Search results for "rush"

showing 10 items of 216 documents

Capillary Rise in Nanotubes Coated with Polymer Brushes

2009

The spontaneous rise of a fluid in a brush-coated nanocapillary is studied by molecular dynamics simulation of a coarse-grained model. The cases of changing wettability of both the capillary walls and the brush were examined. We also investigated the impact of polymer chain length on the transport of fluid along the nanotube. We found that capillary filling takes place in both lyophilic and lyophobic tubes, provided that the polymer brush coating is wetted by the fluid. In all the cases studied, capillary rise proceeds by a time-square law, but the mechanisms behind them (Lucas-Washburn or diffusive propagation) differ, depending on the chain length N. For a wettable wall, the speed of flui…

chemistry.chemical_classificationNanotubeMaterials scienceCapillary actionGeneral NeuroscienceBrushPolymerengineering.materialPolymer brushGeneral Biochemistry Genetics and Molecular Biologylaw.inventionHistory and Philosophy of ScienceCoatingchemistrylawPolymer chemistryengineeringMeniscusWettingComposite materialAnnals of the New York Academy of Sciences
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Structure of bottle brush polymers on surfaces: weak versus strong adsorption.

2011

Large-scale Monte Carlo simulations are presented for a coarse-grained model of cylindrical molecular brushes adsorbed on a flat structureless substrate, varying both the chain length N of the side chains and the backbone chain length N(b). For the case of good solvent conditions, both the cases of weak adsorption (only 10 to 15% of the monomers being bound to the surface) and strong adsorption (~40% of the monomers being bound to the surface, forcing the bottle brush into an almost 2D conformation) are studied. We focus on the scaling of the total linear dimensions of the cylindrical brush with both chain lengths N and N(b), demonstrating a crossover from rod-like behavior (for not very la…

chemistry.chemical_classificationPersistence lengthQuantitative Biology::BiomoleculesChemistryMonte Carlo methodBrushBackbone chainPolymerSurfaces Coatings and Filmslaw.inventionCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundAdsorptionChemical physicslawPolymer chemistryMaterials ChemistrySide chainPhysical and Theoretical ChemistryScalingThe journal of physical chemistry. B
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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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Pulling Single Adsorbed Bottle-Brush Polymers off a Flat Surface: A Monte Carlo Simulation

2013

Force versus extension behavior of flexible chains and semiflexible bottle-brush polymers adsorbed from a good solvent on a planar substrate is studied by Monte Carlo simulation of the bond fluctua...

chemistry.chemical_classificationPhysics::Biological PhysicsQuantitative Biology::BiomoleculesMaterials sciencebusiness.product_categoryPolymers and PlasticsFlat surfaceOrganic ChemistryMonte Carlo methodBrushPolymerMolecular physicslaw.inventionCondensed Matter::Soft Condensed MatterInorganic ChemistrySolventAdsorptionchemistrylawMaterials ChemistryBottlePlanar substrateStatistical physicsPhysics::Chemical PhysicsbusinessMacromolecules
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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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Surfactant-Induced Helix Formation of Cylindrical Brush Polymers with Poly(L-lysine) Side Chains

2008

The complex formation of oppositely charged surfactants with some polypeptides is known to induce β-sheet or helix formation. Here, we report on the complex formation of cylindrical brush polymers with poly(L-lysine) side chains and sodium dodecylsulfate (SDS). With increasing amount of added surfactant the cylindrical polymers first adopt a helical conformation with a pitch of approximately 14-24 nm followed by a spherically collapsed structure before eventually precipitation occurs. CD measurements suggest that the helix formation of the cylindrical brush polymers is driven by the hydrophobicity of the ,8-sheets formed by the PLL side chain-SDS complexes.

