Search results for "Mole fraction"

showing 10 items of 62 documents

Formation of Laves phases in buoyancy matched hard sphere suspensions.

2018

Colloidal Laves phases (LPs) are promising precursors for photonic materials. Laves phases have not yet been observed to form in experiments on colloidal suspensions of hard spheres (HS), even though they have been reported in computer simulations. LP formation so far has been achieved only for binary mixtures of colloidal charged spheres or ligand-stabilized nano-particles after drying. Using static light scattering, we monitored LP formation and annealing in a binary mixture of buoyant hard sphere approximants (size ratio Γ = 0.77, number or molar fraction of small spheres xS = 0.76) for volume fractions in the fluid-crystal coexistence regions. All samples spontaneously formed MgZn2 type…

Materials scienceClose-packing of equal spheresNucleationThermodynamics02 engineering and technologyGeneral ChemistryHard spheres021001 nanoscience & nanotechnologyCondensed Matter PhysicsMole fraction01 natural sciencesColloid0103 physical sciencesVolume fractionSPHERESStatic light scattering010306 general physics0210 nano-technologySoft matter
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Oxidation of pentan-2-ol -Part II: Experimental and modeling study

2021

International audience; The oxidation of pentan-2-ol was investigated at high-pressure in a jet-stirred reactor and in a shock tube. Experiments in the JSR were carried out at 10 atm, between 500-1180 K, for five different equivalence ratios of = 0.35, 0.5, 1, 2, 4 and 1000 ppm of fuel, at a constant residence time of 0.7 s. Reactant, product and intermediate species mole fractions were quantified using Fourier transform infrared spectrometry (FTIR) and gas chromatography (GC). Ignition delay times were measured for pentan-2-ol/O 2 mixtures in argon in a shock tube at 20 and 40 bar, in a temperature range of 1070-1460 K and for equivalence ratios of = 0.5, 1 and 2. Ignition delay times of a…

Materials scienceGeneral Chemical Engineeringpentan-2-olAnalytical chemistrychemistry.chemical_element02 engineering and technologyshock tube010402 general chemistryMole fraction01 natural sciences020401 chemical engineeringAb initio quantum chemistry methods0204 chemical engineeringPhysical and Theoretical ChemistryFourier transform infrared spectroscopyShock tubeArgonMechanical Engineering[SPI.FLUID]Engineering Sciences [physics]/Reactive fluid environmentdetailed mechanismAtmospheric temperature rangebiofuels0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistrykineticsjet-stirred reactorGas chromatographyStoichiometry
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Temperature and pressure dependence of quercetin-3-O-palmitate interaction with a model phospholipid membrane: film balance and scanning probe micros…

2004

The molecular interaction of quercetin-3-O-palmitate (QP) with dimyristoylphosphatidylcholine (DMPC) has been studied. Film balance measurements of the average molecular area vs QP molar fraction in DMPC/QP mixed monolayers showed that relevant positive deviations from ideality, i.e., a less dense monolayer packing, occurred for a temperature of 10 degrees C, below the critical melting transition temperature of DMPC monolayers T c m approximately equal 20 degrees C), while ideal behavior was observed at 37 degrees C, above this phase transition temperature. The positive deviation observed at low temperatures in the average molecular area increased with the surface pressure. Scanning probe m…

Membrane FluiditySurface PropertiesLipid BilayersAnalytical chemistryPhospholipidPalmitic AcidPhase separationPalmitic AcidsSurface pressureMole fractionMicroscopy Atomic ForcePhase TransitionBiomaterialsScanning probe microscopychemistry.chemical_compoundMembrane LipidsColloid and Surface ChemistryMonolayerLangmuir-Blodgett monolayersMolecular StructureTransition temperatureTemperatureQuercetin palmitateSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsLangmuir–Blodgett monolayerMembranechemistryAluminum SilicatesQuercetinMicaStress MechanicalDimyristoylphosphatidylcholineAlgorithmsScanning force microscopy
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Dynamical Properties of Self-Assembled Surfactant-Based Mixtures: Triggering of One-Dimensional Anomalous Diffusion in Bis(2-ethylhexyl)phosphoric Ac…

