Search results for "Catalysis"

showing 10 items of 5944 documents

On the influence of the acid-base character of catalysts on the oxidative dehydrogenation of alkanes

1996

Vanadium oxides supported on metal oxide, i.e. Al2O3, MgO and Mg-Al mixed oxide, and V-containing microporous materials (VAPO-5 and MgVAPO-5) have been tested in the oxidative dehydrogenation of C2-C4 alkanes. In all cases, tetrahedral vanadium species (isolated and/or associated) were mainly observed from51V-NMR and diffuse reflectance spectroscopies. The reducibility of V5+-species, determined from the onset-reduction temperature, decreases as follows: VOx/AL > VAPO-5 > MgVAPO-5 =VOx/MG > VOx/MG + AL. The acid character of catalysts, determined from the FTIR spectra of pyridine adsorbed, decreases as: MgVAPO-5 > VOx/AL > VAPO-5 > VOx/MG + AL > VOx/MG. A similar trend between V-reducibilit…

Alkanechemistry.chemical_classificationInorganic chemistryOxideVanadiumchemistry.chemical_elementGeneral ChemistryCatalysisCatalysischemistry.chemical_compoundchemistryPyridineMixed oxideDehydrogenationSelectivity
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Reaction products and pathways in the selective oxidation of C-2-C-4 alkanes on MoVTeNb mixed oxide catalysts

2010

[EN] The catalytic properties of MoVTeNbO catalysts during the selective oxidation of short chain alkanes and olefins (C-2-C-4) have been comparatively studied The main reaction products have been ethylene from ethane acrylic acid from propane maim anhydride from n-butane and methacrolein from isobutane FTIR studies of the adsorption of the main reaction products i e olefins and aldehydes over MoVTeNbO catalyst has been carried out Accordingly the reaction pathway is explained on the basis of the characteristics of the alkane fed the stability and reactivity of both the intermediates and the reaction products and the nature of the catalytic sites involved in each reaction (C) 2010 Elsevier …

Alkanechemistry.chemical_classificationMaleic anhydrideButaneMethacroleinGeneral ChemistryAldehydeCatalysisCatalysisMoVTeNb mixed oxideschemistry.chemical_compoundchemistryIsobutaneOrganic chemistryReactivity (chemistry)Selective oxidation of alkanesIn situ FTIR spectra
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Catalytic cracking of n-alkane naphtha: The impact of olefin addition and active sites differentiation

2015

An extended dual kinetic model allows to fit the n-heptane cracking results working in a wide range of reaction conditions. The duality of the model is provided by the contribution of monomolecular and bimolecular cracking mechanisms. It takes into account the role played by the olefins formed on the global cracking or added within the feed. Furthermore by means of this model and the kinetic parameters obtained when cracking n-heptane on ZSM-5, it has been observed that, while some characterization techniques show a homogeneous zeolite surface from the point of view of the active sites, rigorous kinetic experiments point to the possibility that the reactant sees a heterogeneous surface with…

Alkanechemistry.chemical_classificationNaphthaOlefin fiberIsosteric heatKinetic modelsChemistryThermal desorption spectroscopyZeolite ZSM-5PhotochemistryFluid catalytic crackingCracking mechanismsCatalysisCatalysisDifferential heatCrackingQUIMICA ORGANICACatalytic crackingChemical physicsTemperature-programmed desorptionPhysical and Theoretical ChemistryZeoliteNaphthaTECNOLOGIA DEL MEDIO AMBIENTE
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Organo-catalyzed synthesis of aliphatic polycarbonates in solvent-free conditions

2012

A new efficient and expeditious route to the synthesis of aliphatic polycarbonates, in solvent-free conditions and using 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) as a catalyst precursor, is described. The protocol consists of a two-step polymerization process involving the transesterification of dimethyl carbonate (DMC) with linear alkane diols and leading to high molecular weight homopolymers. The reaction went to completion quantitatively with the liberation of methanol as the only by-product. The in situ formation of N-heterocyclic carbene species resulting from BMIM-2-CO2 decarboxylation is suggested to be a key feature of the condensation process. The protocol was then …

Alkanechemistry.chemical_classificationPolymers and PlasticsDecarboxylationOrganic ChemistryBioengineeringTransesterificationBiochemistryCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryCopolymerOrganic chemistryMethanolDimethyl carbonatePolymer Chemistry
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Deep oxidation of volatile organic compounds using ordered cobalt oxides prepared by a nanocasting route

2010

Ordered Co3O4 with high surface area (until 173 m2/g) has been successfully obtained through a nanocasting route using mesoporous KIT-6 silica as a hard template and tested in the deep oxidation of a series of representative volatile organic compounds (VOCs): propane as a model of short chain alkane and toluene as a model of monoaromatic hydrocarbon. It has been demonstrated that the catalytic activity for VOC deep oxidation is very elevated and its catalytic stability at moderate temperatures very good. However, the role of the ordered structure in the catalytic performance does not seem to be beneficial. The enhanced catalytic activity has been explained in terms of both the high surface …

Alkanechemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisTolueneCatalysisCatalysischemistry.chemical_compoundHydrocarbonchemistryMesoporous materialCobalt oxideCobalt
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Theoretical characterization of iron and manganese porphyrins for catalyzed saturated alkane hydroxylations

1997

Abstract The theoretical characterization of porphin (H2Por), iron and manganese porphyrins MIII(Por) and their chlorine derivatives MIII(Por)Cl has been carried out. This work represents a first step for modelling catalyzed saturated alkane hydroxylations. The chlorine atom is responsible for the existence of a dipole moment of 1.2–2.0 D in the MIII(Por)Cl molecules and for a negative value of the mean quadrupole moment (−16–(−14)DA). The charge of the metal atom (1.8–2.2 e) is rather varied (to 2.1–2.6 e) and the effective polarizability (2.8–2.9 A3) is increased (to 3.5–3.6 A3) by the addition of the chlorine atom. Starting from the porphin molecule, the presence of the metal atom decrea…

Alkanechemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementManganesePorphyrinCatalysisAccessible surface areaMetalchemistry.chemical_compoundchemistryPolarizabilityvisual_artpolycyclic compoundsvisual_art.visual_art_mediumPhysical chemistryMoleculePhysical and Theoretical ChemistryPorphinJournal of Molecular Catalysis A: Chemical
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Functionalization of CnH2n+2Alkanes: Supercritical Carbon Dioxide Enhances the Reactivity towards Primary Carbon-Hydrogen Bonds

2015

The functionalization of the primary sites of alkanes is one of the more challenging areas in catalysis. In this context, a novel effect has been discovered that is responsible for an enhancement in the reactivity of the primary C-H bonds of alkanes in a catalytic system. The copper complex Cu(NCMe) (=hydrotris{[3,5-bis(trifluoromethyl)-4-bromo]-pyrazol-1-yl}borate) catalyzes the functionalization of CnH2n+2 with ethyl diazoacetate upon inserting the CHCO2Et unit into C-H bonds. In addition, the selectivity of the reaction toward the primary sites significantly increased relative to that obtained in neat alkane upon using supercritical carbon dioxide as the reaction medium. This was attribu…

Alkanechemistry.chemical_classificationSupercritical carbon dioxideChemistryOrganic Chemistrychemistry.chemical_elementPhotochemistryCatalysisSupercritical fluidCatalysisInorganic Chemistrychemistry.chemical_compoundEthyl diazoacetateMoleculeReactivity (chemistry)Physical and Theoretical ChemistryCarbonChemCatChem
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Favoring alkane primary carbon-hydrogen bond functionalization in supercritical carbon dioxide as reaction medium

2019

The selectivity of a catalytic alkane functionalization process can be modified just changing the reaction medium from neat alkane to supercritical carbon dioxide (scCO2). A silica supported copper complex bearing an Nheterocyclic carbene ligand promotes the functionalization of carbon-hydrogen bonds of alkanes by transferring the CHCO2Et group from N2=CHCO2Et (ethyl diazoacetate, EDA). In neat hexane only 3% of the primary C-H bonds (ethyl heptanoate being the product) are functionalized in that manner, whereas the same reaction carried out in scCO2 provides a 30% yield in this linear ester. Such effect seems to be induced by an electronic density flux from the NHC ligand to the surroundin…

Alkanechemistry.chemical_classificationSupercritical carbon dioxideRenewable Energy Sustainability and the EnvironmentGeneral Chemical EngineeringAlkaneCarbon–hydrogen bond activation02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysisHexanechemistry.chemical_compoundchemistryEthyl diazoacetateCarbon dioxidePolymer chemistryEnvironmental Chemistry0210 nano-technologyCarbon-hydrogenCarbeneEthyl heptanoate
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Cracking of n-heptane on a hzsm-5 zeolite. The influence of acidity and pore structure

1985

Abstract The crackino of n-heptane on a HZSM-5 zeolite has been studied in a continuous qlass flow reactor, at atmospheric pressure, up to 470°C. The initial selectivities to the different reaction products, kinetic rate constants, activation energies and decay parameters have been calculated and compared with those obtained using a large pore zeolite (HYUS). A different product distribution is obtained with the two zeolites. In that way, and considering initial selectivities, different C 6 /C 1 , C 5 /C 2 , C 4 /C3, i-C 4 /n-C 4 , ethylene/ethane, propylene/propane ratios have been found on the two zeolite catalysts. The results have been quantitatively explained by considerinq a direct cr…

Alkanechemistry.chemical_classificationchemistry.chemical_compoundHeptaneCrackingEthylenechemistryPropaneInorganic chemistryGeneral EngineeringZeoliteProduct distributionCatalysisApplied Catalysis
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Visible Light Induced Sulfoxidation of Alkanes in the Presence of Titania

2012

Alkanes titanium dioxide C-H activation photocatalysis sulfoxidation sulfur dioxide
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