Search results for " catalyst"

showing 10 items of 292 documents

The roles for a Lewis base and MgCl2 in third-generation Ziegler-Natta catalysts

1998

Activity of a titanium catalyst supported on a bimetallic magnesium-aluminium system, involving a Lewis base [MgCl2(THF) 2 /Al(C 2 H 5 ) 2 Cl], was studied in ethylene polymerization, and the effect of the catalyst composition on the properties of the final polymer produced was investigated. Analysis and discussion of the findings covering also some part of the kinetic study, resulted in defining the roles for MgCl 2 and a Lewis base in the third-generation Ziegler-Natta catalysts. MgCl 2 forms a bimetallic complex with an organoaluminium compound, which involves also a Lewis base. Its reaction with TiCl 4 yields a very active catalyst wherein the Mg: Ti molar ratio is close to 1. This mean…

Polymers and PlasticsbiologyKineticsActive siteGeneral ChemistryPolyethyleneNattabiology.organism_classificationSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundchemistryPolymer chemistryMaterials Chemistrybiology.proteinLewis acids and basesZiegler–Natta catalystBimetallic strip
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Copolymerization of ethylene with 1‐hexene over metallocene catalyst supported on complex of magnesium chloride with tetrahydrofuran

2004

The study of ethylene/1-hexene copolymerization with the zirconocene catalyst, bis(cyclopentadienyl)zirconium dichloride (Cp 2 ZrCl 2 )/methylaluminoxane (MAO), anchored on a MgCl 2 (THF) 2 support was carried out. The influence of 1-hexene concentration in the feed on catalyst productivity and comonomer reactivity as well as other properties was investigated. Additionally, the effect of support modification by the organoaluminum compounds [(MAO, trimethylaluminum (AlMe 3 ), or diethylaluminum chloride (Et 2 AlCl)] on the behavior of the MgCl 2 (THF) 2 /Cp 2 ZrCl/MAO catalyst in the copolymerization process and on the properties of the copolymers was explored. Immobilization of the Cp 2 ZrC…

Polymers and PlasticssupportsOrganic Chemistrymetallocene catalystsMethylaluminoxaneHomogeneous catalysisethylene/1‐hexene copolymersmagnesium supportPost-metallocene catalystzirconocene catalystCatalysischemistry.chemical_compoundcopolymerizationchemistryCyclopentadienyl complexHexenePolymer chemistryMaterials ChemistryMetalloceneTetrahydrofuranJournal of Polymer Science. Part A : Polymer Chemistry
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Electrochemical Abatement of Organic Pollutants in Water by Electro- Fenton with Natural Heterogeneous Catalysts Under Pressure

2020

In recent decades, electrochemical advanced oxidation processes (EAOPs) have proved as alternative technologies to conventional processes. Indeed, EAOPs can often allow to treat wastewater containing toxic and POPs. Among them, electro-Fenton (EF) is considered particularly promising for the treatment of recalcitrant organics, since it presents various advantages, including high abatements for many organic pollutants, simplicity of equipment and operations, relatively low cost and low consumption of chemicals. Recently, the utilization of some natural heterogeneous catalysts was proposed in order to avoid some disadvantages of the conventional EF process. In this frame, in this work EF proc…

Pressure electrochemical advanced oxidation processes EAOPs Electro-Fenton natural heterogeneous catalyst
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Agglomerated non-porous silica nanoparticles as model carriers in polyethylene synthesis

2004

Abstract Non-porous submicron silica particles (250 and 500 nm) with high monodispersity were agglomerated to form spherical agglomerates via spray drying. As a binder, 25 nm sized monodisperse silica spheres were selected from a variety of colloidal systems including Levasil-type and Aerosil-type silica nanoparticles. The use of such binders led to an increase of the specific surface area of the agglomerated carriers. All materials were characterised by nitrogen sorption, mercury intrusion and scanning electron microscopy. The silica agglomerates, with highly defined geometrical and pore structural parameters, were employed as model carriers in the heterogeneous polymerization of ethylene …

Process Chemistry and TechnologyColloidal silicaDispersityNanoparticlePolyethylenePost-metallocene catalystCatalysischemistry.chemical_compoundchemistryChemical engineeringPolymerizationAgglomerateSpecific surface areaPolymer chemistryPhysical and Theoretical ChemistryJournal of Molecular Catalysis A: Chemical
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Novel supported substituted prolinamide as recyclable catalyst for asymmetric aldol reaction

2010

Proline Organocatalysis Stereoselective synthesis Supported catalyst
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Linear, tripodal, macrocyclic: Ligand geometry and ORR activity of supported Pd(II) complexes

2021

Abstract The novel ligand H3L designed to spontaneously adsorb onto MWCNT via electron-deficient pyrimidine residues and bind metal cations is used to prepare an oxygen reduction reaction (ORR) cathode catalyst based on supported Pd(II) complexes. Herein we report the synthesis of the ligand, its solution behaviour (protonation constants, binding constants for the test cation Cu(II), UV evidence of Cu(II) and Pd(II) complexes formation) and ORR performances together with XPS and STEM characterization. Tripodal nature of the H3L ligand frame it in-between previously studied macrocyclic and linear open chain ligands, allowing to draw meaningful comparisons.

