Search results for "styrene"

showing 10 items of 561 documents

NMR Matrix Technique for Detecting Self Diffusion in Polymers

1979

A technique is discussed where monodisperse small spheres or cylindrical fibers of a polymer are embedded in a matrix of the corresponding fully deuterated polymer. On annealing the sample at a temperature above the glass transition the protonated macromolecules diffuse into the deuterated matrix and vice versa. Since the NMR spectrum depends upon the intermolecular proton proton dipolar coupling, the decrease of this coupling can be used to monitor the diffusion process. For particle diameters d ∼ 10−4 cm and annealing times t ∼ 105 s, extremely small diffusion constants D < d2/t are attainable. The NMR analysis of prospective diffusion experiments with polystyrene is discussed in some det…

chemistry.chemical_classificationSelf-diffusionGeneral Chemical EngineeringProtonationNuclear magnetic resonance spectroscopyPolymerchemistry.chemical_compoundchemistryDeuteriumPolymer chemistryPhysical chemistryPolystyreneGlass transitionMagnetic dipole–dipole interactionBerichte der Bunsengesellschaft für physikalische Chemie
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A friction factor analysis of the coupling between polymer/solvent self- and mutual-diffusion: polystyrene/toluene

1996

The Bearman statistical mechanical theory, which couples the mutual-diffusion and self-diffusion coefficients via friction factors, has been applied to polystyrene/toluene solutions with polystyrene molecular weights of 18 kDa and 900 kDa. Toluene and polystyrene self-diffusion coefficients, obtained from the literature and measured here, along with polystyrene/toluene binary mutual-diffusion coefficients and thermodynamic data, were employed to independently calculate the three friction coefficients (ξ 12 , ξ 11 , and ξ 22 ) required to describe transport within binary solutions. Results reveal that the frequently used geometric mean approximation (GMA) for relating the friction coefficien…

chemistry.chemical_classificationSelf-diffusionPolymers and PlasticsChemistryDiffusionThermodynamicsConcentration effectPolymerCondensed Matter PhysicsToluenechemistry.chemical_compoundDynamic light scatteringPolymer chemistryMaterials ChemistryPolystyreneBinary systemPhysical and Theoretical ChemistryJournal of Polymer Science Part B: Polymer Physics
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ChemInform Abstract: Epoxidation of Olefins with a Silica-Supported Peracid.

2012

Anhydrous [2-percarboxyethyl] functionalized silica (2a) is an advantageous oxidant for performing the epoxidation of olefins 1. Epoxides 3 do not undergo the ring-opening reactions catalyzed by the acidic silica surface, except for particularly activated cases such as styrene oxide. The hydrophilic and acidic character of the silica surface does not interfere with the directing effects exerted by allylic H-bond acceptor substituents. The alkenes 1 carrying hydroxyl groups react with silica-supported peracid 2a faster than unsubstituted alkenes, thus reversing the trend known for reactions with soluble peracids. These results are attributed to the H-bond interactions of substrate 1 with the…

chemistry.chemical_classificationSilanolchemistry.chemical_compoundAllylic rearrangementchemistryCarboxylic acidStyrene oxidePolymer chemistryAnhydrousSubstrate (chemistry)General MedicineAcceptorCatalysisChemInform
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Polymer-induced phase separation in suspensions of bacteria

2010

We study phase separation in suspensions of two unrelated species of rod-like bacteria, Escherichia coli and Sinorhizobium meliloti, induced by the addition of two different anionic polyelectrolytes, sodium polystyrene sulfonate or succinoglycan, the former being synthetic and the latter of natural origin. Comparison with the known behaviour of synthetic colloid-polymer mixtures and with simulations show that "depletion" (or, equivalently, "macromolecular crowding") is the dominant mechanism: exclusion of the non-adsorbing polymer from the region between two neighbouring bacteria creates an unbalanced osmotic force pushing them together. The implications of our results for understanding phe…

chemistry.chemical_classificationSinorhizobium melilotiADSORPTIONbiologyBiofilmMIXTURESfood and beveragesGeneral Physics and AstronomyPolymerAGGREGATIONbiology.organism_classificationmedicine.disease_causeLIGHT-SCATTERINGSUCCINOGLYCANPolyelectrolytechemistryESCHERICHIA-COLImedicineBiophysicsMacromolecular crowdingSodium Polystyrene SulfonateEscherichia coliBEHAVIORBacteriaEPL (Europhysics Letters)
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1986

The variation of the Huggins coefficient KH with the relative molecular mass M of the polymers was measured for solutions of polystyrene and of polyisobutylene and found to be most pronounced in the case of thermodynamically good solvents but vanishing at the theta-temperature, where the individual curves kH (T; M) intersect with each other. The experimental results are interpreted as a consequence of the rheological inequality of inter- and intra-molecular contacts between polymer segments. A model is presented according to which kH should be a linear function of M−(a−0,5), where a is the exponent of the intrinsic viscosity-relative molecular mass relationship (Kuhn-Mark-Houwink). The eval…

chemistry.chemical_classificationSolventViscositychemistry.chemical_compoundLinear function (calculus)chemistryVirial coefficientRheologyPolymer chemistryExponentThermodynamicsPolymerPolystyreneDie Makromolekulare Chemie
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Molecular modeling studies of interactions between styrene–butadiene latex and sodium polyacrylate polymer surface

