Nitrit

Ohne Zusammenfassung     

Elliptic semiplanes and group divisible designs with orthogonal resolutions

In this paper we prove that there exists an elliptic semiplaneS(v, k, m) withk –m 2 if and only if there exists a group divisible design GDD _k ((k –m)(k – 1);k –m; 0, 1) withm pairwise orthogonal resolutions. As an example of this theorem, we construct an elliptic semiplaneW(45, 7, 3) and show thatW is isomorphic to the elliptic semiplaneS(45, 7, 3) given by R. D. Baker.     

Why is space three-dimensional and how may groups be seen?

First we propose a model of visual perception essentially based on the Keldysh-Chernavsky-Sossinsky three-channel theorem, from which three-dimensionality of space follows. Second, we associate with a system of subgroups H ₁, ..., H_s of a given group G a geometric object, called a group crystal, in order to visualize G. How this notion works is illustrated via the Burnside problem.     

Observables on hypergraphs

Observables on hypergraphs are described by event-valued measures. We first distinguish between finitely additive observables and countably additive ones. We then study the spectrum, compatibility, and functions of observables. Next a relationship between observables and certain functionals on the set of measures M(H) of a hypergraph H is established. We characterize hypergraphs for which every linear functional on M(H) is determined by an observable. We define the concept of an effect and show that observables are related to effect-valued measures. Finally, we define operational transformations from M(H) to itself and show that they can be described as a certain combination of effects.On leave from University of Berne, Institute of Mathematical Statistics, Sidlerstrasse 5, CH-3012 Berne, Switzerland.     

Distribution of a nonstationary electron beam in a dense gas

The problem of the temporal and spatial dependences of the parameters of the action of a modulated fast-electron beam on a dense gas is posed on the basis of the transport equation. The problem is simplified by making it nondimensional and by transforming to the Fokker-Planck approximation. A Green's function formalism is developed for this problem and is used to express the solution of the general nonstationary problem in the form of a convolution of a nonstationary boundary flow with a stationary Green's function. The use of the derived equation is illustrated using as an example the solution of a problem with the simplest stationary Green's function corresponding to the straight-ahead approximation. This approximation is used to consider a general relativistic case with model scattering cross sections. The methods and results of a numerical computer solution of the nonstationary problem of electron retardation in the upper layer of the atmosphere are surveyed.Translated from Trudy Ordena Lenina Fizicheskogo Instituta im. P. N. Lebedeva AN SSSR, Vol. 145, pp. 172–188, 1984.     

Site-specific core level spectroscopy of CO and NO adsorption on Pt(110)(1×2) and (1×1) surfaces

The adsorption of CO and NO on the (1×2) and (1×1) modifications of the Pt(110) surface was studied by x-ray photoemission spectroscopy, LEED and work-function change measurements. The O(1s) binding energy of adsorbed CO is site-specific and differentiates between on-top and bridge adsorbed species. CO adsorption on Pt(110)(1×2) at 120 K occurred sequentially into on-top and bridge sites yielding an orderedc(8×4) layer at the maximum coverage. At 300 K only on-top bonded CO was present after CO adsorption on the (1×2) surface. CO adsorption on the (1×1) surface at 120 K showed a transient bridge adsorbed CO and on-top CO at saturation, with an ordered (2×1)p1g1 LEED pattern. Heating the (2×1)p1g1 CO layer to 400 K also showed this transient bridge CO species. Work function changes generally correlated with the appearance of different CO species but were complex in detail. The findings for CO adsorption are consistent with the missing row model of the (1×2) surface.Parallel data for NO adsorption on (1×2) and (1×1) surfaces at 120 K were less informative than those for CO because O(1s) spectra showed single broad peaks. Peak contributions due to bridge and on-top bonded NO could be estimated.     

Field dependent critical fluctuations aboveT g in the ESR line width of the spin glassAgMn

The ESR of the spin glassAgMn (2.7 and 9.6 at %) has been investigated below and aboveT _g(0.1T _g<T<5T _g) at various microwave frequencies. The analysis yields:1) No explicit frequency dependence but strong magnetic field effects, inherent with ESR-experiments.2) Part of the excess line width is identified as critical spin fluctuations, following a power law. However, because of the presence of the applied field, the reduced temperaturet is not a good scaling variable. We choose the non-linear susceptibility X _s divided byH ², which scales as the order parameter susceptibility. The experiment yieldsW _ex(X _s /H ²) ^p ,p=0.42. From this we deduce z3.     

Mössbauer effect of iodine at pressures to 30 GPa

We report the first high pressure¹²⁹I Mössbauer measurements with elemental iodine at pressures to 30 GPa. A 20 mg/cm^{2 129}I₂ absorber was mounted in a diamond anvil cell with an effective diameter of 0.21 mm. The source used was Mg₃ ^129mTeO₆. Experiments were performed mainly at 4 K and the pressure was monitored by the ruby fluorescence method. With increasing pressure we observe a gradual decrease in ¦e²qQ¦ and an increase in IS and values of the low pressure, molecular phase; at 16 GPa a new phase (HP1) is detected characterized by a change in sign of e²qQ and a smaller value of ¦e²qQ¦, and a substantial increase in . At 24 GPa a new phase (HP2) is formed that is characterized by a smaller value of . In general the population of the molecular phase decreases from 1.0 near 15 GPa to a value of 0.4 at 30 GPa. The fraction of the high pressure phase (HP1 + HP2) increases at the expense of the molecular phase and that of the HP2 at the expense of the HP1 phase. These observations are discussed in relation to the onset of a metallic phase near 16 GPa and recent x-ray diffraction studies.Work performed under the auspices of the U.S. Department of Energy.