Search results for "free energy"

showing 10 items of 170 documents

Calculation of phase diagrams not requiring the derivatives of the Gibbs energy for multinary mixtures

1996

A method for the calculation of phase diagrams (tie lines and binodal, spinodal, critical points and their stability) based exclusively on the Gibbs energy of mixing with no need of its derivatives with respect to the composition variables is extended to multinary mixtures for any number of components. The mathematical description of the (K-1)-dimensional phase diagram of a K-component mixture is presented. The method is demonstrated for a quinternary blend of five polymers exhibiting a closed miscibility gap; all binary, ternary and quaternary subsystems are completely miscible. The phase separation in the quinternary system is caused by very favorable interactions in the ternary subsystem…

chemistry.chemical_classificationBinodalSpinodalPolymers and PlasticsSpinodal decompositionOrganic ChemistryBinary numberThermodynamicsPolymerCondensed Matter PhysicsGibbs free energyCondensed Matter::Soft Condensed MatterInorganic Chemistrysymbols.namesakechemistryMaterials ChemistrysymbolsTernary operationPhase diagramMacromolecular Theory and Simulations
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High-pressure phases, vibrational properties, and electronic structure ofNe(He)2andAr(He)2: A first-principles study

2009

We have carried out a comprehensive first-principles study of the energetic, structural, and electronic properties of solid rare-gas RG-helium binary compounds, in particular, NeHe2 and ArHe2, under pressure and at temperatures within the range of 0T2000 K. Our approach is based on density-functional theory and the generalized gradient approximation for the exchange-correlation energy; we rely on total Helmholtz freeenergy calculations performed within the quasiharmonic approximation for most of our analysis. In NeHe2, we find that at pressures of around 20 GPa the system stabilizes in the MgZn2 Laves structure, in accordance to what was suggested in previous experimental investigations. In…

Phase transitionMaterials scienceCondensed matter physicsElectronic structureHard spheresLaves phaseCondensed Matter PhysicsElectronic Optical and Magnetic Materialssymbols.namesakeAb initio quantum chemistry methodsHelmholtz free energyPhase (matter)symbolsPhase diagramPhysical Review B
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Equilibrium fluid-crystal interfacial free energy of bcc-crystallizing aqueous suspensions of polydisperse charged spheres

2015

The interfacial free energy is a central quantity in crystallization from the meta-stable melt. In suspensions of charged colloidal spheres, nucleation and growth kinetics can be accurately measured from optical experiments. In previous work, from this data effective non-equilibrium values for the interfacial free energy between the emerging bcc-nuclei and the adjacent melt in dependence on the chemical potential difference between melt phase and crystal phase were derived using classical nucleation theory. A strictly linear increase of the interfacial free energy was observed as a function of increased meta-stability. Here, we further analyze this data for five aqueous suspensions of charg…

fluid-crystalMaterials scienceNucleationFOS: Physical sciencesThermodynamicsNon-equilibrium thermodynamicsCondensed Matter - Soft Condensed Matter01 natural scienceslaw.inventionColloidlawMetastability0103 physical sciencesCrystallization010306 general physicsCondensed Matter - Statistical MechanicsCondensed Matter - Materials ScienceAqueous solutionStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsMaterials Science (cond-mat.mtrl-sci)Condensed Matter::Soft Condensed Matterpolydisperseinterfacial free energySoft Condensed Matter (cond-mat.soft)SPHERESClassical nucleation theoryPhysical Review E
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New QM/MM implementation of the DFTB3 method in the gromacs package.

2015

The approximate density-functional tight-binding theory method DFTB3 has been implemented in the quantum mechanics/molecular mechanics (QM/MM) framework of the Gromacs molecular simulation package. We show that the efficient smooth particle–mesh Ewald implementation of Gromacs extends to the calculation of QM/MM electrostatic interactions. Further, we make use of the various free-energy functionalities provided by Gromacs and the PLUMED plugin. We exploit the versatility and performance of the current framework in three typical applications of QM/MM methods to solve biophysical problems: (i) ultrafast proton transfer in malonaldehyde, (ii) conformation of the alanine dipeptide, and (iii) el…

Theory methodComputer scienceMolecular simulationGeneral ChemistryExtended samplingFree energy simulationMolecular dynamicsDensity-functional tight-bindingComputational scienceQM/MMComputational MathematicsMolecular dynamicsQuantum TheoryThermodynamicsComputer Simulationta116Quantum mechanics/molecular mechanicsSoftwareProtein BindingJournal of computational chemistry
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Techno-economic evaluation of Reverse Electrodialysis process in different real environments

2018

Salinity Gradient Power is a promising renewable energy source based on the recovery of the chemical potential released from the mixing of solutions at different concentrations. Natural salinity gradients are extensively available worldwide in natural reservoirs. Reverse Electrodialysis is an innovative technology able to perform a direct conversion of the energy of mixing into electricity. Salinity gradients coming from natural resources or from human activities are worldwide available. In the present work a number of different scenarios, including natural resources (e.g. rivers, seas, lakes and salt ponds), industrial/urban wastes (e.g. brine and treated wastewaters) are analysed. The aim…

Reverse Electrodialysis Salinity Gradient Power Open-loop RED Gibbs free energy of mixing.
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On the merit of a Central Limit Theorem-based approximation in statistical physics

2012

The applicability conditions of a recently reported Central Limit Theorem-based approximation method in statistical physics are investigated and rigorously determined. The failure of this method at low and intermediate temperature is proved as well as its inadequacy to disclose quantum criticalities at fixed temperatures. Its high temperature predictions are in addition shown to coincide with those stemming from straightforward appropriate expansions up to (k_B T)^(-2). Our results are clearly illustrated by comparing the exact and approximate temperature dependence of the free energy of some exemplary physical systems.

