Search results for "Thermodynamics"

showing 10 items of 2774 documents

Efficient Linear-Scaling Density Functional Theory for Molecular Systems

2013

Despite recent progress in linear scaling (LS) density function theory (DFT), the computational cost of the existing LS methods remains too high for a widespread adoption at present. In this work, we exploit nonorthogonal localized molecular orbitals to develop a series of LS methods for molecular systems with a low computational overhead. High efficiency of the proposed methods is achieved with a new robust two-stage variational procedure or by replacing the optimization altogether with an accurate nonself-consistent approach. We demonstrate that, even for challenging condensed-phase systems, the implemented LS methods are capable of extending the range of accurate DFT simulations to molec…

10120 Department of ChemistryWork (thermodynamics)Mathematical optimization010304 chemical physicsSeries (mathematics)Computer scienceLocalized molecular orbitalsMolecular systems01 natural sciencesComputer Science ApplicationsRange (mathematics)0103 physical sciences540 ChemistryLinear scale1706 Computer Science ApplicationsDensity functional theoryPhysical and Theoretical Chemistry010306 general physics1606 Physical and Theoretical ChemistryAlgorithmOrder of magnitude
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Evaluation of the 2-Methoxyethanol as Entrainer in Ethanol–Water and 1-Propanol–Water Mixtures

2013

In this paper, 2-methoxyethanol (commercially known as methyl cellosolve) is proposed as a potential entrainer for extractive distillation processes involving water–alcohol mixtures. The two alcohols studied in this work are ethanol and 1-propanol. Thereby, isobaric vapor–liquid equilibrium (VLE) data at atmospheric pressure have been measured for the ternary systems ethanol + water + 2-methoxyethanol and 1-propanol + water + 2-methoxyethanol. Moreover, data of the binary systems formed by the 2-methoxyethanol and each of the other chemicals used (ethanol, water, 1-propanol) have been obtained. The well-known local composition models Wilson, UNIQUAC, and NRTL have been used to correlate bin…

2-MethoxyethanolUNIQUACGeneral Chemical EngineeringThermodynamicsGeneral Chemistrychemistry.chemical_compound1-PropanolchemistryAzeotropeNon-random two-liquid modelOrganic chemistryExtractive distillationIsobaric processTernary operationJournal of Chemical & Engineering Data
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Casimir-Lifshitz force out of thermal equilibrium between dielectric gratings

2014

We calculate the Casimir-Lifshitz pressure in a system consisting of two different 1D dielectric lamellar gratings having two different temperatures and immersed in an environment having a third temperature. The calculation of the pressure is based on the knowledge of the scattering operators, deduced using the Fourier Modal Method. The behavior of the pressure is characterized in detail as a function of the three temperatures of the system as well as the geometrical parameters of the two gratings. We show that the interplay between non-equilibrium effects and geometrical periodicity offers a rich scenario for the manipulation of the force. In particular, we find regimes where the force can…

ACS number(s): 12.20.−m42.79.Dj42.50.Ct42.50.Lc[PHYS.MPHY]Physics [physics]/Mathematical Physics [math-ph]Degrees of freedom (physics and chemistry)Non-equilibrium thermodynamicsFOS: Physical sciencesDielectricCasimir Force Out of Thermal equilibrium systems GratingsSettore FIS/03 - Fisica Della Materiasymbols.namesake[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Lamellar structure[PHYS.COND.CM-SM]Physics [physics]/Condensed Matter [cond-mat]/Statistical Mechanics [cond-mat.stat-mech]PhysicsThermal equilibriumQuantum PhysicsCondensed matter physicsScatteringAtomic and Molecular Physics and OpticsCasimir effectFourier transformClassical mechanicssymbolsQuantum Physics (quant-ph)Physics - OpticsOptics (physics.optics)
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Monte Carlo simulations of the solid-liquid transition in hard spheres and colloid-polymer mixtures

2010

Monte Carlo simulations at constant pressure are performed to study coexistence and interfacial properties of the liquid-solid transition in hard spheres and in colloid-polymer mixtures. The latter system is described as a one-component Asakura-Oosawa (AO) model where the polymer's degrees of freedom are incorporated via an attractive part in the effective potential for the colloid-colloid interactions. For the considered AO model, the polymer reservoir packing fraction is eta_p^r=0.1 and the colloid-polymer size ratio is q=sigma_p/\sigma=0.15 (with sigma_p and sigma the diameter of polymers and colloids, respectively). Inhomogeneous solid-liquid systems are prepared by placing the solid fc…

ANISOTROPIC SURFACE-TENSIONMaterials scienceMonte Carlo methodDegrees of freedom (physics and chemistry)General Physics and AstronomyThermodynamicsCondensed Matter - Soft Condensed MatterCAPILLARY WAVESAtomic packing factorCOMPUTER-SIMULATIONVAPOR INTERFACE3-DIMENSIONAL ISING-MODELColloidsymbols.namesakePhase (matter)Physical and Theoretical ChemistryCOEXISTING PHASESchemistry.chemical_classificationCondensed Matter - Materials ScienceINTERFACIAL FREE-ENERGYPROFILESHard spheresPolymerCondensed Matter::Soft Condensed MatterchemistryCRYSTAL-MELT INTERFACESBoltzmann constantsymbolsCRYSTALLIZATIONThe Journal of Chemical Physics
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Low temperature rate coefficients of the H + CH+ → C+ + H2 reaction: New potential energy surface and time-independent quantum scattering

