Search results for "Surfaces"

showing 10 items of 2837 documents

Mass Action Model Applied to the Thermodynamic Properties of Transfer of Nonionic Copolymers from Water to the Aqueous Surfactant Solutions

2003

A thermodynamic model which enables the properties of aqueous copolymer/surfactant mixtures to be fit quantitatively was proposed. Namely, a relationship between the properties of transfer of the unassociated copolymer from water to the aqueous surfactant solutions (DeltaY(t)) and the surfactant concentration was derived. The model was based on the idea that AY, can be expressed in terms of the following contributions: (1) interaction between monomers of copolymer and surfactant, (2) displacement of the monomer-micelle equilibrium induced by the copolymer, (3) formation of the surfactant-copolymer aggregation complex, and (4) formation of the mixed micelles. Such a model was applied to most…

Aqueous solutionChemistryInorganic chemistrySurfaces Coatings and FilmsCondensed Matter::Soft Condensed MatterThermodynamic modelPulmonary surfactantChemical engineeringMaterials ChemistryCopolymerPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAction modelPolyethylene oxides Micelles scattering DLSThe Journal of Physical Chemistry B
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Kinetic and Mechanistic Aspects of a Poly(o-Toluidine)-Modified Gold Electrode. 2. Alternating Current Electrogravimetry Study in H2SO4 Solutions

2012

International audience; Electrodeposited poly(o-toluidine) (POT) on gold electrodes was investigated in 0.5 M H2SO4 aqueous solutions using alternating current electrogravimetry (simultaneous electrochemical impedance and mass transfer functions). The kinetic aspects of the three different redox transitions proposed for this polymer (leucoemeraldine-polaron transition, polaron-bipolaron transition, and bipolaron-pernigraniline transition) and the species involved, cation (hydrated proton), anion (bisulfate ion), and free solvent (water), are studied by means of the mass impedance technique. An ionic transfer model is proposed with coherent results where anion transfer is the fastest process…

Aqueous solutionChemistryIonic transferInorganic chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesRedox0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonGeneral EnergyElectrogravimetryMass transfer[CHIM]Chemical SciencesGrotthuss mechanismPhysical and Theoretical Chemistry0210 nano-technology[CHIM.OTHE]Chemical Sciences/Other
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Mößbauer- und ESCA-Untersuchungen zur Bildung oxidischer Eisenphasen in wäßrigen Medien unter der Einwirkung organischer Korrosionsinhibitoren

1982

Korrosionsschichten auf Stahl nach Exposition in Wasser mit bestimmter Harte und Chloridgehalt wurden hinsichtlich der Wirksamkeit beigefugter organischer Inhibitoren mittels Mosbauer- und ESCA-Spektroskopie untersucht. Es entstehen relativ dicke Schichten mit einem unerwartet niedrigen Eisengehalt in Form von FeOOH. Die Schichten enthalten merkliche Mengen von Ionen aus der Testlosung und auch Abbauprodukte der Inhibitormolekule. Letztere werden anscheinend in dem korrosiven Medium zersetzt. Es ist anzunehmen, das das Gesamtmolekul zwar den Transport des Inhibitors zum Metall beeinflust, die eigentliche Inhibierung aber allein durch funktionelle Gruppen erfolgt. Mossbauer and ESCA investig…

Aqueous solutionChemistryMechanical EngineeringMetals and AlloysGeneral MedicineChlorideSurfaces Coatings and FilmsMechanics of MaterialsIron metalPolymer chemistryIron contentMössbauer spectroscopyMaterials ChemistrymedicineEnvironmental Chemistrymedicine.drugMaterials and Corrosion
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Extended Investigation of the Aqueous Self-Assembling Behavior of a Newly Designed Fluorinated Surfactant

