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Radionuclide

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(Redirected fromRadioisotope)
Atom that has excess nuclear energy, making it unstable

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Not to be confused withradionucleotide.
Chart of knownnuclides as of 2013[update]. The vast majority are radionuclides.

Aradionuclide (radioactive nuclide,radioisotope orradioactive isotope) is anuclide that is unstable and known to undergoradioactive decay into a different nuclide, which may be another radionuclide (seedecay chain) or be stable.Radiation emitted by radionuclides is almost alwaysionizing radiation because it is energetic enough to liberate an electron from another atom.

Radioactive decay is a randomprocess at the level of singleatoms: it is impossible topredict when one particular atom will decay.[1][2] However, for a collection of atoms of a single nuclide, the decay rate (considered as a statistical average), and thus thehalf-life (t1/2) for that nuclide, can be calculated from the measurement of the decay. The range of the half-lives of radioactive atoms has no known limits and spans a time range of over 55 orders of magnitude.

All thechemical elements have radionuclides - even the lightest element,hydrogen, has one well-known radionuclide,tritium (thoughhelium,lithium, andboron have none with half-life over a second). Elements heavier thanlead (Z > 82), and the elementstechnetium andpromethium, have only radionuclides and do not exist in stable forms, thoughbismuth can be treated as stable with the half-life ofits natural isotope being over a trillion times longer than the currentage of the universe.

Production and effects

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Artificial production methods of radionuclides includeneutron sources such asnuclear reactors, as well asparticle accelerators such ascyclotrons.

Exposure to radionuclides generally has, due to their radiation, a harmful effect onorganisms includinghumans, although low levels of exposure occur naturally. The degree of harm will depend on thenature and extent of the radiation produced (alpha,beta,gamma, orneutron), the amount and nature of exposure (close contact,inhalation oringestion), and the biochemical properties of the element (toxicity). Increased risk ofcancer is considered unavoidable, and worse cases experienceradiation-induced cancer,chronic radiation syndrome oracute radiation syndrome. Radionuclides areweaponized by thefallout effects ofnuclear weapons and byradiological weapons.

Radionuclides with suitable properties are used innuclear medicine for both diagnosis and treatment. An imaging tracer made with radionuclides is called aradioactive tracer.Radionuclide therapy is a form ofradiotherapy. Apharmaceutical drug made with radionuclides is called aradiopharmaceutical.

Origins

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Overview

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Radionuclides occur naturally and are artificially produced innuclear reactors,cyclotrons,particle accelerators orradionuclide generators. There are 735 known radionuclides with half-lives longer than an hour (seelist of nuclides); 35 of those areprimordial radionuclides whose presence on Earth has persisted from its formation, and another 62 are detectable in nature, continuously produced either asdaughter products of primordial radionuclides or bycosmic radiation. More than 2400 radionuclides have half-lives less than 60minutes. Most of those are only produced artificially, and have very short half-lives. For comparison, there are 251stable nuclides.

Natural

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On Earth, naturally occurring radionuclides fall into three categories: primordial radionuclides, secondary radionuclides, andcosmogenic radionuclides.

  • Radionuclides are produced instellar nucleosynthesis andsupernova explosions along with stable nuclides. Most decay quickly, but some can be observed astronomically and can play a part in understanding astrophysical processes. Primordial radionuclides, such asuranium andthorium, still exist because theirhalf-lives are so long (>100 million years) that the Earth's initial content has not yet completely decayed. Some radionuclides have half-lives so long (many times the age of the universe) that decay has only recently been detected, and for most practical purposes they can be considered stable, most notablybismuth-209: detection of this decay meant thatbismuth was no longer considered stable. It is possible that decay may be observed in other nuclides now considered stable, adding to the list of primordial radionuclides.[citation needed]
  • Secondary radionuclides are radiogenic isotopes derived from the decay of primordial radionuclides. They have shorter half-lives than primordial radionuclides. They arise in thedecay chain of the primordial isotopesthorium-232,uranium-238, anduranium-235 - such as the natural isotopes ofpolonium andradium - some are also produced by naturalfission and othernucleogenic processes.[citation needed]
  • Cosmogenic isotopes, such ascarbon-14, are present because they are continually being formed on Earth, typically in the atmosphere, due to the action ofcosmic rays.[citation needed]

