Search results for "Isothermal process"

showing 10 items of 114 documents

Thermoconvective instability and local thermal non-equilibrium in a porous layer with isoflux-isothermal boundary conditions

2014

The effects of lack of local thermal equilibrium between the solid phase and the fluid phase are taken into account for the convective stability analysis of a horizontal porous layer. The layer is bounded by a pair of plane parallel walls which are impermeable and such that the lower wall is subject to a uniform flux heating, while the upper wall is isothermal. The local thermal non-equilibrium is modelled through a two-temperature formulation of the energy exchange between the phases, resulting in a pair of local energy balance equations: one for each phase. Small-amplitude disturbances of the basic rest state are envisaged to test the stability. Then, the standard normal mode procedure is…

Thermal equilibriumConvectionHistoryLOCAL THERMAL NONEQUILIBRIUMEIGENPROBLEM FORMULATIONChemistryThermodynamicsLOCAL THERMAL NON-EQUILIBRIUMMechanicsInstabilityIsothermal processComputer Science ApplicationsEducationPhysics::Fluid DynamicsShooting methodThermal conductivityPOROUS MEDIUMLINEAR STABILITY ANALYSISHeat transferBoundary value problemUNIFORM WALL HEAT FLUXJournal of Physics: Conference Series
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Modeling of the catalytic effects of potassium and calcium on spruce wood gasification in CO2

2016

Abstract Using previously reported thermogravimetric analysis measurements, the effects of calcium and potassium on the char gasification rate of spruce wood were modeled. Spruce wood was leached of inorganic ash elements and doped with measured amounts of potassium and calcium. The wood was gasified in an isothermal thermogravimetric analysis device in CO 2 where the devolatilization of the wood, char formation and char gasification all occurred inside the preheated reactor. A new method for separating the effects of devolatilization and char gasification is presented. Kinetic models were evaluated for their ability to describe the observed catalytic effects of potassium and calcium on the…

Thermogravimetric analysis020209 energyGeneral Chemical EngineeringPotassiumEnergy Engineering and Power Technologychemistry.chemical_elementgasification02 engineering and technologyCalciumcomplex mixturesIsothermal processCatalysisChemical kinetics0202 electrical engineering electronic engineering information engineeringCharta116ta215ta218Wood gas generatorbiomasstechnology industry and agriculturemodelingFuel TechnologychemistryChemical engineeringreaction kineticsFuel Processing Technology
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Lifetime predictions of non-ionic and ionic biopolymers: kinetic studies by non-isothermal thermogravimetric analysis

2021

AbstractIn this paper, films based on sustainable polymers with variable charge have been investigated by non-isothermal thermogravimetry in order to predict their lifetime, which is a key parameter for their potential use in numerous technological and biomedical applications. Specifically, chitosan has been selected as positively charged biopolymer, while alginate has been chosen as negatively charged biopolymer. Among non-ionic polymers, methylcellulose has been investigated. Thermogravimetric measurements at variable heating rates (5, 10, 15 and 20 °C min−1) have been performed for all the polymers to study their degradation kinetics by using isoconversional procedures combined with ‘Mas…

Thermogravimetric analysisMaterials scienceDiffusionIonic bondingThermodynamics02 engineering and technologyActivation energyengineering.materialMethylcellulose010402 general chemistry01 natural sciencesIsothermal processBiomaterialsBiopolymersWaste Management and Disposalchemistry.chemical_classificationChitosanRenewable Energy Sustainability and the EnvironmentAlginatePolymer021001 nanoscience & nanotechnology0104 chemical sciencesThermogravimetrychemistrySettore CHIM/03 - Chimica Generale E InorganicaThermogravimetryCeramics and CompositesengineeringBiopolymer0210 nano-technologyLifetime
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Non-isothermal thermogravimetry as an accelerated tool for the shelf-life prediction of paracetamol formulations

2021

Abstract In this work, non-isothermal thermogravimetric studies have been carried out on several paracetamol formulations with the aim to predict their shelf-lives under variable storage conditions. Specifically, paracetamol tablets of different brands have been investigated allowing to estimate their pharmaceutical quality by considering the specific drug stability. The proposed protocol is based on the kinetic study of thermogravimetric data by the combination of isoconversional procedures (Friedman and Kissinger-Akahira-Sunose (KAS) methods) and “Master plot” analysis. Accordingly, the kinetics of the paracetamol degradation is totally explored in terms of activation energy, pre-exponent…

Thermogravimetric analysisMaterials scienceShelf-lifeThermodynamicsExpiration date02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter PhysicsShelf life01 natural sciencesIsothermal process010406 physical chemistry0104 chemical sciencesThermogravimetryDecay timeParacetamolIsoconversional methodsThermogravimetryPhysical and Theoretical Chemistry0210 nano-technologyInstrumentationSettore CHIM/02 - Chimica Fisica
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Thermogravimetric and Sorption Measurement Techniques/Instruments

2002

The survey covers commercially offered instruments for the determination of the surface structure of porous solids based on isothermal measurement of physisorption of inert gases and of thermogravimetric instruments. Basic assumptions, features and experimental uncertainties are compared.

