Search results for "Catalysis"

showing 10 items of 5944 documents

Transition metal complexes of tetradentate and bidentate Schiff bases as catalysts for ethylene polymerization: Effect of transition metal and cocata…

2009

This article compares catalytic performance of ethylene polymerization in similar polymerization conditions of transition metal complexes having two ligands [O,N] (phenoxy-imine) and having one tetradentate ligand [O,N,N,O] (salphen or salen). It is shown that the activity of both complex types as well as the product properties depend in the same way on the type of central metal in the complex and on the cocatalyst used. Although the type of ligand has some effect on the catalyst activity, yet it does not control the properties of the obtained products. The vanadium and zirconium complexes, irrespective of the cocatalyst used, yield linear polyethylene with high molecular weight (a few hund…

polyethyleneZiegler‐Natta polymerizationDenticitySchiff basePolymers and PlasticsChemistryLigandOrganic ChemistryVanadiumchemistry.chemical_elementPolyethyleneCatalysischemistry.chemical_compoundpostmetallocene catalystTransition metalPolymerizationPolymer chemistryMaterials ChemistrySchiff basesoligomersJournal of Polymer Science. Part A : Polymer Chemistry
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Effect of sample preparation on gel permeation chromatography results of determination of molecular weight of polyethylene obtained with using of zir…

2003

Molecular weights of polyethylene (PE) obtained with using of zirconocene catalyst activated with large excess of methylaluminoxane (MAO) were determined by gel permeation chromatography (GPC) method. It was found that repeatability of the measurements is strongly influenced by MAO remained in PE samples as well as time of sample keeping in the apparatus (dissolution + measurement time) at temp. 142 °C. A method of MAO removing from PE samples, before GPC measurement, based on additional washing of the sample with HF in methanol solution has been proposed. This modification leads to better both authenticity and repeatability of the results. Studies on the influence of time of sample keeping…

polyethylenechemistry.chemical_classificationChromatographyPolymers and PlasticsChemistryGeneral Chemical Engineeringgel permeation chromatographyMethylaluminoxanemethylaluminoxanesamples preparationsPolymerzirconocene catalystPolyethyleneCatalysisGel permeation chromatographychemistry.chemical_compoundMaterials ChemistrySample preparationMethanolAluminoxanePolimery
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Effect of immobilization of titanocene catalyst in aralkyl imidazolium chloroaluminate media on performance of biphasic ethylene polymerization and p…

2012

1-(2-Phenylethyl)-3-methylimidazolium and 1-benzyl-3-methylimidazolium chloroaluminates, [Ph-C2mim][AlCl4] and [Bzlmim][AlCl4], were applied as media of the Cp2TiCl2 catalyst for biphasic ethylene polymerization. The studied aralkyl ionic liquids ensure greater stability of the catalyst at higher temperatures and more regular morphology of the produced polyethylene than analogous 1-n-alkyl-3-methylimidazolium chloroaluminates. The alkylaluminium compound participates in the termination reaction of the polymer chain. The catalyst is stable and enables recycling of the ionic liquid phase in the consecutive polymerization reactions. The [Ph-C2mim][AlCl4] ionic liquid and AlEt2Cl alkylaluminium…

polyethylenechemistry.chemical_classificationMaterials scienceChemistry(all)Polymers and PlasticsDispersityGeneral ChemistryPolymermetallocene catalystPolyethylenePost-metallocene catalystCondensed Matter PhysicsCatalysischemistry.chemical_compoundCrystallinityPolymerizationchemistryPolymer chemistryIonic liquidMaterials Chemistryionic liquidPolymer Bulletin
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Preparation of tungstophosphoric acid/cerium-doped NH2-UiO-66 Z-scheme photocatalyst: a new candidate for green photo-oxidation of dibenzothiophene a…

