Search results for "Supported catalyst"

showing 10 items of 40 documents

Enhanced NiO Dispersion on a High Surface Area Pillared Heterostructure Covered by Niobium Leads to Optimal Behaviour in the Oxidative Dehydrogenatio…

2020

[EN] A Nb-containing siliceous porous clay heterostructure (PCH) with Nb contents from 0 to 30 wt %) was prepared from a bentonite and used as support in the preparation of supported NiO catalysts with NiO loading from 15 to 80 wt %. Supports and NiO-containing catalysts were characterised by several physicochemical techniques and tested in the oxidative dehydrogenation (ODH) of ethane. The characterisation studies on Nb-containing supports showed the presence of well-anchored Nb(5+)species without the formation of Nb(2)O(5)crystals. High dispersion of nickel oxide with low crystallinity was observed for the Nb-containing PCH supports. In addition, when NiO is supported on these Nb-containi…

010405 organic chemistryChemistryNiobiumOrganic ChemistryNon-blocking I/OSupported catalystsNiobiumchemistry.chemical_elementHeterojunctionGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesNickelNickelPorous heterostructuresPhysical chemistryDehydrogenationDehydrogenationDispersion (chemistry)Chemistry - A European Journal
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Hydrogenolysis of hydroxymatairesinol on Y derived catalysts: a computational study

2010

Hydrogenolysis of 7-hydroxymatairesinol (HMR) to matairesinol (MAT) occurs on palladium supported acidic catalysts. HMR has three stereochemical centres and naturally exists as a mixture of two diastereoisomers, namely RRR-HMR and SRR-HMR. The latter is significantly more reactive than the former, in the reaction above. In order to elucidate the hydrogenolysis mechanism, simple surface events involving HMR derivatives on aluminated faujasite (H-Y) fragments were simulated by quantum chemical calculations. The metallic function of a Pd/H-Y acidic catalyst was also mimicked by a minimal palladium cluster. Stereochemical evidences pointed already out that water β-elimination on the epimeric ce…

7-HydroxymatairesinolProcess Chemistry and TechnologySupported catalystschemistry.chemical_elementDFT calculationFaujasiteengineering.materialHeterogeneous catalysisMedicinal chemistryHydrogenation/dehydration processeCatalysisCatalysisReaction rateHydroxymatairesinolchemistryHydrogenolysisengineeringOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryPalladiumH-Y zeolite
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Carbons from second generation biomass as sustainable supports for catalytic systems

2018

In this study activated carbons were produced from the wood of three different wood species (pine, birch, spruce). The resulting activated carbons were characterized in bulk for ash content, carbon content (elemental analyses), specific surface area, and pore size distribution, and at the surface by measuring the autogenerated pH and studying their structure by XPS. All the samples presented high surface areas and appeared to be mesoporous materials (mesopores >80%). The carbons were then used as support for AuPt nanoparticles and tested in the liquid phase oxidation of glycerol (GLY) and in the hydrogenation of levulinic acid (LA), two important chemicals from cellulose-based biomass. The …

Activated mesoporous carbonskatalyytitaktiivihiiliLevulinic acid hydrogenationbiomassa (teollisuus)Carbon supported catalystsGlycerol oxidationGVL production
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Solid-State Synthesis of “Bamboo-Like” and Straight Carbon Nanotubes by Thermolysis of Hexa-peri-hexabenzocoronene–Cobalt Complexes

2006

BambooHot TemperatureTime FactorsMaterials scienceSelective chemistry of single-walled nanotubeschemistry.chemical_elementCarbon nanotubelaw.inventionBiomaterialsMicroscopy Electron TransmissionlawNanotechnologyOrganic chemistryPolycyclic CompoundsGeneral Materials ScienceArgonMethylene ChlorideNanotubes CarbonCarbon nanofiberThermal decompositionTemperatureHexa-peri-hexabenzocoroneneCobaltGeneral ChemistryMicroscopy ElectronModels ChemicalchemistryChemical engineeringMicroscopy Electron ScanningCarbon nanotube supported catalystCrystallizationCobaltBiotechnologySmall
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Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water

2009

Several polystyrene-supported proline dipeptides and a prolinamide derivative were prepared by thiol–ene coupling. These materials were used as catalysts for the direct asymmetric aldol reaction in water, and results compared with unsupported catalysts in water. Such an approach gave more active or stereoselective catalysts compared to the unsupported compounds, showing that our immobilization procedure may be useful to develop catalytic materials with enhanced performance. Moreover, these catalysts can be recovered and reused for at least nine times without loss of activity or can be easily regenerated when their activity has decreased. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, …

ChemistryCatalyst supportOrganic ChemistryEnantioselective synthesisSettore CHIM/06 - Chimica OrganicaChemical synthesisCatalysisAldol reactionOrganocatalysisOrganic chemistryDipeptide Organocatalysis Prolinamide Proline Supported catalystAldol condensationStereoselectivityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Recyclable Catalyst Reservoir: Oxidation of Alcohols Mediated by Noncovalently Supported Bis(imidazolium)-Tagged 2,2,6,6-Tetramethylpiperidine 1-Oxyl

