Search results for " Catalyst"

showing 10 items of 292 documents

Biomass-based composite catalysts for catalytic wet peroxide oxidation of bisphenol A:preparation and characterization studies

2019

The wet granulation process was used to prepare new, efficient, and cost-effective granular biomass-based composite catalysts for catalytic wet peroxide oxidation (CWPO) of bisphenol A (BPA). The most stable composite granules was prepared by mixing biomass-based carbon residue (CR) with metakaolin (MK) combined with calcium oxide (CaO) or cement and a solvent (NaOH or KOH). For all the prepared composite granules, the optimized binding agents to carbon ratio was 0.3, the solvent to carbon ratio 1.2, and the agitation rate 1200 rpm. The specific surface area of the prepared catalysts was 152–205 m2/g. The composite granular catalyst (CR + MK + CaO + NaOH) had the most durable and stable str…

Oxidation of bisphenol AGranular activated carbonaktiivihiiliComposite catalystWastewater purificationbiomassa (teollisuus)jätevesiBiomasskomposiititjäteveden käsittely
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Magneli-type tungsten oxide nanorods as catalysts for the selective oxidation of organic sulfides

2021

Selective oxidation of thioethers is an important reaction to obtain sulfoxides as synthetic intermediates for applications in the chemical industry, medicinal chemistry and biology or the destruction of warfare agents. The reduced Magneli-type tungsten oxide WO3−x possesses a unique oxidase-like activity which facilitates the oxidation of thioethers to the corresponding sulfoxides. More than 90% of the model system methylphenylsulfide could be converted to the sulfoxide with a selectivity of 98% at room temperature within 30 minutes, whereas oxidation to the corresponding sulfone was on a time scale of days. The concentration of the catalyst had a significant impact on the reaction rate. R…

OxidesSulfoxideCombinatorial chemistryDecompositionTungstenNanomaterial-based catalystSulfoneCatalysisInorganic ChemistryReaction ratechemistry.chemical_compoundchemistryHydrogen peroxideSelectivityDalton Transactions
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Palladium nanoparticles immobilized on halloysite nanotubes covered by a multilayer network for catalytic applications

2018

The synthesis of pure fine chemicals for industrial purposes is one of the most attractive challenges of chemical research. The use of catalytic pathways mediated by palladium nanoparticles (PdNPs) for C-C bond formation is a useful way to obtain these kinds of compounds. To achieve this objective, the PdNPs can be efficiently loaded on a functionalized natural nanostructured support such as halloysite nanotubes (HNTs). Hybrid materials based on thiol functionalized halloysite nanotubes and highly cross-linked imidazolium salts were successfully developed and used for the stabilization of PdNPs. The HNT/Pd hybrids were thoroughly characterized from a physico-chemical point of view and teste…

Palladium nanoparticles immobilized on halloysite nanotubes02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteCatalysisCoupling reactionCatalysisSuzuki reactionMaterials ChemistrySettore CHIM/02 - Chimica FisicaChemistryPalladium nanoparticlesSettore CHIM/06 - Chimica OrganicaGeneral ChemistryPalladium nanoparticles halloysite nanotubes catalyst021001 nanoscience & nanotechnology0104 chemical sciencesTurnover numberChemical engineeringMicrowave irradiationengineering0210 nano-technologyHybrid materialHalloysite nanotubes cross-coupling reactionsNew Journal of Chemistry
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Growth of Palladium Clusters on a Boron Nitride Nanotube Support

2015

We demonstrated that the migration process of a single palladium atom on the BNNT is not highly energy demanding and can be represented as a hopping mechanism between boron and nitrogen. A model was finally found for the interpretation of the growth energetics, showing that the process is generally favoured increasing the cluster size.

Palladium Boron Nitride Supported Catalyst DFT
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Structural characterization of Pd-Ag and Pd-Cu bimetallic catalysts by means of EXAFS, WAXS and XPS

2000

Bimetallic Pd-Ag and Pd-Cu pumice-supported catalysts have been synthesized following different preparation procedures with the aim of improving the selectivity and reactivity of monometallic Pd/pumice systems. The structural characterization, carried out by X-ray Diffraction, X-ray Absorption and X-ray Photoelectron Spectroscopy, allowed to investigate the importance of the preparation procedures in the alloy formation.

Pd-CuMaterials scienceExtended X-ray absorption fine structureAlloyengineering.materialCatalysisCrystallographyX-ray photoelectron spectroscopyPd-AgengineeringPhysical chemistrybimetallic catalystsReactivity (chemistry)Absorption (chemistry)SelectivityBimetallic strip
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Confined Pt-1(1+) Water Clusters in a MOF Catalyze the Low-Temperature Water-Gas Shift Reaction with both CO2 Oxygen Atoms Coming from Water

2018

[EN] The synthesis and reactivity of single metal atoms in a low-valence state bound to just water, rather than to organic ligands or surfaces, is a major experimental challenge. Herein, we show a gram-scale wet synthesis of Pt-1(1+) stabilized in a confined space by a crystallographically well-defined first water sphere, and with a second coordination sphere linked to a metal-organic framework (MOF) through electrostatic and H-bonding interactions. The role of the water cluster is not only isolating and stabilizing the Pt atoms, but also regulating the charge of the metal and the adsorption of reactants. This is shown for the low-temperature water-gas shift reaction (WGSR: CO + H2O CO2 + H…

