Reflection and transmission at normal incidence onto air-saturated porous materials and direct measurements based on parametric demodulated ultrasonic waves

The present work is related to the characterization of air-saturated porous media by using parametric demodulated ultrasonic waves. One uses two different powerful ultrasonic emitters working either at 47 kHz or at 162 kHz which are electronically amplitude modulated over the 200 Hz-4 kHz or 2 kHz-40 kHz bandwidths respectively. The demodulation process takes place in air, due to its nonlinearity enabling to generate audio range acoustical waves or alternatively low frequency ultrasonic waves which can be used to characterize porous materials in the reflection configuration at normal incidence. Some appropriate theoretical calculations are introduced for three configurations of interest, i.e. a porous slab, a porous layer mounted onto a rigid plate, and a porous half space, in the case of the equivalent-fluid model. Comparisons between theoretical modeling and experimental data are provided and prospective industrial applications are discussed.     

Etude en fonction du temps de l'oxydation des magnetites substituees a l'aluminium et au chrome au moyen de la conductivite electrique

The oxidation of substituted magnetites (Fe²⁺Fe_2?x³⁺M_x³⁺O₄^2?(O < x < 2) into the lacunar phase γ(Fe_1?z³⁺M_z³⁺)O₃^{2 ?} (x = 3z) was followed over time by electrical conductivity over the temperature r Curves σ = f(t) are different according to whether we deal with an n or p-type spinel. However, for intermediate substitution rates (1,1 < x < 1,8), n-type ferrichromites are oxidized after an initial period in the same way as p-type semi-conductors.For the initial period, the chemisorption kinetics of oxygen upon these n-type samples, reduced under vacuum, was found to follow Elovich's law with an activation energy depending on the degree of coverage.     

Photoluminescence processes in LaOCl:Bi and YOCl:Bi

The luminescence of rare earth oxychlorides LnOCL:Bi (with Ln = La and Y) is studied in detail. The main excitation bands, responsible for the blue and UV fluorescences, are attributed to the bismuth activator substituting for Ln³⁺ in the rare earth tetragonal site. The weak shoulder of these bands and the complex decay times are assumed due to a parasitical phase, La₂O₃ or Y₂O₃ doped by bismuth, an X-ray analysis confirming their presence in the samples. Finally, the existence of these phases does not seem to have an important effect upon the interpretation of the luminescence processes of the main center, as shown by the configuration curve model.     

LEED-Auger characterization of GaAs during activation to negative electron affinity by the adsorption of Cs and O

A combination of low energy electron diffraction (LEED) and Auger electron spectroscopy (AES) has been used to study the formation of the negative electron affinity (NEA) condition on surfaces of p-type, degenerate, (100) and (111) GaAs. Activation to NEA is achieved by adsorbing Cs and O onto atomically clean GaAs in repetitive cycles of first Cs and then O. Before activation, the clean GaAs surfaces exhibit their characteristic LEED patterns. However, once obtained, there is no significant correlation between the quality of these LEED patterns and the final activation. The adsorption of both Cs and O during activation to NEA is amorphous. Auger measurements have shown that the first photoemission maximum occurs after the adsorption of about a half monolayer of Cs. The initial O adsorption occurs on the GaAs surface between the Cs atoms. The adsorbed O interacts strongly with Cs at any stage during the activation. Peak photosensitivities, after completion of the Cs and O adsorptions, were in the range 400 to 1100 $\text{μA}\text{lumen}$. The final activation does not correlate with the quantity of Cs and O on the surface. The temperature dependence of the photosensitivity of NEA GaAs (100) activated at ?170°C has a broad maximum at about ?50°C and a subsidiary maximum at about 160°C. In addition, the photoemission at ?170°C can be either increased or decreased by having heated the sample up to 200°C, even though no Cs or O desorption has taken place. These results can be traced to changes in work function rather than to changes in bulk properties. While the LEED patterns from clean GaAs show no structural changes with temperature, such changes are observed when Cs is on the surface. It is suggested that changes both in photoemission and in LEED patterns are due to the temperature-induced mobility of Cs on GaAs. An atomic model for the NEA surface is discussed in terms of a layer of Cs and O atoms about 10 Å thick on the GaAs.     

Les Sels de Bismuth (III) Comme Catalyseurs Dans la Reaction D'ouverture Des Epoxydes Par Les Amines

BiCl 3 and Bi (OTf) 3 catalyze the opening of epoxides ( 1-7 ) by amines ( 8-12 ). High regioselectivities are observed. BiCl 3 et Bi (OTf) 3 catalysent la réaction d'ouverture des époxydes ( 1-7 ) par les amines ( 8-12 ). La réaction est fortement régiosélective.     

Complexes of Tin(IV) Tetrachloride with 3-Formylpyridine Semicarbazone and Thiosemicarbazones

The reaction of tin(IV) tetrachloride with 3-formylpyridine semicarbazone and different 3-formylpyridine thiosemicarbazones produces [Sn(HL)CL 3 ][SnCl 5 ] where HL stands for the neutral ligand. The tin(IV) complexes were characterized using a variety of spectroscopic techniques. Coordination through the pyridine nitrogen occurs in all cases. Solvation studies in DMSO indicated that dissociation of the ligands and their complete replacement by solvent molecules occurs.     

Le Triflate de Bismuth(III) Comme Catalyseur Dans la Reaction de Carbonyl-Diels-Alder

In presence of bismuth(III) triflate, a carbonylated electrophile (ethyl mesoxalate or glyoxylate) and usual diene led selectively (60-100) the hetero carbonyl-Diels-Alder reaction with the ene reaction product. Bi(OTf) 3 exhibits strong catalytic activity and reacts under mild conditions. En présence de triflate de bismuth(III) le mésoxalate et le glyoxylate d'éthyle réagissent avec des diènes usuels pour donner un mélange de carbonyl-Diels-Alder et du produit de la ène réaction. Bi(OTf) 3 présente une forte activité catalytique et réagit dans des conditions douces.