Search results for "ZEOLITES"

showing 10 items of 31 documents

Determination of benzomercaptans in environmental complex samples by combining zeolitic imidazolate framework-8-based solid-phase extraction and high…

2020

[EN] In this work, the synthesis of zeolitic imidazolate framework-8 (ZIF-8) crystals and their subsequent application as effective sorbents for extraction and preconcentration of several benzomercaptans from environmental complex samples is described. These materials were prepared by solvothermal approach varying the concentration of n-butylamine modulator to modify the surface of the metal-organic framework. The resulting materials were characterized by scanning and transmission electron microscopy, powder X-ray diffraction and Fourier transform infrared spectroscopy. The ZIF-8 material that gave the best features was selected as extractive phase and the influence of various parameters (s…

Soil and aqueous samples010402 general chemistry01 natural sciencesBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundSorbentSample preparationImidazolateQUIMICA ANALITICASample preparationSolid phase extractionChromatography High Pressure LiquidDetection limitSolid-phase extractionChromatographyElutionSolid Phase Extraction010401 analytical chemistryOrganic ChemistryExtraction (chemistry)General MedicineMetal-organic frameworks0104 chemical sciencesEnvironmental pollutantschemistryZeolitesWater Pollutants ChemicalZeolitic imidazolate framework
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Rovibrational spectroscopy of ethylene : Stark effect : Application to ethylene in zeolites

2010

The objective of this report is to present a study as complete as possible of the Stark effect in the asymmetric top molecules of X2Y4 type possessing the D2h symmetry group and to apply it to the problem of the spectroscopy of the ethylene molecule trapped in a zeolite. For the first time, a tensorial formalism adapted to the study of the Stark effect for the O(3) D2h group chain was developed. In parallel, a computer package was worked out as a new generation of software called D2hTDS-ST using a simpler basis, allowing an economy in the calculation time. On the basis of the theoretical and computing tools as well as from the experimental spectra, recorded in the laboratory, we made a firs…

Spectroscopie moléculaireD2h point groupNanoporous solidsFormalisme tensorielStark effectZéolithesTensorial formalismSolides nanoporeux[ PHYS.COND.CM-GEN ] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]Effet StarkGroupe ponctuel D2hMolecular spectroscopy[PHYS.COND.CM-GEN] Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other][PHYS.COND.CM-GEN]Physics [physics]/Condensed Matter [cond-mat]/Other [cond-mat.other]Zeolites
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Influence of preparation conditions on the catalytic performance of mo/h-zsm-5 for methane dehydroaromatization

2021

[EN] Methane, the main component of natural gas, is an interesting source of chemicals and clean liquid fuels, and a promising alternative raw material to oil. Among the possible direct routes for methane conversion, its aromatization under non-oxidative conditions has received increasing attention, despite the low conversions obtained due to thermodynamic limitations, because of its high selectivity to benzene. Mo/H-ZSM-5, the first bifunctional zeolite-catalyst proposed for this reaction, is still considered as one of the most adequate and has been widely studied. Although the mono- or bifunctional nature of the MDA mechanism is still under debate, it is generally accepted that the Mo spe…

TechnologyQH301-705.5QC1-999Inorganic chemistryCatalysts preparation010402 general chemistry01 natural sciencesMethaneCatalysischemistry.chemical_compoundMo/ZSM-5General Materials ScienceBiology (General)Methane aromatizationZeoliteBifunctionalBenzeneQD1-999InstrumentationFluid Flow and Transfer Processes010405 organic chemistryTPhysicsProcess Chemistry and TechnologyGeneral EngineeringAromatizationCatalyst activationEngineering (General). Civil engineering (General)0104 chemical sciencesComputer Science ApplicationsChemistrychemistryZeolitesTA1-2040ZSM-5Selectivity
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Use of alkylarsonium directing agents for the synthesis and study of zeolites