PhysicsQuantum PhysicsSettore FIS/02 - Fisica Teorica Modelli E Metodi MatematiciStatistical Mechanics (cond-mat.stat-mech)Physical systemFOS: Physical sciencesStatistical and Nonlinear PhysicsSettore FIS/03 - Fisica Della MateriaIsing modelQuantum statistical mechanicIntermediate temperatureStatistical physicsFree energyQuantum Physics (quant-ph)QuantumCentral Limit TheoremMathematical PhysicsEnergy (signal processing)Condensed Matter - Statistical MechanicsCentral limit theorem
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Peptide Bond Formation Mechanism Catalyzed by Ribosome

2015

In this paper we present a study of the peptide bond formation reaction catalyzed by ribosome. Different mechanistic proposals have been explored by means of Free Energy Perturbation methods within hybrid QM/MM potentials, where the chemical system has been described by the M06-2X functional and the environment by means of the AMBER force field. According to our results, the most favorable mechanism in the ribosome would proceed through an eight-membered ring transition state, involving a proton shuttle mechanism through the hydroxyl group of the sugar and a water molecule. This transition state is similar to that described for the reaction in solution (J. Am. Chem. Soc. 2013, 135, 8708–871…

Models MolecularReaction mechanismProtein ConformationStereochemistryElectronsBiochemistryRibosomeArticleCatalysisCatalysisFree energy perturbationColloid and Surface ChemistryProtein structureComputational chemistryMoleculePeptide bondcatalysisChemistryGeneral Chemistrypeptide bond formationribosomeBiocatalysispeptidesBiocatalysisThermodynamicsPeptidesRibosomesJournal of the American Chemical Society
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Thermodynamics of the spin transition in [FexZn1−x(2-pic)3]Cl2 · EtOH

1992

Abstract With a new type of calorimeter we reinvestigated the specific heat Cp of the mixed crystals [FexZni1−x(2-pic)3]Cl2 · EtOH in the temperature range from 15 to 300 K. On the basis of a phenomenological thermodynamic model the anomaly in the Cp(T) curve of the mixed crystal (x = 0.73) can be quantitatively described as a result of the spin transition (1A1(low spin, LS) → 5T2(high spin, HS)). The parameters of the Gibbs free energy were independently derived from the temperature dependence of the HS fraction γ in [FexZn1−x(2-pic)3]Cl2 · EtOH. The pure iron complex (x = 1) exhibits a two-step spin transition. In the temperature range between the two steps the entropy obtained from the C…

ChemistrySpin transitionThermodynamicsGeneral ChemistryCalorimetryAtmospheric temperature rangeCondensed Matter PhysicsMagnetic susceptibilityGibbs free energyCrystalsymbols.namesakePhenomenological modelsymbolsPhysical chemistryMoleculeGeneral Materials ScienceJournal of Physics and Chemistry of Solids
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Unveiling the regioselectivity in electrophilic aromatic substitution reactions of deactivated benzenes through molecular electron density theory

2021

The origin of the meta regioselectivity in electrophilic aromatic substitution (EAS) reactions of deactivated benzene derivatives is herein analysed through Molecular Electron Density Theory (MEDT). To this end, the EAS reaction of benzenesulfonic acid with the nitronium NO2+ ion in H2SO4 solution has been studied at the ωB97X-D/6-311G(d,p) level. This reaction takes place through a two-step polar mechanism involving the formation of an unstable cation intermediate. The activation Gibbs free energies associated with the three competitive regioisomeric reaction paths are found in the narrow range of 15.5–18.3 kcal mol−1. By using the Eyring–Polanyi equation a relationship of 18.7 (ortho) : 8…

Steric effectsElectron density010405 organic chemistryRegioselectivityGeneral ChemistryElectrophilic aromatic substitution010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesGibbs free energychemistry.chemical_compoundsymbols.namesakeBenzenesulfonic acidchemistryMaterials ChemistrysymbolsBenzeneNew Journal of Chemistry
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Exact Fourier expansion in cylindrical coordinates for the three-dimensional Helmholtz Green function

2009

A new method is presented for Fourier decomposition of the Helmholtz Green Function in cylindrical coordinates, which is equivalent to obtaining the solution of the Helmholtz equation for a general ring source. The Fourier coefficients of the Helmholtz Green function are split into their half advanced+half retarded and half advanced-half retarded components. Closed form solutions are given for these components in terms of a Horn function and a Kampe de Feriet function, respectively. The systems of partial differential equations associated with these two-dimensional hypergeometric functions are used to construct a fourth-order ordinary differential equation which both components satisfy. A s…

42B05Helmholtz equationSeries (mathematics)Applied MathematicsGeneral MathematicsMathematical analysis34B27General Physics and AstronomyFOS: Physical sciencesMathematical Physics (math-ph)Legendre function35J05; 34B27; 42B05symbols.namesake35J05Helmholtz free energysymbolsHypergeometric functionFourier seriesMathematical PhysicsHorn functionBessel functionMathematics
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