability of these polymers. The mechanical properties of isotropic and anisotropic samples have been also reported.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceIsotropytechnology industry and agriculturePolymerBiodegradable polymerIsothermal processCondensed Matter::Soft Condensed MatterRheologychemistryHigh-density polyethyleneComposite materialAnisotropyShear flowbiodegradable filmAIP Conference Proceedings
researchProduct

Molecular modeling studies of interactions between sodium polyacrylate polymer and calcite surface

2013

Abstract The interactions between calcite pigment and sodium polyacrylate dispersing agent, widely used in papermaking as paper coating components, were investigated using classical force field and quantum chemical approaches. The objective was to understand interactions between the calcite surface and sodium polyacrylate polymer at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree–Fock method was also used to obtain detailed information about the sodium polyacrylate polymer structure. The effect of water molecules (moisture) on the interactions was also examined. Calculations showed that molecular weight, branching and the orientation of sodium polyacrylate…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceSodium polyacrylateSodiumInorganic chemistryAb initioGeneral Physics and Astronomychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryPolymerCondensed Matter PhysicsBranching (polymer chemistry)DispersantSurfaces Coatings and FilmsMolecular dynamicschemistry.chemical_compoundchemistryChemical engineeringPhysics::Atomic and Molecular ClustersMoleculePhysics::Chemical Physicsta116Applied Surface Science
researchProduct

Polymer droplets on substrates with striped surface domains: molecular dynamics simulations of equilibrium structure and liquid bridge rupture

2005

The structure of a polymer nanodroplet adsorbed on a flat lyophobic substrate chemically decorated with a lyophilic stripe of width 2RD is studied by molecular dynamics simulation of a coarse-grained bead–spring model of short macromolecules (containing N = 20 effective monomers). Varying the stripe width, the strength of the monomer–wall attraction and the temperature, the equilibrium morphology of the resulting droplets is studied and discussed in terms of current phenomenological theories. In the second part, the behaviour of a liquid bridge connecting two such lyophilic stripes a distance L apart is analysed. It is shown that for large enough L such free-standing films are unstable and …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMorphology (linguistics)NanotechnologyPolymerSubstrate (electronics)Condensed Matter PhysicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicsMonomerAdsorptionchemistryChemical physicsGeneral Materials ScienceThin filmMacromoleculeJournal of Physics: Condensed Matter
researchProduct

Photoinduced electron transfer in molecular organizates at the gas-water interface

1994

Abstract The influence of the molecular geometry is of fundamental importance for a better understanding of the photoinduced electron transfer mechanism. Because of their typical molecular structures, cyclophane rings have proved to be suitable for this purpose as electron acceptor molecules adsorbed under an amphiphile monolayer. We used a pyrene-labelled phospholipid derivative both as molecular anchor for the cyclophane ring and electron donor molecule. The co-spreading technique was used to prepare the complex monolayers. Surface pressure and surface potential measurements have indicated similar monolayer behaviour as with dimyristoylphosphatidic acid as anchor molecule, leading to the …

chemistry.chemical_classificationQuenching (fluorescence)ChemistryMetals and AlloysElectron donorSurfaces and InterfacesElectron acceptorPhotochemistryPhotoinduced electron transferSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferMonolayerMaterials ChemistryPyreneCyclophaneThin Solid Films
researchProduct

Structure and Yielding of Colloidal Silica Gels Varying the Range of Interparticle Interactions.

2016

The relationship between interaction range, structure, fluid-gel transition, and viscoelastic properties of silica dispersions at intermediate volume fraction, Φv ≈ 0.1 and in alkaline conditions, pH = 9 was investigated. For this purpose, rheological, physicochemical, and structural (synchrotron-SAXS) analyses were combined. The range of interaction and the aggregation state of the dispersions were tuned by adding either divalent counterions (Ca(2+)) or polycounterions (PDDA). With increasing calcium chloride concentration, a progressive aggregation was observed which precludes a fluid-gel transition at above 75 mM of calcium chloride. In this case, the aggregation mechanism is driven by s…

chemistry.chemical_classificationRange (particle radiation)Colloidal silicaInorganic chemistrychemistry.chemical_element02 engineering and technologyCalcium010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesViscoelasticity0104 chemical sciencesSurfaces Coatings and FilmsDivalentchemistryChemical engineeringRheologyVolume fractionMaterials ChemistryPhysical and Theoretical ChemistryCounterion[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph]0210 nano-technologyComputingMilieux_MISCELLANEOUSThe journal of physical chemistry. B
researchProduct

On the tribology and rheology of polymer brushes in good solvent conditions: a molecular dynamics study

2003

Tribological and rheological properties of two polymer brushes in relative sliding motion and good solvent conditions are investigated by means of molecular dynamics (MD) simulations. The lateral forces between the brushes are found to decrease logarithmically with increasing relative sliding velocity v0 over a range of more than one decade in v0. We also observe an almost logarithmic relaxation of the end-to-end distance vector that occurs after sliding is stopped. The coincidence of these logarithmic dependencies support the picture that friction between polymer brushes is small due to the retraction of the polymers from the interpenetration zone. The shear stress relaxes almost instantly…

chemistry.chemical_classificationRange (particle radiation)Materials scienceNanotechnologySurfaces and InterfacesPolymerTribologyCondensed Matter PhysicsSurfaces Coatings and FilmsMolecular dynamicschemistryRheologyMechanics of MaterialsChemical physicsMaterials ChemistryLubricationShear stressRelaxation (physics)Wear
researchProduct

Mechanism of Trichloroethene Hydrodehalogenation: A First-Principles Kinetic Monte Carlo Study

2014

A hydrodehalogenation (HDC) reaction of trichloroethene (TCE) has gained a lot of interest due to its possible application in water purification, but the reaction mechanism has been subject to much controversy. In this work, HDC of TCE on Pd(111) was examined by carrying out kinetic Monte Carlo simulations based on DFT-calculated thermodynamic and kinetic parameters. Obtained kMC results show that the HDC follows a so-called direct pathway, which means that, after adsorption on a catalyst, TCE quickly dechlorinates, producing CH–C and then, more slowly, hydrogenates to form hydrocarbon products. This is reflected in the surface coverage snapshots, where intermediates corresponding to the di…

chemistry.chemical_classificationReaction mechanismWork (thermodynamics)ChemistryKinetic energySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisGeneral EnergyAdsorptionHydrocarbonMechanism (philosophy)Computational chemistryOrganic chemistryKinetic Monte CarloPhysical and Theoretical Chemistryta116The Journal of Physical Chemistry C
researchProduct

Impact of aggregates on excitation dynamics in transparent polymer films doped by dipolar molecules

2008

Abstract Optical properties of transparent polymer films of polymethylmethacrylate doped (up to 25 wt.%) by dipolar N , N -dimethylaminobenzylidene 1,3-indandione (DMABI) molecules were studied. Formation of DMABI nanocrystallites, increasing in their density and size with dopant concentration, was revealed by optical microscopy. Transformation of the fluorescence spectrum from the molecular-like emission (for the low dopant concentration below 1 wt.%) to highly red-shifted fluorescence corresponding to self-trapped excitons in the crystallites was observed. It was shown, that due to the resonant energy transfer in the blend, the DMABI nanocrystals can serve as efficient fluorescence marker…

chemistry.chemical_classificationResonant inductive couplingMaterials scienceDopantExcitonDopingMetals and AlloysAnalytical chemistrySurfaces and InterfacesPolymerPhotochemistryFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceNanocrystalchemistryMaterials ChemistryCrystalliteThin Solid Films
researchProduct