Search results for "catalysts"

showing 10 items of 164 documents

Photocatalytic Degradation of 4-Nitrophenol in Aqueous Suspension by Using Polycrystalline TiO2 Impregnated with Lanthanide Double-Decker Phthalocyan…

2007

The photocatalytic activity of polycrystalline TiO2 samples impregnated with rare-earth-metal diphthalocyanines was investigated. The 4-nitrophenol (4-NP) photocatalytic degradation in aqueous suspension was used as a probe reaction. Commercial anatase TiO2 was impregnated with home-prepared double-decker phthalocyanine complexes of the lanthanide metals, such as Ce, Pr, Nd, Sm, Ho, and Gd. In particular, the impregnation with Ho, Sm, and Nd complexes, acting as sensitizers, proved beneficial for the photoactivity of the studied systems. Significant improvements of the TiO2-based catalytic system appeared possible in terms of lower impregnation loading, enhanced photoreactivity under solar …

LanthanideAnataseMaterials scienceInorganic chemistryPhthalocyanineOxides4-NitrophenolDecompositionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundGeneral EnergychemistryPhotocatalystsMineralsIrradiationPhotocatalysisPhthalocyanineCrystallitePhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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Gas-phase hydrogenation of propionitrile on copper-lanthanide oxides

2009

Abstract The hydrogenation of propionitrile on copper-lanthanide oxide catalysts (2Cu·CeO 2 and 4Cu·Ln 2 O 3 (Ln = La, Pr, Nd)) was studied in the gas phase. The activity of the catalysts varies with the lanthanide in the order 2Cu·CeO 2  > 4Cu·Pr 2 O 3  > 4Cu·La 2 O 3  ≥ 4Cu·Nd 2 O 3 , while the activation energies varies in the opposite order, except for 2Cu·CeO 2 . The main product was the primary amine, n -propylamine. The formation of the unstable imine CH 3 CH 2 N CHCH 3 as a major product over 2Cu·CeO 2 seems to be consistent with the acidity of the catalyst. The catalysts were more selective than conventional copper impregnation catalysts, Cu (10 wt.%) on SiO 2 , La 2 O 3 or CeO 2 ,…

LanthanideCopper oxideInorganic chemistryImineprimary aminechemistry.chemical_element010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysisgas-phase hydrogenationPhysical and Theoretical Chemistrysupported catalystsComputingMilieux_MISCELLANEOUS010405 organic chemistryProcess Chemistry and Technologypropionitrile[CHIM.CATA]Chemical Sciences/CatalysisCopper0104 chemical scienceschemistrycopperAmine gas treatingPropionitrile
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Di- and Tetrairon(III) μ-Oxido Complexes of an N3S-Donor Ligand: Catalyst Precursors for Alkene Oxidations

2019

The new di- and tetranuclear Fe(III) μ-oxido complexes [Fe 4 (μ-O) 4 (PTEBIA) 4 ](CF 3 SO 3 ) 4 (CH 3 CN) 2 ] (1a), [Fe 2 (μ-O)Cl 2 (PTEBIA) 2 ](CF 3 SO 3 ) 2 (1b), and [Fe 2 (μ-O)(HCOO) 2 (PTEBIA) 2 ](ClO 4 ) 2 (MeOH) (2) were prepared from the sulfur-containing ligand (2-((2,4-dimethylphenyl)thio)-N,N-bis ((1-methyl-benzimidazol-2-yl)methyl)ethanamine (PTEBIA). The tetrairon complex 1a features four μ-oxido bridges, while in dinuclear 1b, the sulfur moiety of the ligand occupies one of the six coordination sites of each Fe(III) ion with a long Fe-S distance of 2.814(6) A. In 2, two Fe(III) centers are bridged by one oxido and two formate units, the latter likely formed by methanol oxidati…

MECHANISMFe-S interactionoxidation116 Chemical sciencesThio-rautaSULFURHomogeneous catalysis02 engineering and technology010402 general chemistry01 natural sciencesMedicinal chemistrythioetherCatalysislcsh:Chemistrychemistry.chemical_compoundThioetheriron-oxo complexAcetonitrileta116Fe-S interaction; homogeneous catalysis; iron-oxo complex; oxidation; thioetherOriginal Researchchemistry.chemical_classificationeetteritFUNCTIONAL-MODELCOORDINATIONPEROXIDEAlkeneLigandACTIVE-SITEhapettuminenGeneral Chemistrykompleksiyhdisteet021001 nanoscience & nanotechnology540COPPER-COMPLEXEShomogeneous catalysis0104 chemical sciencesChemistrychemistrylcsh:QD1-999katalyysiACIDOXO0210 nano-technologySelectivityNONHEME IRON CATALYSTSFrontiers in Chemistry
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Robust Mesoporous CoMo/γ-Al2O3 Catalysts from Cyclodextrin-Based Supramolecular Assemblies for Hydrothermal Processing of Microalgae: Effect of the P…

