Search results for "thermal [correlation function]"

showing 10 items of 1923 documents

Some fundamentals of the vapor and solution growth of ZnSe and ZnO

1999

Abstract Some fundamentals of ZnSe and ZnO vapor and solution growth are investigated. Residual water present in gases or gaseous mixtures such as H 2 , Ar or H 2 +H 2 O is shown to act as a sublimation activator in the vapor-phase transport of both compounds. The processes involved in the growth by chemically activated sublimation with such gases and gas mixtures have been studied by close-spaced vapor transport (CSVT). The ZnSe growth rate is found to be constant, while in the ZnO case a high initial growth rate is followed by slower growth subsequently. Using a theoretical model, the thermodynamic constants of the transport – energies of activation, sublimation and condensation and entha…

ChemistryInorganic chemistryAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsInorganic ChemistrySolventDifferential thermal analysisActivator (phosphor)Materials ChemistryChlorineSublimation (phase transition)Growth rateStandard enthalpy change of formationPhase diagramJournal of Crystal Growth
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Preparation of multi-nanocrystalline transition metal oxide (TiO2–NiTiO3) mesoporous thin films

2005

Ordered mesoporous TiO2–NiTiO3 thin films, with nickel content x < 0.5, were prepared by dip-coating an acidic solution of hydrolysed transition metal chlorides in controlled humidity, followed by a very careful annealing treatment. These latter treatments were studied by in situ SAXS-WAXS experiments involving synchrotron radiation and TEM analysis. They revealed that the walls can be composed of amorphous, single crystalline or multi crystalline nanoparticles depending on x and the conditions applied during the thermal treatment.

ChemistryInorganic chemistryOxideNanoparticleGeneral ChemistryThermal treatmentCatalysisNanocrystalline materialAmorphous solidchemistry.chemical_compoundTransition metalMaterials ChemistryThin filmMesoporous materialNew J. Chem.
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Evaluation of the Stability of Pure Silica MCM-41 toward Water Vapor

1999

Water vapor adsorption/desorption isotherms at 298 K and XRD measurements and nitrogen isotherms at 77 K before and after exposure to water vapor were determined on pure silica MCM-41 samples; samples had different pore widths and were prepared by different synthesis methods, including hydrothermal and room-temperature procedures. It was found that prolonged exposure to water vapor provoked structural alterations in all of the MCM-41 materials studied, the most significant effects being a loss of pore shape uniformity and a large decrease in pore size and, in consequence, pore volume. Analysis of the results suggests that these alterations are due to expansion of the pore walls as well as, …

ChemistryInorganic chemistrytechnology industry and agriculturechemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsMolecular sieveNitrogenHydrothermal circulationAdsorptionMCM-41Volume (thermodynamics)Chemical engineeringDesorptionElectrochemistryGeneral Materials ScienceSpectroscopyWater vaporLangmuir
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Relations between compression and thermal contraction in 1,2,4-trichlorobenzene and melting of trichlorobenzene isomers

2015

The compression and thermal expansion of crystalline 1,2,4-trichlorobenzene, C6H3Cl3, 124TCB, investigated under isobaric and isothermal conditions, are in reverse relation, as for most of crystals, however, the isochoric strain along direction c is clearly different from those along a and b. Single crystals of 124TCB have been in situ grown under isochoric and isobaric conditions, at 270 K/0.1 MPa and 295 K/0.16 GPa, and also at 100 K/0.1 MPa and 295 K/0.64 GPa, when the unit-cell volume is similar. All crystallizations yielded the same phase, of monoclinic space group P21/n, with two symmetry-independent molecules (Z′ = 2). The structure is governed by Cl⋯Cl and Cl⋯H interactions and the …

ChemistryIsochoric processThermodynamicsTrichlorobenzeneGeneral ChemistryCondensed Matter PhysicsThermal expansionIsothermal processPhase (matter)medicineIsobaric processGeneral Materials Sciencemedicine.drugPhase diagramMonoclinic crystal systemCrystEngComm
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Synthesis, crystal structure, and magnetic characterization of the three-dimensional compound [Co2(cbut)(H2O) 3]n (H4cbut = 1,2,3,4- cyclobutanetetra…

2014

A novel cobalt(II) complex of formula [Co2(cbut)(H 2O)3]n (1) (H4cbut = 1,2,3,4-cyclobutanetetracarboxylic acid) has been synthesized under hydrothermal conditions and its crystal structure has been determined by means of synchrotron radiation and neutron powder diffraction. The crystal structure of 1 consists of layers of cobalt(II) ions extending in the bc-plane which are pillared along the crystallographic a-axis through the skeleton of the cbut 4- ligand. Three crystallographically independent cobalt(II) ions [Co(1), Co(2), and Co(3)] occur in 1. They are all six-coordinate with four carboxylate-oxygens [Co(1)-Co(3)] and two cis-[Co(1)] or trans-water molecules [Co(2) and Co(3)] buildin…

ChemistryLigandchemistry.chemical_elementCrystal structureHydrothermal circulationIonInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronMoleculeCarboxylatePhysical and Theoretical ChemistryCobalt
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On the synthesis and characterization of layered antimony(III) phosphate and its interaction with moist ammonia and amines

