Search results for "Adsorption"

showing 10 items of 1326 documents

Hydration of calcium sulfate hemihydrate (CaSO4·H2O) into gypsum (CaSO4·2H2O). The influence of the sodium poly(acrylate)/surface interaction and mol…

2000

Abstract The retarding influence of sodium poly(acrylate) (PANa) on the hydration of calcium sulfate hemihydrate (CaSO 4 · 1 2 H 2 O) was investigated. This study reports the influence of sodium poly(acrylate) on hemihydrate dissolution, on homogenous and heterogeneous gypsum (CaSO 4 ·2H 2 O) nucleation as well as on gypsum growth. It is shown that adsorption of PANa does not hinder the dissolution of hemihydrate in the present experimental conditions. The specific interaction of PANa with gypsum can explain the oriented growth of gypsum crystal. The gypsum growth is slowed down but cannot be blocked by the adsorption of PANa. On the other hand, PANa can block the heterogeneous and homogeno…

AcrylateGypsumPrecipitation (chemistry)SodiumInorganic chemistryNucleationchemistry.chemical_elementengineering.materialCondensed Matter PhysicsInorganic Chemistrychemistry.chemical_compoundAdsorptionchemistryMaterials ChemistryengineeringHydrateDissolutionJournal of Crystal Growth
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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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Calculation of the chemical potential and the activity coefficient of two layers of CO2 adsorbed on a graphite surface.

2014

We study the adsorption of carbon dioxide at a graphite surface using the new Small System Method, and find that for the temperature range between 300 K and 550 K most relevant for CO2 separation; adsorption takes place in two distinct thermodynamic layers defined according to Gibbs. We calculate the chemical potential and the activity coefficient of both layers directly from the simulations. Based on thermodynamic relations, the entropy and enthalpy of the CO2 adsorbed layers are also obtained. Their values indicate that there is a trade-off between entropy and enthalpy when a molecule chooses for one of the two layers. The first layer is a densely packed monolayer of relatively constant e…

Activity coefficientEntropy (classical thermodynamics)AdsorptionFundamental thermodynamic relationChemistryMonolayerEnthalpyGeneral Physics and AstronomyThermodynamicsGraphitePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtmospheric temperature rangePhysical chemistry chemical physics : PCCP
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Binding of a fluorescent dansylcadaverine-substance P analogue to negatively charged phospholipid membranes.

2000

Abstract We have investigated the binding of a new dansylcadaverine derivative of substance P (DNC-SP) with negatively charged small unilamellar vesicles composed of a mixture of phosphatidylcholine (PC) and either phosphatidylglycerol (PG) or phosphatidylserine (PS) using fluorescence spectroscopic techniques. The changes in fluorescence properties were used to obtain association isotherms at variable membrane negative charges and at different ionic strengths. The experimental association isotherms were analyzed using two binding approaches: (i) the Langmuir adsorption isotherm and the partition equilibrium model, that neglect the activity coefficients; and (ii) the partition equilibrium m…

Activity coefficientVesicleLipid BilayersAnalytical chemistryLangmuir adsorption modelCharge densityGeneral MedicineSubstance PBiochemistryBinding constantFluorescencechemistry.chemical_compoundsymbols.namesakeMembranechemistryModels ChemicalStructural BiologyPhosphatidylcholinePartition equilibriumCadaverinesymbolsMolecular BiologyPhospholipidsFluorescent DyesProtein BindingInternational journal of biological macromolecules
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Interpretive search of optimal isocratic and gradient separations in micellar liquid chromatography in extended organic solvent domains

2020

Abstract Micellar liquid chromatography (MLC) is a reversed-phase mode with mobile phases containing an organic solvent and a micellised surfactant. Most procedures developed in MLC are implemented in the isocratic mode, since the general elution problem in chromatography is less troublesome. However, gradient elution may be still useful in MLC to analyse mixtures of compounds within a wide range of polarities, in shorter times. MLC using gradients is attractive to determine by direct injection moderate to low polar compounds in physiological samples. In these analyses, the use of initial micellar conditions (isocratic or gradient) with a fixed amount of surfactant above the critical micell…

Adrenergic beta-Antagonists1-Propanol010402 general chemistry01 natural sciencesBiochemistryMicelleChemistry Techniques AnalyticalAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantHumansMicellesChromatographyElutionChemistryChemical polarity010401 analytical chemistryOrganic ChemistrySodium Dodecyl SulfateGeneral Medicine0104 chemical sciencesSolventMicellar liquid chromatographyCritical micelle concentrationSolventsIndicators and ReagentsAdsorptionChromatography LiquidJournal of Chromatography A
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Role of Electrical Charges on the Adsorption of Hydrogen: Something Old, Something New.

