Search results for "Thermodynamic"

showing 10 items of 2971 documents

Bisphenol A removal from water by biomass-based carbon: isotherms, kinetics and thermodynamics studies

2018

Biomass-based carbon was modified and used as an efficient bisphenol A (BPA) sorbent. The simple and environmentally friendly modification method produced sorbent with a capacity of 41.5 mg/g. The ...

Bisphenol ASorbent0208 environmental biotechnologyKineticsBiomasschemistry.chemical_element02 engineering and technology010501 environmental sciences01 natural scienceschemistry.chemical_compoundPhenolsmedicineEnvironmental ChemistryBiomassBenzhydryl CompoundsWaste Management and Disposal0105 earth and related environmental sciencesWater Science and TechnologyWaterSorptionGeneral MedicineHydrogen-Ion ConcentrationEnvironmentally friendlyCarbon020801 environmental engineeringKineticsChemical engineeringchemistryThermodynamicsAdsorptionCarbonWater Pollutants ChemicalActivated carbonmedicine.drugEnvironmental Technology
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Hysteretic nonequilibrium Ising-Bloch transition

2005

We show that a parametrically driven cubic-quintic complex Ginzburg-Landau equation exhibits a hysteretic nonequilibrium Ising-Bloch transition for large enough quintic nonlinearity. These results help to understand the recent experimental observation of this pheomenon [A. Esteban-Martin et al., Phys. Rev. Lett. 94, 223903 (2005)].

BistabilityPhase (waves)FOS: Physical sciencesPattern formationNon-equilibrium thermodynamicsPattern Formation and Solitons (nlin.PS)Nonlinear Sciences - Pattern Formation and SolitonsNonlinear systemAmplitudeQuantum mechanicsIsing modelNonlinear Sciences::Pattern Formation and SolitonsSign (mathematics)MathematicsPhysical Review E
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Bollettino di Matematica pura e applicata

2020

The paper emphasizes some the advances of knowledge in mathematics problems ad new applications. The Bollettino is open to the contribution of Italian or foreign researchers.

Block designLebesgue improper integralBmPaSettore MAT/05 - Analisi MatematicaBoll. di mat. Pura ed appl.Liquid Helium II.Hadamard designFirst return integralNon Equilibrium Thermodynamic
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Enhancement of immunohistochemical staining

1982

The present paper describes two simple procedures which enhance immunohistochemical staining. One is to cover the sections with a plastic film to keep the serum uniformly distributed and minimize its evaporation. Secondly, rocking of the slides has been introduced, causing the serum to flow back and forth under the plastic film. Using this system, it has been possible to test for the effect of mixing on an immunohistochemical reaction (the demonstration of calcitonin in thyroid C cells). It has been found that mixing definitely enhances the reaction during the first 8 h. No effect of serum volume was observed.

Blood Specimen CollectionChromatographyStaining and LabelingHistocytochemistryChemistryGoatsImmunochemistryThyroid GlandMixing (process engineering)Plastic filmGeneral MedicineEvaporation (deposition)RatsVolume (thermodynamics)CalcitoninAnimalsImmunohistochemistryRabbitsAnatomyGeneral Agricultural and Biological SciencesHistochemistry
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Physically-Based Approach to the Mechanics of Strong Non-Local Linear Elasticity Theory

2009

In this paper the physically-based approach to non-local elasticity theory is introduced. It is formulated by reverting the continuum to an ensemble of interacting volume elements. Interactions between adjacent elements are classical contact forces while long-range interactions between non-adjacent elements are modelled as distance-decaying central body forces. The latter are proportional to the relative displacements rather than to the strain field as in the Eringen model and subsequent developments. At the limit the displacement field is found to be governed by an integro-differential equation, solved by a simple discretization procedure suggested by the underlying mechanical model itself…

Body forceNon-local elasticityDiscretizationField (physics)Mechanical EngineeringLinear elasticityConstitutive equationMathematical analysisCentral volume forceEquivalent mechanical modelThermodynamic consistencyContact forceLong-range interactionMechanics of MaterialsDisplacement fieldGeneral Materials ScienceBoundary value problemSettore ICAR/08 - Scienza Delle CostruzioniMathematicsJournal of Elasticity
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Dielectric polarization and polarizability of 1-pentanol+n-octane mixtures from static dielectric constant and refractive index data at 0,25 and 45�C

1990

Static dielectric constants and refractive indices of 1-pentanol+n-octane mixtures were measured in the temperature range between 0 and 45°C. Data discussed in terms of Kirkwood correlation factor and Lorentz-Lorenz molar refractivity give information on the short range intermolecular interactions between the components. The role played by the nonpolar n-octane in the destruction of 1-pentanol oligomers is also pointed out.

