Search results for " Films"

showing 10 items of 2599 documents

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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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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Quantitative XPS analysis of leached layers on optical glasses

1993

The corrosion of optical glasses often reduces the utility of uncoated glasses as well as the adhesion of resistive coatings deposited onto corroded glasses. Photoelectron spectroscopy (XPS) was applied to study glass surfaces with respect to their surface corrosion. In particular, leaching by the influence of polish slurries, pure water, air and even residual gases inside a vacuum device was studied in detail. Pure quartz glass and different sodium and barium silicate glasses were broken in ultrahigh vacuum (4 × 10−10 mbar) for the determination of sensitivity factors of the different XPS signals. It was found that a quantitative determination of the surface composition of corroded and lea…

Aqueous solutionHydrogenAnalytical chemistryAttenuation lengthchemistry.chemical_elementMineralogyBariumSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCorrosionchemistryX-ray photoelectron spectroscopyMaterials ChemistryLeaching (metallurgy)QuartzSurface and Interface Analysis
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Solubilization of an Organic Solute in Aqueous Solutions of Unimeric Block Copolymers and Their Mixtures with Monomeric Surfactant: Volume, Surface T…

2008

The ability of aqueous systems, formed by unimeric copolymers and their mixtures with a monomeric surfactant, in solubilizing large quantities of 1-nitropropane (PrNO2) was explored. The copolymers are F68 and L64, which differ for the hydrophilicity, and the surfactant is sodium dodecanoate. For a better understanding of the mechanism of solubilization, thermodynamic (volume and differential scanning calorimetry), spectroscopy (steady-state fluorescence), viscosity, and interfacial investigations were carried out. PrNO2 causes the micellization of the unimeric copolymer, and the required amount of PrNO2 depends on the composition, the copolymer nature, and the temperature. Large quantities…

Aqueous solutionISOTHERMAL TITRATION CALORIMETRYChemistryMICELLAR SYSTEMSDYNAMIC LIGHT-SCATTERINGIONIC SURFACTANTSTRIBLOCK COPOLYMERSMicelleFluorescence spectroscopySurfaces Coatings and FilmsSurface tensionViscosityDifferential scanning calorimetryAGGREGATION BEHAVIORPulmonary surfactantChemical engineeringMIXED MICELLESPolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistrySODIUM DODECYL-SULFATEOXIDE)(13)-(PROPYLENE OXIDE)(30)-(ETHYLENE OXIDE)(13)GEMINI SURFACTANTS
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Thermodynamics of Solubilization of Pentanol in Sodium Dodecyl Sulfate-Dodecyldimethylamine Oxide Mixed Micelles

1994

Abstract Heat capacity and density measurements of pentanol (PeOH)-sodium dodecyl sulfate (NaDS)-dodecyldimethylamine oxide-water mixtures were carried out at 0.03 m PeOH as a function of the total surfactants concentration (mc) at different ratios (XNaDS). From experimental data, the apparent molar volumes (VΦ,R) and heat capacities (CΦ,R) of PeOH in the surfactants mixture solutions were calculated. As a general feature, at a given mixture composition, VΦ,R increases monotonically with mt as observed in pure surfactants. In the cases of XNaDS = 0.1 and 0.3, VΦ,R drops at about 0.1 and 0.15 mt respectively. The decreasing CΦ,R VS mt curve shows peculiarities which were ascribed to the pres…

Aqueous solutionInorganic chemistryDistribution constantAnalytical chemistryPartial molar propertyHeat capacityApparent molar propertySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGibbs free energyBiomaterialschemistry.chemical_compoundsymbols.namesakeColloid and Surface ChemistrychemistrysymbolsSodium dodecyl sulfateSolubilityJournal of Colloid and Interface Science
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Study of Redox Processes in Zeolite Y-Associated 2,4,6-Triphenylthiopyrylium Ion by Square Wave Voltammetry

2003

The electrochemical responses of 2,4,6-triphenylthiopyrylium ion (TTP+) in solution and attached to zeolite Y (TTP@Y) are described using cyclic and square wave voltammetries upon immersion of zeolite-modified polymer film electrodes in MeCN (LiClO4, Et4NClO4, and BuN4PF6 electrolytes) and aqueous (LiNO3, NaNO3, and KNO3 electrolytes) media. The electrochemistry of TTP@Y in contact with Bu4NPF6/MeCN is identical to that of TTP(BF4) in solution, with reduction processes at −0.25, −0.74, and −1.36 V vs SCE, and oxidation steps at +0.85 and +1.11 V. This response differs from those obtained for TTP@Y in Et4NClO4/MeCN and LiClO4/MeCN electrolytes. In contact with aqueous electrolytes, TTP@Y dis…

Aqueous solutionInorganic chemistrychemistry.chemical_elementSquare waveElectrolyteElectrochemistryRedoxSurfaces Coatings and FilmsIonchemistryElectrodeMaterials ChemistryPhysical and Theoretical ChemistryPlatinumThe Journal of Physical Chemistry B
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Ab Initio Liquid Water Dynamics in Aqueous TMAO Solution

2015

Ab initio molecular dynamics (AIMD) simulations in trimethylamine N-oxide (TMAO)-D2O solution are employed to elucidate the effects of TMAO on the reorientational dynamics of D2O molecules. By decomposing the O-D groups of the D2O molecules into specific subensembles, we reveal that water reorientational dynamics are retarded considerably in the vicinity of the hydrophilic TMAO oxygen (O(TMAO)) atom, due to the O-D···O(TMAO) hydrogen-bond. We find that this reorientational motion is governed by two distinct mechanisms: The O-D group rotates (1) after breaking the O-D···O(TMAO) hydrogen-bond, or (2) together with the TMAO molecule while keeping this hydrogen-bond intact. While the orientatio…

Aqueous solutionLiquid waterAb initioTrimethylamineRadial distributionForce field (chemistry)Surfaces Coatings and FilmsAb initio molecular dynamicschemistry.chemical_compoundchemistryComputational chemistryChemical physicsMaterials ChemistryMoleculePhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Fabrication of metal nano-structures using anodic alumina membranes grown in phosphoric acid solution: Tailoring template morphology

2007

Abstract The influence of experimental parameters on the morphology of the porous structure and on the formation kinetics has been investigated for anodic alumina membranes (AAM) grown in aqueous H 3 PO 4 at 160 V. It was found that pore aspect ratio and membrane porosity on the solution-side surface are influenced by tensiostatic charge, bath temperature and the presence of Al 3+ ions in solution. Morphological and kinetic data, recorded in different conditions, give useful information on the growth mechanism of pore channels in phosphoric acid solution. Nickel nano-structures have been fabricated using AAM as template. Electroless deposition, performed by adding the reducing agent to a su…

Aqueous solutionMaterials scienceMetal ions in aqueous solutionNanowireGeneral Physics and AstronomyAlumina membraneNanotechnologySurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsNanowirechemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicataMembraneElectrodepositionChemical engineeringchemistryTransition metalNickelNano-PorosityPhosphoric acidApplied Surface Science
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