Search results for "tammet"

showing 10 items of 409 documents

Mechanism of the palladium-catalysed electrosynthesis of diethyl carbonate from carbon monoxide and ethanol

2004

Abstract A mechanism is proposed for the PdBr2(PPh3)2-catalysed electrosynthesis of diethyl carbonate from carbon monoxide and ethanol, proceeding at room temperature and atmospheric CO pressure. The mechanism is investigated by cyclic voltammetry and 31P NMR spectroscopy. The active Pd0 complex able to coordinate CO is generated by the chemical reduction of PdBr2(PPh3)2 by EtO– ions generated from EtOH at the cathode. After reaction of EtO– ions with Pd0(PPh3)2(CO), the ensuing anionic complex [(PPh3)2Pd0–COOEt]– is oxidized at the anode in a key step leading to BrPdII–COOEt(PPh3)2. A nucleophilic attack of ethoxide on the latter generates diethyl carbonate and the Pd0 complex active in th…

Reaction mechanismGeneral Chemical EngineeringInorganic chemistryDiethyl carbonatechemistry.chemical_elementGeneral ChemistryElectrosynthesisCatalysischemistry.chemical_compoundchemistryCyclic voltammetryCarbonylationCarbon monoxidePalladiumComptes Rendus Chimie
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The electrochemical reduction of thioisonicotinamide in an aqueous medium

1998

Abstract The electrochemical reduction of thioisonicotinamide NRCSNH 2 has been examined in an aqueous medium between H 0 =−1 and pH=13.7. As shown by cyclic voltammetry and polarography, a global 2e − reversible transfer is followed by two successive first-order chemical reactions and a 2e − , 2H + reduction (EC 1 C 2 E process). A mechanism is proposed, beginning with the 2e − reduction of NRCSNH 2 to the formal diionized form NRC − (SH)(NH 3 + ), the first chemical reaction, C 1 , being a formal proton transfer which yields the 4- gem aminosulfanylmethylpyridine; the rate constant of this reaction is 2×10 4  s −1 in acidic medium and diminishes in neutral medium. The second process, C 2 …

Reaction mechanismPolarographyAqueous solutionStereochemistryGeneral Chemical EngineeringInorganic chemistryIsonicotinic acidChemical reactionchemistry.chemical_compoundReaction rate constantchemistryElectrochemistryIsonicotinamideCyclic voltammetryElectrochimica Acta
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Electrochemical Quartz Crystal Microbalance Study of Copper Electrochemical Reaction in Acid Medium Containing Chlorides

2006

Copper electrodissolution and electrodeposition were studied by means of gravimetric quartz crystal microbalance and electric cyclic voltammetry combined measurements. Relevant information on the mechanism of these electrochemical processes is provided by the analysis of experimental data and particularly of the mass change per charge unit. The copper electrodeposition and electrodissolution take place by means of two consecutive monoelectronic transfers where the anion participation in the reaction mechanism is specified. Besides, it is proved that the presence of molecular oxygen in the solution contributes to the formation of a passive layer on the surface of the metallic copper deposit.

Reaction mechanismRenewable Energy Sustainability and the EnvironmentChemistryInorganic chemistrychemistry.chemical_elementQuartz crystal microbalanceCondensed Matter PhysicsElectrochemistryCopperSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonMetalvisual_artMaterials ChemistryElectrochemistryvisual_art.visual_art_mediumGravimetric analysisCyclic voltammetryJournal of The Electrochemical Society
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Magnetoelectrochemical modulation of pre-organization processes in a 4,4′-dinitrobiphenyl azacrown macrocyclic lactam

2004

A magnetoelectrochemical effect consisting on the modulation of the reaction rate of pre-organization reactions in a 4,4′-dinitrobiphenyl azacrown lactam is described. The electrochemical response of that compound in DMSO solution at microelectrodes consists in two successive dinitrobiphenyl-centred one-electron transfer processes at −0.9 and −1.6 V vs. AgCl/Ag involving the transition from the dihedral geometry of the neutral starting compound to the planar geometry of the final dianion, resulting in an overall ECE mechanism. In the presence of moderate (0.05–0.2 T) static magnetic fields, the second electron transfer process decreases significantly, the apparent rate constant of the dihed…

