Search results for "Length scale"

showing 5 items of 75 documents

Detecting self-similarity in surface microstructures

2000

The relative configurational entropy per cell as a function of length scale is a sensitive detector of spatial self-similarity. For Sierpinski carpets the equally separated peaks of the above function appear at the length scales that depend on the kind of the carpet. These peaks point to the presence of self-similarity even for randomly perturbed initial fractal sets. This is also demonstrated for the model population of particles diffusing over the surface considered by Van Siclen, Phys. Rev. E 56 (1997) 5211. These results allow the subtle self-similarity traces to be explored.

Surface (mathematics)Length scalePhysicsCondensed Matter - Materials Scienceeducation.field_of_studySelf-similarityStatistical Mechanics (cond-mat.stat-mech)PopulationConfiguration entropyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesSurfaces and InterfacesFunction (mathematics)Condensed Matter PhysicsSurfaces Coatings and FilmsSierpinski triangleMaterials ChemistryPoint (geometry)Statistical physicseducationCondensed Matter - Statistical Mechanics
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Polymeric alloys: Model materials for the understanding of the statistical thermodynamics of mixtures

1997

Polymeric materials find industrial applications that are comparable to those of metals and ceramics.1 In addition to the great variability via the synthesis of various monomers and the choice of the degree of polymerization (N), alloying of polymers finds increasing attention for combining favorable materials properties.1,2 But polymeric (binary) alloys (A,B) of flexible polymers with chain lengths NA, NB are also most interesting for testing theoretical concepts: changing NA, NB one controls the entropy of mixing, keeping intermolecular forces invariant. Variation of these control parameters thus allows stringent tests of the theories on miscibility, unmixing etc. Furthermore, the large s…

chemistry.chemical_classificationLength scaleBinodalMaterials sciencechemistrySpinodal decompositionCritical point (thermodynamics)Intermolecular forceThermodynamicsPolymer blendPolymerEntropy of mixing
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Dynamics of Glassy Polymer Melts in Confined Geometry: A Monte Carlo Simulation

1996

Dynamic properties of a dense polymer melt confined between two hard walls are investigated over a wide range of temperatures by dynamic Monte Carlo simulation. The temperature interval ranges from the ordinary liquid to the strongly supercooled melt. The influence of temperature, density and confinement on the polymer dynamics is studied by various mean-square displacements, structural relaxation functions and quantities derived from them (relaxation times, apparent diffusion coefficients, monomer relaxation rates), yielding the following results: The motion of the monomers and polymers close to the walls is enhanced in parallel, but reduced in perpendicular direction. This dynamic anisotr…

chemistry.chemical_classificationLength scaleMaterials scienceCondensed matter physicsDiffusionMonte Carlo methodGeneral EngineeringThermodynamicsStatistical and Nonlinear PhysicsPolymerCondensed Matter::Soft Condensed MatterchemistryRadius of gyrationRelaxation (physics)AnisotropySupercoolingJournal de Physique I
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Tracer diffusion properties of core-shell latex films studied by photoinduced grating relaxation

2007

This article reports the application of the Photo-Induced Grating Relaxation technique (also known as Forced Rayleigh Scattering) to investigate the dynamics of films prepared from structured core–shell latex particles via the transport property of the photochromic tracer molecule Aberchrome 540®. The core–shell particles were prepared with a fluoropolymer core (immiscible and impenetrable to the tracer) and a poly(butyl methacrylate) shell. The incompletely dried films (with residual water) manifest their spatial heterogeneity via non-Fickian behavior (spatial scale- dependent apparent diffusion coefficient). The diffusion data was interpreted using the two-state diffusion model, previousl…

chemistry.chemical_classificationLength scaleMaterials sciencePolymers and PlasticsPolymerStrain hardening exponentCondensed Matter PhysicsFick's laws of diffusionchemistry.chemical_compoundsymbols.namesakechemistryChemical physicsPolymer chemistryMaterials ChemistrysymbolsFluoropolymerEffective diffusion coefficientPhysical and Theoretical ChemistryDiffusion (business)Rayleigh scatteringJournal of Polymer Science Part B: Polymer Physics
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Growing range of correlated motion in a polymer melt on cooling towards the glass transition

1999

Many liquids cooled to low temperatures form glasses (amorphous solids) instead of crystals. As the glass transition is approached, molecules become localized and relaxation times increase by many orders of magnitude1. Many features of this ‘slowing down’ are reasonably well described2 by the mode-coupling theory of supercooled liquids3. The ideal form of this theory predicts a dynamical critical temperature T c at which the molecules become permanently trapped in the ‘cage’ formed by their neighbours, and vitrification occurs. Although there is no sharp transition, because molecules do eventually escape their cage, its signature can still be observed in real and simulated liquids. Unlike c…

chemistry.chemical_classificationLength scaleMultidisciplinaryMaterials scienceCondensed matter physicsCritical phenomenaPolymerAmorphous solidCondensed Matter::Soft Condensed MatterchemistryCritical point (thermodynamics)Mode couplingGlass transitionSupercoolingNature
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