Search results for " Dehydrogenation"

showing 10 items of 13 documents

Intermolecular oxidative dehydrogenative 3,3′-coupling of benzo[b]furans and benzo[b]thiophenes promoted by DDQ/H+: total synthesis of shandougenine B

2016

With an excess of a strong acid, 2,3-dichloro-5,6-dicyano-1,4-quinone (DDQ) is shown to promote metal-free intermolecular oxidative dehydrogenative (ODH) 3,3'-coupling of 2-aryl-benzo[b]furans and 2-aryl-benzo[b]thiophenes up to 92% yield as demonstrated with 9 substrates. Based on the analysis of oxidation potentials and molecular orbitals combined with EPR, NMR and UV-Vis observations, the studied reaction is initiated by a DDQ-substrate charge transfer complex and presumably proceeds via oxidation of the substrate into an electrophilic radical cation that further reacts with another molecule of a neutral substrate. The coupling reactivity can easily be predicted from the oxidation potent…

116 Chemical sciencesEFFICIENTfree radicalscoupling reactionsvapaat radikaalit010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryCoupling reactionoxidative dehydrogenationC BOND FORMATIONSCHOLL REACTIONELECTRON-TRANSFERMolecular orbitalReactivity (chemistry)luonnonaineiden synteesiDIPHOSPHINE LIGANDSta116BASIS-SETSCATALYZED STEREOSELECTIVE REACTIONS010405 organic chemistryChemistryOrganic ChemistrykytkentäreaktiotSubstrate (chemistry)Total synthesishapettava dehydroganaatiolaskennallinen kemiaCharge-transfer complex0104 chemical sciencesRadical ionsynthesis of natural productsACIDElectrophileCATION-RADICALSHETEROCYCLESOrganic Chemistry Frontiers
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NiO diluted in high surface area TiO2 as efficient catalysts for the oxidative dehydrogenation of ethane

2017

[EN] Catalysts consisting of NiO diluted in high surface area TiO2 can be as efficient in the oxidative dehydrogenation of ethane as the most selective NiO-promoted catalysts reported previously in the literature. By selecting the titania matrix and the NiO loading, yields to ethylene over 40% have been obtained. In the present article, three different titanium oxides (TiO2) have been employed as supports or diluters of nickel oxide and have been tested in the oxidative dehydrogenation of ethane to ethylene. All TiO2 used present anatase as the main crystalline phase and different surface areas of 11,55 and 85 m(2) g(-1). It has been observed that by selecting an appropriate nickel loading …

AnataseInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysisCatalysisEthyleneSurface coverageNiO diluted in TiO2DehydrogenationOxidative dehydrogenation of ethaneTitanium oxideChemistryProcess Chemistry and TechnologyNickel oxideNon-blocking I/O021001 nanoscience & nanotechnologyNickel oxide catalysts0104 chemical sciencesTitanium oxideNickel(ODH)0210 nano-technologyTitanium
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Oxidative dehydrogenation of ethane over NiO–CeO2 mixed oxides catalysts

2012

[EN] In this paper we present the synthesis, characterization and catalytic behaviour in the oxidative dehydrogenation of ethane of NiO-CeO2 mixed oxides. The addition of cerium oxide to NiO strongly modifies its catalytic performance, although the changes in the catalytic behaviour depend on the catalyst composition. The incorporation of low amounts of cerium oxide to NiO multiplies the productivity to ethylene in the oxidative dehydrogenation of ethane by a factor of ca. 7, which is the result of an increase in both catalytic activity and selectivity to ethylene. The enhanced activity has been related to the remarkable increase of the surface area of catalyst and the low crystal sizes of …

Cerium oxideEthyleneCatalyst characterization (XPS TPR XRD Raman FTIR of adsorbed CO oxygen isotopic-exchange)Inorganic chemistryNon-blocking I/Ochemistry.chemical_elementCerium oxideGeneral ChemistryCatalysisCatalysisCerium(IV) oxide–cerium(III) oxide cycleEthylenechemistry.chemical_compoundCeriumchemistryDehydrogenationOxidative dehydrogenation of ethaneNickel oxideSelectivityCatalysis Today
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The nickel-support interaction as determining factor of the selectivity to ethylene in the oxidative dehydrogenation of ethane over nickel oxide/alum…

