Search results for "Polystyrene"

showing 10 items of 349 documents

Micelles Formed by Cylindrical Brush-Coil Block Copolymers

2005

Amphiphilic cylindrical brush-coil block copolymers consisting of a polystyrene coil and a cylindrical brush block with poly(acrylic acid) side chains are prepared by ATRP of t-butylacrylate from a block comacroinitiator. Upon acidolysis of the poly(t-butylacrylate), water-soluble polymers were obtained that were observed to form micelles consisting of 4-5 block copolymers on average in aqueous solution. The star-like nature of such micelles was clearly visualized by scanning force microscopy.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerMicellechemistry.chemical_compoundchemistryBlock (telecommunications)Polymer chemistryAmphiphileMaterials ChemistryCopolymerSide chainPolystyreneAcrylic acidMacromolecular Rapid Communications
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Mechanical relaxation in miscible polymer systems: the glass transition regime in poly(vinylmethylether) (PVME)-cross-polystyrene (PS) semi-interpene…

1990

Abstract Miscible semi-interpenetrating polymer networks (semi-IPN) of varying composition are prepared by crosslinking polystyrene containing few maleic anhydride groups with a diamine in the presence of linear poly(vinylmethylether) (PVME). The resulting PVME-c-P(ScoMA) semi-IPNs are characterized by their thermal and thermomechanical behaviour. Comparison with the corresponding uncrosslinked material proves that weak crosslinking has a negligible effect on the location of the glass transition as measured by d.s.c. Both the Tg data and the temperatures of the loss modulus maximum E″ (at 1 rad/s) show the same non-linear curved composition dependence. Contrary to this the tan δ maximum var…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRelaxation (NMR)Maleic anhydridePolymerDynamic mechanical analysischemistry.chemical_compoundchemistryDiamineDynamic modulusMaterials ChemistryPolystyreneComposite materialGlass transitionPolymer
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Interpolymer complexes and polymer compatibility.

2012

A reliable method to decide whether two polymers A and B are miscible or incompatible would be very helpful in many ways. In this contribution we demonstrate why traditional procedures cannot work. We propose to use the intrinsic viscosities [η] of the polymer blends instead of the composition dependence of the viscosities as a criterion for polymer miscibility. Two macromolecules A and B are miscible because of sufficiently favorable interactions between the two types of polymer segments. For solutions of these polymers in a joint solvent, this Gibbs energetic preference of dissimilar intersegmental contacts should prevail upon dilution and lead to the formation of interpolymer complexes, …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymersViscosityIntrinsic viscosityOrganic ChemistryThermodynamicsWaterDextransDimethylformamidePolymerMiscibilityDilutionSolventchemistryPolysaccharidesCompatibility (mechanics)Polymer chemistryMaterials ChemistryPolystyrenesPolyvinylsPolymer blendGlucansMacromoleculeMacromolecular rapid communications
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Sorption of n-hexane in amorphous polystyrene

2014

Sorption properties of pure n-hexane vapor in amorphous polystyrene (PS) were studied at 298 K by thermogravimetry under controlled vapor pressure. Two sorption-desorption cycles were performed by varying the relative pressure between 0 and 0.91. Mixing of PS with n-hexane resulted in a strong plasticization, which was evidenced by quite significant depression in the glass transition temperature of the polymer as shown by differential scanning calorimetry. Maximum quantity of n-hexane sorbed in the PS at 298 K and at a pressure close to saturation was about 12.4 wt %. The thermogravimetry yielded an isotherm with a strong hysteresis loop, explanation of which was hypothesized with the help …

chemistry.chemical_classificationMaterials sciencePolymers and Plastics[ SDV ] Life Sciences [q-bio]Vapor pressureamorphous[SDV]Life Sciences [q-bio]Analytical chemistrySorptionPolymerCondensed Matter PhysicsAmorphous solidThermogravimetrychemistry.chemical_compoundswellingDifferential scanning calorimetryGlassy PolystyrenechemistryPolymer chemistryMaterials Chemistrysorption hysteresisPolystyrenestructurePhysical and Theoretical ChemistryGlass transition
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Synthesis and Characterization of Syndiotactic Polystyrene-Polyethylene Block Copolymer

2019

The direct synthesis of syndiotactic polystyrene-block-polyethylene copolymer (sPS-b-PE) with a diblock structure has been achieved. The synthetic strategy consists of the sequential stereocontrolled polymerization of styrene and ethylene in the presence of a single catalytic system: cyclopentadienyltitanium(IV) trichloride activated by modified methylaluminoxane (CpTiCl3/MMAO). The reaction conditions suitable for affording the partially living polymerization of these monomers were identified, and the resulting copolymer, purified from contaminant homopolymers, was fully characterized. Gel permeation chromatography coupled with two-dimensional NMR spectroscopy COSY, HSQC, and DOSY confirme…

chemistry.chemical_classificationMaterials sciencePolymers and Plasticsblock copolymerGeneral ChemistryPolymerBlock copolymer; Poly-insertion catalysis; Syndiotactic polystyrene; Thin film morphologysyndiotactic polystyreneArticlethin film morphologyStyreneGel permeation chromatographylcsh:QD241-441chemistry.chemical_compoundchemistryPolymerizationlcsh:Organic chemistryTacticityPolymer chemistryCopolymerLiving polymerizationPolystyrenepoly-insertion catalysisPolymers
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Main dielectric relaxation of poly(methyl acrylate)–polystyrene interpenetrating polymer networks

