Search results for " Catalyst"

showing 10 items of 292 documents

Direct synthesis of fibrous high molecular weight polyethylene using vanadium catalysts supported on an SiO2ionic liquid system

2015

Polyethylene of fibrous morphology was obtained using Cp2VCl2 and VCl2(salenCl2) catalysts activated by AlEt2Cl and AlEtCl2 and heterogenized on a supported ionic liquid system prepared with SiO2 and 1-(3-triethoxysilyl)propyl-3-methylimidazolium chloroaluminate. The fibre length ranges from 15 to 60 µm, depending on the reaction conditions. The polyethylene is characterized by a high molecular weight ((1.1–2.4) × 106 g mol−1) and a narrow molecular weight distribution (1.4–2.5). It is a linear polymer, properly without branching. The DSC method reveals characteristic changes in melting temperature and crystallinity degree between the first and second scan heating cycles (141 °C and 136 °C,…

Materials sciencePolymers and PlasticsOrganic ChemistryPolyethylenePost-metallocene catalystBranching (polymer chemistry)Catalysischemistry.chemical_compoundCrystallinitychemistryChemical engineeringIonic liquidPolymer chemistryMaterials ChemistryMolar mass distributionFourier transform infrared spectroscopyPolymer International
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Preparation of Catalysts and Photocatalysts Used for Similar Processes

2019

Abstract This chapter reports the main techniques used to synthesize powders and films of heterogeneous catalysts and photocatalysts, often used for similar processes. Traditional preparation processes of bulky (photo)catalysts including precipitation, sol–gel technique, hydrothermal or solvothermal method, solid-state reactions, and flame syntheses were briefly described. The sonochemical method and microwave irradiation technique were also considered. The syntheses of supported catalysts by different techniques, including deposition–precipitation, impregnation, and wet coating technologies were also described. Moreover, a survey is reported of methods to deposit thin films of catalysts on…

Materials sciencePrecipitation (chemistry)Bulk and supported catalystFlame syntheseengineering.materialChemical and physical vapor depositionHydrothermal circulationCatalysisPreparation of heterogeneous (photo)catalystChemical engineeringCoatingWet chemical techniquesPhysical vapor depositionMicrowave irradiationengineeringThin filmSolid-state reaction
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Hydroformylation of 1-Hexene over Rh/Nano-Oxide Catalysts

2013

The effect of nanostructured supports on the activity of Rh catalysts was studied by comparing the catalytic performance of nano- and bulk-oxide supported Rh/ZnO, Rh/SiO₂ and Rh/TiO₂ systems in 1-hexene hydroformylation. The highest activity with 100% total conversion and 96% yield of aldehydes was obtained with the Rh/nano-ZnO catalyst. The Rh/nano-ZnO catalyst was found to be more stable and active than the corresponding rhodium catalyst supported on bulk ZnO. The favorable morphology of Rh/nano-ZnO particles led to an increased metal content and an increased number of weak acid sites compared to the bulk ZnO supported catalysts. Both these factors favored the improved catalytic performan…

Materials scienceScanning electron microscopeInorganic chemistryOxiderodiumchemistry.chemical_elementsupported catalyst02 engineering and technologylcsh:Chemical technology010402 general chemistry7. Clean energy01 natural sciencesCatalysisCatalysisRhodiumlcsh:Chemistrychemistry.chemical_compoundDesorptionlcsh:TP1-1185Physical and Theoretical Chemistryta116hydroformylation of 1-hexenehydroformylointinano-zinc oxide021001 nanoscience & nanotechnology0104 chemical sciences1-Hexenehydroformylation nano-oxidelcsh:QD1-999chemistrykatalyysirhodiumnano-oxidit0210 nano-technologyPowder diffractionHydroformylationCatalysts
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Au/CeO2-SBA-15 catalysts for CO oxidation: Effect of ceria loading on physic-chemical properties and catalytic performances

