Search results for "oxidation"

showing 10 items of 1913 documents

Energetic coupling between plastids and mitochondria drives CO2 assimilation in diatoms.

2015

International audience; Diatoms are one of the most ecologically successful classes of photosynthetic marine eukaryotes in the contemporary oceans. Over the past 30 million years, they have helped to moderate Earth's climate by absorbing carbon dioxide from the atmosphere, sequestering it via the biological carbon pump and ultimately burying organic carbon in the lithosphere. The proportion of planetary primary production by diatoms in the modern oceans is roughly equivalent to that of terrestrial rainforests. In photosynthesis, the efficient conversion of carbon dioxide into organic matter requires a tight control of the ATP/NADPH ratio which, in other photosynthetic organisms, relies prin…

Aquatic Organismschemistry.chemical_compoundAdenosine TriphosphateSettore BIO/04 - Fisiologia VegetaleCYCLIC ELECTRON FLOWPlastidsPhotosynthesisPHAEODACTYLUM-TRICORNUTUMPlant Proteinschemistry.chemical_classificationMultidisciplinarymicroalgaeRespirationCarbon fixationEnergetic interactionsProton-Motive ForceMitochondriametabolic mutantPhenotypeATP/NADPH ratioOXYGEN PHOTOREDUCTIONCarbon dioxideOxidoreductasesOxidation-ReductionOceanOceans and SeasElectron flowMarine eukaryotesBiologyPhotosynthesisCHLAMYDOMONAS-REINHARDTIICarbon cycleCarbon CycleMitochondrial ProteinsEnergetic exchangesBotanyOrganic matterEcosystem[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology14. Life underwaterPlastidEcosystemDiatomsChemiosmosisfungiECSCarbon Dioxidechemistry13. Climate actionNADP
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Proton coupled electron transfer of ubiquinone Q2 incorporated in a self-assembled monolayer.

2011

We present a complete study of the reduction of ubiquinone Q(2) (UQ(2)) in simpler aqueous medium, over a pH range of 2.5 to 12.5. The short isoprenic chain ubiquinones (UQ(2)) were incorporated in a self-assembled monolayer. Under these conditions, the global 2e(-) electrochemical reaction can be described on the basis of a nine-member square scheme. The thermodynamic constants of the system were determined. The global 2e(-) process is controlled by the uptake of the second electron. The elementary electrochemical rate constants obtained by fitting of the experimental rate constant were k(s4) = 1.5 s(-1) for QH˙(+)(2)↔ QH(2), k(s5) = 1.5 s(-1) for QH˙↔ QH(-) and k(s6) = 1 s(-1) for Q˙(-)↔ …

Aqueous mediumChemistrySurface PropertiesUbiquinoneAnalytical chemistryGeneral Physics and AstronomyWaterSelf-assembled monolayerElectronHydrogen-Ion ConcentrationElectrochemistryElectron TransportReaction rate constantCoenzyme Q – cytochrome c reductaseMonolayerElectrochemistryThermodynamicsGoldPhysical and Theoretical ChemistryProton-coupled electron transferProtonsOxidation-ReductionPhysical chemistry chemical physics : PCCP
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Voltammetric behavior of berenil.

1993

Abstract Berenil is reduced on mercury drops electrode in buffered aqueous media. The reduction of —N=N— group is controlled by diffusion. Polarographie waves are of analytical usefulness. The hydrogen discharge is favored by the basic centers of the molecule in Co(ll)/ammonia-buffered media.