2021

International audience; The goal of this study was to introduce an effective visible-light induced photocatalytic system with a good ability for photocatalytic oxidative desulfurization (PODS) and denitrogenation (PODN) using molecular oxygen (O2) as an oxidant. In this regard, tungestophosphoric acid (PW12) was supported onto cerium-doped NH2-UiO-66 (PW12/Ce-NUiO-66) and employed for the photo-oxidation of dibenzothiophene (DBT) and quinoline (Qu). Herein, using cerium (Ce) as a “mediator” facilitated the separation of charge carriers, while NH2-UiO-66 remarkably enhanced the surface area with plentiful adsorption sites and shifted the adsorption edge of PW12to the visible region. The sum …

pore volumeAdsorption edgesLight02 engineering and technology01 natural scienceschemistry.chemical_compound[SPI]Engineering Sciences [physics]quinolineVisible-light irradiationMaterials Chemistryoxidizing agentOxidative desulfurizationirradiationQuinolineCerium021001 nanoscience & nanotechnologyOxidantsFlue-gas desulfurizationCeriumDibenzothiophenePhotocatalysisCharge carrierCarrier mobility0210 nano-technologychemistry.chemical_element010402 general chemistryMaximum EfficiencyCatalysisArticleuraniumAdsorptionphosphotungstic acidpore size distributiondibenzothiophene derivativegreen chemistryphotooxidationDopingdesulfurizationGeneral Chemistrysurface areaPhotocatalytic systems0104 chemical sciencesVisible light inducedDibenzothiophenesTungstophosphoric acidMolecular oxygenPhotocatalytic activitychemistryadsorptiondesorptionoxygenphotocatalysisNuclear chemistrycatalyst
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Inside Cover: Hydrogen-Bonded Open-Framework with Pyridyl-Decorated Channels: Straightforward Preparation and Insight into Its Affinity for Acidic Mo…

2017

International audience; A hydrogen-bonded open framework with pores decorated by pyridyl groups was constructed by off-charge-stoichiometry assembly of protonated tetrakis(4-pyridyloxymethyl)methane and [Al(oxalate)(3)](3-), which are the H-bond donor and acceptor of ionic H-bond interactions, respectively. This supramolecular porous architecture (SPA-2) has 1nm-large pores interconnected in 3D with large solvent-accessible void (53%). It demonstrated remarkable affinity for acidic organic molecules in solution, which was investigated by means of various carboxylic acids including larger drug molecules. Competing sorption between acetic acid and its halogenated homologues evidenced good sel…

porosityabsolute-structureHydrogenSupramolecular chemistrychemistry.chemical_element010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysissupramolecular chemistrycrystalhost-guest systemsPolymer chemistryMoleculesolid-state nmr[CHIM]Chemical Scienceshost frameworkssorption010405 organic chemistryHydrogen bondmicroporous materialsOrganic ChemistryarchitecturesSorptionGeneral Chemistrymetal-organic frameworkenantioselective separationOpen frameworkcations0104 chemical scienceschemistryadsorptionhydrogen bondsCover (algebra)
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.Single-Ion Magnetic Behaviour in an Iron(III) Porphyrin Complex: A Dichotomy Between High Spin and 5/2-3/2 Spin Admixture

2020

International audience; A mononuclear iron(III) porphyrin compound exhibiting unexpectedly slow magnetic relaxation, which is a characteristic of single-ion magnet behaviour, is reported. This behaviour originates from the close proximity (approximate to 550 cm(-1)) of the intermediate-spinS=3/2 excited states to the high-spinS=5/2 ground state. More quantitatively, although the ground state is mostlyS=5/2, a spin-admixture model evidences a sizable contribution (approximate to 15 %) ofS=3/2 to the ground state, which as a consequence experiences large and positive axial anisotropy (D=+19.2 cm(-1)). Frequency-domain EPR spectroscopy allowed them(S)= |+/- 1/2⟩->|+/- 3/2&Rig…

porphyrinoids010402 general chemistry[MATH.MATH-FA]Mathematics [math]/Functional Analysis [math.FA]01 natural sciencesMolecular physicsCatalysislaw.inventionMagnetizationchemistry.chemical_compoundiron[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]lawMössbauer spectroscopy[CHIM.COOR]Chemical Sciences/Coordination chemistryAnisotropyElectron paramagnetic resonanceSpin (physics)010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryExcited statesingle-ion magnetsdensity functional calculationsmagnetic propertiesGround state
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Sponge‐Like Behaviour in Isoreticular Cu(Gly‐His‐X) Peptide‐Based Porous Materials

