Search results for " catalyst"

showing 10 items of 292 documents

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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Synthesis and catalytic performance in ethylene and 1-octene polymerization of chlorotitanium(IV) silsesquioxane complexes. Effect of increasing liga…

2016

Abstract The series of titanasilsesquioxanes that differ in a way of binding to the transition metal ( via one, two or three oxygen atoms) and type of nonreactive substituents bonded to inorganic oxygen-silicon cage ( i -Bu, Ph, c -C 6 H 11 ) were prepared by reacting of TiCl 4 with 1 eqv. of the silsesquioxane ligand. Upon treatment with an appropriate cocatalyst, all titanium precatalysts are active in ethylene and 1-octene polymerization and produce from low to high molecular weight polyethylenes and moderately ([ mmmm ] = 44–74%) isotactic poly(1-octene)s. The influence of polymerization parameters, type of cocatalyst and the silsesquioxane structure on the catalytic behavior of the tit…

Materials scienceDenticityEthylenePolymers and Plastics010405 organic chemistryLigandmicrostructureOrganic ChemistryGeneral Physics and AstronomysilsesquioxaneZiegler-Natta polymerization010402 general chemistry01 natural sciencesSilsesquioxane0104 chemical sciencesCatalysischemistry.chemical_compoundTransition metalchemistryPolymerizationPolymer chemistryMaterials Chemistrytitanium catalystpolyolefins1-OcteneEuropean Polymer Journal
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Ibuprofen degradation using a Co-doped carbon matrix derived from peat as a peroxymonosulphate activator

2021

The wider presence of pharmaceuticals and personal care products in nature is a major cause for concern in society. Among pharmaceuticals, the anti-inflammatory drug ibuprofen has commonly been found in aquatic and soil environments. We produced a Co-doped carbon matrix (Co-P 850) through the carbonization of Co2+ saturated peat and used it as a peroxymonosulphate activator to aid ibuprofen degradation. The properties of Co-P 850 were analysed using field emission scanning electron microscopy, energy filtered transmission electron microscopy and X-ray photoelectron spectroscopy. The characterization results showed that Co/Fe oxides were generated and tightly embedded into the carbon matrix …

advanced oxidation processhapetushajotusBicarbonateIbuprofen010501 environmental sciencespharmaceuticals and personal care productsComputing Methodologies01 natural sciencesBiochemistryChlorideCatalysisCatalysisturveSoil03 medical and health scienceschemistry.chemical_compoundkatalyytit0302 clinical medicineX-ray photoelectron spectroscopyDissolved organic carbonmedicineEnergy filtered transmission electron microscopy030212 general & internal medicineibuprofenjäteveden käsittely0105 earth and related environmental sciencesGeneral Environmental Sciencecarbon-based catalystvedenpuhdistuscobalt oxidesCarbonizationorganic chemicalsAdvanced oxidation processlääkeaineetCarbonPeroxidesibuprofeenichemistryaktiivihiilioksiditQuantum TheoryWater Pollutants ChemicalNuclear chemistrymedicine.drugEnvironmental Research
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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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Effect of hydrogen on the ethylene polymerization process over Ziegler–Natta catalysts supported on MgCl2(THF)2. I. Studies of the chain‐transfer rea…

2001

The effect of hydrogen on the molecular weight of polyethylene obtained over vanadium catalysts (based on VCl4 and VOCl3) supported on MgCl2(THF)2 was studied and the results were compared to those obtained for similar titanium catalysts. It was confirmed that the dependencies of the transfer reaction on the hydrogen concentration are a half‐order in all investigated systems. However, the transition metal of the catalytic site affects the ratio of the transfer rate with hydrogen to the propagation rate (ktr,H/kp) and the results showed that hydrogen is a more effective agent of polyethylene molecular weight control in vanadium‐based systems as compared to the titanium catalyst.

chain transfer with hydrogenvanadium and titanium catalystshydrogenmolecular weightethylene polymerizationJournal of Applied Polymer Science
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ChemInform Abstract: Switchable Palladium-Catalyst Reaction of Bromomethyl Sulfoxides, CO, and N-Nucleophiles: Aminocarbonylation at Csp3versus Oxida…

2013

Pd2(dba)3/ Xantphos-catalyzed coupling of the sulfoxides (I) and (V) with amines and carbon monoxide allows a new and efficient access to amides of type (IV) and (VI).

