Search results for "53"

showing 10 items of 2908 documents

Correlated gluonic hot spots meet symmetric cumulants data at LHC energies

2019

We present a systematic study on the influence of spatial correlations between the proton constituents, in our case gluonic hot spots, their size and their number on the symmetric cumulant SC(2, 3), at the eccentricity level, within a Monte Carlo Glauber framework [1]. When modeling the proton as composed by 3 gluonic hot spots, the most common assumption in the literature, we find that the inclusion of spatial correlations is indispensable to reproduce the negative sign of SC(2, 3) in the highest centrality bins as dictated by data. Further, the subtle interplay between the different scales of the problem is discussed. To conclude, the possibility of feeding a 2+1D viscous hydrodynamic sim…

COLLISIONSNuclear and High Energy PhysicsParticle physicsNuclear TheoryFLOWMonte Carlo methodFOS: Physical sciencesSmall systemshiukkasfysiikka114 Physical sciences01 natural sciences7. Clean energyHigh Energy Physics - ExperimentNuclear Theory (nucl-th)High Energy Physics - Experiment (hep-ex)High Energy Physics - Phenomenology (hep-ph)correlations0103 physical sciencesEntropy (information theory)ddc:530initial state010306 general physicsCumulantPhysicsLarge Hadron Colliderta114010308 nuclear & particles physicselliptic flowElliptic flowhot spotsHigh Energy Physics - Phenomenologysmall systemsSubstructureGlauberNuclear Physics A
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Non-radial pulsations in be stars. Preparation of the corot space mission

2006

The general objective of the present work is to contribute to the knowledge of the physics of Be Stars. In particular, we are interested in studying and characterizing their pulsational properties. A very suitable tool to reach this goal is the study and analysis of photometric time series with the maximum time baseline, density and photometric accuracy.The space mission COROT scheduled to be launched in December 2006, will provide ultra high precision, relative stellar photometry for very long continuous observing runs. Up to ten stars will be observed in the seismology fields with a photometric accuracy of a few 10-4 and color information during 150 days.The observations of Be stars with …

COROT53Be starsAstrophysics::Solar and Stellar AstrophysicsFísicaAstrophysics::Cosmology and Extragalactic AstrophysicsAstrophysics::Earth and Planetary AstrophysicsSmall Magellanic CloudsAstersoseismologyAstrophysics::Galaxy Astrophysics
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Improved limit on the directly measured antiproton lifetime

2017

Continuous monitoring of a cloud of antiprotons stored in a Penning trap for 405 days enables us to set an improved limit on the directly measured antiproton lifetime. From our measurements we extract a storage time of $3.15\times {10}^{8}$ equivalent antiproton-seconds, resulting in a lower lifetime limit of ${\tau }_{\bar{{\rm{p}}}}\gt 10.2\,{\rm{a}}$ with a confidence level of $68 \% $. This result improves the limit on charge-parity-time violation in antiproton decays based on direct observation by a factor of 7.

CPT symmetryPenning trapGeneral Physics and Astronomypenning traps01 natural sciencesLower limit010305 fluids & plasmasNuclear physicsContinuous monitoring0103 physical sciencesddc:530Limit (mathematics)Physics::Atomic Physics010306 general physicsNuclear ExperimentPhysicsCPT invariancePhysicsResearchContinuous monitoringDirect observationsDirect observationConfidence levelsPenning trapCharge parityAntiprotonlifetimesPhysics::Accelerator PhysicsCP violationHigh Energy Physics::ExperimentDewey Decimal Classification::500 | Naturwissenschaften::530 | PhysikPräzisionsexperimente - Abteilung BlaumantiprotonsParticle Physics - Experiment
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Umme Dunia, un romanzo italiano del XIX secolo sulla caduta di Costantinipoli

2006

A partire dal romanzo Umme Dunia di Alberto Furse, si analizzano varie testimonianze sulla conquista turca di Costantinopoli nel 1453.

Caduta di Costantinopoli. 1453. RomanziSettore L-LIN/20 - Lingua E Letteratura Neogreca
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Molecular Self-Assembly Versus Surface Restructuring During Calcite Dissolution.

2016

Organic additives are known to alter the mineral-water interface in various ways. On the one hand, organic molecules can self assemble into ordered structures wetting the surface. On the other hand, their presence can affect the interfacial morphology, referred to as surface restructuring. Here, we investigate the impact, of a class of calcium-complexing azo dyes on the dissolution of calcite (10.4) using high-resolution atomic force microscopy operated in aqueous solution, with a focus on the two constitutional isomers Eriochrome Black T and Eriochrome Black A. A very pronounced surface restructuring is observed in the presence of the dye solution, irrespective of the specific dye used and…

CalciteAqueous solutionMorphology (linguistics)Chemistry02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences5300104 chemical sciencesEriochrome Black Tchemistry.chemical_compoundChemical engineeringElectrochemistryMolecular self-assemblyOrganic chemistryMoleculeGeneral Materials ScienceWetting0210 nano-technologyDissolutionSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Where Is the Most Hydrophobic Region? Benzopurpurine Self-Assembly at the Calcite–Water Interface

