Search results for "Redox"

showing 10 items of 619 documents

Determination of kinetic parameters of redox reactions using CE‐ICP‐MS: A case study for the reduction of Np(V) by hydroxylamine hydrochloride

2018

The rate constants k of the reduction of 5 × 10-5  M Np(V) to Np(IV) by hydroxylamine hydrochloride (HAHCl) in 1 M HCl have been determined by CE-ICP-MS in the temperature range of ϑ = 30-70°C and with varying concentrations of HAHCl from 1 to 7.2 M. The reaction was found to have (pseudo)first order kinetics with respect to HAHCl. The experimental results for k ranged from 0.0029(1) min-1 (ϑ = 40°C, c(HAHCl) = 3 M) to 0.039(7) min-1 (ϑ = 60°C, c(HAHCl) = 7.2 M). The activation energy of the reaction was determined as EA  = (72 ± 10) kJ/mol. These results and a comparison with literature data show that the coupling of CE to ICP-MS provides a powerful analytical tool for the investigation of…

Clinical BiochemistryInorganic chemistrychemistry.chemical_elementHydroxylamine02 engineering and technologyActivation energy01 natural sciencesBiochemistryRedoxMass SpectrometryAnalytical ChemistryNeptuniumReaction rate constantTransition metalChemistryNeptunium010401 analytical chemistryTemperatureElectrophoresis CapillaryActinideRate equationAtmospheric temperature range021001 nanoscience & nanotechnology0104 chemical sciencesKineticsReducing Agents0210 nano-technologyOxidation-ReductionELECTROPHORESIS
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A multi-phase multi-objective genome-scale model shows diverse redox balance strategies in yeasts

2021

Yeasts constitute over 1500 species with great potential for biotechnology. Still, the yeastSaccharomyces cerevisiaedominates industrial applications and many alternative physiological capabilities of lesser-known yeasts are not being fully exploited. While comparative genomics receives substantial attention, little is known about yeasts’ metabolic specificity in batch cultures. Here we propose a multi-phase multi-objective dynamic genome-scale model of yeast batch cultures that describes the uptake of carbon and nitrogen sources and the production of primary and secondary metabolites. The model integrates a specific metabolic reconstruction, based on the consensus Yeast8, and a kinetic mod…

Comparative genomicsFermentation in winemakingbiologyMulti phaseSaccharomyces cerevisiaeGenome scaleBiochemical engineeringbiology.organism_classificationRedoxYeastFlux balance analysis
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A multi-phase multi-objective dynamic genome-scale model shows different redox balancing among yeast species in fermentation

2021

ABSTRACTYeasts constitute over 1500 species with great potential for biotechnology. Still, the yeastSaccharomyces cerevisiaedominates industrial applications and many alternative physiological capabilities of lesser-known yeasts are not being fully exploited. While comparative genomics receives substantial attention, little is known about yeasts’ metabolic specificity in batch cultures. Here we propose a multi-phase multi-objective dynamic genome-scale model of yeast batch cultures that describes the uptake of carbon and nitrogen sources and the production of primary and secondary metabolites. The model integrates a specific metabolic reconstruction, based on the consensus Yeast8, and a kin…

Comparative genomicsbiologyChemistrySaccharomyces cerevisiaeGenome scaleFermentationBiochemical engineeringbiology.organism_classificationSaccharomycesRedoxYeastFlux balance analysis
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Recent Advances in Photocatalytic Functionalization of Quinoxalin‐2‐ones

2020

Quinoxalin‐2(1H)‐one is an important class of nitrogen heterocycle in medicinal and pharmaceutical industry, which became a synthetic target in organic chemistry in recent years. This review covers the recent advances in the functionalization of this particular nitrogen heterocycle through photocatalysis.

Compostos heterocíclicsCatàlisiChemistryRadicalOrganic ChemistryPhotocatalysisPhotoredox catalysisSurface modificationPhysical and Theoretical ChemistryPhotochemistryQuímica orgànicaEuropean Journal of Organic Chemistry
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Charging process in electron conducting polymers: dimerization model

2001

Abstract Theory of the charging and discharging process in electron-conducting polymer films at an electrode surface has been presented. It is based on the concept of two coexisting subsystems at the polymer matrix, ‘usual’ sites P which can exchange with the electrode by the electronic charge in a quasi-reversible manner, and sites D where intermolecular bonds between neighboring polymer molecules can be formed. The charging and discharging of the latter subsystem may be realized along different reaction pathways, e.g. via the bond formation after the generation of two cation radicals within such site D in the course of the anodic scan while the bond dissociation may take place via a parti…

Conductive polymerChemical physicsChemistryGeneral Chemical EngineeringIntermolecular forceElectrochemistryAnalytical chemistryMoleculeElectronCyclic voltammetryElementary chargeRedoxDissociation (chemistry)Electrochimica Acta
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Memory effects in functionalized conducting polymer films: titanocene derivatized polypyrrole in contact with THF solutions

2003

Abstract Films with a polypyrrole matrix and pendant titanocene dichloride centers, p(Tc3Py), have been obtained by potentiostatic electropolymerization of the titanocene-pyrrolyl derivative, Tc3Py=Tc(CH 2 ) 3 NC 4 H 4 (Tc=Cl 2 TiCpCp′, Cp=C 5 H 5 , Cp′=C 5 H 4 ), in acetonitrile (AN) solutions on a Pt surface. The redox activity has been studied after the transfer of the film-coated electrode into the monomer-free solution of the same electrolyte, TBAPF 6 , in THF. Contrary to the case of AN or dichloromethane solutions, one can achieve a stable redox activity of the immobilized Tc centers in THF solutions during a series of cycles. A parallel between the redox properties of the Tc complex…

Conductive polymerGeneral Chemical EngineeringInorganic chemistryTitanocene dichlorideElectrolytePolypyrroleRedoxAnalytical Chemistrychemistry.chemical_compoundTransition metalchemistryElectrochemistryPhysical chemistryAcetonitrileMetalloceneJournal of Electroanalytical Chemistry
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Comprehensive Study of Poly(2,3,5,6-tetrafluoroaniline): From Electrosynthesis to Heterojunctions and Ammonia Sensing.

