Search results for " Catalyst"

showing 10 items of 292 documents

Interface Amorphization of Two‐Dimensional Black Phosphorus upon Treatment with Diazonium Salts

2021

Abstract Two‐dimensional (2D) black phosphorus (BP) represents one of the most appealing 2D materials due to its electronic, optical, and chemical properties. Many strategies have been pursued to face its environmental instability, covalent functionalization being one of the most promising. However, the extremely low functionalization degrees and the limitations in proving the nature of the covalent functionalization still represent challenges in many of these sheet architectures reported to date. Here we shine light on the structural evolution of 2D‐BP upon the addition of electrophilic diazonium salts. We demonstrated the absence of covalent functionalization in both the neutral and the r…

Thermogravimetric analysisred phosphoruschemistry.chemical_element010402 general chemistryPhotochemistryMass spectrometryblack phosphorus01 natural sciencesCatalysislaw.inventionsymbols.namesakeX-ray photoelectron spectroscopylawElectron paramagnetic resonanceMaterialsFull Paper010405 organic chemistryChemistryPhosphorusOrganic ChemistryBalz–Schiemann productGeneral ChemistryQuímicaFull Paperssacrificial catalysts6. Clean waterMaterials Science | Hot Paperamorphization0104 chemical sciencesElectrophilesymbolsSurface modificationRaman spectroscopyddc:547Chemistry – A European Journal
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Dehydration of Fructose to 5-HMF over Acidic TiO2 Catalysts

2020

Different solid sulfonic titania-based catalysts were investigated for the hydrothermal dehydration of fructose to 5-hydroxymethylfurfural (5-HMF). The catalytic behavior of the materials was evaluated in terms of fructose conversion and selectivity to 5-HMF. The surface and structural properties of the catalysts were investigated by means of X-ray diffraction (XRD), N2 adsorption isotherms, thermo-gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and acid capacity measurements. Special attention was focused on the reaction conditions, both in terms of 5-HMF selectivity and the sustainability of the process, choosing water as the solvent. Among the various process condition…

TitaniaSolid acid catalysts02 engineering and technology010402 general chemistrylcsh:Technology01 natural sciencesCatalysischemistry.chemical_compoundAdsorptionX-ray photoelectron spectroscopymedicineGeneral Materials ScienceBiomassDehydrationHydrothermal dehydrationlcsh:MicroscopyHMFlcsh:QC120-168.85lcsh:QH201-278.5lcsh:TChemistryFructose021001 nanoscience & nanotechnologymedicine.disease0104 chemical sciencesSolventlcsh:TA1-2040Yield (chemistry)lcsh:Descriptive and experimental mechanicsSettore CHIM/07 - Fondamenti Chimici Delle Tecnologielcsh:Electrical engineering. Electronics. Nuclear engineeringlcsh:Engineering (General). Civil engineering (General)0210 nano-technologySelectivitylcsh:TK1-9971Nuclear chemistryMaterials
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The selective oxidative dehydrogenation of ethane over hydrothermally synthesised MoVTeNb catalysts

2002

Mo–V–Te–Nb metal oxide catalysts prepared by hydrothermal synthesis and heat-treated in N2 at high temperatures (600–700 °C) show high activity and selectivity for the oxidative dehydrogenation of ethane to ethene. Yields of ethene of 75% have been obtained at 400 °C on the best catalysts. Dejoz Garcia, Ana Maria, Ana.M.Dejoz@uv.es

UNESCO::QUÍMICAOxideOxidative phosphorylation:QUÍMICA [UNESCO]CatalysisCatalysisMetalchemistry.chemical_compoundMaterials ChemistryHydrothermal synthesisOrganic chemistryHigh activityHydrothermal synthesisDehydrogenationEthaneCatalystsUNESCO::QUÍMICA::Química inorgánicaChemistryMetals and AlloysGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOxidative dehydrogenation ; Hydrothermal synthesis ; Ethane ; Catalystsvisual_artCeramics and Compositesvisual_art.visual_art_mediumSelectivityOxidative dehydrogenationChem. Commun.
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A solar photothermo-catalytic combined process for the VOCs combustion and the subsequent CO2 valorization using noble metal-free catalysts

2023

We here investigated a solar photothermo-catalytic combined process where the toluene (as volatile organic compound model) was first oxidized to CO2 which was subsequently converted into solar fuels in a second reactor. For this aim two noble-metal free catalytic systems were used, namely MnOx-ZrO2, which gave the best results for the toluene removal, and brookite TiO2-CeO2 mixed oxides which were the most efficient in the subsequent CO2 conversion. This latter reaction was further improved by the addition of small amounts of copper-based materials on brookite-ceria, acting as co-catalysts. The key point for both the examined reactions was the synergism between the thermocatalytic and the p…

VOCs removal CO2 conversion Photothermo-catalysis Noble metals-free catalysts Brookite MnOxSettore CHIM/07 - Fondamenti Chimici Delle TecnologieGeneral ChemistryCatalysisCatalysis Today
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Insights into the catalytic production of hydrogen from propane in the presence of oxygen: Cooperative presence of vanadium and gold catalysts

2015

7 figures.-- © 2015. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

Vanadium and gold catalystsHydrogenGeneral Chemical EngineeringInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementVanadiumHydrogen catalytic productionPhotochemistryWater-gas shift reactionVanadium oxideCatalysischemistry.chemical_compoundFuel TechnologyVanadium oxidechemistryPropaneDehydrogenationGoldPropane oxidationWGSHydrogen production
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Multilayered supported ionic liquids as catalysts for chemical fixation of carbon dioxide

2011

Multilayered, covalently supported ionic liquid phase (mlc-SILP) materials were synthesized by using a new approach based on the grafting of bis-vinylimidazolium salts on different types of silica or polymeric supports. The obtained materials were characterized and tested as catalysts in the reaction of supercritical carbon dioxide with various epoxides to produce cyclic carbonates. The material prepared by supporting a bromide bis-imidazolium salt on the ordered mesoporous silica SBA-15 was identified as the most active catalyst for the synthesis of cyclic carbonates and displayed improved productivity compared with known supported ionic liquid catalysts. The catalyst retained its high act…

Vinyl CompoundsMaterials scienceGeneral Chemical EngineeringCatalyst supportIndustrial catalystsInorganic chemistryCarbonatesIonic LiquidsHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundsupercritical carbon dioxideEnvironmental ChemistryGeneral Materials ScienceSupported ionic liquidSupercritical carbon dioxidecarbonate synthesiImidazolesSettore CHIM/06 - Chimica OrganicaCarbon DioxideMesoporous silicaSupercritical fluidGeneral EnergychemistryIonic liquidEpoxy CompoundsChemSusChem
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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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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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