Search results for "Molecular sieve"

showing 10 items of 58 documents

Co-adsorption of 1,2-dichloroethane and 1-bromo,2-chloroethane on zeolite ZSM-5 from the liquid and vapour phases, using the Myers-Prausnitz-Dubinin …

2002

Abstract The adsorption/co-adsorption of 1,2-dichloroethane (DCA) and 1-bromo,2-chloroethane (BCA) from the vapour and the liquid phases by zeolite ZSM-5 at ambient temperature is reported, using Dubinin's theory and the recent Myers-Prausnitz-Dubinin (MPD) theory. For adsorption from the liquid phase, the activity coefficients in the adsorbed and the liquid states are the same and no selectivity is observed. This is confirmed by the absence of an excess enthalpy of immersion of ZSM-5 into the mixtures. Adsorption from the vapour phase proceeds in two stages, as indicated by double Dubinin-Astakhov (DA) plots. If one considers only the domain of high relative pressure, co-adsorption is desc…

Activity coefficientEnthalpyThermodynamicsGeneral Chemistry12-DichloroethaneCondensed Matter PhysicsMolecular sievechemistry.chemical_compoundAdsorptionchemistryMechanics of MaterialsPhase (matter)Organic chemistryGeneral Materials ScienceZSM-5ZeoliteMicroporous and Mesoporous Materials
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Investigation on the Adsorption of N2 Ar, CO and CH4 on Aluminophosphates

1994

Abstract Adsorption isotherms at different temperatures and isothermal micro-calorimetric curves were measured for N2 Ar, CO, and CH4 on various molecular sieves as VPI-5, MCM-9, AlPO4-8, AlPO4-H, AlPO4-5, SAPO-5, AlPO4-39, AlPO4-C. It was shown that the isosteric heats of adsorption correlated with the pore-sizes of the studied molecular sieves.

AdsorptionChemistryInorganic chemistryMolecular sieveIsothermal process
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Study and Modelling of the Vacuum Swing Adsorption (VSA) Process Employed in the Production of Oxygen

1999

An isothermal and non-equilibrium mathematical model was provided for the multi-component adsorption process. In addition, the software was developed for the VSA-based production of oxygen with the use of a CaX zeolite molecular sieve. The mathematical model and computer software were verified on the basis of experimental data. The study employed a test stand comprising two adsorption columns. The adsorption pressure P A = 150 and 135 kPa and desorption pressure P D = 20 kPa were adopted in the experiments. The tests produced oxygen with the purity of 90–94% O 2 (vol), at an efficiency of 55–73% and productivity of 570–850 kg O 2 per ton per day. The calculation results showed good consiste…

AdsorptionChromatographyChemistryGeneral Chemical EngineeringDiffusionDesorptionAnalytical chemistrySorptionGeneral ChemistryVacuum swing adsorptionMolecular sieveZeoliteIsothermal processChemical Engineering Research and Design
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Isomerization of C5–C7 n-alkanes on unidirectional large pore zeolites: activity, selectivity and adsorption features

2001

Abstract The hydroisomerization–hydrocracking of nC5–nC7 is studied with a 12MR unidirectional zeolite (ITQ-4). Selectivity and kinetic parameters indicate that differences in pore topology are more important than acidity for determining isomerization selectivity. The adsorption of the paraffins is determined by van der Waals interactions.

Alkanechemistry.chemical_classificationChemistryGeneral ChemistryMolecular sieveCatalysisMordenitesymbols.namesakeAdsorptionsymbolsPhysical chemistryOrganic chemistryvan der Waals forceZeoliteSelectivityIsomerizationCatalysis Today
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New insights in the formation of silanol defects in silicalite-1 by water intrusion under high pressure.

2010

International audience; The "water-silicalite-1" system is known to act as a molecular spring. The successive intrusion-extrusion cycles of liquid water in small crystallites (6 × 3 × 0.5 μm(3)) of hydrophobic silicalite-1 were studied by volumetric and calorimetric techniques. The experiments displayed a decrease of the intrusion pressure between the first intrusion-extrusion cycle and the consecutive ones, whereas the extrusion pressures remained unchanged. However, neither XRD studies nor SEM observations revealed any structural and morphological modifications of silicalite-1 at the long-range order. Such a shift in the value of the intrusion pressure after the first water intrusion-extr…

