Search results for "Surface pressure"

showing 10 items of 20 documents

Physisorption Instabilities during Dynamic Langmuir Wetting

1994

Continuous dynamic Langmuir wetting of lipid monolayers can create regular stripe patterns on the solid substrate surface. Monolayers doped with minor amounts of fluorescence dye may be deposited in stripes of alternating high and low dye concentration. In case of pure monolayers stripes are observed with AFM. The striations run normal to the dipping direction and have widths of typically several micrometres and distances varying from 1 to ≈ 100 μm. The stripe widths, distances, and fluorescence contrast depend on deposition speed, surface pressure, substrate surface preparation, and dye concentration. The patterns probably result from physisorption (meniscus) instabilities caused by a feed…

LangmuirMaterials sciencebusiness.industryfood and beveragesGeneral Physics and AstronomySubstrate (electronics)Surface pressureContact angleOpticsPhysisorptionChemical physicsMonolayerMeniscusWettingbusinessEurophysics Letters (EPL)
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Structural Relationships between Floating and Deposited Monolayers of Docosanoic Acid

1991

Floating docosanoic acid (behenic acid) monolayers in the SmI and SmH phase were deposited with the Langmuir-Blodgett technique onto thin polymethylmethacrylate (PMMA) and Formvar substrates and investigated by electron diffraction. The molecular packing of the monolayers on the substrates vary from those on the water surface and are different for different substrates. On PMMA four phases (H, SmB, SmI, SmL) have been identified, depending on the deposition conditions. While SmB and SmI are known for docosanoic acid on the water surface, H and SmL have only been unequivocally observed in other substances or on other subphases. The monolayer structure on Formvar was identical under all deposi…

Materials scienceGeneral Chemical EngineeringAdhesionSurface pressurechemistry.chemical_compoundAdsorptionFormvarchemistryElectron diffractionChemical engineeringPhase (matter)MonolayerOrganic chemistryBehenic acidBerichte der Bunsengesellschaft für physikalische Chemie
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Temperature and pressure dependence of quercetin-3-O-palmitate interaction with a model phospholipid membrane: film balance and scanning probe micros…

2004

The molecular interaction of quercetin-3-O-palmitate (QP) with dimyristoylphosphatidylcholine (DMPC) has been studied. Film balance measurements of the average molecular area vs QP molar fraction in DMPC/QP mixed monolayers showed that relevant positive deviations from ideality, i.e., a less dense monolayer packing, occurred for a temperature of 10 degrees C, below the critical melting transition temperature of DMPC monolayers T c m approximately equal 20 degrees C), while ideal behavior was observed at 37 degrees C, above this phase transition temperature. The positive deviation observed at low temperatures in the average molecular area increased with the surface pressure. Scanning probe m…

Membrane FluiditySurface PropertiesLipid BilayersAnalytical chemistryPhospholipidPalmitic AcidPhase separationPalmitic AcidsSurface pressureMole fractionMicroscopy Atomic ForcePhase TransitionBiomaterialsScanning probe microscopychemistry.chemical_compoundMembrane LipidsColloid and Surface ChemistryMonolayerLangmuir-Blodgett monolayersMolecular StructureTransition temperatureTemperatureQuercetin palmitateSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsLangmuir–Blodgett monolayerMembranechemistryAluminum SilicatesQuercetinMicaStress MechanicalDimyristoylphosphatidylcholineAlgorithmsScanning force microscopy
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Performance of Thin-Film Lithium Energy Cells under Uniaxial Pressure

2008

The objective of this study was two-fold. The first objective was to determine if the all-solid-state thin-film lithium energy cells could withstand the minimal 550 kPa uniaxial pressure required for composite manufacturing, which both specimens successfully did. The second objective was to determine the upper boundary uniaxial pressure limit of operation for the all-solid-state thin-film lithium energy cells. The two all-solid- state thin-film lithium energy cells tested in the present study under uniaxial pressure performed well even when subjected to uniaxial pressures up to about 2.0 MPa. However, pressures higher than this value led to their degradation. The observed degradation was du…

Microelectromechanical systemsFabricationMaterials sciencechemistry.chemical_elementCondensed Matter PhysicsUniaxial pressureSurface pressureLithium batterythin film batteries mechanical performanceSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryGeneral Materials ScienceLithiumThin filmComposite materialEnergy (signal processing)Advanced Engineering Materials
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Effect of apolar phase dielectric constant on interfacial properties of β-lactoglobulin (dielectric constant and interfacial properties of β-lactoglo…

2005

International audience; In this work, we hypothesized that the difference in the dielectric constant value existing between two non-miscible phases such as oil and water could be partially responsible for both protein unfolding and reorganization of the protein structure at the interface. So, we replaced the oil phase, whose dielectric constant value is 2, by organic solvents chosen for both their non-miscibility with water and their range of dielectric constant values higher (range 6.1-7.2) than that of oil. Using a dynamic drop tensiometer, we studied both surface activity and viscoelastic properties of the milk protein at various interfaces. The aqueous phase (pH7; 25°C) contained the co…

Permittivity030309 nutrition & dieteticsGeneral Chemical EngineeringAnalytical chemistryThermodynamicsDielectricSurface pressureViscoelasticity03 medical and health sciencesProtein structure[SDV.IDA]Life Sciences [q-bio]/Food engineeringOil/water interfaceDielectric constant[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology0303 health sciencesα-LactoglobulinMilk proteinChemistryDrop (liquid)0402 animal and dairy scienceAqueous two-phase system04 agricultural and veterinary sciencesGeneral Chemistry040201 dairy & animal scienceInterfacial water organizationFood Science
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Phospholipid monolayers at water∣oil interfaces: theoretical modelling of surface pressure–molecular area isotherms

