Search results for "Diffusion"

showing 10 items of 1615 documents

New insights into seismic absorption imaging

2020

Abstract In recent years, attenuation has been used as a marker for source and dynamic Earth processes due to its higher sensitivity to small variations of lithospheric properties compared to seismic velocity. From seismic hazard analysis to oil and gas exploration and rock physics, many fields need a better reconstruction of energy absorption, a constituent of seismic attenuation generally considered a reliable marker of fluid saturation in space. Here, we propose absorption tomography (AT), a technique grounded on the principles of scattering tomography and Multiple Lapse Time Window Analysis. We benchmark its efficiency to image absorption in space by comparing its results with those obt…

Seismic attenuationDiffusion (acoustics)010504 meteorology & atmospheric sciencesPhysics and Astronomy (miscellaneous)Seismic attenuation; Scattering; Absorption; Tomography; DiffusionFault (geology)010502 geochemistry & geophysics01 natural sciencesPhysics::GeophysicsCodaAbsorptionScatteringDiffusionAbsorption (electromagnetic radiation)Tomography0105 earth and related environmental sciencesgeographygeography.geographical_feature_categoryAttenuationAstronomy and AstrophysicsTectonicsGeophysicsSeismic hazardSpace and Planetary ScienceTomographySeismology
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Protein diffusion through charged nanopores with different radii at low ionic strength

2014

[EN] The diffusion of two similar molecular weight proteins, bovine serum albumin (BSA) and bovine haemoglobin (BHb), through nanoporous charged membranes with a wide range of pore radii is studied at low ionic strength. The effects of the solution pH and the membrane pore diameter on the pore permeability allow quantifying the electrostatic interaction between the chargedpore and the protein. Because of the large screening Debye length, both surface and bulk diffusion occur simultaneously. By increasing the pore diameter, the permeability tends to the bulk self-diffusion coefficient for each protein. By decreasing the pore diameter, the charges on the pore surface electrostatically hinder …

Self assembled monolayersUltrafiltration membranesSurface PropertiesPHStatic ElectricityAnalytical chemistryGeneral Physics and AstronomyDiffusionHemoglobinsNanoporessymbols.namesakeProtein purificationAnimalsHemoglobinParticle SizePhysical and Theoretical ChemistryBovine serum albuminMolecular transportAqueous solutionsSerum AlbuminDebye lengthChemical PhysicsbiologyNanoporousChemistryOsmolar ConcentrationMicroporous membranesLight scatteringSerum Albumin BovineBovineHydrogen-Ion ConcentrationSurfaceNanoporeMembraneIsoelectric pointBovine serum albuminPermeability (electromagnetism)Chemical physicsFISICA APLICADAPhysical SciencesChemical Sciencesbiology.proteinsymbolsCattlePorosity
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Dynamic anomalies at the glass transition of organic van der Waals liquids

1993

Abstract The paper discusses the question of whether there is a characteristic temperature T c above the calorimetric glass transition temperature T g . Mode-coupling theory (MCT) predicts a crossover from liquid- to solid-like dynamics at T c . Neutron scattering and gradient NMR experiments have been carried out to test MCT using the molecular van der Waals liquid ortho -terphenyl as a model system. A significant anomaly of the Debye—Waller factor and a “decoupling” of self-diffusion from viscosity support the MCT predictions. A critical discussion of the relevance of such tests and of the limitations of neutron scattering is presented.

Self-diffusionCondensed matter physicsOrganic ChemistryNeutron scatteringCondensed Matter::Disordered Systems and Neural NetworksAnalytical ChemistryCondensed Matter::Soft Condensed MatterInorganic Chemistrychemistry.chemical_compoundViscositysymbols.namesakechemistryTerphenylsymbolsPhysics::Chemical PhysicsAnomaly (physics)Debye–Waller factorvan der Waals forceGlass transitionSpectroscopyJournal of Molecular Structure
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Heterogeneity at the Glass Transition:  Translational and Rotational Self-Diffusion

1997

Self-diffusion coefficients, D, have been measured in the glass forming liquids salol, glycerol, phenolphthaleine dimethyl ether (PDE), cresolphthaleine dimethyl ether (CDE), and ααβ-trinaphthylbenzene (TNB) in the supercooled regime. The NMR static magnetic field gradient technique was applied where D >10-14 m2 s-1 can be attained. The results are similar to previous diffusion experiments where an enhancement of translational diffusion was found in comparison with rotational diffusion and shear viscosity. Various models of spatial heterogeneity are related to a phenomenological environmental fluctuation model in view of recent diffusion and relaxation data close to the glass transition.

