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881.
N. Ahmad C. Nanjundayya W. G. Chace M. A. Ssobolew M. M. Tschilikin A. T. Iwanowa F. Kalmanowitsch A. Kolotyrewa C. F. Cross E. J. Bevan A. Eavenson J. W. Creely J. H. Skinkle O. Viertel A. J. Hall W. N. Udalskaja D. A. Clibbens A. H. Little Karin Schulze S. M. Edelstein E. Lindemann F. Schütz W. Klauditz P. Winterfeld F. H. Guernsay L. T. Howells F. Schroeder R. Finlay G. Hasse Niederhauser H. Ris R. D. Nutting W. Lesnianski F. Fabrowicz und Coch 《Fresenius' Journal of Analytical Chemistry》1938,115(1-2):51-57
Ohne Zusammenfassung 相似文献
882.
Ohne ZusammenfassungDie vorliegende Untersuchung wurde im Laboratorium für allgemeine Experimentalchemie und in jenem für analytische Chemie an der technischen Hochschule in Wien durchgeführt. Es ist uns eine angenehme Pflicht, den Vorständen dieser Institute, den Herren Professoren Dr. M. Bamberger und Dr. G. Vortmann für ihr stetes Entgegenkommen unseren wärmsten Dank zu sagen. 相似文献
883.
The orientational relaxation of optically induced anisotropy in rarefied gases and at a damped rotation has been investigated. It has been found that the anisotropy relaxation in rarefied gases is described by a reduced kinetic equation depending only on free rotation integrals. The behavior of the integral anisotropy of luminescence for free symmetric and asymmetric top molecules has been elucidated. The law of luminescence depolarization has been obtained for asymmetric top molecules in the Gordon J-diffusion model. It represents the sum of two Stern–Volmer-type dependences, whose relative contribution is determined by the orientation of the dipole moments of transitions with absorption and emission of light in the molecular coordinate system and by the principal moments of inertia of the molecular top. It has been established that in the limit of a strongly damped rotation, kinetic equations of the general form reduce to equations of rotational diffusion. A number of modified diffusion equations correctly describing the contribution of inertial effects to the orientational relaxation of anisotropy have been obtained. 相似文献
884.
E. E. Roper W. P. White H. P. Brown O. A. Sliskonskaja F. Lieneweg I. Schrodt M. Benedict und P. Neubert 《Fresenius' Journal of Analytical Chemistry》1940,120(1-2):17-18
Ohne Zusammenfassung 相似文献
885.
L. Erlandsen G. Schenck H. Graf R. Wasicky G. Stern M. Zimet W. Schreber W. Hoffmann F. Schoofs V. F. Stewart H. J. Wollner J. R. Matchett und H. Quéré 《Fresenius' Journal of Analytical Chemistry》1940,120(3-4):147-151
Ohne Zusammenfassung 相似文献
886.
F. Despa R. S. Berry 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2003,24(1-3):37-40
Interpretive theoretical tools prove valuable in guiding
the analysis of experiments in the realm of atomic clusters.
Here, we review basic elements of an analytic approach that
makes it possible to find and visualize the effective
electrostatic potential and Coulomb correlations in multicenter
problems. To illustrate the utility of these concepts we apply
them to exploring molecular-doped metallic clusters. This study
is aiming at a systematic, visual assessment of changes induced
in screening, Coulomb correlation and effective potential by
varying the charge of the electronegative impurity and its
position in the cluster cage. 相似文献
887.
888.
889.
S. N. Dorogovtsev A. V. Goltsev J. F. F. Mendes 《The European Physical Journal B - Condensed Matter and Complex Systems》2004,38(2):177-182
We consider the general p-state Potts model on random networks with a given degree distribution (random Bethe lattices). We find the effect of the suppression of a first order phase transition in this model when the degree distribution of the network is fat-tailed, that is, in more precise terms, when the second moment of the distribution diverges. In this situation the transition is continuous and of infinite order, and size effect is anomalously strong. In particular, in the case of p = 1, we arrive at the exact solution, which coincides with the known solution of the percolation problem on these networks.Received: 3 December 2003, Published online: 17 February 2004PACS:
05.10.-a Computational methods in statistical physics and nonlinear dynamics - 05.40.-a Fluctuation phenomena, random processes, noise, and Brownian motion - 05.50. + q Lattice theory and statistics (Ising, Potts, etc.) - 87.18.Sn Neural networks 相似文献
890.
P. Budrugeac J. M. Criado F. J. Gotor J. Malek L. A. Prez‐Maqueda E. Segal 《国际化学动力学杂志》2004,36(6):309-315
The isoconversional method suggested by Friedman and the invariant kinetic parameters method (IKP) were used in order to examine the kinetics of the nonisothermal crystallization of (GeS2)0.3(Sb2S3)0.7. The objective of the paper is to show the usefulness of the IKP method both for determining the activation parameters as well as the model of the investigated process. It was shown that the kinetic triplet [(E, A, f(α), where E is the activation energy, A is the preexponential factor, and f(α) is the differential function of conversion], which results through the application of the IKP method, depends on the set of kinetic models considered. For different sets of kinetic models, proportional values of f(α) are obtained. A criterion for the selection of this set, the use of which lead to the true kinetic triplet corresponding to the analyzed process (E = 163.2 kJ mol?1; A = 2.47 × 1012 min?1 and the Avrami‐Erofeev model, Am, for m = 2.5–2.6 was suggested. © 2004 Wiley Periodicals, Inc. Int J Chem Kinet 36: 309–315, 2004 相似文献