PhysicsWater–gas shift reactionQuímica Inorgánicabiology010405 organic chemistryWater-gas shift reactionSingle atom catalystGeneral MedicineGeneral ChemistryMetal-organic frameworks010402 general chemistrybiology.organism_classification01 natural sciencesCatalysisWater-gas shift reactionSingle-atom catalyst0104 chemical sciencesOxygen atomWater clustersPhysical chemistryValenciaMetal-organic frameworks (MOFs)Platinum
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High crystallinity polyethylene obtained in biphasic polymerization using pyridinium chloroaluminate ionic liquid

2014

A series of N-n-alkylpyridinium chloroaluminate ionic liquids [C n -py][AlCl4] (where n-alkyl = n-butyl, n-hexyl, and n-octyl) was applied as a medium of the Cp2TiCl2 catalyst, activated by AlEtCl2 or AlEt2Cl, to evaluate the influence of the studied ionic liquids on the performance of the biphasic ionic liquid/hexane ethylene polymerization and the properties of the produced polyethylene (PE). The best results were obtained using N-n-butylpyridinium chloroaluminate. The polyethylene obtained in the biphasic polymerization have the high crystallinity, which was confirmed by DSC, WAXS and PALS methods, as well as the bulk density comparable to commercial HDPE. These unique properties results…

Polyethylene . Biphasic process . Ionic liquid . Metallocene catalystMaterials sciencePolymers and PlasticsOrganic Chemistrytechnology industry and agriculturePost-metallocene catalystPolyethyleneCrystallinitychemistry.chemical_compoundPolymerizationChemical engineeringchemistryPhase (matter)Polymer chemistryIonic liquidMaterials ChemistryCoordination polymerizationHigh-density polyethyleneJournal of Polymer Research
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Multi-Alkenylsilsesquioxanes as Comonomers and Active Species Modifiers of Metallocene Catalyst in Copolymerization with Ethylene.

2018

The copolymers of ethylene (E) with open-caged iso-butyl-substituted tri-alkenyl-silsesquioxanes (POSS-6-3 and POSS-10-3) and phenyl-substituted tetra-alkenyl-silsesquioxane (POSS-10-4) were synthesized by copolymerization over the ansa-metallocene catalyst. The influence of the kind of silsesquioxane and of the copolymerization conditions on the reaction performance and on the properties of the copolymers was studied. In the case of copolymerization of E/POSS-6-3, the positive comonomer effect was observed, which was associated with the influence of POSS-6-3 on transformation of the bimetallic ion pair to the active catalytic species. Functionality of silsesquioxanes and polymerization par…

Polymers and Plastics02 engineering and technologyPost-metallocene catalyst010402 general chemistry01 natural sciencesArticlelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPolymer chemistryCopolymerethylenecrosslinkingchemistry.chemical_classificationmetalloceneComonomerGeneral ChemistryPolymer021001 nanoscience & nanotechnologySilsesquioxaneethylene; polyhedral oligomeric silsesquioxanes (POSS); copolymerization; metallocene; crosslinking; active site modifier0104 chemical sciencesactive site modifiercopolymerizationchemistryPolymerization0210 nano-technologyGlass transitionMetallocenepolyhedral oligomeric silsesquioxanes (POSS)Polymers
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An assembly of organic-inorganic composites using halloysite clay nanotubes

2018

Halloysite is natural tubular clay suitable as a component of biocompatible nanosystems with specific functionalities. The selective modification of halloysite inner/outer surfaces can be achieved by exploiting supramolecular and covalent interactions resulting in controlled colloidal stability adjusted to the solvent polarity. The functionalized halloysite nanotubes can be employed as reinforcing filler for polymers as well as carriers for the sustained release of active molecules, such as antioxidants, flame-retardants, corrosion inhibitors, biocides and drugs. The tubular morphology makes halloysite a perspective template for core-shell metal supports for mesoporous catalysts. The cataly…

Polymers and PlasticsHalloysite nanotube02 engineering and technologyReview01 natural sciencesunclassified drug adsorptionFlame retardantcovalent bondColloid and Surface ChemistryhalloysiteControlled drug deliverychemistry.chemical_classificationemulsionquantum dotSurfaces and InterfacesPolymerSelf assembly021001 nanoscience & nanotechnologynanorodPickering emulsionCorrosion inhibitoroil spillSolventSelective modification Kaolinite chemicals and drugNanorodBiocompatibility0210 nano-technologyOil water interfaceYarn Covalent interactionNanotubeMaterials scienceSupramolecular chemistrysustained drug releasecatalysiengineering.material010402 general chemistryHalloysitebioremediationPhysical and Theoretical ChemistryhydrophobicityMesoporous catalystpetroleummetal nanoparticlePhase interfacemetal bindingReinforcing fillerPickering emulsion0104 chemical sciencesOrganic-inorganic compositeNanotubeFilled polymerchemistryChemical engineeringengineeringSelf-assemblyCatalystMesoporous material
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Effect of hydrogen on the ethylene polymerization process over Ziegler-Natta catalysts supported on MgCl2(THF)2. II. Kinetic studies

2000

This article reports on a study of the effects of hydrogen on the activity of vanadium and titanium catalysts supported on MgCl 2 (THF) 2 in ethylene polymerization. It was found that hydrogen did not change the stable nature of the active sites and the polydispersity index of the polyethylene obtained. The propagation rate, expressed as k p , was found to be independent of the presence and concentration of hydrogen, indicating that this reacting agent does not modify the reactivity of the active sites. However, the presence of hydrogen in the polymerization medium is responsible for partial deactivation of the active sites just before polymerization is initiated.

Polymers and PlasticsHydrogenchemistry.chemical_elementGeneral ChemistrySurfaces Coatings and FilmsCatalysisChain-growth polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCoordination polymerizationReactivity (chemistry)Ziegler–Natta catalystIonic polymerizationJournal of Applied Polymer Science
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