Aqueous mediumHydrogenAnalytical chemistryPharmaceutical Sciencechemistry.chemical_elementHydrogen-Ion ConcentrationTrypanocidal AgentsMercury (element)chemistryElectrodeElectrochemistryMoleculeVoltammetryDiminazeneElectrodesOxidation-ReductionPolarographyJournal of pharmaceutical sciences
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Reactor model for fast reactions in the micro-bubble column and validation

2007

A simple reactor model for predicting conversions in a micro-bubble column is described. It assumes fast reactions so that the gaseous component is readily consumed at the gas-liquid interface. Then, gas-liquid mass transfer becomes determining. As input parameters for the model, the hydrodynamics, specific interfacial area, and mass transport need to be described. Two fast model reactions, the catalytic oxidation of butyraldehyde and the absorption of CO2 in aqueous NaOH, show the applicability of the model but also its limits. The model was used for predicting reaction performance in dependence of operating conditions, in particular to get maximum conversion with the antagonistic paramete…

Aqueous solutionGeneral Chemical EngineeringAnalytical chemistryThermodynamicsGeneral ChemistryResidence time (fluid dynamics)TolueneIndustrial and Manufacturing EngineeringVolumetric flow ratechemistry.chemical_compoundchemistryCatalytic oxidationMass transferPhysics::Chemical PhysicsAbsorption (electromagnetic radiation)ButyraldehydeIndustrial and Engineering Chemistry Research
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Chromia on silica and zirconia oxides as recyclable oxidizing system: structural and surface characterization of the active chromium species for oxid…

2004

Chromium oxide samples supported over silica and zirconia were prepared by wet impregnation of the supports with aqueous solution of CrO3. In order to investigate the influence of the preparation method on the chromium dispersion and oxidation state, one sample was prepared by sol-gel technique. The materials were structurally characterized by XRD analysis. The oxidation states of chromium species were investigated by XPS, DRS and TPR/TPO techniques. EPR analyses were also carried out for the sample Cr/SiO2, that due to the low crystalline state exhibits broad XPS signals. In this case, particular attention was paid to the presence of Cr(V) and Cr (III) species and their concentration. The …

Aqueous solutionInorganic chemistrychemistry.chemical_elementGeneral ChemistryRedoxTPR/FPO cycleCatalysisChromiaCatalysisChromiumchemistry.chemical_compoundchemistryOxidation stateBenzyl alcoholOxidizing agentchromium supported oxideXPSbenzyl alcohol oxidation
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Chemical heterogeneities in nanometric titanomagnetites prepared by soft chemistry and studied ex situ : evidence for fe-segregation and oxidation ki…

2001

Nanocrystalline Fe-based spinels with composition Fe3-xTixO4 are synthesized using soft chemistry. Two steps are involved:  precipitation in an aqueous solution followed by thermal annealing under a reducing mixture of N2/H2/H2O gases. Fe-segregation is found inside stoichiometric particles when the powders are studied ex situ; they exhibit a strong surface iron enrichment. This heterogeneity is related to kinetic effects linked to the difference of mobility between Fe2+ and Ti4+ cations during the partial oxidation of cations occurring ex situ. Stresses in the grains induced by oxidation govern the oxidation kinetics and lead to an abrupt compositional variation inside each particle. These…

Aqueous solutionMaterials sciencePrecipitation (chemistry)Analytical chemistry02 engineering and technology[SPI.MAT] Engineering Sciences [physics]/Materials010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSoft chemistryNanocrystalline material0104 chemical sciencesSurfaces Coatings and Films[SPI.MAT]Engineering Sciences [physics]/MaterialsX-ray photoelectron spectroscopyMaterials ChemistryParticlePartial oxidationPhysical and Theoretical Chemistry0210 nano-technologyStoichiometryComputingMilieux_MISCELLANEOUS
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Microheterogeneous electrocatalytic chiral recognition at monoclinic vanadium-doped zirconias: enantioselective detection of glucose.