2005

Abstract Two series of poly(methyl acrylate)–polystyrene sequential interpenetrating polymer networks were prepared by free radical polymerization using ethyleneglycol dimethacrylate as cross-linking agent. In one of them the cross-linking density was very low and the IPNs presented phase separation. The main dielectric relaxation appears in the IPNs in the same position in the frequency axis and almost with the same shape as in the pure PMA network. Nevertheless the ratio of the relaxation strength to the weight fraction of PMA in the IPN decreases slightly with the increase of polystyrene content. The other series of IPNs were highly cross-linked, in these IPNs a dielectric relaxation sti…

chemistry.chemical_classificationMaterials scienceRadical polymerizationPolymerDielectricPoly(methyl acrylate)Condensed Matter PhysicsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryChemical engineeringPolymerizationPolymer chemistryMaterials ChemistryCeramics and CompositesRelaxation (physics)PolystyreneMethyl acrylateJournal of Non-Crystalline Solids
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Switching of Polymer Brushes

1999

Polymer coatings of brushlike monolayers composed of two different polymers, polystyrene and poly(2-vinylpyridine), are grafted by radical polymerization on the surface of silicon wafers. Thickness, grafting density, molecular weight of grafted chains, and the composition of the coatings were regulated by grafting time, monomer concentration, and additional initiator in solution. A typical dry film thickness is between 10 and 100 nm, and the molecular weights of the components range from 100 to 300 kg/mol. The fabricated coatings turn out to be sensitive to the composition of the environment. For instance after exposition to toluene the layer becomes hydrophobic and the top of the layer is …

chemistry.chemical_classificationMaterials scienceRadical polymerizationSurfaces and InterfacesPolymerCondensed Matter PhysicsContact anglechemistry.chemical_compoundMonomerChemical engineeringchemistryX-ray photoelectron spectroscopyMonolayerElectrochemistryGeneral Materials SciencePolystyreneLayer (electronics)SpectroscopyLangmuir
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Synthesis and large scale fractionation of non-linear polymers: brushes and hyperbranched polymers

2002

Polymer brushes with poly(methyl methacrylate) (PMMA) backbone and polystyrene side chains were synthesized by radical polymerization of ω-methacryloyl-polystyrene macromonomers. Hyperbranched PMMA was obtained by means of self-condensing group transfer copolymerization of methyl methacrylate with an initiator-monomer containing a polymerizable methacryloyl moiety and an initiating silylketeneacetal function. Both non-linear products were fractionated using the method of continuous polymer fractionation, consisting in a particular type of continuous countercurrent extraction. The combination of methyl ethyl ketone (solvent) with acetone (AC) (precipitant) turned out to be suitable for the f…

chemistry.chemical_classificationMaterials scienceRadical polymerizationtechnology industry and agriculturePolymerCondensed Matter PhysicsMacromonomerElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCeramics and CompositesSide chainCopolymerPolystyrenePolymer fractionationMethyl methacrylateJournal of Non-Crystalline Solids
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Self-Diffusion in Concentrated Colloid Suspensions Studied by Digital Video Microscopy of Core−Shell Tracer Particles

1998

Optical video microscopy and digital image processing have been used to study the self-diffusion of colloidal particles with a hard-sphere potential. The colloid particles consist of cross-linked polymers and are dispersed in a good solvent to avoid aggregation. To investigate single particle motion in highly concentrated dispersions, a host−tracer system, consisting of two different kinds of polymer particles, has been designed:  the host particles are made of poly-t-butylacrylate (with ethanedioldiacrylate as cross-linker) and have the same refractive index as the employed solvent, 4-fluorotoluene. The tracer particles have a core−shell structure with a polystyrene core (cross-linked with…

chemistry.chemical_classificationMaterials scienceScatteringVideo microscopySurfaces and InterfacesPolymerCondensed Matter Physicslaw.inventionCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundColloidchemistryOptical microscopeChemical engineeringlawPolymer chemistryMicroscopyElectrochemistryGeneral Materials SciencePolystyreneParticle sizeSpectroscopyLangmuir
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Nanowear on Polymer Films of Different Architecture

2007

In this paper, we describe atomic force microscope (AFM) friction experiments on different polymers. The aim was to analyze the influence of the physical architecture of the polymer on the degree and mode of wear and on the wear mode. Experiments were carried out with (1) linear polystyrene (PS) and cycloolefinic copolymers of ethylene and norbornene, which are stabilized by entanglements, (2) mechanically stretched PS, (3) polyisoprene-b-polystyrene diblock copolymers, with varying composition, (4) brush polymers consisting of a poly(methyl methacrylate) (PMMA) backbone and PS side chains, (5) PMMA and PS brushes grafted from a silicon wafer, (6) plasma-polymerized PS, and (7) chemically c…

chemistry.chemical_classificationMaterials scienceSiliconchemistry.chemical_elementSurfaces and InterfacesPolymerCondensed Matter Physicschemistry.chemical_compoundchemistryvisual_artPolymer chemistryElectrochemistryvisual_art.visual_art_mediumCopolymerSide chainGeneral Materials ScienceWaferPolystyrenePolycarbonateMethyl methacrylateComposite materialSpectroscopyLangmuir
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