2012

In this work gold catalysts supported over SBA-15 with different CeO 2 loadings (5-30 wt%) were prepared, characterized by N 2 physisorption analyses, SAXS, XRD, STEM and XPS techniques and their catalytic performances were evaluated in the CO oxidation, chosen as reaction test. Over a selected catalyst, Au/CeO 2(20 wt%)-SBA-15, the effect of CO 2 and of the mixture (CO 2 + H 2O) on the CO conversion to CO 2 was also evaluated. Characterizations by SAXS, XRD, STEM and XPS were carried out on selected spent catalysts after CO oxidation. The results were discussed in terms of relationship between morphological, structural, electronic and catalytic properties as a function of the ceria loading…

Materials scienceSmall-angle X-ray scatteringOxideNucleationSinteringNanotechnologyGeneral ChemistryCatalysisCatalysischemistry.chemical_compoundAu CeO2 SBA-15 catalysts CO oxidationchemistryX-ray photoelectron spectroscopyChemical engineeringPhysisorptionParticle sizeCatalysis Today
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Spin state, electronic structure and bonding on C-scorpionate [Fe(II)Cl2(tpm)] catalyst: An experimental and computational study

2020

Abstract The Fe(II) spin state in the condensed phase of [Fe(II)Cl2(tpm)] (tpm = [tris(pyrazol-1-yl)methane]; 1) catalyst has been determined through a combined experimental and theoretical investigation of X-Ray Absorption Spectroscopy (XAS) at the FeL2,3-edges and NK-edge. Results indicated that in this phase a mixed singlet/triplet state is plausible. These results have been compared with the already know Fe singlet spin state of the same complex in water solution. A detailed analysis of the electronic structure and bonding mechanism of the catalyst showed that the preference for the low-spin diamagnetic ground state, strongly depends upon the ligands, the bulk solvent and the interactio…

Materials scienceSpin statesDFT calculationHomogeneous catalysis02 engineering and technologyElectronic structure010402 general chemistryDFT calculations01 natural sciencesCatalysisSinglet stateTriplet stateDFT calculations.HOMO/LUMOX-ray absorption spectroscopyC-scorpionate catalystX-ray absorption spectroscopyGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSpin statesC-scorpionate catalyst; DFT calculations; Spin states; X-ray absorption spectroscopySpin statePhysical chemistry0210 nano-technologyGround state
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Fe-N/C catalysts for oxygen reduction based on silicon carbide derived carbon

2017

This work was supported by the projects TK141 “Advanced materials and high-technology devices for energy recuperation systems” (2014-2020.4.01.15-0011), NAMUR “Nanomaterials - research and applications” (3.2.0304.12-0397) and by the Estonian Institutional Research Grant No. IUT20-13.

Materials sciencechemistry.chemical_element02 engineering and technology010402 general chemistry7. Clean energy01 natural sciencesCatalysisOxygen reduction reactionlcsh:Chemistrychemistry.chemical_compoundElectrochemistrySilicon carbide:NATURAL SCIENCES:Physics [Research Subject Categories]Aqueous solutionLigandMetallurgyDurability test021001 nanoscience & nanotechnologyNitrogenCarbide derived carbonRotating disc electrode method0104 chemical scienceschemistrylcsh:Industrial electrochemistrylcsh:QD1-999Fe-N/C catalystElectrodeCarbide-derived carbon0210 nano-technologyCarbonNuclear chemistrylcsh:TP250-261Electrochemistry Communications
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Function of titanium oxide coated on carbon nanotubes as support for platinum catalysts

2015

This study describes the outcome of the synthesis of laboratory-made (HM) Pt monometallic, binary and ternary catalysts supported on TiO2/CNT (carbon nanotubes) and based on using the dry-mix method of organometallic chemical vapor deposition (OMCVD). These multicomponent catalysts were investigated and compared with commercial Johnson Matthey (JM) catalysts for electrochemical applications.

