Search results for "dynamics."

showing 10 items of 9637 documents

Information Decomposition in Bivariate Systems: Theory and Application to Cardiorespiratory Dynamics

2015

In the framework of information dynamics, the temporal evolution of coupled systems can be studied by decomposing the predictive information about an assigned target system into amounts quantifying the information stored inside the system and the information transferred to it. While information storage and transfer are computed through the known self-entropy (SE) and transfer entropy (TE), an alternative decomposition evidences the so-called cross entropy (CE) and conditional SE (cSE), quantifying the cross information and internal information of the target system, respectively. This study presents a thorough evaluation of SE, TE, CE and cSE as quantities related to the causal statistical s…

causalityInformation dynamicsTransfer entropyDynamical systems theoryComputationGeneral Physics and Astronomylcsh:AstrophysicsBivariate analysisMultivariate autoregressive processeMachine learningcomputer.software_genreMultivariate autoregressive processesCardiorespiratory interactionsPhysics and Astronomy (all)Systems theoryDynamical systemslcsh:QB460-466Decomposition (computer science)Statistical physicslcsh:ScienceCardiorespiratory interactions; Causality; Dynamical systems; Heart rate variability; Information dynamics; Multivariate autoregressive processes; Transfer entropyHeart rate variabilityMathematicsCardiorespiratory interactions; Causality; Dynamical systems; Heart rate variability; Information dynamics; Multivariate autoregressive processes; Transfer entropy; Physics and Astronomy (all)business.industryCardiorespiratory interactionheart rate variabilitytransfer entropyDynamical systemcardiorespiratory interactionsdynamical systemslcsh:QC1-999CausalityInformation dynamicCross entropySettore ING-INF/06 - Bioingegneria Elettronica E Informaticamultivariate autoregressive processesBenchmark (computing)lcsh:QTransfer entropyArtificial intelligenceinformation dynamicsbusinesscomputerlcsh:PhysicsEntropy
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The dawning of the theory of equilibrium figures: a brief historical account from the 16th through the 20th century

2014

A very brief historical survey of the theory of equilibrium figures is outlined, from the early origins, dating back to the late 1500s, until up the latest 20th century developments. A seen toward physical applications, ranging from relativistic astrophysics through nuclear physics, is also provided.

celestial bodieatomic nucleiSelf-gravitanting fluid; hydrodynamics; celestial bodies; atomic nucleiSelf-gravitanting fluidhydrodynamic
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Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three-Component Complexes

2020

Cethyl-2-methylresorcinarene (A), pyridine (B), and a set of 10 carboxylic acids (Cn) associate to form A·B·Cn ternary assemblies with 1:1:1 stoichiometry, representing a useful class of ternary systems where the guest mediates complex formation between the host and a third component. Although individually weak in solution, the combined strength of the multiple noncovalent interactions organizes the complexes even in a highly hydrogen-bond competing methanol solution, as explored by both experimental and computational methods. The interactions between A·B and Cn are dependent on the pKa values of carboxylic acids. The weak interactions between A and C further reinforce the interactions betw…

chemistry.chemical_classification010405 organic chemistryStereochemistryComponent (thermodynamics)Organic ChemistryComplex formationCarboxylic AcidsCooperative bindingHydrogen Bonding010402 general chemistry01 natural sciences0104 chemical sciencesChemistrychemistry.chemical_compoundMolecular recognitionchemistryPyridineNon-covalent interactionsTernary operationBiochemistry Biophysics and Structural BiologyStoichiometryThe Journal of Organic Chemistry
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Phase Equilibria in the Binary and Ternary Systems Composed of Diethyl Ketone, 2-Pentanone, and 3-Pentanol at 101.3 kPa

2003

New vapor−liquid equilibrium data for the binary systems diethyl ketone + 2-pentanone, diethyl ketone + 3-pentanol and 2-pentanone + 3-pentanol and for the diethyl ketone + 2-pentanone + 3-pentanol ternary system are reported at 101.3 kPa. The data were found to be thermodynamically consistent according to the Van Ness−Byer−Gibbs method for the binary systems and according to the McDermott−Ellis method for the ternary one. The experimental results show that the diethyl ketone + 2-pentanone system is well represented by assuming ideal behavior. The other binary systems exhibit slight positive deviations from ideality, and no azeotrope is present. The VLE data have been correlated with the Wi…

chemistry.chemical_classification3-PentanolTernary numeral systemKetoneUNIQUACGeneral Chemical Engineering2-PentanoneThermodynamicsGeneral Chemistrychemistry.chemical_compoundchemistryAzeotropeNon-random two-liquid modelTernary operationJournal of Chemical & Engineering Data
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Photochemical holes under pressure: Compressibility and volume fluctuations of a protein

1991

From the pressure induced frequency shift of photochemical holes burnt into mesomorphyrin substituted horseradish peroxidase, we determined the compressibility of the protein and the vacuum frequency of the chromophore. From the compressibility, an estimation of the volume fluctuations of the biomolecule is possible.

chemistry.chemical_classificationAbsorption spectroscopybiologyChemistryBiomoleculeGeneral Physics and AstronomyA proteinFrequency shiftChromophorePhotochemistryHorseradish peroxidaseVolume (thermodynamics)biology.proteinCompressibilityPhysical and Theoretical ChemistryThe Journal of Chemical Physics
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Thermodynamic studies of octyltrimethylammonium chloride in water

