Iron-55 Explained

Mass Number:55
Symbol:Fe
Num Neutrons:29
Num Protons:26
Decay Product:Manganese-55
Decay Mass:55
Decay Symbol:Mn
Decay Mode1:Electron capture
Decay Energy1:0.00519

Iron-55 (55Fe) is a radioactive isotope of iron with a nucleus containing 26 protons and 29 neutrons. It decays by electron capture to manganese-55 and this process has a half-life of 2.737 years. The emitted X-rays can be used as an X-ray source for various scientific analysis methods, such as X-ray diffraction. Iron-55 is also a source for Auger electrons, which are produced during the decay.

Decay

Iron-55 decays via electron capture to manganese-55 with a half-life of 2.737 years.[1] The electrons around the nucleus rapidly adjust themselves to the lowered charge without leaving their shell, and shortly thereafter the vacancy in the "K" shell left by the nuclear-captured electron is filled by an electron from a higher shell. The difference in energy is released by emitting Auger electrons of 5.19 keV, with a probability of about 60%, K-alpha-1 X-rays with energy of 5.89875 keV and a probability about 16.2%, K-alpha-2 X-rays with energy of 5.88765 keV and a probability of about 8.2%, or K-beta X-rays with nominal energy of 6.49045 keV and a probability about 2.85%. The energies of the K-alpha-1 and -2 X-rays are so similar that they are often specified as mono-energetic radiation with 5.9 keV photon energy. Its probability is about 28%.[2] The remaining 12% is accounted for by lower-energy Auger electrons and a few photons from other, minor transitions.

Use

The K-alpha X-rays emitted by the manganese-55 after the electron capture have been used as a laboratory source of X-rays in various X-ray scattering techniques. The advantages of the emitted X-rays are that they are monochromatic and are continuously produced over a years-long period.[3] No electrical power is needed for this emission, which is ideal for portable X-ray instruments, such as X-ray fluorescence instruments.[4] The ExoMars mission of ESA used, in 2016,[5] [6] such an iron-55 source for its combined X-ray diffraction/X-ray fluorescence spectrometer.[7] The 2011 Mars mission MSL used a functionally similar spectrometer, but with a traditional, electrically powered X-ray source.[8]

The Auger electrons can be applied in electron capture detectors for gas chromatography. The more widely used nickel-63 sources provide electrons from beta decay.[9]

Occurrence

Iron-55 is most effectively produced by irradiation of iron with neutrons. The reaction (54Fe(n,γ)55Fe and 56Fe(n,2n)55Fe) of the two most abundant isotopes iron-54 and iron-56 with neutrons yields iron-55. Most of the observed iron-55 is produced in these irradiation reactions, and it is not a primary fission product.[10] As a result of atmospheric nuclear tests in the 1950s, and until the test ban in 1963, considerable amounts of iron-55 have been released into the biosphere.[11] People close to the test ranges, for example Iñupiat (Alaska Natives) and inhabitants of the Marshall Islands, accumulated significant amounts of radioactive iron. However, the short half-life and the test ban decreased, within several years, the available amount of iron-55 nearly to the pre-nuclear test levels.[11] [12]

See also

Notes and References

  1. Audi. Georges. The NUBASE Evaluation of Nuclear and Decay Properties. Nuclear Physics A. 729. 1. 3–128. 2003. 10.1016/j.nuclphysa.2003.11.001. 2003NuPhA.729....3A. 10.1.1.692.8504.
  2. Book: Handbook on radiation probing, gauging, imaging and analysis. 978-1-4020-1294-5. Esam M. A. Hussein. Springer. 2003. 26.
  3. 10.1063/1.1754691. Demonstration of X-ray Diffraction by LiF using the Mn Kα X-rays Resulting From 55Fe decay. 1966. Preuss. Luther E.. Applied Physics Letters. 9. 159–161. 1966ApPhL...9..159P. 4 .
  4. Book: Toxic Materials in the Atmosphere, Sampling and Analysis. Himmelsbach, B.. 978-0-8031-0603-1. Portable X-ray Survey Meters for In Situ Trace element Monitoring of Air Particulates. 1982.
  5. Web site: The ESA-NASA ExoMars Programme Rover, 2018. ESA. 2010-03-12. https://web.archive.org/web/20091223032943/http://exploration.esa.int/science-e/www/object/index.cfm?fobjectid=45084. 2009-12-23. dead.
  6. Web site: The ExoMars instrument suite. ESA. 2010-03-12.
  7. An European XRD/XRF Instrument for the ExoMars Mission. Lunar and Planetary Science Conference . 1338 . Marinangeli, L. . Hutchinson, I. . Baliva, A. . Stevoli, A. . Ambrosi, R. . Critani, F. . Delhez, R. . Scandelli, L. . Holland, A. . Nelms, N. . Mars-Xrd Team . 38th Lunar and Planetary Science Conference. March 12–16, 2007. League City, Texas. 1322. 2007LPI....38.1322M .
  8. https://web.archive.org/web/20090320125601/http://msl-scicorner.jpl.nasa.gov/Instruments/CheMin/ Chemistry & Mineralogy (CheMin)
  9. 10.1016/S0021-9673(00)89896-9. Iron-55 as an auger electron emitter : Novel source for gas chromatography detectors. D.J. Dwight . E.A. Lorch . J.E. Lovelock . Journal of Chromatography A. 116 . 1976. 2 . 257–261 . subscription .
  10. Concentrations of iron-55 in commercial fish species from the North Atlantic. 1970. 10.1007/BF00353667. Preston. A.. Marine Biology. 6. 345–349. 4. 91254200.
  11. Iron-55 in Humans and Their Foods. 1965. 10.1126/science.149.3682.431. Palmer. H. E.. Beasley. T. M.. Science. 149. 431–2. 17809410. 3682. 1965Sci...149..431P . 206565239.
  12. Iron-55 in Rongelap people, fish and soils. 1965. 10.1097/00004032-197203000-00005. Conard. R. M.E.. Held. E. E.. Beasley. T. M.. Health Physics. 22. 245–50. 5062744. 3 .