Search results for "interfacial"

showing 10 items of 53 documents

Initial stages of metal oxides thin films growth by MOCVD: physicochemical characterisation of the film/substrate interface

2006

The initial stages of Metalorganic Chemical Vapour Deposition (MOCVD) of TiO2 thin films on Si(100) were studied in situ by surface analyses (XPS, ARXPS, AES). An original experimental set-up was built for this purpose and developed. Information obtained from these in situ experiments was completed by ex situ characterisations (HRTEM, SIMS, GIXRD...).The formation of an interfacial SiOy<2 layer resulting of the interaction of the precursor Ti(OCH(CH3)2)4 with the substrate takes place before the formation of stoichiometric TiO2 and leads to the presence of carbon at the interface. At the deposition temperature, 675 °C, silicon diffusion within the TiO2 external layer was also revealed. Conc…

[CHIM.MATE] Chemical Sciences/Material chemistryinterfacial reactivityin situ surface analysisARXPScrystalline structure[ CHIM.MATE ] Chemical Sciences/Material chemistryMOCVDTEMXPSstructure cristallineMETréactivité interfacialeanalyse de surfaces in situTiO2/Si
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Fabrication and characterization of barium silicate ultrathin films as an alternative gate oxide

2008

Down-scaling of elementary CMOS elements requires the replacement of SiO2 as a gate oxide. By the identification of the formation conditions of barium silicate in direct contact of a silicon substrate, this study revealed a potential candidate. First of all, a reaction between Ba and SiO2 leading to the formation of barium silicate as been evidenced by in-situ XPS and SR-PES analyses. Then, barium silicate films have been elaborated by oxygen and barium co-deposition at 580 °C. Thermal treatments under vacuum showed that barium silicate was thermally stable up to 900 °C. TEM and SIMS ex-situ analyses revealed a sharp interface with the substrate. Finally, an experimental setup dedicated to …

[CHIM.MATE] Chemical Sciences/Material chemistrysilicate de baryuminterfacial reactivity[ CHIM.MATE ] Chemical Sciences/Material chemistrybarium silicateXPS[CHIM.MATE]Chemical Sciences/Material chemistry[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]SR-PESréactivité interfaciale[PHYS.COND] Physics [physics]/Condensed Matter [cond-mat]high-k[ PHYS.COND ] Physics [physics]/Condensed Matter [cond-mat]
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CFRP sheets bonded to natural stone: interfacial phenomena

2004

The effectiveness of the reinforcing technique consisting of fiber reinforced polymer sheets bonded to the structural elements depends on a good connection at the joint. This has to be able to ensure the transfer length of the shear stress in order to avoid a premature failure due to debonding. In this paper, the bond phenomenon at the interface is examined with reference to the calcarenite stone and carbon fiber reinforced polymer (CFRP) sheets in order to evaluate the possibility of utilizing this technique on masonry structural members, consisting of calcarenite ashlars and mortar. An experimental investigation is carried out on nine specimens obtained by applying unidirectional CFRP she…

calcarenite stone composite laminate bond length interfacial phenomenon load transfer.
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Analysis of adsorption of phospholipids at the 1,2-dichloroethane/water interface by electrochemical impedance spectroscopy: A study of the effect of…

2007

Abstract The adsorption behaviour of a series of phosphatidylcholines (PCs) with saturated carbon chains of different length (DLPC, DPPC, DSPC, DAPC, and DBPC) at the electrified 1,2-dichloroethane/water interface was studied by measuring electrochemical impedance spectroscopy at the polarized interface. Two different trends in the interfacial capacitance were observed for any of the PCs the capacity dependence on the applied potential: strong adsorption occurs at negative potential with a marked decrease of C ( E ); increase of capacity is observed at positive potentials. It is demonstrated that the interfacial lipid adsorption was dependent on phospholipid concentration, applied potential…

chemistry.chemical_classificationChemistryGeneral Chemical EngineeringPhospholipid adsorptionPhospholipidAnalytical chemistryLiquid-liquid interfaceCapacitanceAnalytical ChemistryDielectric spectroscopyDichloroethanechemistry.chemical_compoundAdsorptionInterfacial capacitancePhosphatidylcholineElectrochemistrylipids (amino acids peptides and proteins)ITIESElectrochemical impedance spectroscopyAlkyl
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Influence of the modification, induced by zirconia nanoparticles, on the structure and properties of polycarbonate

2013

Melt compounding was used to prepare polycarbonate (PC)–zirconia nanocomposites with different amounts of zirconia. The effect of the zirconia loading, in the range of 1–5 wt.%, on the structure, mechanical properties and thermal degradation kinetics was investigated. The zirconia nanoparticle aggregates were well dispersed in the PC matrix and induced the appearance of a local lamellar order in the polycarbonate as inferred by SAXS findings. This order could be a consequence of the intermolecular interactions between zirconia and the polymer, in particular with the quaternary carbon bonded to the methyl groups and the methyl carbon as inferred from the NMR results. The presence of zirconia…

chemistry.chemical_classificationMaterials scienceNanocompositeNanocompositePolymers and PlasticsOrganic ChemistryGeneral Physics and AstronomyNanoparticlePolymerInterfacial interactionDegradationchemistryPolycarbonatevisual_artMaterials Chemistryvisual_art.visual_art_mediumZirconiaDegradation; Interfacial interaction; Nanocomposites; Polycarbonate; ZirconiaThermal stabilityCubic zirconiaLamellar structurePolycarbonateComposite materialGlass transitionSettore CHIM/02 - Chimica Fisica
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Photoaffinity cross-linking of F1ATPase from the thermophilic bacterium PS3 by 3′-arylazido-β-alanyl-2-azido ATP

