Search results for "interfacial"

showing 10 items of 53 documents

2,8-Diazido-ATP — a short-length bifunctional photoaffinity label for photoaffinity cross-linking of a stable F1 in ATP synthase (from thermophilic b…

1995

Abstract To demonstrate the direct interfacial position of nucleotide binding sites between subunits of proteins we have synthesized the bifunctional photoaffinity label 2,8-diazidoadenosine 5′-triphosphate (2,8-DiN3ATP). UV irradiation of the F1-ATPase (TF1) from the thermophilic bacterium PS3 in the presence of 2,8-DiN3ATP results in a nucleotide-dependent inactivation of the enzyme and in a nucleotide-dependent formation of α-β crosslinks. The results confirm an interfacial localization of all the nucleotide binding sites on TF1.

Models MolecularAzidesNucleotide binding siteLightStereochemistryImmunoblottingBiophysicsDirect interfacial localizationShort lengthBiochemistry8-azidoadenosine 5'-triphosphatechemistry.chemical_compoundAdenosine TriphosphateStructural BiologyGeneticsNucleotide binding sitesBifunctionalMolecular BiologyThermophilic bacterium PS3Photoaffinity cross-linkingchemistry.chemical_classificationATP synthasebiologyBacteriaThermophileAffinity LabelsCell BiologyProton-Translocating ATPasesEnzymeCross-Linking ReagentsBiochemistrychemistrybiology.proteinF1-ATPase: Short-length bifunctional photoaffinity labelFEBS Letters
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Electrical properties of Au/CdZnTe/Au detectors grown by the boron oxide encapsulated Vertical Bridgman technique

2016

Abstract In this work we report on the results of electrical characterization of new CdZnTe detectors grown by the Boron oxide encapsulated Vertical Bridgman technique (B-VB), currently produced at IMEM-CNR (Parma, Italy). The detectors, with gold electroless contacts, have different thicknesses (1 and 2.5 mm) and the same electrode layout, characterized by a central anode surrounded by a guard-ring electrode. Investigations on the charge transport mechanisms and the electrical contact properties, through the modeling of the measured current–voltage ( I – V ) curves, were performed. Generally, the detectors are characterized by low leakage currents at high bias voltages even at room tempera…

Nuclear and High Energy PhysicsTraveling heater method electrical propertie02 engineering and technology01 natural sciencesBoron oxide encapsulated Vertical Bridgman techniqueTraveling heater methodElectrical resistivity and conductivity0103 physical sciencesInstrumentationDeposition (law)010302 applied physicsPhysicsInterfacial layer-thermionic-diffusionbusiness.industryCdZnTe detectorsCdZnTe detectorSettore FIS/01 - Fisica SperimentaleBiasing021001 nanoscience & nanotechnologySettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Electrical contactsAnodeBoron oxideelectrical propertiesElectrodeOptoelectronics0210 nano-technologybusinessVoltageNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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Photoaffinity cross-linking of F1ATPase from spinach chloroplasts by 3'-arylazido-beta-alanyl-8-azido ATP.

1994

UV irradiation of the ATPase (CF1) from spinach chloroplasts in the presence of 3'-arylazido-beta-alanyl-8-azido ATP (8,3'-DiN3ATP) results in a nucleotide-dependent inactivation of the enzyme and in a nucleotide-dependent formation of alpha-beta cross-links. The results demonstrate an interfacial localization of the nucleotide binding sites on CF1.

Nucleotide binding siteAzidesChloroplastsStereochemistryPhotochemistryAffinity labelATPaseBiophysicsBiochemistryChloroplastF1ATPasechemistry.chemical_compoundAdenosine TriphosphateStructural BiologyVegetablesGeneticsBinding siteChenopodiaceaeInterfacial localizationMolecular BiologyPhotoaffinity cross-linkingchemistry.chemical_classificationbiologyfood and beveragesAffinity LabelsCell Biologybiology.organism_classificationChloroplastProton-Translocating ATPasesEnzymeCross-Linking Reagentschemistrybiology.proteinSpinach chloroplastAdenosine triphosphateFEBS letters
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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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Chapter III Phase transitions at surfaces

1995

Abstract The statistical mechanics of phase transitions is briefly reviewed, with an emphasis on surfaces. Flat surfaces of crystals may act as a substrate for adsorption of two-dimensional (d=2) monolayers and multilayers, offering thus the possibility to study phase transitions in restricted dimensionality. Critical phenomena for special universality classes can thus be investigated which have no counterpart in d=3. Also phase transitions can occur that are in a sense “in between” different dimensionalities (e.g., multilayer adsorption and wetting phenomena are transitions in between two and three dimensions, while adsorption of monolayers on stepped surfaces allows phenomena in between o…

Phase transitionsymbols.namesakeGibbs isothermCondensed matter physicsChemistryCritical phenomenasymbolsStatistical mechanicsWettingSuperfluid filmInterfacial PhenomenonUniversality (dynamical systems)
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On the measurement of local gas hold-up and interfacial area in gas–liquid contactors via light sheet and image analysis

2010

Abstract Particle image velocimetry techniques coupled with advanced image processing tools are receiving an increasing interest for measuring flow quantities and local bubble-size distributions in gas–liquid contactors. Aim of this work is that of providing a numerical procedure able to reconstruct local gas hold-up and specific interfacial area from images obtained by laser sheet illumination. A correction for measured quantities accounting for laser sheet thickness is proposed and tested by means of Monte Carlo simulations. The algorithms proposed are robust and independent of any measured parameters of the actual bubble size distribution.