2009

The physicochemical behavior of the newly synthesized fluorinated 5-hydroxyamino-3-perfluoroheptyl-1,2,4-oxadiazin-6-one (PFHO) surfactant was investigated. Thermal analysis showed that the pure surfactant is thermally stable under an inert atmosphere to 135 degrees C, which is several degrees higher than the melting point (99 degrees C). PFHO is rather active at the water/air interface where it assumes a standing up configuration. It exhibits an enhanced self-assembling behavior; accordingly, the critical micellar concentrations at some temperatures are 2 orders of magnitude lower than those of a similar surfactant having the same phobicity, such as sodium perfluorooctanoate. Even in the d…

Aqueous solutionChromatographyChemistrySurfaces and InterfacesCondensed Matter PhysicsMicelleViscosityDifferential scanning calorimetryPulmonary surfactantDynamic light scatteringChemical engineeringElectrochemistryMelting pointGeneral Materials ScienceThermal analysisSpectroscopyFluorinated Surfactant thermodynamic micelle gel
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On the Existence of Different Zeolite-Associated Topological Redox Isomers. Electrochemistry of the Y Zeolite-Associated Mn(Salen)N3 Complex

2002

The electrochemical properties of Y zeolite-associated MnIII(salen)N3 (salen = trans-(R,R)-1,2-bis(salicyldeneamino)cyclohexane) has been investigated using polymer film electrodes immersed into neutral aqueous solutions. Zeolite Y-associated Mn(III)−salen complexes are reduced in one-electron reversible process at −0.25 V versus SCE. The electrochemical response is discussed in terms of the existence of two topological redox isomers:  a weakly boundary-associated Mn(salen) complex, whose electrochemical response corresponds to a reversible one-electron transfer controlled by diffusion of the positive ions of the supporting electrolyte through the zeolite surface windows and channels, and a…

Aqueous solutionCyclohexaneSupporting electrolyteInorganic chemistryReversible processTopologyElectrochemistryRedoxSurfaces Coatings and Filmschemistry.chemical_compoundchemistryMetal salen complexesMaterials ChemistryPhysical and Theoretical ChemistryZeoliteThe Journal of Physical Chemistry B
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A thermodynamic study to evidence the alpha,omega-dichloroalkane/ block copolymer mixed aggregates formation: effect of the copolymer architecture.

2006

Abstract The thermodynamics of α , ω -dichloroalkanes in aqueous solutions of (ethylene oxide)11(propylene oxide)16(ethylene oxide)11 (L35) and (propylene oxide)8(ethylene oxide)23(propylene oxide)8 (10R5) was determined at 298 and 305 K. Modeling the experimental data allowed to calculate the standard free energy ( Δ G D o / w ) and the volume ( Δ V D / w ) for the additive–copolymer mixed aggregates formation per additive molecule. Δ G D o / w for Cl2CH2 and Cl2(CH2)2 evidenced that the process is controlled by the forces exercising between the chlorine atoms and the OH groups of the copolymer micelles protruded into the aqueous phase. Cl2(CH2)3 experiences both the hydrophilic and hydrop…

Aqueous solutionEthylene oxideEthylene oxide)11(propylene oxide)16(ethylene oxide)11TemperatureAqueous two-phase systemMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGibbs free energyBiomaterialsHydrophobic effectsymbols.namesakechemistry.chemical_compoundColloid and Surface Chemistrychemistry(Propylene oxide)8(ethylene oxide)23(propylene oxide)8-DichloroalkanePolymer chemistryCopolymersymbolsStandard free energyPhysical chemistryPropylene oxideJournal of colloid and interface science
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Binding between (Ethylene Oxide)13−(Propylene Oxide)30−(Ethylene Oxide)13 and Sodium Decanoate. Volume, Enthalpy, and Heat Capacity Studies

2002

Volume, enthalpy, and heat capacity of transfer (ΔYt) of (ethylene oxide)13−(propylene oxide)30−(ethylene oxide)13 (L64), at some concentrations, from water to the aqueous sodium decanoate (NaDec) solutions as functions of the surfactant concentration (mS) were determined at 298 K. The copolymer was studied in both the unassociated and associated forms. For a given L64 concentration (mC), the ΔYt vs mS profiles for the volume and the enthalpy are equal but different from that of the heat capacity because the latter contains also the relaxation terms. The experimental data were analyzed by assuming the distribution of L64 between the aqueous and the micellar phases and the shift of micelliza…

