Search results for "Monte Carlo method"

showing 10 items of 1234 documents

Brownian dynamics simulation of grafted polymer brushes

1995

We present results of computer simulations by the method of Brownian dynamics of polymeric brushes attached to impenetrable planes. For testing both model and method we have used one polymer brush attached to a repulsive plane and compare some results with Monte Carlo results of Lai and Binder on the bond fluctuation model. We have also studied two polymeric brushes attached to two parallel planes at different distances between planes, and investigate the interplay between the interpenetration of the brushes and the configurational properties of the grafted chains.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsChemistryPlane (geometry)Organic ChemistryMonte Carlo methodPolymerCondensed Matter PhysicsPolymer brushdigestive systemCondensed Matter::Soft Condensed MatterInorganic ChemistryComputer Science::GraphicsIntermolecular interactionChemical physicsMaterials ChemistryBrownian dynamicsStatistical physicsStructure factorBond fluctuation modelMacromolecular Theory and Simulations
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Structure of a bidisperse polymer brush: Monte Carlo simulation and self-consistent field results

1992

Using the bond-fluctuation model, Monte Carlo simulations are performed for polymer brushes composed of chains of two different chain lengths under good solvent condition. Profiles of monomer density and free end density, chain linear dimensions, and average monomer position along a chain are studied. Quantities measured in the simulations are derived from the analytic self-consistent field (SCF) theory and compared with the simulation data. The structural properties can be quite accurately described by the theory only when both the long and short chains are stretched

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsField (physics)Organic ChemistryMonte Carlo methodStructure (category theory)PolymerPolymer brushMolecular physicsCondensed Matter::Soft Condensed MatterInorganic Chemistrychemistry.chemical_compoundMonomerChain (algebraic topology)chemistryPosition (vector)Materials ChemistryStatistical physicsMacromolecules
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Comb-Branched Polymers:  Monte Carlo Simulation and Scaling

1996

The Monte Carlo simulation technique (the bond fluctuation model) has been used for the study of the equilibrium conformations of comb-branched polymers consisting of a long flexible main chain and side chains grafted at a regular separation onto the main chain. The solvent has been supposed to be good (athermal) for the main and side chains. The global conformation and the gyration radius of the polymer, as well as the local conformational structure of the comb, have been analyzed as functions of the length of the side chains and spacers. The effect of induced rigidity of the comb due to the interaction between side chains has been observed. We have found the results of the simulation to b…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsOrganic ChemistryMonte Carlo methodPhysics::OpticsPolymerGyrationCondensed Matter::Soft Condensed MatterInorganic ChemistryRigidity (electromagnetism)chemistryChemical physicsMaterials ChemistrySide chainRadius of gyrationStatistical physicsScalingBond fluctuation modelMacromolecules
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Monte Carlo simulations of the polymer glass transition: From the test of theories to material modeling

1997

We present results on the glass transition in polymer melts using Monte Carlo simulations of the bond fluctuation lattice model. There are two questions we address in this work. What is the temperature dependence of the entropy density in such a model polymer melt and how well is it described by theories like the Gibbs-DiMarzio theory of the glass transition? And to what degree is one able to map the Hamiltonian of such an abstract lattice model onto a specific polymer material and use it to model the large scale and long time properties of a realistic polymer melt?

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed Mattersymbols.namesakeEntropy densitychemistryMaterials ChemistrysymbolsHamiltonian (quantum mechanics)Glass transitionPolymer meltMacromolecular Symposia
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How does the pattern of grafting points influence the structure of one-component and mixed polymer brushes?

2005

Using Monte Carlo simulations of a coarse-grained bead-spring model we study the lateral structure formation of one-component polymer brushes in a bad solvent and of a mixed polymer brush upon increasing the incompatibility of the two species. We compare the morphology of the brush with a regular distribution of grafting points and with a random arrangement. Density or composition fluctuations of the grafting points enhance the formation of irregular structures but randomness prevents the formation of long-range order. Even small fluctuations of the grafting points are sufficient to pin the lateral structures of the brush.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesStructure formationMaterials scienceMorphology (linguistics)Monte Carlo methodGeneral Physics and AstronomyBrushNanotechnologyPolymerPolymer brushGraftinglaw.inventionCondensed Matter::Soft Condensed MatterComputer Science::GraphicschemistrylawComposite materialRandomnessEurophysics Letters (EPL)
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Entropy theory and glass transition: A test by Monte Carlo simulation

