Trace element concentrations from São Francisco River - PR analyzed with PIXE technique

Summary Kulcsszavak (angolul, ha nem azonos az elozovel)     

Entanglement of Momentum for a Single Photon with a Single Atom

In this talk, the interaction of a single photon injected to a single atom is studied, for which initially the photon is uncorrelated with the atom. The spontaneous emitted photon will then evolve to be entangled with the atom on their continuous kinetic variables （momentum） in the process of resonant scattering. We find the relations between the entanglement and their physical control parameters （such as the linewidth of the injected photon wave packet, and that of the atomic wave packet, etc. ）, which indicates that high entanglement can be reached by broadening the scale of the atomic wave or squeezing the linewidth of the incident single-photon pulse.     

A new approach towards peptidosulfonamides: synthesis of potential inhibitors of bacterial peptidoglycan biosynthesis enzymes MurD and MurE

Peptidosulfonamides are an emerging group of peptidomimetics with a variety of applications in medicinal chemistry. We present a novel approach to the synthesis of peptidosulfonamides, and apply it to a series of new potential inhibitors of the bacterial peptidoglycan biosynthesis enzymes MurD and MurE. The synthesis was conducted via N-phthalimido β-aminoethanesulfonyl chlorides, which are new building blocks for the synthesis of peptidosulfonamides. In the most crucial step, sulfonic acids or their sodium salts were converted into the corresponding sulfonyl chlorides using an excess of either SOCl₂ or SOCl₂/DMF, and then coupled to the C-protected amino acid. None of the compounds significantly inhibited MurD, however, some inhibited MurE; one had an IC₅₀ below 200 μM, which constitutes a promising starting point for further development. Molecular modelling simulations were performed on two analogues to investigate the absence of inhibitory activity of the sulfonamide compounds on MurD.     

基于FPGA+DSP系统的红外图像非均匀校正的实现

首先引述了红外探测器两点法进行图像非均匀校正的原理,给出了基于DSP+FPGA的图像处理系统硬件模块整体实现框图,以及其非均匀校正模块的硬件结构。然后对其非均匀校正模块硬件实现中的芯片选择,工作流程以及实现作了详细的阐述。最后给出了非均匀校正试验的结果。     

Regioselectivity in the ene-reaction of singlet oxygen with cyclic alkenes: photooxygenation of methyl-substituted 1,4-cyclohexadiene derivatives

The photooxygenation of the 1-methyl-, 2,3-dimethyl-, and 1,4-dimethylcyclohexa-1,4-dienes, which are readily available through Birch reduction, yielded the corresponding ene-products. The formed endocyclic dienes were trapped by the addition of singlet oxygen to give the corresponding bicyclic endoperoxy hydroperoxides. In the case of 1-methylcyclohexa-1,4-diene and 1,4-dimethylcyclohexa-1,4,-diene, the cis-effect determined the product distribution. Photooxygenation of 2,3-dimethylcyclohexa-1,4-dienes gave mainly exocyclic olefin, which was attributed to the lowered rotational barrier of the methyl group and increased reactivity of the methyl groups.     

Structural studies of Cr-doped mullite derived from single-phase precursors

Cr-doped mullites were prepared from single-phase precursors containing up to 9.60 wt% Cr₂O₃ using a sol-gel technique followed by thermal treatment. Particle induced X-ray emission spectroscopy and X-ray powder diffraction were used to characterize the samples. Mullites were orthorhombic, space group Pbam. Cr doping caused the increase of unit-cell parameters. Strongest expansion was noticed along c-axis followed by a and b (Δc/c=0.089, Δa/a=0.061, Δb/b=0.045% per mole Cr₂O₃). A second phase, namely θ-(Al,Cr)₂O₃, was revealed by XRD in the sample containing 9.60 wt% Cr₂O₃. The structure of mullites was refined by the Rietveld method, location of Cr³⁺ was performed by the EPR spectroscopy. At low chromium doping level (Cr₂O₃ content less than ∼5 wt%) Cr³⁺ ions were substituted for Al³⁺ in the AlO₆ octahedra of the mullite structure (M1 site). For higher doping level, Cr³⁺ ions were additionally substituted for Al³⁺ in the AlO₆ octahedra of the second phase [θ-(Al,Cr)₂O₃ at 1400 °C, or α-(Al,Cr)₂O₃ at 1600 °C] which segregated in the system. Substitution of Cr³⁺ for Al³⁺ on M1 site in the mullite structure resulted in increase of average distances in (M1)O₆ octahedron and decrease of average distances in T*O₄ tetrahedron, while average distances in TO₄ tetrahedron stayed almost constant.     

椭圆型问题一类广义差分法的L~2模误差估计

1.引 言 广义差分法作为处理偏微分方程的离散技术,能够保持质量,动量,能量等物理量的守恒.广义差分法（有些文献称为box method[3];finite volume element method[4],[5],[6]）利用在对偶剖分体积单元积分原始方程,并将近似解限制于某一有限元空间而得到离散方程.因此,它在局部区域保持了原始方程的物理守恒性和其他重要特性.从而被广泛地应用于数值求解数学物理方程,特别是计算流体力学和热传导问题[11]. 对广义差分法的研究已有许多文献,专著[10]有详细的介绍.早期的工作主要考虑标准的重心对偶剖分.近年来Cai et,al[4],[5],[6],在某些假定下对较一般的对偶剖分给出了能量模误差估计,Huang and Xi[9]去掉了文献[6]中的这些限制.Chou,Li[8]和Li,     

超稳定TO-8型压力传感器在气体导热系数测定实验中的应用

介绍了TO-8型压力传感器的性能及电源电路.以气体导热系数测定实验为例,用TO-8型压力传感器制成的测压装置代替旋转式麦氏真空计,利用可调针孔式放气阀对真空气压进行连续调节,实现了对测试系统真空度的实时监测.     

混杂配体金属簇合物的分子振动光谱与结构

由于原子簇化合物在催化，生物活性，功能材料等方面所呈现的重要性，使其成为无机和物理化学最重要的研究领域之一。文章中和谱学方法对一些具有混配体的过渡金属簇合物的结构及其两者之间的关系进行.