Search results for "polymers"

showing 10 items of 3567 documents

On the Preparation and Characterization of Polyethylene/Polyamide Blends by Melt Processing in the Presence of an Ethylene/Acrylic Acid Copolymer and…

2006

Samples of HDPE and PA6 have been melt-processed in the presence of two new phosphazene compounds, CP-2EPOX and CP-20XA together with an ethylene/acrylic acid copolymer. The blends have been prepared in an industrial twin-screw extruder by using PA6 and PE in weight ratios of 25/75 and 75/25. When used, 5 phr of EAA and 0.2 phr of CP have been added. The materials have been completely characterized from a rheological, morphological, and mechanical point of view. The results indicate that the additives used caused an increase in the rupture tensile properties, of the impact strength and viscosity especially in the PE-rich blend in the presence of CP-2EPOX. This result can be attributed both …

Materials sciencePolymers and PlasticsOrganic ChemistryCompatibilizationPolyethyleneCondensed Matter Physicschemistry.chemical_compoundchemistryPolymer chemistryPolyamideMaterials ChemistryHigh-density polyethylenePolymer blendPhysical and Theoretical ChemistryIonomerPhosphazeneAcrylic acid
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Modelling the Influence of Nanoparticles in the Phase Behaviour of an Epoxy/Polystyrene Mixture, 2

2007

The influences of nanoparticle size and concentration on the thermodynamic behaviour of epoxy/polystyrene blends are evaluated in the framework of Ginzburg's simple analytical theory. Two approaches have been employed: NPEPO (for particles coated with epoxy groups) and NPFEN (for particles coated with phenyl groups). Using NPEPO, the particles are found to prefer the phase richer in epoxy, whereas the opposite occurs for NPFEN. The particles size significantly influences blend compatibility. When the particle radius Rp is about the same size as the radius of gyration R g of PS, the compatibility of blends increases with particle concentration, whereas for R p > R g , higher particle concent…

Materials sciencePolymers and PlasticsOrganic ChemistryConcentration effectNanoparticleEpoxyCondensed Matter PhysicsInorganic Chemistrychemistry.chemical_compoundchemistryChemical engineeringvisual_artPhase (matter)Polymer chemistryMaterials Chemistryvisual_art.visual_art_mediumRadius of gyrationParticleParticle sizePolystyreneMacromolecular Theory and Simulations
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Ellipsoidal core-shell cylindrical microphases in PS-b -PB-b -PCL triblock copolymers with a crystallizable matrix

1997

Polystyrene-block-polybutadiene-block-poly(e-caprolactone) SBC triblock copolymers with a PCL matrix exhibit microphase separation into three different phases within the spherulitic superstructures. Mixing of the PS-block can occur upon melting of the PCL-block if the molecular weight is low enough. Even though the crystallization takes place well below the PS-glass transition, a deformation of the amorphous microphases into ellipsoidal core-shell cylindrical microdomains is observed by TEM. These copolymers have mechanical properties which are dominated by the PCL (Poly(e-caprolactone)) matrix with an influence of the amorphous blocks.

Materials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter PhysicsEllipsoidAmorphous solidlaw.inventionCore shellMatrix (mathematics)lawMaterials ChemistryCopolymerCrystallizationDeformation (engineering)Composite materialMacromolecular Symposia
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Polyelectrolytes on block copolymer surfaces

2004

Soft lithography and properties of amphiphilic block copolymers are combined in a new technique for the generation of patterned substrates, which can be used in different ways as templates for further processing. In these processing steps the deposition of polyelectrolytes, metals and grafting from polymerizations are used for the construction of different structures.

Materials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter PhysicsGraftingPolyelectrolyteSoft lithographyTemplateChemical engineeringPolymer chemistryAmphiphileMaterials ChemistryCopolymerDeposition (phase transition)MetallizingMacromolecular Symposia
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Poly(styrene sulfonate) self-organization: electrostatic and secondary interactions

2004

We investigate the self-organization of PSS in brushes and polyelectrolyte multilayers with X-ray, neutron and optical reflectivity. The electrostatic force dominates brush phases and adsorption behavior, additionally we find evidence of a strong hydrophobic force: (i) within amphiphilic diblock copolymer monolayers, a PSS monolayer adsorbs flatly to the hydrophobic block, (ii) on temperature increase (and with screened electrostatic forces), more PSS is adsorbed onto oppositely charged surfaces, and (iii) a polyelectrolyte multilayers shrinks when heated at 100% r.h. The latter two effects are consistent with the well-known increase of the hydrophobic force on heating: The increased PSS su…

