基于光弹调制的运动斯塔克效应诊断

电流密度分布是等离子体物理研究的关键分布参数,在托卡马克先进运行模式发展,电流驱动,约束与输运等方面发挥着重要的作用。中性束与等离子体相互作用产生的分裂光谱,包括σ分量与π分量,水平观测时,σ分量的偏振方向垂直于等效电场的方向,π分量的偏振方向平行于等效电场的方向,通过测量分裂光谱的偏振方向可以反演出等离子体电流密度分布。基于光弹调制器的偏振检测系统具有检测精度高、时间响应迅速的独特优点,非常适用于等离子体电流快速变化下的电流密度分布测量。光弹调制器的双折射晶体在周期性外部驱动源的作用下发生弹性形变,其折射率会产生周期性的变化,当偏振光通过时,出射光的偏振特性将相应产生周期性变化,再经过偏振片,形成调制的光强变化。运动斯塔克效应(MSE)诊断的偏振检测系统由两个光弹调制器(PEM)和一个偏振片组成,通过检测不同调制频率的调制强度的比值,从而快速、精确地获得分裂光谱的偏振方向的实时变化,进而得到等离子体电流密度分布。详细介绍了东方超环托卡马克(EAST)装置上的MSE诊断,初步完成了离线测试与标定,参与中性束电流本文驱动物理实验,初步获得了等离子体电流密度分布的信息。     

Novel bioactive vic-dioxime ligand containing piperazine moiety: Synthesis,X-ray crystallographic studies, 2D NMR applications and complexation with Ni(II)

A new vic-dioxime ligand bearing an important pharmacophore substituent, anti-1-(4-benzylpiperazine-1-yl) phenylglyoxime (LH₂) (Scheme 1), has been synthesized and its nickel(II) complex was obtained by the reaction of NiCl₂·6H₂O and the ligand. The characterization of the newly formed compounds was performed by elemental analysis, FT-IR, 1D NMR (¹H, ¹³C, DEPT), 2D NMR (HMBC), ESI mass-spectrometry, TG/DTA, X-ray crystallography. The antibacterial activity was also studied against Staphylococcus aureus ATCC 25923, Streptococcus mutans RSHM 676, Enterococcus faecalis ATCC 29212, Lactobacillus acidophilus RSHM 06029, Escherichia coli ATCC 25922, E. coli ATCC 35218, Pseudomonasaeruginosa ATCC 27853. The antimicrobial test results indicated that all the compounds have mild antibacterial activity against both Gram negative and Gram positive bacterial species.     

Analysis of the Effect of Potential Cycles on the Reflective Infrared Signals of Nitro Groups in Nanofilms: Application of the Fractional Moments Statistics

The effect of the potential cycles on the reflective IR signals of nitro‐groups in nanofilms was studied for the statistical characterization of nitrobenzene (NB) and nitroazobenzene (NAB)‐modified glassy carbon (GC) surfaces. Both NB and NAB nanofilms were obtained by the electrochemical reduction of the diazonium tetrafluoroborate salts in acetonitrile using cyclic voltammetry (CV). The modified surfaces were denoted as GC‐(NB)_n and GC‐(NAB)_n, respectively, where n indicates the number of CV cycles performed during modification. Reflective IR signals of the normalized NB and NAB nanofilms and GC were used for the quantitative evaluation of the effect of the potential cycles on the reflective IR signals of nitro‐groups in nanofilms. The detection and quantitative ‘reading’ of the influence of number of CV cycles were realized in the frame of a new error controllable approach that was applied for analysis of all available set of data. This approach includes in itself the following basic steps: (a) the procedure of the division (normalization) on the GC spectra, (b) the comparison of the smoothed spectra for their statistical proximity in the frame of the statistics of the fractional moments, (c) extraction of possible calibration parameters for possible calibration of the normalized spectra with respect to the number of CV cycles. These three basic steps are becoming effective for detection of the influence of some external factors. In our case it is important to detect the influence of the factor n characterizing CV cycles.     