Self-diffusionDiffusionRelaxation (NMR)Rotational diffusionThermodynamicsMagnetostaticsSurfaces Coatings and FilmsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundNuclear magnetic resonancechemistryMaterials ChemistryDimethyl etherPhysical and Theoretical ChemistrySupercoolingGlass transitionThe Journal of Physical Chemistry B
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Surface Self-Diffusion and Mean Displacement of Hydrogen on Graphite and a PEM Fuel Cell Catalyst Support

2009

International audience; Quasielastic neutron scattering (QENS) measurements together with equilibrium molecular dynamic (EMD) simulations have been performed to investigate the surface interaction between hydrogen molecules and a carbon material commonly used in polymer electrolyte membrane fuel cells (PEMFC), called XC-72. Half a monolayer of molecular hydrogen was adsorbed on to the carbon material at 2 K. QENS spectra were recorded at the time-of-flight spectrometer IN5 at 40, 45, 50, 60, 70, 80, and 90 K. Simultaneously the pressure was measured as a function of time to monitor the equilibrium surface coverage at each temperature. By using the Chudley and Elliott model for jump diffusio…

Self-diffusionHydrogenCatalyst supportDiffusionAnalytical chemistryProton exchange membrane fuel cellchemistry.chemical_element02 engineering and technologyElectrolyte010402 general chemistry01 natural sciences7. Clean energy[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]GraphitePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSChemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistry[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]General EnergyQuasielastic neutron scattering[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technology
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Collective and self diffusion of PS microgels in solution as observed by thermal diffusion forced Rayleigh scattering

2007

Thermal diffusion in solutions of polystyrene micro-network spheres (microgels) in toluene has been studied by the holographic scattering technique of thermal diffusion forced Rayleigh scattering (TDFRS) and by photon correlation spectroscopy (PCS). Size distributions of microgels of different crosslink ratios are obtained from TDFRS measurements on dilute solutions at very low q-values around 4000cm−1. At low concentrations a single diffusive mode is observed and the diffusion coefficient increases with concentration. It is attributed to the collective diffusion of the microgels and the solvent. At high concentrations an additional slow mode appears whose diffusion coefficient decreases wi…

Self-diffusionMaterials scienceScatteringDispersityRelaxation (NMR)Analytical chemistryThermal diffusivityCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundchemistryDynamic light scatteringChemical physicsPolystyrenePhysics::Chemical PhysicsDiffusion (business)
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Si self-diffusion in cubic B20-structured FeSi

2008

Self-diffusion of implanted 31Si in the e-phase FeSi (cubic B20-structure) has been determined in the temperature range 660–810 °C using the modified radiotracer technique. With an activation enthalpy of 2.30 eV and a pre-exponential factor of 15×10−8 m2 s−1 the silicon diffusivity was found to be slightly slower than Ge impurity diffusion in FeSi. This difference is proposed to originate from attractive elastic interactions prevailing between the slightly oversized Ge atoms and the Si sublattice vacancies. The results confirm the argument that 71Ge radioisotopes may be used to substitute the short-lived 31Si radiotracers when estimating self-diffusion in silicides.

Self-diffusionMaterials scienceSiliconCondensed matter physicsEnthalpyGeneral Physics and Astronomychemistry.chemical_element02 engineering and technologyAtmospheric temperature range021001 nanoscience & nanotechnologyThermal diffusivity01 natural scienceschemistryImpurity diffusion0103 physical sciences010306 general physics0210 nano-technologyEPL (Europhysics Letters)
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Computer simulation of the glass transition of polymer melts

2007

Bond fluctuation models on square and simple cubic lattices at melt densities are simulated, using potentials depending on the length of the (effective) bond (and also on the bond angle, in d=3 dimensions). Various relaxation functions have the Kohlrausch-Williams-Watts (KWW) form; the associated relaxation time diverges as exp (const/T 2) in d=2 and as exp [const/T−T 0)] in d=3. For d=3 the self-diffusion constant also follows the Vogel-Fulcher law, with T 0=250 K for chain lengths N=20 and potentials adapted to bisphenol-A-polycarbonate [BPA-PC].

Self-diffusionMolecular geometryMaterials scienceComputational chemistryMonte Carlo methodRelaxation (NMR)ThermodynamicsCubic crystal systemGlass transitionConstant (mathematics)Square (algebra)
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Heptane adsorption in silicalite-1 : molecular dynamics simulation.

2009

Molecular dynamics (MD) simulations have been used to study the adsorption process of n-heptane molecules in silicalite-1 at 300 K. MD simulated results were compared to experimental neutron diffraction (ND) and experimental self-diffusion coefficients. The analysis of MD data indicated a packing of the adsorbed molecules around 4 mol./u.c., which is not the consequence of an enthalpic effect but of an entropic effect. The role of the n-heptane chain flexibility (cis–trans conformation) in relation with the silicalite-1 channel type (straight versus sinusoidal) was outlined and enabled to understand the mobility change arising at 4 mol./u.c., according to previous experimental results. The …

Self-diffusionNeutron diffractionThermodynamics02 engineering and technologyNeutron scattering010402 general chemistry01 natural sciences[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]chemistry.chemical_compoundMolecular dynamicsAdsorptionMoleculeGeneral Materials ScienceComputingMilieux_MISCELLANEOUSHeptaneChemistryGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciences[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Mechanics of MaterialsPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyEntropic force
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Dynamics of Copolymer Micelles in a Homopolymer Melt:  Influence of the Matrix Molecular Weight

2000

We have studied the dynamics of styrene−isoprene (SI) block copolymer micelles in a matrix of linear entangled polyisoprene (PI) chains, using forced Rayleigh scattering (FRS) and dynamic mechanica...

Self-diffusionPolymers and PlasticsChemistryOrganic ChemistryDynamics (mechanics)Concentration effectMicelleCondensed Matter::Soft Condensed MatterInorganic ChemistryMatrix (mathematics)Molten stateChemical engineeringPolymer chemistryMaterials ChemistryCopolymerForced Rayleigh scatteringPhysics::Chemical PhysicsMacromolecules
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