Pyrimidine010405 organic chemistryLigandProtonation010402 general chemistry01 natural sciences0104 chemical sciencesCathode catalystInorganic ChemistryMetalchemistry.chemical_compoundAdsorptionX-ray photoelectron spectroscopychemistryvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumMacrocyclic ligandPhysical and Theoretical ChemistryInorganica Chimica Acta
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Benzyl alcohol to benzaldehyde oxidation on MnOx clusters: Unraveling atomistic features

2021

Abstract The catalytic oxidation of benzyl alcohol with O 2 is a promising option for the production of benzaldehyde, from both environmental and economical viewpoints. In particular, highly dispersed MnO x systems feature good activity and selectivity in a wide range of temperatures, although deactivation phenomena by over-oxidation and/or poisoning of active sites are generally recorded. On this account, a density functional theory study was performed on cluster-sized catalyst models, namely Mn 4 O 8 and over-oxygenated Mn 4 O 9 fragments, to predict the reactivity pattern of MnO x catalysts in the selective aerobic oxidation of benzyl alcohol. Several pathways concur to determine the who…

Reaction mechanismCatalyst deactivationReaction mechanismsProcess Chemistry and TechnologyMnOx based catalystsPhotochemistryDFTCatalysisCatalysisBenzaldehydechemistry.chemical_compoundchemistryCatalytic oxidationBenzyl alcoholAlcohol oxidationCatalyst deactivation; DFT; MnO; x; based catalysts; Oxidative dehydrogenation; Reaction mechanismsReactivity (chemistry)Physical and Theoretical ChemistryOxidative dehydrogenationSettore CHIM/02 - Chimica FisicaBenzoic acidMolecular Catalysis
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Trapping AsPh3 via reaction with NiS/γ-Al2O3 in the presence of H2: Reaction mechanism and kinetics

2021

International audience; Removal of As from petroleum feedstocks is an important process which can be realized using As trapping mass containing supported nickel sulfide. In order to understand the mechanism of the trapping we studied the reaction of AsPh3 with NiS/γ-Al2O3 in the presence of H2 in a batch reactor in toluene solution at 230 °C. This reaction results in formation of NiAs, benzene and H2S. Also, the intermediate species, thiophenol and diphenylsulfide, were observed. Despite formation of NiAs layer in the course of reaction, the rate of AsPh3 decomposition is not affected by the solid state diffusion up to ∼ 50 % of nickel conversion. The rate determining step in these conditio…

Reaction mechanismNickel sulfideOrder of reaction010405 organic chemistryProcess Chemistry and TechnologyThiophenolchemistry.chemical_element[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryPhotochemistryRate-determining step01 natural sciences7. Clean energyCatalysisDearsenification0104 chemical sciencesCatalysisAs trapping masschemistry.chemical_compoundNickelchemistry13. Climate actionHydrogenolysisProtection of hydrotreatment catalysts
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Ru(bpy)2Cl2: A catalyst able to shift the course of the photorearrangement in the Boulton-Katritzky reaction

2015

The Boulton-Katritzky reaction represents one of the most popular and efficient strategies used to realize azole-into-azole conversions. For example, under different experimental conditions, it allows the rearrangement of Z-arylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazoles (1) into 2-aryl-4-benzoylamino-5-phenyl-2H-1,2,3-triazoles (2) in very high yields. Moreover, we have recently realized this conversion also by UV-photostimulation. Now we have enlarged the scope of the reaction irradiating with visible or UV light an acetonitrile solution of some Z-arylhydrazones (1a-e) in the presence of catalytic amounts of Ru(bpY)(2)Cl-2. We have observed the unexpected formation of the 1-aryl-5-…

RegiochemistryRuthenium catalystDrug Discovery3003 Pharmaceutical ScienceOrganic ChemistryRegioselectivityRuthenium catalystPhotochemistryDFTBiochemistryCatalysischemistry.chemical_compoundchemistryPhotochemical rearrangementDrug Discovery124-OxadiazoleAcetonitrile
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Preferential CO oxidation over catalysts with well-defined inverse opal structure in microchannels

2008

Catalyst supports of CeO 2 /SiO 2 and Al 2 O 3 with three-dimensionally ordered macroporous structure were fabricated in microchannels by application of PMMA opals as templates. Pt-Rh supported on CeO 2 /SiO 2 showed high efficiency for CO removal in preferential CO oxidation in the presence of excess hydrogen. Pt-Rh supported on Al 2 O 3 with an inverse opal structure showed higher reactivity than that supported on wash-coated Al 2 O 3 layers in microchannel reactor.

Renewable Energy Sustainability and the EnvironmentCatalyst supportInorganic chemistryPt-Rh catalystEnergy Engineering and Power Technologychemistry.chemical_elementPreferential CO oxidationCondensed Matter PhysicsCatalysisRhodiumchemistry.chemical_compoundFuel TechnologychemistryChemical engineeringAluminium oxideInverse opalsReactivity (chemistry)SDG 7 - Affordable and Clean EnergyMicroreactorPlatinumSDG 7 – Betaalbare en schone energieCarbon monoxideInternational Journal of Hydrogen Energy
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