Search results for "Polystyrene"

showing 10 items of 349 documents

Homopolymerization of styrenic monomers and their copolymerization with ethylene using group 4 non‐metallocene catalysts

2020

Homopolymerization of styrenic monomers (St, p ‐Me‐St, p ‐t Bu‐St, p ‐t BuO‐St) and their copolymerization with ethylene, with the use of [( t Bu2O2NN′)ZrCl]2(μ‐O) (1 ) and ( t Bu2O2NN′)TiCl2 (2 ), where t Bu2O2NN′ = Me2N(CH2)2N(CH2‐2‐O−‐3,5‐t Bu2‐C6H2)2, is explored in the presence of MMAO and (i Bu)3Al/Ph3CB(C6F5)4. The ethylene/styrenic monomers copolymerization with 1 /MMAO produces exclusively copolymers with high activity and good comonomer incorporation whereas the other catalytic systems yield mixtures of copolymers and homopolymers. The use of p ‐alkyl styrene derivatives instead of styrene raises the catalytic activity, comonomer incorporation and molecular weights of the copolyme…

EthylenePolymers and Plasticsstructure–property relationshipsGeneral ChemistrypolystyrenecatalystsSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundMonomerchemistryGroup (periodic table)Polymer chemistryMaterials ChemistryCopolymercopolymersPolystyreneMetalloceneJournal of Applied Polymer Science
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Directed Assembly of Soft Colloids through Rapid Solvent Exchange

2015

We studied the directed assembly of soft nanoparticles through rapid micromixing of polymers in solution with a nonsolvent. Both experiments and computer simulations were performed to elucidate the underlying physics and to investigate the role of various process parameters. In particular, we discovered that no external stabilizing agents or charged end groups are required to keep the colloids separated from each other when water is used as the nonsolvent. Furthermore, the size of the nanoparticles can be reliably tuned through the mixing rate and the ratio between polymer solution and nonsolvent. Our results demonstrate that this mechanism is highly promising for the mass fabrication of un…

FabricationMaterials scienceMixing (process engineering)General Physics and AstronomyNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesColloidComputer SimulationGeneral Materials ScienceColloidsParticle Sizechemistry.chemical_classificationGeneral EngineeringWaterPolymer021001 nanoscience & nanotechnology0104 chemical sciencesMicromixingSolutionsSolventKineticsModels ChemicalchemistryColloidal particleNanoparticlesPolystyrenesThermodynamics0210 nano-technologyACS Nano
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A fluorescent molecular sensor for pH windows in traditional and polymeric biocompatible micelles: comicellization of anionic species to shift and re…

2011

A new approach is presented to obtain fluorescent sensors for pH windows that work in water and under biomimetic conditions. A single molecule that features all-covalently linked components is used, thus making it capable of working as a fluorescent sensor with an OFF/ON/OFF response to pH value. The components are a tertiary amine, a pyridine, and a fluorophore (pyrene). The forms with both protonated bases or both neutral bases quench the pyrene fluorescence, whereas the form with the neutral pyridine and protonated amine groups is fluorescent. The molecular sensor is also equipped with a long alkyl chain to make it highly hydrophobic in all its protonated and unprotonated forms, that is,…

FluorophoreTertiary aminePolymersPyridinesInorganic chemistryPhotochemistryMicelleCatalysisPolystyrene sulfonatechemistry.chemical_compoundAmphiphileAminesAlkylMicellesFluorescent Dyeschemistry.chemical_classificationPyrenesfluorescence micelles polymerization potentiometry sensorsOrganic ChemistryMolecular sensorGeneral ChemistryHydrogen-Ion ConcentrationPolyelectrolyteKineticschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoHydrophobic and Hydrophilic InteractionsChemistry (Weinheim an der Bergstrasse, Germany)
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[The in vitro effect of the addition of ion exchange resins on the bioavailability of electrolytes in artificial enteral feeding formulas].

