Search results for "Nolay"

showing 10 items of 588 documents

Behenic Acid as a Structural Model for Fatty Acid Monolayers at the Air/Water Interface: An X-Ray Diffraction Study

1992

We present an X-ray diffraction study of behenic (docosanoic) acid films at the air/water interface. Analysis of the rod profiles parallel and perpendicular to the surface provides detailed information on the unit cells of five different phases.

Diffractionchemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceBiochemistrychemistryAir water interfaceX-ray crystallographyMonolayerPerpendicularAnalytical chemistryFatty acidBehenic acid
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An Analysis of the Broadening Induced by Beam Damage in Transmission Electron Diffraction Spots from an Oriented Aliphatic Monolayer

1991

We have analysed the progressive changes in diffraction spot shape during prolonged transmission electron diffraction observation of a soap monolayer supported on a thin polymer film. The material used to form the monolayer was cadmium eicosanoate (arachidate). The observed changes cannot be explained at all in terms of the chemical crosslinking which is known to occur as a result of beam damage, nor completely in terms of the strain fields caused by unbound dislocation defects of the crystalline lattice. The most plausible explanation involves the formation of linear dislocation aggregates which resemble grain boundaries but yet which are not linked into a continuous network. The evolution…

Diffractionchemistry.chemical_compoundCrystallographyElectron diffractionChemistryMonolayerGrain boundaryCrystal structureDislocationSilicon monoxideMolecular physicsBeam (structure)
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Morphology and structures in double-, triple- and quadruple-chain phospholipid monolayers at the air/water interface

2007

The structure of double-, triple- and quadruple-chain phospholipid monolayers has been studied by Synchrotron x-ray diffraction. The double-chain mixed- linkage species exhibit an oblique structure at all pressures investigated. The triple-chain phospholipids show at lower lateral pressures a rectangular unit cell with a phase transition at higher pressures to a hexagonal packing of vertically arranged chains. The quadruple- chain lipid exhibits only the hexagonal phase structure. The position of the ether linkage and of the branched chain on the glycerol backbone has also a strong influence on the monolayer structures. Fluorescence microscopy shows different domain shapes for the different…

Diffractionchemistry.chemical_compoundCrystallographyPhase transitionchemistrylawMonolayerPhospholipidHexagonal phaseMoleculeAnisotropySynchrotronlaw.invention
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The Phases of Phosphatidyl Ethanolamine Monolayers

1992

For the first time phospholipid monolayers at the air/water interface have been studied by X-ray diffraction and reflection along the whole isotherm from the isotropic fluid to the ordered phases [1]. The model used to analyze the data — and the accuracy of the parameters deduced — were tested by comparing the results obtained with two lipids having the same head group but different chain lengths.

Diffractionchemistry.chemical_compoundCrystallographyReflection (mathematics)chemistryIsotropyMonolayerPhospholipidPhosphatidyl ethanolamineLipid monolayer
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2D shape relaxation dynamics in amphiphile monolayers

2007

The shape relaxation dynamics of the droplets in amphiphile monolayers is studied in Darcy approximation. It is shown by numerical experiments that relaxation from the highly extended dumbbell configurations can be described by simple physical model according to which the dissipation is concentrated on circular tips. By numerical simulation it is illustrated that longrange dipolar interactions lead to the stabilization of the shape relaxation process with respect to the formation of a narrow neck causing the rupture of the droplet when dipolar forces are absent. Effect of the dipolar forces on the shape-relaxation process can be accounted by the slope of the relaxation curve at small deviat…

DipoleHele-Shaw flowComputer simulationComputational chemistryChemistryMonolayerDynamics (mechanics)Relaxation (physics)DumbbellDissipationMolecular physics
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Tilted phases of fatty acid monolayers

1995

X‐ray diffraction data from water‐supported monolayers of fatty acids with chain lengths from 19 to 22 is presented. The structures of the tilted mesophases L2’, L2, and Ov are characterized in detail. The contributions to the unit cell distortion from the tilt and the ordering of the backbone planes of the molecules are separated. It is shown that at the swiveling transition L2’–L2, not only the tilt azimuth but also the packing of the backbone planes change discontinuously. We demonstrate that the tilting transition LS–L2 is accompanied by the ordering of the backbone planes and may be discontinuous. Evidence is presented for a herringbone ordering transition within the L2 region. The dis…

Distortion (mathematics)DiffractionQuantitative Biology::BiomoleculesCrystallographyTilt (optics)ChemistryX-ray crystallographyMonolayerGeneral Physics and AstronomyMoleculePhysical and Theoretical ChemistrySymmetry (geometry)Phase diagramThe Journal of Chemical Physics
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Pd nanoparticles immobilized on the poly-dopamine decorated halloysite nanotubes hybridized with N-doped porous carbon monolayer: A versatile catalys…

