Search results for "Diffusion"

showing 10 items of 1615 documents

Self-Diffusion of Associating Star-Shaped Polymers

2016

The dynamics of associating bonds in transient polymer networks exerts a paramount influence on their relaxation and time-dependent mechanical properties. In particular, diffusive motion of polymers mediated by the dissociation and association equilibrium of reversible junctions can affect the materials’ structural stability, dynamic mechanical properties, and a broad spectrum of functionality that arises from the constant motion of polymer chains. In this work, forced Rayleigh scattering is used to measure the diffusion of terpyridine end-functionalized four-arm poly(ethylene glycol) polymers transiently interlinked by zinc ions in organic solvent across a wide range of length and time sca…

chemistry.chemical_classificationSelf-diffusionPolymers and PlasticsConstant of motionOrganic Chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFick's laws of diffusionDissociation (chemistry)0104 chemical sciencesInorganic ChemistrychemistryStructural stabilityChemical physicsPolymer chemistryMaterials ChemistryExponent0210 nano-technologyScalingMacromolecules
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Observation of Very Narrow Linewidths in the Fluorescence Excitation Spectra of Single Conjugated Polymer Chains at 1.2 K

2007

Fluorescence emission and excitation spectra of single poly[2-methoxy-5-(2'-ethyl-hexyloxy)-1,4-phenylene vinylene] polymer molecules embedded in poly(methylmethacrylate) have been recorded at 1.2 K. The ubiquitous spectral diffusion causes large variations in the spectral shape and apparent linewidth in the emission spectra. Nevertheless, we find very narrow (approximately 0.1 cm(-1)) purely electronic zero-phonon lines in the excitation spectra, which are 2 orders of magnitude smaller than previous estimates of the homogeneous linewidth. These results complement the molecular description of the low energy transitions in conjugated polymers.

chemistry.chemical_classificationVinyl CompoundsMaterials sciencePolymersGeneral Physics and AstronomyPolymerConjugated systemMolecular physicsFluorescenceFluorescenceLaser linewidthNuclear magnetic resonanceOrders of magnitude (time)chemistryPolymethyl MethacrylateMoleculeEmission spectrumDiffusion (business)Physical Review Letters
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Time-monitoring sensor based on oxygen diffusion in an indicator/polymer matrix

2013

Abstract A time-monitoring sensor based on the oxidation of leuco methylene blue (LMB) to methylene blue (MB) was developed. The sensor changes its color from yellow to green in the presence of oxygen and was integrated into a poly(vinyl alcohol) matrix. The diffusion of the oxygen in the polymer matrix as well as the oxygen uptake due to the oxidation reaction determines the time monitoring of the sensor. A physical model has been developed that accounts for both the diffusion as well as the oxidation reaction. For this purpose, the reaction kinetics was determined experimentally. Moreover, the diffusion coefficient of oxygen was determined and concentration profiles in the polymer matrix …

chemistry.chemical_classificationVinyl alcoholChemistryDiffusionMetals and AlloysAnalytical chemistrychemistry.chemical_elementPolymerCondensed Matter PhysicsOxygenRedoxSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (chemical analysis)Chemical kineticschemistry.chemical_compoundMaterials ChemistryElectrical and Electronic EngineeringInstrumentationMethylene blueSensors and Actuators B: Chemical
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LARGE DEFORMATION CREEP BEHAVIOR OF A SOLID POLYMER.

1981

Abstract The effect of loading rate and strain on the creep behavior after sample yielding has been studied in previous communications (14–15) for Mylar in tension and for Lexan in compression. In this work the creep behavior of Lexan samples previously elongated is considered both in tension and in compression. A procedure which collects all the data independently of both loading rate and initial creep strain is proposed.

chemistry.chemical_classificationWork (thermodynamics)Large deformationMaterials sciencePolymers and PlasticsTension (physics)General Chemical EngineeringDiffusion creepPolymerCompression (physics)Analytical ChemistrychemistryCreepLoading rateComposite material
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Factors influencing the transport of tryptophan hydrochloride through supported liquid membranes containing macrocyclic carriers

1997

Commercially available PTFE membranes were used as a support for liquid membranes in amino acid transport. Using tryptophan as a model amino acid, the influence of the type of organic liquid, kind of macrocyclic carrier and counter-ion on transport efficiency was examined. These studies show the strong influence of the kind of the counter-ion co-transported with amino acid cation, and the type of macrocyclic carrier used on the transport efficiency. The transport efficiency depends also on the pH of the source phase and on the nature of the organic liquid used as a membrane solvent. Liquid membranes supported on commercial porous-PTFE-membranes with hydrophobic solvents are stable for more …

chemistry.chemical_classificationamino acidsFacilitated diffusionHydrochlorideInorganic chemistryTryptophanFiltration and SeparationBiochemistrysupported liquid membranesAmino acidmembrane stabilitySolventPartition coefficientchemistry.chemical_compoundMembranechemistryOrganic chemistryGeneral Materials Sciencefacilitated transportPhysical and Theoretical ChemistryCounterionJournal of Membrane Science
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QENS from polymeric micelles in supercritical CO[sub 2]

