Search results for "Faces"

showing 10 items of 3167 documents

Volumes of Polar Additives in Aqueous Solutions of the Poly(ethylene oxide)13−Poly(propylene oxide)30− Poly(ethylene oxide)13 Triblock Copolymer at 2…

1999

Density measurements of poly(ethylene oxide)13−poly(propylene oxide)30−poly(ethylene oxide)13 (L64)−water and alcohol−L64−water systems were carried out at 293 and 301 K. The alcohols studied are propanol to pentanol and 2,2,2-trifluoroethanol (F3EtOH) to 2,2,3,3,4,4,4-heptafluorobutanol (F7BuOH). From the experimental data of the water−L64 binary system as functions of L64 concentration (mC), the partial molar volumes of L64 in the standard state and in the aqueous and micellar phases were calculated. At both temperatures L64 micelle is formed by a core of pure polypropylene oxide units and a hydrated shell of poly(ethylene oxide) units. In the case of the ternary systems, the apparent mol…

Aqueous solutionMaterials scienceEthylene oxideInorganic chemistryOxideSurfaces and InterfacesCondensed Matter PhysicsMicellePropanolchemistry.chemical_compoundchemistryElectrochemistryCopolymerGeneral Materials SciencePropylene oxideBinary systemSpectroscopyLangmuir
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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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Micellization and Micellar Structure of a Poly(ethylene oxide)/Poly(propylene oxide)/Poly(ethylene oxide) Triblock Copolymer in Water Solution, As St…

1997

The micellization of the triblock copolymer Pluronic P85 (poly(oxyethylene)27/poly(oxypropylene)39/poly(oxyethylene)27) in aqueous solution was followed vs temperature and addition of aliphatic alcohols, using the spin probe technique. Different types of probes properly chosen (spin-labeled (SL) poly(oxyethylene(4))nonylphenol, SL-Pluronic L62, TEMPO-laurate, TEMPO-hexanoate, CAT 4, CAT 8, CAT 11, CAT 16, and 5-, 7-, 10-, and 12-doxylstearic acids) provided information about the micellar structure (polarity, viscosity, and order degree) at different radial locations. Micellization was found to be low at room temperature, even for 10% aqueous solutions, but strongly increasing with temperatu…

Aqueous solutionMaterials scienceOxideSurfaces and InterfacesPoloxamerCondensed Matter PhysicsResonance (chemistry)NonylphenolSpin probeViscositychemistry.chemical_compoundchemistryPolymer chemistryElectrochemistryCopolymerGeneral Materials ScienceSpectroscopyLangmuir
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Chemical heterogeneities in nanometric titanomagnetites prepared by soft chemistry and studied ex situ : evidence for fe-segregation and oxidation ki…

2001

Nanocrystalline Fe-based spinels with composition Fe3-xTixO4 are synthesized using soft chemistry. Two steps are involved:  precipitation in an aqueous solution followed by thermal annealing under a reducing mixture of N2/H2/H2O gases. Fe-segregation is found inside stoichiometric particles when the powders are studied ex situ; they exhibit a strong surface iron enrichment. This heterogeneity is related to kinetic effects linked to the difference of mobility between Fe2+ and Ti4+ cations during the partial oxidation of cations occurring ex situ. Stresses in the grains induced by oxidation govern the oxidation kinetics and lead to an abrupt compositional variation inside each particle. These…

Aqueous solutionMaterials sciencePrecipitation (chemistry)Analytical chemistry02 engineering and technology[SPI.MAT] Engineering Sciences [physics]/Materials010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSoft chemistryNanocrystalline material0104 chemical sciencesSurfaces Coatings and Films[SPI.MAT]Engineering Sciences [physics]/MaterialsX-ray photoelectron spectroscopyMaterials ChemistryParticlePartial oxidationPhysical and Theoretical Chemistry0210 nano-technologyStoichiometryComputingMilieux_MISCELLANEOUS
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Study of the Chemical Conversion of Aluminum Alloys by Coupling CFDE and EQCM

2004

The ability of the channel flow double electrode (CFDE) technique and electrochemical quartz crystal microbalance (EQCM) for studying in situ chromate phosphate conversion coating on 5182 aluminum alloys was explored. It was first demonstrated that aqueous Cr(VI) can be analyzed quantitatively with the CFDE technique by reduction into Cr(III) on a graphite electrode. Samples used for EQCM were quartz plated by physical vapor deposition using a 5182 alloy target, allowing thin layers of aluminum alloys with a similar chemical composition to be obtained. EQCM was adapted in order to account for the hydrodynamic conditions in an industrial process, by placing the quartz in a flow cell. In orde…

