Search results for "Monte Carlo method"

showing 10 items of 1234 documents

Dragging a Polymer Chain into a Nanotube and Subsequent Release

2008

We present a scaling theory and Monte Carlo (MC) simulation results for a flexible polymer chain slowly dragged by one end into a nanotube. We also describe the situation when the completely confined chain is released and gradually leaves the tube. MC simulations were performed for a self-avoiding lattice model with a biased chain growth algorithm, the pruned-enriched Rosenbluth method. The nanotube is a long channel opened at one end and its diameter $D$ is much smaller than the size of the polymer coil in solution. We analyze the following characteristics as functions of the chain end position $x$ inside the tube: the free energy of confinement, the average end-to-end distance, the averag…

chemistry.chemical_classificationLattice model (finance)NanotubeCritical distanceMaterials scienceStatistical Mechanics (cond-mat.stat-mech)Polymers and PlasticsOrganic ChemistryMonte Carlo methodFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterMolecular physicsInorganic ChemistrychemistryChain (algebraic topology)Phase (matter)Materials ChemistrySoft Condensed Matter (cond-mat.soft)Tube (fluid conveyance)Condensed Matter - Statistical MechanicsMacromolecules
researchProduct

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
researchProduct

Unmixing of Polymer Blends Confined in Ultrathin Films:  Crossover between Two-Dimensional and Three-Dimensional Behavior

2006

The interplay between chain conformations and phase separation in binary symmetric polymer mixtures confined into thin films by "neutral" hard walls (i.e., walls that do not preferentially attract or repel one of the two components of the mixture) is studied by Monte Carlo simulations. Using the bond fluctuation model on a simple cubic lattice in the semi grand canonical ensemble, we locate the critical temperature of demixing via finite size scaling methods for a wide range of chain lengths (16/= N/= 256 effective monomers per chain) and film thicknesses (2/= D/= 19 lattice spacings). Simultaneously, we investigate the geometrical structure of the chains, showing that despite using melt de…

chemistry.chemical_classificationMaterials scienceCondensed matter physicsMonte Carlo methodPolymerSurfaces Coatings and FilmsGrand canonical ensemblechemistryLattice (order)Materials ChemistryPerpendicularRadius of gyrationPolymer blendPhysical and Theoretical ChemistryScalingThe Journal of Physical Chemistry B
researchProduct

Multi-scale simulations of polymeric nanoparticle aggregation during rapid solvent exchange.

2018

Using a multi-scale approach which combines both molecular dynamics (MD) and kinetic Monte Carlo (KMC) simulations, we study a simple and scalable method for fabricating charge-stabilized nanoparticles through a rapid solvent exchange, i.e., Flash NanoPrecipitation (FNP). This multi-scale approach is based on microscopic information from MD simulations and uses a KMC algorithm to access macroscopic length- and time scales, which allows direct comparison with experiments and quantitative predictions. We find good agreement of our simulation results with the experiments. In addition, the model allows us to understand the aggregation mechanism on both microscopic and macroscopic levels and det…

chemistry.chemical_classificationMaterials scienceMonte Carlo methodGeneral Physics and AstronomyNanoparticle02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesMolecular dynamicsNanolithographychemistryScientific methodParticle sizeKinetic Monte CarloPhysical and Theoretical Chemistry0210 nano-technologyBiological systemThe Journal of chemical physics
researchProduct

Molecular Simulation of Polymer Melts and Blends: Methods, Phase Behavior, Interfaces, and Surfaces

2016

chemistry.chemical_classificationMaterials scienceMonte Carlo methodMolecular simulation02 engineering and technologyPolymer021001 nanoscience & nanotechnology01 natural sciencesMolecular dynamicschemistryChemical physicsPhase (matter)0103 physical sciences010306 general physics0210 nano-technology
researchProduct

Penetrant diffusion in frozen polymer matrices: A finite-size scaling study of free volume percolation

