Search results for "isotherm"

showing 10 items of 268 documents

Factors Controlling the Energy of Nitrogen Monolayer Coverage onHigh Surface Area Catalyst Oxide Carriers

2011

Factors affecting the strength of nitrogen physisorption at monolayer coverage on different catalytic oxide carriers (e.g., ZnO, MgO, Al2O3, ZrO2, TiO2, and SiO2) have been addressed. Isotherm elaboration by the two-parameter BET equation provides C-constant values (80–200) inversely related to the polarizing power (PP) of the oxide adsorbent irrespective of the surface area exposure. The energy of monolayer formation depends on the extent of charge-delocalization characterizing the surface cation-oxygen bond, which determines the acid–base character of the oxide and strength of van der Waals interactions with adsorbate molecules. Density functional theory (DFT) calculations on MgO and TiO2…

Materials scienceInorganic chemistryOxideSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisBET isothermchemistry.chemical_compoundsymbols.namesakenitrogen adsorption DFTGeneral EnergyAdsorptionchemistryPhysisorptionChemical engineeringMonolayersymbolsMoleculeDensity functional theoryPhysical and Theoretical Chemistryvan der Waals force
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Adsorption of CO and N 2 molecules at the surface of solid water. A grand canonical Monte Carlo study

2020

International audience; The adsorption of carbon monoxide and nitrogen molecules at the surface of four forms of solid water is investigated by means of grand canonical Monte Carlo simulations. The trapping ability of crystalline Ih and low-density amorphous ices, along with clathrate hy-drates of structures I and II, are compared at temperatures relevant for astrophysics. It is shown that, when considering a gas phase that contains mixtures of carbon monoxide and nitrogen, the trapping of carbon monoxide is favored with respect to that of nitrogen at the surface of all solids, irrespective of the temperature. The results of the calculations also indicate that some amounts of molecules can …

Materials scienceInterface propertiesClathrate hydrateGeneral Physics and Astronomychemistry.chemical_elementGas phaseTrappingPhysics of gases010402 general chemistryAstrophysics01 natural scienceschemistry.chemical_compoundAmorphous materialsAdsorption0103 physical sciencesCometsMoleculePhysical and Theoretical ChemistryAdsorption isothermCarbon monoxideComputingMilieux_MISCELLANEOUS[PHYS]Physics [physics]010304 chemical physicsMonte Carlo methodsNitrogen0104 chemical sciencesAmorphous solid[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry13. Climate actionChemical physics[SDU]Sciences of the Universe [physics]Complex solidsSelectivityCarbon monoxide
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High Temperature Oxidation of TiAl and TiAl8Nb Alloys in Air

2011

Isothermal oxidation of two g-TiAl-based intermetallic alloys: Ti48Al and Ti46Al8Nb alloys was studied in synthetic air at 1073-1223 K for up to 240 hrs. Mass change per unit area for the oxidized samples followed approximately the parabolic rate law. The kp values for the studied temperature interval were in the range from 7.2×10-13 to 1.8×10-11 g2cm-4s-1. The activation energy for oxidation of Ti48Al alloy in air at 1073-1223 K was Ea = 165±12 kJ/mol. Niobium addition to Ti48Al alloy in the amount of 8% increased its oxidation resistance. Structure and chemical composition of the oxidation products, and morphology of the oxidized samples were investigated using XRD, SEM-EDS, and TEM. The …

Materials scienceMechanical EngineeringAlloyNiobiumIntermetallicOxideAnalytical chemistrychemistry.chemical_elementActivation energyengineering.materialCondensed Matter PhysicsIsothermal processMetalchemistry.chemical_compoundchemistryMechanics of Materialsvisual_artvisual_art.visual_art_mediumengineeringGeneral Materials ScienceTinMaterials Science Forum
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Influence of the mode of introduction of a reactive element on the high temperature oxidation behavior of an alumina-forming alloy. Part I: Isotherma…

2004

Several routes of yttrium introduction were applied to test the high temperature oxidation performance of a FeCrAl alloy. Isothermal oxidation tests were described in a previous paper (Part I of this paper in this journal, 2004, 55, 352). Cyclic oxidation tests were performed in air under atmospheric pressure on blank specimens, Y 2 O 3 sol-gel coated-, Y 2 O 3 metal-organic chemical vapor deposited (MOCVD)-, yttrium ion implanted-alloys, as well as on a steel containing 0.1 wt.% of yttrium as an alloying element. For the 20 hours cycles, all the samples, except FeCrAl-0.1Y, exhibit weight losses after a few cycles, indicating drastic spallation of the oxide scales. The MOCVD coated specime…

Materials scienceMechanical EngineeringHigh-temperature corrosionAlloyMetallurgytechnology industry and agricultureMetals and AlloysAnalytical chemistryOxidechemistry.chemical_elementY alloyGeneral MedicineYttriumengineering.materialIsothermal processSurfaces Coatings and FilmsCorrosionchemistry.chemical_compoundchemistryMechanics of MaterialsMaterials ChemistryengineeringEnvironmental ChemistrySpallationMaterials and Corrosion
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Oxidation behavior of γ-TiAl coated with zirconia thermal barriers