2007

Synthetic tetragonal and monoclinic vanadium-doped zirconias (t- and m-VxZr1-xO2, 0.005x0.150) exert an effective catalytic effect toward the electrochemical oxidation of glucose in aqueous alkaline media. The catalytic effect of monoclinic specimens attached to carbon and fluorine-doped tin oxide electrodes exhibits a remarkable enantioselectivity, so that catalytic currents for the oxidation of L-glucose at +0.92 V vs AgCl/Ag are considerably larger than those obtained for the oxidation of D-glucose. This enantioselectivity can be associated with the existence of a noncentrosymmetric coordination of vanadium centers in the monoclinic crystalline form of zirconia. From the electrochemical …

Aqueous solutionMolecular StructureChemistryInorganic chemistryVanadiumchemistry.chemical_elementElectronsStereoisomerismVanadiumElectrocatalystTin oxideElectrochemistryCatalysisAnalytical ChemistryCatalysisGlucoseMicroscopy Electron TransmissionCalibrationElectrochemistryMicroscopy Electron ScanningCubic zirconiaZirconiumOxidation-ReductionMonoclinic crystal systemAnalytical chemistry
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Dioxygen reduction by cobalt(II) octaethylporphyrin at liquid|liquid interfaces.

2010

Oxygen reduction catalyzed by cobalt(II) (2,3,7,8,12,13,17,18-octaethylporphyrin) [Co(OEP)] at soft interfaces is studied by voltammetry and biphasic reactions. When Co(OEP) is present in a solution of 1,2-dichloroethane in contact with an aqueous acidic solution, oxygen is reduced if the interface is positively polarized (water phase versus organic phase). This reduction reaction is facilitated when an additional electron donor, here ferrocene, is present in excess in the organic phase.

Aqueous solutionPorphyrinsSurface PropertiesInorganic chemistrychemistry.chemical_elementElectron donorOxygenRedoxAtomic and Molecular Physics and OpticsCatalysisCatalysisOxygenchemistry.chemical_compoundchemistryPhase (matter)Organometallic CompoundsPhysical and Theoretical ChemistryCobaltVoltammetryOxidation-ReductionChemphyschem : a European journal of chemical physics and physical chemistry
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Photocatalytic green synthesis of piperonal in aqueous TiO2 suspension

2014

Abstract Piperonal (heliotropine or 3,4-methylenedioxybenzaldehyde) has been synthesized by oxidizing piperonyl alcohol in aqueous UV-irradiated TiO2 suspensions. This compound was identified by GC–MS chromatography, 1H NMR and melting point determination. The other products of the photoprocess were 1,3-bis(3,4-(methylenedioxy)benzyl) ether (found in traces) and CO2, derived from the parallel pathway of photo-mineralization. Commercial and home-prepared TiO2 samples have been tested and the best selectivity (ca. 35%) was obtained by using the home-prepared ones. The reported green process allows to obtain an added value product (piperonal), upon partial oxidation of a cheap reagent.

Aqueous solutionProcess Chemistry and TechnologyEtherCatalysisMethylenedioxyPiperonalchemistry.chemical_compoundchemistryReagentOxidizing agentOrganic chemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePartial oxidationSelectivityPhotocatalysisGreen synthesisPiperonalTiO2suspensionGeneral Environmental ScienceApplied Catalysis B: Environmental
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The influence of ultrasound on the RuI3-catalyzed oxidation of phenol: Catalyst study and experimental design

2009

Abstract The influence of ultrasound at 24 kHz on the heterogeneous aqueous oxidation of phenol over RuI3 with hydrogen peroxide (H2O2) was studied isothermally at 298 K. Effect of ultrasound irradiation on catalytic properties and performance of RuI3 has been studied in details by means of scanning electron microscopy (SEM), X-ray powder diffraction (XRD), dispersion analyzer and a surface analyzer. Turn over frequency of the catalyst was also calculated. In this work, experimental design methodology was applied to optimize the degradation of phenol in aqueous solution, while minimizing an excessive consumption of chemical reagents. The independent variables considered were the catalyst lo…

Aqueous solutionStereochemistryChemistryProcess Chemistry and TechnologyInorganic chemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundCatalytic oxidationReagentPhenolLeaching (metallurgy)Hydrogen peroxideGeneral Environmental ScienceApplied Catalysis B: Environmental
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