сОДЕРжАНИь РАБОт, ОпУБлИкОВАННых тОлькО В ЧЕшскОМ ИжДАНИИ НАстОьЩЕгО жУРНАлА

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Abstracts of Papers which have appeared only in the Czech Edition of this Journal

     

Determination of interdiffusion coefficients in the Co-Ni system with the use of spline functions

The interdiffusion of Co-Ni has been investigated at the temperature 1150 ?C. The concentration dependence curvesc(x, t) obtained with the aid of an JXA-3A electron microprobe were evaluated with the use of smoothing cubic spline by means of the Boltzmann-Matano method. The results are interpreted in terms of Co-Ni equilibrium diagram and compared with the results of other authors. On the basis of this comparison a conclusion was drawn which interdiffusion coefficient values can be taken for most realistic in the given system at 1150 ?C. In the Appendix of this paper a program in the USASI-STANDARD FORTRAN language, generally applicable to the calculations of interdiffusion coefficients with the use of cubic spline, is given.     

Mössbauer effect in the surface layer of Co-57 diffused into an Ni-Al alloy

In this paper a possibility is shown of the surface-layer studies on solids (obtained e.g. in the course of a diffusion anneal) by the Mössbauer effect. The surface layer of the nearly stoechiometric paramagnetic Ni₃Al alloy, on which Co-57 was deposited, became ferromagnetic during the diffusion anneal. Mössbauer spectrum splitting of this layer yields an internal magnetic field value ofH _i =(294.55±0.84) kOe. It has been found that the concentration of cca 3at.% Co in the Ni-Al (29 at.%)-Co alloy is sufficient to transform the paramagnetic Ni-Al phase into a ferromagnetic state.ikova 22, Brno, Czechoslovakia.The authors are indebted to Dr. I. Vagera for the computations on the ZPA-600 computer.     

Distance-dependent quenching of Nile Blue fluorescence byN,N-diethylaniline observed by frequency-domain fluorometry

Fluorescence quenching of Nile Blue by amines is thought to be due to electron transfer to the excited dye molecule from the amine electron donor. We used electron transfer quenching of Nile blue byN,N-diethylaniline in propylene glycol as a model system for an interaction which depends exponentially on distance. We investigated the time dependence of the presumed distance-dependent process using gigahertz harmonic-content frequency-domain fluorometry. The frequency-domain data and the steady-state quantum yield were analyzed globally based on either the Smoluchowski-Collins-Kimball radiation boundary condition (RBC) model or the distancedependent quenching (DDQ) model, in which the rate of quenching depends exponentially on the flourophore-quencher distance. We performed a global analysis which included both the frequencydomain time-resolved decays and the steady-state intensities. The latter were found to be particularly sensitive to the model and parameter values. The data cannot be satisfactorily analyzed using the RBC model for quenching. The analysis shows the excellent agreement of the DDQ model with the experimental data, supporting the applicability of the DDQ model to describe the quenching by the electron transfer process, which depends exponentially on the donor-acceptor distance.     

Mechanisms of the catalytic carbon monoxide oxidation on Pt (110)

The kinetics of the carbon monoxide oxidation on a clean Pt (110) crystal were investigated in an ultra-high vacuum system by utilizing Auger electron spectroscopy, low-energy electron diffraction and residual gas analysis. Two different catalytic reaction mechanisms were found to prevail for the experimental conditions chosen. In the temperature range, 100 < T ? 220°C, where essentially CO was preadsorbed on the Pt surface the subsequent adsorption of O₂ was competitive and the reaction exhibited the characteristics of a Langmuir-Hinshelwood mechanism. In this case the onset of the CO₂ formation was delayed by a characteristic time which depended strongly on temperature (“induction period”). A simple model for the Langmuir-Hinshelwood reaction was developed which permitted a more detailed evaluation of the kinetic curves yielding an activation energy for the catalytic reaction of 2.9 kcal/mole. On the other hand, when oxygen was preadsorbed on the Pt surface (T > 90°C) the subsequent reaction with CO occurred immediately and was temperature independent. This behavior was interpreted in terms of an Eley-Rideal mechanism. Both reactions were used for titration of the adsorbed species. From area measurements under the titration curves it was concluded that the saturation coverage for CO and oxygen on Pt(110) is approximately the same.     

Influence of diffusion on nonradiative energy transfer between FMN molecules in aqueous solutions

Concentration dependence of photoluminescence quantum yield of FMN aqueous solutions (66mM potassium phosphate buffer, pH 7.0) is investigated over the concentration range from 6.31x10(-5) M to 1.8x10(-2) M at temperatures 298.2 and 323.9K. Experimental data are compared with those obtained theoretically based on two different models of excitation energy transfer and migration in the system of FMN monomers and dimers. The first model does not take the material diffusion into account [Acta Phys. Acad. Sci. Hung. 30 (1971) 145] and the second model is based on the second-order transfer rates which are diffusion dependent [Chem. Phys. Lett. 41 (1976) 139; J. Lumin. 27 (1982) 441]. The comparison shows that the process of material diffusion cannot be neglected in the solutions studied as the relative contribution of the diffusion accelerated nonradiative energy transfer to the total drop of the quantum yield can be even higher then 70%. It is also shown, that in order to obtain a good agreement of the experimental and theoretical data it is necessary to introduce into the theory an additional channel of deactivation for the excitation energy. It is proposed that this additional channel can be partial degradation of excitation energy during its migration between the monomers.     

Upper and lower bounds for fundamental natural frequency of beams

A better upper bound than the Rayleigh quotient is the Timoshenko quotient, the evaluation of which depends on a pair of compatible admissible moment and displacement functions. Based on both Rayleigh and Timoshenko quotients, a lower bound is readily computed. By means of an iteration procedure, both the upper and lower bound converge to the fundamental natural frequency.     

Surface energy and solute strain energy effects in surface segregation

Previous models of surface segregation have generally been based on the assumption that a decrease in surface free energy constitutes the predominant driving force for the phenomenon. In contrast, grain boundary segregation models have been founded on the postulate that the major driving force for that phenomenon is the reduction in lattice strain energy which accompanies the transfer of misfitting solute atoms from the lattice to the boundary. These two concepts have been combined here into a single unified formalism of surface segregation. In addition, the temperature dependence of surface composition of both nickel-rich and gold-rich nickelgold alloys has been measured by Auger electron spectroscopy. Comparisons of the predictions of the combined formalism with the experimental results show excellent agreement between measured and calculated heats of adsorption (segregation). Furthermore, the present formalism provides estimates of the entropies of adsorption which can be used to explain apparent incompatibilities between the behavior of gold-rich and nickel-rich alloys.