2018

Hydrothermal liquefaction (HTL) is a promising technology for the production of biocrude oil from microalgae. Although this catalyst-free technology is efficient under high-temperature and high-pressure conditions, the biocrude yield and quality can be further improved by using heterogeneous catalysts. The design of robust catalysts that preserve their performance under hydrothermal conditions will be therefore very important in the development of biorefinery technologies. In this work, we describe two different synthetic routes (i.e., impregnation and cyclodextrin-assisted one-pot colloidal approach), for the preparation in aqueous phase of six high surface area CoMo/γ-Al2O3 catalysts. Cat…

Materials science02 engineering and technology010402 general chemistrybiocrude01 natural sciencesHydrothermal circulationCatalysisCopolymer[CHIM]Chemical SciencesGeneral Materials ScienceComputingMilieux_MISCELLANEOUSbiocrude; cyclodextrin; heterogeneous catalysts; hydrothermal liquefaction; microalgaeheterogeneous catalystsmicroalgaeheterogeneous catalystAqueous two-phase systemhydrothermal liquefaction[CHIM.CATA]Chemical Sciences/CatalysisSettore ING-IND/27 - Chimica Industriale E Tecnologica021001 nanoscience & nanotechnologyBiorefinery0104 chemical sciencesHydrothermal liquefactioncyclodextrinChemical engineeringYield (chemistry)Materials Science (all)0210 nano-technologyMesoporous materialACS Applied Materials & Interfaces
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Nanocatalysts for High Selectivity Enyne Cyclization: Oxidative Surface Reorganization of Gold Sub-2-nm Nanoparticle Networks

2021

International audience; Ultrasmall gold nanoparticles (NPs) stabilized in networks by polymantane ligands (diamondoids) were successfully used as precatalysts for highly selective heterogeneous gold-catalyzed dimethyl allyl(propargyl)malonate cyclization to 5-membered conjugated diene. Such reaction usually suffers from selectivity issues with homogeneous catalysts. This control over selectivity further opened the way to one-pot cascade reaction, as illustrated by the 1,6-enyne cycloisomerization–Diels–Alder reaction of dimethyl allyl propargyl malonate with maleic anhydride. The ability to assemble nanoparticles with controllable sizes and shapes within networks concerns research in sensor…

Materials scienceAlkyneLigands010402 general chemistry01 natural sciencesArticleenyne cyclizationCycloisomerizationCascade reactionSelectivity[CHIM.COOR]Chemical Sciences/Coordination chemistryQD1-999chemistry.chemical_classificationdiamondoidsEnyne010405 organic chemistryCombinatorial chemistryHydrocarbonsNanomaterial-based catalyst0104 chemical sciencesChemistrychemistryCyclizationColloidal goldgold sub-2-nm nanoparticlesPropargylnanocatalystsGoldSelectivityJACS Au
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Reversible oxidation of WOx and MoOx nano phases

2012

International audience; WOx and MoOx nano phases were prepared on TiO2(1 1 0) surfaces by a CVD procedure consisting of adsorption and decomposition of W(CO)(6) or Mo(CO)(6) precursors followed by annealing under UHV. Metal amount involved in each elaborated sample is in the fractional range from 0.1 to 0.35 equivalent monolayer (eqML) of W or Mo. Evolution of sample stoichiometry as a function of subsequent treatment is followed by valence band and core level photoemission as well as work function measurement. In each case, exposure of samples to molecular oxygen at room temperature induces an increase of sample work function in a range of several tenth of eV. Such a work function change i…

Materials scienceAnnealing (metallurgy)Inorganic chemistryAnalytical chemistrychemistry.chemical_elementCATALYSTS02 engineering and technologyTungsten010402 general chemistryTIO2(110) SURFACE01 natural sciencesSTOICHIOMETRYCatalysisTUNGSTEN-OXIDE[ CHIM.OTHE ] Chemical Sciences/OtherMonolayerWork functionHEXACARBONYL ADSORPTIONSOL-GELVISIBLE-LIGHT IRRADIATIONTIO2 110MOLYBDENUMGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryMolybdenumPhotocatalysisPHOTOCATALYSIS[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyStoichiometryTitanium
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Brookite, the Least Known TiO2 Photocatalyst

2013

Brookite is the least studied TiO2 photocatalyst due to the difficulties usually encountered in order to obtain it as a pure phase. In this review, a comprehensive survey of the different methods available for preparing brookite powders and films is reported. Attention has been paid both to the most traditional methods, such as hydrothermal processes at high temperatures and pressures, and to environmentally benign syntheses using water soluble compounds and water as the solvent. Papers reporting the photocatalytic activity of pure and brookite-based samples have been reviewed.

