Search results for "THERMODYNAMICS"

showing 10 items of 2774 documents

Generalized transport coefficients in a gas with large shear rate

1987

We get a solution of the Bhatnagar-Gross-Krook (BGK) model kinetic equation by means of a perturbative expansion of a temperature gradient to study the transport properties in a gas with large shear rate. The irreversible fluxes are evaluated exactly to first order in the expansion for Maxwell molecules. The transport coefficients obtained are highly nonlinear functions of the shear rate. This dependence on shear rate is analysed and compared with previous results for several transport coefficients. Finally, we have found a solution for a simple model of constant collision frequency for which a large shear rate coexists with an arbitrary temperature gradient.

ChemistryBiophysicsThermodynamicsMechanicsCondensed Matter PhysicsFirst orderPhysics::Fluid DynamicsShear rateSimple shearNonlinear systemTemperature gradientCollision frequencyKinetic equationsPhysical and Theoretical ChemistryConstant (mathematics)Molecular BiologyMolecular Physics
researchProduct

Transport equations of electrodiffusion processes in the laboratory reference frame.

2006

The transport equations of electrodiffusion processes use three reference frames for defining the fluxes: Fick's reference in diffusion, solvent-fixed reference in transference numbers, and laboratory fluxes in electric conductivity. The convenience of using only one reference frame is analyzed here from the point of view of the thermodynamics of irreversible processes. A relation between the fluxes of ions and solvent and the electric current density is deduced first from a mass and volume balance. This is then used to show that (i) the laboratory and Fick's diffusion coefficients are identical and (ii) the transference numbers of both the solvent and the ion in the laboratory reference fr…

ChemistryBoundary (topology)ThermodynamicsMechanicsSurfaces Coatings and FilmsIonElectrical resistivity and conductivityMaterials ChemistryPhysical and Theoretical ChemistryElectric currentExperimental methodsDiffusion (business)Volume balanceReference frameThe journal of physical chemistry. B
researchProduct

Capillary Hysteresis in Nanopores: Theoretical and Experimental Studies of Nitrogen Adsorption on MCM-41

1995

Capillary hysteresis in cylindrical nanopores has been studied using MCM-41 as the prime example of a mesoporous material. These materials, due to their regular pore structure, can be considered to be candidates for reference adsorbents for standardizing adsorption measurements and methods for characterization of porous solids. They provide a unique opportunity for verification of theoretical models employed for predicting phase equilibrium in confined geometry. Three samples with monodisperse pore channels have been synthesized and examined using X-ray diffraction (XRD). Nitrogen adsorption isotherms were modeled using nonlocal density functional theory (NLDFT) in a wide range of pore size…

ChemistryCapillary actionDispersityMineralogyThermodynamicsSurfaces and InterfacesCondensed Matter PhysicsCondensed Matter::Materials ScienceNanoporeHysteresisAdsorptionMetastabilityElectrochemistryGeneral Materials ScienceDensity functional theoryMesoporous materialSpectroscopyLangmuir
researchProduct

Mechanistic and kinetic insight into spontaneous cocrystallisation of isoniazid and benzoic acid

2015

Solid-state cocrystallisation is of contemporary interest, because it offers an easy and efficient way to produce cocrystals, which are recognized as prospective pharmaceutical materials. Research explaining solid-state cocrystallisation mechanisms is important, but still too scarce to give a broad understanding of factors governing and limiting these reactions. Here we report an investigation of the mechanism and kinetics of isoniazid cocrystallisation with benzoic acid. This reaction is spontaneous; however its rate is greatly influenced by environmental conditions (humidity and temperature) and pre-treatment (milling) of the sample. The acceleration of cocrystallisation in the presence o…

ChemistryChemistry PharmaceuticalIsoniazidKineticsPharmaceutical Sciencefood and beveragesLimitingBenzoic AcidCocrystalKineticschemistry.chemical_compoundDrug StabilitySolubilityX-Ray DiffractionMechanism (philosophy)MechanochemistryDrug DiscoveryIsoniazidmedicineThermodynamicsMolecular MedicineOrganic chemistryCrystallizationmedicine.drugBenzoic acid
researchProduct

Fourier transform infrared analysis of paint solvents

1991

Abstract The composition of solvent mixtures employed in the paint industry was determined by Fourier transform infrared spectrometry. A procedure based on the use of the ratio between the absorbance of characteristic bands of each component permits the ratio between two solvents in a binary mixture to be determined, independently of the thickness of the sample film. Typical mixtures of xylol with butan-1-ol and with butyl acetate (xylol=mixture of o-, m- and p-xylenes) were used as model systems to develop the proposed procedure and the accuracy was determined using synthetic formulations. Another possible application of the procedure is the characterization of azeotropic mixtures.

