Search results for "LYST"

showing 10 items of 904 documents

Nature of cobalt active species in hydrodesulfurization catalysis: combined support and preparation method effects

2007

Abstract Co/γ-Al2O3, Co/SiO2, Co/MCM-41, Co/ASA and Co/S2 (amorphous aluminosilicate with Al/Si = 0.13 and with Al/Si ≈ 2, respectively) were prepared by the method of wet impregnation and by the method of precipitation in the presence of sodium carbonate. The samples were characterised by XPS, XRD and TPR. The catalytic activity was tested in the hydrodesulfurization of thiophene using a continuous flow reactor. Among the wet impregnated catalysts those supported on the amorphous and ordered mesoporous silica exhibited higher HDS activity as compared to the alumina containing supports. Particularly, the use of the mesoporous, high surface area MCM-41 support, determined the best performing…

inorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementMesoporous silicaCatalysisCatalysischemistry.chemical_compoundchemistryMCM-41Physical and Theoretical ChemistrySodium carbonateMesoporous materialHydrodesulfurizationCobaltNuclear chemistry
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Atomistic Insights into Nitrogen-Cycle Electrochemistry: A Combined DFT and Kinetic Monte Carlo Analysis of NO Electrochemical Reduction on Pt(100)

2017

Electrocatalytic denitrification is a promising technology for the removal of NOx species in groundwater. However, a lack of understanding of the molecular pathways that control the overpotential and product distribution have limited the development of practical electrocatalysts, and additional atomic-level insights are needed to advance this field. Adsorbed NO has been identified as a key intermediate in the NOx electroreduction network, and the elementary steps by which it decomposes to NH4+, N2, NH3OH+, or N2O remain a subject of debate. Herein, we report a combined density functional theory (DFT) and kinetic Monte Carlo (kMC) study of this reaction on Pt(100), a catalytic surface that i…

inorganic chemicalsProtonation02 engineering and technologyOverpotential010402 general chemistryElectrocatalyst01 natural sciencesCatalysisReaction rateelektrokatalyysiComputational chemistryelectrocatalysisKinetic Monte Carlota116density functional theorykinetic Monte CarloNOxta114ChemistrytiheysfunktionaaliteoriaGeneral ChemistryNO electroreduction021001 nanoscience & nanotechnologyProduct distribution0104 chemical sciencesPt(100)Density functional theory0210 nano-technologyACS Catalysis
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Nanolayered Cobalt-Molybdenum Sulfides as Highly Chemo- and Regioselective Catalysts for the Hydrogenation of Quinoline Derivatives

2018

[EN] Herein, a general protocol for the preparation of a broad range of valuable N-heterocyclic products by hydrogenation of quinolines and related N-heteroarenes is described. Interestingly, the catalytic hydrogenation of the N-heteroarene ring is chemoselectively performed when other facile reducible functional groups, including alkenes, ketones, cyanides, carboxylic acids, esters, and amides, are present. The key to successful catalysis relies on the use of a nanolayered cobalt-molybdenum sulfide catalyst hydrothermally synthesized from earth-abundant metal precursors. This heterogeneous system displays a tunable composition of phases that allows for catalyst regeneration. Its catalytic …

inorganic chemicalsSulfidechemistry.chemical_element010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisCatalysisMetalchemistry.chemical_compoundQUIMICA ORGANICAChemo-/regioselective hydrogenationN-heterocycleschemistry.chemical_classificationHeterogeneous catalysis010405 organic chemistryQuinolineRegioselectivityGeneral ChemistryCombinatorial chemistry0104 chemical sciencesCo-Mo-S catalystschemistryMolybdenumvisual_artvisual_art.visual_art_mediumQuinolinesCobalt
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Titanium (IV) chloride complexes with salen ligands supported on magnesium carrier: Synthesis and use in ethylene polymerization

2009

The magnesium support with the formula MgCl 2 (THF) 0.32 (Et 2 AlCl) 0.36 was used for immobilization of salen complexes of titanium [Ti(salen)Cl 2 , Ti(salen(O-Me) 2 )Cl 2 ]. The effects of the catalyst composition (i.e. type of titanium complex and type of activator), polymerization temperature, polymerization time, and the effect of comonomer (1-octene) on the activity of the obtained supported catalysts, on the polymer characteristics (molecular weight, molecular weight distribution, melting point), and on the polymer morphology were studied. The findings were compared to those obtained for corresponding unsupported systems. Catalysts immobilization results in considerable changes in ca…

inorganic chemicalschemistry.chemical_classificationpolyethyleneZiegler‐Natta polymerizationPolymers and PlasticssupportsComonomerOrganic Chemistrychemistry.chemical_elementPolymerPolyethylenecatalystsCatalysischemistry.chemical_compoundchemistryPolymerizationMetal salen complexesPolymer chemistryMaterials ChemistryMolar mass distributiontitanium (IV) salen complexesTitaniumJournal of Polymer Science. Part A : Polymer Chemistry
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Bifunctional Acid-Base Catalysis

