Search results for "SELECTIVITY"

showing 10 items of 1148 documents

Total oxidation of naphthalene with high selectivity using a ceria catalyst prepared by a combustion method employing ethylene glycol.

2009

Abstract During the catalytic combustion of naphthalene, compounds other than CO 2 are often obtained. These products, as polymerized polycyclic aromatic hydrocarbons, oxygenated aromatic compounds and benzene derivate compounds, are usually more toxic than naphthalene. At the present work it is shown a nanocrystalline cerium oxide prepared by a combustion method employing a proper ethylene glycol concentration that exhibits very high activity in the decomposition of naphthalene in the presence of air and, most importantly, a selectivity value towards CO 2 of 100% for any range of conversions and/or temperatures used. In addition, it has been demonstrated that the amount of ethylene glycol …

Cerium oxideEthylene GlycolEnvironmental EngineeringHealth Toxicology and MutagenesisInorganic chemistryCatalytic combustionNaphthalenesCatalysisCatalysischemistry.chemical_compoundX-Ray DiffractionEnvironmental ChemistryBenzeneWaste Management and DisposalNaphthalenechemistry.chemical_classificationAir PollutantsAirTemperatureCarbon DioxidePollutionOxygenHydrocarbonchemistryMicroscopy Electron ScanningNanoparticlesGasesSelectivityCrystallizationEthylene glycolJournal of hazardous materials
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Oxidative dehydrogenation of ethane over NiO–CeO2 mixed oxides catalysts

2012

[EN] In this paper we present the synthesis, characterization and catalytic behaviour in the oxidative dehydrogenation of ethane of NiO-CeO2 mixed oxides. The addition of cerium oxide to NiO strongly modifies its catalytic performance, although the changes in the catalytic behaviour depend on the catalyst composition. The incorporation of low amounts of cerium oxide to NiO multiplies the productivity to ethylene in the oxidative dehydrogenation of ethane by a factor of ca. 7, which is the result of an increase in both catalytic activity and selectivity to ethylene. The enhanced activity has been related to the remarkable increase of the surface area of catalyst and the low crystal sizes of …

Cerium oxideEthyleneCatalyst characterization (XPS TPR XRD Raman FTIR of adsorbed CO oxygen isotopic-exchange)Inorganic chemistryNon-blocking I/Ochemistry.chemical_elementCerium oxideGeneral ChemistryCatalysisCatalysisCerium(IV) oxide–cerium(III) oxide cycleEthylenechemistry.chemical_compoundCeriumchemistryDehydrogenationOxidative dehydrogenation of ethaneNickel oxideSelectivityCatalysis Today
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Enhanced quantum sieving of hydrogen isotopes via molecular rearrangement of the adsorbed phase in chabazite

2020

Coadsorption experiments reveal an unexpected increase of the D2/H2 selectivity with loading in pure silica chabazite at 47 K. This effect is correlated with the appearance of a step in the adsorption isotherms of H2 and D2. Grand canonical Monte Carlo simulations show that this phenomenon is related to a molecular rearrangement of the adsorbed phase induced by its strong confinement. In the case of a H2 and D2 mixture, this rearrangement favors the adsorption of D2 having a smaller size due to quantum effects.

ChabaziteHydrogenchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysisAdsorptionPhase (matter)Materials ChemistryMolecular rearrangementQuantumComputingMilieux_MISCELLANEOUSIsotopeMetals and AlloysGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryChemical physicsCeramics and Composites0210 nano-technologySelectivity
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ChemInform Abstract: o-(Hydroxyalkyl)phenyl P-Chirogenic Phosphines as Functional Chiral Lewis Bases.

2013

The stereoselective synthesis of P-chirogenic phosphines bearing an o-hydroxyalkyl chain is described.

Chain (algebraic topology)ChemistryStereochemistryStereoselectivityGeneral MedicineLewis acids and basesChemInform
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ChemInform Abstract: Bubble Fractionation of Enantiomers from Solution Using Molecularly Imprinted Polymers as Collectors.

2010

Adsorptive bubble separation methods have been used to enrich components from both heterogeneous and homogeneous solutions. These methods are particularly effective for processing large solution volumes at low cost. Previous work demonstrated that chiral, surface-active collectors could be used to enrich enantiomers from homogeneous solution in a foam fractionation process. In a significant extension of this work, the use of highly selective molecularly imprinted polymers (MIPs) and heterogeneous solutions for the bubble flotation of enantiomers was evaluated. The high selectivity and ease of recycling of the MIP make this a potentially powerful approach for process-scale separations from l…

Chemical engineeringHomogeneousChemistryBubbleHigh selectivityMolecularly imprinted polymerSeparation methodFoam fractionationGeneral MedicineFractionationEnantiomerChemInform
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Stereoselective syntheses of piperidinones and their modification by organometallic coupling reactions

2007

Dehydropiperidinones stereoselectively obtained from N-arabinosyl imines were iodinated at the enaminone structure. Knochel iodine-magnesium exchange afforded Grignard compounds of these piperidinone derivatives which reacted, either directly or after transmetalation to zinc or copper intermediates, with alkyl-, aryl- or acylhalides to give correspondingly substituted piperidinones. Stereoselective conjugate allyl cuprate addition to a thus obtained 5-allyl dehydropiperidinone and ring-closing metathesis of the product gave a hydroquinolinone containing three stereogenic centers.