Materials sciencechemistry.chemical_elementCarbon nanotubeChemical vapor depositionCondensed Matter PhysicsElectrochemistryAtomic and Molecular Physics and OpticsCatalysisTitanium oxidelaw.inventionchemistryChemical engineeringlawCarbon nanotube supported catalystPlatinumTernary operationMathematical PhysicsPhysica Scripta
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H2 Transformations on Graphene Supported Palladium Cluster: DFT-MD Simulations and NEB Calculations

2020

Molecular dynamics simulations based on density functional theory were employed to investigate the fate of a hydrogen molecule shot with different kinetic energy toward a hydrogenated palladium cluster anchored on the vacant site of a defective graphene sheet. Hits resulting in H2 adsorption occur until the cluster is fully saturated. The influence of H content over Pd with respect to atomic hydrogen spillover onto graphene was investigated. Calculated energy barriers of ca. 1.6 eV for H-spillover suggest that the investigated Pd/graphene system is a good candidate for hydrogen storage.

Materials sciencespilloverhydrogen reactionchemistry.chemical_elementsupported metal catalysts02 engineering and technology010402 general chemistryKinetic energylcsh:Chemical technology01 natural sciencesDFTCatalysislaw.inventionlcsh:ChemistryMolecular dynamicsHydrogen storagelawCluster (physics)lcsh:TP1-1185Physical and Theoretical Chemistryhydrogenation elementary eventsGraphene021001 nanoscience & nanotechnology0104 chemical scienceschemistrylcsh:QD1-999Chemical physicsDensity functional theoryHydrogen spillover0210 nano-technologyPalladiumCatalysts
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Colloidal lithography and Metal-Organic Chemical Vapor Deposition process integration to fabricate ZnO nanohole arrays

2010

A complete set up of optimal process conditions for an effective colloidal lithography/catalyst assisted MOCVD process integration is presented. It mainly focuses on the determination of the deposition temperature threshold for ZnO Metal-Organic Chemical Vapour Deposition (MOCVD) as well as the concentration of metal-organic silver (Ag) catalyst. Indeed, the optimization of such process parameters allows to tailor the ZnO film morphology in order to make the colloidal lithography/catalyst assisted MOCVD approach a valuable bottom up method to fabricate bi-dimensional ordered ZnO nanohole arrays. (C) 2010 Elsevier B.V. All rights reserved.

Materials sciencezinc oxide; Nanowires and nanohole arrays; Colloidal lithographyMetals and AlloysNanowirezinc oxideNanotechnologyZnO; Catalyst; Nanowires; Nanohole array; Colloidal lithography; MOCVDSurfaces and InterfacesChemical vapor depositionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisNanowireNanohole arrayScientific methodProcess integrationMOCVDMaterials ChemistryNanowires and nanohole arraysZnOColloidal lithographyMetalorganic vapour phase epitaxyCatalystThin filmLithography
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A New Heterogeneous Catalyst Obtained via Supramolecular Decoration of Graphene with a Pd2+ Azamacrocyclic Complex

2019

A new G-(H2L)-Pd heterogeneous catalyst has been prepared via a self-assembly process consisting in the spontaneous adsorption, in water at room temperature, of a macrocyclic H2L ligand on graphene (G) (G + H2L = G-(H2L)), followed by decoration of the macrocycle with Pd2+ ions (G-(H2L) + Pd2+ = G-(H2L)-Pd) under the same mild conditions. This supramolecular approach is a sustainable (green) procedure that preserves the special characteristics of graphene and furnishes an efficient catalyst for the Cu-free Sonogashira cross coupling reaction between iodobenzene and phenylacetylene. Indeed, G-(H2L)-Pd shows an excellent conversion (90%) of reactants into diphenylacetylene under mild conditio…

Models MolecularChemical PhenomenaIodobenzeneMolecular ConformationPharmaceutical ScienceSonogashira couplingLigands010402 general chemistryHeterogeneous catalysiscross coupling01 natural sciencesArticleCoupling reactionAnalytical Chemistrylaw.inventionCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryCoordination ComplexeslawDrug DiscoveryPolymer chemistryPhysical and Theoretical ChemistryDiphenylacetyleneMolecular Structurecatalysis010405 organic chemistryGrapheneSpectrum AnalysisOrganic ChemistrySonogashirapalladium catalystHydrogen-Ion Concentrationsupramolecular interactions0104 chemical sciencesSolutionsazamacrocycleschemistryPhenylacetyleneChemistry (miscellaneous)surface adsorptionMolecular MedicineGraphitecatalysis palladium catalyst; Sonogashira graphenePalladiumMolecules
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