Aqueous solutionEthylene oxideInorganic chemistryEnthalpyFlory–Huggins solution theoryMicelleHeat capacityBinding constantSurfaces Coatings and Filmschemistry.chemical_compoundchemistryMaterials ChemistryPropylene oxidePhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Heat Capacity of Transfer of (Ethylene oxide)13-(propylene oxide)30-(ethylene oxide)13 from Water to the Aqueous Anionic Surfactant Solutions at 298 …

2004

Heat capacities of transfer (ACpt) of unimeric (ethylene oxide)(13)-(propylene oxide)(30)-(ethylene oxide)(13) from water to the aqueous surfactant solutions as functions of the surfactant concentrations (m(S)) were determined at 298 K. The surfactants investigated are sodium hexanoate, sodium heptanoate, sodium octanoate, sodium undecanoate, and sodium dodecanoate. For short alkyl chain surfactants, the profiles of the DeltaCp(t) versus ms curves show maxima and minima; for long alkyl chain surfactants, the maximum becomes sharper and moved to lower ms values whereas the minimum tends to disappear. These experimental trends are different from those of the enthalpy in agreement with the fac…

Aqueous solutionEthylene oxideSodiumInorganic chemistryEnthalpychemistry.chemical_elementThermodynamicsSurfaces and InterfacesCondensed Matter PhysicsHeat capacityGibbs free energysymbols.namesakechemistry.chemical_compoundchemistryPulmonary surfactantElectrochemistrysymbolsGeneral Materials SciencePolyethylene oxides Micelles scattering DLSSpectroscopyEquilibrium constant
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Aqueous nonionic copolymer-functionalized laponite clay. A thermodynamic and spectrophotometric study to characterize its behavior toward an organic …

2006

The affinity of functionalized Laponite clay toward an organic material in the aqueous phase was explored. Functionalization was performed by using triblock copolymers based on ethylene oxide (EO) and propylene oxide (PO) units that are EO(11)PO(16)EO(11) (L35) and PO(8)EO(23)PO(8) (10R5). Phenol (PhOH) was chosen as organic compound, which represents a contaminant prototype. To this purpose, densities and enthalpies of mixing as well as PhOH UV-absorption spectra were determined. The enthalpy and the spectrophotometry revealed PhOH-Laponite interactions whereas the volume did not. It emerged that the area occupied by PhOH on the Laponite surface is equal to that computed from the partial m…

Aqueous solutionEthylene oxideSuspensions (fluids)Aqueous two-phase systemPartial molar propertySurfaces and InterfacesCondensed Matter Physicsyield stresschemistry.chemical_compoundAdsorptionchemistryChemical engineeringPolymer chemistryBentoniteElectrochemistryCopolymerSurface modificationGeneral Materials SciencePropylene oxideSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Aqueous block copolymer-surfactant mixtures and their ability in solubilizing chlorinated organic compounds. A thermodynamic and SANS study.

2006

Within the topic of surfactant enhanced solubilization of additives sparingly soluble in water, volumetric, solubility, conductivity, and small-angle neutron scattering (SANS) experiments on mixtures composed of alpha,omega-dichloroalkane, surfactant, copolymer, and water were carried out at 298 K. The triblock copolymers (ethylene oxide)132(propylene oxide)50(ethylene oxide)132 (F108) and (ethylene oxide)76(propylene oxide)29(ethylene oxide)76 (F68) were chosen to investigate the role of the molecular weight keeping constant the hydrophilic/hydrophobic ratio. The selected surfactants are sodium decanoate (NaDec) and decyltrimethylammonium bromide (DeTAB) with comparable hydrophobicity and …

Aqueous solutionEthylene oxidescattering DLSConductivitySurfaces Coatings and Films| Micelleschemistry.chemical_compoundMonomerchemistryPulmonary surfactantChemical engineeringPolymer chemistryMaterials ChemistryCopolymerPropylene oxidePolyethylene oxidePhysical and Theoretical ChemistrySolubilityThe journal of physical chemistry. B
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