2022

The adsorption of H2 in zeolites by molecular simulations use, in many applications, single sphere model. Although this representation provides coherent results with ex- periments above 77K, below this temperature the usual hydrogen representation fails to reproduce experimental results. The disagreement can be associated to the interplay of the atomistic heterogeneity and the electric field produced by the zeolite faujasite. These aspects are generally excluded in classical force fields. For elucidating the influ- ence of these issues, we performed DFT simulations for the faujasite Na86X at 40K with and without guest hydrogen molecules for determining the electrical field generated by the …

Adsorption Isotherm[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistrydynamique moléculaireDFT
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Specific separation and recovery of phosphate anions by a novel NiFe-LDH/rGO hybrid film based on electroactivity-variable valence

2022

Phosphorus is a non-renewable resource. Supplies are limited and much phosphorus is currently wasted during the production and utilization process, causing concerns about future supplies and widespread environmental problems. To solve these problems, a new type of NiFe-LDH/rGO electrically switched ion-selective (ESIX) film is designed, based on the dominant mechanism of inner-sphere complexation. An ESIX process allows the NiFe-LDH/rGO hybrid film to achieve a controllably selective uptake and release of the phosphate anions. This route involves tuning potential steps to regulate the redox states of the composite film and the variable metal (e.g., Ni, Fe (II)/(III)) in coordination centers…

Adsorption capacityPhosphorusInner-sphere complexationSettore ING-IND/27 - Chimica Industriale E TecnologicaPhosphatesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistryValence state transitionSelective extractionMetalsLayered double hydroxideHydroxidesGraphitePhosphate anion
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Preparation and characterization of bio-organoclays using nonionic surfactant

2015

The present study was aimed at the preparation and characterization of tailor made hybrid materials, whose peculiar hosting capability could be exploited in biotechnological applications. With this purpose, the modification of K10 montmorillonite by intercalation of Tween 20 surfactant, was accomplished. The influence of two internal parameters, namely pH and surfactant/clay ratio, on the surfactant uptake ability by clay was investigated. The adsorption mechanism was elucidated on the basis of complementary kinetic and equilibrium studies and, then, corroborated by the useful information provided by the FT-IR, TGA and XRD characterization. The gathered results allow to draw the conclusion …

Adsorption kineticGeneral Chemical EngineeringIntercalation (chemistry)Drug delivery systemTween 20Dual mode model02 engineering and technology010402 general chemistrycomplex mixtures01 natural scienceschemistry.chemical_compoundAdsorptionPulmonary surfactantOrganic chemistryNonionic surfactantChemical Engineering (all)MontmorilloniteOrgano-clayIsothermHydrophobic drugChemistry (all)Surfaces and InterfacesGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCharacterization (materials science)MontmorillonitechemistryChemical engineering0210 nano-technologyHybrid materialSurfaces and Interface
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General application of Jäntti's method for the fast calculation of sorption equilibrium

2004

On the basis of a molecular model for adsorption kinetics Jantti introduced a method to calculate equilibriums shortly after a change of the pressure of the sorptive gas. In the present paper we show that this method is useful in many more situations than those intended originally.

Adsorption kineticsMolecular modelChemistryKineticsThermodynamicsAdsorption equilibriumSorptionPhysical and Theoretical ChemistryCondensed Matter PhysicsThermal analysis
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Dry adsorbed emulsion: 1. Characterization of an intricate physicochemical structure

2000

Abstract A recent solid pharmaceutical form called “Dry Adsorbed Emulsion” (DAE) was characterized in morphological and structural fields. A DAE is an intricate system initiated by a water‐in‐oil emulsion including the active drug (i.e., theophylline). Each emulsion phase is adsorbed on pulverulent adsorbents with a suitable polarity (silica) to obtain a free‐flowing powder with nonporous particles of size from 125 to 710 μm, with small specific surface area and a spherical shape. Different methods, such as scanning electron microscopy combined with chemical microanalysis, dying tests, and electron spin resonance studies, allow the formulator to follow the behavior of DAE aqueous and oily p…

AdsorptionAqueous solutionChemical engineeringStereochemistryChemistryPhase (matter)Specific surface areaEmulsionPharmaceutical ScienceParticle sizeMicroanalysisDosage formJournal of Pharmaceutical Sciences
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