2019

[EN] Expanding the previously known family of -onium (ammonium, phosphonium, and sulfonium) organic structure-directing agents (OSDAs) for the synthesis of zeolite MFI, a new member, the arsonium cation, is used for the first time. The new group of tetraalkylarsonium cations has allowed the synthesis of the zeolite ZSM-5 with several different chemical compositions, opening a route for the synthesis of zeolites with a new series of OSDA. Moreover, the use of As replacing N in the OSDA allows the introduction of probe atoms that facilitate the study of these molecules by powder X-ray diffraction (PXRD), solid-state nuclear magnetic resonance (MAS NMR), and X-ray absorption spectroscopy (XAS)…

X-ray absorption spectroscopyChemistrySulfoniumOrganic ChemistryGeneral ChemistryOniumAlkylarsoniumCatalysislaw.inventionArsenicchemistry.chemical_compoundCrystallographyCompostos orgànics SíntesiStructure-directing agentslawCationsQUIMICA ANALITICAZeolitesMoleculePhosphoniumCrystallizationZeoliteMaterialsPowder diffraction
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Hemicellulose hydrolysis catalysed by solid acids

2013

Depolymerising hemicellulose into platform sugar molecules is a key step in developing the concept of an integrated biorefinery. This reaction is traditionally catalysed by either enzymes or homogeneous mineral acids. We compared various solid catalysts for hemicellulose hydrolysis, running reactions in water, under neutral pH and relatively mild temperature and pressure (120°C and 10 bar) conditions. Sulphonated resins are highly active, but they leach out sulphonic groups. Sulphonated silicas are less active, but more stable. They have weakly and strongly bound sites and the strongly bound ones do not leach. Zeolites are moderately active and stable. Among them, H-ferrierite especially, d…

chemistry.chemical_classificationChemistryBiorefineryCatalysisCatalysischemistry.chemical_compoundHydrolysisEnzymeHemicellulose heterogeneous catalysis solid acids xylose arabinose zeolitesHomogeneousOrganic chemistryMoleculeQDHemicelluloseSugar
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Heterocyclic rearrangements in constrained media. A zeolite-directed photorearrangement of 1,2,4-oxadiazoles

2005

[reaction: see text] The first intrazeolite-photoinduced rearrangement of a five-membered heterocycle is reported. A completely different behavior compared to solution irradiations has been observed. The zeolite's role in directing the photoreaction of 3-phenyl-1,2,4-oxadiazoles toward the formation of the corresponding 1,3,4-oxadiazoles in a ring contraction-ringexpansion route is discussed.

chemistry.chemical_classificationModels MolecularOxadiazolesRING-PHOTOISOMERIZATIONMolecular StructurePHOTOCHEMICAL BEHAVIORChemistryPhotochemistryUltraviolet RaysOrganic ChemistryPATHWAYSSettore CHIM/06 - Chimica OrganicaRing (chemistry)PhotochemistryHeterocyclic compoundCyclizationZeolitesZeolite
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Photooxidations of Alkenes in Fluorinated Constrained Media:  Fluoro-organically Modified NaY as Improved Reactors for Singlet Oxygen “Ene” Reactions

2007

Creating a stationary fluorinated environment inside the zeolite cavity can increase the reactivity observed for intrazeolite photooxidation of alkenes. Exchanging the zeolite with fluorinated organic cations is a much more effective strategy than simply using a fluorinated solvent for slurry irradiations. Use of cations containing C-F bonds is also more efficient than use of deuterated cations for creation of a singlet oxygen friendly environment where the quenching processes are slowed down. Doping the zeolite with fluoro-organic cation 4 resulted in an increase in the singlet oxygen lifetime to 12 micros.

chemistry.chemical_classificationQuenching (fluorescence)ZEOLITESChemistryAlkeneSinglet oxygenOrganic ChemistryInorganic chemistryINTRAZEOLITE PHOTOOXIDATIONSLIFETIMEOXIDATIONPhotochemistrySolventchemistry.chemical_compoundCHEMISTRYReactivity (chemistry)Singlet stateDEACTIVATIONOLEFINSZeoliteEne reactionThe Journal of Organic Chemistry
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A Novel Zeolite-Induced Population of a Planar Viologen Conformation. New Viologen Charge Transfer Complexes and Alkene/Viologen/Zeolite Arrays

