Search results for "OXIDATION"

showing 10 items of 1913 documents

Polymeric carbon nitride (C3N4) as heterogeneous photocatalyst for selective oxidation of alcohols to aldehydes

2018

Abstract Polymeric carbon nitride (C3N4) is a semiconductor material which is a very promising green photocatalyst with good physico-chemical properties and stability. It is a metal-free carbon based non-toxic material which can be easily obtained from earth-abundant components. The robustness and versatility of C3N4 as a photo-redox catalyst allows its use for selective oxidations by heterogeneous photocatalysis. This paper reviews the state of art in the application of C3N4 as heterogeneous photocatalyst for selective oxidation of alcohols to the corresponding aldehydes.

Materials scienceCarbon nitrideSemiconductor materialsPartial oxidationchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesC3N4CatalysisCatalysischemistry.chemical_compoundCarbon nitridePolymeric photocatalyst2D-materialGeneral Chemistry021001 nanoscience & nanotechnologySelective photo-oxidation0104 chemical scienceschemistryChemical engineeringSettore CHIM/03 - Chimica Generale E InorganicaAlcohol oxidationState of artPhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyAlcoholCarbonPhotocayalysi
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Strontium and iron-doped barium cobaltite prepared by solution combustion synthesis: exploring a mixed-fuel approach for tailored intermediate temper…

2013

Ba0.5Sr0.5Co0.8Fe0.2O3-? (BSCF) powders were prepared by solution combustion synthesis using single and double fuels. The effect of the fuel mixture on the main properties of this well-known solid oxide fuel cell cathode material with high oxygen ion and electronic conduction was investigated in detail. Results showed that the fuel mixture significantly affected the area-specific resistance of the BSCF cathode materials, by controlling the oxygen deficiency and stabilizing the Co2+ oxidation state. It was demonstrated that high fuel-to-metal cations molar ratios and high reducing power of the combustion fuel mixture are mainly responsible for the decreasing of the area-specific resistance o…

Materials scienceCathode materialsInorganic chemistrychemistry.chemical_elementBSCFCombustionlaw.inventionchemistry.chemical_compoundOxidation statelawPhase (matter)Materials ChemistryChatode materialIntermediate temperature solid oxide fuel cellsStrontiumRenewable Energy Sustainability and the EnvironmentPerovskite-type materialsBariumPerovskite-type compoundsCombustion fuel mixtureCathodeElectronic Optical and Magnetic MaterialsCobaltiteFuel TechnologychemistrySolution combustion synthesisSolid oxide fuel cellSettore CHIM/07 - Fondamenti Chimici Delle TecnologieMaterials for Renewable and Sustainable Energy
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Honeycomb supported Co3O4/CeO2 catalysts for CO/CH4 emissions abatement: effect of low Pd-Pt content on the catalytic activity

2007

Abstract A structured Co3O4–CeO2 composite oxide, containing 30% by weight of Co3O4, has been prepared over a cordieritic honeycomb support. The bimetallic, Pd–Pt catalyst has been obtained by impregnation of the supported Co3O4–CeO2 with Pd and Pt precursors in order to obtain a total metal loading of 50 g/ft3. CO, CH4 combined oxidation tests were performed over the catalyzed monoliths in realistic conditions, namely GHSV = 100,000 h−1 and reaction feed close to emission from bi-fuel vehicles. The Pd–Pt un-promoted Co3O4–CeO2 is promising for cold-start application, showing massive CO conversion below 100 °C, in lean condition. A strong enhancement of the CH4 oxidation activity, between 4…

Materials scienceComposite oxideHoneycomb supported Co3O4–CeO2 Promotion effect of Pd–Pt CO and CH4 oxidation Low-temperature activityProcess Chemistry and TechnologyNanotechnologyGeneral ChemistryOxidation ActivityCatalysisCatalysisMetalChemical engineeringvisual_artvisual_art.visual_art_mediumHoneycombBimetallic strip
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Comparison between preparative methodologies of nanostructured carbon nitride and their use as selective photocatalysts in water suspension