1989

AbstractThe photoactivatable bifunctional 3′-arylazido-β-alanyl-2-azido ATP (2,3′-DiN3ATP) has been applied to study the localization of the nucleotide-binding sites of coupling factor 1 (F1ATPase, TF1) from the thermophilic bacterium PS3 by photoaffinity cross-linking. UV irradiation of TF1 in the presence of 2,3′-DiN3ATP results in the nucleotide-dependent formation of various higher molecular mass cross-links formed by two, three or even four α- and/or β-subunits. The differences observed upon photoaffinity cross-linking by the bifunctional 2-azido ATP or 8-azido ATP analog are discussed. They are probably due to the varied maximal distance between both azido groups, or to the different …

chemistry.chemical_classificationMolecular massbiologyStereochemistryProtein subunitNucleotide conformationBiophysicsCell Biologybiology.organism_classificationBiochemistrychemistry.chemical_compoundEnzymechemistryStructural BiologyGeneticsPhotoaffinity crosslinkingATPase F1-NucleotideNucleotide-binding siteBinding siteBifunctionalInterfacial localizationMolecular BiologyThermophilic bacterium PS3BacteriaFEBS Letters
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Improving the properties of polypropylene–wood flour composites by utilization of maleated adhesion promoters

2007

Polymer composites filled with natural organic fillers have gained a significant interest during the last few years, because of several advantages they can offer compared with properties of inorganic-mineral fillers. However, these composites (based, in most cases, on polyolefins) often show a reduction in some mechanical properties. This is mainly due to the problems regarding dispersion of the polar filler particles in the non-polar polymer matrix and their interfacial adhesion with polymer chains. In this work, polypropylene-wood flour composites were prepared and the effect of the addition of a maleated polypropylene was investigated. The two materials were compounded by an industrial c…

chemistry.chemical_classificationPolypropyleneWaxMaterials scienceGeneral Physics and AstronomyWood flourInterfacial adhesionPolymerengineering.materialSurfaces Coatings and FilmsNatural fibers Fibers natural fibrechemistry.chemical_compoundchemistryvisual_artFiller (materials)Ultimate tensile strengthCeramics and Compositesvisual_art.visual_art_mediumengineeringComposite materialDispersion (chemistry)Composite Interfaces
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Macro-micro relationship in nanostructured functional composites

2012

This paper examines the results of the characterization of two functional composites: Poly(methyl methacrylate) (PMMA)-Ce:YAG (yttrium aluminium garnet doped with cerium) and PMMA-cobalt hexacyanoferrate (CoHCF). The composites were prepared as possible emitters in the fields of lighting thermal sensors. The prepared composites were char- acterized using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, thermogravi- metric analysis (TGA), differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) analyses to study the correlation between micro and macro characteristics. We found that the molecular interactions of the two different fill…

cobalt hexacyanoferrateMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringComposite numberchemistry.chemical_elementlcsh:Chemical technologyNanocompositeschemistry.chemical_compoundDifferential scanning calorimetryYttrium aluminium garnetnanocomposites PMMA yttrium aluminium garnet doped with cerium (Ce:YAG) cobalt hexacyanoferrate (CoHCF) interfacial interactionlcsh:TA401-492Materials ChemistryCeYAGlcsh:TP1-1185Physical and Theoretical ChemistryComposite materialMethyl methacrylateSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationOrganic ChemistryPolymerDynamic mechanical analysisPMMACeriumchemistryTransmission electron microscopyYAG) cobalt hexacyanoferrate (CoHCF) interfacial interaction [nanocomposites PMMA yttrium aluminium garnet doped with cerium (Ce]lcsh:Materials of engineering and construction. Mechanics of materialsinterfacial interactionExpress Polymer Letters
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Equilibrium fluid-crystal interfacial free energy of bcc-crystallizing aqueous suspensions of polydisperse charged spheres

2015

The interfacial free energy is a central quantity in crystallization from the meta-stable melt. In suspensions of charged colloidal spheres, nucleation and growth kinetics can be accurately measured from optical experiments. In previous work, from this data effective non-equilibrium values for the interfacial free energy between the emerging bcc-nuclei and the adjacent melt in dependence on the chemical potential difference between melt phase and crystal phase were derived using classical nucleation theory. A strictly linear increase of the interfacial free energy was observed as a function of increased meta-stability. Here, we further analyze this data for five aqueous suspensions of charg…

fluid-crystalMaterials scienceNucleationFOS: Physical sciencesThermodynamicsNon-equilibrium thermodynamicsCondensed Matter - Soft Condensed Matter01 natural scienceslaw.inventionColloidlawMetastability0103 physical sciencesCrystallization010306 general physicsCondensed Matter - Statistical MechanicsCondensed Matter - Materials ScienceAqueous solutionStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsMaterials Science (cond-mat.mtrl-sci)Condensed Matter::Soft Condensed Matterpolydisperseinterfacial free energySoft Condensed Matter (cond-mat.soft)SPHERESClassical nucleation theoryPhysical Review E
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Understanding membrane protein folding and interfaciality

2021

Despite the bast abundance of membrane proteins encoded in the human genome, the understanding of their biosynthesis and folding is far from the knowledge we have of soluble proteins. In the present thesis the main objective is to increase our knowledge on membrane protein biogenesis and folding, from the first steps of folding within the ribosome to the native structure acquisition in the membrane. Hydrophobicity, helicity and length of the polypeptide chain have been stablished as the major determinants for alpha-helical conformation adoption within the ribosome exit tunnel. Also, a 'biological' interfacial scale for the 20 naturally occurring amino acids were determined due to the develo…

foldingmatchingUNESCO::CIENCIAS DE LA VIDAinterfacialhydrophobicproteinmembrane:CIENCIAS DE LA VIDA [UNESCO]
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