2002

Abstract The applicability of the thermal barrier coating concept, which is an established concept for Ni-base alloys, was investigated for the first time for γ-TiAl. As potential bond coats, the following surface treatments were applied: Al-diffusion coating, Al-diffusion coating combined with short term pre-oxidation in air, short term pre-oxidation in oxygen of a rough surface finish γ-TiAl sample without aluminide coating. For the purpose of lowering the temperature of the γ-TiAl substrate surface, and thus, to prolong the life time, a zirconia thermal barrier coating (TBC) was applied on top of the above-mentioned modified TiAl surfaces. Oxidation resistance of the modified γ-TiAl allo…

Materials scienceMechanical EngineeringMetallurgyMetals and AlloysOxidechemistry.chemical_elementGeneral Chemistryengineering.materialOxygenIsothermal processThermal barrier coatingchemistry.chemical_compoundchemistryCoatingMechanics of MaterialsThermalMaterials ChemistryengineeringCubic zirconiaComposite materialAluminideIntermetallics
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XRD Line Broadening Studies on Mullite

1996

An X-ray diffraction microstructural study on 110, 220, 001 and 111 peaks has been performed on mullite in the temperature range of primary mullite formation in order to monitor nucleation and growth process. Considering the crystallinity of the starting kaolinites, a greater disorder of the kaolinite has been found to enhance the mullite formation. Isothermal growth is related to a decrease in the Al 2 O 3 content of mullite.

Materials scienceNucleationMineralogyMulliteCrystal growthGeneral ChemistryAtmospheric temperature rangeCondensed Matter PhysicsMicrostructureIsothermal processCrystallinityChemical engineeringKaoliniteGeneral Materials ScienceCrystal Research and Technology
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Crystallization and melting of fractions of branched polyethylene

1983

Effects of the molecular weight on the crystallization behaviour of branched polyethylene become observable if isothermal crystallization is studied at temperatures near to the melting end. Crystallinities decrease with decreasing molecular weight. Thicknesses of lamellae grown during isothermal crystallization are independent of the molecular weight. They depend only on temperature. Compared to the effect of the branches polydispersity gives only a minor contribution to the broadening of the crystallization and melting range of low density polyethylene.

Materials sciencePolymers and PlasticsDispersitytechnology industry and agricultureIsothermal crystallizationPolyethylenelaw.inventionCondensed Matter::Soft Condensed MatterCondensed Matter::Materials ScienceLow-density polyethylenechemistry.chemical_compoundColloid and Surface ChemistryChemical engineeringchemistrylawCondensed Matter::SuperconductivityMaterials ChemistryPhysical and Theoretical ChemistryCrystallizationColloid & Polymer Science
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Crystallization kinetics of poly(ethylene oxide) from its melt and from mixtures with tetrahydronaphthalene and oligo(ethylene oxide-block-dimethylsi…

2004

The crystallization of poly(ethylene oxide) (PEO) from the pure state and from its mixtures with oligo(dimethyl siloxane-b-ethylene oxide) (COP) and tetrahy- dronaphthalene (THN) was investigated. The crystallization kinetics was studied iso- thermally and nonisothermally with an automated device that monitored the light passing through the corresponding liquids as functions of time and/or temperature. The rate was strongly influenced by the concentration of COP in the mixture. A substantial decrease in the induction time (the time required for the onset of crystallization) and a considerable shift in the crystallization temperature (the transition from a liquid state to a solid state) to h…

Materials sciencePolymers and PlasticsEthylene oxideKineticsOxideCondensed Matter PhysicsIsothermal processlaw.inventionchemistry.chemical_compoundAvrami equationchemistryChemical engineeringlawPolymer chemistryMaterials ChemistryPolymer blendPhysical and Theoretical ChemistryCrystallizationSupercoolingJournal of Polymer Science Part B: Polymer Physics
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Elongational behavior of low density/linear low density polyethylenes

1988

Rheological data have been collected in isothermal elongational flow for three different types of blends, made from one low density polyethylene and three linear low density samples. In addition to the transient curves, elongation at break data are also reported. The influence of the composition and of the molecular weight of the linear low density polyethylene is discussed.

Materials sciencePolymers and PlasticsLinear polymerFlow (psychology)technology industry and agricultureGeneral ChemistryIsothermal processCondensed Matter::Soft Condensed MatterLinear low-density polyethyleneLow-density polyethyleneRheologyMaterials ChemistryLow densityElongationComposite materialPolymer Engineering and Science
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Effect of CTBN rubber inclusions on the curing kinetic of DGEBA–DGEBF epoxy resin

2003

Abstract The curing kinetics of an epoxy resin matrix, based on diglycil ether of bisphenol A and F (DGEBA–DGEBF), associated with an anhydride hardener, at different carboxyl-terminated copolymer of butadiene and acrylonitrile liquid rubber (CTBN) concentration (0–10 phr) are studied using a differential scanning calorimetry (DSC) and a stress-controlled rheometer in isothermal and dynamic conditions. The aim of this work is to correlate the presence of the rubber phase with the transition phenomena that occur during the curing process. The CTBN rubber induces a catalytic effect on the polymerization of the pure resin clearly observed by a significant enhancement of the curing rate. Calori…

Materials sciencePolymers and PlasticsOrganic Chemistrytechnology industry and agricultureGeneral Physics and AstronomyEpoxyChemo-rheologyIsothermal processchemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiDifferential scanning calorimetryEpoxyNatural rubberchemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumCopolymerPultrusionCuringAcrylonitrileComposite materialNitrile rubberCuring (chemistry)European Polymer Journal
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