Search results for "Catalyst"

showing 10 items of 516 documents

Metal-support interaction and redox behavior of Pt(1 wt %)/Ce0.6Zr0.4O2

2006

The catalyst Pt(1 wt %)/Ce(0.6)Zr(0.4)O(2) is studied by CO-temperature programmed reduction (CO-TPR), isothermal oxygen storage complete capacity (OSCC), X-ray absorption spectroscopy (XAS) at the Pt L(III) edge, and in situ X-ray diffraction (in situ XRD), with the aim of elucidating the role of supported metal in CO oxidation by ceria-based three-way catalysts (TWC). The redox behavior of Pt(1 wt %)/Ce(0.6)Zr(0.4)O(2) is compared to that of bare ceria-zirconia. OSCC of redox-aged Pt/ceria-zirconia is twice that of bare ceria-zirconia, and the maximum of CO consumption occurs at a temperature about 300 K lower than redox-aged ceria-zirconia. XAS analysis allows one to evidence the formati…

X-ray absorption spectroscopyMaterials scienceAbsorption spectroscopyOxygen storageAlloyXRD XAFS Pd catalystAnalytical chemistrySinteringengineering.materialRedoxSurfaces Coatings and FilmsCatalysisMetalCrystallographySettore CHIM/03 - Chimica Generale E Inorganicavisual_artMaterials Chemistryvisual_art.visual_art_mediumengineeringPhysical and Theoretical Chemistry
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Solvent-free synthesis of ZIFs: a route toward the elusive Fe(II) analogue of ZIF-8

2019

Herein we report the synthesis of an elusive metal-organic framework, the iron(II) analogue of ZIF-8 with the formula Fe(2-methylimidazolate) , here denoted as MUV-3. The preparation of this highly interesting porous material, inaccessible by common synthetic procedures, occurs in a solvent-free reaction upon addition of an easily detachable template molecule, yielding single crystals of MUV-3. This methodology can be extended to other metals and imidazolate derivatives, allowing the preparation of ZIF-8, ZIF-67, and the unprecedented iron(II) ZIFs Fe(2-ethylimidazolate) and Fe(2-methylbenzimidazolate) . The different performance of MUV-3 toward NO sorption, in comparison to ZIF-8, results …

Zeolitic imidazolate frameworksStorage02 engineering and technologyOverpotential010402 general chemistryMetal-Organic frameworks01 natural sciencesBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryImidazolateMaterialsThermal-StabilityTafel equationNanocompositeChemistryOxygen evolutionElectrocatalystsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemisorptionPhysical chemistryMetal-organic frameworkAdsorptionCristalls0210 nano-technologyOxygen evolutionZeolitic imidazolate framework
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Electrochemistry of vanadium-doped ZrSiO4Site-selective electrocatalytic effect on nitrite oxidation

2004

The electrochemistry of vanadium-doped zircon (VxZrSiO4, 0 < x < 0.10) has been studied using abrasive-conditioned paraffin-impregnated graphite electrodes. It is compared with that of ZrSiO4, ZrO2, and vanadium-doped tetragonal and monoclinic zirconias. In contact with acetic/acetate and HCl + NaCl electrolytes, zirconium materials are reduced to Zr(III) at potentials near to −0.5 versus AgCl/Ag and to Zr metal at potentials more negative than −1.2 V, via proton-assisted reductive processes, influenced by the complexing action of chloride ions. Vanadium-centred oxidation processes appear at potentials from +0.2 to +0.7 V enabling for a distinction between different coordinative arrangement…

ZirconiumGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementVanadiumElectrochemistryElectrocatalystChlorideCatalysisMetalchemistry.chemical_compoundchemistryvisual_artElectrochemistryvisual_art.visual_art_mediummedicineNitritemedicine.drugElectrochimica Acta
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Determination of hydrogen peroxide using glassy carbon and graphite/polyester composite electrodes modified by vanadium-doped zirconias