2015

We report two isoreticular 3D peptide-based porous frameworks formed by coordination of the tripeptides Gly-L-His-Gly and Gly-L-His-L-Lys to Cu(II) which display sponge-like behaviour. These porous materials undergo structural collapse upon evacuation that can be reversed by exposure to water vapour, which permits recovery of the original open channel structure. This is further confirmed by sorption studies that reveal that both solids exhibit selective sorption of H2 O while CO2 adsorption does not result in recovery of the original structures. We also show how the pendant aliphatic amine chains, present in the framework from the introduction of the lysine amino acid in the peptidic backbo…

postsynthetic modificationsPeptideTripeptideCatalysismetal–organic frameworksAdsorptionMetalloproteinsPolymer chemistryUreaMoleculePorositywater adsorptionchemistry.chemical_classificationMolecular Structurenanoporous materialsOrganic ChemistrySorptionGeneral ChemistryFull PaperschemistryChemical engineeringpeptidesMetal-organic frameworkAdsorptionPorous mediumOligopeptidesPorosityCopperChemistry – A European Journal
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Total oxidation of propene at low temperature over Co3O4–CeO2 mixed oxides: Role of surface oxygen vacancies and bulk oxygen mobility in the catalyti…

2008

Liotta, L. F. Ousmane, M. Di Carlo, G. Pantaleo, G. Deganello, G. Marci, G. Retailleau, L. Giroir-Fendler, A.; Co3O4, CeO2 and Co3O4-CeO2 mixed oxides with Co/Ce nominal atomic ratio 0.1:5, prepared by co-precipitation method with sodium carbonate, were tested in the oxidation of propene under lean condition and the catalyst stability was checked by performing three consecutive heating-cooling cycles. Characterization of the textural properties were performed by surface area measurement BET, X-ray diffraction (XRD) and scanning electron microscopy (SEM) measurements. Among the Co3O4-CeO2 mixed oxides, Co3O4 (30 Wt%)-CeO2 (70 wt%) gives the best activity attaining full propene conversion at …

propene oxidation Co3O4 CeO2Process Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementBinary compound[CHIM.CATA]Chemical Sciences/Catalysis02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesOxygenCatalysis0104 chemical sciencesCatalysisPropenechemistry.chemical_compoundchemistryDesorptionAtomic ratio0210 nano-technologySodium carbonateApplied Catalysis A: General
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Interaction of mushroom tyrosinase with aromatic amines, o-diamines and o-aminophenols

2004

3-Amino-L-tyrosine was found to be a substrate of mushroom tyrosinase, contrary to what had previously been reported in the literature. A series of amino derivatives of benzoic acid were tested as substrates and inhibitors of the enzyme. 3-Amino-4-hydroxybenzoic acid, 4-amino-3-hydroxybenzoic acid and 3,4-diaminobenzoic acid were oxidized by this enzyme, as previously reported for Neurospora crassa tyrosinase, but 4-aminobenzoic acid and 3-aminobenzoic acid were not. Interestingly, 3-amino-4-hydroxybenzoic acid was oxidized five times faster than 4-amino-3-hydroxybenzoic acid, confirming the importance of proton transfer from the hydroxyl group at C-4 position. All compounds inhibited the m…

proton transferStereochemistryTyrosinaseBiophysicsPlasma protein bindingDiaminestyrosinaseAminophenolsBiochemistryCatalysisNeurospora crassachemistry.chemical_compoundo-aminophenolSide chainAminesMolecular BiologyBenzoic acidchemistry.chemical_classificationbiologyMonophenol Monooxygenaseo-phenylenediamineSubstrate (chemistry)biology.organism_classificationOxygenEnzymechemistryElectrophoresis Polyacrylamide GelAgaricalesProtein BindingBiochimica et Biophysica Acta (BBA) - General Subjects
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Role of the support and pseudo-liquid phase in the Phosphotungstic Heteropolyacid (photo)catalytic activity

2016

Catalytic and photocatalytic tests for propene hydration to 2-propanol were successfully carried out by using binary materials obtained by supporting a Keggin or Wells-Dawson heteropolyacids via impregnation method to commercial SiO2 or TiO2. (Photo)catalytic hydration was studied in gas-solid regime by using a continuous (photo)reactor working at atmospheric pressure and 80 °C. The alcohol was the main product. The acidity of the cluster accounts for the catalytic role, whereas both the acidity of the cluster and the oxidant ability were responsible for the increase of the reaction rate of the photo-assisted catalytic reaction. Moreover, the presence of a photoactive semiconductor support …

pseudo-liquid phase photocatalysis heteropolyacidSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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