Search results for "Polybutadiene"

showing 10 items of 49 documents

Improvement of the photo-stability of polystyrene-block-polybutadiene-block-polystyrene through carbon nanotubes

2015

Abstract The photo-stability of Polystyrene-Polybutadiene-Polystyrene (SBS) based nanocomposites containing bare multi-walled carbon nanotubes (CNTs) and carbon nanotubes bearing carboxylic functional groups (CNTs-COOH) in comparison to that of pristine SBS has been studied. The photo-oxidation of pristine SBS occurs through crosslinking reactions and oxidized species formation and both these processes begin at early stage of exposure. The formation of crosslinking, formerly in polybutadiene phase, assessed by spectroscopical (FTIR), mechanical, dynamic mechanical and rheological analysis, leads to occurrence of internal mechanical stresses in the solid state and the SBS samples become prem…

Solid-state chemistryPolystyrene-polybutadiene-polystyrene copolymerMaterials sciencePolymers and PlasticsCarbon nanotubesCarbon nanotubes; Photo-stability; Polystyrene-polybutadiene-polystyrene copolymer; Structural changes; Condensed Matter Physics; Mechanics of Materials; Polymers and Plastics; Materials Chemistry; 2506; Metals and AlloysCarbon nanotubeCarbon nanotubelaw.inventionchemistry.chemical_compoundPolybutadieneRheologylawPhase (matter)Structural changeMaterials ChemistryMechanics of MaterialFourier transform infrared spectroscopyComposite materialStructural changesNanocompositePolymers and PlasticMetals and AlloysCondensed Matter PhysicsPhoto-stabilitychemistryChemical engineeringMechanics of MaterialsPolystyrene2506
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Linear versus Three-Arm Star Polybutadiene: Effects of Polymer Architecture on the Thermodynamic Solution Behavior

2012

The interaction of linear and of three-arm star polybutadiene (PB) with THF was studied in the temperature range between 25 and 55 °C. Information for dilute solution rests on light scattering experiments; Flory–Huggins interaction parameter χ stem from vapor pressure measurements as a function of φ, the volume fraction of polymer. Despite the minute divergence in the architecture, the second osmotic virial coefficients of the two PBs differ noticeably. The present work demonstrates that these disparities become much more pronounced as φ increases and that they depend strongly on temperature. These findings are interpreted on the basis of an approach accounting for the effects of chain conn…

Work (thermodynamics)Materials sciencePolymers and PlasticsVapor pressureOrganic ChemistryThermodynamicsPolymer architectureFlory–Huggins solution theoryLight scatteringInorganic ChemistryPolybutadieneVirial coefficientVolume fractionPolymer chemistryMaterials ChemistryMacromolecules
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Non-porous polybutadiene-coated silicas as stationary phases in reversed-phase chromatography

1990

Abstract Non-porous silica of mean particle diameter 1.7 μm (Monospher) was coated with polybutadiene (PBD) following a published procedure. The silicas were prepared with graduated polymer loads up to 8% (w/w). Examination of the PBD-coated packings by means of electron spectroscopy for chemical analysis, scanning electron microscopy, diffuse reflection infrared fourier transform spectroscopy and differential thermal gravimetry indicated that the optimum polymer load was between 1 and 3% (w/w) with regard to a dense coverage corresponding to an average layer thickness of about 4 nm. No silanophilic interactions could be monitored using 1–3% (w/w) coated silicas under reversed-phase conditi…

chemistry.chemical_classificationChromatographyScanning electron microscopeOrganic ChemistryAnalytical chemistryGeneral MedicinePolymerReversed-phase chromatographyBiochemistryElectron spectroscopyFourier transform spectroscopyAnalytical ChemistryPolybutadienechemistryDiffuse reflectionPorosityJournal of Chromatography A
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Organometallic ABC-triblock copolymers

1998

The interaction of Fe and Pd complexes with double bonds of the polybutadiene (PB) block in polystyrene-polybutadiene-poly(methyl methacrylate) block copolymers has been studied. The incorporation of Fe(CO)3 fragments into the PB bloc was found to result in an increase in its rigidity. The presence of iron or palladium complexes in the PB block affects strongly the morphology of the triblock copolymers.

chemistry.chemical_classificationDouble bondInfrared spectroscopychemistry.chemical_elementGeneral Chemistrychemistry.chemical_compoundDifferential scanning calorimetryPolybutadienechemistryTransmission electron microscopyPolymer chemistryCopolymerMethyl methacrylatePalladiumRussian Chemical Bulletin
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Behaviour of modified and unmodified polybutadienes in the semidilute regime

1997

Abstract The association behaviour of polybutadiene modified with 4-phenyl-l,2,4-triazoline-3,5-dione was studied in semidilute solution through static (SLS) and dynamic light scattering (DLS). The results were compared with the unmodified polybutadiene, whose behavior in semidilute solution was also studied as function of the molecular weight. At higher concentrations a small-angle excess scattering in SLS and a slow mode motion in DLS were observed both for modified and unmodified polybutadienes suggesting the presence of large clusters. Increasing the polymer concentration, the mass fraction of the slow motion increases up to values near 1, indicating a proximity to the gel point. For po…

chemistry.chemical_classificationGel pointPolymers and PlasticsScatteringOrganic ChemistryIntermolecular forceAnalytical chemistryGeneral Physics and AstronomyConcentration effectPolymerPolybutadienechemistryDynamic light scatteringPolymer chemistryMaterials ChemistryMass fractionEuropean Polymer Journal
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A model for polybutadiene coatings on porous silica

