Search results for " Catalyst"

showing 10 items of 292 documents

Polymerization of ethylene by oxide-supported titanium halide catalyst: kinetic model with a deactivation of active species

2000

Abstract The effect of the calcination temperature of alumina, which was then used as a support for a titanium halide catalyst [TiCl4/Et2AlCl], on the catalyst activity in ethylene polymerization was investigated. α-Al2O3 was found to make a more advantageous catalyst support as compared to γ-Al2O3 despite the fact that the former offered a clearly lower specific surface area and its content of surface OH groups was inferior. The ethylene polymerization in the presence of the catalytic system on different alumina supports was investigated on the basis of a proposed kinetic model, taking into consideration the deactivation of active sites in the process. The improved activity was found to re…

EthylenePolymers and PlasticsCatalyst supportOrganic Chemistrytechnology industry and agriculturechemistry.chemical_elementPolymerization of ethyleneCatalysisTitanium chloridechemistry.chemical_compoundchemistryPolymerizationSpecific surface areaPolymer chemistryMaterials ChemistryTitanium Ziegler–Natta type catalystZiegler–Natta catalystOxide-type supportTitaniumPolymer
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“Functional Poly(ethylene glycol)”: PEG-Based Random Copolymers with 1,2-Diol Side Chains and Terminal Amino Functionality

2010

A series of poly(ethylene glycol-co-isopropylidene glyceryl glycidyl ether) (P(EO-co-IGG)) random copolymers with different fractions of 1,2-isopropylidene glyceryl glycidyl ether (IGG) units was synthesized. After acidic hydrolysis a new type of "functional PEGs", namely poly(ethylene glycol-co-glyceryl glycerol) (P(EO-co-GG)) was obtained. Using an initiator that releases a terminal amino moiety after deprotection, functional end groups with orthogonal reactivity to the in-chain groups were obtained. All polymers showed narrow molecular weight distributions (1.07-1.19), and control of the molecular weights was achieved in the range 5000-30 000 g/mol. Random incorporation of both comonomer…

EthylenePolymers and PlasticsPolyglycerolDiolHigh-Loading SupportPolymerizationInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerSide chainMoietychemistry.chemical_classificationReagentsTelechelic polymerOxide)Organic ChemistryPolymerSoluble PolymersRecoverable CatalystschemistryPolymerizationGlycidolBlock-CopolymersDerivativesMacromolecules
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Isolated Fe(III)-O Sites Catalyze the Hydrogenation of Acetylene in Ethylene Flows under Front-End Industrial Conditions

2018

[EN] The search for simple, earth-abundant, cheap, and nontoxic metal catalysts able to perform industrial hydrogenations is a topic of interest, transversal to many catalytic processes. Here, we show that isolated FeIII¿O sites on solids are able to dissociate and chemoselectively transfer H2 to acetylene in an industrial process. For that, a novel, robust, and highly crystalline metal¿organic framework (MOF), embedding FeIII¿OH2 single sites within its pores, was prepared in multigram scale and used as an efficient catalyst for the hydrogenation of 1% acetylene in ethylene streams under front-end conditions. Cutting-edge X-ray crystallography allowed the resolution of the crystal structur…

EthylenebiologyChemistryActive site02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundColloid and Surface ChemistryQUIMICA ORGANICAAcetyleneChemical engineeringbiology.proteinCubic zirconiaMetal catalyst0210 nano-technologyEfficient catalyst
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Dichlorovanadium(IV) diamine-bis(phenolate) complexes for ethylene (co)polymerization and 1-olefin isospecific polymerization

2018

Abstract Two vanadium complexes bearing amine-bis(phenolate) ligands with the amino side-arm donor, [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)2}Cl2] (1) and [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)(CH2-2-O-C6H4)}Cl2] (2), were synthesised and characterized by FTIR and 1H NMR spectroscopy. Upon activation with Al(iBu)3/Ph3CB(C6F5)4, these complexes became active catalysts for 1-octene polymerization giving highly stereoregular polymers (mmmm ∼ 90%) having regioirregularly arranged units. The catalytic activity of the catalysts in ethylene homo- and copolymerization, and their ability to incorporate a comonomer were highly dependent on both the activator type and the complex structure. 1/EtAlCl2 exhi…

