Search results for "polyelectrolyte"

showing 10 items of 214 documents

Influence of synthesis conditions on the performance of chitosan–Heteropolyacid complexes as membranes for low temperature H2–O2 fuel cell

2015

Flat, free-standing chitosan/phosphotungstic acid (PTA) polyelectrolyte membranes were prepared by in-situ ionotropic gelation process at room temperature on porous alumina support firstly impregnated by H3PW12O40. Scanning electron microscopy revealed the formation of compact and homogeneous membranes, whose thickness resulted to be dependent on chitosan concentration and reticulation time. X-ray diffraction and Fourier transform infrared spectroscopy (FTIR) evidenced the formation of almost amorphous membrane without appreciable concentration of not protonated NH2 groups and PTA3- ions with preserved Keggin structure. Membranes were tested as proton conductor in low temperature H2-O2 fuel…

ChitosanMaterials scienceProtonconductingRenewable Energy Sustainability and the EnvironmentScanning electron microscopeAnalytical chemistryEnergy Engineering and Power TechnologyHeteropolyacidCondensed Matter PhysicH<inf>2</inf>-O<inf>2</inf> PEMCFCondensed Matter PhysicsElectrochemistryPolyelectrolyteComposite membranechemistry.chemical_compoundKeggin structureSettore ING-IND/23 - Chimica Fisica ApplicataFuel TechnologyMembranechemistryChemical engineeringChitosanHeteropolyacidComposite membraneProton conducting H2 O2 PEMCFPhosphotungstic acidFourier transform infrared spectroscopyProton conductorInternational Journal of Hydrogen Energy
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Chitosan-phosphotungstic acid complex as membranes for low temperature H2-O2 fuel cell

2015

Abstract Free-standing Chitosan/phosphotungstic acid polyelectrolyte membranes were prepared by an easy and fast in-situ ionotropic gelation process performed at room temperature. Scanning electron microscopy was employed to study their morphological features and their thickness as a function of the chitosan concentration. The membrane was tested as proton conductor in low temperature H 2 –O 2 fuel cell allowing to get peak power densities up to 350 mW cm −2 . Electrochemical impedance measurements allowed to estimate a polyelectrolyte conductivity of 18 mS cm −1 .

ChitosanMaterials scienceScanning electron microscopeRenewable Energy Sustainability and the EnvironmentProton conductingH2-O2 PEMCFEnergy Engineering and Power TechnologyHeteropolyacidConductivityElectrochemistryPolyelectrolyteChitosanComposite membranechemistry.chemical_compoundMembraneSettore ING-IND/23 - Chimica Fisica ApplicatachemistryChemical engineeringPolymer chemistryPhosphotungstic acidElectrical and Electronic EngineeringPhysical and Theoretical ChemistryChitosanHeteropolyacidComposite membraneProton conductingH2–O2 PEMFCProton conductor
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Interaction of polyelectrolytes with oppositely charged micelles studied by fluorescence and liquid chromatography

2005

It is studied by spectrofluorimetry the association of ionized cationic micelles (cetyltrimethylammonium bromide, CTAB) with oppositely charged polyelectrolyte [sodium poly(styrenesulfonate), PSSNa]. CTAB provokes a change in the fluorescence intensity emitted by PSSNa. The investigated surfactants form micelle-like aggregates before critical micellar concentration (CMC). Two approaches (binding and partition equilibrium) are used to obtain the association constant, KA, number of CTAB molecules in a binding site, N, and apparent partition coefficient, Γ. Analysis of the parameters as a function of polymer concentration and ionic strength μ is performed. The effect of μ shows an enhancement …

ChromatographyAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryGeneral Physics and AstronomyMicellePolyelectrolytePartition coefficientchemistry.chemical_compoundBromideIonic strengthPartition equilibriumCritical micelle concentrationMaterials ChemistryEuropean Polymer Journal
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Solution Properties of Polyelectrolytes. VI. Secondary Effects in Aqueous Size-Exclusion Chromatography

1990

Abstract An independent analysis of different operational variables in aqueous size exclusion chromatography of poly electrolytes has been carried out using a silica-based support. The effect of polyion concentration, pH and ionic strength on sodium polystyrenesulfonate calibration plots has been investigated. Finally, a novel semi-empirical model has been developed from thermodynamic considerations which relates the support effective pore volume to the polyelectrolyte molecular weight and qualitatively describes secondary effects.

ChromatographyAqueous solutionVolume (thermodynamics)Ionic strengthChemistrySodiumSize-exclusion chromatographyMolecular Medicinechemistry.chemical_elementElectrolytePolyelectrolyteJournal of Liquid Chromatography
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Ionomers in solution: 1. Viscometric and chromatographic studies in cononsolvent and cosolvent mixtures

1997

Abstract The viscosity and elution behaviour of polystyrene sulfonate ionomers with varying ionic content has been studied in the pure solvents chloroform (CHL), tetrahydrofuran (THF), dioxan (DIO), ethyl acetate (EA) and dimethylformamide (DMF) as well as in their cononsolvent mixtures CHL/THF (50:50), DIO/CHL (75:25) and in the cosolvent mixture EA/DMF (50:50). In the pure solvents with low dielectric constant the reduced viscosities of ionomers are lower at low concentrations and higher at moderate ones than the respective viscosities of the polystyrene precursor. These results can be explained by formation of intramolecular and intermolecular associations. Moreover, differences in visco…