1993

Non-wetting viscous liquids such as oligobutadiene prefer “active” sites such as pores during the process of physisorption. Thus, polybutadiene (PBD) coatings on porous silica do not result in a homogeneous polymer film but in an inhomogeneous loading where the bulk polymer is mainly sited in the pores of the silica. An increasing polymer loading leads to increasingly filled pores instead of a thicker polymer film. We cannot exclude the possibility that most of the surface is covered at least with a thin polymer film since the chromatographic behaviour is relatively good for polypeptides, which are highly susceptible to the silanol groups of silica.

chemistry.chemical_classificationMagic angleOrganic ChemistryClinical BiochemistryPolymerViscous liquidBiochemistryAnalytical ChemistrySilanolchemistry.chemical_compoundPolybutadienechemistryPhysisorptionChemical engineeringHomogeneousOrganic chemistryPorosityChromatographia
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1993

4-(4-Carboxyphenyl)-3,5-dioxo-1,2,4-triazolidin-1-yl moieties resulting from 4-(3,5-dioxo-1,2,4-triazolin-4-yl)benzoic acid (U4A) randomly attached to 1,4-polybutadiene form supramolecular aggregates which act as effective junction zones in new thermoplastic elastomers. Deuteron nuclear magnetic resonance (2H NMR) spectroscopy was used to investigate the molecular dynamics of the polymer backbone and the junction zones in selectively labelled samples. The spectra show motional heterogeneity along the polymer chain as well as in the supramolecular domains. Polybutadiene segments which are adjacent to these polar clusters are restricted in their mobility, even at temperatures 100 K above the …

chemistry.chemical_classificationMaterials scienceHydrogen bondSupramolecular chemistryPolymerchemistry.chemical_compoundMolecular dynamicsNuclear magnetic resonanceMonomerPolybutadienechemistryPolymer chemistryThermoplastic elastomerGlass transitionDie Makromolekulare Chemie
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Direct Surface Relief Formation in Polymer Films

2013

Due to active development of nanoelectronics, the studies of methods of nanorelief surface formation in different materials, in particular polymers are very important. Organic polymer films in consequence of their dielectric and optical properties have been used as basis of these devices. In this paper, the possibility of UV optical record and electron beam lithography in different type of polymeric films was studied. Mechanisms of molecular structure changes: photoisomerization, destruction, cross-linking and oxidation have been discussed. The results of UV illumination of polyurethanes, polyacrylates, and some block-copolymers were described. The element analysis of polybutadiene block co…

chemistry.chemical_classificationMaterials sciencePhotoisomerizationbusiness.industryMechanical EngineeringPolymerDielectricPolybutadieneOpticschemistryNanoelectronicsMechanics of MaterialsCopolymerOptoelectronicsMoleculeGeneral Materials SciencebusinessElectron-beam lithographyKey Engineering Materials
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Cooperative self-assembling in statistical copolymers: a new approach to high-temperature thermoplastic elastomers

1994

Based on previous work, where it was shown that 4-urazoylbenzoic acid (U4A) groups, which are attached statistically to polybutadiene, form ordered supramolecular arrays in the unpolar polymer matrix, the present work describes the synthesis of a new molecular building block capable of self-assembling in the unpolar polymer matrix. 5-Urazoylisophthalic acid (U35A) groups attached to 1,4-polybutadiene chains cause the formation of a thermoplastic elastomer of improved properties. The clusters of functional groups show an endothermic transition. The melting temperature increases for low levels of modification from 130°C up to 190°C. The mechanical properties (stress–strain and dynamic mechani…

chemistry.chemical_classificationMaterials sciencePolybutadienePolymers and PlasticschemistryHydrogen bondCopolymerSupramolecular chemistryPolymerThermoplastic elastomerComposite materialMaterial propertiesEndothermic processPolymers for Advanced Technologies
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Competitive Adsorption of Functionalized Polymers

1996

The adsorption and desorption of functionalized polystyrene-block-polybutadiene diblock copolymers from dilute solutions in toluene onto silicon wafers are investigated by means of null ellipsometry. The short polybutadiene block is functionalized by a reaction with 4-(3,5-dioxo-1,2,4-triazolidin-4-yl)benzoic acid. On the average there are six functional groups per chain. The polystyrene block does not adsorb on the surface. The adsorption depends on the length of the polystyrene block, and chains with short polystyrene blocks yield higher surface coverage than larger ones. When short and long chains are put together, the short chains displace the long ones in equilibrium conditions nearly …

chemistry.chemical_classificationMaterials scienceSurfaces and InterfacesPolymerCondensed Matter PhysicsToluenePolyelectrolytechemistry.chemical_compoundAdsorptionPolybutadieneChemical engineeringchemistryDesorptionPolymer chemistryElectrochemistryCopolymerGeneral Materials SciencePolystyreneSpectroscopyLangmuir
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