Search results for "Liquid state"

showing 10 items of 18 documents

Multiple vibrational resonances in the Raman spectra of liquid ethanes

1990

The Raman spectra of liquid ethane, ethane-d3 and ethane-d6 were recorded and analysed. The CH3 and CD3 stretching regions were computer resolved using Cauchy-Gaussian and Voigt functions to account for asymmetric band shapes. Multiple vibrational resonances were investigated using the wavenumbers and observed intensities in these regions. The developed basis functions show strong mixing of the levels in these regions. In general the resonances appear to be less strong in the liquid phase than reported in previous studies of the gaseous state. Some new assignments in the liquid-state spectra of ethanes could be suggested.

010304 chemical physicsChemistryComputer aidLiquid phaseBasis function02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsSpectral linesymbols.namesakeLiquid stateNuclear magnetic resonance0103 physical sciencessymbolsWavenumberGeneral Materials ScienceAstrophysics::Earth and Planetary AstrophysicsPhysics::Chemical Physics0210 nano-technologyRaman spectroscopySpectroscopyMixing (physics)Journal of Raman Spectroscopy
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Temperature dependent properties of environmentally important synthetic musks.

2002

Environmental fate determining physical properties including their temperature dependence for five nitro musks and for seven polycyclic musks were estimated. The properties evaluated were vapor pressure in a solid and liquid state (PS and PL), solubility in water (S), Henry's law coefficient (H = PL/S) and log octanol-water partition coefficient (log KOW). Gas chromatography for starting values of vapor pressure estimation and HPLC experiments at 5-20 degrees C for comparison of the theoretical versus experimental solubilities in water were performed. The values of temperature (T) dependence coefficients (Ai and Bi) in equations: log (Property)i = Ai - Bi/T were determined. Values of proper…

Air PollutantsChromatographyVolatilisationChemical PhenomenaChemistryVapor pressureChemistry PhysicalHealth Toxicology and MutagenesisAnalytical chemistryTemperatureGeneral MedicinePollutionHigh-performance liquid chromatographyHenry's lawPartition coefficientFatty Acids MonounsaturatedLiquid stateEnvironmental ChemistryGas chromatographySolubilityVolatilizationEnvironmental science and pollution research international
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How Do Droplets Depend on the System Size? Droplet Condensation and Nucleation in Small Simulation Cells

2003

Using large scale grandcanonical Monte Carlo simulations in junction with a multicanonical reweighting scheme we investigate the liquid-vapor transition of a Lennard—Jones fluid. Particular attention is focused on the free energy of droplets and the transition between different system configurations as the system tunnels between the vapor and the liquid state as a function of system size. The results highlight the finite size dependence of droplet properties in the canonical ensemble and free energy barriers along the path from the vapor to the liquid in the grandcanonical ensemble.

Condensed Matter::Soft Condensed MatterPhysics::Fluid DynamicsCanonical ensembleLiquid stateMaterials scienceScale (ratio)Monte Carlo methodCondensationNucleationMechanicsSize dependence
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Relation of Interdiffusion and Self-Diffusion in Polymer Mixtures

1986

From different assumptions one obtains linear relationships either between the interdiffusion coefficient and the self-diffusion coefficients or between the inverse interdiffusion coefficient and the inverse self-diffusion coefficients. The nature of these assumptions and possible experiments for discriminating between them are discussed.

Condensed Matter::Soft Condensed Matterchemistry.chemical_classificationCondensed Matter::Materials ScienceSelf-diffusionLiquid stateChemistryInverseThermodynamicsPhysical chemistryPolymerPolymer blendComputer Science::Other
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Heterogeneity at the glass transition: what do we know?

2002

We critically discuss the information that can be obtained from experiments with respect to the existence, the life time, and the length scale of dynamical heterogeneity in glass-forming liquids. The ability to select a dynamically distinguishable subensemble and observe its return to the full equilibrium ensemble is illustrated by examples from multi-dimensional NMR. We also discuss non-resonant hole burning spectroscopy as an example for which two separate time scales are involved.

Length scaleLiquid stateCondensed matter physicsChemistryMaterials ChemistryCeramics and CompositesSpin echoLife timeDynamical heterogeneityCondensed Matter PhysicsGlass transitionSpectroscopyElectronic Optical and Magnetic MaterialsJournal of Non-Crystalline Solids
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Electronic-structure-induced deformations of liquid metal clusters

1995

Ab initio molecular dynamics is used to study deformations of sodium clusters at temperatures $500\cdots 1100$ K. Open-shell Na$_{14}$ cluster has two shape isomers, prolate and oblate, in the liquid state. The deformation is stabilized by opening a gap at the Fermi level. The closed-shell Na$_8$ remains magic also at the liquid state.