ChemistryComponent (thermodynamics)InfraredAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistrySolventAbsorbancechemistry.chemical_compoundsymbols.namesakeFourier transformsymbolsEnvironmental ChemistryFourier transform infrared spectrometryButyl acetateSpectroscopyAnalytica Chimica Acta
researchProduct

On the relaxation mechanisms of 6-azauracil

2011

The nonadiabatic photochemistry of 6-azauracil has been studied by means of the CASPT2//CASSCF protocol and double-ζ plus polarization ANO basis sets. Minimum energy states, transition states, minimum energy paths, and surface intersections have been computed in order to obtain an accurate description of several potential energy hypersurfaces. It is concluded that, after absorption of ultraviolet radiation (248 nm), two main relaxation mechanisms may occur, via which the lowest (3)(ππ*) state can be populated. The first one takes place via a conical intersection involving the bright (1)(ππ*) and the lowest (1)(nπ*) states, ((1)ππ*/(1)nπ*)(CI), from which a low-energy singlet-triplet crossin…

ChemistryConical intersectionPotential energyTransition stateSurfaces Coatings and FilmsMaterials ChemistryEnergy levelQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryAtomic physicsTriplet stateGround stateUracilUltraviolet radiationFOTOQUÍMICA
researchProduct

Structural relaxation in a molten salt probed by time-dependent dc conductivity measurements

1998

Abstract Time-dependent dc conductivity was measured after cooling steps of about 2 K in the glass transformation range of 2Ca(NO 3 ) 2 -3RbNO 3 . The shape and time scale of the structural relaxation function was thus monitored for times 60 s t 6 s. The time scale could be compared with results from scanning calorimetry measurements and good agreement was found. From the heat capacity data and from the solid state conductivity the expected liquid state conductivity relaxation time was calculated using several models. The good compatibility of these calculations with the experimental results provides evidence that near the calorimetric glass transition the mobile ions perform concerted moti…

ChemistryDc conductivityRelaxation (NMR)Analytical chemistryThermodynamicsCalorimetryConductivityCondensed Matter Physics530Heat capacityElectronic Optical and Magnetic MaterialsIonMaterials ChemistryCeramics and CompositesMolten saltGlass transitionJournal of Non-Crystalline Solids
researchProduct

Modelling of thermo-chemical properties over the sub-solidus MgO–FeO binary, as a function of iron spin configuration, composition and temperature

2014

Thermo-chemical properties and T–X phase relations diagram of the (Mg,Fe)O solid solution are modelled using mixing Helmholtz energy, ΔF(T,x)mixing, calculated by quantum mechanical and semi-empirical techniques. The sub-solidus MgO–FeO binary has been explored as a function of composition, with iron either in high-spin (HS) or low-spin (LS) configuration. Only the HS model provides physically sound results at room pressure, yielding a correct trend of cell edge versus composition, whereas LS’s issues are at variance with observations. Mixing Helmholtz energy has been parametrized by the following relationship: ΔF(T,x)mixing = x × y × [U0(T) + U1(T) × (x – y) + U2(T) × (x − y)2]−T × S(x,y)c…

ChemistryDegrees of freedom (physics and chemistry)(MgFe)OThermodynamicsSolidusMixing energyGibbs free energyMixing energy; Ab initio and semi-empirical modelling; (Mg; Fe)Osymbols.namesakeCrystallography(MgFe)O; Ab initio and semi-empirical modelling; Mixing energy; Geochemistry and Petrology; Materials Science (all)Geochemistry and PetrologyPhase (matter)Helmholtz free energysymbolsRelaxation (physics)General Materials ScienceMaterials Science (all)(MgFe)OAb initio and semi-empirical modellingMixing (physics)Solid solutionPhysics and Chemistry of Minerals
researchProduct

Analysis and parametric sensitivity of the behavior of overshoots in the concentration of a charged adsorbate in the adsorbed phase of charged adsorb…

2003

In this work, an analysis of the parametric sensitivity of the overshoot in the concentration of the adsorbate in the adsorbed phase, which occurs under certain conditions during an ion-exchange adsorption process, is presented and used to suggest practical implications of the concentration overshoot phenomenon on operational policies and configurations of chromatographic columns and finite bath adsorption systems. The results presented in this work demonstrate and explain how the development of an overshoot in the concentration of the adsorbate in the adsorbed phase could be enhanced or suppressed by (i) varying the diffusion coefficient, D3, of the adsorbate relative to the diffusion coef…

ChemistryDiffusionAnalytical chemistryLangmuir adsorption modelThermodynamicsElectrolyteCharged particleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialssymbols.namesakeColloid and Surface ChemistryAdsorptionIonic strengthPhase (matter)symbolsDebye lengthJournal of Colloid and Interface Science
researchProduct

Size Dependence of Tracer Diffusion in Supercooled Liquids

1996

We have determined by forced Rayleigh scattering the diffusion coefficients D of several photochromic tracers with van der Waals radii between 0.38 and 8 nm (the largest ones being photolabeled polystyrene micronetworks) in 10 glass-forming liquids at temperatures between the glass temperature Tg and ∼1.2Tg. The results were analyzed in terms of power law plots, D(T) ∝ T/η(T)ξ, where η is the solvent shear viscosity, and temperature shifts, D(T) ∝ T/η(T + ΔT). The shift ΔT was related with the width of the rotational correlation time distribution via the time−temperature superposition principle.

ChemistryDiffusionGeneral EngineeringThermodynamicsPower lawPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Mattersymbols.namesakeSuperposition principlechemistry.chemical_compoundsymbolsVan der Waals radiusPolystyrenePhysical and Theoretical ChemistrySupercoolingGlass transitionRotational correlation timeThe Journal of Physical Chemistry
researchProduct