Materials scienceBrookiteInorganic chemistrybrookite nanostructuresTio2 photocatalystbrookitelcsh:Chemical technologyCatalysisHydrothermal circulationbrookite-based photocatalystslcsh:ChemistrySolventWater solublelcsh:QD1-999visual_artvisual_art.visual_art_mediumPhotocatalysisTiO2lcsh:TP1-1185brookite filmsPhysical and Theoretical Chemistrymixtures of TiO2 phasesCatalysts
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Total oxidation of VOCs on mesoporous iron oxide catalysts: Soft chemistry route versus hard template method

2016

9 figures, 3 tables.-- Supplemantary information available

Materials scienceGeneral Chemical EngineeringCatalytic total oxidationOxalic acidInorganic chemistry02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing EngineeringSoft chemistryCatalysisIron oxide catalysts: Soft chemistry synthesischemistry.chemical_compoundPropaneAdsorptionEnvironmental ChemistryNanocastingTotal oxidatioVOCsMesoporous supportSoft chemistry synthesis [Iron oxide catalysts]General Chemistry021001 nanoscience & nanotechnologyToluene oxidation0104 chemical sciencesMesoporous organosilicachemistry0210 nano-technologyMesoporous materialMesoporous α-Fe2O3Template method patternToluene
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Nanoparticles of AlTiZr mixed oxides as support of hydrodesulfurizaton catalysts: Synthesis and characterisation

2012

Abstract TiAlZr mixed oxides, synthesized using sol–gel method, were characterized and used as supports of hydrodesulfurization catalysts (12 wt% Mo) prepared by impregnation either with molybdenum heteropolyacid H3PMo12O40 or its cobalt salt Co1.5PMo12O40. Structure, morphology and textural properties of oxides and catalysts were characterized using X-ray powder diffraction (XRD), Raman spectroscopy, Nitrogen adsorption porosimetry, TEM-EDS, temperature-programmed desorption (TPD) and temperature-programmed reduction (TPR) techniques. Activity of the catalytic systems was tested in thiophene hydrodesulfurization (HDS). No formation of a new oxide phase was revealed in the synthesized mixed…

Materials scienceMechanical EngineeringInorganic chemistryMetals and AlloysOxidechemistry.chemical_elementCatalysisMixed oxides supports Sol–gel process Co-Mo-P-catalysts Thiophene hydrodesulfurizationchemistry.chemical_compoundchemistryMechanics of MaterialsMolybdenumDesorptionMaterials ChemistryThiopheneCobaltHydrodesulfurizationSol-gelSettore CHIM/02 - Chimica Fisica
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Ni-Based Catalysts for Low Temperature Methane Steam Reforming: Recent Results on Ni-Au and Comparison with Other Bi-Metallic Systems

2013

Steam reforming of light hydrocarbons provides a promising method for hydrogen production. Ni-based catalysts are so far the best and the most commonly used catalysts for steam reforming because of their acceptably high activity and significantly lower cost in comparison with alternative precious metal-based catalysts. However, nickel catalysts are susceptible to deactivation from the deposition of carbon, even when operating at steam-to-carbon ratios predicted to be thermodynamically outside of the carbon-forming regime. Reactivity and deactivation by carbon formation can be tuned by modifying Ni surfaces with a second metal, such as Au through alloy formation. In the present review, we su…

Materials scienceMethane reformerInorganic chemistryIndustrial catalystschemistry.chemical_elementhydrocarbons steam reforminggoldlcsh:Chemical technologysurface alloyCatalysissupport modificationCatalysisSteam reforminglcsh:ChemistryNickelnickelchemistrylcsh:QD1-999bimetalliclcsh:TP1-1185hydrocarbons<b> </b>steam reforming; nickel; gold; bimetallic; surface alloy; support modificationPhysical and Theoretical ChemistryBimetallic stripCarbonHydrogen production
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