Many of these radionuclides exist only in trace amounts in nature, including all cosmogenic nuclides. Secondary radionuclides in adecay chain will occur in proportion to their half-lives, so short-lived ones will be very rare. For example, polonium can be found inuranium ores at a concentration about 1 part 1010 of uranium (0.1 mg permetric ton) by calculating the ratio of half-lives ofpolonium-210 touranium-238, its ultimate parent.[citation needed]

Nuclear fission

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Radionuclides are produced as an unavoidable result ofnuclear fission andnuclear explosions. The process of nuclear fission creates a wide range offission products, most of which are radionuclides. Further radionuclides are created from irradiation of the nuclear fuel (creating a range ofactinides) and of the surrounding structures, yieldingactivation products. This complex mixture of radionuclides with different chemistries and radioactivity makes handlingnuclear waste and dealing withnuclear fallout particularly problematic.[citation needed]

Synthetic

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Americium-241 emittingalpha particles inserted into acloud chamber

Synthetic radionuclides are created innuclear reactors or by particle accelerators (not necesssarily on purpose) or as decay products of such:[3]

  • As well as being extracted from nuclear waste, radioisotopes can be produced deliberately with nuclear reactors, exploiting the high flux ofneutrons present. These neutrons activate elements placed within the reactor. A typical product from a nuclear reactor isiridium-192, from activation ofiridium targets. The elements that have a large propensity to take up neutrons in the reactor are said to have a highneutron cross-section, but even at low cross-sections this process is generally economical.
  • Particle accelerators such ascyclotrons accelerate particles to bombard a target to produce radionuclides. Cyclotrons accelerate (most often) protons at a target to produce positron-emitting radionuclides, e.g.fluorine-18.
  • Radionuclide generators, standard for many medical isotopes, contain a parent radionuclide that decays to produce a shorter-lived radioactive daughter. A typical example is thetechnetium-99m generator, which employsmolybdenum-99 produced in a reactor.

Uses

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Radionuclides are used in two major ways: either for their radiation alone (irradiation,nuclear batteries) or for the combination of chemical properties and their radiation (tracers, biopharmaceuticals). For scientific study they may be used for their chemical properties alone when there is no stable form of that element.

Examples

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The following table lists properties of selected radionuclides illustrating the range of properties and uses.