EthylenemicrostructureDispersityZiegler-Natta polymerization010402 general chemistry01 natural sciencesCatalysisTREFchemistry.chemical_compoundDiaminediamine-bis(phenolate) ligandPolymer chemistryethyleneCopolymerPhysical and Theoretical Chemistrychemistry.chemical_classificationOlefin fiber010405 organic chemistryChemistryComonomerPolymer0104 chemical sciencescopolymerizationVanadium catalystPolymerization1-octeneJournal of Catalysis
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Hydrogen Arrangements on Defective Quasi-Molecular BN Fragments

2019

Considering the ever-increasing interest in metal-free materials, some potential chemical applications of quasi-molecular boron nitride (BN) derivatives were tested. Specifically, the behavior of BN fragments was analyzed when given defects, producing local electron density changes, were introduced by using topological engineering approaches. The inserted structural faults were Schottky-like divacancy (BN-d) defects, assembled in the fragment frame by the subtraction of one pair of B and N atoms or Stone-Wales (SW) defects. This study is aimed at highlighting the role of these important classes of defects in BN materials hypothesizing their future use in H-2-based processes, related to eith…

Exothermic reactionElectron densityMaterials scienceHydrogenGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesEndothermic processArticlechemistry.chemical_compoundAdsorptionFragmentation (mass spectrometry)MoleculeQD1-999General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemistrychemistryBoron nitrideChemical physicsSettore CHIM/03 - Chimica Generale E Inorganica0210 nano-technologyh-BN catalysts hydrogen surface arrangements DFT studiesACS Omega
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Counter anion binding in the phenoxyimine, salan and metallocene olefin polymerization catalysts activated with perfluorophenylborate

2012

Abstract Ion pair separation is a process that may influence the activity of homogeneous catalysts of olefin polymerization. We have studied the energy of separation for selected titanium and zirconium metallocene and post-metallocene catalytic ion pairs by means of DFT, dispersion-corrected DFT and Paired Interacting Orbitals method (PIO). Unusually weak cation–anion interactions in the bis(phenoxyimine) systems were attributed to strong electron-donating properties of the phenoxyimine ligands. Energy decomposition analysis (EDA) revealed that almost 70% of the counter ion binding energy results from electrostatic interactions. The PIO method made it possible to analyze the nature of the c…

FI catalystBinding energyPopulationchemistry.chemical_elementPhotochemistryDFTBiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryAnion bindingeducationchemistry.chemical_classificationZirconiumeducation.field_of_studyOrganic Chemistryphenoxyiminechemistrypaired interacting orbitals (PIO)Counterionolefin polymerizationMetalloceneTitaniumJournal of Organometallic Chemistry
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Fabrication of Porous Hydrogenation Catalysts by a Selective Laser Sintering 3D Printing Technique

2019

Open in a separate window Three-dimensional selective laser sintering printing was utilized to produce porous, solid objects, in which the catalytically active component, Pd/SiO2, is attached to an easily printable supporting polypropylene framework. Physical properties of the printed objects, such as porosity, were controlled by varying the printing parameters. Structural characterization of the objects was performed by helium ion microscopy, scanning electron microscopy, and X-ray tomography, and the catalytic performance of the objects was tested in the hydrogenation of styrene, cyclohexene, and phenylacetylene. The results show that the selective laser sintering process provides an alte…

FabricationMaterials sciencelaser sintering printingGeneral Chemical EngineeringCyclohexene3D printingfabrication02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyArticleCatalysislaw.inventionlcsh:Chemistryhuokoisuuschemistry.chemical_compoundkatalyytitlaw3D-tulostushydrogenation catalystsPorosityPolypropylenebusiness.industry3D printingGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCharacterization (materials science)Selective laser sinteringchemistryChemical engineeringlcsh:QD1-9990210 nano-technologybusinessACS Omega
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Catalytic hydrothermal liquefaction of municipal sludge assisted by formic acid for the production of next-generation fuels