2010

Abstract The interaction between two important paper coating ingredients, sodium polyacrylate polymer dispersing agent and styrene–butadiene latex binder, was studied using classical force field and quantum chemical methods. The objective was to understand the adsorption of styrene–butadiene latex on the sodium polyacrylate polymer model surfaces at 300 K using molecular dynamics simulations. A quantum mechanical ab initio Hartree–Fock method was also used to obtain detailed information about the above interactions. In addition, the effect of moisture was investigated. Calculations showed that the conformation and orientation of styrene–butadiene latex, the number of carboxylate groups in t…

chemistry.chemical_classificationStyrene-butadieneSodium polyacrylateSodiumchemistry.chemical_elementPolymerCondensed Matter PhysicsBiochemistryDispersantchemistry.chemical_compoundMolecular dynamicsAdsorptionchemistryPolymer chemistryMoleculePhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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Surface-Functionalized Latex Particles as Controlling Agents for the Mineralization of Zinc Oxide in Aqueous Medium

2005

Polystyrene latex particles modified at the surface with different hydrophilic functional groups were prepared by miniemulsion polymerization and used as controlling agents in the crystallization of zinc oxide from aqueous medium. The effects of the chemical nature of the surface functionalization and the latex concentration on the crystal growth, morphology, and crystalline structure of the resulting zinc oxide were analyzed. Micro- and submicrosized crystals with a broad variety of morphologies depending on the functionalization were obtained. Among the different latexes studied, the acrylic-acid-derived particles were shown to be a convenient system for further quantitative investigation…

chemistry.chemical_classificationSurface PropertiesChemistryOrganic ChemistryWaterGeneral ChemistryPolymerMicrospheresCatalysislaw.inventionMiniemulsionAdsorptionX-Ray DiffractionChemical engineeringPolymerizationlawPolymer chemistryWettabilityPolystyrenesSurface modificationWettingParticle sizeParticle SizeZinc OxideCrystallizationChemistry - A European Journal
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Interfacial tension of demixed polymer solutions: augmentation by polymer additives

1997

The interfacial tension between phase separated polymer solutions increases pronouncedly upon the addition of asmall amounts of incompatible polymers. This feature is demonstrated by means of measurements with solutions of polystyrene in cyclohexane and the folloowing additives: poly(styrene-block-dimethylsiloxane), polyisobutylene and polydimethylsiloxane. Theoretical considerations based on a correlation between the lenth of the tie lines and the corresponding interfacial tension corroborates this finding

chemistry.chemical_classificationTernary numeral systemMaterials sciencePolymers and PlasticsCyclohexanePolydimethylsiloxaneOrganic ChemistryPolymerSurface tensionchemistry.chemical_compoundchemistryChemical engineeringPhase (matter)Polymer chemistryMaterials ChemistryCopolymerPolystyreneMacromolecular Rapid Communications
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Miscibility of a DGEBA Based Epoxy Resin Blended with Thermoplastic Mixtures of Poly(styrene) and Block Copolymers: Influence of the Copolymer Conten…

2008

The miscibility and phase behavior of ternary systems formed by a DGEBA based epoxy resin, polystyrene (PS), and diblock copolymers has been investigated through phase diagrams experimentally obtai...

chemistry.chemical_classificationThermoplasticMaterials sciencePolymers and PlasticsGeneral ChemistryEpoxyCondensed Matter PhysicsMiscibilityStyrenechemistry.chemical_compoundchemistryChemical engineeringPhase (matter)visual_artPolymer chemistryMaterials ChemistryCopolymervisual_art.visual_art_mediumPolystyreneTernary operationJournal of Macromolecular Science, Part B
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Modification of commercial UF membranes by electrospray deposition of polymers for tailoring physicochemical properties and enhancing filtration perf…

2020

Abstract The main challenge for a widespread use of nanoporous membranes in the removal of ionic contaminants lies in the adjustment of their physicochemical properties to allow adequate ion rejection and mitigate fouling based on the targeted application. Most of the commercial membranes are negatively charged and their use is thus not necessarily relevant for divalent cation rejection. The main objective for researchers is therefore to provide novel tailored membranes by developing specific synthesis or modifying available membranes. It is proposed here to tailor physicochemical properties of a commercial low molecular weight cut-off ultrafiltration membrane by electrospray deposition of …

chemistry.chemical_classificationUltrafiltrationIonic bondingFiltration and Separation02 engineering and technologyPolymerPermeation010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesDivalentPolystyrene sulfonateContact anglechemistry.chemical_compoundMembraneChemical engineeringchemistry[CHIM]Chemical SciencesGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyComputingMilieux_MISCELLANEOUS
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