Search results for "thermal [radiation]"

Preparation of photocatalytic brookite thin films

2007

Pure brookite films were deposited from a brookite dispersion obtained by peptizing a mixture brookite–rutile prepared by thermolysis of TiCl4 in a HCl solution. The films were characterised by X-ray diffraction and Raman spectroscopy. The photoactivity of the samples was tested by using the photo-oxidation of 2-propanol in gas–solid regime as a probe reaction. The brookite films efficiently degraded 2-propanol under UV illumination.

New rotational levels in $^{186}$Re nucleus

2020

International audience; Excited levels of 186 Re have been studied using results of the single γ -ray spectra measurements following the thermal neutron capture reaction. Energies and intensities of more than 500 γ -transitions have been obtained with the high-resolution crystal diffraction spectrometer GAMS5 of ILL. Most of the obtained intense γ -transitions have been placed in the 186 Re level scheme. A number of new levels, as well as the depopulation for levels observed earlier in the 187 Re (p,d)186 Re reaction measurements have been proposed. Structure of 186 Re levels is interpreted in terms of two-quasiparticle plus rotor coupling model and compared with that of the neighbouring do…

Coupling of Benzynezirconocene with 1,4-Diphenyl-1,3-butadiyne

2000

The thermolysis of diphenylzirconocene in the presence of 1,4-diphenyl-1,3-butadiyne to yield the seven-membered zirconacyclocumulene 1 via the intermediacy of benzynezirconocene is described. This complex has been characterized by an X-ray diffraction study. Additionally, better knowledge of the bonding of the cumulene moiety was achieved by DFT calculations. Cleavage of the Zr−C bonds of 1 with methanol provided the corresponding butatriene 2.

Synthesis of single crystalline sub-micron rutile TiO2 rods using hydrothermal treatment in acidic media

2014

Size engineered rutile sub-micron rods were obtained from nanostructured titania under acidic conditions. The synthesis was performed by hydrothermal treatment starting from TiO2-P25 and HCl. The synthesis proceeds in less than two hours and can be up-scaled to several grams in a one-pot reaction by increasing the reaction time. The product is single-phase, and the particles are single crystalline as confirmed by electron diffraction and powder X-ray diffraction analysis. The length of the particles can be varied over a wide range from 100 nm to 1.3 μm by changing the acid concentration. Particle growth is proposed to proceed by a dissolution-recrystallization process via soluble [TiCl6]2− …

Inorganic gels as precursors of TiO2 photocatalysts prepared by low temperature microwave or thermal treatment

2008

Abstract A simple procedure for preparing active TiO2 photocatalysts is presented. The starting materials were unusual TiO2 gels formed from TiCl4. The use of microwaves for a very short time enhanced the TiO2 crystallinity preventing an increase of particle size and minimizing the decrease of specific surface area. This result makes this preparation very attractive. The formation of the gels was monitored through measurements of viscosity. All the samples were characterized by means of X-ray diffraction, diffuse reflectance spectroscopy and BET specific surface area measurements. The photoactivity of the samples was evaluated using the photodegradation of 4-nitrophenol in liquid–solid regi…

Diffusional kinetics of metalliding zinc into solid copper

1982

The process of incorporation of zinc into a copper cathode has been experimentally studied in a molten salt system at 381±2° C and at various current densities. The process is shown to be kinetically controlled by the diffusion of Zn into the solid matrix. A galvanostatic pulse titration technique has been used to determine the chemical diffusion coefficient at various alloy compositions, and an exponential relationship has been found between the diffusivity and the third power of the zinc concentration in the alloy. This relationship was then used in the diffusion equation within the solid matrix and a numerical integration was performed. Very good agreement was found between the calculate…

Diffusion, thermodiffusion, and thermal diffusion of polystyrene in solution

1962

Thermal Diffusion and Partial Molar Enthalpy Variations of n-Butane in Silicalite-1

2008

International audience; We report for the first time the heat of transfer and the Soret coefficient for n-butane in silicalite-1. The heat of transfer was typically 10 kJ/mol. The Soret coefficient was typically 0.006 K−1 at 360 K. Both varied with the temperature and the concentration. The thermal conductivity of the crystal with butane adsorbed was 1.46 ±0.07 W/Km. Literature values of the isosteric enthalpy of adsorption, the concentration at saturation, and the diffusion coefficients were reproduced. Non-equilibrium molecular dynamics simulations were used to find these results, and a modified heat exchange algorithm, Soft-HEX, was developed for the purpose. Enthalpies of butane were al…

Heterobimetallic single-source precursors for MOCVD. Synthesis and characterization of volatile mixed ligand complexes of lanthanides, barium and mag…

1999

Several heterobimetallic complexes of general formula [(M 1 Q) m M 2 (dik) n ], where (M 1 Q) is Cu(salen) or Ni(salen) and M 2 (dik) n is a lanthanide tris(β-diketonate) or an alkali-earth element bis(β-diketonate) with more or less fluorinated diketonato(-) ligands, have been prepared and structurally characterized. Some of them were submitted to thermal and mass spectrometry analyses, and to isothermal vacuum sublimation tests, in view of their potential use as MOCVD single-source precursors for the deposition of heterobimetallic materials. The study stresses upon the influence of the nature of the diketone. of the M 2 cation, and of chemical modification of the salen ligand on the therm…

Die kinetik der allendimerisation, ein beitrag zum mechanismus

1971

Zusammenfassung The reaction kinetics of the dimerization of some polyhalogenated allenes with the general formula Cl2CCCCIX (X = Cl, Br, C6H5, COOEt) and of tetrabromoallene was studied by an IR spectrophotometric method. The reaction was found to be of strictly second order kinetics. The activation parameters were determined and the experimental data and the influence of the substituents were discussed in terms of the accepted general theory of allene cycloaddition. All data are in agreement with a non-concerted two-step electrocyclic addition mechanism. Within the experimental limits no paramagnetic species like a diradical could be detected by the ESR-method during the dimerization re…