Search results for "Statistic"

showing 10 items of 12520 documents

Standard Definitions of Persistence Length Do Not Describe the Local “Intrinsic” Stiffness of Real Polymer Chains

2010

On the basis of extensive Monte Carlo simulations of lattice models for linear chains under good and Θ solvents conditions, and for bottle-brush polymers under good solvent conditions, different me...

chemistry.chemical_classificationPersistence lengthPhysics::Biological PhysicsQuantitative Biology::BiomoleculesPolymers and PlasticsOrganic ChemistryMonte Carlo methodStiffnessPolymerCondensed Matter::Soft Condensed MatterInorganic ChemistrychemistryLattice (order)Materials ChemistrymedicineStatistical physicsPhysics::Chemical Physicsmedicine.symptomWorm-like chainMacromolecules
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One- and two-component bottle-brush polymers: simulations compared to theoretical predictions

2007

Scaling predictions and results from self-consistent field calculations for bottle-brush polymers with a rigid backbone and flexible side chains under good solvent conditions are summarized and their validity and applicability is assessed by a comparison with Monte Carlo simulations of a simple lattice model. It is shown that under typical conditions, as they are also present in experiments, only a rather weak stretching of the side chains is realized, and then the scaling predictions based on the extension of the Daoud-Cotton blob picture are not applicable. Also two-component bottle brush polymers are considered, where two types (A,B) of side chains are grafted, assuming that monomers of …

chemistry.chemical_classificationPhase transitionQuantitative Biology::BiomoleculesPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodFOS: Physical sciencesThermodynamicsPolymerCondensed Matter - Soft Condensed MatterCondensed Matter PhysicsPolymer brushInorganic ChemistryCondensed Matter::Soft Condensed MatterMaterials ChemistrySide chainRadius of gyrationSoft Condensed Matter (cond-mat.soft)Statistical physicsScalingLattice model (physics)
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The intermediate coherent scattering function of entangled polymer melts: a Monte Carlo test of des Cloizeaux' theory

1994

Using the bond fluctuation model for flexible polymer chains in a dense melt the intermediate coherent scattering function for chains containing N=200 monomers is calculated and interpreted in terms of a recent theory of des Cloizeaux. The theory yields an explicit description for the crossover from the Rouse model to the regime where reptation prevails, for the limit N→∞. While the Monte Carlo data are qualitatively compatible with this description, an accurate estimation of the tube diameter is prevented due to the onset of a diffusive decay of the scattering function, not included in the theory. For a full quantitative analysis of the Monte Carlo data (as well as of experiments on chains…

chemistry.chemical_classificationPhysics and Astronomy (miscellaneous)ScatteringMonte Carlo methodCrossoverGeneral EngineeringPolymerFunction (mathematics)Atomic and Molecular Physics and OpticsCondensed Matter::Soft Condensed MatterMonte carlo testReptationchemistryStatistical physicsLimit (mathematics)Journal de Physique II
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Scaling theory of star polymers and general polymer networks in bulk and semi-infinite good solvents

1988

Theorie d'echelle utilisant l'equivalence entre la fonction generatrice du nombre total de configuration et la fonction de correlation a plusieurs spins du modele de Heisenberg classique a n composantes dans la limite n→0

chemistry.chemical_classificationPhysicsCorrelation function (statistical mechanics)Star polymerchemistrySemi-infiniteHeisenberg modelSolid-stateThermodynamicsField theory (psychology)PolymerScaling theoryJournal de Physique
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Long Range Bond-Bond Correlations in Dense Polymer Solutions

2004

The scaling of the bond-bond correlation function $C(s)$ along linear polymer chains is investigated with respect to the curvilinear distance, $s$, along the flexible chain and the monomer density, $\rho$, via Monte Carlo and molecular dynamics simulations. % Surprisingly, the correlations in dense three dimensional solutions are found to decay with a power law $C(s) \sim s^{-\omega}$ with $\omega=3/2$ and the exponential behavior commonly assumed is clearly ruled out for long chains. % In semidilute solutions, the density dependent scaling of $C(s) \approx g^{-\omega_0} (s/g)^{-\omega}$ with $\omega_0=2-2\nu=0.824$ ($\nu=0.588$ being Flory's exponent) is set by the number of monomers $g(\r…

chemistry.chemical_classificationPhysicsLinear polymerGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyPolymerCondensed Matter - Soft Condensed Matter010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPower lawOmega0104 chemical sciencesChemical bondchemistryDensity dependentExponentSoft Condensed Matter (cond-mat.soft)Statistical physicsAtomic physics0210 nano-technologyScaling[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]61.25.Hq 05.10.Ln 05.40.Fb
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Third virial coefficient for 4-arm and 6-arm star polymers