Coupling (electronics)chemistry.chemical_compoundNucleophileChemistryOxidative carbonylationPolymer chemistryGeneral MedicinePalladium catalystPyrrole derivativesCarbon monoxideChemInform
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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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α-d-Glucopyranose Adsorption on a Pd30 Cluster Supported on Boron Nitride Nanotube

2016

Boron nitride nanotube (BNNT) as an innovative support for carbohydrate transformation processes was evaluated, using density functional theory. The α-d-glucopyranose adsorption on a Pd30 cluster, supported on BNNT, was used to check both the local activity of topologically different metallic sites and the effects of the proximity of the BNNT surface to the same metallic sites. Detailed geometrical and electronic analyses performed on Pd30/BNNT and α-d-glucopyranose/Pd30/BNNT systems were discussed. It was observed that the deposition of the Pd30 cluster onto the BNNT support gives rise to an electronic rearrangement, determining a charge transfer from the support to the adsorbed metal clus…

Surface site reactivityChemical substanceNanotechnologyElectron donor02 engineering and technology010402 general chemistryDFT01 natural sciencesBoron nitride nanotubeCatalysisCatalysiCatalysisMetalchemistry.chemical_compoundAdsorptionSupported palladium catalystCluster (physics)Chemistry (all)Molecular electrostatic potentialGeneral Chemistry021001 nanoscience & nanotechnologyBoron nitride nanotube; DFT; Molecular electrostatic potential; Supported palladium catalyst; Surface site reactivity; α-d-Glucopyranose adsorption; Catalysis; Chemistry (all)0104 chemical scienceschemistryChemical physicsvisual_artα-d-Glucopyranose adsorptionvisual_art.visual_art_mediumDensity functional theory0210 nano-technologyScience technology and societyTopics in Catalysis
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Production of ethyl lactate by activated carbon-supported Sn and Zn oxide catalysts utilizing lignocellulosic side streams

2021

In this study, activated carbon-supported Sn and Zn oxide catalysts were prepared from hydrolysis lignin and used for the conversion of model solutions of trioses, hexoses, and lignocellulosic biomass hydrolysates to ethyl lactate. Both catalysts, SnO2@AC and ZnO@AC, were able to produce ethyl lactate in high yields. SnO2@AC was a more active and selective catalyst in triose (dihydroxyacetone) conversion, providing 99% yield to ethyl lactate. ZnO@AC, by contrast, was more selective in glucose and hydrolysate conversion, with a yield of 60% and 85%, respectively. The ethyl lactate yields were significantly higher than those from the optimized model solution experiments when using ZnO@AC cata…

katalyytitsinkkioksidikatalyysiaktiivihiilioksiditkemian tekniikkaheterogeneous catalystactivated carbonbiomassa (teollisuus)metal oxideethyl lactatelaktaatitlignocellulosic biomass
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Studies on the microstructure of ethylene/1-hexene copolymers prepared over heterogeneous Ziegler - Natta catalysts

2000

Three MgCl 2(THF) 2-supported, AlEt 2Cl-activated VOCl 3, VCl 4 and TiCl 4 Ziegler - Natta catalysts were used to copolymerize ethylene with 1-hexene in the presence of hydrogen to prepare low-M well-soluble copolymers that could be analyzed by 13C-NMR. The spectra (Fig. 1) showed resonance signals due to ethylene and 1-hexene units in positions unaffected by catalyst type and with intensities related to the degree of comonomer incorporation into the copolymer. The triad sequence distribution and comonomer reactivity ratios (r) were calculated by the Randall method [11] and Bernoulli statistics based on the known copolymer composition. The latter appeared to be the more valid in predicting …

EthyleneMaterials sciencePolymers and PlasticsbiologyGeneral Chemical EngineeringmicrostructureNattaethylene/1-hexene copolymersbiology.organism_classificationMicrostructurereactivity ciefficientsCatalysis1-Hexenechemistry.chemical_compoundchemistryMgCl2(THF)2-supported V and Ti catalystsMaterials ChemistryCopolymerOrganic chemistryPolimery
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