1992

Densities, heat capacities, enthalpies of dilution at 298 K and osmotic coefficients at 310 K of octyltrimethylammonium chloride were measured as functions of concentration. From the experimental data, the partial molar volumes, heat capacities, relative enthalpies, nonideal free energies and entropies at 298 K were derived as functions of concentration. A comparison between the above data and those of dodecyltrimethylammonium chloride reported in the literature shows that the increase of the alkyl chain length shifts the apparent molar volumevs. concentration curves towards greater values and the heat capacity, relative enthalpy and free energyvs. concentration curves towards smaller value…

chemistry.chemical_classificationActivity coefficientAqueous solutionChemistryEnthalpyThermodynamics of micellizationThermodynamicsOsmotic coefficientHeat capacityAlkylDilutionJournal of thermal analysis
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Thermodynamic properties of some N-alkyl-N-methylpiperidinium chlorides and N-alkylpiperidine hydrochlorides in water

1993

Densities and heat capacities at 25[degrees]C were measured for N-octyl-, N-decyl- and N-dodecyl-N-methylpiperidinium chlorides and for N-octyl- and N-dodecylpiperidine hydrochlorides in water as functions of concentration. Enthalpies of dilution at 25[degrees]C and osmotic coefficients at 37[degrees]C of the N-methyl-N-alkylpiperidinium chlorides were also measured as functions of concentration. The partial molar volumes, heat capacities, relative enthalpies, nonideal Gibbs energies and entropies at 25[degrees]C were derived as functions of the surfactant concentration. By increasing the alkyl chain length of the surfactant, both the apparent molar volume vs. concentration curves are shift…

chemistry.chemical_classificationActivity coefficientThermodynamics of micellizationEnthalpyBiophysicsThermodynamicsBiochemistryHeat capacityGibbs free energysymbols.namesakeMolar volumechemistrysymbolsOrganic chemistryOsmotic coefficientPhysical and Theoretical ChemistryMolecular BiologyAlkylJournal of Solution Chemistry
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Structural organization of surfactant aggregates in vacuo: a molecular dynamics and well-tempered metadynamics study

2015

Experimental investigations using mass spectrometry have established that surfactant molecules are able to form aggregates in the gas phase. However, there is no general consensus on the organization of these aggregates and how it depends on the aggregation number and surfactant molecular structure. In the present paper we investigate the structural organization of some surfactants in vacuo by molecular dynamics and well-tempered metadynamics simulations to widely explore the space of their possible conformations in vacuo. To study how the specific molecular features of such compounds affect their organization, we have considered as paradigmatic surfactants, the anionic single-chain sodium …

chemistry.chemical_classificationAggregation numberChemistryMetadynamicsGeneral Physics and AstronomyIonic bondingmolecular dynamics simulations well-tempered metadynamics simulationsMicellechemistry.chemical_compoundMolecular dynamicsPulmonary surfactantChemical physicsOrganic chemistryPhysical and Theoretical ChemistrySodium dodecyl sulfateAlkylSettore CHIM/02 - Chimica Fisica
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Continuum-uniform approach calculations of the solubility of hydrocarbons in water

1993

Abstract The ransfer free energies from gas phase to water for some hydrocarbons are calculated by means of a continuum-uniform model of the solvent. For the calculation of the cavitation energy a model based on the surface tension is proposed. The calculated values are compared with the experimental free energies obtained with and without a corrective factor that accounts for the difference in the solute—solvent sizes. Good agreement between the theoretical free energies and the corrected experimental data is obtained. Our calculations seem to show that the hydrophobic effect is directly related to the molecular surface area.

chemistry.chemical_classificationAlkaneAqueous solutionGeneral Physics and AstronomyThermodynamicsMineralogySolventHydrophobic effectSurface tensionHydrocarbonchemistryCavitationPhysical and Theoretical ChemistrySolubilityChemical Physics Letters
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A chiral molecular conductor: synthesis, structure, and physical properties of [ET]3[Sb2(L-tart)2].CH3CN (ET = bis(ethylendithio)tetrathiafulvalene; …

2004

The salt [ET](3)[Sb(2)(L-tart)(2)].CH(3)CN (1) has been obtained by electrocrystallization of the organic donor bis(ethylendithio)tetrathiafulvalene (ET or BEDT-TTF) in the presence of the chiral anionic complex [Sb(2)(L-tart)(2)](2-) (L-tart = (2R,3R)-(+)-tartrate). This salt crystallizes in the chiral space group P2(1)2(1)2(1) (a = 11.145(2) angstroms, b = 12.848(2) angstroms, c = 40.159(14) angstroms, V = 5750.4(14) angstroms(3), Z = 4) and is formed by alternating layers of the anions and of the organic radicals in a noncentrosymmetric alpha-type packing. This compound shows a room temperature electrical conductivity of approximately 1 S.cm(-1) and semiconducting behavior with an activa…

chemistry.chemical_classificationAntimonyChemistryStereochemistryRadicalMolecular ConformationTemperatureSalt (chemistry)Activation energyTartrateCrystallography X-RayMagnetic susceptibilityInorganic Chemistrychemistry.chemical_compoundCrystallographyElectrical resistivity and conductivityElectrochemistryOrganometallic CompoundsThermodynamicsPhysical and Theoretical ChemistryElectronic band structureTartratesTetrathiafulvaleneInorganic chemistry
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