Search results for "plastic"

showing 10 items of 7296 documents

Mechanical, structural and magnetic properties of polypropylene/iron ferrite magnetic nanocomposites

2012

In this research, composites of polypropylene (PP) and a relatively small concentrations of iron ferrite (Fe3O4) nanopowder equal to 2, 5 and 10 wt.% have been made. An methacrylate monomer 2,2'-bis-(4-(2-methylprop-2-enoyloxy)phenyl)- propane (BAD) was added at a small amount (3 wt.%) to part of the composites during the thermoplastic mixing. The BAD has been used as a compatibilizing agent on the phase interaction between the filler and the matrix of polypropylene. It has been found that composites have adjustable mechanical, structural and magnetic properties dependent on the content of magnetic filler. Increase of concentration of ferrite particles affects a notable increase of elastic …

chemistry.chemical_classificationPolypropylenechemistry.chemical_compoundCrystallinityNanocompositeMaterials scienceThermoplasticchemistryFerrite (iron)PolymerComposite materialMethacrylateElastic modulusIOP Conference Series: Materials Science and Engineering
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Structure and dynamics of thin polymer films: a case study with the bond-fluctuation model

2002

Abstract This paper reports Monte Carlo simulation results of a polymer melt of short, non-entangled chains which are embedded between two impenetrable walls. The melt is simulated by the bond-fluctuation lattice model under athermal conditions, i.e. only excluded volume interactions between the monomers and between the monomers and the walls are taken into account. In the simulations, the wall separation is varied from about one to about 15 times the bulk radius of gyration R g . The confinement influences both static and dynamic properties of the films: Chains close to the walls preferentially orient parallel to it. This parallel orientation decays with increasing distances from the wall …

chemistry.chemical_classificationPreferential alignmentLattice model (finance)Polymers and PlasticsCondensed matter physicsChemistryOrganic ChemistryMonte Carlo methodPolymerCondensed Matter::Soft Condensed MatterOrientation (geometry)Excluded volumeMaterials ChemistryRadius of gyrationStatistical physicsThin filmPolymer
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Dipolar Relaxation in Functionalized Poly-p-phenylenes Bearing Ultrastrong Dipoles Perpendicular to the Backbone

2018

Local polymer dynamics are studied in polymers bearing dipoles rigidly attached to the backbone. The compounds are based on cyano-substituted dihydrobenzimidazoles bearing ultrastrong dipole moments (∼12 D per repeat unit) incorporated in a poly-p-phenylene backbone, giving rise to polymers with rigid dipoles perpendicular to the chain. They belong to type B polymers according to the Stockmayer classification. They are ideal model systems for studying rotational isomers in the gas phase and the self-assembly and local dynamics in the solid state. Gas phase calculations (DFT) provided the dipole moments, the energetic barriers, and the backbone conformation as a function of the dipole streng…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesBearing (mechanical)Materials sciencePolymers and PlasticsOrganic ChemistryIntermolecular forcePolymerMolecular physicslaw.inventionDielectric spectroscopyInorganic ChemistryDipolechemistrylawMoment (physics)Materials ChemistryPerpendicularPhysics::Atomic PhysicsRepeat unitMacromolecules
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Osmotic pressure of catenanes in solution

1989

We propose a nonuniversal scaling for the osmotic pressure in the case of concatenating ring polymers. The size exponent depends on the molecular weight of the catenans. The effect is more significant the shorter and the stiffer the molecules are.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesChromatographyPolymers and PlasticsChemistryCatenaneThermodynamicsGeneral ChemistryPolymerCondensed Matter PhysicsRing (chemistry)Condensed Matter::Soft Condensed MatterMaterials ChemistryExponentChemical solutionMoleculeOsmotic pressureScalingPolymer Bulletin
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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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Mean square radius of gyration and hydrodynamic radius of jointed star (dumbbell) and H-comb polymers