2015

The observed abundances of the methylidyne cation, CH(+), in diffuse molecular clouds can be two orders of magnitude higher than the prediction of the standard gas-phase models which, in turn, predict rather well the abundances of neutral CH. It is therefore necessary to investigate all the possible formation and destruction processes of CH(+) in the interstellar medium with the most abundant species H, H2, and e(-). In this work, we address the destruction process of CH(+) by hydrogen abstraction. We report a new calculation of the low temperature rate coefficients for the abstraction reaction, using accurate time-independent quantum scattering and a new high-level ab initio global potenti…

Ab initio quantum chemistry methodsChemistryScatteringPotential energy surfaceThermochemistryAb initioGeneral Physics and AstronomyThermodynamicsReactivity (chemistry)Scattering theoryPhysical and Theoretical ChemistryAtomic physicsPotential energyThe Journal of Chemical Physics
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Rat proximal tubule D-glucose transport as a function of concentration, flow, and radius

1972

From earlier microperfusion studies ofD-glucose and water reabsorption in the proximal surface nephron of the rat,D-glucose was found to be removed by a saturable carrier and by an apparent coupling with net fluid reabsorption. Equations appropriate to describe this system were developed. They incorporated carrier-mediatedD-glucose transport, net water transport, and water-coupled solute transport. Water reabsorption was assumed to be constant either per unit surface area, or per unit volume of the nephron, and the rate of carrier-transportedD-glucose was assumed constant per unit length, per unit surface area, or per unit volume of the tubule. The possibility thatD-glucose could be reabsor…

Absorption (pharmacology)medicine.medical_specialtyPhysiologyClinical BiochemistryBiological Transport ActiveRenal functionNephronAbsorptionchemistry.chemical_compoundD-GlucosePhysiology (medical)Internal medicinemedicineAnimalsWater transportReabsorptionChemistryWaterRatsPerfusionGlucoseKidney TubulesTubuleEndocrinologymedicine.anatomical_structureVolume (thermodynamics)BiophysicsGlomerular Filtration RatePflügers Archiv European Journal of Physiology
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Energy analysis of a non-linear dynamic impact using FEM

2014

In the car industry, the Finite Element Method (FEM) is being more and more used to analyze the crashworthiness performance of vehicles. In order to validate the results, these impact simulations are normally compared with real crash footage and acceleration data. This paper studies the deformation- and energy output of a simple dummy model during a non-linear dynamic impact. The dummy model is crashed into an obstacle at three different velocities to observe the energy dissipated through different damping mechanisms. Furthermore, in impact simulations, material damping plays an important role in energy dissipation. However, it can be difficult to determine realistic damping parameter value…

AccelerationEngineeringWork (thermodynamics)business.industryObstacleCrashworthinessStructural engineeringDissipationDeformation (meteorology)businessEnergy (signal processing)Finite element methodProceeding of the 11th World Congress on Intelligent Control and Automation
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Some observations on the determination of total heavy metals in sewage sludge by atomic absorption spectrophotometry after a pressurized acid digesti…

1990

Abstract An economical and simple method for the flame atomic absorption spectrometric determination of Cd, Pb, Ni, Cu, Fe, and Zn in sewage sludges is described. Samples are treated with concentrated HNO 3 in a thermal oven using Pyrex glass tubes hermetically sealed with Bakelite screw caps. The effect of the digestion parameters, such as digestion time, acid volume, sample mass, and temperature, were studied. The precision and accuracy of this procedure were evaluated by the analysis of two BCR (Community Bureau of Reference, European Communities) certified sewage sludge samples (CRM 146 and 144).

Acid digestionChemistrybusiness.industryAnalytical chemistrySewageHeavy metalsAnalytical Chemistrylaw.inventionchemistry.chemical_compoundDigestion (alchemy)Volume (thermodynamics)lawBakelitebusinessAtomic absorption spectroscopySpectroscopySludgeNuclear chemistryMicrochemical Journal
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Isobaric vapour–liquid equilibria for the binary systems 4-methyl-2-pentanone+1-butanol and+2-butanol at 20 and 101.3kPa

2009

Abstract Isobaric vapour–liquid equilibrium (VLE) measurements for the binary systems 4-methyl-2-pentanone + 1-butanol and 4-methyl-2-pentanone + 2-butanol are reported at 20 and 101.3 kPa. The system 4-methyl-2-pentanone + 1-butanol presents a minimum boiling point azeotrope at both pressures (20 and 101.3 kPa) and the system 4-methyl-2-pentanone + 2-butanol presents only a minimum boiling azeotrope at 20 kPa. In both systems, which deviate positively from ideal behaviour, the azeotropic composition is strongly dependent on pressure. The activity coefficients and boiling points of the solutions were correlated with its composition by the Wilson, UNIQUAC, and NRTL models for which the param…

Activity coefficientBoiling pointUNIQUACChemistryGeneral Chemical EngineeringBoilingAzeotropeNon-random two-liquid modelGeneral Physics and AstronomyThermodynamicsIsobaric processBinary systemPhysical and Theoretical ChemistryFluid Phase Equilibria
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Isobaric Vapor−Liquid Equilibria of the Water + 1-Propanol System at 30, 60, and 100 kPa

1996

Isobaric vapor−liquid equilibria for the water + 1-propanol system are reported at 30, 60, and 100 kPa. The results were found to be thermodynamically consistent according to Van Ness−Byer−Gibbs, Kojima, and Wisniak methods. The system shows a minimum boiling azeotrope, and the azeotropic composition is scarcely shifted with pressure. Results were compared with literature values. The data were correlated with Margules, Van Laar, Wilson, NRTL, and UNIQUAC liquid-phase activity coefficient models.

Activity coefficientBoiling pointUNIQUACVapor pressureChemistryGeneral Chemical EngineeringBoilingAzeotropeNon-random two-liquid modelThermodynamicsIsobaric processGeneral ChemistryJournal of Chemical & Engineering Data
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