Search results for "Heterogeneous catalysis"

showing 10 items of 233 documents

Selective oxidative dehydrogenation of ethane over MoVSbO mixed oxide catalysts

2006

Abstract Mo–V–Sb–O mixed metal oxides were prepared, characterized and tested for the oxidative dehydrogenation of ethane (ODH). These catalysts are active and selective in the oxidative dehydrogenation of ethane to ethylene, although their catalytic performance depends strongly on the calcination temperature. The best catalytic results were obtained on samples heat-treated at 600 °C in N 2 (with selectivities to ethylene higher than 80% at ethane conversions about 65%). Moreover, a loss in the catalyst activity is initially observed on these catalysts as a consequence of modifications in the nature of the crystalline phases. Changes on the oxidation state of antimony ions on the surface of…

EthyleneChemistryProcess Chemistry and TechnologyInorganic chemistryOxideHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundlawMixed oxideCalcinationDehydrogenationAntimony oxideApplied Catalysis A: General
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Molybdenum–vanadium supported on mesoporous alumina catalysts for the oxidative dehydrogenation of ethane

2006

Abstract Vanadium and/or molybdenum oxides supported on mesoporous alumina have been prepared by a “wet” impregnation method, characterized (by using several physico-chemical techniques TPR, DR-UV–vis, Raman spectroscopies) and tested in the oxidative dehydrogenation (ODH) of ethane. For comparison Mo–V-mixed oxides supported on γ-Al2O3 have also been studied. The characterization results indicate that the main vanadium species in both Mo-free and Mo-containing V-based samples present low aggregation and coordination, whereas molybdenum is present as monomeric or polymeric tetrahedral molybdenum species. Interestingly, no apparent interaction between molybdenum and vanadia takes place. The …

EthyleneInorganic chemistrychemistry.chemical_elementVanadiumGeneral ChemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundchemistryTransition metalMolybdenumDehydrogenationMesoporous materialCatalysis Today
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Growth and characterization of horizontally suspended CNTs across TiN electrode gaps.

2010

A technique is proposed to grow horizontal carbon nanotubes (CNTs) bridging metal electrodes and to assess their electrical properties. A test structure was utilized that allows for selective electrochemical sidewall catalyst placement. The selectivity of the technique is based on the connection of the desired metal electrodes to the silicon substrate where the potential for electrochemical deposition was applied. Control over the Ni catalyst size (15-30 nm) and density (up to 3 x 10(11) particles cm(-2)) is demonstrated. Horizontal CNTs with controlled diameter and density were obtained by CVD growth perpendicular to the sidewalls of patterned TiN electrode structures. Electrode gaps with …

FabricationMaterials scienceSiliconScanning electron microscopeElectrodeHeterogeneous catalysis at surfacechemistry.chemical_elementBioengineeringNanotechnologyChemical vapor depositionCarbon nanotubeSettore ING-INF/01 - Elettronicalaw.inventionlawGeneral Materials ScienceElectrical and Electronic EngineeringOhmic contactbusiness.industryMechanical EngineeringSurface and interface chemistryGeneral ChemistryNanostructured materials in electrochemistryNanotubechemistryMechanics of MaterialsElectrodeOptoelectronicsTinbusinessScanning electron microscopyNanotechnology
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Palladium-Catalyzed Carbon–Carbon Cross-Coupling Reactions in Thermomorphous Double Emulsions

2015

The method of combining the concept of fluorous biphasic catalysis (FCB) with micro multiple emulsions benefits from the advantages of homogeneous as well as from heterogeneous catalysis in continuous micro flow. In this particular case, three immiscible fluid phases in continuous micro segmented flow were used to perform palladium-catalyzed Heck crosscoupling reactions of styrene with aryl halides. A capillary tube-in-tube coaxial flow setup in combination with a glass micro reactor was used to produce monodisperse aqueous phase/organic phase/perfluorinated phase double emulsions. The resulting emulsions had a core-shell droplet structure composed of a perfluorcarbon fluid in which a palla…

