Search results for "Thermal"

showing 10 items of 3576 documents

Functionalized Fe3O4 nanoparticles: influence of ligand addition sequence and pH during their continuous hydrothermal synthesis

2015

In this study we report various new efficient ways to synthesize and modify in situ magnetite (Fe3O4) iron oxide nanoparticles (NPs). Thanks to an apparatus especially developed for this new method of grafting, the NPs have been synthesized and functionalized by 3,4-dihydroxyhydrocinnamic acid (DHCA) or 3,4-dihydroxy-L-phenylalanine (LDOPA) in one step and under hydrothermal conditions using varying concentration ratios ([organic molecules]/[ferrous and ferric ions]). The organic molecules were added before or after the NP synthesis. The addition of these organic molecules modifies the structure, the morphology, the oxidation degree and the growth of the crystallites. Adding the organic mol…

ChemistryGeneral Chemical EngineeringInorganic chemistryMaghemiteGeneral Chemistryengineering.materialHydrothermal circulationFerrouschemistry.chemical_compoundengineeringmedicineHydrothermal synthesisFerricPartial oxidationIron oxide nanoparticlesmedicine.drugMagnetiteRSC Advances
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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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On-line vapor-phase generation combined with Fourier transform infrared spectrometry

2008

We present a critical review of on-line vapor-phase generation combined with Fourier transform infrared spectrometry for detection. We discuss different experimental approaches developed for generating the vapor phase based on different principles (e.g., thermal volatilization, acid-base, redox reaction and covalent hydride generation). Using examples of applications, we try to demonstrate the analytical potential of on-line vapor-phase generation in vibrational spectrometry in order to improve the selectivity and the sensitivity of the measurement step and to make environmentally-friendly procedures available for problem solving in the analytical laboratory. We pay special attention to int…

ChemistryHydrideVaporizationLine (geometry)ThermalAnalytical chemistrySensitivity (control systems)Mass spectrometryInterference (wave propagation)SpectroscopyFourier transform spectroscopyAnalytical ChemistryComputational physicsTrAC Trends in Analytical Chemistry
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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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Application of solid-state electrochemistry techniques to polyfunctional organic–inorganic hybrid materials: The Maya Blue problem

2013

Abstract The time evolution of indigo plus palygorskite powdered mixtures during isothermal heating at different temperatures between 120 and 180 °C to form Maya Blue-type materials has been monitored by means of infrared spectrometry, diffuse reflectance spectrometry in the visible region and solid state electrochemical techniques. The kinetics of the formation process of such materials can be described in terms of two consecutive reactions, the first one consisting of the loss of zeolitic water of the palygorskite coupled with clay-indigo attachment and partial indigo to denydroindigo oxidation. The palygorskite dehydration acts as a rate-determining step fitting to a 3D Avrami-Erofe’ev k…

ChemistryKineticsInfrared spectroscopyPalygorskiteGeneral ChemistryCondensed Matter PhysicsElectrochemistryIndigoIsothermal processChemical engineeringMechanics of MaterialsmedicineOrganic chemistryGeneral Materials ScienceDiffuse reflectionHybrid materialmedicine.drugMicroporous and Mesoporous Materials
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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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