Search results for "Polyelectrolyte"

showing 10 items of 214 documents

Crosslinked chitosan/poly(vinyl alcohol)-based polyelectrolytes for proton exchange membranes

2019

[EN] The preparation polyelectrolytes based on crosslinked poly(vinyl alcohol) (PVA) and chitosan (CS) was considered as a feasible alternative to develop highly functionalised, cost-effective and eco-friendly membranes for proton exchange fuel cell technologies. CS/PVA-based membranes were combined with sulfosuccinic acid (SSA) as crosslinking and sulfonating agent, and glycerol (GL) to promote flexibility and favour their manageability. The chemical structure, the thermo-oxidative behaviour, the ethanol uptake, the electric, the proton conductivity, and the performance in direct ethanol fuel cell (DEFC) were assessed. In general, all the CS/PVA-based polyelectrolytes showed a synergetic i…

Vinyl alcoholPolymers and PlasticsChitosan (CS)General Chemical Engineering02 engineering and technology010402 general chemistryPoly(vinyl alcohol) (PVA)01 natural sciencesBiochemistryProton exchange membraneChitosanchemistry.chemical_compoundMaterials ChemistryEnvironmental ChemistryEthanolDirect ethanol fuel cell (DEFC)PlasticizerGeneral ChemistryPolyelectrolyte021001 nanoscience & nanotechnologyDirect-ethanol fuel cellPolyelectrolyte0104 chemical sciencesMembranechemistryChemical engineeringMAQUINAS Y MOTORES TERMICOSAbsorption (chemistry)0210 nano-technologyReactive and Functional Polymers
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Some new polyelectrolytes

1989

Revue de methodes de preparation de polyelectrolytes: alkylation du poly(iminohexamethylene), homo- et copolymeres sequences de l'aza-1 bicyclo [4.2.0] octane, polymeres-peignes prepares a partir de macromeres obtenus par polymerisation de la phenyl-2 oxazoline. Preparation de polyampholytes ayant une distribution statistique ou sequencee des motifs ioniques

ViscosityMaterials sciencePolymers and PlasticsOrganic ChemistryPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryCondensed Matter PhysicsMacromonomerPolyelectrolyteMakromolekulare Chemie. Macromolecular Symposia
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Acid−Base Properties of Synthetic and Natural Polyelectrolytes: Experimental Results and Models for the Dependence on Different Aqueous Media

2008

Protonation constants of several natural and synthetic humates and fulvates were determined by ISE-H+ potentiometry in different ionic media (alkali metal halides and tetraethylammonium iodide) at different ionic strengths and T ) 298.15 K. Experimental data obtained in previous studies of different synthetic (polyacrylates, polymethacrylates, polyacrylate-co-maleate) and naturally occurring (alginate, humic substances) polycarboxylates were also taken into account in the general analysis of acid-base properties of polyelectrolytes. Protonation constants were expressed as a function of the dissociation degree (R) using three models, namely, a simple linear model, the Ho¨gfeldt three-paramet…

acid-base properiteAcrylate polymerdiprotic-like modelTetraethylammonium iodideGeneral Chemical EngineeringInorganic chemistryHalideIonic bondingProtonationGeneral ChemistryUronic acidAlkali metalPolyelectrolytethermodynamicchemistry.chemical_compoundchemistrySettore CHIM/01 - Chimica AnaliticapolyelectrolyteJournal of Chemical & Engineering Data
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Protection of living yeast cells by micro-organized shells of natural polyelectrolytes

2015

International audience; Saccharomyces cerevisiae, a eukaryotic model organism, plays a key role in the oxidative stability of fermented products. In order to protect cells against environmental stresses, we report a method of modifying the cell surface architecture while maintaining the internal working properties of the system. The objective was to encapsulate living yeast cells in micro-organized polyelectrolyte shells using layer-by-layer (LbL) assembly. For the first time, the natural polyelectrolytes, β-lactoglobulin and sodium alginate, were alternately deposited on the surface of S. cerevisiae. Transmission electron microscopy coupled with immune-cytochemistry and scanning electron m…

biologyScanning electron microscopeChemistrySaccharomyces cerevisiaeLayer by layerBioengineeringSaccharomyces cerevisiaebiology.organism_classificationLayer-by-layerβ-LactoglobulinApplied Microbiology and BiotechnologyBiochemistryPolyelectrolyteYeastBiochemistryFTIRTransmission electron microscopyFreezing[SDV.IDA]Life Sciences [q-bio]/Food engineeringBiophysicsFermentation[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringFourier transform infrared spectroscopyImmuno-electron microscopy
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Macromolecules in ordered media: 5. Poly(4-vinyl pyridine)—liposome association induced by electrostatic interactions

1997

Abstract The association of water-soluble vinyl polymers to dimyristoyl phosphatidic acid unilamellar vesicles as a function of pH, temperature and salt content using steady-state fluorescence and viscometry has been investigated. Poly(4-vinyl pyridine) fluorescence data were converted to association isotherms and discussed in terms of binding and partition models. The results of this report support previous suggestions: (1) in the case of polyions the inclusion of the activity coefficient in both models is essential; (2) the parameters calculated using the two different theoretical approaches can be directly compared by the relating equation proposed for us. Finally, the excellent agreemen…

chemistry.chemical_classificationActivity coefficientPolymers and PlasticsOrganic ChemistryPolymerVinyl polymerPolyelectrolytePartition coefficientchemistry.chemical_compoundchemistryPyridineMaterials ChemistryPhysical chemistryPyridiniumMacromoleculePolymer
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Ionic polymers based on dextran: hydrodynamic properties in aqueous solution and solvent mixtures.

