Search results for "THERMODYNAMICS"

showing 10 items of 2774 documents

Thermodynamics-based gradient plasticity theories with an application to interface models

2008

AbstractIn the framework of small deformations, the so-called residual-based gradient plasticity theory is reconsidered and improved. Using the notion of moving geometrically necessary dislocations (GNDs), suitable micromechanics interpretations are heuristically given for the higher order boundary conditions and the long distance particle interactions. Also, a comparison is made between this theory and the analogous virtual work principle (VWP)-based one, whereby their respective conceptual and methodological features are pointed out. The conditions under which the two theories lead to a same constitutive model are investigated, showing that, correspondingly, a certain indeterminacy exhibi…

Interface (Java)Mechanical EngineeringApplied MathematicsConstitutive equationDislocationsMicromechanicsResidualCondensed Matter PhysicsGradient plasticityIndeterminacy (literature)Nonlocal continuum thermodynamicsClassical mechanicsMaterials Science(all)Mechanics of MaterialsModeling and SimulationModelling and SimulationGeneral Materials SciencePoint (geometry)Virtual workBoundary value problemStatistical physicsMathematicsInternational Journal of Solids and Structures
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Solutions properties and solute–solvent interactions in ternary sugar–salt–water solutions

2010

International audience; Viscometric constants were used to provide information on solute-solvent interactions in ternary water-sugar-salt solutions. Comparison was made between pure water and aqueous salt solution as solvents affecting the behaviour of small carbohydrates. The determination of intrinsic viscosity was made more accurate by applying triple extrapolation of the three equations (Huggins. Kramer and Meffroy-Biget). Results obtained with this triple extrapolation method were compared to that obtained with the Jones-Dole equation usually used. The B coefficient of the Jones-Dole equation was interpreted in terms of its components (B(size)) and (B(structure)), respectively assigned…

Intrinsic viscositySalt (chemistry)Thermodynamicsinteraction02 engineering and technologyFood chemistry010402 general chemistry01 natural sciencesAnalytical ChemistryViscosityMolar volume020401 chemical engineering[SDV.IDA]Life Sciences [q-bio]/Food engineering0204 chemical engineeringaqueous salt solutionsapparent molar volumechemistry.chemical_classificationAqueous solutionChromatographyGeneral Medicine6. Clean water0104 chemical sciencesSolventchemistrysugarsviscosityTernary operationhydrationFood Science
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Isomerism of [64Cu-NOTA-Bn]-labeled radiotracers: separation of two complex isomers and determination of their interconversion energy barrier using i…

2011

The model complex [(64)Cu((S)-p-NH(2)-Bn-NOTA)](-) ([(64)Cu]1) was used to study the isomerism of [(64)Cu-NOTA-Bn]-labeled radiotracers. Two complex isomers [(64)Cu]1a and [(64)Cu]1b, which were formed at a ratio of 1:9 during the complexation of [(64)Cu]Cu(2+) with (S)-p-NH(2)-Bn-NOTA, were separated using ion pair chromatography. To study the interconversion, the nonradioactive complex isomers Cu1a and Cu1b were separated and thermally treated at 90 °C in both ammonium acetate solution and deionized water. A faster interconversion rate was observed for both isomers with lower concentrations of ammonium ions. At the end of reaction, the thermodynamic Cu1a to Cu1b equilibrium ratio was 6:94…

Ion pair chromatographyAnalytical chemistryMolecular Conformationchemistry.chemical_elementAcetatesChemical Fractionation010402 general chemistry01 natural sciencesMolecular conformationIonInorganic Chemistrychemistry.chemical_compoundHeterocyclic Compounds 1-RingDrug StabilityIsomerismCoordination ComplexesHeterocyclic CompoundsAmmoniumPhysical and Theoretical ChemistryRadioactive TracersChromatography010405 organic chemistryChemistryChemical fractionationTemperatureWaterHydrogen-Ion ConcentrationCopper0104 chemical sciencesSolutionsPositron-Emission TomographyPhysical chemistryThermodynamicsAmmonium acetateCopperInorganic chemistry
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Anomalous and Not-So-Common Behavior in Common Ionic Liquids and Ionic Liquid-Containing Systems

2019

This work highlights unexpected, not so well known responses of ionic liquids and ionic liquid-containing systems, which are reported in a collective manner, as a short review. Examples include: (i) Minima in the temperature dependence of the isobaric thermal expansion coefficient of some ILs; (ii) Viscosity Minima in binary mixtures of IL + Molecular solvents; (iii) Anomalies in the surface tension within a family of ILs; (iv) The constancy among IL substitution of Cp/Vm at and around room temperature; (v) ILs as glass forming liquids; (vi) Alternate odd-even side alkyl chain length effects; (vii) Absolute negative pressures in ILs and IL-containing systems; (viii) Reversed-charged ionic l…

Ionic bondingThermodynamicsReview02 engineering and technology010402 general chemistry01 natural sciencesLower critical solution temperatureodd-even effectsThermal expansionionic liquidslcsh:ChemistrySurface tensionchemistry.chemical_compoundViscosityLCSTsurface tensionAlkylchemistry.chemical_classificationreversed charge ILsunusual behaviorGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemistrylcsh:QD1-999chemistrythermal expansion coefficientviscosityIonic liquidIsobaric process0210 nano-technologyFrontiers in Chemistry
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Classical ionic fluids in the mean spherical approximation

1980

The recently obtained analytical solution of the mean spherical approximation has been used to calculate thermodynamic and structural properties of aqueous solutions of asymmetric electrolytes. The same approximation has also been used to calculate structure functions of pure and mixed molten salts. The agreement between experimental or “quasi-experimental” structure functions and those obtained within the framework of the MSA is quite good especially when the ionic radii are obtained by fitting the long wavelength limit of the structure functions to the isothermal compressibility of the system, under the condition that the diameter ratio is the same as in the crystal.

