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Iron-55

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Artificial radioisotope of iron
Iron-55, Fe
General
SymbolFe
Namesiron-55, 55Fe, Fe-55
Protons (Z)26
Neutrons (N)29
Nuclide data
Half-life (t1/2)2.737 years
Decay productsMn
Decay modes
Decay modeDecay energy (MeV)
Electron capture0.00519
Isotopes of iron
Complete table of nuclides

Iron-55 (Fe) 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. 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%. 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. No electrical power is needed for this emission, which is ideal for portable X-ray instruments, such as X-ray fluorescence instruments. The ExoMars mission of ESA used, in 2016, such an iron-55 source for its combined X-ray diffraction/X-ray fluorescence spectrometer. The 2011 Mars mission MSL used a functionally similar spectrometer, but with a traditional, electrically powered X-ray source.

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.

Occurrence

Iron-55 is most effectively produced by irradiation of iron with neutrons. The reaction (Fe(n,γ)Fe and Fe(n,2n)Fe) 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. 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. 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.

References

  1. Georges, Audi (2003). "The NUBASE Evaluation of Nuclear and Decay Properties". Nuclear Physics A. 729 (1): 3–128. Bibcode:2003NuPhA.729....3A. CiteSeerX 10.1.1.692.8504. doi:10.1016/j.nuclphysa.2003.11.001.
  2. Esam M. A. Hussein (2003). Handbook on radiation probing, gauging, imaging and analysis. Springer. p. 26. ISBN 978-1-4020-1294-5.
  3. Preuss, Luther E. (1966). "Demonstration of X-ray Diffraction by LiF using the Mn Kα X-rays Resulting From Fe decay". Applied Physics Letters. 9 (4): 159–161. Bibcode:1966ApPhL...9..159P. doi:10.1063/1.1754691.
  4. Himmelsbach, B. (1982). "Portable X-ray Survey Meters for In Situ Trace element Monitoring of Air Particulates". Toxic Materials in the Atmosphere, Sampling and Analysis. ISBN 978-0-8031-0603-1.
  5. "The ESA-NASA ExoMars Programme Rover, 2018". ESA. Archived from the original on 2009-12-23. Retrieved 2010-03-12.
  6. "The ExoMars instrument suite". ESA. Retrieved 2010-03-12.
  7. Marinangeli, L.; Hutchinson, I.; Baliva, A.; Stevoli, A.; Ambrosi, R.; Critani, F.; Delhez, R.; Scandelli, L.; Holland, A.; Nelms, N.; Mars-Xrd Team (March 12–16, 2007). An European XRD/XRF Instrument for the ExoMars Mission. 38th Lunar and Planetary Science Conference. Lunar and Planetary Science Conference. No. 1338. League City, Texas. p. 1322. Bibcode:2007LPI....38.1322M.
  8. Chemistry & Mineralogy (CheMin), NASA
  9. D.J. Dwight; E.A. Lorch; J.E. Lovelock (1976). "Iron-55 as an auger electron emitter : Novel source for gas chromatography detectors". Journal of Chromatography A. 116 (2): 257–261. doi:10.1016/S0021-9673(00)89896-9.
  10. Preston, A. (1970). "Concentrations of iron-55 in commercial fish species from the North Atlantic". Marine Biology. 6 (4): 345–349. doi:10.1007/BF00353667. S2CID 91254200.
  11. ^ Palmer, H. E.; Beasley, T. M. (1965). "Iron-55 in Humans and Their Foods". Science. 149 (3682): 431–2. Bibcode:1965Sci...149..431P. doi:10.1126/science.149.3682.431. PMID 17809410. S2CID 206565239.
  12. Beasley, T. M.; Held, E. E.; Conard, R. M.E. (1965). "Iron-55 in Rongelap people, fish and soils". Health Physics. 22 (3): 245–50. doi:10.1097/00004032-197203000-00005. PMID 5062744.

See also

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