On a positive set theory with inequality

We introduce a quite natural Frege‐style set theory, which we call Strong‐Frege‐2 $(\mathsf {SF}_2)$, a sort of simplification of the theory considered in 13 (under the name Strong‐Frege‐3) and 1 (under the name F2). We give a model of a weaker variant of $\mathsf {SF}_2$, called $\mathsf {SF}_2\mathsf {AC}$, where atoms and coatoms are allowed. To construct the model we use an enumeration “almost without repetitions” of the Π¹₁ sets of natural numbers; such an enumeration can be obtained via a classical priority argument much in the style of 5 and 15 . © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim     

Anomalous diffusion governed by a fractional diffusion equation and the electrical response of an electrolytic cell

The electrical response of an electrolytic cell in which the diffusion of mobile ions in the bulk is governed by a fractional diffusion equation of distributed order is analyzed. The boundary conditions at the electrodes limiting the sample are described by an integro-differential equation governing the kinetic at the interface. The analysis is carried out by supposing that the positive and negative ions have the same mobility and that the electric potential profile across the sample satisfies the Poisson's equation. The results cover a rich variety of scenarios, including the ones connected to anomalous diffusion.     

Shears band in the 105Sn nucleus

The structure of ¹⁰⁵Sn has been investigated through the ⁵⁰Cr(⁵⁸Ni,2pn) reaction at a beam energy of 210 MeV. In addition to an extension of the spherical level scheme, a regular sequence of dipole transitions has been found. The experimental results are in agreement with the prediction of Tilted Axis Cranking calculations, which satisfactorily explain the properties of the band.     

Interplay of pairing and quadrupole correlations in deformed nuclei

We study pairing correlations in deformed nuclei in the framework of the Nilsson+BCS theory. As in the spherical case, the pairing interaction is found to induce strong spacial correlations between the partners of each paired couple. The presence of the deformed mean field gives rise to a non-spherical pair field, whose deformation is governed by the properties of a few single-particle orbitals around the Fermi surface and does not necessarily follow the shape of the mean field. Multipole expansion of the pair field yields all the pair densities associated with the direct two-particle transfer processes to the members of the g.s. rotational band in the A+2 system. The interplay of the deformations of the mean and the pair fields can lead to different relative magnitudes and phases of these densities and therefore to different excitation patterns of the rotational bands in two-particle transfer reactions. In the case of non-collective twoquasiparticles and bands the associated pair densities display large components with high multipoles and the associated transfer processes may be favoured in heavy-ion collisions by kinematical conditions. Examples corresponding to both prolate and oblate cases are considered.     

Molal volumes of sucrose in aqueous solutions of NaCl,KCl, or urea at 25°C

The apparent molal volume _v of sucrose in water has been measured at 25°C in the concentration range 0.04–4.4m from precise density measurements. The same property was also determined for dilute solutions of sucrose in mixed aqueous solvents containing NaCl, KCl, or urea. The limiting values _v ^° and the slopesS _v ^* were obtained in each case, and their significance has been discussed briefly. The mean apparent molal volumes _v of the ternary systems were also calculated, and the predictive accuracy of Ward and Millero's modified Young's rule for _v was found to be comparable to that for other electrolyte-nonelectrolyte solutions. For the system H₂O-sucrose-urea, an additivity rule based simply on total molality predicted _v with similar accuracy.Deceased January 15, 1976.     

A theoretical study of the vibronic structure in the electronic spectrum of HNO+

The results of an ab initio study of the vibronic and rotational structure in the ²Π state of HNO⁺ are presented. It is shown that the absorption spectrum at 7200 Å observed by Herzberg could be caused by the transition from the ground to the first excited electronic state of HNO⁺     

Representation of MV-algebras by regular ultrapowers of [0, 1]

We present a uniform version of Di Nola Theorem, this enables to embed all MV-algebras of a bounded cardinality in an algebra of functions with values in a single non-standard ultrapower of the real interval [0,1]. This result also implies the existence, for any cardinal α, of a single MV-algebra in which all infinite MV-algebras of cardinality at most α embed. Recasting the above construction with iterated ultrapowers, we show how to construct such an algebra of values in a definable way, thus providing a sort of “canonical” set of values for the functional representation.