Aqueous solutionMaterials scienceThin layersChromate conversion coatingRenewable Energy Sustainability and the EnvironmentMetallurgyAnalytical chemistryQuartz crystal microbalanceengineering.materialCondensed Matter PhysicsPhosphate conversion coatingSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCoatingPhysical vapor depositionElectrodeMaterials ChemistryElectrochemistryengineeringJournal of The Electrochemical Society
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Structural Characterization of Zirconia Nanoparticles Prepared by Microwave-Hydrothermal Synthesis

2009

Nanocrystalline zirconia powders have been prepared by microwave-hydrothermal synthesis starting from aqueous solution of ZrOCl2·8H2O. Results of investigations on the aqueous suspension stability of the washed zirconia nanopowders by dynamic light scattering showed that the suspension, constituted by superaggregates of nanoparticles (131 ± 10 nm), was stable up to 15 days. Nanopowders were investigated by means of transmission electron microscopy and small angle x-ray scattering measurements which proved that the zirconia nanopowder is constituted by small primary nanoparticles of ca. 8 nm that agglomerate forming bigger aggregates of 50 ± 1 nm.

Aqueous solutionMaterials sciencenanostructurePolymers and PlasticsElectron microscopy; nanostructures; oxides; surface propertiesSmall-angle X-ray scatteringNanoparticleMineralogyNanocrystalline materialSurfaces Coatings and FilmsDynamic light scatteringChemical engineeringTransmission electron microscopynanostructuresoxidesElectron microscopyHydrothermal synthesissurface propertiesCubic zirconiaoxidePhysical and Theoretical ChemistryJournal of Dispersion Science and Technology
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A new method for fluoride determination by using fluorophores and dyes anchored onto MCM-41Electronic supplementary information (ESI) available: IR s…

2002

A new colourimetric and fluorimetric method for fluoride determination in aqueous samples based on the specific reaction between fluoride and silica has been developed and applied on real samples.

Aqueous solutionMetals and AlloysNanotechnologyGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMCM-41Materials ChemistryCeramics and CompositesFluorideNuclear chemistryChemical Communications
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Oxidative transformation of aryls using molybdenum pentachloride.

2012

Molybdenum pentachloride combines a strong Lewis acid character with an unusually high oxidation potential creating a powerful reagent for oxidative transformations. Since the oxidative coupling reaction of aryls is induced at an extraordinarily high reaction rate, a variety of labile groups, e.g. iodo, tert-alkyl, etc., are tolerated on the aromatic core. Furthermore, the co-formed molybdenum salts can either be exploited for template effects to obtain uncommon geometries in a preferred manner, or redox-play starts after aqueous workup. Therefore MoCl(5) represents a unique and easily available reagent.

Aqueous solutionMetals and Alloyschemistry.chemical_elementGeneral ChemistryOxidative phosphorylationMolybdenum pentachlorideCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsReaction ratechemistryMolybdenumReagentMaterials ChemistryCeramics and CompositesOrganic chemistryOxidative coupling of methaneLewis acids and bases
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In-situ characterisation of organosilane films formation on aluminium alloys by electrochemical quartz crystal microbalance and in-situ ellipsometry

2005

Abstract Organosilane pre-treatments have been studied intensively during the last years in order to replace hexavalent chromium conversion treatments. The aim of this study is to follow in-situ the formation of this organosilane layer in solution. Two in-situ techniques, spectroscopic ellipsometry and electrochemical quartz crystal microbalance, were used to investigate the mechanism and the kinetics of this protective film formation. In-situ measurements highlight that the organosilane film observed after the drying process is not formed into the solution, but during the emersion and drying step. Hence, it has been possible to characterise the presence of a very thin organosilane layer in…

Aqueous solutionMetals and Alloyschemistry.chemical_elementMineralogySurfaces and InterfacesQuartz crystal microbalanceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryX-ray photoelectron spectroscopyChemical engineeringAluminiumEllipsometryMonolayerMaterials ChemistryThin filmLayer (electronics)
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Effect of Anions and Oxygen on the Kinetics of the Anodic Dissolution of Nickel

2006

An electrochemical impedance spectroscopy study on electrochemical dissolution and active/passive transition of polycrystalline nickel in acid media has been performed in sulfate and nitrate aqueous solutions. Oxygen favors the nickel electrodissolution in a nitrate aqueous acid medium, but the dissolution decreases in the sulfate medium due to nickel passivation. The anion and oxygen effect is analyzed from a model where Ni(I) species are stabilized on the Ni metal surface and all anions present in the solution compete in the neutralization of Ni(I) and Ni(II) and in the solubilization of Ni(II).

Aqueous solutionPassivationRenewable Energy Sustainability and the EnvironmentChemistryInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsOxygenSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDielectric spectroscopyMetalNickelchemistry.chemical_compoundvisual_artMaterials ChemistryElectrochemistryvisual_art.visual_art_mediumSulfateDissolutionJournal of The Electrochemical Society
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