Fluid Flow and Transfer ProcessesOrganic ChemistryInorganic chemistryAqueous two-phase systemchemistry.chemical_elementHeterogeneous catalysisCoupling reactionCatalysischemistryChemistry (miscellaneous)Heck reactionPhase (matter)MicroreactorPalladiumJournal of Flow Chemistry
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Catalytic hydrothermal liquefaction of municipal sludge assisted by formic acid for the production of next-generation fuels

2021

Abstract Hydrothermal liquefaction (HTL) of municipal sludge (MS) was studied at 325 °C and 30 min at 10 and 30% w/w concentration of MS using formic acid (FA) as a green liquid hydrogen donor both in the absence and in the presence of heterogeneous catalysts. Pellets of commercial NiMo/Al2O3, CoMo/Al2O3 and felt of activated carbon ACF 1600 were used as catalysts. The addition of FA at high MS loading allowed to increase the yields in BC from 41 to 62% and its H/C ratio from 1.80 to 2.01 leading to energy recovery (ER) higher than 100%.When heterogeneous catalysts were used together with FA, a marked improvement of BC yields and quality was obtained at 10% MS loading. This behavior was not…

Formic acidPelletsFormic acidHeterogeneous catalysisHeterogeneous catalystIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundmedicineElectrical and Electronic EngineeringHydrogen donorMunicipal sludgeCivil and Structural EngineeringFoulingChemistryMechanical EngineeringBuilding and ConstructionSettore ING-IND/27 - Chimica Industriale E TecnologicaBiorefineryPollutionBiorefineryHydrothermal liquefactionGeneral EnergyHydrothermal liquefactionActivated carbonmedicine.drugNuclear chemistryEnergy
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Formaldehyde: Catalytic Oxidation as a Promising Soft Way of Elimination

2013

International audience; Compared to other molecules such as benzene, toluene, xylene, and chlorinated compounds, the catalytic oxidation of formaldehyde has been studied rarely. However, standards for the emission level of this pollutant will become more restrictive because of its extreme toxicity even at very low concentrations in air. As a consequence, the development of a highly efficient process for its selective elimination is needed. Complete catalytic oxidation of formaldehyde into CO2 and H2O using noble-metal-based catalysts is a promising method to convert this pollutant at room temperature, making this process energetically attractive from an industrial point of view. However, th…

General Chemical EngineeringFormaldehyde02 engineering and technologyengineering.material010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energyCatalysisCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryFormaldehyde[ CHIM.OTHE ] Chemical Sciences/OtherEnvironmental ChemistryOrganic chemistryGeneral Materials SciencePollutantAir Pollutants[CHIM.ORGA]Chemical Sciences/Organic chemistryXylene[CHIM.CATA]Chemical Sciences/Catalysis021001 nanoscience & nanotechnologyToluene0104 chemical sciencesGeneral EnergychemistryCatalytic oxidation13. Climate actionAir Pollution IndoorengineeringNoble metal[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyOxidation-ReductionChemSusChem
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Transesterification of rapeseed oil over acid resins promoted by supercritical carbon dioxide

2011

The methanolysis of rapeseed oil catalyzed by commercial styrene-divinylbenzene macroporous acid resins was performed in a batch reactor at 100-140 °C and 10-46 MPa to study the effect of supercritical carbon dioxide (scCO2) on the performances of the process. Reaction temperatures of 120-140 °C were necessary to obtain high enough yields of fatty acid methyl esters. Upon addition of scCO2 faster transesterification kinetics was obtained also at the lowest investigated operating pressure (10-11 MPa), working in two fluid phase systems. Experiments performed changing the reaction time indicated that most of the esters were formed during the first 3 h. When the pressure was increased at 38-46…

General Chemical EngineeringMethanolysiKineticsBatch reactorOperating pressurePolymeric acidHeterogeneous catalysisCatalysiCatalysisHeterogeneous catalysiIon exchange resinSupercritical carbon dioxideOrganic chemistryFatty acid methyl esterRapeseed oilEsterPhysical and Theoretical ChemistryVegetable oils Supercritical fluid extractionIon-exchange resinStyreneReaction systemReaction timeBiodieselFluid phasiTwo-fluid Batch reactorSupercritical carbon dioxideEsterificationChemistryReaction kineticTransesterificationSettore ING-IND/27 - Chimica Industriale E TecnologicaFatty acidCondensed Matter PhysicsPhase behaviourTransesterificationCarbon dioxideReaction temperatureMacroporouStyrene-divinylbenzeneBiodieselEnhancement effectIon exchangeThe Journal of Supercritical Fluids
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Heterometallic Titanium-Organic Frameworks as Dual Metal Catalysts for Synergistic Non-Buffered Hydrolysis of Nerve Agent Simulants