2008

Objective: To determine in vitro free ion concentration in 3 standard artificial enteral feeding formulas following the addition of ion exchange resins. Method: Three standard types of AEF were chosen: Osmolite HN®, Nutrison Standard®, and Isosource Standard®. The ion exchange resins used were: sodium polystyrene sulfonate and calcium polystyrene sulfonate. In a beaker were mixed 100 mL of AEF with 1.5 g or 3 g of ion exchange resins for 48 hours at 37oC. Subsequently, the samples were precipitated and the supernatant obtained was used for determining the concentrations of calcium, magnesium, sodium, and potassium ions. Results: The addition of sodium polystyrene sulfonate to different type…

Food FormulatedChromatographyMagnesiumPotassiumSodiumSodiumchemistry.chemical_elementBiological AvailabilityElectrolyteCalciumEnteral NutritionchemistryPotassiumCalciumMagnesiumIon Exchange ResinsIon-exchange resinSodium Polystyrene SulfonateMagnesium ionFarmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalaria
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ChemInform Abstract: Covalently Supported Ionic Liquid Phases: An Advanced Class of Recyclable Catalytic Systems

2016

In this review, the most recent advances in the synthesis and catalytic applications of covalently supported ionic liquid (IL) phases will be discussed. This class of recyclable catalytic materials is based on the covalent attachment of several types of ammonium salts, usually imidazolium, but also thiazolium, triazolium, and pyrrolidinium salts, on the surface of different supports, for example, silica, periodic mesoporous organosilica, polystyrene, magnetic-based materials, carbon nanotubes (NTs), halloysite NTs, polyhedral oligomeric silsesquioxane (POSS), and fullerenes. Moreover, poly(ionic liquid) materials, in which the IL-based structure also acts as a support, will be considered. T…

FullereneGeneral MedicineCarbon nanotubeSilsesquioxaneCatalysislaw.inventionchemistry.chemical_compoundMesoporous organosilicachemistryChemical engineeringCovalent bondlawIonic liquidPolystyreneChemInform
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Solution properties of polyelectrolytes. III. Effect of sodium polystyrene sulfonate concentration on viscometric and size exclusion chromatographic …

1988

The effect of sodium polystyrene sulfonate concentration on the shape of its molecules in aqueous solution at different NaNO3 ionic strengths has been analyzed by viscometry and size-exclusion chromatography (s.e.c). An equation has been developed which predicts the intrinsic viscosity, [η] p.cp.cs, at finite concentration of both polyion (cp) and electrolyte (cs). The experimental results obtained by both techniques can be accounted for in terms of the theory. Several factors involved in the elution mechanism have been considered and the variation of the slopes of s.e.c. calibration curves with cp and cs has been discussed in terms of polyion conformation changes.

Gel permeation chromatographyChromatographyAqueous solutionChemistryIonic strengthIntrinsic viscositySize-exclusion chromatographyGeneral EngineeringGeneral Materials ScienceElectrolyteSodium Polystyrene SulfonatePolyelectrolyteBritish Polymer Journal
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Solution properties of polyelectrolytes. I. Exclusion chromatography of sodium polystyrene sulphonate in salt-free water as eluent

1987

The effect of concentration of sodium polystyrene sulphonate on the elution volume in exclusion chromatography has been investigated using salt-free water as eluent. A non-linear increase in the elution volume has been observed with increasing injected sample concentration. Concentration-dependent calibrations have been obtained which approach the universal calibration for uncharged polymers (dextrans) as polyelectrolyte concentration increases. The separation mechanisms are interpreted in terms of electrostatic and hydrodynamic interactions. A semi-empirical model is proposed to predict concentration effects of linear polyions in exclusion chromatography and good agreement has been found b…

Gel permeation chromatographychemistry.chemical_classificationViscosityColumn chromatographyChromatographyChemistryElutionSize-exclusion chromatographyGeneral EngineeringGeneral Materials SciencePolymerSodium polystyrene sulphonatePolyelectrolyteBritish Polymer Journal
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Zur Gelpermeationschromatographie in organischen Lösungsmitteln

