Search results for "Faujasite"

showing 10 items of 11 documents

Ship-in-a-bottle synthesis of triphenylamine inside faujasite supercages and generation of the triphenylamminium radical ion

2005

Abstract The ship-in-a-bottle synthesis of triphenylamine encapsulated within basic X zeolite has been accomplished by reacting sodium diphenylamide with bromobenzene in the presence of a bifunctional palladium (Hartwig–Buchwald conditions). The presence of incarcerated triphenylamine was demonstrated by dissolving the zeolite with concentrated HF and analyzing the organic material in the dichloromethane extract. Laser flash photolysis (266 nm) gives rise to the generation of triphenylamminium radical cation detected as a transient species decaying in hundreds of microseconds. Upon repetitive cyclic voltammograms, zeolite encapsulated triphenylamine shows a reversible oxidation–reduction pr…

Organic Chemistrychemistry.chemical_elementFaujasiteengineering.materialTriphenylaminePhotochemistryBiochemistryPhotoinduced electron transferchemistry.chemical_compoundchemistryRadical ionDrug DiscoveryengineeringFlash photolysisBifunctionalZeolitePalladiumTetrahedron
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Preparation and conductivity of PEDOT encapsulated inside faujasites

2005

Poly[3,4-(ethylenedioxy)thiophene] (PEDOT) encapsulated inside the faujasite micropores has been prepared by polymerization of the monomer in partially Fe-exchanged faujasites. Faujasites containing PEDOT within the interior exhibit notable electrical conductivity compared to plain faujasite. This conductivity is attributed to the presence of polarons that have been detected by EPR spectroscopy.

Materials scienceInorganic chemistryGeneral Physics and AstronomyFaujasiteengineering.materialConductivitylaw.inventionchemistry.chemical_compoundMonomerchemistryPolymerizationPEDOT:PSSChemical engineeringlawThiopheneengineeringPhysical and Theoretical ChemistryElectron paramagnetic resonanceEthylenedioxyChemical Physics Letters
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Adsorption of hydrogen isotopes in the zeolite NaX: Experiments and simulations

2017

Abstract Among the different methods to separate hydrogen isotopes one is based on the physisorption at low temperature (below 100 K) where quantum effects induce a particular behavior. In the present work, we study the adsorption of single H 2 and D 2 on the zeolite NaX by combining experiments (manometry) from 30 to 150 K and molecular dynamics simulations at 40 and 77 K. Simulations also include the adsorption analysis for T 2 . Adsorption on NaX membranes is simulated and quantum corrections are introduced by using the well-known Feynman–Hibbs approach into the interaction potentials. Experimental adsorption isotherms are reproduced by using the Toth equation and it is shown that the ad…

Work (thermodynamics)HydrogenInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementThermodynamics02 engineering and technologyengineering.material010402 general chemistry7. Clean energy01 natural sciencesMolecular dynamicsAdsorptionPhysisorptionZeoliteComputingMilieux_MISCELLANEOUSRenewable Energy Sustainability and the EnvironmentChemistryFaujasite021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryFuel TechnologyMembraneengineering0210 nano-technology
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Macroscopic and Molecular Insights from CO Adsorption on NaY Zeolite: A Combined FTIR and Manometric Study

2012

International audience; This survey combines both quantitative and IR molecular descriptions and aims to provide new insights for the description of CO adsorption on NaY zeolite at 77 K. Quantitative measurements of the number of CO molecules trapped in the microporous super cage are compared to the corresponding IR spectra of CO as adsorbed species. We demonstrate that polycarbonyls formed during the completion of the accessible S-II Na+ coordinative vacancies result in the formation of mono-, di- and tricarbonyls but not consecutively. Quantitative analysis and measurements of the CO molecules that are adsorbed prove that polycarbonyls coexist with different proportions over the adsorptio…

FAUJASITESPolycarbonylInfrared spectroscopyACIDITY02 engineering and technologychemistry.chemical_compoundAdsorption020401 chemical engineeringPhase (matter)Organic chemistryMolecule0204 chemical engineeringPhysical and Theoretical ChemistryFourier transform infrared spectroscopyZeoliteCOORDINATIONSITESSPECTROSCOPYChemistryMicroporous material021001 nanoscience & nanotechnologySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyIRPhysical chemistry0210 nano-technology
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Molecular simulation studies of water physisorption in zeolites

2006

We report a series of Grand Canonical Monte Carlo simulations of water adsorption in NaY and NaX faujasite, as well as in silicalite-1. Computed adsorption isotherms and heats of adsorption were in good agreement with the available experiments. The existence of cyclic water hexamers in NaX located in the 12-ring windows, recently disclosed by neutron diffraction experiments (Hunger et al., J. Phys. Chem. B, 2006, 110, 342-353) was reproduced in our simulations. Interestingly enough, such cyclic hexamer clusters were also observed in the case of NaY, in which no stabilizing cation is present in the 12-ring window. We also report cation redistribution upon water adsorption for sodium faujasit…

Aqueous solutionChemistryNeutron diffractionGeneral Physics and Astronomy02 engineering and technologyFaujasiteengineering.material010402 general chemistry021001 nanoscience & nanotechnologyMolecular sieve01 natural sciences0104 chemical sciencesSeparation processAdsorptionPhysisorptionengineeringPhysical chemistryPhysical and Theoretical Chemistry0210 nano-technologyZeolitePhysical Chemistry Chemical Physics
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Adsorption of chlorinated volatile organic compounds on hydrophobic faujasite: correlation between the thermodynamic and kinetic properties and the p…

