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Nm Band (nm + band)
Selected AbstractsPeau sèche-rêche et "Hydratation".INTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 4 2004Concept de la capture de l'eau organisée comme de la glace Synopsis About sixty years ago Frank and Evans showed, by entropy measurements, that when a "non-polar molecule dissolves in water it modifies the water structure in the direction of greater ,cristallinity', the water builds a microscopic iceberg around it" Now, we propose the "concept of ice-like-water capture": a lowering of organized ice-like water promotes aggregation (loss of solubility) of the filaggrin/keratin1/keratin10 associations through their hydrophobic patches. The capture of ice-like water may be performed by the glucoceramides-rich bilayers in stratum granulosum. Probably, the same process aggregates the proteins of corneocytes envelope as well as corneodesmosomes proteins. According to the "concept of ice-like-water capture", to regulate the keratinization, it is not total water that must be added to the stratum corneum, but ice-like water that must be removed from stratum granulosum. Both petrolatum (lipophilic ingredient) and glycerol (hydrophilic ingredient) would capture the ice-like water, most probably after combination with the lipid bilayers of stratum corneum. Moisturizing cream, when organized in secondary droplets is likely to perform the same action. Measurements by near-infrared reflectance spectroscopy of the skin show that petrolatum; glycerol and/or moisturizing cream enhance the quantity of bulk water (1890,1897 nm band). As the ice-like water is the complement of bulk water, the enhanced bulk water let presume an ice-like water lessening. Some desynchronization (late or forward) of the keratinization/differentiation which confer the somatosensory problems associated with "dry and flaky skin" may be linked to an excess or lack of ice-like. For instance, the winter xerosis, very common by chilling weather, could be explained by an increase of ice-like water driven by the fall of the temperature. Résumé En s'appuyant: 1°-sur d'anciens travaux de thermodynamique montrant, d'une part que les molécules d'eau autour des zones apolaires en solution dans l'eau s'organise selon une structure d'eau-comme-de-la-glace, d'autre part qu'en l'absence de cette eau-comme-de-la-glace les molécules de protéines s'agrègent par leurs zones hydrophobes; 2°-sur des travaux récents utilisant la spectroscopie de l'infrarouge proche; technique qui permet de mesurer la quantité d'eau-en-vrac, forme que prend l'eau-comme-de-la-glace après sa fusion lors de l"établissement de liaisons/interactions hydrophobes; nous proposons le "concept de la capture de l"eau-comme-de-la-glace" selon lequel : 1° la différenciation des kératinocytes, qui se traduit à la fois par l'agrégation des trios filaggrine/K1/K10 (ainsi que notamment la formation de l'enveloppe des cornéocytes et des cornéodesmosomes) est promue par une baisse de la teneur en eau organisée dans le stratum granulosum. La captation de l'eau-comme-de-la-glace pourrait être assurée in situ par la structure lipidique riche en glucocéramides dont l'apparition dans le stratum granulosum est contemporaine du début de la baisse de la teneur en eau; 2° contrairement à la "tradition", la peau sèche-rêche n'est pas améliorée par une augmentation de l'hydratation du stratum corneum mais par la capture d'eau-comme-de-la-glace dans le stratum granulosum. 3° le glycérol, la Vaseline et les crèmes "hydratantes" peuvent concourir à cette capture d'eau-comme-de-la-glace, vraisemblablement après s"être combinés aux bicouches céramidiques du stratum corneum, et ainsi agir depuis ce stratum sur le stratum granulosum. 4°-la baisse hivernale de la température provoque une baisse de la quantité d'eau organisée et confère une aggravation de la peau sèche-rêche. 