Search results for "Monte Carlo method"

showing 10 items of 1234 documents

Recent Developments in Monte Carlo Simulations of Lattice Models for Polymer Systems

2008

A brief review is given of methodological advances made during the past decade with the Monte Carlo sampling of equilibrium properties of simple lattice models of polymer systems, and representative applications of these new algorithms are summarized. These algorithms include Wang−Landau (WL) sampling, the pruned-enriched Rosenbluth method (PERM), and topology violating dynamic Monte Carlo algorithms such as combinations of local moves, slithering snake moves, and “double bridging” moves for the bond fluctuation model. The applications mentioned concern phase-transition-like phenomena of single chains (collapse and crystallization in bad solvents; interplay of collapse and adsorption; escap…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodBinary numberPolymerCondensed Matter::Soft Condensed MatterInorganic ChemistryIntramolecular forceLattice (order)Materials ChemistryDynamic Monte Carlo methodStatistical physicsPolymer blendBond fluctuation modelMacromolecules
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Stimuli-responsive brushes with active minority components: Monte Carlo study and analytical theory

2015

Using a combination of analytical theory, Monte Carlo simulations, and three dimensional self-consistent field calculations, we study the equilibrium properties and the switching behavior of adsorption-active polymer chains included in a homopolymer brush. The switching transition is driven by a conformational change of a small fraction of minority chains, which are attracted by the substrate. Depending on the strength of the attractive interaction, the minority chains assume one of two states: An exposed state characterized by a stem-crown-like conformation, and an adsorbed state characterized by a flat two-dimensional structure. Comparing the Monte Carlo simulations, which use an Edwards-…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodBrushFOS: Physical sciencesPolymerFlory–Huggins solution theoryCondensed Matter - Soft Condensed Matterlaw.inventionCondensed Matter::Soft Condensed MatterInorganic Chemistrysymbols.namesakelawThermalExcluded volumeMaterials ChemistrysymbolsDynamic Monte Carlo methodSoft Condensed Matter (cond-mat.soft)Statistical physicsHamiltonian (quantum mechanics)
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Glass transition of polymer melts: Test of theoretical concepts by computer simulation.

2003

Abstract Polymers are good glass formers and allow for the study of melts near the glass transition in (meta-)stable equilibrium. Theories of the glass transition imply such an equilibrium and can, hence, be tested by the study of polymer melts. After a brief summary of the basic experimental facts about the glass transition in polymers, the main theoretical concepts are reviewed: mode coupling theory (MCT), entropy theory, free-volume theory, the idea of a growing length describing the size of cooperative regions, etc. Then, two basic coarse-grained models of polymers are described, which have been developed aiming at a test of these concepts. The first model is the bond-fluctuation model …

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodConfiguration entropy02 engineering and technologySurfaces and InterfacesPolymer021001 nanoscience & nanotechnology01 natural sciencesCondensed Matter::Soft Condensed MatterMolecular dynamics0103 physical sciencesMode couplingMaterials ChemistryCeramics and CompositesEntropy (information theory)Kinetic Monte CarloStatistical physics010306 general physics0210 nano-technologyGlass transition[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]
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Adsorption Transition of a Polymer Chain at a Weakly Attractive Surface: Monte Carlo Simulation of Off-Lattice Models

2002

A bead-spring model of a polymer chain with one end attached to a wall is studied by Monte Carlo simulations for chain lengths 16 ≤ N ≤ 256. Two types of adsorption potentials, 9-3 and 10-4 Lennard-Jones (LJ) potentials, between the effective monomers and the wall are assumed. For both cases the adsorption transition where the chain changes its asymptotic statistical properties from a three-dimensional to a two-dimensional configuration is located using a scaling analysis. It is shown that the crossover exponent φ = 0.50 ± 0.02 is the same for both LJ potentials. This value is compatible with recent theoretical predictions and simulation results for lattice models with short-range wall pote…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodCrossoverThermodynamicsStatistical mechanicsPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterInorganic ChemistryAdsorptionLattice (order)Materials ChemistryExponentStatistical physicsScalingMacromolecular Theory and Simulations
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Interfaces between coexisting phases in polymer mixtures: What can we learn from Monte Carlo simulations?