2009

Hydrodynamic properties of a series of ionic polysaccharides with different charge density but the same molecular weight have been evaluated in salt-free aqueous solution and aqueous/organic solvent mixtures by means of capillary viscometry. The polyelectrolytes investigated contain quaternary ammonium salt groups, N-ethyl-N,N-dimethyl-2-hydroxypropylammonium chloride, attached to a dextran backbone. The experimental viscometric data have been plotted in terms of the Wolf method. The results show that the experimental data fit well with this model and allow the calculation of intrinsic viscosities and other hydrodynamic parameters, which provide new information about the dependence of the p…

chemistry.chemical_classificationAqueous solutionChemistryInorganic chemistryIonic bondingCharge densityViscometerPolymerChloridePolyelectrolyteSurfaces Coatings and FilmsSolventChemical engineeringMaterials ChemistrymedicinePhysical and Theoretical Chemistrymedicine.drugThe journal of physical chemistry. B
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Speciation of polyelectrolytes in natural fluids Protonation and interaction of polymethacrylates with major components of seawater.

2002

Acid–base properties of two sodium polymethacrylates (W= 4000 and 5400 Da) were studied potentiometrically in aqueous solution at 25 °C. Measurements were made in different salt solutions: LiCl 0.1–1.5, NaCl 0.1–2, KCl 0.1–2, Et4NI 0.1–0.75 mol l − 1 , and in artificial seawater in the salinity range 10 S 45. Protonation data were analysed by two different models and the dependence of the relative parameters on ionic strength were calculated. Measurements performed in interacting media (alkali metal chlorides and artificial seawater) were interpreted in terms of complex formation, and the relative formation parameters are reported. Previous data on the interaction of a higher molecular weig…

chemistry.chemical_classificationAqueous solutionChemistryIonic strengthInorganic chemistrySalt (chemistry)Artificial seawaterProtonationSeawaterAlkali metalPolyelectrolyteAnalytical ChemistryTalanta
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Solution properties of polyelectrolytes

1993

Abstract Aqueous size-exclusion chromatography was used to analyse the elution behaviour of several standard ionic polymers, including poly( l -glutamic acid), sodium poly(styrene sulphonate) and poly(acrylic acid), different in nature and chain flexibility, as a function of the pH and ionic strength of the eluent. Two organic-based hydrophilic packings, Spherogel TSK PW4000 and Ultrahydrogel 250, were tested in order to select the optimal conditions of macromolecular separation, and the results obtained for each column were compared. A set of calibration graphs for the above polyions as a function of eluent pH and ionic strength were obtained and compared with those obtained for uncharged …

chemistry.chemical_classificationAqueous solutionChromatographyChemistryElutionOrganic ChemistrySize-exclusion chromatographyIonic bondingPolymerGeneral MedicineElectrostaticsBiochemistryPolyelectrolyteAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundColumn chromatographyIonic strengthSurface chargeAcrylic acidJournal of Chromatography A
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Solution properties of polyelectrolytes XII. Semi-quantitative approach to mixed electrostatic and hydrophobic polymer-gel interactions

1996

Abstract Aqueous size-exclusion chromatography of polyanions, where secondary effects affect the total separation mechanism, was investigated. For elution of polyelectrolytes on inorganic silica-based supports, the electrostatic polymer-gel repulsive interactions were evaluated through the values for a hypothetical repulsion layer, X e , according to the model developed by other workers. Using a similar procedure, the existence of an effective barrier defined as X e − X h is proposed for those systems in which electrostatic repulsion and hydrophobic interactions take place simultaneously as secondary mechanisms. X h can be viewed as a measure of the “enlargement” of the geometrical pore rad…

chemistry.chemical_classificationAqueous solutionChromatographyElutionOrganic ChemistryGeneral MedicinePolymerFlory–Huggins solution theoryElectrostaticsBiochemistryPolyelectrolyteAnalytical ChemistryHydrophobic effectchemistryIonic strengthJournal of Chromatography A
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Polyelectrolytes:  Intrinsic Viscosities in the Absence and in the Presence of Salt

2008

Intrinsic viscosities were determined at 25 °C for 10 samples of narrowly distributed sodium polystyrene sulfonate (the molecular weights M ranging from 0.9 to 1000 kg/mol) in pure water and in aqueous solutions containing 0.9 wt % NaCl from the slope of ln ηrel versus polymer concentration. In the middle range of M, the [η] values are in the former case almost 2 orders of magnitude larger than in the latter case. In the absence of salt, the plot of log [η] as a function of log M exhibits a sigmoidal shape, which can be approximated within the interval 3 < M (in kg mol-1) < 30 by log[η] = −0.17 + 2.1 log M. In the presence of salt, the following relation holds true in the entire regime:  lo…

chemistry.chemical_classificationAqueous solutionChromatographyPolymers and PlasticsChemistryIntrinsic viscosityOrganic ChemistryAnalytical chemistryConcentration effectSalt (chemistry)PolymerPolyelectrolyteInorganic ChemistryMaterials ChemistryOrders of magnitude (speed)Sodium Polystyrene SulfonateMacromolecules
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