On Prospects for Exploration of Supersymmetry in Double Beta Decay Experiments

We analyze constraints on the parameters of the R-parity violating supersymmetry which can be extracted from non-observation of the neutrinoless nuclear double beta decay ($0\nu\beta\beta$) at a given half-life lower bound. Our analysis covers a large class of phenomenologically viable R-parity violating SUSY models. We introduce special characteristics: the SUSY sensitivity of a $\beta\beta$ decaying isotope and the SUSY reach of a $0\nu\beta\beta$ experiment. The former provides a physical criterion for a selection of the most promising isotopes for SUSY searches and the latter gives a measure of success for a $0\nu\beta\beta$ experiment in exploring the R-parity violating SUSY parameter space. On this basis we discuss prospects for exploration of supersymmetry in various $0\nu\beta\beta$ experiments.Comment: 11 pages, 5 Postscript figures. Modified and updated version is printed also in Proc. of NANP97 (JINR, Dubna, July 7--11, 1997): Phys. Atom Nucl, 1998, 61, vol. 6, p.1092--109

Electrochemical Reducing of Terbium and Holmium Ions in the Sodium and Potassium Chlorides Melt with Equimolar Composition

Interest to rare-earth metals (REM) and their alloys is due to the possibility of using them for the creation of new materials need for modern technology. For instance, REM as alloying components allows for preparation of material with special magnetic properties. A promising method for forming such coating is the surface treatment of metals. This process has an electrochemical character as such for the organization of technology the knowledge of kinetics and mechanism of these processes is important. Despite significant interest in rare-earth metals, these issues are not well described in the literature. In order to choose an adequate mathematical model for calculation of kinetic primers, preliminary experiments that allow evaluating the reversibility of the electrode process have been conducted. Based on that, it was concluded that cathodic reduction of terbium and holmium ions in equimolar NaCl-KCl melt is irreversible. By means of voltammetric analysis, kinetic parameters (transfer coefficients, heterogeneous constants of charge transfer rate) of terbium and holmium electroreduction in equimolar NaCl-KCl melt were determined. The experiment was conducted in a three-electrode cell under a purified argon atmosphere. A dependency of kinetic parameters on the concentration of terbium and holmium chlorides wt (%): 1, 3, 5, 7, 10, was determined. The experiment was conducted in 1073–1173K temperature range. Values of kinetic parameters increase with temperature but decrease with the increase of REM chloride. Based on obtained data, it was found that electroreduction of chloride complexes LnCl63– (Ln–Tb, Ho) in equimolar NaCl-KCl melt is irreversible in the studied range of temperatures and REM concentrations. In summary of experimental data, in range of temperature and rare-earth chloride concentration, and assumption was made that reduction of terbium and holmium ions occurs in two stages. The process includes the preceding stage of complex dissociation. A mechanism of LnCl63– complex reduction in the mentioned melt is proposed. The obtained results are in agreement with literate data for analogues systems

Determination Of Formation Regimes For Bilayer Cobalt Dysprosium Intermetalic Surface Alloy

High tech industrial fields on modern development stage are in need of construction materials with an optimal ratio of volume and surface properties, along with low cost of material itself. As evidenced by studies, in order to give a set complex of properties to a workpiece that operates under specific conditions, it is often sufficient to only modify its surface area. Over the course of studies, by means of gravimetric, influence of technological parameters (temperature and time samples are kept in the melt) on specific mass change of cobalt samples, that act as substrate, during electroless diffusive saturation with dysprosium in eutectic melt of lithium and potassium chlorides have been studied. A mathematical dependency was established for specific mass change of cobalt samples on time spent in melt for temperature range of 873–973 K. Composition of intermetallic coats obtained on surface of cobalt samples was studied means of EDX and SEM analyses. It was discovered, that for chosen temperature range, diffusion layers formed on surface of cobalt samples consists of two structural zones that correspond to Co-Dy and Cp2Dy phases