1996

Equations for the mean square radius of gyration and the hydrodynamic radius for jointed stars (dumbbells) and H-combs are derived, based on random flight statistics for each subchain. Comparision with literature data on computer simulations and experimental data for H-combs show good agreement for the g-value of the mean square radius of gyration even in good solvents. This suggests that for the mean square radius of gyration the relative dimension of a H-comb relative to the linear molecule of the same degree of polymerization is not altered significantly by long range interactions, as in the case of star polymers. For the hydrodynamic radius the situation is different. Fair agreement is …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesHydrodynamic radiusPolymers and Plasticsbusiness.industryChemistryOrganic ChemistryLinear molecular geometryPolymerDegree of polymerizationCondensed Matter PhysicsRelative dimensionMolecular physicsCondensed Matter::Soft Condensed MatterInorganic ChemistryViscosityOpticsMaterials ChemistryRadius of gyrationDumbbellbusinessMacromolecular Theory and Simulations
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Adsorption of Oligomers and Polymers into a Polymer Brush Formed from Grafted Ring Polymers

2013

The interaction of a ring polymer brush with a solution containing oligomers or free linear flexible macromolecules is studied by Monte Carlo simulation, varying the chain length of the free chains, and in selected cases also the lengths of the rings. Two grafting densities are studied, corresponding to semidilute and very concentrated conditions, and a comparison with the corresponding case of brushes formed from grafted linear chains is made. Although the ring polymer linear dimensions in the brushes show an anomalous scaling with ring length, similar to (noncatenated) ring polymer melts, the concentration profiles of oligomers and long macromolecules in ring polymer brushes differ only v…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceMathematics::Commutative AlgebraPolymers and PlasticsPolymer scienceOrganic ChemistryBrushPolymer architecturePolymerRing (chemistry)GraftingPolymer brushlaw.inventionCondensed Matter::Soft Condensed MatterInorganic ChemistryComputer Science::GraphicsAdsorptionchemistrylawMaterials ChemistryMacromoleculeMacromolecules
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Modeling Studies of the Phase Behavior of Monomer/Polymer/Disk Composites

2008

The model developed by Balazs et al. to explain the phase behavior of polymer/clay composites is extended to monomer/polymer/clay composites, obtaining an expression for the free energy of a monomer/polymer/thin-disk mixture. By minimizing the free energy and calculating the chemical potentials of the three system components, phase diagrams for the monomer/disk and monomer/polymer/disk mixtures are contructed. Through the evolution and comparison of these diagrams, the effects of nanodisk size, polymer molecular mass and interaction parameters (temperature) on mixture stability and attained morphology are then studied.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceMorphology (linguistics)Polymers and PlasticsOrganic ChemistryPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPhase (matter)Materials ChemistryComposite materialPhase diagramMacromolecular Theory and Simulations
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Static and dynamic scaling behavior of a polymer melt model with triple-well bending potential

2018

We perform molecular-dynamics simulations for polymer melts of the coarse-grained polyvinyl alcohol model that crystallizes upon slow cooling. To establish the properties of its high temperature liquid state as a reference point, we characterize in detail the structural features of equilibrated polymer melts with chain lengths $5\le N \le 1000$ at a temperature slightly above their crystallization temperature. We find that the conformations of sufficiently long polymers with $N >50$ obey essentially the Flory's ideality hypothesis. The chain length dependence of the end-to-end distance and the gyration radius follow the scaling predictions of ideal chains and the probability distributions o…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials sciencePolymers and PlasticsCrystallization of polymersThermodynamicsMesophase02 engineering and technologyPolymer021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesGyrationCondensed Matter::Soft Condensed MatterMean squared displacementReptationMolecular dynamicschemistry0103 physical sciencesMaterials ChemistryPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyScalingJournal of Polymer Science Part B: Polymer Physics
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Kinetic Monte Carlo Simulations of Flow-Assisted Polymerization

2012

We performed kinetic Monte Carlo simulations on a model of a polymerization process in the presence of a periodic oscillatory flow to explore the role of mixing in polymerization reactors. Application of an oscillatory flow field helps overcome the diffusive limitations that develop during a polymerization process due to an increase in the molecular weights of polymer chains, thereby giving rise to high rates of polymerization. A systematic increase in the flow strength results in a "dynamic" coil-stretch transition, leading to an elongation of polymer chains. Reactive ends of stretched (polymer) chains react more frequently than the reactive ends of coiled chains, which are screened by oth…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials sciencePolymers and PlasticsField (physics)Organic Chemistrytechnology industry and agricultureMixing (process engineering)NanotechnologyPolymerInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationFlow (mathematics)Chemical physicsMaterials ChemistryKinetic Monte CarloChoked flowACS Macro Letters
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