5°-une désynchronisation de la synthèse ou une modification de la structure et/ou de la composition des bicouches glucocéramidiques du stratum granulosum pourraient être à l'origine de certains types de peau sèche-rêche. [source] The Effect of Decreasing Temperature up to Chilling Values on the in vivo F685/F735 Chlorophyll Fluorescence Ratio in Phaseolus vulgaris and Pisum sativum: The Role of the Photosystem I Contribution to the 735 nm Fluorescence Band ,PHOTOCHEMISTRY & PHOTOBIOLOGY, Issue 1 2000Giovanni Agati ABSTRACT The effect of leaf temperature (T), between 23 and 4°C, on the chlorophyll (Chl) fluorescence spectral shape was investigated under moderate (200 ,E m,2 s,1) and low (30,35 ,E m,2 s,1) light intensities in Phaseolus vulgaris and Pisum sativum. With decreasing temperature, an increase in the fluorescence yield at both 685 and 735 nm was observed. A marked change occurred at the longer emission band resulting in a decrease in the Chl fluorescence ratio, F685/F735, with reducing T. Our fluorescence analysis suggests that this effect is due to a temperature-induced state 1,state 2 transition that decreases and increases photosystem II (PSII) and photosystem I (PSI) fluorescence, respectively. Time-resolved fluorescence lifetime measurements support this interpretation. At a critical temperature (about 6°C) and low light intensity a sudden decrease in fluorescence intensity was observed, with a larger effect at 685 than at 735 nm. This is probably linked to a modification of the thylakoid membranes, induced by chilling temperatures, which can alter the spillover from PSII to PSI. The contribution of photosystem I to the long-wavelength Chl fluorescence band (735 nm) at room temperature was estimated by both time-resolved fluorescence lifetime and fluorescence yield measurements at 685 and 735 nm. We found that PSI contributes to the 735 nm fluorescence for about 40, 10 and 35% at the minimal (F0), maximal (Fm) and steady-state (Fs) levels, respectively. Therefore, PSI must be taken into account in the analysis of Chl fluorescence parameters that include the 735 nm band and to interpret the changes in the Chl fluorescence ratio that can be induced by different agents. [source] Color centers in Yb:YAG crystals grown by temperature-gradient techniquesPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 10 2006Yongjun Dong Abstract Yb:YAG (Yb:Y3Al5O12) crystals have been grown by temperature-gradient techniques (TGT) and their color centers and impurity defects were investigated by means of gamma irradiations and thermal treatment. Two color centers located at 255 and 290 nm were observed in the as-grown TGT-Yb:YAG. Analysis shows that the 255 nm band may be associated with Fe3+ ions. Absorption intensity changes of the 290 nm band after gamma irradiation and thermal treatment indicate that this band may be associated with oxygen-vacancy defects. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Photoelectric properties of lead tungstate crystalsPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 14 2004R. Gamernyk Abstract Room temperature photoconductivity measurements were performed for PbWO4 crystals grown under different conditions. In the near-band-edge region three bands of photoionization absorption (310, 330 and 338 nm) were detected. The intensity of these bands depends on crystal perfection and quality. The value of a photocurrent under excitation within the 330 nm band depends on preceding irradiation of a PbWO4 crystal by a laser beam (,ex = 337 nm). The nature of defect centers related to the photoionization absorption bands is discussed. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Observation of 4F3/2,4I15/2 radiative transition in Nd3+ ions in GaLaS glass using frequency-resolved PL spectroscopyPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue S1 2009Takeshi Aoki Abstract The photoluminescence (PL) emission band corresponding to 4F3/2,4I15/2 transition has been revealed using a double lock-in technique and quadrature frequency resolved spectroscopy (QFRS) at room temperature in Nd3+ in a GaLaS glass. The band is centred around 1840 nm and has a lifetime ,77 ,s, which seems to be the same for all four radiative transitions 4F3/2,4IJ (J = 9/2, 11/2, 13/2 and 15/2). The branching ratios ,J of the four above transitions have been estimated from the PL data and agree well with the results of Judd-Ofelt (JO) analysis. In addition to the 1840 nm band, we have observed another PL band appearing around 1580 nm and having a dominant lifetime ,3.8 ,s. This band may be identified with the radiative transition from the doublet (4F5/2, 2H9/2) to the 4I15/2 manifold. The short lifetime ,3.8 ,s may be caused by effective multiphonon relaxation from the doublet to the 4F3/2 manifold. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Photoluminescence properties of erbium-doped amorphous gallium-germanium-selenium films fabricated by RF sputteringPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue S1 2009Takahiko Imai Abstract Chalcogenide glasses have various useful features for optical devices such as a high refractive index, low-loss transmission in the mid-IR, and low phonon energies. The fabrication of thin films is important for use in waveguide applications and integrated photonics. In this work, we report the properties of vacuum deposited films of gallium-germanium-selenium glasses onto fused silica substrates by an RF magnetron sputtering technique (RF electric power of 40-250 W and growth rate of 0.01-2.1 ,m/min). The concentration of Er3+ ions is controlled by the number of sintered Er2S3 small plates on a target. Samples are shown to be in an amorphous-like state as measured by X-ray diffraction experiments. Film thicknesses are proportional to the RF sputtering power and sputtering time. The compositions of films obtained from energy dispersive X-ray (EDX) analysis. There are much dependent on the condition of the sputtering target, for example whether the target is in the bulk or powder-state. Photoluminescence (PL) spectrum, intensity, and lifetime at 1550 nm band are measured by excitation from a 973 nm laser. The PL band of the films has a similar shape to those of bulk glasses. The PL intensity increased with the RF electric power. The PL lifetime at the 1550 nm band of the film is about 1.8-2.6 ms; the latter values are similar to those of bulk samples. The results show that the RF sputtering is a potential method of fabrication for Er-doped GeGaSe thin films. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Photoluminescence of Ho3+:YVO4 crystalsPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 3 2007S. Polosan Abstract Emission spectra of Ho3+ -doped YVO4 crystals are studied in the visible and infrared spectral regions. Besides the emission bands at 544 nm and at about 1950 and 2017 nm due to Ho3+, we observed a broad emission band at 610 nm at low temperatures like 15 K in the highly doped crystals with the Ho3+ concentrations of more than 0.5 mol%. The excitation band for this broad emission is located at 390 nm which is near the edge of band gap of the crystal. It is suggested that the 610 nm band is attributed to defects related to oxygen vacancies around V4+ ions. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Electronic and Vibrational Properties of Fluorenone in the Channels of Zeolite LCHEMISTRY - A EUROPEAN JOURNAL, Issue 10 2004André Devaux Dr. Abstract Fluorenone (C13H8O) was inserted into the channels of zeolite L by using gas-phase adsorption. The size, structure, and stability of fluorenone are well suited for studying host,guest interactions. The Fourier transform IR, Raman, luminescence, and excitation spectra, in addition to thermal analysis data, of fluorenone in solution and fluorenone/zeolite L are reported. Normal coordinate analysis of fluorenone was performed, based on which IR and Raman bands were assigned, and an experimental force field was determined. The vibrational spectra can be used for nondestructive quantitative analysis by comparing a characteristic dye band with a zeolite band that has been chosen as the internal standard. Molecular orbital calculations were performed to gain a better understanding of the electronic structure of the system and to support the interpretation of the electronic absorption and luminescence spectra. Fluorenone shows unusual luminescence behavior in that it emits from two states. The relative intensity of these two bands depends strongly on the environment and changes unexpectedly in response to temperature. In fluorenone/zeolite L, the intensity of the 300 nm band (lifetime 9 ,s) increases with decreasing temperature, while the opposite is true for the 400 nm band (lifetime 115 ,s). A model of the host,guest interaction is derived from the experimental results and calculations: the dye molecule sits close to the channel walls with the carbonyl group pointing to an Al3+ site of the zeolite framework. A secondary interaction was observed between the fluorenone's aromatic ring and the zeolite's charge-compensating cations. [source] | ||||||||||