2021

Abstract Hydrothermal liquefaction (HTL) of municipal sludge (MS) was studied at 325 °C and 30 min at 10 and 30% w/w concentration of MS using formic acid (FA) as a green liquid hydrogen donor both in the absence and in the presence of heterogeneous catalysts. Pellets of commercial NiMo/Al2O3, CoMo/Al2O3 and felt of activated carbon ACF 1600 were used as catalysts. The addition of FA at high MS loading allowed to increase the yields in BC from 41 to 62% and its H/C ratio from 1.80 to 2.01 leading to energy recovery (ER) higher than 100%.When heterogeneous catalysts were used together with FA, a marked improvement of BC yields and quality was obtained at 10% MS loading. This behavior was not…

Formic acidPelletsFormic acidHeterogeneous catalysisHeterogeneous catalystIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundmedicineElectrical and Electronic EngineeringHydrogen donorMunicipal sludgeCivil and Structural EngineeringFoulingChemistryMechanical EngineeringBuilding and ConstructionSettore ING-IND/27 - Chimica Industriale E TecnologicaBiorefineryPollutionBiorefineryHydrothermal liquefactionGeneral EnergyHydrothermal liquefactionActivated carbonmedicine.drugNuclear chemistryEnergy
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How Proximal Nucleobases Regulate the Catalytic Activity of G-Quadruplex/Hemin DNAzymes

2018

International audience; G-quadruplexes (G4s) are versatile catalytic DNAs when combined with hemin. Despite the repertoire of catalytically competent G4/hemin complexes studied so far, little is known about the detailed catalytic mechanism of these biocatalysts. Herein, we have carried out an in-depth analysis of the hemin binding site within the G4/hemin catalysts, providing the porphyrinic cofactor with a controlled nucleotidic environment. We intensively assessed the position-dependent catalytic enhancement in model reactions and found that proximal nucleobases enhance the catalytic ability of the G4/hemin complexes. Our results allow for revisiting the mechanism of the G4/hemin-based ca…

G4-based catalystDNAzymeproximal nucleobasesDeoxyribozyme010402 general chemistryG-quadruplex01 natural sciencesCatalysisCofactorCatalysisNucleobasechemistry.chemical_compoundG4/hemin complexpolycyclic compoundsNucleotideheterocyclic compoundsBinding sitechemistry.chemical_classificationbiology010405 organic chemistryG-quartetGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysisequipment and suppliesCombinatorial chemistry0104 chemical scienceschemistrybiology.proteinHemin
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Activity of a Heterogeneous Catalyst in Deep Eutectic Solvents: The Case of Carbohydrate Conversion into 5-Hydroxymethylfurfural

2019

Obtaining industrially relevant products from renewable resources and developing processes under the light of sustainable chemistry is a prominent endeavor of present-day chemical research. In this context, herein we investigated the dehydration of fructose and sucrose in deep eutectic solvents promoted by the ion-exchange resin Amberlyst 15 as heterogeneous catalyst. We optimized the reaction conditions in terms of temperature, catalyst loading, and initial amount of substrate. Then, we looked at the effect of structural variations in the solvent components on the reaction outcome. Under the best experimental conditions, we obtained very good yields of 78% at 60 °C and 69% at 80 °C for fru…

Green chemistryChemical researchRenewable Energy Sustainability and the EnvironmentChemistryGeneral Chemical EngineeringSettore CHIM/06 - Chimica Organica02 engineering and technologyGeneral ChemistryCarbohydrate010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciences0104 chemical sciencesChemical engineering5-hydroxymethylfurfuralEnvironmental ChemistryDeep eutectic solvents Amberyst 15 Carbohydrates 5-HMF Catalyst recycling0210 nano-technologyEutectic systemRenewable resourceACS Sustainable Chemistry & Engineering
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