Bond dipole momentChemistryIntermolecular forceBiophysicsThermodynamicsDielectricAtmospheric temperature rangeBiochemistryPolarization densityComputational chemistryMolar refractivityPolarizabilityPhysical and Theoretical ChemistryMolecular BiologyRefractive indexJournal of Solution Chemistry
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The deformation tensor ∊ of the spin transition in the mixed crystal [Fe0.46Zn0.54(ptz)6](BF4)2

2004

The conversion of the spin state of complexes exhibiting thermal spin crossover from the1A1low-spin (LS) state to the5T2high-spin (HS) state is accompanied by a deformation of the lattice due to the larger bond lengths in the HS state as compared with the LS state. In a previous work [Kuszet al.(2000).J. Appl. Cryst.33, 201–205], it has been shown that the deformation of the lattice, corrected for its temperature dependence, can be described by an almost temperature-independent tensor ∊ multiplied by the fraction of molecules in the HS state, γHS. Here the dependence of ∊ in a mixed single crystal of [Fe0.46Zn0.54(ptz)6](BF4)2(ptz = propyltetrazole) with a transition temperature near 110 K …

Bond lengthNuclear magnetic resonanceLattice constantSpin statesChemistrySpin crossoverExcited stateSpin transitionThermodynamicsCrystal structureGeneral Biochemistry Genetics and Molecular BiologyLIESSTJournal of Applied Crystallography
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A theoretical determination of the dissociation energy of the nitric oxide dimer

1994

Multi-reference CI methods have been applied to determine the dissociation energy and structure of thecis-N2O2 molecule. The convergence of the theoretical result has been checked with respect to a systematic expansion of the one-electron basis set and the multi-reference CI wave function. The best calculated value, 13.8 kJ/mol, is in agreement with the experimental value, 12.2 kJ/mol. It has been obtained with an extended ANO-type basis set [6s5p3d2f], including the effect of the basis set superposition error (BSSE) in the geometry optimization, and additional effects, such as the electron correlation of core electrons and relativistic corrections, using the average coupled pair functional…

Bond lengthPhysicsMolecular geometryElectronic correlationCore electronAb initio quantum chemistry methodsThermodynamicsChiropracticsPhysical and Theoretical ChemistryConfiguration interactionBond-dissociation energyBasis setTheoretica Chimica Acta
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AM1 prediction of the equilibrium geometry of Si60

1993

Abstract AM1 calculations have been carried out to determine the equilibrium geometry of Si 60 . The predicted I h geometry shows that bonds may be clearly identified as single (2.297 A) or aromatic (2.092 A). Several analogies and differences between Si 60 and C 60 are pointed out. Especially remarkable is the bigger size of the Si 60 cluster, which is predicted to have a radius 2 A larger than that of the C 60 cluster. Results are compared to other levels of theory.

Bond lengthSiliconChemistryComputational chemistryCluster (physics)General Physics and AstronomyMoleculeThermodynamicschemistry.chemical_elementElectronic structureRadiusPhysical and Theoretical ChemistryEquilibrium geometryChemical Physics Letters
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Comparison of various CI treatments for the description of potential curves for the lowest three states of O2

1972

Abstract Various ab initio CI treatments are reported for the 3 Σ − g , 1 Δ g and 1 Σ + g states of O 2 with particular emphasis on the agreement obtained between calculated and experimental results for binding energies and bond distances of these species and also for transition energies between them. The utility of off-center s and p gaussians in describing the bonding process is stressed and the possibility of optimizing the configurations used in the calculations at each internuclear distance is considered.

Bonding processCrystallographyMaterials scienceBinding energyPotential curvesAb initioGeneral Physics and AstronomyThermodynamicsPhysical and Theoretical ChemistryChemical Physics Letters
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