Search results for "enthalpy"

showing 10 items of 199 documents

Thermodynamics of Surfactant, Block Copolymer and Their Mixtures in Water: The Role of the Isothermal Calorimetry

2009

The thermodynamics of conventional surfactants, block copolymers and their mixtures in water was described to the light of the enthalpy function. The two methodologies, i.e. the van't Hoff approach and the isothermal calorimetry, used to determine the enthalpy of micellization of pure surfactants and block copolymers were described. The van't Hoff method was critically discussed. The aqueous copolymer+surfactant mixtures were analyzed by means of the isothermal titration calorimetry and the enthalpy of transfer of the copolymer from the water to the aqueous surfactant solutions. Thermodynamic models were presented to show the procedure to extract straightforward molecular insights from the …

PolymerssurfactantEnthalpyThermodynamicsReviewCalorimetrycopolymer+surfactant mixtureCalorimetryMicelleenthalpy of injectionCatalysisEnthalpy change of solutionInorganic Chemistrylcsh:ChemistrySurface-Active Agentsenthalpy of copolymer+surfactant aggregationenthalpy of transferCopolymerPhysical and Theoretical ChemistryMolecular Biologylcsh:QH301-705.5MicellesSpectroscopyenthalpy of micellizationchemistry.chemical_classificationAqueous solutioncopolymerOrganic Chemistrycopolymer+surfactant mixturesWaterIsothermal titration calorimetryGeneral MedicinePolymerComputer Science Applicationschemistrylcsh:Biology (General)lcsh:QD1-999Thermodynamics
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High-accuracy extrapolated ab initio thermochemistry. II. Minor improvements to the protocol and a vital simplification

2006

The recently developed high-accuracy extrapolated ab initio thermochemistry method for theoretical thermochemistry, which is intimately related to other high-precision protocols such as the Weizmann-3 and focal-point approaches, is revisited. Some minor improvements in theoretical rigor are introduced which do not lead to any significant additional computational overhead, but are shown to have a negligible overall effect on the accuracy. In addition, the method is extended to completely treat electron correlation effects up to pentuple excitations. The use of an approximate treatment of quadruple and pentuple excitations is suggested; the former as a pragmatic approximation for standard cas…

Protocol (science)Electronic correlationComputer scienceAb initio quantum chemistry methodsComputational chemistryMinor (linear algebra)Ab initioThermochemistryTest suiteGeneral Physics and AstronomyStatistical physicsPhysical and Theoretical ChemistryStandard enthalpy of formationThe Journal of Chemical Physics
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Proton, Hydroxide Ion, and Oxide Ion Affinities of Closed-Shell Oxides: Importance for the Hydration Reaction and Correlation to Electronic Structure

2019

Phenomenologically, the enthalpy of the dissociative water incorporation (hydration) of oxides is often found to be more favorable for more basic oxides. In the present work, we investigate proton,...

ProtonChemistryInorganic chemistryEnthalpy02 engineering and technologyElectronic structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAffinities0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonchemistry.chemical_compoundGeneral EnergyHydration reactionHydroxidePhysical and Theoretical Chemistry0210 nano-technologyOpen shellThe Journal of Physical Chemistry C
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Surface Segregation Entropy of Protons and Oxygen Vacancies in BaZrO3

2016

The perovskite BaZrO3 has attracted considerable attention in the recent decade due to its high temperature proton conducting properties, and possible application as electrolyte in intermediate temperature fuel cells and electrolyzers. In this contribution, we performed, for the first time, first-principles calculations of the phonon contribution to the defect thermodynamics of the ZrO2 terminated (001) surface of BaZrO3. The approach allows us to determine both the segregation enthalpy and entropy of defects, which we apply to two fundamental defects in BaZrO3; fully charged oxygen vacancies (vO••) and protonic defects (OHO•). The calculations show that both defects exhibit favorable segre…

ProtonChemistryPhononGeneral Chemical EngineeringEnthalpyThermodynamicschemistry.chemical_element02 engineering and technologyGeneral ChemistryElectrolyte010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxygen0104 chemical sciencesEntropy (classical thermodynamics)Materials ChemistryFuel cellsIntermediate temperature0210 nano-technologyChemistry of Materials
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PREDICTION OF THERMODYNAMIC INSTABILITIES OF PROTEIN SOLUTIONS FROM SIMPLE PROTEIN-PROTEIN INTERACTIONS

2013

Statistical thermodynamics of protein solutions is often studied in terms of simple, microscopic models of particles interacting via pairwise potentials. Such modelling can reproduce the short range structure of protein solutions at equilibrium and predict thermodynamics instabilities of these systems. We introduce a square well model of effective protein-protein interaction that embeds the solvent's action. We modify an existing model [45] by considering a well depth having an explicit dependence on temperature, i.e. an explicit free energy character, thus encompassing the statistically relevant configurations of solvent molecules around proteins. We choose protein solutions exhibiting dem…