PhysicsWork (thermodynamics)Specific interfacial areaMathematical modellingbusiness.industryApplied MathematicsGeneral Chemical EngineeringBubbleFlow (psychology)Monte Carlo methodMultiphase flowImage processingGeneral ChemistryLocal gas hold-upLaserIndustrial and Manufacturing EngineeringImaginglaw.inventionPhysics::Fluid DynamicsOpticsMixingParticle image velocimetrylawMultiphase flowbusinessChemical Engineering Science
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The apparently anomalous effects of surfactants on interfacial tension in the IBA/water system near its upper critical solution temperature

2016

We studied the effect of anionic, cationic, and nonionic surfactants on the interfacial tension between the two phases of the isobutyric acid/water system using spinning drop tensiometry. It has been found that interfacial tension decreases with increasing concentration of the surfactant in the case of sodium dodecyl sulfate (SDS) and of dodecyltrimethylammonium chloride (DTAC). However, in the case of Triton X-100 an increase of surfactant concentration leads to an increase of the interfacial tension. Such results are consistent with the upper critical solution temperature (UCST) in the presence of these surfactants: the UCST decreases with increasing SDS and DTAC concentrations while it i…

Polymers and Plastics02 engineering and technology01 natural sciencesSpinning drop tensiometry010305 fluids & plasmasIsobutyric acidSurface tensionchemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantUpper critical solution temperature0103 physical sciencesPolymer chemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistrySodium dodecyl sulfateSettore CHIM/02 - Chimica FisicaChemistryDrop (liquid)Cationic polymerizationUpper critical solution temperature (UCST)021001 nanoscience & nanotechnologyChemical engineering0210 nano-technologyInterfacial tensionColloid and Polymer Science
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Local gas-liquid hold-up and interfacial area via light sheet and image analysis

2010

Particle Image Velocimetry techniques coupled with advanced Image Processing tools are receiving an increasing interest for measuring flow quantities and local bubble-size distributions in gas-liquid contactors. In this work, an effective experimental technique for measuring local gas hold-up and interfacial area, as well as bubble size distribution, is discussed. The technique, hereafter referred to as Laser Induced Fluorescence with Shadow Analysis for Bubble Sizing (LIF-SABS) is based on laser sheet illumination of the gas-liquid dispersion and synchronized camera, i.e. on equipment typically available within PIV set-ups. The liquid phase is made fluorescent by a suitable dye, and an opt…

Settore ING-IND/25 - Impianti ChimiciGas-Liquid flows Bubbles BSD LIF-SABS local hold-up interfacial area
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Study on Interfacial Surface in Modified Spray Tower

2019

This paper presents an analysis of the changes in interfacial surface and the size of droplets formed in a spray tower. The interfacial surface and the size of droplets formed are of fundamental importance to the performance of the equipment, both in terms of pressure drop and process efficiency. Liquid film and droplet sizes were measured using a microphotography technique. The confusors studied were classical, with profiled inside surface, and with double profiled inside surface. The liquids studied were water and aqueous solutions of high-molecular polyacrylamide (PAA) of power-law characteristics. The ranges of process Reynolds number studied were as follows: ReG &isin

Surface (mathematics)Materials science020209 energyPolyacrylamideBioengineering02 engineering and technologylcsh:Chemical technologyconfusorlcsh:ChemistryPhysics::Fluid Dynamicschemistry.chemical_compoundsymbols.namesake020401 chemical engineering0202 electrical engineering electronic engineering information engineeringChemical Engineering (miscellaneous)lcsh:TP1-11850204 chemical engineeringComposite materialinterfacial surfacePressure dropAqueous solutionProcess Chemistry and TechnologySauter mean diameterReynolds numberSauter mean diameterlcsh:QD1-999chemistrymodified spray towerSpray towersymbolsDimensionless quantityProcesses
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PMMA-titania nanocomposites: Properties and thermal degradation behavior

2012

Titania nanoparticles were prepared using a solegel method and calcination at 200 and 600 � C in order to obtain anatase and rutile phases, respectively. The obtained powders were used to prepare PMMAe titania nanocomposites by a melt compounding method. The effect of the crystalline phase and the amount of titania, in the range 1e5 wt.%, on the morphology, mechanical properties and thermal degradation kinetics of PMMA was investigated by means of X-ray diffractometry (XRD), transmission electron microscopy (TEM), 13 C cross-polarization magic-angle spinning nuclear magnetic resonance spectroscopy ( 13 C{ 1 H}CP-MAS NMR), including the measurement of proton spinelattice relaxation time in t…

Thermogravimetric analysisAnataseMaterials sciencePolymers and Plasticslaw.inventionlawnanocompositesPMMA Titania Nanocomposites Interfacial interaction Properties Degradation kineticsMaterials ChemistrytitaniaCalcinationFourier transform infrared spectroscopyComposite materialSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationNanocompositePolymerDynamic mechanical analysisCondensed Matter PhysicsPMMAAmorphous soliddegradation kineticsChemical engineeringchemistryMechanics of MaterialspropertiesPMMA; titania; nanocomposites; interfacial interaction; properties; degradation kineticsinterfacial interaction
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