2021

[EN] Nickel oxides supported on gamma-alumina (Ni-loading from 5 to 30 wt% NiO) have been synthesized and tested in the oxidative dehydrogenation (ODH) of ethane in order to determine the importance of the NiO-support interaction. The best performance was achieved by the catalyst with 15 wt% NiO; higher NiO-loadings lead to the formation of unselective bulk-like NiO and lower Ni-loadings present high proportion of free alumina surface sites. The presence of oxalic acid and/or niobium in the synthesis gel resulted in the formation of NiO particles with similar size, but higher crystallinity and reducibility than the standard 15 wt% NiO catalyst. The obtained results have revealed that, in ad…

Ethylene010405 organic chemistryChemistryProcess Chemistry and TechnologyNickel oxideInorganic chemistryNon-blocking I/OOxalic acidAluminachemistry.chemical_elementCatalyst characterization (XPS HREM UV raman and UV-vis-DRS)010402 general chemistry01 natural sciencesCatalysisODH0104 chemical sciencesCatalysisCrystallinitychemistry.chemical_compoundNickelEthyleneDehydrogenationOxidative dehydrogenation of ethaneNickel oxide
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Nickel oxide supported on porous clay heterostructures as selective catalysts for the oxidative dehydrogenation of ethane

2016

[EN] Porous clay heterostructures (PCH) have shown to be highly efficient supports for nickel oxide in the oxidative dehydrogenation of ethane. Thus NiO supported on silica with a PCH structure shows productivity towards ethylene three times higher than if NiO is supported on a conventional silica. This enhanced productivity is due to the increase in the catalytic activity and especially to the drastic increase in the selectivity to ethylene. Additionally, PCH silica partially modified with titanium in the columns (PCH-Ti) have also been synthesized and used as supports for NiO. An enhanced activity and selectivity to ethylene was found over NiO supported over PCH-Ti compared to the corresp…

EthyleneMaterials scienceCatalystsNickel oxideNon-blocking I/OInorganic chemistrychemistry.chemical_elementNickel oxide supported02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryPorous Clay HeterostructuresDehydrogenationOxidative dehydrogenation of ethane0210 nano-technologyDispersion (chemistry)SelectivityTitaniumCatalysis Science & Technology
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Morphological and Chemical Evolution of Gradually Deposited Diamond-Like Carbon Films on Polyethylene Terephthalate: From Subplantation Processes to …

2016

Diamond-like carbon (DLC) films on polyethylene terephthalate (PET) are nowadays intensively studied composites due to their excellent gas barrier properties and biocompatibility. Despite their applicative features being highly explored, the interface properties and structural film evolution of DLC coatings on PET during deposition processes are still sparsely investigated. In this study two different types of DLC films were gradually deposited on PET by radio frequency plasma-enhanced chemical vapor deposition (RF-PECVD) using acetylene plasma. The surface morphology of the deposited samples has been analyzed by atomic force microscopy (AFM). Their chemical composition was investigated by …

Materials sciencefilm dehydrogenationDiamond-like carbonchemistry.chemical_elementgrain analysiNanotechnology02 engineering and technologyChemical vapor deposition01 natural sciencesContact anglechemistry.chemical_compoundsymbols.namesake0103 physical sciencesPolyethylene terephthalateDeposition (phase transition)General Materials ScienceRF-PECVDRaman010302 applied physicsamorphous hydrogenated carbon (a-C:H)Settore FIS/01 - Fisica Sperimentaleinterlayer formation021001 nanoscience & nanotechnologyDRIFTchemistryChemical engineeringsymbolsWettingMaterials Science (all)0210 nano-technologyRaman spectroscopyCarbonACS applied materialsinterfaces
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Benzyl alcohol to benzaldehyde oxidation on MnOx clusters: Unraveling atomistic features

2021

Abstract The catalytic oxidation of benzyl alcohol with O 2 is a promising option for the production of benzaldehyde, from both environmental and economical viewpoints. In particular, highly dispersed MnO x systems feature good activity and selectivity in a wide range of temperatures, although deactivation phenomena by over-oxidation and/or poisoning of active sites are generally recorded. On this account, a density functional theory study was performed on cluster-sized catalyst models, namely Mn 4 O 8 and over-oxygenated Mn 4 O 9 fragments, to predict the reactivity pattern of MnO x catalysts in the selective aerobic oxidation of benzyl alcohol. Several pathways concur to determine the who…

