Search results for "Dubnium"
showing 10 items of 11 documents
Chemical properties of rutherfordium (Rf) and dubnium (Db) in the aqueous phase
2016
Recent experimental studies of the chemical characterization of the first two transactinide elements, rutherfordium (Rf) and dubnium (Db), conducted atom-at-a-time in aqueous phases are reviewed. A short description on experimental techniques based on partition methods, specifically automated rapid chemical separation systems, is also given. Perspectives for aqueous-phase chemistry experiments on heavier elements are briefly discussed.
Fluoride Complexation of Element 104, Rutherfordium
2004
Fluoride complexation of element 104, rutherfordium (Rf), produced in the 248Cm(18O,5n)261Rf reaction has been studied by anion-exchange chromatography on an atom-at-a-time scale. The anion-exchange chromatographic behavior of Rf was investigated in 1.9-13.9 M hydrofluoric acid together with those of the group-4 elements Zr and Hf produced in the 18O-induced reactions on Ge and Gd targets, respectively. It was found that the adsorption behavior of Rf on anion-exchange resin is quite different from those of Zr and Hf, suggesting the influence of relativistic effects on the fluoride complexation of Rf.
Hexafluoro complex of rutherfordium in mixed HF/HNO3 solutions
2008
Formation of anionic fluoride-complexes of element 104, rutherfordium, produced in the 248 Cm( 18 O, 5n) 261 Rf reaction was studied by anion-exchange on an atom-at-a-time scale. It was found that the hexafluoro complex of Rf, [RfF 6 ] 2- , was formed in the studied fluoride ion concentrations of 0.0005-0.013 M. Formation of [RfF 6 ] 2- was significantly different from that of the homologues Zr and Hf, [ZrF 6 ] 2- and [HfF 6 ] 2- ; the evaluated formation constant of [RfF 6 ] 2- is at least one-order of magnitude smaller than those of [ZrF 6 ] 2- and [HfF 6 ] 2- .
Liquid-Phase Chemistry of Superheavy Elements
2013
An overview over the chemical separation and characterization experiments of the four transactinide elements so far studied in liquid phases, rutherfordium (Rf), dubnium (Db), seaborgium (Sg), and hassium (Hs), is presented. Results are discussed in view of the position of these elements in the Periodic Table and of their relation to theoretical predictions. Short introductions on experimental techniques in liquid-phase chemistry, specifically automated rapid chemical separation systems, are also given. Studies of nuclear properties of transactinide nuclei by chemical isolation will be mentioned. Some perspectives for further liquid-phase chemistry on heavier elements are briefly discussed.
Adsorption of Db and its homologues Nb and Ta, and the pseudo-homologue Pa on anion-exchange resin in HF solution
2009
Anion-exchange chromatography of element 105, dubnim (Db), produced in the 206 Cm( 19 F, 5n) 262 Db reaction is investigated together with the homologues Nb and Ta, and the pseudo-homologue Pa in 13.9 M hydrofluoric acid (HF) solution. The distribution coefficient (K d ) of Db on an anion-exchange resin is successfully determined by running cycles of 1702 chromatographic column separations. The result clearly indicates that the adsorption of Db on the resin is significantly different from that of the homologues and that the adsorption of anionic fluoro complexes of these elements decreases in the sequence of Ta ≈ Nb > Db > Pa.
Chemical studies on rutherfordium (Rf) at JAERI
2005
SummaryChemical studies on element 104, rutherfordium (Rf), at JAERI (Japan Atomic Energy Research Institute) are reviewed. The transactinide nuclide261Rf has been produced in the reaction248Cm(18O, 5n) at the JAERI tandem accelerator with the production cross section of about 13 nb. On-line anion-exchange experiments on Rf together with the lighter homologues, group-4 elements Zr and Hf, in acidic solutions have been conducted with a rapid ion-exchange separation apparatus. From the systematic study of the anion-exchange behavior of Rf, it has been found that the properties of Rf in HCl and HNO3solutions are quite similar to those of Zr and Hf, definitely confirming that Rf is a member of …
Anionic Fluoro Complex of Element 105, Db
2009
We report on the characteristic anion-exchange behavior of the superheavy element dubnium (Db) with atomic number Z=105 in HF/HNO3 solution at the fluoride ion concentration [F−]=0.003 M. The resul...
Fluoride complexation of rutherfordium (Rf, element 104)
2000
The fluoride complexation of the group-4 elements Zr, Hf and Rf, and of the pseudo-homolog Th, has been investigated in mixed HNO3/HF solutions by studying Kd values on both cation exchange resins (CIX) and anion exchange resins (AIX) using the automated rapid chemistry apparatus ARCA. On the CIX, the four elements are strongly retained as cations below 10-3M HF. For Zr and Hf, the decrease of the Kd values due to the formation of fluoride complexes occurs between 10-3M HF and 10-2M HF. For Rf and Th, this decrease is observed at one order of magnitude higher HF concentrations. On the AIX, for Zr and Hf, a rise of the Kd values due to the formation of anionic fluoride complexes is observed …
Decay properties of neutron-deficient isotopes 256, 257Db, 255Rf, 252, 253Lr
2001
Isotopes of dubnium (element 105) with mass numbers A = 256, 257, and 258 were produced by the reaction 209Bi(50Ti,xn) 259-xDb (x = 1, 2, 3) at projectile energies of (4.59-5.08) AMeV. Excitation functions were measured for the 1n, 2n and 3n evaporation channels. The same position of the excitation function was observed for the 1n channel as for the previously measured 1n channel of the reaction 208Pb(50Ti,1n)257Rf. The measured α-decay data of 257Db and its daughter products resulted in the identification of α-decaying isomeric states in 257Db and 253Lr. Two new isotopes, 256Db and 252Lr, were produced at the highest bombarding energies of 4.97 AMeV and 5.08 AMeV. They were identified by d…
Calculation of atomic spectra and transition amplitudes for superheavy element Db (Z=105)
2018
Atomic spectra and other properties of superheavy element dubnium (Db, $Z=105$) are calculated using recently developed method combining configuration interaction with perturbation theory [the CIPT method, V. A. Dzuba, J. C. Berengut, C. Harabati, and V. V. Flambaum, Phys. Rev. A 95, 012503 (2017)]. These include energy levels for low-lying states of Db and Db II, electric dipole transition amplitudes between the ground state and low-lying states of opposite parity, isotope shift for these transitions, and the ionization potential of Db. Similar calculations for Ta, which is a lighter analog of Db, are performed to control the accuracy of the calculations.