1998

Samples of antimony(III) phosphate, a layered material, were prepared at room temperature, using the two allotropic forms of Sb2O3, layered valentinite and cubic senarmontite. The compounds were characterized by infrared spectroscopy, X-ray diffraction, and thermogravimetric–differential thermal analysis. Solids exposed to ammonia, ethylenediamine, or hydrazine vapors also were studied. The interaction between SbPO4 and the bases always led to the formation of stoichiometric amounts of Sb2O3 and hydrogen phosphate(–2) salts of the bases. With ammonia, the SbPO4 raw materials gave rise to valentinite or senarmontite, depending on which Sb2O3 allotropic form was used to prepare antimony phosp…

ChemistryMechanical EngineeringInorganic chemistryHydrazineIntercalation (chemistry)Infrared spectroscopychemistry.chemical_elementEthylenediamineCondensed Matter PhysicsPhosphateThermogravimetrychemistry.chemical_compoundAntimonyMechanics of MaterialsDifferential thermal analysisGeneral Materials ScienceMaterials Research Bulletin
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Determination of the first ionization potential of einsteinium by resonance ionization mass spectroscopy (RIMS)

1998

Abstract The first ionization potential of einsteinium (IP Es ) was determined by resonance ionization mass spectroscopy (RIMS) using samples with ≤10 12 atoms of 254 Es ( T 1/2 =276 days). This method is based on the measurement of photoionization thresholds as a function of applied electric field strength, followed by extrapolation to zero field strength to yield IP Es . An atomic beam of Es was created by heating a filament on which einsteinium was electrodeposited from an aqueous solution onto a tantalum backing and covered with titanium metal. Es atoms were ionized via a three-step excitation scheme, and the ions mass-selectively detected in a time-of-flight (TOF) mass spectrometer. Th…

ChemistryMechanical EngineeringMetals and AlloysAnalytical chemistryThermal ionizationPhotoionizationMass spectrometryAtmospheric-pressure laser ionizationMechanics of MaterialsIonizationMaterials ChemistryAtomic physicsIonization energyElectron ionizationAmbient ionizationJournal of Alloys and Compounds
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Determination of the first ionization potential of nine actinide elements by resonance ionization mass spectroscopy (RIMS)

1998

The high sensitivity of RIMS enables the precise determination of the first ionization potential of actinide elements with a sample size of ≤1012 atoms. By multiple resonant laser excitation, the actinide atoms under investigation are ionized in the presence of an electric field, and the ions are mass-selectively detected in a time-of-flight spectrometer. The first ionization potential is obtained by scanning the wavelength of the laser used for the last excitation step across the ionization threshold Wth—indicated by a sudden increase of the ion count rate—at various electric field strengths. Extrapolation of Wth to electric field strength zero leads directly to the first ionization potent…

ChemistryMechanical EngineeringMetals and AlloysThermal ionizationPhotoionizationMolar ionization energies of the elementsIon sourceAtmospheric-pressure laser ionizationMechanics of MaterialsIonizationMaterials ChemistryAtomic physicsElectron ionizationAmbient ionizationJournal of Alloys and Compounds
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Thermal analyses of commercial magnesium stearate pseudopolymorphs

2005

Abstract Two commercial magnesium stearate powders in two well-characterised structural states are investigated using DSC and coupled TGA–DTA under dry nitrogen flow. They consist of either a mixture of crystalline hydrates or a poorly crystallised so-called anhydrate. Following the degassing of unbound water, 1 or 3 weight-loss peaks are observed below about 100 °C, each associated with one heat loss peak at the same temperature. The present results and a review of graphical data from literature show that the so-called anhydrate always contains a significant amount of water. At the beginning of the dehydration process, the heat loss is the same as the standard heat of vaporisation of water…

ChemistryMineralogyCondensed Matter Physicsmedicine.diseaseThermogravimetrychemistry.chemical_compoundDifferential scanning calorimetryChemical engineeringPolymorphism (materials science)medicineGravimetric analysisDehydrationMagnesium stearatePhysical and Theoretical ChemistryThermal analysisHydrateInstrumentationThermochimica Acta
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Chemical modification of porous calcium hydroxyapatite surfaces by grafting phenylphosphonic and phenylphosphite acids

2006

Abstract It is well known that the incorporation of organic molecules can provide an effective route to modify the surface properties of apatite ceramics. The present study shows that phosphonates can react with calcium ions to control the formation of the hydroxyapatite structures. The grafting of C6H5PO(OH)2 (PPOH) and C6H5PO(OH)H (PPH) was used to increase the specific surface area as well as the porosity of hydroxyapatite materials. The higher specific surface area for HAp treated by PPOH is around 267 m2/g compared to the pure HAp (140 m2/g). The phenyl (C6H5) groups are removed by thermal treatment around 500 °C. After treatment at 800 °C, organoapatites (PP-HAp) are converted to stoi…

ChemistryMineralogychemistry.chemical_elementChemical modification02 engineering and technologyThermal treatmentCalcium010402 general chemistry021001 nanoscience & nanotechnologyGrafting01 natural sciencesApatite0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryColloid and Surface Chemistryvisual_artSpecific surface area[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryvisual_art.visual_art_mediumHydroxyapatites0210 nano-technologyPorosityComputingMilieux_MISCELLANEOUSNuclear chemistry
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