Ionic radiusLong wavelength limitChemistryIonic bondingThermodynamicsElectrolyteRadial distribution functionInorganic ChemistryCrystalMaterials ChemistryCompressibilityPhysical chemistryPhysical and Theoretical ChemistryMolten saltInorganica Chimica Acta
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Nonadiabatic transitions between lambda-doubling states in the capture of a diatomic molecule by an ion

2008

The low-energy capture of a dipolar diatomic molecule in an adiabatically isolated electronic state with a good quantum number Hund’s coupling case a by an ion occurs adiabatically with respect to rotational transitions of the diatom. However, the capture dynamics may be nonadiabatic with respect to transitions between the pair of the -doubling states belonging to the same value of the intrinsic angular momentum j. In this work, nonadiabatic transition probabilities are calculated which define the -doubling j-specific capture rate coefficients. It is shown that the transition from linear to quadratic Stark effect in the ion-dipole interaction, which damps the T �1/2 divergence of the captur…

IonsAngular momentumTime FactorsRotationChemistryStatic ElectricityGeneral Physics and AstronomyElectronsElectronDiatomic moleculeIonGood quantum numbersymbols.namesakeDipoleStark effectsymbolsQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryAtomic physicsAdiabatic processAlgorithmsThe Journal of Chemical Physics
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Interactions of the alternating double stranded copolymer poly(dA-dT).poly(dA-dT) with NiCl2 and CdCl2: solution behaviour

2007

The thermal denaturation of the synthetic high molecular weight double stranded polynucleotide poly(dA-dT) x poly(dA-dT) has been studied in aqueous buffered solution (Tris 1.0 mM; pH 7.8+/-0.2) in the presence of increasing concentrations of either Ni(2+) (borderline cation) or Cd(2+) (soft cation) at four different constant ionic strength values (NaCl), making use of UV and circular dichroism (CD) spectroscopies. The experimental results show that the B-type double helix of the polymer is stabilized against thermal denaturation in the presence of both cations at low concentrations, relative to the systems where only NaCl is present, in the same conditions of ionic strength and pH. The eff…

IonsCircular DichroismModel polynucleotideOsmolar ConcentrationUV-spectroscopyNickel (II) and Cadmium (II) ionThermal denaturationModel polynucleotides; Thermal denaturation; Nickel (II) and Cadmium (II) ions; Circular Dichroism; UV-spectroscopySolutionsCadmium ChloridePoly dA-dTNickelNucleic Acid ConformationThermodynamics
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Self-consistent continuum solvation (SCCS): the case of charged systems.

2013

The recently developed self-consistent continuum solvation model (SCCS) [O. Andreussi, I. Dabo, and N. Marzari, J. Chem. Phys. 136, 064102 (2012)] is applied here to charged species in aqueous solutions. Describing ions in solution represents a great challenge because of the large electrostatic interactions between the solute and the solvent. The SCCS model is tested over 106 monocharged species, both cations and anions, and we demonstrate its flexibility, notwithstanding its much reduced set of parameters, to describe charged species in solution. Remarkably low mean absolute errors are obtained with values of 2.27 and 5.54 kcal/mol for cations and anions, respectively. These results are co…

IonsModels MolecularAqueous solutionChemistryMetal ions in aqueous solutionImplicit solvationStatic ElectricitySolvationGeneral Physics and AstronomyWaterElectrostaticsIonSolventSolvation shellChemical physicsComputational chemistryQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryThe Journal of chemical physics
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Do zwitterionic species exist in the non-enzymatic peptide bond formation?

2012

The use of proper computational methods and models has allowed answering the controversial question of whether zwitterionic species exist in the mechanism of peptide bond synthesis in aqueous solution. In fact, the different conformations of zwitterionic species open the door to different mechanistic paths.

IonsModels MolecularAqueous solutionChemistryMetals and AlloysGeneral ChemistryZwitterionicCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPeptide bondNon enzymaticMaterials ChemistryCeramics and CompositesQuantum TheoryThermodynamicsPeptide bondOrganic chemistryPeptidesChemical Communications
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Pattern Formation Kinetics for Charged Molecules on Surfaces: Microscopic Correlation Function Analysis

2011

The kinetics of pattern formation and phase separation in a system of two types of oppositely charged molecules with competing short- and long-range interactions on surfaces/interfaces is studied combining three methods: a microscopic formalism of the joint correlation functions, reverse Monte Carlo, and nonequilibrium charge-screening factors. The molecular ordering occurs on the background of the Ostwald ripening and thus is strongly nonequilibrium. We have demonstrated how initial random distribution of molecules is changed for loose similar-molecule aggregates, with further reorganization into dense macroscopic domains of oppositely charged molecules. Pattern formation process is charac…

IonsModels MolecularOstwald ripeningChemistryKineticsMonte Carlo methodNon-equilibrium thermodynamicsPattern formationReverse Monte CarloSurfaces Coatings and FilmsKineticsCorrelation function (statistical mechanics)symbols.namesakeCrystallographyChemical physicsMaterials ChemistrysymbolsMoleculePhysical and Theoretical ChemistryMonte Carlo MethodThe Journal of Physical Chemistry B
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