1997

This article reviews the results of a test of the Gibbs-DiMarzio theory by Monte Carlo Simulation. The simulation employed the bond-fluctuation model on a simple cubic lattice. This model incorporates two kinds of interactions: the excluded volume interaction among all monomers of the melt and an internal energy of the chains, which favors large bonds and makes the chains stiffen with decreasing temperature. The stiffening of the chains leads to an increase of their volume requirements, which competes with the packing constraints at low temperatures. This competition strongly slows down the structural relaxation of the melt and induces the glassy behavior. The model therefore takes into acc…

chemistry.chemical_classificationQuantitative Biology::Biomoleculesbond-fluctuation modelMaterials scienceInternal energyMonte Carlo methodGibbs-DiMarzio theoryGeneral EngineeringThermodynamicsSimple cubic latticePolymerArticleStiffeningCondensed Matter::Soft Condensed Matterentropy measurementchemistryExcluded volumeAdam-Gibbs theoryEntropy (information theory)chemical potentialglass transitionStatistical physicsdiffusion coefficientGlass transitionMonte Carlo simulation
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Interfacial properties of glassy polymer melts: A Monte Carlo study

1996

The properties of the interface between a polymer melt and a solid wall are studied over a wide range of temperatures by dynamic Monte Carlo simulations. It is shown that in the supercooled state near the glass transition of the melt an “interphase” forms, the structure of which is influenced by the wall. The thickness of this interphase is determined from the monomer density profile near the surface and is strongly temperature dependent. At low glass-like temperatures it is larger than the bulk radius of gyration of the chains.

chemistry.chemical_classificationRange (particle radiation)Materials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerCondensed Matter PhysicsCondensed Matter::Disordered Systems and Neural NetworksCondensed Matter::Soft Condensed MatterCrystallographychemistry.chemical_compoundMonomerchemistryMaterials ChemistryRadius of gyrationInterphaseSupercoolingGlass transitionMacromolecular Symposia
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Polymer translocation through a nanopore induced by adsorption: Monte Carlo simulation of a coarse-grained model

2004

Dynamic Monte Carlo simulation of a bead-spring model of flexible macromolecules threading through a very narrow pore in a very thin rigid membrane are presented, assuming at the cis side of the membrane a purely repulsive monomer-wall interaction, while the trans side is attractive. Two choices of monomer-wall attraction epsilon are considered, one choice is slightly below and the other slightly above the "mushroom to pancake" adsorption threshold epsilon(c) for an infinitely long chain. Studying chain lengths N=32, 64, 128, and 256 and varying the number of monomers N(trans) (time t=0) that have already passed the pore when the simulation started, over a wide range, we find for epsiloneps…

chemistry.chemical_classificationRange (particle radiation)Monte Carlo methodGeneral Physics and AstronomyPolymerNanoporeAdsorptionMembranechemistryChemical physicsStatistical physicsPhysical and Theoretical ChemistryPorosityScalingThe Journal of Chemical Physics
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Conformational studies of bottle-brush polymers absorbed on a flat solid surface.

2010

The adsorption of a bottle-brush polymer end-grafted with one chain end of its backbone to a flat substrate surface is studied by Monte Carlo simulation of a coarse-grained model, that previously has been characterized in the bulk, assuming a dilute solution under good solvent conditions. Applying the bond fluctuation model on the simple cubic lattice, we vary the backbone chain length $N_b$ from $N_b=67$ to $N_b = 259$ effective monomeric units, the side chain length $N$ from N=6 to N=48, and the grafting density $\sigma=1$, i.e., parameters that correspond well to the experimentally accessible range. When the adsorption energy strength $\epsilon$ is varied, we find that the adsorption tra…

chemistry.chemical_classificationRange (particle radiation)Quantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodGeneral Physics and AstronomyBackbone chainThermodynamicsFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterGyrationCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerAdsorptionchemistrySide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryThe Journal of chemical physics
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From orientational glasses to structural glasses: What computer simulations have contributed to understand experiments

2002

Abstract Orientational glasses, produced by random dilution of molecular crystals, exhibit a freezing transition of the quadrupole moments. Monte Carlo simulations of lattice models (generalization of the Edwards–Anderson spin glass model) have been used to elucidate this behavior. While short range models exhibit a static glass transition at zero temperature only, the infinite range Potts glass exhibits a transition where a glass order parameter appears discontinuously. At higher temperature, a dynamical transition occurs, described by mode-coupling theory (MCT). MCT has also been tested by Monte Carlo and molecular dynamics simulations of coarse-grained models of glass-forming polymers. W…

chemistry.chemical_classificationSpin glassCondensed matter physicsMonte Carlo methodPolymerCondensed Matter PhysicsCondensed Matter::Disordered Systems and Neural NetworksElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed MatterMolecular dynamicschemistryLattice (order)Materials ChemistryCeramics and CompositesGlass transitionAnderson impurity modelPotts modelJournal of Non-Crystalline Solids
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