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971.
The Coulomb drag of electrons in spatially separated two-dimensional layers is considered under conditions of electron heating when the nonequilibrium distribution of electrons in the first layer can be described by macroparameters, such as the effective temperature. The nonequilibrium response is calculated using a projection operator that is an obvious generalization of the Mori operator to the case of nonequilibrium systems. 相似文献
972.
Using the thermodynamical approach and the method of York, the back-reaction of anti-de Sitter Schwarzschild black hole in thermal equilibrium with conformal spin-2 field is studied. It is found that both approaches give identical results. 相似文献
973.
Solichová D Melichar B Klejna M Jurašková B Královská L Bláha V Zd'ánský P Zadák Z 《Talanta》2003,60(2-3):459-465
Twelve self-sustaining nonagenarians, 10 women and two men, aged 94+/-3 years, and eight institutionalised nonagenarians, eight women, aged 91+/-1 year as well as 11 control subjects, seven women and four men, aged 84+/-5 years entered the study. Urinary neopterin, an indicator of systemic immune activation, and serum thiobarbituric acid reactive substances (TBARS), a marker of lipoperoxidation, were determined initially, and collection of the blood and urine samples was repeated at 3-month interval. Neopterin was measured in the urine specimens by reversed-phase high performance liquid chromatography. A C(18) reversed-phase column 3.3x150 mm, 5 mum-diameter packing Separon SGX was used. Potassium phosphate buffer (15 mmol l(-1), pH 6.4) at flow rate of 0.8 ml min(-1) was used as mobile phase. After centrifugation (5 min, 1300xg) and diluting 100 mul of urine specimens with 1.0 ml of mobile phase containing 2 g of disodium-EDTA per litre, a 20 mul sample was injected on a column. Neopterin was identified by its native fluorescence (353 nm excitation, 438 nm emission). Creatinine was determined by Jaffé kinetic reaction after dilution of sample 1:50 (v/v). The concentration of neopterin in urine was expressed as neopterin/creatinine ratio (mumol mol(-1) creatinine). TBARS were determined spectrofluorometrically using LS-5 spectrofluorimeter (excitation wavelength 528 nm, emission wavelength 558 nm) after extraction with n-butanol treatment with thiobarbituric acid. The significance of differences between nonagenarians and control group was examined by ANOVA-Kruskal-Wallis tests, using statistical software NCSS 6.0.21 (Kaysville, UT, 1996). The decision on significance was based on P=0.05. Urinary neopterin was significantly higher in institutionalised compared to self-sustaining subjects and controls (625+/-565 vs. 203+/-63 mumol mol(-1) creatinine, and 198+/-128 mumol mol(-1) creatinine, respectively, P=0.006). The serum TBARS were higher in both groups of nonagenarians (3.23+/-1.16 mumol l(-1) and 2.69+/-0.39 vs. 2.12+/-0.83 mumol l(-1) for the self-sustaining, institutionalised and controls, respectively, P=0.023). We conclude that the fluorimetric determinations of urinary neopterin and serum TBARS can be useful for the monitoring health status in the elderly patients. 相似文献
974.
A. N. Dovbnya K. V. Korytchenko M. A. Krasnogolovets Yu. Ya. Volkolupov Yu. D. Tur S. M. Shkirida A. I. Kosoi 《Technical Physics》2003,48(12):1586-1589
The influence of the discharge conditions on the dynamics of energy release is considered for pulsed arcs in air at initial pressures from 105 to 8×105 Pa and a low-voltage capacitor voltage of up to 400 V. A novel method for determining the resistance of the discharge channel in the final stage of a spark discharge is proposed. The method is applied to estimating the discharge channel parameters. 相似文献
975.
Periodica Mathematica Hungarica - 相似文献
976.
We solve the problem of describing compatible nonlocal Poisson brackets of hydrodynamic type. We prove that for nonsingular pairs of compatible nonlocal Poisson brackets of hydrodynamic type, there exist special local coordinates such that the metrics and the Weingarten operators of both brackets are diagonal. The nonlinear evolution equations describing all nonsingular pairs of compatible nonlocal Poisson brackets of hydrodynamic type are derived in these special coordinates, and the integrability of these equations is proved using the inverse scattering transform. The Lax pairs with a spectral parameter for these equations are found. We construct various classes of integrable reductions of the derived equations. These classes of reductions are of an independent differential-geometric and applied interest. In particular, if one of the compatible Poisson brackets is local, we obtain integrable reductions of the classical Lamé equations describing all orthogonal curvilinear coordinate systems in a flat space; if one of the compatible brackets is generated by a constant-curvature metric, the corresponding equations describe integrable reductions of the equations for orthogonal curvilinear coordinate systems in a space of constant curvature. 相似文献
977.
A. V. Vypirailenko I. B. Dzvinchuk M. O. Lozinskii 《Chemistry of Heterocyclic Compounds》2003,39(1):123-125
2-Phenacylbenzothiazole reacts with hydrazines and o-hydroxybenzaldehydes to give hydrazones and chalcones. These compounds tend to isomerize to benzothiazole-2-spiro-3'-pyrazoles and benzo[b]pyran-2-spiro-2'-benzothiazoles, respectively. 相似文献
978.
Equations that simulate the magnetic induction and current density distributions in half-space in view of the power I-V characteristic are derived. The magnetization front velocity is determined for a given mean rate of external magnetic field variation at the boundary of the sample. An integral condition for the electrical resistance (nonlinearly depending on the magnetic field) under which the magnetic flux penetrates into the sample with a finite rate is found. An analytical solution that simulates the power variation of the magnetic field at the boundary is given. The Bean generalized model describing the current density distribution near the critical current is considered. It is shown that solutions like shock waves may arise beyond the applicability domain of the Bean model. 相似文献
979.
980.
Photoinduced NH tautomerism, along with the reaction pathways of phototautomerization in tetrabenzoporphin and porphin free bases in n-octane polycrystalline matrices at 77 K, is studied by simulation of kinetic processes and their experimental observation. The simulation of the processes is performed by the numerical solution of the system of kinetic equations describing the populations of electronic levels and transitions between them. Kinetic dependences are obtained by measuring the perturbation of stationary fluorescence of one component of the 0-0 doublet origin upon pulsed selective photoexcitation of the other component. For two tautomeric forms related by the reversibility of the photochemical reaction, under the assumption of synchronism of the NH rearrangement, (i) analytical solutions governing the reaction rate are found, (ii) a method of measuring the rate constants of the proton rearrangement is suggested and the constants themselves are estimated, and (iii) direct evidence of the participation of T 1 levels in the photochemical reaction is obtained. With the aid of numerical simulations, the specific features of kinetic manifestation of an asynchronous mechanism of the photoinduced NH rearrangement are studied. 相似文献