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201.
Solutions of the equations v x+v 3?tv+x=0 and v xx=v 3? tv+x, which describe the nucleation of domain walls occurring in the neighborhood of cusps of slowly varying equilibriums, are analyzed. Examples related to the diffusion in smoothly inhomogeneous media are considered.  相似文献   
202.
The solution of the Poisson-Boltzmann equation for a cloud of charges surrounding two charged dust particles treated as Debye atoms forming a Debye molecule is investigated numerically using Cassini coordinates. The electric force exerted on a dust particle by the other dust particle was determined by integrating the electrostatic pressure on the surface of the dust particle. It is shown that attractive forces appear when the following two conditions are satisfied. First, the Debye radius (corresponding to the electron density at half the mean distance between the dust particles) must be approximately equal to half the mean distance between the dust particles. Attraction between the dust particles emerges at a distance equal approximately to half the mean distance between the dust particles. Second, attraction takes place when like charges are concentrated predominantly on the dust particles. If the particles carry a small fraction of charge of the same polarity, repulsion between the particles takes place at all distances.  相似文献   
203.
In the present work, a quantitative analysis of the phase compositions by Mössbauer effect spectroscopy of solid and conventional hydrogen disproportionated Pr13.7Fe80.3B6.0 and Pr13.7Fe63.5Co16.7Zr0.1B6.0 alloys was carried out. Significant amounts of intermediate borides t-Fe3B and Pr(Fe, Co)12B6 were detected after solid hydrogen disproportionation treatment in Pr13.7Fe80.3B6.0 and Pr13.7Fe63.5Co16.7Zr0.1B6.0 alloys, respectively. After conventional hydrogenation–disproportionation–desorption–recombination treatment these phases were not detected and in no case residual Pr2Fe14B-phase was found. It was observed that the amount of intermediate borides after disproportionation can be correlated with the degree of texture after recombination at various temperatures.  相似文献   
204.
The first experimental observation of the propagation dynamics of a short broadband acoustic pulse in a resonance medium with gas bubbles is carried out. The probing pulse is generated using the optoacoustic effect. It is shown that the theory of short pulse propagation in media with generalized resonance relaxation adequately and accurately describes the dynamics of short pulse dispersion. A possibility to determine the relaxation and resonance parameters of media by the pulsed testing technique is demonstrated.  相似文献   
205.
The efficiency of suppression of the generation of a photon echo response depending on the mutual spatial orientation of gradients of external nonumform electric fields acting on a resonant medium is studied. The possibility of creating an associative memory where the mutual orientation of the gradients of external electric fields is an associative key is discussed.  相似文献   
206.
It is shown that the small-scale Rossby waves in a shallow rotating fluid placed in a gravitational field can generate large-scale zonal flows by means of a two-stream-like mechanism. This mechanism is revealed under the conditions when the Lighthill instability criterion is not satisfied. The text was submitted by the authors in English.  相似文献   
207.
The interaction of water-soluble cationic 5,10,15,20-tetrakis(4-N-methyl pyridyl) porphyrin (H2TMPyP4) with some mono-and polynucleotides is studied by time-resolved and steady-state fluorescence spectroscopy, as well as by steady-state absorption spectroscopy. The fluorescence decay kinetics are analyzed by reconstructing the decay time distributions, which made it possible to describe in more detail than previously the complexes formed due to the interaction. The main effect of binding of H2TMPyP4 adenosine 5′-monophosphate and to poly(dA-dT)2 is shown to be an increase in the fluorescence lifetime from 4.6 ns in the solution to 8.3 and 12.3 ns, respectively. This effect is explained by a less polar (in comparison with water) environment of porphyrin in complexes, which leads to a decrease in the quenching action of the intramolecular charge transfer state between the porphyrin macrocycle and methyl pyridyl groups. In the case of complex formation with guanine-containing nucleotides (guanosine 5′-monophosphate and poly(dG-dC)2), the effect of decrease in the quenching action of the intramolecular charge transfer state caused by a decrease in the medium polarity is superimposed by a stronger effect of decrease in the fluorescence lifetime of porphyrin as a result of intermolecular electron transfer from guanine to excited porphyrin. A high sensitivity of this intermolecular quenching to the mutual arrangement of the electron donor and the electron acceptor makes it possible to reveal four types of complexes between H2TMPyP4 and guanosine 5′-monophosphate, which differ in the positions of four broad peaks in the porphyrin fluorescence decay time distribution (0.1, 0.7, 2.4, and 6.1 ns). For the complex with poly(dG-dC)2, a narrow peak at 2.8 ns prevails in the fluorescence decay time distribution, with the contributions from two additional narrow peaks at 1.0 and 6.2 ns being small.  相似文献   
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