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151.
Maxwell’s equations in the Majorana representation are generalized to the case of a chiral medium. A relation between the dynamic variables and the parameters of a chiral medium is found. An expression for the current density 4-vector is obtained for the medium under consideration.  相似文献   
152.
The fluorescence of solid solutions of CdSe/ZnS quantum dots and the organic dye DODCI is investigated. It is shown that nonradiative transfer of electronic excitation energy to dye molecules, which with some probability lose their acceptor properties as a result of photoisomerization or photodegradation, is responsible for a significant increase in the fluorescence intensity of a donor. The degree of polarization of the donor fluorescence attains values exceeding 0.5, which is due to the difference in the fluorescence quantum yields of donors with different orientations of the oscillator with respect to the electric vector of an excitation light wave. A numerical simulation of the experimentally observed dependences is performed.  相似文献   
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155.
The initial stage of propagation of a vertical hydraulic fracture in an impermeable or low-permeability stratum is considered within the framework of the pseudo-three-dimensional Perkins-Kern model.Moscow. Translated from Izvestiya Rossiiskoi Akademii Nauk, Mekhanika Zhidkosti i Gaza, No. 6, pp. 79–86, November–December, 1995.  相似文献   
156.
S. P. Timoshenko Institute of Mechanics, National Academy of Sciences of the Ukraine. Translated from Prikladnaya Mekhanika, Vol. 31, No. 9, pp. 15–23, September, 1995.  相似文献   
157.
We have measured the concentration dependence of the average magnetic moment per Fe atom Fe(x) in microcrystalline and amorphous Fe-P alloys obtained over a wide concentration range using electrochemical deposition. The model of local magnetic moments has been used to described Fe(x). On the basis of this model the effects of phosphorus on the value Fe are explained in terms of the parameters of the local environment of the Fe atom.  相似文献   
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159.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 994–996, July, 1992.  相似文献   
160.
Sulfonic cation exchangers with two ion exchange group concentrations (0.5 and 2.4 mmol/g, samples A and B, respectively) were obtained by sulfonation of a porous styrene (S) and divinylbenzene (DVB) copolymer with chlorosulfonic acid. Strong thermal decomposition of the sulfonated copolymer A, accompanied by significant changes in its porous structure, starts at ca. 400°C. The char has no sulfonic groups. After heat treatment at 400°C in steam, a sorbent was obtained (yield 65%) that shows higher phenol sorption than the untreated sample when related to the bed volume. The chlorosulfonic derivatives of the initial copolymer were less thermally resistant than the sulfonic ones obtained by hydrolysis. Pyrolysis of the cation exchanger B, in its H+ and Ca2+ forms, was carried out at 900°C (yield of both chars close to 30%). By subsequent steam activation at 800°C to a 50% burn-off of the char, sorbents with well-developed, but distinctly different, porous structures were obtained. The activated char from the sulfonated copolymer in its hydrogen form was highly microporous and indicated an effective surface area of 1180 m2/g. However, because of a low contribution of mesopores, its ability to adsorb phenol from the liquid phase was not very high. The activated char from the calcium-doped copolymer, indicating a smaller surface area (580 m2/g) but characterized by a well-developed mesoporosity, was a better sorbent for phenol. © 1994 John Wiley & Sons, Inc.  相似文献   
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