2002

Abstract Synthetic monoclinic and tetragonal vanadium-doped zirconias (VZrO2) with vanadium loading ranging from 0.5 to 15 mol% are used to modify glassy carbon and graphite/polyester composite electrodes able to detect oxygen and hydrogen peroxide in neutral aqueous media. Electrodes modified by monoclinic VZrO2 decrease the overpotential for the reduction of oxygen and hydrogen peroxide in neutral and alkaline media and enhance their reduction currents with respect to unmodified carbon electrodes. This is associated to seven-coordinated vanadium centers isomorphously substituting zirconium ones in the ZrO2 lattice. The catalytic effect shows site-selectivity, since it is almost entirely a…

ZirconiumInorganic chemistryVanadiumchemistry.chemical_elementOverpotentialGlassy carbonElectrocatalystBiochemistryAnalytical ChemistryCatalysischemistry.chemical_compoundchemistryEnvironmental ChemistryGraphiteHydrogen peroxideSpectroscopyAnalytica Chimica Acta
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Functionalised Imidazoporphyrins and their application in catalysis

2017

A broad series of functionalized imidazo[4,5-b]porphyrins was synthesized by the acid-catalyzed condensation of 2,3-dioxo-5,10,15,20-tetraarylchlorins with aromatic aldehydes. Both steric and electronic features of meso-aryl substituents influence on the product yield ranging from 18% to 90%.Single-crystal X-ray diffraction analysis of the structure of zinc(II) 5,10,15,20-tetramesityl-2-(4-pyridyl)-1H-imidazo[4,5-b]porphyrinate showed that this compound forms 1D coordination chains in the solid state.The post-synthetic modifications of imidazo[4,5-b]porphyrins were investigated by performing the Suzuki-Miyaura coupling reaction, preparing water-soluble imidazoporphyrins and linear/angular b…

[CHIM.ORGA]Chemical Sciences/Organic chemistry5-b]porphyrineMatériaux hybrides organiques-inorganiquesCatalyse hétérogène[CHIM.ORGA] Chemical Sciences/Organic chemistryPhosphonate[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryPorphyrin[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryRéaction d'oxydationL'auto-assemblage supramoléculaireCatalystImidazole annelationMatériaux poreuxGreffage de métalloporphyrinesImidazo[4
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Cannabinoid ligands sorting out by a 3D-QSAR approach using catalyst/hypogen

2009

National audience; Understanding how molecular structures are involved in recognition by a biological receptor is a decisive step in drug design, and could constitute an intricate problem because of existence of several binding sites, as is the case of GPCRs (1) that constitute the largest class of membrane receptors. In this context, identification of pharmacophores that should differentiate multiple binding modes is of particular interest. We have recently applied to ligands of a human olfactory receptor an original sorting-out procedure carried out using Catalyst/HypoGen software (Accelrys Ltd) (2). We aimed to validate this sorting out procedure using literature data, and in this way, w…

[SDV] Life Sciences [q-bio]CANNABINOID LIGANDS[SDV]Life Sciences [q-bio]CATALYST/HYPOGEN3D-QSAR APPROACH
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Pd-Cu catalysts supported on anion exchange resin for the simultaneous catalytic reduction of nitrate ions and reductive dehalogenation of organochlo…

2019

International audience; The present work proposes the simultaneous removal of these classes of pollutants by a catalytic hydrotreatment processes. For this purpose, bimetallic Pd-Cu catalysts (with mass ratio Pd:Cu of 4:1) supported on macroporous strong base anion resin were prepared by different methods. The catalysts were characterized (by XRD, SEMEDX, XPS, AAS and H-2 chemisorption) and tested in a continuous flow system. The selected catalyst preparation protocol consists in a two-step method, which implies the deposition of palladium by ion exchange and the subsequent deposition of copper by controlled reaction on the surface of the pre-reduced palladium. The effectiveness of the cata…

[SDV]Life Sciences [q-bio]Inorganic chemistrypd-cu catalystchemistry.chemical_element010402 general chemistry7. Clean energy01 natural sciencesCatalysisCatalysis[CHIM]Chemical SciencesIon-exchange resinBimetallic stripComputingMilieux_MISCELLANEOUShydrodechlorinationAqueous solutionIon exchange010405 organic chemistryChemistryProcess Chemistry and Technologyanion exchange resinSelective catalytic reductionwater treatmentnitrate reduction0104 chemical sciences13. Climate actionChemisorptionPalladiumApplied Catalysis A: General
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Switch in Relative Stability between cis and trans 2-Butene on Pt(111) as a Function of Experimental Conditions: A Density Functional Theory Study

