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791.
J. Feldhaus E. L. Saldin J. R. Schneider E. A. Schneidmiller M. V. Yurkov 《Optics Communications》1997,140(4-6):341-352
A new design for a single pass X-ray Self-Amplified Spontaneous Emission (SASE) FEL is proposed. The scheme consists of two undulators and an X-ray monochromator located between them. The first stage of the FEL amplifier operates in the SASE linear regime. After the exit of the first undulator the electron bunch is guided through a non-isochronous bypass and the X-ray beam enters the monochromator. The main function of the bypass is to suppress the modulation of the electron beam induced in the first undulator. This is possible because of the finite value of the natural energy spread in the beam. At the entrance to the second undulator the radiation power from the monochromator dominates significantly over the shot noise and the residual electron bunching. As a result the second stage of the FEL amplifier operates in the steady-state regime when the input signal bandwidth is small with respect to that of the FEL amplifier. Integral losses of the radiation power in the monochromator are relatively small because grazing incidence optics can be used. The proposed scheme is illustrated for the example of the 6 nm option SASE FEL at the TESLA Test Facility under construction at DESY. As shown in this paper the spectral bandwidth of such a two-stage SASE FEL (Δλ/λ 5 × 10−5) is close to the limit defined by the finite duration of the radiation pulse. The average brilliance is equal to 7 × 1024 photons/(s × mrad2 × mm2 × 0.1% bandw.) which is by two orders of magnitude higher than the value which could be reached by the conventional SASE FEL. The monochromatization of the radiation is performed at a low level of radiation power (about 500 times less than the saturation level) which allows one to use conventional X-ray optical elements (grazing incidence grating and mirrors) for the monochromator design. 相似文献
792.
793.
S. M. Kelly 《Liquid crystals》1991,10(2):273-287
Three separate series of new materials of weak to strongly positive dielectric anisotropy have been prepared. Each series contains four sub-sets of materials each incorporating a different four unit linking group (i.e., C4H8, C4H6, C3H6O and C3H4O) and the same series of end groups (i.e. F, CN and OCF3) in various substitution patterns. The synthesis and liquid crystal transition temperatures of these novel substances are described and compared with those of the corresponding materials incorporating standard central linkages (i.e.-, C2H4, CH2O, COO). The effect of an additional trans carbon-carbon double bond in the terminal alkyl chain and in the central linking unit has also been studied. 相似文献
794.
A new porphyrin, peroxyacetic acid uroporphyrin I, has been isolated from the urine of patients with congenital erythropoietic porphyria by reversed phase high performance liquid chromatography. The porphyrin was characterized by high resolution mass spectrometry and by typical chemical reactions of a peroxyacid. 相似文献
795.
The kinetics and mechanism of the oxidation of 3,3′-dimethoxybenzidine (oda, o-dianisidine) by potassium bromate in aqueous acidic medium were studied by monitoring the formation rate of the reaction product, 3,3′-dimethoxy 4,4′-diphenoquinone at 447 nm. The reaction is, first order with respect to both the substrate and oxidant, and second order with respect to H+. The oda: bromate stoichiometric ratio is 1:1. Plausible mechanism and rate laws are proposed accounting the experimental findings. Computer simulations were done using the proposed mechanism. 相似文献
796.
The 2-meter liquid-hydrogen bubble chamber is exposed to a separated beam of α particles from the ITEP synchrotron. The momentum of the incident 4He nuclei, averaged over the fiducial volume of the chamber, is 5 GeV/c (the kinetic energy of initial protons in the nucleus rest frame is T
p
=620 MeV). The spectral functions of decays α→tp and α→τn) are extracted in the 4π geometry (the latter is extracted for the first time) from the exclusive reactions αp→tpp and αp→τpn in the spectator momentum region 0<q<0.3 GeV/c. The pole dominance criteria are carefully checked. Extrapolation of the nuclear vertex function to the pole gives a lower
bound on the nuclear vertex constant. Our experimental data are compared with the results of other studies and with theoretical
calculations.
Pis’ma Zh. éksp. Teor. Fiz. 66, No. 2, 69–74 (25 July 1997)
Published in English in the original Russian journal. Edited by Steve Torstveit. 相似文献
797.
M. Keane 《Applied Acoustics》2007,68(10):1104-1117
A new method is presented for splitting musical notes into tonal and broadband components by removing the harmonic peaks from the spectra. This method was used to analyse the key vibrations of eight pianos (four grand and four upright). The broadband component of vibrations was found to be more intense in the upright pianos than in the grand pianos, while no such difference was found in the tonal component. As grands are considered to be superior to uprights, this suggests that it may be possible to improve upright pianos by reducing the strength of the broadband component of vibrations. 相似文献
798.
Brad M. Rosen Virgil Percec 《Journal of polymer science. Part A, Polymer chemistry》2007,45(21):4950-4964
Atom transfer radical polymerization (ATRP) and single electron‐transfer living radical polymerization (SET‐LRP) both utilize copper complexes of various oxidation states with N‐ligands to perform their respective activation and deactivation steps. Herein, we utilize DFT (B3YLP) methods to determine the preferred ligand‐binding geometries for Cu/N‐ligand complexes related to ATRP and SET‐LRP. We find that those ligands capable of achieving tetrahedral complexes with CuI and trigonal bipyramidal with axial halide complexes with [CuIIX]+ have higher energies of stabilization. We were able to correlate calculated preferential stabilization of [CuIIX]+ with those ligands that perform best in SET‐LRP. A crude calculation of energy of disproportionation revealed that the same preferential binding of [CuIIX]+ results in increased propensity for disproportionation. Finally, by examining the relative energies of the basic steps of ATRP and SET‐LRP, we were able to rationalize the transition from the ATRP mechanism to the SET‐LRP mechanism as we transition from typical nonpolar ATRP solvents to polar SET‐LRP solvents. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4950–4964, 2007 相似文献
799.
A molecular dynamics method has been used to simulate the argon ion-assisted deposition of Cu/Co/Cu multilayers and to explore ion beam assistance strategies that can be used during or after the growth of each layer to control interfacial structures. A low-argon ion energy of 5–10 eV was found to minimize a combination of interfacial roughness and interlayer mixing (alloying) during the ion-assisted deposition of multilayers. However, complete flattening with simultaneous ion assistance could not be achieved without some mixing between the layers when a constant ion energy approach was used. It was found that multilayers with lower interfacial roughness and intermixing could be grown either by modulating the ion energy during the growth of each metal layer or by utilizing ion assistance only after the completion of each layers deposition. In these latter approaches, relatively high-energy ions could be used since the interface is buried and less susceptible to intermixing. The interlayer mixing dependence upon the thickness of the over layer has been determined as a function of ion energy. 相似文献
800.