2017

Carbon nitride photocatalysts have been prepared by different methodologies, such as chemical ultrasonic irradiation (sonochemical treatment), hydrothermal and ball milling and thermoexfoliation, and have been used for the selective oxidation of 5-hydroxymethyl-2-furaldehyde (HMF) to form 2,5-furandicarboxyaldehyde (FDC) in water suspension both under UV and natural solar irradiation. The physico-chemical features of the photocatalysts have been studied by X-ray diffraction, infrared spectroscopy, UV–Vis diffuse reflectance spectroscopy, photoluminescence spectroscopy, scanning electron microscopy, and specific surface area measurements. The results indicate that exfoliation of carbon nit…

Materials scienceDiffuse reflectance infrared fourier transformCarbon nitrideInorganic chemistryInfrared spectroscopychemistry.chemical_element02 engineering and technologyNitride010402 general chemistry01 natural scienceschemistry.chemical_compoundPhotocatalysiSpecific surface areaSonochemical treatmentCarbon nitrideChemistry (all)General Chemistry021001 nanoscience & nanotechnology5-(Hydroxymethyl)-2-furaldehydeExfoliation joint0104 chemical scienceschemistryChemical engineeringPhotocatalysisSelective oxidationSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyCarbon
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Structure of the Metal–Support Interface and Oxidation State of Gold Nanoparticles Supported on Ceria

2012

An Au/CeO2 model catalyst was prepared by deposition–precipitation, with the aim of obtaining a sample suitable for a detailed X-ray absorption fine structure (XAFS) analysis of the gold–ceria interface structure. The results demonstrate the existence of a large interface between the gold particle and the support oxide, characterized by well-defined Au–O and Au–Ce interactions extending up to ∼6.4 A. The complex interface structure is retained after CO treatment up to 250 °C and subsequent reoxidation at 400 °C. The analysis of the XANES spectra, and the Au–O distance of 2.21 A, longer than Au–O bond lengths previously reported for Au/ceria catalysts, suggest a low oxidation state for the g…

Materials scienceExtended X-ray absorption fine structureOxideXANESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisX-ray absorption fine structureMetalCrystallographychemistry.chemical_compoundGeneral EnergychemistryChemical engineeringColloidal goldOxidation statevisual_artEXAFS ceria catalysis goldvisual_art.visual_art_mediumPhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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Total oxidation of VOCs on mesoporous iron oxide catalysts: Soft chemistry route versus hard template method

2016

9 figures, 3 tables.-- Supplemantary information available

Materials scienceGeneral Chemical EngineeringCatalytic total oxidationOxalic acidInorganic chemistry02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing EngineeringSoft chemistryCatalysisIron oxide catalysts: Soft chemistry synthesischemistry.chemical_compoundPropaneAdsorptionEnvironmental ChemistryNanocastingTotal oxidatioVOCsMesoporous supportSoft chemistry synthesis [Iron oxide catalysts]General Chemistry021001 nanoscience & nanotechnologyToluene oxidation0104 chemical sciencesMesoporous organosilicachemistry0210 nano-technologyMesoporous materialMesoporous α-Fe2O3Template method patternToluene
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Methyl-3-Hexenoate Combustion Chemistry: Experimental Study and Numerical Kinetic Simulation

2020

International audience; This work represents a detailed investigation of combustion and oxidation of methyl-3-hexenoate (CAS Number 2396-78-3), including experimental studies of combustion and oxidation characteristics, quantum chemistry calculations and kinetic model refinement. Following experiments have been carried out: Speciation measurements during oxidation in a jet-stirred reactor at 1 atm; chemical speciation measurements in a stoichiometric premixed flame at 1 atm using molecular-beam mass-spectrometry; ignition delay times measurements in a shock tube at 20 and 40 bar; and laminar burning velocity measurements at 1 atm using a heat-flux burner over a range of equivalence ratios. …

Materials scienceGeneral Chemical EngineeringFlame structureGeneral Physics and AstronomyEnergy Engineering and Power TechnologyThermodynamics02 engineering and technologyKinetic energyCombustion01 natural sciences7. Clean energylaw.invention020401 chemical engineeringlawOxidation mechanisms0103 physical sciencesOxidationJet stirred reactor0204 chemical engineeringShock tubePremixed flame010304 chemical physics[SPI.FLUID]Engineering Sciences [physics]/Reactive fluid environmentBurning velocityLaminar flowGeneral Chemistrykinetic modelingIgnitionbiofuelsIgnition system[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryFuel TechnologyFlame structureCombustorMethyl-3-hexenoate
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Electrochemical oxidation of organics at metal oxide electrodes: The incineration of oxalic acid at IrO2-Ta2O5 (DSA-O2) anode