1965

Die Gelpermeationschromatographie hat sich vor allem mittels der Sephadexgele fur die Trennung polymerhomologer wasserloslicher Makromolekule als sehr erfolgreich erwiesen. Die Trennung nur in organischen Losungsmitteln loslicher Polymerer ist erst in jungster Zeit gelungen, wobei vernetzte Polystyrol-, Polymethacrylat- und Dextranderivatgele benutzt werden. Der Mechanismus dieses chromatographischen Prozesses wird untersucht. Ein Vergleich dieses Vorganges, bei dem das Polymere nur in einer Phase vorliegt, mit den klassischen Methoden, die mit Auftrennung in zwei Phasen arbeiten, wird durchgefuhrt. Insbesondere werden die Methoden der Dreiecks-Fallungsfraktionierung, der Kolonnentechnik mi…

Gel permeation chromatographychemistry.chemical_classificationchemistry.chemical_compoundChemistryElutionGeneral Chemical EngineeringPolymer chemistryDextran DerivativesPolymerPolystyreneFractionationGeneral expressionSephadex gelsBerichte der Bunsengesellschaft für physikalische Chemie
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Flavobacterium columnare colony types: connection to adhesion and virulence?

2008

Four different colony morphologies were produced by Flavobacterium columnare strains on Shieh agar plate cultures: rhizoid and flat (type 1), non-rhizoid and hard (type 2), round and soft (type 3), and irregularly shaped and soft (type 4). Colonies produced on AO agar differed from these to some extent. The colony types formed on Shieh agar were studied according to molecular characteristics [Amplified Fragment Length Polymorphism (AFLP), Automated Ribosomal Intergenic Spacer Analysis (ARISA), and whole cell protein SDS-PAGE profiles], virulence on rainbow trout fingerlings, and adhesion on polystyrene and fish gills. There were no molecular differences between colony types within one strai…

Gillsfood.ingredientRibosomal Intergenic Spacer analysisVirulenceBiologyMicrobiologyFlavobacteriumVirulence factorBacterial AdhesionMicrobiologyAgar plateFish DiseasesfoodBacterial ProteinsFlavobacteriaceae InfectionsDNA Ribosomal SpacerAgarAnimalsPhase variationVirulencebiology.organism_classificationCulture MediaAgarInfectious DiseasesOncorhynchus mykissFlavobacterium columnarePolystyrenesElectrophoresis Polyacrylamide GelFlavobacteriumPolymorphism Restriction Fragment LengthMicrobial pathogenesis
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Pd nanoparticles formation inside porous polymeric scaffolds followed by in situ XANES/SAXS

2015

International audience; Simultaneous time-resolved SAXS and XANES techniques were employed to follow in situ the formation of Pd nanoparticles from palladium acetate precursor in two porous polymeric supports: polystyrene (PS) and poly(4-vinyl-pyridine) (P4VP). In this study we have investigated the effect of the use of different reducing agents (H-2 and CO) from the gas phase. These results, in conjunction with data obtained by diffuse reflectance IR (DRIFT) spectroscopy and TEM measurements, allowed us to unravel the different roles played by gaseous H-2 and CO in the formation of the Pd nanoparticles for both PS and P4VP hosting scaffolds

HistoryMaterials scienceAbsorption spectroscopyNanoparticlechemistry.chemical_elementreduction02 engineering and technologypolystyrene010402 general chemistry01 natural sciencesEducationP4VPchemistry.chemical_compoundPdPd nanoparticles formation inside porous polymeric scaffoldspaladumchemistry.chemical_classification[PHYS]Physics [physics]Small-angle X-ray scatteringnanoparticlein situSAXS XANES Pd paladum nanoparticle polystyrene P4VP DRIFT TEM reduction in situSAXSPolymer021001 nanoscience & nanotechnologyXANESXANES0104 chemical sciencesComputer Science ApplicationsCrystallographyDRIFTchemistryChemical engineeringTEMPolystyreneDiffuse reflection0210 nano-technologyPalladium
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