Analytical chemistryGeneral Physics and AstronomyInfrared spectroscopy02 engineering and technologyCalorimetry010402 general chemistryMolecular sieve01 natural scienceschemistry.chemical_compoundX-Ray DiffractionSpectroscopy Fourier Transform InfraredPressure[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyPhysical and Theoretical ChemistryFourier transform infrared spectroscopyZeoliteSilicatesWaterSilanes021001 nanoscience & nanotechnology0104 chemical sciencesSilanolchemistryChemical engineeringSiloxaneX-ray crystallographyZeolitesCrystallite0210 nano-technologyCrystallizationPhysical chemistry chemical physics : PCCP
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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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Novel pathways for the preparation of mesoporous MCM-41 materials: control of porosity and morphology

1999

Two novel synthesis routes for the preparation of mesoporous MCM-41 materials are introduced. Both methods use tetra-n-alkoxysilanes such as tetraethoxysilane (TEOS) or tetra-n-propoxysilane (TPS) as a silica source which are added to an aqueous solution of a cationic surfactant in the presence of ammonia as catalyst. In this study, n-alkyltrimethylammonium bromides and n-alkylpyridinium chlorides were employed as templates. The addition of an alcohol (e.g. ethanol or isopropanol) leads to a homogeneous system which allows the formation of spherical MCM-41 particles. The main advantages of these methods are short reaction times, excellent reproducibility and easy preparation of large batche…

Aqueous solutionStereochemistryChemistryCationic polymerizationGeneral ChemistryCondensed Matter PhysicsMolecular sieveCatalysisChemical engineeringMCM-41Mechanics of MaterialsGeneral Materials ScienceMesoporous materialZeolitePorosityMicroporous and Mesoporous Materials
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Sorption of argon and nitrogen on network types of zeolites and aluminophosphates

1991

Abstract Synthetic zeolites and aluminophosphates comprising 10- and 12- membered ring openings, unidimensional and network type of pore systems (MFI, MEL, ERI, LTA, AEL, AFI and FAU) were used as model adsorbents to examine the impact of micropore structure on the sorption properties. Argon and nitrogen were employed as adsorptives. Adsorption measurements were carried out on gravimetric and volumetric sorption devices and also monitored by microcalorimetry. From the low coverage regime of the isotherm Henry's constants and isosteric heats of adsorption were derived. Both quantities allowed the discrimination between 10- and 12- membered ring systems. Unidimensional 10- and 12- membered ri…

ArgonAdsorptionchemistryInorganic chemistryNeutron diffractionchemistry.chemical_elementPhysical chemistryGravimetric analysisSorptionMicroporous materialMolecular sieveNitrogen
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High Resolution Sorption Studies of Argon and Nitrogen on Large Crystals of Aluminophosphate AlPO4-5 AND ZEOLITE ZSM-5

1989

High resolution adsorption (HRADS) with argon and nitrogen at 77 K in the pressure range of 10−6 < p/p° < 0.5 were performed on large crystals of zeolite ZSM-5 (180 μm) and aluminophosphate AlPO4-5 (150 μm) using a novel volumetric device. Multi-step isotherms of both adsorptives on ZSM-5 could be observed for the first time. The adsorption followed by low temperature microcalorimetry resulted in distinct exothermic signals at the steps in the adsorption isotherms. Based on the results of atom-atom potential energy calculations (AAP) as well as independent model building it was shown that 24 ‘kinetic’ adsorbate molecules can be filled into a ZSM-5 unit cell. Experimental results are reasona…

ArgonChemistryInorganic chemistryAnalytical chemistrychemistry.chemical_elementLangmuir adsorption modelSorptionMolecular sieveNitrogensymbols.namesakeAdsorptionsymbolsZSM-5Zeolite
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Pore Size Analysis of MCM-41 Type Adsorbents by Means of Nitrogen and Argon Adsorption

1998

Methods of nonlocal density functional theory (NLDFT), proposed recently for predictions of adsorption equilibrium and calculations of pore size distributions in micro- and mesoporous materials, were tested on reference MCM-41 materials. Five newly synthesized MCM-41 adsorbents with presumably uniform pore channels varying from 32 to 45 Å were characterized by X-ray diffraction (XRD), nitrogen adsorption at 77 K, and argon adsorption at 77 and 87 K. New sets of intermolecular interaction parameters of the NLDFT model for N2 and Ar adsorption on MCM-41 were determined. The parameters were specified to reproduce the bulk liquid-gas equilibrium densities and pressures, liquid-gas interfacial t…

Capillary condensationNanoporousChemistryMineralogyThermodynamicsFlory–Huggins solution theoryMolecular sieveSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistryAdsorptionDesorptionZeoliteMesoporous materialJournal of Colloid and Interface Science
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