2017

Control of molecular self-assembly at solid–liquid interfaces is challenging due to the complex interplay between molecule–molecule, molecule–surface, molecule–solvent, surface–solvent, and solvent–solvent interactions. Here, we use in-situ dynamic atomic force microscopy to study the self-assembly of Benzopurpurine 4B into oblong islands with a highly ordered inner structure yet incommensurate with the underlying calcite (10.4) surface. Molecular dynamics and free energy calculations provide insights by showing that Benzopurpurine 4B molecules do not anchor to the surface directly but instead assemble on top of the second hydration layer. This seemingly peculiar behavior was then rationali…

CalciteChemistryAtomic force microscopy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHydrophobeMolecular dynamicschemistry.chemical_compoundCrystallographyGeneral EnergyAdsorptionChemical physicsMoleculeSelf-assemblyPhysical and Theoretical Chemistry0210 nano-technologyLayer (electronics)The Journal of Physical Chemistry C
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Stabilization of Polar Step Edges on Calcite (10.4) by the Adsorption of Congo Red

2015

In this work, we present the stabilization of polar step edges along the [010] direction of calcite (10.4) by the presence of a water-soluble organic molecule, namely Congo Red. While characteristic etch pits are observed on the surface in the absence of the additive, no etch pits can be found in the presence of the additive. Using atomic force microscopy, we can directly follow the restructuring of the surface. Upon addition of Congo Red, the charge-neutral step edges confining the characteristic etch pits vanish, while polar step edges along the [010] direction appear on the surface, which are entirely decorated by well-ordered molecular islands of the additive. After the restructuring ha…

CalciteChemistryDirect evidenceAtomic force microscopyMineralogySurfaces and InterfacesCondensed Matter Physics530Congo redchemistry.chemical_compoundAdsorptionChemical physicsElectrochemistryPolarStep edgesMoleculeGeneral Materials ScienceSpectroscopy
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Structure-Dependent Dissolution and Restructuring of Calcite Surfaces by Organophosphonates

2017

Organophosphonates are well-known to strongly interact with the surfaces of various minerals, such as brucite, gypsum, and barite. In this work, we study the influence of six systematically varied organophosphonate molecules (tetraphosphonates and diphosphonates) on the dissolution process of the (10.4) surface of calcite. In order to pursue a systematic study, we have selected organophosphonates that exhibit similar structural features, but also systematic architectural differences. The effect of this class of additives on the dissolution process of the calcite (10.4) surface is evaluated using in situ dynamic atomic force microscopy. For all of the six organophosphonate derivatives, we ob…

CalciteGypsumAtomic force microscopyBruciteDiphosphonates02 engineering and technologyGeneral Chemistryengineering.material010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics53001 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryChemical engineeringengineeringMoleculeGeneral Materials ScienceOrganophosphonates0210 nano-technologyDissolutionCrystal Growth & Design
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Deposition order controls the first stages of a metal-organic coordination network on an insulator surface

2016

| openaire: EC/FP7/610446/EU//PAMS We report on first stages toward the formation of a surface-confined metal-organic coordination network (MOCN) by sequential deposition of biphenyl-4,4′-dicarboxylic acid and iron atoms on the surface of a bulk insulator, calcite (10.4). The influence of the deposition order on the structure formation is studied by noncontact atomic force microscopy operated in ultrahigh vacuum at room temperature. It is found that sequential deposition facilitates MOCN formation when the organic linker molecules are first adsorbed on the surface, followed by iron deposition. This observation is explained by first-principles computations, indicating that the metal-molecule…

CalciteStructure formationta114Atomic force microscopyIron deposition02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundGeneral EnergyAdsorptionchemistryChemical physicsLattice (order)Coordination networkMoleculePhysical and Theoretical Chemistry0210 nano-technologyJournal of Physical Chemistry C
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Three-dimensional hydration layer mapping on the (10.4) surface of calcite using amplitude modulation atomic force microscopy

2014

Calcite, the most stable modification of calcium carbonate, is a major mineral in nature. It is, therefore, highly relevant in a broad range of fields such as biomineralization, sea water desalination and oil production. Knowledge of the surface structure and reactivity of the most stable cleavage plane, calcite (10.4), is pivotal for understanding the role of calcite in these diverse areas. Given the fact that most biological processes and technical applications take place in an aqueous environment, perhaps the most basic - yet decisive - question addresses the interaction of water molecules with the calcite (10.4) surface. In this work, amplitude modulation atomic force microscopy is used…

CalciteSurface (mathematics)Work (thermodynamics)solid-liquid interfaceAqueous solutionMineralMaterials sciencehydration layerMechanical EngineeringMineralogyBioengineeringGeneral Chemistry530chemistry.chemical_compoundCalcium carbonatechemistry3D mappingMechanics of MaterialsMoleculeGeneral Materials ScienceAFMElectrical and Electronic EngineeringcalciteBiomineralizationNanotechnology
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