ChromatographyPolymers and PlasticsOrganic ChemistryConcentration effectIonic bondingPolyelectrolytePolystyrene sulfonatechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryDimethylformamidePolystyreneIonomerTetrahydrofuranPolymer
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Inducing mixing of water-in water BSA/dextran emulsion by a strong polyelectrolyte

2015

Abstract We examine whether a small amount of strong polyelectrolyte (dextran sulfate sodium salt/DSS/) can induce mixing in water-in-water bovine serum albumin/dextran (BSA/DEX) emulsion and how intermacromolecular interactions affect its the rheological properties. Addition of DSS to water-in-water emulsion at pH 5.4 leads to its mixing at the DSS/BSA weight ratio, ( q ( DSS / BSA ) ) ≥ 0.07 , a noticeable increase in viscosity and storage modulus (G′). Mixing is reversible: increasing the ionic strength leads to phase separation in the water/BSA/DEX/DSS system. The increase in viscoelasticity results from the interaction of DSS with both macromolecular compounds of the emulsion. We assum…

Chromatographybiologyanimal diseasesGeneral Chemical EngineeringGeneral ChemistryCompatibilizationdigestive systemdigestive system diseasesPolyelectrolytecarbohydrates (lipids)stomatognathic diseaseschemistry.chemical_compoundDextranchemistryChemical engineeringIonic strengthEmulsionCopolymerbiology.proteinPolymer blendBovine serum albuminFood ScienceFood Hydrocolloids
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Titration of poly(dA-dT) · poly(dA-dT) in solution at variable NaCl concentration

2004

CD and uv absorption data showed that high molecular weight poly(dA-dT) . poly(dA-dT), at 298 K, undergoes an acid-induced transition from B-double helix to random coil in NaCl solutions of different concentrations, ranging from 0.005 to 0.600M. Similarly, titration of the polynucleotide with a strong base causes duplex-to-single strands transition. The base- and acid-induced transitions were both reversible by back-titration (with an acid or, respectively, with a base): the apparent pKa were the same in both directions. However, the number of protons per titratable site (adenine N1) required to reach half-denaturation was in great excess over the stoichiometric value; to a much larger exte…

Circular dichroismOrganic ChemistryBiophysicsGeneral MedicineBiochemistryPolyelectrolyteRandom coilThymineBiomaterialsCrystallographychemistry.chemical_compoundDeprotonationchemistryPolynucleotideCounterion condensationOrganic chemistryTitrationBiopolymers
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Complex Formation between Polyelectrolytes and Oppositely Charged Oligoelectrolytes

2016

We study the complex formation between one long polyanion chain and many short oligocation chains by computer simulations. We employ a coarse-grained bead-spring model for the polyelectrolyte chains, and model explicitly the small salt ions. We systematically vary the concentration and the length of the oligocation, and examine how the oligocations affects the chain conformation, the static structure factor, the radial and axial distribution of various charged species, and the number of bound ions in the complex. At low oligocation concentration, the polyanion has an extended structure. Upon increasing the oligocation concentration, the polyanion chain collapses and forms a compact globule,…

Complex formationGeneral Physics and AstronomySalt (chemistry)FOS: Physical sciences02 engineering and technologyCondensed Matter - Soft Condensed Matter010402 general chemistry01 natural sciencesIonChain (algebraic topology)Physics - Biological PhysicsPhysical and Theoretical Chemistrychemistry.chemical_classificationIonsMolecular StructureChemistryCharge (physics)021001 nanoscience & nanotechnologyPolyelectrolytesPolyelectrolyte0104 chemical sciencesModels ChemicalChemical physicsBiological Physics (physics.bio-ph)Soft Condensed Matter (cond-mat.soft)Counterion0210 nano-technologyStructure factor
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Structural Study of Star Polyelectrolytes and Their Porous Multilayer Assembly in Solution

2015

Star polyelectrolytes with responsive properties to external stimuli, such as pH, temperature and ionic condition, were utilized to fabricate layer-by-layer (LbL) microcapsules . The microstructure of star polyelectrolytes was first studied in semi-dilute solution by in situ small-angle neutron scattering (SANS). These measurements show that with the addition of salts, arms of strong cationic star polyelectrolytes will contract and the spatial ordering of the stars would be interrupted. SANS measurements were also performed on the microcapsules in order to study their internal structure and responsive properties in solution. The results show that with the increase of shell thickness, microc…

Condensed Matter::Soft Condensed MatterMaterials scienceFractalChemical engineeringPolymer chemistryShell (structure)Ionic bondingNeutron scatteringPorosityMicrostructureFractal dimensionPolyelectrolyte
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Mesoscopic Simulations of Polyelectrolyte Electrophoresis in Nanochannels

2011

We present the results of mesoscopic dissipative particle dynamics (DPD) simulations of coupled electrohydrodynamic phenomena on the micro- and nanoscale. The effects of electroosmotic flow and slippage combined with polyelectrolyte electrophoresis are investigated in detail, taking full account of hydrodynamic and electrostatic interactions. Our numerical results are in excellent agreement with analytical calculations.

Condensed Matter::Soft Condensed MatterMesoscopic physicsElectrophoresisChemical physicsComputer scienceDissipative particle dynamicsElectrohydrodynamicsElectrostaticsNanoscopic scalePolyelectrolyte
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