IsotopeZNhalf-lifeDMDE
keV
Mode of formationComments
Tritium (3H)1212.3 yβ19Cosmogeniclightest radionuclide, used in artificialnuclear fusion, also used forradioluminescence and as oceanic transient tracer. Synthesized from neutron bombardment oflithium-6 ordeuterium
Beryllium-10461,387,000 yβ556Cosmogenicused to examine soil erosion, soil formation from regolith, and the age of ice cores
Carbon-14685,700 yβ156Cosmogenicused forradiocarbon dating
Fluorine-1899110 minβ+,EC633/1655Cosmogenicpositron source, synthesised for use as a medicalradiotracer inPET scans.
Aluminium-261313717,000 yβ+,EC4004Cosmogenicexposure dating of rocks, sediment
Chlorine-361719301,000 yβ,EC709Cosmogenicexposure dating of rocks, groundwater tracer
Potassium-4019211.24×109 yβ,EC1330 /1505Primordialused forpotassium-argon dating, source of atmosphericargon, source ofradiogenic heat, largest source of natural radioactivity
Calcium-41202199,400 yECCosmogenicexposure dating ofcarbonate rocks
Cobalt-6027335.3 yβ2824Syntheticproduces high energy gamma rays, used for radiotherapy, equipment sterilisation, food irradiation
Krypton-813645229,000 yβ+Cosmogenicgroundwater dating
Strontium-90385228.8 yβ546Fission productmedium-lived fission product; probably most dangerous component of nuclear fallout
Technetium-994356210,000 yβ294Fission productmost common isotope of the lightest unstable element, most significant oflong-lived fission products
Technetium-99m43566 hrγ,IC141Syntheticmost commonly used medical radioisotope, used as a radioactive tracer
Iodine-129537615,700,000 yβ194Cosmogeniclongest livedfission product; groundwater tracer
Iodine-13153788 dβ971Fission productmost significant short-term health hazard from nuclear fission, used in nuclear medicine, industrial tracer
Xenon-13554819.1 hβ1160Fission productstrongest known "nuclear poison" (neutron-absorber), with a major effect on nuclear reactor operation.
Caesium-137558230.2 yβ1176Fission productother majormedium-lived fission product of concern
Gadolinium-1536489240 dECSyntheticcalibrating nuclear equipment, bone density screening
Bismuth-209831262.01×1019yα3137Primordiallong considered stable, decay only detected in 2003
Polonium-21084126138 dα5307Decay producthighly toxic, used inpoisoning of Alexander Litvinenko
Radon-222861363.8 dα5590Decay productgas, responsible for the majority of public exposure to ionizing radiation, second most frequent cause of lung cancer
Thorium-232901421.4×1010 yα4083Primordialbasis ofthorium fuel cycle
Uranium-235921437×108yα4679Primordialfissile, main nuclear fuel
Uranium-238921464.5×109 yα4267Primordialmain uranium isotope
Plutonium-2389414487.7 yα5593Syntheticused in radioisotope thermoelectric generators (RTGs) and radioisotope heater units as an energy source for spacecraft
Plutonium-2399414524,110 yα5245Syntheticused for most modern nuclear weapons
Americium-24195146432 yα5486Syntheticused in household smoke detectors as an ionising agent
Californium-252981542.64 yα/SF6217Syntheticundergoes spontaneous fission (3% of decays), making it a powerful neutron source, used as a reactor initiator and for detection devices
Lutetium-177711066.6443(9) dβ497 (78.6 %), 384 (9.1 %), 176 (12.2 %)Syntheticused predominantly in targeted radionuclide therapy (TRT) against somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs)

Key:Z = atomic number;N = neutron number; DM = decay mode; DE = decay energy; EC = electron capture

Householdsmoke detectors

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Americium-241 container in a smoke detector.
Americium-241 capsule as found in smoke detector. The circle of darker metal in the center is americium-241; the surrounding casing is aluminium.

Radionuclides are present in many homes as they are used inside the most common householdsmoke detectors. The radionuclide used isamericium-241, which is created by bombarding plutonium with neutrons in a nuclear reactor. It decays by emittingalpha particles andgamma radiation to becomeneptunium-237. Smoke detectors use a very small quantity of241Am (about 0.29 micrograms per smoke detector) in the form ofamericium dioxide.241Am is used as it emits alpha particles which ionize the air in the detector'sionization chamber. A small electric voltage is applied to the ionized air which gives rise to a small electric current. In the presence of smoke, some of the ions are neutralized, thereby decreasing the current, which activates the detector's alarm.[8][9]

Impacts on organisms

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Radionuclides that find their way into the environment may cause harmful effects asradioactive contamination. They can also cause damage if they are excessively used during treatment or in other ways exposed to living beings, byradiation poisoning. Potential health damage from exposure to radionuclides depends on a number of factors, and "can damage the functions of healthy tissue/organs. Radiation exposure can produce effects ranging from skin redness and hair loss, toradiation burns andacute radiation syndrome. Prolonged exposure can lead to cells being damaged and in turn lead to cancer. Signs of cancerous cells might not show up until years, or even decades, after exposure."[10]

Summary table for classes of nuclides, stable and radioactive

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Following is a summary table for thelist of 986 nuclides with half-lives greater than one hour. A total of 251 nuclides have never been observed to decay, and are classically considered stable. Of these, 90 are believed to be absolutely stable except toproton decay (which has never been observed), while the rest are "observationally stable" and theoretically can undergo radioactive decay with extremely long half-lives.[citation needed]

The remaining tabulated radionuclides have half-lives longer than 1 hour, and are well-characterized (seelist of nuclides for a complete tabulation). They include 31 nuclides with measured half-lives longer than the estimated age of the universe (13.8 billion years[11]), and another four nuclides with half-lives long enough (> 100 million years) that they are radioactiveprimordial nuclides, and may be detected on Earth, having survived from their presence in interstellar dust since before the formation of theSolar System, about 4.6 billion years ago. Another 60+ short-lived nuclides can be detected naturally as daughters of longer-lived nuclides or cosmic-ray products. The remaining known nuclides are known solely from artificialnuclear transmutation.[citation needed]

Numbers may change slightly in the future as some nuclides now classified as stable are observed to be radioactive with very long half-lives.[citation needed]

This is a summary table[12] for the 986 nuclides with half-lives longer than one hour (including those that are stable), given inlist of nuclides.

