Search results for "Roche"

showing 10 items of 2666 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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Electrochemical reduction of graphene oxide films in aqueous and organic solutions

2013

Abstract Electrochemical reduction of graphene oxide (GO) films cast on tin oxide glass substrates were carried out in aqueous solutions and in propylene carbonate and acetonitrile. Cyclic voltammetric measurements indicate successful reduction of GO films. The reduction process begins in aqueous solutions at less negative potentials than in organic solutions. Additionally the pH value of the aqueous solutions influences the reduction potential. According to spectroscopic analysis the reduction process of the GO film can be controlled by the choice of reduction potential and electrolyte medium. The potential window in this work was made broader by increasing pH or by using organic electroly…

Aqueous solutionMaterials scienceGrapheneGeneral Chemical EngineeringInorganic chemistryOxideElectrolyteElectrochemistryTin oxidelaw.inventionchemistry.chemical_compoundchemistrylawPropylene carbonateElectrochemistryAcetonitrileta116Electrochimica Acta
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Solid-State Electrochemical Method for Determining Core and Shell Size in Pd@PdO Nanoparticles

2010

Electrochemical characterization of palladium nanoparticles surrounded by a palladium oxide shell (Pd@PdO) is described from a combination of voltammetry plus electrochemical quartz crystal microbalance experiments at nanoparticle deposits on graphite electrodes in contact with aqueous H2SO4 and NaOH solutions. A method for determining the metal core size and oxide shell thickness of the Pd@PdO nanoparticles, based on a combination of conventional voltammetry of nanoparticles in DMSO solution and voltammetry of nanoparticle deposits in contact with 0.10 M aqueous NaOH solution, is described.

Aqueous solutionMaterials scienceInorganic chemistryShell (structure)OxideNanoparticleQuartz crystal microbalanceElectrochemistryAnalytical ChemistryMetalchemistry.chemical_compoundchemistryvisual_artElectrochemistryvisual_art.visual_art_mediumVoltammetryElectroanalysis
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Reversible Cluster Formation of Colloidal Nanospheres by Interparticle Photodimerization

2004

Crosslinked spherical nanoparticles based on trimethoxysilane monomers have been prepared by polycondensation in aqueous emulsion. These particles have been labeled chemically at their surface region with two different types of organic dye molecules (cinnamate, coumarin), which both are well known for their ability to undergo a reversible photodimerization if irradiated with light of a suitable wavelength. Upon irradiation of dilute solutions of these nanoparticles with UV light, the photodimerization of labels belonging to different colloidal nanoparticles caused the formation of large colloidal clusters consisting of chemically bound individual nanospheres. This process has been quantitat…

Aqueous solutionMaterials scienceNanoparticleCondensed Matter PhysicsPhotochemistryLight scatteringElectronic Optical and Magnetic MaterialsBiomaterialsColloidchemistry.chemical_compoundMonomerchemistryEmulsionElectrochemistryMoleculeIrradiationAdvanced Functional Materials
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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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Cation and anion electrochemically assisted solid-state transformations of malachite green

2020

[EN] The possibility of the electrochemical promotion of different solid-to-solid transformations including the performance of successive cation and anion insertion processes has been tested using malachite green, a triphenylmethane dye, in contact with aqueous NaCl electrolyte. Electrochemical data using the voltammetry of microparticles methodology reveal significant differences with the solution phase electrochemistry of the dye. Voltammetric data, combined with atomic force microscopy, focusing ion beam-field emission scanning electron microscopy, and high-resolution field emission scanning electron microscopy permit characterization of the oxidative dissolution, oxidation with anion in…

Aqueous solutionMaterials scienceScanning electron microscopeInorganic chemistryGeneral Physics and Astronomy02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciences0104 chemical sciencesIonchemistry.chemical_compoundchemistryPINTURAPhysical and Theoretical ChemistryMalachite green0210 nano-technologyDissolutionVoltammetry
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Electrochemical conversion of pressurized CO2 at simple silver-based cathodes in undivided cells: study of the effect of pressure and other operative…

2020

Abstract Electrochemical reduction of pressurized CO2 is proposed as an interesting approach to overcome the main hurdle of the CO2 electrochemical conversion in aqueous solution, its low solubility (ca. 0.033 M), and to achieve good faradaic efficiency in CO using simple sheet silver cathodes and undivided cells, thus lowering the overall costs of the process. The effect on the process of CO2 pressure (1–30 bar), current density, nature of the supporting electrolyte and other operative conditions, such as the surface of the cathode or the mixing rate, was studied to enhance the production of CO. It was shown that pressurized conditions allow to improve drastically the current efficiency o…

Aqueous solutionMaterials scienceSilverSupporting electrolyteGeneral Chemical EngineeringSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryCathodelaw.inventionChemical engineeringlawElectrodeMaterials ChemistryElectrochemistryPressureCO2SolubilityCarbon monoxideCurrent densityFaraday efficiencyReduction
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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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Microheterogeneous electrocatalytic chiral recognition at monoclinic vanadium-doped zirconias: enantioselective detection of glucose.

2007

Synthetic tetragonal and monoclinic vanadium-doped zirconias (t- and m-VxZr1-xO2, 0.005x0.150) exert an effective catalytic effect toward the electrochemical oxidation of glucose in aqueous alkaline media. The catalytic effect of monoclinic specimens attached to carbon and fluorine-doped tin oxide electrodes exhibits a remarkable enantioselectivity, so that catalytic currents for the oxidation of L-glucose at +0.92 V vs AgCl/Ag are considerably larger than those obtained for the oxidation of D-glucose. This enantioselectivity can be associated with the existence of a noncentrosymmetric coordination of vanadium centers in the monoclinic crystalline form of zirconia. From the electrochemical …

Aqueous solutionMolecular StructureChemistryInorganic chemistryVanadiumchemistry.chemical_elementElectronsStereoisomerismVanadiumElectrocatalystTin oxideElectrochemistryCatalysisAnalytical ChemistryCatalysisGlucoseMicroscopy Electron TransmissionCalibrationElectrochemistryMicroscopy Electron ScanningCubic zirconiaZirconiumOxidation-ReductionMonoclinic crystal systemAnalytical chemistry
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Effect of temperature on the growth of alfa-PbO2 nanostructures

2010

Abstract Ordered arrays of α-PbO 2 nanostructures were grown by galvanostatic anodic deposition into the channels of alumina templates. Electrodepositions were performed in an aqueous solution containing lead acetate and sodium acetate at pH 5.4. Bath temperature and electrodeposition time were varied to check their effect on the growth of nanostructures. It has been found that filling of alumina pores is independent of the time and electrodeposition temperature, whilst height and growth kinetics of nanostructures vary with both parameters. Temperature greatly influences morphology: wires grown at room temperature consisted of clusters of particles, leading to poorly compact structures, whi…

Aqueous solutionNanostructureMaterials scienceLead dioxide Nanostructures Template electrosynthesis Alumina membranes Metal oxideGeneral Chemical EngineeringNanowireLead dioxideNanotechnologyCrystal structureGrain sizechemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicatachemistryChemical engineeringElectrochemistryCrystalliteDeposition (law)
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