1998

This work deals with a thermodynamic and kinetic study of the adsorption of single volatile organic compounds (VOCs) (dichloromethane (DCM), 1,2-dichloroethane (DCA), trichloroethene (TCE) and tetrachloroethene (PCE)) on a dealuminated faujasite Y by simultaneous measurements of the adsorbed amounts, adsorption heats and diffusivities. The type V isotherms and the weak values of derivative enthalpies allowed us to predict that the competitive adsorption of their mixture would be similar to a distillation. This prediction was verified experimentally: the breakthrough curves of VOC mixtures showed that the adsorbate with the higher boiling point displaced the adsorbate with the lower boiling …

chemistry.chemical_classificationInorganic chemistryGeneral ChemistryFaujasiteengineering.materialCondensed Matter PhysicsMolecular sievelaw.inventionchemistry.chemical_compoundBoiling pointAdsorptionchemistryMechanics of MaterialslawengineeringOrganic chemistryGeneral Materials ScienceVolatile organic compoundZeoliteDistillationDichloromethaneMicroporous and Mesoporous Materials
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Anionic Organic Guests Incorporated in Zeolites: Adsorption and Reactivity of a Meisenheimer Complex in Faujasites

2005

Zeolites are suitable microporous hosts for positively charged organic species, but it is believed that they cannot adsorb organic anions. Pure Meisenheimer complex, derived from reduction of 2,4-dinitroaniline with NaBH4, was adsorbed inside faujasite cavities. Evidence for the internal incorporation of this negatively charged reaction intermediate comes from 1) XPS elemental analysis as a function of the depth of penetration into the particle, 2) the remarkable blue shift in lambda(max) of the Meisenheimer complex adsorbed on zeolite (ca. 470 nm) as compared to that in acetonitrile (580 nm) and 3) from the lack of reactivity with size-excluded hydride-acceptor reagents. Evidence is provid…

AnionsAniline CompoundsMolecular StructurebiologyChemistryOrganic ChemistryInorganic chemistryGeneral ChemistryReaction intermediateMicroporous materialFaujasiteengineering.materialCatalysisMeisenheimer complexAdsorptionZeolitesbiology.proteinengineeringReactivity (chemistry)AdsorptionZeoliteOxidation-ReductionOrganic anionChemistry - A European Journal
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Hydrogenolysis of hydroxymatairesinol on Y derived catalysts: a computational study

2010

Hydrogenolysis of 7-hydroxymatairesinol (HMR) to matairesinol (MAT) occurs on palladium supported acidic catalysts. HMR has three stereochemical centres and naturally exists as a mixture of two diastereoisomers, namely RRR-HMR and SRR-HMR. The latter is significantly more reactive than the former, in the reaction above. In order to elucidate the hydrogenolysis mechanism, simple surface events involving HMR derivatives on aluminated faujasite (H-Y) fragments were simulated by quantum chemical calculations. The metallic function of a Pd/H-Y acidic catalyst was also mimicked by a minimal palladium cluster. Stereochemical evidences pointed already out that water β-elimination on the epimeric ce…

7-HydroxymatairesinolProcess Chemistry and TechnologySupported catalystschemistry.chemical_elementDFT calculationFaujasiteengineering.materialHeterogeneous catalysisMedicinal chemistryHydrogenation/dehydration processeCatalysisCatalysisReaction rateHydroxymatairesinolchemistryHydrogenolysisengineeringOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryPalladiumH-Y zeolite
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Selective adsorption of ethyl mercaptan on NaX zeolite.

2008

Adsorption on microporous solid is an alternative technique to remove mercaptans from natural gases. The present study gives equilibrium adsorption data on NaX faujasite for some pure gases representative of natural gas impurities (ethyl mercaptan, toluene and n-heptane) and their binary mixtures. The first part of the paper is devoted to the adsorption of pure gases. Experimental results show that the zeolite has a high adsorption affinity for ethyl mercaptan, toluene and n-heptane. In the second part, we examine adsorption isotherms for binary mixtures of ethyl mercaptan and toluene or n-heptane over a large domain of composition. Coadsorption enthalpies are also determined. These experim…

Inorganic chemistry02 engineering and technologyengineering.material010402 general chemistryMolecular sieve01 natural sciences[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]chemistry.chemical_compoundAdsorptionGeneral Materials ScienceZeoliteComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationGeneral ChemistryMicroporous materialFaujasite021001 nanoscience & nanotechnologyCondensed Matter PhysicsToluene0104 chemical sciences[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]HydrocarbonchemistryMechanics of MaterialsSelective adsorptionengineering[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technology
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Exploratory Synthesis of Low-Silica Nanozeolites through Geopolymer Chemistry

2019

Nanozeolites are of great interest with the premise of their efficiency in traditional applications such as catalysis and separation, as well as their emerging applications including chemical sensors, medicine, and food industry. We report a new geopolymerization route for the synthesis of nanozeolites with different crystal structures by exploring the Na–Al–Si–H2O quaternary phase space under a mild hydrothermal condition. Nanostructured faujasite (FAU), cancrinite (CAN), and sodalite (SOD) zeolites with a crystallite size smaller than 40 nm were successfully produced from our exploration, as well as a submicron-sized Linde-Type A (LTA) zeolite. The transmission electron microscopy and nit…

010405 organic chemistryGeneral ChemistryFaujasiteengineering.material010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesCancriniteCatalysisGeopolymerchemistry.chemical_compoundChemical engineeringchemistryengineeringSodaliteGeneral Materials ScienceCrystalliteMesoporous materialZeoliteCrystal Growth & Design
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