Search results for "electrolyte"

showing 10 items of 746 documents

Electrocatalytic properties of manganese and cobalt polyporphine films toward oxygen reduction reaction

2018

International audience; Novel member of polymetalloporphines, namely manganese polymetalloporphine of type I (pMnP-I) obtained by ion exchange from magnesium polyporphine of type I (pMgP-I) is reported for the first time and compared to its cobalt analogue (pCoP-I). Both polymer films have been obtained via two-step procedure: demetaladon of the pMgP-I electrode film via its exposure to trifluoroacetic acid solution, resulting in formation of the metal-free polyporphine of type I (pH(2)P-I) followed by electrochemically induced incorporation of Co or Mn ions from the acetonitrile solution of cobalt and manganese perchlorates. A further oxidative transformation of pCoP-I, polymer films has l…

conjugated porphyrin polymerGeneral Chemical EngineeringInorganic chemistryFOS: Physical scienceschemistry.chemical_element02 engineering and technologyElectrolyteManganesepositive potentialsphthalocyanines010402 general chemistry01 natural sciencescatalystsAnalytical ChemistryCatalysisporphine[CHIM.ANAL]Chemical Sciences/Analytical chemistryframeworksElectrochemistry[CHIM]Chemical Sciencesdioxygen reductionCondensed Matter - Materials SciencemetalloporphyrinsAqueous solutionIon exchangeMagnesiumElectroactive polymersMaterials Science (cond-mat.mtrl-sci)Oxygen electroreductionelectropolymerizationfuel-cell cathode021001 nanoscience & nanotechnologyMetalloporphines0104 chemical sciencesPolymer film coated electrodechemistry0210 nano-technologyPlatinumCobaltMg(II) porphineJournal of Electroanalytical Chemistry
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Electrocatalytic rate constants from DFT simulations and theoretical models: Learning from each other

2022

Electrochemical interfaces present an extraordinarily complex reaction environment and several, often counter-acting, interactions contribute to rate constants of electrocatalytic reactions. We compile a short review on how electrode potential, solvent, electrolyte, and pH effects on electrocatalytic rates can be understood and modelled using computational and theoretical methods. We address the connections between computational models based on DFT and (semi)analytical model Hamiltonians to extract physical or chemical insights, identify some omissions in present DFT simulation approaches and analytic models, and discuss what and how simulations and models could learn from each other. peerR…

elektrokatalyysielectrode potentialpHtermodynamiikkaelektroditElectrochemistryelectrolyterate constantlaskennallinen kemiasolventsähkökemialiuottimetAnalytical ChemistryCurrent Opinion in Electrochemistry
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Direct Measurement of Particle−Bubble Interactions in Aqueous Electrolyte:  Dependence on Surfactant

1998

The aim of this study was to determine the influence of surfactant on the particle−bubble interaction. Therefore we constructed an experimental setup with which the interaction between colloidal pa...

endocrine systemChromatographyChemistryBubbledigestive oral and skin physiologytechnology industry and agricultureSurfaces and InterfacesAqueous electrolyteCondensed Matter Physicscomplex mixturesColloidPulmonary surfactantChemical engineeringotorhinolaryngologic diseasesElectrochemistryParticleGeneral Materials ScienceSpectroscopyLangmuir
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Electrostatically Driven Complexation of Liposomes with a Star-Shaped Polyelectrolyte to Low-Toxicity Multi-Liposomal Assemblies

2013

Anionic liposomes are electrostatically complexed to a star-shaped cationic polyelectrolyte. Upon complexation, the liposomes retain their integrity and the resulting liposome-star complexes do not dissociate in a physiological solution with 0.15 M NaCl. This provides a multi-liposomal container for possible use as a high-capacity carrier.

endocrine systemLiposomePolymers and PlasticsLow toxicityChemistryCationic polymerizationBioengineeringPolyelectrolyteBiomaterialsStar polymerChemical engineeringMaterials ChemistryOrganic chemistryBiotechnologyMacromolecular Bioscience
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Structural analysis, phase stability and electrochemical characterization of Nb doped BaCe0.9Y0.1O3−x electrolyte for IT-SOFCs

