Search results for "Electrolyte"

showing 10 items of 746 documents

Unexpected high robustness of electrochemical cross-coupling for a broad range of current density

2017

Solvent effect enables electrosynthesis of organic compounds with strong variation of electric current at constant efficacy.

CouplingMultidisciplinaryMaterials science010405 organic chemistrySciAdv r-articlesNanotechnologyElectrolyte010402 general chemistry01 natural sciences0104 chemical sciencesAnodeChemical physicsRobustness (computer science)Yield (chemistry)ElectrochemistryConstant currentCurrent densityOrder of magnitudeResearch ArticlesResearch ArticleScience Advances
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Cathodic reduction of hexavalent chromium coupled with electricity generation achieved by reverse-electrodialysis processes using salinity gradients

2014

Abstract A new approach for the simultaneous generation of electric energy and the treatment of waters contaminated by recalcitrant pollutants using salinity gradients was proposed. Reverse electrodialysis allows for the generation of electric energy from salinity gradients. Indeed, the utilization of different salt concentrations gives a potential difference between the electrodes which allows the generation of electric energy by using suitable electrolytes and an external circuit. The simultaneous generation of electric energy and the treatment of waters contaminated by Cr(VI) was successfully achieved for the first time by reverse electrodialysis processes using salinity gradients and pr…

Cr(VI)ChemistrySupporting electrolyteGeneral Chemical EngineeringElectrolytesalinity gradientVolumetric flow rateSalinitychemistry.chemical_compoundElectricity generationChemical engineeringStack (abstract data type)Waste water treatmentenergy generationEnvironmental chemistryReversed electrodialysisElectrochemistryreverse electrodialisyHexavalent chromium
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The solid-state architecture of a metallosupramolecular polyelectrolyte

2006

Self-assembly of Fe(II) and the ditopic ligand 1,4-bis(2,2′:6′,2″-terpyridine-4′-yl)benzene results in equilibrium structures in solutions, so-called metallosupramolecular coordination polyelectrolytes (MEPEs). It is exceedingly difficult to characterize such macromolecular assemblies, because of the dynamic nature. Therefore, hardly any structural information is available for this type of material. Here, we show that from dilute solutions, where small aggregates predominate, it is possible to grow nanoscopic crystals at an interface. A near atomic resolution structure of MEPE is obtained by investigating the nanoscopic crystals with electron diffraction in combination with molecular model…

CrystallographyMultidisciplinaryElectron diffractionMolecular modelLigandChemistryPhysical SciencesSupramolecular chemistryNanoscopic scalePolyelectrolyteCoordination geometryMonoclinic crystal systemProceedings of the National Academy of Sciences
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Model for Solid State Voltammetry of Zeolite-Associated Species

2004

The electrochemical reduction/oxidation of zeolite-associated species is described from the model of Lovric and Scholz for redox conductive microcrystals and the model of Andrieux and Saveant for redox polymers. It is assumed that the reaction starts at the three-phase boundary between electrode, zeolite particle, and electrolyte. From this point, the reaction zone grows while electrons and charge-balancing cations diffuse perpendicularly along the zeolite. As a result, at short times, a Cottrell-type behavior, controlled by the diffusion of electrolyte countercations in the zeolite can be expected. At larger times, a thin-layer response in which electron hopping between adjacent redox site…

CyclohexaneDiffusionInorganic chemistryElectrolyteElectrochemistryRedoxSurfaces Coatings and Filmschemistry.chemical_compoundchemistryElectrodeMaterials ChemistryPhysical and Theoretical ChemistryZeoliteVoltammetryThe Journal of Physical Chemistry B
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Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups

2019

Abstract We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans.

Denticityoxidation010405 organic chemistryChemistrySupporting electrolyteCommunicationC−C couplingoxygen heterocyclesSubstrate (chemistry)General Chemistry010402 general chemistryElectrochemistry01 natural sciencesEnvironmentally friendlyCombinatorial chemistryCommunicationsCatalysisCoupling reaction0104 chemical scienceschemistry.chemical_compoundElectrochemistry | Hot Paperelectrochemistrycross-couplingPolar effectPhenolsAngewandte Chemie International Edition
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Chiral separation of bupivacaine enantiomers by capillary electrophoresis partial-filling technique with human serum albumin as chiral selector

2004

Abstract Capillary electrophoresis (CE) is a powerful technique for enantiomer separations due to its intrinsic high separation efficiencies, speed of analysis, low reagent consumption and small sample requirements. However, some chiral selectors present strong background UV absorption providing high detection limits. The present paper deals with the application of the partial-filling technique to the separation of bupivacaine enantiomers by capillary electrophoresis using human serum albumin (HSA) as chiral selector. In this procedure the cationic surfactant cetyltrimethylammonium bromide (CTAB) was used as a dinamic capillary coating in order to reduce the electro-osmotic flow and detect …

Detection limitChromatographyChemistryCapillary actionOrganic ChemistryAnalytical chemistryElectrophoresis CapillaryStereoisomerismGeneral MedicineElectrolyteHuman serum albuminBupivacaineBiochemistryAnalytical ChemistryCapillary electrophoresisPharmaceutical PreparationsReagentmedicineAnesthetics LocalEnantiomerEnantiomeric excessmedicine.drugJournal of Chromatography A
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Determination ofl-Ascorbic Acid and Total Ascorbic Acid in Vascular and Nonvascular Plants by Capillary Zone Electrophoresis