1998

Abstract The phospholipid adsorption and surface pressure–molecular area isotherms at interfaces are interpreted theoretically from two-dimensional (2D) lattice and real gas models that incorporate a minimum number of adjustable parameters. The first model is based on the lattice statistics of binary solutions and the molecular parameters introduced are the energy changes involved in the mixing process of the phospholipid and organic solvent molecules and the effective phospholipid head area. The surface pressure is interpreted in terms of the difference between the two liquid surface tensions. The second model makes use of (i) a non-localised adsorption model with a square-well potential e…

Physics::Biological PhysicsReal gasChromatographyChemistryGeneral Chemical EngineeringPhospholipidThermodynamicsInteraction energySurface pressurePotential energyAnalytical ChemistryCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundAdsorptionMonolayerElectrochemistrylipids (amino acids peptides and proteins)Physics::Chemical PhysicsOrder of magnitudeJournal of Electroanalytical Chemistry
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2D dynamical arrest transition in a mixed nanoparticle-phospholipid layer studied in real and momentum spaces

2015

AbstractWe investigate the interfacial dynamics of a 2D self-organized mixed layer made of silica nanoparticles interacting with phospholipid (DPPC) monolayers at the air/water interface. This system has biological relevance, allowing investigation of toxicological effects of nanoparticles on model membranes and lung surfactants. It might also provide bio-inspired technological solutions, exploiting the self-organization of DPPC to produce a non-trivial 2D structuration of nanoparticles. The characterization of interfacial dynamics yields information on the effects of NPs on the mechanical properties, important to improve performances of systems such as colloidosomes, foams, creams. For thi…

Surface PropertiesComputer sciencePhospholipidNanoparticleRELAXATIONCOLLOIDOSOMESRespiratory physiologySurface pressureArticleMomentumchemistry.chemical_compoundPhase (matter)MonolayerParticle SizeSILICA NANOPARTICLESPhospholipidsBrownian motionSimulation[PHYS]Physics [physics]MultidisciplinaryAirRelaxation (NMR)WaterPulmonary SurfactantsModels TheoreticalSilicon DioxideSURFACTANTCharacterization (materials science)MembranechemistryChemical physicsNanoparticlesWater chemistryParticle sizeCOLLOIDAL GLASS-TRANSITIONAlgorithmsScientific Reports
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The binding of G-protein to rod outer segment phospholipids at the nitrogen–water interface

1989

In the visual process, one photoexcited rhodopsin (R*) catalyzes the activation of hundreds of G-proteins. It remains to be determined whether G-protein and R* find one another by membrane surface diffusion of these components (diffusion model) or by diffusion of G-protein through the aqueous phase (hopping model). A monolayer of each main rod outer segment (ROS) phospholipid interacting with a subphase containing G-protein, has been used to simulate the interaction of G-protein with the cytoplasmic surface of discal membranes. The possible diffusion of G-protein through the aqueous phase was then measured by observing its adsorption–desorption in the monolayer of each main ROS phospholipi…

biologyChemistryAqueous two-phase systemPhospholipidMembrane ProteinsCell BiologySurface pressureBiochemistryCrystallographychemistry.chemical_compoundMembraneGTP-Binding ProteinsCytoplasmRhodopsinMonolayerbiology.proteinAnimalsCattlePhotoreceptor CellsDiffusion (business)Molecular BiologyPhospholipidsBiochemistry and Cell Biology
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Two-Dimensional Assembly Formation of Hydrophobic Helical Peptides at the Air/Water Interface: Fluorescence Microscopic Study

1995

Monolayer formation of hydrophobic α-helical peptides, X-(Ala-Aib) 8 -Y (X=Boc-, HOOCCH 2 CH 2 CO-, biotinyl, biotinyl-(Sar) 3 -; Y=OMe, OBzl, OH), at the air/water interface was studied by the fluorescence microscopic method. Some peptides showed a mound in the π-A isotherm. When the monolayer containing a small amount of FITC-labeled peptide was held at the surface pressure corresponding to the top of the mound, bright and dark domains were observed by fluorescence microscopy. Domain formation was also observed by the addition of a cationic dye (DiIC 1 ) into the subphase underneath the peptide monolayer. The mound in the π-A isotherm is, therefore, ascribed to the phase transition from a…

chemistry.chemical_classificationPhase transitionStereochemistryfungiCationic polymerizationPeptideSurfaces and InterfacesCondensed Matter PhysicsSurface pressureFluorescencelaw.inventionCrystallographychemistrylawMonolayerElectrochemistryFluorescence microscopeGeneral Materials ScienceCrystallizationSpectroscopyLangmuir
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Separation of Enantiomers in a Monolayer of Racemic 3-Hexadecyl-oxy-propane-1,2-diol

1993

Monolayers of a racemic mixture and of the pure S enantiomer of 3-hexadecyloxy-propane-1,2-diol have been characterized by thermodynamic measurements at the air/water interface as well as by fluorescence microscopy. The critical temperatire T c , the limiting molecular area at high pressure and the pressure π c corresponding to the observed main phase transition, derived from the isotherms, slightly depend on chiral purity

chemistry.chemical_compoundAqueous solutionchemistryStereochemistryPropaneGeneral Chemical EngineeringDiolMonolayerPhysical chemistryRacemic mixtureEnantiomerSurface pressureEnantiomeric excessBerichte der Bunsengesellschaft für physikalische Chemie
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