Search results for "Dynamic"

showing 10 items of 12329 documents

Dynamical Scaling in Polymer Solutions Investigated by the Neutron Spin-Echo Technique

1979

Chain dynamics in polymer solutions was investigated by means of the recently developed neutron spin echo spectroscopy. — By this technique, it was possible for the first time to verify unambiguously the scaling predictions of the Zimm model in the case of single chain behaviour and to observe the cross over to many chain behaviour. The segmental diffusion of single chains exhibits deviations from a simple exponential law, indicating the importance of memory effects. Mit Hilfe der erst kurzlich entwickelten Neutronen-Spin-Echo-Spektroskopie wurde die Kettendynamik von Polymermolekulen im gelosten Zustand untersucht. - Die Methode eroffnete die Moglichkeit, zum ersten Mal fur das Einzelkette…

chemistry.chemical_classificationPhysicsDynamical scalingCondensed matter physicsGeneral Chemical EngineeringCrossoverGeneral Physics and AstronomyPolymerOmegaNeutron spin echochemistryPolymer chemistryExponentNeutronAtomic physicsExponential decaySpectroscopyScalingPhysical Review Letters
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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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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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KINETICS OF POLYMER EJECTION FROM CAPSID CONFINEMENT: SCALING CONSIDERATIONS AND COMPUTER EXPERIMENT

2012

We investigate the ejection dynamics of a flexible polymer chain out of confined environment by means of scaling considerations and Monte Carlo simulations. Situations of this kind arise in different physical contexts, including a flexible synthetic polymer partially confined in a nanopore and a viral genome partially ejected from its capsid. In the case of cylindric confinement the entropic driving force which pulls the chain out of the pore is argued to be constant once a few persistent lengths are out of the pore. We demonstrate that in this case the ejection dynamics follows a [Formula: see text]-law with elapsed time t. The mean ejection time τ depends nonmonotonically on chain length…

chemistry.chemical_classificationPhysicsQuantitative Biology::BiomoleculesMonte Carlo methodDynamics (mechanics)General Physics and AstronomyStatistical and Nonlinear PhysicsNanotechnologyPolymerMechanicsComputer experimentComputer Science ApplicationsNanoporeComputational Theory and MathematicschemistryChain (algebraic topology)Constant (mathematics)ScalingMathematical PhysicsInternational Journal of Modern Physics C
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Scaling behavior of topologically constrained polymer rings in a melt

2014

Large scale molecular dynamics simulations on graphic processing units (GPUs) are employed to study the scaling behavior of ring polymers with various topological constraints in melts. Typical sizes of rings containing $3_1$, $5_1$ knots and catenanes made up of two unknotted rings scale like $N^{1/3}$ in the limit of large ring sizes $N$. This is consistent with the crumpled globule model and similar findings for unknotted rings. For small ring lengths knots occupy a significant fraction of the ring. The scaling of typical ring sizes for small $N$ thus depends on the particular knot type and the exponent is generally larger than 0.4.

chemistry.chemical_classificationPhysicsStatistical Mechanics (cond-mat.stat-mech)Mathematics::Commutative AlgebraCatenaneFOS: Physical sciencesGeometryPolymerCondensed Matter - Soft Condensed MatterCondensed Matter PhysicsMathematics::Geometric TopologyMolecular dynamicsKnot (unit)chemistryExponentSoft Condensed Matter (cond-mat.soft)General Materials ScienceScalingCondensed Matter - Statistical MechanicsJournal of Physics: Condensed Matter
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Publisher’s Note: “Polymer-specific effects of bulk relaxation and stringlike correlated motion in the dynamics of a supercooled polymer melt” [J. Ch…

2004

a! Present address: Department of Physics, Wesleyan University, Middletown, CT 06459. b!Author to whom correspondence should be addressed. Electronic mail: baschnag@ics.u-strasbg.fr c!Author to whom correspondence should be addressed. Electronic mail: sglotzer@umich.edu FIG. 8. Temperature dependence of the ratio of ^sseg(tstr )& and ^s(tstr )&. tstr max is the peak time of ^sseg& and ^s& at different temperatures. TMCT 50.45. JOURNAL OF CHEMICAL PHYSICS VOLUME 120, NUMBER 14 8 APRIL 2004

chemistry.chemical_classificationPhysicschemistryGeneral Physics and AstronomyThermodynamicsMotion (geometry)Relaxation (physics)PolymerPhysical and Theoretical ChemistrySupercoolingPolymer meltElectronic mailThe Journal of Chemical Physics
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Polymer-induced shape changes and capping in giant liposomes