2008

We discuss the computation of the third virial coefficient in polymer systems, focusing on an additional contribution absent in the case of monoatomic fluids. We determine the interpenetration ratio and several quantities that involve the third virial coefficient for star polymers with 4 and 6 arms in the good-solvent regime, in the limit of a large degree of polymerization.

chemistry.chemical_classificationPhysicsMonatomic gasStatistical Mechanics (cond-mat.stat-mech)Polymers and PlasticsOrganic ChemistryMonte Carlo methodFOS: Physical sciencesThermodynamicsPolymerStatistical mechanicsDegree of polymerizationCondensed Matter - Soft Condensed MatterCondensed Matter Physicsmonte carlo simulations; star polymers; statistical mechanics; statistical thermodynamics; virial expansionInorganic ChemistrychemistryVirial coefficientMaterials ChemistryVirial expansionSoft Condensed Matter (cond-mat.soft)Limit (mathematics)Condensed Matter - Statistical Mechanics
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Phase transitions in a single polymer chain: A micro-canonical analysis of Wang–Landau simulations

2008

Abstract We present simulation results for the phase behavior of a single chain for a flexible lattice polymer model using the Wang–Landau sampling idea. Using the micro-canonical density of states obtained with this method we will discuss the ability of an analysis in the micro-canonical ensemble to locate the coil-globule (continuous) and liquid–solid (first-order) transitions found for this problem using a canonical analysis.

chemistry.chemical_classificationPhysicsPhase transitionMonte Carlo methodGeneral Physics and AstronomyPolymerSingle chainCanonical analysischemistryHardware and ArchitectureLattice (order)Density of statesStatistical physicsPhase diagramComputer Physics Communications
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GPU Based Molecular Dynamics Simulations of Polymer Rings in Concentrated Solution: Structure and Scaling

2011

We report on equilibrium properties of a concentrated solution of non-concatenated ring polymers by Molecular dynamics simulations using HooMD-blue, a fast implementation on graphics processor units (GPUs). We are able to identify the intermediate scaling regime for the radius of gyration Rg ∝ N as well as indication for a crossover to Rg ∝ N for rings with chain length N in our fully flexible off-lattice polymer model. This crossover takes place between a ring size of 2500 and 7500 monomers for monomer density ρ = 0.5. Our results are in agreement with recent studies for lattice and stiff off-lattice models and show once again that this scaling is not model dependent at all. Furthermore th…

chemistry.chemical_classificationPhysicsPhysics and Astronomy (miscellaneous)CrossoverPolymerComputational physicsRing sizeMolecular dynamicschemistryLattice (order)Radius of gyrationStatistical physicsGraphicsScalingProgress of Theoretical Physics Supplement
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A Monte Carlo Study of Living Polymers in 2D: Effect of Small Chains on Static Properties

1996

A slithering snake algorithm is combined with a binding and breaking chain algorithm to simulate the static behavior of living polymers according to Cates' description. It is shown that this simple two-dimensional simulation on a square lattice gives good agreement with the mean field theory. However, the large amount of small contour length chains for small values of the mean average length 〈L 〉 appears to be one of the reasons for the discrepancies observed between the simulated results and the mean field theory. This finding could explain disagreements between experimental observation and theory. Also, the results are not in favor of a swelling of the greater chains by the smaller one.

chemistry.chemical_classificationPhysicsPhysics and Astronomy (miscellaneous)Monte Carlo methodGeneral EngineeringPolymerSquare latticeAtomic and Molecular Physics and OpticschemistryChain (algebraic topology)Mean field theoryContour lengthStatistical physicsStatic behaviorArithmetic meanJournal de Physique II
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Structure and dynamics of amorphous polymers: computer simulations compared to experiment and theory

2004

This contribution considers recent developments in the computer modelling of amorphous polymeric materials. Progress in our capabilities to build models for the computer simulation of polymers from the detailed atomistic scale up to coarse-grained mesoscopic models, together with the ever-improving performance of computers, have led to important insights from computer simulations into the structural and dynamic properties of amorphous polymers. Structurally, chain connectivity introduces a range of length scales from that of the chemical bond to the radius of gyration of the polymer chain covering 2–4 orders of magnitude. Dynamically, this range of length scales translates into an even larg…

chemistry.chemical_classificationPhysicsQuantitative Biology::BiomoleculesMesoscopic physicsIntermolecular forceGeneral Physics and AstronomyObservableNanotechnologyPolymerAmorphous solidCondensed Matter::Soft Condensed MatterReptationchemistryRadius of gyrationStatistical physicsGlass transitionReports on Progress in Physics
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