Search results for "Styrene"

showing 10 items of 561 documents

Statistical Characterization of Self-Assembled Colloidal Crystals by Single-Step Vertical Deposition

2014

Abstract We have statistically characterized the self-assembly of multi-layer polystyrene colloidal crystals, using the technique of vertical deposition, with parameters chosen to produce thick layers of self-assembled crystals in one deposition step. The size distribution of domains produced with this technique was seen to follow a log-normal distribution, hinting that aggregation or fragmentation phenomena play a role. In addition, using a lithographically directed self-assembly method, we have shown that the size of multi-layer, continuous crack-free domains in lithographically defined areas can be many times larger than in the surrounding areas. In a single deposition step, we have prod…

Polystyrene spheresCondensed Matter - Materials ScienceMaterials scienceta114Condensed Matter - Mesoscale and Nanoscale Physicsbusiness.industryta221Materials Science (cond-mat.mtrl-sci)FOS: Physical sciencesSingle stepNanotechnologyColloidal crystalSelf assembledchemistry.chemical_compoundColloid and Surface ChemistrychemistryMesoscale and Nanoscale Physics (cond-mat.mes-hall)OptoelectronicsPolystyreneSelf-assemblybusinessLithography
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Photo-Stability Improvement of Polystyrene-block-Polybutadiene-block-Polystyrene through Carbon Nanotubes

2015

The photo-oxidation stability of Polystyrene-Polybutadiene-Polystyrene (SBS) based nanocomposites containing bare multi-walled carbon nanotubes (CNTs) and carbon nanotubes bearing hydroxyl functional groups (CNTs-OH) in comparison to that of pristine SBS has been widely investigated. 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 be…

Polystyrene-block-Polybutadiene-block-Polystyrene Carbon Nanotubes Photo-Stability
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Attachment of Marine Sponge Cells of Hymeniacidon perleve on Microcarriers

2003

Toward the development of an in vitro cultivation of marine sponge cells for sustainable production of bioactive metabolites, the attachment characteristics of marine sponge cells of Hymeniacidon perleve on three types of microcarriers, Hillex, Cytodex 3, and glass beads, were studied. Mixed cell population and enriched cell fractions of specific cell types by Ficoll gradient centrifugation (6%/8%/15%/20%) were also assessed. Cell attachment ratio (defined as the ratio of cells attached on microcarrier to the total number of cells in the culture) on glass beads is much higher than that on Cytodex 3 and Hillex for both mixed cell population and cell fraction at Ficoll 15-20% interface. The h…

PopulationCell Culture TechniquesFicollMarine BiologyBeadMicrobiologyMaterials TestingCell AdhesionAnimalsCentrifugationBovine serum albumineducationCells Culturededucation.field_of_studyChromatographybiologyMicrocarrierDextransMembranes Artificialbiology.organism_classificationMicrospheresPoriferaSpongeCell culturevisual_artvisual_art.visual_art_mediumbiology.proteinPolystyrenesGlassBiotechnologyBiotechnology Progress
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Polystyrene Sulfonate–Porphyrin Assemblies: Influence of Polyelectrolyte and Porphyrin Structure

2011

In this study, electrostatic self-assembly of different polystyrene sulfonates and a set of tetravalent cationic porphyrins is investigated. It is shown that association of linear polystyrene sulfonates of different molar masses yields finite size nanoscale assemblies that are stable in aqueous solution. Aggregates are compared to the ones of cylindrical brushes, revealing that both form assemblies in the 100 nm range with the charge ratio (molar ratio of porphyrin charges to polyelectrolyte charges) being determining, while the morphology of the resulting network-like assemblies is different for both polyelectrolyte architectures. For the smallest 8k polystyrene sulfonate, in addition, sto…

PorphyrinsLightStatic ElectricityMicroscopy Atomic ForcePorphyrin structurePolystyrene sulfonatechemistry.chemical_compoundScattering Small AnglePolymer chemistryMaterials ChemistryScattering RadiationPhysical and Theoretical ChemistryCationic polymerizationPorphyrinPolyelectrolyteNanostructuresSurfaces Coatings and FilmsQuaternary Ammonium CompoundsNeutron DiffractionZincchemistryPolystyrenesSpectrophotometry UltravioletSelf-assemblyPolystyreneCopperThe Journal of Physical Chemistry B
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1976

The phenomenon of “true cosolvency”, which has only recently been observed in the system acetone/diethyl ether/polystyrene (AC/DEE/PS), is investigated with regard to its pressure dependence and compared with the thermodynamic behaviour of the corresponding binary sub-systems. For the determination of the limits of complete solubility, a pressure apparatus was used which had been constructed, in order to measure the turbidity of fluids in the temperature range of −70 to +500°Cand in the pressure range of 1 to 4000 bar (105 to 4·108 Nm−2). The critical line observed for the system DEE/PS (MPS=20400) looks similar to that reported for AC/PS in the literature, i.e. the upper critical solution …

Pressure rangechemistry.chemical_compoundchemistryHomogeneousPolymer chemistryAcetonePolystyrenePressure dependenceSolubilityBar (unit)Die Makromolekulare Chemie
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Polystyrene-supported proline and prolinamide. Versatile heterogeneous organocatalysts both for asymmetric aldol reaction in water and α-selenenylati…

2007

A simple and efficient synthesis of polystyrene-supported proline and prolinamide has been carried out. Polystyrene-supported proline has been used as organocatalyst in the asymmetric aldol reaction between cyclohexanone and substituted benzaldehydes in water without any additive. High yields, diastereoselectivities and ee values have been observed. The versatility of this resin was demonstrated in the α-selenenylation of aldehydes. Both proline and prolinamide resins gave high yields. Recycling studies showed that the proline resin gave better results than prolinamide resin.