chemistry.chemical_classificationPolymers and PlasticsChemistryPrecipitation (chemistry)Organic ChemistryLysineBrushPolymerPolyelectrolytelaw.inventionPulmonary surfactantlawPolymer chemistryHelixMaterials ChemistrySide chainMacromolecular Rapid Communications
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Solvent-Induced Length Variation of Cylindrical Brushes

2001

Communication: Polymacromonomers with a main chain much larger than the side-chain length adopt the form of cylindrical brush polymers the contour length per mainchain monomer of which depends on the side-chain length. In the present investigation it is demonstrated that the length per monomer also depends on the solvent quality, i.e., the cylinders are shorter in a poor solvent as compared to a good solvent. It is argued that the repulsion of the side chains represents the extension force, which acts against the entropic contraction force of the main chain. Thus, cylindrical brushes may be suitable as responsive materials for sensors, actuators or soft machines.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesHydrodynamic radiusPolymers and PlasticsPolymer scienceOrganic ChemistryBrushPolymerlaw.inventionCondensed Matter::Soft Condensed MatterSolventchemistry.chemical_compoundMonomerchemistrylawChemical physicsMaterials ChemistrySide chainRadius of gyrationSolvent effectsMacromolecular Rapid Communications
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Selfdiffusion of polymer chains in solutions and melts

2005

Anomalous diffusion of monomers of polymer chains, as well as motion of these chains as a whole, is discussed with an emphasis on Monte Carlo simulations and simple scaling concepts. While the behavior of isolated chains in good solvents or Theta-solvents without excluded volume interactions is fully accounted for by the Rouse model, the behavior is less clear both for isolated chains in bad solvents and for chains in dense melts. Collapsed chains are shown to diffuse as g3(t) = <([rCM (t) -rCM(0)]2〉 ∝ tξ3 where the (effective?) exponent ξ3 simply seems to be linearly temperature-dependent for temperatures T lower than the Σ-temperature, ξ3 T/Θ. A relaxation time τ oc N3 is found, and scali…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceAnomalous diffusionMonte Carlo methodThermodynamicsPolymerPolymer brushCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerchemistryExcluded volumeExponentPhysical chemistryScaling
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Scaling concepts for polymer brushes and their test with computer simulation

2004

After a brief review of the scaling concepts for static and dynamic properties of polymer brushes in good solvents and Theta solvents, the Monte Carlo evidence is discussed. It is shown that under typical conditions the diameter of the last blob is of the order of 10-20% of the brush height, and therefore pronounced deviations from the self-consistent field predictions occur. In bad solvents, lateral microphase separation occurs leading to an irregular pattern of "dimples". Particularly interesting is the response of brushes to shear deformation, and the interaction between two interpenetrating brushes. Recent attempts to understand the resulting shear forces via molecular-dynamics simulati…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceField (physics)Shear forceMonte Carlo methodBiophysicsBrushSurfaces and InterfacesGeneral ChemistryPolymerlaw.inventionCondensed Matter::Soft Condensed MatterchemistrylawDimpleGeneral Materials ScienceStatistical physicsSoft matterScalingBiotechnologyThe European Physical Journal E
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Interactions between polymer brush-coated spherical nanoparticles: the good solvent case.

2011

The interaction between two spherical polymer brushes is studied by molecular dynamics simulation varying both the radius of the spherical particles and their distance, as well as the grafting density and the chain length of the end-grafted flexible polymer chains. A coarse-grained bead-spring model is used to describe the macromolecules, and purely repulsive monomer-monomer interactions are taken throughout, restricting the study to the good solvent limit. Both the potential of mean force between the particles as a function of their distance is computed, for various choices of the parameters mentioned above, and the structural characteristics are discussed (density profiles, average end-to…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceGeneral Physics and AstronomyNanoparticleInteraction energyPolymerPolymer brushCondensed Matter::Soft Condensed MatterMolecular dynamicschemistryComputational chemistryChemical physicsDensity functional theoryPhysical and Theoretical ChemistryPotential of mean forceSolvent effectsThe Journal of chemical physics
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