Reaction mechanismStereochemistryDihedral angleElectrochemistryReaction ratelcsh:ChemistryCrystallographychemistry.chemical_compoundElectron transferReaction rate constantchemistrylcsh:Industrial electrochemistrylcsh:QD1-999ElectrochemistryLactamCyclic voltammetrylcsh:TP250-261Electrochemistry Communications
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A chemical and electrochemical multivalent memory made from FeNi3-graphene nanocomposites

2014

FeNi3-graphene nanocomposites present in acetonitrile solutions a redox couple with an electrochemical hysteresis of 2.4 V between the oxidation and the reduction maxima. In view of the high energy required for the reverse transitions, they are here proposed as chemical multilevel memories: permanent, after drying, or erasable in electrolytes, respectively. Keywords: FeNi3-graphene nanocomposites, Voltammetry, Coulovoltammetry, Redox couple, Redox hysteresis

Redox hysteresisHigh energyMaterials scienceInorganic chemistryRedox coupleFeNi3-graphene nanocompositesElectrolyteElectrochemistryRedoxlcsh:ChemistryHysteresischemistry.chemical_compoundlcsh:Industrial electrochemistrylcsh:QD1-999Graphene nanocompositeschemistryChemical engineeringCoulovoltammetryElectrochemistryVoltammetryAcetonitrileVoltammetrylcsh:TP250-261Electrochemistry Communications
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Electrochemical characterization of mangrove sediments: A proposal of new proxies for organic matter oxidation

2019

Abstract The voltammetric response of microparticulate deposits resulting from solvent evaporation of ethanolic extracts of mangrove sediments in contact with aqueous acetate buffer is hereby described. Dated sediment cores sampled from the Peruvian mangrove system (“Manglares de Tumbes” National Sanctuary) presented voltammetric responses dominated by oxidative signals of organic components that exhibit significant variations depending on the depth. Voltammetric data allowed for the definition of electrochemical indexes representative of the electrochemically oxidable organic matter fraction. These electrochemical indexes were fEAOM (for the total amount of organic matter being electrochem…

Redox state010501 environmental sciences010502 geochemistry & geophysicsElectrochemistryMangrove sediments01 natural sciencesevaporationPeruElectrochemistryChemical analysisInfrared spectroscopyorganic matterchemistry.chemical_classificationAqueous solutionChemistryBiogeochemistryPollutionOrganic matter oxidationEnvironmental chemistryOrganic matter degradationsMangroveoxidationInfrared spectroscopyredox conditionssolventSedimentsVoltammetric responseGeochemistry and PetrologyOrganic compoundsOrganic matter fractionEnvironmental ChemistryOrganic matter14. Life underwaterSpectroscopyOxidation proxies0105 earth and related environmental sciencesparticulate mattermangrove//purl.org/pe-repo/ocde/ford#1.05.00 [https]SedimentBiological materials15. Life on landcoastal sedimentElectrochemical characterizationssediment coreSolvent evaporationVoltammetryethanolacetateaqueous solutionReactive oxygen species
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Rare trinuclear NiII2MII complexes (MII = Mn, Fe and Co) with a reduced Schiff base ligand: Synthesis, structures and magnetic properties

2018

Abstract Three new trinuclear hetero-metallic NiII2MII complexes with MII = Mn, Fe and Co have been synthesized using a [NiLR] “metalloligand”, where H2LR = N,N′-bis(2-hydroxybenzyl)-1,3-propanediamine. All complexes have been characterized by elemental analysis, spectroscopic methods, single crystal XRD and magnetic and electrochemical studies. In the three complexes, in addition to the double phenoxido bridges, the two terminal NiII atoms are linked to the central MII [M = Mn(1), Fe(2) and Co(3)] ion by means of a bridging carboxylato co-anion, giving rise to a linear NiII-MII-NiII structure. Variable temperature magnetic susceptibility measurements show the presence of weak ferromagnetic…