Thermogravimetric analysisPhysisorptionChemical engineeringChemistryAnalytical chemistrySurface structureSorptionPorous solidsIsothermal process
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Analysis of the oxidation process and mechanical evolution in nanosized copper spinel ferrites. Role of stresses on the coercivity

1997

Isothermal oxidations of the iron(II) and copper(I) cations in nanosized copper spinel ferrites which were oxidized in cation-deficient spinels have been studied by thermogravimetric analysis. The low temperature kinetics of oxidation of each oxidizable cation has been explained on the basis of a diffusion-induced stress effect, these stresses being generated in the ferrite particles by the chemical gradient induced during the oxidation process where the cations at the surface are more oxidized than those in the bulk. A reaction mechanism coupling the chemical and the mechanical effects has been proposed. When the Cu-ferrites contain some Co-cations, it has also been revealed that the stres…

Thermogravimetric analysisReaction mechanismMaterials scienceSpinelKineticsInorganic chemistrychemistry.chemical_elementCoercivityengineering.materialCondensed Matter PhysicsCopperIsothermal processchemistryengineeringFerrite (magnet)General Materials ScienceMaterials Chemistry and Physics
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The effect of Mo and Ge reactive elements on high-temperature oxidation of higher manganese silicide

2021

Abstract Higher manganese silicide (HMS) alloys (Mnx-αMoαSiy-βGeβ (x = 0.99–1.011, α = 0.005–0.02, y = 1.75, β = 0.005–0.01)) were studied to elucidate the effect of Mo and Ge pertaining to oxidation. Oxidation experiments were conducted using thermogravimetry and characterized using x-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). Isoconversion experiments below 450 °C, shows that doping (up to 2 at%) raises the oxidation potential of HMS. Isothermally, the oxidation rate reduces buy one order of magnitude by doping on Mn and/or Si sites from 0.5 to 2 at%, revealing that the dopants-based oxides do not lessen the robustness of SiO2 oxide.

VDP::Teknologi: 500::Materialteknologi: 520Materials scienceDopantScanning electron microscopeGeneral Chemical EngineeringDopingInorganic chemistrytechnology industry and agricultureOxideGeneral ChemistryIsothermal processCorrosionThermogravimetrychemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyGeneral Materials ScienceCorrosion Science
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(Vapour + liquid) equilibria of (water + dimethylformamide): application of the headspace-gas chromatography for the determination of thermodynamic i…

1998

Abstract Isothermal measurements of the partial vapour pressures have been carried out on {water + dimethylformamide (DMF)} at temperatures betweenT=305.15 K andT=323.15 K using an apparatus composed of a headspace sampler and a normal gas chromatograph. These data were simultaneously evaluated in one step with respect to the (composition dependent, integral) Flory-Huggins interaction parametergby means of a new method which minimizes the Gibbs energy of mixing and does not require chemical potentials. The expression forggiven by Koningsveld and Kleintjens, originally designed for polymer solutions, describes the present results best.

Vapor pressureThermodynamicsFlory–Huggins solution theoryEntropy of mixingAtomic and Molecular Physics and OpticsIsothermal processGibbs free energychemistry.chemical_compoundsymbols.namesakechemistrysymbolsDimethylformamideGeneral Materials ScienceGas chromatographyBinary systemPhysical and Theoretical ChemistryThe Journal of Chemical Thermodynamics
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Interdependence of enthalpic and entropic contributions to the second osmotic virial coefficient

1972

The interdependence of the enthalpic contribution A2, H and the entropic contribution A2, s to the second osmotic virial coefficient for a given polymer-solvent system has been investigated from the experimental and the theoretical point of view. Experimentally, the following common facts were observed for various systems at temperatures and pressures below the critical values for the solvent. Both the isobaric and isothermal dependences can be approximated over relatively wide ranges of A2, H by linear relations with a slope deviating only slightly, but in a characteristic manner from a value of −1. When the temperature is increased at constant pressure one moves along an isobar towards hi…

Virial coefficientConstant pressureChemistryIsobarIsobaric processThermodynamicsConstant (mathematics)Isothermal processJournal of Polymer Science Part A-2: Polymer Physics
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Determination of water intrusion heat in hydrophobic microporous materials by high pressure calorimetry

2010

International audience; The understanding of interactions between a solid surface and a non-wetting liquid still remains of fundamental interest in numerous research fields, from chemistry to biology. This work focuses on the mechanisms of water intrusion in hydrophobic microporous materials through the thermal analysis of the phenomenon. A specific calorimetric technique coupled to high pressure equipment has been developed to investigate equilibrium thermal effects in such thermodynamic systems from 0 to 400 MPa under isothermal conditions. First validation tests of this method were carried out by compressing degassed water in a constant volume V with successive small pressure increments …

Work (thermodynamics)Non-wetting surface[SDV]Life Sciences [q-bio]Thermodynamics02 engineering and technologyCalorimetry010402 general chemistry01 natural sciencesEndothermic processIsothermal process[CHIM]Chemical SciencesGeneral Materials SciencePorosityThermal analysisChemistryIntrusionWaterGeneral ChemistryMicroporous materialHigh pressure calorimetry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSilicalite-113. Climate actionMechanics of MaterialsIsobaric process0210 nano-technology
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