2012

Abstract To improve the chemical stability of high temperature proton conductors based on barium cerate, electrolyte powders doped with different amounts of niobium were synthesized by the citrate–nitrate auto-combustion method. Pure single phases of BaCe 0.9− x Nb x Y 0.1 O 3− x (BCYN, 0.03 ≤  x  ≤ 0.12) were obtained by thermal treatment at 1000 °C. Sintering at 1450 °C for 10 h produced dense pellets. X-ray absorption spectroscopy allowed to define the dopant ion insertion site and the co-dopant valency. Treatments in pure CO 2 atmosphere at 700 °C for 3 h and subsequent XRD analysis were carried out to probe the chemical stability of the produced electrolytes. The influence of the prese…

exafMaterials scienceHigh temperature proton conductors (HTPCs)Absorption spectroscopyDopantNb-dopingRenewable Energy Sustainability and the EnvironmentBarium ceratesofcSettore ING-IND/22 - Scienza e Tecnologia dei MaterialiStructural analysiSettore CHIM/07 - Fondamenti Chimici delle TecnologieAnalytical chemistryEnergy Engineering and Power TechnologyElectrolyteElectrochemical performancefuel cellsHigh temperature proton conductors (HTPCs) Barium cerates Nb-doping Structural analysis Electrochemical performanceConductivityAtmospheric temperature rangeDielectric spectroscopyChemical stabilityElectrical and Electronic EngineeringPhysical and Theoretical ChemistryPolarization (electrochemistry)
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Characterization of hydroxyaromatic compounds in vegetable oils by capillary electrophoresis with direct injection in an oil-miscible KOH/propanol/me…

2005

The separation of hydroxyaromatic compounds in vegetable oils, including synthetic antioxidants (3-tert-butyl-4-hydroxyanisol and 2,6-di-tert-butyl-4-hydroxytoluene), E-vitamers and other natural oil components, by nonaqueous capillary electrophoresis in an oil-miscible background electrolyte (BGE) was investigated. The BGE contained 40 mM KOH in a methanol/1-propanol (PrOH) mixture (15:85 v/v). The oil samples were 1:1 diluted with PrOH and directly injected in the capillary. Under negative polarity (cathode at the injection end), the anionic solutes moved faster than the electroosmotic flow, being well-resolved among them and from the triacylglycerols. Using virgin palm, extra virgin oliv…

food.ingredientChromatographyCapillary actionPotassium CompoundsMethanolClinical Biochemistryfood and beveragesElectrophoresis CapillaryWheat germElectrolyte1-PropanolBiochemistrySoybean oilAnalytical ChemistryPropanolchemistry.chemical_compoundCapillary electrophoresisfoodchemistryPhenolsSolubilityYield (chemistry)HydroxidesPlant OilsMethanolElectrophoresis
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Tuning the Electrochemistry of Free-Base Porphyrins in Acidic Nonaqueous Media: Influence of Solvent, Supporting Electrolyte, and Ring Substituents

2016

International audience; A detailed study of reduction potentials, electroreduction mechanisms and acid-base chemistry was carried out on two series of free-base porphyrins in nonaqueous media. The first series is represented by four-pyrrole substituted tetraphenylporphyrin (TPP) derivatives, two of which are planar and two of which are nonplanar in their non-protonated form. The second comprises porphyrins with 0-4 meso-phenyl groups on the macrocycle. Equilibrium constants for conversion of each neutral porphyrin to its diprotic [H4P] 2+ form were determined and the electrochemistry was then elucidated as a function of: (i) type of nonaqueous solvent, (ii) anion of supporting electrolyte, …

free-base porphyrinsSupporting electrolyteprotonationInorganic chemistry010402 general chemistryElectrochemistry[ CHIM ] Chemical Sciences01 natural sciencesCatalysistetraphenylporphyrin monoacidschemistry.chemical_compoundconformational-analysismetal derivativesTetraphenylporphyrin[CHIM]Chemical SciencesReactivity (chemistry)tetraarylporphyrinsEquilibrium constantcomplexes010405 organic chemistryFree basecrystal-structurespectroelectrochemistryanionDiprotic acidPorphyrin0104 chemical sciencessupporting electrolytechemistryelectrochemistryexpanded porphyrindiacids[CHIM.OTHE]Chemical Sciences/Otherabsorption
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The adsorption of water vapor on super absorbent product at low temperatures and low mass.

