Search results for "Free Energy"

showing 10 items of 170 documents

Application of headspace analysis to the study of aroma compounds-lipids interactions

1998

Taking into account interactions between aroma compounds and food components is necessary to better manage the flavoring of food products. These interactions occur at a molecular level and reflect changes, at a macroscopic level, in thermodynamic equilibria, such as solubility or volatility. The rate of transfer of an aroma compound from the liquid to the vapor phase can be affected as well. The behavior of aroma compounds in water and lipid solutions was studied in two complementary ways, a thermodynamic and a kinetic approach (head-space analysis). The transfer rate of volatiles at the liquid-water interface does not only depend on the hydrophobicity of the aroma compounds. Vapor-liquid p…

chemistry.chemical_classificationActivity coefficientbiologyGeneral Chemical EngineeringOrganic Chemistryfood and beveragesbiology.organism_classificationGibbs free energyPartition coefficientchemistry.chemical_compoundsymbols.namesakechemistryComputational chemistryMass transfersymbolsAroma compoundOrganic chemistryVolatile organic compoundSolubilityAromaJournal of the American Oil Chemists' Society
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Increased Acid Dissociation at the Quartz/Water Interface.

2018

As shown by a quite significant amount of literature, acids at the water surface tend to be “less” acid, meaning that their associated form is favored over the conjugated base. What happens at the solid/liquid interface? In the case of the silica/water interface, we show how the acidity of adsorbed molecules can instead increase. Using a free energy perturbation approach in combination with electronic structure-based molecular dynamics simulations, we show how the acidity of pyruvic acid at the quartz/water interface is increased by almost two units. Such increased acidity is the result of the specific microsolvation at the interface and, in particular, of the stabilization of the deprotona…

chemistry.chemical_classificationBase (chemistry)Chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAcid dissociation constant0104 chemical sciencesFree energy perturbationMolecular dynamicsAdsorptionDeprotonationChemical engineeringMoleculeGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyQuartzThe journal of physical chemistry letters
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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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Excess free energy, enthalpy and entropy of surfactant-surfactant mixed micelle formation

1996

Enthalpies of dilution and osmotic coefficients of sodium decylsulfate (NaDeS)-dodecyldimethylamine oxide (DDAO) mixtures in water were determined at 298 and 310 K, respectively. From the enthalpies of dilution, the apparent and then the partial molar relative enthalpies of the surfactant mixtures were calculated. From the osmotic coefficients, calculated at 298 K, the non-ideal free energies were derived. The latter were combined with the partial molar relative enthalpies to obtain the non-ideal entropies. From the apparent molar properties, using a previously reported approach, the excess thermodynamic properties for the surfactant-surfactant mixed micelle formation in water were evaluate…

chemistry.chemical_classificationChemistryGeneral Chemical EngineeringSodiumEnthalpyInorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementThermodynamicsMicelleDilutionGibbs free energysymbols.namesakePulmonary surfactantsymbolsOsmotic coefficientPhysical and Theoretical ChemistryAlkylFluid Phase Equilibria
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Interfacial tension between polymer-containing liquids - Predictability and influences of additives

1999

The first part of the contribution deals with the interfacial tension, σ, of phase-separated polymer solutions in single or mixed solvents and of binary polymer blends as a function of the relative distance to the critical temperature of the system, special attention being paid to the possibilities of theoretical prediction. Two methods are discussed in more detail. One is based on a realistic description of the Gibbs energy of mixing as a function of composition, the second correlates σ with the length of the measured tie line. The second part is devoted to another aspect, namely the effects of additives on the interfacial tension between the coexisting phases of demixed polymer solutions …

chemistry.chemical_classificationChromatographyPolymers and PlasticsOrganic ChemistryMixing (process engineering)ThermodynamicsPolymerCondensed Matter PhysicsGibbs free energySurface tensionchemistry.chemical_compoundsymbols.namesakeMonomerchemistryMaterials ChemistryCopolymersymbolsPolymer blendTie lineMacromolecular Symposia
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Quick and reliable routes to phase diagrams for polyethersulfone and polysulfone membrane formation

2000

Phase diagrams were measured and calculated for the ternary membrane forming systems DMF/water/polysulfone and DMF/water/polyethersulfone at different temperatures. Customary experiments yielded cloud point curves, tie lines, and critical compositions. The theoretical computation starts from the Flory-Huggins theory and employs binary interaction parameters g ij that vary with the composition. This information was mainly obtained by means of Headspace-Gas Chromatography (HSGC, yielding the partial pressures of the volatile components); these data were complemented by light scattering and swelling experiments. The calculation of binodals, spinodals, tie lines, and critical points avoids the …

chemistry.chemical_classificationCloud pointPolymers and PlasticsOrganic ChemistryPolymerFlory–Huggins solution theoryCondensed Matter PhysicsLight scatteringGibbs free energychemistry.chemical_compoundsymbols.namesakechemistryPolymer chemistryMaterials ChemistrysymbolsPolysulfonePhysical and Theoretical ChemistryTernary operationPhase diagramMacromolecular Chemistry and Physics
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Shear Effects on the Phase Diagrams of Solutions of Highly Incompatible Polymers in a Common Solvent. 1. Equilibrium Behavior and Rheological Propert…