2004

A rare example of a novel zeolite-induced conformational change and a mechanism for this process are suggested in order to rationalize an unexpected spontaneous intrazeolite reduction observed during preparation of a new viologen (MQ2+)-doped zeolite (NaY). In addition, the formations of six new alkene/viologen/ zeolite charge transfer (CT) arrays using NaMQY and the previously reported NaMVY are also reported. The binding constants between MQ2+ and MV2+ and 2,3-dimethyl-2-butene (TME) were determined using the Benesi-Hildebrand approach, and the stabilities of these CT complexes are compared to their intrazeolite analogue.

chemistry.chemical_classificationeducation.field_of_studyConformational changeChemistryAlkenePopulationViologenCharge (physics)Settore CHIM/06 - Chimica OrganicaPhotochemistrySurfaces Coatings and FilmsPlanarMaterials ChemistrymedicinePhysical and Theoretical ChemistryeducationZeolitemedicine.drugZeolites Binding constants Electrochromic display devices Oxygenation
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Enhanced Heterogeneous Catalytic Conversion of Furfuryl Alcohol into Butyl Levulinate

2014

We study the catalytic condensation of furfuryl alcohol with 1-butanol to butyl levulinate. A screening of several commercial and as-synthesized solid acid catalysts shows that propylsulfonic acid-functionalized mesoporous silica outperforms the state-of-the-art phosphotungstate acid catalysts. The catalyst is prepared via template-assisted sol-gel polycondensation of TEOS and MPTMS. It gives 96 % yield (and 100 % selectivity) of butyl levulinate in 4h at 110 °C. Reaction profiles before and after a hot filtration test confirm that the active catalytic species do not leach into the solution. The catalyst synthesis, characterization, and mode of operation are presented and discussed. Sour ca…

inorganic chemicalsCondensation polymerGeneral Chemical EngineeringesterificationNiobiumHeterogeneous catalysisCatalysisCatalysisFurfuryl alcoholalcoholschemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryGeneral Materials ScienceFuransbiomassorganic chemicalsCondensationMesoporous silicasolid acidsSilicon DioxideLevulinic AcidsGeneral Energyheterogeneous catalysischemistryYield (chemistry)ZeolitesPolystyrenesSulfonic AcidsSelectivityChemSusChem
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Ammonium adsorption, desorption and recovery by acid and alkaline treated zeolite

2021

In this study, the suitability of zeolite as a possible medium for ammonium adsorption, desorption and recovery from wastewater was investigated. Specifically, batch adsorption and desorption studies with solutions enriched in NH$_4^+$ were conducted employing zeolite to evaluate how the chemical treatment and contact time affect adsorption and desorption. Several experimental tests were carried out considering both untreated and treated zeolite. Untreated and HCl-Na treated zeolite adsorbed up to 11.8 mg NH$_4^+$ g$^{-1}$ and showed the highest efficiency in recovering NH$_4^+$ from aqueous solution. Regardless of pre-treatment, treatments with NaCl resulted in higher and faster adsorption…

inorganic chemicalsEnvironmental EngineeringSettore AGR/13 - Chimica Agraria0207 environmental engineeringFOS: Physical sciencesBioengineering02 engineering and technologyApplied Physics (physics.app-ph)010501 environmental sciencesWastewater01 natural sciencesAmmonium adsorptionWater PurificationAdsorptionDesorptionPhysics - Chemical PhysicsAmmonium CompoundsAlkaline and acid treatments Ammonium exchange capacity Ammonium kinetic adsorption Clinoptilolite Resource recovery020701 environmental engineeringZeoliteWaste Management and Disposal0105 earth and related environmental sciencesResource recoveryChemical Physics (physics.chem-ph)ClinoptiloliteAqueous solutionSettore ICAR/03 - Ingegneria Sanitaria-AmbientaleRenewable Energy Sustainability and the EnvironmentChemistryfood and beveragesGeneral MedicinePhysics - Applied Physics6. Clean waterWastewaterZeolitesAdsorptionWater Pollutants ChemicalNuclear chemistryBioresource Technology
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