Search results for "Equilibrium"

showing 10 items of 1021 documents

Synthesis, Characterization, and Electrochemistry of Open-Chain Pentapyrroles and Sapphyrins with Highly Electron-Withdrawing meso -Tetraaryl Substit…

2017

International audience; A series of open-chain pentapyrroles and sapphyrins with highly electron-withdrawing substituents (i.e., CN, CF3 , or CO2 Me) on the meso-phenyl rings was synthesized and characterized as to the spectral properties, protonation reactions, and electrochemistry in non-aqueous media. The investigated compounds are represented as (Ar)4 PPyH3 and (Ar)4 SapH3 where PPy and Sap correspond to the tri-anion of the open-chain pentapyrrole and sapphyrin, respectively, and Ar=p-CNPh, p-CF3 Ph, or p-CO2 MePh. UV/Vis and 1 H NMR spectroscopy as well as mass spectrometry data are given for the confirmation of the structures for the newly synthesized compounds. An X-ray structure fo…

Absorption spectroscopyprotonationInorganic chemistryporphyrinoidsProtonationpentapyrroles010402 general chemistry01 natural sciencesRedox[ CHIM ] Chemical SciencesCatalysischemistry.chemical_compound[SPI]Engineering Sciences [physics]PyridinePolymer chemistryTrifluoroacetic acid[CHIM]Chemical SciencesEquilibrium constantsapphyrins010405 organic chemistryOrganic ChemistryGeneral Chemistry0104 chemical scienceschemistryelectrochemistryProton NMRCyclic voltammetry
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Dependence of plasma pH on oxygen saturation

1969

Abstract The influence of haemoglobin oxygenation on the pH value of the blood plasma of healthy adolescents was investigated at 38°C by varying the parameters CO2 pressure, Hb concentration and buffer bases. A total of 5000 measurements gave the following results: 1. 1. The pHs difference between oxygenated and deoxygenated blood increases with diminishing CO2 pressure and with increasing Hb concentration. There is a linear relation between the pHs changes and the O2 saturation of the haemoglobin. 2. 2. Quantitatively these relationships can be expressed by the following equation: δpHs = (8 − pH ox − log 0.03 Pco 2 ) · [Hb] 225 · (100 − So 2 100 where ΔpHs is the pHs difference between par…

Acid-Base EquilibriumPulmonary and Respiratory MedicineAdolescentPhysiologyChemistryPartial PressureAnalytical chemistryOxygenationVenous bloodPlasmaBuffersCarbon DioxideHydrogen-Ion ConcentrationOxygenBicarbonatesHemoglobinsBloodBiochemistryBlood plasmaLinear relationHumansBase excessOxygen saturationBlood phRespiration Physiology
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Dioxouranium(VI) hydrolysis at 75 and 100°C in 3.6 molkg-1 LiClO4

2008

This work concerns the acidic properties of uranyl ion UO22+ at 75 and 100 °C in 3.6 molal (molkg-1 solvent) LiClO4 aqueous medium. The investigation was carried out by a coulometric-potentiometric technique. Direct and reverse acid base titrations were carried out in order to check the achievement of actual equilibrium conditions. Moreover, in order to reveal oversaturation conditions, a further check was carried out on clean saturated hydrolyzed solutions.

Acid-base titrations check of equilibrium conditions hydrolysis in hot LiClO4 aqueous medium.Settore CHIM/01 - Chimica Analitica
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A radiometric and petrographic approach to risk assessment at Alte Madonie Mounts region (Sicily, Italy)

2013

The main goal of this work was to assess the radiological hazard at Alte Madonie Mounts region (north-central Sicily, Italy) in response to rumours of an increase in the incidence of cancer in this area. A correlation between the natural radionuclide contents and the petrographic features of the soil and rock samples was also evaluated. A total of 41 samples of selected soils and rocks were collected, powdered, dried and sealed in 'Marinelli' beakers for 20 d prior to measurement to ensure that a radioactive equilibrium between (226)Ra and (214)Bi had been reached. A gamma-ray spectrometer was used to quantify the radioactivity concentrations. To determine (238)U and (232)Th activities, the…

ActiniumSettore ING-IND/20 - Misure E Strumentazione NucleariMineralogychemistry.chemical_elementRisk AssessmentNuclear physicsPetrographyRadiation MonitoringBackground RadiationSoil Pollutants RadioactiveRadiology Nuclear Medicine and imagingRadiometrySicilyRadioisotopesRadionuclideRadiationGeographyRadiological and Ultrasound TechnologyCarbonate radiaoctivity petrographyThoriumSettore GEO/07 - Petrologia E PetrografiaPublic Health Environmental and Occupational HealthThoriumGeneral MedicineSecular equilibriumUraniumSpectrometry GammaLinear relationshipchemistrySoil waterLinear ModelsPotassiumUraniumEnvironmental scienceRadiometric datingBismuthRadiumRadiation Protection Dosimetry
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Control of irregular cardiac rhythm

2018

International audience; The aim of this work is to investigate the chaos control of the one di- mensional map which modelizes the duration of the current cardiac action potential (APD) as a function of the previous one. Using OGY control method, we obtain very satisfactory numerical results to stabilize the irregular heart rhythm into the normal rhythm.

