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Z.J. Yang T.H. Johansen H. Bratsberg G. Helgesen A.T. Skjeltorp 《Physica C: Superconductivity and its Applications》1989,160(5-6):461-465
Based on a dipole-dipole interaction model, we discuss the levitation force and related vibration problems to understand the effects of flux pinning in type-II superconductors, and the applications of levitation in superconducting systems. 相似文献
3.
Tom H. Johansen 《Journal of Crystal Growth》1987,80(2):465-468
Crystal diameter monitoring in liquid encapsulated Czochralski (LEC) growth using the weighing method is investigated. An analytical expression for the differential weight gain signal is derived for stationary growth conditions accounting for bouyancy. For the GaAs/B2O3 system the buoyancy component of the signal can easily amount to 30%. The formula can be applied to determine the crystal/melt interface area, provided the radius of the part emerging from the encapsulant is known, either in advance as the seed dimension, or by separate monitoring using, e.g., conventional optical methods. 相似文献
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K. K. Karukstis R. M. Moision S. K. Johansen K. E. Birkeland S. M. Cohen 《Photochemistry and photobiology》1992,55(1):125-132
We have previously used chlorophyll fluorescence measurements at Fmax conditions (i.e. with Photosystem II electron acceptor QA reduced) to monitor the action of 9,10-anthraquinones on photosynthetic electron transport in plant chloroplasts. The present investigation employs two additional techniques to characterize the extent of electron transport inhibition induced by the addition of substituted anthraquinones to the suspending medium of spinach chloroplasts. Results are presented for spectrophotometric assays of the rate of electron transfer to an exogenous electron acceptor, 2,6-dichloroindophenol (DCIP) and for electrochemical determinations of the rate of oxygen evolution in anthraquinone-treated chloroplasts. In general, amino-substituted anthraquinones are ineffective inhibitors, maintaining electron transfer rates to DCIP at levels ranging from 50 to 90% of normal rates and yielding rates of O2 evolution averaging at 70% of the rate in untreated chloroplasts. In contrast, hydroxy-substituted anthraquinones efficiently block Photosystem II electron transport, resulting in low rates of DCIP photoreduction ranging from 0 to 20% of normal values and reducing O2 evolution rates to an average of 30% of the rate observed for untreated chloroplasts. Relative rates of DCIP photoreduction for anthraquinone-treated chloroplasts show a strong linear correlation with the reported relative Fmax chlorophyll fluorescence intensities. Relative O2 evolution rates are observed to correlate with the Stern-Volmer fluorescence quenching parameter Ksv. We suggest that slight differences in the extent of inhibitory activity of an anthraquinone as measured by the three techniques are consistent with certain known Photosystem II heterogeneities. The similarities in relative rankings of inhibitory effects for the 9, 10-anthraquinones, however, demonstrate that the three techniques employed (measurements of Fmax chlorophyll fluorescence, DCIP photoreduction rates, and O2 evolution rates) are alternative assays of anthraquinone-induced Photosystem II electron transport inhibition. 相似文献
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N. H. Tea R. -C. Yu M. B. Salamon D. C. Lorents R. Malhotra R. S. Ruoff 《Applied Physics A: Materials Science & Processing》1993,56(3):219-225
We have performed thermal conductivity measurements on C60 and C70 crystals grown by sublimation. For single crystal C60, the thermal conductivity k is 0.4 W/m K at room temperature and is nearly temperature independent down to 260K. We observed a sharp orientational phase transition at 260K, indicated by a 25% jump in k. Below 90K, k is time dependent, which manifests itself as a shoulder-like structure at 85K. The temperature and time dependence of k below 260K can be described by a simple model which accounts for the thermally activated hopping of C60 molecules between two nearly degenerate orientations, separated by an energy barrier of 240 meV. It is found that solvents have a strong influence on the physical properties of C70 crystals. For solvent-free C70 crystal, k is about constant above 300K. There is a broad first-order phase transition in k at 300K with a 25% jump. We associate this transition with the aligning of the fivefold axes of the C70 molecules along the c-axis of the hexagonal lattice. Upon further cooling, k increases and is time independent. 相似文献
10.
The electronic structure of the permanganate ion has been investigated, using a semiquantitative LCAO MO method without empirical parameters. The atomic orbital basis set for the central ion has been varied systematically, and the effect of symmetric changes of bond distances has also been examined. In addition, calculations have been performed in which the regions around the ligands have been made more attractive for electrons, to simulate the presence of cations in solution and in the crystalline state. The electronic absorption spectrum of MnO
4
–
has been tentatively assigned, on the basis of predicted band shapes and transition energies.
Zusammenfassung Die Elektronenstruktur des Permanganations wurde mit einer halbquantitativen LCAO-MO Methode ohne empirische Parameter behandelt. Die Zustandsfunktionen des Zentralatoms wurden variiert und der Einflu\ symmetrische Änderungen der BindungsabstÄnde untersucht. Um die Gegenwart von Kationen in Lösung und im Kristall zu simulieren, wurden daneben auch Rechnungen durchgeführt, bei denen einer stÄrkeren Elektronenanziehung durch die Liganden Rechnung getragen wird. Ferner wurde versucht, das Absorptionsspektrum von MnO 4 – auf Grund der vorausgesagten Bandenform und übergangsenergien zu deuten.
Résumé La structure électronique de l'ion permanganate est étudiée à l'aide d'une méthode LCAO MO semi-quantitative sans paramètres empiriques. La base d'orbitales atomiques pour l'ion central a été systématiquement variée et l'effet de changements symétriques des longueurs de liaison a été aussi examiné. Pour simuler la présence des cations dans la solution et dans le cristal on a fait des calculs dans lesquels la région autour des ligands était rendue plus attractive pour les électrons. Le spectre d'absorption de MnO 4 –1 est interprété à l'aide des prédictions sur les formes des bandes et les énergies de transition.相似文献