1996

The diffusion of penetrant particles in frozen polymer matrices is investigated by means of Monte Carlo simulations of the bond fluctuation model. By applying finite-size scaling to data obtained from very large systems it is demonstrated that the diffusion process takes place on a percolating free volume cluster describable by a correlated site percolation model which falls into the same universality class as random percolation. The diverging correlation length entails a pronounced dependence of the diffusion constant on the size of the simulated system. It is shown that this dependence is appreciable for a wide range of parameters around the transition. \textcopyright{} 1996 The American …

chemistry.chemical_classificationMaterials sciencePenetrant (mechanical electrical or structural)Condensed matter physicschemistryDiffusion processMonte Carlo methodThermodynamicsPolymerRenormalization groupScalingBond fluctuation modelFick's laws of diffusionPhysical Review E
researchProduct

The glass transition in polymer melts

1994

This paper presents some results of a Monte Carlo simulation for the glass transition in two- and three-dimensional polymer melts. The melt was simulated by the bond-fluctuation model on a d-dimensional cubic lattice which was combined with a two-level hamiltonian favouring long bonds in order to generate a competition between the energetic and topological constraints in the system. This competition prevents crystallization and makes the melt freeze in an amorphous structure as soon as the internal relaxation times match the observation time of the simulation set by the cooling rate. The freezing point of the melt, i.e the glass transition temperature Tg, thus depends upon the cooling rate …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerCondensed Matter PhysicsFreezing pointAmorphous solidlaw.inventionCrystallographychemistrylawLattice (order)Mode couplingMaterials ChemistryCrystallizationGlass transitionMacromolecular Symposia
researchProduct

Strategy for good dispersion of well-defined tetrapods in semiconducting polymer matrices.

2014

The morphology or dispersion control in inorganic/organic hybrid systems is studied, which consist of monodisperse CdSe tetrapods (TPs) with grafted semiconducting block copolymers with excess polymers of the same type. Tetrapod arm-length and amount of polymer loading are varied in order to find the ideal morphology for hybrid solar cells. Additionally, polymers without anchor groups are mixed with the TPs to study the effect of such anchor groups on the hybrid morphology. A numerical model is developed and Monte Carlo simulations to study the basis of compatibility or dispersibility of TPs in polymer matrices are performed. The simulations show that bare TPs tend to form clusters in the m…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymersOrganic ChemistryMonte Carlo methodDispersityPolymerHybrid solar cellMatrix (mathematics)chemistryMicroscopy Electron TransmissionSemiconductorsTransmission electron microscopyMaterials ChemistryCopolymerCadmium CompoundsComposite materialWell-definedSelenium CompoundsMonte Carlo MethodMacromolecular rapid communications
researchProduct

Grafted polymer layers under variable solvent conditions: A Monte Carlo simulation

1993

Polymer chains anchored with one end at a hard wall under variable solvent conditions are investigated by Monte Carlo simulations using the bond- fluctuation model. Detail information on the structural properties are obtained above, at, and below the Θ-point and discussed in terms of the appropriate theories. In particular, the scaling of the brush thickness is formulated and verified by the simulation data. For the dynamics at the Θ-point, both the relaxation time of the chain configuration and the mean-square time displacement are studied. At temperatures distinctly below the Θ-point, we find that the layer develops considerable lateral inhomogeneity in its density, which has not been pre…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsTime displacementOrganic ChemistryMonte Carlo methodMechanicsPolymerCondensed Matter PhysicsSolventChain (algebraic topology)chemistryMaterials ChemistryStatistical physicsScalingVariable (mathematics)Makromolekulare Chemie. Macromolecular Symposia
researchProduct

Monte Carlo simulation of polymer mixtures: recent progress

2000

chemistry.chemical_classificationMaterials sciencePolymers and PlasticschemistryCondensed matter physicsOrganic ChemistryMonte Carlo methodMaterials ChemistryPolymerCondensed Matter PhysicsComputational physicsMacromolecular Symposia
researchProduct