2018

International audience; The adsorption of cis and trans 2-butenes on Pt(111) has been studied as a function of hydrogen coverage OH by means of calculations based on density functional theory (DFT) with the inclusion of dispersion forces. All hydrogen coverages have been considered, from 0 to 1.00 monolayer (ML). For each case, the di-sigma and pi adsorption geometries of the olefins have been compared at a surface coverage of theta(C4H8) = 0.11 ML. Calculations of the Gibbs free energies of these systems have identified the most stable 2-butene isomer (cis or trans) as a function of coverage, temperature, and pressure. In particular, focus was placed on two sets of conditions, namely, one …

ab-initioMaterials scienceHydrogenmolecular-dynamicschemistry.chemical_element010402 general chemistryenergy recoil scattering7. Clean energy01 natural sciencesDFTCatalysischemistry.chemical_compoundsymbols.namesakecis-trans isomerizationAdsorptionPt(111)Monolayersingle-crystal surfaces[CHIM]Chemical Sciences[PHYS]Physics [physics]1st-principles calculationsethylene hydrogenation010405 organic chemistrymetal-surfacesheterogeneous catalystsGeneral ChemistryAtmospheric temperature range2-Butenefree energyhydrogenation catalysisCis trans isomerization0104 chemical sciencesGibbs free energyH coveragechemistry13. Climate actionadsorptionsymbolsPhysical chemistryDensity functional theory2-butenesolid-surfacestemperature diagram
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Comparison of the generation II with IV heterogeneous Ziegler-Natta catalysts used in propylene polymerizations

1998

An unsupported TiCl3-based catalyst (generation II), modified with n-butyl ether and AlEt2Cl3, was compared with a MgCl2/dibutyl phthalate/AlEt3/cyclohexylmethyldimethoxysilane catalyst system (generation IV) in propylene polymerizations. The latter (magnesium-supported) was fund to be more than 20 times as active as the former and more stereospecific, but to yield PP with a lower molecular weight (Table 2). The kinetics of the polymerizations studied with either of the catalyst, and involving the determination of concentrations of active sites [C0*] and elementary reaction rate constants (Table 4) based on earlier kinetic models, showed the C0*-values in the magnesium-supported catalyst to…

active sitestitanium catalyst of generation IIelementary reaction ratesTi-Mg catalyst of generation IVkinetics of propylene polymerizationPolimery
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Simulations on the mechanism of CNT bundle growth upon smooth and nanostructured Ni as well as θ-Al2O3 catalysts

2011

Abstract In the current study, we have performed ab initio DFT calculations on the gradually growing 2D periodic models of capped single-wall carbon nanotubes (SW CNTs) upon their perpendicular junctions with the Ni(111) substrate, in order to understand the peculiarities of the initial stage of their growth on either smooth or nanostructured catalytic particles. Appearance of the adsorbed carbon atoms upon the substrate follows from the dissociation of CVD hydrocarbon molecules, e.g., CH4: (CH4)ads → (CH)ads+3Hads and (CH)ads → Cads+Hads. (Since the effective growth of CNTs upon Ni nanoparticles occur inside the nanopores of amorphous alumina, we have also simulated analogous surface react…

adsorption and dissociation of ch4Materials scienceQC1-999General Physics and AstronomyNanoparticleNanotechnology02 engineering and technologyCarbon nanotubeflat and nanostructured surfaces of ni and θ-al2o3 catalystsarcmchair and zigzag-type chiralities01 natural sciencesdft calculationsDissociation (chemistry)Catalysislaw.inventionNanoclusterslaw0103 physical sciencesMoleculemechanism of cnt growth010306 general physicsbundles of single-wall cntsPhysics021001 nanoscience & nanotechnologyAmorphous solidChemical bondChemical engineeringcnt-ni junction0210 nano-technologyCentral European Journal of Physics
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