Experimental and DFT studies of ethyl N′-3-(1H-imidazol-1-yl) propylcarbamoyl benzohydrazonate monohydrate

The Imidazole compound, Ethyl N′-3-(1H-imidazol-1-yl) propylcarbamoyl benzohydrazonate monohydrate, has been synthesized and characterized by IR, NMR, electronic spectroscopy, and X-ray single-crystal determination. Molecular geometry from X-ray experiment of the title compound in the ground state has been compared using the density functional method (B3LYP) with 6-31G+(d) basis set. To determine conformational flexibility, molecular energy profile of the title compound was obtained by DFT calculations with respect to two selected degrees of torsional freedom, which were varied from −180° to +180° in steps of 10°. Besides, molecular electrostatic potential (MEP), natural bond orbitals (NBO), frontier molecular orbitals (FMO), and thermodynamic properties were performed at B3LYP/6-31G+(d) level of theory.     

Three-dimensional opal-like silica foams

The synthesis of novel meso-/macroporous SiO2 monoliths by combining a nano-building-blocks-based approach with the confined geometry of a tailored air-liquid foam structure is described. The resulting macrostructure in which ordered close-packed colloidal silica nanoparticles constitute the monolith's scaffolds very closely resembles the tailored periodic air-liquid foam template. The void spaces between adjacent particles create textural mesoporosity; therefore, the as-prepared silica networks are characterized by hierarchical porosity at the macroscopic and mesoscopic length scales. The fine-tuning of both the liquid foam's fraction and the bubble size allows a rational design over the macroscopic cell morphologies (shape, Plateau border's length, and width). Striking results of this approach are the weak shrinkage of the as-synthesized opal-like scaffolds during the thermally induced sintering process and, in contrast with previous studies, the formation of closed-cell structures. Particle organization and the foam film surface roughness are investigated by atomic force microscopy (AFM), showing the influence of the liquid flow, within the foams' Plateau borders and films, on the final assemblies.     

The invertibility of adapted perturbations of identity on the Wiener space

Let $(W,H,\mu )$ be the classical Wiener space. Assume that $U=I_W+u$ is an adapted perturbation of identity, i.e., $u:W\to H$ is adapted to the canonical filtration of W. We give some sufficient analytic conditions on u which imply the invertibility of the map U. To cite this article: A.S. Üstünel, M. Zakai, C. R. Acad. Sci. Paris, Ser. I 342 (2006).     

The Picard Theorem on S-metric spaces

Recently, the notion of an S-metric space is defined and extensively studied as a generalization of a metric space. In this paper, we define the notion of the S∞-space and prove its completeness. We obtain a new generalization of the classical "Picard Theorem".     

Polyelectrolytes in thin liquid films

The review addresses the influence of polyelectrolytes on the statics and dynamics of thin liquid films. Both, changes of interfacial and bulk properties, contribute to the overall behaviour of thin films formed from aqueous polyelectrolyte solutions. Therefore, the chapter is separated into two parts: polyelectrolytes at film interfaces and polymers in film bulk.     

Spectroscopy and dynamics of the isolated sp2 CH chromophore in trideuteroacetaldehyde CD3CHO as derived from extrapolated SDCI ab initio calculations

Ab initio CI potential energy (PES) and dipole moment (DMS) surfaces have been calculated with singles and doubles excitation configuration interaction (SDCI) for the 2-dimensional isolated sp² CH chromophore subspace of trideuteroacetaldehyde (CD₃CHO). Different extrapolation schemes to full-CI have been applied after the extrapolation to full-SDCI. Vibrational band centres and absolute intensities are determined variationally on six extrapolated surfaces. The band centres are analysed within the effective Hamiltonian model for isolated CH chromophores and the effective spectroscopic parameters are compared for the different extrapolation schemes. Time dependent population evolution for vibrational quantum motion with a pure CH stretching state being initially populated is calculated for some of the extrapolated surfaces within the effective Hamiltonian model.