Search results for "thermal [radiation mechanism]"

showing 10 items of 2571 documents

Enhanced nonlinear optical properties and thermal stability of donor-acceptor substituted oligothiophenes

1997

Abstract Linear and nonlinear optical properties of a series of novel donor-acceptor substituted α-oligothiophenes were investigated by means of electrooptical absorption measurements (EOAM) and electric field induced second harmonic generation (EFISH). The second-order polarizabilities β(−2ω; ω, ω) were related to dipole changes Δμ ag and transition dipoles μ ag associated with low-lying charge-transfer (CT) excitations by using the perturbational two-level approximation. Systematic variation of the donor and acceptor groups led to compounds with exceptional nonlinearity and thermal stability. Too strong donor/acceptor pairs, however, yielded structures in the charge-resonance (CR) limit w…

ChemistryGeneral Physics and AstronomySecond-harmonic generationMolecular physicsAcceptorCondensed Matter::Materials ScienceNonlinear systemDipoleNonlinear opticalComputational chemistryElectric fieldThermal stabilityPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)Chemical Physics
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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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Selective oxidation of ethane: Developing an orthorhombic phase in Mo–V–X (X=Nb, Sb, Te) mixed oxides

2009

Abstract Mo–V–X (X = Nb, Sb and/or Te) mixed oxides have been prepared by hydrothermal synthesis and heat-treated in N2 at 450 °C or 600 °C for 2 h. The calcination temperature and the presence or absence of Nb determines the nature of crystalline phases in the catalyst. Nb-containing catalysts heat-treated at 450 °C are mostly amorphous solids, while Nb-free catalysts heat-treated at 450 °C and samples treated at 600 °C clearly contain crystalline phases. TPR-H2 experiments show higher H2-consumption on catalysts with amorphous phases. Catalytic results in the oxidative dehydrogenation of ethane indicate that the selective production of the olefin is strongly related to the development of …

ChemistryInorganic chemistryGeneral ChemistryCatalysisCatalysisAmorphous solidlaw.inventionCrystallographylawPhase (matter)Mixed oxideHydrothermal synthesisDehydrogenationOrthorhombic crystal systemCalcinationCatalysis Today
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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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