ProlineOrganocatalysisOrganic Chemistrytechnology industry and agricultureCyclohexanoneSettore CHIM/06 - Chimica OrganicaGeneral MedicineBiochemistrychemistry.chemical_compoundHeterogeneous Catalysisstomatognathic systemchemistryAldol reactionDrug DiscoveryOrganic chemistryProlinePolystyreneTetrahedron Letters
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Valence Topological Charge-Transfer Indices for Dipole Moments

2003

Valence topological charge-transfer (CT) indices are applied to the calculation of dipole moments. The dipole moments calculated by algebraic and vector semisums of the CT indices are defined. The combination of the CT indices allows the estimation of the dipole moments. The model is generalized for molecules with heteroatoms. The ability of the indices for the description of the molecular charge distribution is established by comparing them with the dipole moment of the valence-isoelectronic series of benzene and styrene. Two CT indices, μ v e c (vector semisum of vertex-pair dipole moments) and μ V v e c (valence μ v e c ) are proposed. μ v e c and μ V v e c are important for the predicti…

Protein ConformationHeteroatomPharmaceutical ScienceBiochemistryAnalytical ChemistryElectricityComputational chemistryDrug DiscoveryPhysicsvalence topological charge-transfer indexChemistryCharge densityGeneral Medicinemolecular charge distributionCondensed Matter Physicstransdermal drug deliveryChemistry (miscellaneous)Molecular MedicineAtomic physicsInformation SystemsSteric effectsBond dipole momentStatic ElectricityTransition dipole momentBiophysicsElectronsFractal dimensionMolecular physicsBiophysical PhenomenaArticleCatalysislcsh:QD241-441Inorganic Chemistrylcsh:Organic chemistryAtomic orbitalMoleculePhysical and Theoretical ChemistryMolecular BiologyStyreneTopological quantum numberDipole momentModels StatisticalValence (chemistry)Chemical polarityOrganic ChemistryBenzeneModels Theoreticalvalence topological chargetransfer indexElectric dipole momentDipolephenyl alcoholModels ChemicalMoment (physics)Electric dipole transitionMolecules
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Shear induced deformation of polystyrene coils in dilute solution from small angle neutron scattering

1985

The deformation of the overall conformation of polystyrene,Mw=280000 g/ mole in dilute solution in a constant shear gradient has been investigated by small angle neutron scattering (SANS).

Quantitative Biology::BiomoleculesMaterials sciencePolymers and PlasticsTesting equipmentNeutron scatteringSmall-angle neutron scatteringCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryShear (geology)Materials ChemistryPolystyrenePhysical and Theoretical ChemistryComposite materialCouette flowColloid & Polymer Science
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Quantitative evaluation of the preferential orientation ofpara-phenylene vinylene pentamers in polystyrene films by optically detected magnetic reson…

2007

The morphology of drop-casted and spin-coated films of blends ofpara-phenylene vinylenederived pentamers with polystyrene is investigated by means of X-band optically detected magnetic resonance (ODMR) of the triplet excited states. Adapting an electron spin resonance simulation program to ODMR, the orientation distribution function of the oligomers in the films could be quantified. After drop casting or spin coating the pentamers from a solution, the oligomers tend to lie with their backbones in the plane of the film. The parameters of film preparation and the type of pentamer strongly influence the orientation distribution function. Also, the study of preferentially oriented films allows …

Quantitative Biology::BiomoleculesSpin coatingMaterials sciencePentamerPhysicsAnalytical chemistryZero field splittingAtomic and Molecular Physics and Opticslaw.inventionChemistrychemistry.chemical_compoundCrystallographychemistrylawPhenyleneExcited stateMoleculePolystyreneElectron paramagnetic resonanceApplied Magnetic Resonance
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Kinetics of phase separation in polymer blends for deep quenches

1986

Electro microscopy was used to study the phase separation kinetics of a polystyrene/polyvinylmethylether system subjected to a critical deep quench. The size of the phase-separated domains was found to increase linearly with time, implying that hydrodynamic effects control the rate of growth of the domains in the time scale and temperature range under consideration. From these measurements the growth velocity and approximate diffusion constants can be determined for three different temperatures. Comparison of these results with those obtained by light scattering on other systems and with theoretical predictions is possible by replotting in dimensionless units.

QuenchingSpinodalPolymers and PlasticsChemistryKineticsMineralogyThermodynamicsAtmospheric temperature rangeCondensed Matter PhysicsLight scatteringchemistry.chemical_compoundCritical point (thermodynamics)Materials ChemistryPolystyrenePhysical and Theoretical ChemistryDimensionless quantityJournal of Polymer Science Part B: Polymer Physics
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