Chemistry OrganicMolecular ConformationStereoisomerismCrystallography X-RayMetathesisBiochemistryCoupling reactionStereocenterchemistry.chemical_compoundTransmetalationOrganometallic CompoundsOrganic chemistryMagnesiumPhysical and Theoretical ChemistryPiperidonesGroup 2 organometallic chemistryMolecular StructureChemistryArylOrganic ChemistryStereoisomerismZincModels ChemicalStereoselectivityIminesCopperIodineOrg. Biomol. Chem.
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Comparison of quantum dot-binding protein tags: Affinity determination by ultracentrifugation and FRET

2013

Abstract Background Hybrid complexes of proteins and colloidal semiconductor nanocrystals (quantum dots, QDs) are of increasing interest in various fields of biochemistry and biomedicine, for instance for biolabeling or drug transport. The usefulness of protein–QD complexes for such applications is dependent on the binding specificity and strength of the components. Often the binding properties of these components are difficult and time consuming to assess. Methods In this work we characterized the interaction between recombinant light harvesting chlorophyll a / b complex (LHCII) and CdTe/CdSe/ZnS QDs by using ultracentrifugation and fluorescence resonance energy transfer (FRET) assay exper…

ChemistryBinding proteinBiophysicsNanoparticleProtein tagBiochemistryCrystallographyB vitaminsFörster resonance energy transferQuantum dotQuantum DotsFluorescence Resonance Energy TransferNanoparticlesUltracentrifugeChlorophyll Binding ProteinsUltracentrifugationMolecular BiologyBinding selectivityProtein BindingBiochimica et Biophysica Acta (BBA) - General Subjects
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Corrigendum to: α-Conotoxins EpI and AuIB switch subtype selectivity and activity in native versus recombinant nicotinic acetylcholine receptors (FEB…

2003

Corrigendum to: K-Conotoxins EpI and AuIB switch subtype selectivity and activity in native versus recombinant nicotinic acetylcholine receptors (FEBS 27779) [FEBS Letters 554 (2003) 219^223]C Annette Nickea;1, Marek Samochockib, Marion L. Loughnana, Paramjit S. Bansala, Alfred Maelickeb, Richard J. Lewisa; aInstitute for Molecular Bioscience, University of Queensland, Brisbane, Qld. 4072, Australia bInstitute for Physiological Chemistry and Pathobiochemistry, University of Mainz, D-55099 Mainz, Germany First published online 24 December 2003

ChemistryBiophysicsSubtype selectivityCell BiologyPharmacologyBiochemistrylaw.inventionNicotinic agonistGanglion type nicotinic receptorStructural BiologylawPhysiological chemistryGeneticsRecombinant DNAAlpha-4 beta-2 nicotinic receptorMolecular BiologyAcetylcholine receptorα conotoxinFEBS Letters
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High activity of brookite TiO2 nanoparticles in the photocatalytic abatement of ammonia in water

2015

Abstract The effects of the TiO 2 crystal structure and its surface modification with Pt nanoparticles on the photocatalytic oxidation of NH 3 in the aqueous phase were studied with home-made TiO 2 photocatalyst powders synthesized by a thermo-hydrolysis approach that allowed a fine control of the crystallographic phase composition. Ammonia conversion and the selectivity toward mildly oxidized N 2 and highly oxidized nitrite and nitrate anions were monitored during the runs. Pure brookite powders modified by Pt nanoparticles, deposited either from a colloidal suspension or by deposition–precipitation, were found to be the most efficient photocatalysts in NH 3 degradation, with a desired goo…

ChemistryBrookiteInorganic chemistryGeneral ChemistryCrystal structureCatalysisCatalysisColloidAmmoniachemistry.chemical_compoundvisual_artvisual_art.visual_art_mediumPhotocatalysisSurface modificationSelectivityCatalysis Today
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Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water

2009

Several polystyrene-supported proline dipeptides and a prolinamide derivative were prepared by thiol–ene coupling. These materials were used as catalysts for the direct asymmetric aldol reaction in water, and results compared with unsupported catalysts in water. Such an approach gave more active or stereoselective catalysts compared to the unsupported compounds, showing that our immobilization procedure may be useful to develop catalytic materials with enhanced performance. Moreover, these catalysts can be recovered and reused for at least nine times without loss of activity or can be easily regenerated when their activity has decreased. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, …

ChemistryCatalyst supportOrganic ChemistryEnantioselective synthesisSettore CHIM/06 - Chimica OrganicaChemical synthesisCatalysisAldol reactionOrganocatalysisOrganic chemistryDipeptide Organocatalysis Prolinamide Proline Supported catalystAldol condensationStereoselectivityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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