2020

A hybrid catalyst, Pd@Hal-pDA-NPC, with the utility for promoting both C–C coupling reactions (Sonogashira, Heck and Suzuki reactions) and hydrogenation of nitrocompounds is prepared through two main steps. First, Pd(0) nanoparticles was immobilized on the poly-dopamine decorated halloysite nanotubes (Hal-pDA) and then Pd@Hal-pDA was hybridized with the layers of a novel multi-N-doped porous carbon monolayer derived from 4,4′,4″-((1,3,5-triazine-2,4,6-triyl)tris(azanediyl))tribenzonitrile. The results established that the catalyst could catalyze all the reactions efficiently under mild reaction condition. Moreover Pd@Hal-pDA-NPC exhibited high recyclability (up to ten reac…

DopamineN-doped porous carbonOxideNanoparticleSonogashira coupling02 engineering and technologyengineering.material01 natural sciencesHalloysiteHeterogeneous catalystCatalysisCatalysischemistry.chemical_compoundMonolayerPdPhysical and Theoretical ChemistrySettore CHIM/02 - Chimica Fisica010405 organic chemistryGraphitic carbon nitrideHalloysite021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringHeterogeneous catalystsengineeringLeaching (metallurgy)0210 nano-technology
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Stability and magnetic properties of Fe double layers on Ir (111)

2018

We investigate the interplay between the structural reconstruction and the magnetic properties of Fe doublelayers on Ir (111)-substrate using first-principles calculations based on density functional theory and mapping of the total energies on an atomistic spin model. We show that, if a second Fe monolayer is deposited on Fe/Ir (111), the stacking may change from hexagonal close-packed to bcc (110)-like accompanied by a reduction of symmetry from trigonal to centered rectangular. Although the bcc-like surface has a lower coordination, we find that this is the structural ground state. This reconstruction has a major impact on the magnetic structure. We investigate in detail the changes in th…

Double layer (biology)Condensed Matter - Materials ScienceMaterials scienceCondensed matter physicsMagnetic structureStackingMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences02 engineering and technology021001 nanoscience & nanotechnologyMagnetocrystalline anisotropy01 natural sciencesCondensed Matter::Materials Science0103 physical sciencesMonolayerCondensed Matter::Strongly Correlated ElectronsDensity functional theory010306 general physics0210 nano-technologyGround stateAnisotropyPhysical Review B
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On the Electrostatic Component of the Adhesional Interaction between Solid Substrates and Langmuir Monolayers

1991

The work of adhesion between Langmuir monolayers and solid surfaces in a hydrophilic Langmuir-Blodgett configuration has been measured as function of the surface charge densities σ of the contacting surfaces. It was derived from the equilibrium meniscus height which was measured with the transfer fluorescence microscope. The surface charge density of the contacting surfaces was varied by changing the subphase pH. With both surfaces negatively charged (dimyristoylphosphatidylethanolamine onto SiO2-substrates) and low charge densities (σ < 1 e−/100 A2)) we observe a decrease of the adhesion with increasing charge density. At high charge densities (dimyristoylphosphatidic acid onto SiO2-substr…

Double layer (biology)Langmuirchemistry.chemical_compoundChemistryGeneral Chemical EngineeringDipalmitoylphosphatidylcholineMonolayerAnalytical chemistryCharge densityAdhesionSurface chargeDouble layer forcesBerichte der Bunsengesellschaft für physikalische Chemie
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Studies of monolayer/substrate adhesion as function of the monolayer headgroup charge: DMPE and DMPA

1991

The variation of the work of adhesion between lipid monolayers and a plane silicon oxide surface in a typical LB-configuration is measured as function of the subphase pH. The adhesion energy is deduced via fluorescence microscopy from the equilibrium meniscus height. With increasing pH the negative headgroup charge of both, dimyristoylphosphatidylethanolamine (DMPE) and dimyristoylphosphatidic acid (DMPA) monolayers increases. The increasing charge of DMPE is reflected in a measured decrease of the work of adhesion at higher pH. The DMPA/SiO2 interaction is not affected by increasing headgroup charges. These results are qualitatively understood in terms of an electrostatic double layer inte…

Double layer (biology)Polymers and PlasticsChemistryStereochemistryOrganic ChemistryCharge (physics)AdhesionSubstrate (electronics)Condensed Matter PhysicsCrystallographyMonolayerMaterials ChemistryMeniscusSurface chargeSilicon oxideMakromolekulare Chemie. Macromolecular Symposia
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