Stability classNumber of nuclidesRunning totalNotes on running total
Theoretically stable to all butproton decay9090Includes first 40 elements. Proton decay yet to be observed.
Theoretically stable toalpha decay,beta decay,isomeric transition, anddouble beta decay but notspontaneous fission, which is possible for "stable" nuclides ≥niobium-9356146All nuclides that arepossibly completely stable (spontaneous fission has never been observed for nuclides with mass number < 232).
Energetically unstable to one or more known decay modes, but no decay yet seen. All considered "stable" until decay detected.105251Total of classicallystable nuclides.
Radioactiveprimordial nuclides35286Total primordial elements includeuranium,thorium,bismuth,rubidium-87,potassium-40,tellurium-128 plus all stable nuclides.
Radioactive nonprimordial, but naturally occurring on Earth62348Carbon-14 (and other isotopes generated bycosmic rays) and daughters of radioactive primordial elements, such asradium andpolonium, of which 32 have a half-life of greater than one hour, also long-livedfission products.
Radioactive synthetic half-life ≥ 1.0 hour). Includes most usefulradiotracers.638986These comprise the remainder of thelist of nuclides.
Radioactive synthetic (half-life < 1.0 hour).>2400>3300Includes all well-characterized synthetic nuclides.

See also

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Notes

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  1. ^"Decay and Half Life". Retrieved14 December 2009.
  2. ^Loveland, W.; Morrissey, D.;Seaborg, G.T. (2006).Modern Nuclear Chemistry. Wiley-Interscience. p. 57.Bibcode:2005mnc..book.....L.ISBN 978-0-471-11532-8.
  3. ^"Radioisotopes".www.iaea.org. 15 July 2016. Retrieved25 June 2023.
  4. ^Ingvar, David H.[in Swedish];Lassen, Niels A. (1961)."Quantitative determination of regional cerebral blood-flow in man".The Lancet.278 (7206):806–807.doi:10.1016/s0140-6736(61)91092-3.
  5. ^Ingvar, David H.[in Swedish]; Franzén, Göran (1974)."Distribution of cerebral activity in chronic schizophrenia".The Lancet.304 (7895):1484–1486.doi:10.1016/s0140-6736(74)90221-9.PMID 4140398.
  6. ^Lassen, Niels A.;Ingvar, David H.[in Swedish];Skinhøj, Erik[in Danish] (October 1978). "Brain Function and Blood Flow".Scientific American.239 (4):62–71.Bibcode:1978SciAm.239d..62L.doi:10.1038/scientificamerican1078-62.PMID 705327.
  7. ^Severijns, Nathal; Beck, Marcus; Naviliat-Cuncic, Oscar (2006). "Tests of the standard electroweak model in nuclear beta decay".Reviews of Modern Physics.78 (3):991–1040.arXiv:nucl-ex/0605029.Bibcode:2006RvMP...78..991S.doi:10.1103/RevModPhys.78.991.S2CID 18494258.
  8. ^"Smoke Detectors and Americium".world-nuclear.org. Archived fromthe original on 12 November 2010.
  9. ^Office of Radiation Protection – Am 241 Fact Sheet – Washington State Department of HealthArchived 2011-03-18 at theWayback Machine
  10. ^"Ionizing radiation, health effects and protective measures". World Health Organization. November 2012. Retrieved27 January 2014.
  11. ^"Cosmic Detectives". The European Space Agency (ESA). 2 April 2013. Retrieved15 April 2013.
  12. ^Table data is derived by counting members of the list; seeWP:CALC. References for the list data itself are given below in the reference section inlist of nuclides

References

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Further reading

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External links

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