Search results for "Polymers"

showing 10 items of 3567 documents

Scattering function and the dynamics of phase separation in polymer mixtures under shear flow

1988

The phenomenological mean-field theory describing concentration fluctuations and spinodal decomposition of binary mixtures of long flexible macromolecules is generalized to mixtures under steady shear flow. This shear flow leads to a partial orientation and stretching of the coils, as well as to an anisotropic deformation of concentration fluctuations. Generalizing the approach of Onuki and Kawasaki, we obtain the collective scattering function describing these concentration fluctuations in the mixture under shear flow. Both the steady-state situation in the one-phase region and the initial stages of spinodal decomposition for concentrations inside of the spinodal curve are considered.

chemistry.chemical_classificationScattering functionSpinodalPolymers and PlasticsSpinodal decompositionChemistryDynamics (mechanics)ThermodynamicsPolymerPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterColloid and Surface ChemistryMaterials ChemistryField theory (psychology)Physical and Theoretical ChemistryShear flowStructure factorColloid & Polymer Science
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Chlorotitanium (IV) tetradentate Schiff-base complex immobilized on inorganic supports: Support type and other factors having effect on ethylene poly…

2009

A titanium complex with [O,N,N,O]-type tetradentate Schiff base (LTiCl2), never used before in polymerization of olefins, was immobilized on silica- and magnesium-type carriers, and it was used in ethylene polymerization. The conducted research revealed that the catalytic properties of the complex LTiCl2 supported on those carriers were different for both the catalytic systems studied, and simultaneously they turned out different from those of the unsupported system. The supported catalysts require the use of Me3Al, Et3Al, or MAO as the activator to be able to offer high catalytic activities, whereas Et2AlCl is needed for the nonsupported catalyst. This finding, together with considerable c…

chemistry.chemical_classificationSchiff basePolymers and PlasticsMagnesiumOrganic Chemistrychemistry.chemical_elementPolymerPolyethyleneCatalysischemistry.chemical_compoundchemistryPolymerizationEthylene polymerizationPolymer chemistryMaterials ChemistrySupport systemJournal of Polymer Science Part A: Polymer Chemistry
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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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Self-Diffusion of Small Molecules into Rubbery Polymers: A Lattice Free-Volume Theory

2010

In the framework of the Free Volume Theory, a new equation was derived for the evaluation of self-diffusion coefficients of small molecules in polymers above the mixture glass transition temperature. The derivation of the equation turned out to be straightforward once the equivalence between the free-volume and the unoccupied volume given by Thermodynamic Lattice Theories is assumed. A parameter evaluation scheme is proposed, which is substantially simpler compared to the conventional Vrentas-Duda approach, even without losing generality. The key assumption is discussed and its consistency is verified from a numerical viewpoint. A comparison with experimental solvent self-diffusion coeffici…

chemistry.chemical_classificationSelf-diffusionPolymers and PlasticsChemistrydiffusionThermodynamicsConcentration effectBinary numbermodelingPolymerCondensed Matter PhysicsSmall moleculeAmorphous solidfree-volumethermodynamicLattice (order)Materials ChemistryamorphouPhysical and Theoretical ChemistryGlass transition
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Self-Diffusion of Associating Star-Shaped Polymers

2016

The dynamics of associating bonds in transient polymer networks exerts a paramount influence on their relaxation and time-dependent mechanical properties. In particular, diffusive motion of polymers mediated by the dissociation and association equilibrium of reversible junctions can affect the materials’ structural stability, dynamic mechanical properties, and a broad spectrum of functionality that arises from the constant motion of polymer chains. In this work, forced Rayleigh scattering is used to measure the diffusion of terpyridine end-functionalized four-arm poly(ethylene glycol) polymers transiently interlinked by zinc ions in organic solvent across a wide range of length and time sca…

chemistry.chemical_classificationSelf-diffusionPolymers and PlasticsConstant of motionOrganic Chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFick's laws of diffusionDissociation (chemistry)0104 chemical sciencesInorganic ChemistrychemistryStructural stabilityChemical physicsPolymer chemistryMaterials ChemistryExponent0210 nano-technologyScalingMacromolecules
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Polymeric scaffolds based on blends of poly-l-lactic acid (PLLA) with poly-d-l- lactic acid (PLA) prepared via thermally induced phase separation (TI…