1997

Phase diagrams (cloud points, tie lines, critical compositions) and viscosities of homogeneous solutions were determined at temperatures ranging from 20 to 100 °C for three representatives of the ternary system cyclohexanone/polystyrene/poly(n-butyl methacrylate) [CHO/PS/PBMA] in preparation of a study on shear influences. An only moderate increase of the two-phase region observed upon heating (LCST behavior) witnesses little heat effects upon mixing. Tie lines which are nearly parallel to the PS/PBMA edge of the Gibbs phase triangle indicate comparable solvent quality of CHO for both polymers. The quantitative mathematical description of the equilibrium behavior-required for a theoretical …

chemistry.chemical_classificationCloud pointTernary numeral systemPolymers and PlasticsChemistryOrganic ChemistryThermodynamicsMineralogyPolymerLower critical solution temperatureGibbs free energyInorganic Chemistrysymbols.namesakechemistry.chemical_compoundRheologyMaterials ChemistrysymbolsPolystyrenePhase diagramMacromolecules
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Pressure dependence in the methyl vinyl ketone + OH and methacrolein + OH oxidation reactions: an electronic structure study.

2005

High-level electronic structure calculations were carried out for the study of the reaction pathways in the OH-initiated oxidations of methyl vinyl ketone (MVK) and methacrolein (MACR). For the two conformers of MVK (called synperiplanar and antiperiplanar), the addition channels of OH to the terminal and central carbon atom of the double bond dominate the overall rate constant, whereas the abstraction of the methyl hydrogen atoms has no significant kinetic role. In the case of MACR, only the antiperiplanar conformer is important in its reactivity. In addition, the lower Gibbs free energy barrier for MACR corresponds to the aldehydic hydrogen abstraction reaction, which will be somewhat mor…

chemistry.chemical_classificationDouble bondChemistryHydroxyl RadicalMethacroleinElectronsHydrogen atom abstractionPhotochemistryAtomic and Molecular Physics and OpticsButanonesGibbs free energysymbols.namesakechemistry.chemical_compoundReaction rate constantModels ChemicalAlkane stereochemistryMethyl vinyl ketonesymbolsPressureOrganic chemistryThermodynamicsReactivity (chemistry)Physical and Theoretical ChemistryAcroleinOxidation-ReductionChemphyschem : a European journal of chemical physics and physical chemistry
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Understanding the domino reactions of alkyne-tethered N-tosylhydrazones yielding fused polycyclic pyrazoles. An MEDT study

2019

Abstract The domino reactions of alkyne-tethered N-mesylhydrazones yielding fused polycyclic pyrazoles have been studied within the Molecular Electron Density Theory (MEDT). Analysis of the Gibbs free energies indicates that the more favourable reactive path is the one in which the elimination of mesylate anion takes place before the intramolecular [3 + 2] cycloaddition (IM32CA) reaction, which corresponds with the rate-determining step of these domino processes. ELF topological analysis of the bond formation along the IM32CA reaction indicates that in spite of the high activation energy associated to this intramolecular reaction, it shows a pmr-type mechanism characterised by the presence …

chemistry.chemical_classificationIntramolecular reaction010405 organic chemistryChemistryOrganic ChemistryAlkyneBond formation010402 general chemistry01 natural sciencesBiochemistryCycloadditionDomino0104 chemical sciencesIonGibbs free energysymbols.namesakeComputational chemistryIntramolecular forceDrug DiscoverysymbolsTetrahedron
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Modelling the hydrogen-bonding interactions in a copolymer/biodegradable homopolymer blend through excess functions

2008

A recent theoretical approach based on the coupling of both the Flory-Huggins (FH) and the Association Equilibria thermodynamic (AET) theories was modified and adapted to study the miscibility properties of a multi- component system formed by two polymers (a proton-donor and a proton-acceptor) and a proton-acceptor solvent, named copolymer(A)/solvent(B)/polymer(C). Compatibility between polymers was mainly attained by hydrogen- bonding between the hydroxyl group on the phenol unit of the poly(styrene-co-vinyl phenol) (PSVPh) and the car- bonyl group of the biodegradable and environmentally friendly poly(3-hydroxybutyrate) (PHB). However, the self- association of PSVPh and specific interacti…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsHydrogen bondGeneral Chemical EngineeringOrganic ChemistryPolymerMiscibilityPolymer engineeringGibbs free energySolventsymbols.namesakechemistryPolymer chemistryMaterials ChemistryCopolymersymbolsPolymer blendMacromolecular Research
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