A fundamental question in nuclear physics is what combinations of neutrons and protons can make up a nucleus. Many hundreds of exotic neutron-rich isotopes have never been observed; the limit of how many neutrons a given number of protons can bind is unknown for all but the lightest elements, owing to the delicate interplay between single particle and collective quantum effects in the nucleus. This limit, known as the neutron drip line, provides a benchmark for models of the atomic nucleus. Here we report a significant advance in the determination of this limit: the discovery of two new neutron-rich isotopes--40Mg and 42Al--that are predicted to be drip-line nuclei. In the past, several attempts to observe 40Mg were unsuccessful; moreover, the observation of 42Al provides an experimental indication that the neutron drip line may be located further towards heavier isotopes in this mass region than is currently believed. In stable nuclei, attractive pairing forces enhance the stability of isotopes with even numbers of protons and neutrons. In contrast, the present work shows that nuclei at the drip line gain stability from an unpaired proton, which narrows the shell gaps and provides the opportunity to bind many more neutrons.
The periodic table provides a classification of the chemical properties of the elements. But for the heaviest elements, the transactinides, this role of the periodic table reaches its limits because increasingly strong relativistic effects on the valence electron shells can induce deviations from known trends in chemical properties. In the case of the first two transactinides, elements 104 and 105, relativistic effects do indeed influence their chemical properties, whereas elements 106 and 107 both behave as expected from their position within the periodic table. Here we report the chemical separation and characterization of only seven detected atoms of element 108 (hassium, Hs), which were generated as isotopes (269)Hs (refs 8, 9) and (270)Hs (ref. 10) in the fusion reaction between (26)Mg and (248)Cm. The hassium atoms are immediately oxidized to a highly volatile oxide, presumably HsO(4), for which we determine an enthalpy of adsorption on our detector surface that is comparable to the adsorption enthalpy determined under identical conditions for the osmium oxide OsO(4). These results provide evidence that the chemical properties of hassium and its lighter homologue osmium are similar, thus confirming that hassium exhibits properties as expected from its position in group 8 of the periodic table.
The decay of extremely neutron-deficient 45Fe has been studied in detail by means of a novel type of a gaseous detector employing digital imaging to record tracks of charged particles. The two-proton radioactivity channel was clearly identified. For the first time, the angular and energy correlations between two protons emitted from the nuclear ground state were determined, indicating the genuine three-body character of this decay. The half-life of 45Fe was found to be 2.6+/-0.2 ms and the observed 2p decay branching ratio is 70+/-4%.
We have measured fragment cross-sections of projectile fragmentation reactions using primary beams of 40 Ca, 48 Ca, 58 Ni, and 64 Ni at 140 MeV/nucleon on 9 Be and 181 Ta targets. The cross-sections were obtained by integrating the momentum distributions of isotopes with Z 5 measured in the A1900 fragment separator. We compare the extracted cross-sections to the predictions of the empirical parametrization of fragmentation cross-sections (EPAX).
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