Schiff base010405 organic chemistryInorganic chemistry010402 general chemistryElectrochemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesIonInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryFerromagnetismMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryCyclic voltammetrySingle crystalInorganica Chimica Acta
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Copper(II) complexes with 1,5-bis(2-hydroxybenzaldehyde)carbohydrazone

2014

Abstract The acid–base properties of 1,5-bis(2-hydroxybenzaldehyde)carbohydrazone (H4L) and its thioanalogue 1,5-bis(2-hydroxybenzaldehyde)thiocarbohydrazone (H4LS) have been studied experimentally by pH-potentiometry and UV–Vis spectrophotometry and theoretically by using DFT methods. Copper(II) complexes [Cu2(HL)(DMSO)2(H2O)]NO3·H2O (1), [{Cu2(HL)(DMF)(H2O)}n][{Cu2(HL)(DMF)NO3}n](NO3)n (2), [Cu2(HL)(DMF)2(H2O)]HSO4·H2O (3), [Cu2(HL)(DMF)2(H2O)][Cu2(HL)(SO4)(H2O)(DMF)2]·2H2O (4) and [Cu4(HL)2(HSO4)(DMF)2]HSO4 (5), where H4L = 1,5-bis(2-hydroxybenzaldehyde)carbohydrazone, have been synthesised. Complexes 1–3 have been characterised by elemental analysis, IR spectroscopy, ESI mass spectromet…

Schiff basemedicine.diagnostic_testLigandStereochemistryInfrared spectroscopychemistry.chemical_elementMagnetic susceptibilityCopperInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistrySpectrophotometryMaterials ChemistrymedicinePhysical and Theoretical ChemistryCyclic voltammetryPolyhedron
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A voltammetric e-tongue tool for the emulation of the sensorial analysis and the discrimination of vegetal milks

2018

[EN] The relevance of plant-based food alternatives to dairy products, such as vegetable milks, has been growing in recent decades, and the development of systems capable of classifying and predicting the sensorial profile of such products is interesting. In this context, a methodology to perform the sensorial analysis of vegetable milks (oat, soya, rice, almond and tiger nut), based on 12 parameters, was validated. An electronic tongue based on the combination of eight metals with pulse voltammetry was also tested. The current intensity profiles are characteristic for each non-dairy milk type. Data were processed with qualitative (PCA, dendrogram) and quantitative (PLS) tools. The PCA stat…

Sensorial analysisTECNOLOGIA DE ALIMENTOSElectronic tonguePulse voltammetryContext (language use)02 engineering and technologyRaw material01 natural sciencesTECNOLOGIA ELECTRONICAQUIMICA ORGANICAMaterials ChemistryStatistical analysisFood scienceElectrical and Electronic EngineeringInstrumentationMathematicsHomogeneity (statistics)010401 analytical chemistryDendrogramElectronic tongueQUIMICA INORGANICAMetals and Alloys021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsVegetable milkPrincipal component analysisTiger nut0210 nano-technology
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Sequestering ability of landfill leachate towards toxic metal ions

2017

The great part of municipal solid wastes is worldwide stored in sanitary landfills. The interaction of organic and inorganic wastes with rainwater produces in the landfill a leachate of extremely variable composition. It depends on several variables such as the type of wastes, the age of landfill, the pH, the redox potential, etc [1-2]. Four are the recognized categories of pollutants in landfill leachate: inorganic macrocomponents, dissolved organic matter (DOM), heavy metals and xenobiotic organic compounds [3]. In particular, heavy metals (arsenic, cadmium, copper, lead, mercury, etc.) are usually present at concentration of few ppb and up to some ppm. A variable but consistent fraction …

Settore CHIM/01 - Chimica AnaliticaLandfill leachate sequestration toxic metal ions speciation Differential Pulse Anodic Stripping Voltammetry
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