Decay scheme: Difference between revisions
Chapter moved |
I think the article has been sufficiently improved |
||
Line 1: | Line 1: | ||
{{cleanup-rewrite|date=May 2013}} |
|||
The '''decay scheme''' of a [[Radioactive decay|radioactive]] substance is a graphical presentation of all the transitions occurring in a decay, and of their relationships. Examples are shown below. |
The '''decay scheme''' of a [[Radioactive decay|radioactive]] substance is a graphical presentation of all the transitions occurring in a decay, and of their relationships. Examples are shown below. |
||
Revision as of 06:55, 16 August 2015
The decay scheme of a radioactive substance is a graphical presentation of all the transitions occurring in a decay, and of their relationships. Examples are shown below.
It is useful to think of the decay scheme as placed in a coordinate system, where the ordinate axis is energy, increasing from bottom to top, and the abscissa is the proton number, increasing from left to right. The arrows indicate the emitted particles. For the gamma rays (vertical arrows), the gamma energies are given; for the beta decay (oblique arrow), the maximum beta energy.
Examples
These relations can be quite complicated; a simple case is shown here: the decay scheme of the radioactive cobalt isotope cobalt-60.[1] 60Co decays by emitting an electron (beta decay) with a half-life of 5.272 years into an excited state of 60Ni, which then decays very fast to the ground state of 60Ni, via two gamma decays.
All known decay schemes can be found in the Table of Isotopes.,[2][3]
Nickel is to the right of cobalt, since its proton number (28) is higher by one than that of cobalt (27). In beta decay, the proton number increases by one. For a positron decay and also for an alpha decay (see below), the oblique arrow would go from right to left since in these cases, the proton number decreases.
Since energy is conserved and since the particles emitted carry away energy, arrows can only go downward (vertically or at an angle) in a decay scheme.
A somewhat more complicated scheme is shown here: the decay of the nuclide 198Au [4] which can be produced by irradiating natural gold in a nuclear reactor. 198Au decays via beta decay to one of two excited states or to the ground state of the mercury isotope 198Hg. In the figure, mercury is to the right of gold, since the atomic number of gold is 79, that of mercury is 80. The excited states decay after very short times (2.5 and 23 ps, resp.; 1 picosecond is a millionth of a millionth of a second) to the ground state.
While excited nuclear states are usually very short lived, decaying almost immediately after a beta decay (see above), the excited state of the technetium isotope shown here to the right is comparatively long lived. It is therefore called "metastable" (hence the "m" in 99mTc [5]). It decays to the ground state via gamma decay with a half-life of 6 hours.
Here, to the left, we now have an alpha decay. It is the decay of the element Polonium [6] discovered by Marie Curie, with mass number 210. The isotope 210Po is the penultimate member of the uranium-radium-decay series; it decays into a stable lead-isotope with a half-life of 138 days. In almost all cases, the decay is via the emission of an alpha particle of 5.305 MeV. Only in one case of 100000, an alpha particle of lower energy appears; in this case, the decay leads to an excited level of 206Pb, which then decays to the ground state via gamma radiation.
Selection Rules
Alpha- beta- and gamma rays can only be emitted if the conservation laws (energy, angular momentum, parity) are obeyed. This leads to so-called selection rules. Applications for gamma decay can be found in Multipolarity of gamma radiation.
References
- ^ K.H.Lieser Einführung in die Kernchemie (1991) S.223, Abb. (7-22); ISBN 3-527-28329-3
- ^ C.M. Lederer, J.M. Hollander, I. Perlman: Table of Isotopes, Wiley (1968)
- ^ ie.lbl.gov/toi/
- ^ K.H.Lieser, Nuclear and Radiochemistry (2001), p.61, Fig 5.12; ISBN 3-527-30317-0
- ^ H.Krieger, Grundlagen der Strahlungsphysik und des Strahlenschutzes (2007), S.117, Fig 3.15; ISBN 978-3-8351-0199-9
- ^ K.H.Lieser, Nuclear and Radiochemistry (2001), p.52, Fig 5.4; ISBN 3-527-30317-0