2018

In this work, we report for the first time on a comprehensive study of poly(2,3,5,6-tetrafluoroaniline) (PTFANI). Contrary to the nonfluorinated polyaniline (PANI) or its analogues bearing one fluorine atom, PTFANI is a poorly conductive material. We present a comprehensive study of the electrosynthesized PTFANI from its monomer in an acidic aqueous medium. PTFANI was fully characterized by a potential-pH diagram, spectroelectrochemistry, and electrochemical quartz crystal microbalance (EQCM) measurements, as well as by a morphological study. Combined with the X-ray photoelectron spectroscopy (XPS) analysis, it allowed us to understand the redox properties of this polymer compared to those …

Conductive polymerMaterials scienceInorganic chemistry02 engineering and technologyQuartz crystal microbalance010402 general chemistry021001 nanoscience & nanotechnologyElectrosynthesisElectrochemistry01 natural sciencesRedox0104 chemical scienceschemistry.chemical_compoundElectron transferchemistryX-ray photoelectron spectroscopyPolyaniline[CHIM]Chemical SciencesGeneral Materials Science0210 nano-technologyComputingMilieux_MISCELLANEOUSACS applied materialsinterfaces
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Solid-state electrochemistry of LDH-supported polyaniline hybrid inorganic–organic material

2008

Abstract The solid-state electrochemistry of a Zn–Al layered double hydroxide-supported polyaniline material (LDH-PANI) in contact with aqueous electrolytes is described. Interconversion processes between different forms (emeraldine, protoemeraldine, leucoemeraldine, nigraniline and pernigraniline) of the LDH-supported polyaniline units are involved in redox processes. This material exhibits significant variations of impedance upon application of different conditioning potentials, acting as an electrochemical frequency filter. Using Fe (CN) 6 4 - as redox probe, LDH-PANI can be used as a chemical–electrochemical information processing system equivalent to different combinational logic circu…

Conductive polymerPolyaniline nanofibersGeneral Chemical EngineeringInorganic chemistryInfrared spectroscopyElectrochemistryRedoxAnalytical ChemistryDielectric spectroscopychemistry.chemical_compoundchemistryPolyanilineElectrochemistryHybrid materialJournal of Electroanalytical Chemistry
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Design of experiment approach applied to reducing and oxidizing tolerance of anode supported solid oxide fuel cell. Part I: Microstructure optimizati…

2011

The main drawback of Ni/YSZ anode supports for solid oxide fuel cell application is their low tolerance to reducing and oxidizing (RedOx) atmosphere changes, owing to the Ni/NiO volume variation. This work describes a structured approach based on design of experiments for optimizing the microstructure for RedOx stability enhancement. A full factorial hypercube design and the response surface methodology are applied with the variables and their variation range defined as: (1) NiO proportion (40-60 wt% of the ceramic powders), (2) pore-former proportion (0-30 wt% corresponding to 0-64 vol.%), (3) NiO particle size (0.5-8 mu m) and (4) 8YSZ particle size (0.6-9 mu m).

ConductivityMaterials scienceDesign of experimentRenewable Energy Sustainability and the EnvironmentNon-blocking I/OEnergy Engineering and Power TechnologyRedOx stabilityCermetMicrostructureAnodeChemical engineeringSolid oxide fuel cellOxidizing agentCermetsSolid oxide fuel cellNi-YSZ anode supported cellResponse surface methodologyParticle sizeElectrical and Electronic EngineeringPhysical and Theoretical ChemistrySurface response methodologySofc AnodeReduction
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Synthesis and characterization of vanadyl(IV) complexes of Schiff bases derived from anthranilic acid and salicylaldehyde (or its derivatives) or ace…

1997

Anhydrous, dimeric vanadyl(IV) complexes of Schiff bases derived from [1+1] condensation of salicylaldehyde (or its derivatives) and anthranilic acid, have been synthesized from CH3CN and were characterized by elemental analysis, FTIR, EPR, absorption, TGA, cyclic voltammetry and room temperature magnetic susceptibility measurements. These complexes were found to be oxidized by air in polar solvents like MeOH and DMF to V-V products. The E(1/2) values were found to be around 660 mV indicating that the carboxylate group favours vanadyl(IV) binding when compared to the alkoxo-bound vanadium complexes. Oxidative instability of these complexes are dependent on the substituent on the salicylalde…

Coordination sphereAcetylacetoneDimeric Vanadyl(Iv)Inorganic chemistryDecavanadateVanadiumchemistry.chemical_elementRedoxSingle Crystal X-RayInorganic Chemistrychemistry.chemical_compoundOxidationPyridinePolymer chemistryMaterials ChemistryAnthranilic acidPhysical and Theoretical ChemistrySchiff BasesSchiff baseReactivityVanadiumBindingMononuclear Octahedral Vo3+chemistrySalicylaldehydeDecavanadatesPyridiniumOxidative InstabilityOxovanadium(Iv)Polyhedron
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