Quantitative Biology::BiomoleculesSpinodalRange (particle radiation)Liquid–liquid demixingSpinodal lineChemistrySolvent mediated protein-protein interactionEnthalpyProtein solutionGeneral Physics and AstronomyThermodynamicsEntropy driven phase transitionLiquid-liquid demixingAction (physics)Settore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Solvent mediated protein–protein interactionProtein–protein interactionSpinodal lines SW potential free energy parametrizationPhysics and Astronomy (all)Mean field theoryFinite potential wellMoleculePhysical and Theoretical ChemistrySquare well potential
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QSPR prediction of chromatographic retention times of pesticides: Partition and fractal indices

2014

The high-performance liquid-chromatographic retentions of red-wine pesticide residues are modeled by structure-property relationships. The effect of different types of features is analyzed: geometric, lipophilic, etc. The properties are fractal dimensions, partition coefficient, etc., in linear and nonlinear correlation models. Biological plastic evolution is an evolutionary perspective conjugating the effect of acquired characters and relations that emerge among the principles of evolutionary indeterminacy, morphological determination and natural selection. It is applied to design the co-ordination index that is used to characterize pesticide retentions. The parameters used to calculate th…

Quantitative structure–activity relationshipChromatographyChemistryEnthalpyNonlinear correlationQuantitative Structure-Activity RelationshipGeneral MedicinePesticidePollutionFractal dimensionPartition coefficientFractalsFractalPartition (number theory)PesticidesChromatography LiquidFood ScienceJournal of Environmental Science and Health, Part B
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Thermochemical analysis of the OH+C2H4→C2H4OH reaction using accurate theoretical methods

2001

Abstract The radical addition of hydroxyl radical to ethene has been investigated using ab initio methods and density functional theory. The structure and energetics of reactants, prereaction complex, transition state structure and radical product have been optimized and vibrational frequencies have been calculated at the HF, MP2, B88, and B3LYP level using 6-31G* and 6-311G** basis sets. The energetics of the reaction is characterized within the MP2, DFT, G2, CBS, and BAC approaches. The evolution of the barrier height and reaction enthalpy has been systematically investigated with respect to the methodological approach employed. The best agreement with experimental results for the barrier…

RadicalEnthalpyEnergeticsAb initioCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundState structurechemistryTheoretical methodsPhysical chemistryHydroxyl radicalDensity functional theoryPhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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An Ab Initio Study on the Mechanism of the Atmospheric Reaction NH2+O3→H2NO+O2

2003

The atmospheric reaction NH 2 +0 3 →H 2 NO+O 2 has been investigated theoretically by using MP2, QCISD, QCISD(T), CCSD(T), CASSCF, and CASPT2 methods with various basis sets. At the MP2 level or theory, the hypersurface of the potential energy (HPES) shows a two step reaction mechanism. Therefore, the mechanism proceeds along two transition states (TS1 and TS2), seperated by an intermediate disignated as Int. However, when the single-reference higler correlated QCISD and the multiconfigurational CASSCF methodologies have been employed, the minimum structure Int and TS2 are not found on the HPES, which thus confirms a direct reaction mechanism. Single-reference high correlated and multiconfi…

Reaction mechanismHypersurfaceChemistryAb initio quantum chemistry methodsEnthalpyAb initioPhysical chemistryPhysical and Theoretical ChemistryPotential energyChemical reactionAtomic and Molecular Physics and OpticsTransition stateChemPhysChem
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Exploring two-state reaction pathways in the photodimerization of cyclohexadiene.

2006

The ground- (S0) and lowest triplet-state (T1) pathways associated with dimerization of cyclohexadiene to give [2+2] and [4+2] cycloadducts have been theoretically studied at the UBLYP and UB3LYP levels of theory with the 6-31G* basis set. The DFT energies were validated by CCSD(T) single-point energy calculations. These cycloaddition reactions follow stepwise mechanisms with formation of bis-allylic biradical (BB) intermediates. In the S0 ground state, the interaction between two cyclohexadiene molecules with formation of BB intermediate IN(S0) has a large activation enthalpy of 32.0 kcal mol(-1). On the other hand, C-C bond-formation in the lowest triplet state (T1) leading to BB intermed…

Reaction mechanismIntersystem crossingComputational chemistryChemistryEnthalpyMoleculePhysical and Theoretical ChemistryTriplet stateGround stateMedicinal chemistryAtomic and Molecular Physics and OpticsBasis setCycloadditionChemphyschem : a European journal of chemical physics and physical chemistry
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Ab initiostudy of the mechanism of the atmospheric reaction: NO2+ O3→ NO3+ O2

2003

The atmospheric reaction NO2 + O3 --> NO3 + O2 (1) has been investigated theoretically by using the MP2, G2, G2Q, QCISD, QCISD(T), CCSD(T), CASSCF, and CASPT2 methods with various basis sets. The results show that the reaction pathway can be divided in two different parts at the MP2 level of theory. At this level, the mechanism proceeds along two transition states (TS1 and TS2) separated by an intermediate, designated as A. However, when the single-reference higher correlated QCISD methodology has been employed, the minimum A and the transition state TS2 are not found on the hypersurface of potential energy, which confirms a direct reaction mechanism. Single-reference high correlated and mu…

Reaction rateComputational MathematicsReaction mechanismHypersurfaceAb initio quantum chemistry methodsChemistryEnthalpyAb initioPhysical chemistryGeneral ChemistryPotential energyTransition stateJournal of Computational Chemistry
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