2013

Bis(imidazolium)-tagged 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) catalysts were adsorbed on different supports such as silica gel, silica gel modified with highly cross-linked polymeric imidazolium networks, and highly cross-linked polymeric imidazolium networks entrapping magnetic particles. These systems provided a convenient tool for the oxidation of both primary and secondary alcohols working as recyclable reservoirs for the bis(imidazolium)-tagged TEMPO catalysts. By using EPR spectroscopy it was demonstrated that the catalyst was released as the corresponding oxoammonium salt in the solution during the recycling step, thus promoting the oxidative process in a homogeneous fashion. …

ChemistryalcoholoxidationOrganic ChemistryketoneALCOHOLSSettore CHIM/06 - Chimica OrganicaRecyclable catalystCatalysisaldehydelaw.inventionInorganic Chemistry2 2 6 6 tetramethylpiperidine 1 oxyllawAlcohol oxidationKETONESOrganic chemistryPhysical and Theoretical Chemistrysupported catalystsElectron paramagnetic resonanceEPR spectroscopy
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Sol–gel material as a support of organometallic catalyst for ethylene polymerization

2008

Abstract The sol–gel procedure was applied to obtain powdery materials with different structures and morphology. It was possible to produce almost non-porous silica powder, with an extremely low surface area (ca. 4 m 2 /g) and very high uniformity of spherical particles as well as materials with various uniformity of particles and different porosity, most likely associated with increasing pore volume. Dependent on the properties of the carrier, the resulting supported vanadium catalysts (VOCl 3 /AlEt 2 Cl) showed significant differences concerning activity and stability. It was confirmed that improved hydrophobicity of the carrier’s surface may be useful and improve the activity of the syst…

Ethylene polymerizationPolymers and PlasticsOrganic ChemistrySupported catalystsGeneral Physics and AstronomyVanadiumchemistry.chemical_elementSilicaPolyethyleneSol–gelChlorideCatalysischemistry.chemical_compoundReaction rate constantchemistryPolymerizationChemical engineeringPolymer chemistryMaterials ChemistrymedicinePorosityPolymerization kineticmedicine.drugSol-gelEuropean Polymer Journal
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Effect of silica-type sol–gel carrier’s structure and morphology on a supported Ziegler–Natta catalyst for ethylene polymerization

2006

Abstract Silica xerogels with different structures and morphology, synthesized using a sol–gel procedure, were used as a carrier of vanadium catalysts (VOCl 3 /AlEt 2 Cl) for ethylene polymerization. Two techniques of catalyst synthesis were applied: slurry impregnation and gas-phase adsorption and the relevant polymerization methods were then employed. The effect of the carrier structure and morphology on the vanadium loading in the catalysts, the catalyst’s activity and kinetic stability were investigated.

Ethylene polymerizationPolymers and PlasticsSilica gelCatalyst supportUHMWPEOrganic ChemistrySupported catalystsGeneral Physics and AstronomyVanadiumchemistry.chemical_elementSilicaPolyethyleneSol–gelCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryZiegler–Natta catalystSol-gelEuropean Polymer Journal
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Carbon dioxide conversion to dimethyl carbonate: The effect of silica as support for SnO2 and ZrO2 catalysts

2011

International audience; Abundant in nature, CO2 poses few health hazards and consequently is a promising alternative to phosgene feedstock according with the principles of Green Chemistry and Engineering. The synthesis organic carbonates from CO2 instead of phosgene is highly challenging as CO2 is much less reactive. As part of our ongoing research on the investigation of catalysts for dimethyl carbonate (DMC) synthesis from methanol and CO2, we herein report results aimed at comparing the catalytic behavior of new SnO2-based catalysts with that of ZrO2. Silica-supported SnO2 and ZrO2 exhibit turnover numbers which are an order of magnitude higher than those of the unsupported oxides. Tin-b…

Green chemistryZirconiumCarbon dioxide fixation010405 organic chemistryGeneral Chemical EngineeringSupported catalystschemistry.chemical_elementGeneral Chemistry010402 general chemistryHeterogeneous catalysis01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryTinOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistrySustainable chemistryZirconiumMethanolDimethyl carbonatePhosgeneTinComptes Rendus Chimie
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New Hybrid Organic-inorganic Multifunctional Materials Based on Polydopamine-like Chemistry

2021

Taking inspiration from the chemistry of dopamine, a simple and economic synthetic approach toward the synthesis of a series of silica-based polydopamine-like materials has been developed. Mild conditions and easy manipulation are the strongest aspects of this methodology. Such hybrid materials were successfully used as recyclable catalysts for Knoevenagel reactions.

Heterogeneous catalysisSilanesChemistryOrganic ChemistrySupported catalystsNanotechnologypolydopamine like chemistrySettore CHIM/06 - Chimica OrganicaSilanesHeterogeneous catalysisDopamineschemistry.chemical_compoundImmobilizationOrganic inorganichybrid organic-inorganic multifunctional materials
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