Liquid metalCondensed Matter - Materials ScienceMaterials scienceFermi levelMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesElectronic structureProlate spheroidMolecular physicsAb initio molecular dynamicssymbols.namesakeLiquid stateCluster (physics)symbolsPhysics::Atomic and Molecular ClustersDeformation (engineering)
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Precise measurement of 1H 90° pulse in solid-state NMR spectroscopy for complex and heterogeneous molecular systems

2007

The 90 degrees pulse calibration is essential in NMR spectroscopy to prevent artefacts in the liquid state or to enhance cross-polarization efficiency in the solid state. We verified pulse-angle (PA) errors due to circuit impedances in solid-state NMR and suggested a possible solution to prevent the inconvenience of PA errors. The classic pulse sequences used to calibrate (1)H 90 degrees pulse lengths by direct detection of protons or by cross-polarization were modified in order to replace single (1)H pulses with (1)H pulse trains. Pulse trains were found to decrease the effect of PA imperfections in the calibration of basic pulses (i.e. 90 degrees and 180 degrees ) for a number of organic …

Magnetic Resonance SpectroscopyMagic angleChemistrySettore AGR/13 - Chimica AgrariaAnalytical chemistryReproducibility of ResultsNuclear magnetic resonance spectroscopyBiochemistryAnalytical ChemistryPulse (physics)Liquid stateSolid-state nuclear magnetic resonanceCalibrationCross polarization magic angle spinning NMR 1H 90° pulse Pulse calibration Circuit impedance Complex molecular systemsCalibrationSpectroscopyElectrical impedanceAnalytical and Bioanalytical Chemistry
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Solvation parameters of solutes: an attempt of improvements in characterization and determination

2008

We are presenting here an updated version of our predictive model of solvation parameters of solutes, based on a simplified molecular topology (J. Chem. Inf. Model, 2006, 46, 1723-1734). The learning experimental database of this model is presently larger than in our first version and includes more compounds with more than one functional group of the same type. This experimental database is also surer, in the sense that it only includes compounds in liquid state at room temperature, when the polarizability of a compound in solution is established via its refractive index in gas or crys- talline state. Indeed, we demonstrate in this paper, a bias in this case.

Materials science[SCCO.NEUR]Cognitive science/Neuroscience[SCCO.NEUR] Cognitive science/NeuroscienceSolvationThermodynamicsState (functional analysis)Type (model theory)Characterization (materials science)Liquid statePolarizability[ SCCO.NEUR ] Cognitive science/NeuroscienceMolecular topologyRefractive indexComputingMilieux_MISCELLANEOUS
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Advances in Microwave and Submillimeter-Wave Dielectric Spectroscopic Techniques and their Applications

2007

Measurement methodOpticsLiquid stateSpectrometerChemistrybusiness.industryDielectric lossDielectricbusinessRefractive indexMicrowaveSubmillimeter wave
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DNP in MRI: an in-bore approach at 1.5 T.

2011

Abstract We have used liquid state (“Overhauser”) Dynamic Nuclear Polarization (DNP) to significantly enhance the signal to noise ratio (SNR) of Magnetic Resonance Imaging (MRI). For the first time this was achieved by hyperpolarizing directly in the MRI-scanner field of 1.5 T in continuous flow mode and immediately delivering the hyperpolarized substance to the imaging site to ensure maximum contrast between hyperpolarized sample and sample at thermal polarization. We achieve a maximum absolute signal enhancement factor of 98; while the hyperpolarized sample is transported at a flow rate of up to 30 ml/h yielding an average flow speed up to 470 mm/s over a distance of approximately 80 mm. …

Nuclear and High Energy PhysicsContrast enhancementMagnetic Resonance Spectroscopymedicine.diagnostic_testContinuous flowChemistryPhantoms ImagingBiophysicsMagnetic resonance imagingSignal-To-Noise RatioCondensed Matter PhysicsPolarization (waves)BiochemistryMagnetic Resonance ImagingVolumetric flow rateSignal enhancementCyclic N-OxidesLiquid stateNuclear magnetic resonanceFlow velocitymedicineImage Processing Computer-AssistedSpin LabelsMicrowavesCopperJournal of magnetic resonance (San Diego, Calif. : 1997)
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