Search results for "Electrolyte"

showing 10 items of 746 documents

Metal-free electrochemical fluorodecarboxylation of aryloxyacetic acids to fluoromethyl aryl ethers

2020

Electrochemical decarboxylation of aryloxyacetic acids followed by fluorination provides easy access to fluoromethyl aryl ethers. This electrochemical fluorodecarboxylation offers a sustainable approach with electric current as traceless oxidant. Using Et3N·5HF as fluoride source and as supporting electrolyte, this simple electrosynthesis affords various fluoromethoxyarenes in yields up to 85%.

Chemistrychemistry.chemical_compoundchemistryMetal freeSupporting electrolyteDecarboxylationArylGeneral ChemistryElectrochemistryElectrosynthesisCombinatorial chemistryFluorideChemical Science
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Fuel Cell Performances of Bio-Membranes Made of Chitosan-Polyelectrolyte Thin Films and Nanowires into Anodic Alumina Membranes

2012

Chitosan (CS) / Phosphotungstic acid (PTA) polyelectrolytes in the shape of thin films and nanowires supported by Anodic Alumina Membranes (AAM) have been fabricated through solution cast and filtration techniques, respectively. Their ability to function in a H2/O2 fuel cell under mild conditions (room temperature, low humidity and low Pt loading) is proved for the first time. The fabricated membrane electrode assemblies produce power peaks of ~20 mW cm-2 for both films and nanowires. The CS/PTA films (20-40 μm thick) are able to produce a quite constant power density of ~10 mW cm-2 recorded for at least 7 h. The gradual decrease of the power output with time observed for CS/PTA nanowires i…

ChitosanMaterials scienceChitosan (CS)Alumina membranesNanowireAnodic Alumina Membranes (AAM)Phosphotungstic acid (PTA) polyelectrolyteChitosan-polyelectrolytePolyelectrolyteAnodeAnodic Alumina membraneChitosanfuel cellbio-membranechemistry.chemical_compoundMembranethin films and nanowireSettore ING-IND/23 - Chimica Fisica ApplicataChemical engineeringchemistryFuel cellsThin filmAnodic Alumina MembranesECS Meeting Abstracts
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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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Abatement of Acid Orange 7 in macro and micro reactors. Effect of the electrocatalytic route

2014

Abstract The electrochemical treatment of aqueous solutions contaminated by Acid Orange 7 (AO7) was widely studied with the main objective to evaluate as the electrocatalytic route affects the performances of the degradation process in macro and microfluidic cells. Direct anodic oxidation (EO), electro-Fenton (EF), electro-generation of active chlorine (IOAC) and coupled processes were investigated in macro and microfluidic reactors in order to select more effective conditions for the treatment of such compound. The effect of numerous operative parameters (such as nature of the electrode materials, coupling of processes, flow rate, current density and inter-electrode distance) on the perfor…

ChromatographyAqueous solutionSupporting electrolyteChemistryProcess Chemistry and TechnologyElectrocatalysiElectrochemistryElectrocatalystCatalysisCatalysisVolumetric flow rateChemical engineeringMass transferActive chlorineAcid Orange 7Electro-FentonMicroreactorMicro reactorBDDGeneral Environmental Science
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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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Simulation Analysis of the Influence of Hemodialysis Control Parameters on Exchange Processes during Therapy

1992

The effect of dialysis control parameters (dialysate composition, ultrafiltration rate, blood flow rate) on the patient's internal milieu were studied using a mathematical model for the description of the dynamic exchange processes during hemodialysis. This model simulates the electrolyte and water distribution, the acid-base and the oxygenation state as well as the ventilation. The dialysate sodium concentration affects mainly the intra-/ extracellular water and the potassium distribution. The dialysate bicarbonate and acetate concentrations control the acid-base state and the electrolyte distribution (sodium and potassium). In addition, the dialysate acetate concentration has a strong ef…

ChromatographyBicarbonatemedicine.medical_treatmentPotassiumSodium030232 urology & nephrologyBiomedical EngineeringMedicine (miscellaneous)chemistry.chemical_elementBioengineeringGeneral MedicineOxygenationElectrolyte030204 cardiovascular system & hematologyBiomaterials03 medical and health scienceschemistry.chemical_compoundUltrafiltration (renal)0302 clinical medicinechemistryExtracellular fluidmedicineDialysisThe International Journal of Artificial Organs
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Isobaric vapor–liquid equilibria for 1-propanol+water+copper(II) chloride at 100kPa

2005

Abstract Isobaric vapor–liquid equilibria for the ternary system 1-propanol + water + copper(II) chloride has been measured at 100 kPa using a recirculating still. The addition of copper(II) chloride to the solvent mixture produced a salting-out effect of the alcohol, but the azeotrope did not tend to be eliminated when the salt content increased. The experimental data sets were fitted with the electrolyte NRTL model and the parameters of Mock's model were estimated. This model has proved to be suitable to represent experimental data in the entire range of compositions. The effect of copper(II) chloride on the vapor–liquid equilibrium of the 1-propanol + water system has been compared with …

ChromatographyChemistryGeneral Chemical EngineeringAnalytical chemistryGeneral Physics and AstronomyElectrolyteChloridePropanolchemistry.chemical_compoundAzeotropemedicineNon-random two-liquid modelCopper(II) chlorideIsobaric processPhysical and Theoretical ChemistryCopper chloridemedicine.drugFluid Phase Equilibria
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Gibbs' Dividing Surface between a Fixed-Charge Membrane and an Electrolyte Solution. Application to Electrokinetic Phenomena in Charged Pores

1999

The Gibbs model for the boundary between two phases consists of replacing the finite interfacial region, where the properties of the system change gradually, by a dividing surface which acts as a third phase of zero volume in which some magnitudes change abruptly. This thermodynamic concept was recently applied to a planar interface between a fixed charge membrane and an electrolyte solution.1 The continuous decrease of counterions with the distance from the charged surface is replaced by a step function, so that the diffuse double layer is ideally represented by a charged region depleted of all co-ions. Here the cylindrical geometry is analyzed, and the planar case is revisited by proposin…

ChromatographyChemistryThermodynamicsSurfaces and InterfacesElectrolyteConductivityCondensed Matter PhysicsSpace chargeStreaming currentIonElectrokinetic phenomenaMembraneStep functionElectrochemistryGeneral Materials ScienceSpectroscopyLangmuir
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