2006

The adsorption isotherms of water vapor on super absorbent product have the same form of type III isotherm at ambient temperature with the hysteresis phenomena. For temperatures lower than ambient, the isotherms become deformed because of the chains effect. The polymer is characterized by a multilayer adsorption, which occurs before a full-course is complete. During adsorption reactions, the polymer undergoes rearrangement polymeric network, which results from a cooperative diffusion of the water molecules and from a chain spacing followed by an expansion of the polymeric network. Three types of water molecules adsorbed on polymer were identified: strongly dependent water, adsorbed water, a…

gelPolymers and PlasticsDiffusionpolymervaporwater02 engineering and technology010402 general chemistry01 natural sciencesCondensed Matter::Materials ScienceAdsorptionPolymer chemistryMaterials ChemistryBound waterPhysics::Chemical PhysicsWater contentPhysics::Atmospheric and Oceanic PhysicsComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationQuantitative Biology::BiomoleculesChemistryisothermtechnology industry and agriculturesuper absorbentGeneral ChemistryPolymer[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPolyelectrolyte0104 chemical sciencesSurfaces Coatings and FilmsCondensed Matter::Soft Condensed MatterHysteresis[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Chemical engineeringadsorption[ CHIM.MATE ] Chemical Sciences/Material chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]isobarheat0210 nano-technologyWater vapor
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Mechanistic Origins of the pH Dependency in Au-Catalyzed Glycerol Electro-oxidation: Insight from First-Principles Calculations

2021

Electrocatalytic oxidation of glycerol (EOG) is an attractive approach to convert surplus glycerol to value-added products. Experiments have shown that EOG activity and selectivity depend not only on the electrocatalyst but also on the electrode potential, the pH, and the electrolyte. For broadly employed gold (Au) electrocatalysts, experiments have demonstrated high EOG activity under alkaline conditions with glyceric acid as a primary product, whereas under acidic and neutral conditions Au is almost inactive producing only small amounts of dihydroxyacetone. In the present computational work, we have performed an extensive mechanistic study to understand the pH and potential dependency of …

hapetusglycerolelectrolyte02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical scienceskatalyysiorgaaninen kemiaglyserolielectrocatalystelektrolyytit0210 nano-technologyelectro-oxidationACS Catalysis
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Self-Assembled Molecular Rafts at Liquid|Liquid Interfaces for Four-Electron Oxygen Reduction

2011

The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetramethylpyridinium porphyrin (CoTMPyP(4+)) and cobalt tetrasulphonatophenyl porphyrin (CoTPPS(4-)), at the interface with an organic solvent to form molecular "rafts", provides an excellent catalyst to perform the interfacial four-electron reduction of oxygen by lipophilic electron donors such as tetrathiafulvalene (TTF). The catalytic activity and selectivity of the self-assembled catalyst toward the four-electron pathway was found to be as good as that of the Pacman type cofacial cobalt porphyrins. The assembly has been characterized by UV-visible spectroscopy, Surface Second Harmonic Generation, and Scanning …

inorganic chemicals2Nd-Harmonic Generationchemistry.chemical_elementPhotochemistryBiochemistryOxygenCatalysisCatalysischemistry.chemical_compoundWater-Soluble PorphyrinsColloid and Surface ChemistryCobalt Porphyrinsheterocyclic compoundsLiquid/Liquid Interface2Nd DerivativesEnergyDioxygenPolarizable Continuum ModelGeneral ChemistryPorphyrinRadical CationchemistryRadical ionSurface second harmonic generationDensity functional theoryImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
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