2000

We report QENS measurements from PS-b-PFOA aggregates in supercritical CO2. These consist of dense cores of CO2-insoluble polystyrene surrounded by a ‘corona’ of PFOA surfactant molecules whose CO2-philic groups interface with supercritical CO2. Lineshapes are dominated by localized diffusive modes and segmental dynamics of the anchored, finite-length PFOA chains. For Q∼0.6 A−1, we obtain effective diffusion coefficients of ≈0.8×10−6 cm2/sec. At higher Q, a single component is not sufficient as shown by excess intensity on the flanks. For Q>1.5 A−1, the wings reflect contributions due to a distribution of faster, more localized chain modes.

chemistry.chemical_classificationchemistry.chemical_compoundCrystallographychemistryChemical physicsDiffusionMoleculePolymerPolystyreneCrystal structureNeutron scatteringSupercritical fluidPhase diagramAIP Conference Proceedings
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Transport of amino acids and their phosphonic acid analogues through supported liquid membranes containing macrocyclic carriers. Experimental paramet…

1991

Abstract Amino acid hydrochlorides are well transported through 1-decanol membranes containing Kryptofix 5 or 222 and supported in a porous polyacrylonitrile hollow fiber matrix. Factors which influence the transport of phenylalanine hydrochloride were studied in some detail using this sheet- as well as hollow fibre-supported liquid membranes. These studies show that the choice of the membrane phase, the kind of polymeric support and the mode of membrane preparation are of great importance for the efficiency of the process. The most vital step in the membrane preparation appears to be its activation by soaking in a solution of phenylalanine hydrochloride in a water-ethanol or water-propanol…

chemistry.chemical_classificationorganic separationsamino acid transportChemistryHydrochloridediffusiontechnology industry and agricultureIonophoreAqueous two-phase systemPolyacrylonitrileFiltration and SeparationPhenylalanineBiochemistryMembrane technologyAmino acidchemistry.chemical_compoundMembraneliquid membranePolymer chemistrymembrane carriersOrganic chemistryGeneral Materials Sciencefacilitated transportsupported liquid membranePhysical and Theoretical ChemistryJournal of Membrane Science
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Effect of Temperature on Isobutyric Acid Loss during Roasting of Carob Kibble

1997

The high content of isobutyric acid in carob (Ceratonia siliqua L.) constitutes a handicap for some of its potential uses due to the undesirable smell produced by that compound. In this study the loss of isobutyric acid during roasting was approached by heating the carob kibble at temperatures from 120 to 180 °C in two local cultivars (Matalafera and Lisa). The initial content of isobutyric acid varied between 6.3 (Lisa) and 9.4 (Matalafera) g isobutyric acid/kg dry solid. Results showed that the process can be described by a diffusive model. The activation energy of the process is about 55 kJ/mol for both cultivars. Keywords: Carob pod; roasting; isobutyric acid; diffusion

chemistry.chemical_compoundCeratonia siliquafoodChemistryDiffusionBotanyGeneral ChemistryActivation energyFood scienceGeneral Agricultural and Biological Sciencesfood.foodIsobutyric acidRoastingJournal of Agricultural and Food Chemistry
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Glucose Diffusion Coefficients Determined from Concentration Profiles in Emt6 Tumor Spheroids Incubated in Radioactively Labeled L-Glucose

1994

In order to theoretically assess tissue energetic status, conditions for substance exchange need to be known. One group of parameters important in this context are diffusion coefficients of nutrients and metabolic waste products which may be assessed by incubating spheroids in a medium containing tracer amounts of the radioactively labeled substance in question, for a defined period of time. In previous studies, the overall amount of 14C-labeled substance taken up by the spheroids was measured by scintillation counters (e.g.[1]), or the concentration of 3H-labeled substance in the spheroid center was determined by autoradiography and grain counting (e.g. [4]). From a number of such measurem…

chemistry.chemical_compoundChromatographyL-GlucoseChemistryTRACERDiffusionembryonic structuresScintillation counterTumor spheroidSpheroidContext (language use)Densitometry
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Effects of VTE Treatment on Composition of Lithium Tantalate Single Crystals

2011

The vapour transport equilibration (VTE) is used to change the Li/Ta ratio in lithium tantalate single crystals of different crystallographic orientations (Z-cut and Y/128°-cut). Treatment by VTE is shown to provide thin layers in lithium tantalate plates composition of which is close to stoichiometric while the values of the coercive field are different, much smaller compared with congruent single crystals. There are several mechanisms of diffusion of the Li+ ions in LiTaO3 under conditions of VTE the contribution of each being dependent on the crystallographic orientation of the sample.

chemistry.chemical_compoundMaterials scienceThin layerschemistryDiffusionLithium tantalateAnalytical chemistryCoercivityCondensed Matter PhysicsStoichiometryElectronic Optical and Magnetic MaterialsIonFerroelectrics
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