2008

Abstract The electrochemical incineration of oxalic acid (OA) at Ti/IrO2–Ta2O5 (DSA-O2) anode was investigated to find the influence of the operative parameters on the performances of the process. Polarization curves and chronoamperometric measurements indicate the probable occurrence of a direct electrochemical oxidation of OA at the surface of the DSA anode. In incineration electrolyses, the performances of the process in terms of OA conversion and current efficiency dramatically depend on the adopted operative conditions. Interestingly, very high OA removal and current efficiency were obtained when the process was performed at relatively high temperatures (50 °C) or in the presence of Na…

Materials scienceGeneral Chemical EngineeringInorganic chemistryOxalic acidOxideElectrochemistryAnodeIncinerationMetalchemistry.chemical_compoundchemistryelectrochemical incineration oxalic acid carboxylic acid IrO2 DSA oxidation of organicsvisual_artElectrodeElectrochemistryvisual_art.visual_art_mediumPolarization (electrochemistry)
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Structure and the metal-support interaction of the Au/Mn oxide catalysts

2010

Gold catalysts with loading 1 and 10 wt % were-prepared by deposition precipitation method with urea over mesoporous manganese oxide, obtained through a surfactant-assisted procedure by using cetyltrimethylammonium bromide (CTAB), followed by treatment with sulphuric acid. For comparison, Au(10 wt %) was also deposited over commercial CeO2 and SiO2 supports. The materials were characterized by XRD and EXAFS at the Mn K and Au L-III edges and XPS. Moreover, the analyses were performed on the samples treated under 1%CO/He, at 250 degrees C for 90 min. The structural and surface results of the as prepared manganese oxide confirmed the formation of gamma-MnO2 along with some amorphous Mn3O4 upo…

Materials scienceGeneral Chemical EngineeringInorganic chemistryTEMPERATURE CO OXIDATIONOxideBixbyiteAEROBIC ALCOHOL OXIDATIONCatalysisMetalENHANCED ACTIVITYchemistry.chemical_compoundX-ray photoelectron spectroscopyBromideMANGANESE OXIDERAY-ABSORPTION SPECTROSCOPYBODY DISTRIBUTION-FUNCTIONSMaterials ChemistryCONDENSED MATTERCERIAGeneral ChemistryTEMPERATURE CO OXIDATION; RAY-ABSORPTION SPECTROSCOPY; BODY DISTRIBUTION-FUNCTIONS; AEROBIC ALCOHOL OXIDATION; GOLD NANOPARTICLES; NANOCRYSTALLINE CEO2; ENHANCED ACTIVITY; CONDENSED MATTER; MANGANESE OXIDE; CERIAchemistryvisual_artGOLD NANOPARTICLESNANOCRYSTALLINE CEO2visual_art.visual_art_mediumMesoporous materialHausmannite
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Effects of anion size on the electrochemical behavior of H2SO4-structured poly(o-toluidine) films. An ac-electrogravimetry study in acid solutions

2014

International audience; ac -Electrogravimetry has allowed an easy separation of kinetic information to be evaluated for all the transferred species in three different H2SO4-structured poly(o-toluidine) or POT films, View the MathML sourcePOT-NO3−, View the MathML sourcePOT-ClO4− and POT-Cl− films when they are polarized between the pernigraniline (oxidized) and leucoemeraldine (reduced) forms. It is clear that larger anions slow down the electrochemical transitions of POT films, but the effects of anion transfer on hydrated protons and free solvent transfers are affected. For the same polymeric structure of a POT film, the kinetics of all specie transfers have been evaluated considering the…

Materials scienceGeneral Chemical EngineeringKineticsInorganic chemistryAnalytical chemistry02 engineering and technology010402 general chemistryElectrochemistry01 natural sciencesac-ElectrogravimetryOxidation stateElectrogravimetryElectrochemistryMoleculeElectrochemical quartz crystal microbalance[CHIM]Chemical Scienceschemistry.chemical_classificationac-Electrogravimetry.Polymer021001 nanoscience & nanotechnology0104 chemical sciencesDielectric spectroscopySolventchemistryIntrinsically conducting polymer0210 nano-technology[CHIM.OTHE]Chemical Sciences/OtherElectrochemical impedance spectroscopyPoly(o-toluidine)
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