2012

Porous scaffolds based on blends of high crystalline Poly-L-lactic acid (PLLA) with low crystalline poly-D-L-lactic acid (PLA) were prepared via Ther- mally Induced Phase Separation (TIPS), with the aim of exploring the possibility to control the degradation behaviour of the PLA-based scaffold, simultaneously pre- serving the morphological characteristics required for tissue engineering applica- tions. Porous foams with different PLLA/PLA weight ratios (from 95/5 to 60/40) were produced and characterised in terms of pore size, porosity, and thermal properties. The scaffolds present an open porosity, with average pore sizes ranging from 30 to 70 lm. Results showed that, when dealing with a P…

chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaMorphology (linguistics)Materials sciencePolymers and Plasticstechnology industry and agricultureSettore ING-IND/34 - Bioingegneria IndustrialeGeneral ChemistryPolymerBiodegradationCondensed Matter PhysicsBiodegradable polymerTissue engineering Biodegradable polymers Poly-L-lactic-acid (PLLA) Polymer blendsLactic acidCrystallinitychemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistrySettore BIO/10 - BiochimicaMaterials ChemistryPolymer blendComposite materialPorosity
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Investigation of Multicomponent Sorption in Polymers from Fluid Mixtures at Supercritical Conditions:  The Case of the Carbon Dioxide/Vinylidenefluor…

2008

The simultaneous sorption of carbon dioxide and vinylidene fluoride (VDF) in poly(vinylidenefluoride) from their supercritical (sc) mixtures was studied using an experimental method, already described in a previous publication, based on the gas-chromatographic determination of the equilibrium composition of the fluid phase in contact with the polymer. Argon was added to the system as a nonabsorbable molecular probe in the polymer to take into account the effect of the volume swelling on the measurement. Sorption behavior has been studied at 50 °C by changing the composition and the density of the supercritical phase. We have found that VDF dissolves in its polymer with concentrations much l…

chemistry.chemical_classificationSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciPolymers and PlasticsOrganic ChemistryRadical polymerizationSorptionPolymerSettore ING-IND/27 - Chimica Industriale E TecnologicaSupercritical fluidInorganic Chemistrychemistry.chemical_compoundChemical reaction kineticsMonomerchemistryChemical engineeringCarbon dioxideMaterials ChemistryOrganic chemistryFluorideFluid mechanicsGas chromatographyPolymerizationPolymersSorptionMacromolecules
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No-Flow Temperature in Injection Molding Simulation

2010

Most injection molding simulation packages use the no-flow temperature (NFT) as a means of determining whether the polymer flows or is solid. The NFT is not well defined, and a standard method for measuring it does not exist. A sensitivity analysis of the filling stage has been carried out with two different packages [VISI Flow (Vero Software Limited, Gloucestershire, UK) and Moldflow (Autodesk, Inc., San Rafael, CA)] to estimate the influence of the NFT on the main processing parameters. The NFT has a large influence on the thickness of the frozen layer, but it does not appreciably affect the filling pressure. Because the NFT affects the frozen layer, an effect on the estimation of shrinka…

chemistry.chemical_classificationSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciSettore ING-IND/24 - Principi Di Ingegneria ChimicaMaterials sciencePolymers and Plasticsinjection moldingFlow (psychology)General ChemistryPolymerMolding (process)Surfaces Coatings and FilmsAmorphous solidCrystallinitySettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMaterials ChemistryForensic engineeringprocessingSensitivity (control systems)simulationsWell-definedComposite materialShrinkage
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Ferrocenyl-functionalized long chain branched polydienes

2009

A convenient two-step approach for the synthesis of ferrocenyl-functionalized long chain branched polydienes, based on both butadiene and isoprene, respectively, is presented. Classical living anionic polymerization was used to synthesize different AB n type poly(diene) macromonomers with moderate molecular weights between 1700 and 3200 g/mol and narrow polydispersity. Quantitative end-capping with chlorodimethylsilane resulted in the desired AB n macromonomer structures. In the ensuing Pt-catalyzed hydrosilylation polyaddition, branched, functionalized polydienes were obtained by a concurrent AB n + AR type of copolymerization with mono-and difunctional ferrocenyl silanes (fcSiMe 2 H or fc…

chemistry.chemical_classificationSilanesPolymers and PlasticsHydrosilylationOrganic ChemistryPolymerBranching (polymer chemistry)Macromonomerchemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryMaterials ChemistryCopolymerLiving anionic polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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Synthesis of a rod-based porous coordination polymer from a nucleotide as a sequential chiral inductor

2021

We report the two-step synthesis of a novel chiral rod-based porous coordination polymer (PCP). The chemical approach consists of the use of a previously prepared bis(ethylenediamine) copper monomer [Cu(en)]2(NO3)2 [where en = ethylenediamine] reacting with the cytidine 5′-monophosphate (CMP) nucleotide. The bis(ethylenediamine) copper compound—stabilized by axial coordination of nitrate counter-anions—reacts in the presence of sodium salt of CMP to yield right-handed copper(II) chains of P helicity with formula [Cu2(en)2(CMP)2]·5H2O (1). The axial coordination of the CMP2- ligands through the N3 and O2 sites (free nitrogen and carbonyl groups) of the cytosine nucleobase and oxygen atoms of…

chemistry.chemical_classificationSolucions polimèriquesCoordination polymertechnology industry and agriculturePorous Coordination Polymerschemistry.chemical_elementEthylenediamineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistryInductor01 natural sciencesCopper0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryNucleotideCristallsPhysical and Theoretical ChemistryPorosity
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