Reaction mechanismCatalyst deactivationReaction mechanismsProcess Chemistry and TechnologyMnOx based catalystsPhotochemistryDFTCatalysisCatalysisBenzaldehydechemistry.chemical_compoundchemistryCatalytic oxidationBenzyl alcoholAlcohol oxidationCatalyst deactivation; DFT; MnO; x; based catalysts; Oxidative dehydrogenation; Reaction mechanismsReactivity (chemistry)Physical and Theoretical ChemistryOxidative dehydrogenationSettore CHIM/02 - Chimica FisicaBenzoic acidMolecular Catalysis
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Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts

2012

[EN] Ni-Sn-O mixed oxides catalysts have been investigated for the oxidative dehydrogenation of ethane. The catalysts were prepared through the evaporation of aqueous solutions of nickel nitrate and tin oxalate and finally calcined in air at 500 degrees C for 2 h. These materials have been characterized by several techniques (N-2-adsorption, X-ray diffraction, High-Resolution Electron Microscopy, temperature programmed reduction, X-Ray Photoelectron Spectroscopy, Fourier Transformed Infrared Spectroscopy of adsorbed CO and O-18/O-16 isotope exchange). The addition of just a tiny amount of tin highly increases the selectivity to ethylene (from ca. 40% to 80-90%). Thus, high selectivity to et…

SnO2-promotedInorganic chemistrychemistry.chemical_elementInfrared spectroscopyTin oxideCatalysisOxalateCatalysisEthane ODHNiO catalystsEthane oxidationchemistry.chemical_compoundNickelEthyleneTin oxidechemistryDehydrogenationPhysical and Theoretical ChemistryTemperature-programmed reductionTinOxidative dehydrogenation of ethaneNickel oxideCatalyst characterization (XPS HREM oxygen isotope exchange FTIR CO adsorbed)
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The selective oxidative dehydrogenation of ethane over hydrothermally synthesised MoVTeNb catalysts

2002

Mo–V–Te–Nb metal oxide catalysts prepared by hydrothermal synthesis and heat-treated in N2 at high temperatures (600–700 °C) show high activity and selectivity for the oxidative dehydrogenation of ethane to ethene. Yields of ethene of 75% have been obtained at 400 °C on the best catalysts. Dejoz Garcia, Ana Maria, Ana.M.Dejoz@uv.es

UNESCO::QUÍMICAOxideOxidative phosphorylation:QUÍMICA [UNESCO]CatalysisCatalysisMetalchemistry.chemical_compoundMaterials ChemistryHydrothermal synthesisOrganic chemistryHigh activityHydrothermal synthesisDehydrogenationEthaneCatalystsUNESCO::QUÍMICA::Química inorgánicaChemistryMetals and AlloysGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOxidative dehydrogenation ; Hydrothermal synthesis ; Ethane ; Catalystsvisual_artCeramics and Compositesvisual_art.visual_art_mediumSelectivityOxidative dehydrogenationChem. Commun.
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Support effects on NiO-based catalysts for the oxidative dehydrogenation (ODH) of ethane

2019

[EN] We report on the effect of NiO-support interactions on the chemical nature of Ni species in a series of supported NiO catalysts for the ODH of ethane. SiO2, TiO2-anatase, a high surface area TiO2 and a porous clay hetero-structure (PCH) with TiO2 and SiO2 pillars were used as supports, which led to a selectivity to ethylene in the range 30-90% over supported NiO catalysts. The catalysts were characterized by means of XRD, N-2-Adsorption, H-2-TPR, XPS and in situ (under H-2 reductive atmosphere) and ex situ XAS spectroscopy. The catalytic performance of supported materials is discussed in terms of their reducibility and specific reduction kinetics, but also taking into account the speci…

X-ray absorption spectroscopyMaterials scienceEthyleneExtended X-ray absorption fine structureNon-blocking I/OOxidative dehydrogenation (ODH)02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesCatalysisSupported NiOchemistry.chemical_compoundEthyleneEXAFSChemical engineeringchemistryX-ray photoelectron spectroscopyDehydrogenation0210 nano-technologySelectivity
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