2013

The dynamic features of bis(2-ethylhexyl)phosphoric acid (HDEHP)/n-octylamine (NOA) mixtures have been investigated as a function of the NOA mole fraction and temperature by (1)H NMR spectroscopy and rheometry. All data consistently suggest a composition-induced glass-forming behavior. The microscopic factors responsible for this behavior have been highlighted and have been explained in terms of driving forces given by HDEHP-to-NOA proton transfer, the tendency of the resulting species to establish H bonds and to spatially segregate the alkyl chains. The study sheds light on the molecular mechanism responsible for the peculiar behavior of transport properties in such systems and furnishes b…

Models Molecularsurfactant mixtures self-assembly dynamical propertiesProtonAnomalous diffusionMole fractionSelf assembledDiffusionSurface-Active Agentschemistry.chemical_compoundPulmonary surfactantElectrochemistryOrganic chemistryGeneral Materials ScienceAminesPhosphoric acidSpectroscopyAlkylSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationMolecular StructureRheometryChemistrySurfaces and InterfacesCondensed Matter PhysicsOrganophosphatesThermodynamicsPhysical chemistryRheologyLangmuir
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Volumes and heat capacities of anionic-nonionic surfactant mixtures

1995

Density, heat capacity and surface tension measurements of sodium decylsulfate (NaDeS)-dodecyldimethylamine oxide (DDAO)-water mixtures were carried out as functions of the surfactants total molality mt at fixed stoichiometric mixture compositions XNaDeS. From the surface tension data, the critical micelle concentration of NaDeS-DDAO mixtures as a function of XNaDeS were obtained. From density and heat capacity data, the apparent molar volume VΦ,2 and heat capacity CΦ,2 of NaDeS-DDAO mixtures in water were calculated, respectively. At a given mole fraction, VΦ,2 and CΦ,2 monotonically increases and decreases, respectively, with increasing mt. However, anomalies were observed at XNaDeS=0.1 a…

MolalityAqueous solutionChromatographyChemistryBiophysicsThermodynamicsMole fractionBiochemistryHeat capacityMicelleSurface tensionMolar volumeCritical micelle concentrationPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Demixing of Mixed Micelles. Thermodynamics of Sodium Perfluorooctanoate−Sodium Dodecanoate Mixtures in Water

1997

Conductivity, density, heat capacity, enthalpy of dilution, and osmotic coefficient measurements of water−sodium perfluorooctanoate (NaPFO)−sodium dodecanoate systems were carried out as functions of the surfactants' total molality (mt) at different mole fractions (XNaPFO). From conductivity data, the critical micelle concentration (cmc) and the degree of ionization (β) of the micelles were derived. The cmc's of the micelles are higher than those of the pure surfactants while β depends linearly on XNaPFO. At a given mole fraction, the apparent molar volume (VΦ) and heat capacity (CΦ) of the mixture increases and decreases monotonically with mt, respectively. From data in the premicellar reg…

MolalityChemistryThermodynamicsPartial molar propertySurfaces and InterfacesCondensed Matter PhysicsMole fractionHeat capacityMicelleMolar volumeCritical micelle concentrationElectrochemistryGeneral Materials ScienceOsmotic coefficientSpectroscopyLangmuir
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Thermodynamic Studies of Sodium Dodecyl Sulfate–Sodium Dodecanoate Mixtures in Water

1996

Abstract Conductivity, density, heat capacity, enthalpy of dilution, and osmotic coefficient measurements of water–sodium dodecyl sulfate (NaDS)–sodium dodecanoate systems were carried out as functions of the surfactants total molality ( m t ) at different mole fractions ( X NaDS ). From conductivity data, the critical micelle concentration (cmc) and the degree of ionization of the micelles (β) were calculated. The cmc vs X NaDS profile deviates negatively from that predicted on the basis of the Clint approach, while the β vs X NaDS profile deviates positively from the line correlating the values for pure surfactants. At a given mole fraction, the profiles of all the investigated properties…