2020

Heterometallic metal-organic frameworks (MOFs) can offer important advantages over their homometallic counterparts to enable targeted modification of their adsorption, structural response, electronic structure, or chemical reactivity. However, controlling metal distribution in these solids still remains a challenge. The family of mesoporous titanium-organic frameworks, MUV-101(M), displays heterometallic TiM2 nodes assembled from direct reaction of Ti(IV) and M(II) salts. We use the degradation of nerve agent simulants to demonstrate that only TiFe2 nodes are capable of catalytic degradation in non-buffered conditions. By using an integrative experimental-computational approach, we rational…

General Chemical Engineeringchemistry.chemical_element02 engineering and technology010402 general chemistryHeterogeneous catalysis01 natural sciencesBiochemistryCatalysisMetalchemistry.chemical_compoundHydrolysisMaterials ChemistryEnvironmental ChemistrySynergistic catalysisLewis acids and basesBimetallic stripBiochemistry (medical)General ChemistryPurple acid phosphatases021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryvisual_artvisual_art.visual_art_mediumChemical stabilityTrimesic acid0210 nano-technologyBrønsted–Lowry acid–base theoryTitanium
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New heterogeneous catalysts for greener routes in the synthesis of fine chemicals

2007

Abstract New strong Lewis acid SnTf-MCM-41 and SnTf-UVM-7 catalysts with unimodal and bimodal pore systems were prepared in a two-step synthesis in which the triflic acid (Tf) was incorporated to previously synthesized mesoporous tin-containing silicas. The Sn incorporation inside the pore walls was carried out through the Atrane method. The SnTf-UVM-7 catalysts were prepared by aggregating nanometric mesoporous particles defining a hierarchic textural-type additional pore system. Following these procedures, catalysts with different Si/Sn ratios—21.8 to 50.8 for SnTf-MCM-41 and 18.4 for SnTf-UVM-7—were prepared. These new materials were tested in the acylation of aromatic sulfonamides using…

Green chemistryAcylationchemistry.chemical_compoundAtranechemistryOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistryMesoporous materialHeterogeneous catalysisTriflic acidCatalysisCatalysisJournal of Catalysis
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Sustainable Approach to Waste-Minimized Sonogashira Cross-Coupling Reaction Based on Recoverable/Reusable Heterogeneous Catalytic/Base System and Ace…

2016

In this contribution, we present a chemically efficient and sustainable protocol for the palladium-catalyzed copper-free Sonogashira cross-coupling reaction, based on the use of a heterogeneous catalytic system. This consists in the combination of a palladium catalyst on highly cross-linked thiazolidine network on silica and a polystyrene-supported base. The solid catalyst/base system acts as a palladium scavenger avoiding leaching of the metal and consequent product contamination. The reaction can be conducted in safe and easily recoverable acetonitrile/water azeotrope as reaction medium. This proved to be an efficient greener alternative to the classic toxic aprotic media commonly used in…

Green chemistryAzeotrope media; Green chemistry; Heterogeneous catalysis; Sonogashira reaction; Waste minimization; Chemistry (all); Environmental Chemistry; Chemical Engineering (all); Renewable Energy Sustainability and the EnvironmentGeneral Chemical EngineeringWaste minimizationchemistry.chemical_elementSonogashira coupling010402 general chemistryHeterogeneous catalysis01 natural sciencesCoupling reactionCatalysisHeterogeneous catalysichemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryChemical Engineering (all)Renewable EnergyAcetonitrileHeterogeneous catalysisSustainability and the Environment010405 organic chemistryRenewable Energy Sustainability and the EnvironmentChemistry (all)Settore CHIM/06 - Chimica OrganicaGeneral ChemistryAzeotrope mediaCombinatorial chemistry0104 chemical scienceschemistryGreen chemistryLeaching (metallurgy)Sonogashira reactionPalladiumACS Sustainable Chemistry and Engineering
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