Effects of Lorentz violation in the Bose-Einstein condensation

In this paper we study the corrections emergent from a Lorentz-violating CPT-odd extension of the complex scalar sector to the Bose-Einstein condensation and to the thermodynamics parameters. We initially discussed some features of the model to only then compute the corrections to the Bose-Einstein condensation. The calculations were done by computing the generating functional, from which we extract the thermodynamics parameters. We also obtained a Lorentz-violating correction for the critical temperature $T_c$ that sets the Bose-Einstein Condensation.Comment: 6 pages. 2 figures. Version accepted by EPL. Minor typo corrections. arXiv admin note: text overlap with arXiv:2009.0230

Dressing approach to the nonvanishing boundary value problem for the AKNS hierarchy

We propose an approach to the nonvanishing boundary value problem for integrable hierarchies based on the dressing method. Then we apply the method to the AKNS hierarchy. The solutions are found by introducing appropriate vertex operators that takes into account the boundary conditions.Comment: Published version Proc. Quantum Theory and Symmetries 7 (QTS7)(Prague, Czech Republic, 2011

Higher order effects in the 16O(d,p)17O^{16}O(d,p)^{17}O and 16O(d,n)17F^{16}O(d,n)^{17}F transfer reactions

Full Coupled Channels Calculations were performed for the $^{16}O(d,n)^{17}F$ and $^{16}O(d,p)^{17}O$ transfer reactions at several deuteron incident energies from $E_{lab}=2.29$ MeV up to 3.27 MeV. A strong polarization effect between the entrance channel and the transfer channels $^{16}O(d,n)^{17}F(1/2^{+},0.495)$ and $^{16}O(d,p)^{17}O(1/2^{+},0.87)$ was observed. This polarization effect had to be taken into account in order to obtain realistic spectroscopic factors from these reactions.Comment: 15 papes, 13 figures, accepted for publication in Phys. Rev.

New extractants for separation of platinium-group metals from chloride solutions and their application to recycling processes

In this paper some results on the application of four N,N’-tetrasubstituted malonamide derivatives for the extraction and separation of platinum-group metals (PGMs) are presented. The above mentioned extractants were specifically synthesized in order to evaluate their efficiency for the extraction of a specific metal, or group of metals, from aqueous chloride matrices. Different behaviours were obtained towards platinum(IV) and/or palladium(II) extraction, all the N,N’-tetrasubstituted malonamide derivatives allowing the mutual separation of the two metal ions, depending on the HCl concentration. Generally, extraction experiments were carried out involving initial aqueous phases containing 100 mg/L of each metal isolate, in varying 1M to 8M HCl concentration ranges, and 0.05M extractant in 1,2- dichloroethane solutions. From the preliminary results obtained, one can conclude that HCl concentrations and the structure of the malonamide derivative play a crucial role on the efficiency shown for Pt(IV) and/or Pd(II) extraction. The efficiency of the stripping stage of the loaded organic phases is variable, depending on the N,N’-tetrasubstituted malonamide derivative, as well as on the metal ion involved; for Pt(IV), distilled water and 1M HCl were generally successful, whereas for Pd(II), thiourea in HCl gave better results. The overall data already achieved suggest that these extractants may be good candidates for further evaluation in PGMs separations from real solutions resulting from recycling processes