1999

Symmetric binary polymer mixtures are studied by Monte Carlo simulation of the bond fluctuation model, considering both interfaces between coexisting bulk phases and interfaces confined in thin films. It is found that the critical behavior of interfacial tension and width is compatible with that of the Ising model, as expected from the universality principle. In the strong segregation limit, only qualitative but not quantitative agreement with the self-consistent field (SCF) theory is found. It is argued that the SCF theory requires √ 6 X √D for short-range forces, in agreement with experiment.

chemistry.chemical_classificationPolymers and PlasticsCondensed matter physicsOrganic ChemistryMonte Carlo methodBinary numberPolymerCondensed Matter PhysicsUniversality (dynamical systems)Condensed Matter::Soft Condensed MatterSurface tensionchemistryMaterials ChemistryIsing modelPolymer blendStatistical physicsThin filmMacromolecular Symposia
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Computer simulation of macromolecular materials

1988

Computer simulation of model systems with Monte Carlo methods enables the detailed study of structure and thermodynamic properties of these systems and thus constitutes a link between analytic theory and experiment. Typical applications that are discussed include polymer blends, dynamics of local motions in polymer melts, and the adsorption of polymers on walls.

chemistry.chemical_classificationPolymers and PlasticsPolymer scienceMonte Carlo methodPolymerCondensed Matter::Soft Condensed MatterReptationMolten stateColloid and Surface ChemistrychemistryMaterials ChemistryPolymer blendStatistical physicsPhysical and Theoretical ChemistryDiffusion (business)Phase diagramMacromoleculeColloid & Polymer Science
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Structure and dynamics of thin polymer films: a case study with the bond-fluctuation model

2002

Abstract This paper reports Monte Carlo simulation results of a polymer melt of short, non-entangled chains which are embedded between two impenetrable walls. The melt is simulated by the bond-fluctuation lattice model under athermal conditions, i.e. only excluded volume interactions between the monomers and between the monomers and the walls are taken into account. In the simulations, the wall separation is varied from about one to about 15 times the bulk radius of gyration R g . The confinement influences both static and dynamic properties of the films: Chains close to the walls preferentially orient parallel to it. This parallel orientation decays with increasing distances from the wall …

chemistry.chemical_classificationPreferential alignmentLattice model (finance)Polymers and PlasticsCondensed matter physicsChemistryOrganic ChemistryMonte Carlo methodPolymerCondensed Matter::Soft Condensed MatterOrientation (geometry)Excluded volumeMaterials ChemistryRadius of gyrationStatistical physicsThin filmPolymer
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Anomalous diffusion in polymer melts

2002

Abstract We present a study of the anomalous diffusion regimes in polymer melt dynamics performing a Monte Carlo (MC) simulation of the bond-fluctuation lattice model. Special emphasis is laid on the crossover from a Rouse-like motion to the behavior predicted by reptation theory. For the longest chains of N=400 the high statistical accuracy of the data allows for clear identification of the subdiffusive regimes in the center of mass motion and the monomer displacement. They are well compatible with those predicted by reptation theory. Furthermore a detailed analysis of the different short time anomalous diffusion regimes in the melt dynamics of polymer chains is presented and it is shown t…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesAnomalous diffusionMonte Carlo methodCrossoverGeneral Physics and AstronomyThermodynamicsPolymerDisplacement (vector)Condensed Matter::Soft Condensed MatterReptationchemistryStatistical physicsCenter of massPhysical and Theoretical ChemistryLattice model (physics)Chemical Physics
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Interfaces in immiscible polymer blends: A Monte Carlo simulation approach on the CRAY T3E

1999

Polymeric materials pose a challenge for Monte Carlo simulations because of the widely spread length and time scales involved. Using large scale computer simulations we investigate the interfacial structure in a partially compatible polymer mixture. The problem is studied in the framework of a coarse grained lattice model - the bond fluctuation model on the simple cubic lattice, choosing N = 32 and lattice linear dimensions L × L × D up to 512 × 512 × 64. We employ a two dimensional geometric decomposition scheme to implement this algorithm on the CRAY T3E. The algorithm scales very well with the number of processors. The structure of polymer coils near interfaces between coexisting phases …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesCapillary waveComputer scienceMonte Carlo methodPolymerComputational scienceCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerDistribution functionchemistryChemical physicsLattice (order)CopolymerPolymer blend
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Structure and dynamics of grafted polymer layers: A Monte Carlo simulation

1991

The bond fluctuation model of polymer chains on lattices is used to study layers of polymers anchored with one end at a hard wall, assuming good solvent conditions and repulsive interactions between the monomers and the wall. Chain lengths from N=10 to N=80 and grafting densities σ from 0.025 to 0.20 are considered, both for the ‘‘quenched’’ case, where the anchor points are kept fixed at randomly chosen surface sites, and the ‘‘annealed’’ case, where lateral diffusion of the anchored ends at the wall is considered. Profiles of monomer density and free end density, chain linear dimensions parallel and perpendicular to the wall, as well as corresponding mean square displacements of inner and…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesChemistryMonte Carlo methodRelaxation (NMR)General Physics and AstronomyPolymerMolecular physicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerChain (algebraic topology)Chemical bondPerpendicularStatistical physicsPhysical and Theoretical ChemistryScalingThe Journal of Chemical Physics
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