1995

We studied the coupling of a polymeric amphiphile undergoing a transition from an expanded to a collapsed state of the hydrophilic polymer chain upon heating above 29°C with free and solid supported lipid bilayers. Lateral diffusion measurements and studies of vesicle shape-changes confirmed previous calorimetric studies, suggesting that the amphiphile remains incorporated in the giant vesicles and the supported bilayer during the transition. The two-dimensional hydrodynamic radii of the amphiphile in the expanded and collapsed state was measured by making use of the strong quadratic dependence of the diffusion coefficient on the radius of the diffusant (D ∞ r−2) due to the frictional coupl…

chemistry.chemical_classificationPhysics::Biological PhysicsLiposomeHydrodynamic radiusVesicleBilayerDiffusionOrganic ChemistryAnalytical chemistryCell BiologyPolymerBiochemistryQuantitative Biology::Subcellular ProcessesCondensed Matter::Soft Condensed MatterchemistryChemical physicsAmphiphilesense organsLipid bilayerMolecular BiologyChemistry and Physics of Lipids
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Composite soy lecithin–decylpolyglucoside vesicles: A theoretical and experimental study

2008

In the present work, vesicles made with soy lecithin and a commercial mixture of alkyl polyglucosides were prepared and characterized. Vesicles with a constant amount of soy lecithin and an increasing amount of a decylpolyglucoside surfactant, (OrNS10), were formulated and their physicochemical properties were studied with the aim to design a drug delivery system suitable for different applications. To this purpose, morphology, size distribution, ζ-potential and apparent viscosity of the prepared vesicles were studied. Vesicles were also characterized by using optical and light polarized microscopy, transmission electron microscopy and photon correlation spectroscopy. A stability study was …

chemistry.chemical_classificationPolarized light microscopyfood.ingredientChromatographyAPPARENT VISCOSITY QUITARVesicleDECYLPOLYGLUCOSIDELECITINAApparent viscosityΖ-POTENTIALLecithinVESICULASVESICLESchemistry.chemical_compoundColloid and Surface ChemistryfoodchemistryDynamic light scatteringPulmonary surfactantPhosphatidylcholineLECITHINAlkylColloids and Surfaces A: Physicochemical and Engineering Aspects
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Characterization of Micelles of Polyisobutylene-block-poly(methacrylic acid) in Aqueous Medium

2000

Four amphiphilic block copolymers polyisobutylene-block-poly(methacrylic acid) (IBm-MAAn; m = 70−134, n = 52−228) were synthesized and transferred into aqueous medium at pH 10−12. Their structure in solution was characterized by fluorescence correlation spectroscopy (FCS), static and dynamic light scattering (SLS, DLS), analytical ultracentrifuge (AUC), and by transmission electron microscopy (TEM) with freeze-fracturing and staining techniques. DLS data, AUC sedimentation traces, and TEM images indicate at least two different kinds of particles. TEM shows spherical micelles; however, especially for polymers with larger hydrophobic blocks, additional particles are observed. FCS shows extrem…

chemistry.chemical_classificationPoly(methacrylic acid)Aqueous solutionPolymers and PlasticsOrganic ChemistryAnalytical chemistryFluorescence correlation spectroscopyPolymerMicelleInorganic Chemistrychemistry.chemical_compoundchemistryMethacrylic acidDynamic light scatteringPolymer chemistryMaterials ChemistryCopolymerMacromolecules
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1989

A series of combined main-chain side-group liquid-crystalline polymers was synthesized by melt polycondensation from trans-1,4-cyclohexanedicarboxylic acid, chloro-1,4-phenylene diacetate and 6-(4-methoxy-4′-biphenylyloxy)hexyl-1,4-phenylene diacetate. These polyesters combine the features of rigid-rod main-chain LC-polymers and of side-group LC-polymers. Polymers with small fractions of mesogenic side-groups (5 and 10 mol-%) have lower melting points than the parent polymer poly(chloro-1,4-phenylene 1,4-cyclohexanedicarboxylate) but are still liquid crystalline up to their decomposition at T ≥ 400°C. In polymers with larger fractions of mesogenic side-groups (50 and 100 mol-%) partial isom…

chemistry.chemical_classificationPolyesterCondensation polymerMaterials sciencechemistryLiquid crystalMesogenPolymer chemistryMelting pointThermomechanical analysisPolymerDynamic mechanical analysisDie Makromolekulare Chemie
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