Search results for "FILMS"

showing 10 items of 2839 documents

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
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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
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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
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Aggregation Processes and Formation of Silico-calco-alkaline Gels under High Ionic Strength

2002

This paper presents a systematic in situ study of the process of formation of silico-calco-alkaline gels starting from a liquid colloidal solution containing different alkaline ions and different calcium concentration until the final gel state. The combined use of X-ray and neutron small-angle scattering (SAS) and dynamical rheometry techniques lead to a consistent description of the structure of the aggregates and of the mechanisms of aggregation involved in gel formation. SAS results indicate that the aggregates are fractal objects, their structure strongly depending on calcium ion concentration. The differences in gelation kinetics for systems containing different alkaline ions were attr…

chemistry.chemical_classificationRheometryKineticsInorganic chemistryConcentration effectFractal dimensionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCondensed Matter::Soft Condensed MatterBiomaterialsColloid and Surface ChemistrychemistryChemical engineeringIonic strengthMoleculeCounterionJournal of Colloid and Interface Science
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No-Flow Temperature in Injection Molding Simulation

2010

Most injection molding simulation packages use the no-flow temperature (NFT) as a means of determining whether the polymer flows or is solid. The NFT is not well defined, and a standard method for measuring it does not exist. A sensitivity analysis of the filling stage has been carried out with two different packages [VISI Flow (Vero Software Limited, Gloucestershire, UK) and Moldflow (Autodesk, Inc., San Rafael, CA)] to estimate the influence of the NFT on the main processing parameters. The NFT has a large influence on the thickness of the frozen layer, but it does not appreciably affect the filling pressure. Because the NFT affects the frozen layer, an effect on the estimation of shrinka…

chemistry.chemical_classificationSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciSettore ING-IND/24 - Principi Di Ingegneria ChimicaMaterials sciencePolymers and Plasticsinjection moldingFlow (psychology)General ChemistryPolymerMolding (process)Surfaces Coatings and FilmsAmorphous solidCrystallinitySettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMaterials ChemistryForensic engineeringprocessingSensitivity (control systems)simulationsWell-definedComposite materialShrinkage
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The influence of counterions and hydrophobic moieties on the thermostability of Langmuir-Blodgett multilayers

1994

Abstract Langmuir-Blodgett (LB) multilayers with various counterions and different organic moieties (one- and two-chain fatty acids, polymeric acid) are prepared to investigate on line temperature-dependent structural changes and desorption by small-angle X-ray scattering (SAXS), interference-enhanced reflection and Nomarsky microscopy. On temperature increase a sequence of phase transitions can be observed. A crystalline LB film melts to a fluid phase and eventually desorbs either from droplets or from a homogeneous film. The phase sequence depends on the counterion: nickel stearate and magnesium stearate melt while the layered structure is conserved; SAXS measurements reveal a continuous,…

chemistry.chemical_classificationSmall-angle X-ray scatteringMetals and AlloysSurfaces and InterfacesLangmuir–Blodgett filmSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryChemical engineeringStearatePhase (matter)Materials ChemistryOrganic chemistryThermal stabilityMagnesium stearateStearic acidCounterionThin Solid Films
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Fluorescence excitation and emission spectroscopy on single MEH-PPV chains at low temperature.

2008

Fluorescence emission and excitation spectra of single MEH-PPV polymer molecules dispersed in thin PMMA films have been recorded at 1.2 and 20 K. We observe single as well as multichromophore emission in single chain emission spectra, whereby the relative fractions depend on the two different molecular weights (50 and 350 kDa) studied. The molecular weight also affects the distribution of peak emission maxima, which is monomodal (bimodal) for the low (high) molecular weight. The appearance of an additional "red" subpopulation for the high molecular weight sample is attributed to interactions of multiple chromophores from a sufficiently flexible single chain. The comparison of emission spect…

chemistry.chemical_classificationSpectral shape analysisMolecular massAnalytical chemistryAstrophysics::Cosmology and Extragalactic AstrophysicsPolymerChromophoreFluorescenceSurfaces Coatings and FilmschemistryMaterials ChemistryMoleculeEmission spectrumPhysical and Theoretical ChemistryAstrophysics::Galaxy AstrophysicsExcitationThe journal of physical chemistry. B
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Pressure-induced cooperative spin transition in ironII 2D coordination polymers: room-temperature visible spectroscopic study.

2011

For the 2D coordination polymers [Fe(3-Fpy)(2)M(II)(CN)(4)] (M(II) = Ni, Pd, Pt), the pressure-induced spin crossover behavior has been investigated at 298 K by monitoring the distinct optical properties associated with each spin state. Cooperative first-order spin transition characterized by a piezohysteresis loop ca. 0.1 GPa wide was observed for the three derivatives. Application of the mean field regular solution theory has enabled estimation of the cooperative parameter, Γ(p), and the enthalpy, ΔH(HL)(p), associated with the spin transition for each derivative. These values, found in the intervals 6.8-7.9 and 18.6-20.8 kJ mol(-1), respectively, are consistent with those previously repo…

chemistry.chemical_classificationSpin statesCondensed matter physicsEnthalpySpin transitionElastic energyPolymerSurfaces Coatings and FilmschemistryMean field theorySpin crossoverMaterials ChemistryPhysical chemistryPhysical and Theoretical ChemistrySpin-½The journal of physical chemistry. B
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Internal rotation of 1,2-dichloroethane in haloalkane dehalogenase. A test case for analyzing electrostatic effects in enzymes

2003

1,2-Dichoroethane (DCE) is a prototypical molecule for studying electrostatic solvent effects on molecular conformation as far as rotation around the carbon−carbon bond notably changes the electric...

chemistry.chemical_classificationStereochemistryInternal rotation12-DichloroethaneRotationMolecular conformationSurfaces Coatings and Filmschemistry.chemical_compoundEnzymechemistryComputational chemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistrySolvent effectsHaloalkane dehalogenase
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The cyclic [N(PiPr2E)2]+ (E = Se, Te) cations: a new class of inorganic ring system.

2006

The two-electron oxidation of [(tmeda)NaN(PiPr2E)2] with iodine produces the cyclic [N(PiPr2E)2]+ (E = Se, Te) cations, which exhibit long E–E bonds in the iodide salts. peerReviewed

chemistry.chemical_classificationStereochemistryIodideMetals and Alloyschemistry.chemical_elementliganditGeneral ChemistryRing (chemistry)IodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsdikalkogenoimidodifosfinaatitdichalcogenoimidodiphosphinateschemistryMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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