2011

Acid-base catalysis with bifunctional catalysts is a very prominent catalytic strategy in both small-molecule organocatalysts as well as enzyme catalysis. In both worlds, small-molecule catalysts and enzymatic catalysis, a variety of different general acids or hydrogen bond donors are used. In this chapter, important parallels between small molecule catalysts and enzymes are discussed, and a comparison is also made to the emerging field of frustrated Lewis pair catalysis.

inorganic chemicalschemistry.chemical_compoundchemistryHydrogen bondTetrahedral carbonyl addition compoundOxyanion holeBifunctionalCombinatorial chemistryFrustrated Lewis pairBifunctional catalystCatalysisEnzyme catalysis
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Direct arylation of heteroaromatic compounds with congested, functionalised aryl bromides at low palladium/triphosphane catalyst loading.

2011

International audience; A new ferrocenyl triphosphane ligand associated to palladium was found to be an efficient catalyst for the direct coupling of highly congested, functionalised aryl bromides with a variety of heteroarenes. These coupling reactions can generally be performed by using a low-loading (0.1-0.5 mol%) of the catalyst. The present protocol tolerates important and useful functional groups, which allows for further elaboration into more sophisticated heterocyclic molecules. The straightforward arylation of heteroaromatic compounds with congested ortho-substituted aryl bromides may permit further convergent syntheses of diverse ligands, biologically active molecules and molecula…

inorganic chemicalschemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisCoupling reactionCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundMoleculeOrganic chemistryEfficient catalystaryl bromidesheterocycles010405 organic chemistryChemistryLigandArylOrganic Chemistryferrocenyl polyphosphaneGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysispalladium0104 chemical sciencesC[BOND]H activationTriphosphanePalladium
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Lignin-based activated carbon-supported metal oxide catalysts in lactic acid production from glucose

2021

In this study, heterogeneous biomass-based activated carbon-supported metal oxide catalysts were prepared and tested for lactic acid production from glucose in aqueous solution. Activated carbons were produced from hydrolysis lignin by chemical (ZnCl2) or steam activation and modified with a nitric acid treatment and Sn, Al, and Cr chlorides to obtain carbon-based metal oxide catalysts. The modification of the carbon support by nitric acid treatment together with Sn and Al oxides led to an increase in lactic acid yield. The highest lactic acid yield (42%) was obtained after 20 minutes at 180 °C with the Sn/Al (5/2.5 wt.%) catalyst on steam-activated carbon treated by nitric acid. Reusabilit…

inorganic chemicalsmaitohappobiomasskemialliset reaktiotheterogeneous catalystlactic acidfood and beveragesmetal oxidecomplex mixturesglukoosikatalyytitkatalyysiaktiivihiilioksiditkemian tekniikkaactivated carbonbiomassa (teollisuus)aqueous solutionmuuntaminen
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Total oxidation of naphthalene using bulk manganese oxide catalysts

2013

Several Mn2O3 catalysts have been synthesized using different preparation methods and tested for the total oxidation of naphthalene, a model polycyclic aromatic compound. The catalysts have been characterized by several physico-chemical techniques such as XRD, TPR, XPS, EDX and TEM. The surface area of the catalyst seems to be of paramount importance, since the mass normalized activity of catalysts increases as the surface area of the Mn2O3 catalysts increases. Consequently, a high surface area ordered mesoporous Mn2O3 catalyst, obtained through a nanocasting route using mesoporous KIT-6 silica as a hard template, was the most efficient catalyst for the deep oxidation of naphthalene. In add…

inorganic chemicalsorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistryCatalysisCatalysisHopcalitechemistry.chemical_compoundchemistryCatalytic oxidationX-ray photoelectron spectroscopyPhase (matter)heterocyclic compoundsMesoporous materialNaphthaleneApplied Catalysis A: General
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Gas-Phase Hydrogenation of Propionitrile Catalyzed by LnCu2 (Ln = La, Ce, Pr, Nd)

2007

The hydrogenation of propionitrile over binary copper−lanthanide intermetallic compounds (LnCu2, Ln = La, Ce, Pr, Nd) was studied in the gas phase. The results show that the reaction main product is the primary amine, the n-propylamine. To our knowledge, it is the first time that such behavior is reported for copper catalysts.

intermetallicInorganic chemistryKineticsIntermetallicchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencescatalystsGas phaseCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysislanthanum-copperPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSChemistrypropionitrile[CHIM.CATA]Chemical Sciences/Catalysis021001 nanoscience & nanotechnologyCopper0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergykineticsPhysical chemistryAmine gas treatingPropionitrilegas phasehydrogenation0210 nano-technology
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Palladium supported on cross-linked imidazolium network on silica as highly sustainable catalysts for the Suzuki reaction

2013

ionic liquidspalladium catalystcatalysi
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