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851.
H. Arenhövel W. Leidemann E. L. Tomusiak 《Zeitschrift für Physik A Hadrons and Nuclei》1988,331(2):123-138
The influence of the neutron electric form factor on various observables in two-body break-up of deuterons by electrons such as differential cross section, beam, target and beam-target asymmetries and outgoing nucleon polarization as well is investigated for different kinematic regions. The electron-deuteron vector asymmetryA ed V and the outgoing nucleon polarization component P′x(n) are the most promising observables in and off the quasi-free region for a determination ofG En. Also the single polarization observablesA d T and Py 0(p) and the double polarization observable P′z(n) show significant influences fromG En. 相似文献
852.
R. Suntz H. Becker P. Monkhouse J. Wolfrum 《Applied physics. B, Lasers and optics》1988,47(4):287-293
Two-dimensional laser-induced fluorescence (2D-LIF) imaging of OH radicals, excited at 308 nm, has been employed to visualize the flame front in an internal combustion engine burning air/propane mixtures. Light sheet thicknesses down to 70 m have been attained for excitation. Hydroxyl radicals were detected up to pressures of 7.5 bar at engine speeds of 500 rpm. An upper limit of 300 m for the flame front thickness was obtained from line intensity profiles. 相似文献
853.
H. Zacharias 《Applied Physics A: Materials Science & Processing》1988,47(1):37-54
In this article the application of tunable dye lasers to desorption phenomena is illuminated. These lasers provide radiation continuously tunable from 105 nm in the vacuum ultraviolet to about 10 m in the mid-IR. By employing either laser induced fluorescence (LIF) or resonance enhanced multiphoton ionization (REMPI) spectroscopy almost all diatomic and many polyatomic molecules can be probed with the sensitivity required to detect desorbing molecules under UHV conditions. The spectral resolution of the lasers is sufficiently high that rotational state selectivity is achieved. Recent developments permit in addition the velocity distributions of molecules to be determined with internal quantum state resolution. Therefore very detailed information about the molecular dynamics has been obtained. In most experiments so far reactive recombinations off surfaces have been investigated. In this paper special emphasis will be given to the recombination of hydrogen on copper and palladium surfaces. For these systems very detailed data about the internal state populations at various surface temperatures have been obtained. The rotational cooling previously observed in molecular beam scattering has also been established for desorption. Strong vibrational excitation has been observed, which in the case of desorption from copper may be associated with the recombination dynamics, whereas for desorption of D2 from Pd(100) a molecular precursor state might be responsible. By measuring the velocity distribution in each quantum state, the complete energetics of the desorbing molecules has been determined. Some first experiments on laser induced desorption with state selective detection of the desorbing molecules will also be discussed. Finally, making use of the polarization analysis of the signal, alignment effects in the desorption can be observed, permitting observation of molecular dynamics with a magnifying glass.Heisenberg fellow of the Deutsche Forschungsgemeinschaft 相似文献
854.
T. S. Baller G. N. A. van Veen H. A. M. van Hal 《Applied Physics A: Materials Science & Processing》1988,46(3):215-220
Thin layers YBa2Cu3O7–x. are deposited by a laser ablation technique using a pulsed excimer laser operating at 308 nm. The influence of the substrate material and the annealing procedure on the superconducting behaviour of the 123 film and the reactions between the film and the substrate are studied by resistance, X-ray patterns and TEM measurements. The best results are obtained for deposition on (100) SrTiO3 substrates. The resistance of the 1 m thick film shows a metallic behaviour, an onset in superconductivity at a temperature of 90 K, and has zero resistance at 86 K. The 123 material has a preferential oriented c-axis perpendicular to the surface plane. 相似文献
855.
