Determination de la structure de perfluoroalcenes a chaines longues par R.M.N. du19F : lère Partie : pefluoroalcenes-1

After a review of 1-perfluoroalkene R_FCFCF₂ synthesis, with R_FC₄F₉, C₅F₁₁, C₆F₁₃, we have studied their fine structures by ¹⁹F N.M.R. This study has led us to first generalize the rules set for the chemical shifts and coupling constants of olefinic fluorine atoms of fluoropropene and their derivatives. Then, we have been able to determinate unambiguously the chemical shifts of the difluoromethylene groups of the perfluorinated chains. We have thus shown, by irradiation, that inversions may take place in the chemical shifts of the CF₂ groups at the β and γ position of the double bond.     

Remarques sur un article de Israel Aharoni sur les prolongements lipschitziens dansc 0

We give a purely metric proof of the following result: let (X,d) be a separable metric space; for all ?>0 there is an injectionf ofX inC ₀ ⁺ such that: $$\forall x,y \in X,d(x, y) \leqq \parallel f(x) - f(y)\parallel _\infty \leqq (3 + \varepsilon )d(x, y).$$ It is a more precise version of a result of I. Aharoni. We extend it to metric space of cardinal α⁺ (for infinite α).     

Velocimetry microsensors driven by linearly polarized optical tweezers

We report on a new type of single-point velocimetry microsensor that can be positioned in microfluidic devices by use of optical tweezers. The flag-shaped microsensor is readily made by a low-cost two-photon polymerization technique. At rest the linearly polarized optical tweezer traps the microsensor at the focal point, and the flag-plate gets aligned in the polarization direction. Under a fluid flow, the plate rotates to an equilibrium angle that is used to measure the fluid velocity with a micrometer-size spatial resolution. Experimental results are in good agreement with theoretical calculations of optical and hydrodynamic torques on such a flag-shaped microsensor.     

Study of tryptophan assisted synthesis of gold nanoparticles by combining UV–Vis, fluorescence, and SERS spectroscopy

We developed a rapid and non-toxic method for the preparation of colloidal gold nanoparticles (GNPs) by using tryptophan (Trp) as reducing/stabilizing agent. We show that the temperature has a major influence on the kinetics of gold ion reduction and the crystal growth, higher temperatures favoring the synthesis of anisotropic nanoparticles (triangles and hexagons). The as-synthesized nanostructures were characterized by UV–Vis absorption spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), fluorescence, and surface-enhanced Raman scattering (SERS) spectroscopy. The UV–Vis measurements confirmed that temperature is a critical factor in the synthesis process, having a major effect on the shape of the synthesized GNPs. Moreover, fluorescence spectroscopy was able to monitor the quenching of the Trp fluorescence during the in situ synthesis of GNPs. Using Trp as molecular analyte to evaluate the SERS efficiency of as-prepared GNPs at different temperatures, we demonstrated that the Raman enhancement of the synthesized gold nanoplates is higher than that of the gold spherical nanoparticles.     

Investigation on laser brazing AA6056 Al alloy to XC18 low-carbon steel

Based on the studies of influence of YAG laser heating conditions for Al alloy melt and steel on wettability,the mechanics of the laser overlap braze welding of 6056 Al and XC18 steel sheet has been investigated.Under the temperature range which is above the melting point of the Al alloy and below the melting point of the steel, two dissimilar metals can be joined by means of laser braze welding. There is no crack observed in the joining area, i.e. Al-Fe intermetallic phase (Fe3Al/FeAl/FeAl3/Fe2Al5) layer formed by solution and diffusion between liquid-solid interface. The temperature range can be defined as the process temperatures of laser braze welding of Al-Fe materials. Selecting a higher laser heating temperature can improve the wettability of Al melt to steel surface, but the intermetallic phase layer is also thicker. When the laser heating temperature is so high that the joining surface of steel is melted, there is a crack trend in the joining area.     

Three-dimensional microfabrication by two-photon-initiated polymerization with a low-cost microlaser

Fabrication of submicrometer structures by two-photon-initiated polymerization is performed with an inexpensive and low-power microlaser. This is made possible by the design of photoinitiators with strong two-photon absorption cross sections. We analyze the influence of both material properties and irradiation conditions on the two-photon polymerization rate and show that resins based on our highly sensitive two-photon photoinitiator can be solidified with microlaser excitation, whereas commercial UV photoresins require ultrashort and intense laser pulses.     

Theoretical and experimental study of differential group delay and polarization dependent loss of Bragg gratings written in birefringent fiber

In this paper, we completely study the wavelength dependency of differential group delay (DGD) and polarization dependent loss (PDL) for Bragg gratings written in birefringent fibers. Based on the coupled mode theory, we present analytical expressions for the evolution with wavelength of the transmission coefficient, the DGD and the PDL. The wavelength dependencies of these evolutions on the birefringence are then discussed. Experimental results are finally presented for an apodized FBG written in a bow-tie fiber. A very good agreement between theory and experience is reported, confirming the validity of the theoretical analysis.     

无零级衍射干扰的彩色数字全息研究

彩色数字全息研究中,用球面波为重建波及角谱衍射公式进行波前重建是一种有效的方法.然而,重建图像上通常伴有强烈的零级衍射干扰.本文通过理论分析,对波前重建过程作了重要改进.用改进后的方法进行彩色数字全息的实验研究表明,重建彩色图像的质量获得显著改善. 关键词： 彩色数字全息 波前重建 零级衍射干扰     

Complex concentration dependence of SERS and UV–Vis absorption of glycine/Ag‐substrates because of glycine‐mediated Ag‐nanostructure modifications

Complex concentration‐dependence of surface‐enhanced Raman scattering (SERS) and UV–Vis absorption of Ag‐nanoparticles (AgNPs) mixed with Gly has been observed. Surprisingly, with decreasing Gly concentration, a new band in UV–Vis absorption of AgNPs/Gly mixtures is found to red‐shift with increasing intensity, until a turning point at a critical concentration. Further diluting Gly, the new band blue‐shifts with decreasing intensity. Similarly, the SERS intensities of Gly bands at 615 and 905 cm^–1 consistently increase with decreasing Gly concentrations, reaching maxima at the critical concentration. This agrees consistently with the variation in position and intensity of the new developing plasmon absorption band. Interestingly, transmission electron microscopy (TEM) revealed Gly‐induced modifications of AgNPs, including a reassembling and increasing aspect ratio with deceasing Gly concentration. The concentration‐dependent behavior of UV–Vis absorption, SERS, and TEM of AgNPs/Gly mixtures could be due to the complex nature of Gly‐AgNPs interaction depending on the molecular density, as supported by TEM images. Copyright © 2012 John Wiley & Sons, Ltd.