Materials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter PhysicsPolyelectrolyteStyrenestomatognathic diseaseschemistry.chemical_compoundAdsorptionSulfonatechemistryChemical engineeringPolymer chemistryMonolayerAmphiphileMaterials ChemistryCopolymerSelf-assemblyMacromolecular Symposia
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Studies on the solution behaviour of self-assembling polymeric systems

1993

Functional groups were attached to styrene-butadiene copolymers with different polymeric architectures and a low molecular weight compound. These polar stickers form binary, chelate-like contacts or extended juntion zones depending on their chemical nature. The solution properties of these amphiphilic species in toluene were studied by static light scattering.

Materials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter PhysicsToluenechemistry.chemical_compoundChemical engineeringchemistrySelf assemblingAmphiphilePolymer chemistryMaterials ChemistryCopolymerPolarStatic light scatteringMakromolekulare Chemie. Macromolecular Symposia
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Thermal behavior and spherulitic superstructures of SBC triblock copolymers based on polystyrene (S), polybutadiene (B) and a crystallizable poly(ɛ-c…

1996

The dynamic crystallization and the melting behavior of polystyrene-block-poly(e-caprolactone) (PS-b-PCL, short notation SC), polybutadiene-block-poly(e-caprolactone) (PB-b-PCL, BC) and polystyrene-block-polybutadiene-block-poly(e-caprolactone) (PS-b-PB-b-PCL, SBC) have been studied using differential scanning calorimetry. The copolymers with high molecular weight exhibit microphase separation into microphases consisting of polystyrene, polybutadiene and poly(e-caprolactone) and partial crystallization of the corresponding PCL block. The crystallization occurs at temperatures below the PS glass transition. Depending on the block copolymer composition, crystallization takes place through a c…

Materials sciencePolymers and PlasticsOrganic ChemistryCondensed Matter Physicslaw.inventionAvrami equationchemistry.chemical_compoundPolybutadieneDifferential scanning calorimetrychemistrylawPolymer chemistryMaterials ChemistryMelting pointCopolymerPolystyrenePhysical and Theoretical ChemistryCrystallizationGlass transitionMacromolecular Chemistry and Physics
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Amphipolar core-shell cylindrical brushes

1999

Methacryloyl-endfunctionalized block copolymers consisting of styrene and 2-vinylpyridine were polymerized to polyblockcomacromonomers with a much higher main chain than side chain degree of polymerization. Like homopolymacromonomers these molecules exhibit the structure of cylindrical brushes. Since the vinylpyridine block is coupled to the polymerizable group, the resulting cylindrical macromolecules exhibit a core of vinylpyridine and a shell of polystyrene, thus resembling an amphipolar unimolecular micelle of cylindrical shape. The micellar character of the structure is demonstrated by loading the cylindrical brushes with tetrachloroauric acid in toluene. Subsequent reduction leads to …

Materials sciencePolymers and PlasticsOrganic ChemistryDegree of polymerizationMacromonomerMicelleStyrenechemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerSide chainPolystyreneMacromolecular Rapid Communications
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Linear-Hyperbranched Amphiphilic AB Diblock Copolymers Based on Polystyrene and Hyperbranched Polyglycerol

2005

A convenient three-step strategy has been developed for the preparation of well-defined amphiphilic, linear hyperbranched block copolymers by hypergrafting. The synthetic procedure is based on a combination of carbanionic polymerization with the alkoxide-based controlled ring-opening multibranching polymerization of glycidol. A linear AB diblock copolymer polystyrene-block-polybutadiene (PS-b-PB) with narrow polydispersity was obtained by anionic copolymerization. Subsequent hydroxylation by hydroboration led to PS 508 -b-(PB-OH) 56 , used as macro--initiator for the polymerization of glycidol under slow monomer addition conditions.

Materials sciencePolymers and PlasticsOrganic ChemistryDispersityGlycidolRing-opening polymerizationchemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerPolystyreneMacromolecular Rapid Communications
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Using Copolymers to Design Tunable Stimuli-Reponsive Brushes

2020

Recently, a new design for switch sensors has been proposed that exploits a conformational transition of end-grafted minority adsorption-active homopolymers in a monodisperse polymer brush [Klushin...

Materials sciencePolymers and PlasticsOrganic ChemistryDispersityNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPolymer brush01 natural sciences0104 chemical sciencesInorganic ChemistryMaterials ChemistryCopolymer0210 nano-technologyMacromolecules
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