Action Potential Duration (APD)chaos[MATH.MATH-DS]Mathematics [math]/Dynamical Systems [math.DS][ MATH.MATH-DS ] Mathematics [math]/Dynamical Systems [math.DS][MATH.MATH-DS] Mathematics [math]/Dynamical Systems [math.DS][ SPI.SIGNAL ] Engineering Sciences [physics]/Signal and Image processing[ SDV.MHEP.CSC ] Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular systemequilibrium point[SDV.MHEP.CSC] Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system[SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular systemnormal rhythmirregular heart rhythm[SPI.SIGNAL]Engineering Sciences [physics]/Signal and Image processingcontrol[SPI.SIGNAL] Engineering Sciences [physics]/Signal and Image processing
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Activity coefficients and Donnan coion exclusion in charged membranes with weak-acid fixed charge groups

1998

Abstract We have studied theoretically the effects that the dissociation equilibrium of weak-acid fixed charge groups (e.g. carboxyl groups) exerts on the mean activity coefficients in charged membranes using a Donnan formalism. The model calculations indicate that unless carbon dioxide is excluded from the external aqueous solution, the pH of the membrane solution can be low enough to affect significantly the effective fixed charge concentration and the coion exclusion when the membrane fixed charge concentration is high compared with the external solution salt concentration. Although this problem was already pointed out in previous studies, the possibility that the pH and salt concentrati…

Activity coefficientChromatographyAqueous solutionChemistrySalt effectThermodynamicsFiltration and SeparationEquilibrium equationBiochemistryDissociation (chemistry)Formalism (philosophy of mathematics)MembraneFixed chargeGeneral Materials SciencePhysical and Theoretical ChemistryJournal of Membrane Science
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A series expansion of the extended Debye-H�ckel equation and application to linear prediction of stability constants

1996

The Debye-Hückel semiempirical extended equation is frequently used to calculate activity coefficients of chemical species and equilibrium constants at ionic strengths different from those used in their experimental evaluation. A series expansion of the extended Debye-Hückel equation is proposed here and checked with experimental data taken from the literature. The expansion is linear in the ionic parameters and yields a geometrical series which converges rapidly and that enables the accurate calculation of interpolated and extrapolated activity coefficients and equilibrium constants by simple and multiple linear regression without previous knowledge of the ionic parameters.

Activity coefficientSeries (mathematics)ChemistryThermodynamicsLinear predictionAnalytical Chemistrysymbols.namesakeIonic strengthComputational chemistryDebye–Hückel equationLinear regressionPhysics::Atomic and Molecular ClusterssymbolsSeries expansionEquilibrium constantTalanta
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Isobaric vapor–liquid equilibrium for binary mixtures of 2-methylpentane+ethanol and +2-methyl-2-propanol

1999

Abstract Vapor–liquid equilibrium (VLE) data for the binary systems, 2-methylpentane+ethanol and 2-methylpentane+2-methyl-2-propanol (TBA), are reported at 101.3 kPa, including pure component vapor pressures. The systems deviate remarkably from ideal behaviour presenting one positive azeotrope. The activity coefficients and boiling points of the solutions were correlated with its composition by Wilson, UNIQUAC, NRTL, and Wisniak–Tamir equations.

Activity coefficientUNIQUACChemistryGeneral Chemical EngineeringGeneral Physics and AstronomyThermodynamicsPropanolchemistry.chemical_compoundBoiling pointAzeotropeNon-random two-liquid modelVapor–liquid equilibriumIsobaric processPhysical and Theoretical ChemistryFluid Phase Equilibria
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Isobaric vapor-liquid equilibria and densities for the system methyl 1,1-dimethylethyl ether+2-propanol

2002

Vapor-liquid equilibrium data at 50, 75 and 94 kPa have been determined for the binary system methyl 1,1-dimethylethyl ether + 2-propanol, in the temperature range 308-344 K. The measurements were made in an equilibrium still with circulation of both the vapor and liquid phases. Excess volumes have been also determined from density measurements using a vibrating tube densimeter at 298.15 K. The system exhibits positive deviation from ideal behavior and does not present azeotropy within the range of pressures studied. The excess volume of the system is negative over the whole mole fraction range. The activity coefficients and boiling points of the solutions were well correlated with the mole…

Activity coefficientUNIQUACChemistryThermodynamicsCondensed Matter PhysicsMole fractionElectronic Optical and Magnetic MaterialsPropanolBoiling pointchemistry.chemical_compoundMolar volumeMaterials ChemistryNon-random two-liquid modelVapor–liquid equilibriumPhysical and Theoretical Chemistry
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Binding of a fluorescent dansylcadaverine-substance P analogue to negatively charged phospholipid membranes.

2000

Abstract We have investigated the binding of a new dansylcadaverine derivative of substance P (DNC-SP) with negatively charged small unilamellar vesicles composed of a mixture of phosphatidylcholine (PC) and either phosphatidylglycerol (PG) or phosphatidylserine (PS) using fluorescence spectroscopic techniques. The changes in fluorescence properties were used to obtain association isotherms at variable membrane negative charges and at different ionic strengths. The experimental association isotherms were analyzed using two binding approaches: (i) the Langmuir adsorption isotherm and the partition equilibrium model, that neglect the activity coefficients; and (ii) the partition equilibrium m…

Activity coefficientVesicleLipid BilayersAnalytical chemistryLangmuir adsorption modelCharge densityGeneral MedicineSubstance PBiochemistryBinding constantFluorescencechemistry.chemical_compoundsymbols.namesakeMembranechemistryModels ChemicalStructural BiologyPhosphatidylcholinePartition equilibriumCadaverinesymbolsMolecular BiologyPhospholipidsFluorescent DyesProtein BindingInternational journal of biological macromolecules
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