L. Käubler W. Enghardt H. Prade P. Carlé L. O. Norlin K. -G. Rensfelt U. Rosengård 《Zeitschrift für Physik A Hadrons and Nuclei》1988,329(2):143-150
Using the reaction138Ba(α,2n)140Ce the magnetic moment of the 10 1 + isomer atE x =3714.7 keV in theN=82 nucleus140Ce has been determined by means of the TDPAD method toμ=+10.3(4)μ N . Measuredg-factors in140Ce are compared to calculations within the shell model with configuration mixing. For the 10 1 + isomer in140Ce the four proton configuration π(1g 7 2/2 ,2d 5 2/2 ) has been found to be dominant. From theg-factor measurement strong contributions of multiparticle excitations to thegp2d 3/2,π3s 1 2 or π1h 11 2 shells and admixtures of neutron excitations to the wave function of the 10 1 + state could be excluded. The strongE1γ-branch of the deexcitation of the 10 1 + isomer in140Ce can be explained by means of small admixtures of configurations which contain the outer subshell excitationsπ2f 7/2 andπ1h 9/2. On this basisE1 transitions experimentally observed in theN=82 nuclei140Ce,141Pr and145Eu may be understood. 相似文献
856.
K. -H. Speidel M. Knopp W. Karle U. Kilgus M. -L. Dong H. -J. Simonis F. Hagelberg J. Gerber 《Zeitschrift für Physik A Hadrons and Nuclei》1988,331(1):29-36
Transient field precessions have been measured with the first excited 2 1 + -state as probe for ions of28Si traversing Fe at vion?1v0 and 13v0(v0=c/137) and62Ni being stopped in Fe. The degree of polarization deduced for the Si ions, p1s=0.19(6), is consistent with low-velocity data. There is clear evidence that the field strength is attenuated by heavy ion beams. For the62Ni(2 1 + ) state at 1.173 MeV a g-factor value of g=0.34(7) was obtained in good agreement with a previous result. 相似文献
857.
The three proteins phosphorylase b, calmodulin and fibrinogen are adsorbed onto thioalkyl derivatives of Sepharose much more strongly than onto gels carrying the same alkyl residue coupled via a carbamate linkage. This enhancement of binding onto alkyl-S-Sepharoses compared with alkyl-N-agaroses is not primarily due to an increase in the extent of conformational changes of the proteins occurring on the gel surface. This can be shown in experiments with the tripeptide Trp-Trp-Trp. The Trp tripeptide is also adsorbed with a much higher affinity to butyl-S-Sepharose than to butyl-N-Sepharose, showing that the primary interaction between the immobilized alkyl residue and the amino acids of the protein is decisive for adsorption. A model stressing the strong influence of an atom or a group of atoms at the base of an immobilized alkyl residue is described as "base-atom recognition". 相似文献
858.
859.
Egyptian Portland Cement in the form of one inch cube was hydrated at different times of hydration. Nine cubes of each period of hydration were heated for five minutes 200, 300, 400 up to 1000°C then were quenched in air. The compressive strength was measured for these samples and related to unheated ones. These cubes were ground and measured by Mössbauer spectrometry to correlate the effect of dehydration of cement pastes on the states of iron, with the decrease of compressive strength. It was observed that starting from 400°C the central doublet characteristic of the hydration process decreased as the dehydration temperature was increased. At 1000°C the dehydration process was complete, the central doublet disappeared and the compressive strength vanished. The hydration process was found to be reversible. The application of Mössbauer spectrometry to estimate the degree of fire in concrete building was demonstrated. 相似文献
860.
R. Bacaud M. Besson D. Brodzki P. Bussière H. Charcosset G. Diega-Mariadassou M. Oberson B. K. Sharma 《Hyperfine Interactions》1989,46(1-4):583-589
Mössbauer Spectroscopy, X-Ray Diffraction and Electron Microscopy were applied to the study of solid residues of coal hydroliquefaction, for which tin-based catalysts were used. In the general case hydroliquefaction runs were performed in the presence of added sulphur and of finely dispersed SnO2 as a catalyst precursor. The only observed tin species were SnO2 and SnS, the former with percentages higher than expected from XRD, due to its large f factor, the latter as a symmetric doublet, which suggests that any asymmetry should be ascribed to small particle sizes rather than to structure. When the S content was only that of coal and the catalyst precursor β-Sn, FeSn2 occurred together with Sn sulfides and oxides, while no β-Sn was detected. The main catalytic role is ascribed to SnS. 相似文献