1998

A capillary zone electrophoresis (CZE) procedure for the determination of l-ascorbic acid (AA) and total ascorbic acid (TAA, as the sum of AA and dehydroascorbic acid) in vascular plants, lichens, bryophytes, and liverworts is described. The samples were frozen in liquid nitrogen and extracted with 2% metaphosphoric acid. To determine AA, an aliquot was directly injected in a fused-silica capillary. The determination of TAA was performed upon its reduction with dl-homocysteine at pH 7. The background electrolyte contained 60 mM sodium chloride, 60 mM sodium dihydrogen phosphate, 1 x 10(-4)% hexadimetrine bromide, and NaOH up to pH 7. The procedure was rapid and highly reproducible; the limi…

Detection limitChromatographySodiumBiophysicsElectrophoresis CapillaryReproducibility of Resultschemistry.chemical_elementAscorbic AcidCell BiologyElectrolytePlantsAscorbic acidSensitivity and SpecificityBiochemistryElectrophoresischemistry.chemical_compoundCapillary electrophoresischemistryBromideDehydroascorbic acidMolecular BiologyAnalytical Biochemistry
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Direct determination of oleic acid in soybean oil by capacitively coupled contactless conductivity detection capillary electrophoresis in an oil-misc…

2014

Este trabalho teve por objetivo desenvolver um método analítico direto e rápido para a determinação de ácido oleico em óleo de soja por eletroforese capilar com detecção condutométrica sem contato. O eletrólito de corrida empregado foi uma mistura metanol/1-propanol (1:6 v/v) contendo 4 × 10-2 mol L-1 de KOH e 10% (v/v) em etileno glicol. As amostras foram preparadas pela solubilização de 50 g L-1 de óleo de soja e 1,33 × 10-3 de ácido salicílico (padrão interno) no eletrólito de corrida. Os ensaios quantitativos foram realizados adicionando ácido oleico puro às amostras, na faixa entre 0,53 e 2,13 × 10-3 mol L-1. Sob polaridade negativa, os solutos aniônicos deslocaram-se mais rapidamente …

Detection limitChromatographyfood.ingredientcontactless capacitively coupled contactless conductivity detection (C4D)soybean oilGeneral ChemistryElectrolyteontactless capacitively coupled contactless conductivity detection (C4D)Soybean oilOleic acidchemistry.chemical_compound1-PropanolCapillary electrophoresisfoodchemistryoleic acidÓleo de sojanon-aqueous capillary electrophoresis (NACE)MethanolEletroforese capilarÁcido oléicoEthylene glycol
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Separation and determination of homologues of linear alkylbenzenesulfonates by nonaqueous capillary zone electrophoresis using alkylammonium salts in…

2001

The separation of linear alkylbenzene sulfonates (LAS) by nonaqueous capillary electrophoresis (NACE) using negative polarity, and a buffer containing acetic acid and an alkylamine in nonaqueous ethanol, has been investigated. Several primary, secondary, and tertiary alkylamines with alkyl chains of different length were compared. The solutes travelled against the electroosmotic flow (EOF), and at the same time were braked by association with the alkylamine molecules or with the alkylammonium ions. The best resolution between adjacent LAS homologues (R approximately 2.1), partial isomer resolution in two peaks, and at the same time an excellent repeatability, was obtained with a small dipen…

Detection limitchemistry.chemical_classificationChromatographyEthanolResolution (mass spectrometry)Linear alkylbenzeneClinical BiochemistryAnalytical chemistryElectrolyteBiochemistryAnalytical Chemistrychemistry.chemical_compoundAcetic acidCapillary electrophoresischemistryAlkylELECTROPHORESIS
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Defect interaction and local structural distortions in Mg-doped LaGaO3: A combined experimental and theoretical study

2017

A combined experimental and theoretical study of Mg-doped LaGaO3 electrolyte was carried out, with the aim to unveil the interaction between oxygen vacancy (Vo) and perovskite B site cations. LaGaO3 (LG) and LaGa0.875Mg0.125O2.938 (LGM0125) samples were comprehensively characterized by X-ray absorption spectroscopy (XAS) and X-ray diffraction, in order to investigate short- and long-range structures of both undoped and Mg-doped materials. XAS analysis evidenced a preferential Ga-Vo interaction in LGM0125, confirmed by periodic hybrid density functional theory calculations, which were combined with a symmetry-independent classes (SICs) approach in order to (a) obtain a detailed picture of th…

DiffractionAbsorption spectroscopyGeneral Physics and Astronomy02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesCHEMISTRY1ST PRINCIPLESRAY-ABSORPTION SPECTROSCOPYBODY DISTRIBUTION-FUNCTIONSPhysical and Theoretical ChemistryOXIDE FUEL-CELLSION CONDUCTIVITYPerovskite (structure)CONDENSED MATTERX-ray absorption spectroscopyELECTROLYTESChemistryDoping021001 nanoscience & nanotechnologyTRANSPORT0104 chemical sciencesCrystallographyX-ray crystallographyDensity functional theory0210 nano-technologyLANTHANUM GALLATE PEROVSKITEThe Journal of Chemical Physics
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