MolalitySodiumEnthalpyInorganic chemistryAnalytical chemistrychemistry.chemical_elementMole fractionMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryCritical micelle concentrationOsmotic coefficientSodium dodecyl sulfateJournal of Colloid and Interface Science
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A study of the refractive index and surface tension synergy of the binary water/ethanol: influence of concentration

2005

Pure alcohols or alcohols mixed with water are the most widely used solvents in a great variety of industrial applications, including the formulation of pharmaceutical and cosmetic products. As a result of water/alcohol molecular associations, variations result in the physico-chemical characteristics of the system, such as density, viscosity, refractive index and surface tension. The present study investigates the refractive index and the surface tension of ethanol and water mixtures at a temperature of 25°C, for different molar fractions. The data obtained allow us to study the corresponding refractive index and the surface tension synergies; in this sense, an absolute maximum refractive i…

MolarEthanolChromatographyAnalytical chemistryBinary numberAlcoholCondensed Matter PhysicsMole fractionElectronic Optical and Magnetic MaterialsSurface tensionchemistry.chemical_compoundViscositychemistryMaterials ChemistryPhysical and Theoretical ChemistryRefractive indexPhysics and Chemistry of Liquids
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Emissions and spatial variability of N2O, N2 and nitrous oxide mole fraction at the field scale, revealed with 15N isotopic techniques.

2006

Abstract The accurate measurement of nitrous oxide (N 2 O) and dinitrogen (N 2 ) during the denitrification process in soils is a challenge which will help to estimate the contribution of soil N 2 O emissions to global warming. Oxygen concentration, nitrate concentration and carbon availability are generally the main factors that control soil denitrification rate and the amount of N 2 O or N 2 emitted. The aim of this paper is to present a database of the N 2 O mole fraction measured at the field scale, and to test hypotheses concerning its regulation. A 15 N-nitrate tracer solution was added to 36 undisturbed soil cores on a 20 m×20 m cultivated field plot. Fluxes of CO 2 , N 2 O and N 2 f…

Mole fractionDenitrificationDinitrogen[SDE.MCG]Environmental Sciences/Global ChangesSoil Sciencechemistry.chemical_elementMole fractionMicrobiologySpatial variabilitychemistry.chemical_compoundNitrate[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/Geochemistry[ SDU.ENVI ] Sciences of the Universe [physics]/Continental interfaces environment[SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces environmentWater contentSpatial dependenceNitrous oxideEcology15NNitrous oxide[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/Geochemistryequipment and suppliesNitrogen[ SDE.MCG ] Environmental Sciences/Global ChangeschemistryEnvironmental chemistrySoil waterDenitrificationLimiting oxygen concentration
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Nano-demixing as a novel strategy for magnetic field responsive systems: the case of dibutyl phosphate/bis(2-ethylhexyl)amine systems

2016

Pure surfactant liquids and their binary mixtures, owing to the amphiphilic nature of the molecules involved, can exhibit nano-segregation and peculiar transport properties. The possibility of opportunely choosing the amphiphiles should lead to the formation of anisotropic aggregates that can be oriented by an external factor like a magnetic field. In this case some properties, like optical birefringence, can be induced by the use of a magnetic field. Dynamic features of dibutyl phosphate (DBP)/bis(2-ethylhexyl)amine (BEEA) mixtures have been investigated by FT-IR, NMR, rheometry, Brillouin scattering, and magnetically-induced birefringence measurements as a function of the BEEA mole fracti…

Molecular diffusionsurfactant mixtures nanodemixingBirefringenceRheometryChemistryGeneral Chemical Engineering02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyMole fraction01 natural sciencesMicelle0104 chemical sciencesChemical physicsAmphiphilePolarOrganic chemistryMolecule0210 nano-technologySettore CHIM/02 - Chimica Fisica
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